Morphological and molecular analysis of the freshwater bivalve Anodonta anatina in Iran and Finland
Downloads
Duck mussel, Anodonta anatina is a habitat generalist inhabiting both lentic and lotic aquatic ecosystems. Due to high morphological similarity and phenotypic plasticity, A. anatina has sometimes been misidentified as A. cygnea. Here, morphological and molecular studies were conducted on Anodonta mussels inhabiting North Iran and Finland. The individuals were collected from Anzali Wetland, Tajan River (North Iran) and Jyväsjärvi Lake (Finland). The COI sequence analysis showed the existence of A. anatina in the sampling areas. The Iranian and Finland specimens showed three and two haplotypes, respectively. The Iranian haplotypes were placed in a single clade, while the Finland haplotypes were clustered with those of Central Europe. The mean P-distance between these two clades was 2.4. The median-joining network showed that the Iranian haplotypes were lumped into a single haplogroup, while the Finland ones were in the same haplogroup as those from Central Europe. The Mediterranean haplotypes were the most divergent haplogroup from both Iranian and Central European haplogroups. In morphological characteristics, the shell pattern of all individuals from both Iranian and Finland specimens was stretched and slightly compact with light/dark brown periostracum. The mean length of the specimens from Anzali Wetland was significantly higher than those of Tajan and Jyväsjärvi. No significant difference was observed in morphometric characteristics between Tajan and Jyväsjärvi populations. The results did not indicate significant variation in shell morphology in the studied groups. In this regard, the conventional linear measurements can be supplemented using more complex geometric morphology in further studies.
Downloads
Akaike H. (1973). Information theory and an extension of the maximum likelihood principle. In: B.N. Petrov, F. Csáki (Ed.). Second International Symposium on Information Theory. Akadémiai Kiadó, Budapest. pp: 267-281.
Alyakrinskaya I.O. (2005). Functional significance and weight properties of the shell in some mollusks. Biology Bulletin, 32(4): 397-418.
Araujo R., Reis J., Machordom A., Toledo C., Madeira M.J., Gómez I., Velasco J.C., Morales J., Barea J.M., Ondina P., Ayala I. (2009). The naiades of the Iberian Peninsula. Iberus, 27(2): 7-72.
Araujo R., Buckley D., Nagel K.O., Machordom A. (2017). Potomida littoralis (Bivalvia, Unionidae) evolutionary history: Slow evolution or recent speciation? Zoological Journal of Linnean Society, 179(2): 277-290.
Bespalaya Y.V., Bolotov I.N., Aksenova O.V., Gofarov M.Y., Kondakov A.V., Vikhrev I.V., Vinarski M.V. (2018). DNA barcoding reveals invasion of two cryptic Sinanodonta mussel species (Bivalvia: Unionidae) into the largest Siberian river. Limnologica, 69: 94-102.
Bolotov I.N., Bespalaya Y.V., Gofarov M.Y., Kondakov A.V., Konopleva E.S., Vikhrev I.V. (2016). Spreading of the Chinese pond mussel, Sinanodonta woodiana, across Wallacea: One or more lineages invade tropical islands and Europe. Biochemical Systematics and Ecology, 67: 58-64.
Bontes B.M., Verschoor A.M., Dionisio Pires L.M., van Donk E., Ibelings B.W. (2007). Functional response of Anodonta anatina feeding on a green alga and four strains of cyanobacteria, differing in shape, size and toxicity. Hydrobiologia, 584: 191-204.
Ferreira-Rodríguez N., Akiyama Y.B., Aksenova O.V., Araujo R., Barnhart M.C., Bespalaya Y.V., Bogan A.E., Bolotov I.N., Budha P.B., Clavijo C., Clearwater S.J., Darrigran G., Do V.T., Douda K., Froufe E., Gumpinger C., Henrikson L., Humphrey C.L., Johnson N.A., Klishko O., Klunzinger M.W., Kovitvadhi S., Kovitvadhi U., Lajtner J., Lopes-Lima M., Moorkens E.A., Nagayama S., Nagel K.O., Nakano M., Negishi J.N., Ondina P., Oulasvirta P., Prié V., Riccardi N., Rudz?te M., Sheldon F., Sousa R., Strayer D.L., Takeuchi M., Taskinen J., Teixeira A., Tiemann J.S., Urba?ska M., Varandas S., Vinarski M.V., Wicklow B.J., Tadeusz Zaj?c T., Vaughn C.C. (2019). Research priorities for freshwater mussel conservation assessment. Biological Conservation, 231: 77-87.
Froufe E., Sobral C., Teixeira A., Sousa R., Varandas S., Aldridge D., Lopes-Lima M. (2014). Genetic diversity of the pan-European freshwater mussel Anodonta anatina (Bivalvia: Unionoida) based on CO1: new phylogenetic insights and implications for conservation. Aquatic Conservation: Marine and Freshwater Ecosystems, 24(4): 561-574.
Ghozzi K., Dhiab R.B., Challouf R., Bradai M.N. (2022). Morphometric Variation among Four Local Ruditapes decussatus Populations in Monastir Bay (Eastern Coast, Tunisia). Brazilian Archives of Biology and Technology, 65: e2221023.
Girgibo N. (2013). Morphological variation of the Unionidae mussel Anodonta anatina. M.Sc. thesis, Department of Biological and Environmental Science, University of Jyväskylä. 35 p.
Gopko M., Mironova E., Pasternak A., Mikheev V., Taskinen J. (2017). Freshwater mussels (Anodonta anatina) reduce transmission of a common fish trematode (eye fluke, Diplostomum pseudo-spathaceum). Parasitology, 144(14): 1971-1979.
Graf D.L. (1998). Freshwater pearly mussels: Pigtoes and Ortmann's Law. American Conchologist, 26(2): 20-21.
Graf D.L. (2007). Palearctic freshwater mussel (Mollusca: Bivalvia: Unionoida) diversity and the comparatory method as a species concept. Proceedings of the Academy of Natural Sciences of Philadelphia, 156(1): 71-88.
Graf D., Cummings K. (2019). The MUSSEL Project Database. Available from: http://musselproject.uwsp. edu/db/.
Guerra D., Lopes-Lima M., Froufe E., Gan H.M., Ondina P., Amaro R., Klunzinger M.W., Callil C., Prié V., Bogan A.E., Stewart D.T., BretonS. (2019). Variability of mitochondrial ORFans hints at possible differences in the system of doubly uniparental inheritance of mitochondria among families of freshwater mussels (Bivalvia: Unionida) .BMC Evolutionary Biology, 19(1): 229.
Haas F. (1969). Superfamilia Unionacea. In: R. Martens, W. Hennig (Ed.). Das Tierreich. Walter de Gruyter, Berlin. 663 p.
Hall T.A. (1999). BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series, 41: 95e98.
Hajisafarali M., Aaltonen S., Pulkkinen K., Taskinen J. (2022). Does the freshwater mussel Anodonta anatina remove the fish pathogen Flavobacterium columnare from water? Hydrobiologia, 849(4): 1067-1081.
Hinzmann M., Lopes-Lima M., Teixeira A., Varandas S., Sousa R., Lopes A., Froufe E., Machado J. (2013). Sexual strategy and reproductive cycle of Anodonta anatina (L., 1758): notes on hermaphroditism. Journal of Experimental Zoology Part A, 309(7): 378-390.
Hornbach D.J., Kurth V.J., Hove M.C. (2010). Variation in freshwater mussel shell sculpture and shape along a river gradient. The American Midland Naturalist, 164(1): 22-36.
Huelsenbeck J.P., Ronquist F. (2001). MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics, 17(8): 754-755.
Inoue K., Hayes D.M., Harris J.L., Christian A.D. (2013). Phylogenetic and morphometric analyses reveal ecophenotypic plasticity in freshwater mussels Obovaria jacksoniana and Villosa arkansasensis (Bivalvia: Unionidae). Ecology and Evolution, 3(8): 2670-2683.
Klishko O.K., Lopes-Lima M., Bogan A.E., Matafonov D.V., Froufe E. (2018). Morphological and molecular analyses of Anodontinae species (Bivalvia, Unionidae) of Lake Baikal and Transbaikalia. PLoS One, 13(4): e0194944.
Kondakov A.V., Konopleva E.S., Vikhrev I.V., Bespalaya Y.V., Gofarov M.Y., Kabakov M.B., Tomilova A.A., Vinarski M.V., Bolotov I.N. (2020). Phylogeographic affinities, distribution and population status of the non-native Asian pond mussels Sinanodonta lauta and S. woodiana in Kazakhstan. Ecologica Montenegrina, 27: 22-34.
Leigh J.W., Bryant D. (2015). PopART: Full-feature software for haplotype network construction. Methods in Ecology and Evolution, 6 (9): 1110-1116.
Lopes-Lima M., Froufe E., Do Tu V., Ghamizi M., Mock K.E., Kebapçi Ü., Klishko O., Kovitvadhi S., Kovitvadhi U., Paulo O.S., Pfeiffer J.M., Raley M., Riccardi N., ?erefli?an H., Sousa R., Teixeira A., Varandas S., Wu X., Zanatta D.T., Zieritz A., Bogan A.E. (2017). Phylogeny of most species-rich freshwater bivalve family (Bivalvia: Unionida: Unionidae): defining modern subfamilies and tribes. Molecular Phylogenetics and Evolution, 106: 174-191.
Lopes-Lima M., Burlakova L.E., Karatayev A.Y., Mehler K., Seddon M., Sousa R. (2018). Conservation of freshwater bivalves at the global scale: diversity, threats and research needs. Hydrobiologia, 810(1): 1-14.
Mirzoeva A.T., Demchenko N.A. (2022). Morphological response of lagoon cockle Cerastoderma glaucum (Poiret, 1789) to eutrophication in the Sea of Azov. IOP Conference Series: Earth and Environmental Science, 1049(1): 012059.
Minton R.L., Norwood A.P., Hayes D.M. (2008). Quantifying phenotypic gradients in freshwater snails: a case study in Lithasia (Gastropoda: Pleuroceridae) Hydrobiologia, 605(1): 173-182.
Modestin E. (2017). Morphological variations of the shell of the bivalve Lucina pectinata (Gmelin, 1791). Journal of Advances in Biology, 10(2): 2092-2107.
Modesto V., Ilarri M., Souza A.T., Lopes-Lima M., Douda K., Clavero M., Sousa R. (2018). Fish and mussels: Importance of fish for freshwater mussel conservation. Fish and Fisheries, 19 (2): 244-259.
Morais P., Rufino M.M., Reis J., Dias E., Sousa R. (2014). Assessing the morphological variability of Unio delphinus Spengler, 1783 (Bivalvia: Unionidae) using geometric morphometry. Journal of Molluscan Studies, 80(1): 17-23.
Nagel K.O., Badino O., Alessandria B. (1996). Population genetics of European Anodontinae (Bivalvia: Unionidae). Journal of Molluscan Studies, 62(3): 43-357.
Posada D., Crandall K.A. (1998). Modeltest: testing the model of DNA substitution. Bioinformatics, 14(9): 817-818.
Rambaut A. (2008). FigTree v1.1.1: Tree figure drawing tool. Available from: http://tree.bio.ed.ac.uk/ software/.
Riccardi N., Froufe E., Bogan A.E., Zieritz A., Teixeria, A., Vanetti I., Varandas S., Zaccara S., Nagel K., Lopes-Lima M. (2019). Phylogeny of European Anodontini (Bivalvia: Unionidae) with a redescription of Anodonta exulcerata. Zoological Journal of the Linnean Society, 189(3): 745-761.
Sambrook J., Fritschi E.F., Maniatis T. (1989). Molecular cloning: a laboratory manual. USA: Cold Spring Harbor Laboratory Press. New York. 1659 p.
Selin N.I. (2007). Shell form, growth and life span of Astarte arctica and A. borealis (Mollusca: Bivalvia) from the subtidal zone of northeastern Sakhalin. Russian Journal of Marine Biology, 33(4): 232-237.
Swofford D.L. (2003). PAUP: Phylogenetic analysis using parsimony (and other methods), Version 4. Sunderland: Sinauer Associates.
Tamura K., Stecher G., Peterson D., Filipski A., Kumar S. (2013). MEGA6: molecular evolutionary genetics analysis version 6.0. Molecular Biology and Evolution, 30(12): 2725-2729.
Tomilova A.A., Lyubas A., Kondakov A.V., Vikhrev I.V., Gofarov M.Y., Kolosova Y.S., Vinarski M.V., Palatov D.M., Bolotov I.N. (2020). Evidence for Plio-Pleistocene Duck Mussel Refugia in the Azov Sea River Basins. Diversity, 12(118): 1-13.
Vaghun C.C. (2010). Biodiversity losses and ecosystem function in freshwaters: Emerging conclusions and research directions. Bioscience, 60(1): 25-35.
Vaughn C.C. (2018). Ecosystem services provided by freshwater mussels Hydrobiologia, 810(1): 15-27.
Villesen P. (2007). FaBox: an online toolbox for matrix choice. Nucleic Acids Research, 22: 4673-4680.
Walker J.M., Curole J.P., Wade D.E., Chapman E.C., Bogan A., Watters G., Hoeh W.R. (2006). Taxonomic distribution and phylogenetic utility of gender-associated mitochondrial genomes in the Unionoida (Bivalvia). Malacologia, 48(1/2): 265-282.
Walker J.M., Bogan A.E., Bonfiglio E.A., Campbell D.C., Christian A.D., Curole J.P., Harris J.L., Wojtecki R.J., Hoeh W.R. (2007). Primers for amplifying the hypervariable, male-transmitted COII-COI junction region in amblemine freshwater mussels (Bivalvia: Unionoidea: Ambleminae). Molecular Ecology Notes, 7 (3): 489-491.
Williams J.D., Bogan A.E., Butler R.S., Cummings K.S., Garner J.T., Harris J.L., Johnson N.A., Watters G.T. (2017). A revised list of the freshwater mussels (Mollusca: Bivalvia: Unionida) of the United States and Canada. Freshwater Mollusk Biology and Conservation, 20(2): 35-58.
Wu R., Liu X., Guo L., Zhou, C., Ouyang S., Wu X. (2022). DNA barcoding, multilocus phylogeny, and morphometry reveal phenotypic plasticity in the Chinese freshwater mussel Lamprotula caveata (Bivalvia: Unionidae). Ecology and Evolution, 12(7): e9035.
Zieritz A., Aldridge D.C. (2009). Identification of ecophenotypic trends within three European freshwater mussel species (Bivalvia: Unionoida) using traditional and modern morphometric techniques. Biological Journal of the Linnean Society, 98(4): 814-825.
Zieritz A., Hoffman J.I., Amos W., Aldridge D.C. (2010). Phenotypic plasticity and genetic isolation-by-distance in the freshwater mussel Unio pictorum (Mollusca: Unionidae). Evolutionary Ecology, 24(4): 923-938.
Zieritz A., Froufe E., Bolotov I., Gonçalves D.V., Aldridge D.C., Bogan A.E., Gan H.M., Gomes-Dos-Santos A., Sousa R., Teixeira A., Varandas S., Zanatta D., Lopes-Lima M. (2020). Mitogenomic phylogeny and fossil-calibrated mutation rates for all F- and M-type mtDNA genes of the largest freshwater mussel family, the Unionidae (Bivalvia). Zoological Journal of Linnean Society, 193(3): 1088-1107.
Copyright (c) 2022 International Journal of Aquatic Biology
This work is licensed under a Creative Commons Attribution 4.0 International License.