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m.3Aquatic plants

m.3.1MMT


No information was available on the toxicity of MMT to aquatic plants.

m.3.2Manganese


Manganese is widely distributed in the earth’s crust, most commonly as MnO2. It is present in natural waters in suspended form (similar to iron) although soluble forms may persist at low pH or low dissolved oxygen (ANZECC and ARMCANZ, 2000).

The information presented below indicate that Mn is slightly to moderately toxic to freshwater and marine aquatic plants with acute LC(EC)50 values in the range of 4.98 mg/L or greater (Mensink et al., 1995).

Freshwater aquatic toxicity data for Mn were available for 7 aquatic plant species including 2 macrophytes and 5 species of algae. The data are summarised in Table 15.

Table 15. Summary of aquatic phytotoxicity data for manganese


Species

Endpoint

Result (mg/L)

Reference

Duckweed Lemna minor


96-hour EC50 (growth)

31

Wang ,1986, as cited by USEPA, 2000

Rice Oryza sativa


144-day IC50 (growth)

100

Wang ,1994, as cited by USEPA, 2000

Green algae Scenedesmus quadricauda


12-day EC50 (growth)
12-day EC50 values (chlorophyll content)


4.98
1.91 - 2.28

Fargasova et al., 1999
Fargasova et al., 1999

Algae Chlorella vulgaris

NOEC (population growth)
LOEC (population growth)

4.5

11


Den Dooren & de Jong, 1965, as cited by USEPA, 2000

Den Dooren & de Jong, 1965, as cited by USEPA, 2000




Algae Chlorella pyrenoidosa, C. salina & S. quadricauda

84-hour
144-hour LT50

100
50

Wong et al., 1980, as cited by USEPA, 2000

Wong et al., 1980, as cited by USEPA, 2000



Two studies have investigated the effects of Mn to marine diatoms (Fisher and Jones, 1981, as cited by USEPA, 2000; Rosko and Rachlin, 1975, as cited by USEPA, 2000). The 96-hour EC50 (growth) values for diatoms (Asterionella japonica and Nitzschia closterium) range from 25.7 to 53.8 mg/L.

m.4Aquatic invertebrates

m.4.1MMT


The acute (48 hour) toxicity of MMT (95% purity) was studied in cultured neonates (<24 hours old) of the freshwater crustacean Daphnia magna (waterfleas) under static test conditions (Analytical Bio-chemistry Laboratories, Inc., 1990). The study was undertaken with measured MMT concentrations (means) of 0, 0.29, 0.65, 1.0, 2.0, and 3.5 mg/L. Measured concentrations were less than estimated nominal concentrations, presumably due to photodegradation of MMT. Test dilution water had hardness 172 mg/L (as CaCO3), alkalinity 192 mg/L (as CaCO3), pH 7.9, and conductivity 325 Mhos/cm. The 48-hour EC50 was 0.83 mg/L (95% C.I. 0.70 to 0.99 mg/L). The 4-hour and 24-hour EC50 were 0.87 and 0.94 mg/L, respectively. The 48-hour NOEL, based on the absence of immobility and abnormal effects, was 0.29 mg/L. Abnormal effects including immobility and surfacing were observed with the mean measured MMT concentrations of 0.65 mg/L and greater under test concentrations.

Acknowledging data limitations, these results for Daphnia magna suggest that MMT may be considered highly toxic to aquatic invertebrates, with acute LC(EC)50 values in the range of <1 mg/L (Mensink et al., 1995).


m.4.2Manganese


The information presented below indicates that Mn is slightly to moderately toxic to freshwater and marine invertebrates with acute and chronic LC(EC)50 values in the range of 1 to 10 mg/L (Mensink et al., 1995).

Manganese is a neurotoxin and can block the release of neurotransmitters such as acetylcholine, while inhibiting acetylcholine esterase activity (Skukla and Singhal, 1984, as cited by MacDonald et al., 1988).

Acute and chronic toxicity data for Mn are available for several species of freshwater invertebrates with acute and chronic LC50 values ranging from 12.6 and 9 mg/L, respectively. Sublethal effects including intoxication and aberrant reproduction have been recorded above 4.7 mg/L. The data are summarised in Table 16.

Table 16. Summary of freshwater invertebrate toxicity data for manganese


Species

Endpoint

Result (mg/L)

Reference

Crayfish Austropotamobius pallipes & Orconectes limosus

4-day LC50

30-day LC50



28 - 51

17 - 34


Boutet and Chaisemartin, 1973, as cited by USEPA, 2000

Boutet and Chaisemartin, 1973, as cited by USEPA



Rotifer Brachionus calyciflorus

24-hour LC50

38.7

Couillard et al., 1989, as cited by USEPA, 2000.

Waterfleas Daphnia magna

Acute LC50

12.6

Sorvari and Sillanpaa, 1996, as cited by USEPA, 2000; Kimball, 1978, as cited by USEPA, 2000; Cabejszek and Stasiak, 1960, as cited by USEPA, 2000




21-day LC50

9

Kimball , 1978, as cited by USEPA, 2000




EC50 (intoxication)

4.7

Baird et al., 1991; Anderson, 1948 as cited by USEPA, 2000; Biesinger and Christensen, 1972 as cited by USEPA, 2000; Khangarot and Ray, 1989 as cited by USEPA, 2000; Rossini and Ronco, 1996 as cited by USEPA, 2000




48-hour NOEC (intoxication)

48-hour EC50 (intoxication)



28

40


Bowmer et al., 1998 as cited by ANZECC and ARMCANZ, 2000

Bowmer et al., 1998, as cited by ANZECC and ARMCANZ, 2000






21-day EC50 (intoxication)

5.7

Biesinger and Christensen, 1972 as cited by USEPA, 2000



Table 16. Summary of freshwater invertebrate toxicity data for manganese (cont.)

Species

Endpoint

Result (mg/L)

Reference




21-day EC50 (reproduction)

5.2

Biesinger and Christensen, 1972 as cited by USEPA, 2000




28-day NOEC

7-day NOEC



1.1

3.9


Kimball, 1978 as cited by USEPA, 2000

Kimball , 1978 as cited by USEPA, 2000






28-day MATC a

7-day MATC



1.1

5.5


Kimball, 1978 as cited by USEPA, 2000

Kimball, 1978 as cited by USEPA, 2000



Tubificid worm Tubifex tubifex

24- and 96-hour EC50 (intoxication)

301 & 270

Khangarot, 1991 as cited by USEPA, 2000

Khangarot, 1991 as cited by USEPA, 2000



Sowbugs Asellus aquaticus: Crustacea

48-hour EC50
(intoxication)

96-hour EC50 (intoxication)



771
333

Martin and Holdich, 1986 as cited by USEPA, 2000

Martin and Holdich, 1986 as cited by USEPA, 2000



Aamphipods Cragonyx pseudogracilis

48-hour EC50 (intoxication)

96-hour EC50 (intoxication)



1389
694

Martin and Holdich, 1986 as cited by USEPA, 2000

Martin and Holdich, 1986 as cited by USEPA, 2000



Protozoa Spirostomum ambiguum

24-hour LC50
48-hour LC50

92.8
109

Nalecz-Jawecki and Sawicki, 1998 as cited by USEPA, 2000

Nalecz-Jawecki and Sawicki, 1998 as cited by USEPA, 2000






24-hour EC50 (development)

48-hour EC50 (development)



148
146

Nalecz-Jawecki and Sawicki, 1998 as cited by USEPA, 2000

Nalecz-Jawecki and Sawicki, 1998 as cited by USEPA, 2000



Ciliates Tetrahymena pyriformis

3-hour IC50

6-hour IC50

9-hour IC50


152

117


106

Sauvant et al., 1995 as cited by USEPA, 2000

Sauvant et al., 1995 as cited by USEPA, 2000

Sauvant et al., 1995 as cited by USEPA, 2000


a. Maximum acceptable threshold concentration (MATC) is a hypothetical threshold concentration that is the geometric mean between the NOEC and LOEC concentration.

Manganese toxicity data are available for several species of marine invertebrates with acute toxicity (mortality) in the range of between 16 to 75 mg/L and chronic EC50 values in the range of 1 to 10 mg/L (refer Table 17).


Table 17. Summary of saltwater/marine invertebrate toxicity data for Manganese


Species

Endpoint

Result (mg/L)

Reference

American oyster Crassostrea virginica

48-hour LC50

16

Calabrese et al., 1973 as cited by USEPA, 2000

Blue mussel Mytilus edulis

48-hour EC50

30

Morgan et al., 1986 as cited by USEPA, 2000

Harpacticoid copepod Nitocra spinipes

96-hour LC50

70

Bengtsson, 1978 as cited by ANZECC and ARMCANZ, 2000

Brine shrimps Artemia spp.

24-hour LC50

48-hour LC50



75

51.8


Gajbhiye and Hirota, 1990 as cited by USEPA, 2000

Gajbhiye and Hirota , 1990 as cited by USEPA, 2000



Starfish Asterias rubens

72-hour LT50

50

Hansen and Bjerregaard, 1995 as cited by USEPA, 2000

Yellow Crabs Cancer anthonyi

96-hour LD50 (embryo mortality)

96-hour EC50 (hatching success)*



10 - 100

1 to 10


MacDonald et al., 1988

MacDonald et al., 1988



Oyster Crassostrea gigas

NOEC (larval settlement & behaviour)

0.02

Watling (1983)

* ANZECC and ARMCANZ (2000) noted the apparent spurious data generated in this study for lower tested concentrations of manganese.

MacDonald et al. (1988) noted that embryos of the crab species Cancer anthonyi live on the outside of the adult crab and may receive a higher exposure than many other aquatic organisms, explaining the higher sensitivity compared to other aquatic organisms. MacDonald et al. (1988) suggest that adverse effects of metals such as Mn may not be expressed within the typical time frame of standard toxicity tests (e.g. 96 hours), and that effects of Mn may not be fully expressed until at least 120 hours. However as they indicated, the increased rate of effects they noted at 120 hours in the toxicity test coincided with a peak in metamorphosis and hatching of viable embryos, which may be a more sensitive life stage. Other confounding factors in the tests, such as disease, cannot be excluded.

Eggs of the marine crab Carcius maenas can accumulate Mn during ovogenesis (Martin, 1976a, as cited in MacDonald et al., 1988). Further, eggs of the marine crab Cancer irroratus can accumulate Mn following exclusion, due to their selective adsorption to the chitinous vitelline membrane (Martin, 1976b, as cited in MacDonald et al., 1988). Bioconcentration of Mn by these crab species, may explain the high sensitivity of these species to Mn relative to other marine organisms (e.g. Rao and Saxema, 1981, as cited in MacDonald et al., 1988; Morgan et al., 1986, as cited in USEPA, 2000).

Watling (1983) investigated the effects of Mn on settlement of the oyster Crassostrea gigas, finding no effects on larval settlement or larval behaviour (as evidenced by foot extension and crawling movement) when exposed to 0.02 mg/L. This was the highest concentration tested. The author suggested that minor effects in growth of 51-day old young (spats) may have been evident following 14-days exposure to Mn at the lowest concentration tested (i.e. 0.01 mg/L). However, further testing would be required to verify this hypothesis, and spat growth recovered following removal to clean seawater for 14 days.




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