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J Exp Biol (2020) 223 (17): jeb227074.
Published: 03 September 2020
...Alexander A. Venn; Coralie Bernardet; Apolline Chabenat; Eric Tambutté; Sylvie Tambutté ABSTRACT Coral calcification relies on the transport of ions and molecules to the extracellular calcifying medium (ECM). Little is known about paracellular transport (via intercellular junctions) in corals and...
Includes: Supplementary data
J Exp Biol (2020) 223 (11): jeb206961.
Published: 29 May 2020
... external skeletons. However, initial predictions of wide-scale sensitivity are changing as we understand more about the mechanisms underpinning skeletal production (biomineralization). These studies demonstrate the complexity of calcification pathways and the cellular responses of animals to these altered...
J Exp Biol (2019) 222 (22): jeb211128.
Published: 15 November 2019
... development, coincident with expansion of the intracellular compartment through the development of gills and other organs. Ca 2+ influx across the nuchal organ and body surface of neonates but not embryos is presumably related to calcification of the exoskeleton. Increases in the levels of Na + and Ca 2+ in...
Includes: Supplementary data
Christabel Y. L. Chan, Kum C. Hiong, Celine Y. L. Choo, Mel V. Boo, Wai P. Wong, Shit F. Chew, Yuen K. Ip
J Exp Biol (2019) 222 (7): jeb195644.
Published: 09 April 2019
... Calcification Nitrogen Symbiodinium Urea Zooxanthellae Tropical waters are poor in nutrients owing to a lack of overturn, and therefore referred to as ‘deserts’ of the sea. To compensate for nutrient shortage in tropical waters, some marine invertebrates, including giant clams and scleractinian...
Christabel Y. L. Chan, Kum C. Hiong, Mel V. Boo, Celine Y. L. Choo, Wai P. Wong, Shit F. Chew, Yuen K. Ip
J Exp Biol (2018) 221 (8): jeb176313.
Published: 19 April 2018
... transporter, DUR3-like, in its ctenidium which may participate in light-enhanced urea absorption. Amino acid Ammonia Calcification Nitrogen Symbiodinium Zooxanthellae Tropical waters are often referred to as ‘deserts’, characterized by poor nutrient content due mainly to the lack of...
J Exp Biol (2017) 220 (23): 4399–4409.
Published: 01 December 2017
... exhibit unique resilience to future ocean acidification. This is achieved through plastic shifts in reproductive investment, calcification and skeletal composition. Phenotypic plasticity Acclimatization Colonial growth forms Calcification Global environmental change Regional oceanography...
Includes: Supplementary data
Gary H. Dickinson, Anna V. Ivanina, Omera B. Matoo, Hans O. Pörtner, Gisela Lannig, Christian Bock, Elia Beniash, Inna M. Sokolova
J Exp Biol (2012) 215 (1): 29–43.
Published: 01 January 2012
... acidification salinity calcification shell mechanical properties energy status mollusks 1 H-NMR spectroscopy Ocean acidification associated with increasing atmospheric CO 2 levels is an urgent problem in the present and future state of oceans. An increase in dissolved CO 2 reduces seawater pH...
J Exp Biol (2011) 214 (21): 3570–3576.
Published: 01 November 2011
... cycles via the release of organic matter. Nevertheless, our current knowledge on basic CWC properties, such as feeding ecology and key physiological processes (i.e. respiration, calcification and organic matter release), is still very limited. Here, we show evidence for the trophic significance of...
J Exp Biol (2011) 214 (16): 2791–2798.
Published: 15 August 2011
... calcification intestine estrogen marine teleost endocrine Marine teleost fish are osmoregulators, maintaining their body fluids (∼300 mOsm kg –1 ) hypo-osmotic to seawater (∼1000 mOsm kg –1 ), and thus face the problem of osmotic water loss and the passive gain of ions ( Evans et al., 2005...
Sophie Martin, Sophie Richier, Maria-Luiza Pedrotti, Sam Dupont, Charlotte Castejon, Yannis Gerakis, Marie-Emmanuelle Kerros, François Oberhänsli, Jean-Louis Teyssié, Ross Jeffree, Jean-Pierre Gattuso
J Exp Biol (2011) 214 (8): 1357–1368.
Published: 15 April 2011
... seawater at six pH levels, i.e. pH T 8.1, 7.9, 7.7, 7.5, 7.25 and 7.0. Fertilization success, survival, growth and calcification rates were monitored over a 3 day period. The expression of genes coding for key proteins involved in development and biomineralization was also monitored. Paracentrotus lividus...
J Exp Biol (2010) 213 (23): 4092–4098.
Published: 01 December 2010
... uptake of Ca 2+ via voltage-dependent Ca 2+ channels and possibly an electrogenic Ca 2+ /1H + exchanger. Additionally, CO 2 hydration provides an endogenous source of HCO – 3 . Thus, hydration of endogenous CO 2 forms HCO – 3 for calcification while hydrogen ions are excreted, contributing to continued...
J Exp Biol (2010) 213 (15): 2602–2609.
Published: 01 August 2010
... invasions bivalve calcification common-garden experiment functional morphology Great Lakes moment of inertia phenotypic plasticity temperature Following their introduction into North America, zebra ( Dreissena polymorpha Pallas) and quagga mussels ( Dreissena bugensis Andrusov) have caused...
Christine Ferrier-Pagès, Eric Tambutté, Thamilla Zamoum, Natacha Segonds, Pierre-Laurent Merle, Nathaniel Bensoussan, Denis Allemand, Joaquim Garrabou, Sylvie Tambutté
J Exp Biol (2009) 212 (18): 3007–3015.
Published: 15 September 2009
... special interest in its photosynthetic and calcification response to the stress. Two populations collected at 15 and 35 m depths were studied in order to determine whether there was a difference in sensitivity to thermal stress between living depths. Our results show: (a) that calcification and...
J Exp Biol (2006) 209 (17): 3413–3419.
Published: 01 September 2006
...Aurélie Moya; Sylvie Tambutté; Eric Tambutté; Didier Zoccola; Natacha Caminiti; Denis Allemand SUMMARY This work, performed on the scleractinian coral Stylophora pistillata , aims at providing new information on the `light-enhanced calcification' process. In a first step, in controlled...
J Exp Biol (2004) 207 (9): 1461–1469.
Published: 01 April 2004
... during the experiment, and fed corals (FC), which were abundantly fed with Artemia salina nauplii and freshly collected zooplankton. Changes in tissue growth, photosynthesis and calcification rates were measured after 3 and 8 weeks of incubation. Calcification is the deposition of both an organic matrix...
G. Borelli, M. E. Guibbolini, N. Mayer-Gostan, F. Priouzeau, H. De Pontual, D. Allemand, S. Puverel, E. Tambutte, P. Payan
J Exp Biol (2003) 206 (15): 2685–2692.
Published: 01 August 2003
...G. Borelli; M. E. Guibbolini; N. Mayer-Gostan; F. Priouzeau; H. De Pontual; D. Allemand; S. Puverel; E. Tambutte; P. Payan SUMMARY Ionic and organic parameters of the otolith calcification process in the trout Oncorhynchus mykiss were analysed in plasma and endolymph over the day:night cycle...
J Exp Biol (2002) 205 (14): 2107–2113.
Published: 15 July 2002
...Alan T. Marshall; Peta L. Clode SUMMARY The relationship between calcification and photosynthesis in coral was investigated using standard sea water with enhanced calcium concentration. In standard sea water at 23°C with the calcium concentration increased by 2.5 mmol l -1 , incorporation of...
J Exp Biol (1992) 171 (1): 283–299.
Published: 01 October 1992
... whole body were 4.6, 15.6 and 3.0%, respectively, of their intermoult values. During the time of most rapid calcification, calcium uptake was 5.4±1.4mmoll −1 , which is comparable to the maximum rate found in seawater-acclimated crabs. The concentrations of bound and free calcium in the blood changed...
J Exp Biol (1989) 143 (1): 285–304.
Published: 01 May 1989
... gain begins about 4 h before ecdysis, accelerates rapidly to a maximum rate at about the time of ecdysis, and is essentially complete by 2h after ecdysis. Both calcification and net H + excretion remain at control (intermoult) levels until 1–2 h post-moult, whereupon a very rapid increase in both...
J Exp Biol (1985) 119 (1): 275–285.
Published: 01 November 1985
... that inward calcium transport is accompanied by both inward HCO 3 − transport and outward H + transport, probably by separate exchanges with ions of like charge such as Na + and Cl − . Crustecdysone (β-ecdysone) does not appear to be involved in control of these post-moult fluxes and calcification...