Callot J.P. & Geoffroy L. (2004). Magma flow in the East Greenland dyke swarm inferred from AMS study: Magmatic growth of volcanic margin. Geophysical journal international, 159(2), 816–830.
Abstract: Volcanic passive margins (VPMs) are characterized by large volumes of melt emplaced within the lithosphere during break-up processes. Several data and a recently proposed conceptual model of volcanic margin development suggest that VPMs are fed from localized crustal zones of magma storage, underlying large polygenetic volcanoes localized above diapir-like instabilities of the asthenosphere. We investigated the magma flow pattern within the coast-parallel dyke swarm of the East Greenland VPM, which is the only outcropping VPM, over a distance of 125 km. The 44 sampled dykes are representative of the successive families of intrusions. Igneous petrofabrics are constrained by the measurements of the anisotropy of magnetic susceptibility. The magnetic fabrics are of medium to low anisotropy (P' < 1.08) and show moderately oblate ellipsoids (T > 0) . Flow-related fabrics are recorded in 75 per cent of the sampled dykes. We infer the flow directions from the imbrication geometry of the magnetic foliation planes at the dyke margins, and check the results by measuring the preferred orientation of plagioclase in thin sections cut in the magnetic principal planes. Due to probable fabric superposition, the magnetic lineation represents the zone axis for the distribution of magnetic foliation plane. We obtained 23 reliable flow directions that are predominantly horizontal and directed away from identified crustal reservoirs. This flow pattern supports the proposed model of VPM growth, and emphasizes the localized nature of the magma sources in the mantle. The entire flood basalt sequence appears to have been fed by a restricted number of crustal reservoirs and associated dyke swarms.
Programme: 290
|
Cherel Y. (2008). Mar. Biol., 154, 813–821.
|
Crouzet, N., Guillot, T., Fressin, F., Blazit, A. (2007). the A STEP team 2007, Front- vs. back-illuminated CCD cameras for photometric surveys: a noise budget analysis. Astronomische nachrichten, 328, 805.
|
Belviso S., Moulin C., Bopp L. & Stefels J. (2004). Assessment of a global climatology of oceanic dimethylsulfide (DMS) concentrations based on SeaWiFS imagery (1998-2001). Can. J. Fish. Aquat. Sci., 61(5), 804–816.
|
Corbel H, Morlon F, Groscolas R. (2008). Is fledging in king penguin chicks related to changes in metabolic or endocrinal status? Gen Comp Endocrinol., 155(3), 804–13.
Abstract: This study examines the possibility that metabolic or endocrinal factors initiate fledging in the king penguin, a semi-altricial seabird species breeding a single chick on the ground. Chick fledging (departure to sea) occurred 5d after completion of the molt. It was preceded by a 16d fasting period and by a 7-fold increase in locomotor activity. From the measurement of the plasma concentration of metabolites and of glucagon and insulin, pre-fledging king penguin chicks were found to adapt to fasting in a classical way, i.e. by sparing body protein and mobilizing fat stores. At fledging, chicks were in phase II of fasting and their departure to sea was not stimulated by reaching critical energy depletion (phase III), in contrast to that which has been reported in breeding-fasting adults. The plasma level of corticosterone remained unchanged throughout the whole pre-fledging period, providing no support for a role of this stress-hormone in the facilitation of fledging. Thus, king penguin fledglings did not appear to be environmentally or nutritionally stressed. The plasma levels of thyroid hormones were elevated during the pre-fledging molt, in accordance with their key role in molt control in adult penguins. These levels declined by the time of the molt end, the plasma level of T4 thereafter being directly related to the time left before fledging. These results do not support the view that chronically elevated levels of thyroid hormones are required for the energy-demanding transition between being ashore and in cold water, but they suggest that the maintenance of high T4 levels may delay fledging.
Programme: 119
|
Frezzotti M., Pourchet M., Flora O., Gandolfi S., Gay M., Urbini S., Vincent C., Becagli S., Gragnani R., Proposito M., Severi M.,Traversi R., Udisti R., Fily M. (2004). New estimations of precipitation and surface sublimation in East Antarctica from snow accumulation measurements,. Climate dynamics, 23, 803–813.
|
Poulin E. & Feral J.P. (1998). Genetic structure of the brooding sea urchin Abatus cordatus, an endemic of the subantarctic Kerguelen Island, and the origin of the diversity of antarctic echinoids..
Abstract: : San Francisco, Proc.9th Intn.Echinoderm Conf.
Programme: 195
|
. (2004). Linking the foraging performance of a marine predator with local prey abundance. Functional ecology, 18, 793–801.
|
Van Camp M., Steim J., Rapagnani G. and Rivera L. (2008). Connecting a Quanterra Datalogger Q330 on the GWR C021 Superconducting Gravimeter. SEISMOLOGICAL RESEARCH LETTERS, 79, 785–796.
|
Ann Marie Aglionby Harding, Carsten Egevang, Wojciech Walkusz, Flemming Merkel, Stephane Blanc & David Gremillet. (2009). Estimating prey capture rates of a planktivorous seabird, the little auk (Alle alle), using diet, diving behaviour, and energy consumption. Polar Biol., 32, 785–793.
|