about
Importance of salt fingering for new nitrogen supply in the oligotrophic ocean.Large mesopelagic fishes biomass and trophic efficiency in the open ocean.Annual trend patterns of phytoplankton species abundance belie homogeneous taxonomical group responses to climate in the NE Atlantic upwelling.Dispersal similarly shapes both population genetics and community patterns in the marine realm.The relative effects of upwelling and river flow on the phytoplankton diversity patterns in the ria of A Coruña (NW Spain).Oceanic Sink and Biogeochemical Controls on the Accumulation of Polychlorinated Dibenzo-p-dioxins, Dibenzofurans, and Biphenyls in Plankton.Variability in δ¹⁵N of intertidal brown algae along a salinity gradient: differential impact of nitrogen sources.The effect of the "Prestige" oil spill on the plankton of the N-NW Spanish coast.Stable nitrogen isotopes in coastal macroalgae: geographic and anthropogenic variability.Dissolved organic nitrogen release and bacterial activity in the upper layers of the Atlantic Ocean.Functional differences in the allometry of the water, carbon and nitrogen content of gelatinous organismsNew and regenerated production and ammonium regeneration in the western Bransfield Strait region (Antarctica) during phytoplankton bloom conditions in summerToward a mechanistic understanding of trophic structure: inferences from simulating stable isotope ratiosForaging ecology of five toothed whale species in the Northwest Iberian Peninsula, inferred using carbon and nitrogen isotope ratiosBridging the gap between marine biogeochemical and fisheries sciences; configuring the zooplankton linkDegree of oligotrophy controls the response of microbial plankton to Saharan dustTemporal variability of diazotroph community composition in the upwelling region off NW IberiaTaurine Is a Major Carbon and Energy Source for Marine Prokaryotes in the North Atlantic Ocean off the Iberian Peninsula
P50
Q30402059-FAF29723-B402-49F2-A333-304B22B66385Q30442802-1DADCE06-03D5-46E5-98BF-4FD800E6A3AFQ33465847-7AA8DEC5-35D5-4EF3-B698-72C6CF076DADQ37039882-BFDDA1F4-DB47-4D04-BEBA-8F46CFF201F0Q37730975-E77D1816-1BBD-4567-8E94-D3373E6C2EC4Q38991125-12EF0696-8633-4DD7-8039-7DE76D9DA825Q41532493-9F3603A3-F98F-4473-8D03-8651AECA5DE8Q42021126-B82D4DC0-F9B4-47A6-8D24-9EF30D070D6AQ43529123-799BAFD6-11E4-4E76-9F02-C7643C0BAB23Q43530094-3715B2F6-1988-4DF5-8F85-2ECEB1912EDAQ57208789-C5495DB6-03A4-4F7B-BE36-3035E40762E8Q58400420-D096A7FC-095A-4DE5-8756-38B9334F5A38Q58711292-22C7D304-87CF-4A7A-8C9F-2CE54B159F89Q59280870-133265A3-BACC-42A5-A84D-9FB233EC081BQ60330711-EA61D9FF-B79D-4247-A35D-D167B04132A0Q62609599-720896F7-6654-4695-9B53-B01E238BDE0CQ64059445-E3BF10D1-1366-4DCA-8F89-F5C160E96467Q91149641-C6772286-D28F-466C-9460-9F10A1165C13
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Antonio Bode
@ast
Antonio Bode
@en
Antonio Bode
@es
Antonio Bode
@nl
type
label
Antonio Bode
@ast
Antonio Bode
@en
Antonio Bode
@es
Antonio Bode
@nl
prefLabel
Antonio Bode
@ast
Antonio Bode
@en
Antonio Bode
@es
Antonio Bode
@nl
P1053
B-7949-2009
P106
P1153
7101850601
P21
P31
P3829
P496
0000-0002-9535-2548