Ocean chemistry

Ocean chemistry, also known as marine chemistry, is influenced by plate tectonics and seafloor spreading, turbidity currents, sediments, pH levels, atmospheric constituents, metamorphic activity, and ecology. The field of chemical oceanography studies the chemistry of marine environments including the influences of different variables. Ocean chemistry, also known as marine chemistry, is influenced by plate tectonics and seafloor spreading, turbidity currents, sediments, pH levels, atmospheric constituents, metamorphic activity, and ecology. The field of chemical oceanography studies the chemistry of marine environments including the influences of different variables. Colored dissolved organic matter (CDOM) is estimated to range 20-70% of carbon content of the oceans, being higher near river outlets and lower in the open ocean. Marine life is largely similar in biochemistry to terrestrial organisms, except that they inhabit a saline environment. One consequence of their adaptation is that marine organisms are the most prolific source of halogenated organic compounds. The ocean provides special marine environments inhabited by extremophiles that thrive under unusual conditions of temperature, pressure, and darkness. Such environments include hydrothermal vents and black smokers and cold seeps on the ocean floor, with entire ecosystems of organisms that have a symbiotic relationship with bacteria and hydrocarbon compounds that provided energy through a process called chemosynthesis. Seafloor spreading on mid-ocean ridges is a global scale ion-exchange system. Hydrothermal vents at spreading centers introduce various amounts of iron, sulfur, manganese, silicon and other elements into the ocean, some of which are recycled into the ocean crust. Helium-3, an isotope that accompanies volcanism from the mantle, is emitted by hydrothermal vents and can be detected in plumes within the ocean. Spreading rates on mid-ocean ridges vary between 10 and 200 mm/yr. Rapid spreading rates cause increased basalt reactions with seawater. The magnesium/calcium ratio will be lower because more magnesium ions are being removed from seawater and consumed by the rock, and more calcium ions are being removed from the rock and released to seawater. Hydrothermal activity at ridge crest is efficient in removing magnesium. A lower Mg/Ca ratio favors the precipitation of low-Mg calcite polymorphs of calcium carbonate (calcite seas). Slow spreading at mid-ocean ridges has the opposite effect and will result in a higher Mg/Ca ratio favoring the precipitation of aragonite and high-Mg calcite polymorphs of calcium carbonate (aragonite seas). Experiments show that most modern high-Mg calcite organisms would have been low-Mg calcite in past calcite seas, meaning that the Mg/Ca ratio in an organism's skeleton varies with the Mg/Ca ratio of the seawater in which it was grown. The mineralogy of reef-building and sediment-producing organisms is thus regulated by chemical reactions occurring along the mid-ocean ridge, the rate of which is controlled by the rate of sea-floor spreading.