M. Zuykov, E. Pelletier, and D. Harper, Bivalve mollusks in metal pollution studies: From bioaccumulation to biomonitoring, Chemosphere, vol.93, issue.2, pp.201-208, 2013.
DOI : 10.1016/j.chemosphere.2013.05.001

P. Leung, J. Ip, S. Mak, J. Qiu, P. Lam et al., De novo transcriptome analysis of Perna viridis highlights tissue-specific patterns for environmental studies, BMC Genomics, vol.15, issue.1, p.25239240, 2014.
DOI : 10.1007/s00244-012-9868-y

A. Bouetard, C. Noirot, A. Besnard, O. Bouchez, D. Choisne et al., Pyrosequencing-based transcriptomic resources in the pond snail Lymnaea stagnalis, with a focus on genes involved in molecular response to diquat-induced stress, Ecotoxicology, vol.28, issue.8, pp.2222-2234, 2012.
DOI : 10.1007/s10646-012-0977-1

URL : https://hal.archives-ouvertes.fr/hal-01210141

M. Notten, A. Oosthoek, J. Rozema, and R. Aerts, Heavy metal pollution affects consumption and reproduction of the landsnail Cepaea nemoralis fed on naturally polluted Urtica dioica leaves, Ecotoxicology, vol.7, issue.3, pp.295-304, 2006.
DOI : 10.1007/s10646-006-0059-3

K. Webb, C. Craft, and E. Elswick, The Evaluation of the Freshwater Western Pearl Mussel, Margaritifera falcata (Gould, 1850), as a Bioindicator Through the Analysis of Metal Partitioning and Bioaccumulation, Northwest Science, vol.82, issue.3, pp.163-173, 2008.
DOI : 10.3955/0029-344X-82.3.163

M. Young, P. Cosgrove, L. Hastie, G. Bauer, and K. Wachtler, The Extent of, and Causes for, the Decline of a Highly Threatened Naiad: Margaritifera margaritifera, In Ecological Studies, vol.145, pp.337-357, 2001.
DOI : 10.1007/978-3-642-56869-5_19

H. Frank and S. Gerstmann, Declining populations of freshwater pearl mussels (Margaritifera margaritifera) are burdened with heavy metals and DDT/DDE, Ambio, vol.36, pp.571-574, 2007.

K. Walsh, R. Dunstan, and R. Murdoch, Differential bioaccumulation of heavy metals and organopollutants in the soft tissue and shell of the marine Gastropod, Austrocochlea constricta, Archives of Environmental Contamination and Toxicology, vol.9, issue.1, pp.35-39, 1995.
DOI : 10.1007/BF00213966

X. Puente, R. Villares, E. Carral, and A. Carballeira, Nacreous shell of Mytilus galloprovincialis as a biomonitor of heavy metal pollution in Galiza (NW Spain), Science of The Total Environment, vol.183, issue.3, pp.205-211, 1996.
DOI : 10.1016/0048-9697(96)05066-8

A. Jaouen, C. Galap, C. Minier, R. Tutundjian, and F. Leboulenger, Bioaccumulation of pollutants and measures of biomarkers in the Zebra mussel (Dreissena polymorpha) from downstream river Seine, Bull Soc Zool France, vol.125, pp.239-249, 2000.

P. Muller, D. Geary, and I. Magyar, The endemic molluscs of the Late Miocene Lake Pannon: their origin, evolution, and family-level taxonomy, Lethaia, vol.42, issue.Supplement, pp.47-60, 1999.
DOI : 10.1111/j.1502-3931.1999.tb00580.x

M. Harzhauser and O. Mandic, Neogene dreissenids in Central Europe: evolutionary shifts and diversity changes. Chapter 2 The zebra mussel in Europe, pp.11-28, 2010.

D. Minchin, F. Lucy, and M. Sullivan, Zebra Mussel: Impacts and Spread, Aquatic Invasive Species of Europe. Distribution, Impacts and Management. Netherlands, pp.135-146, 2002.
DOI : 10.1007/978-94-015-9956-6_15

R. Bias and L. Karbe, Bioaccumulation and Partitioning of Cadmium within the Freshwater MusselDreissena polymorpha Pallas, Internationale Revue der gesamten Hydrobiologie und Hydrographie, vol.261, issue.1, pp.113-125, 1985.
DOI : 10.1002/iroh.19850700110

A. Hendriks, H. Pieters, and J. De-boer, Accumulation of metals, polycyclic (halogenated) aromatic hydrocarbons, and biocides in zebra mussel and eel from the rhine and meuse rivers, Environmental Toxicology and Chemistry, vol.22, issue.10, pp.1885-1898, 1998.
DOI : 10.1002/etc.5620171001

M. Garaud, J. Trapp, S. Devin, C. Cossu-leguille, S. Pain-devin et al., Multibiomarker assessment of cerium dioxide nanoparticle (nCeO2) sublethal effects on two freshwater invertebrates, Dreissena polymorpha and Gammarus roeseli, Aquatic Toxicology, vol.158, pp.63-74, 2015.
DOI : 10.1016/j.aquatox.2014.11.004

URL : https://hal.archives-ouvertes.fr/hal-01159543

H. Reeders, A. De-vaate, and F. Slim, The fitration rate of Dreissena polymorpha (Bivalvia) in three Dutch lakes with reference to biological water quality management, Freshwater Biology, vol.1, issue.1, pp.133-141, 1989.
DOI : 10.1007/BF00345709

H. Reeders and A. De-vaate, Zebra mussels (Dreissena polymorpha): a new perspective for water quality management, Hydrobiologia, vol.200201, pp.437-450, 1990.

B. Marie, C. Joubert, A. Tayale, I. Zanella-cleon, C. Belliard et al., Different secretory repertoires control the biomineralization processes of prism and nacre deposition of the pearl oyster shell, Proceedings of the National Academy of Sciences, vol.109, issue.51, pp.20986-20991, 2012.
DOI : 10.1073/pnas.1210552109

URL : https://hal.archives-ouvertes.fr/hal-00786507

Y. Shi, C. Yu, Z. Gu, X. Zhan, Y. Wang et al., Characterization of the Pearl Oyster (Pinctada martensii) Mantle Transcriptome Unravels Biomineralization Genes, Marine Biotechnology, vol.8, issue.2, pp.175-187, 2013.
DOI : 10.1007/s10126-012-9476-x

K. Mann, E. Edsinger-gonzales, and M. Mann, In-depth proteomic analysis of a mollusc shell: acid-soluble and acid-insoluble matrix of the limpet Lottia gigantea, Proteome Science, vol.10, issue.1, p.22540284, 2012.
DOI : 10.1016/0014-5793(88)80054-1

G. Zhang, X. Fang, X. Guo, L. Li, R. Luo et al., The oyster genome reveals stress adaptation and complexity of shell formation, Nature, vol.10, issue.7418, pp.49-54, 2012.
DOI : 10.1038/nature11413

F. Marin, G. Luquet, M. B. Medakovic, and D. , Molluscan Shell Proteins: Primary Structure, Origin, and Evolution, Curr Top Dev Biol, vol.80, pp.209-276, 2008.
DOI : 10.1016/S0070-2153(07)80006-8

URL : https://hal.archives-ouvertes.fr/hal-00197133

R. Bettencourt, M. Pinheiro, C. Egas, P. Gomes, M. Afonso et al., High-throughput sequencing and analysis of the gill tissue transcriptome from the deep-sea hydrothermal vent mussel Bathymodiolus azoricus, BMC Genomics, vol.11, issue.1, p.20937131, 2010.
DOI : 10.1186/1471-2164-11-559

D. Niu, L. Wang, F. Sun, Z. Liu, and J. Li, Development of Molecular Resources for an Intertidal Clam, Sinonovacula constricta, Using 454 Transcriptome Sequencing, PLoS ONE, vol.6, issue.353, p.23935831, 2013.
DOI : 10.1371/journal.pone.0067456.s002

S. Artigaud, M. Thorne, J. Richard, R. Lavaud, F. Jean et al., Deep sequencing of the mantle transcriptome of the great scallop Pecten maximus, Marine Genomics, vol.15, p.24731930, 2014.
DOI : 10.1016/j.margen.2014.03.006

URL : https://hal.archives-ouvertes.fr/hal-01022918

F. Marin, L. Roy, N. , and M. B. , The formation and mineralization of mollusk shell, Frontiers in Bioscience, vol.4, issue.3, pp.1099-1125, 2012.
DOI : 10.2741/s321

URL : https://hal.archives-ouvertes.fr/hal-00657792

R. Devol, C. Sun, M. Marcus, S. Coppersmith, S. Myneni et al., Nanoscale Transforming Mineral Phases in Fresh Nacre, Journal of the American Chemical Society, vol.137, issue.41, pp.13325-13333, 2015.
DOI : 10.1021/jacs.5b07931

G. Moura, L. Vilarinho, and J. Machado, The action of Cd, Cu, Cr, Zn, and Pb on fluid composition of Anodonta cygnea (L.): organic components, Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, vol.127, issue.1, pp.105-112, 2000.
DOI : 10.1016/S0305-0491(00)00241-8

A. Poustka, A. Kuhn, D. Groth, V. Weise, S. Yaguchi et al., A global view of gene expression in lithium and zinc treated sea urchin embryos: new components of gene regulatory networks, Genome Biology, vol.8, issue.5, pp.85-17506889, 2007.
DOI : 10.1186/gb-2007-8-5-r85

T. Therriaud, M. Docker, M. Orlova, D. Heath, and H. Macisaac, Molecular resolution of the family Dreissenidae (Mollusca: Bivalvia) with emphasis on Ponto-Caspian species, including first report of Mytilopsis leucophaeata in the Black Sea basin, Molecular Phylogenetics and Evolution, vol.30, issue.3, pp.479-489, 2004.
DOI : 10.1016/S1055-7903(03)00240-9

B. Marie, G. Luquet, P. De-barros, J. Guichard, N. Morel et al., The shell matrix of the freshwater mussel Unio pictorum (Paleoheterodonta, Unionoida), FEBS Journal, vol.82, issue.11, pp.2933-2945, 2007.
DOI : 10.1111/j.1742-4658.2007.05825.x

URL : https://hal.archives-ouvertes.fr/hal-00197094

J. Balmain, B. Hannoyer, and E. Lopez, Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction analyses of mineral and organic matrix during heating of mother of pearl (nacre) from the shell of the molluscPinctada maxima, Journal of Biomedical Materials Research, vol.155, issue.5, pp.749-754, 1999.
DOI : 10.1002/(SICI)1097-4636(1999)48:5<749::AID-JBM22>3.0.CO;2-P

D. Paula, S. Silveira, and M. , Studies on molluscan shells: Contributions from microscopic and analytical methods, Micron, vol.40, issue.7, pp.669-690, 2009.
DOI : 10.1016/j.micron.2009.05.006

J. Mccoy, J. Varani, and I. Goldstein, Enzyme-linked lectin assay (ELLA), Experimental Cell Research, vol.151, issue.1, pp.437-444, 1983.
DOI : 10.1016/0014-4827(84)90359-8

M. Monsigny, C. Sene, A. Obrenovitch, A. Roche, F. Delmotte et al., Properties of Succinylated Wheat-Germ Agglutinin, European Journal of Biochemistry, vol.16, issue.1, pp.39-45, 1979.
DOI : 10.1016/0005-2795(74)90174-3

H. Debray, D. Decout, G. Strecker, G. Spik, and J. Montreuil, Specificity of Twelve Lectins Towards Oligosaccharides and Glycopeptides Related to N-Glycosylproteins, European Journal of Biochemistry, vol.149, issue.14, pp.41-55, 1981.
DOI : 10.1111/j.1432-1033.1981.tb06300.x

P. Kaladas, E. Kabat, A. Kimura, and B. Ersson, The specificity of the combining site of the lectin from Vicia villosa seeds which reacts with cytotoxic T-lymphoblasts, Molecular Immunology, vol.18, issue.11, pp.969-77, 1981.
DOI : 10.1016/0161-5890(81)90114-0

R. Cummings and S. Kornfeld, Characterization of the structural determinants required for the high affinity interaction of asparagine-linked oligosaccharides with immobilized Phaseolus vulgaris leukoagglutinating and erythroagglutinating lectins, J Biol Chem, vol.257, pp.11230-11234, 1982.

H. Debray, J. Montreuil, H. Lis, and N. Sharon, Affinity of four immobilized Erythrina lectins toward various n-linked glycopeptides and related oligosaccharides, Carbohydrate Research, vol.151, pp.359-370, 1986.
DOI : 10.1016/S0008-6215(00)90355-0

K. Hagiwara, D. Collet-cassart, K. Kobayashi, and J. Vaerman, Jacalin: isolation, characterization, and influence of various factors on its interaction with human IgA1, as assessed by precipitation and latex agglutination, Molecular Immunology, vol.25, issue.1, pp.69-83, 1988.
DOI : 10.1016/0161-5890(88)90092-2

H. Kawashima, S. Sueyoshi, H. Li, K. Yamamoto, and T. Osawa, Carbohydrate binding specificities of several poly-N-acetyllactosamine-binding lectins, Glycoconjugate Journal, vol.7, issue.4, pp.323-334, 1990.
DOI : 10.1007/BF01073376

L. Ameye, D. Becker, G. Killian, C. Wilt, F. Kemps et al., Proteins and Saccharides of the Sea Urchin Organic Matrix of Mineralization: Characterization and Localization in the Spine Skeleton, Journal of Structural Biology, vol.134, issue.1, pp.56-66, 2001.
DOI : 10.1006/jsbi.2001.4361

S. Kirkeby and D. Moe, Binding of Griffonia simplicifolia 1 isolectin B4 (GS1 B4) to alpha-galactose antigens, Immunology and Cell Biology, vol.32, issue.2, pp.121-127, 2001.
DOI : 10.1016/0966-3274(95)80024-7

S. Oguri, Analysis of sugar chain-binding specificity of tomato lectin using lectin blot: recognition of high mannose-type N-glycans produced by plants and yeast, Glycoconjugate Journal, vol.90, issue.7-9, pp.453-461, 2005.
DOI : 10.1007/s10719-005-5329-4

E. Laboratories, Available: http://eylabs

J. Kanold, N. Guichard, F. Immel, L. Plasseraud, M. Corneillat et al., - a comparative characterization of their sugar signature, FEBS Journal, vol.21, issue.10, pp.1891-1905, 2015.
DOI : 10.1111/febs.13242

A. Wheeler, J. George, and C. Evans, Control of Calcium Carbonate Nucleation and Crystal Growth by Soluble Matrx of Oyster Shell, Science, vol.212, issue.4501, pp.1397-1398, 1981.
DOI : 10.1126/science.212.4501.1397

S. Albeck, J. Aizenberg, L. Addadi, and S. Weiner, Interactions of various skeletal intracrystalline components with calcite crystals, Journal of the American Chemical Society, vol.115, issue.25, pp.11691-11697, 1993.
DOI : 10.1021/ja00078a005

J. Morrissey, Silver stain for proteins in polyacrylamide gels: A modified procedure with enhanced uniform sensitivity, Analytical Biochemistry, vol.117, issue.2, pp.307-310, 1981.
DOI : 10.1016/0003-2697(81)90783-1

R. Wall and T. Gyi, Alcian blue staining of proteoglycans in polyacrylamide gels using the ???Critical electrolyte concentration??? approach, Analytical Biochemistry, vol.175, issue.1, pp.298-299, 1988.
DOI : 10.1016/0003-2697(88)90392-2

K. Campbell, D. Maclennan, and A. Jorgensen, Staining of the Ca 2+ -binding proteins, calsequestrin, calmodulin , troponin C, and S-100, with the cationic carbocyanine dye 'Stains-all', J Biol Chem, vol.258, pp.11267-11273, 1983.

A. Shevchenko, S. Sunyaev, A. Loboda, A. Shevehenko, P. Bork et al., Charting the Proteomes of Organisms with Unsequenced Genomes by MALDI-Quadrupole Time-of-Flight Mass Spectrometry and BLAST Homology Searching, Analytical Chemistry, vol.73, issue.9, pp.1917-1926, 2001.
DOI : 10.1021/ac0013709

J. Kanold, F. Immel, C. Broussard, N. Guichard, L. Plasseraud et al., The test skeletal matrix of the black sea urchin Arbacia lixula, Comparative Biochemistry and Physiology Part D: Genomics and Proteomics, vol.13, pp.24-34, 2015.
DOI : 10.1016/j.cbd.2014.12.002

URL : https://hal.archives-ouvertes.fr/hal-01108760

F. Immel and F. Marin, Data Mining Approaches to Identify Biomineralization Related Sequences, Key Engineering Materials, vol.672, pp.191-214, 2015.
DOI : 10.4028/www.scientific.net/KEM.672.191

URL : https://hal.archives-ouvertes.fr/hal-01194591

G. Jones and J. B. , Infrared Transmission Spectra of Carbonate Minerals, 1993.
DOI : 10.1007/978-94-011-2120-0

J. Archambault-guezou, Comparaison microstructurale des tests de diverses espèces actuelles des genres Dreissena et Congeria (Dreissenidae: Mollusca: Bivalvia), Malacologia, vol.22, pp.325-332, 1982.

J. Taylor, W. Kennedy, and A. Hall, The shell structure and mineralogy of the Bivalvia. II Lucinacea?Clavagellacea?Conclusions, Bull Br MusNat Hist) Zool, vol.22, pp.255-294, 1973.

A. Barth, Infrared spectroscopy of proteins, Biochimica et Biophysica Acta (BBA) - Bioenergetics, vol.1767, issue.9, pp.1073-1101, 2007.
DOI : 10.1016/j.bbabio.2007.06.004

W. Jastrzebski, M. Sitarz, M. Rokita, and K. Bulat, Infrared spectroscopy of different phosphates structures, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, vol.79, issue.4, pp.722-727, 2011.
DOI : 10.1016/j.saa.2010.08.044

B. Morton, The Evolution of the Heteromyarian Condition in the Dreissenacea (Bivalvia), Palaeontology, vol.13, pp.563-572, 1970.

R. Theodory, The distribution of stable isotopes and heavy metals in Dreissena polymorpha (zebra mussel)?chemical tracers for environmental contamination in Lake St. Clair. A thesis submitted to the College of Graduate Studies and Research through the Department of Earth Sciences in partial fulfilment of the requirements for the degree of Master of Science, 1999.

W. Mcintire, Trace element partition coefficients???a review of theory and applications to geology, Geochimica et Cosmochimica Acta, vol.27, issue.12, pp.1209-1264, 1963.
DOI : 10.1016/0016-7037(63)90049-8

J. Zemann and . Chemistry, Handbook of Geochemistry, Volume l, pp.12-36, 1969.

J. Loreau, Sédiments aragonitiques et leur diagenèse Mémoire du Muséum National d'Histoire Naturelle . Nouvelle Série. Série C. Géologie tome XLVII, 1982.

S. Boggs and . Jr, Petrology of Sedimentary Rocks, 2009.
DOI : 10.1017/CBO9780511626487

M. Menadakis, G. Maroulis, and P. Koutsoukos, Incorporation of Mg2+, Sr2+, Ba2+ and Zn2+ into aragonite and comparison with calcite, Journal of Mathematical Chemistry, vol.38, issue.144, pp.484-491, 2009.
DOI : 10.1007/s10910-008-9490-4

C. Mclaughlan, P. Rose, and D. Aldridge, Making the Best of a Pest: The Potential for Using Invasive Zebra Mussel (Dreissena Polymorpha) Biomass as a Supplement to Commercial Chicken Feed, Environmental Management, vol.56, issue.4, pp.1102-1109, 2014.
DOI : 10.1007/s00267-014-0335-6

F. Marin, P. Narayanappa, and S. Motreuil, Acidic Shell Proteins of the Mediterranean Fan Mussel Pinna nobilis, Prog Mol Subcell Biol, vol.52, pp.353-395, 2011.
DOI : 10.1007/978-3-642-21230-7_13

URL : https://hal.archives-ouvertes.fr/hal-00618992

C. Pavat, I. Zanella-cléon, M. Becchi, D. Medakovic, G. Luquet et al., The shell matrix of the pulmonate land snail Helix aspersa maxima, Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, vol.161, issue.4, pp.303-314, 2012.
DOI : 10.1016/j.cbpb.2011.12.003

URL : https://hal.archives-ouvertes.fr/hal-00672366

A. Osuna-mascaro, T. Cruz-bustos, S. Benhamada, N. Guichard, M. B. Plasseraud et al., The shell organic matrix of the crossed lamellar queen conch shell (Strombus gigas), Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, vol.168, pp.76-85, 2014.
DOI : 10.1016/j.cbpb.2013.11.009

URL : https://hal.archives-ouvertes.fr/hal-00923994

A. Palmer, Relative cost of producing skeletal organic matrix versus calcification: Evidence from marine gastropods, Marine Biology, vol.45, issue.2-3, pp.287-292, 1983.
DOI : 10.1007/BF00406014

A. Palmer, Calcification in marine molluscs: how costly is it?, Proceedings of the National Academy of Sciences, vol.89, issue.4, pp.1379-1382, 1992.
DOI : 10.1073/pnas.89.4.1379

P. Ramos-silva, J. Kaandorp, F. Herbst, L. Plasseraud, G. Alcaraz et al., The Skeleton of the Staghorn Coral Acropora millepora: Molecular and Structural Characterization, PLoS ONE, vol.11, issue.13, p.24893046, 2014.
DOI : 10.1371/journal.pone.0097454.s001

URL : https://hal.archives-ouvertes.fr/hal-01001694

G. Goffinet and C. Jeuniaux, Distribution et importance quantitative de la chitine dans les coquilles de mollusques, Cah Biol Mar, vol.20, pp.341-349, 1979.

F. Zentz, L. Bedouet, M. Almeida, C. Milet, E. Lopez et al., Characterization and Quantification of Chitosan Extracted from Nacre of the Abalone Haliotis tuberculata and the Oyster Pinctada maxima, Marine Biotechnology, vol.3, issue.1, pp.36-44, 2001.
DOI : 10.1007/s101260000042

A. Osuna-mascaro, T. Cruz-bustos, F. Marin, and A. Checa, Ultrastructure of the Interlamellar Membranes of the Nacre of the Bivalve Pteria hirundo, Determined by Immunolabelling, PLOS ONE, vol.3, issue.4, p.25909912, 2015.
DOI : 10.1371/journal.pone.0122934.g005

URL : https://hal.archives-ouvertes.fr/hal-01150482

L. Addadi, D. Joester, F. Nudelman, and S. Weiner, Mollusk shell formation: A source of new concepts for understanding biomineralization processes, Chemistry, vol.12, pp.981-987, 2006.

B. Morton, The evolution and success of the heteromyarian form in the Mytiloida, editor. The mussel Mytilus: ecology, physiology, genetics and culture, Amsterdam, pp.21-52, 1992.

B. Marie, L. Roy, N. , M. A. Dubost, L. Milet et al., Nacre Evolution : A Proteomic Approach, MRS Proceedings, vol.130, pp.3-8, 2009.
DOI : 10.1186/1471-2148-7-160

URL : https://hal.archives-ouvertes.fr/hal-00441257

M. Shi, Y. Lin, G. Xu, L. Xie, X. Hu et al., Characterization of the Zhikong Scallop (Chlamys farreri) Mantle Transcriptome and Identification of Biomineralization-Related Genes, Marine Biotechnology, vol.14, issue.6, pp.706-715, 2013.
DOI : 10.1007/s10126-013-9517-0

P. Tompa, Intrinsically unstructured proteins, Trends in Biochemical Sciences, vol.27, issue.10, pp.527-533, 2002.
DOI : 10.1016/S0968-0004(02)02169-2

C. Mcdougall, F. Aguilera, and B. Degnan, Rapid evolution of pearl oyster shell matrix proteins with repetitive, low-complexity domains, Journal of The Royal Society Interface, vol.97, issue.6, p.23427100, 2013.
DOI : 10.1002/bip.22007

L. Roy, N. Jackson, D. , M. B. Ramos-silva, P. Marin et al., The evolution of metazoan ??-carbonic anhydrases and their roles in calcium carbonate biomineralization, Frontiers in Zoology, vol.23, issue.5, p.75, 2014.
DOI : 10.1186/s12983-014-0075-8

URL : https://hal.archives-ouvertes.fr/hal-01100241