Organic carbon fluxes and ecological recovery from the cretaceous-tertiary mass extinction

Differences between the carbon isotopic values of carbonates secreted by planktic and benthic organisms did not recover to stable preextinction levels for more than 3 million years after the Cretaceous-Tertiary mass extinction. These decreased differences may have resulted from a smaller proportion of marine biological production sinking to deep water in the postextinction ocean. Under this hypothesis, marine production may have recovered shortly after the mass extinction, but the structure of the open-ocean ecosystem did not fully recover for more than 3 million years.     

Calibrating the end-Permian mass extinction

The end-Permian mass extinction was the most severe biodiversity crisis in Earth history. To better constrain the timing, and ultimately the causes of this event, we collected a suite of geochronologic, isotopic, and biostratigraphic data on several well-preserved sedimentary sections in South China. High-precision U-Pb dating reveals that the extinction peak occurred just before 252.28 ± 0.08 million years ago, after a decline of 2 per mil (‰) in δ(13)C over 90,000 years, and coincided with a δ(13)C excursion of -5‰ that is estimated to have lasted ≤20,000 years. The extinction interval was less than 200,000 years and synchronous in marine and terrestrial realms; associated charcoal-rich and soot-bearing layers indicate widespread wildfires on land. A massive release of thermogenic carbon dioxide and/or methane may have caused the catastrophic extinction.     

Atmospheric carbon dioxide and carbon reservoir changes

The net release of CO(2) from the biosphere to the atmosphere between 1850 and 1950 is estimated to amount to 1.2 x 10(9) tons of carbon per year. During this interval, changes in land use reduced the total terrestrial biomass by 7 percent. There has been a smaller reduction in biomass over the last few decades. In the middle 19th century the air had a CO(2) content of approximately 268 parts per millon, and the total increase in atmospheric CO(2) content since 1850 has been 18 percent. Major sinks for fossil fuel CO(2) are the thermocline regions of large oceanic gyres. About 34 percent of the excess CO(2) generated so far is stored in surface and thermocline gyre waters, and 13 percent has been advected into the deep sea. This leaves an airborne fraction of 53 percent.     

End-cretaceous mass extinction event: argument for terrestrial causation

The end-Cretaceous mass extinctions were not a geologically instantaneous event and were selective in character. These features are incompatible with the original Alvarez hypothesis of their being caused by a single asteroid impact that produced a world-embracing dust cloud with devastating environmental consequences. By analysis of physical and chemical evidence from the stratigraphic record it is shown that a modified extraterrestrial model in which stepwise extinctions resulted from encounter with a comet shower is less plausible than one intrinsic to the earth, involving significant disturbance in the mantle.     

Atmospheric carbon tetrachloride: another man-made pollutant

On the basis of an analysis of historic worldwide emissions and removal mechanisms for carbon tetrachloride, a possible precursor for stratospheric ozone destruction, it has been demonstrated that the present atmospheric loading and distribution of carbon tetrachloride is primarily attributable to man-made emissions and no natural sources need be invoked to explain its presence in the atmosphere.     

Atmospheric carbon dioxide levels over phanerozoic time

A new model has been constructed for calculating the level of atmospheric CO(2) during the past 570 million years. A series of successive steady states for CO(2) is used in order to calculate CO(2) level from a feedback function for the weathering of silicate minerals. Processes considered are: sedimentary burial of organic matter and carbonates; continental weathering of silicates, carbonates, and organic matter; and volcanic and metamorphic degassing of CO(2). Sediment burial rates are calculated with the use of an isotope mass-balance model and carbon isotopic data on ancient seawater. Weathering rates are calculated from estimates of past changes in continental land area, mean elevation, and river runoff combined with estimates of the effects of the evolution of vascular land plants. Past degassing rates are estimated from changes in the rate of generation of sea floor and the shift of carbonate deposition from platforms to the deep sea. The model results indicate that CO(2) levels were high during the Mesozoic and early Paleozoic and low during the Permo-Carboniferous and late Cenozoic. These results correspond to independently deduced Phanerozoic paleoclimates and support the notion that the atmospheric CO(2) greenhouse mechanism is a major control on climate over very long time scales.     

A multispecies overkill simulation of the end-Pleistocene megafaunal mass extinction

A computer simulation of North American end-Pleistocene human and large herbivore population dynamics correctly predicts the extinction or survival of 32 out of 41 prey species. Slow human population growth rates, random hunting, and low maximum hunting effort are assumed; additional parameters are based on published values. Predictions are close to observed values for overall extinction rates, human population densities, game consumption rates, and the temporal overlap of humans and extinct species. Results are robust to variation in unconstrained parameters. This fully mechanistic model accounts for megafaunal extinction without invoking climate change and secondary ecological effects.     

Sudden productivity collapse associated with the Triassic-Jurassic boundary mass extinction

The end-Triassic mass extinction is one of the five most catastrophic in Phanerozoic Earth history. Here we report carbon isotope evidence of a pronounced productivity collapse at the boundary, coincident with a sudden extinction among marine plankton, from stratigraphic sections on the Queen Charlotte Islands, British Columbia, Canada. This signal is similar to (though smaller than) the carbon isotope excursions associated with the Permian-Triassic and Cretaceous-Tertiary events.     

A double mass extinction at the end of the paleozoic era

Three tests based on fossil data indicate that high rates of extinction recorded in the penultimate (Guadalupian) stage of the Paleozoic era are not artifacts of a poor fossil record. Instead, they represent an abrupt mass extinction that was one of the largest to occur in the past half billion years. The final mass extinction of the era, which took place about 5 million years after the Guadalupian event, remains the most severe biotic crisis of all time. Taxonomic losses in the Late Permian were partitioned among the two crises and the intervening interval, however, and the terminal Permian crisis eliminated only about 80 percent of marine species, not 95 or 96 percent as earlier estimates have suggested.     

Atmospheric carbon tetrafluoride: a nearly inert gas

An analysis of existing thermodynamic, photochemical, and kinetic data indicates that the dominant sinks for atmospheric carbon tetrafluoride (CF(4)) are in and above the mesosphere. Theoretical calculations predict an atmospheric residence time for CF(4) of over 10,000 years, about 100 times that for dichlorodifluoromethane (CF(2)Cl(2)) and monofluorotrichloromethane (CFC1(3)). It is predicted that CF(4) will be well mixed through the stratosphere and mesosphere; only one or two parts of hydrogen fluoride in 10(12) are predicted in the high stratosphere as a result of the decomposition of CF(4). Although natural sources of CF(4) cannot be ruled out, there are several likely industrial sources that may account for its present concentration. The principal environmental effect of CF(4) could be the trapping of outgoing planetary infrared energy in its intense bands near 8 micrometers.     

Atmospheric input of carbon dioxide from burning wood

The atmospheric input of carbon dioxide from burning wood, in particular from forest fires in boreal and temperate regions resulting from both natural and man-made causes and predominantly from forest fires in tropical regions caused by shifting cultivation, is estimated to be 5.7 x 10(15) grams of carbon per year as gross input and 1.5 x 10(15) grams of carbon per year as net input. This is a significant amount as compared to the fossil fuel carbon dioxide produced from the utilization of oil, gas, coal, and limestone, and bears on the hypothesis of the enhanced sedimentation of marine detritus as a removal mechanism of excess atmospheric carbon dioxide.