Dead zones in the coastal oceans have spread exponentially since the 1960s and have serious consequences for ecosystem functioning. The formation of dead zones has been exacerbated by the increase in primary production and consequent worldwide coastal eutrophication fueled by riverine runoff of fertilizers and the burning of fossil fuels. Enhanced primary production results in an accumulation of particulate organic matter, which encourages microbial activity and the consumption of dissolved oxygen in bottom waters. Dead zones have now been reported from more than 400 systems, affecting a total area of more than 245,000 square kilometers, and are probably a key stressor on marine ecosystems.

Supporting Online Material for Spreading Dead Zones and Consequences for Marine Ecosystems

https://homepages.uc.edu/~algeot/Tribovillard-Algeo-etal-CG-2006.pdf

Trace metals as paleoredox and paleoproductivity proxies: An update

In this chapter, we will restrict our attention to the ferrites and a few other closely related materials. The great interest in ferrites stems from their unique combination of a spontaneous magnetization and a high electrical resistivity. The observed magnetization results from the difference in the magnetizations of two non-equivalent sub-lattices of the magnetic ions in the crystal structure. Materials of this type should strictly be designated as “ferrimagnetic” and in some respects are more closely related to anti-ferromagnetic substances than they are to ferromagnetics in which the magnetization results from the parallel alignment of all the magnetic moments present. We shall not adhere to this special nomenclature except to emphasize effects, which are due to the existence of the sub-lattices.

Ferromagnetic materials

Matrix-related pore networks in mudrocks are composed of nanometer- to micrometer-size pores. In shale-gas systems, these pores, along with natural fractures, form the flow-path (permeability) network that allows flow of gas from the mudrock to induced fractures during production. A pore classification consisting of three major matrix-related pore types is presented that can be used to quantify matrix-related pores and relate them to pore networks. Two pore types are associated with the mineral matrix; the third pore type is associated with organic matter (OM). Fracture pores are not controlled by individual matrix particles and are not part of this classification. Pores associated with mineral particles can be subdivided into interparticle (interP) pores that are found between particles and crystals and intraparticle (intraP) pores that are located within particles. Organic-matter pores are intraP pores located within OM. Interparticle mineral pores have a higher probability of being part of an effective pore network than intraP mineral pores because they are more likely to be interconnected. Although they are intraP, OM pores are also likely to be part of an interconnected network because of the interconnectivity of OM particles. In unlithifed near-surface muds, pores consist of interP and intraP pores, and as the muds are buried, they compact and lithify. During the compaction process, a large number of interP and intraP pores are destroyed, especially in ductile grain-rich muds. Compaction can decrease the pore volume up to 88% by several kilometers of burial. At the onset of hydrocarbon thermal maturation, OM pores are created in kerogen. At depth, dissolution of chemically unstable particles can create additional moldic intraP pores.

Spectrum of pore types and networks in mudrocks and a descriptive classification for matrix-related mudrock pores

Hydrothermal technologies are broadly defined as chemical and physical transformations in high-temperature (200–600 °C), high-pressure (5–40 MPa) liquid or supercritical water. This thermochemical means of reforming biomass may have energetic advantages, since, when water is heated at high pressures a phase change to steam is avoided which avoids large enthalpic energy penalties. Biological chemicals undergo a range of reactions, including dehydration and decarboxylation reactions, which are influenced by the temperature, pressure, concentration, and presence of homogeneous or heterogeneous catalysts. Several biomass hydrothermal conversion processes are in development or demonstration. Liquefaction processes are generally lower temperature (200–400 °C) reactions which produce liquid products, often called “bio-oil” or “bio-crude”. Gasification processes generally take place at higher temperatures (400–700 °C) and can produce methane or hydrogen gases in high yields.

/pdf/thermochemical-biofuel-production-in-hydrothermal-media-a-57itjyvhnt.pdf

H.L. Barnes

Papers

The kinetics of silica-water reactions

The size distribution of framboidal pyrite in modern sediments : an indicator of redox conditions

Formation processes of framboidal pyrite

Oxidation of pyrite in low temperature acidic solutions: Rate laws and surface textures

Pyrite formation by reactions of iron monosulfides with dissolved inorganic and organic sulfur species