Results 41 to 50 of about 4,722 (202)
Drivers of fluorescent dissolved organic matter in the global epipelagic ocean [PDF]
AbstractFluorescent dissolved organic matter (FDOM) in open surface waters (< 200 m) of the Atlantic, Pacific, and Indian oceans was analysed by excitation‐emission matrix (EEM) spectroscopy and parallel factor analysis (PARAFAC). A four‐component PARAFAC model was fit to the EEMs, which included two humic‐ (C1 and C2) and two amino acid‐like (C3 ...
Catalá, T. S. +13 more
openaire +4 more sources
Bacteria richness estimates (Chao1) by type of samples: epipelagic samples from eruption (eruption), epipelagic samples from post-eruption (post-eruption) and mesopelagic samples (deep).
José M. González (249835) +5 more
core +1 more source
These data were used for the development of the paper "Biodiversity patterns of epipelagic copepods in the South Pacific Ocean: data constraints and drivers". Especifically, we added ecological and environmental data that were used for modeling.
Manuela Isabel Pérez Aragón (16845672) +3 more
core +1 more source
Checklist of the shore and epipelagic fishes of Tonga [PDF]
A checklist is given below of 1162 species of shore and epipelagic fishes belonging to 111 families that occur in the islands of Tonga, South Pacifie Ocean; 40 of these are epipelagic species. As might be expected, the fish fauna of Tonga is most similar
Clua, E. +8 more
core +1 more source
Epipelagic $$L$$ L -packets and rectifying characters
We provide an explicit construction of the local Langlands correspondence for general tamely-ramified reductive p-adic groups and a class of wildly ramified Langlands parameters. Furthermore, we verify that our construction satisfies the expected properties of such a correspondence.
openaire +3 more sources
Langlands parameters for epipelagic representations of GLn
Let F be a non-Archimedean local field. An irreducible cuspidal representation of is epipelagic if its Swan conductor equals . We give a full and explicit description of the Langlands parameters of such representations, in terms of elementary ...
Guy Henniart +3 more
core +1 more source
While many visual predators feed exclusively during the day, others exploit foraging opportunities at night, although the efficiency with which they do so is strongly influenced by ambient light levels. We investigated the influence of variation in nocturnal light on the foraging behaviour of a small pelagic seabird, the European Storm‐petrel ...
Darren Wilkinson +3 more
wiley +1 more source
First record of the pelagic stingray Pteroplatytrygon violacea (Bonaparte, 1832) from the Red Sea
The pelagic stingray, Pteroplatytrygon violacea (Bonaparte, 1832), is the only fully pelagic member of the family Dasyatidae and is distributed across tropical and subtropical oceanic habitats worldwide. Despite its occurrence throughout the Indian Ocean
Ashlie J. McIvor +4 more
doaj +1 more source
Abstract Maximum longevity varies widely among marine‐occurring fishes, but the form of its relationship with body size and the contribution of broad environmental gradients remain uncertain. We analysed 757 species, using maximum length as the primary size metric and completed mass only in sensitivity analyses.
Longyu Li, Zenghui Xu
wiley +1 more source
Impact of light pollution on fishes: Mechanisms and ecological consequences
Abstract The increasing prevalence of artificial light at night (ALAN) is of growing ecological concern. By altering natural light regimes, ALAN affects the behaviour, physiology and life‐history of organisms. While research has largely focused on terrestrial ecosystems, aquatic ecosystems are increasingly exposed.
Hanxi Chen, Ulrika Candolin
wiley +1 more source

