The toxic effects of copper on larvae of the barnacle species Chthamalus challengeri

Leilei Qi; Ying Wang; Jingjing Sha; You Wang; Xuexi Tang

doi:10.1007/s00343-015-4158-y

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The toxic effects of copper on larvae of the barnacle species Chthamalus challengeri

OriginalPaper | Updated：2023-05-16

- The toxic effects of copper on larvae of the barnacle species Chthamalus challengeri
- The toxic effects of copper on larvae of the barnacle species Chthamalus challengeri
- 海洋湖沼学报（英文） 2015年33卷第2期页码：400-409
- Affiliations：
  
  Department of Ecology College of Marine Life Sciences Ocean University of China
- Author bio：
- Funds：
  
  Supported by the National Natural Science Foundation of China (No. 3107045820) and the State Oceanic Administration Public Welfare Project (Nos. 201305009, 201305009-4, 201005007)
- DOI：10.1007/s00343-015-4158-y
  中图分类号：
- 网络首发：2015-01-08，
  
  纸质出版：2015
- Accepted：
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The toxic effects of copper on larvae of the barnacle species Chthamalus challengeri[J]. 海洋湖沼学报（英文）, 2015,33(2):400-409.

Qi, L., Wang, Y., Sha, J. et al. The toxic effects of copper on larvae of the barnacle species Chthamalus challengeri, ., Chin. J. Ocean. Limnol. 33, 400–409 (2015). https://doi.org/10.1007/s00343-015-4158-y
The toxic effects of copper on larvae of the barnacle species Chthamalus challengeri[J]. 海洋湖沼学报（英文）, 2015,33(2):400-409. DOI： 10.1007/s00343-015-4158-y.

Qi, L., Wang, Y., Sha, J. et al. The toxic effects of copper on larvae of the barnacle species Chthamalus challengeri, ., Chin. J. Ocean. Limnol. 33, 400–409 (2015). https://doi.org/10.1007/s00343-015-4158-y DOI：

摘要

Abstract

With the increased use of copper (Cu)-based antifouling (AF) paints

copper has become a potential threat to marine organisms. Experiments were performed to investigate the effects of copper on larvae of the barnacle Chthamalus challengeri. These experiments attempted to identify a more sensitive index to monitor copper pollution in marine environments. The 24 h LC50 ranged from 156.07 μg/L (nauplius II) to 817.15 μg/L (cypris) and the no observed effect concentration (NOEC) ranged from 81.75 μg/L (nauplius II) to 571.04 μg/L (cypris). The cypris settlement rate declined significantly when copper concentrations ≥135 μg/L. No cypris was found in the copper concentration of 60 and 75 μg/L treatment groups stressed for 22 d. Nauplius II moulting was not affected by exposure to copper for 24 h; however

when extended to 48 h

the percent moulted in 75 μg/L treatment group was declined to 37.12%

which was significant lower (P <0.05) than that in the control group. The phototaxis of nauplius II decreased significantly when copper concentrations ≥45 μg/L. Despite an initial significant increase at copper concentrations of 30 μg/L

ammonia excretion rate decreased when copper concentrations ≥60 μg/L. These results suggested that: (1) nauplius II could not develop to the cypris when the copper concentration ≥60 μg/L; (2) cypris settlement is more susceptible to copper than cypris mortality rate; (3) nauplius II is the most sensitive larval stage; (4) nauplius II ammonia excretion rate is the most sensitive index to copper and might be as the indicator for copper pollution monitoring.

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references

Bao W Y, Lee O O, Chung H C et al. 2010. Copper affects biofilm inductiveness to larval settlement of the serpulid polychaete Hydroides elegans (Haswell). Biofouling, 26(1): 119–128.

Blackmore G. 1998. An overview of trace metal pollution in the coastal waters of Hong Kong. Science of the Total Environment, 214(1): 21–48.

Burrows M T, Hawkins S J, Southward A J. 1999. Larval development of the intertidal barnacles Chthamalus stellatus and Chthamalus montagui. Journal of the Marine Biological Association of the UK, 79(01): 93–101.

Chai X J, Hu Z H, Xu J Z et al. 2009. Effect of salinity and pH on oxygen consumption rate and ammonia excretion rate in juvenile Nibea japonica. Journal of Zhejiang Ocean University (Natural Science), 28(2): 146–150. (in Chinese with English abstract)

Cheang C C, Tsang L M, Ng W C et al. 2012. Phylogeography of the cold-water barnacle Chthamalus challengeri in the north-western Pacific: effect of past population expansion and contemporary gene flow. Journal of Biogeography, 39(10): 1 819–1 835.

Desai D V, Anil A C. 2004. The impact of food type, temperature and starvation on larval development of Balanus Amphitrite Darwin (Cirripedia: Thoracica). Journal of Experimental Marine Biology and Ecology, 306(1): 113–137.

Donahue W H, Wang R T, Welch M et al. 1977. Effects of water-soluble components of petroleum oils and aromatic hydrocarbons on barnacle larvae. Environmental Pollution, 13(3): 187–202.

Feng D Q, KE C H, Lu C Y et al. 2008. Laboratory rearing and settlement behavior of Balanus albicostatus cyprid—an model animal for screening natural antifouling agents. Oceanologia et Limnologia Sinica, 39(4): 395–400. (in Chinese with English abstract)

Ferrando M D, Andreu E. 1993. Feeding behavior as an index of copper stress in Daphnia magna and Brachionus calyciflorus. Comparative Biochemistry and Physiology Part C: Pharmacology, Toxicology and Endocrinology, 106(2): 327–331.

Frost B W. 1972. Effects of size and concentration of food particles on the feeding behavior of the marine planktonic copepod Calanus pacificus. Limnol. Oceanogr., 17(6): 805–815.

Gaonkar C A, Anil A C. 2010. What do barnacle larvae feed on? Implications in biofouling ecology. Journal of the Marine Biological Association of the United Kingdom, 90(06): 1 241–1 247.

Gaonkar C A, Anil A C. 2012. Gut fluorescence analysis of barnacle larvae: an approach to quantify the ingested food. Estuarine, Coastal and Shelf Science, 111: 147–150.

Garnacho E, Peck L S, Tyler P A. 2000. Variations between winter and summer in the toxicity of copper to a population of the mysid Praunus flexuosus. Marine Biology, 137(4): 631–636.

King C K, Riddle M J. 2001. Effects of metal contaminants on the development of the common Antarctic sea urchin Sterechinus neumayeri and comparisons of sensitivity with tropical and temperate echinoids. Marine Ecology Progress Series, 215: 143–154.

Kitano Y, Nogata Y, Matsumura K et al. 2005. Design and synthesis of anti-barnacle active fluorescence-labeled probe compounds and direct observation of the target region in barnacle cypris larvae for dimethyl-isocyanoalkyl compounds. Tetrahedron, 61(42): 9 969–9 973.

Lang W H, Forward Jr R B, Miller D C et al. 1980. Acute toxicity and sublethal behavioral effects of copper on barnacle nauplii (Balanusimprovisus). Marine Biology, 58(2): 139–145.

Lee C. 1999. Larval development of Chthamalus challenger Hoek (Cirripedia: Thoracica: Chthamalidae) with keys to barnacle larvae of Korean coastal waters. Korean Journal of Biological Sciences, 3(1): 59–68.

Lewis A G, Cave W R. 1982. The biological importance of copper in oceans and estuaries. Oceanography and Marine Biology, 20: 471–695.

Li H, Miao S, Yan Y et al. 2011. Larval development of the barnacle, Microeuraphiawithersi (Cirripedia, Thoracica, Chthamalidae) reared in the laboratory. Crustaceana, 84(2): 129–152.

Li Z M, Liu Z G, Xie L et al. 2010. Effect of body weight and temperature on oxygen consumption and ammonia-n excretion rates of Chlamys nobilis. Oceanologia et Limnologia Sinica, 1: 015. (in Chinese with English abstract)

Liu S M, Zhu L Y, Xu F F et al. 2012. Effect of tetrabromobisphenol A on the ingestion, respiration and ammonia excretion of Calanus sinicus. Periodical of Ocean University of China, 42(12): 49–53. (in Chinese with English abstract)

Lorenzo J I, Nieto O, Beiras R. 2002. Effect of humic acids on speciation and toxicity of copper to Paracentrotus lividus larvae in seawater. Aquatic Toxicology, 58(1): 27–41.

Luo J, Liu C, Tang H et al. 2008. Effects of temperature on oxygen consumption rate and ammonia excretion rate of Hemifusus tuba (Gelin). Journal of Guangdong Ocean University, 1: 021. (in Chinese with English abstract)

Maki J S, Rittschof D, Costlow J D et al. 1988. Inhibition of attachment of larval barnacles, Balanus amphitrite, by bacterial surface films. Marine Biology, 97(2): 199–206.

Mao Y, Zhou Y, Yang H et al. 2006. Seasonal variation in metabolism of cultured Pacific oyster, Crassostrea gigas, in Sanggou Bay, China. Aquaculture, 253(1): 322–333.

McCoy D L, Brown K M. 1998. Hydrocarbon pollutants alter short-term recruitment in the barnacle Balanus eburneus. Marine Environmental Research, 45(3): 209–224.

Mora S, Fowler S W, Wyse E et al. 2004. Distribution of heavy metals in marine bivalves, fish and coastal sediments in the Gulf and Gulf of Oman. Marine Pollution Bulletin, 49(5): 410–424.

Newman W A, Abbott D P. 1980. Cirripedia: the Barnacles. Intertidal Invertebrates of California. Stanford University Press, Stanford. p.504–535.

Omae I. 2003. General aspects of tin-free antifouling paints. Chemical Reviews, 103(9): 3 431–3 448.

Pineda J, DiBacco C, Starczak V R. 2005. Barnacle larvae in ice: survival, reproduction, and time to post settlement metamorphosis. Limnology and Oceanography, 50: 1 520–1 528.

Pipe R K, Coles J A, Carissan F M M et al. 1999. Copper induced immunomodulation in the marine mussel, Mytilusedulis. Aquatic Toxicology, 46(1): 43–54.

Qiu J W, Qian P Y. 1997. Effects of food availability, larval source and culture method on larval development of Balanusamphitrite Amphitrite Darwin: implications for experimental design. Journal of Experimental Marine Biology and Ecology, 217(1): 47–61.

Qiu J W, Thiyagarajan V, Cheung S et al. 2005. Toxic effects of copper on larval development of the barnacle Balanus Amphitrite. Marine Pollution Bulletin, 51(8): 688–693.

Semmler H, Høeg J T, Scholtz G et al. 2009. Three-dimensional reconstruction of the naupliar musculature and a scanning electron microscopy atlas of nauplius development of Balanus improvises (Crustacea: Cirripedia: Thoracica). Arthropod Structure & Development, 38(2): 135–145.

Shariff M, Jayawardena P, Yusoff F M et al. 2001. Immunological parameters of Javanese carp Puntius gonionotus (Bleeker) exposed to copper and challenged with Aeromona shydrophila. Fish & Shellfish Immunology, 11(4): 281–291.

Srinivasan M, Swain G W. 2007. Managing the use of copperbased antifouling paints. Environmental Management, 39(3): 423–441.

Stebbing A R D. 2002. Tolerance and hormesis-increased resistance to copper in hydroids linked to hormesis. Marine Environmental Research, 54(3): 805–809.

Tang B, Yan W, Wang H et al. 2010. Effects of salinity on oxygen consumption and ammonia-N excretion rate of different-size of Trachycardium flavum. Marine Fisheries, 1: 004. (in Chinese with English abstract)

Tie D, Liu G C, Liu X J et al. 2010. Influence of environmental temperature on vital status of barnacle: Chthamalus challengeri. Marine Environmental Science, 29(2): 191–195. (in Chinese with English abstract)

Tunnicliffe V. 1991. The biology of hydrothermal vents—ecology and evolution. Oceanography and Marine Biology, 29: 319–407.

Turner J T, Levinsen H, Nielsen T G et al. 2001. Zooplankton feeding ecology: grazing on phytoplankton and predation on protozoans by copepod and barnacle nauplii in Disko Bay, West Greenland. Marine Ecology Progress Series, 221: 209–219.

Voulvoulis N, Scrimshaw M D, Lester J N. 1999. Alternative antifouling biocides. Applied Organometallic Chemistry, 13(3): 135–143.

White S L, Rainbow P S. 1985. On the metabolic requirements for copper and zinc in molluscs and crustaceans. Marine Environmental Research, 16(3): 215–229.

Wu W G, Zhang J X, Fang J G et al. 2013. Effects of salinity on oxygen consumption and ammonia excretion rate of different sizes of Bullacta exarata. Chinese Journal of Ecology, 32(9): 2 457–2 461. (in Chinese with English abstract)

Wu Y, Yuan L, Huang J. 2004. Comparison of phototaxis index with acute toxicity test (LC 50) using Daphnia carinata. Acta Scientiae Circumstantiae, 24(5): 905–909. (in Chinese with English abstract)

Xie Z C, Wong N C, Qian P Y et al. 2005. Responses of polychaete Hydroides elegans life stages to copper stress. Marine Ecology Progress Series, 285: 89–96.

Yan Y, Chan B K K. 2004. Larval morphology of a recently recognized barnacle, Chthamalus neglectus (Cirripedia: Thoracica: Chthamalidae), from Hong Kong. Journal of Crustacean Biology, 24(4): 519–528.

Yin L Y, Gao Y L, Yang Z C et al. 2013. Effects of body size on respiration and excretion of Hong Kong oyster Crassostrea hongkongensis. Journal of Tropical Oceanography, 32(1): 60–63. (in Chinese with English abstract)

Yuan L, Michels E, De M L. 2003. Changes in phototactic behavior of Daphnia magna clone C1 242 in response to copper, cadmium and pentachlorophenol. Journal of Environmental Sciences, 15(6): 841–847.

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