2013
DOI: 10.5194/bg-10-3127-2013
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Unravelling the environmental drivers of deep-sea nematode biodiversity and its relation with carbon mineralisation along a longitudinal primary productivity gradient

Abstract: Alongside a primary productivity gradient between the Galicia Bank region in the Northeast Atlantic and the more oligotrophic eastern Mediterranean Basin, we investigated the bathymetric (1200–3000 m) and longitudinal variation in several measures for nematode taxon (Shannon–Wiener genus diversity, expected genus richness and generic evenness) and functional diversity (trophic diversity, diversity of life history strategies, biomass diversity and phylogenetic diversity). Our goals were to establish the form of… Show more

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Cited by 31 publications
(28 citation statements)
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References 82 publications
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“…The species belonging to the monhysterid family were assigned to the C-P 2 class ("general opportunists") as advised by Bongers et al (1995) and later restated by Pape et al (2013); no nematodes belonged to C-P class 1 ("enrichment opportunists").…”
Section: Life History (C-p Score)mentioning
confidence: 99%
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“…The species belonging to the monhysterid family were assigned to the C-P 2 class ("general opportunists") as advised by Bongers et al (1995) and later restated by Pape et al (2013); no nematodes belonged to C-P class 1 ("enrichment opportunists").…”
Section: Life History (C-p Score)mentioning
confidence: 99%
“…The relative abundance (Bongers et al, 1991(Bongers et al, , 1995Pape et al, 2013); 1: species exhibiting trait; 0: species not exhibiting trait.…”
Section: Functional Traitsmentioning
confidence: 99%
“…Since functional diversity provides a direct mechanistic link between diversity and ecosystem functioning, a growing amount of research is being devoted to assessing the effect of functional-rather than taxon-diversity on ecosystem functioning (Petchey et al, 2004;Reiss et al, 2009). Numerous independent variables of functional traits, including feeding guilds, reproduction strategy, bioturbation mode and/or body shape (e.g., Ieno et al, 2006;Carvalho et al, 2013;Pape et al, 2013;Piot et al, 2014;Quéiros et al, 2015), and biological traits analysis (e.g., Bremner et al, 2003;Bolam and Eggleton, 2014) have been applied to express functional diversity. Nevertheless, there is currently no universally accepted methodology for selecting the most appropriate traits for a given study (Bolam, 2013), and quite often the selection is heavily affected by the limited biological information that is available for benthic invertebrate taxa (Bremner, 2008).…”
Section: Introductionmentioning
confidence: 99%
“…Even though the amount of marine systems investigation has risen steeply over the past few years (Worm et al, 2006;Mora et al, 2011), deep-sea BEF studies (>200 m depth) are quite recent (Danovaro et al, 2008a;Leduc et al, 2013;Narayanaswamy et al, 2013;Pape et al, 2013;Zeppilli et al, 2016). A positive and exponential BEF relationship, reported for deep-sea benthic communities (e.g., Danovaro et al, 2008a;Narayanaswamy et al, 2013), has been explained by the prevalence of mutualistic rather than competitive interactions between organisms (Loreau, 2008).…”
Section: Introductionmentioning
confidence: 99%
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