Melanoidins—kerogen precursors and geochemical lipid sinks: a study using pyrolysis gas chromatography (PGC)

Melanoidins, acidic polymeric products of amino acid/sugar condensation reactions, are shown to be capable of reacting with and binding functionalized lipid molecules. Pyrolysis gas chromatography is used to monitor the inclusion of lipids (alcohols and acids) into, and to monitor the changes in composition caused by artificial diagenesis of, the melanoidins. Artificial diagenesis of the lipidcontaining melanoidins produces a material resembling kerogen. The possible role of melanoidins in the formation of kerogens is discussed as are internal transformations within kerogens during diagenesis.     

Diversity of recent planktonic foraminifera in the southern Indian Ocean and Late Pleistocene paleotemperatures

Planktonic foraminiferal assemblages have been examined in 25 trigger core top samples and 51 piston core top samples collected between latitudes 28° S and 55° S and longitudes 79° E and 120° E from the southern Indian Ocean during cruises of the U.S.N.S. Eltanin. Samples taken from water depths exceeding 4000 m and/or showing evidence of calcium carbonate dissolution were eliminated from further analysis. The final piston core data set consists of 34 samples; the trigger core data set containing 21 samples. A close relationship exists between changes in the planktonic foraminiferal assemblages in the surface sediments and surface water temperatures. Species diversity values were computed for each of the core top assemblages using the Shannon-Wiener Index and the Brillouin Index, each of which takes into consideration the number of species and the proportionment of individuals among the species. The Shannon and Brillouin diversity values for all samples are positively correlated (correlation coefficient (r) = +.999). Regression analysis of latitude versus Shannon diversity values in the trigger core samples clearly shows a decrease in diversity with increasing latitude (r = ?.979). Furthermore, a strong correlation (r = +.977) exists between decreasing species diversity (Shannon) and decreasing average summer-winter temperature of the overlying surface waters. A paleotemperature equation derived from the relationship of diversity in trigger core samples and surface water temperature was used to generate paleotemperature curves for five trigger cores and a 6 m piston core of Late Pleistocene age, located beneath the present position of the Subtropical Convergence. A 7–8° C temperature range is suggested between the interglacial and glacial episodes in this Late Pleistocene sequence, and probably reflects latitudinal shifts of the Subtropical Convergence and Australasian Front during the Late Pleistocene.     

Trace element distribution in mineral separates of the Allende inclusions and their genetic implications

Concentrations of the REE, Sc, Co, Fe, Zn, Ir, Na and Cr were determined by instrumental neutron activation and mass spectrometric isotope dilution analysis for mineral separates of the coarseand fine-grained types (group I and II of Martin and Mason's classification) of the Allende inclusions.These data, combined with data on mineral/liquid partition coefficients, oxygen isotope distributions and diffusion calculations, suggest the following: (1) Minerals in the coarse-grained inclusions (group I) crystallized in a closed system with respect to refractory elements. On the other hand, differences in oxygen isotope distributions among minerals preclude a totally molten stage in the history of the inclusion. Group I inclusions were formed by rapid condensation (either to liquid or solid) in a supercooled solar nebula; extrasolar pyroxene and spinel dust were included but not melted in the condensing inclusions, thus preserving their extrasolar oxygen isotope composition. REE were distributed by diffusion during the subsequent heating at subsolidus temperatures; because oxygen diffuses much more slowly at these temperatures, the oxygen isotope anomalies were preserved. (2) The fine-grained (group II) inclusions were also formed by condensation from a super-cooled nebular gas; however, REE-rich clinopyroxene and spinel were formed early and REE-poor sodalite and nepheline were formed later and mechanically mixed with clinopyroxene and spinel to form the inclusions. The REE patterns of the bulk inclusions and the mineral separates are fractionated, indicating that REE abundances in the gaseous phase were already fractionated at the time of condensation of the minerals. (3) Pre-existing Mg isotope anomalies in the coarse-grained inclusions must have been erased during the heating stage thus resetting the ²⁶Al-²⁶Mg chronometer.     

Robust kriging—A proposal

Geological data frequently have a heavy-tailed normal-in-the-middle distribution, which gives rise to grade distributions that appear to be normal except for the occurrence of a few outliers. This same situation also applies to log-transformed data to which lognormal kriging is to be applied. For such data, linear kriging is nonrobust in that (1)kriged estimates tend to infinity as the outliers do, and (2)it is also not minimum mean squared error. The more general nonlinear method of disjunctive kriging is even more nonrobust, computationally more laborious, and in the end need not produce better practical answers. We propose a robust kriging method for such nearly normal data based on linear kriging of an editing of the data. It is little more laborious than conventional linear kriging and, used in conjunction with a robust estimator of the variogram, provides good protection against the effects of data outliers. The method is also applicable to time series analysis.     

The age,origin, and volcanological significance of the Y-5 ash layer in the Mediterranean

The Y-5 ash is the most widespread layer in deep-sea sediments from the eastern Mediterranean. This ash layer was previously correlated with the Citara-Serrara tuff on Ischia Island and dated at approximately 25,000 yr B.P. New data on the glass chemistry of the Y-5 ash and pyroclastic deposits from the Neopolitan volcanic province suggest that the layer is correlative with the large-volume Campanian ignimbrite and not with the deposit from Ischia Island. The volume of the Y-5 ash is approximately 65 km³ which is comparable in magnitude to the volume of the Campanian ignimbrite. An interpolated age of approximately 38,000 yr B.P. is estimated based on sedimentation rates derived from δ¹⁸O stratigraphy. There is a discrepancy between this estimate and previously reported radiocarbon ages which range from 24,000 to 35,000 yr B.P. We propose that the “Campanian tuff ash layer” should be adopted as the full stratigraphic name for the Y-5 ash. The deep-sea ash layer is divisible into two units in proximal localities, probably correlating with two major phases of the eruption: plinian and ignimbrite.     

Lacustrine sedimentation in a semiarid alpine setting: An example from Ladakh, northwestern Himalaya

The Lamayuru lacustrine strata in Ladakh typify many of the carbonate-rich Pleistocene alpine lakes found in the semiarid environment of the northern Himalaya. Created by a 200-m-thick landslide, the lake was in existence by at least 35,000 yr ago, and may have persisted until 500–1000 yr ago. Represented in the center by thin turbidites and laminated muds, the lacustrine sedimentation along the lake margins and low-relief deltas characteristically displays a marked contrast between (1) clastic lenses representing rapid, sporadic, matrix-poor debris flows and periglacial inputs from the alpine slopes and (2) abundant, diverse, shallow-water, biologically dominated carbonate strata, among which organism-rich, chalky beds and oncolithic and encrusted stem-rich strata predominate. Resemblances of the Lamayuru lacustrine strata and their setting to those of former lakes throughout areas north of the Greater Himalayan crest suggest that the alpine, semi-arid environment would favor diversified, spacially restricted carbonate sedimentation punctuated by occasional clastic influxes. Such a depositional regime contrasts strongly with that found immediately south of the Himalayan crest where more humid conditions promote a more continuous clastic influx into intramontane lakes.     

Strontium-calcium ratios in Cenozoic planktonic foraminifera

The $\text{Sr}\text{Ca}$ ratio and other parameters have been measured in fossil planktonic foraminifera from the Atlantic and Pacific Ocean basins in order to evaluate the $\text{Sr}\text{Ca}$ ratio of seawater during the last 75 million years. Results on well-preserved samples indicate that the ratio has increased to its present value by 10–15% during the Cenozoic, and that minima occurred between 55-45 Ma and 10-5 Ma, when the ratio was 15–25% less than at present. The long-term increase may reflect either decreasing deposition of aragonite with a high $\text{Sr}\text{Ca}$ ratio in shallow seas, or decreasing seafloor spreading rates and consequently decreasing hydrothermal supply of Ca during the Cenozoic. Other geologic evidence suggests that the Eocene minimum (near 50 Ma) may have resulted from increased aragonite sedimentation, while the Late Miocene minimum (between 10-5 Ma) may have been caused by an increased rate of seawater-basalt exchange when seafloor spreading rates increased on the East Pacific Rise near 10 Ma.     

Long-term monitoring of the behavior of a talus-colluvium deposit

Landslides - This article describes the behavior of a talus-colluvium deposit up to 70-m thick located in the Serra dos Orgaos, Rio de Janeiro/RJ, Brazil. The monitoring dataset of 13 years...     

The influence of minerals on the pyrolysis of kerogens

The effect of mineral matter on the laboratory pyrolysis of sediments, kerogens and coals, and of coal macerals mixed with either alumina, bentonite, kaolinite, or calcium carbonate has been investigated. Some minerals are more active than others in effecting changes in the composition of the pyrolysate. The relative content of low molecular weight pyrolysis products is higher for kerogens pyrolyzed in a mineral matrix than for isolated kerogens. Our limited data suggests that this is due to both condensation and gasification of higher molecular weight constituents in the ‘primary’ pyrolysate. Differences in the content of aromatic versus aliphatic compounds have been noted when pyrograms from coal macerals are compared with pyrograms from coal maceral-mineral mixtures. We conclude that mineralogy is important in controlling the composition of kerogen pyrolysis products.