The DOI matches its Crossref record; 16 of the 16 references it cites were found in a registry or an index.
Effects of natural and human-induced hypoxia on coastal benthos
Open accessAbstract
Abstract. Coastal hypoxia (defined here as <1.42 ml L−1; 62.5 μM; 2 mg L−1, approx. 30% oxygen saturation) develops seasonally in many estuaries, fjords, and along open coasts as a result of natural upwelling or from anthropogenic eutrophication induced by riverine nutrient inputs. Permanent hypoxia occurs naturally in some isolated seas and marine basins as well as in open slope oxygen minimum zones. Responses of benthos to hypoxia depend on the duration, predictability, and intensity of oxygen depletion and on whether H2S is formed. Under suboxic conditions, large mats of filamentous sulfide oxidizing bacteria cover the seabed and consume sulfide. They are hypothesized to provide a detoxified microhabitat for eukaryotic benthic communities. Calcareous foraminiferans and nematodes are particularly tolerant of low oxygen concentrations and may attain high densities and dominance, often in association with microbial mats. When oxygen is sufficient to support metazoans, small, soft-bodied invertebrates (typically annelids), often with short generation times and elaborate branchial structures, predominate. Large taxa are more sensitive than small taxa to hypoxia. Crustaceans and echinoderms are typically more sensitive to hypoxia, with lower oxygen thresholds, than annelids, sipunculans, molluscs and cnidarians. Mobile fish and shellfish will migrate away from low-oxygen areas. Within a species, early life stages may be more subject to oxygen stress than older life stages. Hypoxia alters both the structure and function of benthic communities, but effects may differ with regional hypoxia history. Human-caused hypoxia is generally linked to eutrophication, and occurs adjacent to watersheds with large populations or agricultural activities. Many occurrences are seasonal, within estuaries, fjords or enclosed seas of the North Atlantic and the NW Pacific Oceans. Benthic faunal responses, elicited at oxygen levels below 2 ml L−1, typically involve avoidance or mortality of large species and elevated abundances of enrichment opportunists, sometimes prior to population crashes. Areas of low oxygen persist seasonally or continuously beneath upwelling regions, associated with the upper parts of oxygen minimum zones (SE Pacific, W Africa, N Indian Ocean). These have a distribution largely distinct from eutrophic areas and support a resident fauna that is adapted to survive and reproduce at oxygen concentrations <0.5 ml L−1. Under both natural and eutrophication-caused hypoxia there is loss of diversity, through attrition of intolerant species and elevated dominance, as well as reductions in body size. These shifts in species composition and diversity yield altered trophic structure, energy flow pathways, and corresponding ecosystem services such as production, organic matter cycling and organic C burial. Increasingly the influences of nature and humans interact to generate or exacerbate hypoxia. A warmer ocean is more stratified, holds less oxygen, and may experience greater advection of oxygen-poor source waters, making new regions subject to hypoxia. Future understanding of benthic responses to hypoxia must be established in the context of global climate change and other human influences such as overfishing, pollution, disease, habitat loss, and species invasions.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Spreading dead zones and consequences for marine ecosystems
Diaz, R. J., & Rosenberg, R. (2008) · Science · doi:10.1126/science.1156401 · Cited by 6,626
Climate change affects marine fishes through the oxygen limitation of thermal tolerance
Pörtner, H. O., & Knust, R. (2007) · Science · doi:10.1126/science.1135471 · Cited by 2,030
Thresholds of hypoxia for marine biodiversity
Vaquer-Sunyer, R., & Duarte, C. M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803833105 · Cited by 1,971
Effects of hypoxia and organic enrichment on the coastal marine environment
Gray, J., Wu, R., & Or, Y. (2002) · Marine Ecology Progress Series · doi:10.3354/meps238249 · Cited by 1,002
Submerged aquatic vegetation in relation to different nutrient regimes
Duarte, C. M. (1995) · Ophelia · doi:10.1080/00785236.1995.10422039 · Cited by 924
Grantham, B. A., Chan, F., Nielsen, K. J., Fox, D. S., Barth, J. A., Huyer, A., Lubchenco, J., & Menge, B. A. (2004) · Nature · doi:10.1038/nature02605 · Cited by 587
Oxygen declines and the shoaling of the hypoxic boundary in the California Current
Bograd, S. J., Castro, C. G., Di Lorenzo, E., Palacios, D. M., Bailey, H., Gilly, W., & Chavez, F. P. (2008) · Geophysical Research Letters · doi:10.1029/2008gl034185 · Cited by 420
Effects of periodic hypoxia on distribution of demersal fish and crustaceans
Pihl, L., Baden, S. P., & Diaz, R. J. (1991) · Marine Biology · doi:10.1007/bf01313644 · Cited by 404
Physiological and metabolic responses to hypoxia in invertebrates
Grieshaber, M. K., Hardewig, I., Kreutzer, U., & Pörtner, H.-O. (1993) · Reviews of Physiology, Biochemistry and Pharmacology · doi:10.1007/bfb0030909 · Cited by 398
Macrobenthic community structure within and beneath the oxygen minimum zone, NW Arabian Sea
Levin, L. A., Gage, J. D., Martin, C., & Lamont, P. A. (2000) · Deep Sea Research Part II: Topical Studies in Oceanography · doi:10.1016/s0967-0645(99)00103-4 · Cited by 236
Self-citation
Cited by
Deoxygenation of the Baltic Sea during the last century
Carstensen, J., Andersen, J. H., Gustafsson, B. G., & Conley, D. J. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323156111 · Cited by 684
Assessing ocean alkalinity for carbon sequestration
Renforth, P., & Henderson, G. (2017) · Reviews of Geophysics · doi:10.1002/2016rg000533 · Cited by 655
“Hypoxia alters benthic ecosystem structure and function, in which smaller taxa are more resilient than larger [Levin et al., 2009].”
BackgroundCoastal ocean acidification: The other eutrophication problem
Wallace, R. B., Baumann, H., Grear, J. S., Aller, R. C., & Gobler, C. J. (2014) · Estuarine, Coastal and Shelf Science · doi:10.1016/j.ecss.2014.05.027 · Cited by 607
Future ocean acidification will be amplified by hypoxia in coastal habitats
Melzner, F., Thomsen, J., Koeve, W., Oschlies, A., Gutowska, M. A., Bange, H. W., Hansen, H. P., & Körtzinger, A. (2013) · Marine Biology · doi:10.1007/s00227-012-1954-1 · Cited by 501
Projected impacts of climate change on marine fish and fisheries
Hollowed, A. B., Barange, M., Beamish, R. J., Brander, K., Cochrane, K., Drinkwater, K., Foreman, M. G. G., Hare, J. A., Holt, J., Ito, S.-I., et al. (2013) · ICES Journal of Marine Science · doi:10.1093/icesjms/fst081 · Cited by 339
Metadata
- Authors
- Levin, L. A., Ekau, W., Gooday, A. J., Jorissen, F., Middelburg, J. J., Naqvi, S. W. A., Neira, C., Rabalais, N. N., & Zhang, J.
- Venue
- Biogeosciences
- Publisher
- Copernicus GmbH
- Published
- 2009-10-08
- Volume
- 6
- Issue
- 10
- Pages
- 2063-2098
- ISSN
- 1726-4170 (ISSN-L)
- 1726-4189
- OpenAlex
- W2106839118
- Cited by
- 755
- References
- 16
- FWCI
- 17.21
- Type
- journal article
- Language
- en
- Open access
- gold
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Effects of natural and human-induced hypoxia on coastal benthos. https://app.cochat.ai/papers/10.5194/bg-6-2063-2009
- The paper
- Levin, L. A., Ekau, W., Gooday, A. J., Jorissen, F., Middelburg, J. J., Naqvi, S. W. A., Neira, C., Rabalais, N. N., & Zhang, J. (2009). Effects of natural and human-induced hypoxia on coastal benthos. Biogeosciences. https://doi.org/10.5194/bg-6-2063-2009
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.