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Large Benthic Foraminifera are a crucial component of coral-reef ecosystems, which are currently threatened by ocean acidification. We conducted culture experiments to evaluate the impact of low pH on survival and test dissolution of the symbiont-bearing species Peneroplis spp., and to observe potential calcification recovery when specimens are placed back under reference pH value (7.9). We found that Peneroplis spp. displayed living activity up to 3 days at pH 6.9 (Ωcal cal > 1), despite the dark and unfed conditions. Dissolution features were observed under low Ωcal values, such as changes in test density, peeled extrados layers, and decalcified tests with exposed organic linings. A new calcification phase started when specimens were placed back at reference pH. This calcification’s resumption was an addition of new chambers without reparation of the dissolved parts, which is consistent with the porcelaneous calcification pathway of Peneroplis spp. The most decalcified specimens displayed a strong survival response by adding up to 8 new chambers, and the contribution of food supply in this process was highlighted. These results suggest that porcelaneous LBF species have some recovery abilities to short exposure (e.g., 3 days to 1 month) to acidified conditions. However, the geochemical signature of trace elements in the new calcite was impacted, and the majority of the new chambers were distorted and resulted in abnormal tests, which might hinder the specimens’ reproduction and thus their survival on the long term.

With 4 to 12 million tons of plastic entering the marine environment each year, plastic pollution has become one of the most ubiquitous sources of pollution of the Anthropocene threatening the marine environment. Beyond the conspicuous physical damages, plastics may release a cocktail of harmful chemicals, i.e. monomers, additives and persistent organic pollutants. Although known to be highly toxic, plastic leachates seemingly appear, however, as the "somewhat sickly child" of the plastic pollution literature. We reviewed the only 26 studies investigating the impact of plastic leachates on marine microbes and invertebrates, and concluded that the observed effects essentially depend on the species, polymer type, plastic composition, accumulated contaminants and weathering processes. We identified several gaps that we believe may hamper progress in this emerging area of research and discussed how they could be bridged to further our understanding of the effects of the compounds released by plastic items on marine organisms. We first stress the lack of a consensus on the use of the term 'leachate', and subsequently introduce the concepts of primary and secondary leachates, based on the intrinisic or extrinsic origin of the products released in bulk seawater. We discuss how methodological inconsistencies and the discrepancy between the polymers used in experiments and their abundance in the environment respectively limit comparison between studies and a comprehensive assessment of the effects leachate may actually have in the ocean. We also discuss how the imbalanced in the variety of both organisms and polymers considered, the mostly unrealistic concentrations used in laboratory experiments, and the lack of investigation on key ecosystem engineers may considerably narrow the spectrum of our understanding of the plastic leachates' effects. We finally discuss how increasing multi-disciplinarity through collaborations between different research fields may benefit to an area of research which is still in its early infancy.

Evolutionary novelties require rewiring of transcriptional networks and/or the evolution of new gene functions. Sex determination (SD), one of the most plastic evolutionary processes, requires such novelties. Studies on the evolution of vertebrate SD revealed that new master SD genes are generally recruited from genes involved in the downstream SD regulatory genetic network. Only a single exception to this rule is currently known in vertebrates: the intriguing case of the salmonid master SD gene (sdY), which arose from duplication of an immune-related gene. This exception immediately posed the question of how a gene outside from the classical sex differentiation cascade could acquire its function as a male SD gene. Here we show that SdY became integrated in the classical vertebrate sex differentiation cascade by interacting with the Forkhead box domain of the female-determining transcription factor, Foxl2. In the presence of Foxl2, SdY is translocated to the nucleus where the SdY:Foxl2 complex prevents activation of the aromatase (cyp19a1a) promoter in cooperation with Nr5a1 (Sf1). Hence, by blocking a positive loop of regulation needed for the synthesis of estrogens in the early differentiating gonad, SdY disrupts a preset female differentiation pathway, consequently allowing testicular differentiation to proceed. These results also suggest that the evolution of unusual vertebrate master sex determination genes recruited from outside the classical pathway like sdY is strongly constrained by their ability to interact with the canonical gonadal differentiation pathway.

A microfluidic on-chip imaging cell sorter has several advantages over conventional cell sorting methods, especially to identify cells with complex morphologies such as clusters. One of the remaining problems is how to efficiently discriminate targets at the species level without labelling. Hence, we developed a label-free microfluidic droplet-sorting system based on image recognition of cells in droplets. To test the applicability of this method, a mixture of two plankton species with different morphologies (Dunaliella tertiolecta and Phaeodactylum tricornutum) were successfully identified and discriminated at a rate of 10 Hz. We also examined the ability to detect the number of objects encapsulated in a droplet. Single cell droplets sorted into collection channels showed 91 ± 4.5% and 90 ± 3.8% accuracy for D. tertiolecta and P. tricornutum, respectively. Because we used image recognition to confirm single cell droplets, we achieved highly accurate single cell sorting. The results indicate that the integrated method of droplet imaging cell sorting can provide a complementary sorting approach capable of isolating single target cells from a mixture of cells with high accuracy without any staining.

The Census for Antarctic Marine Life (CAML, IPY Project 53) aimed to investigate the distribution and abundance of Antarctic marine biodiversity and how it will be affected by climate change. It was a major ship-based research programme in the austral summer of 2007-2008 involving scientists from 30 countries and 19 vessels. The Collaborative East Antarctic Marine Census (CEAMARC) was a multinational contribution to CAML involving scientists and students from several nations using three ships from Australia, Japan and France surveying the one area. This collaboration was a highly coordinated and comprehensive survey of the plankton, fish, benthos, oceanography and geophysical conditions of the waters north of Terre Adelie and George V Land of Eastern Antarctica. CEAMARC has provided a robust benchmark of the marine life in this poorly studied sector and will help to establish the monitoring of future changes in this region. Crown Copyright (C) 2011 Published by Elsevier B.V. and NIPR. All rights reserved.

The spermatogonia of fish can be classified as being either undifferentiated type A spermatogonia or differentiated type B spermatogonia. Although type A spermatogonia, which contain spermatogonial stem cells, have been demonstrated to be a suitable material for germ cell transplantation, no molecular markers for distinguishing between type A and type B spermatogonia in fish have been developed to date. We therefore sought to develop a molecular marker for type A spermatogonia in rainbow trout. Using GFP-dependent flow cytometry (FCM), enriched fractions of type A and type B spermatogonia, testicular somatic cells, and primordial germ cells were prepared from rainbow trout possessing the green fluorescent protein (GFP) gene driven by trout vasa regulatory regions (pvasa-GFP rainbow trout). The gene-expression profiles of each cell fraction were then compared with a microarray containing cDNAs representing 16,006 genes from several salmonid species. Genes exhibiting high expression for type A spermatogonia relative to above-mentioned other types of gonadal cells were identified and subjected to RT-PCR and quatitative PCR analysis. Since only the rainbow trout notch1 homologue showed significantly high expression in the type A spermatogonia-enriched fraction, we propose that notch1 may be a useful molecular marker for type A spermatogonia. The combination of GFP-dependent FCM and microarray analysis of pvasa-GFP rainbow trout can therefore be applied to the identification of potentially useful molecular markers of germ cells in fish.

There is a need to isolate different populations of spermatogenic cells to investigate the molecular events that occur during spermatogenesis. Here we developed a new method to identify and purify testicular germ cells from rainbow trout (Oncorhynchus mykiss) carrying the green fluorescent protein gene driven by trout vasa regulatory regions (pvasa-GFP) at various stages of spermatogenesis. Rainbow trout piwi-like (rtili), rainbow trout scp3 (rt-scp3), and rainbow trout shippo1 (rt-shippo1) were identified as molecular markers for spermatogonia, spermatocytes, and spermatids, respectively. The testicular cells were separated into five fractions (A-E) by flow cytometry (FCM) according to their GFP intensities. Based on the molecular markers, fractions A and B were found to contain spermatogonia, while fractions C and D contained spermatocytes, and fraction E contained spermatids. We also classified the spermatogonia into type A, which contained spermatogonial stem cells (SSCs), and type B, which did not. As none of the molecular markers tested could distinguish between the two types of spermatogonia, we subjected them to a transplantation assay. The results indicated that cells with strong GFP fluorescence (fraction A) colonized the recipient gonads, while cells with weaker GFP fluorescence (fraction B) did not. As only SSCs could colonize the recipient gonads, this indicated that fraction A and fraction B contained mainly type A and type B spermatogonia, respectively. These findings confirmed that our system could identify and isolate various populations of testicular cells from rainbow trout using a combination of GFP-dependent FCM and a transplantation assay.

International audience; We report a modified top-seeded melt-growth technology for processing high performance Gd–Ba–Cu–O trapped field magnets (TFMs) by providing an additional liquid source during the melt-textured growth. The enriched liquid source allows sufficient growth in the a−b plane with an increased growth rate, and depresses the accumulation of Gd2BaCuO5 (Gd211) particles, which largely suppresses the formation of sub-grain boundaries in the a-growth sectors. An average trapped magnet field of 1.2 T is achieved for the 32 mm Gd–Ba–Cu–O TFMs at 77 K. These Gd–Bd–Cu–O TFMs exhibit superior in-field flux trapping performance, thanks to the significant second peak effect of the critical current density (Jc). The additional liquid source intensifies the Gd–Ba substitution, and therefore increases the in-field Jc, especially at the temperature range of 30–70 K, which is meaningful for practical applications.