about
A quantitative assessment of Arctic shipping in 2010-2014.Phenology and Growth dynamics of Avicennia marina in the Central Red SeaLight penetration structures the deep acoustic scattering layers in the global ocean.Large scale patterns in vertical distribution and behaviour of mesopelagic scattering layers.Large mesopelagic fishes biomass and trophic efficiency in the open ocean.Acoustics reveals the presence of a macrozooplankton biocline in the Bay of Biscay in response to hydrological conditions and predator-prey relationshipsMultiple SNP markers reveal fine-scale population and deep phylogeographic structure in European anchovy (Engraulis encrasicolus L.).Biomass changes and trophic amplification of plankton in a warmer ocean.The Arctic Ocean as a dead end for floating plastics in the North Atlantic branch of the Thermohaline Circulation.Plastic debris in the open ocean.Plastic accumulation in the Mediterranean sea.Assessment of Zooplankton Community Composition along a Depth Profile in the Central Red Sea.Extracellular DNA amplicon sequencing reveals high levels of benthic eukaryotic diversity in the central Red Sea.Please mind the gap - Visual census and cryptic biodiversity assessment at central Red Sea coral reefs.A bacterial community-based index to assess the ecological status of estuarine and coastal environments.Born small, die young: Intrinsic, size-selective mortality in marine larval fish.Dispersal similarly shapes both population genetics and community patterns in the marine realm.Sex Change in Clownfish: Molecular Insights from Transcriptome Analysis.Exploring the larval fish community of the central Red Sea with an integrated morphological and molecular approach.Microbial planktonic communities in the Red Sea: high levels of spatial and temporal variability shaped by nutrient availability and turbulence.Climate oscillations reflected within the microbiome of Arabian Sea sediments.Carotenoid metabolic profiling and transcriptome-genome mining reveal functional equivalence among blue-pigmented copepods and appendicularia.RAD-seq derived genome-wide nuclear markers resolve the phylogeny of tunas.Population structure of Atlantic mackerel inferred from RAD-seq-derived SNP markers: effects of sequence clustering parameters and hierarchical SNP selection.Permanent genetic resources added to Molecular Ecology Resources Database 1 October 2011-30 November 2011.Low Carbon sink capacity of Red Sea mangroves.Pushing the limits of photoreception in twilight conditions: The rod-like cone retina of the deep-sea pearlsides.Large-scale ocean connectivity and planktonic body size.High-Throughput Sequencing and Linkage Mapping of a Clownfish Genome Provide Insights on the Distribution of Molecular Players Involved in Sex Change.Modelling the future biogeography of North Atlantic zooplankton communities in response to climate changeCarbon stocks and accumulation rates in Red Sea seagrass meadowsDecadal stability of Red Sea mangrovesNutrient Limitation in Central Red Sea MangrovesFunctional differences in the allometry of the water, carbon and nitrogen content of gelatinous organismsZooplankton diversity across three Red Sea reefs using pyrosequencingGlobal habitat preferences of commercially valuable tunaBenchmarking DNA Metabarcoding for Biodiversity-Based Monitoring and AssessmentThe contribution of migratory mesopelagic fishes to neuston fish assemblages across the Atlantic, Indian and Pacific OceansAre Calanus spp. shifting poleward in the North Atlantic? A habitat modelling approachLatitudinal phytoplankton distribution and the neutral theory of biodiversity
P50
Q27321472-F8594A9E-73AB-4C1B-98CC-DA2425B97322Q28592698-92833D0A-8ECE-4F03-8D4B-1D57A88E5132Q30354933-7017A667-0236-45E9-8995-4D82916DADC1Q30392057-58D0D59F-D644-468C-9615-D43F71B7F9A7Q30442802-BE0F82F5-433E-4804-AFA4-F63FEC157737Q30443308-01B2E451-D3E2-44DE-A868-F52304B2211AQ30464996-94E6764B-F691-44C9-AC66-2F6204B52484Q30772891-87D19021-2ABE-4BBE-B4EF-13A44E4373BEQ33580230-9BF1FB87-E23B-4646-8879-B85866432355Q33925670-DC0D7405-E955-487F-92D5-ECE718191297Q35242074-EF0F6498-940C-4773-A7C3-59602B325A5FQ35694511-C2DD42B8-3087-404B-A29F-2BA7F60478DFQ35829442-4331163B-7151-43D4-9CEB-D6FEFCF0F8A2Q36009736-4DB8FED9-0750-4877-AED1-0E75A08B5D29Q36175422-15CC5465-24BE-430D-B49F-CFFBFBB3BE72Q36310181-44F45D10-43D1-4D43-B03B-300AA929A24AQ37039882-630E3E46-2095-451A-9579-F8AB09CF2777Q37343070-6A02F98F-62D5-470B-B05E-C337910C11B9Q38644320-58FB7CE7-AF09-4E1F-B80A-4200E2DC3829Q38659105-9EA8BDAD-7CD5-47A6-B62E-5F826BA1D183Q38669062-4FB24A83-9CD5-4AF5-976D-8E34E3871478Q39260387-2D8E972D-047F-4509-84D4-050165F2C261Q39693112-360926F1-E8A3-49FD-86B0-704D23CCC94DQ39952715-C1663D7F-DF95-4A0F-A605-E6F912932B62Q41078000-E8298F21-2A0E-48B0-B1BD-D5AE05D6EDF2Q41547331-B688F422-403E-484F-886C-98CA05B5BCDCQ46262071-2BAB1944-9FC8-4327-ADC6-A0DDA3658537Q48267530-8AFD297C-E9AE-457F-8377-648454452ABBQ55381634-52D99FAC-97CE-4DB2-BD7F-AEA1D65F20A4Q56948049-05167EEF-8DD3-4642-8764-D8D8AD1BED98Q57208646-2D0DE8E8-097D-4762-8236-B85EAE70B9A5Q57208756-4DDF3650-2991-415F-AB32-004DA25F813BQ57208768-AE3B2A80-9998-4709-A66F-DE04774C3B7DQ57208789-8F77DBB0-6C0E-4D9C-9CA7-FD41884A0CD9Q57900076-506320A5-C7D1-4F86-94BE-D3883B7DAF49Q58059553-0B805E74-1353-4A0C-B3BD-0B407272362FQ58634090-AC683A00-B545-48DF-981A-23477C1FECF9Q59987486-EAF53E5D-B129-47D7-81AA-BD4D904B53B7Q59987519-B95D6C7C-4ACE-4C09-8AF0-6C9D7F7BD3F5Q59987568-44561692-5C9A-4A5A-B5BD-C8746508E968
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Xabier Irigoien
@ast
Xabier Irigoien
@en
Xabier Irigoien
@es
Xabier Irigoien
@nl
Xabier Irigoien
@sl
type
label
Xabier Irigoien
@ast
Xabier Irigoien
@en
Xabier Irigoien
@es
Xabier Irigoien
@nl
Xabier Irigoien
@sl
prefLabel
Xabier Irigoien
@ast
Xabier Irigoien
@en
Xabier Irigoien
@es
Xabier Irigoien
@nl
Xabier Irigoien
@sl
P1053
B-8171-2009
L-7909-2014
P106
P21
P2798
P31
P3829
P496
0000-0002-5411-6741