Paleobiological Perspectives on Early Eukaryotic Evolution

Eukaryotic organisms radiated in Proterozoic oceans with oxygenated surface waters, but, commonly, anoxia at depth. Exceptionally preserved fossils of red algae favor crown group emergence more than 1200 million years ago, but older (up to 1600–1800 million years) microfossils could record stem group eukaryotes. Major eukaryotic diversification ∼800 million years ago is documented by the increase in the taxonomic richness of complex, organic-walled microfossils, including simple coenocytic and multicellular forms, as well as widespread tests comparable to those of extant testate amoebae and simple foraminiferans and diverse scales comparable to organic and siliceous scales formed today by protists in several clades. Mid-Neoproterozoic establishment or expansion of eukaryophagy provides a possible mechanism for accelerating eukaryotic diversification long after the origin of the domain. Protists continued to diversify along with animals in the more pervasively oxygenated oceans of the Phanerozoic Eon.Earth and Planetary SciencesOrganismic and Evolutionary Biolog

Lynn Margulis, 1938--2011

Organismic and Evolutionary Biolog

The Effects of Various Adhesives and Adhesive Levels on the Scattering Coefficient of Pigmented Coatings: An Attempt to Predict Scattering Coefficients

The object of this study was to determine the effect of various levels of different adhesives on the scattering coefficients of a coating. Once the relationship of the adhesive effect on the scattering coefficient was determined an equation was to be developed to predict the optical properties of the coated sheet. This study shows that there is an increase in scattering coefficient from 5 to 10pph adhesive and after 10pph a steady decrease in the scattering coefficient as more adhesive is added. The increase is theorized to be due to flocculation of fines within the coating and the decrease due to the filling of voids in the coating. The scattering coefficient of the coating can be predicted for the adhesive addition range of 10 to 30pph by a linear equation. The data obtained in this work correlates with results of other workers using black glass and foil substrates

MICROPALEONTOLOGY OF THE LOWER MESOPROTEROZOIC ROPER GROUP, AUSTRALIA, AND IMPLICATIONS FOR EARLY EUKARYOTIC EVOLUTION

ELiTE: Early Life Traces, Evolution, and Implications for Astrobiolog

Non-Skeletal Biomineralization by Eukaryotes: Matters of Moment and Gravity

Skeletal biomineralisation by microbial eukaryotes significantly affects the global biogeochemical cycles of carbon, silicon and calcium. Non-skeletal biomineralisation by eukaryotic cells, with precipitates retained within the cell interior, can duplicate some of the functions of skeletal minerals, e.g., increased cell density, but not the mechanical and antibiophage functions of extracellular biominerals. However, skeletal biomineralisation does not duplicate many of the functions of non-skeletal biominerals. These functions include magnetotaxis (magnetite), gravity sensing (intracellular barite, bassanite, celestite and gypsum), buffering and storage of elements in an osmotically inactive form (calcium as carbonate, oxalate, polyphosphate and sulfate; phosphate as polyphosphate) and acid-base regulation, disposing of excess hydroxyl ions via an osmotically inactive product (calcium carbonate, calcium oxalate). Although polyphosphate has a wide phylogenetic distribution among microbial eukaryotes, other non-skeletal minerals have more restricted distributions, and as yet there seems to be no definitive evidence that the alkaline earth components (Ba and Sr) of barite and celestite are essential for completion of the life cycle in organisms that produce these minerals.Organismic and Evolutionary Biolog

Anomalous Carbonate Precipitates: Is the Precambrian the Key to the Permian?

Late Permian reefs of the Capitan complex, west Texas; the Magnesian Limestone, England; Chuenmuping reef, south China; and elsewhere contain anomalously large volumes of aragonite and calcite marine cements and seafloor crusts, as well as abundant microbial precipitates. These components strongly influenced reef growth and may have been responsible for the construction of rigid, open reefal frames in which bryozoans and sponges became encrusted and structurally reinforced. In some cases, such as the upper biostrome of the Magnesian Limestone, precipitated microbialites and inorganic crusts were the primary constituents of the reef core. These microbial and inorganic reefs do not have modern marine counterparts; on the contrary, their textures and genesis are best understood through comparison with the older rock record, particularly that of the early Precambrian. Early Precambrian reefal facies are interpreted to have formed in a stratified ocean with anoxic deep waters enriched in carbonate alkalinity. Upwelling mixed deep and surface waters, resulting in massive seafloor precipitation of aragonite and calcite. During Mesoproterozoic and early Neoproterozoic time, the ocean became more fully oxidized, and seafloor carbonate precipitation was significantly reduced. However, during the late Neoproterozoic, sizeable volumes of deep ocean water once again became anoxic for protracted intervals; the distinctive "cap carbonates" found above Neoproterozoic tillites attest to renewed upwelling of anoxic bottom water enriched in carbonate alkalinity and ^(12)C. Anomalous late Permian seafloor precipitates are interpreted as the product, at least in part, of similar processes. Massive carbonate precipitation was favored by: 1) reduced shelf space for carbonate precipitation, 2) increased flux of Ca to the oceans during increased continental erosion, 3) deep basinal anoxia that generated upwelling waters with elevated alkalinities, and 4) further evolution of ocean water in the restricted Delaware, Zechstein, and other basins. Temporal coincidence of these processes resulted in surface seawater that was greatly supersaturated by Phanerozoic standards and whose only precedents occurred in Precambrian oceans