scholarly journals Effects of natural and human-induced hypoxia on coastal benthos

2009 ◽  
Vol 6 (10) ◽  
pp. 2063-2098 ◽  
Author(s):  
L. A. Levin ◽  
W. Ekau ◽  
A. J. Gooday ◽  
F. Jorissen ◽  
J. J. Middelburg ◽  
...  

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.

2009 ◽  
Vol 6 (2) ◽  
pp. 3563-3654 ◽  
Author(s):  
L. A. Levin ◽  
W. Ekau ◽  
A. J. Gooday ◽  
F. Jorissen ◽  
J. J. Middelburg ◽  
...  

Abstract. Coastal hypoxia (<1.42 ml L−1; 62.5 μM; 2 mg L−1, approx. 30% oxygen saturation) occurs seasonally in many estuaries, fjords, and along open coasts subject to upwelling or excessive riverine nutrient input, and permanently in some isolated seas and marine basins. Underlying causes of hypoxia include enhanced nutrient input from natural causes (upwelling) or anthropogenic origin (eutrophication) and reduction of mixing by limited circulation or enhanced stratification; combined these lead to higher surface water production, microbial respiration and eventual oxygen depletion. Advective inputs of low-oxygen waters may initiate or expand hypoxic conditions. Responses of estuarine, enclosed sea, and open shelf 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, thereby providing 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.


2009 ◽  
Vol 7 (5) ◽  
pp. 371-381 ◽  
Author(s):  
Niels Peter Revsbech ◽  
Lars Hauer Larsen ◽  
Jens Gundersen ◽  
Tage Dalsgaard ◽  
Osvaldo Ulloa ◽  
...  

2019 ◽  
Vol 16 (22) ◽  
pp. 4337-4356 ◽  
Author(s):  
Ulrike Hanz ◽  
Claudia Wienberg ◽  
Dierk Hebbeln ◽  
Gerard Duineveld ◽  
Marc Lavaleye ◽  
...  

Abstract. Thriving benthic communities were observed in the oxygen minimum zones along the southwestern African margin. On the Namibian margin, fossil cold-water coral mounds were overgrown by sponges and bryozoans, while the Angolan margin was characterized by cold-water coral mounds covered by a living coral reef. To explore why benthic communities differ in both areas, present-day environmental conditions were assessed, using conductivity–temperature–depth (CTD) transects and bottom landers to investigate spatial and temporal variations of environmental properties. Near-bottom measurements recorded low dissolved oxygen concentrations on the Namibian margin of 0–0.15 mL L−1 (≜0 %–9 % saturation) and on the Angolan margin of 0.5–1.5 mL L−1 (≜7 %–18 % saturation), which were associated with relatively high temperatures (11.8–13.2 ∘C and 6.4–12.6 ∘C, respectively). Semidiurnal barotropic tides were found to interact with the margin topography producing internal waves. These tidal movements deliver water with more suitable characteristics to the benthic communities from below and above the zone of low oxygen. Concurrently, the delivery of a high quantity and quality of organic matter was observed, being an important food source for the benthic fauna. On the Namibian margin, organic matter originated directly from the surface productive zone, whereas on the Angolan margin the geochemical signature of organic matter suggested an additional mechanism of food supply. A nepheloid layer observed above the cold-water corals may constitute a reservoir of organic matter, facilitating a constant supply of food particles by tidal mixing. Our data suggest that the benthic fauna on the Namibian margin, as well as the cold-water coral communities on the Angolan margin, may compensate for unfavorable conditions of low oxygen levels and high temperatures with enhanced availability of food, while anoxic conditions on the Namibian margin are at present a limiting factor for cold-water coral growth. This study provides an example of how benthic ecosystems cope with such extreme environmental conditions since it is expected that oxygen minimum zones will expand in the future due to anthropogenic activities.


2020 ◽  
Author(s):  
J.M. Beman ◽  
S.M. Vargas ◽  
J.M. Wilson ◽  
E. Perez-Coronel ◽  
S. Vazquez ◽  
...  

AbstractOceanic oxygen minimum zones (OMZs) occur where microorganisms deplete dissolved oxygen (DO) to exceptionally low levels, and are globally significant sites of biogeochemical cycling. Amid the intense competition for DO and other substrates occurring in these metabolically challenging environments, aerobic nitrite oxidation may consume significant amounts of DO, but this has not been examined comprehensively. Using parallel measurements of oxygen consumption rates and 15N-nitrite oxidation rates applied to water column profiles and to oxygen manipulation experiments, we show that nitrite oxidation is a substantial sink for DO in the ocean’s largest OMZ. The contribution of nitrite oxidation to overall DO consumption increased at low DO concentrations, tracking gradients and variations within and across multiple stations in the eastern tropical North Pacific Ocean. Oxygen manipulation experiments produced highly consistent effects, with nitrite oxidation responsible for progressively more DO consumption (up to 97%) as DO was experimentally decreased. Natural abundance stable isotope data indicated coupling of nitrite oxidation and nitrate reduction, while 16S rRNA and metagenome sequencing revealed that Nitrospina ecotypes possessing high-affinity cytochrome oxidase genes were prevalent and active within the OMZ. Collectively, our results demonstrate that nitrite oxidation consumes significant amounts of DO, and that this proportion increases as DO declines—indicating that nitrite oxidation is critically important to the formation and maintenance of OMZs.SignificanceOceanic oxygen minimum zones (OMZs) are naturally-occuring regions of low oxygen found in select areas of the ocean. Lack of dissolved oxygen has important implications for both the distribution of marine organisms and global biogeochemical cycles, yet we have a limited understanding of how oxygen is depleted to such low levels. Here we comprehensively quantify the contribution of nitrite oxidation to oxygen depletion in the ocean’s largest OMZ. We observed highly consistent patterns across depth profiles, and in multiple experiments where we manipulated oxygen concentrations, finding that nitrite oxidation consumes progressively more oxygen at lower oxygen concentrations. Our findings demonstrate that nitrite oxidation plays a pivotal role in exhausting oxygen to the low levels found in OMZs.


2012 ◽  
Vol 9 (1) ◽  
pp. 203-215 ◽  
Author(s):  
E. Ryabenko ◽  
A. Kock ◽  
H. W. Bange ◽  
M. A. Altabet ◽  
D. W. R. Wallace

Abstract. We present new data for the stable isotope ratio of inorganic nitrogen species from the contrasting oxygen minimum zones (OMZs) of the Eastern Tropical North Atlantic, south of Cape Verde, and the Eastern Tropical South Pacific off Peru. Differences in minimum oxygen concentration and corresponding N-cycle processes for the two OMZs are reflected in strongly contrasting δ15N distributions. Pacific surface waters are marked by strongly positive values for δ15N-NO3–) reflecting fractionation associated with subsurface N-loss and partial NO3– utilization. This contrasts with negative values in NO3– depleted surface waters of the Atlantic which are lower than can be explained by N supply via N2 fixation. We suggest the negative values reflect inputs of nitrate, possibly transient, associated with deposition of Saharan dust. Strong signals of N-loss processes in the subsurface Pacific OMZ are evident in the isotope and N2O data, both of which are compatible with a contribution of canonical denitrification to overall N-loss. However the apparent N isotope fractionation factor observed is relatively low (&amp;varepsilon;d=11.4 ‰) suggesting an effect of influence from denitrification in sediments. Identical positive correlation of N2O vs. AOU for waters with oxygen concentrations ([O2] < 5 μmol l−1) in both regions reflect a nitrification source. Sharp decrease in N2O concentrations is observed in the Pacific OMZ due to denitrification under oxygen concentrations O2 < 5 μmol l−1.


2015 ◽  
Vol 112 (35) ◽  
pp. 10979-10984 ◽  
Author(s):  
Wei Qin ◽  
Laura T. Carlson ◽  
E. Virginia Armbrust ◽  
Allan H. Devol ◽  
James W. Moffett ◽  
...  

Marine ammonia-oxidizing archaea (AOA) are among the most abundant of marine microorganisms, spanning nearly the entire water column of diverse oceanic provinces. Historical patterns of abundance are preserved in sediments in the form of their distinctive glycerol dibiphytanyl glycerol tetraether (GDGT) membrane lipids. The correlation between the composition of GDGTs in surface sediment and the overlying annual average sea surface temperature forms the basis for a paleotemperature proxy (TEX86) that is used to reconstruct surface ocean temperature as far back as the Middle Jurassic. However, mounting evidence suggests that factors other than temperature could also play an important role in determining GDGT distributions. We here use a study set of four marine AOA isolates to demonstrate that these closely related strains generate different TEX86–temperature relationships and that oxygen (O2) concentration is at least as important as temperature in controlling TEX86values in culture. All of the four strains characterized showed a unique membrane compositional response to temperature, with TEX86-inferred temperatures varying as much as 12 °C from the incubation temperatures. In addition, both linear and nonlinear TEX86–temperature relationships were characteristic of individual strains. Increasing relative abundance of GDGT-2 and GDGT-3 with increasing O2limitation, at the expense of GDGT-1, led to significant elevations in TEX86-derived temperature. Although the adaptive significance of GDGT compositional changes in response to both temperature and O2is unclear, this observation necessitates a reassessment of archaeal lipid-based paleotemperature proxies, particularly in records that span low-oxygen events or underlie oxygen minimum zones.


2019 ◽  
Author(s):  
Ulrike Hanz ◽  
Claudia Wienberg ◽  
Dierk Hebbeln ◽  
Gerard Duineveld ◽  
Marc Lavaleye ◽  
...  

Abstract. Fossil cold-water coral mounds overgrown by sponges and bryozoans were observed in anoxic conditions on the Namibian margin, while mounds colonized by thriving cold-water coral reefs were found in hypoxic conditions on the Angolan margin. These low oxygen conditions do not meet known environmental ranges favoring cold-water corals and hence are expected to provide unsuitable habitats for cold-water coral growth and therefore reef formation. To explain why the living fauna can nevertheless thrive in both areas, present day environmental conditions at the southwestern African margin were assessed. Downslope CTD transects and the deployment of bottom landers were used to investigate spatial and temporal variations of environmental properties. Temporal measurements in the mound areas recorded oscillating low dissolved oxygen concentrations of 0–0.17 ml l−1 (≙ 0–9 % saturation) on the Namibian and 0.5–1.5 ml l−1 (≙ 7–18 % saturation) on the Angolan margin, which were associated with relatively high temperatures (11.8 13.2 °C and 6.4–12.6 °C respectively). Semi-diurnal barotrophic tides were found to interact with the margin topography producing internal waves with excursions of up to 70 and 130 m for the Namibian and Angolan margins, respectively. These tidal movements temporarily deliver water with more suitable characteristics to the coral mounds from below and above the hypoxic zone. Concurrently, the delivery of high quantity and quality of suspended particulate organic matter was observed, which serves as a food source for cold-water corals. On the Namibian slope organic matter indicates a completely marine source and originates directly from the surface productive zone, whereas on the Angolan margin the geochemical signature of organic material suggest an additional mechanisms of food supply. A nepheloid layer observed above the cold-water coral mound area on the Angolan margin may constitutes a reservoir of fresh organic matter, facilitating a constant supply of food particles by tidal mixing. This suggests that the cold-water coral communities as well as the associated fauna may compensate unfavorable conditions induced by low oxygen levels and high temperatures with an enhanced availability of food. With the expected expansion of oxygen minimum zones in the future due to anthropogenic activities, this study provides an example on how ecosystems could cope with such extreme environmental conditions.


2016 ◽  
Author(s):  
Daniela Niemeyer ◽  
Tronje P. Kemena ◽  
Katrin J. Meissner ◽  
Andreas Oschlies

Abstract. Observations indicate an expansion of oxygen minimum zones (OMZs) over the past 50 years, likely related to ongoing deoxygenation caused by reduced solubility, changes in stratification and circulation, and a potential acceleration of organic matter turnover in a warming climate. Higher temperatures also lead to enhanced weathering on land, which, in turn, increase the phosphorus and alkalinity flux into the ocean. The overall area of ocean sediments that are in direct contact with low oxygen bottom waters also increases with expanding OMZs. This leads to an additional release of phosphorus from ocean sediments and therefore raises the ocean's phosphorus inventory even further. Higher availability in phosphorus enhances biological production, remineralisation and oxygen consumption, and might therefore lead to further expansions of OMZs, representing a positive feedback. A negative feedback arises from the enhanced productivity-induced drawdown of carbon and also increased uptake of CO2 due to increased alkalinity, which, in turn, got there through weathering. This feedback leads to a decrease in atmospheric CO2 and weathering rates. Here we quantify these two competing feedbacks on millennial timescales for a high CO2 emission scenario. Using the UVic Earth System Climate Model of intermediate complexity, our model results suggest that the positive benthic phosphorus release feedback has only a minor impact on the size of OMZs in the next 1000 years, although previous studies assume that the phosphorus release feedback was the main factor for anoxic conditions during Cretaceous period. The increase in the marine phosphorus inventory under assumed business-as-usual global warming conditions originates, on millennial timescales, almost exclusively from the input via terrestrial weathering and causes a 4 to 5-fold expansion of the suboxic water volume in the model.


2013 ◽  
Vol 10 (6) ◽  
pp. 9451-9492 ◽  
Author(s):  
L. A. Levin ◽  
A. L. McGregor ◽  
G. F. Mendoza ◽  
C. Woulds ◽  
P. Cross ◽  
...  

Abstract. There is a growing need to understand the ability of bathyal assemblages to recover from disturbance and oxygen stress, as human activities and expanding oxygen minimum zones increasingly affect deep continental margins. The effects of a pronounced oxygen minimum zone (OMZ) on slope benthic community structure have been studied in both the Western and Eastern Arabian Sea; however, little is known about the dynamics or resilience of these benthic populations. To examine the influence of oxygen and phytodetritus on short-term settlement patterns we conducted colonization experiments along two cross-OMZ transects on the West Indian continental margin. Four colonization trays were deployed at each depth for 4 days at 542 and 802 m (16°58′ N) and for 9 days at 817 m and 1147 m (17°31′ N). Oxygen concentrations ranged from 0.9 μM (0.02 mL L−1) at 542 m to 22 μM (0.5 mL L−1) at 1147 m. All trays contained local defaunated sediments; half of the trays at each depth also contained 13C/15N-labeled phytodetritus mixed into the sediments. Sediment cores were collected between 535 m and 1140 m for analysis of background (source) macrofaunal (> 300 μm) densities and composition. Background densities ranged from 0 ind. m−2 (at 535–542 m) to 7400 ind. m−2, with maximum values on both transects at 700–800 m. Macrofaunal colonizer densities ranged from 0 ind. m−2 at 542 m, where oxygen was lowest, to average values of 142 ind. m−2 at 800 m, and 3074 ind. m−2 at 1147 m, where oxygen concentration was highest. These were equal to 4.3% and 151% of the ambient background community at 800 m and 1147 m, respectively. Community structure of settlers showed no response to the presence of phytodetritus. Increasing depth and oxygen concentration, however, significantly influenced the community composition and abundance of colonizing macrofauna. Polychaetes constituted 92.4% of the total colonizers, followed by crustaceans (4.2%), mollusks (2.5%), and echinoderms (0.8%). The majority of colonizers were found at 1147m; 88.5% of these were Capitella sp., although they were rare in the background community. Colonists at 800 and 1147 m also included ampharetid, spionid, syllid, lumbrinerid, cirratulid, cossurid and sabellid polychaetes. Consumption of δ13C/ δ15N-labeled phytodetritus was observed for macrofaunal foraminifera (too large to be colonizers) at the 542 and 802/817 m sites, and by metazoan macrofauna mainly at the deepest, better oxygenated site. Calcareous foraminifera (Uvigerina, Hoeglundina sp.), capitellid polychaetes and cumaceans were among the major consumers. These preliminary experiments suggest that bottom-water oxygen concentrations may strongly influence ecosystem services on continental margins, as reflected in rates of colonization by benthos and colonizer processing of carbon following disturbance.


2012 ◽  
Vol 9 (12) ◽  
pp. 5007-5022 ◽  
Author(s):  
L. M. Zamora ◽  
A. Oschlies ◽  
H. W. Bange ◽  
K. B. Huebert ◽  
J. D. Craig ◽  
...  

Abstract. The eastern tropical Pacific (ETP) is believed to be one of the largest marine sources of the greenhouse gas nitrous oxide (N2O). Future N2O emissions from the ETP are highly uncertain because oxygen minimum zones are expected to expand, affecting both regional production and consumption of N2O. Here we assess three primary uncertainties in how N2O may respond to changing O2 levels: (1) the relationship between N2O production and O2 (is it linear or exponential at low O2 concentrations?), (2) the cutoff point at which net N2O production switches to net N2O consumption (uncertainties in this parameterisation can lead to differences in model ETP N2O concentrations of more than 20%), and (3) the rate of net N2O consumption at low O2. Based on the MEMENTO database, which is the largest N2O dataset currently available, we find that N2O production in the ETP increases linearly rather than exponentially with decreasing O2. Additionally, net N2O consumption switches to net N2O production at ~ 10 μM O2, a value in line with recent studies that suggest consumption occurs on a larger scale than previously thought. N2O consumption is on the order of 0.01–1 mmol N2O m−3 yr−1 in the Peru-Chile Undercurrent. Based on these findings, it appears that recent studies substantially overestimated N2O production in the ETP. In light of expected deoxygenation and the higher than previously expected point at which net N2O production switches to consumption, there is enough uncertainty in future N2O production that even the sign of future changes is still unclear.


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