Draft
                                                           2/18/86
AMBIENT AQUATIC LIFE WATER QUALITY CRITERIA FOR

                     NICKEL
      U.S. ENVIRONMENTAL PROTECTION AGENCY
       OFFICE OF RESEARCH AND DEVELOPMENT
       ENVIRONMENTAL RESEARCH LABORATORIES
               DULUTH, MINNESOTA
           NARRAGANSETT, RHODE ISLAND

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                                 NOTICES
This document has been reviewed by Che Criteria and Standards Division,
Office of Water Regulations and Standards, U.S. Environmental Protection
Agency, and approved for publication.

Mention of trade names or commercial products does not constitute
endorsement or recommendation for use.

This document is available to the public through the National Technical
Information Service (NTIS), 5285 Port Royal Road,  Springfield, VA 22161.
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                                 FOREWORD
     Section 304(a)(l) of the Clean Water Act of 1977 (P.L. 95-217)
requires the Administrator of the Environmental Protection Agency to
publish water quality criteria that accurately reflect the latest
scientific knowledge on the kind and extent of all identifiable effects
on health and welfare that might be expected from the presence of pollutants
in any body of water, including ground water.  This document is a revision
of proposed criteria based upon a consideration of comments received from
other Federal agencies, State agencies, special interest groups, and
individual scientists.  Criteria contained in this document replace
any previously published EPA aquatic life criteria for the same pollutant(s).

     The term "water quality criteria" is used in two sections of the
Clean Water Act, section 304(a)(l) and section 303(c)(2).  The term has a
different program impact in each section.  In section 304, the term
represents a non-regulatory, scientific assessment of ecological effects.
Criteria presented in this document are such scientific assessments.
If water quality criteria associated with specific stream uses are adopted
by a State as water quality standards under section 303, they become
enforceable maximum acceptable pollutant concentrations in ambient waters
within that State.  Water quality criteria adopted in State water quality
standards could have the same numerical values as criteria developed
under section 304.  However, in many situations States might want to
adjust water quality criteria developed under section 304 to reflect
local environmental conditions and human exposure patterns before incorporation
into water quality standards.  It is not until their adoption as part of
State water quality standards that criteria become regulatory.

     Guidelines to assist States in the modification of criteria presented
in this document, in the development of water quality standards, and in
other water-related programs of this Agency, have been developed by EPA.
                                    James M. Conlon
                                    Acting Director
                                    Office of Water Regulations and Standards

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                             ACKNOWLEDGMENTS
Loren J. Larson
Judy L. Crane
(freshwater authors)
University of Wisconsin-Superior
Superior, Wisconsin
                           Jeffrey L. Hyland
                           Robert E. HilLman
                           (saltwater authors)
                           Battelle New England Laboratory
                           Duxbury, Massachusetts
Charles E. Stephan
(document coordinator)
Environmental Research Laboratory
Duluth, Minnesota
                           David J. Hansen
                           (saltwater coordinator)
                           Environmental Research Laboratory
                           Narragansett, Rhode Island
Clerical Support:
Terry L. Highland
Shelley A. Heintz
                                    IV

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                                 CONTENTS
                                                                         Page
Foreword	     ill

Acknowledgments  	      iv

Tables	      vi


Introduction 	       1

Acute Toxicity to Aquatic Animals   	       5

Chronic Toxicity to Aquatic Animals   	       8

Toxicity to Aquatic Plants 	      10

Bioaccumulation  	      11

Other Data	      12

Unused Data	      14

Summary	      15

National Criteria  	      16


References	      50

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                                  TABLES
                                                                        Page

1.  Acute Toxicity of Nickel to Aquatic Animals  	  19

2.  Chronic Toxicity of Nickel To Aquatic Animals 	  29

3.  Ranked Genus Mean Acute Values with Species Mean Acute-Chronic

    Ratios	31

4.  Toxicity of Nickel to Aquatic Plants	35

5.  Bioaccumulation of Nickel by Aquatic Organisms  	  37

6.  Other Data on Effects of Nickel on Aquatic Organisms	39

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Introduction*

     Nickel is one of the most common of the heavy metals occurring in

surface waters (Forstner 1984; Hutchinson et al. 1975; Kopp and Kroner 1967;

Martin and Knauer 1972; Mathis and Cummings 1973; McCabe et al. 1970; Portman

1972; Solbe 1973; Trollope and Evans 1976; Young 1982).  Although nickel

can exist in oxidation states of -1, 0, +1, +2, +3, and +4, under usual

conditions in surface waters the divalent cation greatly predominates

and is generally considered the most toxic.  Alkalinity, hardness, salinity,

pH, temperature, and complexing and adsorbing agents such as humic acids

influence the oxidation state, toxicity, and availability of the total

nickel pool.

     Natural sources of the nickel in surface waters include weathering

of rocks, inflow of particulate matter, and precipitation.  Anthropogenic

sources of nickel include industries, such as electroplating and smelting,

and the burning of coal and other fossil fuels.  Although fly ash can

contain as much as 960 Mg/g (Swaine 1980), lake restoration projects have

experimented with the use of fly ash to remove nutrients.

    Mechanisms of nickel toxicity are varied and complex (Mushak 1980) ,

and as with other heavy metals, significant effects occur at cell membranes

and membranous tissues, such as gills.  In fish, hematological effects

such as hyperglycemia, hepatic glycogenolysis, lymphopenia, and erythrocytosis

have been reported in association with nickel intoxication (Agrawal et

al. 1979; Chaudhry 1984; Gill and Pant 1981).
* An understanding of the "Guidelines for Deriving Numerical National Water
  Quality Criteria for the Protection of Aquatic Organisms and Their Uses"
  (Stephan et al.  1985), hereafter referred to as the Guidelines, is necessary
  in order to understand the following text, tables, and calculations.

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     Because of the variety of forms of nickel (Callahan et al. 1979;




Nriagu 1980) and lack of definitive information about their relative




toxicities, no available analytical measurement is known to be ideal for




expressing aquatic life criteria for nickel.  Previous aquatic life




criteria for nickel (U.S. EPA 1980) were expressed in terms of total




recoverable nickel (U.S. EPA 1983a), but this measurement is probably too




rigorous in some situations.  Acid-soluble nickel (operationally defined




as the nickel that passes through a 0.45 ^m membrane filter after the




sample is acidified to pH = 1.5 to 2.0 with nitric acid) is probably the




best measurement at the present for the following reasons:




1.  This measurement is compatible with nearly all available data




    concerning toxicity of nickel to, and bioaccumulation of nickel by,




    aquatic organisms.  No test results were rejected just because it was




    likely that they would have been substantially different if they had




    been reported in terms of acid-soluble nickel.  For example, results




    reported in terms of dissolved nickel would not have been used if the




    concentration of precipitated nickel had been substantial.




2.  On samples of ambient water,  measurement of acid-soluble nickel will




    probably measure all forms of nickel that are toxic to aquatic life or




    can be readily converted to toxic forms under natural conditions.  In




    addition, this measurement probably will not  measure several forms, such




    as nickel that is occluded in minerals, clays, and sand or is strongly




    sorbed to particulate matter, that are not toxic and are not likely




    to become toxic under natural conditions.  Although this measurement




    (and many others) will measure soluble complexed forms of nickel,




    such as the EDTA complex of nickel, that probably have low toxicities

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    to aquatic life, concentrations of these forms probably are negligible




    in most ambient water.




3.  Although water quality criteria apply to ambient water, the measurement




    used to express criteria is likely to be used to measure nickel in aqueous




    effluents.  Measurement of acid-soluble nickel probably will be applicable




    to effluents because it will measure precipitates, such as carbonate




    and hydroxide precipitates of nickel, that might exist in an effluent




    and dissolve when the effluent is diluted with receiving water.  If




    desired, dilution of effluent with receiving water before measurement




    of acid-soluble nickel might be used to determine whether the receiving




    water can decrease the concentration of acid-soluble nickel because




    of sorption.




4.  The acid-soluble measurement is probably useful for most metals, thus



    minimizing the number of samples and procedures that are necessary.




5.  The acid-soluble measurement does not require filtration at the time




    of collection, as does the dissolved measurement.




6.,  The only treatment required at the time of collection is preservation




    by acidification to pH = 1.5 to 2.0, similar to that required for the




    total recoverable measurement.




7.  Durations of 10 minutes to 24 hours between acidification and filtration




    of most samples of ambient water probably will not affect the result




    substantially..




8.  The carbonate system has a much higher buffer capacity from pH = 1.5 to




    2.0 than it does from pH = 4 to 9 (Weber and Stumm 1963).




9.  Differences in pH within the range of 1.5 to 2.0 probably will not




    affect the result substantially.

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10.   The acid-soluble measurement  does  not require a digestion step,  as  does




     the total recoverable measurement.




11.   After acidification and filtration of the sample to isolate  the  acid-




     soluble nickel,  the analysis  can be performed using either atomic




     absorption spectrophotometric or ICP-atomic emission spectrometric




     analysis (U.S. EPA 1983a),  as with the total recoverable measurement.




 Thus,  expressing aquatic life  criteria for nickel in terms  of the  acid-




 soluble measurement  has both toxicological and practical advantages.  On




 the other hand,  because no measurement is known to be ideal for  expressing




 aquatic life criteria for nickel  or for measuring nickel in ambient  water




 or  aqueous effluents, measurement of both acid-soluble nickel and  total




 recoverable nickel in ambient  water or effluent or both might be useful.




 For example,  there might be cause for  concern if total recoverable nickel




 is  much above an applicable limit,  even though acid-soluble nickel is




 below  the limit.




     Unless otherwise noted,  all concentrations reported herein are expected




 to  be  essentially equivalent to acid-soluble  nickel concentrations.  All




 concentrations are expressed as nickel,  not as the chemical tested.  The




 criteria presented herein supersede previous  national aquatic life water




 quality criteria for nickel  (U.S.  EPA  1976, 1980)  because these  new



 criteria were derived using improved procedures and additional information.




 Whenever adequately  justified, a  national criterion may be  replaced  by  a




 site-specific criterion (U.S.  EPA 1983b), which may include not  only



 site-specific criterion concentrations (U.S.  EPA 1983c), but also  site-specific




 durations of  averaging periods and  site-specific frequencies of  allowed



 excursions (U.S.  EPA 1985).  The  latest  literature search for information



 for this document was conducted in  February,  1985; some newer information




 was also used.



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Acute Toxicity to Aquatic Animals




    Lind et al. (manuscript) conducted studies on the effects of both




hardness and TOC on the acute toxicity of nickel to both Daphnia pulicaria




and the fathead minnow (Table 6).  With both species, hardness was the




only significantly correlated parameter.  Nebeker et al. (1985) reported




that rainbow trout were more sensitive when 12-months old than when 3-months




old.  Rehwoldt et al. (1973) observed that embryos were more sensitive




than adult snails.  One of the most sensitive vertebrate species is the




narrow-mouthed toad.  In 7-day tests, the EC50 with embryos and larvae




was 30 ug/L (Table 6).  The 8-day EC50 with embryos and larvae of the




marbled salamander was 410 to 420 ng/L (Birge and Black 1980; Birge et al.




1978).  With channel catfish, Birge and Black (1980) and Birge et al.



(1981) obtained a 7-day EC50 of 710 (Jg/L with embryos and larvae, whereas




Wilford (1966) obtained a 48-hr LC50 of 36,840 pg/L with 1 to 2-gram fish.




     Many factors might affect the results of tests of the toxicity of




nickel to aquatic organisms (Sprague, 1985), but water quality criteria




can quantitatively take into account such a factor, only if enough data




are available to show that the factor similarly affects the results of




tests with a variety of species.  Hardness is often thought of as having




a major effect on the toxicity of nickel in fresh water although the




observed effect is probably due to one or more of a number of usually




interrelated ions, such as hydroxide, carbonate, calcium, and magnesium.




Hardness (expressed as mg CaC03/L) is used here as a surrogate for the




ions that affect the results of toxicity tests on nickel.  An analysis




of covariance (Dixon and Brown 1979; Neter and Wasserman 1974) was performed




using the natural logarithm of the acute value as the dependent variable,




species as the treatment or grouping variable, and the natural logarithm

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 of hardness  as  Che covariate  or  independent variable.   This  analysis of


 covariance model was  fit  to the  data  in Table  1  for  the four  species for


 which  acute  values are  available over a range  of hardness  such  that the


 highest hardness is at  least  three times  the lowest  and the highest is


 also at least 100 mg/L  higher than the lowest.   The  slopes for  all four


 species are  between 0.69  and  1.19 (see end of  Table  1)  and are  close to the


 slope  of 1.0 that is  expected on the  basis that  nickel,  calcium, magnesium,


 and carbonate all have  a  charge  of two.   An F-test showed  that, under the


 assumption of equality  of slopes, the probability of obtaining  four slopes


 as dissimilar as these  is P = 0.26.   This was  interpreted  as  indicating


 that it is not  unreasonable to assume that the slopes for  these four species


 are the same..


    Where possible, the pooled slope  of 0.8460 was used  to adjust the


 acute values in Table 1 to hardness = 50 mg/L.   Species  Mean  Acute Values


 were calculated as geometric means of the adjusted acute values.  Genus Mean


 Acute Values at hardness = 50 mg/L were then calculated  as geometric


 means of the available  freshwater Species Mean Acute Values  (Table 3).


 Of the eighteen genera  for which freshwater acute values are  available,


 the most sensitive genus, Daphnia, was 29 times more sensitive  than the


most resistant,  Fundulus.  The freshwater Final Acute Value for nickel at


hardness = 50 mg/L was calculated to be 1,578 pg/L using the  procedure


 described in the Guidelines and  the Genus Mean Acute Values in Table 3.


 Thus, the freshwater Criterion Maximum Concentration (in pg/L) =

 (0.8460(ln(hardness)]+3.3612)
 e

    The acute toxicity of nickel to saltwater organisms  has been determined


 with 18 species of invertebrates and  4 species of fish  (Table 1).  The


 LCSOs and ECSOs for invertebrates range from 151.7 pg/L  for juveniles of

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the mysid Heteromysis formosa (Gentile et al. 1982) to 1,100,000 pg/L for




late juvenile to adult stages of the clam Macoma balthica (Bryant et al.




1985).  Fish are not as sensitive or as resistant to nickel.  The 96-hr




LC50s range from 7,958 Mg/L f°r larval stages of the Atlantic silverside,




Menidia menidia (Cardin 1985) to 350,000 (jg/L for adult stages of the




mummichog, Fundulus heteroclitus (Eisler and Hennekey 1977).




    Although data are limited, relationships might exist between both




salinity and temperature and the toxicity of nickel to some saltwater species.




For example, the LC50 for the mummichog is 55,000 ug/L at a salinity of




6.9 g/kg, and 175,000 (jg/L at a salinity of 21.6 g/kg (Dorfman 1977).  In




a series of tests with the amphipod, Corophium volutator (Bryant et al.




1985), the LC50 increased with salinity at 5s C, 10* C, and 15" C.  At




salinities of 5, 10, and 15 g/kg, temperature did not seem to affect the




LC50, but at salinities of 25 and 35 g/kg, the LC50 decreased as temperature




increased.  Bryant et al. (1985) found similar effects of salinity and




temperature on nickel toxicity with the clam Macoma balthica (Table 6).




Regressions of toxicity on salinity for the above data show strong correlations,




However, analysis of covariance reveals that the slopes for the individual




species are too dissimilar (P < 0.05) to justify expressing nickel toxicity




as a function of salinity.

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    Of  the nineteen saltwater genera  for which  acute values  are  available,




 the most  sensitive genus, Heteromysis, was over 2,000  times  more sensitive




 than  the  most  resistant, Mya (Table 3).  Acute  values  are available  for




 more  than one  species  in each of three genera,  and the  range of  Species




 Mean  Acute Values within each genus is less than a factor of 4.8.  Genus




 Mean  Acute Values for  the four most sensitive genera, Heteromysis,




 Mercenaria, Mysidopsis, and Crassest rea, were within a  factor of 7.8 even




 though  the acute tests were conducted with juveniles of the  crustaceans




 and with  embryos of the bivalves.  The saltwater Final Acute Value was




 calculated to  be 141.9
Chronic Toxicity to Aquatic Animals




     Data are available on the freshwater chronic toxicity of nickel to




a cladoceran, a caddisfly, and two species of fish (Table 2).  Nebeker




et al. (1985) conducted two early life-stage tests beginning with rainbow




trout embryos 4 hours after fertilization and one with trout embryos 25




days after fertilization.  In the first test weight was significantly




reduced by all tested concentrations including the lowest of 35 ^ig/L.  In




the second test weight was significantly reduced by 62 and 431 |Jg/L, but




not by 35, 134, and 238 \ig/l»  In this second test survival was reduced




at nickel concentrations of 134 Mg/L and higher.  In the third test weight




was significantly reduced at 431 Mg/L and higher, but the reduction in




survival was significant only at 1,680 |Jg/L and higher.




    The influence of hardness on chronic toxicity of nickel was investigated




by Chapman et al . (manuscript).  In life-cycle tests with Daphnia magna,




they observed an increase in chronic values with increased hardness.




Least squares regression of ln[chronic value] on ln[hardness] produced a




slope of 2.3007 with wide confidence limits (Table 2).  A similar




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 regression with data  for the  fathead minnow produced  a  slope  of 0.5706,




 but  confidence limits could not be calculated because only  two points were




 available for use  in  the regression.  An F-test  showed  that,  under the




 assumption of equality of slopes, the probability of  obtaining two




 slopes as dissimilar  as these  is P a 0.19.  This was  interpreted  as




 indicating that it is not unreasonable to assume that the two slopes are




 the  aame.  The pooled slope is 1.3418 with 95% confidence limits  of




 -1.3922 and 4.0760.   The confidence limits on the pooled acute slope are




 well within the confidence limits on the pooled  chronic slope.




     The mysid Mysidopsis bahia is the only saltwater  species  with which




 an acceptable chronic test has been conducted on nickel (Table 2).




 Chronic exposure to nickel resulted in a reduced survival and number of




 young at 141 pg/L  and above but not at 61 pg/L and  lower (Lussier et al.



 1985).  Thus the chronic value for nickel with this species is 92.74




>ig/L and the acute-chronic ratio is 5.478.




     The three available species mean acute-chronic  ratios range from 5.478  to




 35.58 and were all determined with species that  are acutely sensitive to




 nickel (Table 3).  The Final Acute-Chronic Ratio of 17.99 was calculated




 as the geometric mean of the three ratios.  Division  of the freshwater




 Final Acute Value by  the Final Acute-Chronic Ratio  results  in a freshwater




 Final Chronic Value of 87.72 ug/L at hardness =  50 mg/L.  Some data




 (Tables 2 and 6) concerning the chronic toxicity of nickel  to rainbow




 trout indicate that embryos and larvae of this species  will probably be




 affected at this concentration, whereas other data  (Table 2)  indicate




 that embryos and larvae of the species might not be adversely affected.




 Use  of an acute-chronic ratio  that is independent of  hardness

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is equivalent to assuming that the chronic slope is equal to the acute

slope.  Thus the freshwater Final Chronic Value (in yg/L) =

 (0.8460[ln(hardness) 1+1.645)
e

     Division of the saltwater Final Acute Value by 17.99 results in a
saltwater Final Chronic Value of 7.888 Mg/L.  Three of the four acutely


most sensitive saltwater species are in the same family as the species


with which the saltwater acute-chronic ratio was determined.  In addition,


the two other most sensitive species are bivalve molluscs for which the


acute values were obtained from tests on embryos and larvae.



Toxicity to Aquatic Plants


    Data on the toxicity of nickel to aquatic plants are found in Table 4.


Nickel concentrations resulting in a 40-601 reduction in growth of fresh-


water algae range from 50 ug/L for the green algae, Scenedesmus acuminatz,


to 5,000 Mg/L for the green algae, Ankistrodesmus falcatus and Chlorbcoccum


sp.  Wang and Wood (1984) indicate that toxicity of nickel to plants is

pH dependent.  Although lack of hardness values makes comparisons difficult,


general comparison of data in Table 4 with chronic toxicity data in Table 2


suggests that nickel concentrations high enough to produce chronic effects

in freshwater animals will also have deteriorative effects on freshwater


algal populations.

    Patrick et al . (1975) found a decrease in diatom diversity and a

shift to green and blue-green algae as a community effect of nickel

exposure.  Their findings are in agreement of a field study by Spencer and


Greene (1981) in which an increase in blue-green algae was observed.  Using

EDTA to manipulate Ni+^ concentrations, Spencer and Nichols (1983) reported

algal growth to be inversely related to free divalent nickel and independent

of total nickel concentrations.



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    Brown and Rattigan (1979) studied nickel toxicity Co two freshwater




vascular plants, duck weed and Elodea (Anacharis).   Despite the presence




of a thick cuticle, which protects it from many pollutants (e.g., herbicides),




duck weed was much more susceptible to nickel than was Elodea.




    Data on the toxicity of nickel to saltwater plants and algae are




found in Tables 4 and 6.  The test with the giant kelp, Macrocystis




pyrifera, lasted four days and resulted in a 50% reduction in photosynthesis




at 2,000 Mg/L (Clendenning and North 1959).  The lowest concentrations




affecting growth of phytoplankton ranged from 17 to 1,800 Mg/L and were




salinity and temperature dependent (Wilson and Freeberg 1980).  Concentrations




that affect most saltwater plants apparently are higher than those that are




chronically toxic to saltwater animals.






Bioaccumulation




    Data are available on            bioaccumulation of nickel by a




freshwater alga, a cladoceran, and two species of fish (Table 5).  The lowest




factor, 0.8, was obtained for muscle of rainbow trout.  All other studies




where conducted on whole body samples and the factors ranged from 9.3 for




the alga to 193 for the cladoceran.  In studies with the fathead minnow,




Lind et al. (Manuscript) found that the BCF decreased as the concentration




of nickel in water increased.  This same trend was observed by Hall




(1982), who studied the accumulation of nickel in various tissues of




Daphnia magna and used a model to describe uptake at different exposure




concentrations.  Jennett et al. (1982) examined physical and biological




variables affecting uptake by algae.  Although their study does not




demonstrate that steady-state was attained, Taylor and Crowder (1983)
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studied differential uptake of nickel of various portions of an emergent




aquatic plant, the cattail.




    Data on bioaccumulation of nickel by saltwater organisms are available




for two species of algae and two species of bivalves (Table 5).  BCFs for




algae collected from the field are 675 for the rockweed, Fucus vesiculosis.




and 458.3 for Ascophyllum nodosum (Foster 1976).  BCFs for bivalves




exposed for 9 days in the laboratory were 472.7 and 328.6 for the blue mussel




and 458.1 and 261.8 for the Eastern oyster (Zaroogian and Johnson 1984).




     No U.S. FDA action level or other maximum acceptable concentration in




tissue is available for nickel, and, therefore, no Final Residue Value




can be calculated.






Other Data




    Data in Table 6 suggest a high toxicity to nickel in the single-celled




organisms.   Bringmann and Kuhn (1959a,b; 1977a; 1979; 1980a,b; 1981)




reported that concentrations of 2.5 to 1,500 |Jg/L resulted in incipient




inhibition of algae, bacteria, and protozoans.  Babich and Stotzky (1983)




observed delayed effects after a 24-hr exposure.




    Willford (1966) reported 48-hr LCSOs for six fishes tested in the




same water.  Although the fish differed in size, neither this nor taxonomic



differences produced a clear trend in relative toxicity.  Blaylock and




Frank (1979) observed LCSOs for carp larva at 3 and 10.5 days to be 8,460




and 750 pg/L, respectively.




    Shaw and Brown (1971) studied the effect of nickel on laboratory




fertilization of rainbow trout eggs.  They did not find a statistically




significant effect at 1000 Mg/L (hardness = 260 to 280 rag/L), and noted a




stimulation in development after fertilization compared to controls.




    Several studies have investigated associated effects of nickel intox-




ication.  Whitley and Sikora (1970) and Brkovic-Popovic and Popovic




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 (1977b) studied effects on respiration in tubificid worms.  Influence of




 nickel on thermal resistance of salmonids was examined by Becker and




 Wolford (1980).  The effect of complexing agents on toxicity of nickel to




 carp was studied by Muramoto (1983).  Smith-Sonneborn et al. (1983)




 studied the toxicity of ingested nickel dust particles in Paramecium.




 Anderson and Weber (1975) derived an expression relating body size to




 sensitivity of the guppy.




    In a field study, Havas and Hutchinson (1982) worked with acidified




 and control ponds and suggested that the lowered pH increased the




 concentrations of heavy metals such as nickel and stressed resident




 aquatic invertebrates.




    Available data that were not used directly in the derivation of




 saltwater criterion for nickel (Table 6) do not indicate a need to lower




 the criterion.  In addition to affecting survival of saltwater animals,




 nickel affects growth, development, reproduction, and biochemical responses.




 A 19% reduction in growth of juvenile Pacific oysters, Crassostrea gigas,




 exposed to 10 |Jg/L for 14 days at a salinity of 34 g/kg was reported by




 Watling (1983).  The ecological significance of this reduction is unknown,




 but after 14 days in clean water size was similar to that of the controls.




 Petrich and Reish (1979) found that 100 to 500 ug/L suppressed reproduction




 of the polychaete Ctenodrilus serratus.  Zaroogian et al. (1982) showed a




 significant reduction in ATP activity in the adductor muscle of the blue




mussel, but not the Eastern oyster, after a 10-week exposure to 10 Mg/L.




 Abnormal development in embryos of the sea urchins, Arbacia punctulata and




 Lytechinus pictus, occurred at several concentrations of nickel (Timourian




 and Watchmaker 1972; Waterman 1937), and concentrations as low as 58.69
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     depressed sperm motility in gametes of the purple urchin, Strongylocentrotus




purpuratus (Timourian and Watchmaker 1977).






Unused Data




    Some data on the effects of nickel on aquatic organisms were not used




because the studies were conducted with species that are not resident in North




America (e.g. , Ahsanullah 1982; Ballester and Castellvi 1979; Baudouin




and Scoppa 1974; Khangarot et al. 1982; Saxena and Parashari 1983; Van




Hoof and Nauwelaers 1984; Verma et al. 1981; Wilson 1983).  Data were




also not used if nickel was a component of a mixture (e.g., Anderson 1983;




Besser 1985; Eisler 1977b; Hutchinaon and Sprague 1983; Markarian et al.




1980; Muska 1978; Phelps et al. 1981; Stratton and Corke 1979b; Wong et




al. 1978,1982) or an effluent (e.g., Abbe 1982).




    Babich and Stotzky (1985), Birge and Black (1980), Chapman et al.




(1968), Kaiser (1980), Phillips and Russo (1978), Rai et al. (1981),




Thompson et al. (1972), and U.S. EPA (1978) only present data that




have been published elsewhere.  Studies reporting no data or data in an




unusable form for deriving criterion include Braginskiy and Shcherban




(1978), Jones (1939), Muska and Weber (1977a,b), Scheherban (1977), and




Whitton and Shehata (1982).  Data were not used if the organisms were




exposed to nickel in food (e.g., Windom et al. 1982).  Results were not




used if the test procedures were not adequately described (e.g., Bean and




Harris 1977; Brown 1968; Petukov and Ninonenko 1982; See et al. 1974,1975;




Sirover and Loeb 1976; Wang et al. 1984).  The 96-hr values reported




by Buikema et al. (1974a,b) were subject to error because of possible




reproductive interactions (Buikema et al. 1977).




    Results of some laboratory tests were not used because the tests were




conducted in distilled or deionized water without addition of appropriate




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salts (e.g., Jones 1935; Shaw and Grushkin 1957) or were conducted in




chlorinated or "tap" water (e.g., Grande and Andersen 1983).  Dilution




waters in studies by  Mann and Fyfe (1984) and Stratton and Corke (1979a)




contained excessive amounts of EDTA.  Stokes (1975) used algae from a




lake containing high concentrations of nickel.  The data by Girhards and




Weller (1977) on accumulation of nickel by algae were not used because




the test concentrations of nickel adversely affected the growth of the algae.




     Bringraann and Kuhn (1982) cultured Daphnia magna in one water and




conducted tests in another.  Tests conducted with too few test organisms




(e.g., Applegate et al. 1957; Tarzwell and Henderson 1960) were not used.




    Reports of the concentrations of nickel in wild aquatic organisms




(e.g., Abo-Rady 1979; Brezina and Arnold 1977; Bryan et al. 1983; Dunstan



et al. 1980; Gordon et al. 1980; Hall et al. 1978; Jenkins 1980; Kawamata




et al. 1983; LaTouche and Mix 1982; Martin 1979; Mathis and Cummings




1973; Mears and Eisler 1977; O'Conner 1976; Pennington et al. 1982; Pulich




1980; Reynolds 1979; Tong et al. 1974; Trollope and Evans 1976; Uthe and




Bligh 1971; Wachs 1982; Wehr and Whitton 1983; Wren et al. 1983) were not




used to calculate bioaccumulation factors due to the absence or insufficient




number of measurements of nickel in water.






Summary




    Acute values with twenty-one freshwater species in 18 genera range




from 1,101 yg/L for a cladoceran to 43,240 Mg/L for a fish.  Fishes and




invertebrates are both spread throughout the range of sensitivity.  Acute




values with four species are significantly correlated with hardness.




    Data are available concerning the chronic toxicity of nickel to two




invertebrates and two fishes in fresh water.  Data available for two




species indicates that chronic toxicity decreases as hardness increases.




                                    15

-------
The measured chronic values ranged  from  14.77 \ig/L with Daphnia magna
in soft water to 526.7 pg/L with the fathead minnow in hard water.  Five
acute-chronic ratios are available  for two species in soft and hard water
and range from 14 to 122.
    Nickel appears to be quite toxic to  freshwater algae, with concentrations
as low as 50 Mg/L producing significant  inhibition.  Bioconcentration
factors for nickel range from 0.8 for fish muscle to 193 for a cladoceran.
    Acute values for 22 saltwater species in 19 genera range from 151.7
gg/L with juveniles of a raysid to 1,100,000 ug/L with juveniles and adults
of a clam.  The acute values for the four species of fish range from
7,598 to 350,000 Mg/L.  The acute toxicity of nickel appears to be related
to salinity, but the form of the relationship appears to be species-
dependent .
    Mysidop8Js bahia is the only saltwater species with which an acceptable
chronic test has been conducted on nickel.  Chronic exposure to 61 yg/L
and greater resulted in reduced survival and reproduction.   The measured
acute-chronic ratio was 5.478.
    Bioconcentration factors in salt water range from 261.8 with a oyster
to 675 with a brown alga.

National Criteria
    The procedures described in the "Guidelines for Deriving Numerical
National Water Quality Criteria for the Protection of Aquatic Organisms
and Their Uses" indicate that, except possibly where a locally important
species is very sensitive,  freshwater aquatic organisms and their uses
should not be affected unacceptably if the four-day average concentration
(in |Jg/L) of nickel does not exceed the numerical value given by
e(0.8460[ln(hardnessmi.l645) mQre

                                    16

-------
average and if the one-hour average concentration (in pg/L) does not



exceed the numerical value given by e(0.8460[ln(hardness)1+3.3612)




than once every three years on the average.  For example, at hardnesses




of 50, 100, and 200 mg/L as CaC03 the four-day average concentrations of




nickel are 88, 160, and 280 Mg/L» respectively, and the one-hour average




concentrations are 790, 1400, and 2500 Mg/L.




    The procedures described in the "Guidelines for Deriving Numerical




National Water Quality Criteria for the Protection of Aquatic Organisms




and Their Uses" indicate that, except possibly where a locally important




species is very sensitive, saltwater aquatic organisms and their uses




should not be affected unacceptably if the four-day average concentration




of nickel does not exceed 7.9 (Jg/L more than once every three years on the




average and if the one-hour average concentration does not exceed 71 pg/L




more than once every three years on the average.




    EPA believes that "acid-soluble" is probably the best measurement at




present for expressing criteria for metals and the criteria for nickel




were developed on this basis.  However, at this time, no EPA approved




method for such a measurement is available to implement criteria for metals




through the regulatory programs of the Agency and the States.  The Agency




is considering development and approval of a method for a measurement such




as "acid-soluble."  Until one is approved, however, EPA recommends applying




criteria for metals using the total recoverable method.  This has two impacts:




(1) certain species of some metals cannot be measured because the total




recoverable method cannot distinguish between individual oxidation




states, and (2) in some cases these criteria might be overly protective




when based on the total recoverable method.
                                    17

-------
     The allowed average excursion  frequency of three years  is  the Agency's


best scientific judgment of  the average amount of time it will  take an un-


stressed aquatic ecosystem to recover from a pollution event in which


exposure to nickel exceeds Che criterion.  Stressed systems, for example one


in which several outfalls occur in  a limited area, would be expected to require

                           i
more time for recovery.  The resiliencies of ecosystems and their abilities


to recover differ greatly, however, and site-specific criteria  may be


established if adequate justification is provided.


    Use of criteria for developing  water quality-based permit limits and


for designing waste treatment facilities requires selection of  an appropriate


wasteload allocation model.  Dynamic models are preferred for the application


of these criteria.  Limited data or other considerations might make their


use impractical, in which case one must rely on a steady-state model.


The Agency recommends the interim use of 1Q5 or 1Q10 for the Criterion


Maximum Concentration (CMC) design  flow and 7Q5 or 7Q10 for the Criterion


Continuous Concentration (CCC) design flow in steady-state models for


unstressed and stressed systems respectively.  These matters are discussed


in more detail in the Technical Support Document for Water Quality-Based


Toxics Control (U.S. EPA 1985).
                                    18

-------
Table I.  Acute Toxlclty  of Nickel  to Aquatic Animals
Species
Worm,
Nats sp.
Snai 1 (embryo) ,
Amnlcola sp.
Snail (adult),
Amnlcola sp.
Cladoceran,
Daphn la maqna
C ladoceran,
Daphnla magna
Cladoceran,
Daphnla maqna
Cladoceran,
Daphnla magna
Cladoceran,
Oaphnla magna
Cladoceran,
Daphnla magna
Cladoceran,
Daphnla magna
Cladoceran,
Daphnla pul Icar la
Cladoceran,
Daphnla pul Icaria
C 1 adoceran ,
Daphnla pul Icaria
Method8 Checnica!
S, M
S, M
S, M
. S, U Nickel
chloride
S, U Nickel
chloride
S. M Nickel
nitrate
S, M Nickel
chloride
S. M Nlcke,!
chloride
S, M Nickel
chloride
S, M Nickel
chloride
S, M Nickel
sul fate
S, M Nickel
sul fate
S, M Nickel
suit ate
Hardness LC50
(mg/L as or EC50
CaC05)_ (ug/L)»»
FRESHWATER SPECIES
50 14,100
50 11,400
50 14,300
<317
45.3 510
51.1 915
51 1,800
100 2,360
104 1 ,920
206 4,970
48 2.182
48 1.813
44 1 ,836
Adjusted
LC50 or EC50
(Hg/L)»«
14,100
11,400
14,300
554.4
898.3
1,770
1,313
1,033
1,500
2,259
1,877
2.046
Species Mean
Acute Value
(M9/L)*"** Reference
14,100 Rehwoldt et al .
Rehwo 1 dt et al .
12,770 Rehwoldt et al .
Anderson 1948
Bleslnger and
Chrlstensen 1972
Cal 1 et al . 1983
Chapman et al .
Manuscript
Chapman et al .
Manuscript
Chapman et al .
Manuscript
1 , 102 Chapman et al .
Manuscript
Llnd et al .
Manuscr ipt
L 1 nd et al .
Manuscr Ipt
L 1 nd et al .
Manuscript
1973
1973
1973







-------
Table 1.  (Continued)
Species

Cladoceran,
Daphnla pullcarla

Amph I pod,
Gammarus sp.

Mayfly,
Ephemeral la subvarla

Damsel fly,
Unidentified sp.

Stonefly,
Acroneurla  lycorlas

Caddlsfly.
Unidentified sp.

AmerI can eaI,
Angullla rostrata

American eel,
Angullla rostrata

Rainbow trout (2 tnos),
Salmo galrdnerl

Rainbow trout (juvenile),
Salmo galrdnerl

Rainbow trout (juvenile),
Salmo galrdnerl

Rainbow trout (juvenile),
Salmo 'galrdnerl

Rainbow trout (juvenile),
Salmo galrdnerI

Rainbow trout (juvenile),
Salmo galrdnerl
                             Method*    Chemical
s.

s,
s.

s,
s,

s.
s,

s,
F.

F,

F.

F,

F,.

F,

M

M
U

M
U

M
M

M
M

M

M

M

M

M

Nickel
sul fate
-
Nickel
sul fate
-
Nickel
•sul fate
-
Nickel
nitrate
-
Nickel
nitrate
Nickel
sul fate
Nickel
sul fate
Nickel
sulf ate
Nickel
sul fate
Nickel
sul fate
Hardness
(mg/L as
CaCO})
47
50
42
50
40
50
53
55
-
-
-
-
-
_
LC50
or EC50
(iig/l)**
1.901
13,000
4.000
21,200
33.500
30,200
13.000*
13.000
35.500
20,100*
12,700*
28.000*
30,900*
16,900*
Adjusted Species Mean
LC50 or EC50 Acute Value
(iig/L>«** (i.g/L)««M
2,003 2,042
13,000 13,000
4,636 4,636
21,200 21,200
40,460 40,460
30.200 30,200
12,370
11,990 12,180
-
-
-
-
-
— -.
Reference
Llnd et al .
Manuscript
Rehwoldt et al .
Warnlck and Bel 1
1969
Rehwoldt et al .
Warnlck and Bel 1
1969
Rehwoldt et al .
1973
Rehwoldt et al .
1971
Rehwoldt et al .
1972
Haje 1977
Anderson 1981
Anderson 1981
Anderson 1981
Anderson 1981
Anderson 1981

-------
Table 1.  (continued!
Species
Rainbow trout (juvenile),
Salmo qairdnerl
Rainbow trout (juvenile),
Salmo galrdneri
Rainbow trout (juvenile),
Salmo galrdneri
Rainbow trout (3 mos),
Salmo galrdner 1
Rainbow trout (3 mos),
Salmo galrdneri
Rainbow trout (12 mos),
Salmo qairdnerl
Rainbow trout (12 mos),
Salmo qalrdneri
Goldfish (1-2 q),
Carasslus auratus
Common carp (<20 cm),
Cyprlnus carplo
Common carp,
Cyprlnus carplo
Fathead minnow (1-2 g) ,
Plmephales promelas
Fathead minnow (1-2 q) ,
Plmephales promelas
Fathead minnow (1-2 q) ,
Plmephales promelas
Fathead minnow (1-2 g),
Plmephales promelas
Method*
F.
F.
F,
F,
F,
F.
F,
s,
S,
s,
s.
S,
s.
S.
M
M
M
M
M
M
M
U
M
M
U
I
U
U
U
Chemical
Nickel
sulfate
Nickel
sulfate
Nickel
su If ate
Nickel
chlor ide
Nickel
chloride
Nickel
chloride
Nickel
chlor Ide
Nickel
chlor Ide
Nickel
nitrate
-
Nickel
chlor Ide
Nickel
chloride
Nickel
chloride
Nickel
chl or Ide
Hardness
(mg/L as
27-
39
27-
39
27-
39
27-
39
20
53
55
20
20
360
360
LC50
or EC50
(u9/L)*«
15,900*
11.300*
11; 100*
10,000
10,900
8,900
8,100
9,820
10,600*
10
5
4
42
44
.400
,180
,580
,400
,500
Adjusted
LC50 or EC5O
14,210
15,490
12,650
11,510
21,320
10,090
9,594
11,250
9,943
7,981
8,376
Species Mean
Acute Value
(ng/L>«««» Reference
Anderson 1981
Anderson 1981
Anderson 1981
Nebeker et al .
Nebeker et al .
Nebeker et al .
13,380 Nebeker et al .
21,320 Pickering and
Henderson 1966
Rehwoldt et al ,
1971
9,839 Rehwoldt et al ,
1972
Pickering and
Henderson 1966
P 1 cker 1 ng and
Henderson 1966
Pickering and
Henderson 1966
Pickering and
Henderson 1966
1985
1985
1985
19b5
>
•





-------
    Table 1.   (continued)
Xi
V-
Species
Fathead minnow (Immature),
Pltnephales promelas
Fathead minnow (Immature),
Plmephales promelas
Fathead minnow (Immature),
Plmephales promelas
Fathead minnow ( Immature) ,
Plmephales promelas
Fathead minnow,
Plmephales promelas
Fathead minnow,
Plmephales promelas
Banded kllllflsh (<20 cm),
Fundulus dlaphanus
Banded kll 1 If Ish,
Fundulus dlaphanus
Guppy (6 mo) ,
Poecl 1 la retlculata
White perch «20 cm) ,
Morone amerlcana
White perch,
Morone amerlcana
Striped bass ( finger 1 Inq) ,
Morone saxat Ills
Striped bass,
Morone saxat 1 1 Is
Striped bass (63 day),
Morone saxat 1 1 Is
Method*
S, U
s.
F,
F,
F,
F,
s,
s,
s,
s,
s,
s,
s.
s.
M
M
M
M
M
M
M
U
i
M
M
M
M
U
Chemical
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
sulfate
Nickel
sulfate
Nickel
nitrate
Nickel
chloride
Nickel
nitrate
Nickel
nitrate
Nickel
chlor Ide
Hardness
(mg/L as
CaCO^L
210
210
210
210
45
44
53
55
20
53
55
53
55
40
LC50
or EC50
(ng/L)**
27,000
32,200
28,000
25,000
5.209
5.163
46.200t
46.100
4,450
13.600*
13,700
6,200f
6,300
3,900
Adjusted
LC50 or EC50
(Mg/L)«««
8,019
9,563
8,316
7,425
5,695
5,753
43,980
42 , 530
9,661
12,950
12,640
5,902
5,812
4,710
Species Mean
Acute Value
(iig/L)**** Reference
Pickering 1974
Pickering 1974
Pickering 1974
Pickering 1974
Llnd et al .
Manuscript
8,027 Llnd et al.
Manuscript
Rahwoldt et al .
1971
43,250 Rehwoldt et al .
1972
9,661 Pickering and
Henderson 1966
Rehwoldt et al .
1971
12,790 Rehwoldt et al .
1972
Rehwoldt et al .
1971
Rehwoldt et al .
1972
Pa lawskl et al .

-------
Table 1.  (continued)
Species
Striped bass (63 day),
Morone saxat Ills
Rock bass,
Ambloplltes rupestrls
Pumpkin seed (<20 cm),
Lepomls qlbbosus
Pumpklnseed ,
Lepomls glbbosus
Bluegl'll (1-2 g) ,
Lepomls macrochlrus
Blueglll (1-2 g) ,
Lepomls macrochlrus
Blueglll (1-2 g) .
Lepomls macrochlrus
Blueglll ,
Lepomls macrochlrus
Method"
S, U
F, M
S, M
S, M
S, U
S, U
S, U
Fu
> n
Chemical
Nickel
chloride
Nickel
sulfate
Nickel
n Itrate
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Hardness
(mg/L as
CaCOj)
285
26
53
55
20
20
360
49
LC50
or EC50
33,000
2,480
8,100*
8,000
5,180
5,360
39,600
21.200
Adjusted
LC50 or EC50
7,569
4,312
7,710
7,380
11,250
11,640
7,454
21,570
Species Mean
Acute Value

-------
Table 1.  (continued)
Species
Method*
Chemical
Salinity
LC50 Species Mean
or EC50 Acute Value
(tig/L)** (MQ/L)
SALTWATER SPECIES
Polychaete worm (adult).
Nereis arenaceodentata
Polychaete worm (adult).
Nereis vlrens
Polychaete worm (adult),
Ctenodrllus serratus
Polychaete worm (adult),
Capltel la capltata
Mud snail (adult),
Nassarlus obsoletus
Eastern oyster (embryo) ,
Crassostrea vlrqlnlca
Clam,
Macoma balthlca
Clam,
Macoma balthlca
Clam,
Macoma balthlca
Clam,
Macoma balthlca
Clam,
Macoma balthlca
Clam,
Macoma balthlca
Clam,
Macoma balthlca
S, U
S, U
S, U
s, u
s, u
s, u
s, u
s, u
s, u
s. u
s. u
s. u
s, u
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
. chloride
Nickel
chlor Ide
Nickel
chlor Ide
Nickel
chloride
Nickel
chloride
Nickel
chloride
20
20
25
15
25
35
15
25
35
15
49,000
25,000
17,000
>50,000
72,000
1,180
100,000 (5°C)
380,000 (5°C)
700,000 (5'C)
95,000 (10"C)
560,000 (10"C)
1,100,000 (10"C)
110,000 (I5°C)
49,000
25 ,000
17,000
>50,000
72 ,000
1,180
                                                                                                         Reference
                                                                                                         Petrlch  and Relsh 1979
                                                                                                         Elsler  and  Hennekey 1977
                                                                                                         Petrlch  and Relsh 1979
                                                                                                         Petrlch and Relsh 1979
                                                                                                          Elsler  and  Hennekey 1977
                                                                                                          Calabrese et al . 1973
                                                                                                          Bryant et al. 1985
                                                                                                          Bryant et aI. 1985
                                                                                                          Bryant et al. 1985
                                                                                                          Bryant et al. 1985
                                                                                                          Bryant et al. 1985
                                                                                                          Bryant et al. 1985
                                                                                                          Bryant et al. 1985

-------
Table 1.  (continued)
Species
Clam,
Macoma balthlca
Clam,
Macoma balthlca
Quahog clam (embryo),
Mercenarla mercenarla
Soft-shel 1 clam (adult),
Mya arenaria
Soft-shell clam (adult),
Mya arenaria
Copepod (adult) ,
Eury femora at fin Is
Copepod (adult) ,
Eurytemora aft In Is
Copepod (adult) ,
Acartla clausl
Copepod (adult),
Nltocra splnlpes
Mysld (juvenile) ,
Heteromysls formosa
Mysld (juvenile),
Mysldopsls bah la
Mysld (juvenile),
Mysldopsls bl gel owl
Amph 1 pod ,
Corophlum volutator
Amph 1 pod,
Corophlum volutator
Method*
s.
1 s,
s,
s,
S,
s.
s,
s,
s,
s,
F,
s.
s,
s.
U
U
U
U
U
U
U
U
U
M
M
M
U
U
Chemical
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chlor Ide
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
ch 1 or 1 de
Nickel
chloride
Nickel
chlor Ide
Nickel
chloride
SsHnity
50 ,000
13,180
9,593
3,466
6,000
151.7
508
634
5,000 (5°C)
21,000 (5°C)
Acute Value
(iig/L)
-
294 , 500
310
-
320,000
-
11,240
3,466
6,000
151.7
508
634
-
-
                                                                                                          Reference

                                                                                                          Bryant et  at.  1985
                                                                                                          Calabrese  and Nelson
                                                                                                          1974

                                                                                                          Elsler  and Hennekey  1977
                                                                                                          Elsler  1977a
                                                                                                          Lussler  and Card In  1985
                                                                                                           Lussler  and  Card In  1985
                                                                                                          Lussler  and Card In 1985
                                                                                                          Bengtsson  1978
                                                                                                151.7     Gentile  et al .  1982
                                                                                                          Gentile  et al .  1982;
                                                                                                          Lussler  et al.  1985

                                                                                                          Gentile  et al .  1982
                                                                                                          Bryant  et al .  1985
                                                                                                          Bryant  et  al .  1985

-------
Table 1.  (continued)
Species

Amph i pod,
Corophlum volutator

AmphI pod,
Corophlum volutator

AmphI pod,
Corophlum volutator

AmphI pod,
CorophI urn volutator

AmphI pod,
Corophlum volutator

Amph I pod,
CorophIum volutator

AmphI pod,
Corophlum volutator

AmphI pod,
Corophlum volutator

Amphi pod,
CorophIum volutator

Amphi pod,
Corophlum volutator

AmphI pod,
Corophlum volutator

Amphi pod,
Corophlum volutator

AmphI pod,
Corophlum volutator

Hermit crab (adult),
Paqurus lonqlcarpus
Method*
S, U
s.
s.
s.
s.
s,
s.
s.
s.
s,
s.
s,
s.
s,
U
U
U
U
U
U
U
U
U
U
U
1)
U
Chemical
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chlor Ide
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chlor Ide
Nickel
chlor Ide
Nickel
chloride
Nickel
chlor Ide
Nickel
chloride
Salinity

-------
       Table 1.  (continued)
\J
Species
Starfish (adult),
Aster las forbesll
Mummlchoq (adult),
Fundulus heteroclltus
Mumm 1 chog ( adu 1 t) ,
Fundulus heteroclltus
Mummlchoq (adult),
Fundulus heteroclltus
Atlantic sllverslde
( larva) ,
Menldla men Id la
Tidewater sllverslde
(juvenile) ,
Menldla peninsulas
Spot ( juvenl le) ,
Lelostomus xanthurus

LC50 Species Mean
Salinity or EC50 Acute Value
Method* Chemical (g/kg) dig/D" (pg/L) Reference
S, U Nickel 20 150,000 150,000 Elsler and Hennekey 1977
chlor Ide
S, U Nickel 6.9 55,000 - Dorftnan 1977
chloride
S, U Nickel 21.6 175,000 - Dor f man 1977
chloride
S, U Nickel 20 350,000 149,900 Eisler and Hennekey 1977
chlor Ide
S, U Nickel 30 7,958 7,958 Cardln 1982
chloride
S, U Nickel 20 38,000 38,000 Hansen 1983
chloride
S, U Nickel 21 70,000 70,000 Hansen 1983
chloride
       *    S = static, R = renewal, F = flow-through, M = measured, U = unmeasured.



       **   Results are expressed as nickel, not as the chemical.



       ***  Freshwater LCSOs and EC50s were adjusted to hardness = 50 mg/L using  the  pooled slope of 0.8460 (see text).



       »«»* Freshwater Species Mean Acute Values are calculated at hardness = 50  mg/L.



       *    In river water.

-------
Table 1.  (continued)
Ki
                                   Results of Covarlance Analysis of Freshwater Acute Toxic Ity versus Hardness
Species
Daphnla
Fathead
Striped
Blueglll

roagna
minnow
bass

All of above
n
6
10
4
4
24
Slope
1
0
1
0
0
.1810
.8294
.0459
.6909
.8460»
95* Confidence Limits
0
0
0
-0
0
.3187.
.6755,
.7874.
.1654,
.7004,
2
0
1
1
0
.0433
.9833
.3045
.5472
.9915
Degrees of Freedom
4
8
2
2
19
                                * P = 0.26 for equality of slopes with 16 degrees of  freedom.

-------
                                            Table 2.  Chronic Toxlclty of Nickel  to Aquatic Animals
V)
Species
Cladoceran,
Daphnla magna
Cladoceran,
Daphnla magna
Cladoceran,
Daphnla magna
Caddlsfly,
Cllstoronla magnlflca
Rainbow trout,
Salmo galrdnerl
Rainbow trout,
Salmo galrdnerl
Rainbow trout,
Salmo galrdnerl
Fathead minnow,
Plmephales promelas
Fathead minnow,
Plmephales promelas
Mysld,
Mysldopsls bah I a

Test*
LC
LC
LC
LC
ELS
ELS
ELS
LC
ELS
LC
. Chemical
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
sul fate
Nickel
chloride
Hardness
(mg/L as
CaCOiL
FRESHWATER SPECIES
51
105
205
54
53
52
49 .
210
44
451
SALTWATER SPECIES
30"
Llatts
10.2-
21.4
101-
150
220-
578
66-
250
<35*«»
62-
134
134-
431
380-
730
108.9-
433.5
61-
141
Chronic Value

14.77
123.1
356.6
128.4
<35
91.15
240.3
526.7
217.3
92.74
Reference
Chapman et al.
Manuscript
Chapman et al .
Manuscript
Chapman et al .
Manuscript
Nebeker et al. 1984
Nebeker et al. 1985
Nebeker et al . 1985
Nebeker et al . 1985
Pickering 1974
Llnd et al .
Manuscript
Gentile et al . 1982;
Lussler et al. 1985
       *    LC = life-cycle or partial  life-cycle;  ELS = early life-stage.



       **   Results are based on measured concentrations of nickel.



       ***  Unacceptable effects occurred at all  concentrations tested.



            Values from acute tests In Table 1.



       tf   Sal Inlty (g/kg).

-------
Table 2.  (Continued)
                          Results of Regression Analysis of Freshwater Chronic Toxlcltv versus Hardness
Species n
Daphnla maqna 3
Fathead minnow 2
Al 1 of above 5
Slope
2.3007
0.5706
1.3418**
* Cannot be calculated because degrees
*« P = 0.19 for equality of
slopes with
95< Confidence Limits Degrees
-2.6551. 7.2568
•
-1.3922, 4.0760
of freedom = 0.
1 degree of freedom.
of Freedom
1
0
2


Acute-Chronic Ratio


Species
Cladoceran,
Daphnla maqna
Cladoceran,
Daphnla maqna
Cladoceran,
Daphnla magna
Fathead minnow.
Plmephales promelas
Fathead minnow.
Plmephales promelas
Mysld,
Mysldopsls bah la

Hardness
(mg/L as
CaCOj)
51

104-
105
205-
206
210

44-
45
30***


Acute- Value Chronic Value
(uq/L) (Mg/L)
1,800 14.77

1,920 123.1

4,970 356.6

27,930» 526.7

5.186" 217.3

508 92 .74



Ratio
122.4

15.60

13.94

53.03

23.87

5.478

                           *   Geometric mean of four values In Table 1.



                           **  Geometric mean of two values In Table I.



                           *** Salinity (g/kg).

-------
Table 3.  Ranked Genus Mean Acute Values ulth Species Mean Acute-Chronic Ratios
iank»
18
17
16
15
14
13
12
11
10
9
a
7
6
Genus Mean
Acute Value
(uq/L)"
43,250
40,460
30,200
21,320
21,200
14,100
13,380
13,000
12,770
12,180
9,839
9,661
8,697
Species Mean
Acute Value
Species (|i9/D*»«
FRESHWATER SPECIES
Banded kllllflsh,
Fundulus dlaphanls
Stonefly,
Acroneurla lycorlas
Caddlsfly,
Unidentified sp.
Goldfish,
Carasslus auratus
Damsel f ly,
Unidentified sp.
Worm,
Nals sp.
Rainbow trout,
Salmo galrdnerl
Amphlpod,
Gammarus sp.
Snal 1,
Ann 1 co la sp.
American eel ,
Anqullla rostrata
Common carp,
Cyprlnus carplo
• Guppy.
Poecl 1 la reticulata
White perch,
Morone amerlcana
Striped bass,
43,250
40,460
30 ,200
21,320
21,200
14,100
13,380
13,000
12,770
12,180
9,839
9,661
12,790
5,914
Species Mean
Acute-Chronic
Rat 1 <>•»••
-
                        Morone saxatiI Is

-------
                        Table 3.  (Continued)
VXJ
ank*
5
4
3
2
1
19
18
17
16
15
14
Genus Mean
Acute Value
"»
9,530
8,027
4,636
4,312
1,500
320,000
294,500
150,000
149,900
72,000
70,000
Species Mean Species Mean
Acute Value Acute-Chronic
Species (ugA.)"*« Ratlo««««
Pumpklnseed,
Leporols glbbosus
Blueglll,
Lepomls macrochlrus
Fathead minnow,
Plmephales promelas
Mayfly,
Ephemeral la subvarla
Rock bass,
Ambloplltes rupestrls
Cl adoceran,
Daphnla pul Icarla
Cl adoceran,
Daphnla maqna
SALTWATER SPECIES
Soft-shell clam,
Mya arenarla
Clam,
Macoma balthlca
Starfish,
Aster las forbesl 1
Mummlchog,
Fundulus heteroclltus
Mud snal 1 ,
Nassarlus obsoletus
Spot.
7,544
12,040
8,027 35.58f
4.636
4.312
2.042
1.102 29.86tf
320,000
294,500
150,000
149,900
72 ,000
70,000
                                                  Lelostomus xanthurus

-------
                             Table 3.  (Continued)
 ~ V
VlSl
Rank"
13
12
11
10
9
8
7
6
5
4
3
2
Genus Mean
Acute Value
>50,000
47,000
35,000
17,390
17,000
18,950
11,240
6,000
3,466
1,180
567.5
310
Species
Polychaete worm,
Capltel la capltata
Hermit crab,
Pagurus long! carpus
Polychaete worm,
Nereis arenaceodentata
Polychaete worm.
Nereis vlrens
Atlantic sllverslde.
Men Id I a men Id la
Tidewater sllverslde,
Menldla peninsulas
Polychaete worm,
Ctenodrilus serratus
Amph 1 pod ,
Corophlum volutator
Copepod ,
Eurytemora aftinls
Copepod ,
Nltocra splnlpes
Copepod ,
Acartla clausl
Eastern oyster,
Crassostrea vlrglnlca
Mysld,
Mysldopsls bah la
Mysld,
Mysldopsls blgelowl
Qua hog clam,
Species Mean
Acute Value
>50,000
47,000
49.000
25,000
7.958
38.000
17,000
18,950
11,240
6,000
3,466
.1.180
508
634
310
Species Mean
Acute-Chron 1 c
Ratio""
5.478
                                                       Mercenarla mercenarla

-------
                               Table 3.  (Continued)
VJJ
Rank*
1
Genus Mean
Acute Value
diq/D"
151.7
Species
Mysld.
Heteromysls formosa

Species Mean
Acute Value

-------
Table 4.  Toxic Ity of Nickel  to Aquatic Plants
Species
Blue-green alga,
Anabaena flos-aquae .
Blue-green alga,
Mlcrocystls aeruglnosa
Green alga,
Ank 1 strodesmus falcatus
Green alga,
Ank 1 strodesmus falcatus
Green alga,
Ank 1 strodesmus falcatus
var. aclcularls
Green alga,
Ch lamydomonas euqametos
Green alga,
Chloral la vulgar Is
Green alga,
Chlorococcum sp.
Green alga,
Haematococcus capensls
Green alga,
Pediastrum tetras
Green alga,
Scenedesmus acumlnata
Chemical
Nickel
nitrate
Nickel
chloride
Nickel
chloride
Nickel
nitrate
Nickel
nitrate
Nickel nitrate or
Nickel sulfate
Nickel nitrate or
Nickel sulfate
Nickel
ch lor Ide
Nickel nitrate or
Nickel sulfate
Nickel
nitrate
Nickel nitrate or
Nickel sulfate
Hardness
(mg/L as Duration
CaCOjL (days)
FRESHWATER SPECIES
14
8
10
14
14
47.5 12
47.5 12
10
47.5 12
14
47.5 12
Effect
84$ reduction
In growth
Incipient
Inhibition
45$ reduction
In growth
98$ reduction
In growth
42$ reduction
In growth
91$ reduction
In growth
53$ reduction
In growth
52$ reduction
In growth
85$ reduction
In growth
Increased
growth
54$ reduction
. In growth
Resu I t
600
5
5,000
100
100
700 »«
300 »»
5,000
300*«
100
50 »*
Reference
Spencer and Greene
1981
Brlngmann and Kuhn
1978a,b
Devi Prasad and
Devi Prasad 1982
Spencer and Greene
1981
Spencer and Greene
1981
Hutchlnson 1973;
Hutchlnson and
Stokes 1975
Hutchlnson 1973;
Hutchlnson and
Stokes 1975
Devi Prasad and
Devi Prasad 1982
Hutchlnson 1973;
Hutchlnson and
Stokes 1975
Spencer and Greene
1981
Hutchinson 1973;
Hutchlnson and

-------
         Table 4.  (Continued)
vw
Species
Green alga,
Scenedesmus acumlnata
Green alga,
Scenedesmus dlmorphus
Green alga,
Scenedesmus obi Iquus
Green alga,
Scenedesmus quadrlcauda
Green alga,
Scenedesmus quadrlcauda
Diatom,
Navlcula pell leu losa
Duckweed,
Lemna minor
Macrophyte,
E lodea (Anacharls) canadensls
Giant kelp (young fronds),
Hacrocystls pyrlfera
Chemical
Nickel nitrate or
Nickel sulfate
Nickel
nitrate
Nickel
chloride
Nickel
chloride
Nickel
nitrate
Nickel
nitrate
Nickel
chloride
Nickel
chloride
Hardness
(mg/L as Duration
CaC03) (days)
47.5 13
14
10
8
14
14.96 14
28
28
SALTWATER SPECIES
4
Effect
Reduced
growth
30$ reduction
In growth
47$ reduction
In growth
Incipient
Inhibition
60$ reduction
In growth
82$ reduction
In growth
EC50
EC50
EC 50 (reduc-
tion In
. photosynthesis)
Result
(wfl/L)"
500
100
3,000
1,300
100
100
340
2,800
2,000
Reference
Stokes et al. 1973;
Hutchlnson and
Stokes 1975
Spencer and Greene
1981
Dev 1 Prasad and
Devi Prasad 1982
Brlngmann and Kuhn
1977a; 1978a,b;
1979; 1980b
Spencer and Greene
1981
Fezy et al. 1979
Brown and Rattlgan
1979
Brown and Rattlgan
1979
Clendennlng and North
1959
          *  Results are expressed as nickel,  not as the chemical.

-------
                                               Table 5.  Bloaccumulaton of Nickel by Aquatic Organisms
M
Species
Green alga,
Scenedesmus acumlnata
C 1 adocer an ,
Daphnla magna
Cl adocer an,
Dapjuilja magna
Cladoceran,
Daphnla magna
Rainbow trout,
Salmo galrdnerl
Fathead minnow,
P 1 mep_haies_ prome l__as_
Fathead minnow,
Plmephales prome las
Fathead minnow,
Plmephales prome las
Rockweed ,
Fucus veslculosls
Brown macroalga,
Ascophyllum nodosum
Blue mussel ,
Mytl lus edulls
Blue mussel ,
Mytl lus edul Is
Chemical
Nickel nitrate or
Nickel sulfate
63NI In
0.1M HCI
-
-
Nickel
chloride
Nickel
sulfate
Nickel
sul fate
Nickel
sulfate
Nickel
sulfate
Nickel
sulfate
Concentration
In Mater (nq/D*
1,000
50
750
1,000
21
44.4
108.9
1.2
1.2
4.4
10.0
Hardness
(mg/L as Duration
CaCO3) (days)
FRESHWATER SPECIES
6
20.1 3.75
20.1 3.75
320 180
30
30
30
SALTWATER SPECIES
Field
col lections
Field
col lections
84
84
Tissue BCF or BAF«
Whole 9.3
body
Whole 100
body
Whole 192 **»
body
Whole 123***
body
Muscle 0.8
Whole 106
body
Whole 79
body
Whole 47
body
Whole 675f
plant
Whole 458. 3t
plant
Soft parts 472.7
Soft parts 328.6
Reference
Hutch Inson and Stokes
1975
Hal 1 1978
Hall 1982
Hall 1982
Calamarl et al . 1982
Llnd et al . Manuscript
Llnd et al . Manuscript
Llnd et al . Manuscript
Foster 1976
Foster 1976
Zarooglan and Johnson
1984
Zarooglan and Johnson
1984

-------
Table 5.  (Continued)
Species
Eastern oyster,
Crassostrea vlrqlnlca
Eastern oyster,
Crassostrea vlrqlnlca

Hardness
Concentration (mg/L as Duration
Che*1cal In Water (ii9/L>* CaCO.) (days) Tissue BCF or BAF** Reference
Nickel
sul fate
Nickel
sulfate
4.2 - 84 Soft parts 458.1 Zarooglan
1984
9.9 - 84 Soft parts 261.8 Zarooglan
1984
and Johnson
and Johnson
*   Measured concentration of nickel.
**  Bloconcentratlon factors (BCFs) and bloaccuraulatlon  factors (BAFs) are  based on measured concentrations of  nickel  In water and In tissue.
*** Estimated from graph.
    Factor was converted from dry weight to wet weight basis.

-------
Table 6.  Other Data on Effects of  Nickel on Aquatic Organisms
Species
Alga,
Chiorella pyrenoldosa
Green alga,
Scenedesmus quadricauda
Green alga,
Scenedesmus quadricauda
Alga,
(mixed population)
Bacterium,
Aeromonas sobrla
Bacterium,
Bacl 1 lus brevls
Bacter i um,
Bacl 1 lus cereus
Bacterium,
Escherlchla col 1
Bacterium,
Escherlchla col 1
Bacterium,
Pseudomonas put Ida
Bacterium,
Serratla marcescens
Protozoan,
Entoslphon sulcatum
Chemical
Nickel
chloride
Nickel
ammon 1 um
sulfate
Nickel
nitrate
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
ammon 1 um
sulfate
Nickel
chlor Ide
Nickel
chloride
Nickel
chlor Ide
Hardness

-------
Table 6.  (Continued)
Species
Protozoan,
Mlcroreqma heterostoma
Protozoan,
Mlcroreqma heterostoma
Protozoan ,
Ch 1 lomonas paramecluro
Protozoan,
Uronema parduezl
Tub! field worm,
Tublfex tublfex
Cladoceran,
Daphnla maqna
Cladoceran,
Daphnla maqna
Cladoceran ,
Daphnla maqna
Cladoceran,
Daphnla maqna
Cladoceran,
Daphnla maqna
Cladoceran,
Daphnla maqna
Cladoceran,
Daphnla pul Icarla
Cladoceran,
Daphnla pul Icarla
Cladoceran,
Daphnla pul Icarla
Hardness
(mg/L as
Chemical CaCO5)
Nickel
chloride
Nickel
ammon 1 urn
sul fate
Nickel
chloride
Nickel
chloride
Nickel 34.2
sul fate
Nickel
chloride
Nickel
ammon 1 urn
sul fate
Nickel 288
chloride
Nickel 45.3
chloride
Nickel 45.3
chloride
Nickel 45.3
chloride
Nickel 25
sul fate
Nickel 28
sul fate
Nickel 28
sul fate
Duration
28 hrs
28 hrs
48 hrs
20 hrs
48 hr
48 hrs
48 hrs
24 hrs
48 hrs
21 days
21 days
48 hrs
48 hrs
48 hrs
Effect
Incipient
Inhibition
Incipient
Inhibition
Incipient
Inhibition
Incipient
Inhibition
LC50
EC50 (river
water)
EC50 (river
water)
EC50
(swimming)
EC50 (Immobll-
zatlon) (fed)
EC50 (Immobll-
zat Ion)
\6t reproduc-
tive Impairment
LC50 (TOC =
39 mg/L)
LC50 (TOC =
15 mg/L)
LC50 (TOC =
13 mg/L)
Result
*
50
70
820
42
8.70
7.00
6,000
6,000
1 1 ,000
1,120
130
30
2,171
1,140
1,034
Reference
Brlngmann and Kuhn
1959b
Brlngmann and Kuhn
1959b
Brlngmann et al . 1980;
Br 1 ngmann and Kuhn
1981
Brlngmann and Kuhn
I980a, 1981
Br kov 1 c-Popov 1 c and
Popov Ic 1977a
Brlngmann and Kuhn
1959a,b
Brlngmann and Kuhn
1959a,b
Brlngmann and Kuhn
1977b
Bleslnger and
Chrlstensen 1972
Bleslnger and
Chrlstensen 1972
Bleslnger and
Chrlstensen 1972 .
Llnd et al . Manuscript
Llnd et al . Manuscript
Llnd et al . Manuscript

-------
Table 6.  (Continued).

Species
Cladoceran,
Daphnla pulicarla
Cladoceran,
Daphnla pu 1 Icarla
Cladoceran,
Daphnla pul Icarla
Cladoceran,
Daphnla pul Icarla
Cladoceran,
Daphnla pul Icarl a
Cladoceran,
Daphnla pul Icarla
Cladoceran,
Daphnla pulicarla
Cladoceran,
Daphnla pul Icarla
Cladoceran,
Daphnla pul Icarla
Cladoceran,
Daphnla pul Icarla
Midge,
Chlronomus sp.
Coho salmon (yearling),
Oncorhynchus klsutch
Rainbow trout (0.5-0.9 g) ,
Salmo qalrdner 1
Rainbow trout (1 yr) ,
Salmo qalrdner 1

Chemical
Nickel
sul fate
Nickel
sul fate
Nickel
sul fate
Nickel
sul fate
Nickel
sul fate
Nickel
sul fate
Nickel
sul fate
Nickel
sul fate
Nickel
sul fate
Nickel
sulfate
_

Nickel
chloride
Nickel
sul fate
Nickel
sulfate
Hardness
(mg/L as
CnCO?)
29

73

74

84

86

89

89

100

114

120

50

90

42

240


Duration
48 hrs

48 hrs

48 hrs

48 hrs

48 hrs

48 hrs

48 hrs

48 hrs

48 hrs

48 hrs

96 hrs

144 hrs

48 hrs

48 hrs


Effect
LC50 
-------
Table 6.  (Continued)
Species
Rainbow trout
(embryo, larva),
Salmo galrdnerl
Rainbow trout (embryo),
Salmo gairdneri
Rainbow trout
(embryo, larva),
Salmo qalrdnerl
Rainbow trout
(embryo, larva),
Salmo gairdneri
Rainbow trout,
Salmo qairdnerl
Rainbow trout (adult),
Salmo gairdneri
Rainbow trout (10 g),
Salmo qairdnerl
Rainbow trout,
Salmo qalrdnerl
Brown trout (0.8-1.2 g) ,
Salmo trutta
Brook trout (0.4-0.6 g),
Salvellnus fontinalls
Lake trout (2.5-3.2 g) ,
Salvelinus namaycush
Goldfish,
Carasslus auratus
Goldfish (embryo, larva),
Carasslus auratus
Chemical
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
sul fate
Nickel
chloride
Nickel
chloride
Nickel
sul fate
Nickel
sul fate
Nickel
sul fate
Nickel
sul fate
Nickel
chloride
Nickel
chloride
Hardness
(mg/L as
CaCO;>
104
(92-110)
104
125
174
240
320
28.4
22.5
42
42
42
195
Duration
28 days
28 days
28 days
28 days
3.5 days
6 mos
20 mlns
48 hr
48 hrs
48 hrs
48 hrs
19-50 hrs
200-210 hrs
7 days
Effect
EC5O (death
and deformity)
LC50
EC 50 (death
and deformity)
EC 50 (death
and deformity)
Decreased gill
diffusion
Increase in
liver proteoly-
tlc activity of
males
Avoidance
threshold
LC50
LC50
LC50
LC50
LT
LT
EC50 (death
and deformity)
Result
(M9/L)»
50
50
60
90
2.000
1,000
23.9
54.963
60,290
54,040
16,750
100,000
10,000
2,140
Reference
Blrqe 1978; Blrge and
Black 1980; Blrge et al
1978, 1980. 1981
Blrqe et al . 1979
Birge et al . 1981
Blrge et al . 1981
Hughes et al . 1979
Aril lo et al . 1982
Glattlna et al. 1982
Bornatowlcz 1983
Ml II ford 1966
Mil Iford 1966
Mil Iford 1966
Ellis 1937
Blrge 1978

-------
Table 6.  (Continued)
Species
Goldfish (embryo, larva),
Carasslus auratus
Common carp (embryo),
Cyprlnus carplo
Common carp (larva),
Cyprlnus carplo
Common carp (embryo),
Cyprlnus carplo
Fathead minnow,
Plmephales promelas
Fathead minnow,
Plmephales promelas
Fathead minnow,
Plmephales promelas
Fathead minnow,
Plmephales promelas
Fathead minnow,
Pimephales promelas
Fathead minnow,
Plmephales promelas
Channel catfish (1.2-1.5 g) ,
Ictalurus punctatus
Channel catfish,
Ictalurus punctatus
Guppy,
Poec Ilia ret i cu 1 at a
Guppy ( 184 mg) ,
Poecilia retlculata
Chemical
Nickel
chloride
Nickel
sulfate
Nickel
sulfate
Nickel
sulfate
Nickel
sulfate
Nickel
sulfate
Nickel
sul fate
Nickel
sulfate
Nickel
sulfate
Nickel
sulfate
Nickel
sulfate
Nickel
chloride
Nickel
sulfate
Nickel
chloride
Hardness
(mg/L as
CaC05)
93-
105
128
128
360
28
29
77
86
89
91
42
93-
105
260
260
Duration Effect
7 days EC50 (death
and deformity)
72 hrs LC50
72 hrs LC50
257 hrs
EC50 (hatch)
96 hrs LC50 (TOC =
14 mg/L)
96 hrs LC50 (TOC =
12 mg/L)
96 hrs LC50 (TOC =
32 mg/L)
96 hrs LC50 (TOC =
15 mg/L)
96 hrs LC50 (TOC =
33 mg/L)
96 hrs LC50 (TOC =
30 mg/L)
48 hrs LC50
7 days EC 56 (death
and deformity)
96 hrs LC50 (high
sol Ids)
48 hrs LC50
Result
(MS/L)«
2,780
6,100
8,460
750
22,000
2,923
2,916
12,356
5,383
17,678
8,617
36,840
710
34,900
37,000
Reference
Blrge and Black 1980;
Blrge et al . 1981
B lay lock and Frank
1979
B lay lock and Frank
1979
Kapur and Yadov 1982
Llnd et al . Manuscript
Llnd et al . Manuscript
Llnd et al. Manuscript
Lind et al . Manuscript
Llnd et al . Manuscript
Llnd et al . Manuscript
Mil Iford 1966
Blrge and Black 1980;
Blrge et al. 1981
Khangarot 1981
Khangarot et al. 1981

-------
Table 6.  (Continued)
Species
Blueglll (0.7-1.1 g),
Lepomls macrochlrus
Largemouth bass
(embryo, larva),
Mlcropterus sal mo Ides
Narrow-mouthed toad
(embryo, larva),
Gastrophryne carol Inens Is
Narrow- mouthed toad
(embryo, larva),
Gastrophryne carol Inens Is
Fowler's toad,
Bufo fowlerl
Marbled salamander
(embryo, larva),
Chemical
Nickel
sul fate
Nickel
chlor Ide
Nickel
chlor Ide
Nickel
chloride
Nickel
chloride
Nickel
chloride
Hardness
(mg/L as
42
93-
105
195
95-
103
93-
105
93-
105
Duration
48 hrs
8 days
7 days
7 days
7 days
8 days
Effect
UC50
EC50 (death
and deformity)
EC50 (death
and deformity)
EC50 (death
and deformity)
EC50 (death
and deformity)
EC50 (death
and deformity)
Result
110,500
2,020
(2,060)
50
50
11,030
420
(410)
Reference
Will ford 1966
Blrge and Black 1980;
Blrge et al. 1978, 1981
Birqe 1978; Blrge et al
1979
Blrge and Black 1980
Birge and Black 1980
Blrge and Black 1980;
Blrge et al . 1978
Ambystoma opacum

-------
Table 6.  (Continued)
Species Chemical
Salinity
(q/hg) Duration
Effect
Result
(ug/D*
SALTWATER SPECIES
Golden brown alga,
Isochrysls galbana
Golden brown alga,
Isochrysls galbana
Diatom, Nickel
Phaeodacty lum trlcornutum chloride
Diatom,
Thalassloslra pseudonana
Diatom,
Thalassloslra pseudonana
Diatom,
Tha lass los Ira pseudonana
Diatom,
Thalassloslra pseudonana
Diatom,
Thalassloslra pseudonana
Diatom,
Thalassiosira pseudonana
Diatom,
Thalassiosira pseudonana

28 2 days
28 9 days
26 7 days
14 2 days
14 2 days
14 2 days
14 2 days
14 2 days
28 2 days
28 2 days
Lowest concen-
tration reducing
chlorophyll a_
Lowest concen-
tration reducing
eel 1 numbers
Reduced growth
Ch 1 orophy 1 1 a_
reduced about
65* at 12"C
Chi orophy 1 1 _a_
reduced about
65* at 16"C
Chlorophyll a
reduced about
65* at 20°C
Ch 1 orophy 1 1 a
reduced about
65* at 24 "C
Chi orophy 1 1 a_
red uced about
65* at 28*C
Chi orophy 1 1 j*_
reduced about
65* at 12°C
Chi orophy 1 1 _a_
reduced about
65* at 16°C
500
80
1,000
100
31
28
17
80
72
140
                                                                                                 Reference
                                                                                                 Wilson  and Freeberg 1980
                                                                                                 Wilson  and Freeberg I960
                                                                                                 Skaar  et al. 1974
                                                                                                 Wilson and Freeberg 1980
                                                                                                 Wilson and Freeberg 1980
                                                                                                 Wilson and Freeberg 1980
                                                                                                 Wilson and Freeberg 1980
                                                                                                 Wilson and Freeberg 1980
                                                                                                 Wilson and Freeberg 1980
                                                                                                 Wilson and Freeberg 1980

-------
Table 6.  (Continued)
Species Chemical
Diatom,
Thalassloslra pseudonana
Diatom,
Thalassloslra pseudonana
Diatom,
Thalassloslra pseudonana
Diatom,
Thalassloslra pseudonana
D Inof lagel late,
6 lenodlnlum hal 1 1
Dlnof lagel late,
Glenod Inlum hal 1 1.
D Inof lagel late,
Gymnod In lum sp lendens
Dlnof lagel late,
Gymnod Inlum splendens
Dlnof lagel late,
Gymnod In lum splendens ,
Salinity
(g/kg)
28
28
28
28
28
28
28
28
28
Duration
2 days
2 days
2 days
2 days
5 days
2 days
2 days
2 days
2 days
Effect
Result
«
Ch 1 orophy 1 1 JJ^ 30
reduced about
65* at 20 °C
Chi orophy 1 1 _a 21
reduced about
65* at 24 "C
Chi orophy 1 1 _a_ 18
reduced about
65* at 30 °C
Lowest concen- 100
tratlon reducing
chlorophyll a
Reduced chloro- 50
phy 1 1 a^ and
population
numbers 1 n chemo-
stat cultures
Lowest concen- 200
tratlon reducing
chl orophy 1 1 _a
Chi orophy 1 1 _a 1,000
reduced about
65* at 16 "C
Chlorophyll J^ 950
reduced about
65* at 20 °C
Chl orophy 1 1 a^ 560
reduced about
65* at 24 °C
Reference
Wilson and Freeberg 1980
Wilson and Freeberg 1980
Wilson and Freeberg 1980
Wilson and Freeberg 1980
Wilson and Freeberg 1980
Wilson and Freeberg 1980
Wilson and Freeberg 1980
Wilson and Freeberg 1980
Wilson and Freeberg 1980

-------
Table 6.  (Continued)
Species
Dlnof lagel late,
Gymnod Inlum spendens
Dlnof lagel late,
Gymnod In lum splendens
Dl not lagel late,
Gymnod In lum splendens
Dlnof lagel late,
Gymnod In lum splendens
Dlnof lagel late,
Gymnod Inlum splendens
Polychaete worm (adult),
Ctenodrllus serratus
Blue mussel ,
Mytl lus edulls
Pacific oyster (juvenile),
Crassostrea glgas
Eastern oyster (larva),
Crassostrea virgin lea
Eastern oyster (larva),
Crassostrea virgin lea
Eastern oyster,
Crassostrea virgin lea
Clam ( larva) ,
Mu 1 Ina lateral Is
Chemical
-
—
—
-
—
Nickel
chloride
Nickel
chloride
Nickel
chlor Ide
Nickel
chloride
Nickel
chloride
Nickel
chloride
Nickel
chloride
Salinity
(g/kg)
28
28
14
14
28
29-
32
34
24+2
24+2
29-
32
35
Duration
2 days
2 days
2 days
2 days
2 days
28 days
10 weeks
14 days
12 days
12 days
10 weeks
48 hrs
Effect
Chlorophy 1 1 a
reduced about
65V at 28°C
Ch 1 orophy 1 1 ^
reduced about
65* at 30 °C
Chi orophy 1 1 ^
reduced about
65* at 16*C
Chlorophyll a±
reduced about
65% at 30*C
Lowest concen-
tration reducing
Chlorophy 1 1 _a
Inhibited
reproduction
ATP reduced
19* reduction
In growth
LC50
54.8* reduction
In growth
No effect on
AEC and
components
Reduced calcium
uptake
Result
Cufl/D"
130
1,800
1,800
400
200
100-
500
10
20
1,200
1,200
10
2,000
Reference
Wl (son and
W 1 1 son and
W 1 1 son and
W 1 1 son and
Wilson and
Freeberg 1980
Freeberg 1980
Freeberg 1980
Freeberg 1980
Freeberg 1980
Petrlch and Relsh 1979
Zarooglan et al . 1982
Wat ling 1983
Calabrese et al . 1977
Calabrese et al . 1977
Zarooglan et al . 1982
Ho and Zubkoff 1983

-------
Table 6.  (Continued)
                                           Salinity
Species                       Chemical      (g/kg)       Duration

Quahoq olam (larva),            Nickel       24j*2        8-10 days
Mercenarla mercenarla         chloride

Common Pacific llttleneck       Nickel         31          48 hrs
(adult),                      nitrate
Protothaca stamlnea

Common Pacific llttleneck       Nickel         31          48 hrs
(adult),                      nitrate
Protothaca stamlnea

Copepod (adult),                Nickel         30          72 hrs
Pseudodlaptomus coronatus      chloride

Copepod (adult).                Nickel         30          72 hrs
Acartla clausl                chloride

Copepod (adult).                Nickel         30          72 hrs
Acartla tonsa                 chloride

Pink shrimp (adult).            Nickel           -          48 hrs
Panda I us montaguI              sulfate

Green crab (adult).            Nickel           -          48 hrs
Carclnus maenas               sulfate

Sea urchin (embryo),            Nickel           -          21 hrs
Arbacla punctulata            chloride

Sea urchin (embryo),            Nickel           -          42 hrs
Arbacla punctulata            chloride

Sea urchin (embryo).            Nickel           -        18-26 hrs
Lytechlnus pIctus             chloride
Sea urchin (embryo).            Nickel          -          48 hrs
Lytechlnus plctus              chloride
                                                                                       Result
Effect
   •
LC50
No growth

BCF = 4.3
(gill)
BCF = 4.0
(whole  clam)
LC50
LC50
 LC50
 LC50
 LC50
 Stunted
 development
                 5,700
                 5,700
                14,570
                 6,010
                    747
                56,880
               170,600
                 7,562


>50* mortalIty   7,562
 Totally
 arrested
 development

 AbnormaI
 development
               586,900
                                                                                          586.9
Reference

Calabrese et al.  1977


Hardy and Roes I jad I  1982



Hardy and Roes I j ad I  1982



Lussler and Card In  1985


Lussler and Cardln  1985


Lussler and Cardln  1985


Portmann  1968


Portmann  1968


Waterman  1937


Waterman  1937
 Tlmourlan  and Watchmaker
 1972
                             Tlmourlan  and  Watchmaker
                             1972

-------
Table 6.  (Continued)
Species Chemical
Sea urchin (gamete),
Stronqy locentrotus purpuratus
Salinity
(g/kg)
-
Duration
300 mlns
Effect
Depressed sperm
motlllty
Result
(iig/L)«
58.69
Reference
Tl mount an and
1977
Matchmaker
*  Results are expressed as nickel, not as the chemical.



** Incubated for 2 to 4 days after exposure.

-------
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