RECEIVED
CLERK’S~OFFICE
ILLINOIS POLLUTION CONTROL BOARD
AU~°
0
August 30, 2005
V J
STATE OF ILLINOIs
ll’4
THE MATTER OF:
)
Pollution Control Board
)
PROPOSED AMENDMENTS TO
)
R04-25
DISSOLVED OXYGEN STANDARD 35 ILL.)
(Rulemaking
-
Water)
ADM. CODE 302.206
)
HEARING
OFFICER ORDER
On August 25, 2005, in Chicago, the Board held the third hearing in this rulemaking. The
rulemaking proponent, the Illinois Association ofWastewater Agencies, seeks to amend the
Board’s rule establishing general use water quality standards for dissolved oxygen (35 Ill. Adm.
Code 302.206). In this order, the hearing officer discusses two rulings made at the third hearing.
First, the Illinois Environmental Protection Agency (Agency) asked at hearing to have the
opportunity to continue stakeholder discussions regarding the dissolved oxygen standard and to
submit a status report on those discussions in two months. The hearing officer granted the
Agency’s request, and required that the Agency file the status report with the Board by
November 1, 2005. The hearing officer also noted that the “mailbox rule” (35 Ill. Adm. Code
101 .300(b)(2)) would not apply to this filing, and that, accordingly, the Board must receive the
Agency’s status report by November 1, 2005. This filing may be made electronically through the
Board’s Web-based Clerk’s Office On-Line (COOL) at www.ipcb.state.il.us. Any filing with the
Board must also be served on the hearing officer and on those persons on the Service List.
Second, the Illinois Department ofNatural Resources (DNR) stated at hearing that it
would not be presenting, at the third hearing, the witness for whom it had prefiled testimony, Dr.
David L. Thomas. DNR represented that it, like the Agency, wished to pursue stakeholder
discussions regarding the dissolved oxygen standard. DNR also stated that Dr. Thomas’ prefiled
testimony, filed with the Board on August 4, 2005, no longer represents DNR’s position. DNR
therefore made a motion to withdraw the prefiled testimony ofDr. Thomas, which the hearing
officer granted.
Although Dr. Thomas’ August 4, 2005 prefiled testimony is withdrawn, the filing itself
remains part ofand physically present in the official Clerk’s office record ofthis rulemaking
proceeding. Accordingly, when reading another document in this record that refers to Dr.
Thomas’ prefiled testimony, such as Public Comment 81, a member ofthe public will be able to
locate the referenced DNIR filing. To avoid any potential confusion, however, the R04-25 docket
sheet entry for Dr. Thomas’ prefiled testimony will reflect that the hearing officer granted DNR’s
motion to withdraw the prefiled testimony, as it no longer represents DNR’s position. For fUrther
2
clarity, the Clerk’s office has been instructed to physically and electronically attach this hearing
officer order to the front of Dr. Thomas’ August 4, 2005 prefiled testimony.
IT IS SO ORDERED.
Richard R. McGi,
Hearing Officer
Illinois Pollution Control Board
100 West Randolph Street, Suite 11-500
Chicago, Illinois 60601
(312) 814-6983 mcgil1r4i~ipcb.state.il.us
BEFORE THE ILLINOIS POLLUTION CONTROL BOARLA
E CE IV ED
CLERK’S
OFFICE
AUG 04 2005
IN THE MATTER OF:
)
STATE OF ILUNOIS
PROPOSED AMENDMENTS TO
)
R 04-25
PollutIon
Control Board
DISSOLVED OXYGEN STANTARD
)
35 Ill. Adm. Code 302.206
)
)
NOTICE OF FILING
See attached Service List
PLEASE TAKE NOTICE that on Wednesday, August 3, 2005, we filed the attached
Testimony ofDavid L. Thomas, PhD. with the Clerk of the Illinois Pollution Control Board, a copy
of which is herewith served upon you.
Stanley Yonkauski, Jr.
Illinois Department ofNatural Resources
One Natural Resources Way
Springfield, Illinois 62702-127 1
Respectfully submitted,
ILLINOIS DEPARTMENT OF
NATURAL RESOURCES
By:
torn eys
This filling being submitted on recycled paper.
CERTIFICATE OF SERVICE
The undersigned certifies that a copy of the foregoing Testimony was filed by hand deliver
to the Clerk of the Illinois Pollution Control Board and served upon the parties to whom said Notice
is directed by first class mail, postage prcpaid, by depositing in the U.S. Mail at One Natural
Resources, Springfield, Illinois on Wednesday, August 3, 2005.
SEE ATTACHED SERVICE LIST
Stan
ki, Jr.
SERVICE LIST
Fred L. Hubbard
415 North Gilbert Street
Danville, IL 62834-00 12
Benard Sawyer
Metropolitan Water Reclamation District
6001 W. Pershing Rd.
Cicero, IL 60650-4112
Claire A. Manning
Posegate & Denes, P.C.
111 N. Sixth Street
Springfield, IL 62705
Deborah J. Williams
IEPA
1021 North Grand Avenue
P.O. Box 19276
Springfield, IL 62794-9276
Dorothy M. Gunn
Illinois Pollution Control Board
100 W. Randolph St., Suite 11-500
Chicago, IL 60601
Frederick D. Keady
Vermilion Coal
1979 Johns Drive
Glenview, IL 60025
James T. Harrington
Ross & Hardies
150 North Michigan
Chicago, IL 6060 1-7567
John Donahue
City ofGeneva
22 South First Street
Geneva, IL 60 134-2203
Alex Messina
Illinois Environmental Regulatory Group
3150 Roland Avenue
Springfield, IL 62703
Charles W. Wesselhoft
Ross & Hardies
150 North Michigan Avenue, Suite 2500
Chicago, IL 6060 1-7567
Connie L. Tonsor
IEPA
1021 North Grand Avenue
P.O. Box 19276
Springfield, IL 62794-9276
Dennis L. Duffield
City of Joliet
Department of Public Works and Utilities
921 E. Washington Street
Joliet, IL 60431
Erika K. Powers
Barnes & Thomburg
1 N. Wacker, Suite 4400
Chicago, IL 60606
James L. Daugherty
Thom Creek Basin Sanitary District
700 West End Avenue
Chicago Heights, IL 60411
Joel J. Stemstein
Office of the Attorney General
188 West Randolph,
20th
Floor
Chicago, IL 60601
William Richardson
Illinois Department of Natural Resources
One Natural Resources Way
Springfield, IL 62702-127 1
Avenue, Suite 2500
Katherine D. Hodge
Hodge Dwyer Zeman
3150 Roland Avenue
P.O. Box 5776
Springfield, IL 62705-5776
Lisa Frede
Chemical Industry Council of
2250 E. Devan Avenue, Suite
Des Plaines, IL 600 18-4509
Matthew J. Dunn
Office of the Attorney General
188 West Randolph,
20th
Floor
Chicago, IL 60601
Mike Callahan
Bloomington Normal
Water Reclamation District
P.O. Box 3307
Bloomington, 16 1702-3307
Richard McGill
Illinois Pollution Control Board
100W. Randolph St., Suite 11-500
Chicago, IL 60601
Stephanie N. Diers
IEPA
1021 North Grand Avenue
P.O. Box 19276
Springfield, IL 62794-9276
Susan M. Franzetti
10 South LaSalle Street, Suite 3600
Chicago, IL 60603
Vicky McKinley
Evanston Environment Board
23 Grey Avenue
Evanston, IL 60202
Lany Cox
Downers Grove Sanitary District
2710 Curtis Street
Downers Grove, IL 60515
Margaret Hedinger
2601 South Fifth Street
Springfield, IL 62703
Michael 0. Rosenberg, Esq.
Metropolitan Water Reclamation District
100 East Erie Street
Chicago, IL 60611
Richard Lanyon
Metropolitan Water Reclamation District
100 East Erie Street
Chicago, IL 60611
Sanjay K. Sofat
EPA
1021 North Grand Avenue
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
Tom Muth
Fox Metro Water Reclamation district
682 State Route 31
Oswego, IL 60543
W.C. Blanton
Blackwell Sanders Peper Martin LLP
2300 Main Street, suite 1000
Kansas City, MO 64108
Illinois
239
Edward Hammer
U.S. Environmental Protection Agency
WQ-16J
77 W. Jackson Boulevard
Chicago, IL 60604
TESTIMONY
AUG 042005
David L. Thomas, PhD
STATE OF
IWN0IS
Chief, Illinois
Natural
History
Survey
POllutiOn Control Bo&tj
August 3, 2005
My name is David
L.
Thomas, and lam Chief of the Illinois Natural History Survey, a
Division of the Department of Natural Resources (Department). I received my Masters degree in
Ecology from the University of Illinois in 1967, where! worked on the Percina darters of the Kaskaskia
River for my thesis. I completed my PhD from Cornell in 1971 in Ecology and Systemmatics, and my
thesis was on the drums (Sciaenidae) ofthe upper Delaware Bay and lower Delaware River. I also
taught the laboratories for Ichthyology and Advanced Ichthyology whie at Cornell, and was curator of
the Cornell fish collection.
This testimony is presented on behalf of the Illinois DNR and based on my experience as a
trained ichthyologist, on my more than 35 years of evaluating the effects of various environmental
parameters on aquatic biota, and my first-hand knowledge and experience on Illinois fishes. I have
regularly measured DO as part ofthe physical/chemical parameters measured during field collections,
and
have
experience evaluating the effects of this parameter on aquatic resources in Illinois. I interact
with our Ichthyologist at the Survey on a regular basis, and have made numerous collections with him
over the last 5 years. I deal with a variety of issues with our fisheries staff, particularly regarding
invasive species. I have also conducted field work with DNR fisheries staff, and assisted in their basin
surveys.
The present DO standard requires that at no time shall concentrations decline below 5mg/Land
for at least 16 hours each day they must remain above 6 ma/L. The LAWA, based on testimony and
recommendations ofDrs. Garvey and Whiles, recommended the following changes to the DO standard:
A 1-day minimum* of 5.0 mg/L spring through summer (ie.. March 1 through June 30)
A 7-day mean** of 6.0 mg/L spring through early summer (i.e. March 1 through June 30)
A 1-day minimum of3.5 mg/L the remainder ofthe year (i.e., July 1 through February 28 or 29)
A 7-day mean minimum*** of4.0 mg/Lthe remainder ofthe year (i.e., July 1 through February
28 or 29)
*
I-day minimum is the lowest measured value of DO during a
24-hour
calendar day
**
7-day mean DO is the average of the daily mean DO values from the current and previous 6
calendar days.
~**
7-cla~’mean nzhiimunz is the arithmetic average oft/ic dat/v fninh?nlLni DO valuesfrom the current
cindprevious
6
calendar
days.
The DNR believes that while we should recognize that some rivers and streams could maintain
present aquatic populations under a revised standard like that proposed by the IAWA, there are many
streams and rivers in Illinois that would not be able to maintain present aquatic populations. If one
statewide standard is going to be put into place. it needs to be high enough to protect sensitive species.
The IAWA proposal does not accomplish this level of protection. We believe the present standard
should be maintained until
it
can be demonstrated that the biota in particular water bodies will not be
negatively affected by a lower standard.
Since the second hearing on this matter, conducted on August 12, 2004, the Department has
been actively participating in status conference calls and stakeholder meetings addressing the merits
of the rulemaking proposal. Though the stake holders meetings did not result in an agreed upon
regulatory proposal, it helped the DNR understand the state of knowledge in Illinois as it relates to
dissolved oxygen and aquatic life needs.
The DO standard in Illinois needs to account for the natural DO levels in the water body in
question and the presence or absence of DO sensitive species. Initially, the opposite approach was
attempted, that is, to designate streams that needed greater protection than proposed by the IAWA,
however, our level of knowledge of all streams and the species that they contain is not sufficiently
developed to come up with a complete list. Without a complete list of streams needing to maintain at
least the present standard, implementation ofa lower standard could prove to be detrimental to sensitive
aquatic species. Justification for needing greater protection (than those proposed by the IAWA) of
some of our aquatic resources are presented below.
There are a significant number of rivers and streams in Illinois that contain fish species
considered to be oxygen sensitive (see Table 1). This list represents 25 fish species that are sensitive
to low DO based on life history and distribution data for Illinois (Smith, 1979) andWisconsin (Becker,
1983). These species were considered good indicators for waters that contain DO sensitive aquatic
biota. Other species could be added to this list as indicated below.
A list of 30 “DO” tributaries and 10 “DO” major rivers is contained in Table 2. These were
selected based on the presence of at least 5 DO sensitive indicator fish species for major river
mainstems, and 4 DO sensitive indicator species for tributary streams, and represents the kinds of
streams that would need greater protection than the proposal from IAWA. All streams are perennial
according to 7Q10 flow maps from the Illinois State Water Survey. Rankin recently (2004) provided
data for Ohio that showed that Exceptional Warmwater Habitat streams (described below) maintained
fairly high DO levels and could have 10 or more sensitive species. Those streams with mean DO values
between 6-7 mg/I rarely had more than
5
intolerant species.
The Ohio EPA (1996) made a good rationale for why some warmwater streams needed a greater
level of protection, and higher DO standards, than other ~varmwaterstreams. This document developed
arationale for designation of DOcriteriaforExceptional \Varmwater Habitat (EWH), and theirstandard
for these streams was a 6.0 mg/I daily average and aS mg/I minimum. EWH designation was reserved
for waters which support ‘unusual and exceptional” assemblages of aquatic organisms which are
characterized by a high diversity of species, particularly those which are highly intolerant and/or rare,
threatened, endangered, or special status (i.e., declining species). These waters were characterized by
Index of Biotic Integrity (WI) values above 46. In a summary of individual Ohio streams and rivers
(page 17), they state the following: “The results ofthe comparison of continuously measured D.O. and
E’Wl-I attainment in six steams and rivers of varying sizes shows that the latter can he compatible with
minimum D.O. values less than 6 mg/I. However, values less that S mg/I were either infrequent, did
not frequently correlate with full EWH use attainment, or were measured only under extreme low flow
conditions. Thus, the analysis would appear to support a minimum EWU D.O. standard less that 6
mg/I, but not less than S mg/I.”
Illinois has many streams that meet the Ohio standard for Exceptional WarmwaterHabitat, and
we list 40 ofthese as “DO sensitive streams” based on the presence ofDO sensitive species. Eighteen
ofthe streams selected had IBI scores with an average weighted score of 50. Only two of these streams
had an IBI under 46 (one with a value of40 and one with a value of43). There were 29 other streams
on the larger list provided that had IBI values of over 46, and on closer examination these too might
be considered for greater protection.
There are other fishes found in Illinois, other than those listed in Table 1, that are found in
“higher” DO waters. Rankin (2004) produced a table of variOus fishes and the weighted mean DO
values at which they were captured. I went through the list and noted all fish species that I was sure
also occurred in Illinois that were found at DO levels areater than Smallmouth bass (which was found
at a weighted mean DO of 6.61 mg/I). This list is included as Table 3, and includes four species (Black
Redhorse, Blacknose Dace, Northern Hog Sucker and Rosyface Shiner) listed as DO sensitive in Table
1. One of the species on this list, the Slenderhead darter, was a species that I had worked on for my
master’s theses at University of Illinois. I found in tests I conducted that this species had a higher rate
ofrespiration, and was found in higheroxygen waters, than the Blacksided darter, another species that
I studied. In Ohio the weighted mean DO valuefor all collections ofSlenderhead darter was 6.7 mg/I,
whereas it was 5.6 mg/I for Blacksided darter.
The Department has given strong consideration to the Ohio data for this testimony because they
are on the same latitude as much ofIllinois, and have many of the same Ohio River drainage fishes as
are found in Illinois. Ohio EPA has developed one ofthe better databases that we have found on field
measurements of DO with individual fish collections. The Ohio data corroborates our field
observations in Illinois, and fish that are DO sensitive in Ohio, will be DO sensitive in illinois and
across their range.
The IAWA recommended an end date for the sensitive season (spawning and earlydevelopment
of fish) of June 30 statewide. This date will not be protective of many species that spawn up through
late June, or are summer spawners. Table 4 is a summary of Illinois fishes that spawn primarily in the
summer. This list does not include late spring spawners such as Smallmouth bass which may spawn
into late June. It also does not include the Channel catfish, although Simon and Wallus (2003) stated
that yolk-sac larvae andearlyjuveniles were collected mid-May through August with peaks in June and
July in the Tennessee and lower Ohio rivers. Six of the “summer” spawners in Table 4 are also listed
in Table 3 as being found in Ohio in higher oxygen waters
-
Emerald shiner, Ironcolor shiner. Bigmouth
shiner, Weed shiner, River redhorse, and Stonecat. One of these species, the Bigmouth shiner, was
studied by a student (Clinton Kowalik) atUniversity of Illinois that I helped advise. He found that peak
gonad development occurred on June26 and small young (under 20mm) were collected in July.
Ohio EPA (1996) stated that while Smg/l (their recommended minimum for Exceptional
Warmwater Habitat) is more stringent than that proposed by U.S. EPA (1986) for adults and juveniles,
it is necessary to protect younger life stages. They go on to state that “the EW’H DO. criterion that we
propose lies between the U.S. EPA recommended wanriwater and coldwaterlevels (non-embryonic life
stages only) of protection which also seems reasonable given that some of the sensitive warmwater
species that comprise the assemblages representative of EWH may well approach the sensitivity of
salmonids”. With the information provided, it is evident the standard, as proposed. will not he
protective for all the waters of the state.
The Ohio EPA document addresses an issue that we have struggled with in Illinois. and that is
that thereis a group of fishes that fall in DO sensitivity between cold-water andthe more typical warm-
water fauna. The Ohio Exceptional Warmwater Habitat category recognizes that a number of species
found in their biologically diverse warm water streams require very good water quality including well
oxygenated waters, We recognizethat Illinois also has waters that could be considered as needing extra
protection because theycontain diverse fish populations. threatened andendangered species. and many
DO sensitive species. If one statewide standard is going to be put in place, then it needs to he high
enough to protect these sensitive species. The IAWA proposal does not accomplish that and should
not be adopted.
The Ohio EPA document cites FWPCA (1968) as stating that “In some cases, good populations
of warmwater fish, including game and pan fishes, occur in waters in which dissolved oxygen may be
as low as 4 mg/I for short periods...(and)...Five and 4 mg/I are close to the borderline of oxygen
concentrations that are tolerable for extended periods. For a good population of game and pan fishes
the concentration should be considerably more than this.”
In light of the above statements it seems particularly important that we provide greater
protection for warm water streams that have high biotic integrity, good game and pan fishes, and
oxygen sensitive fishes.
The focus of this testimony has been on fishes, but there are a number of mussels and other
invertebrates that are also sensitive to low DO (see Rankin 2004). In addition, we have a number of
state threatened and endangered species in Illinois, and for many we know little about their oxygen
requirements. All of the above indicates that we should maintain our present standard, unless we can
show for particular water bodies that a lower standard will not negatively affect aquatic species in that
system.
References:
Becker, G.C. 1983. Fishes of Wisconsin. University of Wisconsin Press, Madison, Wisconsin.
lOS2p.
FederalWater Pollution Control Administration (FWPCA). 1968. Waterquality criteria. Report
of the National Technical Committee to the Secretary of Interior. Washington, D.C. 234p.
Ohio Environmental Protection Agency (OEPA). 1996. Justification andrationale forrevisions
to the dissolved oxygen criteria in the Ohio Water Quality Standards. OEPA Technical Bulletin
MAS.1995-12-S, 25p.
Rankin, E.T. 2004.
Notes on associations between dissolved oxygen and fish and
macroinvertebrate assemblages in wadeable Ohio streams. (Draft iact Sheet)
Simon, T.P. and R.Wallace. 2003. Ictaluridae
-
catfish and madtom. Vol 3, in Wallus, Yeager
and Simon. Reproductive biology and early life history of fishes in the Ohio River drainage. TVA.
Chattanooga, Tenn.
Smith, P.W. 1979. The Fishes of Illinois. University of Illinois Press. (Published forthe Illinois
Natural History Survey). 314p.
Table 1: Species of fish found in Illinois that require higher dissolved oxygen levels
Common Name
American brook
lamprey
Banded sculpin
Bigeye
chub
Bigeye shiner
Black redhorse
Blacknose dace
Brook stickleback
Fourhorn sculpin
lroncolor shiner
Least brook lamprey
Longnose dace
Mottled sculpin
Ninespine stickleback
Northern brook
lamprey
Northern hog sucker
Northern pike
Ozark minnow
River redhorse
Rock bass
Rosyface
shiner
Slimy sculpin
Southern redbelly dace
Spoonhead seulpin
Threespine stickleback
Weed
shiner
Table 2 - TESTIMONY OF DAVID L. THOMAS, AUGUST 2005
lB-BASIN
CATCHMENT NAME OR MAINSTEM
PROPOSED
DO
WATERS
DO
MAJOR
RIVER
NUMBER OF
HIGH DO
HIGH DO
FISH
FISH
DO
INDICATOR INDICATOR
TRIBUTARY SPECIES
SPECIES
IBI
ABASH RIVER MS
WABASH RIVER MS
X
X
X
6
53
~RMILION(SOUTH) RVR LITTLE VERMILION (SOUTH) RIVER
X
X
x
6
54
ERMILION (SOUTH) RVR VERMILION (SOUTH) RIVER MS
X
ERMILION (SOUTH) RVR SALT FORK
X
ERMILION (SOUTH) RVR MIDDLE FORK
X
\CKINAW RIVER
MACKINAW RIVER MS
X
\CKINAW RIVER
LITTLE MACKINAW RIVER
X
3 BUREAU CREEK
BIG BUREAU CREEK .
X
ERMILION (NORTH) RVR VERMILION (NORTH) RIVER MS
X
X
x
5
45
x
5
51
X
X
4
5~
X
X
7
55
Xx
6
X
x
6
50
x
X
5
48
)X RIVER
FOX RIVER Ms
X
X
X
7
40
)X RIVER
INDIAN CREEK
X
X
X
4
)X RIVER
BIG ROCK CREEK
X
X
X
4
)X RIVER
NIPPERSINK CREEK
X
X
X
4
\NGAMON RIVER
KICKAPOO CREEK
X
X
X
4
XNKAKEE RIVER
KANKAKEE RIVER MS
X
X
X
10
so
\NKAKEE RIVER
FORKED CREEK
X
X
X
4
45
\NKAKEE RIVER
HORSE CREEK
X
X
X
4
5Q
\NKAKEE RIVER
ROCK CREEK
X
X
X
4
5~
OOUOIS RIVER
IROOUOIS RIVER MS
X
X
X
5
OQUOIS RIVER
BEAVER CREEK
X
X
X
4
OOUOIS RIVER
SUGAR CREEK
X
X
X
5
~PLERIVER
APPLE RIVER MS
X
X
X
5
‘PLE RIVER
FURNACE CREEK
X
X
X
6
~PLERIVER
SOUTH FORK
X
X
X
6
3PLE RIVER
CLEAR CREEK
X
~______
X
X
5
JCK RIVER
GREEN RIVER
X
X
X
5
JCK RIVER
FRANKLIN CREEK
X
X
X
6
JCK RIVER
LEAF RIVER
X
X
X
5
50
OCK RIVER
KYTE RIVER
X
X
X
4
43
OCK RIVER
STILLMAN CREEK
X
X
X
6
OCK RIVER
KISHWAUKEE RIVER
X
X
X
7
56
OCK RIVER
KILLBUCK CREEK
X
X
X
7
OCK RIVER
PISCASAW CREEK
X
X
X
5
51
OCK RIVER
COON CREEK
X
X
X
5
OCK RIVER
RUSH CREEK
X
X
X
5
56
OCK RIVER
SOUTH BRANCH-EAST KISHWAUKEI
X
X
X
6
OCK RIVER
NORTH BRANCH-KISHWAUKEE RVR
X
X
X
4
OCK RIVER
PINE CREEK
X
X
X
4
OCK RIVER
SUGAR RIVER
X
X
X
4
51
OCKRIVER
ROCKRIVERMS
X
-
X
X
5
TOTALS BY
CATEGORY =
40
10
30
Table 3: The weighted mean DO
for various
fishes collected in Ohio streams. Fish listed are
ones that occur in Illinois, and were found at DO levels equivalent to or higher than for
Smallmouth Bass*
Weighted DO Means (MglI) for Ohio Streams
Smallmouth Bass
6.61
Central Stoneroller
6.62
Black
Crappie
6.63
Golden Redhorse
6.70
Slenderhead Darter
6.71
Silver Redhorse
6.72
Silverjaw Minnow
6.81
Hornyhead Chub
6.52
Emerald Shiner
6.83
Black Redhorse
6.93
Shorthead Redhorse
6.96
Blacknose Dace
6.96
Northern Hog Sucker
7.02
Rosyface Shiner
7.18
Bigmouth Shiner
7.22
Stonecat Madtom
7.41
River Chub
749
*Rankin E,T. 2004. Draft Notes on Associations between Dissolved Oxygen and Fish and
Macroinvertebrate Assemblages in Wadeable Ohio Streams.
Table 4. Summary of the fishes of Illinois thought to spawn through summer (based in
part on Smith 1979. The Fishes of Illinois)
Table 1. List of summertime (June —August) fish spawners in Illinois.
Scaphirhynchus albus
LyEhrurus furn eus
Pallid shiner
Ribbon shiner
Dorosorna cepedian urn
Gizzard shad
Lythrurus urn bratilis
Redfin shiner
Notetnigonus crysoleucas
Golden shiner
Macrh vbopsis hyostoma
Shoal chub
Pirnephales notatus
Bluntnose minnow
Pirnephales prornelas
Fathead minnow
Platygobio gracilis
Flathead chub
Pimephales vigilax
Bullhead minnow
Phenacobius rnirabills
Suckermouth minnow
Carpiodes carpio
River carpsucker
Notropis atherinoides
Emerald shiner
Carpiodes ve4fer
Highfin carpsucker
Notropis blennius
River shiner
Moxostorna carinaturn
River redhorse
Noturusfiavus
Stonecat
Fundulus olivaceus
Spotted topminnow
Gambusia affInis
Western
mo~qtuitofis~~
Notropis boops
Bigeye shiner
Notropis buchanani
Ghost shiner
Notropis chalybaeus
Ironcolor shiner
Labidesthes sicculus
Brook silverside
Notropis dorsalis
Bigmouth shiner
Notropis heterodon
Blackchin shiner
Men idia beryllina
Inland silverside
Notropis shwnardi
Silverband shiner
Lepornis cyanellus
Green sunfish
Lepornis gibbosus
Pumpkinseed
Notropis strarnineus
Sand shiner
Lepornis gulosus
Warmouth
Notropis texanus
Weed shiner
Opsopoeodus emiliae
Pugnose minnow
Lepornis hurnilis
Orangespotted sunfish
Cyprinella lutrensis
Red shiner
Lepornis rniniat:.is
Redspotted sunfish
Cyprinella spiloptera
Spotfin shiner
Arnmocrypta clara
Western sand darter
Cyprinella whipplei
Steelcolor shiner
REFERENCES
FISHES
OF
WISCONSIN
GEORGE C. BECKER
The University of Wisconsin Press
Published 1983
The University of Wisconsin Press
114 North
Murray Street
Madison, Wisconsin 53715
The University of Wisconsin Press. Ltd.
1 Gower Street
London WC1E 6HA, England
Copyright © 1983
The Board of Regents of the University of Wisconsin System
Al) rights reserved
First printing
Printed in the United States of America
For LC CII’ information see the colophon
ISBN 0—299—08790—5
Work on this book was funded in part by the University of Wisconsin Sea Grant
College Program under a grant from the Office of Sea Grant, National Oceanic
and Atmospheric Administration, U.S. Department of Commerce, and by the State
of Wisconsin (Fed. grant #NASOAA—D—00086, Project #E/E—5). The U.S. government
is authorized to produce and distribute reprints for government purposes not-
withstanding any copyright notation that may appear hereon.
Water
Quality Criteria
Report of the
National Technical Advisory Committee
to the
Secretary of the Interior
APRIL I, 1968
WASHINGTON, D.C.
FEDERAL WATER POLLUTION CONTROL ADMINISTRATION
.,unencaeict’.(t:C:cec
ct’e:v:u
•cc number ot
aud carrot:
destrcvec. c:’’.uiote
‘‘tod if this resource is to be preserred:
I) Inland trout streams, headwatert of
cams, trout and salmon lakes and reservoir’s. roe’ the
polirnnior. of lakes one reservoirs containtag so.-
‘usnids should not be warmed, No heated e~stents
!,ould be discharged in the vicinity of sPawning areas.
For other types and reaches of cold-xvesier streams,
‘-~on’oirs, and lakes, the following restrictions ore
ircommended,
(2) During any month of the vet:’. neaL should cc-
added to a stream in excess of the amount that v-il:
ike the temperature of the ,‘,ater mere thor. S 1°
hosed on the minimum expected flow for that month).
in
lakes and reservoirs, the temperature of the api-
iilunion should not be raised more than 3 F by the ad-
dillon of heat of artificial origin.
(3) The normal daily and seasonal tomperature
lisictuations that existed before the addition of heat due
ii
other than natural causes should be maintained.
(4)
The recommended maximum temperatures that
•‘re not
to he exceeded for various speoiec of cold water
lish
are
given in toble Ill—h
NoTE—For streams, totai added heat
(ir,
ETU’s..
‘night be specified as an allowable increase in tempera-
lure of the minimum daily flow expected for the month
nr period in question. This would ahoy addition of a
constant amount of heat throughout the period. Ap-
proached in this Way for all periods of the year, sea-
ronal variation, would be maintained. For lakes thc
‘ituation is more complex and cannot he spocified in
~imple terms.
TABLE Ill—i
‘‘royjsjonal maximum temperatures recommended as compati.
bie with the weII.being of various species of fish and
their associated btotaj
V~
F: Growth of
catfish,
gar, white or yellow bass,
spotted bass,
buffalo, carpsucker, threadfin shad.
and gizzard shad.
‘G F: Growth of largemouth bass, drum, bluegill, and
crappie.
‘4 F: Growth of pike, perch,
walleye, sniallmouth bass,
and
sauger.
.0 F: Spawning and
egg development of
catfish.
buffalo,
threadfin shad, and gizzard shad.
‘5 F:
Spawning and egg development of largernouth
bass,
white, yellow, and spotted bass,
SF: Growth
or migration routes of salmonids and for
egg development
of perch and smallmouth bass.
• 5 F: Spawning
and egg
development
of
salmon, and
trout
(other
than
lake trout).
18 F:
5pawning
and egg
development
of lake trout.
walleye,
northern
pike,
sauger.
and Atlantic
salmon.
Note.~Recornmended temperatures icr other species, ncr
t5d above, may be established if and when necessary in-
,,rmaticn becomes available
Dissolved oxygen
Oxygen requirements ot actuatic life have beer.
•:xtensively studied, Excellent survey papers ate
and
1-f
i0H~
(AuCIT
on :imuera:ot’o
:00:100 F~CPt5
050 cc:-
siders oxygen or5o those iriiiio.granhies are eettaiiv
‘•;aiuob~e.
Most oi’ the research concerning oxygen require-
ments for freshwater organisms deals with fish, loot:
since fiSh depend upon other aquatic species
tot
food and would no: remain inar~area war. ar
adequate food supPly. it seems reasonable to as-
sunie that a requirement for fisfl would serve also
for the rest of the conarnunity. The fish themsel’’es
oar be srouped into three categories according
t:neir temperature ar.d oxygen requirements:
0) the cold-water fish (e.g.. salmon and trout:’.
(2)
the warm~watergame and pan fish (e.g.. bass
and sunfish). and (3) the warm-water “coarse”
flsh (e.g.. carp and buffalo). The cold-water fish.
seem to require higher oxygen concentrations than
the warm-water varieties. The reason is not knowr,,
but it may be related to the fact that, for half
saturation, trout hemoglobin requires an oxygen
partial pressure thrce or four times that required
by carp hemoglobin under similar circumstances.
Warm-water game and pan fish seem to require a
higher concentration than the “coarse” fish, prob-
ably because the former are more active and
predatory.
Relatively little of the research on the oxygen
requirements of fish in any of these three categories
is applicable to the problem of establishing oxygen
criteria
because the endpoints have usually been
too crude. It is useless in the present context tc
know how long an animal can resist death by as-
phyxiation at low’ dissolved oxygen concentrations;
we must know instead the oxygen concentration
that will permit an aquatic population to thrive. We
need data on the oxygen requirements for egg de-
velopment, for newly hatched larvae, for normaj
growth and activity, and for completing all stages
of the reproductive cycle. It is only recently that
experimental -work has been undertaken on the
effects of oxygen concentration on these more
subtle endpoints. As yet, only a few species have
been studied.
One of the first signs that a fish is being affected
by a reduction of dissolved oxygen (DO) concen-
tration is an increase in the rate at which it r’er.ti-
lates its gills. a process. accomplished in part by an
increase in the frequency of the opercular move-
men
The half dozen or so species (chiefly
warm-water game and pan flsh) that have beer
t-eported so far snot’: o significant increase 1: fre-
quency as the DO concentration is reduced from
6 to
5
mg/i (at about
F, and a greater increase
from 5 to
4
mg/i. If the opereular rate is taken as
the criterion by which the adequacy of an oxygen
concentration is to he judged, then such evidence
as we have indicates 6 mu/I as the required dis-
solved oxygen concentration. Several field studius
have shown, however, that good and diversified
fish populations can occur in waters in which the
dissolved oxygen concentration is bettveen 6 and
S
mg/I in the summer, suggesting that a minimum
of 6 mg/I is probably more stringent than neces-
sary for warm-water fishes. Because the oxygen
content of a body of water does not remain con-
stant, it follows that if the dissolved oxygen is
never less than 5 mg/I it must be higher part of
the time. In some cases, good populations of
warm-water fish, including game and pan fishes,
occur in waters in which the dissolved oxygen may
be as low as
4
mg/I for short periods. Three mg/I
is much too low, however, if normal growth and
activity are to be maintained. It has been reported
that the growth of young fish is slowed markedly if
the oxygen concentration falls to 3 mg~lfor part
of the day, even if it rises as high as S mg 1 at
other times, It is for such reasons as this that oxy-
gen criteria cannot be based on averages. Five and
4 mg/I
are close to the borderline of oxygen con-
centrations that are tolerable for extended periods.
For a good population of game and pan fishes,
the concentration should be considerably more
than this.
The requirements of the different stages in thc
life cycles of aquatic organisms must he taken into
account. An oxygen concentration that can he
tolerated by an adult animal, with fully developed
respiratory apparatus, less intense metabolic re-
quirements, and the ability to move away from
adverse conditions, could easily be too lo’v for eggs
and larval stages. The eggs are especially vulner-
able to oxygen lack because they have to depend
upon oxygen diffusing into them at a rate sufficient
to maintain the developing embryos. Hatching,
too, is a critical time; recently hatched young need
relatively more oxygen than adults, but until they
become able to swim for themselves (unless they
are in flowing water) they must depend upon the
oxygen supply in the limited zone around them.
These problems are not as great among species
that tend their eggs and young, suspend their eggs
from plants, or have pelagic eggs, as they are for
salmonids. Salmonids bury their eggs in the gravel
of the stream away from the main flow of the water
thereby requiring a relatively high oxygen concen-
tration in the water that does reach them.
Recommendation: In view of the above considerations
and with the nroviso that future research may make
revision necessary, the following environmental con-
ditions are considered essential for maintaining
fl
tive populations of fish and other aquatic life,
(I) For a diversified warm’water biota, includir
came fish, daily DO concentration should be abo’
S
mg/i, assuming that there are normal seasonal ar
daily variations above this concentration. Under
trenie conditions, however, and with the same stipul.
lion for seasonal and daily fluctuations, the DO mE
range between 5 mg/I and 4 mg/I for short periods
linac, provided that the water quality is favorable
alt other respects. In stratified eutrophic and dystroph
lakes, the DO requirements may not apply to ti
h~polininion.In shallow unstratified lakes, they shou
apply to the entire circulating water mass.
These requirements should apply to all waters
cept administratively established mixing a.ones. In lake
such mixing zones must be restricted so as to limit tl
effect on the biota. In streams, there must be no bloc
to migration and there must be adequate and sa
passageways for naigrating forms. These zones of pa
sage must be extensive enough so that the majority
plankton and other drifting organisms are protecti
see section on zones of passage).
(2) For the cold water biota, it is desirable that D
concentrations be at or near saturation. This is esp
cially important in spawning areas where DO leve
must not be below
7
mg/I at any time, For good grow
and the general well-being of trout, salmon, and oth
species of the hiota, DO concentrations should not
below 6 mg/I. Under extreme conditions they ml
range between 6 and S mg/I for short periods providt
that the water quality is favorable and normal dai
and seasonal fluctuations occur. In large streams th
have some stratification or that serve principally as
if
gratory routes, DO levels may be as low as
S
mg/I
periods up to 6 hours, but should never be below
ing/lat any tnae or place.
13) DO levels in the hypolim::,on of oligotropt’
small inland lakes and in large lakes should not I
lowered below 6 mg/I at any time due to the additit
of oxygen-demanding wastes or other materials.
Carbon dioxide
An excess of “free” carbon dioxide (as disti
guished from that present as carbonate and bica
bonate) may have adverse effects on aquatic ar
mals. These effects range from avoidance reactio:
and changes in respiratory movements at low co
centrations, through interference with gas e
change at higher concentrations, to narcosis ai
death if the concentration is increased further. TI
respiratory effects seem’ the most likely to be
concern in the present connection,
Since the carbon dioxide resulting from met
holic processes leaves the organisms by diffusio
an increase in external CO2 concentration w
make it more difficult for it to diffuse out of tl
organism. Thus, it begins to accumulate internall
The consequences of this internal accumulatb
are best known for fish, but presumably the print
pIes are the same for other organisms. As the C(
accumulates, it depresses the blood pH, and U
44
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0
Justification and Rationale for Revisions to the Dissolved Oxygen
Criteria in the Ohio Water Quality Standards
OEPA Technical Bulletin MAS/1995-12-5
January31, 1996
State of
Ohio Environmental Protection Agency
Division ofSurface Water
Monitoring & Assessment Section
1685 Westbelt Drive
Columbus, Ohio 43228
MAS/ 1995-12-5
D.O. Criteria Revision
Justification
January 3!, 1996
TABLE OF CONTENTS
NOTICE TO USERS
iii
Summary and Conclusions
v
Introduction
~.
.
Dissolved
Oxygen Criteria
2
The Need for A Revised EWH D.O. Criterion....
...~,
RationalefortheCurrentEWHD.O. Criterion
Rationale for A Revised EWH D.O. Criterion.
6
Analysis ofthe Statewide Database
.
6
Observations in Individual Rivers and Streams
7
Scippo Creek
9
Big
Darby
Creek
9
Upper Great Miami River
12
Little Micrnii River
12
Waihonding River
16
Scioto River
16
Summary of Individual Streams and Rivers
16
Synthesis of Information
20
REFERENCES
23
ACKNOWLEDGEMENTS
24
ii
MAS/L995-12-5
0.0. Criteria Revision Justification
January 31, 1996
NOTICE
TO USERS
Ohio EPA incorporated biological criteria into the Ohio Water Quality Standards (WQS; Ohio
Administrative Code 3745-1) regulations inFebruary 1990 (effective May 1990). These criteria
consist ofnumeric values forthe Index ofBiotic Integrity (IBJ) and Modified Index ofWell-Being
(MIwb), both ofwhich are based on fish assemblage data, and the Invertebrate Community Index
(id), which is based on macroinvertebrate assemblage data. Criteria for each index are specified
for each of Ohio’s five ecoregions (as described by Omernik 1987), and are further organized by
organism group, index, site type, and aquatic life use designation. These criteria, along with the
existing chemical and whole effluent toxicity evaluation methods and criteria, figure prominently
in the monitoring and assessment ofOhio’s surface water resources.
The following Ohio EPA documents support the use of biological criteria by outlining the
rationale for using biological information, the methods by
which
the biocriteria were derived and
calculated, the field methods by which sampling must be conducted, and the process for
evaluating results:
Ohio Environmental Protection Agency. 1987a. Biological criteria for the protection of aquatic
life: Volume!. The role ofbiological data in water quality assessment. Division ofWater
Qual. Monit. & Assess.~Surface Water Section, Columbus, Ohio.
Ohio Environm~nta1Protection Agency. 1987b. Biological criteria for the protection ofaquatic
life: Volume II. Users manual for biological field assessment of Ohio surface waters.
Division of Water Qual. Monit. & Assess., Surface Water
Section, Columbus,
Ohio.
Ohio Environmental Protection Agency. 1989b.
Addendum to Biological criteria for the
protection of aquatic life: Volume II. Users manual for biological field assessment of
Ohio surface waters. Division of Water Qua!. Plan. & Assess., Ecological Assessment
Section, Columbus, Ohio.
Ohio Environmental Protection Agency. 1989c. Biological criteria for the protection of aquatic
life: Volume III. Standardized biological field sampling and laboratory methods for
assessing fish and macroinvertebrate communities. Division of Water Quality Plan. &
Assess., Ecot. Assess. Sect., Columbus, Ohio.
Ohio Environmental Protection Agency. 1990. The use of biological criteria in the Ohio EPA
surface water monitoring and assessment program. Division of Water Qua!. Plan. &
Assess., Ecol. Assess. Sect., Columbus, Ohio.
Rankin, E.T. 1989. The qualitative habitat evaluation index (QHEI): rationale,methods, and
application. Division of Water Qual. Plan. & Assess., Ecol. Assess. Sect., Columbus,
Ohio.
III
MAS/ 1995-12-5
D.O. Criteria
Revision Justification
January
31,
1996
Since the publication of
the
preceding guidance documents
new
publications by Ohio EPA
have
become
available.
The following publications
should also
be consulted
as
they represent the
latest
information
and
analyses
used
by Ohio
EPA
to
implement
the
biological
criteria.
Deshon, J.D. 1995. Development and application of the invertebrate community index (Id),
pp. 2 17-243. in W.S. Davis and T. Simon (eds.). Biological Assessment and Criteria:
Tools for Risk-based Planning
and
Decision Making. Lewis Publishers,
Boca
Raton, FL.
Rankin, E. T. 1995. The use of habitat assessments in water resource management programs,
pp. 181-208. in W. Davis and T. Simon (eds.). Biological Assessment and Criteria:
Tools for Water Resource Planning and Decision Making. Lewis Publishers, Boca Raton,
FL.
Yoder, C.O. and E.T. Rankin.
1995.
BioLogical criteria program development and
implementation in Ohio, pp. 109-144. in W. Davis and T. Simon (eds.). Biological
Assessment and Criteria: Tools for Water Resource Planning and Decision Making.
Lewis Publishers, Boca Raton, FL.
Yoder, CD. and E.T. Rankin. 1995. Biological response signatures and the area of degradation
value: new tools for interpreting multimetric data, pp. 263-286. in W. Davis and T.
Simon (eds.). Biological Assessment and Criteria: Tools for Water Resource Planning
and Decision Making. Lewis Publishers, Boca Raton, FL.
Yoder, CO.
1995.
Policy issues and management applications for biological criteria, pp. 327-
344.
in W. Davis and T. Simon (eds.). Biological Assessment
and
Criteria: Tools for
Water Resource Planning and Decision Making. Lewis Publishers, Boca Raton, FL.
Yoder, CO. and E.T. Rankin. 1995. The role of biological criteria in water quality monitoring,
assessment,
and
regulation. Environmental Regulation in Ohio: How to Cope With the
Regulatory Jungle. Inst. of Business Law, Santa Monica, CA. 54 pp.
These documents and this report can be obtained by writing to:
Ohio EPA, Division of Surface Water
Monitoring and Assessment Section
1685 Westbelt Drive
Columbus, Ohio 43228-3809
(614) 728-3377
iv
MAS/ 1995-12-5
DO. Criteria Revision Justification
January 31. 1996
Several of the major water quality criteria compendia
(e.g..
U.S. EPA 1986) were also examined
during the course of this study. The information contained in this literature strongly suggests
that the proposed revision to the EWH D.O. criterion is both protective and appropriate. Based
on the information presented by U.S. EPA (1986) there is also justification for bringing the Cold
Water Habitat (CWH) DO. criterion (presently 6 mg/I minimum only) into line with the two-
number average/minimum hierarchy of the Ohio WQS. In practical terms the proposed two-
number criteria for EWH and CWH
are
consistent with the hierarchy of D.O. criteria between the
WWH, MWH, and LRW use designations. The adoption of a 6 mg/i daily average, 5 mg/i
minimum two-number D.O. criterion for EWU and a 7 mg/I daily average, 6 mg/I minimum two-
number D.O. criterion for CWH is supported by the scientific evidence (both field and
laboratory) examined by this study.
vi
MASR99S-12-5
DO. Criteria Revision Justification
January 31. 1996
Summary
and Conclusions
The principal
objective
of this study
is to
present a rationale for revising
the
existing 6 mg/I
minimum dissolved oxygen
(DO.) criterion
for the Exceptional Warmwater Habitat (EWH) use
designation. The need for a revised EWH
D.O.
criterion has been recognized by Ohio EPA for
more than a decade. DO. criteria have traditionally been expressed as a period average (usually
daily) along with a minimum below which D.O. values should not fall. The need for both is
evident in the literature on the effects of D.O. on aquatic life. Such a two-number criterion is
exemplified by the current Wamiwater Habitat (WWH), Modified Warmwater Habitat (MWI-I),
and Limited Resource Water (LRW) DO. criteria, an approach which is recognized as
appropriate by U.S. EPA (1986). Unlike these criteria, the existing EWH and Coidwater Habitat
(CWH) DO. criteria were adopted in 1978 as minimum only values. One reason cited by Ohio
EPA for needing a two-number D.O. criterion, the daily average value in particular, was a more
meaningful target for steady-state D.O. modeling efforts. The very nature of D.O. regimes in
warmwater rivers and streams also substantiates the need for a two-number criterion. DO.
concentrations are subject to natural, did changes which are influenced by the daily cycles of algal
photosynthesis and respiration. The magnitude of change between the minimum and maximum
D.O. during any 24-hour period is dependent on several factors including flow, ambient
temperature, solar insolation, and the abundance and activity of photosynthetic algae andlor
higher aquatic plants. In the warmwater rivers and streams of Ohio and the midwest U.S. a did
swing of as much as 3-5 mg/I may be considered “typicaL” during normal summer low flow and
ambient temperature conditions. Thus, the relationship of the dynamic D.O. regime to an average
value over a24-hour period is as important as the minimum.
The need for a revised EWH DO. criterion is also indicated by the frequent and widespread
observation of hill attainment of the EWH biological criteria where D.O. values less than the
current 6.0 mgIl (minimum) criterion have been measured. The results of comparing continuously
measured D.O. data and EWH use attainment in six streams and rivers of varying size shows that
the latter is compatible with D.O. values less than 6 mg/I. However, values less than 5 mgIl were
either infrequent, did not correlate with full EWH use attainment, or were measured only under
extreme low flow conditions. The results of this analysis tends to support a minimum EWH
DO. criterion of less than 6 mg/I, but not less than
5
mg/I.
V
MAS/1995-12-5
DO. Criteria Revision
Justilication
January 31,
1996
Justification and Rationale for Revisions to the Dissolved Oxygen
Criteria in the Ohio Water Quality Standards
Chris
0.
Yoder
Ohio EPA, Division of Surface Water
Monitoring & Assessment Section
1685 Westbelt Drive
Columbus, Ohio 43228
Introduction
The Ohio Water Quality Standards (WQS; Ohio Administrative Code 3745-1) consist of
designated uses and chemical, physical, and biological criteria designed to represent measurable
properties of the environment that are consistent with the goals specified by each use
designation. Use designations consist of two broad groups, aquatic life and non-aquatic life uses.
In applications of the Ohio WQS to the management of water resource issues in Ohio’s rivers and
streams, the aquatic life use criteria frequently result in the most stringent protection and
restoration requirements.
The five major aquatic life uses which have broad application
throughout Ohio are currently defined in the Ohio WQS. A brief description of each follows:
1)
Wannwater Habitat (WWH)
-
this use designation defines the “typical” warmwater
assemblage
of
aquatic organisms for Ohio rivers and streams and represents the principal
restoration target for water resource management efforts.
2)
Exceptional Wannwater habitat (EWH)
-
this use designation is reserved for waters which
support “unusual and exceptional” assemblages of aquatic organisms which are characterized
by a high diversity of species, particularly those which are highly intolerant and/or nrc,
threatened, endangered, or special status
(i.e.,
declining species); this designation usually
represents a protection target for water resource management efforts.
3)
Coidwater Habitat (C WI!)
-
this use is intended for waters which support assemblages of
cold water organisms and/or those which are stocked with salmonids with the intent of
providing a put-and-take fishery on a year round basis which is further sanctioned by the
Ohio DNR, Division of Wildlife; thisuse should not be confused with the Seasonal Salmonid
Habitat (SSI-I) use which applies to the Lake Erie tributaries which support periodic “runs”
of salmonids during the spring, summer, and/or fall.
4)
Mod(/Ied Warmwater Habitat (MW!!)
-
this use applies to streams and rivers which have
been subjected to extensive, maintained, and essentially permanent hydromodifications such
that the biocriteria for the WWH use are not attainable; the representative aquatic
assemblages are generally composed of species which are tolerant to low dissolved oxygen,
silt, nutrient enrichment, and poor quality habitat.
MAS/995-1 2-5
D.O. Criteria Revision
Justification
January 31, 1996
5) Limited Resource Water (LRW)
-
this use applies to streams (usually 3 mi.2 drainage area)
which have been irretrievably altered to the extent that no appreciable assemblage of aquatic
life can be supported; such streams generally occur in extensively urbanized areas and/or
completely lack water during normally recurring dry weather periods; other waters subjected
to acidic runoff from past surface mining activities may also be designated LRW.
Chemical, physical, and/or biological criteria are generally assigned to each use designation in
accordance with the broad goals defined by each. As such the system of use designations
employed in the Ohio WQS constitutes a “tiered” approach in that varying and graduated levels
of protection are provided by each. This hierarchy is especially apparent for parameters such as
dissolved oxygen, ammonia-nitrogen, temperature, and the biological criteria.
For other
parameters such as heavy metals, the technology to construct an equally graduated set of criteria
has been lacking, thus the same criteria may apply to two or more different use designations.
Dissolved Oxygen Criteria
Dissolved oxygen (D.Oj is one of the most important parameters in the protection and
management of aquatic ecosystems since all of the higher life forms
(i.e.,
vertebrates.
macroinvertebrates including Unionidac) are dependent on minimum levels of oxygen not only
for survival, but critical life cycle lIrnctions such as growth, maintenance, and reproduction. As
such, the DO. criteria for each of the beneficial aquatic life uses1 have been established in light of
these protection end points. The DO. criteria for the MWH and LRW use designations (Ohio
EPA 1987a) are. designed to maintain generally tolerant and lower value aquatic assemblages and
for the prevention of nuisance conditions
(e.g.,
anoxia, odors, fish kills). The current DO.
criteria for each aquatic life use designation is listed in Table 1. The principal objective of this
analysis is to present a rationale for revising the DO. criterion for the Exceptional Warmwater
Habitat (EWH) use designation. However, the lack of a daily average D.O. criterion for the Cold
Water Habitat (CWH) use designation was also examined.
The Need for A Revised
EWH D.O. Criterion
The need for a revised D.O. criterion for the EWH use designation has been sporadically
recognized and considered by Ohio EPA for more than a decade. Dissolved oxygen (DO.)
criteria have traditionally been expressed as a period average (usually daily) along with a
minimum below which 0.0. values should not fall. This is exemplified by the current WWH,
MWH, and LRW DO. criteria (Table 1), an approach which is also recognized as appropriate by
U.S. EPA (1986). The current WWH DO. criterion was originally adopted in the
1985
revisions
A
beneficial use meets either
the interim fishable/swimmable or biological integrity goals specified by the Clean
WaterAct (Section 1O1I(2).
In the
Ohio WQS. the
following aquatic life usesare considered beneficial:
EWH, WWH,
and
CWH.
2
MAS11995-12-5
0.0. Criteria Revision Justification
January 3!, 1996
Table 1.
Current dissolved oxygen (DO.)
criteria
for the major aquatic life use designations as
presently codified
in
the Ohio Water Quality Standards (WQS: Ohio Administrative
Code 3745-1).
Daily Aver-
Minimum
Use Designation
age (mg/i)
(mg/i)
Protection Endpoint
Coidwater Habitat
-
6.Oa
Coidwater organisms;
periodic stocking of
salmonids (maintenance,
growth).
Exceptional Warmwater
-
6.Oa
Highly sensitive aquatic
organisms; growth and
reproduction of recreationally
and commercially important
species; maintenance of
populations of imperiled
S~CC
‘Cs.
Warmwater Habitat
5.0
4.0
Maintenance of typically
representative warmwater
aquatic organisms and
recreationally important
species.
Modified Warmwater
4.0
3.0
Maintenance of moderately
and generally tolerant species
which are
common in highly
modified stream habitats.
Limited Resource Water
3.0
2.0
Prevention of nuisance
conditions (odors, anoxia,
acute toxicity).
a the
present criterion is expressed as a minimum value
only -
no
avenge is
specified.
3
MAS/ 995-12-5
0.0. Criteria Revision
Justification
January
3!, 1996
to
the Ohio
WQS and emanated from the original
introduction of tiered aquatic life
uses in the
1978
WQS revisions. The current MWH
and
LRW
criteria were
adopted in the May
1990
revisions
to the Ohio WQS.
The existing EWH
and
CWH
D.O. criteria were adopted in 1978 as
minimum only values.
The need for a “two-number” D.O. criterion for each designated aquatic life use was recognized
when Ohio EPA initiated the adoption of two-number criteria for most of the heavy metals and
other toxic constituents for which a sufficient database existed (bC by Dick Robertson dated
August 8. 1983). The principal reason cited was that a two-number criterion, the daily average
value in particular, would result in a more meaningful target for the steady-state D.O. modeling
efforts which were widely employed by Ohio EPA in the early and mid 1980s. The present
policy employed for water quality modeling is to target a daily average criterion value under an
assumed set of critical, steady-state stream flow and discharge conditions. In the case of the
existing D.O. criteria for EWH and CWH, a default value 0.5 mg/I above the daily minimum
criterion is used as the target for steady-state modeling efforts. However, an average criterion is
best suited for the steady-state modeling techniques which are commonly employed in the
wasteload
allocation process.
In addition to the aforementioned practical reasons for a two-number criterion forD.0., the very
nature of DO. regimes is more amenable to this type of approach. DO. concentrations are
subject to natural, did changes which are influenced by the daily cycles of algal photosynthesis
and respiration. The highest DO. values in a 24-hour period occur during the daylight hours
(usually in the late afternoon) and the lowest values occur in the early morning, pre-dawn hours.
This naturally occurring cycle is sometimes referred to as the “did D.O. swing”. The extent or
size of the “swing” between the minimum and maximum D.O. concentration recorded during a
24-hour
period is dependent on several factors including stream or river flow, ambient
temperature, solar insolation, and the relative abundance and activity of photosynthetic algal
and/or higher aquatic plants. In Ohio’s warmwater rivers and streams, a diel swing of as much as
2-4 mg/I may be considered “typical” during normal summer low flow and ambient temperature
conditions. Variations outside of this range likely signify increased nutrient enrichment and the
potential for negative effects to aquatic life, particularly for the most sensitive assemblages
(i.e.,
those representative of EWH). However, the relationship of the dynamic D.O. regime to an
average value over a 24-hour period is also important. Thus, in using ambient DO. data to
analyze the causes of aquatic life use impairment, it is also important to consider the average in
relation to minimum and maximum values
and
the width ofthe did variation.
The need for a revised DO. criterion for the EWH use designation is also evident in the repeated
observation of fi.ill attainment of the EWH biological criteria when D.O. values less than the
current 6.0 mg/I (minimum) criterion have occurred. Several examples from the Ohio EPA
4
MAS11995-12-5
0.0. Criteria Revision Justification
January 31, 1996
biological
and water quality assessment database were used to illustrate this point.
Rationale for the Current F 0W 110. Criterion
In attempting to determine the origin of the current 6 mgil minimum criterion, several sources
were consulted. The Ohio EPA WQS files contained little explicit information about the origins
of the 6 mg/I criterion and much of the documentation found pertained to justifications for the S
mg/I average/4 mg/I minimum criterion for the WWH designation. There were references to the
CWH and EWH DO. criteria needing to be more stringent than WWFI
“.
in order to give
protection to more sensitive fish species” (bC by Bob Monsarrat dated February 8, 1978).
Ohio has had a 6 mg/I criterion (applied to specific rivers and streams) since 1967 (Ohio Water
Poll. Contr. Sd. Resolutions), but the origins and level of protection specified remain unclear.
Some of the contemporary water quality criteria compendia of that time period allude to the
range of D.O. between
5
mg/i and 6 mg/I as being a critical threshold for sensitive fish species,
especially coidwater species (FWPCA 1968). This same study also established a hierarchy of
decreasing sensitivity from coidwater fish
(e.g.,
salmon, trout) to warmwater game and pan fish
(e.g.,
bass, sunfish) to warmwater “coarse” fish
(e.g.,
carp, buffalo). While some of these
categorizations do not necessarily parallel a species sensitivity
(i.e.,
“coarse” fish, several of
which are actually sensitive species) the hierarchy remains an appropriate way to categorize
levels of protection consistent with that specified by the Ohio EPA aquatic life uses
(e.g.,
CWHEWFLWWHMWHLRW).
Thus, a hierarchical set of D.O. criteria consistent with the
hierarchy of the designated aquatic life uses seems appropriate.
None of this, however, sheds much more than indirect light on the origins of the EWH 6 mgIl
minimum D.O. criterion. The FWPCA (1968) summary on D.O. was one of the documents
available to Ohio EPA to support the development of the 1978 WQS which is where the EWH
DO. minimum of 6 mg/I first appeared. This study indicates that one of the first signs of stress
on fish from declining DO. concentrations is increased respiration
(i.e..
gill movement) and that
this becomes evident for the “half-dozen or so warmwater game and pan fish” as DO. is reduced
from 6 mg/i to 5 mg/I and the effects are further exacerbated from 5 mg/I to 4mg/I. However, the
FWPCA (1968) report also stated the following:
“Several field studies have shown that good and diversified fish populations can occur in
waters in which the dissolved oxygen concentration is between 6 and 5 mg/I in the
summer,
suggesting that a minimum of 6 mg/i is probably more stringent than necessary
Jbr warrnwaterJishes
(italics added). Because the oxygen content of a body of water does
not remain constant, it follows that if the dissolved oxygen is never less than 5 mg/I it
must be higher part of the time. In some cases, good populations of warmwater fish,
including game and pan fishes, occur in waters in which the dissolved oxygen may be as
5
MAS/995-12-5
0.0. Criteria Revision Justification
January 31, 1996
low as 4 mg/I for short periods.
.
(and).
Five and 4 mg/I are close to the borderline of
oxygen concentrations that are tolerable for extended periods. For a good population of
game and pan fishes the concentration should be considerably more than this.”
The recommendations forthcoming from the FWPCA (1968) were
5
mg/I for a diversified
warmwater biota assuming that there are normal seasonal and daily variations above this
concentration. The DO. could range between 5 and 4 mg/I for “short periods of time” provided
other water quality conditions are favorable. However, the growth of young fish was markedly
impaired if the D.O. dropped to 3 mg/I even for a part of the day when maximum values as high
as
18 mg/I occurred. This is one of the reasons cited for needing a daily minimum criterion in
addition to an average.
Based on an
examination of Ohio EPA files and conversations with some of the key staff who
developed the 1978 WQS (R. Shank, pets. comm.) the origin of the 6mg/I minimum criterion was
based on assuring the protection of a set of ecological values that were higher than “typical”
(i.e.,
WWH). Given that the tools
and techniques now available to discriminate between the WWF!
and
EWH uses were lacking,
it is not surprising that a clear justification for the 6 mg/I criterion
cannot be found. In one sense, the 6 mg/i minimum was largely a best professional judgenient
decision employing a generous margin of safety given the resource value implied by EWH. Thus,
the proposed minor adjustment to the original 6mg/I minimum criterion seemsjustified given the
existence of new information resulting from the availability of improved assessment tools
(i.e.,
multimetric biok’gical indices, bicAogical criteria, etc.) and databases 18 years hence.
Rationale for A Revised EWH 0.0. Criterion
Part of the rationale for a revised EWH DO. criterion is based largely on the observation of flu
attainment of the EWH biological criteria under D.O. regimes which include minimum daily
values less than 6 mg/i. Other information including the U.S. EPA
Ambient Water Quality
Criteria for Dissolved arygen
(U.S. EPA 1986) was also examined to verify the efficacy of this
criterion revision.
Analysis of the
Statewide
Database
One approach
used to determine the appropriateness of the proposed EWH D.O. criterion was
to
examine the Ohio EPA statewide database for DO. and biological community performance
indicators
(i.e.,
Index of Biotic Integrity, Invertebrate Community Index). This was accomplished
by plotting various expressions of D.O. levels (raw values, means, percentiles) in Ohio rivers and
streams against the biological indices which comprise the Ohio EPA biological criteria (Ohio EPA
1987b, 1989a,b). After examining a number of different statewide comparisons, three stood out
as offering both meaningful and representative information.
6
MASIt99S-12-5
0.0. Criteria Revision
Justification
January 31, 1996
Raw D.O. values (instantaneous measurements) from the statewide database spanning the period
of 1981-1992 were plotted against the Index of Biotic Integrity (1BI) values recorded at linked
locations
(i.e.,
the D.O. value was deemed representative of the biological sampling location).
The resultant scatterplot (Figure 1, upper tier) reveals a cluster of data points which we term a
“wedge” of data points. The left surface of the wedge represents a boundary between which IBI
values representative of a given level of biological community performance at a given DO.
concentration have been observed to occur. A 95 line of best fit was drawn across the left
surface boundary with
5
of the data points falling to the left of the line (Figure 1). The 95
tine corresponds to the lowest D.O. value at which a given level of biological community
performance as measured by the IBI has regularly occurred
-
coincidences of DO. and iBI values
to the left of this line are by comparison rare. Thus, any proposed “new” criterion for D.O. can
be evaluated for precedence against this historically and spatially robust database. As such this
represents a “one-sided” analysis in that a proposed criterion can be evaluated to determine if it
is under-protective moreso than evaluating if it is over-protective.
Shaded areas representing the boundaries of “representative” numerical biological criteria for the
respective EWH, WWH, and MWH aquatic life uses were superimposed on the scatterplot to
determine the DO. levels at which attainment or non-attainment of these criteria have been
observed. The existing 4mg/i mthimum DO. criterion for the WWH use and the proposed
5
mg/I
minimum for the EWU use were also superimposed to determine the D.O. concentrations at
which IBI values consistent with the attainment of each use designation occurred. The results
indicate that lB! values consistent with the EWH use designation at DO. concentrations as low
as 5 mg/I have precedence with some sporadic occurrences less than 5 mg/i (Figure 1, upper tier).
A similar plot of median DO. values (Figure 1, lower tier) shows that EWH attainment with
median DO. values as low as 6 mg/I also has precedence. Figure Ia is a box-and-whisker plot
analysis by narrative biological performance ranges
(i.e.,
exceptional, good, fair, poor, and very
poor) of the IBI showing the median, 10th, 25th. 75th, and 90th peicentiles, and outliers for 10th
percentile DO. values. This analysis shows that the proposed
5
mg/i minimum corresponds to
exceptional performance at the 10th percentile of DO. values. The majority of the D.O. data in
Figure 1 arc comprised of daytime readings meaning that potentially lower readings, which would
occur in the early morning hours, are not ~ve1Irepresented. Thus, minimum daily values lower
than those in Figures 1 and la probably occurred at the sites where full attainment of the EWH
use was observed. As such, Figures 1 and Ia represent conservative analyses in that the data
points do not necessarily represent all of the daily minimum values which likely occurred. While
these analyses
alone
are not entirely conclusive regarding the efficacy of the proposed 6 mg/I
average/5 mg/I minimum EWH 0.0. criterion, the occurrence of daytime DO. values less than
the present 6 mgII minimum criterion with full attainment of the EWH use is certainly not
unprecedented in a historically, spatially, and observationally (n=14,992) robust database.
7
DO.
Criteria Revision Justification
~MNH
i:io.
Rtrised EWH
D~O~
O*stri
(4 nTrN.~
,.~/
(5 rrql IT*L)
:2.-.
IndividuäDaytim& csamples
a
n=14,992
0_nfl
0
00 O~
the
~:
88°8
___
I
0
0
•
I
~
_______
9
0
0
___
___ ~1
0
__________
o
o
~
1
10
~ico
0
January31. 1996
Re~
xese,tatM)
i~i(46-50)
R~afl~e
~1-I
181(38-42)
Reçzascflative
MWH IBI (22-24)
DissoIv~xy~j~m8/l)
Figure 1. Relationship between the Index of Biotic Integrity (IBI) and individual
(upper) and median (lower) dissolved oxygen (D.O.) concentrations at
sampling sites in rivers and streams throughout Ohio based on
daytime DO. readings and biological sampling conducted between
1979
and
1992.
60
50
MASt 1995-12-5
12j
LI
40
30
20
RD
EWH
D.C. Citer4on
I
60
50
40
30
20
10
Reçrnseflative
181(46-50)
Dissolved Oxygen (mg/I)
8
MAS/1995-12-5
DO. Criteria Revision Justification
January31. 1996
12-19
20-29
30-39
40-49
50-60
INDEX OF
BKYI1C
INTEGRI1Y
Rq~s&EV~
Mit DO. crtthr
Figure Ia. Box-and-whisker plot of 10th percentile daytime D.O. values
arranged by narrative biological performance categories based
on the Index of Biotic of Integrity (IBI) and the Ohio EPA
statewide DO.
database.
2
I
12
10
8
6
4
2
0
9
MAS/1995-12-S
DO. Criteria Revision Justification
January 31, 1996
Observations in Individual Rivers and Streams
Another analysis undertaken in this study was an examination of the occurrence of attainment of
the EWH biocriteria in designated (or recommended) EWH streams and rivers with an adequate
continuous DO. database. This analysis provides a comparison of the IBI and Invertebrate
Community Index (IC!; DeShon 1995; Ohio EPA 1987a, 1989) with the D.O. results obtained
using Datasonde continuous monitors. Information from six streams and rivers either presently
designated as EWH (or where the biological
data
indicates a redesignation to EWH is
appropriate) was examined. These represent a cross-section of different stream and river sizes as
well. Full attainment of the EWH use designation over an extended length of river or stream
and/or over multiple years under D.O. levels which are periodically below the present 6 mg/I
minimum D.O. criterion represents additional evidence that the criterion should be revised.
Scippo Creek
Scippo Creek is a small tributary of the Scioto River located within the Eastern Corn Belt Plains
(ECBP) ecoregion (Omernik and Gallant 1988) and drains
52
square miles of land area. Land use
is predominantly row crop agriculture and one major point source (PPG Industries) discharges to
the mainstem. Based on results obtained through monitoring
conducted
in 1992 and 1993,
Scippo Creek is being recommended for redesignation as EWH. Both the 18! and IC! attain the
EWH biological criteria at nearly all sites sampled, thus meeting the Ohio EPA requirement that
the ability to attain EWH be demonstrated (Figure 2; Ohio EPA 1987b). Continuous DO.
readings taken in August 1993 indicate that minimum values below 6 mgI! occurred at most sites.
No values below
5
mg/I were observed.
Big
Darby
Creek
Big Darby Creek is a major tributary of the Scioto River located within the Eastern Corn Belt
Plains (ECBP) ecoregion (Omernik and Gallant 1988) and drains approximately 560 square miles
of land area. Land use is predominantly row crop agriculture, but several small point sources
(mostly WWTPs) discharge to the mainstem and tributaries. The existing use designation of the
mainstem is EWH with the exception of the extreme headwaters which are designated as WWH.
Big Darby Creek has long been recogi~izedfor supporting an unusually diverse and unique
assemblage of aquatic life and is a nationally designated Scenic River and one of The Nature
Conservancy’s “Last Great Places”. Biological performance as measured by the 181 and IC!
indicate that the biological criteria for the EWH are largely met with the exceptiontf-hxalized
reaches of impairment (Figure 3). The latest contiguous set of data (1992) indicates the strongest
showing of lull attainment and show the highest biological index scores to occur in the tower4O-
50 miles of the mainstem. Several sets of continuous D.O. data have been collected between
1988 and 1992. The D.O. data collected in August 1992 covers the longest reach, but represents
an elevated flow year (Figure 4). The D.O. data collected in 1988 represents the opposite
extreme as critically low flows occurred during an extended drought period. The D.O. results
10
MASt 1995-12-5
110. Criteria Revision Justification
January 3!, 1996
Figure 2. Biological and D.O. monitoring results from Scippo Creek during 1992 and
1993; D.O. (upper) as measured by Datasonde continuous monitors in August
1993 and the Index of Biotic Integrity (WI; middle) and Invertebrate
Community Index (id; lower).
11
C,
C
0,
0
-D
U)
0U,
U,
C
14
12
10
8
6
4
2
0
60
50
40
30
20
12
60
50
40
30
20
10
0
I
I
I
AugusIl 993
H
T
I
I
a-
I
:
:
.
RM 0.4
RM 0.1
1993
—s——
1992
.
I
‘‘
fl:
—w-——
1993
:
I
.
I
—
EWH fln~
QBI=50)
W~MOtHt~
QBt=40)
EWH(ICI=46)
C~
~II
cAatn
(CI=36)
20
15
10
5
0
RIVEFaIILE
MAS/1995-12-5
DO. Criteria Revision
Justification
January 31, 1996
Bi~Darbçreeki988-1993
80
70
60
50
40
30
20
RIVEF~1ILE
EW~CA~th
(IC
1=46)
~H O~th
fla=36)
Figure 3. Index of Riotic Integrity (IB1; upper) and Invertebrate Community Index (ICI;
lower) results for the mainstem of Rig Darby Creek during 1988, 1990, 1992, and
1993.
40
—
m
60
~5O
I
30
20
12
0
C)
V
~5o
~4o
E
0
Co
-o
a)
t
a)
C
30
20
10
0
10
0
12
MAS/1995-12-5
D.O. Criteria
Revision Justification
January 31, 1996
indicate that values less than the existing 6 mg/I EWH D.O. criterion have occurred in the lower
mainstem while biological performance consistent with the EWH use designation also occurred
(Figures 3 and 4). The site at RM 13.36 showed extremely low D.O. values during the extended
low flow period in 1988 with minimum values less than 3 mg/I and a 25th percentile value of 4
mg/I (Figure 4). Long-term monitoring with macroinvertebrates at this same site shows IC!
values well above the EWH biological criteria with similar values persisting in 1990 and 1992
(Figure 4). 181 values were also well above the EWH criteria at this same site in 1988 with
similarly high values extending into 1990 and 1992.
Upper Great Miami River
The Great Miami River is a major tributary of the Ohio River located within the Eastern Corn
Belt Plains (ECEP) ecoregion (Omernik and Gallant 1988). Our focus here is with the upper
mainsteni which drains approximately 1150 square miles of land area. Land use is predominantly
row crop agriculture, but several major point sources (mostly WWTPs) discharge to the
mainstem. The existing use designation of the inainstem is WWH. but the results obtained in
1994 strongly suggest a redesignation to EWH is in order. IBI and ICI values along most of the
mainstem between RM 85 and 140 were above the EWH biological criteria (Figure
5).
Minimum
D.O. values less than 6 mg/I were measured at three sites, two of which were either close to or at
biological sampling locations which met the EWH biological criteria (Figure
5).
Values less than 5
mg/I occurred at only one site which was in a localized impoundment on the mainstem which will
remain designated WWH.
Little MiamiRiver
The Little Miami River is a major tributary of the Ohio River located within the Eastern Corn
Belt Plains (ECBP) and Interior Plateau ecoregions (Omernik and Gallant 1988) and drains
approximately 1760 square miles of land area. Land use is predominantly row crop agriculture,
but numerous major point sources (mostly WWTPs) discharge to the mainstem. The volume of
municipal WWTP effluent is the largest of any EWH designated river in Ohio (50 million
gallons/day) and is projected to increase. Full attainment ofthe EWH biological criteria occurs in
two disjunct reaches and the cumulative distance in full attainment increased substantially
between 1983 and 1993 (Figure 6).
Three other reaches including the lower mainstem
(downstream from RM 20), a reach between RM 50 and 65. and the headwaters upstream from
RM 80-85 were in partial attainment due primarily to organic enrichment from municipal WWTP
discharges and combined sewer ovefflows (lower reach only; Ohio EPA 1995). Biological
performance along most ofthe mainstem has improved significantly since 1983, reflecting loading
reductions from point sources. Reaches of full EWH attainment were correlated with D.O.
values less than the current 6 mg/I criterion, but very few values were found to be less than
5
mg/I
(Figure 6). Because most of the WWTPs are submitting expansion plans, the Little Miami River
is a case in point as to the appropriate D.O. target for wasteload allocation purposes. The
13
MAS/1995-12-5
D.O. Criteria Revision Justification
January 3!, 1996
EWlSegment
15 _________________________________
0
0
0’ ~
•0)
________
_______
0) 0) 0) 0) 0~
00
:~
~
Augusl992
~
S
—
~
—,
sc
0-(I)
== —
=
a
-,
(I)
_
(I).
a,
C
ci~
a,
0
a)
-ö
Proposed 6 mg/I Average:
o
S mg/I
Minimum EWH Criterion
(0
I 111111.1
~
U~) C’J
N
U~)•
liii’,!.’,
~
N
N
(N
liii’,’’’’
(N
(N (N Ij) LU
LU
~
çyjCCj
th
~-
~h
thr~r
cvi”~ “?“?
~
(I)
r
U)
r
CM
N
(V)
(fl
~
U)
U)
CL)
CD
CD
CD
W
r
r
(N C’J
22~
~
N-
N N N N N
~
~6O
:
I
~ I
I
I
I
EWHCrIscn
-~5o
E30:
E
E40
/
o
:
~HCItSiDn
~2O
:
0036)
Bi4,arbfreeklcwrend
-
.0
s~10
-
—cn——
a)
I....
1975
1980
1985
1990
1995
YEAR
Figure 4. DO. results (upper) obtained with Datasonde continuous monitors during
the summer months of 1988 and 1992 from the mainstem of Big Darby
Creek and Invertebrate Community Index (ICI; lower) results obtained at a
long-term fixed monitoring location (RM 13.4) between 1976 and 1992.
14
MAS/1995-!2-5
January31. 1996
~nnmflxWWH
S~ot
‘4-
-
th16 -
A&~-S~1994
P.~.Se41i994
I
S~t94 --
4
~
Proposed 6 mg/I Average:
— -
S mgII
Minimum
EWH
Criteri
ii
2
II
IIIII
~D
U~
0
~
(0
U~
(0
N
~
-~
U
~
UI
~
0N
~
0
•g~o
C)
-D
I
@160
C
Figure
5.
Biological and D.O. monitoring results from the upper Great Miami
River during 1982 and
1994; D.O.
(upper) as measured by Datasonde
continuous monitors during June-September 1994 and the Index of
Biotic Integrity (IBI; middle) and Invertebrate Community Index (ICI
lower) based on results obtained in 1982 and 1994.
D.O. Criteria Revision
Justification
150 140
130
120 110 100
90
80
RIVER MILE
15
MASh 995-12-5
January 3!, 1996
LittldvliamRiveri
993
LittlcMiamRi 983/Si 993
20
0
EWH Cr~tr
((0=46)
vw~
at~
QCI=36)
Figure 6. Biological and D.O. monitoringresults from the Little Miami River during 1983
and 1993; D.O. (upper) as measured by Datasonde continuous monitors during
June-September 1993 and the Index of Biotic Integrity (181; middle) and
Invertebrate Coniinunity Index (ICI; lower) based on results obtained in 1983
and 1993. The entire mainstem to RM 3.0 is designated EWH.
DO. Criteria Revision Justification
15
C,
E
C
wiG
C
-o
F
0
Proposed 6
mg/I Avgerage:
—
5 mg/I Minimum EWH Criterion
-1--~-.-•
—
t.J
0
U,
e) o~ C F— 0
In
a, e1 c’J
in u~
c~’
.n
~i
C
cn
~
0) r-
CC ~
t’~ °
~ 2 ~
~6O
40
230
P
-oU)
20
0
Lo
g4o
~3o
~2O
~1o
0)
EU
100
80
60
40
RIVER IvILE
16
MASt1995-12-S
0.0. Criteria Revision Justification
January 31. 1996
problems associated with the WWTP impacts
included
excessive nutrient concentrations (mostly
total phosphorus) and the influence of this on diet 110. patterns. The available information
suggests that protecting for the proposed 6 mg/I
averagel5
mg/I minimum EWH 0.0. criterion
would be appropriate for maintaining and ftirther restoring the EWH use designation.
Waihonding River
The Waihonding River is a major tributary of the Muskingum River located within the Western
Allegheny Plateau (WAP) ecoregion (Omemik and Gallant 1988) and drains approximately 2250
square miles of land area. Land use is predominantly row crop agriculture, but point sources
discharge to the upper sections of several major tributaries which feed the Waihonding. The
existing use designation of the mainstem is EWH and the biological results easily reaffirm this
(Figure 7). Continuous D.O. data collected during three different years show some minimum
values less than 6 mg/I, but above
5
mg/I (Figure 7). The Walhonding is probably the largest river
in Ohio with no direct point source discharges and only a few scattered concentrations of such in
thc upper parts of the watershed.
Scioto River
The Scioto River is a major tributary of the Ohio River thcated within the Eastern Corn Belt
Plains (ECBP) ecoregion (Omemik and Gallant 1988). Our
focus here is with the
central
mainstem which drains approximately
3200
square miles of
land area
making it
the largest
river
among the six examples. Land use in
the
upper
watershed
is predominantly
row
crop agriculture,
but
two major
~ointsources (both
WWTPs) and
several smaller sources
(WWTPs, industries)
discharge
to
the mainstem. The existing
use designation
of
the mainstem
is WWH, but results
obtained
since the mid and
late
1980s
strongly suggest a redesignation to
EWH for an
approximately
eight
mile
long reach
of the lower central mainstem. IBI and IC! values in the
reach between
RM 106.1 and
97.9
indicate lull attainment ofthe EWH biological
criteria
at most
locations (Figure
8).
Continuous
DO. data
collected in
1988
shows values less than 6 mg/I and
even
5
mg/I during an
extended
drought. Daytime
grab
samples during other years
also
show
minimum values less than 6 mg/I
at sites which
attain the EWH
biocriteria.
Long-term results
for
the
ICI and
TB!
both
show values approaching and
exceeding
EWH biological criteria as early as
1986
and generally persisting through
1992
(Figure 9).
Summary ofIndividual Streams and Rivers
The results of the comparison of continuously measured D.O. and EWH use attainment in six
streams and rivers of varying sizes shows that the latter can be compatible with minimum DO.
values less than 6 mg/I. However, values less than
5
mg/ were either infrequent, did not
frequently correlate with full EWH use attainment, or were measured only under extreme low
flow conditions. Thus, this analysis would appear to support a minimum EWH D.O. criterion
less than 6 mg/I, but not less than
5
mg/i.
17
MAS/1995-12-5
January 31, 1996
II
.
~-
—m-—19941B1
—s— i~i~
m
.
—W--— 1994
—s-—
1988
H
II
20
15
10
5
0
RiVER MLE
EWHQ~
QBI=48)
/
~HOI&tn
(181=40)
EVM Q~tn
(ICI=46)
QCI=36)
Figure 7. Biological and D.O. monitoring results from the Waihonding River during 1983-
1994; D.O. (upper) as measured by Datasonde continuous monitors during August
1988, July 1989, and September 1994 and the Index of Biotic Integrity (IBI;
middle) and Invertebrate Community Index (ICI; lower) based on results obtained
in 1983, 1988, and 1994. The Waihonding River is designated EWI-I.
18
110. Criteria Revision
Justification
16
a)
=
12
a,
a)
08
-o
a)
0)
b
0
=~60
c
t
~4o
630
50
p
C)
~12
~‘6O
~,5o
~4o
~3o
‘c)
C
MAS/1995-1 2-5
January 31, 1996
—~14
0)
E12
C
olO
0,
C
-D
3)6
U,
0
~6O
~ 50
0)
C)
t
E3o
C)
S 12
E~ O~
(IBI=48)
0
-~
EWlQtetr
50
QCI=46)
~4o
~3o
~
140
Figtire 8. Results of continuous D.O. Monitoring in 1988 (upper) compared to Index
ofBiotic Integrity (IBI; middle) and Invertebrate Community Index (id:
lower) results forthe central Scioto River mainstem during 1980, 1988,
1991. and 1992.
19
DO. Criteria
Revision Justification
II
-
Rexininmied -V
-
EWSegment
-
July1928
__
TE
iii
_
-
__
I
I-
-
Proposed 6 mg/I Average:
-
-
5 mg/I Minimum
EWH
Criterion
-
II
RM119.9 RM115.31 RM1O9.37 RM1O2.14
I
I
I
p
120
110
RIVER tYkE
MAS/1995-12-5
January 3!, 1996
C)
E 12
C
e
10
0)
,
0
‘8
-c
0,
02
0
60
50
I-
~4Oa,
C
-~3o
-o
9o20
C
—
12
o 60
40-
~2O
Ct
I-
-o
t
a)
a)
10
0
C
R~nnme~ded
EWisegment
JuI~4
988
H
J_I
J~
Proposed 6 mg/I Average:
-
5 mg/I Minimum EWH Criterion
I
I
I
I
I
I
RM119.9
RM115.31
RM1O9.37
RM1O2.14
1979-7994
—m--—
I~V11O2fl
-
1980
1985
1990
1995
YEAR
LWI O~
081=48)
Iv,
~HQ~tn
(IBI=42)
EW~Q~
2C1=46)
W~H
Q*st~
QO=36)
Figure 9. Comparison of Dii (upper) concentrations in the Scioto River as
measured by Datasonde continuous monitors during July 1988 and the
Index of Biotic Integrity (IBI; middle) and Invertebrate Community
Index (JEll; lower) based on results obtained at fixed locations (RM
100.0 and 102.0) during 1974-1994.
0.0. Criteria Revision
Justification
19741993
I’’’!’
1975
—0--— l~v1lcflCVlO2.O
20
MASII99S-12-5
D.O.
Criteria Revision
Justification
January 31, 1996
Synthesis
of Information
The information presented thus far from the Ohio EPA database consists mostly of field
observations with the goal of evaluating the
efficacy of a 6 mg/I average/5 mg/I minimum two-
number EWH 110. criterion. These observations (Figures 1-9) tend to support changing the
current 6 mg/I minimum LW!-! DO. critedon to the proposed two-number criterion. Not only
have there been observations of EWH use attainment with minimum D.O.
values
less than 6 mg/I,
the evidence also suggests the relative absence ofthis occurrence when instantaneous DO. levels
drop below
5
mgfl and median 1eve~sdrop below6 mg/I (see Figures 1 and la). These results also
seem to correlate with the findings of Ellis (1937) and Coble (1982) who both found that fish
communities characterized by a high divershy and a significant proportion of sport-species
(e.g.,
percids, bass, sunfish) occurred at sites
averaging
greater than
5
mg/I. The latter study by Coble
(1982) is particularly supportive as it focused on what arc sometimes referred to as “cool water’
fish assemblages. In distinguishing between EWH and WWH communities in Ohio, the
qualitative association of “cool water” fish species with EWH is one way of describing some of
the species which are the significant biological attributes of this use designation. In a review of
these field studies U.S. EPA (1986) concluded
“.
. .
that
increases in dissolved oxygen
concentrations above 5 mg/I do not produce noteworthy improvements in the composition,
abundance, or condition of non-sairnonid fish populations
(italics added). but that sites with
dissolved oxygen concentrations below 5 mgI have fish assemblages with increasingly poorer
population characteristics”.
While these studies essentially pit-dated the development of
multimetric indiées such as the IBI, the qualitative characteristics of the fish populations which
are described by each are consistent with some of the key differences between the WWH and
EWH uses which are discriminated and quantified by multimetric indices such as the IBI and ICI.
The most recent and comprehensive compendium of the effects of DO. on fish and other aquatic
organisms is the U.S. EPA
Ambient Water Quality Criteria for Dissolved Oxygen
(U.S. EPA
1986). This document included the findings and conclusions of some noteworthy reviews such
as Davis (1975) and Doudoroff and Shumway (1967, 1970), the latter being cited by the water
quality criteria compendia of that time
(e.g.,
National Academy of Sciences/Engineering 1973).
While the U.S. EPA (1986) study only distinguished between warmwater and coidwater criteria,
it did refer to varying degrees of protection within each category
(e.g.,
degrees of fish production
impairment). One analysis correlated the percent survival of embryonic and larval stages of
warmwater fish with mean DO. which showed complete survival of eight species when the
mean
DO. was greater than 6 mg/I (Figure 10). It was further noted that the minima in the
laboratory experiments averaged about 0.3 mg/I less than the mean, The U.S. EPA (1986)
recommendations for DO. criteria specified three temporal thresholds for early life stages and
other life stages including adults. For warmwater applications this consisted of the criteria listed
in Table 2. Based on the thresholds developed by U.S. EPA (1986) a 6 mg/I average/5 mg/I
21
MAS/1995-12-5
0.0. Criteria Revision Justification
January 31, 1996
120
I
~ oI~ ‘i
a
•,—
2
80—
‘I
.0
V
-~
.
:~o 60—
V
U
0 Largemouth Bass
o
0 Block Crappie
—
A
a White Sucker
•
Boss
—
S
Northern Pike
20
U Channel Catfish
i
?lSWctleye
•
VSmci?Imouth Bass
(I)
____
I Li till
2
3
4 5678910
Dissolved Oxygen (rng/L)
Figure 11. The effect of continuous exposure to various mean dissolved oxygen concentrations on
survival of embryonic and larval stages of eight species of non-salmonid fish. Minima
recorded in these tests averaged about 0.3 mg/I below
the
mean concentrations (reproduced
from
Ambient Water Quality CriteriaJbr Dissolved Oxygen,
U.S. EPA 1986)
22
MASh
995-12-5
DO. Criteria Revision Justification
January 31, 1996
Table 2. Water quaLity criteria for ambient dissolved oxygen concentrations to protect
warmwater aquatic life as proposed by U.S. EPA (1986).
Life Stages
30-Day Mean
7-Day Mean
7-Day Mean
Minimum
I-Day Minimuma
Early Life Stages
(embryos, larvae,
juveniles 30 days)
NA
6.0
NA
5.0
Other Life Stages
(juveniles, adults)
5.5
NA
4.0
3.0
a
instantaneous minimum.
minimum EWH D.O. criterion appears to be protective of all life stages. While a
5
mg/I minimum
is more stringent than that proposed by US. EPA (1986) for adults andjuveniles, it is necessary
to protect younger life stages. It also seems a reasonabk minimum given that EWH criteria
should be more protective than those for WWH. The EWH DO. criterion that we propose lies
between the U.S. EPA recommended warmwater and coidwater levels (non-embryonic life stages
only) of protection which also seems reasonable given that some of the sensitive warmwater
species that comprise the assemblages representative of EWH may well approach the sensitivity
of
salmonids.
The adoption of a 6 mg/I average/5 mgi minimum two-number D.O. criterion for EWH seems
supported by the scientific evidence (both field and laboratory) examined by this study. In
practical terms the proposed two-number criterion is also consistent with the hierarchy of DO.
criteria between the WWH, MWH, and LRW use designations. Based on the information
presented by U.S. EPA (1986) there is also justification for bringing the Coidwater Habitat
(CWH) D.O. criterion (presently 6 mg/I minimum) into line with the two-number
average/minimum hierarchy ofthe other use designations. The addition of a 7mg/i average seems
to be supported by the U.S. EPA (1986) study which specifics a 6.5 mg/I 30-day mean for life
stages other than embryos and larvae which are not at issue in Ohio’s CWFI designated streams.
These life stages are not applicable protection end points for CWF! in Ohio as this use is focused
on maintaining adult andjuvenile salmonids on a put-and-take basis, thus a 7 mgJl
averagel6
mg/i
minimum criterion should be protective of the CWH use designation.
23
MAS/ 1995-12-5
D.O. Criteria
Revision
Justification
January 31. 1996
REFERENCES
Coble, D.W. 1982. Fish populations in relation to dissolved oxygen in the Wisconsin River.
Trans. Am. Fish. Soc. 111:612-623.
Ellis, M.M. 1937. Detection and measurement of stream pollution. Bull. U.S. Bureau of Sport
Fisheries and Wildlife. 48(22): 365-437.
Davis, J.C. 1975. Minima! dissolved oxygen requirements of aquatic life with emphasis on
Canadian species: a review. J. Fish. Res. Bd. Can. 32:2295-2232.
Doudoroff, P. and DL. Shumway. 1967. Dissolved oxygen criteria for the protection of fish.
Amer. Fish. Soc. Spec. Pubi. No. 4: 13-19.
Doudoroff, P. and D.L. Shurnway. 1970. Dissolved oxygen requirements of freshwater fishes.
Food Agric. Org. United Nations, Rome, Italy. FAO Tech. Paper 86. 291 pp.
DeShon, J.D. 1995. Development and application of the invertebrate community index (IC!),
pp. 217-244.
in
W.S. Davis and T. Simon (eds.). BioIogica~Assessment and Criteria:
Tools for Risk-based Planning and Decision Making. Lewis Publishers, Boca Raton, FL.
Federal Water Pollution Control Administration (FWPCA). 1968. Water quality criteria. Rept.
of the National Tech. Advisory Comm. to the Secy. of Interior, Washington, D.C. 234 pp.
National Academy of Sciences/Engineering. 1973. Water quality criteria. National Research
Council, Washington, D.C.
594 pp.
Ohio Environmental Protection Agency. 1995. Biological and water quality study of the Linle
Miami River and selected tributaries. OEPA Tech. Rept. MAS/1994-12-11. Division of
Surface Water, Monitoring and Assessment Section, Columbus, Ohio. Vols. I and II.
Ohio Environmental Protection Agency. 1989a. Biological criteria for the protection of aquatic
life. Volume III: standardized biological field sampling and laboratory methods for assessing
fish and macroinvertebrate communities. Div. Water Qual. Plan. Assess., Columbus, Ohio.
Ohio Environmental Protection Agency.
1989b. Addendum to biological criteria for the
protection of aquatic life, Volume II: users manual for biological field assessment of Ohio
surface waters. Div. Water Qual. Plan. Assess.. Surface Water Section, Columbus, Ohio.
24
MAS/ 1995-12-5
DO. Criteria Revision Justification
January 3 L, 1996
Ohio Environmental Protection Agency. I 987a. Justification and rationale for the modified
warm-water habitat aquatic life use and associated dissolved oxygen criteria. Division of
Water Quality Monitoring and Assessment, Surface Water Section, Columbus, Ohio. 26
pp.
Ohio Environmental Protection Agency. 1987b. Biological criteria for the protection of aquatic
life: Volume II. users manual for biological field assessment of Ohio surface waters.
Division of Water Quality Monitoring and Assessment, Surface Water Section, Columbus,
Ohio.
Omernik, J. M., and Gallant, A. L. 1988. Ecoregions of the upper Midwest States, U. S. EPA,
Environmental Research Lab, Corvallis, OR. EPA/600/3-88/037.
Omernik, J. M. 1987. Ecoregions of the conterminous United States. Ann. Assoc. Amer.
Geogr. 77(1): 118425.
U.S. EPA. 1986. Ambient water quality criteria for dissolved oxygen. Offe. Water Reg. Stds.,
Criteria and Stds. Div., Washington, D.C. EPA 440/5-86-003. 46 pp.
ACKNOWLEDGEMENTS
Chris Skaiski is acknowledged for his aitical review of all drafts ofthis report and helpfiut advice
and comments. Jeff DeShon and Marc Smith are acknowledged for their review of an earlier draft
of the report.
25
Notes on Associations Between DissoWed Oxygen
and Fish and Macroinvertebrate Assemblages
in Wadeable Ohio Streams
DRAFT
Nov 12, 2004
Edward T. Rankin
Center for Applied Bioassessment and Biocriteria
introduction
Dissolved oxygen (DO) is perhaps the most important chemical constituent limiting to
aquatic life in streams across the U.S. streanis because of its obvious importance for
respiration. Most flowing waters have sufficient dissolved oxygen to support natural
populations of aquatic life and certain habitats with low natural levds of dissolved oxygen
during some portion of a year have species adapted to obtain dissolved oxygen from other
sources (gulping of atmospheric oxygen in the mudminnow, grass pickerel in certain
wetland conditions). Most state water quality standards have devdoped dissolved oxygen
requirement based on the U.S. EPA (1986) criteria derivation guidelines using the most
sensitive species (to low DO) that inhabit these waters based on a relatively abundant
literature related to DO requirements. Ohio has incorporated field data associating
biological condition indices, such as the Index of Biotic Integrity (IBI) and the Invertebrate
Community Index (id), with ambient dissolved oxygen measurements to adjust dissolved
oxygen criteria by aquatic 1fe use and, in some cases, ecoregion differences (Appendix 1).
Data
This fact
sheet discusses two types of ambient dissolved oxygen data collect from Ohio
streams.
The largest database is composed of daytinie grab sanipks (ORB) collected during
intensive watershed surveys. Biological and chemical data were matched on a case by case
where the exact location denoted by a river mile (RM) differed slightly. This can occur
because water chemistry data is a point sample, macroinvertebrates sites are a combination
of
a point (artificial substrates) and short reach (natural substrates) and fish are sampled
along a I 5O-500m transect. Chemical and biological data were linked if chemical data were
deemed to be representative of the chemical conditions to which the biology was exposed
and when no significant source of pollutants or dilution entered between sampling
locations (e.g., tributary, discharge). Data also had to be collected during the sante year and
during the same summer period (June 15-October 15).
The second type of data was collected by Ohio EPA using Datasonde continuous
tnoniroring samplers (CND that record parameters such as DO, temperature and pH every
15 minutes; these were typically set for 48 hours. This data, which we obtained from Ohio
EPA, was collected between 1988 and 1994 and should encompass or include time periods
where dissolved oxygen levels had both very high and very low values. There were fewer
linked macroli-ivet-tebrate sites than fish sites with the continuous data so we focused on
the
ORB data when examining macroinvertebrate responses. The ORB database was
extremely large so we used one subset that matched the continuous monitoring sites, a
second subset from the Eastern Corn Belt Plains and 1-luron Erie Lake Nains ecoregions
front 1994-200? for fish, and the statewide data for the macroinvertebrates where there
were somewhat fewer data points.
Day Time Grab Data (GRB) vs. Continuous (CNT) DO Data
Although CNT dissolved oxygen data collection is fairly widespread, it is often not
collected at the same sites as biological, habitat, and other grab water chemistry data. ORB
sample data are important because they have been used to determine whether ambient data
meet or exceed water chemistry criteria in State Water Quality Standards (WQS). ORB
samples in the Ohio EPA database arc composed of approximately 6-8 samples during a
summer period (mean 6.6, median 6.0)
lypically
collected during daytime hours. Samples
were processed in the Ohio EPA laboratory according to U.S. EPA approved methods.
Datasonde
samplers
were
generally set
~
ror
‘to
An
flours,
i
out
bata-1994-2001
-
ECBP & HELP Ecoreguons
were occasionally set for long
periods. Each Datasonde set
averaged 94 samples (e.g., DO
measures) with a median oI
52
samples per set.
We compared ORB vs. UNT
data from the same stations to
explore how they compared in
:~
characterizing a station’s DO
*
2
regime. Figure 1 illustrates a
scatter plot of minimum values
a
0
2
468
from
C’4T
samples
vs.
bolnscnde
Minimum
minimum
values
of ORB
-
bissolved
Oxy9en
samples
at
these
stations
collected during the same
summer period, but likely on
different days. Although there
is scatter these values are
positivejy correlated (R2=O.26).
Quadrant A on Figure 1
illustrates
situations
where
minimum ORB samples are ~ 4 mg/I (Ohio Warmwater Habitat IWWHJ minimum
criteria value), but CNT values are less than 4. Less frequent are values in quadrant B
where
CNT values are ~ 4, but ORB samples are tess than 4 mg/i. These are concentrated
above 3 rug/I (Figure 1). This pattern can also be illustrated with cumulative frequency
FIguve I. Plot of Dawson& cunlingous
dissolved
oxygen
~.
grab
zanipk data for
minimitm
clissoh’cd
oxygn,
data.
Q.wchnnt
A
has
CNT vat
un 4m but
GRB ta(ua 4
uli4e
qiw&aut 8
has
ORB t&ues C 4m but CNT
values
4.
Dashed line is a
regression
hue and
the
solid line
ha predicted line
if
data
were
pe4ectty
matdwct
plots that illustrate the percentage distribution values of dissolved oxygen for minimum
values (Figure 2, tight) and for
10rh
percentile values (Figure 2, left). These graphs contain
the same information as Figure 1, but make it easier to estimate the overall differences
between the methods. For example, the CNT sampling identified about 15 more values
4 mg/i than did the GRB sampling. This is expected, but identifying the magnitude of
difference can be important when applying ORB data for deriving field based targets.
10th Pccer*ile
Dissolnd
0xy9e0
Mirunum bissolved Oxygen
ORB
vs.
CNT
&RB vs. CNT
10
-
___
0
______
0,
C
~
6-
C
.
-u
4
2’
1
2
a
0’
0!
-
-
-
I
01 .1
I
5~O 2O~ ~
7Q~ 9096 99
99999.99
P*rant
Percent
Figute 2. Cumulatiw
frequenty plot
of
lath
~CTCCThÜIC
(top) and mininiu,n
(bottom) dissolved
oflgen
values
from CNT
(dashed)
and GRB (solid) ‘amp6
Ass
ociatüms
Between BiologicalIndicaums and Ambient Dissolved (hygen
Although there is some variability related to multiple stressors that influence the
relationship of DO to aquatic communities in Ohio, there is still a clear threshold
relationship between biological indicators of aquatic condition and ambient dissolved
oxygen. Figure 3 illustrates scatter plots of dissolved oxygen (ORB data) at sites in the
ECBP and HELP ecoregions vs. IBI scores (top) and statewide data and ICI scores
(bottom). The relationship between the ORB and 04T data indicates that diurnal data
would push the threshold relationships to the kft slightly if this were based on CNT data.
There are sites that evidently support Exceptional Warmwater Habitat (EWH) or WWH
IBI and ICI scores
(
50
and 40, respectively) with individual DO concentrations below the
minimum criteria established in Ohio for these uses (EWI+5 rug/I min WWH4 mg/i
mm). The grab sample data represent a snap shot of the actual DO regime. The furthest
outlier on Figure 3 (top) where the IBI scores are greater than 40 is a DO of 1.6 mg/I. This
was found in the headwaters of the Olentangy River. This area has had a history or relative
severe impacts with nearby stations in 1979 with IBI scores below 20. Much of this has
been abated and IBI scores in these areas are now in WWH ranges in the ‘lOs. There were
several DO sensitive species in this community (e.g., rainbow darter) although perhaps at
lower abundances than expected. In addition, certain microhabitats such as riffles could
have slightly higher DO regimes than pooi areas where the DO sample was likely collected.
In the macroinvertebrate data there is an extreme value in the Stiliwater River with a DO
of 1.3 mill that had an ICI of 40 in 1982. This was considered an impairment at that time
and the data collected in 1990 had DO values above 6 mill and the id rebounded to a
to
CNT
a
9o9~ 99 99999.99
score of 50. We suggest that extreme examples or outliers should not be used to detive or
support towed DO critetia especially based on grab samples. Grab samples on average
however are likely protective or conservative estimates because CNT identifies about 15
more low values than (3KB samples do (Figure 2). Biological signatures (e.g., presence or
absence a1 DO sensitive species or tan) can be useful however, in determining whether an
exceedance oi the dissolved oxygen criteria is biological significant and should be identified
as an area that needs some restoration (e.g., placed on a TMDL list).
Figures 4 and 5 illustrate the distributions of
10th
percentile or minimum dissolved oxygen
values for ORB samples (Figures 4 and 5) and CNT samples (Figure 4). These graphs are
another method of illustrating the relationship between IBI or ICI and disscilved oxygen.
The more frequent low values collected in CNTvs. ORB samples are reflected in the lower
ranges
of
the open boxes which represent
10th
percentile values across all stations. The
ONT sampling picks up the diurnal swings that the ORB samples miss, although the grab
samples cover more periods of time across a summer sampling period (when low DO values
are more likely due to high temperatures, algal activity, and increase organic production).
The biokgical data integrate stressor influences across multiple time periods (e.g., weeks to
years), and the absence of ‘ow DO in either the CNT or ORB data can miss events or
underestimate the severity of the DO influences. Biological signatures of low DO from
impaired assemblages can compensate for the lack of “exceedences” of DO criteria and in
fact the identification of DO as a cause of imp&rment in the Ohio 305(b) report (Ohio
EPA 2000) is often accomplished without a specific chemical exceedence.
Figures ôa-f provides some insight into species sensitivity or tolerance to dissolved oxygen
stress. These are plots of catch per unit effort (relative number per 300m) of individual
species counts from electrofishing surveys paired with individual dissolved oxygen vaLues
for wadeabk streams ( 200 sq mO. Each species count can be repeated for each ORB at a
station. The DO tolerant species (carp, Figure
61
and creek chub, Figure 6e) provide a good
illustration
of
the range
of
dissolved oxygen values distributed throughout this database
which comprises the entire range of possible DO values. Moderately sensitive species (e.g.,
sand shiner and golden redhorse) are not found or found at reduced abundance at sites
with less than 3-4 mill of dissolved oxygen. Two highly sensitive species, black redhorse
and variegate darter are rarely (black redhorse), if ever (variegate darter) found at dissolved
oxygen concentrations tess than
5
mill. These types are data are important in helping
establishing or verifying the appropriate minimum criteria for a given aquatic life use in
Ohio. There is a continuum of sensitivity to ambient concentrations of dissolved oxygen
across species and taxa that occur across Ohio. The presence of such sensitive species could
be used to help identify reaches or watersheds that might be especially sensitive to factors
that influence dissolved oxygen such as nutrient enrichment, habitat degradation and
seditnentation. As has been outlined by us and others, these “nonpoint” stressors should
typically be dealt with in combination and not separately as is often done in TMDL efforts.
I-4
I-I
60
50
bata
-
1994-2001
ECBP & HELP Ecoregions
60
50
40,
•
a •~
•
S.:.
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.:...:
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024
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8
Dissolved Oxygen (mg/I)
Grab Data
Grab Data
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.
.
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• _•
.
• • •
• . U
Se
•* •• •• •• .
e...e
~. — .
. . •.* •.
S.ee •a*..
Ia.
•
•a
• .e
—•
0.
• •
0
•
• ~fl.a
S~
.._.
. .•ø
~.
.
.
- 0 -
0
2
4
6
8
10
Minimum Dissolved Oxygen
(mg/I)
Figure
3. WI
(top) ami IC! (bottom)
15.
minimum dissolved axygen (indevkhwl
grab
samples) at
statiom
in
the
ECBP
and EOLP
ecaregion from I 9942001 (top)
and sratewkk data from
1978-2000 (bottom)
Daswd
line
refneserns
Ohio’s iaimaoatcr aitS~zJot average w,wentratjon of
d~ssoivedux~ger~
Solid
line is an
95th
percentile tATCShOId
line drata, by
ge.
C:.?.
.
I
—.
10
10
Ohio EPA
Survey
bota
10th
Percentile,
Grab bata
C’
&
0’
6 I
U
I
0-8
~
L
£~
2
0
12-19
20-29
30-39
40-49
50-60
IBI
Range
Ohio EPA Survey
Data
Minimum Values, Grab bate
10
C’
E
c~.
6
01 t
0-6
I~
12-19
20-29
L
11
35
10
8
6
4
2
0
IBI Range
Ohio
EPA
Survey
Data
Minimum Values,
batosonde Data
1o_
B
6
4
2
0
12-19
20-29
30-39
4049
~O-6O
Ohio EPA Survey bath
10th
Percentile
Datosonde Data
12-19
20-29
30-39
40-49
50-60
30-39
40-49
~O4O
IBI Range
IBI Range
Figure 4. Box ~locsof I Cr percentile (wp) andminimum (bottom)
thssokd oxygen
conccnwations
b~
IRI
ranges
far
GRB
samples (left)
and
fin
Datasomie
continuous
monitor
data fright)
at sites
where
b0th data
types were
coUecwd
between
1988
and 1994
by
Ohio EPA.
Ohio EPA Survey
bata
Grab Data
10
b
____
I~I!
:1
~
I
0
-
-
0
—
ro
to
&
9
?
N
9
CO
aa
In
Range
Ohio EPA Survey Data
Means,
Grab
bata
10
~
iCt
Narrative Pon9e
•
o
9
0
5. Box plots
of
,ninim,jm
dusolved oxygen
wnannatiom ~
Ed
Tanga (top and ngnatñ~
id
equiwlenrs
(bottom))foc GRB
samples
collected in Ohio
from 1978-2000.
Red
line
7E~resents
Ohio’s
waymwatn cSeria for average
cornrntration
of
dàsolvcd
oxygew
Ii-
Dl
=0
0)01
O~
-o
VI
-°
a
it
-o t
0
-—
o
C
0
-U
‘I
3
~
!
=
In
Wadeoble Streams
100
••,
¶0.1.P
10
:i~!~~L~i4.
24
bissolved Oxygen (mg/I)
Wadeable Streoms
1000
-
-
-
I
- -.
y,.*.r•
...
-
.r
:r.J~’q.
.
•4
•~
1~j~
100.
-
:;.4fl3~
•pz
ret.’
10
•
___
-
.•,
..
O
2
4
6
B
10
12
bissolved Oxygen
(mg/I)
Wadeable Streams
i
o~
1000
100
10
Dissolved Oxygen
(mg/I)
c_
‘-
1
•
w ‘~
•
•~
:, s~_
t- -0
-C =
-w
—
Wodeable Streams
100
‘“-sq..
..
.
10 -
1:
~
• ..•
_0•
I.
•••
•
.‘~
...:
.~.
-
•
. ..
. .._.t.•..
o
2
4
6
8
¶0
12
Dissolved Oxygen
(mg/I)
Wadeable
Streams
1000
-
-
-
•
—
.
..
I
•S
I
~
;4n1t44p?(.,J.
100 I
a-
he
•
S •~
•—4__-
.4
.
-tl
-;\-i
- ~
•S
-
o
2
4
6
8
10
12
bissolved Oxygen (mg/I)
Wadeable
Streams
-~ ~
=
z
-
t
¼,
• •I’ .*wu~rl
~
—‘p--
t
bissolved Oxygen (mg/I)
1-
-C ~
--
a
I- -0
-cz
‘I)
-a
C
at
a
-~ -a
-C ~
-~ U
w
a
-4
I.-..
Figute
4. PIot~
of sekcrr4
specks idative
ab,rndances vs.
dissolved
oxygen
mixes
at
~wdeabk,t,nm
sites
in Ohio.
Dashed
line
wpTrJcnts
Ohio’, twznmmun aiwña
for average concentration
of
dissoh’ed
nygen.
Ohio
EPA
Survey
buta
20
-c-u
-~
I
LL
ç,
15
S
0
I—. ~
•.
U
..
“a
.
..
ot,
..
0
•
1—
I
•
•
•••
“a—
E~
S
. —..
—
0.
-
.. __.._
.C.If)
*
•
•
0
— • •~ •*
.
e..._e..
• •
0
1
~•••
••
o
2
4
6
8
10
AverQge
bissolved Oxygen (mg/I)
in Hucil Watershed
Ohio EPA Survey
Data
—
50
t4~
~b
4O~
—
30
• •
U)Q
-
S
..
S
~
3;
.
Q~.
20
—
el:
10
•
*
1—I
•t:~’
~‘••
-
l••~
I
~
-
o
2
4
6
8
10
Average
bissolved Oxygen (mg/I)
in Hucli Watershed
F~rc
5.
Cwmdaüve
total
intolnant
fish
specin
(top)
and
,eusidw
uizcwintzenebyuw
taxa bottom) in
Oil, HucI
I scab,
watersheds).
Thuhed line i’ejneseuts
OhM waymuwn
cyftnia for
ateage conc~ntyaSnof
dissolved
ox~gen.
Solid
lines are
95th percentile
threshold lines
drawn
fry
eye.
QHED62.B
Mean Hugh
Mean Hucli
0.076
~
257
6
&
&
28.3
33.5
FF
____M~4jsw
~POI65~
.-.-~.._.
P4QQ9&~
46.0
40.4
E6
39.3
29.1
&F
Figiue
8.
Example
regression (Tees
fat
TnLLjoT NI’S stYaion
to
WjudtIC 14e in
the FCBP a,2
HELP ecoTegons of
Ohio. Data afrom 1994-2001 and TC~TOCnCS smtiom
tail
mpafred or injLcna
by
nonpotnt zouirn of
tioUusn.
Response
variable
on top is
fBI and
on bottom is IC!.
IRE
and
IC!
scores
with nanacivc codes
are
at
the
end of
each
node (F
—
Excellent, C
—
Good. F
-
Fair,
P
- Poor,
VP
—
Vn~
Poor.
Multiple Stresso-is
and Cumulative Impacts
to WatershecLs
The accrual of multiple stressors at a watershed scale can hinder restoration of
aquatic
life
in stream reaches within such watersheds. In Midwest streams, iow DO, especially from
NPS is typically associated with increased organic enrichment, increase nutrients, and
degraded
habitats. Figures 7 (top, bottom) identifr a
limiting
threshokl oIclissolved oxygen
associated with the maximum, cumulative number of intolerant fish species (top) and
sensitive ruacroinvertebrate taxa (bottom) expected in a watershed. Watersheds with mean
dissolved oxygen values greater than 7 mg/I (indicates a high proportion olsites with DO
values
5
mg/fl can have 10 or more sensitive species, a number typically associated with
Ohio’s EWLI aquatic life use. Watersheds with mean DO values between 6-7 mg 1’ rarely
have more than
5
intolerant species in these watersheds indicating an increasing number of
sites likely exceeding
wannwater
DO criteria in Ohio (X
=
5 mg t’,
ruin.
4
rug F1).
Average watershed DO values 6 mill rarely have more than I intolerant species and
these watersheds are likely those with high nutrients, high siltation and degraded habitats.
The biological response variables in areas affected by NPS stressors are more strongly
associated with habitat conditions and nutrients such as total phosphorus (TP) than with
DO concentrations, at least as they are reflected in the sampled DO regime. Regression
tree analyses and other triultivariate exploration techniques have identified some of these
associations for the ECBP and HELP ecoregions (Rankin and Arrnitage 2004). Typical
regression trees are illustrated in Figure 8 for 181 (top) and ICI (bottom). These analyses do
not eliminate the important of DO as ecological mechanism of impairment, but identify
the strong controlling influence of habitat and nutrients in explaining observed fish and
macroinvertebrate impainnent and reinforce the need to incorporate habitat in NPS
restoration scenarios.
Species and Tarn
Specific DO Tolerance
Valttes
One of the more challenging wrts of an assessment is identifying the stressor responsible
for aquatic life impairment. While laboratory tests can provide useful data, often such data
is only available for a handful of macroinvertebrate taxa or fish species. Data sets like the
one we used here are usefu’ for “mining” stressor-response relationships between stressor
variables and abundances of a species or tan. A ranking of species responses allow
consideration of biological signatures for these stressors. Taxa that are abundant in the
ambient environment at depressed concentrations oi dissolved oxygen and remain after
other taxa disappear can help distinguish situations where DO is a primary stressor.
Conversely, high populations of taxa that only occur at high, background DO levels can
provide evidence that DO is not an important stressor. Parameter specific tolerance
rankings can provide an improvement over “general” tolerance rankings where
identification of multiple stressors is difficult.
One method to calculate parameter-specific tolerance ratings is to calculate weighted mean
stressor values for parameters where the weighting is done based on the relative abundance
of a specific organism at a site. This requires data with consistent quantitative methods to
control for error due to sampling variability. Organism that are common at high stressor
levels will have higher weighted average parameter values than
an
organism that has its
populations depressed or eliminated at a similar parameter concentrations. ‘Where data is
sufficient the organisms can be ranked and divided into quartiles or some other
distribution as way to assign narrative tolerance rankings (e.g.. tolerant, moderately
tolerant, moderate intolerant, intolerant). ‘When this is done for multiple taxa the
“biological signatures” become more compelling (Ranicin and Yoder 1995). Dissolved
oxygen is somewhat problematic because although low oxygen
is
clearly a stressor to
respiration, very high DO concentrations may be an indicator that nighttime DO is
depressed related to high algal respiration. Tables 1 and 2 provide data on weighted
dissolved oxygen values for ruacroinvertebrate tan and fish species in Ohio. Ohio’s general
tolerance rankings1 are provided for comparison. We excluded tan where there were iess
than 100 DO data points or about 20 stations that had biological and DO data. We used
the minimum dissolved oxygen value from each station to generate the weighed parameter
value as the best indicator of stress conditions and this was paired with taxa or species
abundances collected at these same sites during the same summer period. We also
generated unweighted statistics from all of the DO data associated with each species from
all samples at all sites (means,
25th
and
10th
percentiles).
We
compared the general tolerance ratings ior fish and macroirwertebrate taxa with the
weighted DO values we generated to examine concordance between these tanking methods
(Tables 3 and 4). We divided the weighted DO rankings into quintiles and assigned them
the same narrative ratings used in the general tolerance rankings: intolerant, sensitive or
moderatdy intolerant, intermediate, moderately tolerant, and tolerant Agreement among
rankings indicates a general correspondence between general tolerance and DO-specific
tolerance (Tables 3
and
4) with some variability.
Table 3. Comparison of general tolerance
vs.
DO tolerance
for
93 Ohio fish species where
there were at least 20 sites with DO data and a species occunence. General tolerance
based on Ohio EPA’s tolerance rankings for the IBI.
DO Tolerance
General Tolerance
Tolerant
Mod.
Tolerant
Intermediate
Sensitive
Intolerant
Intolerant
1
6
3
!
8
Sensitive
1
7
6
Intermediate
2
9
6
1
Mc,d.Tolerant
3
.
3 —.
13
Tolerant
j....
:7
.
3
9
“General” tolerance rankings are assessment of a taxa or species tolerance to a wide range of stressors and
are typically used in ID! and
other mtiltimetric indkes.
These are often species that have declined in
abundance compared to their
histork
geographic nnges and often in response to multiple stressors
including
habitat degradation, siltation, organic enrichment, and toxic chemicals. These assignments are typically made
from a combination of fish
distribution texts and data, literature, examination
oi ambient datasets, acid best
professional judgment.
Outliers can be useful to explain vanation between general and specific tolerances. In the
fish comparison, one species, bladcnose dace, is an outlier with a general tolerance rating
of tolerant, but a DO rating oi intolerant. This species is generally associated with cool
headwater streams, but can be extremely tolerant of industrial discharges and is not a
generally a habitat specialist.
Table 4. Comparison of general tolerance vs. DO tolerance for 171 Ohio macroinvertebrare
taxa where there were at least 20 sites with DO data and a vaxa occurrence. General
tolerance based on recent Ohio EPA’s rankings of general tolerance.
DO
Tolerance
General Tolerance
Tolerant
Mod.
Tolerant
Intermediate
Sensitive
Intolerant
Intolerant
1
6
3
.~
Sensitive
1
7
5
6
Intermediate
2
9
6
1
Mod.
Tolerant
3
3
13
Tolerant
.~ .
7
3
9
The greatest
variability was in comparisons between intermediate rankings of general
tolerance and dissolved oxygen tolerance rankings where intermediate general sensitivity
was broadly distributed with both DO intolerant as well as DO tolerant species and taxa
(Tables 3 and 4). Some of this was variation was related to coidwater species considered
generally interniediate to certain general impacts (e.g., mottled sculpin, trout sp. stocked),
but sensitive to temperature and DO and ~mother group of species associated with wetland
and prairie habitats that are habitat specialists, but are associated with naturally lower DO
regimes (tadpole madtorn, warmouth, least darter) than found in more common high
gradient Midwest streams.
Derivation of Dissolved Orygen Criteria
Criteria for dissolved oxygen for streams are typically structured as a two number criteria
with a minimum (never to be exceeded) vaiue and as daily average values. Even though
most state dissolved oxygen criteria are based on methodologies generated from controlled
studies as outline in the 1986 EPA guidelines (U.S. EPA 1986) some states have modified
criteria on the basis of ambient field data (Ohio EPA 1996) or have methodologies for site
specific derivation of criteria due to natural conditions (SCDHEC 1999; MO DNR 2004)
that are were considered either over or under-protected by existing statewide criteria. These
modifications of criteria typically rely on reference sites without substantial anthropogenic
impacts.
12
12
ID
8
6
4 I
&RB
boto
a
0
a
E
C
I
I.
a
6RB ban
59
58
51
56
55
54
53
52
5!
50
181 Score
Figure 8.
Box and whisker plots of
dissolwd oxygen
(ORB, top andbottom, CNT
middk) m. IC!
(top)
and 1131 (middle
and kuom)
flOTes
above 50.
Dotted
tine
TC~TCSCHC5
the
WV/H average SitS and
the solid line the
minimum aitcria fbi DO.
ia Score
CNT
bate
IBI Score
60
58
56
54
R
5C
59
58 57 56
55
54
53
52
51
50
Ohio EPA’s origina’ EWH dissolved oxygen criteria was odginally based on best
professional judgment related to the perceived need that the biota of EWH streams were
more sensitive to iow DO than the biota typical oIWWH streams (Ohio EPA 1996). The
minimum DO criteria for EWH streams was then set to be equivalent to Ohio’s coidwater
aquatic life use (6 mg/I minimum). Ambient data similar to that presented here was used
to provide evidence that EWH index scores (fBI, ICI) occurred commonly at DO values
between 5-6 mg/I, but not iess than
5
mg/I (Ohio EPA 1996) to justifr a
5
mg/I minimum
value for these waters. This is also supported with additional data examined here. For
example, the intolerant black redhorse and variegate darters that are associated with EWH
streams and rivers show abundant populations down to 5 mill, but quicidy disappear
below that level (see Figure 6). These species-based graphs were done with ORB data and
are conservative because they miss some of the lower nighttime values measured in the
CNT data.
WWH Dissolved Oxygen Criteria
The same approach used to examine and provide justification for the EWFI criteria can be
applied to the WWH criteria as well. Ambient biological data indicates that attainment of
WWH biological index scores occurs at stations with DO values of 4 mg/I or above, but
much less frequently when DO is less than 4 mg/i. Interestingly, there was a slight
difference in the range of minimum dissolved oxygen values at stations with WWH 181
scores (40-49) between stations with grab data at sites with datasonde data (see Figure 4a)
and grab samples at a broad range of sites represented by the statewide data set. The
distribution of minimum DO values at stations with IBI scores of 40-49 are summathed in
the histograms for stations in the statewide data set (Figure 9, top) and a subset a1 this data
that also had datasonde data. The presence of lower DO values at statewide sites is partly a
result of larger sample sizes, but may also be related to datasortde samplers being more
commonly set at complex sites where multiple stressors are common and point sources
occur. At such sites, lower DO values are more likely to co-occur with toxicants and other
acute stressors, and thus they less frequently co-occured with IBI scores of 40-49. The
statewide data includes more sites where DO is the predominant stress and low DO values
co-occur more frequently with IBI scores of 40-49.
Stations with DO values less than 4 mg/I primarily comprise the “tail” of the distribution
(Figure 9, top). An examination of sensitive species that are charactistic of WWH streams
such as the golden redhorse and rainbow darter show fewer organisms below a DO of 4
mg/I although populations do occur at lower DO values. Some data points below the
criteria should be expected because the chemical grab samples are an imperfect estimate of
the magnitude and duration of a chemical stress. The abundance of a fish species
characteristic of EWH streams (variegate darter, Figure 10, bottom) illustrates the greater
restriction in abundance along the DO gradient observed in EWI-! streams justifying the
higher minimum DO (5 mg/I vs. 4 mg/I) for these waters.
Grab Data
Statewide,
All
Years
4
§
6
7 8 9 101112
bissolved
Oxygen (mg/I)
10
6
•1-
6.
C
0
4
Grab bota at
Sites with
Datasonde bum
bissolved Oxygen (mg/I)
200
150
100
•1-
C
‘3
50:
~
123
10
11
12
Figure
9.
Hislogrwns
ofminimum
dissolved
oxgen
data (mg/i) at
stations
with IBI
values
of40-49 (WWH range)
from a statewide
Ohio data set (lop) and a
subset
ofsites that
also had
datcisonde data (bottom).
Ohio EPA
5.rvey beta
Rthrtow Darter Collections
Wodeobk Streams
200
I5O~
~Ioo~
a
I
r
Minimum
USso
lyS Oxy9en
(mg/I)
),io
B’A
Survey
bat
a
Golden Reã,orse
Collections
Wodectk
5trearns
I
60:
I
1
1
I
!
~
:‘r ~1~ti1~~
Minimum
bissolved Oxygen
(mg/I)
Ohio
EPA Survey Data
Vonegote Dcrter Collections
Wodcthk Streams
100
~ H
60j
~~
Minimum Dissolved Oxygen (mg/I)
Figure &
Box
and whiskerplots of
rainbow
darter,
golden ret/horse, ami
variegate darter vs. minimum dissolved oxygen concentrations in Ohio
strewns.Red lines
denote
the minimum DO
criteria
for
WWH streams;
hhie linesfor EWH streams.
Figure
10
probably underestimates the effects of the lowest DO because it does not include
sites where a
species should occur, but has been eliminated because of low DO or other
stressors. The development of species distribution and abundance models along natural
gradients of habitat, elevation, stream gradient, and flow could provide estimates of
expected abundance of an organism. Rektionships between stressors like DO and expected
abundance could result in more precise estimates of the influence of a stressor such as DO
on individual species or tan
Using ambient biological data to help or adjust criteria such as dissolved oxygen takes
advantage of the strength of well-founded biological monitoring to integtate the often
complex pathways of influence of DO. The selection of the biological target is a critical
choice in this effort. Ohio has developed biological targets through their development of
biological criteria. The difficuky is in determining which chemical number is a protective
and reasonable target for protection of aquatic life. The appropriate role of the biological
data is as a response indicators to the suite of stressor that occur in the environment and
the chemical stressors are best used as design endpoints and to help identify cause of
biological impairments. The iocus on this paper was to identify DO values that can be
protective and reasonable design criteria and provide information for various management
efforts on cause of impairment. We know that a reliance on chemical assessment of aquatic
life use attainment and impairment, in the absence of biological data, outside of where
values will obviously result in acute impacts, can result in large errors in identifying
impairment with the error tendencies strongly skewed to missing impairments (Rankin
2003).
A reliance on biological data for assessment impairment is consistent with the NRC
TMDL
Committee that argued that indicators should be as direct measures of the
designated use as
possible (NRC 2001). There is more concern with the precision of the
criteria number when using DO data alone to estimate impairment, than when using DO
data as a support to biological assessments to identifj impairment.
There are a number of methods being explored as tools for deriving accurate criteria from
ambient data. Paul (2004) has proposed a conditional probability approach using
probabilistic survey data. As with other methods it relies on the ability to derive sound
biological targets or endpoints. Such advances are compatible with U.S. EPA’s strategy for
its WQS and Criteria programs because and touches a number of the 28 “Strategic
Actions” in the Draft Strategy for Water Quality Standards and Criteria (U.S. EPA 2002).
Here we outlined what is a muftiple line of evidence approach to determine DO
concentrations that appear to protective on the basis of large scale analyses of databases,
site specific examples of attainment of a tiered use at various DO levels, and the
identification of DO sensitive or tolerant tan that can be used to support attainment
decisions where data is ambiguous. Because many of the stressors are moderately to highly
correlated the choice of the numeric chemical target can be difficult and often depends on
multiple tines of evidence. Some of the newer approaches may provide more standardized
methods to achieve ambient based aiteria.
Perhaps as important a process as the derivation of criteria is consideration of how
attainment and impairment decisions are made. Some of the weakness with attainment
decisions, as for example the 305(b) and 303(d) process, lies with the inappropriate reliance
on stressor indicators to identify impairment rather than on response indicators. The
strength of stressor criteria is with the derivation of appropriate treatment and
management strategies and causes of impairment. Because of weaknesses with using
stressor data to identifij impairment, outside of where values will obviously result in acute
impacts, biological data should be the indicator of choice to determine aquatic life use
impairment. As mentioned above, the DO sampling regime does not always clearly identify
impairments and there is a risk of identifying a water as attaining an aquatic life use with
this data when it is actually impaired (Rankin 2003). Many olthese concerns fade when an
adequate monitoring approach is used that provides confidence in identifying impairment
and is able to employ multiple approaches to identi~ingthe cause of impairment.
Summary
In this paper we explored the relationships between CNT and ORB DO data and the
response of biological data to gradients of DO data across Ohio. Ohio EPA (1996) used a
similar approach to justify a two-number criteria for its EWH aquatic life use including a
addition oi a minimum criteria of 5 mg/I for EWH streams. Both community-level and
taxa and species specific data were used to identify that attainment of an EWH aquatic life
use was rare
below a DO
of
5
mg/I, but became
more
common
between
DO
values of
5-6
mg/I.
Similarly, for V/Wi-I streams, attainment of the
use
was uncommon
below a DO
of 4
mg/i, but
became more common between
DO values
of 45 mg/I.
Ohio
EPA
(1996)
provided more
case
examples supporting the
5
mg/I minimum value for DO for EWH
streams
and
the
standard
laboratory-based
approach supports the WWH criteria. We
also
derived a fish species and a macroinvertebrate taxa sensitivity list
for DO
that shows
differences from
the general
tolerance sensitivities. We
envision
this as a
tool
for use in the
stressor identification process. It is clear from the watershed scale patterns
we
have
presented that restoration
of
streams can
be
limited by watershed
scale
influences and that
muftiple
stressors are the
nile rather than exception.
It is
also clear that aquatic life have a
continuum of response
to DO
and that tiered aquatic life
uses
provide
great advantages
for
water
resource
management and the derivation
of
reasonable and protective
DO
criteria.
References
MO DNR. 2004. Deriving Site-Specific Criteria to Protect Missouri’s Aquatic Life. Water
Protection Program Technical Bulletin, Missouri Department of Natural Resources.
4/2004.
Ohio
Environmental Protection Agency (Ohio EPA). 1996. Justification
and
Rationale for
Revisions
to the
Dissolved Oxygen
Criteria
in the Ohio Water
Quality Standards,
OEPA Technical Bulletin
MAS/1995-12-5, State
of Ohio Environmental
Protection Agency, Division
of Surface
Water, Columbus,
Ohio 43228.
Ohio Environmental Protection Agency (Ohio EPA). 2000. Ohio Water Resource
Inventory, Volume I: Summary, Status and Trends, E. T. Rankin, C. 0. Yoder, and
D.Mishne, (editors). Division of Surface Water, Ecological Assessment Section.
Columbus, Ohio.
Paul, J. F. 2004. Geographic-specific water quality criteria development: A conditional
probability approach. Presented at the EMAP Symposium: Integrated Monitoring
and Assessment for Effective Water Quality Management, May 3-7, Newport
Rhode Island.
Rankin, E. T. 2003. Comparison of Biological-based and Water Chemistry-based Aquatic
Life AttainrnenVlrnpairrnent Measures under a Tiered Aquatic Life Use System
Aquatic Life Use Attainment Fact Sheet 3—CABB-03 prepared for U. S.
Environmental Protection Agency, Region V, Chicago, IL.
Rankin, E. T. and B. Arrnitage. 2004. Associations Between Stream Habitat
Characteristics, Biological Condition, And Nutrient Concentrations in Wadeable
Streams Of The Eastern Corn Belt Plain And Huron Erie Lake Plain Ecoregions.
CABB Technical Report I-CABB-04 prepared for U. S. Environmental Protection
Agency, Region V. Chicago, IL
SCDHEC. 1999. Methodology for Determining a Permitted Dissolved Oxygen Deficit
Allowance for Waters Not Meeting Numeric Standards Due to Natural Conditions.
South Carolina Department of Health and Environmental Control.
US Environmental Protection Agency (EPA) 1986. Ambient Water Quality Criteria for
Dissolved Oxygen. Criteria and Standards Division. US Environmental Protection
Agency, Washington, D.C. EPA. 440/5-86.003.
US Environmental Protection Agency (EPA). 2002. Draft Strategy for Water Quality
Standards and Criteria: Strengthening the Foundation of Programs to Protect and
Restore the Nation ‘s Waters. United States Environmental Protection Agency,
Office of Water. EPA-823-R-02-OO 1.
Yoder, C. 0. and E. T. 1&ankirt. 1995. Biological response signatures and the area of
degradation value: new tools for interpreting multimetric data. Pages 263-286 in W.
S. Davis and T. P. Simon (editors). Biological assessment and criteria: tools for
water resource planning and decision making. CRC Press, Boca Raton, FL.
Table
1.
Weighted
mean
and
other
statistics
for
dissolved
concentrations
by
macoinvertebrate
taxa
ranked
by
the
weighted
mean
bO
cIue.
No.
Weighted
25th
10th
Species
Stations
Mean
Mean
Median
tile
tile
(04935-
Erpobdello
punctato
punctata
TI
74
3.4882
5.4007
7.50000
5.00000
3.04000
(05800-
Coecidotea
sp
(MT
301
3.6346
5.7784
7.70000
6.10000
4.20000
(83600-
Kiefferulus
(K.)
dux
Ml
26
3.6364
4.2731
6.20000
4.22500
3.10000
(82770-
Chironomus
(C.)
riparius
group
(VT
117
3.6609
52152
7.70000
6.12000
4.20000
82730-
Chironomus
(C.)
decorus
group
(T
353
3.6880
5.2856
7.60000
6.00000
4.1
0000
(06201-
Hyalella
azteca
F
211
4.2822
5.3877
7.00000
5.40000
4.20000
78401
-
Natarsia
species
A
(sensu
Roback,
1978)
(MI
70
4.3925
5.7471
6.40000
4.17500
2.70000
04664-
Helobdella
stagnalis
T
71
4.4502
4.8470
6.30000
3.70000
2.50000
(83051
-
bicrotendipes
simpsoni
T
375
4.5597
4.9994
6.85000
5.20000
3.80000
08200-
Orconectes
sp
F
53
4.6024
5.1
070
7.10000
5.80000
4.1
0000
(77355-
Clinotonypus
pinguis
MT
24
4.6058
5.2500
6.80000
4.70000
3.38000
04666-
Helobdello
triserialis
1
86
4.6132
5.0440
7.40000
5.30000
3.80000
(84010
-
Parochironomus
“aborti~w”
(sensu
Simpson
&
50
4.6981
5.1760
7.00000
5.30000
4.20000
(77130-
Ablabesmyia
rhamphe
group
MT
167
4.7572
5.5494
7.20000
5.90000
4.70000
83002-
Dicrotendipes
modestus
F
29
4.8260
5.3497
7.80000
6.20000
4.30000
(77115
-
Ablobesmyic
janta
F
37
5.0363
57524
7.10000
5.90000
4.79000
(84790-
Tribelos
fuscicorne
(F
158
5.0533
5.6172
6.70000
5.70000
4.90000
(84800-
Tribelos
jucundum
(F
149
5.1
060
5.5517
6.80000
5.60000
4.60000
(03600-Oligochaeto
T
1927
5.1247
6.0965
7.70000
6.30000
4.60000
78101-
Labrundinia
becki
(
25
5.21
74
57800
7.20000
6.1
0000
5.00000
(83158
-
Endochironomus
nigricans
F
64
5.2762
5.5247
6.90000
5.30000
4.00000
84520
-
Polypedilum
(Tripoduro)
halterale
group
(F
77
5.3000
5.9468
7.50000
6.20000
5.40000
(80510
-
Cricotopus
(Isocladius)
sylvestris
group
VT
58
5.3106
5.4724
7.10000
5.40000
4.20000
(85200-
Cladotanytarsus
sp
(F
70
5.3675
5.71
29
7.30000
6.10000
4.70000
(81630-
Porakiefferiella
sp
25
5.3765
5.8920
7.1
0000
5.90000
4.96000
83050
-
bicrotendipes
lucifer
MI
271
5.4008
5.3974
7.20000
5.60000
4.20000
(01200
-
Cordylophora
lacustris
F
59
5.4125
5.6695
7.50000
6.30000
5.30000
81240
-
Nanocladius
(N.)
distinctus
MT
503
5.4790
5.7290
7.40000
5.90000
4.40000
(81201
-
Nanocladius
(N.)
sp
I
88
5.4973
5.7489
7.60000
6.30000
4.80000
78650-
Procladius
sp
(MI
229
5.5312
57576
7.20000
5.80000
4.20000
(84020-
Parachironomus
carinatus
(F
63
5.5542
5.6365
6.90000
5.70000
4.40000
(84540-
Polypedilum
(Tripodura)
scalaenum
group
F
1161
5.5646
6.1448
7.70000
6.30000
4.80000
78600-
Pentaneura
incanspicuo
F
64
5.5950
5.8755
8.20000
6.40000
5.00000
Table
1.
Weighted
mean
and
other
statistics
for
dissolved
concentrations
by
mocoinvertebrate
toxa
ranked
by
the
weighted
mean
bO
cIue.
No.
Weighted
25th
10th
Species
Stations
Mean
Mean
Median
tile
tile
(01801-
Turbellaria
MI
1285
5.6051
6.1104
7.80000
6.40000
4.80000
(78100-
Labrundinia
sp
F
107
5.6500
5.9850
7.80000
6.30000
5.10000
(79100
-
Thienencnnimyia
group
F
449
5.6665
5.8318
7.70000
6.30000
4.60000
06810
-
Gammarus
fasciatus
(F
64
5.6962
6.01
75
7.80000
6.40000
5.1
0000
(85500-
Paratanytarsus
sp
F
696
5.7031
61429
7.40000
6.20000
4.90000
07701-
Cambaridae
(1
31
5.7087
5.5871
7.40000
6.22500
4.60000
(81631
-
Parakiefferiella
n.sp
1
(MI
67
5.7121
6.6104
7.55000
6.40000
5.70000
81260-
Nanoclodius
(N.)
“rectinervis”
(old)
55
5.7245
5.6727
7.90000
6.10000
4.44000
(18100-
Anthopotamus
sp
(MI
74
5.7313
6.1216
7.80000
6.60000
5.73000
(22001
-
Coenag’ionidae
MI)
448
5.7388
5.741
2
7.40000
5.80000
4.30000
(84470-
Polypedilum
(P.)
illinoense
(1
643
5.7576
5.9490
7.40000
5.90000
4.40000
(84300-
Phoenopsectra
obedier~
group
F
498
5.8176
6.3501
7.80000
6.30000
4.60000
22300-
Argia
.sp
F
1116
5.8194
6.0036
7.70000
6.30000
4.80000
(08260
-
Orconectes
(Crokerinus)
sonbornii
sonbornii
(F
88
5.8246
6.0420
7.50000
5.90000
4.50000
(84210
-
Paratendipes
albimanus
or
P.
duplicatus
MI
479
5.8994
62339
7.80000
6.50000
5.30000
(04964-
Mooreobdella
tnicrostoma
1
87
5.9005
5.8548
7.50000
6.22500
4.60000
(83300
-
Glyptotendipes
(G.)
sp
MI
854
5.9360
57444
7.60000
6.20000
4.80000
06700
-
Crangonyx
sp
MI
252
5.9383
5.9930
7.30000
6.00000
4.60000
(85803-
Tanytarsus
Type
3
(F
46
5.9423
63065
7.10000
6.02500
5.10000
(85201
-
Cladotanytarsus
species
group
A
(MI
24
5.9628
5.6025
6.80000
5.72500
4.90000
(80350-
Corynoneura
sp
(
107
5.9857
6.3252
8.00000
6.90000
5.96000
83003-
bicrotendipes
fumidus
F
40
5.9897
6.6150
7.50000
6.30000
5.00000
(83040)
-
bicrotendipes
neomodestus
F
999
5.9948
6.1
303
7.80000
6.30000
4.80000
(80420
-
Cricotopus
(C.)
bicinctus
MI
768
6.0105
6.1920
7.70000
6.40000
4.90000
84302
-
Phaenopsectra
punctipes
F
29
6.0357
6.0241
7.40000
6.50000
5.43000
11200
-
Callibaetis
sp
F
53
6.0461
5.7175
7.05000
4.80000
3.10000
(83900-
Nilothauma
sp
(F
55
6,0556
61509
7.30000
6.30000
5.40000
(85400-
Micropsectra
sp
F
72
6,0563
6.1046
8.30000
6.77500
5.30000
84460-
Polypedilum
(P.)
faliax
group
F
1287
6.0621
6.2470
7.60000
6.40000
5.10000
(14950
-
Leptophlebia
sp
or
Paroleptophlebia
sp
(MI
84
6.0624
6.1979
7.20000
6.10000
4.90000
(11651
-.
Procloeon
sp
(w/o
hind~ng
pads)
MI
75
6,0681
6.0360
7.30000
6.50000
5.40000
84960
-
Pseudochironomus
sp
F
56
6.0726
5.9982
8.00000
6.45000
5.69000
78200-
Larsia
sp
(F
91
6.0753
6.0253
7.50000
5.70000
3.68000
Table
1.
Weighted
mean
and
other
statistics
for
dissolved
concentrations
by
macoinvertebrate
taxa
ranked
by
the
weighted
mean
bO
~lue.
No.
Weighted
25th
10th
Species
Stations
Mean
Mean
Median
°Iotile
Votile
(78140-
Labrundinia
pilosella
MI
330
6.0859
6.0976
7.30000
6.20000
5.10000
13521
-
Stenonema
femoratum
F
444
6.0933
62165
7.70000
6.60000
5.50000
(85230
-
Cladotanytarsus
mancus
group
F)
43
6.0971
6.3395
7.50000
6.40000
5.70000
(77120-
Ablabesmyio
mallochi
F
728
6.1064
6.0008
7.50000
6.20000
4.80000
(18750-
Hexagenia
limbata
MI
21
6.1121
5.9571
7.25000
6.50000
5.80000
81825-
Rheocricotopus
(Psilocricotopus)
robacki
MI
476
6.1
286
6.5722
7.80000
6.60000
5.50000
(21200-
Calopteryx
sp
(F
438
6.1412
61279
7.60000
6.40000
5.20000
83840-
Microtendipes
pedellus
group
(MI
472
6.1446
6.2353
7.60000
6.40000
5.20000
(81230
-
Nanocladiug
(N.)
crassicornus
(old)
296
6.1533
6.0186
7.80000
6.40000
5.08000
01320)-
Hydra
sp
F
1099
6.1653
6.1094
7.80000
6.40000
5.20000
(81632-
Parakiefferiella
n.sp
2
(MI
70
6.1
836
62983
7.60000
6.50000
5.62000
(84155-
Paralauterborriella
nigrohalteralis
(MI)
51
6.2051
62451
7.40000
6.20000
5.10000
84315-
Phaenopsectra
flavipes
MI)
213
6.2059
6.1683
7.30000
5.90000
4.20000
(77750-
Hayesomyio
senata
or
Thieneimnnimyio
norena
1005
6.2095
6.3178
7.80000
6.40000
4.90000
(82820-
Cryptochironomus
sp
(F
258
6.2207
6.3291
7.80000
6.60000
5.50000
81690
-
Paratrichocladius
sp
(MI
45
6.2544
71538
8.30000
7.40000
6.80000
81231-
Nanocladius
(N.)
crassicornus
or
N.
(N.)
320
6.2664
6.3248
7.70000
6.62500
5.60000
11650-
Proclocon
sp
(w/
hindwing
pads)
MI
51
6.2684
61020
7.65000
6.50000
5.41000
(79400-
Zavrelimyio
sp
F
72
6.2737
62894
7.95000
6.50000
5.10000
(03360-
Piumatella
sp
F
826
6.2818
62965
7.90000
6.70000
5.50000
03040)-
Fredericella
sp
MI
29
6.2915
63728
7.75500
6.80000
6.00000
(13400-
Stenacron
sp
F
1507
6.3213
63213
7.80000
6.50000
5.00000
777403-
Hayesomyia
senata
F
1
94
6.3252
62809
7.60000
6.60000
5.30000
(11020-
Acerpenna
pygmaeus
1
173
6.3335
63401
7.70000
6.60000
5.70000
17200)
-
Caenis
sp
(F)
1408
6.3501
62785
7.90000
6.50000
5.00000
(81229-
Nanocladius
(N.)
crassicornus
(F
52
6.3511
6.2558
7.60000
6.50000
5.26000
(84750-
Stictochironomus
sp
(F
48
6.3665
6.3717
7.70000
6.60000
5.30000
03337)-
Hyalinella
punctata
F
26
6.3699
5.9538
9.40000
7.80000
6.37000
(08250
-
Orconectes
(Procericarnbarus)
rusticus
F
154
6.3823
6.1558
7.80000
6.40000
5.10000
(16700-
Tricorythodessp
(MI
909
6.3895
6.6733
8.20000
7.10000
6.10000
086013-
Hydracarina
(MI
627
6.4030
65133
7.90000
6.80000
5.70000
82121)
-
Thienemanniello
Jobapodema
MI)
235
6.4160
6.2729
7.50000
6.40000
5.70000
(82710-
Chironomus
(C.)sp
1
116
6.4230
5.8314
7.50000
6.20000
4.50000
Table
1.
Weighted
mean
aid
other
statistics
for
dissolved
concentrations
by
macoinvertebrate
taxa
ranked
by
the
weighted
mean
bO
value.
No.
Weighted
25th
10th
Species
Stations
Mean
Mean
Median
tile
°Iotile
(11400
-
Centroptilum
sp
or
Procloeon
sp
(formerly
in
167
6.4293
62287
7.80000
6.40000
5.20000
13560
-
Stenonema
puichellum
group
(
138
6.4524
61529
7.80000
6.70000
5.70000
(85800-
lanytarsus
sp
MI
623
6.4548
6.4312
7.80000
6.40000
4.61600
77500-
Conchapelopia
sp
F
908
6.4562
6.4307
7.80000
6.40000
4.70000
(84700-
Stenochironomus
sp
F
178
6.4851
6.4394
7.80000
6.90000
6.08000
(11100-
Baetis
sp
656
6.51
08
6.3796
7.90000
6.50000
4.90000
85814-
Tanytarsus
glabrescens
group
(F
1184
6.5127
6.3247
7.80000
6.40000
4.90000
(03451
-
Urnatella
gracilis
F
226
6.5263
64492
8.40000
7.30000
6.20000
77800-
Helopelopia
sp
F)
633
6.5361
6.4823
7.80000
6.70000
5.70000
(18700
-
Hexagenia
sp
MI)
21
6.5506
6.6571
7.80000
6.80000
6.13000
80370
-
Corynoneura
lobata
MI
973
6.5700
6.4344
7.70000
6.55000
5.50000
(85710
-
Stempellinella
sp
MI
52
6.5908
6.6962
7.90000
7.00000
6.20000
11300-
Procloeon
sp
(formerly
in
Centroptilum)
88
6.6027
6.4625
7.90000
6.80000
5.80000
(84040-
Parachironomus
frequens
(F
124
6.6091
62485
8.10000
6.80000
5.60000
21300
-
Hetaerina
sp
(F
171
6.61
20
6.7719
8.00000
7.00000
6.00000
(13000-
Leucrocuta
sp
I
422
6.6139
6.6788
8.10000
7.10000
6.20000
82141-
Thienemanniella
xena
F
630
6.6141
6.5022
7.80000
6.70000
5.50000
(05900-
Lirceus
sp
F
235
6.6320
6.0894
7.80000
6.40000
5.20000
(13550
-
Stenonema
mexicanum
integrum
(MI
353
6.6333
6.6083
8.20000
7.1
0000
6.1
0000
82130
-
Thienevmnniella
similis
I)
86
6.6498
6.7687
8.00000
7.00000
6.20000
(85802-
lanytarsus
curticornis
group
MI
242
6.6513
6.6555
7.80000
6.60000
5.50000
(844501-
Polypedilum
(P.)
flavum
(F
1350
6.6602
6.5412
8.1
0000
6.90000
5.80000
13570-
Stenonema
terminatum
(MI
629
6.6692
6.6610
8.00000
6.60000
5.00000
(78750-
Rheopelopia
paramaculipennis
MI
132
6.6737
6.8205
8.70000
7.50000
6.50000
(78450-
Nilotanypus
fimbriatus
(MI
691
6.6800
6.5535
8.00000
6.90000
5.90000
(85625-
Rheotanytarsus
exiguus
group
(MI
1491
6.6807
6.5038
8.00000
6.80000
5.80000
(80410-
Cricotopus
(C.)sp
(F
668
6.6833
6.61
27
8.00000
6.90000
5.90000
83310
-
Glyptotendipes
(Trichotendipes)
amplus
F
36
6.6853
6.2861
8.40000
7.00000
6.00000
(13510-
Stenonema
exiguum
(1
376
6.6868
65894
8.1
0000
7.00000
6.1
0000
(80430-
Cricotopus
(C.)
tremulus
group
(F
685
6.6916
6.61
53
7.90000
6.90000
5.80000
(03121-
Paludicellaarticulata
MI
93
6.6997
6.5678
8.20000
7.10000
6.10500
(11130
-
Baetis
intercalaris
(MI
721
6.7058
6.6364
7.90000
6.90000
6.00000
79085
-
Telopelopia
okoboji
F
86
6.7558
6.6110
8.40000
7.20000
5.84000
Table
1.
Weighted
mean
and
other
statistics
for
dissolved
concentrations
by
macoinvertebrate
taxa
ranked
by
the
weighted
mean
bQ
value.
No.
Weighted
25th
10th
Species
Stations
Mean
Mean
Median
tile
tile
11700-
Acentrella
sp
or
Plauditus
sp
(formerly
in
41
6.7575
6.8610
8.80000
7.60000
6.24000
84060-
Parachironomus
pectinatellae
MI
41
6.7718
6.6415
8.30000
7.30000
6.07000
(23909-
Boyeria
vinosa
(F
120
6.7826
6.5200
7.80000
6.80000
5.80000
(12200
-
Isonychia
sp
I
838
6.7866
6.7911
8.20000
7.20000
6.30000
(13580
-
Stenonema
tripunctatum
305
6.8237
62413
7.80000
6.38750
4.60000
81270-
Nanocladius
(N.)spiniplenus
MI
130
6.8252
65410
7.90000
6.90000
6.00000
83820
-
Microtendipes
slcaelumll
(sensu
Simpson
&
Bode,
154
6.8302
6.7748
8.00000
7.00000
6.10000
15000-
Paraleptophlebia
sp
(MI
260
6.8341
6.3125
7.80000
6.50000
5.20000
83000-
bicrotendipes
sp
52
6.8674
5.9423
7.70000
6.10000
4.66000
(85615-
Rheotanytarsus
distinctissimus
group
MI
311
6.8688
67564
7.90000
7.00000
6.10000
(80204-
Brillia
flavifrons
group
F
118
6.8824
6.8076
8.20000
7.20000
6.10000
(80351-
Corynoneura
n.sp
1
MI
36
6.9143
6.9000
8.20000
7.02500
6.10000
(18600-
Ephemera
sp
MI
107
6.9317
6.6271
8.00000
6.90000
6.00000
(13540-
Stenonema
mediopunctatum
(I
111
6.9488
6.6946
8.20000
7.1
7500
6.20000
78350-
Meropelopia
sp
F
72
6.9517
6.9503
8.00000
6.80000
5.40000
(80360-
Corynoneura
“celeripes”
(sensu
Simpson
&
Bode,
238
6.9746
6.8375
8.1
0000
7.20000
6.30000
(13590-
Stenonema
vicurium
MI
305
6.9956
6.8807
8.1
0000
7.00000
6.00000
(85720-
Stempellinella
n.sp
nr.
flavidula
MI
113
6.9999
6.6885
7.90000
6.70000
5.90000
(13561
-
Stenonema
pulchellum
I
777
7.0343
6.8568
8.30000
7.30000
6.40000
16324
-
Serratella
deficiens
I
51
7.0570
71980
8.50000
7.50000
6.72000
84430-
Polypedilum
(P.)
albicorne
(F
21
7.0740
7.0476
8.10000
7.30000
6.48000
(80440-
Cricotopus
(C.)trifascia
group
(F
54
7.1006
7.0407
8.40000
7.30000
5.80000
(81650
-
Parametriocnemus
sp
MI
201
7.1515
7.0805
8.40000
7.30000
6.20000
(11120-
Baetis
flavistriga
MI
378
7.1
774
6.9175
8.20000
7.20000
6.30000
(82101-
Thienemanniella
taurocapita
(I
179
7.2049
7.1
067
8.20000
7.40000
6.50000
(81250-
Nanocladius
(N.)
minimus
F
145
7.2780
64120
7.90000
6.70000
5.40000
(82200-
Tvetenia
bavarica
group
(MI
70
7.3119
72629
8.50000
7.55000
6.71000
85752-
Sublettea
coffmani
(MI
66
7.3567
72491
8.50000
7.67500
6.90000
(85600-
Rheotanytarsus
sp
35
7.3791
7.3457
8.50000
7.60000
6.80000
(80310-
Cardiocladius
obscurus
MI
78
7.3822
7.3992
8.70000
7.80000
7.13000
(84440
-
Polypedilum
(P.)
aviceps
MI
37
7.4003
7.5054
8.90000
7.80000
7.00000
85261-
Cladotanytarsw
vcnderwulpi
group
Type
1
1
71
7.4872
7.1
408
8.50000
7.50000
6.50000
15501-
Ephemerellidae
MI
28
7.4951
7.2786
8.50000
7.62500
7.00000
Table
1.
Weighted
mean
and
other
statistics
for
dissolved
concentrations
by
macoinvertebrate
taxa
ranked
by
the
weighted
mean
bO
value.
No.
Weighted
25th
10th
Species
Stations
Mean
Mean
Median
7otile
tile
(82220-
Tvetenia
discoloripes
group
I
164
7.5254
7.3468
8.70000
7.70000
7.00000
(16200
-
Eurylophella
sp
(MI
79
7.5532
7.0266
8.40000
7.40000
6.50000
(80400-
Cricotopus
sp
(
30
7.8019
7.6200
8.70000
7.67500
6.86000
(11430
-
biphetor
hagerè
I
55
8.0279
74964
8.80000
7.70000
6.55000
(85501-
Paratanytarsus
n.sp
1
MI
71
8.3383
7.2296
8.70000
7.50000
6.14000
11018
-
Acerpenna
macdunnoughi
I
31.
8.5008
7.3268
8.60000
7.30000
6.00000
Table
2.
Weighted
mean
DO
and
other
statistics
for
DO
concentrations
by
fish
species
ranked
by
the
weighted
mean
DO
value.
No.
Weighted
25th
10th
Species
Stations
Mean
Mean
Median
tile
°Iotile
(43-002-
GOLDFISH
1
262
4.1318
52274
6.50000
4.50000
2.80000
34-001-
CENTRAL
MUDMINNOW(T
352
4.1623
5.4271
6.50000
4.80000
3.15000
43-042
-
FAThEAD
MINNOW
(T
1174
4.4812
5.5290
7.10000
5.30000
3.60000
(47-0061
-
BLACK
BULLHEAD
(P
498
4.6736
52842
6.90000
5.40000
4.00000
(43-003
-
GOLDEN
SHINER
(T
517
4.7203
4.9787
6.50000
5.00000
3.30000
47-005
-
BROWN
BULLHEAD
in
325
4.7991
5.3660
6.80000
5.40000
3.80000
43-028
-
SPOTTAIL
SHINER
P
30
4.8268
4.6567
6.00000
4.90000
3.60000
74-003
-
WHITE
PERCH
43
.
4.9496
4.9614
6.30000
5.00000
3.20000
43-045
-
COMMON
CARP
X
GOLDFISH
1
105
4.9791
4.8686
6.50000
4.90000
3.50000
(47-013-
TADPOLE
MADTOM
189
5.0569
4.9556
6.50000
5.20000
3.80000
80-001-
SAUGER
39
5.0615
5.8667
7.60000
6.40000
5.40000
77-012
-
REDEAR
SUNFISH
27
5.2204
6.0222
7.30000
6.10000
5.03000
(74-001-
WHITE
BAS5
64
5.2217
5.7188
6.80000
5.65000
4.50000
(43-001
-
COMMON
CARP
1
2075
5.2995
5.8171
7.30000
6.00000
4.50000
43-023
-
REDFIN
SHINER
622
5.3079
5.3991
6.90000
5.60000
4.20000
77-010
-
ORANGESPOTTED
SUNFISH
(
386
5.3873
5.5105
740000
6.00000
4.50000
(37-003
-
NORTHERN
PIKE
(
65
5.3984
5.3754
6.90000
5.35000
3.83000
(37-001
-
GRASS
PICKEREL
P
771
5.4259
5.6674
7.00000
5.60000
4.10000
(40-020
-
CREEK
CHUBSUCKER
(
65
5.4449
5.0969
6.80000
4.80000
3.70000
47-004
-
YELLOW
BULLHEAD
T
2591
5.5331
5.8874
7.40000
6.00000
4.50000
40-018
-
SPOTTED
SUCKER
342
5.5496
5.5791
6.95000
5.70000
4.70000
(77-008
-
GREEN
SUNFISH
~1
4044
5.5742
5.9769
740000
5.90000
4.20000
(54-002
-
BLACKSTRIPE
TOPMINNOW
(
641
5.6034
5.1
951
7.1
0000
5.60000
4.10000
80-005
-
BLACKSIDE
DARTER
1003
5.6262
5.8214
7.30000
6.20000
5.00000
(85-001
-
FRESHWATER
DRUM
(P
176
5.6642
5.9935
7.60000
6.27500
4.94000
(77-013-
PUMPKINSEED
SUNFISH
P1
798
5.6938
6.0121
7.30000
6.10000
4.60000
77-007)
-
WARMOUTH
SUNFISH
(
284
5.7176
5.7888
7.00000
5.80000
4.50000
(80-025
-
LEAST
DARTER
32
5.7540
5.3344
7.30000
6.20000
4.50000
(63-001
-
TROUT-PERCH
158
5.7917
6.0652
7.60000
6.37500
5.30000
77-001
-
WHITE
CRAPPIE
565
5.8141
57192
7.30000
6.00000
4.60000
(20-003
-
GIZZARD
SHAD
825
5.8202
6.01
97
7.50000
6.10000
4.80000
(47-007
-
FLATHEAD
CATFISH
48
5.8245
6.1
938
8.00000
6.80000
6.00000
77-009
-
BLUEGILL
SUNFISH
P
2889
5.8582
6.1255
7.50000
6.20000
4.90000
Table
2.
Weighted
mean
DO
and
other
statistics
for
DO
concentrations
by
fish
species
ranked
by
the
weighted
mean
DO
value.
No.
Weighted
25th
10th
Species
Stations
Mean
Mean
Median
7otile
tile
77-006
-
LARGEMOUTH
BASS
2228
5.9103
61253
7.50000
6.30000
5.00000
(10-004
-
LONGNOSE
GAR
(
52
5.9175
6.5442
8.20000
7.10000
6.00000
80-014
-
JOHNNY
DARTER
(
2913
6.0059
62295
7.60000
6.31000
5.00000
(40-016
-
WHITE
SUCKER
T
4256
6.0484
6.1
273
7.50000
6.20000
4.60000
95-001
-
BROOK
STICKLEBACK
192
6.0538
6.0108
7.20000
5.60000
3.80000
(77-011
-
LONGEAR
SUNFISH
M
1
303.
6.0558
6.1109
7.40000
6.20000
4.80000
(40-005
-
QUILLBACK
CARPSUCKER
375
6.0604
6.2428
8.00000
6.30000
4.80000
(43-043
-
BLUNTNOSE
MINNOW
1
4304
6.0833
6.1582
7.60000
6.20000
4.80000
(70-001
-
BROOK
SILVERSIDE
M
164
6.0842
6.0868
7.60000
6.40000
5.20000
43-013
-
CREEK
CHUB
T
4293
6.1248
6.1424
7.50000
6.10000
4.40000
(80-023
-
ORANGETHROAT
DARTER
450
6.1386
6.0576
7.40000
6.00000
4.40000
43-035)
-
MIMIC
SHINER
I
180
6.2736
6.6972
8.1
0000
7.00000
6.10000
(80-011
-
LOGPERCH
(M
961
6.2921
6.3048
7.50000
6.40000
5.40000
47-002
-
CHANNEL
CATFISH
(
374
6.3442
6.2429
7.80000
6.50000
5.50000
43-032)
-
SPOTFIN
SHINER
1628
6.3794
62976
7.80000
6.50000
5.30000
80-003
-
YELLOW
PERCH
148
6.3928
6.1
054
7.60000
6.30000
5.25200
(43-024)
-
ROSEFIN
SHINER
M
606
6.4063
62957
7.70000
6.50000
5.30000
77-003
-
ROCK
BASS
(
2251
6.4072
6.3763
7.80000
6.60000
5.50000
(43-025
-
STRIPED
SHINER
2742
6.4319
6.3580
7.70000
6.40000
5.1
0000
(80-004
-
DUSKY
DARTER
(M
46
6.4418
67022
7.60000
6.70000
5.80000
01-006-
LEAST
BROOK
LAMPREY
162
6.4472
6.3673
7.90000
6.62500
5.1
0000
(43-009
-
GRAVEL
CHUB
(M
22
6.4669
6.6000
9.10000
7.60000
6.70000
(43-015
-
SUCKERMOUTH
MINNOW
(
625
6.5159
61645
7.90000
6.50000
5.40000
43-034
-
SAND
SHINER
(M
1520
6.52
14
6.5285
8.10000
6.90000
6.00000
(43-026
-
COMMON
SHINER
766
6.5332
62388
7.60000
6.40000
5.00000
(43-007
-
BIGEYE
CHUB
(I
91
6.5414
6.8659
8.50000
7.50000
6.20000
77-005
-
SPOTTED
BASS
(
338
6.6085
67308
7.60000
6.42500
5.40000
(77-004-
SMALLMOUTH
BASS(M
1586
6.6104
6.5713
8.00000
6.80000
5.70000
80-015
-
GREENSIDE
DARTER
M
2405
6.6157
64821
7.80000
6.70000
5.50000
(43-044
-
CENTRAL
STONEROLLER
3853
6.6294
6.3416
8.00000
6.40000
5.00000
(43-044
-
CENTRAL
STONEROLLER
(3
3853
6.6294
6.3416
8.00000
6.40000
5.00000
77-002
-
BLACK
CRAPPIE
284
6.6345
57687
7.20000
6.00000
4.70000
(40-010
-
GOLDEN
REDHORSE
M
1392
6.6966
6.5323
7.90000
6.70000
5.70000
Table
2.
Weighted
mean
DO
and
other
statistics
for
DO
concentrations
by
fish
species
ranked
by
the
weighted
mean
DO
value.
No.
Weighted
25th
10th
Species
Stations
Mean
Mean
Median
Yotile
Yotile
(80-024
-
FANTAIL
DARTER
(
1920
6.6977
6.5064
7.90000
6.70000
5.50000
(43-021-
SILVER
SHINER
I
719
6.7098
6.6523
8.1
0000
6.90000
6.00000
(80-007
-
SLENDERHEAD
DARTER
(R
27
6.7104
6.6296
8.40000
7.02500
6.40000
(47-012
-
BRINDLED
MADTOM
1
201
6.7257
6.5478
840000
7.30000
6.36000
(40-008
-
SILVER
REDHORSE
M
258
6.7290
6.4643
7.90000
6.70000
5.76000
(80-016
-
BANDED
DARTER
1
828
6.7564
67268
8.00000
6.90000
5.90000
(43-039
-
SILVERJAW
MINNOW
1
550
6.8125
6.5634
7.90000
6.70000
5.30000
(43-031-
STEELCOLOR
SHINER
(P
83
6.81
97
6.4699
8.70000
7.40000
6.50000
(43-004)
-
HORNYHEAD
CHUB
I
255
6.8261
6.6009
8.00000
6.90000
5.99000
43-020
-
EMERALD
SHINER
(
297
6.8326
6.5404
7.90000
6.40000
5.20000
80-022
-
RAINBOW
DARTER
(M
2016
6.8488
6.6788
8.1
0000
6.90000
5.90000
40-009
-
BLACK
REDHORSE
(I
482
6.9339
6.8943
8.20000
7.20000
6.40000
40-011)
-
SHORTHEAD
REDHORSE
M
163
6.9547
6.6055
7.90000
6.80000
5.70000
43-011-
BLACKNOSE
DACE
T
1965
6.9595
6.5343
7.80000
6.50000
4.70000
40-015)
-
NORTHERN
HOG
SUCKER
M
2502
7.0205
6.6912
8.00000
6.80000
5.80000
43-016
-
SOUTH.
REDBELLY
DACE
332
7.0376
6.5361
8.00000
6.50000
4.91000
80-017
-
VARIEGATE
DARTER
I
139
7.0680
7.071
2
8.60000
7.60000
6.80000
(43-022-
ROSYFACE
SHINER
I
573
7.1774
7.1
568
8.50000
7.50000
6.70000
(43-033
-
BIGMOUTH
SHINER
40
7.2239
6.1
725
7.90000
7.00000
5.60000
(43-017-
REDSIDE
DACE
I
151
7.2335
7.0391
8.40000
6.75000
4.70000
47-008-
STONECATMADTOM
(1
623
7.4144
6.9350
8.30000
7.20000
6.30000
43-005
-
RIVER
CHUB
(I
423
7.4902
7.2622
8.50000
7.50000
6.60000
90-002
-
MOTTLED
SCULPIN
(
855
7.6656
7.0913
8.30000
7.30000
6.20000
25-001
-
BROWN
TROUT
53
7.9166
7.9906
9.40000
8.40000
7.40000
01-007
-
AMER
BROOK
LAMPREY
(R
85
8.4789
8.0682
9.30000
8.40000
7.30000
43-014
-
TONGUETIED
MINNOW
5
35
8.6464
8.5314
9.75000
9.1
0000
8.38000
(25-002
-
RAINBOW
TROUT
1
59
8.6895
77805
9.00000
7.47500
5.40000
REPRODUCTIVE BIOLOGY
AND
EARLY LIFE HISTORY
OF
FISHES
IN THE
OHIO RIVER DRAINAGE
Ictaluridae—Catfish and Madtoms
VOLUME
3
Thomas P. Simon
Robert Wallus
CRC PRESS
Boca Raton London New
York Washington, D.C.
Library of Congress Cataloging-in-Publication Data
Simon,
Thomas P.
Reproductive biology and early life history of fishes in the Ohio River drainage
I
Thomas
P. Simon and Robert
Wallus.
p. cm.
Resc ed, of
Reproductive biology and early life history of fishes in the Ohio River
drainage
/
principal authors, Robert
Wallus, Bruce L. Yeager. 1990.
Description based on:
v. 3
published in 2003.
Includes
bibliographical references (p.
).
ISBN
0-8493-1919-6
(alk. paper)
I. Fishes—Ohio River—Reproduction.
2. Fishes—Ohio River—Development.
1. Walluc.
Robert, II. Wallus, Robert. Reproductive biology and early life history of fishes in the
Ohio
River drainage. III. Title,
QL628.033556 2003
57l,S’ll—dc22
2003055777
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100 —
REPRODUCTIVE BIOLOGY AND EARLY LIFE HISTORY OF FISHES
CHANNEL CATFISH
Ictalurus punctatus
(Rafinesque)
Ictalllrtts,
Greek:
“fish cat”;
punctatus,
Latin: “spotted.”
RANGE
Native range is central drainages of the U.S. into
southern Canada, and possibly parts of the Atlantic
coast; from west TX, northern Mexico along Gulf
slope into peninsular FL.1 Newly recorded from
Lake Michigan drainage of IL.’05
HABITAT AND MOVEMENT
Occupies a variety of substrates.78’10° Occurs pre-
dominantly in streams, rivers, and big rivers in
deep pools near cover or in areas with current over
a firm sand or gravel, rocky bottom; also occupies
the open waters of impoundments; avoids clear,
cool upland streams and rivers.’~Seeks deep pools,
submerged logs, and overhanging banks by day, and
at night moves to shallow areas to feed.24’106 Spawn-
ers may not migrate into nearby rivers.2’82 Prefers
bendway and tailwater habitats of large rivers over
main channel habitats.87 Runoff (fraction of stream
area consisting of runs) and water temperature
account for nearly half the variability in biomass.lOt
In IL, correlations for channel catfish 100 mm TL
were not found; however, the presence of 300 mm
fish was highly correlated with water velocity, per-
centTagginginstreamstudies
cover,
have
and
shown
percent
varied
pool.
and
103
often dis-
crepant movement patterns.53 Approximately 50
of recaptured (tagged) fish moved less than 2.5
miles during a 2-year period; the remainder were
evenly dispersed upstream and downstream with
mean distances of movement of 5.1 and 5.6 miles,
respectively. The greatest distances recorded were
Moves70
milesgreaterdownstreamdistancesandin
the155springmiles thanupstream.in the67
fall, usually moving upstream in the spring and
downstream in the fall.~Winter survival is high
and
DISTRIBUTION
may cause little loss in
AND
total body weight.a3
OCCURRENCE IN THE
OHIO RIVER SYSTEM
Common to abundant5’6’t1 and distributed almost
uniformly throughout the Ohio River.45 In KY, gen-
erally distributed and common throughout the
state.3 Occurs throughout IL, abundant in larger
streams and major rivers.4 In PA, occurs in the
Allegheny and Monongahela Rivers.7 Tn WV, occurs
in the Little Kanawha and Kanawha Rivers below
the Falls, possibly native but may be introduced
above the Falls.8’8° Widespread and abundant in
TN.~’Present in most Tennessee River system trib-
utaries of AL,IOS western NC,5’ and VA.78
SPAWNING
Location
In cavities under logs, rocks, undercut banks, or
drift;9’10’25’2~’°8in burrows of muskrats and bea-
vers;25 in artifical nests, such as nail kegs, in
ponds;32 at depths ranging from a few inches to
several feet;9~also° in small streams;5 sometimes in
very swift water.’t Successful spawning in cans has
been reported at depths of 5 m.8’
Season
Late spring in NY;9 June—August in upper Missis-
sippi River;65 March and April, but mostly June and
July in SC;14 June and July in OK;’5 early to late
June in WI;108 prior to mid-June in SD;1° May to
July in MO25 and AR;21 sometimes with two spawn-
ing peaks per season.31 Yolk-sac larvae and early
juveniles were collected mid-May through August
with peaks in June and July in the Tennessee and
lower Ohio Rivers;* gravid females collected as late
as August in AL.109 Begins in late May and peaks
in
Temperature
late June—early July in VA.78
Between 21 and 29.4°C;Z9.1a24.sass in TX, usually
between 21 and 27°C,with most spawning at
21.7°C,but
spawning occurred at 15.9°C,after the
water temperature had exceeded 21°C;19optimum
about 27°C;1°in the low to mid-70s (F) in WI.~
Based on yolk-sac larval and early juvenile collec-
tions, estimated range of spawning temperatures is
19—31°C(optimum 22_28oC).*
Fecundity
Females 1—4 lbs produced approximately 4000 eggs;
estimated fecundity for a female 660 mm was 34,500
eggs;2 other reports of 1052’~to 70,QQQtt and 1500 to
52,000.2&4~53In IA, number of eggs per mature
PhilipW Smith
THE FISHES OF ILLINOIS
Fubiishedfor the Illinois State Natural Histoiy Survey by the
UNIVERSITY
OF ILLINOIS PRESS
Urbana Chicago London
©
1979 by the
Board of Trustees of the University of I liii1ois
Mann factui-ed in die United States of .A merica
Publication 6of this hook has been linde possible b’ funds plo’ ideci by the
Illinois
Department
of Conservation and generous grail
N
from Illinois
Power Conlpan v, N ALC() Foundation, Commonwealth Edison Company,
and Mr. Sanlnel C. Dennison
Library of Congress Cataloging in Publication Data
Smith, Philip Wayne, 1921—
The fishes of Illinois,
Bibliography. p.
I. Fishes— Illitiois.
2.
Fishes—Illinois—
Identification. I. Illinois. Natural History Survey.
II. Title.
QL628.13S58
597.0920773
78-12741
ISBN 0-252-00682-8