Ocean fertilization or ocean nourishment is a type of technology for carbon dioxide removal from the ocean based on the purposeful introduction of plant nutrients to the upper ocean to increase marine food production and to remove carbon dioxide from the atmosphere. [1] [2] Ocean nutrient fertilization, for example iron fertilization, could stimulate photosynthesis in phytoplankton. The phytoplankton would convert the ocean's dissolved carbon dioxide into carbohydrate, some of which would sink into the deeper ocean before oxidizing. More than a dozen open-sea experiments confirmed that adding iron to the ocean increases photosynthesis in phytoplankton by up to 30 times. [3]
This is one of the more well-researched carbon dioxide removal (CDR) approaches, and supported by the Climate restoration proponents. However, there is uncertainty about this approach regarding the duration of the effective oceanic carbon sequestration. While surface ocean acidity may decrease as a result of nutrient fertilization, when the sinking organic matter remineralizes, deep ocean acidity could increase. A 2021 report on CDR indicates that there is medium-high confidence that the technique could be efficient and scalable at low cost, with medium environmental risks. [4] The risks of nutrient fertilization can be monitored. Peter Fiekowsy and Carole Douglis write "I consider iron fertilization an important item on our list of pottential climate restoration solutions. Given the fact that iron fertilization is a natural process that has taken place on a massive scale for millions of years, it is likely that most of the side effects are familiar ones that pose no major threat" [5]
A number of techniques, including fertilization by the micronutrient iron (called iron fertilization) or with nitrogen and phosphorus (both macronutrients), have been proposed. Some research in the early 2020s suggested that it could only permanently sequester a small amount of carbon. [6] More recent research publlications sustain that iron fertilization shows promise. A NOAA special report rated iron fertilization as having "a moderate potential for cost, scalability and how long carbon might be stored compared to other marine sequestration ideas" [7]
The marine food chain is based on photosynthesis by marine phytoplankton that combine carbon with inorganic nutrients to produce organic matter. Production is limited by the availability of nutrients, most commonly nitrogen or iron. Numerous experiments [8] have demonstrated how iron fertilization can increase phytoplankton productivity. Nitrogen is a limiting nutrient over much of the ocean and can be supplied from various sources, including fixation by cyanobacteria. Carbon-to-iron ratios in phytoplankton are much larger than carbon-to-nitrogen or carbon-to-phosphorus ratios, so iron has the highest potential for sequestration per unit mass added.
Oceanic carbon naturally cycles between the surface and the deep via two "pumps" of similar scale. The "solubility" pump is driven by ocean circulation and the solubility of CO2 in seawater. The "biological" pump is driven by phytoplankton and subsequent settling of detrital particles or dispersion of dissolved organic carbon. The former has increased as a result of increasing atmospheric CO2 concentration. This CO2 sink is estimated to be approximately 2 GtC yr−1. [9]
The global phytoplankton population fell about 40 percent between 1950 and 2008 or about 1 percent per year. The most notable declines took place in polar waters and in the tropics. The decline is attributed to sea surface temperature increases. [10] A separate study found that diatoms, the largest type of phytoplankton, declined more than 1 percent per year from 1998 to 2012, particularly in the North Pacific, North Indian and Equatorial Indian oceans. The decline appears to reduce pytoplankton's ability to sequester carbon in the deep ocean. [11]
Fertilization offers the prospect of both reducing the concentration of atmospheric greenhouse gases with the aim of slowing climate change and at the same time increasing fish stocks via increasing primary production. The reduction reduces the ocean's rate of carbon sequestration in the deep ocean.
Each area of the ocean has a base sequestration rate on some timescale, e.g., annual. Fertilization must increase that rate, but must do so on a scale beyond the natural scale. Otherwise, fertilization changes the timing, but not the total amount sequestered. However, accelerated timing may have beneficial effects for primary production separate from those from sequestration. [9]
Biomass production inherently depletes all resources (save for sun and water). Either they must all be subject to fertilization or sequestration will eventually be limited by the one mostly slowly replenished (after some number of cycles) unless the ultimate limiting resource is sunlight and/or surface area. Generally, phosphate is the ultimate limiting nutrient. As oceanic phosphorus is depleted (via sequestration) it would have to be included in the fertilization cocktail supplied from terrestrial sources. [9]
Phytoplankton require a variety of nutrients. These include macronutrients such as nitrate and phosphate (in relatively high concentrations) and micronutrients such as iron and zinc (in much smaller quantities). Nutrient requirements vary across phylogenetic groups (e.g., diatoms require silicon) but may not individually limit total biomass production. Co-limitation (among multiple nutrients) may also mean that one nutrient can partially compensate for a shortage of another. Silicon does not affect total production, but can change the timing and community structure with follow-on effects on remineralization times and subsequent mesopelagic nutrient vertical distribution. [9]
High-nutrient, low-chlorophyll (HNLC) waters occupy the oceans' subtropical gyre systems, approximately 40 per cent of the surface, where wind-driven downwelling and a strong thermocline impede nutrient resupply from deeper water. Nitrogen fixation by cyanobacteria provides a major source of N. In effect, it ultimately prevents the ocean from losing the N required for photosynthesis. Phosphorus has no substantial supply route, making it the ultimate limiting macronutrient. The sources that fuel primary production are deep water stocks and runoff or dust-based. [9]
Iron fertilization is the intentional introduction of iron-containing compounds (like iron sulfate) to iron-poor areas of the ocean surface to stimulate phytoplankton production. This is intended to enhance biological productivity and/or accelerate carbon dioxide (CO2) sequestration from the atmosphere. Iron is a trace element necessary for photosynthesis in plants. It is highly insoluble in sea water and in a variety of locations is the limiting nutrient for phytoplankton growth. Large algal blooms can be created by supplying iron to iron-deficient ocean waters. These blooms can nourish other organisms.
Ocean iron fertilization is an example of a geoengineering technique. [12] Iron fertilization [13] attempts to encourage phytoplankton growth, which removes carbon from the atmosphere for at least a period of time. [14] [15] This technique is controversial because there is limited understanding of its complete effects on the marine ecosystem, [16] including side effects and possibly large deviations from expected behavior. Such effects potentially include release of nitrogen oxides, [17] and disruption of the ocean's nutrient balance. [12] Controversy remains over the effectiveness of atmospheric CO
2 sequestration and ecological effects. [18] Since 1990, 13 major large scale experiments have been carried out to evaluate efficiency and possible consequences of iron fertilization in ocean waters. A study in 2017 considered that the method is unproven; the sequestering efficiency was low and sometimes no effect was seen and the amount of iron deposits needed to make a small cut in the carbon emissions would be in the million tons per year. [19] However since 2021, interest is renewed in the potential of iron fertilization, among other from a white paper study of NOAA, the US National Oceanographic and Atmospheric Administration, which rated iron fertilization as having "moderate potential for cost, scalability and how long carbon might be stored compared to other marine sequestration ideas"
In the very long term, phosphorus "is often considered to be the ultimate limiting macronutrient in marine ecosystems" [21] and has a slow natural cycle. Where phosphate is the limiting nutrient in the photic zone, addition of phosphate is expected to increase primary phytoplankton production. This technique can give 0.83 W/m2 of globally averaged negative forcing, [22] which is sufficient to reverse the warming effect of about half the current levels of anthropogenic CO
2 emissions. One water-soluble fertilizer is diammonium phosphate (DAP), (NH
4)
2HPO
4, that as of 2008 had a market price of 1700/tonne−1 of phosphorus. Using that price and the C : P Redfield ratio of 106 : 1 produces a sequestration cost (excluding preparation and injection costs) of some $45 /tonne of carbon (2008), substantially less than the trading price for carbon emissions. [9]
This technique proposes to fertilize the ocean with urea, a nitrogen rich substance, to encourage phytoplankton growth. [23] [24] [25] Concentrations of macronutrients per area of ocean surface would be similar to large natural upwellings. Once exported from the surface, the carbon remains sequestered for a long time. [26]
An Australian company, Ocean Nourishment Corporation (ONC), planned to inject hundreds of tonnes of urea into the ocean, in order to boost the growth of CO
2-absorbing phytoplankton, as a way to combat climate change. In 2007, Sydney-based ONC completed an experiment involving one tonne of nitrogen in the Sulu Sea off the Philippines. [27] This project was criticized by many institutions, including the European Commission, [28] due to lack of knowledge of side effects on the marine ecosystem. [29]
Macronutrient nourishment can give 0.38 W/m2 of globally averaged negative forcing, [22] which is sufficient to reverse the warming effect of current levels of around a quarter of anthropogenic CO
2 emissions.
The two dominant costs are manufacturing the nitrogen and nutrient delivery. [30]
In waters with sufficient iron micro nutrients, but a deficit of nitrogen, urea fertilization is the better choice for algae growth. [31] Urea is the most used fertilizer in the world, due to its high content of nitrogen, low cost and high reactivity towards water. [32] When exposed to ocean waters, urea is metabolized by phytoplankton via urease enzymes to produce ammonia. [33]
The intermediate product carbamate also reacts with water to produce a total of two ammonia molecules. [34]
Another cause of concern is the sheer amount of urea needed to capture the same amount of carbon as eq. iron fertilization. The nitrogen to iron ratio in a typical algae cell is 16:0.0001, meaning that for every iron atom added to the ocean a substantial larger amount of carbon is captured compared to adding one atom of nitrogen. [35] Scientists also emphasize that adding urea to ocean waters could reduce oxygen content and result in a rise of toxic marine algae. [35] This could potentially have devastating effects on fish populations, which others argue would be benefiting from the urea fertilization (the argument being that fish populations would feed on healthy phytoplankton). [36]
Local wave power could be used to pump nutrient-rich water from hundred- metre-plus depths to the euphotic zone. However, deep water concentrations of dissolved CO2 could be returned to the atmosphere. [9]
The supply of DIC in upwelled water is generally sufficient for photosynthesis permitted by upwelled nutrients, without requiring atmospheric CO2. Second-order effects include how the composition of upwelled water differs from that of settling particles. More nitrogen than carbon is remineralized from sinking organic material. Upwelling of this water allows more carbon to sink than that in the upwelled water, which would make room for at least some atmospheric CO2 to be absorbed. the magnitude of this difference is unclear. No comprehensive studies have yet resolved this question. Preliminary calculations using upper limit assumptions indicate a low value. 1,000 square kilometres (390 sq mi) could sequester 1 gigatonne/year. [9]
Sequestration thus depends on the upward flux and the rate of lateral surface mixing of the surface water with denser pumped water. [9]
Volcanic ash adds nutrients to the surface ocean. This is most apparent in nutrient-limited areas. Research on the effects of anthropogenic and aeolian iron addition to the ocean surface suggests that nutrient-limited areas benefit most from a combination of nutrients provided by anthropogenic, eolian and volcanic deposition. [37] Some oceanic areas are comparably limited in more than one nutrient, so fertilization regimes that includes all limited nutrients is more likely to succeed. Volcanic ash supplies multiple nutrients to the system, but excess metal ions can be harmful. The positive impacts of volcanic ash deposition are potentially outweighed by their potential to do harm.[ citation needed ]
Clear evidence documents that ash can be as much as 45 percent by weight in some deep marine sediments. [38] [39] In the Pacific Ocean estimates claim that (on a millennial-scale) the atmospheric deposition of air-fall volcanic ash was as high as the deposition of desert dust. [40] This indicates the potential of volcanic ash as a significant iron source.
In August 2008 the Kasatochi volcanic eruption in the Aleutian Islands, Alaska, deposited ash in the nutrient-limited northeast Pacific. This ash (including iron) resulted in one of the largest phytoplankton blooms observed in the subarctic. [41] [42] Fisheries scientists in Canada linked increased oceanic productivity from the volcanic iron to subsequent record returns of salmon in the Fraser River two years later [43]
The approach advocated by Ocean Nutrition Corporation is to limit the distribution of added nutrients to allow phytoplankton concentrations to rise only to the values seen in upwelling regions (5–10 mg Chl/m3). Maintaining healthy phytoplankton levels is claimed to avoid harmful algal blooms and oxygen depletion. Chlorophyll concentration is an easily measured proxy for phytoplankton concentration. The company stated that values of approximately 4 mg Chl/m3 meet this requirement. [44] SS
While manipulation of the land ecosystem in support of agriculture for the benefit of humans has long been accepted (despite its side effects), directly enhancing ocean productivity has not. Among the reasons are:
According to Lisa Speer of the Natural Resources Defense Council, "There is a limited amount of money, of time, that we have to deal with this problem....The worst possible thing we could do for climate change technologies would be to invest in something that doesn't work and that has big impacts that we don't anticipate." [45]
In 2009 Aaron Strong, Sallie Chisholm, Charles Miller and John Cullen opined in Nature "...fertilizing the oceans with iron to stimulate phytoplankton blooms, absorb carbon dioxide from the atmosphere and export carbon to the deep sea – should be abandoned." [46]
In Science, Warren Cornwall mentions "Tests have shown the iron does stimulate plankton growth. But key questions remain,says Dave Siegel, a marine scientist at the University of California, Santa Barbara, who served on the NASEM panel. How much of the absorbed carbon makes it to the deep ocean is uncertain", while Wil Burns, an ocean law expert at Northwestern University declares that "...making iron fertilization a research priority is "barking mad" since "...a recent survey of 13 past fertilization experiments found only one that increased carbon levels deep in the ocean." [47]
Algal cell chemical composition is often assumed to respect a ratio where atoms are 106 carbon: 16 nitrogen: 1 phosphorus (Redfield ratio [48] ): 0.0001 iron. In other words, each atom of iron helps capture 1,060,000 atoms of carbon, while one nitrogen atom only 6. [49]
In large areas of the ocean, such organic growth (and hence nitrogen fixation) is thought to be limited by the lack of iron rather than nitrogen, although direct measures are hard. [48]
On the other hand, experimental iron fertilisation in HNLC regions has been supplied with excess iron which cannot be utilized before it is scavenged. Thus the organic material produced was much less than if the ratio of nutrients above were achieved. Only a fraction of the available nitrogen (because of iron scavenging) is drawn down. In culture bottle studies of oligotrophic water, adding nitrogen and phosphorus can draw down considerably more nitrogen per dosing. The export production is only a small percentage of the new primary production and in the case of iron fertilization, iron scavenging means that regenerative production is small. With macronutrient fertilisation, regenerative production is expected to be large and supportive of larger total export. Other losses can also reduce efficiency. [50]
In addition, the efficiency of carbon sequestration through ocean fertilisation is heavily influenced by factors such as changes in stoichiometric ratios and gas exchange make accurately predicting the effectiveness of ocean feralization projects. [51]
Fertilisation also does not create a permanent carbon sink. "Ocean fertilisation options are only worthwhile if sustained on a millennial timescale and phosphorus addition may have greater long-term potential than iron or nitrogen fertilisation." [22]
Beyond biological impacts, evidences suggests that plankton blooms can affect the physical properties of surface waters simply by absorbing light and heat from the sun. Watson added that if fertilization is done in shallow coastal waters, a dense layer of phytoplankton clouding the top 30 metres or so of the ocean could hinder corals, kelps or other deeper sea life from carrying out photosynthesis (Watson et al. 2008). In addition, as the bloom declines, nitrous oxide is released, potentially counteracting the effects from the sequestering of carbon. [52]
Toxic algal blooms are common in coastal areas. Fertilization could trigger such blooms. Chronic fertilization could risk the creation of dead zones, such as the one in the Gulf of Mexico. [53]
Adding urea to the ocean can cause phytoplankton blooms that serve as a food source for zooplankton and in turn feed for fish. This may increase fish catches. [54] However, if cyanobacteria and dinoflagellates dominate phytoplankton assemblages that are considered poor quality food for fish then the increase in fish quantity may not be large. [55] Some evidence links iron fertilization from volcanic eruptions to increased fisheries production. [43] [41] Other nutrients would be metabolized along with the added nutrient(s), reducing their presence in fertilized waters. [45]
Krill populations have declined dramatically since whaling began. [53] Sperm whales transport iron from the deep ocean to the surface during prey consumption and defecation. Sperm whales have been shown to increase the levels of primary production and carbon export to the deep ocean by depositing iron-rich faeces into surface waters of the Southern Ocean. The faeces causes phytoplankton to grow and take up carbon. The phytoplankton nourish krill. Reducing the abundance of sperm whales in the Southern Ocean, whaling resulted in an extra 2 million tonnes of carbon remaining in the atmosphere each year. [56]
Many locations, such as the Tubbataha Reef in the Sulu Sea, support high marine biodiversity. [57] Nitrogen or other nutrient loading in coral reef areas can lead to community shifts towards algal overgrowth of corals and ecosystem disruption, implying that fertilization must be restricted to areas in which vulnerable populations are not put at risk. [58]
As the phytoplankton descend the water column, they decay, consuming oxygen and producing greenhouse gases methane and nitrous oxide. Plankton-rich surface waters could warm the surface layer, affecting circulation patterns. [45]
Many phytoplankton species release dimethyl sulfide (DMS), which escapes into the atmosphere where it forms sulfate aerosols and encourages cloud formation, which could reduce warming. [45] However, substantial increases in DMS could reduce global rainfall, according to global climate model simulations, while halving temperature increases as of 2100. [59] [60]
In 2007 Working Group III of the United Nations Intergovernmental Panel on Climate Change examined ocean fertilization methods in its fourth assessment report and noted that the field-study estimates of the amount of carbon removed per ton of iron was probably over-estimated and that potential adverse effects had not been fully studied. [61]
In June 2007 the London Dumping Convention issued a statement of concern noting 'the potential for large scale ocean iron fertilization to have negative impacts on the marine environment and human health', [62] but did not define 'large scale'. It is believed that the definition would include operations.[ citation needed ]
In 2008, the London Convention/London Protocol noted in resolution LC-LP.1 that knowledge on the effectiveness and potential environmental impacts of ocean fertilization was insufficient to justify activities other than research. This non-binding resolution stated that fertilization, other than research, "should be considered as contrary to the aims of the Convention and Protocol and do not currently qualify for any exemption from the definition of dumping". [63]
In May 2008, at the Convention on Biological Diversity, 191 nations called for a ban on ocean fertilization until scientists better understand the implications. [64]
In August 2018, Germany banned the sale of ocean seeding as carbon sequestration system [65] while the matter was under discussion at EU and EASAC levels. [66]
International law presents some dilemmas for ocean fertilization.[ citation needed ] The United Nations Framework Convention on Climate Change (UNFCCC 1992) has accepted mitigation actions.[ citation needed ]
According to United Nations Convention on the Law of the Sea (LOSC 1982), all states are obliged to take all measures necessary to prevent, reduce and control pollution of the marine environment, to prohibit the transfer of damage or hazards from one area to another and to prohibit the transformation of one type pollution to another. How this relates to fertilization is undetermined. [67]
Fertilization may create sulfate aerosols that reflect sunlight, modifying the Earth's albedo, creating a cooling effect that reduces some of the effects of climate change. Enhancing the natural sulfur cycle in the Southern Ocean [68] by fertilizing with iron in order to enhance dimethyl sulfide production and cloud reflectivity may achieve this. [69] [70]
Phytoplankton are the autotrophic (self-feeding) components of the plankton community and a key part of ocean and freshwater ecosystems. The name comes from the Greek words φυτόν, meaning 'plant', and πλαγκτός, meaning 'wanderer' or 'drifter'.
The biological pump (or ocean carbon biological pump or marine biological carbon pump) is the ocean's biologically driven sequestration of carbon from the atmosphere and land runoff to the ocean interior and seafloor sediments. In other words, it is a biologically mediated process which results in the sequestering of carbon in the deep ocean away from the atmosphere and the land. The biological pump is the biological component of the "marine carbon pump" which contains both a physical and biological component. It is the part of the broader oceanic carbon cycle responsible for the cycling of organic matter formed mainly by phytoplankton during photosynthesis (soft-tissue pump), as well as the cycling of calcium carbonate (CaCO3) formed into shells by certain organisms such as plankton and mollusks (carbonate pump).
The iron cycle (Fe) is the biogeochemical cycle of iron through the atmosphere, hydrosphere, biosphere and lithosphere. While Fe is highly abundant in the Earth's crust, it is less common in oxygenated surface waters. Iron is a key micronutrient in primary productivity, and a limiting nutrient in the Southern ocean, eastern equatorial Pacific, and the subarctic Pacific referred to as High-Nutrient, Low-Chlorophyll (HNLC) regions of the ocean.
High-nutrient, low-chlorophyll (HNLC) regions are regions of the ocean where the abundance of phytoplankton is low and fairly constant despite the availability of macronutrients. Phytoplankton rely on a suite of nutrients for cellular function. Macronutrients are generally available in higher quantities in surface ocean waters, and are the typical components of common garden fertilizers. Micronutrients are generally available in lower quantities and include trace metals. Macronutrients are typically available in millimolar concentrations, while micronutrients are generally available in micro- to nanomolar concentrations. In general, nitrogen tends to be a limiting ocean nutrient, but in HNLC regions it is never significantly depleted. Instead, these regions tend to be limited by low concentrations of metabolizable iron. Iron is a critical phytoplankton micronutrient necessary for enzyme catalysis and electron transport.
The Redfield ratio or Redfield stoichiometry is the consistent atomic ratio of carbon, nitrogen and phosphorus found in marine phytoplankton and throughout the deep oceans.
Iron fertilization is the intentional introduction of iron-containing compounds to iron-poor areas of the ocean surface to stimulate phytoplankton production. This is intended to enhance biological productivity and/or accelerate carbon dioxide sequestration from the atmosphere. Iron is a trace element necessary for photosynthesis in plants. It is highly insoluble in sea water and in a variety of locations is the limiting nutrient for phytoplankton growth. Large algal blooms can be created by supplying iron to iron-deficient ocean waters. These blooms can nourish other organisms.
Carbon sequestration is the process of storing carbon in a carbon pool. It plays a crucial role in limiting climate change by reducing the amount of carbon dioxide in the atmosphere. There are two main types of carbon sequestration: biologic and geologic.
In the deep ocean, marine snow is a continuous shower of mostly organic detritus falling from the upper layers of the water column. It is a significant means of exporting energy from the light-rich photic zone to the aphotic zone below, which is referred to as the biological pump. Export production is the amount of organic matter produced in the ocean by primary production that is not recycled (remineralised) before it sinks into the aphotic zone. Because of the role of export production in the ocean's biological pump, it is typically measured in units of carbon. The term was coined by explorer William Beebe as observed from his bathysphere. As the origin of marine snow lies in activities within the productive photic zone, the prevalence of marine snow changes with seasonal fluctuations in photosynthetic activity and ocean currents. Marine snow can be an important food source for organisms living in the aphotic zone, particularly for organisms that live very deep in the water column.
Bacterioplankton refers to the bacterial component of the plankton that drifts in the water column. The name comes from the Ancient Greek word πλαγκτός (planktós), meaning "wandering" or "drifting", and bacterium, a Latin term coined in the 19th century by Christian Gottfried Ehrenberg. They are found in both seawater and fresh water.
The North Pacific Subtropical Gyre (NPSG) is the largest contiguous ecosystem on earth. In oceanography, a subtropical gyre is a ring-like system of ocean currents rotating clockwise in the Northern Hemisphere and counterclockwise in the Southern Hemisphere caused by the Coriolis Effect. They generally form in large open ocean areas that lie between land masses.
The oceanic carbon cycle is composed of processes that exchange carbon between various pools within the ocean as well as between the atmosphere, Earth interior, and the seafloor. The carbon cycle is a result of many interacting forces across multiple time and space scales that circulates carbon around the planet, ensuring that carbon is available globally. The Oceanic carbon cycle is a central process to the global carbon cycle and contains both inorganic carbon and organic carbon. Part of the marine carbon cycle transforms carbon between non-living and living matter.
Whale feces, the excrement of whales, has a vital role in the ecology of oceans, earning whales the title of "marine ecosystem engineers." This significant ecological role stems from the nutrients and compounds found in whale feces, which have far-reaching effects on marine life.
Haida Eddies are episodic, clockwise rotating ocean eddies that form during the winter off the west coast of British Columbia's Haida Gwaii and Alaska's Alexander Archipelago. These eddies are notable for their large size, persistence, and frequent recurrence. Rivers flowing off the North American continent supply the continental shelf in the Hecate Strait with warmer, fresher, and nutrient-enriched water. Haida eddies are formed every winter when this rapid outflow of water through the strait wraps around Cape St. James at the southern tip of Haida Gwaii, and meets with the cooler waters of the Alaska Current. This forms a series of plumes which can merge into large eddies that are shed into the northeast Pacific Ocean by late winter, and may persist for up to two years.
The CO2 fertilization effect or carbon fertilization effect causes an increased rate of photosynthesis while limiting leaf transpiration in plants. Both processes result from increased levels of atmospheric carbon dioxide (CO2). The carbon fertilization effect varies depending on plant species, air and soil temperature, and availability of water and nutrients. Net primary productivity (NPP) might positively respond to the carbon fertilization effect. Although, evidence shows that enhanced rates of photosynthesis in plants due to CO2 fertilization do not directly enhance all plant growth, and thus carbon storage. The carbon fertilization effect has been reported to be the cause of 44% of gross primary productivity (GPP) increase since the 2000s. Earth System Models, Land System Models and Dynamic Global Vegetation Models are used to investigate and interpret vegetation trends related to increasing levels of atmospheric CO2. However, the ecosystem processes associated with the CO2 fertilization effect remain uncertain and therefore are challenging to model.
Marine biogeochemical cycles are biogeochemical cycles that occur within marine environments, that is, in the saltwater of seas or oceans or the brackish water of coastal estuaries. These biogeochemical cycles are the pathways chemical substances and elements move through within the marine environment. In addition, substances and elements can be imported into or exported from the marine environment. These imports and exports can occur as exchanges with the atmosphere above, the ocean floor below, or as runoff from the land.
Nutrient cycling in the Columbia River Basin involves the transport of nutrients through the system, as well as transformations from among dissolved, solid, and gaseous phases, depending on the element. The elements that constitute important nutrient cycles include macronutrients such as nitrogen, silicate, phosphorus, and micronutrients, which are found in trace amounts, such as iron. Their cycling within a system is controlled by many biological, chemical, and physical processes.
The lipid pump sequesters carbon from the ocean's surface to deeper waters via lipids associated with overwintering vertically migratory zooplankton. Lipids are a class of hydrocarbon rich, nitrogen and phosphorus deficient compounds essential for cellular structures. This lipid carbon enters the deep ocean as carbon dioxide produced by respiration of lipid reserves and as organic matter from the mortality of zooplankton.
The viral shunt is a mechanism that prevents marine microbial particulate organic matter (POM) from migrating up trophic levels by recycling them into dissolved organic matter (DOM), which can be readily taken up by microorganisms. The DOM recycled by the viral shunt pathway is comparable to the amount generated by the other main sources of marine DOM.
The Great Calcite Belt (GCB) refers to a region of the ocean where there are high concentrations of calcite, a mineral form of calcium carbonate. The belt extends over a large area of the Southern Ocean surrounding Antarctica. The calcite in the Great Calcite Belt is formed by tiny marine organisms called coccolithophores, which build their shells out of calcium carbonate. When these organisms die, their shells sink to the bottom of the ocean, and over time, they accumulate to form a thick layer of calcite sediment.
Low-nutrient, low-chlorophyll (LNLC)regions are aquatic zones that are low in nutrients and consequently have low rate of primary production, as indicated by low chlorophyll concentrations. These regions can be described as oligotrophic, and about 75% of the world's oceans encompass LNLC regions. A majority of LNLC regions are associated with subtropical gyres but are also present in areas of the Mediterranean Sea, and some inland lakes. Physical processes limit nutrient availability in LNLC regions, which favors nutrient recycling in the photic zone and selects for smaller phytoplankton species. LNLC regions are generally not found near coasts, since coastal areas receive more nutrients from terrestrial sources and upwelling. In marine systems, seasonal and decadal variability of primary productivity in LNLC regions is driven in part by large-scale climatic regimes leading to important effects on the global carbon cycle and the oceanic carbon cycle.
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: CS1 maint: multiple names: authors list (link)In early August, Germany decided that ocean seeding will only be allowed for research purposes and under strict conditions.[ permanent dead link ]