Oceanic Uptake of Fossil Fuel CO2: Carbon-13 Evidence

The delta(13)C value of the dissolved inorganic carbon in the surface waters of the Pacific Ocean has decreased by about 0.4 per mil between 1970 and 1990. This decrease has resulted from the uptake of atmospheric CO(2) derived from fossil fuel combustion and deforestation. The net amounts of CO(2) taken up by the oceans and released from the biosphere between 1970 and 1990 have been determined from the changes in three measured values: the concentration of atmospheric CO(2), the delta(13)C of atmospheric CO(2) and the delta(13)C value of dissolved inorganic carbon in the ocean. The calculated average net oceanic CO(2) uptake is 2.1 gigatons of carbon per year. This amount implies that the ocean is the dominant net sink for anthropogenically produced CO(2) and that there has been no significant net CO(2) released from the biosphere during the last 20 years.     

Carbon isotope constraints on the deglacial CO₂ rise from ice cores

The stable carbon isotope ratio of atmospheric CO(2) (δ(13)C(atm)) is a key parameter in deciphering past carbon cycle changes. Here we present δ(13)C(atm) data for the past 24,000 years derived from three independent records from two Antarctic ice cores. We conclude that a pronounced 0.3 per mil decrease in δ(13)C(atm) during the early deglaciation can be best explained by upwelling of old, carbon-enriched waters in the Southern Ocean. Later in the deglaciation, regrowth of the terrestrial biosphere, changes in sea surface temperature, and ocean circulation governed the δ(13)C(atm) evolution. During the Last Glacial Maximum, δ(13)C(atm) and atmospheric CO(2) concentration were essentially constant, which suggests that the carbon cycle was in dynamic equilibrium and that the net transfer of carbon to the deep ocean had occurred before then.     

A 23,000-year record of surface water pH and PCO2 in the western equatorial Pacific Ocean

The oceans play a major role in defining atmospheric carbon dioxide (CO2) levels, and although the geographical distribution of CO2 uptake and release in the modern ocean is understood, little is known about past distributions. Boron isotope studies of planktonic foraminifera from the western equatorial Pacific show that this area was a strong source of CO2 to the atmosphere between approximately 13,800 and 15,600 years ago. This observation is most compatible with increased frequency of La Ni?a conditions during this interval. Hence, increased upwelling in the eastern equatorial Pacific may have played an important role in the rise in atmospheric CO2 during the last deglaciation.     

500,000-year stable carbon isotopic record from devils hole, nevada

The record of carbon-13 (delta(13)C) variations in DH-11 vein calcite core from Devils Hole, Nevada, shows four prominent minima near glacial terminations (glacial-interglacial transitions) V to II. The delta(13)C time series is inversely correlated with the DH-11 oxygen isotope ratio time series and leads it by as much as 7000 years. The delta(13)C variations likely record fluctuations in the delta(13)C of dissolved inorganic carbon of water recharging the aquifer. How such variations are transported 80 kilometers to Devils Hole without obliteration by water-rock reaction remains an enigma. The record may reflect (i) global variations in the delta(13)C of atmospheric CO(2) and, hence, the delta(13)C of continental biomass or (ii) variations in extent and density of vegetation in the southern Great Basin. In the latter case, delta(13)C minima at 414, 334, 246, and 133 thousand years ago mark times of maximum vegetation.     

A Large Drop in Atmospheric 14C/12C and Reduced Melting in the Younger Dryas, Documented with 230Th Ages of Corals

Paired carbon-14 ((14)C) and thorium-230((230)Th) ages were determined on fossil corals from the Huon Peninsula, Papua New Guinea. The ages were used to calibrate part of the (14)C time scale and to estimate rates of sea-level rise during the last deglaciation. An abrupt offset between the (14)C and (230)Th ages suggests that the atmospheric (14)C/(12)C ratio dropped by 15 percent during the latter part of and after the Younger Dryas (YD). This prominent drop coincides with greatly reduced rates of sea-level rise. Reduction of melting because of cooler conditions during the YD may have caused an increase in the rate of ocean ventilation, which caused the atmospheric (14)C/(12)C ratio to fall. The record of sea-level rise also shows that globally averaged rates of melting were relatively high at the beginning of the YD. Thus, these measurements satisfy one of the conditions required by the hypothesis that the diversion of meltwater from the Mississippi to the St. Lawrence River triggered the YD event.     

Global carbon sinks and their variability inferred from atmospheric O2 and delta13C

Recent time-series measurements of atmospheric O2 show that the land biosphere and world oceans annually sequestered 1.4 +/- 0.8 and 2.0 +/- 0.6 gigatons of carbon, respectively, between mid-1991 and mid-1997. The rapid storage of carbon by the land biosphere from 1991 to 1997 contrasts with the 1980s, when the land biosphere was approximately neutral. Comparison with measurements of delta13CO2 implies an isotopic flux of 89 +/- 21 gigatons of carbon per mil per year, in agreement with model- and inventory-based estimates of this flux. Both the delta13C and the O2 data show significant interannual variability in carbon storage over the period of record. The general agreement of the independent estimates from O2 and delta13C is a robust signal of variable carbon uptake by both the land biosphere and the oceans.     

Loss of carbon from the deep sea since the Last Glacial Maximum

Deep-ocean carbonate ion concentrations ([CO(3)(2-)]) and carbon isotopic ratios (δ(13)C) place important constraints on past redistributions of carbon in the ocean-land-atmosphere system and hence provide clues to the causes of atmospheric CO(2) concentration changes. However, existing deep-sea [CO(3)(2-)] reconstructions conflict with one another, complicating paleoceanographic interpretations. Here, we present deep-sea [CO(3)(2-)] for five cores from the three major oceans quantified using benthic foraminiferal boron/calcium ratios since the last glacial period. Combined benthic δ(13)C and [CO(3)(2-)] results indicate that deep-sea-released CO(2) during the early deglacial period (17.5 to 14.5 thousand years ago) was preferentially stored in the atmosphere, whereas during the late deglacial period (14 to 10 thousand years ago), besides contributing to the contemporary atmospheric CO(2) rise, a substantial portion of CO(2) released from oceans was absorbed by the terrestrial biosphere.     

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.     

Ice record of delta13C for atmospheric CH4 across the Younger Dryas-Preboreal transition

We report atmospheric methane carbon isotope ratios (delta13CH4) from the Western Greenland ice margin spanning the Younger Dryas-to-Preboreal (YD-PB) transition. Over the recorded approximately 800 years, delta13CH4 was around -46 per mil (per thousand); that is, approximately 1 per thousand higher than in the modern atmosphere and approximately 5.5 per thousand higher than would be expected from budgets without 13C-rich anthropogenic emissions. This requires higher natural 13C-rich emissions or stronger sink fractionation than conventionally assumed. Constant delta13CH4 during the rise in methane concentration at the YD-PB transition is consistent with additional emissions from tropical wetlands, or aerobic plant CH4 production, or with a multisource scenario. A marine clathrate source is unlikely.     

Recent changes in atmospheric carbon monoxide

Measurements of carbon monoxide (CO) in air samples collected from 27 locations between 71 degrees N and 41 degrees S show that atmospheric levels of this gas have decreased worldwide over the past 2 to 5 years. During this period, CO decreased at nearly a constant rate in the high northern latitudes. In contrast, in the tropics an abrupt decrease occurred beginning at the end of 1991. In the Northern Hemisphere, CO decreased at a spatially and temporally averaged rate of 7.3 (+/-0.9) parts per billion per year (6.1 percent per year) from June 1990 to June 1993, whereas in the Southern Hemisphere, CO decreased 4.2 (+/-0.5) parts per billion per year (7.0 percent per year). This recent change is opposite a long-term trend of a 1 to 2 percent per year increase inferred from measurements made in the Northern Hemisphere during the past 30 years.     

Timing of atmospheric CO2 and Antarctic temperature changes across termination III

The analysis of air bubbles from ice cores has yielded a precise record of atmospheric greenhouse gas concentrations, but the timing of changes in these gases with respect to temperature is not accurately known because of uncertainty in the gas age-ice age difference. We have measured the isotopic composition of argon in air bubbles in the Vostok core during Termination III (approximately 240,000 years before the present). This record most likely reflects the temperature and accumulation change, although the mechanism remains unclear. The sequence of events during Termination III suggests that the CO2 increase lagged Antarctic deglacial warming by 800 +/- 200 years and preceded the Northern Hemisphere deglaciation.     

Unexpected changes to the global methane budget over the past 2000 years

We report a 2000-year Antarctic ice-core record of stable carbon isotope measurements in atmospheric methane (delta13CH4). Large delta13CH4 variations indicate that the methane budget varied unexpectedly during the late preindustrial Holocene (circa 0 to 1700 A.D.). During the first thousand years (0 to 1000 A.D.), delta13CH4 was at least 2 per mil enriched compared to expected values, and during the following 700 years, an about 2 per mil depletion occurred. Our modeled methane source partitioning implies that biomass burning emissions were high from 0 to 1000 A.D. but reduced by almost approximately 40% over the next 700 years. We suggest that both human activities and natural climate change influenced preindustrial biomass burning emissions and that these emissions have been previously understated in late preindustrial Holocene methane budget research.     

Potential magnitude of future vegetation change in eastern north america: comparisons with the past

Increases in atmospheric trace gas concentrations could warm the global average temperature 1.5 degrees to 4.5 degrees C by the end of the next century. Application of climate-pollen response surfaces to three climate model simulations of doubled preindustrial atmospheric CO(2) levels shows that the change in the equilibrium distribution of natural vegetation over eastern North America over the next 200 to 500 years could be larger than the overall change during the past 7,000 to 10,000 years and equivalent to the change that took place over the 1,000- to 3,000-year period of most rapid deglaciation. Some plant ranges and abundance maxima could shift as much as 500 to 1000 km during the next 200 to 500 years; such changes would have dramatic impacts on silvicultural and natural ecosystems. Although unprecedented vegetation change is likely if climate changes as predicted, forecasting the exact timing and patterns of change will be difficult.     

The last deglaciation event in the eastern central arctic ocean

Oxygen isotope records of cores from the central Arctic Ocean yield evidence for a major influx of meltwater at the beginning of the last deglaciation 15.7 thousand years ago (16,650 calendar years B.C.). The almost parallel trends of the isotope records from the Arctic Ocean, the Fram Strait, and the east Greenland continental margin suggest contemporaneous variations of the Eurasian Arctic and Greenland (Laurentide) ice sheets or increased export of low-saline waters from the Arctic within the East Greenland Current during the last deglaciation. On the basis of isotope and carbon data, the modern surface- and deep-water characteristics and seasonally open-ice conditions with increased surface-water productivity were established in the central Arctic at the end of Termination lb about 7.2 thousand years ago or 6,000 calendar years B.C.).     

Southern Hemisphere and deep-sea warming led deglacial atmospheric CO2 rise and tropical warming

Establishing what caused Earth's largest climatic changes in the past requires a precise knowledge of both the forcing and the regional responses. We determined the chronology of high- and low-latitude climate change at the last glacial termination by radiocarbon dating benthic and planktonic foraminiferal stable isotope and magnesium/calcium records from a marine core collected in the western tropical Pacific. Deep-sea temperatures warmed by approximately 2 degrees C between 19 and 17 thousand years before the present (ky B.P.), leading the rise in atmospheric CO2 and tropical-surface-ocean warming by approximately 1000 years. The cause of this deglacial deep-water warming does not lie within the tropics, nor can its early onset between 19 and 17 ky B.P. be attributed to CO2 forcing. Increasing austral-spring insolation combined with sea-ice albedo feedbacks appear to be the key factors responsible for this warming.     

Venting of carbon dioxide-rich fluid and hydrate formation in mid-okinawa trough backarc basin

Carbon dioxide-rich fluid bubbles, containing approximately 86 percent CO(2), 3 percent H(2)S, and 11 percent residual gas (CH(4) + H(2)), were observed to emerge from the sea floor at 1335- to 1550-m depth in the JADE hydrothermal field, mid-Okinawa Trough. Upon contact with seawater at 3.8 degrees C, gas hydrate immediately formed on the surface of the bubbles and these hydrates coalesced to form pipes standing on the sediments. Chemical composition and carbon, sulfur, and helium isotopic ratios indicate that the CO(2)-rich fluid was derived from the same magmatic source as dissolved gases in 320 degrees C hydrothermal solution emitted from a nearby black smoker chimney. The CO(2)-rich fluid phase may be separated by subsurface boiling of hydrothermal solutions or by leaching of CO(2)-rich fluid inclusion during posteruption interaction between pore water and volcanogenic sediments.     

Influence of carbonic anhydrase activity in terrestrial vegetation on the 18O content of atmospheric CO2

The oxygen-18 (18O) content of atmospheric carbon dioxide (CO2) is an important indicator of CO2 uptake on land. It has generally been assumed that during photosynthesis, oxygen in CO2 reaches isotopic equilibrium with oxygen in 18O-enriched water in leaves. We show, however, large differences in the activity of carbonic anhydrase (which catalyzes CO2 hydration and 18O exchange in leaves) among major plant groups that cause variations in the extent of 18O equilibrium (theta(eq)). A clear distinction in theta(eq) between C3 trees and shrubs, and C4 grasses makes atmospheric C18OO a potentially sensitive indicator to changes in C3 and C4 productivity. We estimate a global mean theta(eq) value of approximately 0.8, which reasonably reconciles inconsistencies between 18O budgets of atmospheric O2 (Dole effect) and CO2.     

Temperature and surface-ocean water balance of the mid-holocene tropical western pacific

Skeletal Sr/Ca and 18O/16O ratios in corals from the Great Barrier Reef, Australia, indicate that the tropical ocean surface approximately 5350 years ago was 1 degrees C warmer and enriched in 18O by 0.5 per mil relative to modern seawater. The results suggest that the temperature increase enhanced the evaporative enrichment of 18O in seawater. Transport of part of the additional atmospheric water vapor to extratropical latitudes may have sustained the 18O/16O anomaly. The reduced glacial-Holocene shift in seawater 18O/16O ratio produced by the mid-Holocene 18O enrichment may help to reconcile the different temperature histories for the last deglaciation given by coral Sr/Ca thermometry and foraminiferal oxygen-isotope records.     

Isotopic evidence for neogene hominid paleoenvironments in the kenya rift valley

Bipedality, the definitive characteristic of the earliest hominids, has been regarded as an adaptive response to a transition from forested to more-open habitats in East Africa sometime between 12 million and 5 million years ago. Analyses of the stable carbon isotopic composition (delta(13)C) of paleosol carbonate and organic matter from the Tugen Hills succession in Kenya indicate that a heterogeneous environment with a mix of C3 and C4 plants has persisted for the last 15.5 million years. Open grasslands at no time dominated this portion of the rift valley. The observed delta(13)C values offer no evidence for a shift from more-closed C3 environments to C4 grassland habitats. If hominids evolved in East Africa during the Late Miocene, they did so in an ecologically diverse setting.     

Large variations in Southern Hemisphere biomass burning during the last 650 years

We present a 650-year Antarctic ice core record of concentration and isotopic ratios (δ(13)C and δ(18)O) of atmospheric carbon monoxide. Concentrations decreased by ~25% (14 parts per billion by volume) from the mid-1300s to the 1600s then recovered completely by the late 1800s. δ(13)C and δ(18)O decreased by about 2 and 4 per mil (‰), respectively, from the mid-1300s to the 1600s then increased by about 2.5 and 4‰ by the late 1800s. These observations and isotope mass balance model results imply that large variations in the degree of biomass burning in the Southern Hemisphere occurred during the last 650 years, with a decrease by about 50% in the 1600s, an increase of about 100% by the late 1800s, and another decrease by about 70% from the late 1800s to present day.