1. BEFORE THE ILLINOIS POLLUTION CONTROL BOARD
      2. NOTICE OF FILING•
      3. WRITTEN TESTIMONY OFJ. MICHAEL CALLAHAN;
      4. WRITTEN TESTIMONY OF DENNIS STREICHER; and
      5. IAWA Exhibit List
      6. THIS FILING PRINTED ON RECYCLED PAPER
      7. CERTIFICATE OF SERVICE
      8. WRITTEN TESTIMONY OF J. MICHAEL CALLAHAN;
      9. WRITTEN TESTIMONY OF DENNIS STRIEICHER; and
      10. IAWA Exhibit List
      11. Service List
      12. Service List
      13. Service List
      14. WRITTEN TESTIMONY OF J. MICHAEL CALLAHAN
    1. WRITTEN TESTIMONY OF DENNIS STREICHER
  1. 11111
  2. ~,EPA Ambient
  3. Water Quality
  4. Criteria
  5. Dissolved Oxygen
  6. F~lS86 20 8 2 5 31~3
  7. A Walleye
  8. Reproduced by NTIS
  9. ~-~‘,-to
      1. Department of Zoology
      2. Phone: (618) 453-7639

BEFORE THE ILLINOIS POLLUTION CONTROL BOARD
REcE~vED
IN THE MATTER OF:
)
CLERKS OFFICE
PROPOSED AMENDMENTS TO
)
R 04-25
~
2004
DISSOLVED OXYGEN STANDARD
)
STATE OF ILL ~O~S
35 Iii. Adm. Code 302.206
)
PoUut~onControl Bowc~
NOTICE OF FILING•
TO: See Attached Service List
PLEASE TAKE NOTICE that I have today filed with the Office ofthe Clerk ofthe
Pollution Control Board the following documents:
WRITTEN TESTIMONY
OF DR.
JAMES E. GARVEY
FISHERIES AND
ILLINOIS
AQUACULTURE CENTER
SOUTHERN ILLINOIS UNIVERSITY, CARBONDALE,
ILLINOIS;
WRITTEN TESTIMONY OFJ. MICHAEL CALLAHAN;
WRITTEN TESTIMONY OF DENNIS STREICHER; and
IAWA Exhibit List
a copy ofwhich is served upon you.
ILLINOIS ASSOCIATION OF WASTEWATER
AGENCIES,
By:
~
~
One ofIts Attorneys
Dated: June 15, 2004
Sheila H. Deely
Roy M. Harsch
GARDNER CARTON
&
DOUGLAS LLP
191 Wacker Drive
Suite 3700
Chicago, Illinois 60606
(312) 569-1000
THIS FILING PRINTED ON RECYCLED PAPER

CERTIFICATE OF SERVICE
The undersigned certifies that a copy ofthe foregoing:
WRITTEN TESTIMONY OF DR. JAMES E. GARVEY
FISHERIES
AND
ILLINOIS AQUACULTURE CENTER
SOUTHERN ILLINOIS UNIVERSITY, CARBONDALE,
ILLINOIS;
WRITTEN TESTIMONY OF J. MICHAEL CALLAHAN;
WRITTEN TESTIMONY OF DENNIS STRIEICHER; and
IAWA Exhibit List
was filed by hand delivery with the Clerk ofthe Illinois Pollution Control Board and served upon
the.parties to whom said Notice is directed by first class mail, postage prepaid, by depositing in
the U.S. Mail at 191 Wacker Drive, Chicago, IL on Tuesday, June
15,
2004.
CHO2/ 22319687.1

Service List
R2004-025
Fred L. Hubbard
Alex Messina
415 North Gilbert Street
Illinois Environmental Regulatory Group
Danville, IL 61834-0012
3150 Roland Avenue
Springfield, IL 62703
Bernard Sawyer
Metropolitan Water Reclamation District
6001 W. Pershing Rd.
Cicero, IL 60650-4112
Charles W. Wesselhofl
Ross & Hardies
150 North Michigan Avenue
Suite 2500
Chicago, IL 6060
1-7567
Claire A. Maiming
Posegate & Denes, P.C.
111 N. Sixth Street
Springfield, IL 62705
Connie L. Tonsor
JEPA
1021 North Grand Avenue
P.O. Box 19276
Springfield, IL 62794-9276
Deborah J. Williams
IEPA
1021 North Grand Avenue
P.O. Box 19276
Springfield, IL 62794-9276
DennisL. Duffield
City ofJoliet, Department ofPublic Works and
Utilities
921 E. Washington Street
Joliet, IL 60431
Dorothy M. Gunn
Illinois Pollution Control Boark
100 W. Randolph St.
Suite 11-500
Chicago, IL 60601
Erika K. Powers
Barnes & Thornburg
1 N. Wacker
Suite 4400
Chicago, IL 60606
Frederick D. Keady
Vermilion Coal
1979 Johns Drive
Glenview, IL 60025
James L. Daugherty
Thorn Creek Basin SanitaryDistrict
700 West End Avenue
Chicago Heights, IL 60411
James T. Harrington
Ross & Hardies
150 North Michigan Avenue
Suite 2500
Chicago, IL 60601-7567
Joel J. Sternstein
Office ofthe Attorney General
188 West Randolph
20th Floor
Chicago, IL 60601

Service List
R2004-025
John Donahue
City ofGeneva
22 South First Street
Geneva, IL 60134-2203
Jonathan Furr
Illinois Department ofNatural Resources
One Natural Resources Way
Springfield, IL 62702-1271
Ketherine D. Hodge
Hodge Dwyer Zeman
3150 Roland Avenue
P.O. Box 5776
Springfield, IL 62705-5776
Larry Cox
Downers Grove Sanitary District
2710 Curtiss Street
Downers Grove, IL 60515
Lisa Frede
Chemical Industry Council ofIllinois
2250 B. Devon Avenue
Suite 239
Des Plaines, IL 60018-4509
Margaret Hedinger
2601 South Fifth Street
Springfield, IL 62703
.
.
Matthew J. Dunn
Office ofthe Attorney General
188 West Randolph
20th Floor
Chicago, IL 60601
Michael G. Rosenberg, Esq.
Metropolitan Water Reclamation District
100 East Erie Street
Chicago, IL 60611
Mike Callahan
Bloomington Normal Water Reclamation
District
P0 Box 3307
Bloomington, IL 6 1702-3307
Richard Lanyon
Metropolitan Water Reclamation District
100 East Erie Street
Chicago, IL 60611
Richard McGill
Illinois Pollution Control Board
100 W. Randolph St.
Suite 11-500
Chicago, IL 60601
Sanjay K. Sofat
IEPA
1021 North Grand Avenue East
P.O. Box .19276
Springfield, IL 62794-9276
Stephanie. N. Diers
IEPA
1021 North Grand Avenue East
P.O. Box 19276
Springfield, IL 62794-9276
Sue Schultz
Illinois American Water Company
300 North Water Works Drive
P.O. Box 24040
Belleville, IL 62223-9040

Service List
R2004-025
Susan M. Franzetti
10 South LaSalle Street
.
Suite 3600
Chicago, IL 60603
Tom Muth
Fox Metro Water Reclamation District
682 State Route 31
Oswego, IL 60543
Vicky McKinley
Evanston Environment Board
23 Grey Avenue
Evanston, IL 60202
,
W.C. Blanton
Blackwell Sanders Peper Martin LLP
2300 Main Street
Suite 1000
Kansas City, MO 64108
CHO2/ 22319597.1

CE~VED
CLERK’S OFFICE
BEFORE THE ILLINOIS POLLUTION CONTROL
BOARD
j~j~~
r
2004
IN THE MATTER OF:
))
PQIj~t~onSTATE OFControlILLiNOISboard
PROPOSED AMENDMENTS TO
)
R 04-25
DISSOLVED OXYGEN STANDARD
)
35 Iii. Adm. Code 302.206
)
WRITTEN TESTIMONY OF DR. JAMES E. GARVEY
FISHERIES AND ILLINOIS AQUACULTURE CENTER
SOUTHERN ILLINOIS UNIVERSITY, CARBONDALE, ILLINOIS
I am Dr. James Garvey, Assistant Professor in the Fisheries and Illinois
Aquaculture Center at Southern Illinois University in Carbondale. I have been engaged
by the Illinois Association of Wastewater Agencies (IAWA), along with my colleague,
Dr. Matt Whiles, to scientifically evaluate the current State ofIllinois dissolved oxygen
standard and to provide recommendations about how the Illinois standard might be
revised and updated, if warranted by our scientific evaluation.
Both Dr. Whiles and I are broadly trained in aquatic ecology. My specialty is the
ecology offishes, with much ofmy research focusing on how environmental conditions
affect fish physiology, abundance, and distribution. My Short Curriculum Vita has been
submitted as IAWA’s Exhibit
5.
Dr. Whiles, a professor in the Department ofZoology,
is an expert on the ecology ofaquatic invertebrates and their role in streams and lakes.
His Resume has been submitted as IAWA’s Exhibit 6. Our combined experience
qualified us to provide an objective assessment ofthe current state ofknowledge about
how dissolved oxygen affects aquatic organisms and to evaluate the current statewide,
one-day minimum standard of
5
mgIL. We did not intensively evaluate the application of
the state standards to Lake Michigan, and JAWA has not proposed to revise that standard.

Dr. Whiles and Ibegan our assessment by reviewing published, typically peer-reviewed
research on how dissolved oxygen affects aquatic organisms and how dissolved oxygen
varies in lakes and streams. We also reviewed the National Ambient Water Quality
Criteria Document for Dissolved Oxygen (NCD) published by the United States
Environmental Protection Agency (USEPA) in 1986, and submitted as IAWA’s Exhibit
In the final report, Dr. Whiles and I emphasize that using biological- and habitat-
2. We evaluated the current monitoring ofwater quality in Illinois and conferred with
quality criteria to evaluate suitability for aquatic life use in the surface waters ofIllinois
Illinois EPA concerning the scientific basis for the current Illinois dissolved oxygen
is ofparamount importance and should be continued to be emphasized in monitoring
standard. We then prepared a written report of our findings, which is submitted as IAWA
programs. It is unlikely that any one water quality parameter such as dissolved oxygen
Exhibit 1.
concentration will capture the capacity ofa stream or lake to support aquatic life.
Although ourrecommended dissolved oxygen standards are sufficiently protective of
aquatic life in Illinois, we recommend that regulators strive to maintain dissolved oxygen
concentrations well above these minima when possible. We agree with the concerns
voiced by some colleagues that the state should move toward a region-specific set of
water-quality criteria and aquatic life goals, although comprehensive regional data to
guide these decisions for Illinois are not yet available.
As the NCD suggests, dissolved oxygen concentrations in lakes and streams
fluctuate diurnally. During warm, summer months, dissolved oxygen concentrations
decline due to water’s reduced capacity to hold oxygen at elevated temperatures and the
high respiratory demand ofaquatic communities. A single dissolved oxygen standard
such as that in Illinois does not realistically capture these diurnal and seasonal
fluctuations. Although comprehensive surface water data are lacking forthe state, many
pristine aquatic systems largely unaffected by agricuitural~run-offor municipal
2

discharges most likely experience occasional, non-lethal declines in dissolved oxygen
below the state’s current minimum of
5
mgIL.
Our recommendations in the report include seasonally appropriate means and
minima that more realistically account for natural fluctuations in dissolved oxygen
concentrations, while remaining sufficiently protective ofaquatic life. These
recommendations are based largely on potential responses of all life stages ofnative
Illinois fishes that fall in the NCD’s non-salmonid category. As with the NCD, we define
these as typically warm-water fishes, although much variation in temperature and oxygen
tolerance occurs among taxa in this group.
Research summarized in the 1986 NCD was used to set our recommended
dissolved oxygen standards above those concentrations expected to slightly impair
production offishes. Research conducted since publication ofthe report generally
confirms that the seasonal standards we recommend are sufficiently protective offishes
and other aquatic organisms in Illinois surface waters. During spring through early
summer, most early life stages offishes and other aquatic organisms are produced. These
early reproducing organisms are typically the most susceptible to low dissolved oxygen
concentrations and thus require the most stringent protection. Our reanalysis ofdata
within the NCD and our review ofthe literature led to the development ofa standard
proposed to be applicable during March 1 through June 30, which specifically protects
these early life stages and includes both a one-day minimum identical to the current
Illinois standard of
5
mg/L and a seven-day mean of6 mg!L. During warmer, productive
months throughout the remainder ofthe year when species with sensitive early life stages
have largely completed reproduction, we recommend a one-day minimum of3.5 mg/L
3

and a seven-day mean minimum of4 mgIL, which is a more realistic general expectation
for Illinois surface waters than the current minimum standard of
5
mg/L.
Our recommended standards are based on our current understanding ofthe short-
and long-term responses ofaquatic organisms to low dissolved oxygen. In most natural
aquatic systems, habitat use by juvenile and adult fish is largely unaffected by dissolved
oxygen until concentrations decline below 3 mg/L. Acute lethal effects on post-larval,
warm-water fishes do not occur until concentrations decline below 2 mg/L. As wenote
in the report, chronic effects oflong-term exposure to low dissolved oxygen
concentrations are not well understood. See IAWA Ex. 1 at 18. Some impairment of
growth likely occurs in many warm-water species when dissolved oxygen concentrations
are chronically below 4 mgIL, which none ofour recommended standards allow.
Initially, Dr. Whiles and I summarized our findings and outlined our
recommendations in a draft report that was distributed to IAWA and the Illinois
Department ofNatural Resources (IDNR). Dr. Whiles also presented our findings to a
special meeting ofIAWA this spring, where representatives from Illinois EPA (ILEPA)
and Prairie Rivers Network were present. During this time, I also distributed the draft
report to the U.S. Fish and Wildlife Service, Region 3, Carterville Fisheries Resource
Office; the U.S. Fish and Wildlife Service, Region 3, Ecological Services Sub-Office; the
IDNR, Office ofResource Conservation; the IDNR, Office ofRealty and Environmental
Planning, Division ofNatural Resource Review and Coordination; the Illinois Natural
History Survey/U.S. Geological Service, Long-Term Resource Monitoring Program,
Great Rivers Field Station; and the Illinois Chapter ofthe American Fisheries Society
(ILAFS). On June 10, 2004, I met with the extended Executive Committee ofthe ILAFS
4

to discuss the report. Questions voiced by many ofthe participants ofthe IAWA meeting
held this spring were answered in the final draft ofthe report. After circulating the draft,
I received informal comments from the IDNR Office ofResource Conservation, which
also were addressed in the final draft. The IDNR Office ofRealty and Planning
informally found the science to support the recommended changes. During my recent
meeting with the Executive Committee ofthe ILAFS, I answered questions about the
report and the proposed changes to the current Illinois standards. I agreed with the
primary conclusion ofthe group that a set ofregional standards are needed for Illinois.
The other groups have provided neither informal nor formal feedback to me to date.
A letter dated 28 May 2004 written by Ms. Beth Wentzel ofPrairie Rivers
Network to the Division ofWater Pollution ContrOl, ILEPA raised several specific
concerns about our report. Ms. Wentzel noted that ourreport was not entirely consistent
with the NCD. Although the NCD recommends adopting the most conservative
standards for all early life stages offish through thirty-days post hatching whenever these
life stages occur, our report only recommends adopting these conservative standards
through June. Of the forty-eight fish taxa in Illinois that we surveyed, forty likely
complete the reproductive portion oftheir life cycle by the end of June or earlier
throughout Illinois. Given that fluctuating oxygen concentrations occur naturally in
Midwestern streams and lakes during summer, the remainder of species that continue to
reproduce during these months must have adaptations that allow them to persist when
ambient oxygen concentrations occasionally approach our recommended summer
minimum. Hence, our report indeed departs from the NCD in that it attempts to generate
5

more realistic expectations for dissolved oxygen concentrations and the responses of
native aquatic life in Illinois.
Another criticism voiced by Ms. Wentzel was that we failed to address the
responses ofcool-water species such as smailmouth bass in our recommended criteria.
This is untrue. These species were generally grouped under our warm-water
categorization, because temperature requirements ofnon-salmonid fishes are not well-
delineated. Rather, species-specific temperature needs vary widely along a gradient from
cool to warm water among fish in the Midwest. Although cold-water salmonids can be
categorized by their high oxygen and low temperature requirements, I know ofno
specific research that identifies Midwestern cool-water fishes as having substantially
different oxygen requirements during non-reproductive periods than warm-water
counterparts. The main difference between species with cool- and warm- water
requirements appears to be their temperature-dependent growth optima and lethal
maximum temperatures, which is a separate issue regarding the interaction between
habitat quality and temperature. Interestingly, although smallmouth bass is specifically
listed in the NCD as a sensitive, cool-water fish, it has similar temperature requirements
as many conventional warm-water fishes. Further, smallmouth bass adults have a
minimum lethal dissolved oxygen limit of 1.2 mg!L (see Table I, IAWA Ex. 1), which is
well below our recommended Illinois minimum standard.
Ms. Wentzel noted that we omitted a thirty-day mean standard from our
recommendations, although such a long-term moving average is recommended in the
NCD. In our view, fishes and other aquatic organisms will respond at a much shorter
time scale to declining oxygen than thirty days, requiring a more frequently updated
6

moving average of seven days. A thirty-day mean may erroneously miss periods of
chronically low dissolved oxygen if high concentrations occur during the remainder of
the thirty-day monitoring period.
Another argument made against our report’s validity is that it focuses primarily on
fish. Fish were selected as the regulatory focus because they were the model in the NCD
and, as it was in 1986, most research on dissolved oxygen is available for this group.
Fish are also ofrecreational and economic importance. Although the data for other taxa
are indeed quite limited, we did address the influence ofdissolved oxygen on other
organisms, specifically mussels and aquatic insects, and have found a pattern that appears
to be consistent with that for fish. As we outline in the report, species that have high
oxygen requirements tend to inhabit areas ofconsistently high and environmentally
predictable dissolved oxygen concentrations. In a stream, this would be a riffle habitat in
which high gaseous exchange occurs between the water and the atmosphere. In our
report, we recommend quantifying oxygen in areas and during times when dissolved
oxygen concentrations are expected to be lowest such as a stream pool before dawn.
These locations should be more susceptible to declining oxygen than areas in which high
exchange elevates oxygen concentrations and typically harbors the most sensitive species
such as darters and mayflies.
We take issue with Ms. Wentzel’s supposition that our recommendations would
render Illinois’s dissolved oxygen standards the weakest in the nation. I have assessed
the standards for ourpeer State ofOhio. From what I understand, Ohio has various
aquatic use designations that are similar to but more specific than those recommended for
Illinois. Each ofthese specific designations has a different daily minimum and one-day
7

average dissolved oxygen concentration. Probably the most common designation for
surface waters in Ohio is “warm water” which includes a daily minimum of4 mgIL and a
one-day average of
5
mgIL, which appears to applyto the entire year. Clearly, Ohio’s
general standard is less conservative than our recommended statewide standard during
spring, because its minimum of4 mgIL is 1 mg/L less than our proposed minimum
standard. And Ohio’s minimum is not significantly different than ourproposed minimum
standard of3.5 mg/L during the remainder ofthe year. Ohio’s seasonal salmonid and
coldwater designations are analogous to the Lake Michigan standards, which we do not
recommend modifying.
In my assessment, the largest difference between current standards within Ohio
and Illinois is that Ohio has developed more regional-specific criteria to protect waters
that they deem important. Ohio’s “exceptional warm water” criteria are very similar to
those that Illinois currently has adopted for the entire state, where Ohio’s daily minimum
is
5
mg!L and its one-day average is 6 mg/L. Given that all the surface waters in Illinois
would certainlynot be categorized as “exceptional”, it is clear that the current general
aquatic use Illinois dissolved oxygen standard is too strict. Our recommended standards
do provide similar protection as Ohio’s “exceptional” waters during the critical peak
reproductive times ofthe year.
During my conversations with other scientists, resource managers, and water
regulators, I have received many comments about how the recommended standards are
based on sound science and needed in the state. I recognize and somewhat understand
the perception by some individuals that our recommendations would weaken the Illinois
standards. However, the weight of information available for aquatic organisms suggests
8

that the proposed standards set more realistic expectations for surface waters in Illinois
and will not degrade the biological integrity ofthese systems. I agree that more research
is needed in many areas and hope that the proposed standard changes will be viewed as
one step in a dynamic, continuing process. It is my view that the state should move
toward developing region-specific biotic integrity, habitat quality, and water quality
criteria, as credible long-term data sets become available.
CHO2/ 22318249.2
9

CLERKS OFFICE
JUN 15 2004
BEFORE THE ILLINOIS POLLUTION CONTROL BOARBTATE
OF ILLINOIS
Pollution Control Board
IN THE MATTER OF:
)
)
PROPOSED AMENDMENTS TO
)
R 04-25
DISSOLVED OXYGEN STANDARD
)
35 Iii. Adm. Code 302.206
)
WRITTEN TESTIMONY OF J. MICHAEL CALLAHAN
My name is John M. Callahan. I am the Executive Director ofthe Bloomington and
Normal Water Reclamation District (BNWRD) ofMcLean County, Illinois. I have been in the
employment ofthe BNWRD for thirty one years during which time I have held positions of
increasing responsibility from that ofChemist to my current position ofExecutive Director. I
have received a B.S. Degree from Illinois State University with majors in Biological Sciences
and Environmental Health. I have also received an M.A. Degree from the University ofMissouri
(Columbia) in Ecology with an emphasis on nutrient cycling. I pursued Doctoral Studies in
Biological Sciences at Illinois State University, again with an emphasis on nutrient cycling. I
hold an Illinois Environmental Protection Agency Class I Wastewater Treatment Plant Operator
License. I have been a member ofthe Phi Sigma National Biological Honor Society for thirty
years and a member ofthe Sigma Xi Scientific Research Society for twenty three years. I have
been actively involved in professional organizations representing various aspects ofthe
wastewatertreatment industry and have held positions ofleadership in such organizations. These
organizations include the Illinois Association ofWastewaterAgencies, the Illinois Water
Pollution Control Operators Association and the Central States Water Environment Association.
I have been a member ofthe Water Environment Federation for more than twenty five years.
During my career I have served in several stakeholder study groups organized by the Illinois

Environmental Protection Agency to assist in the formulation ofstandards and policies
concerning both Illinois water quality and various issues regarding wastewater treatment within
the State. I have published and/or presented numerous papers on various aspects ofwastewater
treatment throughout my career.
It has been my privilege to previously appear before the Illinois Pollution Control Board
to offer input on key issues ofwidespread importance to our state. I thank the Illinois Pollution
Control Board for the opportunity to appear again today to discuss the need for a re-evaluation of
the Illinois dissolved oxygen water quality standard. I am offering testimony on behalfofthe
Illinois Association ofWastewater Agencies (IAWA) and in support ofMr. Dennis Streicher
who is directing this IAWA initiative. The need for a revised Illinois dissolved oxygen standard
has existed for some time. However, two relatively new initiatives in water quality improvement
within the State have mandated that the issue ofrevising the dissolved oxygen standard be
undertaken at this time. These mandates are in response to the need to develop scientifically
derived nutrient standards and to more precisely direct the adoption oftotal maximum daily load
allocations to Illinois waters listed as not attaining designated use support.
Since its inception, approximately four years ago, I have been a member ofthe IEPA
Nutrient Science Advisory Workgroup. This workgroup was assembled by IEPA to develop a
strategy for scientifically deriving water quality standards fornitrogen and phosphorus.
Historically the Workgroup was chaired by Mr. Robert Mosher of IEPA. Recently, Mr. Paul
Terrio ofthe U.S Geological Survey has replaced Mr. Mosher as Workgroup Chair. The water
quality degradation ascribed to phosphorus and nitrogen is a phenomenon called eutrophication.
2

condition which develops when the naturally limiting nutrient ofan ecosystem is increased to the
extent that the overall balance ofecosystem dynamics is upset. The limiting nutrient of most
freshwater ecosystems is phosphorus. Degrading concentrations ofphosphorus effectively “over
fertilize” the fresh water aquatic system and result in enhanced algal growth. Such algae are
aerobic organisms. During daylight hours algae photosynthesize. A by product of
photosynthesis is oxygen. As a result ofthis photosynthesis, during early stages in the
development of eutrophication, daytime dissolved oxygen levels can be maintained such that
little negative effect is realized in an aquatic system. However, during the night, when no
sunlight is present to power photosynthesis, the increased algae population must continue cellular
respiration as must the remaining aerobic biota ofa freshwater ecosystem. Ultimately, the total
oxygen demand required by these respiring organisms exceeds the ambient night time re-aeration
capability ofa water body. Consequently, oxygen sensitive species are put at stress and
population levels ofsuch organisms may significantly diminish. A self-perpetuating downward
spiral of aquatic organism diversity can thus easily develop as eutrophic conditions continue to
persist.
The IEPA Nutrient Science Advisory Workgroup immediately recognized the
determination ofthe concentration ofphosphorus at which the eutrophication cycle begins to
cause problematic dissolved oxygen depletion to be one ofthe first essential steps in developing
an effective and scientifically derived phosphorus standard. Regrettably, it was also recognized
that this critical concentration ofdissolved oxygen was not known. However, many
professionals throughout Illinois agreed that the current Illinois dissolved oxygen water quality
3

standard does not represent the dissolved oxygen concentration which is critical to preventing the
onset of eutrophication. In fact, there exists general agreement among professionals that the
ambient dissolved oxygen concentrations ofthe waters ofIllinois frequently naturally fall
beneath the existing dissolved oxygen water quality standard. Mr. Mosher, as Chair ofthe
workgroup, was one ofthe individuals that initially suggested a re-evaluation ofthe Illinois
dissolved oxygen water quality standard was a timely consideration.
Although there existed widespread agreement several years ago within the Workgroup
that a reassessment ofour state’s dissolved oxygen water quality standard was warranted, IEPA
indicated the Agency did not have the resources or manpower to undertake such an effort at that
time. Realizing this need and the lack of available IEPA resources, I asked Mr. Mosher if EPA
would be receptive to and supportive of a third party investigation into the issue ofthe dissolved
oxygen standard issue. Such action was not unprecedented. The EPA had supported the IAWA
in a previous issue brought before the Illinois Pollution Control Board involving the ammonia
nitrogenwater quality standard. I was advised that EPA would support such an undertaking, but
definitely wanted input into the design ofthe research investigation. Ithen approached the
IAWA membership asking if sufficient interest existed for IAWA to fund a third party analysis of
both the existing Illinois dissolved oxygen standard as well as an investigation that would
provide a recommendation for an appropriate dissolved oxygen standard for Illinois. The JAWA
membership readily agreed to fund such work and directed me to investigate both the methods by
which such a research study could be undertaken as well as the willingness ofqualified
professionals within Illinois to undertake the study.
4

I initially contacted Dr. Mat Whiles ofthe Southern Illinois University Fisheries Research
Laboratory to both inquire ofhis possible interest in undertaking such work as well as his
recommendation ofany other qualified individuals ofwhich he was aware that might be
interested in the research. Dr. Whiles indicated that he was quite interested in the project and
that he thought a colleague ofhis, Dr. James Garvey, would be very interested in assisting him
with the work. I reported back to the IAWA membership that Dr. Whiles and Dr. Garvey had
expressed considerable interest in undertaking the project. The JAWA membership then
unanimously voted to retain the services ofthe two gentlemen. This agreement was reached in
the summer of2002.
On September 30, 2002, Dr. Whiles and I met with Mr. Mosher, Mr. Greg Goode and
other EPA staff to discuss aspects of the issue that IEPA felt were critical to the investigation
such that a technicallyjustifiable dissolved oxygen standard supportable by sound science could
be developed. Agreement was reached among those in attendance on the key issues which Dr.
Whiles and Dr. Garvey should investigate to satisfactorily address all concerns. I had previously
suggested to the IAWA membership that the conclusions ofthe work done by Dr. Whiles and Dr.
Garvey should not be released publicly until both the EPA and the IAWA had opportunity to
review them. The IAWA readily agreed to this qualification. I advised those in attendance at the
EPA meeting that such was the qualification JAWA had placed on the work to be done by Dr.
Whiles and Dr. Garvey. Again, this was the procedure previously agreed upon between EPA
and JAWA during the ammonia nitrogenwater quality standard development. The EPA
representatives were appreciative ofthis consideration.
5

Dr. Whiles and Dr. Garvey presented their initial draft report on their investigation to me
in early January of2004. I immediately circulated copies ofthe report to the JAWA Executive
Committee and the IAWA Nutrient Subcommittee as well as to IEPA. It was at this point in the
proceedings that I withdrew from a lead role in the development ofthe standard and Mr.
Streicher volunteered to coordinate the upcoming rule making proposal.
The previous discussion presents the need for a sound understanding of dissolved oxygen
dynamics in the waters ofour state such that meaningful and technicallyjustifiable nutrient
standards can be developed. Addressing either water quality parameter, nutrients or oxygen,
without consideration and a sound understanding ofthe other will not result in a comprehensive
and effective resolution ofthe eutrophication problem. I personally find it quite surprising and
very sad that we know no more about the interaction ofthese parameters than we presently do.
However, such is indeed the situation. I assure everyone present that the cost ofaddressing the
nutrient issue in Illinois will be extreme. However, I suggest that we look beyond the actual
monetary cost of suchrequirements. A statistic I have heard often quoted regarding the
wastewater treatment industry states that for every pound ofcarbonaceous waste we currently
remove from wastewater, four pounds ofcarbon in the form ofcarbon dioxide are released to the
atmosphere through the energy generation required for removal ofthat pound ofwaste. Nutrient
removal will only add to this energy requirement. A thorough understanding ofthe dynamics and
interaction ofnutrients and oxygen is absolutely essential for effective and efficient stewardship
which addresses this issue. A valid and scientifically based dissolved oxygen standard is
fundamental to this understanding.
6

The second mandate involving the need for a current reassessment ofthe dissolved
oxygen standard, to which I earlier referred, involves the effort currently under way to develop
total maximum daily load allocations (TMDLs) for waters ofthe State which are determined not
to be achieving full use designation. The TMDL procedure evaluates a watershed in an attempt
to determine what the assimilation rate ofthat watershed is for various parameters.
Hypothetically, both point source and non-point source contributions ofvarious parametersare
considered in determining the reduction in loading necessary to realize use attainment for each
parameter ofconcern. However, there regrettably exists little apparent regulatory control other
than voluntary best management practices that can force non-point contributions ofvarious
parameters to be reduced to levels which are not detrimental to a watershed. The readily
controlled and regulated contributions to a waterbody come from point sources.
There may or maynot be effective additional controls which can be applied to point
sources that will assist in achieving full use attainment. I believe that a specific solution for a
specific location will not universally solve the problems experienced by all use impaired waters
across the State. The dynamics and physical conditions ofeach waterbody must be assessed and
considered as unique to that particular location. However, inadequate dissolved oxygen is listed
on the EPA draft 3 03(d) list as a fairly universal parameter contributing to non use attainment
and subsequent inclusion ofwater bodies on that list. The draft 2004 303(d) list contains
approximately 300 waterbody segments in Illinois listed as impaired, at least in part, by
inadequate dissolved oxygen concentrations. Approximately 800 water bodies are listed on the
draft 2004 303(d) list. Therefore approximately one third ofthe water bodies listed on the draft
7

303(d) list are listed, at leastin part, because of a dissolved oxygen standard which many
professionals have indicated is overly protective and not specific to the needs ofthe waters of
Illinois.
This dissolved oxygen contribution to non-attainment is based on the current Illinois
dissolved oxygen water quality standard which, as previously discussed, has long been
considered to be ofquestionable validity. Some point source dischargers are now having a
minimum dissolved oxygen limit included in theirNPDES permits. In many situations I believe
that compliance with an effluent dissolved oxygen permit limit of6.0 mg/i will have virtually no
effect on improving receiving stream dissolved oxygen -concentration-s when the naturally
occurring ambient diurnal dissolved oxygen minima ofthat stream might easily be 4.5 mg/I. One
might speculate that over-protection is not necessarily unwarranted in its own right. However, I
again respectfu~llyremind the Board that compliance with a standard, over protective or not, has a
cost inherently associated with it. Increased dissolved oxygen concentrations in effluents require
that air be supplied to these waters before discharge. This air comes from blowers which are
powered by electricity.
As I previously mentioned, a rule ofthumb in our industry currently estimates that one
pound ofcarbonaceous waste removed from wastewaterresults in fourpounds ofcarbon in the
form of carbon dioxide released to the atmosphere. Are we as a society, through the TMDL
program, going to require that we aerate treatment plant effluents or provide additional treatment
within our plants to comply with a flawed dissolved oxygen standard and thereby perhaps
contribute another pound ortwo ofcarbon dioxide to the atmosphere forthe energy required to
8

do so on a per unit basis? I certainly hope that our society chooses not to follow that path.
Rather, I strongly encourage the Board to adopt the dissolved oxygen standard beingproposed in
this proceeding. It has been developed by professional aquatic biologists in consideration ofthe
requirements ofthe aquatic biota ofour state. The proposed standard is based upon, and more
conservative than, the USEPA recommended guidance for development ofdissolved oxygen
standards. Thank you for this opportunity to again provide testimony and appear before the
Illinois Pollution Control Board.
CHO2I
22319412.1
9

RECEIVED
BEFORE THE ILLINOIS POLLUTION CONTROL BOARDLERK’S
OFFICE
IN THE MATTEROF:
- )
JUN 152004
PROPOSED AMENDMENTS TO
-
)
R 04-25
Pollution
STATE OFControlILLINO~SBoard
DISSOLVED OXYGEN STANDARD
)
35 Iii. Adm. Code 302.206
)
WRITTEN TESTIMONY OF DENNIS STREICHER
My name is Dennis Streicher, and
I
am Director of Water and
Wastewater with the City of Elmhurst, Illinois. I have been employed by the
City of Elmhurst at the Wastewater Treatment Plant since 1972. I began my
career in Elmhurst as a chemist graduated with a biology degree. I worked
in the lab for approximately 15 years and was promoted to plant
superintendent, then to Assistant Director of Public Works, then to Director
of a newly created Department of Water & Wastewater. My responsibilities
include, in addition to operation of the wastewater treatment plant, operation
of the public water supply and of all storm water pumping utilities in the
City. I hold an Illinois Environmental Protection Agency Class 1 Operators
License and an Illinois Environmental Protection Agency Class “A” Potable
Water Operators License. A copy of my resume has been submitted as
IAWA Exhibit 3. I come before you today, however, representing the
Illinois Association ofWastewater Agencies (IAWA) as the committee chair
for dissolved oxygen standards in Illinois. I am also the current vice
president of administration with the IAWA.
1

The IAWA is a professional association representing the major
wastewater treatment plants in the state of Illinois. We have about 100
members and affiliate members, which includes approximately
55
districts
and municipalities throughout the state. These agencies operate dozens of
publicly owned treatment works (POTWs). In addition to these POTWs,
water reclamation districts and municipalities, the largest Illinois private
wastewater treatment utility, which operates 12 plants, is also a member.
The representatives ofthese organizations are public officials, and include
both elected and appointed trustees of districts and appointed officials at
municipalities throughout the state. Our constituents are the citizens and
taxpayers of Illinois and are the same constituents as any other state or
public agency.
My goal is not to present the technical aspects of the proposed rule
change; Dr. James Garvey is the expert in that area. My hope is to present
the IAWA perspective on the existing dissolved oxygen regulations in
Illinois and why we feel that it is time to update those standards.
The managers of the POTWs in Illinois have two interests in mind:
one is the integrity of the environment in which they work; the second is to
responsibly represent their constituents and charge reasonable rates for
service. Our jobs as managers of the states’ POTWs are the real life
2

application of the water quality standards as promulgated in Illinois to the
operation of sometimes large but always-complex water treatment facilities.
These POTWs have an excellent record of producing treated effluent in
conformance with applicable NPDES permit limitations, due in large part to
the investment of public dollars to construct and upgrade the facilities and
the experience and dedication of those that operate and maintain the plants.
This proposed rulemaking is consistent with IAWA’s purpose and
past practice, to ensure that the standards by which it operates are based on
sound science and to take action to update standards where scientific
information supports such a change. IAWA has engaged the highest
qualified experts consistent with its purpose, and has performed a variety of
assessments that have been used by Illinois EPA and the Board to assess
Illinois standards governing the discharges of its members. IAWA proposed
the rulemaking that resulted in revision of certain water quality standards
governing ammonia nitrogen in R02- 19, and the Board adopted a revised
rule in 2002.
IAWA had participated in a prior rulemaking brought by the Illinois
EPA to revise the ammonia regulations. During the pendency of that
rulemaking, U.S. EPA revised the national criteria document for ammonia.
After discussing this revision with representatives of the Illinois EPA, it
3

became apparent that the Illinois EPA did not have the interest or resources
to initiate rulemaking to again revise the ammonia regulations. Because of
the impact that the recently adopted ammonia regulations had on wastewater
treatment plants and because the regulations were in fact based upon
outdated science, IAWA initiated and saw to completion the rulemaking in
R02- 19 and ultimately the accompanying Illinois EPA implementation
regulations to ensure that Illinois’ ammonia effluent limitations were
consistent with U.S. EPA’s national criteria document and based upon sound
current science. The managers and officials who operate wastewater
treatment plants and who needed to invest in upgrades for their facilities,
were able to make the case to their respective District Boards and City
Councils for authorization for the necessary dollars to meet an appropriate
and justifiable ammonia standard.
IAWA is committed to following the same course of action as it did in
the ammonia rules whenever it is apparent that effluent limitations and water
quality standards that have a significant impact on POTWs are in need of
revision and the Illinois EPA does not have the resources or the inclination
to initiate the appropriate evaluation and ultimate regulatory proceedings.
This dissolved oxygen rulemaking is IAWA’s second such effort. Various
IAWA members were involved in a series of discussions with
4

representatives of the Illinois EPA and other regulators, many of whom had
publicly stated that the existing Illinois dissolved oxygen water quality
standard found at 35 Iii. Admin. Code Section 203 was not based on sound
science was inconsistent with USEPA’s national criteria document and was
too stringent. At the same time, JAWA was aware that many water bodies
throughout Illinois were not in compliance with the existing dissolved
oxygen water quality standard or would not be found to be in compliance if
dissolved oxygen measurements were taken early in the morning due to the
naturally occurring diurnal dissolved oxygen fluctuation cycle.
IAWA decided to undertake a scientific assessment of the dissolved
oxygen standard almost three years ago. In 2002, IAWA engaged Dr. James
Garvey and Dr. Matt Whiles, who concluded that the Illinois standard was
too rigid and not consistent with the U.S. EPA’s National Criteria Document
(NCD) for dissolved oxygen. Dr Jim Garvey and Dr. Matt Wiles have done
an excellentjob in putting together a review of data that has been generated
since the 1980’s, have applied their knowledge and skills and training to
their understanding of all of the data generated since that time, and have
made recommendations that the IAWA feels are reasonable and accurate.
Because revision of the dissolved oxygen standard was not a priority of
5

Illinois EPA, the IAWA elected to itself bring this petition to the Illinois
Pollution Control Board.
The JAWA is very concerned that the existing dissolved oxygen
standard is triggering other legal requirements that are not warranted by
scientific information. The Illinois EPA is currently insisting on imposition
of a dissolved oxygen water quality effluent limitation in NPDES Permits of
6 mg/L to be met continuously. It is IAWA’s understanding that this
effluent limitation is being placed in NPDES Permits to ensure that the
existing water quality standard is not violated. In instances where POTWs
are unable to comply with this limitation, the Illinois EPA has granted
construction schedules requiring investment of public dollars to meet it.
Illinois EPA is required by Section 305(b) of the Clean Water Act to
assess the water quality of Illinois waters and prepare a report, commonly
known as the 305(b) report. Based on this report, Illinois EPA is
additionally required by Section 303(d) ofthe Clean Water Act to develop a
list of impaired waters in Illinois, commonly known as the 303(d) List.
While IAWA has not counted the water body segments in the 305(b) report
or the stream segments in the 303(d) report for purposes of reference there
were 741 segments listed in the 1998 303(d) report and 798 segments in the
final 2002 303(d) report.
6

The Illinois EPA is in the process of finalizing the 2004 Section
305(b) and Section 303(d) reports. IAWA has reviewed the. draft reports.
The Illinois EPA lists approximately 251 water body segments as not
complying with the dissolved oxygen standard in the draft 305(b) report.
There-are 302 segments listed in the 3 03(d) report as impaired for dissolved
oxygen. The 305(b) and 303(d) reports are then used to determine the
waters and parameters for which Total Maximum Daily Loads (TMDLs)
will be established, establishing load limits for dischargers to each listed
waterway. All of these requirements adhere to the current standards, even if
those standards are not scientifically based, as we believe to be the case with
the Illinois dissolved oxygen standard. This can only result in unrealistic and
unwarranted permit limits requiring expensive capital improvements and
modifications to wastewater treatment facilities at taxpayer expense, or
unjustified reasons for plant expansion.
In my position at the City of Elmhurst, I together with other IAWA
member agencies have watched and participated with great interest in the
Illinois EPA’s efforts to establish TMDLs for the West Branch of the
DuPage River, East Branch of the DuPage River and Salt Creek Basins.
These three TMDLs mark the first effort by the Illinois EPA to develop
TMDLs in urban areas with significant potential impact from POTWs,
7

combined sewer overflows, storm sewer discharges, and other urban
impacts. In the initial drafts the TMDLs for the East Branch of the DuPage
River and Salt Creek would have required limitations on CBOD and
ammonia because these streams were listed as impaired under the existing
standard for dissolved oxygen. The potential for the TMDLs to be finalized
with an ultimate requirement for more restrictive CBOD and ammonia
limitations in existing NPDES Permits could have a significant impact on
POTW discharges. Either expensive capital investment would be required
with increased operational expenses or a loss in the existing treatment plant
capacity that has been built to service future growth may be required.
Additional efforts were discussed as well including stream re-aeration and
dam removal as additional potential means of meeting the existing dissolved
oxygen water quality standard. The IAWA and I believe that these
consequences of failure to meet the standard should only result if there is an
actual environmental problem applying a scientifically sound dissolved
oxygen water quality limitation. Let me illustrate with a description of what
is happening today in the Salt Creek basin. The plant I manage discharges to
Salt Creek in DuPage County. As I said, the Illinois EPA has or is about to
submit a completed TMDL on Salt Creek to the USEPA. That TMDL has
found Salt Creek to be impaired for dissolved oxygen and had recommended
8

that significant additional effluent limits on CBOD and ammonia be
imposed on POTWs in the watershed. The TMDL estimated costs for those
improvements to be about 18 million dollars. These are costs that the
POTWs will bear alone. At this time stakeholders in the basin, and I am one
of them, are deeply involved in an effort to form a watershed committee, one
of the goals of this committee will be to attempt to develop more meaningful
data, including biotic data, to further refine the TMDL study and hopefully
mitigate the future costs. There is no guarantee that we will be successful.
The cost of this effort in time and dollars will certainly be significant.
IAWA believes that given the large number of water body and stream
segments that are listed as non-compliant with the current dissolved oxygen
standard or impaired for dissolved oxygen reasons, Illinois should insure that
the existing dissolved oxygen water quality standard is an appropriate
standard based upon sound science and consistent with USEPA’s national
criteria document. The costs now being incurred on the Salt Creek and East
Branch of the DuPage River basin could be multiplied by each of those
additional basins identified as impaired for dissolved oxygen using the
existing inappropriate standard.
JAWA believes this proposed dissolved oxygen rulemaking is
consistent with Section 303(c) of the Clean Water Act, 33 U.S.C. 13 13(c),
9

which requires the states review and re-evaluate existing water quality
standards within three years of adoption of revised national criteria by
USEPA. To date, despite the acknowledgement by many within the Illinois
EPA that the existing dissolved water quality standard is out of date and
inconsistent with the NCD, Illinois has not undertaken such a review.
Dr. Garvey points out in
“An Assessment of National and Illinois
Dissolved Oxygen Water Quality Criteria”
that dissolved oxygen
concentrations fluctuate in natural systems. Dissolved oxygen has a diel
fluctuation, it has a seasonal fluctuation, and concentrations could be
different through the water column. Animals living in those conditions have
evolved a tolerance for those fluctuations. The current regulation does not
take into account seasonal fluctuations.
My own career began at the same time as the development of many of
today’s water quality regulations. I have been able to observe that
development from the inception of the Clean Water Act to today. I observed
the infant Illinois EPA and the Illinois Pollution Control Board struggling
with the proposal and adoption of water quality standards and were faced
with almost insurmountable demands to develop them quickly. At that time
there was a rash of new standards being developed with the aim of quickly
attaining water quality goals. Many of those standards are still in effect
10

today. The dissolved oxygen standard used in Illinois today was
promulgated during that initial period almost three decades ago and has not
been revised since.
When the work of Dr. Garvey and Dr. Whiles and the proposed
regulation were completed, I was excited to volunteer to represent the
IAWA in the effort to see this study through rules making at the pollution
control board and to be a part of the process to develop realistic dissolved
oxygen standards in Illinois. As part of this effort I contacted and shared the
report with a number of other groups within the state to look for their
support and for their comments on the study. I sent letters to the Illinois
Department of Agriculture, the Illinois Farm Bureau (ILFB), the Illinois
Environmental Regulatory Group (IERG), and the Illinois State Water
Survey. I personally spoke to members of all of those agencies that I
mentioned and asked them for their thoughts and if they had concerns to let
me know and to follow up on my letters sent to them. Those letters are
submitted as IAWA’s Exhibit 4. In every single instance the persons I spoke
to expressed support and a hope that the board would adopt this rule.
I also copied many of the citizen advocacy groups such as the Sierra
Club, Prairie Rivers Network, The Salt Creek Watershed Alliance, DuPage
Conservation Foundation and the Environmental Law and Policy Center.
11

Our goal was to offer those folks an opportunity to comment as well. The
goal of IAWA was to be as inclusive as possible.
In summary, it is commonly known throughout the state that the
current dissolved oxygen regulation is not scientifically justifiable. Because
of its importance in the regulatory regime in Illinois, an accurate and
realistic dissolved oxygen standard is critical. IAWA has spent considerable
time and incurred significant expense to ensure that it has the most recent
and strongest scientific data to support its rulemaking. I urge the Board to
proceed with the rulemaking as proposed by the IAWA. Thank you for this
opportunity to address this issue before the Board.
CHO2/ 22319408.1
12

RVED
CLERK’S OFFICE
-
JUN 152004
BEFORE THE ILLINOIS POLLUTION CONTROL BOAR~TATE
OF ILLINOIS
Pollution Contro’ Board
IN THE MATTER OF:
)
)
PROPOSED
AMENDMENTS
TO
)
R 04-25
DISSOLVED OXYGEN STANDARD
)
35 Iii. Adm. Code 302.206
)
IAWA EXHIBIT LIST
-
The Illinois Association ofWastewater Agencies (“IAWA”), by its attorneys Gardner
Carton & Douglas, submits these exhibits to the pre-filed written testimony ofits witnesses for
the hearings in this matter.
1.
An Assessment ofNational and Illinois Dissolved Oxygen Water Quality Criteria,
Dr. James E. Garvey and Dr. Matt R. Whiles ofSouthern Illinois University (previously filed).
2.
United States Environmental Protection Agency’s National Criteria Document
(“NCD”) for Dissolved Oxygen (1986).
-
3.
Resume ofDennis Streicher.
4.
Copies ofletters from Dennis Streicher to various organizations concerning the
proposed rulemaking.
5.
Resume ofDr. James Garvey.
6.
Resume ofDr. Matt Whiles.
Respectfully submitted,
~‘Oneofthe Attorneys ~

Roy M. Harsch
Sheila H. Deely
GARDNER CARTON & DOUGLAS LLP
191 N. Wacker— Suite 3700
Chicago, IL 60606
312-569-1000
CHO2/ 22319686.1
2

m
—1-

An Assessment ofNational and Illinois Dissolved Oxygen Water Quality Criteria, Dr.
James E. Garvey and Dr. Matt R. Whiles ofSouthern Illinois University
(Appended to Petition).

m
:3-
-4
N)

United
States
Office of
Water
EPA
440/586.003
Environmental Protection
Regulations
and
Standarc~
April 1986
Agency
Criteria and ~andards
Div~siOl1
Water
Weshington,DC
20460
pB86-2082
III
liii~IIIIIIIIIlIIIIIIIIIIIII
53

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11111

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~,EPA
Ambient

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Water Quality

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Criteria
for
.

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Dissolved Oxygen
-~---—~—.--—---—----~-~--——
-—--~

~O272 -101
(SseANS~.-Z39.18)
Sli
Instructions on Reverse
OP~W~ALI’ORM
272
(4—77)
(For.~,,rIyNTIS.—35)
0i~-,,”n~ntofCommerc.~
REPORT
DOCUMENTATION 1.
REPORT
NO.
2.
-
EPA 440/5-86-003
4. lIti. and SubtitlI
j~.
Recipient~sAct,ssion No.

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F~lS86 20 8 2 5 31~3
5.
Report
Datn
Ambient
Water Quality Criteria for Dissolved Oxygen.
.
April, 1986
6.
7. Author(s)
~ç~~man, Gary
g. performêng Organization
N.m.
an& Addr.ss
.
U. S. Environmental Protection Agency
Office of Research and Development
Environmental Research Laboratories
Duluth,.Minnesota
Narragansett, Rhode Island
S.
?er~rrnin~Or~anizot~or,
Rept. No.
10. Project/Task/Work Unit No.
.
11.
contract(C) or
Grant(G) No.
(C)
(G)
12. Sponsoring Organization Nams and Address
U. S. Environmental Protection Agency
Office qf Water Regulations and Standards
.
Criteria and Standards Division (WH—585)
401 M St., S.W.
Washington, D. C. 20460
1~.Type of
Report
& Period C~vera~
I
.
14.
15.
Supplementary
Not.s
1~
Abstract (Limit:
200 words)
The Document reviews data which are currently available on the effects of low
levels of dissolved oxygen on the health, growth and reproduction of freshwater
aquatic organisms. Criteria for the protection of freshwater aquatic organisms are
developed, based principally on data derived from studies on fish. The Criteria
are presented in terms of cold and warm water species, early life stages and other
life stages, as well as the length of exposure to low D. 0. concentrations.
11.
Document Analysis a.
Descriptors
Dissolved Oxygen; Oxygen; Water Quality; rreshwater; Aquatic Life; Fish.
-.
b.
lderttlfl.rs/Open.Ended
Terms
~Ambient Water Quality Criteria; Surface Water Quality
C.
COSATI Field/Group
1$. AvailabilIty Statement
19. Security Class (This
Report)
.J21.
o. of Pages
Release Unl.irnited
20.
Security
Class (This Page)
4.~.
22.
“rice
.—.

Ambient Aquatic Life Water Quaflty
Criteria for Dissolved Oxygen
(Freshwater)
U.S. Environmental Protection Agency
Office of Research and Development
Environmental Research Laboratories
Duluth, Minnesota
Narragansett, Rhode Island

NOTICES
This document has been reviewed by the Criteria and Standards Division,
Office of Water Regulations and Standards, U.S. Environmental Protection
Agency, and approved for publication.
Mention of trade names or commercial products does not constitute
endorsement or recommendation for use.
This document is available to the public through the National Technical
Information Service (NTIS), 5285 Port Royal Road, Springfield, Virginia 22161.
ii

FOREWORD
Section 304(a)(1) of the Clean Water Act of 1977 (PL 95-217) requires the-
Administrator of the Environmental Protection Agency to publish water quality
criteria that accurately reflect the latest scientific knowledge on the kind
and extent-of all identifiable effects on health and welfare that might be
expected from the presence of pollutants in any body of water, including
groundwater.
-
This document is a revision of proposed criteria based- upon a
consideration of comments received from other Federal agencies, State
agencies, special interest groups, and individual scientists. Criteria
cor~tained in this document replace any previously published EPA aquatic life
criteria for the same pollutant(s).
-
The term “water quality criteria” is used in two sections of the Clean
Water Act, Section 304(a)(1) and Section 303(c)(2). This term has a different
program impact in each section. In Section 304, the term represents a non—
regulatory, scientific assessment of ecological effects. Criteria presented
in- this document are such scientific assessments. If water quality criteria
associated with specific stream uses are adopted by a State as water quality
standards under Section 303, they become enforceable maximum acceptable
pollutant concentrations in ambient waters within that State. Water quality
criteria adopted in State water quality standards could have the same numer-
ical values as criteria developed under Section 304. However, in many
situations States might want to adjust water quality criteria developed under
Section 304 to reflect local environmental conditions and human exposure
patterns before incorporation into water quality standards. It is not until
their adoption as part of State water quality standards that criteria become
regulatory.
Guidelines to assist States in the modification of criteria presented in
this document, in the development of water quality, standards, and in other
water-related programs of this agency, have been developed by EPA.
William A. Whittington
Director
Office of Water Regulations and Standards
lii

ACKNOWLEDGEMENTS
Gary Chapman
Author
Environmental Research Laboratory
Narragansett, Rhode Island
Clerical Support: Nancy Lanpheare
iv

CONTENTS
Page
Foreword
iii
Acknowledgements
.
iv
Tables
vi
Figures
vii
Introduction
1
Salmonids
4
Physiology
4
Acute Lethal Concentrations
5
Growth
5
Reproduction
8
Early Life Stages
8
Behavior
10
Swimming
11
Field Studies
11
Non-Salmonids
12
Physiology
12
Acute Lethal Concentrations
12
Growth
13
Reproduction
17
Early Life Stages
17
Behavior
18
Swimming
19
Field Studies
19
Invertebrates
20
Other Consideration
23
Effects of Fluctuations
23
Temperature and Chemical Stress
25
Disease Stress
26
Conclusions
27
National -Criterion
33
References
39
V

TABLES,
Page
1. Percent reproduction in growth rate of salmonids at various dissolved
oxygen concentrations expressed as the median value from n tests with
-
each species
6
2. Influence of temperature on growth rate of chinook salmon held at
various dissolved oxygen concentrations
7
3. Influence of temperature on growth rate of coho salmon held at
various dissolved oxygen concentrations
7
4. Percent reduction in growth rate of some nonsalmonid fish held at
various dissolved oxygen concentrations expressed as the median value
from n tests with each species
-
15
5. Effects of temperature on the percent reduction in growth rate of
largemouth bass exposed to various dissolved oxygen concentrations in
ponds
16
6. Acutely lethal concentrations of dissolved oxygen to aquatic insects.. 22
7. Survival of rainbow trout embryos as a function of intergravel
dissolved oxygen concentrations and water velocity as compared to
dissolved oxygen concentrations established as criteria or estimated
as producting various levels of production impairment
32
8. Water quality criteria for ambient dissolved oxygen concentrations..
.
34
9. Sample calculations for determining daily means and 7-day mean
dissolved oxygen concentrations (30-day averages are calculated in a
similar fashion using 30-day data)
35
Vi

FIGURES
Page
1. Effect of continuous exposure to various mean dissolved oxygen
-
concentrations on survival of embryos and larval stages of eight
species of nonsalmonid fish
14
vii

Ambient Water Quality Criteria for Dissolved Oxygen
FRESHWATER AQUATIC LIFE
I. Introduction
A sizable body of literature on the oxygen requirements of freshwater
aquatic life has been thoroughly summarized (Doudoroff and Shuinway, 1967,
1970; Warren et al., 1973; Davis, 1975a,b; and Alabaster and Lloyd, 1980).
These reviews and other documents describing the dissolved oxygen requirements
of aquatic organisms (U.S. Environmental Protection Agency, 1976; Inter-
national Joint Commission, 1975; Minnesota Pollution Control Agency, 1980) and
more recent data were considered in the preparation of this document. The
references cited below are limited to those considered to be the most defin-
itive and most representative of the preponderance of scientific evidence
concerning the dissolved oxygen requirements of freshwater organisms. The
guidelines used in deriving aquatic life criteria for toxicants (Federal
Register, 45 FR 79318, November 28, 1980) are not applicable because of the
different nature of the data bases. Chemical toxicity data bases rely on
standard 96-h LC5O tests and standard chronic tests; there are very few data
of either type on dissolved oxygen.
Over the last 10 years the dissolved oxygen criteria proposed by various
agencies and researchers have generally reflected two basic schools of
thought. One maintained that a dynamic approach should be used so that the
criteria would vary with natural ambient dissolved oxygen minima in the waters
of concern (Doudoroff and Shumway, 1970) or with dissolved oxygen requirements
of fish expressed in terms of percent saturation (Davis, 1975a,b). The other
maintained that, while not ideal, a single minimum allowable concentration
should adequately protect the diversity of aquatic life in fresh waters (U.S.
Environmental Protection Agency, 1976). Both approaches relied on a simple
minimum allowable dissolved oxygen concentration as the basis for their
criteria. A simple minimum dissolved oxygen concentration was also the most
practicable approach in waste load allocation models of the time.
Expressing the criteria in terms of the actual amount of dissolved oxygen
available to aquatic organisms in milligrams per liter (mg/i) is considered
more direct and easier to administer compared to expressing the criteria in
terms of percent saturation. Dissolved oxygen criteria expressed as percent
saturation, such as discussed by Davis (1975a,b), are more complex and could
often result in unnecessarily stringent criteria in the cold months and
potentially unprotective criteria during periods of high ambient temperature
or at high elevations. Oxygen partial pressure is subject to the same
temperature problems as percent saturation.
1

The approach recommended by Doudoroff and Shumway (1970), in which the
criteria vary seasonally with the natural minimum dissolved oxygen concentra-
-
tions in the waters of concern, was adopted by the National Academy of
Sciences and National Academy of Engineering (NAS/NAE, 1973). This approach
has some merit, but the lack of data (natural minimum concentrations) makes
its application difficult, and it can also produce unnecessarily stringent or
unprotective criteria during periods of extreme temperature.
The more simplistic approach to dissolved oxygen criteria has bee-n
supported by the findings of a select committee of scientists specifically
established by the Research Advisory Board of the International. Joint
Commission to review the dissolved oxygen criterion for the Great Lakes
(Magnuson et al., 1979). The committee concluded that a simple criterion (an
average criterion of 6.5 mg/i and a minimum criterion of 5.5 mg/i) was
preferable to one based on percent saturation (or oxygen partial pressure) and
was scientifically sound because the rate of oxygen transfer across fish gills
is directly dependent on the mean difference in oxygen partial pressure across
the gill. Also, the total amount of oxygen delivered to the gills is a more
specific limiting factor than is oxygen partial pressure ~ Se. The format
of this otherwise simple criterion was more sophisticated than earlier
criteria with the introduction of a two-concentration criterion comprised of
both a mean and a minimum. This two-concentration criteria structure is
similar to that currently used for toxicants (Federal Register, 45 FR 79318,
November 28, 1980). EPA agrees with the International Joint Commission’s
conclusions and will recommend a—two-number criterion for dissolved oxygen.
The national criteria presented herein represent the best estimates,
based on the data available, of dissolved oxygen concentrations necessary to
protect aquatic life and its uses. Previous water quality criteria have
either emphasized (Federal Water Pollution Control Administration, 1968) or
rejected (National Academy of Sciences and National Academy of Engineering,
1972) separate dissolved oxygen criteria for coidwater and warmwater biota. A
warmwater-coldwater dichotomy is made in this criterion. To simplify discus-
sion, however, the text of the document is split into salmonid and non-
salmonid sections. The salmonid-nonsalmonid dichotomy is predicated on the
much greater knowledge regarding the dissolved oxygen requirements of
salmonids and on the critical influence of intergravel dissolved oxygen
concentration on salmonid embryonic and larval development. Nonsalmonid fish
include many other coidwater and coolwater fish plus all warmwater fish. Some
of these species are known to be less sensitive than salmonids to low dis-
solved oxygen concentrations. Some other nonsalmonids may prove to be at
least as sensitive to low dissolved oxygen concentrations as the salmonids;
among the nonsalmonids of likely sensitivity are the herrings (Clupeidae), the
smelts (Osmeridae), the pikes (Esocidae), and the sculpins (Cottidae).
Although there is little published data regarding the dissolved oxygen
requirements of most nonsalmonid species, there is apparently enough anecdotal
information to suggest that many coolwater species are more sensitive to
dissolved oxygen depletion than are warmwater species. According to the
American Fisheries Society (1978), the term “coolwater fishes” is not vigor-
ously defined, but it refers generally to those species which are distributed
by temperature preference between the “coldwater” salmonid communities to the
north and the more diverse, often centrarchid-dominated “warmwater” assem-
2

blages •to the south. Many states have more stringent dissolved oxygen
standards for colder waters, waters that contain either salmonids, nonsalmonid
coolwater fish, or the sensitive centrarchid, the smallmouth bass.
The research and sociological emphasis for dissolved oxygen has been
biased towards fish, especially the more economically important species in the
family Salmonjdae. Several authors
-
(Doudoroff and Shumway, 1970; Davis,
.975a,b) have discussed this bias in considerable detail and have drawn
similar conclusions regarding the effects of low dissolved oxygen on fresh-
water invertebrates. Doudoroff and Shumway (1970) stated that although some
invertebrate species are about as sensitive as the moderately susceptible
fishes, all invertebrate species need not be protected in order to protect the
food source for fisheries because many invertebrate species, inherently more
tolerant than fish, would increase in abundance. Davis (1975a,b) also
concluded that invertebrate species would probably be adequately protected if
the fish populations are protected. He stated that the composition of
invertebrate communities may shift to more tolerant forms selected from the
resident community or recruited from outside the community. In general,
stream invertebrates that are requisite riffle-dwellers probably have a higher
dissolved oxygen requirement than other aquatic invertebrates. The riffle
habitat maximizes the potential dissolved oxygen flux to organisms living in
the high water velocity by rapidly replacing the water in the immediate
vicinity of the organisms. This may be especially important for organisms
that exist clinging to submerged substrate in the riffles. In the absence of
data to the contrary, EPA will follow the assumption that a’dissolved oxygen
criterion protective of fish will be adequate.
One of the most difficult problems faced during this attempt to gather,
interpret, assimilate, and generalize the scientific data base for dissolved
oxygen effects on fish has been the variability in test conditions used by
investigators. Some toxicological methods for measuring the effects of
chemicals on aquatic life have been standardized for nearly 40 years; this has
riot been true of dissolved oxygen research. Acute lethality tests with
dissolved oxygen vary in the extreme with respect to types of exposure
(constant vs. declining), duration of exposure (a few hours vs. a week ~r
more), type of endpoint (death vs. loss of equilibrium), type of oxygen
control (nitrogen stripping vs. vacuum degassing), and type of exposure
chamber (open to the atmosphere vs. sealed). In addition there are the normal
sources of variability that influence standardized toxicity tests, including
seasonal differences in the condition of test fish, acclimation or lack of
acclimation to test conditions, type and level of feeding, test temperature,
age of test fish, and.stresses due to test conditions. Chronic toxicity tests
are typically of two types, full life cycle tests or early life stage tests.
These have come to be rather rigorously standardized and are essential to the
toxic chemical criteria established by EPA. These tests routinely are assumed
to include the most sensitive life stage, and the criteria then presume to
protect all life stages. With dissolved oxygen research, very few tests would
be considered legitimate chronic tests; either they fail to include a full
life cycle, they fail to include both embryo and larval stages, or they fail
to include an adequate period of post-larval feeding and growth.
3

Instead of establishing year-round criteria to protect all life stages,
it may be possible to establish seasonal criteria based on the life stages
present. Thus, special early life stage criteria are routinely accepted for
salmonid early life stages because of their usual intergravel environment.
The same concept may be extended to any species that appear to have more
stringent dissolved oxygen requirements during one period of their life
history. The flexibility afforded by such a dichotomy in criteria carries
with it the responsibility to accurately determine the presence or absence of
the more sensitive stages prior to invocation of the less stringent criteria..
Such presence/absence data must be more site-specific than national in scope,
so that temperature, habitat, or calendar specifications are not possible in
this document. In the absence of such site-specific determinations the
default criteria would be those that would protect all life stages year-round;
this is consistent with the present format for toxic chemical criteria.
II. Salmonids
The effects of various dissolved oxygen concentrations on the well—being
of aquatic organisms have been studied more extensively for fish of the family
Salmonidae (which includes the genera Coregonus, Oncorhynchus, Prosopium,
Salmo, Salvelinus, Stenodus, and Thymallus) than for any other family of
organisms. Nearly all these studies have been conducted under laboratory
conditions, simplifying cause and effect analysis, but minimizing or eliminat-
ing potentially important environmental factors, such as physical -and chemical
stresses associated with suboptimal water quality, as well, as competition,
behavior, and other related activities. Most laboratory studies on the
effects of dissolved oxygen concentrations on salmonids have emphasized
growth, physiology, or embryonic development. Other studies have described
acute lethality or the effects of dissolved oxygen concentration on swimming
performance.
A. Physiology
Many studies have reported a wide variety of physiological responses to
low dissolved oxygen concentrations. Usually, these investigations were of
short duration, measuring cardiovascular and metabolic alterations resulting
from hypoxic exposures of relatively rapid onset.
While these data provide
only minimal guidance for establishing environmentally acceptable dissolved
oxygen concentrations, they do provide considerable insight into the mechan-
isms responsible for the overall effects observed in the entire organism. For
example, a good correlation exists between oxygen dissociation curves for
rainbow trout blood (Cameron, 1971) and curves depicting the reduction in
growth of salmonids (Brett and Blackburn, 1981; Warren et al., 1973) and the
reduction in swimming ability of salmonids (Davis et al., 1963). These
correlations indicate that the blood’s reduced oxygen loading capacity at
lower dissolved oxygen concentrations limits the amount of oxygen delivered to
the tissues, restricting the ability of fish to maximize metabolic perform-
ance.
In general, the significance of metabolic and physiological studies on
the establishment of -dissolved oxygen criteria must be indirect, because their
applicability to environmentally acceptable dissolved oxygen concentrations
requires greater extrapolation and more assumptions than those required for
data on growth, swimming, and survival.
4

B. Acute Lethal Concentrations
Doudoroff and Shumway (1970) summarized studies on lethal concentrations
-
of dissolved oxygen for salmonids; analysis of these data indicates that the
test procedures were highly variable, differing in duration, exposure regime,
and reported endpoints. Only in a few cases could a 96-hr LC5O be calculated.
Mortality or loss of equilibrium usually occurred at concentrations between 1
and 3 mg/i.
Mortality of brook trout has occurred in less than one hour at 10°Cat
dissolved oxygen concentrations below 1.2 mg/i, and no fish survived exposure
at or below 1.5 mg/i for 10 hours (Shepard, 1955). Lethal dissolved oxygen
concentrations increase at higher water temperatures and longer exposures. A
3.5 hr exposure killed all trout at 1.1 and 1.6 mg/i at 10 and 20°C,respec-
tively (Downing and Merkens, 1957). A 3.5-day exposure killed all trout at
1.3 and 2.4 mg/i at 10 and 20°C, respectively. The corresponding no-mortality
levels were 1.9 and 2.7 mg/i. The difference between dissolved oxygen
concentrations causing total mortality and those allowing complete survival
was about 0.5 mg/i when exposure duration was less than one week. If the
period of exposure to low dissolved oxygen concentrations is limited to less
than 3.5 days, concentrations of dissolved oxygen of 3 mg/i or higher should
produce no direct mortality of salmonids.
More recent studies confirm these lethal levels in chronic tests with
early life stages of salmonids (Siefert et al., 1974; Siefert’ and Spoor, 1973;
Brooke and Colby, 1980); although studies with lake trout (Carison and
Siefert, 1974) indicate that 4.5 mg/i is lethal at 10°C(perhaps a marginally
acceptable temperature for embryonic lake trout).
C. Growth
Growth of salmonids is most susceptible to the effects of low dissolved
oxygen concentrations when the metabolic demands or opportunities are great-
est. This is demonstrated by the greater sensitivity of growth to low
dissolved oxygen concentrations when temperatures are high and food most
plentiful (Warren et al., 1973). A total of more than 30 growth tests have
been reported by Herrmann et al. (1962), Fisher (1963), Warren et al. (1973),
Brett and Blackburn (1981), and Spoor (1981). Results of these tests are not
easily compared because the tests encompass a wide range of species, tempera-
tures, food types, and fish sizes. These factors produced a variety of
control growth rates which, when combined with a wide range of test durations
and fish numbers, resulted in an array of statistically diverse test results.
The results from most of these 30-plus tests were converted to growth
rate data for fish exposed to low dissolved oxygen concentrations and were
compared to control growth rates by curve-fitting procedures (JRB Associates,
1984). Estimates of growth rate reductions were similar regardless of the
type of curve employed, but the quadratic model was judged to be superior and
was used in the growth rate analyses contained in this document. The apparent
relative sensitivity of each species to dissolved oxygen depletion may be
influenced by fish size, test duration, temperature, and diet. Growth rate
data (Table 1) from these tests with salmon and trout fed unrestricted rations
indicated median growth rate reductions of 7, 14, and 25 percent for fish held
5

at 6, 5., and 4 mg/i, respectively (JRB Associates, 1984). However, median
growth rate reductions for the various species ranged from 4 to 9 percent at 6
mg/i, 11 to 17 percent at 5 mg/i, and 2. to 29 percent at 4 mg/i.
Table 1. Percent reduction in growth rate of salmonids at various dissolved
oxygen concentrations expressed as the median value from n tests
with each species (calculated from JRB Associates, 1984).
Dissolved
Species (number of tests)
-
Oxygen
Chinook
Coho
Sockeye
Rainbow
Brown
Lake
(mg/i) Salmon (6)
Salmon (12) Salmon (1) Trout (2)
Trout (1) Trout (2)
90
0
0000
80
0
0100
71
1
2512
674
6967
5
16
11
12
17
13
16
4
29
2.
22
25
23
29’
3
47
-
37
33
37
‘36
47
Median
Temp. (°C) 15
18
15
12
12
12
Considering the variability inherent in growth studies, the apparent
reductions -in growth rate sometimes seen above 6 mg/i are not usually statist-
ically significant. The reductions in growth rate occurring at dissolved
oxygen concentrations below about 4 mg/i should be considered severe; between
4 mg/i and the threshold -of effect, which variably appears to be between 6 and
10 mg/i in individual tests, the effect on growth rate is moderate to slight
if the exposures are sufficiently long.
Within, the growth data presented by Warren et al. (1973), the greatest
effects and highest thresholds of effect occurred at high temperatures (17.8
to 21.7°C). In two tests conducted at about 8.5°C,the growth rate reduction
at 4 mg/i of dissolved oxygen averaged 12 percent. Thus, even at the maximum
feeding levels in these tests, dissolved oxygen levels down to 5 mg/i probably
have little effect on growth rate at temperatures below 10°C.
Growth data from Warren et al. (1973) included chinook salmon tests
conducted at various temperatures. These data (Table 2) indicated that growth
tests conducted at 10-15°C would underestimate the effects of low dissolved
oxygen concentrations at higher temperatures by a significant margin. For
example, at 5 mg/i growth was not affected at 13°Cbut was reduced by 34
percent if temperatures were as high as 20°C. Examination of the test
temperatures associated with the growth rate reductions listed in Table 1
shows that most data represent temperatures between 12 and 15°C. At the
higher temperatures often associated with low dissolved oxygen concentrations,
the growth rate reductions would have been greater if the generalizations of
6

the chinook salmon data are applicable to salmonids in general. Coho salmon
growth studies (Warren et al., 1973) showed a similar result over a range of
temperatures from 9 to 18°C,but the trend was reversed in two tests near 22°C
(Table 3). Except for the 22°Ccoho tests, the coho and chinook salmon
results support the idea that effects of low dissolved oxygen become more
severe at higher temperatures. This conclusion is supported by data on
iargemouth bass (to be discussed later) and by the increase
in
metabolic rate
produced by high temperatures.
-
.
-
Table 2. Influence of temperature on growth rate of chinook salmon held at
various dissolved oxygen concentrations (calculated from Warren et
al., 1973; JRB Associates, 1984).
Dissolved
Percent Reduction in Growth Rate at
Oxygen
(mg/i)
-
8.4°C 13.0°C 13.2°C
17.8°C 18.6°C 21.7°C
9
00000
0
8
00002
0
7
-0
0
4
0
8
2
6
0
0
8
5
19
14
5
0
0
16
16
34
34
4
7
4
-
25
33
‘53
65
3
26
22
36
57
77
100
Table 3. Influence of temperature
various dissolved oxygen
al., 1973; JRB Associates,
on growth rate of coho salmon
concentrations (calculated from
1984).
held at
Warren et
Dissolved
Oxygen
(mg/l)
-
Percent Reduction in Growth Rate at
-
8.6°C 12.9°C 13.0°C 18.0°C 21.6°C 21.8°C
10
0
0
0
0
0
0
9
00050
0
8
0
1
2
10
0
0
7
1
4
6
17
0
6
6
4
10
13
27
0
1
5
9
18
23
38
0
7
4
17
29
36
51
4
19
3
28
42
51
67
6
37
Effects of dissolved oxygen concentration on the growth rate of salmonids
fed restricted rations have been less intensively investigated. Thatcher
(1974) conducted a series of tests with coho salmon at 15°Cover a wide range
of food consumption rates at 3, 5, and 8 mg/l of dissolved oxygen. The only
significant reduction in growth rate was observed at 3 mg/i and food consump-
7

tion rates greater than about 70 percent of maximum, in these studies,
Thatcher noted that fish at 5 mg/i appeared to expend less energy in swimming
activity than those at 8 mg/i. In natural conditions, where fish may be
rewarded for energy expended
-
defending preferred territory or searching for
food, a dissolved oxygen concentration of 5 mg/i may restrict these activ—
i ties.
The effect of forced activity and dissolved oxygen concentration on the
growth of coho salmon was studied by Hutchins (1974). The growth rates of
salmon fed to repletion at a dissolved oxygen concentration of 3 mg/i and held
at current velocities of 8.5 and 20 cm/sec were reduced by 20 and 65 percent,
respectively. At 5 mg/i, no reduction of growth rate was seen at the slower
velocity, but a 15 percent decrease occurred at the higher velocity.
The effects of various dissolved oxygen concentrations on the growth rate
of coho salmon (“~ 5 cm long) in laboratory streams with an average current
velocity of 12 cm/sec have been reported by Warren et al. (1973). In this
series of nine tests, salmon consumed aquatic invertebrates living in the
streams. Results at temperatures from 9.5°to 15.5°Csupported the res~1tsof
earlier laboratory studies; at higher growth rates (40 to 50 mg/g/day),
dissolved oxygen levels below 5 mg/i reduced growth rate, but at lower growth
rates (0 to 20 mg/g/day),
rio
effects were seen at concentrations down to 3
mg/i.
The applicability of these growth data from laboratory tests depends on
the available food and required activity in natural situations. Obviously,
these factors will be highly variable depending on duration of exposure,
growth rate, species, habitat, season, and size of fish. However, unless
effects of these variables are examined for the site in question, the labora-
tory results should be used. The attainment of critical size is vital to the
smolting of anadromous salmonids and may be important for all salmonids if
size-related transition to feeding on larger or more diverse food organisms is
an advantage. In the absence of more definitive site—specific, species—
specific growth data, the data summary in Tables 1, 2, and 3 represent the
best estimates of the effects of dissolved oxygen concentration on the
potential growth of salmon-id fish.
D. Reproduction
No studies were found that described the effects of low dissolved oxygen
on the reproduction, fertility, or fecundity of salmonid fish.
E. Early Life Stages
Determining the dissolved oxygen requirements for salmonids, many of
which have embryonic and larval stages that develop while buried in the gravel
of streams and lakes, is complicated by complex relationships between the
dissolved oxygen supplies in the gravel and the overlying water. The dis-
solved oxygen supply of embryos and larvae can be depleted even when the
dissolved oxygen concentration in the overlying body of water is otherwise
acceptable. Intergravel dissolved oxygen is dependent upon the balance
between the combined respiration of gravel-dwelling organisms, from bacteria
8

to fish embryos, and the rate of dissolved oxygen supply, which is dependent
upon rates of water percolation and convection, and dissolved oxygen dif-
fusion.
Water flow past salmonid eggs influences the dissolved oxygen supply to
the microenvironment surrounding each egg. Regardless of dissolved oxygen
concentration in the gravel, flow rates below 100 cm/hr directly influence the
oxygen supply in the microenvironment and hence the size at hatch of salmonid
fish. At dissolved oxygen levels below 6 mg/i the time from fertilization to
hatch is longer as water flow decreases (Silver et al., 1963; Shumway et a.,
1964).
-
The dissolved oxygen requirements for growth of salmonid embryos and
larvae have not been shown to differ appreciably from those of older sal-
monids. Under conditions of adequate water flow (~100cm/hr), the weight
attained by salmon and trout larvae prior to feeding (swimup) is decreased
less than 10 percent by continuous exposure to concentrations down to 3 mg/i
(Brannon, 1965; Chapman and Shumway, 1978). The considerable developmental
delay which occurs at low dissolved oxygen conditions could have survival and
growth implications if the time of emergence from gravel, or first feeding, is
critically related to the presence of specific food organisms, stream flow, or
other factors (Carlson and Siefert, 1974; Siefert and Spoor, 1974). Effects
of low dissolved oxygen on early life stages are probably most significant
during later embryonic development when critical dissolved.oxygen concentra-
tions are highest (Alderdice et a., 1958) and during the first few months
post-hatch when growth rates are usually highest. The latter authors studied
the effects of 7-day exposure of embryos to low dissolved oxygen at various
stages during incubation at otherwise high dissolved oxygen concentrations.
They found no effect of 7-day exposure at concentrations above 2 mg/i (at a
water flow of 85 cm/hr).
Embryos of mountain whitefish suffered severe mortality at a mean
dissolved oxygen concentration of 3.3 mg/i (2.8 mg/l minimum) and some
reduction in survival was noted at 4.6 mg/i (3.8 mg/i minimum); at 4.6 mg/i,
hatching was delayed by 1 to 2 weeks (Sieffert et al., 1974). Delayed
hatching resulted in poorer growth at the end of the test, even at dissolved
oxygen concentrations of 6 mg/i.
Evaluating intergravel dissolved oxygen concentrations is difficult
because of the great spatial and temporal variability produced by differences
in stream flow, bottom topography, and gravel composition. Even within the
same redd, dissolved oxygen concentrations can vary by 5 or 6 mg/i at a given
time (Koski, 1965). Over several months, Koski repeatedly measured the
dissolved oxygen concentrations in over 30 coho salmon redds and the overlying
stream water in three small, forested (unlogged) watersheds. The results of
these measurements indicated that the average intraredd dissolved oxygen
concentration was about 2 mg/i below that of the overlying water. The minimum
concentrations measured in the redds averaged about 3 mg/i below those of the
overlying water and probably occurred during the latter period of intergravel
development when water temperatures were warmer, larvae larger, and overlying
dissolved oxygen concentrations lower.
9

Coble (1961) buried steelhead trout eggs in streambed gravel, monitored
nearby intergravel dissolved oxygen and water velocity, and noted embryo
survival. There was a positive correlation between dissolved oxygen concen-
tration, water velocity, and embryo survival. Survival ranged from 16 to 26
percent whenever mean intergravel dissolved oxygen concentrations were below 6
mg/i or velocities were below 20 cm/hr; at dissolved oxygen concentrations
above 6 mg/l and velocities over 20 cm/hr, survival ranged from 36 to 62
percent. Mean reductions in dissolved oxygen concentration between stream and
intergravel waters averaged about 5 mg/i as compared to the 2 mg/i average
reduction observed by Koski (1965) in the same stream. One explanation for
the different results is that the intergravel water flow may have been higher
in the natural redds studied by Koski (not determined) than in the artificial
redds of Coble’s investigation. Also, the density of eggs near the sampling
point may have been greater in Coble’s simulated redds.
A study of dissolved oxygen concentrations in brook trout redds was
conducted in Pennsylvania (Hoilander, 1981). Brook trout generally prefer
areas of groundwater upwelling for spawning sites (Witzel and MacCrimmon,
1983). Dissolved oxygen and temperature data offer no indication of ground-
water flow in Holiender’s study areas, however, so that differences between
water column and intergravel dissolved oxygen concentrations probably repre-
sent intergravel dissolved oxygen depletion. Mean dissolved oxygen concentra-
tions in redds averaged 2.1, 2.8, and 3.7 mg/liter less than the surface water
in the three portions of the study. Considerable variation of intergravel
dissolved oxygen concentration was observed between redds and within a single
redd. Variation from one year to another suggested that dissolved oxygen
concentrations will show greater intergravei depletion during years of low
water flow.
Until more data are available, the dissolved oxygen concentration in the
intergravel environment should be considered to be at least 3 mg/i lower than
the oxygen concentration in the overlying water. The 3 mg/i differential is
assumed in the criteria, since it reasonably represents the only two available
studies based on observations in natural redds (Koski, 1965; Holiender, 1981).
When siltation loads are high, such as in logged or agricultural watersheds,
lower water velocity within the gravel could additionally reduce dissolved
oxygen concentrations around the eggs. If either greater or lesser differen-
tials are known or expected, the criteria should be altered accordingly.
F. Behavior
Ability of chinook and coho salmon to detect and avoid abrupt differences
in dissolved oxygen concentrations was demonstrated by Whitmore et al. (1960).
In laboratory troughs, both species showed strong preference for oxygen levels
of 9 mg/i or higher over those near 1.5 mg/i; moderate selection against 3.0
mg/i was common and selection against 4.5 and 6.0 mg/i was sometimes detected.
The response of young Atlantic salmon and brown trout to low dissolved
oxygen depended on their age; larvae were apparently unable to detect and
avoid water of low dissolved oxygen concentration, but fry 6-16 weeks of age
showed a marked avoidance of concentrations up to 4 mg/i (Bishai, 1962).
Older fry (26 weeks of age) showed avoidance of concentrations up to 3 mg/i.
10

In a recent study of the rainbow trout sport fishery of Lake Taneycomo,
Missouri, Weithman and Haas (1984) have reported that reductions in minimum
daily dissolved oxygen concentrations below 6 mg/i are related to a decrease
in the harvest rate of rainbow trout from the lake. Their data suggest that
lowering the daily minimum from 6 mg/i to 5, 4, and 3 mg/i reduces the harvest
rate by 20, 40, and 60 percent, respectively. The authors hypothesized that
the reduced catch was a result of reduction in feeding activity. This mechan-
ism of action is consistent with Thatcher’s (1974) observation of lower
activity of coho salmon at 5 mg/i in laboratory growth studies and the finding
of Warren et al. (1973) that growth impairment produced by low dissolved
oxygen appears to be primarily a function of lower food intake.
A three-year study of a fishery on planted rainbow trout was published by
Heimer (1984). This study found that the catch of planted trout increased
during periods of low dissolved oxygen in American Falls reservoir, on the
Snake River in Idaho. The author concluded that the fish avoided areas of low
dissolved oxygen and high temperature and the increased catch rate was a
result of the fish concentrating in areas of more suitable oxygen supply and
temperature.
G.
-
Swimming
Effects of dissolved oxygen ‘concentrations on swimming have been demon-
strated by Davis et a. (1963). In their studies, the maximum sustained
swimming speeds (in the range of 30 to 45 cm/sec) of juvenile coho salmon were
reduced by 8.4, 12.7, and 19.9 percent at dissolved oxygen concentrations of
6, 5, and 4 mg/i, respectively. Over a temperature range from 10 to 20°C,
effects were slightly more severe at cooler temperatures. Jones (1971)
reported 30 and 43 percent reductions of maximal swimming speed of rainbow
trout at dissolved oxygen concentrations of 5.1 (14°C) and 3.8 (22°C) mg/i,
respectively. At lower swimming speeds (2 to 4 cm/sec), coho and chinook
salmon at 20°Cwere generally able to swim for 24 hours at dissolved oxygen
concentrations of 3 mg/i and above (Katz et al., 1958). Thus, the signif-
icance of lower dissolved oxygen concentrations on swimming depends on the
level of swimming performance required for the survival, growth, and reproduc-
tion of salmonids. Failure to escape from predation or to negotiate a swift
portion of a spawning migration route may be considered an indirect lethal
effect and, in this regard, reductions of maximum swimming performance can be
very important. With these exceptions, moderate levels of swimming activity
required by saimonids are apparently little affected by concentrations of
dissolved oxygen that are otherwise acceptable for growth and reproduction.
H. Field Studies
Field studies of salmonid populations are almost non-existent with
respect to effects of dissolved oxygen concentrations. ,Some of the systems
studied by Ellis (1937) contained trout, but of those river systems in which
trout or other salmonids were most likely (Columbia River and Upper Missouri
River) no stations were reported with dissolved oxygen concentrations below 5
mg/i, and 90 percent of the values exceeded 7 mg/i.
11

III. Non-Salmonids
The amount of data describing effects of low dissolved oxygen on non-
saimonid fish is more limited than that for salmonids, yet must cover a group
of fish with much greater taxonomic and physiological variability. Salmonid
criteria must provide for the protection and propagation of 38 species in 7
closely related genera; the non-salmon-id criteria must provide for the protec-
tion and propagation of some 600 freshwater species in over 40 diverse
taxonomic families. Consequently, the need for subjective technical judgment
is greater for the non-salmonids.
Many of the recent, most pertinent data have been obtained for ‘several
species of Centrarchidae (sunfish), northern pike, channel catfish, and the
fathead minnow. These data demonstrate that the larval stage is generally the
most sensitive life stage. Lethal effects on larvae have been observed at
dissolved oxygen concentrations that may only slightly affect growth of
juveniles of the same species.
A. Physiology
Several studies of the relationship between low dissolved oxygen concen-
trations and resting oxygen consumption rate constitute the bulk of the
physiological data relating to the effect of hypoxia on nonsalmonid fish. A
reduction in the resting metabolic rate of fish ,is generally believed to
represent a marked decrease in the scope for growth and• activity, a net
decrease in the supply of oxygen to the tissues, and perhaps a partial shift
to anaerobic energy sources. The dissolved oxygen concentration at which
reduction in resting metabolic rate first appears is termed the critical
oxygen concentration.
Studies with brown bullhead (Grigg, 1969), largemouth bass (Cech et al.
1979), and goldfish and carp (Beamish, 1964), produced estimates of critical
dissolved oxygen concentrations for these species. For largemouth bass, the
critical dissolved oxygen concentrations were 2.8 mg/i at 30°C, 2.6 mg/i at
25°C, and 2.3 mg/i at 20°C. For brown bullheads the critical concentration
was about 4 mg/i. Carp displayed critical oxygen concentrations near 3.4 and
2.9 mg/i -at 10 and 20°C,respectively, and goldfish critical concentrations of
dissolved oxygen were about 1.8 and 3.5 mg/i at 10 and 20°C, respectively. A
general summary of these data suggest critical dissolved oxygen concentrations
between 2 and 4 mg/l, with higher temperatures usually causing higher critical
concentrations.
-
Critical evaluation of the data of Beamish (1964) suggest that the first
sign of t-iypoxic stress is not the decrease in oxygen consumption, but rather
an increase, perhaps as a result of metabolic cost of passing an increased
ventilation volume over the gills. These increases were seen in carp at 5.8
mg/i at 20°Cand at 4.2 mg/i at 10°C.
B. Acute Lethal Concentrations
Based on the sparse data base describing acute effects of low dissolved
oxygen concentrations on nonsalmonids, many non—salmonids appear to be
considerably less sensitive than salmonids. Except for larval forms, no
12

non-salmonids appear to be more sensitive than saimonids. ‘Spoor (1977)
observed lethality of largemouth bass larvae at a dissolved oxygen concentra-
tion of 2.5 mg/i after only a 3-hr exposure. Generally, adults and juveniles
of all species studied survive for at least a few hours at concentrations of
dissolved oxygen as low as 3 mg/I. In most cases, no mortality results from
acute exposures to 3 mg/i for the 24- to 96-h duration of the acute tests.
Some non-salmonid fish appear to be able to survive a several-day exposure to
concentrations below 1 mg/i (Moss and Scott, 1961; Downing and Merkens, 1957),
but so little is known about the latent effects of such exposure that short—
term survival cannot now be used as an indication of acceptable dissolved
oxygen concentrations. In addition to the unknown latent effects of exposure
to very low dissolved oxygen concentrations, there are no data on the effects
of repeated short-term exposures. Most importantly, data on the tolerance to
low dissolved oxygen concentrations are available for only a few of the
numerous species of non-salmonid fish.
C. Growth
Stewart et al. (1967) conducted several growth studies with juvenile
iargemouth bass and observed reduced growth at 5.9 mg/i and lower concentra-
tions. Five of six experiments included dissolved oxygen concentrations
between 5 and 6 mg/i; dissolved oxygen concentrations of 5.1 and 5.4 mg/i
produced reductions in growth rate of 20 and 14 percent, respectively, but
concentrations of 5.8 and 5.9 mg/i had essentially no effect on growth. The
efficiency of food conversion was not reduced until dissolved oxygen concen-
trations were much lower, indicating that decreased food consumption was the
primary cause of reduced growth.
When channel catfish fingerlings held at 8, 5, and 3 mg/i were fed as
much as they could eat in three daily feedings, there were significant
reductions in feeding
arid weight gain
(22 percent) after a 6 week exposure to
5 mg/i (Andrews et al., 1973). At a lower feeding rate, growth after 14 weeks
was reduced only at 3 mg/i. Fish exposed to 3 mg/i swam lethargically, fed
poorly and had reduced response to loud noises. Raible (1975) exposed channel
catfish to several dissolved oxygen concentrations for up to 177 days and
observed a graded reduction in growth at each concentration below 6 mg/i.
However, the growth pattern for 6.8 mg/i was comparable to that at 5.4 mg/i.
He concluded that each mg/i increase in dissolved oxygen concentrations
between 3 and 6 mg/i increased growth by 10 to 13 percent.
Carlson et al. (1980) studied the effect of dissolved oxygen concentra-
tion on the growth of juvenile channel catfish and yellow perch. Over periods
of about 10 weeks, weight gain of channel catfish was lower than that of
control fish by 14, 39, and 54 percent at dissolved oxygen concentrations of
5.0, 3.4, and 2.1 mg/i, respectively. These differences were produced by
decreases
,
in growth rate of 5, 18, and 23 percent (JRB Associates, 1984),
pointing out the importance of differentiating between effects on weight gain
and effects~ on growth rate. When of sufficient duration, small reductions in
growth rate can have large effects on relative weight gain. Conversely, large
effects on growth rate may have little effect on annual weight gain if they
occur only over a small proportion of the annual growth period. Yellow perch
appeared to be more tolerant to low dissolved oxygen concentrations, with
reductions in weight gain of 2, 4, and 30 percent at dissolved oxygen concen-
trations of 4.9, 3.5, and 2.1 mg/i, respectively.
13

120
i ±I i ii
D
0
Largemouth Bass
C)
C.)
U
0
Black -Crappie
A
s~
White Sucker
V
White Bass
• Northern Pike
~
20
U
U Channel Catfish
-

Back to top


A
Walleye
S
VSmallmouth Bass
(I)
0_~,g~~I~l
I I I I III
2
3
4 5678910
Dissolved Oxygen (mg/L)
Figure 1. Effect of continuous exposure to various mean dissolved oxygen
concentrations on survival of embryonic and larval stages of eight
species of nonsalmonid fish. Minima recorded in these tests
averaged about 0.3 mg/i below the mean concentrations.
14-

-
The data of Stewart et al. (1967), Carison et a. (1980), and Adelman and
Smith (1972) were analyzed -to determine the relationship between growth rate
and dissolved oxygen concentration (JRB Associates, 1984). Yellow perch
appeared to be very resistant to influences of low dissolved oxygen concentra-
tions, northern pike may be about as sensitive as salmonids, while largemouth
bass and channel catfish are intermediate in their response (Table 4). The
growth rate relations modeled from Adelman and Smith are based on only four
data points, with none in the critical dissolved oxygen region from 3 to.5
rng/l. Nevertheless, these growth data for northern pike are the best avail-
able for nonsalmonid coidwater fish. Adelman and Smith observed about a 65
percent reduction in growth of juvenile northern pike after 6-7 weeks at
dissolved oxygen concentrations of 1.7 and 2.6 mg/i. At the next higher
concentration (5.4 mg/i), growth was reduced 5 percent.
Table 4. Percent reduction in growth rate of some nonsaimonid fish held at
various dissolved oxygen concentrations expressed as the median
value from n tests with each species (calculated from JRB
Associates, 1984).
Dissolved
Oxygen
(mg/i)
Species (number of tests)
Northern
Pike (1)
,
Largemouth
Bass (6)
Channel
Catfish (1),
Yellow
Perch (1)
900
0
0
810
0
0
740
1
0
690
3
0
5
16
1
7
0
4
25
9
13
0
3
35
17
20
7
2
--
51
29
22
Median
Temp (°C)
19
26
25
20
Brake (1972) conducted a series of studies on juvenile largemouth bass in
two artificial ponds to determine the effect of reduced dissolved oxygen
concentration on consumption of mosquitofish and growth during 10 2-week
exposures. The dissolved oxygen in the control pond was maintained near
air-saturation (8.3 to 10.4 mg/i) and the other pond contained mean dissolved
oxygen concentrations from 4.0 to 6.0 mg/i depending upon the individual test.
The temperature, held near the same level in both ponds for each test, ranged
from 13 to 27°C. Food consumption and growth rates of the juvenile bass,
maintained ‘on moderate densities of forage fish, increased with temperature
and decreased at the reduced dissolved oxygen concentrations except at 13°C.
Exposure to that temperature probably slowed metabolic processes of the bass
so much that their total metabolic rates were not limited by dissolved oxygen
except at very low concentrations. These largemouth bass studies clearly
support the idea that higher temperatures exacerbate the adverse effects of
15

low dissolved oxygen on the growth rate of fish (Table 5). Comparisons of
Brake’s pond studies with the laboratory growth studies of Stewart et a.
(1967) suggest that laboratory growth studies may significantly underestimate
the adverse effect of low dissolved oxygen on fish growth. Stewart’s six
studies with largemouth bass are summarized in Table 4 and Brake’s data are
presented in Table 5. All of Stewart’s tests were conducted at 26°C,about
the highest temperature in Brake’s studies, but comparison of the data show
convincingly that at dissolved oxygen concentrations between 4 and 6 mg/i the
growth rate of bass in ponds was reduced 17 to 34 percent rather than the 1 to
9 percent seen in the laboratory studies. These results suggest that the ease
of food capture in laboratory studies may result in underestimating effects of
low dissolved oxygen on growth rates in nature.
Table 5. Effect of temperature on the percent reduction in growth rate of
largemouth bass exposed to various dissolved oxygen concentrations
in ponds (after Brake, 1972; JRB Associates, 1984).
Temperature
(°C)
Percent Reduction in Growth Rate at
4.2 ±0.2 mg/i
4.9 ±0.2
mg/i
5.8 ±0.2 mg/i
13.3
0
--
13.6
--
--
,
7
16.3
--
18
--
16.7
--
--
15
18.1
--
19
--
18.6
--
34
--
18.7
18
--
—-
23.3
26
--
--
26.7
--
--
17
27.4
31
--
Brett and Blackburn (1981) reanalyzed the growth data previously pub-
lished by other authors for largemouth bass, carp, and coho salmon in addition
to their own results for young coho and sockeye salmon. They concluded for
all species that above a critical
level ranging from 4.0 to 4.5
mg/l,
decreases in growth rate and food conversion
efficiency were not statistically
significant in these tests of relatively short duration (6 to 8
weeks) under
the pristine conditions of laboratory testing.
EPA believes that a more
accurate estimate of the dissolved oxygen concentrations that have no effect
on growth and a
better estimate of concent~ation:effect relationships can be
obtained by curve-fitting procedures (JCB Associates, 1984) and by examining
these results from a large number of studies. Brett and Blackburn added an
additional qualifying statement that it was not the purpose of their study to
seek evidence on the acceptable level of dissolved oxygen in nature because of
the problems of environmental complexity involving all life stages and
functions, the necessary levels of activity to survive in a competitive world,
and the interaction of water quality (or lack of it) with varying dissolved
16

oxygen concentrations. Their cautious concern regarding the extrapolation to
the real world of results obtained under laboratory conditions is consistent
with that of numerous investigators.
D. Reproduction
-
A life-cycle exposure of the fathead minnow beginning with 1- to 2-month
old juveniles was conducted and effects of continuous low dissolved oxygen
concentrations on various life stages indicated that the most sensitive stage
was the larval stage (Brungs, 1971). No spawning occurred at 1 mg/i, and the
number of eggs produced per female was reduced at 2 mg/i but not at higher
concentrations. Where spawning occurred, the percentage hatch of embryos
(81-89 percent) was not affected when the embryos were exposed to the same
concentrations as their parents. Hatching time varied with temperature, which
was not controlled, but with decreasing dissolved oxygen concentration the
average incubation time increased gradually from the normal 5 to nearly 8
days. Mean larval survival was 6 percent at 3 mg/i and 25 percent at 4 mg/i.
Mean survival of larvae at 5 mg/l was 66 percent as compared to 50 percent at
control dissolved oxygen concentrations. However, mean growth of surviving
larvae at 5 mg/l was about 20 percent lower than control larval growth.
Siefert and Herman (1977) exposed mature black crappies to constant dissolved
oxygen concentrations from 2.5 mg/i to saturation and temperatures of 13-20°C.
Number of spawnings, embryo viability, hatching success, and survival through
swim-up were similar at all exposures.
E. Early Life Stages
Larval and juvenile non-saimonids are frequently more sensitive to
exposures to low dissolved oxygen than are other life stages. Peterka and
Kent (1976) conducted semi-controlled experiments at natural spawning sites of
northern pike, bluegill, pumpkinseed, and smallmouth bass in Minnesota.
Dissolved oxygen concentrations were measured 1 and 10 cm from the bottom,
with observations being made on hatching success and survival of embryos, sac
larvae, and, in some instances, larvae. Controlled exposure for up to 8 hours
was performed in situ in small chambers with the dissolved oxygen controlled
by nitrogen stripping. For all species tested, tolerance to short-term
exposure •to low concentrations decreased from embryonic to larval stages.
Eight-hour exposure of embryos and larvae’of northern pike to dissolved oxygen
concentrations caused no mortality of embryos at 0.6 mg/i but was 100 percent
lethal to sac-larvae and larvae. The most sensitive stage, the larval stage,
suffered complete mortality following 8 hours at 1.6 mg/i; the next higher
concentration, 4 mg/i, produced no mortality. Smailmouth bass were at least
as sensitive, with nearly complete mortality of sac-larvae resulting from
6-hour exposure to 2.2 mg/i, but no mortality occurred after exposure to 4.2
mg/i. Early life stages of bluegill were more hardy, with embryos tolerating
4-hour exposure to 0.5 mg/i, a concentration lethal to sac—larvae; sac-larvae
survived similar exposure to 1.8 mg/i, however. Because the most sensitive
stage of northern pike was the later larval stage, and because the younger
sac-larval stages of smallmouth bass and bluegill were the oldest stages
tested, the tests with these latter species may not have included the most
sensitive stage. Based on these tests, 4 mg/i is tolerated, at least briefly,
by northern pike and may be tolerated by smallmouth bass, but concentrations
as high as 2.2 mg/i are lethal.
17

Several studies have provided evidence of mortality or other significant
damage to young non-salmonids as a result of a few weeks exposure to dissolved
oxygen concentrations in the 3 to 6 mg/i range. Siefert et ai. (1973) exposed
-
larval northern pike to various dissolved oxygen concentrations at 15 and 19°C
and observed reduced survival at concentrations as high as 2.9 and 3.4 mg/l.
Most of the mortality at these concentrations occurred at the time the larvae
-
initiated feeding. Apparently the added stress of activity at that time or a
greater oxygen requirement for that life stage was the determining factor.
There was a marked decrease in growth at concentrations below 3 mg/i. In-a
similar study lasting 20 days, survival of walieye embryos and larvae was
reduced at 3.4 mg/i (Siefert and Spoor, 1974), and none survived at lower
concentrations. A 20 percent
reduction in the survival of srnalimouth bass
embryos and larvae occurred at a concentration of 4.4 mg/i (Siefert et al.,
1974) and at 2.5 mg/i all larvae died in the first 5 days after hatching. At
4.4 mg/i hatching occurred earlier than in the controls and growth among
survivors was reduced. Carlson and Siefert (1974) concluded that concentra-
tions from 1.7 to 6.3 mg/i reduced the growth of early stages of the large-
mouth bass by 10 to 20 percent. At concentrations as high as 4.5 mg/i,
hatching was premature and feeding was delayed; both factors could indirectly
influence survival, especially if other stresses were to occur simultaneously.
Carlson et a. (1974) also observed that embryos and larvae of channel catfish
are sensitive to low dissolved oxygen during 2— or 3-week exposures. Survival
at 25°Cwas slightly reduced at 5 mg/i and significantly reduced at 4.2 mg/l.
At 28°C survival was slightly reduced at 3.8, 4.6, and 5.4 mg/i; total
mortality occurred at 2.3 mg/l. At all reduced dissolved oxygen concentra-
tions at both temperatures, embryo pigmentation was lighter, incubation period
was extended, feeding was delayed, and growth was reduced. No effect of
dissolved oxygen concentrations as low as 2.5 mg/i was seen on survival of
embryonic and larval black crappie (Sieffert and Herman, 1977). Other
tolerant species are the white bass and the white sucker, both of which
evidenced adverse effect to embryo larva exposure only at dissolved oxygen
concentrations of 1.8 and 1.2 mg/i, respectively (Sieffert et al., 1974;
Sieffert and Spoor, 1974).
Data (Figure 1) on the effects of dissolved oxygen on the survival of
embryonic and larval •nonsalmonid fish show some species to be tolerant
(largemouth bass, white sucker, black crappie, and white bass) and others
nontoierant (channel catfish, waiieye, northern pike, smailmouth bass). The
latter three species are often included with salmonids in a grouping of
sensitive coidwater fish; these data tend to support that placement.
F. Behavior
Largemouth bass in laboratory studies (Whitmore et al., 1960) showed a
slight tendency to avoid concentrations of dissolved oxygen of 3.0 and 4.6
mg/l and a definite avoidance of 1.5 mg/i. Bluegills avoided a concentration
of 1.5 mg/i but not higher concentrations. The environmental significance of
such a response is unknown, but if large areas are deficient in dissolved
oxygen this avoidance would probably not greatly enhance survival. Spoor
(1977) exposed largemouth bass embryos and larvae to low dissolved oxygen for
brief exposures of afew hours. At 23 to 24°Cand 4 to 5 mg/i, the normally
quiescent, bottom-dwelling yolk-sac larvae became very active and swam
18

vertically to a few inches above the substrate. Such behavior in natural
systems would probably cause significant losses due to predation and simple
displacement from the nesting area.
G. Swimming
Effects of low dissolved oxygen on the swimming performance of largemouth
bass were studied by Katz et al. (1959) and Dahlberg et a. (1968). The
results in the former study were highly dependent upon season and temperature,
with summer tests at 25°Cfinding no effect on continuous swimming for 24 hrs
at 0.8 ft/sec unless dissolved oxygen concentrations fell below 2 mg/i. In
the fall, at 20°C,no fish were able to swim for a day at 2.8 mg/i, and in the
winter and 16° no fish swam for 24 hours at 5 mg/i. These results are
consistent with those seen in saimonids in that swimming performance appears
to be more sensitive to low dissolved oxygen at lower temperatures.
Dahlberg et ai. (1968) looked at the effect of dissolved oxygen on
maximum swimming speed at temperatures near 25°C. They reported slight
effects (less than 10 reduction in maximum swimming speed) at concentrations
between 3 and 4.5 mg/i, moderate reduction (16-20) between 2 and 3 mg/i and
severe reduction (30-50) at 1 to 1.5 mg/i.
H. Field Studies
Ellis (1937) reported results of field studies conducted at 982 stations
on freshwater streams and rivers during the months of June through September,
1930-1935. During this time, numerous determinations of dissolved oxygen
concentrations were made. He concluded that 5 mg/i appeared to be the lowest
concentration which may reasonably be expected to maintain varied warmwater
fish species in good condition in inland streams. Ellis (1944) restated his
earlier conclusion and also added that his study had included the measurement
of dissolved oxygen concentrations at night and various seasons. He did not
specify the frequency or proportion of diurnal or seasonal sampling, but the
mean number of samples over the 5-year study was about seven samples per
stati on.
Brinley (1944) discussed a 2-year biological’ survey of the Ohio River
Basin. He concluded that in the zone where dissolved oxygen is between 3 and
5 mg/i the fish are more abundant than at lower concentrations, but show a
tendency to sickness, deformity, and parasitization. The field results show
that the concentration of 5 mg/i seems to represent a general dividing line
between good and bad conditions for fish.
A three—year study of fish populations in the Wisconsin River indicated
that sport fish (percids and centrarchids) constituted a significantly greater
proportion of the fish population at sites Shaving mean summer dissolved oxygen
concentrations greater than 5 mg/i than at sites averaging below 5 mg/i
(Coble, 1982).
The differences could not be related to any observed habitat
variables other than dissolved oxygen concentration.
These three field studies all indicate that increases in dissolved oxygen
concentrations above 5 mg/i do not produce noteworthy improvements in the
composition, abundance, or condition of non-saimonid fish populations, but
19

that sites with dissolved oxygen concentrations below 5 mg/i have fish
assemblages with increasingly poorer population characteristics as the
dissolved oxygen concentrations become lower. It cannot be stressed too
strongly that these field studies lack definition with respect to the actual
exposure conditions experienced by the resident populations and the lack of
good estimates for mean and minimum exposure concentrations Over various
periods precludes the establishment of numerical criteria based on these
studies. The results of these semi—quantitative field studies are consistent
with the criteria derived later in this document.
IV. Invertebrates
As stated earlier, there is a general paucity of information on the
tolerance of the many forms of freshwater invertebrates to low dissolved
oxygen. Most available data describe the relationship between oxygen concen-
tration and oxygen consumption or short-term survival of aquatic larvae of
insects. These data are further restricted by their emphasis on species
representative of relatively fast-fl-owing mountain streams.
One rather startling feature of these data is the apparently -high
dissolved oxygen requirement for the survival of some species. Before
extrapolating from these data one should be cautious in evaluating the
respiratory mode(s) of the species, its natural environment, and the test
environment. Thus, many nongilled species respire over their. entire body
surface while many other species are gilled. Either form is dependent upon
the gradient of oxygen across the respiratory surface, a gradient at least
partially dependent upon the rate of replacement of the water immediately
surrounding the organism. Some insects, such as some members of the mayfly
genus, Baetis, are found on rocks in extremely swift currents; testing their
tolerance to low dissolved oxygen in iaboratory apparatus at slower flow rats
may contribute to their inability to survive at high dissolved oxygen concen-
trations. In addition, species of insects that utilize gaseous oxygen, either
from bubbles or surface atmosphere, may not be reasonably tested for tolerance
of hypoxia if their source of gaseous oxygen is deprived in the laboratory
tests.
In Spite of, these potential problems, the dissolved oxygen requirements
for the survival of many species of aquatic insects are almost certainly
greater than those of most fish species. Early indication of the high
dissolved oxygen requirements of some aquatic insects appeared in the research
of Fox et a. (1937) who reported critical dissolved oxygen concentrations for
mayfiy nymphs in a static test system. Critical concentrations for six
species ranged from 2.2 mg/i to 17 mg/l; three of the species had critical
concentrations in excess of air saturation. These data suggest possible
extreme sensitivity of some species and also the probability of unrealistic
conditions of water flow. More recent studies in water flowing at 10 cm/sec
indicate critical dissolved oxygen concentrations for four species of stonefly
are between 7.3 and 4.8 mg/i (Benedetto, 1970).
In a recent study of 22 species of aquatic insects, Jacob et al. (1984)
reported 2-5 hour LC5O values at unspecified “low to moderate” flows in a
stirred exposure chamber, but apparently with no flow of replacement water.
Tests were run at one or more of five temperatures from 12 to 30°C;some
20
-

species were tested at only one temperature, others at as many as four. The
median of the 22 species mean LC5Os was about 3 mg/l, with eight species
having an average LC5O below 1 mg/i and four in excess of 7 mg/i. The four
most sensitive species were two mayfly species and two caddisfly species. The
studies of Fox et a. (1937), Benedetto (1970), and Jacob et al. (1984) were
all conducted with European species, but probably have general relevance -to
North American habitats. A similar oxygen consumption study of a North
American stonefly (Kapoor and Griffiths, 1975) indicated a possible critical
dissolved oxygen concentration of about 7 mg/i at a flow rate of 0.32 cm/sec
and a temperature of 20°C.
One type of behavioral observation provides evidence of hypoxic stress in
-
aquatic insects. As dissolved oxygen concentrations decrease, many species of
aquatic insects can be seen to increase their respiratory movements, movements
that provide for increased water flow over the respiratory surfaces. Fox and
Sidney (1953) reported caddisfiy respiratory movements over a range of
dissolved oxygen from 9 to 1 mg/i. A dissolved oxygen decrease to 5 mg/i
doubled the number of movements and at 1 to 2 mg/i the increase was 3- to
4-fold.
-
Similar
data were published by Knight and Gaufin (1963) who studied a
stonefly common in the western United States. Significant increases occurred
-
below 5 mg/i at 16°Cand below 2 mg/i at 10°C. Increases in movements
occurred at higher dissolved oxygen concentrations when water flow was 1.5
cm/sec than 7.6 cm/sec, again indicating the importance o’f water flow rate on
the respiration of aquatic insects. A subsequent paper by Knight and Gaufin
(1965) indicated that species of stonefly lacking gills are more sensitive to
low dissolved oxygen than are gilled forms.
Two studies that provide the preponderance of the current data on the
acute effects of low dissolved oxygen concentrations on aquatic insects are
those of Gaufin (1973) and Nebeker (1972) which together provide reasonable
96-hr LC5O dissolved oxygen concentrations for 26 species of aquatic insects
(Table 6). The two studies contain variables that make them difficult to
compare or evaluate fully. Test temperatures~were 6.4°Cin Gauf in’s study and
18.5°C in Nebeker’s. Gaufin used a vacuum degasser while Nebeker used a
30-foot stripping column that probably produced an unknown degree of super-
saturation with nitrogen. The water velocity is not given in either paper,
although flow rates are given but test chamber dimensions are not clearly
specified. The overall similarity of the test results suggests that potential
supersaturation and iower flow volume in Nebeker’s tests did not have a
significant effect on the results.
Because half of the insect species tested had 96-h LCSO dissolved oxygen
concentrations between 3 and 4 mg/i it,appears that these species (collected
in Montana and Minnesota) would require at least 4 mg/i dissolved oxygen to
ensure their survival. The two most sensitive species represent surprisingly
diverse habitats, Ephemerelia doddsi is found in swift rocky streams and has
an LC5O of 5.2 mg/i while the pond mayfly, Callibaetis montanus, has an LC5O
of 4.4 mg/i. It is possible that the test conditions represented too slow a
flow for E. doddsi and too stressful flow conditions for C. montanus.
21

Table 6. Acutely lethal concentrations of dissolved oxygen to aquatic
insects.
-
-
Species
96-h LC5O
(mg/i)
Source*
Stonef~y
Acroneuria
pacifica
1.6 (H)**
-
G
-
Acroneuria lycorias
3.6
N
Acrynopté~yxaurea
3.3 (H)
G
Arcynopteryx parallela
Diura knowitoni
2 (H)
3.6 (1)
~
G
G
Nemoura cinctipes
3.3 (H)
G
Pteronarcys californica
3.9 (L)
G
Pteronarcys caiifornica
3.2 (H)
G
Pteronarcys dorsata
2.2
N
Pteronarcelia badia
Mayfly
2.4 (H)
.
G
Baetisca laurentina
3.5
N
Caliibaetjs mo~tanus
4.4 (L)
G
Ephemerelia doddsi
5.2 (L)
G
Ephemerella grandis
3.0 (H)
G
~phemereilasubvaria
3.9
.
N
Hexagenia limbata
1.8 (H)
G
Hexagenia limbata
1.4
N
LeptophTébia nebulosa
2.2
N
Caddi sfly
Brachycentrus occidentalis
2 (L)
1.8 (H)
G
Drusinus sp.
G
f~ydropsychesp.
3.6 (L)
G
~!ydropsychebetteri
2.9(21°C)
N
Hydropsyche betteri
2.6 (18.5°C)
N
Hydropsyche betteri
2.3 (17°C)
N
f~ydropsychebetteri
1.0 (10°C)
N
Lepidostoma sp.
3 (H)
G
Limnophilus ornatus
3.4 (L)
G
Neophylax sp.
3.8 (L)
G
Neothremma alicia
1.7 (L)
G
~jp~era
Simulium vittatum
3.2 (1)
G
Tanytarsus dissimilis
0.6
N
*
G
=
Gaufin (1973) —-
all tests at 6.4°C.
N
=
Nebeker (1972)
-- all tests at
18.5°Cexcept as noted/flow 125
mi/mm.
~ H
=
high flow (1000 mi/mm); L
=
low flow (500 mi/mm).
22

Other freshwater invertebrates have been subjected to acute hypoxic
stress and their LC5O values determined. Gaufin (1973) reported a 96—h LC5O
for the amphipod Gamnmnarus iimnaeus of 3 mg/i. Four other crustaceans were
studied by Sprague (1963) who reported the following 24-h LC5Os: 0.03 mg/i,
Aseilus intermedius 0.7 mg/i, fjyaleila azteca 2.2 mg/i, Gammarus ~eudo-
iimnaeus and 4.3 mg/i, Gammarus fasciatus. The range of acute sensitivitTés
of these species appears similar to that reported for aquatic insects.
There are few long-term studies of freshwater invertebrate tolerance to
low dissolved oxygen concentrations. Both Gaufin (1973) and Nebeker (1972)
conducted long-term survival studies with insects, but both are -questioned
because of -starvation and potential nitrogen supersaturation, respectively.
Gaufin’s data for eight Montana species and 17 Utah species suggest- that 4.9
mg/i and 3.3 mg/l, respectively, would provide for 50 percent survival for
from 10 to 92 days. Nebeker lists 30-d LC5O values for five species, four
between 4.4 and 5.0 mg/l and one 0.5 mg/i. Overall, these data indicate
that prolonged exposure to dissolved oxygen concentrations below 5 mg/i would
have deterimentai effects on a large proportion of the aquatic insects common
in areas like Minnesota, Montana, and Utah. Information from other habitat
types and geographic locations would provide a broader picture of invertebrate
dissolved oxygen requirements.
A more classic toxicological protocol was used by Homer and Wailer (1983)
in a study of the effects of low dissolved oxygen on Daphna magna. In a 26-d
chronic exposure test, they reported that 1.8 mg/i significantly reduced
fecundity and 2.7 mg/i caused a 17 percent reduction in final weight of
adults. No effect was seen at 3.7 mg/i.
In summarizing the state of knowledge regarding the relative sensitivity
of fish and invertebrates to low dissolved oxygen, it seems that some species
of insects and other crustaceans are killed at concentrations survived by all
species of fish tested. Thus, while most fish will survive exposure to 3
mg/i, many species of invertebrates are killed by concentrations as high as 4
mg/i. The extreme sensitivity of a few species of aquatic inects may be an
artifact of the testing environment. Those sensitive species common to swift
flowing, coidwater streams may require very high concentrations of dissolved
oxygen. -On the other hand, those stream habitats’are probably among the least
likely to suffer significant dissolved oxygen depletion.
Long-term impacts of hypoxia are less well known for invertebrates than
for fish. Concentrations adequate to avoid impairment of fish production
probably will provide reasonable protection for invertebrates as long as
lethal concentrations are avoided.
V. Other Considerations
A. Effects of Fluctuations
Natural dissolved oxygen concentrations fluctuate on a seasonal and daily
basis, while in most laboratory studies the oxygen levels are held essentially
constant. In two studies on the effects of daily oxygen cycles the authors
concluded that growth of fish fed unrestricted rations was markedly less than
would be estimated from the daily mean dissolved oxygen concentrations
23

(Fisher, 1963; Whitworth, 1968). The growth of these fish was only slightly
above that attainable during constant exposure to the minimum concentrations
of the daily cycles. A diurnal dissolved oxygen pulse to 3 mg/i for 8 hours
per day for 9 days, with a concentration of 8.3 mg/i for the remainder of the
time, produced a significant stress pattern in the serum protein fractions of
bluegill and iargemouth bass but not yellow bullhead (Bouck and Bail, 1965).
During periods of low dissolved oxygen the fish lost their natural color,
increased their ventilation rate, and remained very quiet. At these times
food was ignored. Several times, during the low dissolved oxygen concentra-
tion part of the cycle, the fish vomited food which they had eaten as much as
12 hours earlier. After comparable exposure of the rock bass, Bouck (1972)
observed similar results on electrophoretic patterns and feeding behavior.
Stewart et al. (1967) exposed juvenile largemnouth bass to patterns of
diurnally—variable dissolved oxygen concentrations with daily minima near 2
mg/i and daiiy maxima from 4 to 17 mg/i. Growth under any fluctuation pattern
was almost always less than the growth that presumably would have occurred had
the fish been held at a constant concentration equal to the mean concentra-
tion.
• Carison et al. (1980) conducted constant and diurnally fluctuating
exposures with juvenile channel catfish and yellow perch. At mean constant
concentrations of 3.5 mg/i or less, channel catfish consumed less food and
growth was significantly reduced. Growth of this species was not reduced at
fluctuations from about 6.2 to- 3.6 and 4.9 to 2 mg/i, b-ut was significantly
impaired at a fluctuation from about 3.1 to 1 mg/i. Similarly, at mean
constant concentrations near 3.5 mg/i, yellow perch consumed less food but
growth was not impaired until concentrations were near 2 mg/i. Growth was not
affected by fluctuations from about 3.8 to 1.4 mg/i. No dissolved oxygen-
related mortalities were observed. In both the channel catfish and the yellow
perch experiments, growth rates during the tests with fluctuating dissolved
oxygen were considerably below the rate attained in the constant exposure
tests. As a result, the fluctuating and constant exposures could not be
compared. Growth would presumably have been more sensitive in the fluctuating
tests if there had been higher rates of control growth.
MatUre black crappies were exposed to constant and fluctuating dissolved
oxygen concentrations (Carison and Herman, 1978). Constant concentrations
were near 2.5, 4, 5.5, and 7 mg/i and fluctuating concentrations ranged from
0.8 to 1.9 mg/i above and below these original concentrations. Successful
spawning occurred at all exposures except the fluctuation between 1.8 and 4.1
mg/i.
In considering daily or longer-term cyclic exposures to low dissolved
oxygen concentrations, the minimum values may be more important than the mean
levels. The importance of the daily minimum as a determinant of growth rate
is common to the results of Fisher (1963), Stewart (1967), and Whitworth
(1968). S’ince annual low dissolved oxygen concentrations normally occur
during warmer months, the significance of reduced growth rates during the
period in question must be considered. If growth rates are normally low, then
the effects of low dissolved oxygen concentration on growth could be minimal;
if normal growth rates are high, the effects could be significant, especially
if the majority of the annual growth occurs during the period in question.
24

B. Temperature and Chemical Stress
When fish were exposed to lethal temperatures, their survival times were
reduced when the dissolved oxygen concentration was lowered from 7.4 to 3.8
mg/i (Alabaster and Welcomme, 1962). Since high temperature and low dissolved
oxygen commonly occur together in natural environments, this likelihood of
additive or synergistic effects of these two potential stresses is a most
important consideration.
-
High temperatures almost certainly increase the adverse effects of low
dissolved oxygen concentrations. However, the spotty, irregular acute
lethality data base provides little basis for quantitative, predictive
analysis. Probably the most complete study is that on rainbow trout, perch,
and roach conducted by Downing and Merkens (1957). Because their study was
spread over an 18-month period, seasonal effects could have influenced the
effects at the various test temperatures. Over a range from approximately 10
to 20°C, the lethal dissolved oxygen concentrations increased by an average
factor of about 2.6, ranging from 1.4 to 4.1 depending on fish species tested
and test duration. The influence of temperature on chronic effects, of low
dissolved oxygen concentrations are not well known, but requirements for
dissolved oxygen probably increase to some degree with increasing temperature.
-This generalization -is supported by analysis of saimon studies reported by
Warren et al. (1973) and the largemouth bass studies of Brake (1972).
Because most laboratory tests are conducted at temperatures near the
mid-range of a species temperature tolerance, criteria based on these test
-
data will tend to be under-protective at higher temperatures and over-
protective at lower temperatures. Concern for this temperature effect was a
consideration in establishing these criteria, especially in the establishing
of those criteria intended to prevent short-term lethal effects.
A detailed discussion and model for evaluating interactions among
temperature, dissolved oxygen, ammonia, fish size, and ration on the resulting
growth of individual fish (Cuenco et al., 1985a,b,c) provides an excellent,
in-depth evaluation of potential effects of dissolved oxygen on fish growth.
Several laboratory studies evaluated the effect of reduced dissolved
oxygen concentrations on the toxicity of various chemicals, some of which
occur commonly in oxygen-demanding wastes. Lloyd (1961) observed that the
toxicity of zinc, lead, copper, and monohydric phenols was increased at
dissolved oxygen concentrations as high as approximately 6.2 mg/i as compared
to 9.1 mg/i. At 3.8 mg/l, the toxic effect of these chemicals was even
greater. The toxicity of ammonia was enhanced by low dissolved oxygen more
than that of other toxicants. Lloyd theorized that the increases in toxicity
of the chemicals were due to increased ventilation at low, dissolved oxygen
concentrations; as a consequence of increased ventilation, more water, and
therefore more toxicant, passes the fish’s gills. Downing and Merkens (1955)
reported that survival times of rainbow trout at lethal ammonia concentrations
increased markedly over a range of dissolved oxygen concentrations from 1.5 to
8.5 mg/i. Ninety-six-hr LC5O values for rainbow trout indicate that ammonia
became more toxic with decreasing dissolved oxygen concentrations from 8.6 to
2.6 mg/i (Thurston et al., 1981). The maximum increase in toxicity was by
about a factor of 2. They also compared ammonia LC5O values at reduced
25

dissolved oxygen concentrations after’12, 24, 48, and 72 hrs. The shorter the
time period, the more pronounced the positive relationship between the LC5O
and dissolved oxygen concentration. The authors recommended that dissolved
oxygen standards for the protection of salmonids should reflect background
concentrations of ammonia which may be present and the likelihood of temporary
increases in those concentrations. Adelman and Smith (1972) observed that
decreasing dissolved oxygen concentrations increased the toxicity of hydrogen
sulfide to goldfish. When the goldfish were acclimated to the reduced-
dissolved oxygen concentration before the exposure to hydrogen sulfide began,
mean 96-hr LC5O values were 0.062 and 0.048 mg/i at dissolved oxygen concen-
trations of 6 and 1.5 mg/i, respectively. When there was no prior acclima-
tion, the LC5O values were 0.071 and 0.053 mg/i at the same dissolved oxygen
concentrations. These results demonstrated a less than doubling in -toxicity
of hydrogen sulfide and little difference with regard to prior acclimation to
reduced dissolved oxygen concentrations. Cairns and Scheier (1957) observed
that bluegiiis were less tolerant to zinc, naphthenic acid, and potassium
cyanide at periodic low dissolved oxygen concentrations. Pickering (1968)
reported that an increased mortality of bluegilis exposed to zinc resulted
from the added stress of low dissolved oxygen concentrations. The difference
in mean LC5O vaiues between low (1.8 mg/i) and high (5.6 mg/i) dissolved
oxygen concentrations was a factor of 1.5.
Interactions between other stresses and low dissolved oxygen concentra-
tions can greatly increase mortality of trout larvae. For example, sublethal
concentrations of pentachlorophenol and oxygen combined to produce 100 percent
mortality of trout larvae held at an oxygen concentration of 3 mg/i (Chapman
and Shumway, 1978). The survival of chinook salmon embryos and larvae reared
at marginally high temperatures was reduced by any reduction in dissolved
oxygen, especially at concentrations below 7 mg/i (Eddy, 1972).
In general, the occurrence of toxicants in the water mass, in combination
with low dissolved oxygen concentration, may lead to a potentiation of stress
responses on the part of aquatic organisms (Davis, 1975a,b). Doudoroff and
Shumway (1970) recommended that the disposal of toxic pollutants must be
controlled so that their concentrations would not be -unduly harmful at
prescribed, acceptable concentrations of dissolved oxygen, and these accept-
able dissolved oxygen concentrations should be ‘independent of existing or
highest permitted concentrations of toxic wastes.
-
C. Disease Stress
In a study of 5 years of case records at fish farms, Meyer (1970)
observed that incidence of infection with Aeromonas iiquefasciens (a common
bacterial pathogen of fish) was most prevalent during June, July, and August.
He considered low oxygen stress to be a major factor in outbreaks of Aeromonas
disease during summer months. Haley et al. (1967) concluded that a kill of
American and threadfin shad in the San Joaquin River occurred as a result of
Aeromonas infection the day after the dissolved oxygen was between 1.2 and 2.6
mg/i. In this kill the lethal agent was Aeromonas but the additional stress
of the low dissolved oxygen may have been a significant factor.
26

Wedemeyer (1974) reviewed the role of stress as a predisposing factor in
fish diseases and concluded that facultative fish pathogens are continuously
present in most- waters. Disease problems seldom occur, however, unless
environmental quality and the host defense systems of the fish also deter-
iorate. He listed furunculosis, Aeromonad and Pseudomonad hemorrhagic
septicemia, and vibriosis as diseases for which low dissolved oxygen is one
environmental factor predisposing fish to epizootics. He stated that to
optimize fish health, dissolved oxygen concentrations should be 6.9 mg/l or
higher. Snieszko (1974) also stated that outbreaks of diseases are probably
more likely if the occurrence of stress coincides with the presence of
pathogenic microorganisms.
VI. Conclusions
-
-The primary determinant for the criteria is laboratory data describing
effect on growth, with developmental rate and survival included in embryo and
larva production levels. For the purpose of deriving criteria, growth in the
laboratory and production in nature are considered equally sensitive to-low
dissolved oxygen. Fish production in natural communities actually may be
significantly more, or less, sensitive than growth in the laboratory-, which
represents only one simplified facet of production.
The dissolved oxygen criteria are based primarily on data developed in
the laboratory under conditions which are usually artificial in several
important respects. First, they routinely preclude or minimize most environ-
mental stresses and biological interactions that under natural conditions are
iikely to increase, to a variable and unknown extent, the effect of low
dissolved oxygen concentrations. Second, organisms are usually given no
L
opportunity to acclimate to low dissolved oxygen concentrations prior to tests
nor can they avoid the test exposure. Third, food availability is unnatural
because the fish have easy, often unlimited, access to food without signif-
icant energy expenditure for search and capture. Fourth, dissolved oxygen
concentrations are kept nearly constant so that each exposure represents both
a minimum and an average concentration. This circumstance complicates
application of the data to natural systems with fluctuating dissolved oxygen
concentrations.
Considering the latter problem only, if the laboratory data are applied
H-
directly as minimum allowable criteria, the criteria will presumably be higher
than necessary because the mean dissolved oxygen concentration will often be
significantly higher than the criteria. If applied as a mean, the criteria
could allow complete anoxia and total mortality during brief periods of very
low dissolved oxygen or could allow too many consecutive daily minima near the
lethal threshold. If only a minimum or a mean can be given as a general
criterion, the minimum must be chosen because averages are too independent of
the extremes.
Obviously, biological effects of low dissolved oxygen concentrations
depend upon means, minima, the duration and frequency of the minima, and the
period of averaging. In many respects, the effects appear to be independent
of the maxima; for example, including supersaturated dissolved oxygen values
in the average may produce mean dissolved oxygen concentrations that are
misleadingly high and-unrepresentative of the true biological stress of the
dissolved oxygen minima.
-
27

Because most experimental exposures have been constant, data on the
effect of exposure to fluctuating dissolved oxygen concentrations is sketchy.
The few fluctuating exposure studies have used regular, repeating daily cycles
of an on-off nature with 8 to 16 hours at low dissolved oxygen and the
remainder of the 24 hr period at intermediate or high dissolved oxygen. This
is an uncharacteristic exposure pattern, since most daiiy dissolved oxygen
cycles are of a sinusoidal curve shape and not a square-wave variety.
The existing data allow a tentative theoretical dosing model for fluctu-
ating dissolved oxygen only as applied to fish growth. The EPA believes that
the data of Stewart et a. (1967) suggest that effects on growth are reason-
ably represented by calculating the mean of the daily cycle using as’ a maximum
value the dissolved oxygen concentration which represents the threshold effect
concentration during continuous exposure tests. For example, with an effect
threshold of 6 mg/i, all values in excess of 6 mg/i should be averaged as
though they were 6 mg/i. Using this procedure, the growth effects appear to
be a reasonable function of the mean, as long as the minimum is not lethal.
-Lethal thresholds are highly dependent upon exposure duration, species, age,
-
life stage, temperature, and a wide variety of other factors. Generally the
threshold is between 1 and 3 mg/i.
A most critical-and poorly documented aspect of a dissolved oxygen cri-
terion is the question of acceptable and unacceptable minima during dissolved
oxygen cycles of varying periodicity. Current ability to predict effects of
exposure to a constant dissolved oxygen level is only fair; the effects of
regular, daily dissolved oxygen cycies can only be poorly estimated; and
predicting the effects of more stochastic patterns of dissolved oxygen
fluctuations requires an ability to integrate constant and cycling effects.
Several general conclusions result from the synthesis of available field
and iaboratory data. Some of these conclusions differ from earlier ones in
the literature, but the recent data discussed in this document have provided
additional detail and perspective.
°
Naturally-occurring dissolved oxygen concentrations may occasionally fall
beiow target criteria levels due to a combination of low flow, high
temperature, and natural oxygen demand. These naturally-occurring’
conditions represent a normal situation in which the productivity of fish
or other aquatic organisms may not be the maximum possible under ideal
circumstances, but which represent the maximum productivity under the
particular set of natural conditions. Under these circumstances the
numerical criteria should be considered unattainable, but naturally—
occurring conditions which fail to meet criteria should not be inter-
preted
as violations of criteria. Although further reductions in dis-
solved oxygen may be inadvisable, effects of any reductions should be
compared to natural ambient conditions and not to ideal conditions.
o
Situations during which attainment of appropriate criteria is most
critical include periods when attainment of high fish growth rates is a
priority, when temperatures approach upper-lethal levels, when pollutants
are present in near-toxic quantities, or when other significant stresses
are suspected.
-
28

Reductions in growth rate produced by a given low dissolved oxygen
concentration are probably more severe as temperature increases. Even
during periods when growth rates are normally low, high temperature
stress increases the sensitivity of aquatic organisms to disease and
toxic pollutants, making the attainment of proper dissolved oxygen
criteria particularly important. For these reasons, periods of highest
temperature represent a critical portion of the year with respect to
dissolved oxygen requirements.
o
In salmonid spawning habitats, intergravei dissolved oxygen concentra-
tions are significantly reduced by respiration of fish embryos -and other
organisms. Higher water column concentrations of dissolved oxygen are
required to provide protection of fish embryos and larvae which develop
in the intergravel environment. A 3 mg/i difference is used in the
criteria to account for this factor.
The early life stages, especialiy the larval stage, of non-saimonid fish
are usually most sensitive to reduced dissolved oxygen stress. Delayed
development, reduced larval survival, and reduced larval and post—larval
growth are the observed effects. A separate early life stage criterion
for non-salmonids is established to protect these more sensitive stages
and is to apply from spawning through 30 days after hatching.
Other life stages of- salmonids appear to be somewhat more sensitive than
other life stages of the non-salmonids, but this difference, resulting in,
a 1.0 mg/i difference in the criteria for other life stages, may be due
to a more complete and precise data base for saimonids. Also, this
difference is at least partially due to the colder water temperatures at
which salmonid tests are conducted and the resultant higher dissolved
oxygen concentration in oxygen-saturated control water.
Few appropriate data are available on the effects of reduced dissolved
oxygen on freshwater invertebrates. However, historical concensus states
that, if all life stages of fish are protected, the invertebrate commu-
nities, although not necessarily unchanged, should be adequately pro-
tected. This is a generalization to which there may be exceptions of
environmental significance. Acutely lethal concentrations of dissolved
oxygen appear to be higher for many aquatic insects than for fish.
Any dissolved oxygen criteria should include absolute minima to prevent
mortality due to the direct effects of hypoxia, but such minima alone may
not be sufficient protection for the long-term persistence of sensitive
populations under natural conditions. Therefore, the criteria minimum
must also provide reasonable assurance that regularly repeated or
prolonged exposure for days or weeks at the allowable minimum will avoid
significant physiological stress of sensitive organisms.
Several earlier dissolved oxygen criteria were presented in the form of a
family of curves (Doudoroff and Shumway, 1970) or equations (NAS/NAE, 1973)
which yielded various dissolved oxygen requirements depending on the quali-
tative degree of fishery protection or risk deemed suitable at a given site.
Although dissolved oxygen concentrations that risk significant loss of fishery
production are not consistent with the intent of water quality criteria, a
29

qualitative protection/risk assessment for a range of dissolved oxygen
concentrations has considerable value to resource managers. Using qualitative
descriptions similar to those presented in earlier criteria of Doudoroff and
Shumway (1970) and Water Quality Criteria 1972 (NAS/NAE, 1973), four levels of
risk are listed below:
No Production Impairment. Representing nearly maximal protection of fishery
resources.
Slight Production Impairment. Representing a high level of protection of
important fishery resources, risking only slight impairment of production
in most cases.
-
Moderate Production Impairment. Protecting the persistence of existing fish
populations but causing considerable loss of production.
Severe Production Impairment. For low level protection of fisheries of some
value but whose protection in comparison with other water uses cannot be
a major objective of pollution control.
• Selection of dissolved oxygen concentrations equivalent to each of these
levels of effect requires some degree of judgment based largely upon examina-
tion of growth and survival data, generalization of response curve shape, and
assumed applicability of laboratory responses to natural populations. Because
nearly all data on the effects of low dissolved oxygen on aquatic organisms
relate to continuous exposure for relatively short duration (hours to weeks),
the resultant dissolved oxygen concentration-biological effect estimates are
most applicable to essentially constant exposure levels, although they may
adequately represent mean concentrations as well.
The production impairment values are necessarily subjective, and the
definitions taken from Doudoroff and Shumway (1970) are more descriptive than
the accompanying terms “slight,” “moderate,” and “severe.” The impairment
values for other life stages are derived predominantly from the growth data
summarized in the text and tables in Sections II and III. In general, slight,
-
moderate, and severe impairment are equivalent to 10, 20, and 40 percent
growth impairment, respectively. Growth impairment of 50 percent or greater
is often accompanied by mortality, and conditions allowing a combination of
severe growth impairment and mortality are considered as no protection.
Production impairment levels for early life stages are quite subjective
and should be viewed as convenient divisions of the range of dissolved oxygen
concentrations between the acute mortality ‘limit and the no production
impairment concentrations.
Production impairment values for invertebrates are based on survival in
both long-term and short-term studies. There are no studies of warmwater
species and few of lacustrine species.
The following is a summary of the dissolved oxygen concentrations (mg/i)
judged to be equivalent to the various qualitative levels of effect described
earlier; the value cited as the acute mortality limit is the minimum dissolved
oxygen concentration deemed not to risk direct mortality of sensitive
organisms:
-
30

1. Salmonid Waters
-
a. Embryo and Larval Stage5
o
No Production Impairment
=
11* (8)
°
Siight Production Impairment
9* (6)
o
Moderate Production Impairment B~(5)
o
Severe Production Impairment
=
7* (4)
o
Limit to Avoid Acute Mortality
=
6* (3)
-
(* Note: These are water column concentrations recommended to achieve the
required intergravel dissolved oxygen concentrations shown in
parentheses. The 3 mg/i difference is discussed in the criteria
document.)
b. Other Life Stages
o
No Production Impairment
=
8
°
Slight Production Impairment
6
°
Moderate Production Impairment 5
°
Severe Production Impairment
=
4
°
Limit to Avoid Acute Mortality
=
3
2. Nonsalmonid Waters
a. Early Life Stages
°
No Production Impairment
=
6.5
o
Slight Production Impairment
=
5.5
o
Moderate Production Impairment
=
5
°
Severe Production Impairment
=
4.5
o
Limit to •Avoid Acute Mortality
=
4
b. Other Life Stages
°
No Production Impairment
6
0
Slight Production Impairment
=
5
o
Moderate Production Impairment
4
°
Severe Production Impairment
=
3.5
°
Limit to Avoid Acute Mortality
=
3
3. Invertebrates
o
No Production Impairment
=
8
°
Some Production Impairment
=
5
°
Acute Mortality Limit
=
4
Added Note
Just
prior to final publication of this criteria document, a paper
appeared (Sowden and Power, 1985) that provided an interesting field valida-
tion of the salmonid early life stage criterion and production impairment
estimates. A total of 19 rainbow trout redds were observed for a number of
31

parameters including percent survival of embryos, dissolved oxygen concentra-
tion, and calculated intergravel water velocity. The results cannot be
considered a rigorous’ evaluation of the criteria because of the paucity of
dissolved oxygen determinations per redd (2-5) and possible inaccuracies in
determining percent survival and velocity. Nevertheless, the qualitative
validation is striking.
The generalization drawn from Coble’s (1961) study that good survival
occurred when mean intergravel dissolved oxygen concentrations exceeded 6.0
mg/i and velocity exceeded 20 cm/hr was confirmed; 3 of the 19 redds met this
criterion and averaged 29 percent embryo survival. The survival in the other
16 redds averaged only 3.6 percent. The data from the study are summarized in
Table 7. The critical intergravel water velocity from this study appears to
be about 15 cm/hr. Below this velocity even apparently good dissolved oxygen
Table 7. Survival of rainbow trout embryos as a function of intergravel
dissolved oxygen concentration and water velocity (Sowden and Power,
1985) as compared to dissolved oxygen concentrations established as
criteria or estimated as producing various levels of production
-
impairment.
-
Dissolved Oxygen
Concentration
mg/i
Percent
Water
Velocity,
Mean
Survival
(Flow
Criteria Estimates
Mean Minimum
Survival
cm/hr
15 cm/hr)
Exceeded Criteria
8.9
8.0
22..
53.7
-
7.7
7.0
7.0
6.4
6.9
5.4
43.5
1.1
21.3
83.2
9.8
20.6
29.0
Sli~htProduction
7.4
4.1
0.5
7.2
Impairment
7.1
4.3
21.5
16.3
.
6.7
4.5
6.4
4.2
6.0
4.2
4.3
0.3
-
9.6
5.4
7.9
17.4
15.6
Moderate Production 5.8
3.1
13.4
21.6
Impairment
5.3
3.6
5.2
3.9
5.6
0.4
16.8
71.0
6.5
Severe Production
4.6
4.1
0.9
18.3
0.9
Impairment
4.2
3.3
0.0
0.4
Acute Mortality
-
3.9
2.9
3.6
2.1
2.7
1.2
2.4
0.8
2.0
0.8
0.0
0.0
0.0
0.0
0.0
111.4
2.6
4.2
1.1
192.0
-
0.0
32

characteristics do not produce reasonable survival. At water velocities in
excess of 15 cm/hr the average percent survival in the redds that had
dissolved oxygen concentrations that met the criteria was 29.0 percent. There
was no survival in redds that had dissolved oxygen minima below the acute
mortality limit. Percent survival in redds with greater than 15 cm/hr flow
averaged 15.6, 6.5, and 0.9 percent for redds meeting slight, moderate, and
severe production impairment levels, respectively.
Based on an average redd of 1000 eggs, these mean percent survivals woUld
be equivalent to 290, 156, 65, 9, and 0 viable larvae entering the environment
to produce food for other fish, catch for fishermen, and eventually a new
generation of spawners to replace the parents of the embryos in the redd.
Whether or not these survival numbers ultimately represent the impairment
definitions is moot in the light of further survival and growth uncertainties,
but the quantitative field results and the qualitative and quantitative
impairment and criteria values are surprisingly similar.
VII. National Criterion
The natioñál criteria for ambient dissolved oxygen concentrations for the
protection of freshwater aquatic life are presented in Table 8. The criteria
are derived from the production impairment estimates on the preceding page
which are in turn based primarily upon growth data and information on tempera-
ture, disease, and pollutant stresses. The average dissolved oxygen concen-
trations selected are values 0.5 mg/i above the slight production impairment
values and represent values between no production impairment and slight
production impairment. Each criterion may thus be viewed as an estimate of
the threshold concentration below which detrimental effects are expected.
Criteria for coldwater fish are intended to apply to waters containing a
population of one or more species in the family Salmonidae (Bailey et a.,
-
1970) or to waters containing other coidwater or coolwater fish deemed by the
user to be closer to salmonids in sensitivity than to most warmwater species.
Although the acute lethal -limit for salmonids is at or below 3 mg/i, the
coldwater minimum has been established at 4 mg/i because a significant
proportion of the insect species common to salmonid habitats are less tolerant
of acute exposures to low dissolved oxygen than are salmonids. Some coolwater
species may require more protection than that afforded by the other life stage
criteria for warmwater fish and it may be desirable to protect sensitive
coolwater species with the coidwater criteria. Many states have more
stringent dissolved oxygen standards for cooler waters, waters that contain
either salmonids, nonsalmonid coolwater fish, or the sensitive centrarchid,
the smalimouth bass. The warmwater criteria are necessary to protect early
life stages of warmwater fish as sensitive as channel catfish and to protect
other life stages of fish as sensitive as largemouth bass. Criteria for early
life stages are intended to apply only where and when these stages occur.
These criteria represent dissolved oxygen concentrations which EPA believes
provide a reasonable and adequate degree of protection for freshwater aquatic
ii fe.
The criteria do not represent assured no-effect levels. However, because
the criteria represent worst case conditions (i.e., for wasteload allocation
and waste treatment plan design), conditions will be better than the criteria
-
33-

Tabie 8. Water quality criteria for ambient dissolved oxygen concentration.
Coldwater Criteria
Warmwater Criteria
Early Life
Stages1’2
Other Life
Stages
Early Life
Stages2
Other Life
Stages
30 Day Mean
NA3
6.5
NA
5.5
7 Day Mean
9.5 (6.5)
NA
6.0
NA
7 Day Mean
Minimum
NA
5.0
NA
4.0
-
1 Day Minimum4’5
8.0 (5.0)
4.0
5.0
3.0
1
These are water column concentrations recommended to achieve the required
intergravel dissolved oxygen concentrations shown in parentheses. The 3
mg/i differential is discussed in the criteria document. For species-that
have early life stages exposed directly to the -water column, the figures in
parentheses apply.
2
Includes all embryonic and larval stages and all juvenile forms to 30-days
following hatching.
~ NA (not applicable).
~ For highly manipulatable discharges, further restrictions apply (see page
37)
~ All minima should be considered as instantaneous concentrations to be
achieved at all times.
nearly all the time at most sites. In situations where criteria conditions
are just maintained for considerable periods, the criteria represent some risk
of production impairment. This impairment would probably be slight, but would
depend on innumerable other factors. If slight production impairment or a
small but undefinable risk of moderate production impairment is unacceptable,
then continuous exposure conditions should use the no production impairment
values as means and the slight production impairment values as minima.
The criteria represent annual worst case dissolved oxygen concentrations
believed to protect the more sensitive populations of organisms against
potentially damaging production impairment. The dissolved oxygen concentra-
tions in the criteria are intended to be protective at typically high seasonal
environmental temperatures for the appropriate taxonomic and life stage
classifications, temperatures which are often higher than those used. in the
research from which the criteria were generated, especially for other than
early life stages.
-
34

Where natural conditions alone create dissolved oxygen concentrations
less than 110 percent of the applicable criteria means or minima or both, the
minimum acceptable concentration is 90 percent of the natural concentration.
These values are similar to those presented graphically by Doudoroff and
Shumway (1970) and those calculated from Water Quality Criteria 1972 (NAS/NAE,
1973). Absolutely no anthropogenic dissolved oxygen depression in the
potentially lethal area below the 1-day minima should be allowed unless
special care is taken to ascertain the tolerance of resident species to low
dissolved oxygen.
-
-
If daily cycles of dissolved oxygen are essentially sinusoidal, a
reasonable daily average is calculated from the day’s high and low dissolved
oxygen values. A time—weighted average may be required if the dissolved
oxygen cycles are decidedly non-sinusoidal. Determining the magnitude of
daily dissolved oxygen cycles requires
at least two appropriately timed
measurements daily, and characterizing the shape
of the cycle requires several
more appropriately spaced measurements.
Once a series -of daily mean dissolved oxygen concentrations are calcu-
lated, an average of these daily means can be calculated (Table 9).
-
For
embryonic, larval, and early life stages, the averaging period should not
exceed 7 days. This short time is needed to adequately protect these often
Table 9. Sample calculations for determining daily means, and 7—day mean
dissolved oxygen concentrations (30-day averages are calculated in a
similar fashion using 30 days data).
Dissol ved Oxygen (mg/1)
Day
Daily Max.
Daily Mm.
Daily Mean
12
-
10.09.0
3
11.0
4
12~0a
5
10.0
6
11.0
7
120a
7.0
7.0
8.0
8.0
8.0
10.09.0
8.0
8.5
9.5
9.5
-
9.0
10.0
lO.5c
X
57.0
65.0
1-day Minimum
7.0
7-day Mean Minimum
8.1
7—day Mean
-
9.3
a Above air saturation concentration
b example).
(11.0
+
8.0) ÷2.
-
C
(110 +10.0)
÷
2.
(assumed
.
to be 11.0 mg/i--for this
35

short duration, most sensitive life stages. Other life stages can probably be
adequately protected by 30-day averages. Regardless of the averaging period,
the average should be considered a moving average rather than a calendar-week
or calendar-month average.
The criteria have been established on the basis that the maximum dis-
solved oxygen value actually used in calculating any daily mean should not
exceed the air saturation value. This consideration is based primarily on
analysis of studies of cycling dissolved oxygen and the growth of largernouth
bass (Stewart et al., 1967), which indicated that high dissolved oxygen levels
( 6 mg/i) had no beneficial effect on growth.
During periodic cycles of dissolved oxygen concentrations, minima lower
than acceptable constant exposure levels are tolerable so long as:
1. the average concentration attained meets or exceeds the criterion;
2. the average dissolved oxygen concentration is calculated as recommended
in Table 9; and
3.
-
the minima are not unduly stressful and clearly are not lethal.
A daily minimum has been included to make certain that no acute mortality
of sensitive species occurs as a result of lack of oxygen. Because repeated
exposure to dissolved oxygen concentrations at or near the acute lethal
threshold will be stressful and because stress can indirectly produce mortal-
ity or other adverse effects (e.g., through disease), the criteria are
designed to prevent significant episodes of
continuous
or regularly recurring
exposures to dissolved oxygen concentrations at or near the lethal threshold.
This protection has been achieved by setting the daily minimum for early life
stages at the subacute lethality threshold, by the use of a 7-day averaging
period for early life stages, by stipulating a 7-day mean minimum value for
other life stages, and by recommending additional limits for manipulatable
di scharges.
The previous EPA criterion for dissolved oxygen published in Quality
Criteria for Water (USEPA, 1976) was a minimum of 5 mg/i (usually applied as a
7Q10) which is similar to the current criterion minimum except for other life
stages of warinwater fish which now allows a 7-day mean minimum of 4 mg/i. The
new criteria are similar to those contained in the 1968 “Green Book” of the
Federal Water Pollution Control Federation (FWPCA, 1968).,
A. The Criteria and Monitoring and Design Conditions
The acceptable mean concentrations should be attained most of the time,
but some deviation below these values would probably not cause significant
harm. Deviations below the mean wiil probably be serially correlated and
hence apt to occur on consecutive days. The significance of deviations below
the mean will depend on whether they occur continuously or in daily cycles,
the former being more adverse than the latter. Current knowledge”regarding
such deviation-s is limited primarily to laboratory growth experiments and by
extrapolation to other activity-related phenomena.
r
36.
-

Under conditions where large daily cycles of dissolved oxygen occur, it
is possible to meet the criteria mean values and consistently violate the mean
minimum criteria. Under these conditions the mean minimum criteria will
clearly be the limiting regulation unless alternatives such as nutrient
control can dampen the daily cycles.
The significance of conditions which fail to meet the recommended
dissolved oxygen criteria depend largely upon five factors: (1) the duration
of the event; (2) the magnitude of the dissolved oxygen depression; (3) the
frequency of recurrence; (4) the proportional area of the site failing to meet
the criteria; and (5) the biological significance of the site where the event
occurs. Evaluation of an event’s significance must be largely case- and
site—specific. Common sense would dictate that the magnitude of the depres-
sion would be the single most important factor in general, especially if the
acute value is violated. A logical extension of these considerations is that
the event must be considered in the context of the level of resolution of the
monitoring or ‘modeling effort. Evaluating the extent, duration, and magnitude
of an event must be a function of the spatial and temporal frequency of the
data. Thus, a single deviation below the criterion takes on considerably less
significance where continuous monitoring occurs than where sampling is
comprised of once-a-week grab samples. This is so because based on continuous
monitoring the, event is provably small, but with the much less frequent
sampling the event is not provably small and can be considerably worse than
indicated by the sample.
The frequency of recurrence is of considerable interest to those modeling
dissolved oxygen concentratiàns because the return period, or period between
recurrences, is a primary modeling consideration contingent upon probabilities
of receiving water volumes, waste loads, temperatures, etc. It should be
apparent that return period cannot be isolated from the other four factors
discussed above. Ultimately, the question of return period may be decided on
-
a site-specific basis taking into account the other factors (duration,
magnitude, areal extent, and biological significance) mentioned above. Future
studies of temporal patterns of dissolved oxygen concentrations, both within
and between years, must be conducted to provide a better basis for selection
of the appropriate return period.
In conducting waste load allocation and treatment plant design computa-
tions, the choice of temperature in the models will be important. Probably
the best option would be to use temperatures consistent with those expected in
the receiving water over the critical dissolved oxygen period for the biota.
B. The Criteria and Manipulatable Discharges
If daily minimum dissolved oxygen concentrations are perfectly serially
correlated, i.e., if the annual lowest daily minimum dissolved oxygen concen-
tration is adjacent in time to the next lower daily minimum dissolved oxygen
concentration and one of these two minima is adjacent to the third lowest
daily minimum dissolved oxygen concentration, etc., then in order to meet the
7-day mean minimum criterion it is unlikely that there will be more”thah three
or four consecutive daily minimum values below the acceptable 7-day mean
minimum. Unless the dissolved oxygen pattern is extremely erratic, it is also
unlikely that the lowest dissolved oxygen concentration will be appreciably
37

S
below the acceptable 7-day mean minimum or that daily minimum values below the
7-day mean minimum will occur in more than one or two weeks each year. For
some discharges, the distribution of dissolved oxygen concentrations can be
manipulated to varying degrees. Applying the daily minimum to manipulatable
-
discharges would allow repeated weekly cycles of minimum acutely acceptable
dissolved oxygen values, a condition of probable stress and possible adverse
biological effect. If risk of protection impairment is to be minimized, the
application of the one day minimum criterion to manipulatable discharges
should either limit the frequency of occurrence of values below the acceptable
7-day mean minimum or impose further limits on the extent of excursions below
the 7-day mean minimum. For such controlled discharges, it is recommended
that the occurrence of daily minima below the acceptable 7-day mean minimum be
limited to 3 weeks per year or that the acceptable one-day minimum be
increased to 4.5 mg/i for coidwater fish and 3.5 mg/l for warmwater fish.
Such decisions could be site-specific based upon the extent of control, serial
correlation, and the resource at risk.
-
38

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Whitworth, W. R. 1968. Effects of diurnal fluctuations of dissolved oxygen
on the growth of brook trout. J. Fish. Res. Bd. Canada, 25:579—584.
Witzel, L. D., and H. R. McCrimmon. 1983. Redd-site seiection by brook trout
and brown trout in southwestern Ontario streams. Trans. Amer. Fish.
Soc., 112:760-771.
46

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0)

DENNIS STREICHER
City of Elmhurst, Illinois
209 North York Street
Elmhurst, Illinois 60126
630.530.3046
EDUCATION and
CERTIRCATION
B.S. in Biology from Northern Illinois University.
Illinois Class I Sewage Treatment Works Operator
Illinois Class “A” Public Water Supply Operator
WORK
EXPERIENCE
City of Elmhurst, May 1972 to present
1972-1 981
WWTP Chemist
1981-1982
Assistant Superintendent
1982-1990
Superintendent
1991-2000
Assistant Director of Public Works/Water and
Wastewater.
2000-Present
Director of Water & Wastewater
PROFESSIONAL
ACT~VITJES
Member of the A.W.W.A.
Member Water Environment Federation
Member of Central States Water Environment Assoc.
Chairman of the Central States Education Committee
Past president of the Central States Illinois Section
Vice-president of the Illinois Association of Wastewater Agencies
Served as the northeast representative on the Operators
Certification Committee for six years.
AWARDS
2000 Illinois EPA Operator of the Year
1996
CSWEA
Operations Award
INTERESTS
Active in local environmental groups especially bird watching
(bird ing) organizations. Wildlife photography especially birds in
wild habitats. Natural history studies.

Exhibit 4

April 2, 2004
Mr. Dennis P. McKenna
Deputy Administrator
Illinois Department ofAgriculture
P.O. Box 19281
Springfield, IL 62794-9281
Re: Illinois Association ofWastewater Agencies Dissolved Oxygen Study
Dear Dennis,
As a follow up on our conversation ofApril 1, 2004, I’d like to thank you for your
interest in the Illinois Association WastewaterAgencies (IAWA) dissolved oxygen study.
As you are aware IAWA is very interested in implementing this study and modifying the
Illinois water quality standards as regards to dissolved oxygen. It is our opinion that
many other water quality standards will be enhanced by a scientifically well founded
dissolved oxygen standard in Illinois. We feel the study has followed closelythe USEPA
protocols and builds upon the previous water quality standard. In addition it incorporates
the special features ofthe Illinois warm water chemistry. Note that the study specifically
excludes Lake Michigan and wetlands from consideration for DO limits changes.
The IAWA commissioned this study with the goal ofincorporating a previous study by
Chapman in 1986; then adding new datathat has been developed since that time. The
final draft will then make recommendations to modify Illinois water quality standards for
DO based on natural fluctuations in aquatic systems and physiological tolerances of
native aquatic life. The most significant recommendations are the incorporation ofseven
day nilming averages for the mean and minimum DO concentrations. The mean would be
7-d mean of6.0 mg/L when most early life stages of fish are present and a 7-d mean
minimum of4.0 mgIL when most early life stages offish are absent. This feature alone
adds significantly to the standards as it recognizes the seasonality ofthe natural aquatic
systems in Illinois. The recommended standards are either equivalent to or more
conservative than the previously established national dissolved oxygen standards.
I have transmitted a copy ofthe report to you; we would appreciate your thoughts on the
study. Also, please don’t hesitate to share the study with others in the agricultural
communities to elicit their responses as well. The goal ofTAWA is to include comments

ofall interested stakeholders. Further we wish to sure that the concerns of the agricultural
community are answered before the IAWA makes the move to ask the pollution control
board to modify the standards in Illinois.
Once again it was enjoyable speaking with you and if you have any questions don’t
hesitate to give me a call at (630)
530-3046.
Sincerely,
Dennis Streicher
Director ofWater & Wastewater
630.530.3046
office
630.834.0298 fax
Cc:
JAWA DO file

June 14, 2004
Ms. Nancy Erickson
Director ofNatural and Environmental Research
Illinois Farm Bureau
1701 Towanda Avenue
Bloomington, IL 61701
Re:
Illinois Association ofWastewater Agencies Dissolved Oxygen Study
IPCB DocketNumber R04-25
Dear Ms. Erickson,
As a follow up to our conversation ofMay
25,
2004, I’d like to thank you for your
interest in the Illinois Association Wastewater Agencies (JAWA) dissolved oxygen study.
Earlier in April of2004 I had transmitted a copy ofthe study to you for comments.
As you are aware IAWA is very interested in implementing this study and modifying the
Illinois water quality standards as regards to dissolved oxygen. It is our opinion that
many other water quality standards will be enhanced by a scientifically well founded
dissolved oxygen standard in Illinois. We feel the study has followed closely the USEPA
protocols and builds upon the previous water quality standard. In addition it incorporates
the special features ofthe Illinois warm water chemistry. Note that the study specifically
excludes Lake Michigan and wetlands from consideration forDO limits changes.
The IAWA commissioned this study with the goal ofincorporating a previous study by
Chapman in 1986; then adding new data that has been developed since that time. The
final draft will then make recommendations to modify Illinois water quality standards for
DO based on natural fluctuations in aquatic systems and physiological tolerances of
native aquatic life. The most significant recommendations are the incorporation ofseven
day running averages for the mean and minimum DO concentrations. The mean would be
7-d mean of6.0 mg!L when most early life stages offish are present and a 7-d mean
minimum of4.0 mg!L when most early life stages of fish are absent. This feature alone
adds significantly to the standards as it recognizes the seasonality ofthe natural aquatic
systems in Illinois. The recommended standards are either equivalent to or more
conservative than the previously established national dissolved oxygen standards.

At this time the IAWA has filed a petition with the Illinois Pollution Control Board
(IPCB) to incorporate the studies results into Illinois general use water standards. The
IPCB has agreed to hear the petition and has set dates in June and August to receive
testimony from interested stakeholders. We would appreciate your thoughts on the study.
Also, please don’t hesitate to share the study with others in the agricultural communities
to elicit their responses as well. The goal ofIAWA is to include comments ofall
interested stakeholders.
Once again it was enjoyable speaking with you and if you have any questions don’t
hesitate to give me a call at (630) 530-3046.
Sincerely,
Dennis Streicher
Director ofWater & Wastewater
630.530.3046 office
630.834.0298 fax
Cc:
IAWA DO file

April 2, 2004
Alec Messina
IL Environmental Regulatory Group
3150 Roland Avenue
Springfield, IL 62703
Re: Illinois Association ofWastewater Agencies Dissolved Oxygen Study
Dear Alec,
As a follow up on our conversation ofApril 2, 2004, I’d like to thank you for your
interest
in the Illinois Association Wastewater Agencies (IAWA) dissolved oxygen study.
As you are aware IAWA is very interested in implementing this study and modifying the
Illinois water quality standards as regards to dissolved oxygen. It is our opinion that
many other water quality standards will be enhanced by a scientifically well founded
dissolved oxygen standard in Illinois. We feel the study has followed closely the USEPA
protocols and builds upon the previous water quality standard. In addition it incorporates
the special features of the Illinois warm water chemistry. Note that the study specifically
excludes Lake Michigan and wetlands from consideration for DO limits changes.
The IAWA commissioned this study with the goal ofincorporating a previous study by
Chapman in 1986; then adding new data that has been developed since that time. The
final draft will then make recommendations to modify Illinois waterquzditystandards for
DO based on natural fluctuations in aquatic systems and physiological tolerances of
native aquatic life. The most significant recommendations are the incorporation ofseven
day running averages for the mean and minimum DO concentrations. The mean would be
7-d mean of6.0 mg/L when most earlylife stages of fish are present and a 7-d mean
minimum of4.0 mg/L when most early life stages offish are absent. This feature alone
adds significantly to the standards as it recognizes the seasonality ofthe natural aquatic
systems in Illinois. The recommended standards are either equivalent to or more
conservative than the previously established national dissolved oxygen standards.
I have transmitted a copy ofthe report to you; we would appreciate your thoughts on the
study. Also, please don’t hesitate to share the study with others that you represent to elicit
their responses as well. The goal ofIAWA is to include comments of all interested

stakeholders. Further we wish to sure that the concerns ofthe industrial discharger
community are answered before the IAWA makes the move to ask the pollution control
board to modify the standards in Illinois.
Once again it was enjoyable speaking with you and if you have any questions don’t
hesitate to give me a call at (630) 530-3046.
Sincerely,
Dennis Streicher
Director of Water & Wastewater
630.530.3046 Office
630.834.0298 fax
Cc:
IAWA DO file

April 12, 2004
Dr. Edward Krug
Illinois State Water Survey
2204 Griffith Dr
Champaign, IL 61820
Re: Illinois Association of Wastewater Agencies Dissolved Oxygen Study
Dear Dr. Krug,
As a follow up on our conversation ofApril 12, 2004, I’d like to thank you for your
interest in the Illinois Association WastewaterAgencies (JAWA) dissolved oxygen study.
As you are aware IAWA is very interested in implementing this study and modifying the
Illinois water quality standards as regards to dissolved oxygen. It is our opinion that
many other water quality standards will be enhanced by a scientifically well founded
dissolved oxygen standard in Illinois. We feel the study has followed closely the USEPA
protocols and builds upon the previous water quality standard. In addition it incorporates
the special features ofthe Illinois warm water chemistry. Note that the study specifically
excludes Lake Michigan and wetlands from consideration for DO limits changes.
The IAWA commissioned this study with the goal ofincorporating a previous study by
Chapman in 1986; then adding new datathat has been developed since that time. The
final draft will then make recommendations to modify Illinois water quality standards for
DO based on natural fluctuations in aquatic systems and physiological tolerances of
native aquatic life. The most significant recommendations are the incorporation ofseven
day running averages for the mean and minimum DO concentrations. The mean would be
7-d mean of6.0 mg/L when most early life stages offish are present and a 7-d mean
minimum of 4.0 mg!L when most early life stages offish are absent. This feature alone
adds significantly to the standards as it recognizes the seasonality ofthe natural aquatic
systems in Illinois. The recommended standards are either equivalent to or more
conservative than the previously established national dissolved oxygen standards.
I have transmitted a copy ofthe report to you; we would appreciate your thoughts on the
study. Also, please don’t hesitate to share the study with others that you represent to elicit
their responses as well. The goal ofIAWA is to include comments ofall interested
stakeholders. Further we wish to sure that the concerns ofthe industrial discharger

community are answered before the IAWA makes the move to ask the pollution control
board to modify the standards in Illinois.
Once again it was enjoyable speaking with you and if you have any questions don’t
hesitate to give me a call at (630) 530-3046.
Sincerely,
Dennis Streicher
Director ofWater & Wastewater
630.530.3046 Office
630.834.0298 fax
Cc:
IAWA DO file

Exhibit 5

James E. Garvey 1
Short Curriculum Vita
Name
James E. Garvey
Title
Assistant Professor
Address
Fisheries and Illinois Aquaculture Center
Department ofZoology
Southern Illinois University
Carbondale
jgarvey@siu.edu
http://www.science.siu.edu/zoology/garvey/index.html
Degrees
1997 Ph.D., Zoology, The Ohio State University, Ohio
1992 M.S., Zoology, The Ohio State University, Ohio
1990 B.A.,
cum laude,
Zoology, Miami University, Ohio
Experience
2000-
Assistant Professor, Department ofZoology, Southern Illinois
University
1998-2000 Assistant Professor, Division ofBiology, Kansas State University
1997-1998 Postdoctoral Fellow, Department ofBiology, Queen=s University,
Ontario
1997
Research Associate, Department ofZoology, The Ohio State
University
1996-1997 Presidential Fellow, Graduate School, The Ohio State University
1990-1996 Graduate Research Associate, Department ofZoology, The Ohio
State University
1990-1996 Graduate Teaching Associate, Department ofZoology, The Ohio
State University
1988-1990 Research Technician, Department ofZoology, Miami University
1988
Student Researcher, School for Field Studies, St. John, U.S. Virgin
Islands
Fields ofResearch Competence
Aquatic ecology, fish ecology, basic and applied fish biology, limnology,iood
web dynamics, bioenergetics, life history modeling
Honors and Awards
2001 Best Oral Presentation, Annual Meeting ofthe Illinois Chapter of the
American Fisheries Society, February 2001
2000 Best Oral Presentation, 2000 Annual Meeting ofthe Kansas Chapter ofthe
American Fisheries Society, Manhattan, Kansas
1999 Article titled ACompetition between larval fishes in reservoirs: the role of
Revised 2-Jun-04

James E. Garv~y 2
relative timing of appearance@ (co-author, R.A. Stein) was among
5
nominated by a selection committee for Best Paper in Transactions of the
American Fisheries Society (out of —100 articles)
1999 American Society ofLimnology and Oceanography=s DIALOG III
Symposium, Bermuda, October 1999
1998 Graduate Faculty Status, Kansas State University, November 1998
1996 Best Poster, Annual Meeting ofthe American Fisheries Society, Dearborn,
Michigan, August 1996
1996 University Presidential Fellowship, July 1996
1995
Honorable Mention, Best Oral Presentation, Annual Meeting of the
American Fisheries Society, Tampa, Florida, August 1995
Student Awards
2004 Dean Sherman, Honorable Mention, Best Poster Award, Undergraduate
Research Forum, Southern Illinois University, Carbondale, March 2004
2004 Laura Csoboth, Student Travel Award, Illinois American Fisheries Society
Meeting, Champaign, Illinois, March 2004
Selected Professional Service (last five years)
2004
Reviewer, National Science Foundation proposal, Ecology Panel
(RUI proposal)
2004
Member, Skinner Award Committee, American Fisheries Society
(second term)
2004
North Central Representative, Early Life History Section,
American Fisheries Society.
2003
Workshop Presenter, Analysis ofFisheries Data, Illinois Chapter
ofthe American Fisheries Society Continuing Education
Workshop, Springfield, Illinois, April 2003
2003
Moderator, River Session, Illinois Chapter ofthe American
Fisheries Society, Rend Lake, IL, February 2003
2002
Reviewer, National Science Foundation proposal, Ecology Panel,
August 2002
2002
Chair, Student Judging of Oral Presentations, National American
Fisheries Society Meeting, Baltimore, Maryland, August 2002
2002-present Associate Editor,
Transactions of the American Fisheries Society
(handle 10 manuscripts per year)
200 1-2003
Judge, Regional Science Fair, SIUC campus, February 2001-2003
1999-2001
Member, Skinner Award Committee, American Fisheries Society
(first term)
2001
Reviewer, National Science Foundation proposal, Ecology Panel,
February 2001
2001
Moderator, Fisheries Session, Illinois Renewable Natural
Resources Meeting, February 2001
2000
Judge, Student Paper Presentations, American Fisheries Society
Revised 2-Jun-04

James
E.
Garvey
3
National Meeting, August 2000
1994-present Peer Reviewer,
Behaviour, Biological Invasions, Canadian
Journal ofZoology Transactions of the American Fisheries
Society, North American Journal ofFisheries Management,
Ecology, Ecological Applications, Great Basin Naturalist,
American MidlandNaturalist, PrairieNaturalist, Journal of
Plankton Research, Animal Behaviour, Journal ofthe North
American Benthological Society, Northwest Science, North
American Journal ofAquaculture, Proceedings of the Royal
Academy ofScience —Great Britain
Current Society Memberships
2003-present
Honorary Member, American Institute of Biological
Sciences
1 990-present
Ecological Society ofAmerica
1990-present
American Fisheries Society
1990-1996,
North American Benthological Society
1999-present
2001-present
Illinois Chapter ofthe American Fisheries Society
1999-present
Full Member, Sigma Xi
Invited Presentations
2003 Upper Mississippi Conservation Committee, Prairie du Chien, Wisconsin,
August 2003
2002 Ecology Consortium, Southern Illinois University, Carbondale, November
2002
2000 Sam Parr Biological Station, Illinois Natural History Survey, June 2000
2000 Northeast Division Meeting of the American Fisheries Society, April 2000
2000 Department of Zoology, University of Wisconsin
-
Madison, February
2000
1999 Department ofBiology, William Jewell College, Missouri, September
1999
1998 Department ofBiology, Queen=s University, Kingston, Ontario, January
1998
1997 Apple Valley Fishing Club, Apple Valley, Ohio, October 1997
1996 Department ofBiological Sciences, University ofPittsburgh, December
1996.
Technical Reports
Garvey, J.E., and M.R Whiles. 2003. An assessment ofnational and Illinois dissolved
oxygen water quality criteria. Illinois Association of Wastewater Agencies. 52
pages
Garvey, J.E., B.D. Dugger, M.R. Whiles, S.R. Adams, M.B. Flinn, B.M. Burr, and R.J.
Revised 2-Jun-04

James E. Garvey 4
Sheehan. 2003. Responses offish, waterbirds, invertebrates, vegetation, and
water quality to environmental pool management: Mississippi River Pool
25.
U.S. Army Corps ofEngineers. 181 pages.
Garvey,
J.E.
2002. Winter habitat used by fishes in Smithland Pool, Ohio River. U.S.
Fish and Wildlife Service and U.S. Army Corps ofEngineers, 90 pages.
Garvey, J.E., and R.J. Sheehan. 2001. Winter habitat associations ofriverine fishes:
predictions for the Ohio River, U.S. Fish and Wildlife Service and U.S. Army
Corps ofEngineers, 39 pages.
Garvey, J.E.,
R.A. Wright, R.A. Stein, E.M. Lewis, K.H. Ferry, and S.M. Micucci. 1998.
Assessing the influence ofsize on overwinter survival oflargemouth bass in Ohio
on-stream impoundments. Ohio Division of Wildlife Final Report. Federal Aid
in Sport Fish Restoration Program 29, 288 pages.
Stein, R.A., and
J.E. Garvey.
1996. A review ofa technical report prepared for the
Cuyahoga River (Ohio) Community Planning Organization by EnvironScience
Inc.
Theses and Dissertations
Garvey, J.E.
1997. Strong interactors and community structure: testing predictions for
reservoir food webs, Ph.D. dissertation, 235 pages.
Garvey, J.E.
1992. Selective predation as a mechanism ofcrayfish species replacement
in northern Wisconsin lakes. M.S. thesis, The Ohio State University, 88 pages.
Book Chapters
S.R. Chipps, and J.E.
Garvey.
In press. Assessment offood habits and feeding patterns.
In
M.L. Brown and C.S. Guy, editors. Analysis and Interpretation of Freshwater
Fisheries Data. 41 MS pages, 2 tables, 4 figures, 13 boxes. 1 April 2001.
Book Reviews
Garvey, J.E.
2003. Searching for scales in fisheries. Review of “Hierarchical
Perspectives on Marine Complexities: Searching for Systems in the Gulfof
Maine” by Spencer Apollonio. Columbia University Press, New York. 2002.
229 pp. Appeared in BioScience 53(10):1004-1006. (Invited)
Peer-Reviewed Publications (Selected Abstracts at
http://www.science.siu.edu/zoology/garvey/pubs.htmi)
Garvey,
J.E.,
K.G. Ostrand, and D.H. Wahl, In press. Interactions among allometric
scaling, predation and ration affect size-dependent growth and mortality offish
during winter. Ecology. Aug. 2003.
Ostrand, K.G., S.J. Cooke, J.E. Garvey, and D.H. Wahl. In press. The energetic impact
ofoverwinter prey assemblages on age-0 largemouth bass. Environmental
Biology ofFishes.
Colombo, R.E., P.S. Wills, and
J.E. Garvey.
2004. Use ofultrasound imaging to
Revised 2-Jun-04

James E. Garvey
5
determine sex ofshovelnose sturgeon
Scaphirhynchusplatorynchus
from the
Middle Mississippi River. North American Journal ofFisheries Management
24:322-326.
Roberts, M.R., JE. Wetzel, III, R.C. Brooks, and
J.E. Garvey.
2004. Daily
incrementation in the otoliths ofthe red spotted sunfish,
Lepomis miniatus.
North
American Journal ofFisheries Management 24:270-274.
Garvey, J.E.,
and E.A. Marschall. 2003. Understanding latitudinal trends in fish body
size through models ofoptimal seasonal energy allocation. Canadian Journal of
Fisheries and Aquatic Sciences 60(8):938-948.
Micucci, S.M.,
J.E. Garvey, R.A.
Wright, and R.A. Stein. 2003. Individual growth and
foraging responses ofage-0 largemouth bass to mixed prey assemblages during
winter. Environmental Biologyof Fishes
67(2):157-168.
Garvey, J.E., J.E. Rettig, R.A. Stein, D.M. Lodge, and S.P. Klosiewski. 2003. Scale-
dependent associations among fish predation, littoral habitat, and distributions of
native and exotic crayfishes. Ecology 84(12): 3339-3348.
Whiles, M.J., and J.E. Garvey. In press. Aquatic resources ofthe Shawnee and Hoosier
National Forests, USDA Forest Service.
Garvey,
J.E., R.A.
Stein, R.A. Wright, and M.T Bremigan. 2003. Largemouth bass
recruitment in North America: quantifying underlying ecological mechanisms
along environmental gradients Black bass: ecology, conservation and
management. Edited by D. Philipp and M. Ridgway. American Fisheries Society
Symposium 3 1:7-23.
Garvey, J.E., D.R. DeVries, R.A. Wright, and J.G. Miner. 2003. Energetic adaptations
along a broad latitudinal gradient: implications for widely distributed
communities. BioScience 53(2): 141-150.
Garvey, J.E., T.P. Herra, and W.C. Leggett. 2002. Protracted reproduction in sunfish:
the temporal dimension in fish recruitment revisited. Ecological Applications
12:194-205.
Garvey, J.E., R.A. Wright, K.H. Ferry, and R.A. Stein. 2000. Evaluating how local-
and regional- scale processes interact to regulate growth of age-U largemouth
bass. Transactions ofthe American Fisheries Society 129:1044-1059.
Fullerton, A.H., J.E. Garvey, R.A. Wright, and R.A. Stein. 2000. Overwinter growth
and survival oflargemouth bass: interactions among size, food, origin, and winter
duration. Transactions ofthe American Fisheries Society 129:1-12.
Wright, R.A.,
J.E. Garvey, A.H.
Fullerton, and R.A. Stein. 1999. Using bioenergetics
to explore how winter conditions affect growth and consumption of age-U
largemouth bass. Transactions ofthe American Fisheries Society 128:603-6 12.
Garvey, J.E., and R.A. Stein. 1998. Competition between larval fishes in reservoirs:
the role ofrelative timing ofappearance. Transactions ofthe American Fisheries
Society 127:1023-1041.
Garvey, J.E.,
R.A. Wright, and R.A. Stein. 1998. Overwinter growth and survival of
age-0 largemouth bass: revisiting the role ofbody size. Canadian Journal of
Fisheries and Aquatic Sciences 55:2414-2424.
Garvey, J.E., N.A. Dingledine, N.S. Donovan, and R.A. Stein. 1998. Exploring spatial
and temporal variation within reservoir food webs: predictions for fish
assemblages. Ecological Applications 8:104-120.
Revised 2-Jun-04

James E. Garvey 6
Garvey, J.E., and R.A. Stein. 1998. Linking bluegill and gizzard shad assemblages to
growth of age-0 largemouth bass in reservoirs. Transactions ofthe American
Fisheries Society 127:70-83.
Lodge, D.M., R.A. Stein, K.M. Brown, A.P. Covich, C. Brönmark,
J.E. Garvey,
and S.P.
Klosiewski. 1998. Predicting impact offreshwater exotic species on native
biodiversity: challenges in spatial and temporal scaling. Australian Journal of
Ecology 23:53-67.
Garvey, J.E.,
E.A. Marschall, and R.A. Wright. 1998. From star charts to stoneflies:
detecting relationships in continuous bivariate data. Ecology 79(2):442 447.
Schaus, M.H., M.J. Vanni, T.E. Wissing, M. Bremigan, J.E. Garvey, and R.A. Stein.
1997. Nitrogen and phosphorus excretion by the detritivorous gizzard shad
(Dorosoma cepedianum)
in a reservoir ecosystem. Limnology and Oceanography
42(6):1386-1397.
Garvey, J.E., R.A. Stein, and H.M. Thomas. 1994. Assessing how fish predation and
interspecific prey competition influence a crayfish assemblage. Ecology
75:532-
547.
Garvey, J.E., and R.A. Stein. 1993. Evaluating how chela size influences the invasion
potential ofan introduced crayfish,
Orconectes rusticus.
American Midland
Naturalist 129:172-181.
Garvey,
J.E.,
H.A. Owen, and R.W. Winner. 1991. Toxicity ofcopper to the green alga,
Chiamydomonas reinhardtii
(Chiorophycea), as affected by humic substances of
terrestrial and freshwater origin. Aquatic Toxicology 19:89-96.
Oral Presentations and Posters (Last Five Years)
Williamson, C.J., and
J.E.
Garvey. Growth and mortality of silver carp: implications for
its rise to dominance in the Middle Mississippi River. Illinois Chapter of the
American Fisheries Society, Champaign, IL, March 2004. (Oral presentation by
Williamson)
Koch, B.T., J.E.
Garvey,
and M. Lydy. The effects ofland use on organochiorine
accumulation in middle Mississippi River shovelnose sturgeon: intersexuality
and reproductive consequences. Illinois Chapter of the American Fisheries
Society, Champaign, IL, March 2004. (Oral presentation by Koch)
Csoboth, L.A., D.W. Schultz, K. DeGrandChamp,
J.E. Garvey,
and R.M. Neumann.
Fish response at a backwater-river interchange: the Swan Lake rehabilitation and
enhancement project. Illinois Chapter of the American Fisheries Society,
Champaign, IL, March 2004. (Poster presentation)
Colombo, R.E., J.E. Garvey, and R.C. Heidinger. Comparing demographics of channel
catfish in fished and un-fished reaches of the Wabash River. 64~Meeting ofthe
Midwest Fish and Wildlife Conference. Kansas City, December 2003. (Oral
presentation by Colombo)
Spier, T.,
J.E. Garvey,
R.C. Heidinger, R.J. Sheehan, P. Wills, K. Hurley, R.E.
Colombo, R.C. Brooks. Pallid and shovelnose sturgeon movement and habitat
usage in the middle Mississippi River.
64th
Meeting of the Midwest Fish and
Wildlife Conference. Kansas City, December 2003 (Oral presentation by Spier)
Marschall, E.A., and
J.E. Garvey.
Understanding latitudinal trends in fish body size
Revised 2-Jun-04

James E. Garvey 7
through models Of optimal seasonal energy allocation. 88th Meeting ofthe
Ecological Society ofAmerica, Savannah, Georgia, July 2003 (Oral presentation
by Marschall)
Braeutigam, B.J., and J.E. Garvey. Winter habitat used by fish in Smithland Pool, Ohio
River. Ohio River Research Review, Indiana, August 2003. (Oral presentation
by Braeutigam)
Garvey, J.E.
Importance offlood-plain connectivity to fish assemblages in the
Mississippi River. Middle Mississippi River Workgroup Meeting, Carbondale,
IL, June 2003. (Oral presentation by Garvey)
O’Neill, B.J.,
J.E. Garvey,
M.R. Whiles, and K.R. Lips. Scale-dependent
interrelationships among, fish, landscape characteristics, and arnbystomatid
salamanders in forest ponds. Annual Meeting ofthe American Society of
Ichthyologists and Herpetologists, Manaus, Brazil, June 2003 (Oral presentation
by O’Neill)
Spier, T.,
J. Garvey, R.
Heidinger, R. Sheehan, P. Wills, and K. Hurley. Demographics
and habitat usage ofpallid sturgeon in
the Middle Mississippi River. Meeting of
the Illinois Chapter ofAmerican Fisheries Society, Rend Lake, IL, February 2003
(Oral
presentation
by Spier)
Jackson, N.D., J.E. Garvey, R.C. Heidinger, and R.J. Sheehan. Age and mortality of
shovelnose sturgeon,
Scaphirhynchus platorynchus,
in the Middle Mississippi
River and Lower Wabash Rivers, Illinois. Meeting ofthe Illinois Chapter of
American Fisheries Society, Rend Lake, IL, February 2003 (Oral presentation by
Jackson)
Flmnn, M.B., S. R. Adams, M.R. Whiles, J.E. Garvey, B.M. Burr, and R.J. Sheehan. Fish
and macroinvertebrate responses to environmental pooi management in
Mississippi River Pool
25.
Meeting ofthe Illinois Chapter ofAmerican Fisheries
Society, Rend Lake, IL, February 2003 (Oral presentation by Flmnn)
Colombo, R.E., J.E. Garvey, R.C. Heidinger and R.J. Sheehan. Population
demographics of channel catfish
Ictalurus pun ctatus
in the Wabash River.
Meeting ofthe Illinois Chapter ofAmerican Fisheries Society, Rend Lake, IL,
February 2003 (Oral presentation by Colombo)
Garvey, J.E. Early growth ofcentrarchids along a productivity gradient: setting the
stage for future interactions. American Fisheries Society Meeting, Baltimore,
MD, August 2002 (Oral presentation)
Ostrand, K.G., S.J. Cooke, J.E. Garvey, D.H. Wahl. Age-0 largernouth bass: the
overwinter effects ofprey type on growth and spring swimming performance.
American Fisheries Society Meeting, Baltimore, MD, August 2002 (Oral
presentation by Ostrand)
Garvey, J.E.,
S.M. Micucci, R.A. Wright, and R.A. Stein. Prey assemblage structure
during winter influences the condition ofage-0 largemouth bass. Midwest Fish
and Wildlife Meeting, Des Moines, IA, December 2001 (Oral presentation)
Garvey, i.E. Using optimal allocation models to explain latitudinal trends in recruitment
oflargemouth bass. Illinois Renewable Natural Resources Conference, Peoria,
IL, February 2001 (Oral presentation; received Best Oral Presentation)
Bremigan, M.T., R.A. Stein, and J.E. Garvey. Variable gizzard shad recruitment and its
effects along a reservoir productivity gradient. American Society ofLimnology
Revised 2-Jun-04

James E. Garvey 8
and Oceanography Meeting
-
Copenhagen, Denmark, June 2000 (Poster
presentation).
Evans-White, M., W.K. Dodds, and J.E. Garvey. Crayfish biomass, growth, and
production in a tallgrass prairie stream. North American Benthological Society
Meeting, Colorado, May 2000 (Oral presentation by Dodds).
Garvey, J.E. Patterns ofsportfish recruitment in natural lakes and reservoirs: do
generalities exist? Kansas Chapter ofthe American Fisheries Society Meeting,
February 2000 (Oral presentation; received Best Oral Presentation).
Garvey, J.E. From fish in lakes to crayfish in prairie streams: searching for general
recruitment mechanisms and ecosystem consequences. KSU Ecology Research
Seminar Series, November 1999 (Oral presentation).
Garvey, J.E., T.P.
Herra, and W.C. Leggett. Mechanisms underlying the spatial
distribution oflarval sunfish
(Lepomis
spp.) in Lake Opinicon, Ontario.
American Fisheries Society Meeting
-
Charlotte, North Carolina, August 1999
(Oral presentation).
Garvey, i.E. Interactions between ecosystems and life histories: predicting fish
community structure in lakes. Kansas EPSCoR Conference, Topeka, KS, April
1999 (Poster presentation).
Revised 2-Jun-04

ni
0~

MATT ROWLAND
WHILES
Department of Zoology
Southern Illinois University
Carbondale,
Illinois
62901-6501
Phone: (618) 453-7639
PERSONAL INFORMATION
Born December 4, 1964; Kansas City, Missouri.
Married 1998, 1 daughter and 1 son
EDUCATION
9/91-6/95
University ofGeorgia, Athens, Georgia;
Ph.D.
Ecology.
Dissertation: Disturbance, recovery, and invertebrate communities
in southern Appalachian headwater streams.
9/88-9/91
University ofGeorgia, Athens, Georgia; M.S. Entomology.
Thesis: First-year recovery ofa southern Appalachian headwater stream
following an insecticide induced disturbance.
8/84-8/88
Kansas State University, Manhattan, Kansas; B.S. Biology.
AREAS OF SPECIALIZATION
Ecosystem ecology with emphasis on freshwater ecosystem structure and function (mainly
streams and wetlands), the role ofinvertebrates in ecosystems, ecosystem-level consequences
ofextinctions, energetic linkages between aquatic and terrestrial systems, the role of
disturbance, and biological assessment offreshwater habitats.
PROFESSIONAL EXPERIENCE
2003-
Associate
Professor of
Zoology, Southern Illinois University
Teaching Freshwater Invertebrates, Stream Ecology, and General Ecology.
Advising graduate research in freshwater ecosystem ecology.
2000-
Assistant Professor of Zoology, Southern Illinois University
Teaching Freshwater Invertebrates, Stream Ecology, and General Ecology.
Advising graduate research in freshwater ecosystem ecology.
2000-
Adjunct Assistant Professor of Entomology, Kansas State University
Serving as a graduate committee member for students pursuing studies in the
area ofaquatic invertebrate ecology

2
PROFESSIONAL EXPERIENCE (continued)
1997-00
Assistant Professor ofEntomology’
(non-tenure track), Kansas State University
Taught Insect Ecology, Insects and People, Economic Entomology,
and an interdisciplinary Environmental Concerns course. Advised graduate
research in invertebrate ecology.
1995-97
Assistant Professor of
Biology, Wayne State College
Taught Introductory Zoology, Invertebrate Zoology, Entomology, Vertebrate
Zoology, Ecology, and General Biology (majors and non-majors). Advised
undergraduate research in freshwater invertebrate ecology.
1996-
Adjunct Graduate Faculty,
University ofMemphis
Graduate committee member for students working in aquatic ecology.
1989-95
Graduate Teaching Assistant,
University ofGeorgia
Instructed numerous laboratory courses including General Biology, Entomology,
Animal Behavior, Aquatic Entomology, General Ecology, and Insect Ecology.
1994
Laboratory
Coordinator, University ofGeorgia
Instructed, scheduled, and supervised graduate teaching assistants for the
General Biology program.
1988-94
Research Assistant, University ofGeorgia
Investigated the role ofaquatic invertebrates in stream ecosystem function.
Participated in all aspects of a long-term study including sampling and
processing ofinvertebrate communities, organic matter, and water chemistry.
1987-88
Research Assistant, Kansas State University
Investigated effects ofnutrient enrichment on algal growth and invertebrate
grazer densities in streams on LTER sites across the country.
1987-87
Undergraduate Research Assistant,
Kansas State University
Investigated small mammal behavior on islands in the Sea ofCortez with and
without reptilian predators.
1985-87
Undergraduate Research
Assistant, Kansas State University
Examined macroinvertebrate community dynamics
in streams with contrasting
hydrologic
regimes on
the Konza Prairie Research Natural Area.
HONORS AND AWARDS
1997
Professor ofthe Year, Math and Sciences Division, Wayne State College.
1996
Professor ofthe Year, Math and Sciences Division, Wayne State College.
1995
Outstanding Teaching Assistant, University ofGeorgia.
1994-1995 University-Wide Assistantship Award, University ofGeorgia.
1994-1995
Merit Assistantship Award; Outstanding Teaching and Research, Univ. of GA.
1993-1994 Merit Assistantship Award; Outstanding Teaching and Research, Univ. of GA
1988
Nominee for Outstanding Senior Biology Student, Kansas State University.
1987
Hydrolab Award; best poster, North American Benthological Society meetings
1984
Designated Kansas State Scholar.

3
PROFESSIONAL PUBLICATIONS
Dodds, W. K.,
and M. R. Whiles.
Inpress.
Factors related to quality and quantity ofsuspended
particles in rivers: general continent-scale patterns in the United States.
Environmental
Management:
Whiles, M. R., J. B.
Jensen, J. G. Palis, and W. G. Dyer.
Inpress.
Diets oflarval flatwoods
salamanders,
Ambystoma cingulatum,
from Florida and South Carolina.
Journal of
Herpetology.
Whiles, M. R., and J. E. Garvey.
Inpress.
Freshwater resources within the Shawnee-Hoosier
Ecological Assessment Region. Special Publication of the USDA Forest Service:
Dodds, W. K., K. Gido, M. R. Whiles, K. M. Fritz, and W. J. Matthews. 2004. Life on the
Edge: Ecology ofPrairie Streams.
Bioscience 54:
205-216
Ranvestel, A. W., K. R. Lips, C. M. Pringle, M. R. Whiles, and R. J. Bixby. 2004. Neotropical
tadpoles influence stream benthos: evidence for ecological consequences of amphibian
declines.
Freshwater Biology
49: 274-285.
Webber, J. A., K. W. J. Williard, M. R. Whiles, M. L. Stone, J. J. Zaczek, and K. D. Davie.
2004. Watershed scale assessment ofthe impact offorested riparian zones on
stream
water quality. Pages 114-120 In: Van Sambeek, J.W.; J.O. Dawson; F. Ponder, Jr.; E.F.
Loewenstein; and J.S. Fralish, eds. Proceedings, 13th Central Hardwood Forest
Conference; Urbana, IL. Gen. Tech. Rep. NC-234. St. Paul, MN: USDA Forest Service,
North Central Research Station.
Evans-White, M. A., W. K. Dodds, and M. R.
Whiles.
2003. Ecosystem significance of
crayfishes and central stonerollers in a tallgrass prairie stream: functional differences
between co-occurring omnivores.
Journal ofthe North American Benthological Society:
22: 423-441.
Callaham, M. A., Jr., J. M. Blair, T. C. Todd, D. J. Kitchen, and M. R. Whiles. 2003.
Macroinvertebrates in North American tallgrass prairie soils: Effects offire, mowing, and
fertilization on density and biomass.
Soil Biology and Biochemistry
35:1079-1093.
Whiles, M. R., and W. K. Dodds. 2002. Relationships between stream size, suspended
particles, and filter-feeding macroinvertebrates in a Great Plains drainage network.
Journal ofEnvironmental Quality
31: 1589-1600.
Jonas, J., M. R. Whiles, and R. E. Charlton. 2002. Aboveground invertebrate responses to land
management differences in a central Kansas grassland.
Environmental Entomology
31:
1142-1152.
Stagliano, D. M., and M. R. Whiles. 2002. Macroinvertebrate production and trophic structure
in a taligrass prairie headwater stream.
Journal ofthe North American Benthological
Society2l:
97-113.
Callaham, M. A., M. R. Whiles, and J. M. Blair. 2002. Annual fire, mowing, and fertilization
effects on two annual cicadas (Homoptera: Cicadidae) in taligrass prairie.
American
Midland Naturalist
148: 90-101.
Meyer, C. K., M. R. Whiles, and R. E. Charlton. 2002. Life history, secondary production, and
ecosystem significance ofacridid grasshoppers in annually burned and unburned tallgrass
prairie.
American Entomologist
48:
52-61.

4
PROFESSIONAL PUBLICATIONS (continued)
Whiles, M. R., and B. S. Goldowitz. 2001. Hydrologic influences on insect emergence
production from central
Platte River wetlands.
EcologicalApplications
11: 1829-1842.
Whiles, M. R. M. A. Callaham, C. K. Meyer, B. L. Brock, and R. E. Charlton. 2001.
Emergence ofperiodical cicadas from a Kansas riparian forest: densities, biomass, and
nitrogen flux.
American MidlandNaturalist 145:
176-187.
Schrank, S. J., C. S. Guy, M. R. Whiles, and B. L. Brock. 2001. Assessment of
Physicochemical and watershed features influencing Topeka shiner
Notropis topeka
distribution in Kansas streams.
Copeia
2001: 413-42 1.
Dodds, W. K., M. A. Evans-White, N. M. Gerlanc, L. J. Gray, D. A.Gudder, M. J. Kemp, A. L.
Lopez, D. Stagliano, E. A. Strauss, J. L. Tank, M. R.
Whiles, W. M. Wollheim.
2001.
Quantification ofthe nitrogen cycle in a prairie stream.
Ecosystems:
3: 574-589.
Whiles, M. R., B. L. Brock, A. C. Franzen, and S. Dinsmore II. 2000. Stream invertebrate
communities, water quality, and land use patterns in an agricultural drainage basin of
northenNebraska.
Environmental Management:
26:
5
63-576.
Jensen, J. B., and M. R. Whiles. 2000. Diets ofsympatric
Plethodonpetraeus
and
Plethodon
giutinosus. Journal ofthe Elisha MitchellScientific Society
116: 245-250.
Callaharn, M. A., Jr., M.
R.
Whiles, C. K. Meyer, B. L. Brock, and R. B. Charlton. 2000.
Feeding ecology and emergence production of annual cicadas (Homoptera: Cicadidae) in
taligrass prairie.
Oecologia
123: 535-542.
Alexander, K. A., and M. R. Whiles. 2000. A new species of
Ironoquia
Banks (Trichoptera:
Limnephilidae) from the central Platte River, Nebraska.
Entomological News:
111: 1-7.
Whiles, M. R., B. S. Goldowitz, andR. Chariton. 1999. Life history and production of a semi-
terrestrial limnephilid caddisily in a Platte River wetland.
Journal of the North American
Benthological Society
18: 533-544.
Goldowitz, B. S., and M. R. Whiles. 1999. Investigations offish, amphibians, and aquatic
invertebrates within the middle Platte River system. Published final Report, Platte
Watershed Program, Cooperative Agreement X99708 101, USEPA.
Whiles, M. R., and B. S. Goldowitz. 1998. Biological responses to hydrologic fluctuation in
wetland sloughs of the central Platte River.
In
Lingle, G. (ed.)
Proceedings ofthe Ninth
Platte River Basin Ecosystem Symposium.
USFWS and USEPA Region VII.
Whiles, M. R., and J. B. Wallace. 1997. Litter decomposition and macroinvertebrate
communities in headwater streams draining pine and hardwood catchments.
Hydrobiologia 353:
107-119.
Wallace, J. B., T. F. Cuffney, S. L. Eggert, and M. R. Whiles. 1997. Stream organic matter
inputs, storage, and export for Satellite Branch at Coweeta Hydrologic Laboratory, North
Carolina, USA.
Journal of the North American Benthological Society
16: 67-74.
Whiles, M. R. and J. B. Wallace. 1996. Macroinvertebrate production in a headwater stream
during recovery from anthropogenic disturbance and hydrologic extremes.
C’anadian
Journal ofFisheries and Aquatic Sciences
52: 2402-2422.
Wallace, J. B., J. W. Grubaugh, and M. R. Whiles. 1996. The influence of coarse woody debris
on stream habitats and invertebrate biodiversity.
In
McMinn, J. W. and D. A. Crossley, Jr.

5
(eds.). Biodiversity and coarse woody debris in southern
forests.
Gen. Tech. Rept. SE-94.
USDA Forest Service, Southeastern Forest Experiment Station.
PROFESSIONAL PUBLICATIONS (continued)
Wallace, J. B., J. W. Grubaugh, and M. R. Whiles. 1996. Biotic indices and stream ecosystem
processes: results from an experimental study.
Ecological Applications 6:
140-151
Whiles, M. R. and J. W. Grubaugh. 1996. Coarse woody debris and amphibian and reptile
biodiversity in southern forests.
In
McMinn, J. W. and D. A. Crossley, Jr. (eds.).
Biodiversity and coarse woody debris in southern forests. Gen. Tech. Rept. SE-94.
USDA Forest Service, Southeastern Forest Experiment Station.
Wallace, J. B., M. R. Whiles, S. Eggert, T. F. Cuffriey, G. J.Lugthart, and K. Chung. 1995.
Long-term dynamics ofcoarse particulate organic matter in three Appalachian Mountain
streams.
Journal ofthe North American Benthological Society
14: 2 17-232.
Whiles, M. R., K. Chung, and J. B. Wallace. 1993. Influence of
Lepidostoma
(Trichoptera:
Lepidostornatidae) on leaflitter processing in disturbed streams.
American Midland
Naturalist
130: 356-363.
Wallace, J. B., M. R. Whiles, J. R. Webster, T. F. Cuffney, G. J. Lugthart, and K. Chung.
1993.
Dynamics ofparticulate inorganic matter in headwater streams: linkages with
invertebrates.
Journal ofthe’ North American Benthological Society
12: 112-125.
Whiles, M. R. and J. B. Wallace. 1992. First-year benthic recoveryof a southern Appalachian
stream following three years of insecticide treatment.
Freshwater Biology
28: 81-91.
Hooker, K. L. and M. R. Whiles. 1988. A technique for collection and study ofsubterranean
invertebrates.
Southwestern Naturalist
33: 375-376.
ORAL PRESENTATIONS
Meyer, C. K., M. R. Whiles, S. G. Baer, and B. S. Goldowitz. 2004. Macroinvertebrate
communities and ecosytem function in backwater sloughs ofthe central Platte River:
influence of hydrologic gradients and restoration activities. Invited symposia:
Entomology in Prairie Ecosystems. Annual meetings ofthe North Central Branch of the
Entomological Society ofAmerica, Kansas City, MO.
Regester, K.J., K. R. Lips, and M. R. Whiles. 2004. The significance ofpond-breeding
salamanders to energy flow and subsidies in an Illinois forest ecosystem. Midwest
Ecology and Evolution Conference, University ofNotre Dame, March
5-7.
Walther, D. A., M. R. Whiles, D. W. Butler, and M. B. Flmnn. 2004. Community level
estimation ofnon-predatory chironomid production in a southern Illinois stream. Annual
meetings ofthe North Central Branch ofthe Entomological Society ofAmerica, Kansas
City, MO.
Meyer, C. K., M. R. Whiles, and S. G. Baer. 2003. Aboveground production and belowground
biomass in natural and restored Platte River slough wetlands. Annual meetings ofthe
Society for Ecological Restoration, Austin, TX.
Whiles, M. R.
2003. Freshwater macroinvertebrate communities and disturbance: tools for
basic and applied investigations in freshwater ecosystems. Invited seminar speaker,
Purdue University Department ofForestry, Fisheries, and Wildlife.

6
Callaham, M.A., Jr.,
M.R. Whiles, P.F.
Hendrix, and J.M. Blair. 2003. Using natural
abundance stable isotopes to examine the feeding ecology ofcicadas in tallgrass prairie.
Invited symposium presentation, Entomological Society ofAmerica Annual Meetings,
Cincinnati OH.
Whiles, M. R. 2003. Biological responses to hydrologic variability and restoration activities in
central Platte River backwater wetlands. Invited seminar speaker, Eastern Illinois
University Dept. of Biology.
Callaham, M.A., Jr., P.F.
Hendrix,
J.M. Blair, and
M.R. Whiles.
2003. Natural abundance and
tracer applications of stable isotopes for examination ofsoil invertebrate feeding ecology.
Invited symposium presentation at Soil Science Society ofAmerica Annual Meetings,
Denver, CO.
Whiles, M. R. 2003. Biological responses to hydrologic variability in Platte River backwater
wetlands. Invited seminar speaker, University ofIllinois Dept. ofNatural Resources and
Environmental Sciences.
Flmnn, M. B., M. R. Whiles, and S. R. Adams. 2003. Response ofaquatic macroinvertebrates to
environmental pooi management and vegetation in Mississippi River backwater wetlands.
Annual Meetings ofthe North American Benthological Society, Athens, GA.
Stone, M. L., M. R. Whiles, J. A. Webber, and K. J. Williard. 2003. Influence ofriparian
vegetation on water quality, in-stream habitat, and macroinvertebrates in southern Illinois
agricultural streams. Annual Meetings ofthe North American Benthological Society,
Athens, GA.
Oneill, B. J., S. E. Garvey, M. R. Whiles, and K. A. Lips. 2003. Scale-dependent
interrelationships among fish, landscape characteristics, and ambystomatid salamanders
in forest ponds. Joint meeting of ichthyologists and herpetologists, Manaus, Brazil.
Flinn, M. B., S. R. Adams, M. R. Whiles, S. E. Garvey, B. M. Burr, and R. S. Sheehan. 2003.
Fish and macroinvertebrate responses to environmental pool management in Mississippi
River pool 25. Illinois Chapter ofthe American Fisheries Society, Rend Lake, IL.
Adams, S. R. M. B. Flinn, B. M. Burr, R. S. Sheehan, and M. R. Whiles. 2002. Larval ecology
ofblue sucker
(Cycleptus elongatus)
in the Mississippi River. American Society of
Ichthyologists and Herpetologists meetings, Kansas City, MO.
Whiles, M. R.
2002. Ecology and ecosystem significance ofcicadas in a tallgrass prairie
landscape. Invited seminar speaker, Dept. ofBiology, University ofMemphis.
Whiles, M. R.,
and B. S. Goldowitz. 2002. Influence ofhydrology and fish on
macroinvertebrate communities in backwater sloughs ofthe central Platte River,
Nebraska. Annual Meetings of the North American Benthological Society, Pittsburgh.
Whiles, M. R., M. L. Stone, S. Webber, and K. Williard. 2001. The influence offorested
riparian buffers on water quality and stream invertebrates in Sugar Creek drainage,
Illinois. Governor’s Conference on Management ofthe Illinois river system, Peoria, Ii.
Webber, J. A., K. W. Williard, M. R. Whiles, and M. L. Stone. 2001. Watershed-scale
assessment ofthe impact of forested riparian buffer strips on stream water quality and
biotic integrity. Ecological Society of America 2’~International Nitrogen Conference,
Potomac, MD.
Evans-White, M. A., W. K. Dodds, and M. R. Whiles. 2001. Trophic basis ofproduction of
crayfish and central stonerollers in a prairie stream. Annual Meetings ofthe North
American Benthological Society, Lacrosse, WI.

7
Whiles, M. R., and W. K. Dodds. 2001. Relationships between stream size, suspended
particles, and filter-feeding macroinvertebrates in a Great Plains river system. Annual
Meetings ofthe North American Benthological Society, Lacrosse, WI.
Whiles, M. R. and M. L. Stone. 2001. Relationships between riparian zone vegetation, water
quality, and stream invertebrate communities. Midwestern Renewable Natural Resources
Conference, Peoria, Illinois.
Jensen, J. B., C. Camp, S. L. Marshall, and M. R. Whiles. 2001. Recent advances in the
knowledge ofdistribution and natural history ofthe Pigeon Mountain salamander
(Plethodon petraeus).
Joint annual meeting ofthe Herpetologists League and the Society
forthe Study of Amphibians and Reptiles, Indianapolis, Indiana.
Stagliano, D. M. and M. R. Whiles. 2000. Aquatic invertebrate trophic structure and secondary
production in a tallgrass prairie stream. Annual Meetings of the North American
Benthological Society, Keystone, Colorado.
Meyer, C. K., Whiles, M. R., and R. E. Chariton. 2000. Secondary production and energetics of
grass-feeding acridids in tallgrass prairie. Annual meetings of the Southwestern Branch
ofthe Entomological Society ofAmerica, Dallas, TX.
Jonas, J. L., M. R. Whiles, and R. E. Charlton. 2000. Land use patterns and insect diversity in a
central Kansas grassland. Annual meetings ofthe Southwestern Branch ofthe
Entomological Society ofAmerica, Dallas, TX.
Dodds, W. K., M. Evans-White, N. M. Gerlanc, L. Gray, D. Gudder, M. J. Kemp, A. Lopez, D.
M. Stagliano, E. A. Strauss, S. L. Tank, M. R. Whiles, and W. M. Wollheim. 2000.
Quantification ofthe nitrogen cycle in a prairie stream: Konza LINX. Annual Meetings
ofthe North American Benthological Society, Keystone, Colorado.
Whiles, M. R., and B. S. Goldowitz. 1999. Influence ofhydrology on aquatic insect emergence
production from backwater sloughs ofthe central Platte River, Nebraska. Annual
meetings ofthe North American Benthological Society, Duluth, MN.
Meyer, C. K., M. R. Whiles, and R. E. Charlton. 1999. Secondary production and energetics of
a dominant grass-feeding grasshopper in tallgrass prairie. Annual meetings ofthe
Entomological Society ofAmerica, Atlanta.
Stagliano, D., M. R. Whiles, and R. E. Charlton. 1999. Aquatic insect production and
functional structure in a tallgrass prairie headwater stream. Annual meetings ofthe
Entomological Society ofAmerica, Atlanta.
Whiles, M. R. 1999. Natural History and emergence production patterns of cicadas
(Hornoptera: Cicadidae) on the Konza Prairie Research Natural Area, Kansas. Invited
seminar speaker, University of Kansas, November 4, 1999.
Jeffrey, J. D., and M. R. Whiles. 1999. Effects ofthe PGA-class Colbert Hills golf course
construction on prairie amphibians.
26th
meetings ofthe KS Herp. Society, Pratt.
Whiles, M. R. 1999. Ecology and significance ofcicadas in a tallgrass prairie ecosystem.
Invited seminar speaker, University of Maine, October 21, 1999.
Evans-White, M. A., W. K. Dodds, M. J. Kemp, L. A. Gray, A. Lopez, S. L. Tank, and M. R.
Whiles.
1999. Patterns ofnitrogen cycling in a prairie stream food web. Annual
meetings ofthe North American Benthological Society, Duluth, MN.
Goldowitz, B. S., and M. R. Whiles. 1999. Influence ofhydrologic fluctuations on aquatic
vertebrate communities in central Platte River Wetlands. Annual meetings of the
Ecological Society ofAmerica, Spokane, WA.

8
Whiles, M. R. 1999. Significance ofarthropods to prairie ecosystem function. Invited
symposium speaker, annual meetings ofthe Central States Entomological Society,
Manhattan, KS.
Whiles, M. R. 1999. Aquatic invertebrate communities and disturbance: tools for basic and
applied investigations. Invited seminar speaker, Southern Illinois University.
Whiles, M. R., A. Franzen, S. Dinsmore, and B. L. Brock. 1998. Use ofinvertebrate rapid
bioassessment for identification of stream reaches contributing to water quality
degradation in a northeast Nebraska reservoir. Joint meetings of the Association of
Limnologists and Oceanographers and the Ecological Society ofAmerica, St. Louis, MO.
Evans-White, M. A., W. K. Dodds, M. J. Kemp, L. A. Gray, J. L. Tank, M. R. Whiles, and A.
Lopez. 1998. Nitrogen transfer through a prairie stream food web. Annual meetings of
the Great Plains Limnological Society, Pittsburg, KS.
Whiles, M. R. and B. S. Goldowitz. 1998. Biological responses to hydrologic fluctuation in
wetland sloughs ofthe central Platte River. The 9th Platte River Basin Ecosystem
Symposium, Kearney, NE.
Whiles, M. R. 1997. Invertebrate bioassessment: advantages, techniques, and applications.
Invited speaker, ann. meetings ofthe Nebraska Natural Resource Districts, Kearney, NE.
Whiles, M. R. 1997. Invertebrate communities and ecosystem processes in disturbed lotic
systems. Invited seminar speaker, Kansas State University, Manhattan, KS.
Whiles, M. R. 1996. Disturbance, invertebrate con~imunities,and stream ecosystem processes in
southern Appalachian streams. Invited seminar speaker, Texas Tech University,
Lubbock.
Whiles, M. R. 1995. Stream ecosystem research at Coweeta Hydrologic Laboratory. Invited
seminar speaker, Southeastern Oklahoma State University, Durant, Oklahoma.
Whiles, M. R., and S. Bruce Wallace. 1995. Leaf litter decomposition and shredder
communities in streams draining mixed hardwood and white pine watersheds. Annual
meetings ofthe North American Benthological Society, Keystone, Colorado.
Wallace, J. B., J. W. Grubaugh, and M. R. Whiles. 1995. Biotic indices and stream ecosystem
processes: results from an experimental study. Annual meetings ofthe North American
Benthological Society, Keystone, Colorado.
Whiles, M. R. 1995. Disturbance and aquatic invertebrate communities in southern
Appalachian Mountain streams. Invited seminar speaker, University ofTennessee at
Chattanooga.
Whiles, M. R. 1994. Recovery dynamics ofinvertebrate communities and litter processing in
southern Appalachian streams following disturbance. Invited seminar, Berry College,
Mount Berry, Georgia.
Whiles, M. R. and J. B. Wallace. 1994. Long-term measurements ofcoarse particulate organic
matter export from headwater streams. Annual meeting ofthe North American
Benthological Society, Orlando, Florida.
Grubaugh, S. W., Wallace, S. B., and M. R. Whiles. 1994.
1956-57
versus 1991-92: A
comparison ofmacroinvertebrate communities and potential effects of changing land
usage in a Georgia piedmont river. Annual meeting ofthe North American Benthological
Society, Orlando, Florida.

9
Whiles, M. R.
1993. Coarse woody debris and amphibian and reptile diversity in southern
forests. Conference on coarse woody debris in southern forests: effects on biodiversity,
University ofGeorgia, Institute ofEcology.
Whiles, M. R., and G. S. Lugthart. 1993. Secondary production in a headwater stream during
record dry and wet years. Annual meeting ofthe North American Benthological Society,
Calgary, Alberta, Canada.
Whiles, M. R., Wallace, J. B., and K. Chung 1992. Use of a refractory litter species by a
caddisfly: the role of
Lepidostoma
in stream recovery from disturbance. Annual meeting
ofthe North American Benthological Society, Louisville, Kentucky.
Whiles, M. R., and S. B. Wallace 1991. First-year macroinvertebrate community recovery in a
southern Appalachian stream following an insecticide induced disturbance. Annual
meeting ofthe North American Benthological Society, Santa Fe, New Mexico.
Whiles, M. R., Tate, C. M., and K. L. Hooker 1988. The influence ofnutrient enrichments and
grazers on periphyton growth in Konza Prairie streams.
Annual Division of Biology
Graduate Student Forum, Kansas State University.
Tate, C.M., Whiles,
M.R.,
and K. L. Hooker 1988. Influence of nutrients and grazers on
periphyton biomass in prairie streams. Annual meeting
ofthe North American
Benthological Society, Tuscaloosa, Alabama.
Tate, C.M., Hooker, K.L., and M. R. Whiles 1987. Seasonal response ofperiphyton to nutrient
enrichment in prairie streams. Annual meeting ofthe North American Benthological
Society, Orono, Maine.
POSTER PRESENTATIONS
Rowlett, S. H., D. A. Walther, and M. R. Whiles. 2004. A comparison ofmacroinvertebrate
community structure on artificial rock riffles to snag and exposed streambed habitats in
Cache River, Illinios. Annual meetings of the North Central Branch ofthe Entomological
Society ofAmerica, Kansas City, MO.
Whiles, M. R., D. W. Butler, D. A. Waither, and M. B. Flmnn. 2003. Temperature-dependent
growth rates ofnon-predatory chironomids from a southern Illinois stream. Annual
meeting ofthe North American Benthological Society, Athens, GA.
Stone, M. L., M. R. Whiles, S. A. Webber, and K. Williard. 2002. Relationships between
riparian vegetation, water chemistry, and stream invertebrates in a southern Illinois
agricultural landscape. Annual meeting of the North American Benthological Society,
Pittsburgh.
Flinn, M. B., R. Adams, M. R.
Whiles, B.
Burr, and R. Sheehan. 2002. Feeding ecology of
larval blue suckers
(cycleptus elongatus):
a direct benefit of riverine backwater
invertebrates to a main channel fish. Annual meeting ofthe North American
Benthological Society, Pittsburgh.
Flinn, M. B., R. Adams, M. R.
Whiles, B. Burr,
and R. Sheehan. 2002. Feeding ecology of
larval blue suckers in Mississippi River backwaters. Mississippi River Research
Consortium meetings, LaCrosse, WI.
Meyer, C. K., M. R. Whiles, andR. E. Charlton. 2001. Secondary production and energetics of
grasshoppers as affected by annual burning in taligrass prairie. Annual meetings of the
North Central Branch of the Entomological Society ofAmerica, Fort Collins, CO.

10
Callaham, M. A., J. M. Blair, T. C. Todd, D. J. Kitchen, and M. R. Whiles. 2001. Fire,
mowing, and fertilization effects on macroinvertbrate assemblages in tallgrass prairie
soils. Soil Ecology Society Conference, Atlanta, Georgia.
Whiles, M. R., M. A. Callaham, Sr., C. K. Meyer, and S. M. Blair. 2000. Land Management
Influences on Grassland Cicada Emergence Dynamics. Ecological Society ofAmerica
All Scientists meetings, Snowbird, Utah.
Corum, R. A., W. K. Dodds, and M. R. Whiles. 2000. Distribution offilter-feeding
invertebrates in central Kansas rivers and streams. Midwest Limnological Society
Meetings, Lawrence, KS.
Whiles, M. R., D. M. Stagliano, and R. B. Charlton. 2000. Bioassessment ofdisturbed prairie
streams: problems with traditional fish and aquatic invertebrate metrics. Annual
Meetings ofthe North American Benthological Society, Keystone, Colorado.
Callaham, M. A., M. R.
Whiles,
C. K. Meyer, B. L. Brock, and R. E. Charlton. 1999.
Emergence production and ecology ofannual cicadas (Homoptera: Cicadidae) in taligrass
prairie. Annual meetings ofthe Entomological Society ofAmerica, Atlanta, GA.
Callaham, M. A., M. R. Whiles, C. K. Meyer, B. L. Brock, and R. E. Charlton. 1999. Feeding
ecology ofcicadas (Homoptera: Cicadidae) in tallgrass prairie. Soil Ecology Society
Conference, Chicago, IL.
Jonas, S. L., M. R. Whiles, and R. E. Charlton. 1999. Influence ofland use patterns on insect
diversity in a central Kansas grassland. Annual meetings ofthe Entomological Society of
America, Atlanta, GA.
Whiles, M. R., M. A. Callaham, C. K. Meyer, B. L. Brock, and R. E. Charlton. 1998. Periodical
cicada emergence production in a northeast Kansas riparian forest. Annual meetings of
the Entomological Society of America, Las Vegas, NV.
Stagliano, D., R. E. Chariton, and M. R. Whiles, 1998. Assessing environmental impacts on
Colbert Hills using fish and aquatic insect communities. Kansas State Research and
Extension Annual Conference, Manhattan, KS.
Alexander, K. A. and M. R. Whiles. 1998. A new species of
Ironoquia
Banks (Trichoptera:
Limnephilidae) from backwaters ofthe central Platte River, Nebraska. North American
Prairie Conference, Kearney, NE.
Dinsmore, S., M. R. Whiles, and R. Roberts. 1997. Use ofbioassessment for identification of
stream reaches contributing to eutrophication ofa northeastNebraska reservoir. Annual
meetings ofthe Southwestern Association ofNaturalists, Fayetteville, Arkansas.
Dinsmore, S., M. R. Whiles, and R. Roberts. 1996. Biological and chemical analysis of
agriculturally impacted streams in northeastNebraska. 31st regional meetings ofthe
American Chemical Society, Sioux Falls, SD.
Whiles, M. R. 1993. Secondary production in a headwater stream during wet and dry years.
Annual meetings ofthe Coweeta LTER site, Athens, Georgia.
Whiles, M. R. and K. L. Hooker 1987. Subterranean invertebrates from an artesian spring on
Konza Prairie. Annual meeting of the NA Benthological Soc., Orono, Maine.
GRANT REVIEWER
NSF, USDA, USEPA, USGS-BRD, Illinois Groundwater Consortium (IGC)
EPA STAR Fellowships, invited review panel member (2002)

11
BOOK REVIEWER
Fundamentals of Ecology, 5th ed., E. P. Odum and G. Barrett
Ecology, Concepts and Applications, 2’~ed., M. C. Molles
Freshwater Ecology, W. K. Dodds
MANUSCRIPT REVIEWER
BioScience, Ecology, Ecological Applications, Limnology and Oceanography
Archiv furHydrobiologie, Journal of the North American Benthological Society
Environmental Management, Prairie Naturalist, American Entomologist
Environmental Entomology, Journal ofInsect Science, Journal ofEcology
Journal ofthe Kansas Entomological Society, Bulletin of Marine Science
Journal ofCave and Karst Studies, Wetlands, Environmental Toxicology and Chemistry,
New Zealand Journal ofMarine and Freshwater Research, Restoration Ecology
PROFESSIONAL SERVICE and MEMBERSHIPS
2002-03
Program Committee, North American Benthological Society
2002-03
Membership Director, American Water Resources Assoc., Illinois chapter
2000-
Entomological Society ofAmerica
1997-
Sigma Xi
1986-
North American Benthological Society

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