The 100,000-year ice-Age cycle identified and found to lag temperature, carbon dioxide, and orbital eccentricity

The deep-sea sediment oxygen isotopic composition (delta(18)O) record is dominated by a 100,000-year cyclicity that is universally interpreted as the main ice-age rhythm. Here, the ice volume component of this delta(18)O signal was extracted by using the record of delta(18)O in atmospheric oxygen trapped in Antarctic ice at Vostok, precisely orbitally tuned. The benthic marine delta(18)O record is heavily contaminated by the effect of deep-water temperature variability, but by using the Vostok record, the delta(18)O signals of ice volume, deep-water temperature, and additional processes affecting air delta(18)O (that is, a varying Dole effect) were separated. At the 100,000-year period, atmospheric carbon dioxide, Vostok air temperature, and deep-water temperature are in phase with orbital eccentricity, whereas ice volume lags these three variables. Hence, the 100,000-year cycle does not arise from ice sheet dynamics; instead, it is probably the response of the global carbon cycle that generates the eccentricity signal by causing changes in atmospheric carbon dioxide concentration.     

Global warming and marine carbon cycle feedbacks on future atmospheric CO2

A low-order physical-biogeochemical climate model was used to project atmospheric carbon dioxide and global warming for scenarios developed by the Intergovernmental Panel on Climate Change. The North Atlantic thermohaline circulation weakens in all global warming simulations and collapses at high levels of carbon dioxide. Projected changes in the marine carbon cycle have a modest impact on atmospheric carbon dioxide. Compared with the control, atmospheric carbon dioxide increased by 4 percent at year 2100 and 20 percent at year 2500. The reduction in ocean carbon uptake can be mainly explained by sea surface warming. The projected changes of the marine biological cycle compensate the reduction in downward mixing of anthropogenic carbon, except when the North Atlantic thermohaline circulation collapses.     

Ice core records of atmospheric N2O covering the last 106,000 years

Paleoatmospheric records of trace-gas concentrations recovered from ice cores provide important sources of information on many biogeochemical cycles involving carbon, nitrogen, and oxygen. Here, we present a 106,000-year record of atmospheric nitrous oxide (N2O) along with corresponding isotopic records spanning the last 30,000 years, which together suggest minimal changes in the ratio of marine to terrestrial N2O production. During the last glacial termination, both marine and oceanic N2O emissions increased by 40 +/- 8%. We speculate that our records do not support those hypotheses that invoke enhanced export production to explain low carbon dioxide values during glacial periods.     

Sulfur isotopic composition of cenozoic seawater sulfate

A continuous seawater sulfate sulfur isotope curve for the Cenozoic with a resolution of approximately 1 million years was generated using marine barite. The sulfur isotopic composition decreased from 19 to 17 per mil between 65 and 55 million years ago, increased abruptly from 17 to 22 per mil between 55 and 45 million years ago, remained nearly constant from 35 to approximately 2 million years ago, and has decreased by 0.8 per mil during the past 2 million years. A comparison between seawater sulfate and marine carbonate carbon isotope records reveals no clear systematic coupling between the sulfur and carbon cycles over one to several millions of years, indicating that changes in the burial rate of pyrite sulfur and organic carbon did not singularly control the atmospheric oxygen content over short time intervals in the Cenozoic. This finding has implications for the modeling of controls on atmospheric oxygen concentration.     

Amplification of Cretaceous warmth by biological cloud feedbacks

The extreme warmth of particular intervals of geologic history cannot be simulated with climate models, which are constrained by the geologic proxy record to relatively modest increases in atmospheric carbon dioxide levels. Recent recognition that biological productivity controls the abundance of cloud condensation nuclei (CCN) in the unpolluted atmosphere provides a solution to this problem. Our climate simulations show that reduced biological productivity (low CCN abundance) provides a substantial amplification of CO2-induced warming by reducing cloud lifetimes and reflectivity. If the stress of elevated temperatures did indeed suppress marine and terrestrial ecosystems during these times, this long-standing climate enigma may be solved.     

Physical model for the decay and preservation of marine organic carbon

Degradation of marine organic carbon provides a major source of atmospheric carbon dioxide, whereas preservation in sediments results in accumulation of oxygen. These processes involve the slow decay of chemically recalcitrant compounds and physical protection. To assess the importance of physical protection, we constructed a reaction-diffusion model in which organic matter differs only in its accessibility to microbial degradation but not its intrinsic reactivity. The model predicts that organic matter decays logarithmically with time t and that decay rates decrease approximately as 0.2 x t(-1) until burial. Analyses of sediment-core data are consistent with these predictions.     

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.     

Carbon dioxide exchange between air and seawater: no evidence for rate catalysis

It has been suggested that enzymatic catalysis plays a major role in regulating the mass transport of carbon dioxide from the atmosphere into the oceans. Evidence for this mechanism was not found in a series of gas exchange experiments in which the gas transfer rate coefficients for samples obtained from various natural seawaters, with and without the addition of carbonic anhydrase, were compared with those from artificial seawater. Wind-induced turbulence appears to be the major factor controlling the ocean's response to anthropogenic increases in atmospheric carbon dioxide.     

Seawater sulfur isotope fluctuations in the Cretaceous

The exogenic sulfur cycle is tightly coupled with the carbon and oxygen cycles, and therefore a central component of Earth's biogeochemistry. Here we present a high-resolution record of the sulfur isotopic composition of seawater sulfate for the Cretaceous. The general enrichment of isotopically light sulfur that prevailed during the Cretaceous may have been due to increased volcanic and hydrothermal activity. Two excursions toward isotopically lighter sulfur represent periods of lower rates of pyrite burial, implying a shift in the location of organic carbon burial to terrestrial or open-ocean settings. The concurrent changes in seawater sulfur and inorganic carbon isotopic compositions imply short-term variability in atmospheric oxygen partial pressure.     

Evidence for upwelling of corrosive "acidified" water onto the continental shelf

The absorption of atmospheric carbon dioxide (CO2) into the ocean lowers the pH of the waters. This so-called ocean acidification could have important consequences for marine ecosystems. To better understand the extent of this ocean acidification in coastal waters, we conducted hydrographic surveys along the continental shelf of western North America from central Canada to northern Mexico. We observed seawater that is undersaturated with respect to aragonite upwelling onto large portions of the continental shelf, reaching depths of approximately 40 to 120 meters along most transect lines and all the way to the surface on one transect off northern California. Although seasonal upwelling of the undersaturated waters onto the shelf is a natural phenomenon in this region, the ocean uptake of anthropogenic CO2 has increased the areal extent of the affected area.     

Isotopic evidence for variations in the marine calcium cycle over the Cenozoic

Significant variations in the isotopic composition of marine calcium have occurred over the last 80 million years. These variations reflect deviations in the balance between inputs of calcium to the ocean from weathering and outputs due to carbonate sedimentation, processes that are important in controlling the concentration of carbon dioxide in the atmosphere and, hence, global climate. The calcium isotopic ratio of paleo-seawater is an indicator of past changes in atmospheric carbon dioxide when coupled with determinations of paleo-pH.     

Growth of Western Australian corals in the anthropocene

Anthropogenic increases of atmospheric carbon dioxide lead to warmer sea surface temperatures and altered ocean chemistry. Experimental evidence suggests that coral calcification decreases as aragonite saturation drops but increases as temperatures rise toward thresholds optimal for coral growth. In situ studies have documented alarming recent declines in calcification rates on several tropical coral reef ecosystems. We show there is no widespread pattern of consistent decline in calcification rates of massive Porites during the 20th century on reefs spanning an 11° latitudinal range in the southeast Indian Ocean off Western Australia. Increasing calcification rates on the high-latitude reefs contrast with the downward trajectory reported for corals on Australia's Great Barrier Reef and provide additional evidence that recent changes in coral calcification are responses to temperature rather than ocean acidification.     

Rapid variability of seawater chemistry over the past 130 million years

Fluid inclusion data suggest that the composition of major elements in seawater changes slowly over geological time scales. This view contrasts with high-resolution isotope data that imply more rapid fluctuations of seawater chemistry. We used a non-steady-state box model of the global sulfur cycle to show that the global δ(34)S record can be explained by variable marine sulfate concentrations triggered by basin-scale evaporite precipitation and dissolution. The record is characterized by long phases of stasis, punctuated by short intervals of rapid change. Sulfate concentrations affect several important biological processes, including carbonate mineralogy, microbially mediated organic matter remineralization, sedimentary phosphorous regeneration, nitrogen fixation, and sulfate aerosol formation. These changes are likely to affect ocean productivity, the global carbon cycle, and climate.     

Assessment of oceanic productivity with the triple-isotope composition of dissolved oxygen

Plant production in the sea is a primary mechanism of global oxygen formation and carbon fixation. For this reason, and also because the ocean is a major sink for fossil fuel carbon dioxide, much attention has been given to estimating marine primary production. Here, we describe an approach for estimating production of photosynthetic oxygen, based on the isotopic composition of dissolved oxygen of seawater. This method allows the estimation of integrated oceanic productivity on a time scale of weeks.     

Land floras: the major late phanerozoic atmospheric carbon dioxide/oxygen control

Since at least the late Mesozoic, the abundance of terrestrial vegetation has been the major factor in atmospheric carbon dioxideloxygen fluctuations. Of modern ecosystem types occupying more than 1 percent of the earth's surface, productivity/area ratios of terrestrial ecosystems (excepting tundra and alpine meadow, desert scrub, and rock, ice, and sand) exceed those of marine ecosystems and probably have done so for much of late Phanerozoic time. Reduction of terrestrial ecosystems during marine transgression would decrease the world primary productivity, thus increasing the atmospheric carbon dioxide concentration and decreasing the oxygen concentration. Regression would produce opposite effects.     

Role of marine biology in glacial-interglacial CO2 cycles

It has been hypothesized that changes in the marine biological pump caused a major portion of the glacial reduction of atmospheric carbon dioxide by 80 to 100 parts per million through increased iron fertilization of marine plankton, increased ocean nutrient content or utilization, or shifts in dominant plankton types. We analyze sedimentary records of marine productivity at the peak and the middle of the last glacial cycle and show that neither changes in nutrient utilization in the Southern Ocean nor shifts in plankton dominance explain the CO2 drawdown. Iron fertilization and associated mechanisms can be responsible for no more than half the observed drawdown.     

Impacts of atmospheric anthropogenic nitrogen on the open ocean

Increasing quantities of atmospheric anthropogenic fixed nitrogen entering the open ocean could account for up to about a third of the ocean's external (nonrecycled) nitrogen supply and up to approximately 3% of the annual new marine biological production, approximately 0.3 petagram of carbon per year. This input could account for the production of up to approximately 1.6 teragrams of nitrous oxide (N2O) per year. Although approximately 10% of the ocean's drawdown of atmospheric anthropogenic carbon dioxide may result from this atmospheric nitrogen fertilization, leading to a decrease in radiative forcing, up to about two-thirds of this amount may be offset by the increase in N2O emissions. The effects of increasing atmospheric nitrogen deposition are expected to continue to grow in the future.     

Phanerozoic Earth system evolution and marine biodiversity

The Phanerozoic fossil record of marine animal diversity covaries with the amount of marine sedimentary rock. The extent to which this covariation reflects a geologically controlled sampling bias remains unknown. We show that Phanerozoic records of seawater chemistry and continental flooding contain information on the diversity of marine animals that is independent of sedimentary rock quantity and sampling. Interrelationships among variables suggest long-term interactions among continental flooding, sulfur and carbon cycling, and macroevolution. Thus, mutual responses to interacting Earth systems, not sampling biases, explain much of the observed covariation between Phanerozoic patterns of sedimentation and fossil biodiversity. Linkages between biodiversity and environmental records likely reflect complex biotic responses to changing ocean redox conditions and long-term sea-level fluctuations driven by plate tectonics.     

The Southern Ocean's role in carbon exchange during the last deglaciation

Changes in the upwelling and degassing of carbon from the Southern Ocean form one of the leading hypotheses for the cause of glacial-interglacial changes in atmospheric carbon dioxide. We present a 25,000-year-long Southern Ocean radiocarbon record reconstructed from deep-sea corals, which shows radiocarbon-depleted waters during the glacial period and through the early deglaciation. This depletion and associated deep stratification disappeared by ~14.6 ka (thousand years ago), consistent with the transfer of carbon from the deep ocean to the surface ocean and atmosphere via a Southern Ocean ventilation event. Given this evidence for carbon exchange in the Southern Ocean, we show that existing deep-ocean radiocarbon records from the glacial period are sufficiently depleted to explain the ~190 per mil drop in atmospheric radiocarbon between ~17 and 14.5 ka.     

Stable carbon cycle-climate relationship during the Late Pleistocene

A record of atmospheric carbon dioxide (CO2) concentrations measured on the EPICA (European Project for Ice Coring in Antarctica) Dome Concordia ice core extends the Vostok CO2 record back to 650,000 years before the present (yr B.P.). Before 430,000 yr B.P., partial pressure of atmospheric CO2 lies within the range of 260 and 180 parts per million by volume. This range is almost 30% smaller than that of the last four glacial cycles; however, the apparent sensitivity between deuterium and CO2 remains stable throughout the six glacial cycles, suggesting that the relationship between CO2 and Antarctic climate remained rather constant over this interval.