Marinebiotech Catalogue

www.marinebiotech.eu/
log in
[ meld een fout in dit record ] Print deze pagina
Association of European marine biological laboratories
www.assemblemarine.org/
Identifier financieringsorganisatie: FP7-CAPACITIES-INFRA-2008 (Other contract id)
Acroniem: ASSEMBLE
Periode: Maart 2009 tot Februari 2013
Status: Afgelopen
 Instituten | Publicaties 
Instituten (10)  Top | Publicaties 
  • University of Gothenburg, coördinator
  • University of Gothenburg; Sven Lovén Centre for Marine Sciences, partner
  • Scottish Marine Institute; Scottish Association for Marine Science (SAMS), partner
  • Sorbonne Université; Sorbonne Université/CNRS, Station Biologique de Roscoff (SBR), partner
  • Observatoire Océanologique de Banyuls-Sur-Mer (OOB), meer, partner
  • Stazione Zoologica 'Anton Dohrn' of Naples (SZN), meer, partner
  • University of Algarve; Faculty of Marine and Environmental Sciences; Centre of Marine Sciences (CCMAR), meer, partner
  • The Hebrew University of Jerusalem (HUJI), partner
  • Pontifical Catholic University of Chile, partner
  • Max-Planck-Gesellschaft (MPG), partner
Abstract
ASSEMBLE is a research infrastructure initiative, funded within the European Union's 7th framework programme for Research and Technological Development, comprising a network of marine research stations. The joint research activities of ASSEMBLE are designed to improve the quality of provision of marine organisms with an emphasis on models for marine genomics. This includes multi-cellular organisms, unicellular eukaryotic organisms and cell lines as well as genetic and molecular resources. The research projects in ASSEMBLE will focus on:

  • Improving the provision of whole, multi-cellular organisms, including such activities as tank development, flow control, filtration and containment, feeding, breeding, and distribution of marine plants and animals;
  • Improving the provision of unicellular eukaryotic organisms and cell lines, including such activities as development of new cell lines, development of techniques for cryopreservation.
  • Improving the provision of genetic and molecular resources, including such activities as the development of mutant lines, and the curation and arraying of libraries prior to their archiving into a common genomic resource centre (MPI-MG, Berlin).
Publicaties (234)  Top | Instituten 
  • Filker, S. et al. (2014). "Candidatus Haloectosymbiotes riaformosensis" (Halobacteriaceae), an archaeal ectosymbiont of the hypersaline ciliate Platynematum salinarum. Syst. Appl. Microbiol. 37(4): 244-251. https://dx.doi.org/10.1016/j.syapm.2014.01.001
  • Probert, I. et al. (2014). Brandtodinium gen. nov. and B. nutricula comb. nov. (Dinophyceae), a dinoflagellate commonly found in symbiosis with polycystine radiolarians. J. Phycol. 50(2): 388-399. https://dx.doi.org/10.1111/jpy.12174
  • Maibam, C. et al. (2015). Centropages typicus (Crustacea, Copepoda) reacts to volatile compounds produced by planktonic algae. Mar. Ecol. (Berl.) 36(3): 819-834. https://dx.doi.org/10.1111/maec.12254
  • Kalampoki, L.G.; Flytzanis, C.N. (2014). Cis-regulatory control of the nuclear receptor Coup-TF gene in the sea urchin Paracentrotus lividus embryo. PLoS One 9(11): e109274. https://dx.doi.org/10.1371/journal.pone.0109274
  • Giordano, M. et al. (2014). Dunaliella salina (Chlorophyceae) affects the quality of NaCl crystals. Cryptogam., Algol. 35(3): 285-302. https://dx.doi.org/10.7872/crya.v35.iss3.2014.285
  • Schreiber, L. et al. (2016). Endozoicomonas are specific, facultative symbionts of sea squirts. Front. Microbiol. 7. https://dx.doi.org/10.3389/fmicb.2016.01042
  • Plagge, C. et al. (2016). Liocarcinus corrugatus (Pennant, 1777) (Crustacea: Brachyura: Portunidae): a cosmopolitan brachyuran species? Raffles Bull. Zool. 64: 374-388
  • Marti-Solans, J. et al. (2015). Oikopleura dioica culturing made easy: a Low-Cost facility for an emerging animal model in EvoDevo. Genesis 53(1): 183-193. https://dx.doi.org/10.1002/dvg.22800
  • Castellani, C. et al. (2016). Oithona similis likes it cool: evidence from two long-term time series. J. Plankton Res. 38(3): 703-717. https://dx.doi.org/10.1093/plankt/fbv104
  • Siano, R. et al. (2010). Pelagodinium gen. nov. and P. béii comb. nov., a dinoflagellate symbiont of planktonic Foraminifera. Protist 161(3): 385-399. https://dx.doi.org/10.1016/j.protis.2010.01.002
  • Muñoz-Marín, M. et al. (2013). Prochlorococcus can use the Pro1404 transporter to take up glucose at nanomolar concentrations in the Atlantic Ocean. Proc. Natl. Acad. Sci. U.S.A. 110(21): 8597-8602. https://dx.doi.org/10.1073/pnas.1221775110
  • Foissner, W. et al. (2014). Schmidingerothrix salinarum nov. spec. is the molecular sister of the large oxytrichid clade (Ciliophora, Hypotricha). J. Eukaryot. Microbiol. 61(1): 61-74. https://dx.doi.org/10.1111/jeu.12087
  • Egge, E. et al. (2013). 454 pyrosequencing to describe microbial eukaryotic community composition, diversity and relative abundance: a test for marine haptophytes. PLoS One 8(9): e74371. https://dx.doi.org/10.1371/journal.pone.0074371
  • Neves, R.C. et al. (2013). A complete three-dimensional reconstruction of the myoanatomy of Loricifera: comparative morphology of an adult and a Higgins larva stage. Front. Zool. 10. https://dx.doi.org/10.1186/1742-9994-10-19
  • Kuhlisch, C. et al. (2017). A fast and direct liquid chromatography-mass spectrometry method to detect and quantify polyunsaturated aldehydes and polar oxylipins in diatoms. Limnol. Oceanogr., Methods 15(1): 70-79. https://dx.doi.org/10.1002/lom3.10143
  • Svensson, A.; Schön, T.B. (2017). A flexible state-space model for learning nonlinear dynamical systems. Automatica 80: 189-199. https://dx.doi.org/10.1016/j.automatica.2017.02.030
  • Weinberg, I. et al. (2015). A halocarbon survey from a seagrass dominated subtropical lagoon, Ria Formosa (Portugal): flux pattern and isotopic composition. Biogeosciences 12(6): 1697-1711. https://dx.doi.org/10.5194/bg-12-1697-2015
  • Zhang, J. et al. (2016). A highly efficient layered double hydroxide catalyst for direct ethoxylation of butyl acetate to oligo-ethylene glycol butyl ether acetates. Appl. Organometal. Chem. 30(6): 451-457. https://dx.doi.org/10.1002/aoc.3454
  • Pardo, C et al. (2014). A multilocus species delimitation reveals a striking number of species of coralline algae forming maerl in the OSPAR maritime area. PLoS One 9(8). https://dx.doi.org/10.1371/journal.pone.0104073
  • Schockaert, E.R. et al. (2014). A new genus with six new species of Typhlopolycystidinae Evdonin, 1977 (Platyhelminthes, Kalyptorhynchia, Polycystididae). Zootaxa 3755(3): 259-272. https://dx.doi.org/10.11646/zootaxa.3755.3.4
  • Horká, I. et al. (2014). A new species of shrimp of the genus Anachlorocurtis Hayashi, 1975 from the Red Sea, with range extension of A. commensalis Hayashi, 1975 (Crustacea, Decapoda, Pandalidae). ZooKeys 407: 9-28. https://dx.doi.org/10.3897/zookeys.407.7457
  • Gillis, J.A.; Modrell, M.S.; Baker, C.V.H. (2012). A timeline of pharyngeal endoskeletal condensation and differentiation in the shark, Scyliorhinus canicula, and the paddlefish, Polyodon spathula. J. Appl. Ichthyol. 28(3): 341-345. https://dx.doi.org/10.1111/j.1439-0426.2012.01976.x
  • Dunlop, K.M. et al. (2015). Absolute abundance estimates from shallow water baited underwater camera surveys; a stochastic modelling approach tested against field data. J. Exp. Mar. Biol. Ecol. 472: 126-134. https://dx.doi.org/10.1016/j.jembe.2015.07.010
  • Blom, E.-L. et al. (2016). Acoustic and visual courtship traits in two sympatric marine Gobiidae species - Pomatoschistus microps and Pomatoschistus minutus. Environ. Biol. Fish. 99(12): 999-1007. https://dx.doi.org/10.1007/s10641-016-0550-5
  • Calosi, P. et al. (2013). Adaptation and acclimatization to ocean acidification in marine ectotherms: an in situ transplant experiment with polychaetes at a shallow CO2 vent system. Phil. Trans. R. Soc. Lond. (B Biol. Sci.) 368(1627). https://dx.doi.org/10.1098/rstb.2012.0444
  • Nogueira, P. et al. (2017). Altered epiphyte community and sea urchin diet in Posidonia oceanica meadows in the vicinity of volcanic CO2 vents. Mar. Environ. Res. 127: 102-111. https://dx.doi.org/10.1016/j.marenvres.2017.04.002
  • Scarpa, F. et al. (2015). An 18S and 28S-based clock calibration for marine Proseriata (Platyhelminthes). J. Exp. Mar. Biol. Ecol. 463: 22-31. https://dx.doi.org/10.1016/j.jembe.2014.10.020
  • Lindgren, J.F. et al. (2013). Analyzing changes in sediment meiofauna communities using the image analysis software ZooImage. J. Exp. Mar. Biol. Ecol. 440: 74-80. https://dx.doi.org/10.1016/j.jembe.2012.12.001
  • Conzelmann, M.; Jékely, G. (2012). Antibodies against conserved amidated neuropeptide epitopes enrich the comparative neurobiology toolbox. EvoDevo 3. https://dx.doi.org/10.1186/2041-9139-3-23
  • Küpper, F.C. et al. (2016). Arctic marine phytobenthos of northern Baffin Island. J. Phycol. 52(4): 532-549. https://dx.doi.org/10.1111/jpy.12417
  • Kádár, E. et al. (2013). Are reproduction impairments of free spawning marine invertebrates exposed to zero-valent nano-iron associated with dissolution of nanoparticles? Nanotoxicology 7(2): 135-143. https://dx.doi.org/10.3109/17435390.2011.647927
  • Kleyer, M. et al. (2012). Assessing species and community functional responses to environmental gradients: which multivariate methods? J. Veg. Sci. 23(5): 805-821. https://dx.doi.org/10.1111/j.1654-1103.2012.01402.x
  • Ramajo, L. et al. (2016). Biomineralization changes with food supply confer juvenile scallops (Argopecten purpuratus) resistance to ocean acidification. Glob. Chang. Biol. 22(6): 2025-2037. https://dx.doi.org/10.1111/gcb.13179
  • Higgs, N.D. et al. (2011). Bone-boring worms: characterizing the morphology, rate, and method of bioerosion by Osedax mucofloris (Annelida, Siboglinidae). Biol. Bull. 221(3): 307-316. https://dx.doi.org/10.1086/BBLv221n3p307
  • Hiddink, J.G. et al. (2016). Bottom trawling affects fish condition through changes in the ratio of prey availability to density of competitors. J. Appl. Ecol. 53(5): 1500-1510. https://dx.doi.org/10.1111/1365-2664.12697
  • Josef, N. et al. (2015). Camouflage during movement in the European cuttlefish (Sepia officinalis). J. Exp. Biol. 218(21): 3391-3398. https://dx.doi.org/10.1242/jeb.122481
  • Memmola, F. et al. (2014). Carbon allocation and element composition in four Chlamydomonas mutants defective in genes related to the CO2 concentrating mechanism. Photosynth. Res. 121(2-3): 201-211. https://dx.doi.org/10.1007/s11120-014-0005-9
  • Jaspers, C. et al. (2015). Carbon content of Mnemiopsis leidyi eggs and specific egg production rates in northern Europe. J. Plankton Res. 37(1): 11-15. https://dx.doi.org/10.1093/plankt/fbu102
  • Lecointe, A. et al. (2016). Cell proliferation and migration during early development of a symbiotic scleractinian coral. Proc. - Royal Soc., Biol. Sci. 283(1831). https://dx.doi.org/10.1098/rspb.2016.0206
  • Grob, C. et al. (2015). Cell-specific CO2 fixation rates of two distinct groups of plastidic protists in the Atlantic Ocean remain unchanged after nutrient addition. Environmental Microbiology Reports 7(2): 211-218. https://dx.doi.org/10.1111/1758-2229.12228
  • Meron, D. et al. (2013). Changes in microbial communities associated with the sea anemone Anemonia viridis in a natural pH gradient. Microb. Ecol. 65(2): 269-276. https://dx.doi.org/10.1007/s00248-012-0127-6
  • Rousseau, V. et al. (2013). Characterization of Phaeocystis globosa (Prymnesiophyceae), the blooming species in the Southern North Sea. J. Sea Res. 76: 105-113. https://dx.doi.org/10.1016/j.seares.2012.07.011
  • Zupo, V. et al. (2015). Chemoreception of the seagrass Posidonia oceanica by benthic invertebrates is altered by seawater acidification. J. Chem. Ecol. 41(8): 766-779. https://dx.doi.org/10.1007/s10886-015-0610-x
  • Zambounis, A.; Strittmatter, M.; Gachon, C.M.M. (2013). Chronic stress and disease resistance in the genome model marine seaweed Ectocarpus siliculosus. Aquat. Bot. 104: 147-152. https://dx.doi.org/10.1016/j.aquabot.2012.07.008
  • Rubin-Blum, M. et al. (2014). Cold seep biogenic carbonate crust in the Levantine basin is inhabited by burrowing Phascolosoma aff. turnerae, a sipunculan worm hosting a distinctive microbiota. Deep-Sea Res., Part 1, Oceanogr. Res. Pap. 90: 17-26. https://dx.doi.org/10.1016/j.dsr.2014.04.014
  • Richter, S. et al. (2017). Comparative analyses of glycerotoxin expression unveil a novel structural organization of the bloodworm venom system. BMC Evol. Biol. 17. https://dx.doi.org/10.1186/s12862-017-0904-4
  • Marques, C.L. et al. (2016). Comparative analysis of zebrafish bone morphogenetic proteins 2, 4 and 16: molecular and evolutionary perspectives. Cellular and molecular life sciences 73(4): 841-857. https://dx.doi.org/10.1007/s00018-015-2024-x
  • Marques, J.P. et al. (2017). Comparative mitogenomic analysis of three species of periwinkles: Littorina fabalis, L. obtusata and L. saxatilis. Marine Genomics 32: 41-47. https://dx.doi.org/10.1016/j.margen.2016.10.006
  • Herranz, M. et al. (2014). Comparative myoanatomy of Echinoderes (Kinorhyncha): a comprehensive investigation by CLSM AND 3D reconstruction. Front. Zool. 11. https://dx.doi.org/10.1186/1742-9994-11-31
  • De Oliveira, A.L. et al. (2016). Comparative transcriptomics enlarges the toolkit of known developmental genes in mollusks. BMC Genom. 17. https://dx.doi.org/10.1186/s12864-016-3080-9
  • Boavida, J. et al. (2016). Comparison of small remotely operated vehicles and diver-operated video of circalittoral benthos. Hydrobiologia 766(1): 247-260. https://dx.doi.org/10.1007/s10750-015-2459-y
  • Sildever, S. et al. (2016). Competitive advantage and higher fitness in native populations of genetically structured planktonic diatoms. Environ. Microbiol. 18(12): 4403-4411. https://dx.doi.org/10.1111/1462-2920.13372
  • Balzano, S. et al. (2012). Composition of the summer photosynthetic pico and nanoplankton communities in the Beaufort Sea assessed by T-RFLP and sequences of the 18S rRNA gene from flow cytometry sorted samples. ISME J. 6(8): 1480-1498. https://dx.doi.org/10.1038/ismej.2011.213
  • Magnhagen, C. et al. (2014). Context consistency and seasonal variation in boldness of male two-spotted gobies. PLoS One 9(3): e93354. https://dx.doi.org/10.1371/journal.pone.0093354
  • Lauritano, C. et al. (2012). Copepod population-specific response to a toxic diatom diet. PLoS One 7(10): e47262. https://dx.doi.org/10.1371/journal.pone.0047262
  • Burdett, H.L.; Hatton, A.D.; Kamenos, N.A. (2015). Coralline algae as a globally significant pool of marine dimethylated sulfur. Global Biogeochem. Cycles 29(10): 1845-1853. https://dx.doi.org/10.1002/2015GB005274
  • Pedroso, S.S. et al. (2013). Courtship sounds advertise species identity and male quality in sympatric Pomatoschistus spp. gobies. PLoS One 8(6): e64620. https://dx.doi.org/10.1371/journal.pone.0064620
  • Gäbler-Schwarz, S. et al. (2013). Cryopreservation of Phaeocystis antarctica. Cryoletters 34(6): 561-570
  • Heesch, S. et al. (2012). Cryopreservation of the model alga Ectocarpus (Phaeophyceae). Cryoletters 33(5): 327-336
  • Steglich, C. et al. (2015). Dataset for metatranscriptome analysis of Prochlorococcus-rich marine picoplankton communities in the Gulf of Aqaba, Red Sea. Marine Genomics 19: 5-7. https://dx.doi.org/10.1016/j.margen.2014.10.009
  • Sierra, R. et al. (2013). Deep relationships of Rhizaria revealed by phylogenomics: a farewell to Haeckel’s Radiolaria. Mol. Phylogenet. Evol. 67(1): 53-59. https://dx.doi.org/10.1016/j.ympev.2012.12.011
  • Filker, S. et al. (2015). Deep sequencing uncovers protistan plankton diversity in the Portuguese Ria Formosa solar saltern ponds. Extremophiles 19(2): 283-295. https://dx.doi.org/10.1007/s00792-014-0713-2
  • Egge, E.S. et al. (2015). Deep-branching novel lineages and high diversity of Haptophytes in the Skagerrak (Norway) uncovered by 454 pyrosequencing. J. Eukaryot. Microbiol. 62(1): 121-140. https://dx.doi.org/10.1111/jeu.12157
  • Pfreundt, U. et al. (2014). Depth dependent metatranscriptomes of the marine pico-/nanoplanktonic communities in the Gulf of Aqaba/Eilat during seasonal deep mixing. Marine Genomics 18(Part B): 93-95. https://dx.doi.org/10.1016/j.margen.2014.06.005
  • Schreiber, L. et al. (2016). Description of Endozoicomonas ascidiicola sp. nov., isolated from Scandinavian ascidians. Syst. Appl. Microbiol. 39(5): 313-318. https://dx.doi.org/10.1016/j.syapm.2016.05.008
  • Kerbl, A. et al. (2015). Detailed reconstruction of the nervous and muscular system of Lobatocerebridae with an evaluation of its annelid affinity. BMC Evol. Biol. 15. https://dx.doi.org/10.1186/s12862-015-0531-x
  • Peña, V et al. (2014). Detection of gametophytes in the maerl-forming species Phymatolithon calcareum (Melobesioideae, Corallinales) assessed by DNA barcoding. Cryptogam., Algol. 35(1): 15-25. https://dx.doi.org/10.7872/crya.v35.iss1.2014.15
  • Galante-Oliveira, S. et al. (2015). Detection of periodic Sr Ca-1 cycles along gastropod statoliths allows the accurate estimation of age. Mar. Biol. (Berl.) 162(7): 1473-1483. https://dx.doi.org/10.1007/s00227-015-2684-y
  • Varela-Álvarez, E. et al. (2017). Development and characterization of twelve microsatellite markers for Porphyra linearis Greville. Genetica 145(1): 127-130. https://dx.doi.org/10.1007/s10709-016-9941-y
  • Vijayakumar, P. et al. (2013). Development of an in vitro cell system from zebrafish suitable to study bone cell differentiation and extracellular matrix mineralization. Zebrafish 10(4): 500-509. https://dx.doi.org/10.1089/zeb.2012.0833
  • Quintana-Urzainqui, I. et al. (2014). Development of the terminal nerve system in the shark Scyliorhinus canicula. Brain Behav. Evol. 84(4): 277-287. https://dx.doi.org/10.1159/000367839
  • Piredda, R. et al. (2017). Diatom resting stages in surface sediments: a pilot study comparing Next Generation Sequencing and Serial Dilution Cultures. Cryptogam., Algol. 38(1): 31-46. https://dx.doi.org/10.7872/crya/v38.iss1.2017.31
  • Bartish, I.V. et al. (2016). Different habitats within a region contain evolutionary heritage from different epochs depending on the abiotic environment. Glob. Ecol. Biogeogr. 25(3): 274-285. https://dx.doi.org/10.1111/geb.12408
  • Shaked, Y.; Lis, H. (2012). Disassembling iron availability to phytoplankton. Front. Microbiol. 3. https://dx.doi.org/10.3389/fmicb.2012.00123
  • Arslan, D. et al. (2011). Distant Mimivirus relative with a larger genome highlights the fundamental features of Megaviridae. Proc. Natl. Acad. Sci. U.S.A. 108(42): 17486-17491. https://dx.doi.org/10.1073/pnas.1110889108
  • Stolfi, A. et al. (2014). Divergent mechanisms regulate conserved cardiopharyngeal development and gene expression in distantly related ascidians. eLIFE 3: e03728. https://dx.doi.org/10.7554/eLife.03728
  • Prioretti, L. et al. (2014). Diversity and regulation of ATP sulfurylase in photosynthetic organisms. Front. Plant Sci. 5. https://dx.doi.org/10.3389/fpls.2014.00597
  • Balzano, S. et al. (2012). Diversity of cultured photosynthetic flagellates in the northeast Pacific and Arctic Oceans in summer. Biogeosciences 9(11): 4553-4571. https://dx.doi.org/10.5194/bg-9-4553-2012
  • Bittner, L. et al. (2013). Diversity patterns of uncultured Haptophytes unravelled by pyrosequencing in Naples Bay. Mol. Ecol. 22(1): 87-101. https://dx.doi.org/10.1111/mec.12108
  • Carro, B. et al. (2014). DNA barcoding allows the accurate assessment of European maerl diversity: a Proof-of-Concept study. Phytotaxa 190(1): 176-189
  • Segovia-Viadero, M. et al. (2016). Do hatchery-reared sea urchins pose a threat to genetic diversity in wild populations? Heredity 116(4): 378-383. https://dx.doi.org/10.1038/hdy.2015.109
  • Bradassi, F. et al. (2013). Early reproductive stages in the crustose coralline alga Phymatolithon lenormandii are strongly affected by mild ocean acidification. Mar. Biol. (Berl.) 160(8): 2261-2269. https://dx.doi.org/10.1007/s00227-013-2260-2
  • Sykes, A.V. et al. (2013). Early weaning of cuttlefish (Sepia officinalis, L.) with frozen grass shrimp (Palaemonetes varians) from the first day after hatching. Aquac. Res. 44(12): 1815-1823. https://dx.doi.org/10.1111/j.1365-2109.2012.03186.x
  • Myhre, L.C. et al. (2013). Effects of habitat complexity on mating behavior and mating success in a marine fish. Behav. Ecol. 24(2): 553-563. https://dx.doi.org/10.1093/beheco/ars197
  • Norling, P. et al. (2015). Effects of live and post-mortem shell structures of invasive Pacific oysters and native blue mussels on macrofauna and fish. Mar. Ecol. Prog. Ser. 518: 123-138. https://dx.doi.org/10.3354/meps11044
  • Dahlke, F.T. et al. (2017). Effects of ocean acidification increase embryonic sensitivity to thermal extremes in Atlantic cod, Gadus morhua. Glob. Chang. Biol. 23(4): 1499-1510. https://dx.doi.org/10.1111/gcb.13527
  • Lozano, J.-C. et al. (2014). Efficient gene targeting and removal of foreign DNA by homologous recombination in the picoeukaryote Ostreococcus. Plant J. 78(6): 1073-1083. https://dx.doi.org/10.1111/tpj.12530
  • Forsgren, E. et al. (2013). Elevated CO2 affects embryonic development and larval phototaxis in a temperate marine fish. Ecol. Evol. 3(11): 3637-3646. https://dx.doi.org/10.1002/ece3.709
  • Turner, L.M. et al. (2015). Energy metabolism and cellular homeostasis trade-offs provide the basis for a new type of sensitivity to ocean acidification in a marine polychaete at a high-CO2 vent: adenylate and phosphagen energy pools versus carbonic anhydrase. J. Exp. Biol. 218(14): 2148-2151. https://dx.doi.org/10.1242/jeb.117705
  • Pawlowski, J. et al. (2014). Environmental monitoring through protist next-generation sequencing metabarcoding: assessing the impact of fish farming on benthic foraminifera communities. Mol. Ecol. Resour. 14(6): 1129-1140. https://dx.doi.org/10.1111/1755-0998.12261
  • Schalkhausser, B. et al. (2014). Escape performance of temperate king scallop, Pecten maximus under ocean warming and acidification. Mar. Biol. (Berl.) 161(12): 2819-2829. https://dx.doi.org/10.1007/s00227-014-2548-x
  • Olivier, D. et al. (2017). Evolution and diversity of ram-suction feeding in damselfishes (Pomacentridae). Org. Divers. Evol. 17(2): 497-508. https://dx.doi.org/10.1007/s13127-017-0329-3
  • Bertrand, S.; Escriva, H. (2011). Evolutionary crossroads in developmental biology: amphioxus. Development 138(22): 4819-4830. https://dx.doi.org/10.1242/dev.066720
  • Hartmann, S. et al. (2012). Exploiting gene families for phylogenomic analysis of myzostomid transcriptome data. PLoS One 7(1): e29843. https://dx.doi.org/10.1371/journal.pone.0029843
  • Czarkwiani, A. et al. (2013). Expression of skeletogenic genes during arm regeneration in the brittle star Amphiura filiforrnis. Gene expression patterns (Tokyo) 13(8): 464-472. https://dx.doi.org/10.1016/j.gep.2013.09.002
  • Berkovic, B. et al. (2014). Extending the life history of a clonal aquatic plant: Dispersal potential of sexual and asexual propagules of Zostera noltii. Aquat. Bot. 113: 123-129. https://dx.doi.org/10.1016/j.aquabot.2013.10.007
  • Neves, R.C. et al. (2016). First account on kinorhynchs from Portugal, with the description of two new species: Echinoderes lusitanicus sp. nov. and E. reicherti sp. nov. Mar. Biol. Res. 12(5): 455-470. https://dx.doi.org/10.1080/17451000.2016.1154973
  • Dupont, S. et al. (2014). First evidence of altered sensory quality in a shellfish exposed to decreased pH relevant to ocean acidification. J. Shellfish Res. 33(3): 857-861. https://dx.doi.org/10.2983/035.033.0320
  • Marquina, D. et al. (2015). Five new records and one new species of Polycladida (Platyhelminthes) for the Cantabrian coast (North Atlantic) of the Iberian Peninsula. J. Mar. Biol. Ass. U.K. 95(2): 311-322. https://dx.doi.org/10.1017/S0025315414001106
  • Ramajo, L. et al. (2016). Food supply confers calcifiers resistance to ocean acidification. NPG Scientific Reports 6(19374): 6 pp. https://dx.doi.org/10.1038/srep19374
  • Unwin, N.; Fujiyoshi, Y. (2012). Gating movement of acetylcholine receptor caught by plunge-freezing. J. Mol. Biol. 422(5): 617-634. https://dx.doi.org/10.1016/j.jmb.2012.07.010
  • Godhe, A. et al. (2014). Genetic and microscopic evidence for sexual reproduction in the centric diatom Skeletonema marinoi. Protist 165(4): 401-416. https://dx.doi.org/10.1016/j.protis.2014.04.006
  • Bendif, E.M. et al. (2014). Genetic delineation between and within the widespread coccolithophore morpho-species Emiliania huxleyi and Gephyrocapsa oceanica (Haptophyta). J. Phycol. 50(1): 140-148. https://dx.doi.org/10.1111/jpy.12147
  • Kogame, K. et al. (2015). Genetic diversity and mitochondrial introgression in Scytosiphon lomentaria (Ectocarpales, Phaeophyceae) in the north-eastern Atlantic Ocean. Phycologia 54(4): 367-374. https://dx.doi.org/10.2216/15-016.1
  • Krueger-Hadfield, S.A. et al. (2011). Genetic population structure and mating system in Chondrus crispus (Rhodophyta). J. Phycol. 47(3): 440-450. https://dx.doi.org/10.1111/j.1529-8817.2011.00995.x
  • Collén, J. et al. (2013). Genome structure and metabolic features in the red seaweed Chondrus crispus shed light on evolution of the Archaeplastida. Proc. Natl. Acad. Sci. U.S.A. 110(13): 5247-5252. https://dx.doi.org/10.1073/pnas.1221259110
  • Godfroy, O. et al. (2015). Genome-wide comparison of ultraviolet and ethyl methanesulphonate mutagenesis methods for the brown alga Ectocarpus. Marine Genomics 24(1): 109-113. https://dx.doi.org/10.1016/j.margen.2015.03.007
  • Richardson, E. et al. (2014). Genome-wide transcript profiling reveals the coevolution of plastid gene sequences and transcript processing pathways in the fucoxanthin dinoflagellate Karlodinium veneficum. Mol. Biol. Evol. 31(9): 2376-2386. https://dx.doi.org/10.1093/molbev/msu189
  • Edgar, G.J. et al. (2014). Global conservation outcomes depend on marine protected areas with five key features. Nature (Lond.) 506(7487): 216-220. https://dx.doi.org/10.1038/nature13022
  • Ratti, S. et al. (2013). Grazers and phytoplankton growth in the oceans: an experimental and evolutionary perspective. PLoS One 8(10): e77349. https://dx.doi.org/10.1371/journal.pone.0077349
  • Sigwart, J.D.; Carey, N. (2014). Grazing under experimental hypercapnia and elevated temperature does not affect the radula of a chiton (Mollusca, Polyplacophora, Lepidopleurida). Mar. Environ. Res. 102: 73-77. https://dx.doi.org/10.1016/j.marenvres.2014.05.004
  • Vannier, J. (2012). Gut contents as direct indicators for trophic relationships in the Cambrian marine ecosystem. PLoS One 7(12): e52200. https://dx.doi.org/10.1371/journal.pone.0052200
  • Pansch, C. et al. (2014). Habitat traits and food availability determine the response of marine invertebrates to ocean acidification. Glob. Chang. Biol. 20(3): 765-777. https://dx.doi.org/10.1111/gcb.12478
  • Ritter, A. et al. (2017). Herbivore-induced chemical and molecular responses of the kelps Laminaria digitata and Lessonia spicata. PLoS One 12(3): e0173315. https://dx.doi.org/10.1371/journal.pone.0173315
  • Gerecht, A.C. et al. (2014). High temperature decreases the PIC/POC ratio and increases phosphorus requirements in Coccolithus pelagicus (Haptophyta). Biogeosciences 11(13): 3531-3545. https://dx.doi.org/10.5194/bg-11-3531-2014
  • Zambounis, A. et al. (2012). Highly dynamic exon shuffling in candidate pathogen receptors ... What if brown algae were capable of adaptive immunity? Mol. Biol. Evol. 29(4): 1263-1276. https://dx.doi.org/10.1093/molbev/msr296
  • Lejzerowicz, F. et al. (2015). High-throughput sequencing and morphology perform equally well for benthic monitoring of marine ecosystems. NPG Scientific Reports 5. https://dx.doi.org/10.1038/srep13932
  • Giordano, M. (2013). Homeostasis: an underestimated focal point of-ecology and evolution. Plant Sci. 211: 92-101. https://dx.doi.org/10.1016/j.plantsci.2013.07.008
  • Fritsch, M. et al. (2016). Hox and ParaHox gene expression in early body plan patterning of polyplacophoran mollusks. Journal of experimental zoology. Part B, Molecular and developmental evolution 326(2): 89-104. https://dx.doi.org/10.1002/jez.b.22671
  • Härnström, K. et al. (2011). Hundred years of genetic structure in a sediment revived diatom population. Proc. Natl. Acad. Sci. U.S.A. 108(10): 4252-4257. https://dx.doi.org/10.1073/pnas.1013528108
  • Clark, M.S. et al. (2013). Identification of molecular and physiological responses to chronic environmental challenge in an invasive species: the Pacific oyster, Crassostrea gigas. Ecol. Evol. 3(10): 3283-3297. https://dx.doi.org/10.1002/ece3.719
  • Helm, C. et al. (2014). Immunohistochemical investigations of Myzostoma cirriferum and Mesomyzostoma cf. katoi (Myzostomida, Annelida) with implications for the evolution of the myzostomid body plan. Zoomorphology 133(3): 257-271. https://dx.doi.org/10.1007/s00435-014-0221-z
  • Borell, E.M. et al. (2014). Increasing pCO2 correlates with low concentrations of intracellular dimethylsulfoniopropionate in the sea anemone Anemonia viridis. Ecol. Evol. 4(4): 441-449. https://dx.doi.org/10.1002/ece3.946
  • Bach, L.T. et al. (2016). Influence of ocean acidification on a natural winter-to-summer plankton succession: first insights from a long-term mesocosm study draw attention to periods of low nutrient concentrations. PLoS One 11(8): e0159068. https://dx.doi.org/10.1371/journal.pone.0159068
  • Weber, A.A.-T. et al. (2015). Influence of the larval phase on connectivity: strong differences in the genetic structure of brooders and broadcasters in the Ophioderma longicauda species complex. Mol. Ecol. 24(24): 6080-6094. https://dx.doi.org/10.1111/mec.13456
  • Annunziata, R. et al. (2013). Intact cluster and chordate-like expression of ParaHox genes in a sea star. BMC Biology 11. https://dx.doi.org/10.1186/1741-7007-11-68
  • Stuart-Smith, R.D. et al. (2013). Integrating abundance and functional traits reveals new global hotspots of fish diversity. Nature (Lond.) 501(7468): 539-542, + methods (12 pp). http://dx.doi.org/10.1038/nature12529
  • Krueger-Hadfield, S.A. et al. (2013). Intergametophytic selfing and microgeographic genetic structure shape populations of the intertidal red seaweed Chondrus crispus. Mol. Ecol. 22(12): 3242-3260. https://dx.doi.org/10.1111/mec.12191
  • Strittmatter, M. et al. (2013). Intracellular eukaryotic pathogens in brown macroalgae in the Eastern Mediterranean, including LSU rRNA data for the oomycete Eurychasma dicksonii. Dis. Aquat. Org. 104(1): 1-11. https://dx.doi.org/10.3354/dao02583
  • Kremp, A. et al. (2012). Intraspecific variability in the response of bloom-forming marine microalgae to changed climate conditions. Ecol. Evol. 2(6): 1195-1207. https://dx.doi.org/10.1002/ece3.245
  • Tait, K.; Havenhand, J. (2013). Investigating a possible role for the bacterial signal molecules N-acylhomoserine lactones in Balanus improvisus cyprid settlement. Mol. Ecol. 22(9): 2588-2602. https://dx.doi.org/10.1111/mec.12273
  • Sorrenti, G. et al. (2014). Investigating sperm cryopreservation in a model tunicate, Ciona intestinalis sp. A. Cryobiology 68(1): 43-49. https://dx.doi.org/10.1016/j.cryobiol.2013.11.005
  • Lis, H. et al. (2015). Iron bioavailability to phytoplankton: an empirical approach. ISME J. 9(4): 1003-1013. https://dx.doi.org/10.1038/ismej.2014.199
  • Bjærke, O. et al. (2015). Is chain length in phytoplankton regulated to evade predation? J. Plankton Res. 37(6): 1110-1119. https://dx.doi.org/10.1093/plankt/fbv076
  • Achilles-Day, U.E.M.; Day, J.G. (2013). Isolation of clonal cultures of endosymbiotic green algae from their ciliate hosts. J. microbiol. methods 92(3): 355-357. https://dx.doi.org/10.1016/j.mimet.2013.01.007
  • Dylus, D.V. et al. (2016). Large-scale gene expression study in the ophiuroid Amphiura filiformis provides insights into evolution of gene regulatory networks. EvoDevo 7. https://dx.doi.org/10.1186/s13227-015-0039-x
  • Simakov, O. et al. (2013). Linking micro- and macro-evolution at the cell type level: a view from the lophotrochozoan Platynereis dumerilii. Brief. Funct. Genomics 12(5): 430-439. https://dx.doi.org/10.1093/bfgp/els049
  • d'Angelo, C. et al. (2012). Locally accelerated growth is part of the innate immune response and repair mechanisms in reef-building corals as detected by green fluorescent protein (GFP)-like pigments. Coral Reefs 31(4): 1045-1056. https://dx.doi.org/10.1007/s00338-012-0926-8
  • Caputi, L. et al. (2015). Long-term demographic and reproductive trends in Ciona intestinalis sp. A. Mar. Ecol. (Berl.) 36(1): 118-128. https://dx.doi.org/10.1111/maec.12125
  • Schockaert, E.R. (2014). Marine Macrostomorpha (Platyhelminthes, Rhabditophora) from the Algarve (Southern Portugal). Zootaxa 3872(5): 577-590. https://dx.doi.org/10.11646/zootaxa.3872.5.8
  • Wacker, S.; Amundsen, T. (2014). Mate competition and resource competition are inter-related in sexual selection. J. Evolution. Biol. 27(3): 466-477. https://dx.doi.org/10.1111/jeb.12314
  • Scarpa, F. et al. (2016). Meiofaunal cryptic species challenge species delimitation: the case of the Monocelis lineata (Platyhelminthes: Proseriata) species complex. Contributions to Zoology 85(2): 123-145
  • Turner, L.M. et al. (2016). Metabolic responses to high pCO2 conditions at a CO2 vent site in juveniles of a marine isopod species assemblage. Mar. Biol. (Berl.) 163(10). https://dx.doi.org/10.1007/s00227-016-2984-x
  • Weydmann, A. et al. (2014). Microsatellite markers for the Arctic copepod Calanus glacialis and cross-amplification with C. finmarchicus. Conservation Genetics Resources 6(4): 1003-1005. https://dx.doi.org/10.1007/s12686-014-0269-6
  • Gimmler, A.; Stoeck, T. (2015). Mining environmental high-throughput sequence data sets to identify divergent amplicon clusters for phylogenetic reconstruction and morphotype visualization. Environmental Microbiology Reports 7(4): 679-686. https://dx.doi.org/10.1111/1758-2229.12307
  • Tiago, D.M. et al. (2014). Mir-20a regulates in vitro mineralization and BMP signaling pathway by targeting BMP-2 transcript in fish. Arch. Biochem. Biophys. 543: 23-30. https://dx.doi.org/10.1016/j.abb.2013.12.009
  • Geoffroy, A. et al. (2015). Molecular evidence for the coexistence of two sibling species in Pylaiella littoralis (Ectocarpales, Phaeophyceae) along the Brittany coast. J. Phycol. 51(3): 480-489. https://dx.doi.org/10.1111/jpy.12291
  • Laakkonen, H.M. et al. (2015). Molecular lineage diversity and inter-oceanic biogeographical history in Hiatella (Mollusca, Bivalvia). Zoologica Scri. 44(4): 383-402. https://dx.doi.org/10.1111/zsc.12105
  • Torode, T.A. et al. (2015). Monoclonal antibodies directed to fucoidan preparations from brown algae. PLoS One 10(2): e0118366. https://dx.doi.org/10.1371/journal.pone.0118366
  • Balzano, S. et al. (2017). Morphological and genetic diversity of Beaufort Sea diatoms with high contributions from the Chaetoceros neogracilis species complex. J. Phycol. 53(1): 161-187. https://dx.doi.org/10.1111/jpy.12489
  • Bendif, E.M. et al. (2015). Morphological and phylogenetic characterization of new Gephyrocapsa isolates suggests introgressive hybridization in the Emiliania/Gephyrocapsa complex (Haptophyta). Protist 166(3): 323-336. https://dx.doi.org/10.1016/j.protis.2015.05.003
  • Sánchez, N. et al. (2016). Morphology disentangles the systematics of a ubiquitous but elusive meiofaunal group (Kinorhyncha: Pycnophyidae). Cladistics (Print) 32(5): 479-505. https://dx.doi.org/10.1111/cla.12143
  • Foissner, W. et al. (2014). Morphology, ontogenesis and molecular phylogeny of Platynematum salinarum nov. spec., a new scuticociliate (Ciliophora, Scuticociliatia) from a solar saltern. Eur. J. Protistol. 50(2): 174-184. https://dx.doi.org/10.1016/j.ejop.2013.10.001
  • Young, J.R. et al. (2014). Morphospecies versus phylospecies concepts for evaluating phytoplankton diversity: the case of the coccolithophores. Cryptogam., Algol. 35(4): 353-377. https://dx.doi.org/10.7872/crya.v35.iss4.2014.353
  • Gabriel, D. et al. (2016). Multilocus phylogeny reveals Gibsmithia hawaiiensis (Dumontiaceae, Rhodophyta) to be a species complex from the Indo-Pacific, with the proposal of G. eilatensis sp. nov. Phytotaxa 277(1): 1-20. https://dx.doi.org/10.11646/phytotaxa.277.1.1
  • Merkel, J. et al. (2015). Muscular anatomy of an entoproct creeping-type larva reveals extraordinary high complexity and potential shared characters with mollusks. BMC Evol. Biol. 15. https://dx.doi.org/10.1186/s12862-015-0394-1
  • Crocetta, F. et al. (2015). Mutation studies in ascidians: a review. Genesis 53(1): 160-169. https://dx.doi.org/10.1002/dvg.22837
  • Horwitz, R. et al. (2015). Natural high pCO2 increases autotrophy in Anemonia viridis (Anthozoa) as revealed from stable isotope (C, N) analysis. NPG Scientific Reports 5(8779): 9 pp. http://dx.doi.org/10.1038/srep08779
  • Pennati, R. et al. (2013). Neural system reorganization during metamorphosis in the planula larva of Clava multicornis (Hydrozoa, Cnidaria). Zoomorphology 132(3): 227-237. https://dx.doi.org/10.1007/s00435-013-0188-1
  • Casado-Amezúa, P. et al. (2014). New insights into the genetic diversity of zooxanthellae in Mediterranean anthozoans. Symbiosis 63(1): 41-46. https://dx.doi.org/10.1007/s13199-014-0286-y
  • Nilsson, K.S. et al. (2011). New species of Acoela from the Mediterranean, the Red Sea, and the South Pacific. Zootaxa 2867: 1-31
  • Giordano, M.; Raven, J.A. (2014). Nitrogen and sulfur assimilation in plants and algae. Aquat. Bot. 118: 45-61. https://dx.doi.org/10.1016/j.aquabot.2014.06.012
  • Robalo, J.I. et al. (2012). Northern refugia and recent expansion in the North Sea: the case of the wrasse Symphodus melops (Linnaeus, 1758). Ecol. Evol. 2(1): 153-164. https://dx.doi.org/10.1002/ece3.77
  • Jørgensen, A.; Møbjerg, N. (2015). Notes on the cryptobiotic capability of the marine arthrotardigrades Styraconyx haploceros (Halechiniscidae) and Batillipes pennaki (Batillipedidae) from the tidal zone in Roscoff, France. Mar. Biol. Res. 11(2): 214-217. https://dx.doi.org/10.1080/17451000.2014.904883
  • Krueger-Hadfield, S.A. et al. (2015). O father where art thou? Paternity analyses in a natural population of the haploid-diploid seaweed Chondrus crispus. Heredity 114(2): 185-194. https://dx.doi.org/10.1038/hdy.2014.82
  • Thor, P.; Oliva, E.O. (2015). Ocean acidification elicits different energetic responses in an Arctic and a boreal population of the copepod Pseudocalanus acuspes. Mar. Biol. (Berl.) 162(4): 799-807. https://dx.doi.org/10.1007/s00227-015-2625-9
  • Milazzo, M. et al. (2014). Ocean acidification impairs vermetid reef recruitment. NPG Scientific Reports 4(4189): 7 pp. https://dx.doi.org/10.1038/srep04189
  • Bendif, E.M. et al. (2013). On the description of Tisochrysis lutea gen. nov. sp. nov. and Isochrysis nuda sp. nov. in the Isochrysidales, and the transfer of Dicrateria to the Prymnesiales (Haptophyta). J. Appl. Phycol. 25(6): 1763-1776. https://dx.doi.org/10.1007/s10811-013-0037-0
  • Tsadok, R. et al. (2015). On the occurrence and identification of Abudefduf saxatilis (Linnaeus, 1758) in the easternmost Mediterranean Sea. Aquat. Invasions 10(1): 101-105. https://dx.doi.org/10.3391/ai.2015.10.1.10
  • Lindgren, J.F. et al. (2014). PAH effects on meio- and microbial benthic communities strongly depend on bioavailability. Aquat. Toxicol. 146: 230-238. https://dx.doi.org/10.1016/j.aquatox.2013.11.013
  • Weydmann, A. et al. (2016). Pan-Arctic population of the keystone copepod Calanus glacialis. Polar Biol. 39(12): 2311-2318. https://dx.doi.org/10.1007/s00300-016-1898-x
  • Philippe, N. et al. (2013). Pandoraviruses: amoeba viruses with genomes up to 2.5 Mb reaching that of parasitic eukaryotes. Science (Wash.) 341(6143): 281-286. https://dx.doi.org/10.1126/science.1239181
  • Bjærke, O. et al. (2016). Paternal energetic investments in copepods. Limnol. Oceanogr. 61(2): 508-517. https://dx.doi.org/10.1002/lno.10229
  • Annunziata, R. et al. (2014). Pattern and process during sea urchin gut morphogenesis: the regulatory landscape. Genesis 52(3): 251-268. https://dx.doi.org/10.1002/dvg.22738
  • Blanco-Ameijeiras, S. et al. (2016). Phenotypic variability in the coccolithophore Emiliania huxleyi. PLoS One 11(6): e0157697. https://dx.doi.org/10.1371/journal.pone.0157697
  • Zheng, Y. et al. (2015). Photochemical responses of the diatom Skeletonema costatum grown under elevated CO2 concentrations to short-term changes in pH. Aquat. Biol. 23(2): 109-118. https://dx.doi.org/10.3354/ab00619
  • Jenkins, H.L. et al. (2017). Phylogenetically widespread polyembryony in cyclostome bryozoans and the protracted asynchronous release of clonal brood-mates. PLoS One 12(1): e0170010. https://dx.doi.org/10.1371/journal.pone.0170010
  • Martínez, A. et al. (2015). Phylogeny and systematics of Protodrilidae (Annelida) inferred with total evidence analyses. Cladistics (Print) 31(3): 250-276. https://dx.doi.org/10.1111/cla.12089
  • Hague, T. et al. (2013). Preliminary in vitro functional evidence for reflex responses to noxious stimuli in the arms of Octopus vulgaris. J. Exp. Mar. Biol. Ecol. 447: 100-105. https://dx.doi.org/10.1016/j.jembe.2013.02.016
  • Sefbom, J. et al. (2015). Priority effects in a planktonic bloom-forming marine diatom. Biol. Lett. 11(5): 20150184. https://dx.doi.org/10.1098/rsbl.2015.0184
  • Saxena, S. et al. (2013). Proteome map of the neural complex of the tunicate Ciona intestinalis, the closest living relative to vertebrates. Proteomics 13(5): 860-865. https://dx.doi.org/10.1002/pmic.201200148
  • Ramanathan, N. et al. (2015). Quantifying preferences and responsiveness of marine zooplankton to changing environmental conditions using microfluidics. PLoS One 10(10): e0140553. https://dx.doi.org/10.1371/journal.pone.0140553
  • Bendif, E.M. et al. (2016). Recent reticulate evolution in the ecologically dominant lineage of Coccolithophores. Front. Microbiol. 7. https://dx.doi.org/10.3389/fmicb.2016.00784
  • Soler, G.A. et al. (2015). Reef fishes at all trophic levels respond positively to effective marine protected areas. PLoS One 10(10): e0140270. https://dx.doi.org/10.1371/journal.pone.0140270
  • Kuplik, Z. et al. (2015). Regulation of Cyanea capillata populations by predation on their planulae. J. Plankton Res. 37(5): 1068-1073. https://dx.doi.org/10.1093/plankt/fbv064
  • Jaspers, C. et al. (2015). Reproduction rates under variable food conditions and starvation in Mnemiopsis leidyi: significance for the invasion success of a ctenophore. J. Plankton Res. 37(5): 1011-1018. https://dx.doi.org/10.1093/plankt/fbv017
  • Pereira, T.R. et al. (2015). Response of kelps from different latitudes to consecutive heat shock. J. Exp. Mar. Biol. Ecol. 463: 57-62. https://dx.doi.org/10.1016/j.jembe.2014.10.022
  • Tomas, F. et al. (2015). Responses of seagrass to anthropogenic and natural disturbances do not equally translate to its consumers. Glob. Chang. Biol. 21(11): 4021-4030. https://dx.doi.org/10.1111/gcb.13024
  • Pennati, R. et al. (2013). Retinoic acid influences antero-posterior positioning of peptidergic neurons in the planula larva of the hydrozoan Clava multicornis. Mar. Ecol. (Berl.) 34(s1): 143-152. https://dx.doi.org/10.1111/maec.12032
  • Bernal-Bayard, P. et al. (2014). RNase P RNA from the recently evolved plastid of Paulinella and from algae. International Journal of Molecular Sciences 15(11): 20859-20875. https://dx.doi.org/10.3390/ijms151120859
  • Carey, N. et al. (2016). Sea hare Aplysia punctata (Mollusca: Gastropoda) can maintain shell calcification under extreme ocean acidification. Biol. Bull. 231(2): 142-151. https://dx.doi.org/10.1086/690094
  • Godhe, A. et al. (2013). Seascape analysis reveals regional gene flow patterns among populations of a marine planktonic diatom. Proc. - Royal Soc., Biol. Sci. 280(1773). https://dx.doi.org/10.1098/rspb.2013.1599
  • Egge, E.S. et al. (2015). Seasonal diversity and dynamics of haptophytes in the Skagerrak, Norway, explored by high-throughput sequencing. Mol. Ecol. 24(12): 3026-3042. https://dx.doi.org/10.1111/mec.13160
  • Fox, C.J. et al. (2014). Size variation of 0-group plaice: are earlier influences on growth potential a contributing factor? J. Sea Res. 88: 59–66. https://dx.doi.org/10.1016/j.seares.2013.12.015
  • Czarkwiani, A. et al. (2016). Skeletal regeneration in the brittle star Amphiura filiformis. Front. Zool. 13. https://dx.doi.org/10.1186/s12983-016-0149-x
  • Wangensteen, O.S. et al. (2013). Some like it hot: temperature and pH modulate larval development and settlement of the sea urchin Arbacia lixula. J. Exp. Mar. Biol. Ecol. 449: 304-311. https://dx.doi.org/10.1016/j.jembe.2013.10.007
  • Marques, C.L. et al. (2014). Spatiotemporal expression and retinoic acid regulation of bone morphogenetic proteins 2, 4 and 16 in Senegalese sole. J. Appl. Ichthyol. 30(4): 713-720. https://dx.doi.org/10.1111/jai.12539
  • Ozinga, W.A. et al. (2013). Specialists leave fewer descendants within a region than generalists. Glob. Ecol. Biogeogr. 22(2): 213-222. https://dx.doi.org/10.1111/j.1466-8238.2012.00792.x
  • Eyal, G. et al. (2015). Spectral diversity and regulation of coral fluorescence in a mesophotic reef habitat in the Red Sea. PLoS One 10(6): e0128697. https://dx.doi.org/10.1371/journal.pone.0128697
  • Trimmer, M. et al. (2013). Stark contrast in denitrification and anammox across the deep Norwegian trench in the Skagerrak. Appl. Environ. Microbiol. 79(23): 7381-7389. https://dx.doi.org/10.1128/AEM.01970-13
  • Brito, A.C. et al. (2015). Structure of late summer phytoplankton community in the Firth of Lorn (Scotland) using microscopy and HPLC-CHEMTAX. Est., Coast. and Shelf Sci. 167(Part A): 86-101. https://dx.doi.org/10.1016/j.ecss.2015.07.006
  • Römermann, C. et al. (2009). Substitutes for grazing in semi-natural grasslands - do mowing or mulching represent valuable alternatives to maintain vegetation structure? J. Veg. Sci. 20(6): 1086-1098. https://dx.doi.org/10.1111/j.1654-1103.2009.01106.x
  • Borisenko, I. et al. (2016). Surprisingly rich repertoire of Wnt genes in the demosponge Halisarca dujardini. BMC Evol. Biol. 16. https://dx.doi.org/10.1186/s12862-016-0700-6
  • Edgar, G.J.; Stuart-Smith, R.D. (2014). Systematic global assessment of reef fish communities by the Reef Life Survey program. Scientific Data 1: 140007. http://dx.doi.org/10.1038/sdata.2014.7
  • Candelier, Y. et al. (2013). Temperature dependence of oxygen isotope fractionation in coccolith calcite: a culture and core top calibration of the genus Calcidiscus. Geochim. Cosmochim. Acta 100: 264-281. https://dx.doi.org/10.1016/j.gca.2012.09.040
  • Werbrouck, E. et al. (2016). Temperature impact on the trophic transfer of fatty acids in the congeneric copepods Acartia tonsa and Acartia clausi. J. Sea Res. 112: 41-48. https://dx.doi.org/10.1016/j.seares.2016.03.001
  • Kulk, G. et al. (2012). Temperature-dependent growth and photophysiology of prokaryotic and eukaryotic oceanic picophytoplankton. Mar. Ecol. Prog. Ser. 466: 43-55. https://dx.doi.org/10.3354/meps09898
  • Wollesen, T. et al. (2015). The ParaHox gene Gsx patterns the apical organ and central nervous system but not the foregut in scaphopod and cephalopod mollusks. EvoDevo 6. https://dx.doi.org/10.1186/s13227-015-0037-z
  • Gachon, C.M.M. et al. (2013). The CCAP KnowledgeBase: linking protistan and cyanobacterial biological resources with taxonomic and molecular data. Syst. Biodiv. 11(4): 407-413. https://dx.doi.org/10.1080/14772000.2013.859641
  • Gabre, J.L. et al. (2015). The coelomic epithelium transcriptome from a clonal sea star, Coscinasterias muricata. Marine Genomics 24(3): 245-248. https://dx.doi.org/10.1016/j.margen.2015.07.010
  • Oliveri, P. et al. (2014). The Cryptochrome/Photolyase Family in aquatic organisms. Marine Genomics 14: 23-37. https://dx.doi.org/10.1016/j.margen.2014.02.001
  • Mattiello, T. et al. (2012). The dynamic nitric oxide pattern in developing cuttlefish Sepia officinalis. Developmental Dynamics 241(2): 390-402. https://dx.doi.org/10.1002/dvdy.23722
  • Andrews, P.L.R. et al. (2013). The identification and management of pain, suffering and distress in cephalopods, including anaesthesia, analgesia and humane killing. J. Exp. Mar. Biol. Ecol. 447: 46-64. https://dx.doi.org/10.1016/j.jembe.2013.02.010
  • Zheng, Y. et al. (2015). The impact of fluctuating light on the dinoflagellate Prorocentrum micans depends on NO3- and CO2 availability. J. Plant Physiol. 180: 18-26. https://dx.doi.org/10.1016/j.jplph.2015.01.020
  • Purser, A. et al. (2014). The influence of flow velocity and suspended particulate concentration on net prey capture rates by the scleractinian coral Balanophyllia europaea (Scleractinia: Dendrophylliidae). J. Mar. Biol. Ass. U.K. 94(4): 687-696. https://dx.doi.org/10.1017/S0025315414000046
  • Perea-Atienza, E. et al. (2015). The nervous system of Xenacoelomorpha: a genomic perspective. J. Exp. Biol. 218(4): 618-628. https://dx.doi.org/10.1242/jeb.110379
  • Raikova, O.I. et al. (2016). The plastic nervous system of Nemertodermatida. Org. Divers. Evol. 16(1): 85-104. https://dx.doi.org/10.1007/s13127-015-0248-0
  • Munro, C. et al. (2015). The role of ontogeny in physiological tolerance: decreasing hydrostatic pressure tolerance with development in the northern stone crab Lithodes maja. Proc. - Royal Soc., Biol. Sci. 282(1809). https://dx.doi.org/10.1098/rspb.2015.0577
  • Huang, R.-J. et al. (2013). The seaweeds Fucus vesiculosus and Ascophyllum nodosum are significant contributors to coastal iodine emissions. Atmos. Chem. Phys. 13(10): 5255-5264. https://dx.doi.org/10.5194/acp-13-5255-2013
  • Wysocka-Kapcinska, M. et al. (2013). The suppressor of AAC2 lethality SAL1 modulates sensitivity of heterologously expressed Artemia ADP/ATP carrier to bongkrekate in yeast. PLoS One 8(9): e74187. https://dx.doi.org/10.1371/journal.pone.0074187
  • Russo, M.T. et al. (2015). The upstream regulatory sequence of the light harvesting complex Lhcf2 gene of the marine diatom Phaeodactylum tricornutum enhances transcription in an orientation- and distance-independent fashion. Marine Genomics 24(1): 69-79. https://dx.doi.org/10.1016/j.margen.2015.06.010
  • Gonçalves, R.A. et al. (2012). The use of different anaesthetics as welfare promoters during short-term human manipulation of European cuttlefish (Sepia officinalis) juveniles. Aquaculture 370-371: 130-135. https://dx.doi.org/10.1016/j.aquaculture.2012.10.014
  • Richter, S. et al. (2015). The utility of genome skimming for phylogenomic analyses as demonstrated for glycerid relationships (Annelida, Glyceridae). Genome Biology and Evolution 7(12): 3443-3462. https://dx.doi.org/10.1093/gbe/evv224
  • Stuart-Smith, R.D. et al. (2015). Thermal biases and vulnerability to warming in the world’s marine fauna. Nature (Lond.) 528(7580): 88-92. http://dx.doi.org/10.1038/nature16144
  • Bahlmann, E. et al. (2015). Tidal controls on trace gas dynamics in a seagrass meadow of the Ria Formosa lagoon (southern Portugal). Biogeosciences 12(6): 1683-1696. https://dx.doi.org/10.5194/bg-12-1683-2015
  • Hubas, C. et al. (2011). Tools providing new insight into coastal anoxygenic purple bacterial mats: review and perspectives. Research in Microbiology 162(9): 858-868. https://dx.doi.org/10.1016/j.resmic.2011.03.010
  • Horwitz, R. et al. (2014). Trace element profiles of the sea anemone Anemonia viridis living nearby a natural CO2 vent. PeerJ 2: e538. https://dx.doi.org/10.7717/peerj.538
  • Purushothaman, S. et al. (2015). Transcriptomic and proteomic analyses of Amphiura filiformis arm tissue-undergoing regeneration. J. Proteomics 112: 113-124. https://dx.doi.org/10.1016/j.jprot.2014.08.011
  • Borisenko, I.E. et al. (2015). Transdifferentiation is a driving force of regeneration in Halisarca dujardini (Demospongiae, Porifera). PeerJ 3: e1211. https://dx.doi.org/10.7717/peerj.1211
  • Thor, P.; Dupont, S. (2015). Transgenerational effects alleviate severe fecundity loss during ocean acidification in a ubiquitous planktonic copepod. Glob. Chang. Biol. 21(6): 2261-2271. https://dx.doi.org/10.1111/gcb.12815
  • Lehmacher, C. et al. (2016). Ultrastructural differences in presumed photoreceptive organs and molecular data as a means for species discrimination in Polygordius (Annelida, Protodriliformia, Polygordiidae). Org. Divers. Evol. 16(3): 559-576. https://dx.doi.org/10.1007/s13127-016-0272-8
  • Fritsch, M. et al. (2015). Unexpected co-linearity of Hox gene expression in an aculiferan mollusk. BMC Evol. Biol. 15. https://dx.doi.org/10.1186/s12862-015-0414-1
  • Almada, V.C. et al. (2012). Unexpected high genetic diversity at the extreme northern geographic limit of Taurulus bubalis (Euphrasen, 1786). PLoS One 7(8): e44404. https://dx.doi.org/10.1371/journal.pone.0044404
  • Gavilán, B. et al. (2016). Xenacoelomorpha: a case of independent nervous system centralization? Phil. Trans. R. Soc. Lond. (B Biol. Sci.) 371(1685). https://dx.doi.org/10.1098/rstb.2015.0039
Alle informatie in het Integrated Marine Information System (IMIS) valt onder het VLIZ Privacy beleid Top | Instituten | Publicaties 

Website developed and maintained by VLIZ