Plastic waste is a distinctive indicator of the world-wide impact of anthropogenic activities. Both macro- and micro-plastics are found in the ocean, but as yet little is known about their ultimate fate and their impact on marine ecosystems. In this study we present the first evidence that microplastics are already becoming integrated into deep-water organisms. By examining organisms that live on the deep-sea floor we show that plastic microfibres are ingested and internalised by members of at least three major phyla with different feeding mechanisms. These results demonstrate that, despite its remote location, the deep sea and its fragile habitats are already being exposed to human waste to the extent that diverse organisms are ingesting microplastics.
Aim Three‐quarters of Octocorallia species are found in deep waters. These cold‐water octocoral colonies can form a major constituent of structurally complex habitats. The global distribution and the habitat requirements of deep‐sea octocorals are poorly understood given the expense and difficulties of sampling at depth. Habitat suitability models are useful tools to extrapolate distributions and provide an understanding of ecological requirements. Here, we present global habitat suitability models and distribution maps for seven suborders of Octocorallia: Alcyoniina, Calcaxonia, Holaxonia, Scleraxonia, Sessiliflorae, Stolonifera and Subselliflorae. Location Global. Methods We use maximum entropy modelling to predict octocoral distribution using a database of 12,508 geolocated octocoral specimens and 32 environmental grids resampled to 30 arc‐second (approximately 1 km2) resolution. Additionally, a meta‐analysis determined habitat preferences and niche overlap between the different suborders of octocorals. Results Suborder Sessiliflorae had the widest potential habitat range, but all records for all suborders implied a habitat preference for continental shelves and margins, particularly the North and West Atlantic and Western Pacific Rim. Temperature, salinity, broad scale slope, productivity, oxygen and calcite saturation state were identified as important factors for determining habitat suitability. Less than 3% of octocoral records were found in waters undersaturated for calcite, but this result is affected by a shallow‐water sampling bias. Main conclusions The logistical difficulties, expense and vast areas associated with deep‐sea sampling leads to a gap in the knowledge of faunal distributions that is difficult to fill without predictive modelling. Global distribution estimates are presented, highlighting many suitable areas which have yet to be studied. We suggest that approximately 17% of oceans are suitable for at least one suborder but 3.5% may be suitable for all seven. This is the first global habitat suitability modelling study on the distribution of octocorals and forms a useful resource for researchers, managers and conservationists.
Despite the deep sea being the largest habitat on Earth, there are just 77 population genetic studies of invertebrates (115 species) inhabiting non-chemosynthetic ecosystems on the deep-sea floor (below 200 m depth). We review and synthesize the results of these papers. Studies reveal levels of genetic diversity comparable to shallow-water species. Generally, populations at similar depths were well connected over 100s-1,000s km, but studies that sampled across depth ranges reveal population structure at much smaller scales (100s-1,000s m) consistent with isolation by adaptation across environmental gradients, or the existence of physical barriers to connectivity with depth. Few studies were ocean-wide (under 4%), and 48% were Atlanticfocused. There is strong emphasis on megafauna and commercial species with research into meiofauna, "ecosystem engineers" and other ecologically important species lacking. Only nine papers account for~50% of the planet's surface (depths below 3,500 m). Just two species were studied below 5,000 m, a quarter of Earth's seafloor.Most studies used single-locus mitochondrial genes revealing a common pattern of non-neutrality, consistent with demographic instability or selective sweeps; similar to deep-sea hydrothermal vent fauna. The absence of a clear difference between vent and non-vent could signify that demographic instability is common in the deep sea, or that selective sweeps render single-locus mitochondrial studies demographically uninformative. The number of population genetics studies to date is miniscule in relation to the size of the deep sea. The paucity of studies constrains meta-analyses where broad inferences about deep-sea ecology could be made.
Seamounts are proposed to be hotspots of deep-sea biodiversity, a pattern potentially arising from increased productivity in a heterogeneous landscape leading to either high species co-existence or species turnover (beta diversity). However, studies on individual seamounts remain rare, hindering our understanding of the underlying causes of local changes in beta diversity. Here, we investigated processes behind beta diversity using ROV video, coupled with oceanographic and quantitative terrain parameters, over a depth gradient in Annan Seamount, Equatorial Atlantic. By applying recently developed beta diversity analyses, we identified ecologically unique sites and distinguished between two beta diversity processes: species replacement and changes in species richness. The total beta diversity was high with an index of 0.92 out of 1 and was dominated by species replacement (68%). Species replacement was affected by depth-related variables, including temperature and water mass in addition to the aspect and local elevation of the seabed. In contrast, changes in species richness component were affected only by the water mass. Water mass, along with substrate also affected differences in species abundance. This study identified, for the first time on seamount megabenthos, the different beta diversity components and drivers, which can contribute towards understanding and protecting regional deep-sea biodiversity.
Mesophotic coral ecosystems (MCEs) and temperate mesophotic ecosystems (TMEs) have received increasing research attention during the last decade as many new and improved methods and technologies have become more accessible to explore deeper parts of the ocean. However, large voids in knowledge remain in our scientific understanding, limiting our ability to make scientifically based decisions for conservation and management of these ecosystems. Here, we present a list of key research and con-servation questions to enhance progress in the field. Questions were generated following an initial open call to MCE and TME experts, representing a range of career levels, interests, organizations (including academia, governmental, and nongovernmental), and geographic locations. Questions were refined and grouped into eight broad themes: (1) Distribution, (2) Environmental and Physical Processes, (3) Biodiversity and Community Structure, (4) Ecological Processes, (5) Connectivity, (6) Physiology, (7) Threats, and (8) Management and Policy.
Given the current extinction crisis coupled with the shortfall in funding, there is a pressing need to establish species conservation priorities. The prioritization of phylogenetic diversity and evolutionary distinctiveness is one approach; however, taking such an approach requires more phylogenetic data than are currently available for most taxa. Here, we investigate the effects of increased phylogenetic knowledge on the accuracy of evolutionary distinctiveness (ED) scores over time using scleractinian corals as a case study. ED scores were calculated from four molecular-based phylogenies from 2008 to 2013, each one representing a chronological step of increased phylogenetic knowledge for scleractinian corals, finally resulting in a full species-level phylogeny which is used here as the reference dataset. As expected, the most complete and up-to-date phylogenies performed well at predicting scores taken from a recent, full-coverage species-level phylogeny of scleractinian corals. Surprisingly, however, older phylogenies and scores derived from expert opinion also performed well. More unexpectedly, the expert opinion-led scores, when used as a basis for imputing scores for missing species, achieved a close second in terms of prediction accuracy compared with the most recent and largest tree, which had nearly 10 times more taxonomic coverage. We recommend, once tested further, that ED score imputation be considered for assessing the conservation priorities for other poorly studied groups.
Biogeochemical cycling in high-latitude regions has a disproportionate impact on global nutrient budgets. Here, we introduce a holistic, multidisciplinary framework for elucidating the influence of glacial meltwaters, shelf currents, and biological production on biogeochemical cycling in high-latitude continental margins, with a focus on the silica cycle. Our findings highlight the impact of significant glacial discharge on nutrient supply to shelf and slope waters, as well as surface and benthic production in these regions, over a range of timescales from days to thousands of years. Whilst biological uptake in fjords and strong diatom activity in coastal waters maintains low dissolved silicon concentrations in surface waters, we find important but spatially heterogeneous additions of particulates into the system, which are transported rapidly away from the shore. We expect the glacially-derived particles-together with biogenic silica tests-to be cycled rapidly through shallow sediments, resulting in a strong benthic flux of dissolved silicon. Entrainment of this benthic silicon into boundary currents may supply an important source of this key nutrient into the Labrador Sea, and is also likely to recirculate back into the deep fjords inshore. This study illustrates how geochemical and oceanographic analyses can be used together to probe further into modern nutrient cycling in this region, as well as the palaeoclimatological 3 approaches to investigating changes in glacial meltwater discharge through time, especially during periods of rapid climatic change in the Late Quaternary.
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