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Hyalella azteca, an amphipod crustacean, is frequently used in freshwater toxicity tests. Since the mid-1980s, numerous organizations have collected and established cultures of H. azteca originating from localities across North America. However, H. azteca is actually a large cryptic species complex whose members satisfy both the biological and the phylogenetic species concepts. Recently, two publications reported that members of the H. azteca cryptic species complex have different toxicity responses to anions and an insecticide. In this study, four members of the H. azteca species complex were identified with DNA barcoding. The genetic variation among the four clades was consistent with interspecific distances between species. These lineages (clades 1, 3, 6, and 8) were cultured in identical conditions and monitored on a weekly basis to determine two life history traits: adult mortality and juvenile production. The large-bodied clades had significantly better survival and juvenile production compared to the small-bodied clade 3. Clade 6 had very low juvenile production and high mortality; therefore, was not included in this study. Unique culture protocols may be required for each clade to optimize growth, survival, and juvenile production in laboratory conditions. Genetic barcoding has identified only two clades in a survey of 17 laboratories. Therefore these two clades (1 and 8) were compared after exposure to copper and nickel 14-day toxicity tests. Clade 8 was 2.3-2.6 times more tolerant to copper exposure than clade 1 based on their LC50 and LC25. Similarly, clade 8 was more tolerant to nickel exposure than clade 1: LC50 was 1.8 times higher for the former. Nickel LBC50 and LBC25 were significantly different between clades by a factor of 2.1-2-8. Mortality (relative to copper concentrations in tissue), growth, and bioaccumulation responses were not significantly different based on overlapping confidence intervals. Although clades 1 and 8 are both large-bodied ecomorphs, these lineages had significantly different body mass (i.e., dry weight) after 14 days. The results of this study indicate that genetically characterized cultures of H. azteca should be used in toxicity tests.

Echinocardium cordatum (Pennant 1777) oursin irrégulier abondant des zones côtières tempérées a longtemps été considéré comme une espèce cosmopolite dont la vaste aire de distribution était la conséquence directe des capacités de dispersion de sa larve planctotrophe. L’étude couplée des caractéristiques génétiques [génomes mitochondrial et nucléaire (introns+microsatellites)], morphologiques (étude basée sur 20 indices morphométriques) et écologiques (distribution géographique à petite ou grande échelle, et cycle de maturation gonadique) a révélé la présence d’un complexe d’espèces jumelles dont la différenciation génétique est accompagnée d’une différenciation morphologique statistique ainsi que de différenciations écologiques plus ou moins fines. Ces espèces occupent des aires de distribution limitées (clade A : Atlantique, clade SP : Pacifique Sud, clade NP : Pacifique Nord, clade B2 : Méditerranée, et clade B1 : Méditerranée et côtes atlantiques de l’Ibérie). D’après la reconstruction de l’histoire évolutive de ce complexe, à partir des données paléontologiques et moléculaires, ces espèces auraient divergé il y a 3 (B1-B2) à 10 (A-reste) millions d’années sous l’effet de perturbations géologiques et paléoclimatiques (fermeture de la Téthys, crise messinienne de salinité et glaciations Plio-Pléistocène). Le polymorphisme morphologique et moléculaire apparaît réduit chez B1 suggérant un effectif efficace historique de cette espèce réduit. L’analyse des flux géniques contemporains révèle que les clades A et B1 échangent toujours des gènes, alors que les clades B1 et B2, ont mis en place un isolement reproducteur efficace empêchant l’hybridation. Par ailleurs, les capacités de dispersion des espèces de ce complexe sont importantes (plus de 3000 km), mais moindres comparées à d’autres espèces du genre, notamment E. mediterraneum, qui bien qu’ayant subi les mêmes évènements géologiques n’a pas formé d’espèce depuis son apparition il y aurait 28 millions d’années. D’un point de vue évolutif, les taxons à forte capacité de dispersion présenteraient des tailles efficaces de populations importantes, ainsi qu’une aire de répartition étendue et peu de différentiation génétique entre localités ; autant de caractéristiques qui devraient ralentir la vitesse de spéciation dans ces taxons. Si cette hypothèse semble se vérifier chez E. mediterraneum, il n’en est pas de même chez E. cordatum qui malgré des effectifs efficaces apparemment importants et une différenciation des populations à l’échelle régionale faible, présente une dynamique se spéciation plus rapide. Il faut envisager que d’autres caractéristiques soient à l’origine de cette différence de dynamique de spéciation, et la comparaison des exigences écologiques des deux taxons ainsi que l’isolement de la molécule responsable de la réaction acrosomique, la bindine, pourraient apporter des éléments de réponse aux nouvelles questions soulevées. / Echinocardium cordatum (Pennant 1777) an abundant irregular sea urchin from the coastal temperate zones has long been considered as a cosmopolitan species which wide distribution area was the direct consequence of its planktotrophic larvae high dispersal abilities. A combined study of the genetic [mitochondrial and nuclear genomes (introns+microsatellites)], morphologic (based on 20 morphometric indices) and ecologic (geographic distribution at fine or large scale, and gonad maturation cycle) characteristics reveals that this taxon is a complex of cryptic species for which genetic differentiations concurred with morphological and ecological ones. The different species each occupy a limited geographic areas (clade A : Atlantic, clade SP : South Pacific, clade NP : North Pacific, clade B2 : Mediterranean sea, et clade B1 : Mediterranean sea and Atlantic coasts of Iberia). According to the complex species evolutionary history reconstruction, based on fossils and molecular data, the different species diverged between 3 (B1-B2) and 10 (A-rest) million years ago, driven by geologic and paleoclimatic perturbations (Tethys closure, messinian salinity crisis, Plio-Pleistocene glaciations). Molecular and morphologic polymorphisms appear reduced in B1, suggesting a reduced historical effective size. The contemporaneous genetic flux analysis reveals that clades A and B1 exchange genes whereas clades B1 and B2 developed an efficient reproductive isolation preventing hybridization. Though dispersal abilities of the complex species are high (more than 3000 km), they appear to be smaller than those of other species of the same genera, particularly E. mediterraneum which undergone the same geological perturbations without splitting into several species since its appearance some 28 million years ago. From an evolutionary point of view, taxa with high dispersal abilities should exhibit important population effective sizes, wide distribution areas and weak genetic differentiation between localities, properties that should slow species formation within these taxa. If this hypothesis seems verified in E. mediterraneum, it is not the case in E. cordatum for which the apparent high effective size and weak regional structure contrast with the fast speciation dynamics. It seems that other characteristics might be responsible for the speciation dynamic differences, and the comparison of the two taxa ecological requirements, as well as the isolation of the gene coding for the protein responsible of the sperm specific attachment, the bindin, should bring elements to answer these questions.