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Association of European marine biological laboratories
www.assemblemarine.org/
Funder identifier: FP7-CAPACITIES-INFRA-2008 (Other contract id)
Acronym: ASSEMBLE
Period: March 2009 till February 2013
Status: Completed
 Institutes | Publications 
Institutes (10) Top | Publications 
  • University of Gothenburg, more, co-ordinator
  • University of Gothenburg; Sven Lovén Centre for Marine Sciences, more, partner
  • Scottish Marine Institute; Scottish Association for Marine Science (SAMS), more, partner
  • Sorbonne Université; Sorbonne Université/CNRS, Station Biologique de Roscoff (SBR), more, partner
  • Observatoire Océanologique de Banyuls-Sur-Mer (OOB), more, partner
  • Stazione Zoologica 'Anton Dohrn' of Naples (SZN), more, partner
  • University of Algarve; Faculty of Marine and Environmental Sciences; Centre of Marine Sciences (CCMAR), more, partner
  • The Hebrew University of Jerusalem (HUJI), more, partner
  • Pontifical Catholic University of Chile, more, partner
  • Max-Planck-Gesellschaft (MPG), more, 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).
Publications (234) Top | Institutes 
  • Filker, S.; Kaiser, M.; Rosselló-Mora, R.; Dunthorn, M.; Lax, G.; Stoeck, T. (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, more
  • Probert, I.; Siano, R.; Poirier, C.; Decelle, J.; Biard, T.; Tuji, A.; Suzuki, N.; Not, F. (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, more
  • Maibam, C.; Fink, P.; Romano, G.; Buia, M.C.; Butera, E.; Zupo, V. (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, more
  • 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, more
  • Giordano, M.; Bargnesi, F.; Mariani, P.; Ratti, S. (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, more
  • Schreiber, L.; Kjeldsen, K.U.; Funch, P.; Jensen, J.; Obst, M.; López-Legentil, S.; Schramm, A. (2016). Endozoicomonas are specific, facultative symbionts of sea squirts. Front. Microbiol. 7. https://dx.doi.org/10.3389/fmicb.2016.01042, more
  • Plagge, C.; Son, N.T.; Ng, P.L.K.; Türkay, M.; Streit, B.; Klaus, S. (2016). Liocarcinus corrugatus (Pennant, 1777) (Crustacea: Brachyura: Portunidae): a cosmopolitan brachyuran species? Raffles Bull. Zool. 64: 374-388, more
  • Marti-Solans, J.; Ferrández-Roldán, A.; Godoy-Marin, H.; Badia-Ramentol, J.; Torres-Aguila, N.P.; Rodríguez-Marí, A.; Bouquet, J.-M.; Chourrout, D.; Thompson, E.M.; Albalat, R.; Cañestro, C. (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, more
  • Castellani, C.; Licandro, P.; Fileman, E.; Di Capua, I.; Mazzocchi, M.G. (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, more
  • Siano, R.; Montresor, M.; Probert, I.; Not, F.; de Vargas, C. (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, more
  • Muñoz-Marín, M.; Luque, I.; Zubkov, M.V.; Hill, P.G.; Diez, J.; Garcia-Fernandez, J.M. (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, more
  • Foissner, W.; Filker, S.; Stoeck, T. (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, more
  • Egge, E.; Bittner, L.; Andersen, T.; Audic, S.; de Vargas, C.; Edvardsen, B. (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, more
  • Neves, R.C.; Bailly, X.; Leasi, F.; Reichert, H.; Sørensen, M.V.; Kristensen, R.M. (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, more
  • Kuhlisch, C.; Deicke, M.; Ueberschaar, N.; Wichard, T.; Pohnert, G. (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, more
  • 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, more
  • Weinberg, I.; Bahlmann, E.; Eckhardt, T.; Michaelis, W.; Seifert, R. (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, more
  • Zhang, J.; Shi, L.; Meng, Y.; Fu, Y.; Liu, Z.; Zhu, J. (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, more
  • Pardo, C; Lopez, L; Peña, V.; Hernandez-Kantun, J; Le Gall, L; Barbara, I; Barreiro, R (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): -. dx.doi.org/10.1371/journal.pone.0104073, more
  • Schockaert, E.R.; Martens, P.; Revis, N.; Janssen, T.; Willems, W.; Artois, T.J. (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, more
  • Horká, I.; De Grave, S.; Duris, Z. (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, more
  • 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, more
  • Dunlop, K.M.; Ruxton, G.D.; Scott, E.M.; Bailey, D.M. (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, more
  • Blom, E.-L.; Mück, I.; Heubel, K.; Svensson, O. (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, more
  • Calosi, P.; Rastrick, S.P.S.; Lombardi, C.; de Guzman, H.J.; Davidson, L.; Jahnke, M.; Giangrande, A.; Hardege, J.D.; Schulze, A.; Spicer, J.I.; Gambi, M.C. (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, more
  • Nogueira, P.; Gambi, M.C.; Vizzini, S.; Califano, G.; Tavares, A.M.; Santos, R.; Martínez-Crego, B. (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, more
  • Scarpa, F.; Cossu, P.; Sanna, D.; Lai, T.; Norenburg, J.L.; Curini-Galletti, M.; Casu, M. (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, more
  • Lindgren, J.F.; Hassellöv, I.-M.; Dahllöf, I. (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, more
  • 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, more
  • Küpper, F.C.; Peters, A.F.; Shewring, D.M.; Sayer, M.D.J.; Mystikou, A.; Brown, H.; Azzopardi, E.; Dargent, O.; Strittmatter, M.; Brennan, D.; Asensi, A.O.; Van West, P.; Wilce, R.T. (2016). Arctic marine phytobenthos of northern Baffin Island. J. Phycol. 52(4): 532-549. https://dx.doi.org/10.1111/jpy.12417, more
  • Kádár, E.; Dyson, O.; Handy, R.D.; Al-Subiai, S.N. (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, more
  • Kleyer, M.; Dray, S.; De Bello, F.; Leps, J.; Pakeman, R.J.; Strauss, B.; Thuiller, W.; Lavorel, S. (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, more
  • Ramajo, L.; Marba, N.; Prado, L.; Peron, S.; Lardies, M.A.; Rodriguez-Navarro, A.B.; Vargas, C.A.; Lagos, N.A.; Duarte, C.M. (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, more
  • Higgs, N.D.; Glover, A.G.; Dahlgren, T.G.; Little, C.T.S. (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, more
  • Hiddink, J.G.; Moranta, J.; Balestrini, S.; Sciberras, M.; Cendrier, M.; Bowyer, R.; Kaiser, M.J.; Sköld, M.; Jonsson, P.; Bastardie, F.; Hinz, H. (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, more
  • Josef, N.; Berenshtein, I.; Fiorito, G.; Sykes, A.V.; Shashar, N. (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, more
  • Memmola, F.; Mukherjee, B.; Moroney, J.V.; Giordano, M. (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, more
  • Jaspers, C.; Costello, J.H.; Colin, S.P. (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, more
  • Lecointe, A.; Domart-Coulon, I.; Paris, A.; Meibom, A. (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, more
  • Grob, C.; Jardillier, L.; Hartmann, M.; Ostrowski, M.; Zubkov, M.V.; Scanlan, D.J. (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, more
  • Meron, D.; Buia, M.C.; Fine, M.; Banin, E. (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, more
  • Rousseau, V.; Lantoine, F.; Rodriguez, F.; LeGall, F.; Chretiennot-Dinet, M.J.; Lancelot, C. (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, more
  • Zupo, V.; Maibam, C.; Buia, M.C.; Gambi, M.C.; Patti, F.P.; Scipione, M.B.; Lorenti, M.; Fink, P. (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, more
  • 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, more
  • Rubin-Blum, M.; Shemesh, E.; Goodman-Tchernov, B.; Coleman, D.F.; Ben-Avraham, Z.; Tchernov, D. (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, more
  • Richter, S.; Helm, C.; Meunier, F.A.; Hering, L.; Campbell, L.I.; Drukewitz, S.H.; Undheim, E.A.B.; Jenner, R.A.; Schiavo, G.; Bleidorn, C. (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, more
  • Marques, C.L.; Fernández, I.; Viegas, M.N.; Cox, C.J.; Martel, P.; Rosa, J.; Cancela, M.L.; Laizé, V. (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, more
  • Marques, J.P.; Sotelo, G.; Larsson, T.; Johannesson, K.; Panova, M.; Faria, R. (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, more
  • Herranz, M.; Boyle, M.J.; Pardos, F.; Neves, R.C. (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, more
  • De Oliveira, A.L.; Wollesen, T.; Kristof, A.; Scherholz, M.; Redl, E.; Todt, C.; Bleidorn, C.; Wanninger, A. (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, more
  • Boavida, J.; Assis, J.; Reed, J.; Serrão, E.A.; Gonçalves, J.M.S. (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, more
  • Sildever, S.; Sefbom, J.; Lips, I.; Godhe, A. (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, more
  • Balzano, S.; Marie, D.; Gourvil, P.; Vaulot, D. (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, more
  • Magnhagen, C.; Wacker, S.; Forsgren, E.; Myhre, L.C.; Espy, E.; Amundsen, T. (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, more
  • Lauritano, C.; Carotenuto, Y.; Miralto, A.; Procaccini, G.; Ianora, A. (2012). Copepod population-specific response to a toxic diatom diet. PLoS One 7(10): e47262. https://dx.doi.org/10.1371/journal.pone.0047262, more
  • 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, more
  • Pedroso, S.S.; Barber, I.; Svensson, O.; Fonseca, P.J.; Amorim, M.C.P. (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, more
  • Gäbler-Schwarz, S.; Rad-Menéndez, C.; Achilles-Day, U.E.M.; Campbell, C.N.; Day, J.G. (2013). Cryopreservation of Phaeocystis antarctica. Cryoletters 34(6): 561-570, more
  • Heesch, S.; Day, J.G.; Yamagishi, T.; Kawai, H.; Müller, D.G.; Küpper, F.C. (2012). Cryopreservation of the model alga Ectocarpus (Phaeophyceae). Cryoletters 33(5): 327-336, more
  • Steglich, C.; Stazic, D.; Lott, S.C.; Voigt, K.; Greengrass, E.; Lindell, D.; Hess, W.R. (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, more
  • Sierra, R.; Matz, M.V.; Aglyamova, G.; Pillet, L.; Decelle, J.; Not, F.; de Vargas, C.; Pawlowski, J. (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, more
  • Filker, S.; Gimmler, A.; Dunthorn, M.; Mahé, F.; Stoeck, T. (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, more
  • Egge, E.S.; Eikrem, W.; Edvardsen, B. (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, more
  • Pfreundt, U.; Miller, D.; Adusumilli, L.; Stambler, N.; Berman-Frank, I.; Hess, W.R. (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, more
  • Schreiber, L.; Kjeldsen, K.U.; Obst, M.; Funch, P.; Schramm, A. (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, more
  • Kerbl, A.; Bekkouche, N.; Sterrer, W.; Worsaae, K. (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, more
  • Peña, V; Hernandez-Kantun, J; Grall, J; Pardo, C; Lopez, L; Barbara, I; Le Gall, L; Barreiro, R (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, more
  • Galante-Oliveira, S.; Marçal, R.; Espadilha, F.; Sá, M.; Abell, R.; Machado, J.; Barroso, C.M. (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, more
  • Varela-Álvarez, E.; Paulino, C.; Serrão, E.A. (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, more
  • Vijayakumar, P.; Laizé, V.; Cardeira, J.; Trindade, M.; Cancela, M.L. (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, more
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