Anoxic conditions result from a combination of environmental conditions, including density stratification,[11] inputs of organic material or other reducing agents, and physical barriers to water circulation. In fjords, shallow sills at the entrance may prevent circulation. In contrast, at continental boundaries, the circulation may be especially low while the organic material input from production at upper levels is exceptionally high.[12] In wastewater treatment, the absence of oxygen alone is indicated anoxic while the term anaerobic is used to indicate the absence of any common electron acceptor such as nitrate, sulfate or oxygen.
When oxygen is depleted in a basin, bacteria first turn to the second-best electron acceptor, which in seawater is nitrate. Denitrification occurs, and the nitrate will be consumed relatively rapidly. After reducing some other minor elements, the bacteria will turn to reducingsulfate. This results in the byproduct of hydrogen sulfide (H2S), a chemical toxic to most biota and responsible for the characteristic "rotten egg" smell and dark black sediment color:[13][14]
2 CH2O + SO2− 4 → 2 HCO− 3 + H2S + chemical energy
These sulfides will mostly be oxidized to either sulfates (~90%) in more oxygen-rich water or precipitated and converted into pyrite (~10%), according to the following chemical equations:[14]
Some chemolithotrophs can also facilitate the oxidation of hydrogen sulfide into elemental sulfur, according to the following chemical equation:[15]
H2S + O2 → S + H2O2
Anoxia is quite common in muddy ocean bottoms where there are both high amounts of organic matter and low levels of inflow of oxygenated water through the sediment. Below a few centimetres from the surface, the interstitial water (pore water between sediment grains) is oxygen-free.
Anoxia is further influenced by biochemical oxygen demand (BOD), which represents the amount of oxygen utilised by marine organisms during the process of breaking down organic matter. BOD is influenced by the type of organisms present, the pH of the water, temperature, and the type of organic matter present in the area. BOD is directly related to the amount of dissolved oxygen available, especially in smaller bodies of water such as rivers and streams. As BOD increases, available oxygen decreases. This causes stress on larger organisms. BOD comes from natural and anthropogenic sources, including: dead organisms, manure, wastewater, and urban runoff.[16]
The temperature of a body of water directly affects the amount of dissolved oxygen it can hold. Following Henry's law, as water becomes warmer, oxygen solubility decreases. This property leads to daily anoxic cycles on small geographic scales and seasonal cycles of anoxia on larger scales. Thus, bodies of water are more vulnerable to anoxic conditions during the warmest period of the day and during summer months. This problem can be further exacerbated in the vicinity of industrial discharge, where warm water used to cool machinery is less able to hold oxygen than the basin to which it is released.
The activity of photosynthetic organisms also influences daily cycles. The lack of photosynthesis during nighttime hours in the absence of light can result in anoxic conditions intensifying throughout the night, with a maximum shortly after sunrise.[18]
Biological adaptation
The reactions of individual species to eutrophication can vary widely. For example, some organisms, such as primary producers, can adapt quickly and even thrive under anoxic conditions. However, most organisms are highly susceptible to slight changes in aquatic oxygen levels. When a respiring organism is presented with little to no oxygen, the chances of survival decrease. Therefore, eutrophication and anoxic conditions in water lead to a reduction in biodiversity.
For example, the soft coral Xenia umbellata can resist some anoxic conditions for short periods. Still, after about three weeks, mean survival decreases to about 81%, and about 40% of surviving species experience size reductions, a lessening in coloration, and compromised pinnate structures.[19] Another example of a susceptible organism is the Sydney cockle, Anadara trapezia. Enriched sediments have lethal and sublethal effects on this cockle, and, as stated in Vadillo Gonzalez et al. (2021), "movement of cockles was reduced in enriched sediments compared to natural treatments."[20]
A study collecting over 850 published experiments "reporting oxygen thresholds and/or lethal times for a total of 206 species spanning the full taxonomic range of benthicmetazoans."[21]
Individual species will exhibit different adaptive responses to anoxic conditions, depending on their biological makeup and the condition of their habitat. While some can pump oxygen from higher water levels down into the sediment, other adaptations include specific haemoglobins for low-oxygen environments, slow movement to reduce the rate of metabolism, and symbiotic relationships with anaerobic bacteria. In all cases, the prevalence of excess nutrients results in low levels of biological activity and a lower level of species diversity, unless the area is ordinarily anoxic.[13]
↑Bjork, Mats; Short, Fred; McLeod, Elizabeth; Beer, Sven (2008). Managing Sea-grasses for Resilience to Climate Change. Volume 3 of IUCN Resilience Science Group Working Papers. Gland, Switzerland: International Union for Conservation of Nature (IUCN). p.24. ISBN978-2-8317-1089-1.
↑Vadillo Gonzalez, Sebastian; Johnston, Emma L.; Dafforn, Katherine A.; O’Connor, Wayne A.; Gribben, Paul E. (2021). "Body size affects lethal and sublethal responses to organic enrichment: Evidence of associational susceptibility for an infaunal bivalve". Marine Environmental Research. 169 105391. Bibcode:2021MarER.16905391V. doi:10.1016/j.marenvres.2021.105391. PMID34217096. S2CID235728608.
Hallberg, R.O. (1974). "Paleoredox conditions in the Eastern Gotland Basin during the recent centuries". Merentutkimuslait. Julk./Havsforskningsinstitutets Skrift, 238: 3–16.
Jerbo, A (1972). "Är Östersjöbottnens syreunderskott en modern företeelse?". Vatten. 28: 404–408.
Fenchel, Tom & Finlay, Bland J. (1995). Ecology and Evolution in Anoxic Worlds (Oxford Series in Ecology and Evolution), Oxford University Press. ISBN0-19-854838-9
Richards, F.A. (1965). "Anoxic basins and fjords", in Riley, J.P., and Skirrow, G. (eds) Chemical Oceanography, London, Academic Press, 611–643.
Sarmiento, J. A. et al. (1988b). "Ocean Carbon-Cycle Dynamics and Atmospheric pCO2". Philosophical Transactions of the Royal Society of London, Series A, Mathematical and Physical Sciences, Vol. 325, No. 1583, Tracers in the Ocean (May 25, 1988), pp.3–21.
Van Der Wielen, P. W. J. J.; Bolhuis, H.; Borin, S.; Daffonchio, D.; Corselli, C.; Giuliano, L.; d'Auria, G.; De Lange, G. J.; Huebner, A.; Varnavas, S. P.; Thomson, J.; Tamburini, C.; Marty, D.; McGenity, T. J.; Timmis, K. N.; Biodeep Scientific, P. (2005). "The Enigma of Prokaryotic Life in Deep Hypersaline Anoxic Basins". Science. 307 (5706): 121–123. Bibcode:2005Sci...307..121V. doi:10.1126/science.1103569. PMID15637281. S2CID206507712..