ELEMENTAL COMPOSITION OF GONADS, GAMETES AND LARVAE IN THE BLACK AND BROWN MORPHS OF THE BIVALVE MOLLUSK MYTILUS GALLOPROVINCIALIS LAM.
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Keywords

mussel Mytilus galloprovincialis
morphs
gonads
sperm
eggs
larvae
trace elements
bulk structural elements
Black Sea

Abstract

Concentrations of the bulk and trace elements were determined in male and female gonads, gametes (sperm and eggs), and larvae (trochophores) of black and brown morphs of the Mediterranean mussel Mytilus galloprovincialis using energy dispersive X-ray spectroscopy and inductively coupled plasma mass spectrometry. The mollusks were collected in spring 2019 on a mussel-and-oyster farm (Black Sea, Crimea, Sevastopol, Karantinnaya Bay). In the male and female gonads of black and brown morphs, no statistically significant differences were detected in concentrations of the bulk structural elements (C, N, O, P, S), while in gametes and trochophores, these differences were significant. Trace elemental analysis revealed that in the female gonads of both black and brown morphs, Cu, Fe, and As were dominant, however in brown morphs, concentrations of these elements were significantly lower than in black mussels. Zn and Se concentrations in the gonads of black morphs were significantly higher than in brown mussels. Most of the statistically significant differences were found between trochophores and eggs of black vs. brown morphs. These data show that the two M. galloprovincialis morphs differ in their elemental composition.

https://doi.org/10.31857/S004445292106005X
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References

Rainbow PS (2002) Trace metal concentrations in aquatic invertebrates: why and so what? Environmental Pollution 120(3):497–507. https://doi.org/10.1016/S0269–7491(02)00238–5

Casas S, Gonzalez JL, Andral B, Cossa D (2008) Relation between metal concentration in water and metal content of marine mussels (Mytilus galloprovincialis): impact of physiology. Environmental Toxicology and Chemistry (ET&C) 27(7):1543–1552. https://doi.org/10.1897/07–418

Varotto L, Domeneghetti S, Rosani U, Manfrin C, Cajaraville MP, Raccanelli S, Pallavicini A, Venier P (2013) DNA damage and transcriptional changes in the gills of Mytilus galloprovincialis exposed to nanomolar doses of combined metal salts (Cd, Cu, Hg). PLOS One 8(1):e54602. https://doi.org/10.1371/journal.pone.0054602

Bezuidenhout J, Dames N, Botha A, Frontasyeva MV, Goryainova ZI, Pavlov D (2015) Trace elements in mediterranean mussels Mytilus galloprovincialis from the South African West coast. Ecological Chemistry and Engineering Society 22(4):489–498. https://doi.org/ 10.1515/eces–2015–0028

Fengjie Liu, Wen-Xiong Wang (2015) Linking trace element variations with macronutrients and major cations in marine mussels Mytilus edulis and Perna viridis. Environmental Toxicology and Chemistry 34(9):2041–2050. https://doi.org/10.1002/etc.3027

Richir J, Gobert S (2014) The effect of size, weight, body compartment, sex and reproductive status on the bioaccumulation of 19 trace elements in rope–grown Mytilus galloprovincialis. Ecological Indicators 36:33–47. https://doi.org/10.1016/j.ecolind.2013.06.021

Chelyadina NS (2018) Phenotypic and sexual structure of Mytilus galloprovincialis Lam., cultivated on the mussel-oyster farm in the outer harbor of Sevastopol city (Crimea, Black Sea). Marine Biological Journal 3(3):86–93. https://doi.org/10.21072/mbj.2018.03.3.09

Nikonova LL, Nekhoroshev MV, Ryabushko VI (2017) Total testosterone and estradiol in the gonads and gametes of the mussel Mytilus galloprovincialis Lam. Journal of Evolutionary Biochemistry and Physiology 53(6):519–522. https://doi.org/10.1134/S0022093017060114

Kapranov SV, Karavantseva NV, Bobko NI, Ryabushko VI, Kapranova LL (2021) Sex- and sexual maturation-related aspects of the element accumulation in soft tissues of the bivalve Mytilus galloprovincialis Lam. collected off coasts of Sevastopol (southwestern Crimea, Black Sea). Environmental Science and Pollution Research 28(17):21553–21576. https://doi.org/10.1007/s11356–020–12024–z

Kapranova LL, Malakhova LV, Nekhoroshev M, Lobko VV, Ryabushko VI (2020) Fatty acid composition in trochophores of mussel Mytilus galloprovincialis grown under contamination with polychlorinated biphenyls. Marine Biological Journal 5(2):38–49. https://doi.org/ 10.21072/mbj.2020.05.2.04

Kapranova LL, Nekhoroshev MV, Malakhova LV, Ryabushko VI, Kapranov SV, Kuznetsova TV (2019) Fatty acid composition of gonads and gametes in the black sea bivalve mollusk Mytilus galloprovincialis Lam. at different stages of sexual maturation. Journal of Evolutionary Biochemistry and Physiology 55(6):448–455. https://doi.org/10.1134/S0022093019060024

Welborn JR, Manahan DT (1995) Taurine metabolism in larvae of marine molluscs (Bivalvia, Gastropoda). Journal of Experimental Biology 198:1791–1799

Allen K, Awapara J (1960) Metabolism of sulfur amino acids in Mytilus edulis and Rangia cuneata. Biology Bulletin 118:173–182

Ducháteau G, Sarlet H, Camien MN, Florkin M (1952) Acides amines non protéiniques des tissus chez les Mollusques Lamellibranches et chez les Vers. Comparaison des formes marines et des formes dulcicoles. Archives Internationales de Physiologie 60(1):124–125. https://doi.org/10.3109/13813455209145044

Slynko YuV, Kulikova AD, Slynko E, Soldatov AA (2018) Genetic changeability by loci COI mtDNA for different coloring of shell phenotypes of black sea mussel Mytilus galloprovincialis Lam. Russian Journal of Genetics 54(8):944–949. https://doi.org/ 10.1134/S1022795418080112

Bonnard M, Cantel S, Boury B, Parrot I (2020) Chemical evidence of rare porphyrins in purple shells of Crassostrea gigas oyster. Scientific Reports 10:12150. https://doi.org/10.1038/s41598–020–69133–5

Kulikova AD, Soldatov AA, Andreenko TI (2015) The activity of transaminases in the tissues of the Black-Sea mollusk Mytilus galloprovincialis. Journal of Evolutionary Biochemistry and Physiology 51(1):23–31. https://doi.org/10.1134/S0022093015010044

Kulikova AD, Andreenko TI, Soldatov AA (2015) Activity of aldolase in tissues of Mytilus galloprovincialis with different shells color. Hydrobiological Journal 51(6):53–59. https://doi.org/10.1615/HydrobJ.v51.i6

Shcherban SA, Melnik AV (2020) Size and Age Characteristics and Phenotypic Peculiarities of Somatic Growth of the Black Sea Mollusk Flexopecten glaber ponticus (Bivalvia, Pectinidae). Biology Bulletin 47(8):920–929. https://doi.org/ 10.1134/S1062359020080129

Fisher NS, Teyssié JL, Fowler SW, Wang WX (1996) Accumulation and retention of metals in mussels from food and water: a comparison under field and laboratory conditions. Environmental Science & Technology (ES&T) 30(11):3232–3242. https://doi.org/10.1021/es960009u

Wang W-X, Fisher NS (1997) Modeling the influence of body size on trace element accumulation in the mussel Mytilus edulis. Marine Ecology Progress Series 161:103–115. https://doi.org/10.3354/meps161103

Ahsan U, Kamran Z, Raza I, Ahmad S, Babar W, Riaz MH, Iqbalb Z (2014) Role of selenium in male reproduction — A review. Animal Reproduction Science 146(1–2):55–62. https://doi.org/10.1016/j.anireprosci.2014.01.009

Mehdi Y, Hornick J-L, Istasse L, Dufrasne I (2013) Selenium in the environment, metabolism and involvement in body function. Molecules 18:3292–3311. https://doi.org/10.3390/molecules18033292

Lee BG, Lee JS, Luoma SN (2006) Comparison of selenium bioaccumulation in the clams Corbicula fluminea and Potamocorbula amurensis: a bioenergetic modeling approach. Environmental Toxicology and Chemistry 5:1933–1940. https://doi.org/10.1897/05–540R.1

Seeler JF, Ajay S, Zaluzec NJ, Bleher R, Lai B, Schultz EG, Hoffman BM, LaBonne C, Woodruff TK, O’Halloran TV (2021) Metal ion fluxes controlling amphibian fertilization. Nature Chemistry 13:683–691. https://doi.org/10.1038/s41557–021–00705–2

Keith AM, Huang C-C, Carol A (2000) Function and mechanism of zinc metalloenzymes. The Journal of Nutrition 130(5):1437S–1446S. https://doi.org/10.1093/jn/130.5.1437S