Quartz-amethyst hosted hydrocarbon-bearing fluid inclusions from the green ridge breccia in the snoqualmie granite, North Cascades,WA, USA

We wish to acknowledge the constructive criticisms made by the three anonymous reviewers.Their suggestions and comments greatly improved the first version of the manuscript.Peer reviewedPublisher PD

Petroleum evolution within the Tarim Basin, northwestern China: Insights from organic geochemistry, fluid inclusions, and rhenium–osmium geochronology of the Halahatang oil field

The newly discovered Halahatang oil field in the northern Tarim Basin has a potential resource of more than 70 billion bbl of oil. Oil organic geochemical data from the Halahatang oil field indicate that the oils are of moderate maturity, biodegraded, and represent one oil family, derived from the same Paleozoic marine source. Modeling of coeval aqueous and hydrocarbon-bearing inclusion data provide fluid trapping temperatures and pressures of 100°C to 110°C and approximately 39 to 59 MPa (∼5656–8557 psi), respectively. The fluid inclusion data coupled with the previous basin model studies suggest a single prolonged oil migration event during the Permian. The Re–Os isotope data of the oil yields an early Permian Re–Os age of 285 ± 48 Ma. The age agrees with the timing of maturation of the Paleozoic source via burial history modeling but is slightly older (∼5–55 m.y.) than the oil migration and accumulation timing implied by the basin modeling coupled with fluid inclusion analysis and the published reservoir illite K–Ar dates. Thus, the oil Re–Os date suggests that oil generation in the Halahatang depression of the Tarim Basin occurred during the early Permian rather than the Silurian as previously proposed, with subsequent oil migration and accumulation occurring during the middle–late Permian as recorded by basin modeling, coupled with fluid inclusion analysis and illite K–Ar dating. In addition to promoting petroleum exploration in the Tarim Basin, this study, which combines crude oil Re–Os isotope dating and traditional analytical methods (organic geochemistry and fluid inclusion analysis) to constrain petroleum evolution, is applicable to hydrocarbon systems worldwide

Satellite-based prediction of pCO2 in coastal waters of the eastern North Pacific

Continental margin carbon cycling is complex, highly variable over a range of space and time scales, and forced by multiple physical and biogeochemical drivers. Predictions of globally significant air–sea CO2 fluxes in these regions have been extrapolated based on very sparse data sets. We present here a method for predicting coastal surface-water pCO2 from remote-sensing data, based on self organizing maps (SOMs) and a nonlinear semi-empirical model of surface water carbonate chemistry. The model used simple empirical relationships between carbonate chemistry (total dissolved carbon dioxide (TCO2) and alkalinity (TAlk)) and satellite data (sea surface temperature (SST) and chlorophyll (Chl)). Surface-water CO2 partial pressure (pCO2) was calculated from the empirically-predicted TCO2 and TAlk. This directly incorporated the inherent nonlinearities of the carbonate system, in a completely mechanistic manner. The model’s empirical coefficients were determined for a target study area of the central North American Pacific continental margin (22–50°N, within 370 km of the coastline), by optimally reproducing a set of historical observations paired with satellite data. The model-predicted pCO2 agreed with the highly variable observations with a root mean squared (RMS) deviation of 0.8 (r = 0.81; r2 = 0.66). This level of accuracy is a significant improvement relative to that of simpler models that did not resolve the biogeochemical sub-regions or that relied on linear dependences on input parameters. Air–sea fluxes based on these pCO2 predictions and satellite-based wind speed measurements suggest that the region is a ∼14 Tg C yr−1 sink for atmospheric CO2 over the 1997–2005 period, with an approximately equivalent uncertainty, compared with a ∼0.5 Tg C yr−1 source predicted by a recent bin-averaging and interpolation-based estimate for the same area.Fil: Hales, Burke. State University of Oregon; Estados UnidosFil: Strutton, Peter G.. University Of Tasmania; AustraliaFil: Saraceno, Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones del Mar y la Atmosfera. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones del Mar y la Atmosfera; ArgentinaFil: Letelier, Ricardo. State University of Oregon; Estados UnidosFil: Takahashi, Taro. Lamont-Doherty Earth Observatory; Estados UnidosFil: Feely, Richard. National Oceanic and Atmospheric Administration. Pacific Marine Environmental Laboratory; Estados UnidosFil: Sabine, Christopher. National Oceanic and Atmospheric Administration. Pacific Marine Environmental Laboratory; Estados UnidosFil: Chavez, Francisco. Monterey Bay Aquarium Research Institute; Estados Unido

Detection of reduced carbon in a basalt analogue for martian nakhlite : a signpost to habitat on Mars

C. W. Taylor and J. Still are thanked for skilled technical support. J. Parnell, H.G.M. Edwards, I. Hutchinson and R. Ingley acknowledge the support of the UKSA and the STFC Research Council in the UK ExoMars programme. L. V. Harris and S. McMahon acknowledge STFC studentship funding.Peer reviewedPublisher PD

Satellite-based prediction of pCO₂ in coastal waters of the eastern North Pacific

Continental margin carbon cycling is complex, highly variable over a range of space and time scales, and forced by multiple physical and biogeochemical drivers. Predictions of globally significant air–sea CO₂ fluxes in these regions have been extrapolated based on very sparse data sets. We present here a method for predicting coastal surface-water pCO₂ from remote-sensing data, based on self organizing maps (SOMs) and a nonlinear semi-empirical model of surface water carbonate chemistry. The model used simple empirical relationships between carbonate chemistry (total dissolved carbon dioxide (T[subscript CO₂]) and alkalinity (T[subscript Alk])) and satellite data (sea surface temperature (SST) and chlorophyll (Chl)). Surface-water CO₂ partial pressure (pCO₂) was calculated from the empirically-predicted T[subscript CO₂] and T[subscript Alk]. This directly incorporated the inherent nonlinearities of the carbonate system, in a completely mechanistic manner. The model’s empirical coefficients were determined for a target study area of the central North American Pacific continental margin (22–50°N, within 370 km of the coastline), by optimally reproducing a set of historical observations paired with satellite data. The model-predicted pCO₂ agreed with the highly variable observations with a root mean squared (RMS) deviation of 0.8 (r = 0.81; r² = 0.66). This level of accuracy is a significant improvement relative to that of simpler models that did not resolve the biogeochemical sub-regions or that relied on linear dependences on input parameters. Air–sea fluxes based on these pCO₂ predictions and satellite-based wind speed measurements suggest that the region is a ∼14 Tg C yr⁻¹ sink for atmospheric CO₂ over the 1997–2005 period, with an approximately equivalent uncertainty, compared with a ∼0.5 Tg C yr⁻¹ source predicted by a recent bin-averaging and interpolation-based estimate for the same area

Effects of ocean acidification on invertebrate settlement at volcanic CO<inf>2</inf> vents

We present the first study of the effects of ocean acidification on settlement of benthic invertebrates and microfauna. Artificial collectors were placed for 1 month along pH gradients at CO2 vents off Ischia (Tyrrhenian Sea, Italy). Seventy-nine taxa were identified from six main taxonomic groups (foraminiferans, nematodes, polychaetes, molluscs, crustaceans and chaetognaths). Calcareous foraminiferans, serpulid polychaetes, gastropods and bivalves showed highly significant reductions in recruitment to the collectors as pCO2 rose from normal (336-341 ppm, pH 8.09-8.15) to high levels (886-5,148 ppm) causing acidified conditions near the vents (pH 7.08-7.79). Only the syllid polychaete Syllis prolifera had higher abundances at the most acidified station, although a wide range of polychaetes and small crustaceans was able to settle and survive under these conditions. A few taxa (Amphiglena mediterranea, Leptochelia dubia, Caprella acanthifera) were particularly abundant at stations acidified by intermediate amounts of CO2 (pH 7. 41-7.99). These results show that increased levels of CO2 can profoundly affect the settlement of a wide range of benthic organisms. © 2010 Springer-Verlag

Rapid Environmental Change over the Past Decade Revealed by Isotopic Analysis of the California Mussel in the Northeast Pacific

The anthropogenic input of fossil fuel carbon into the atmosphere results in increased carbon dioxide (CO2) into the oceans, a process that lowers seawater pH, decreases alkalinity and can inhibit the production of shell material. Corrosive water has recently been documented in the northeast Pacific, along with a rapid decline in seawater pH over the past decade. A lack of instrumentation prior to the 1990s means that we have no indication whether these carbon cycle changes have precedence or are a response to recent anthropogenic CO2 inputs. We analyzed stable carbon and oxygen isotopes (δ13C, δ18O) of decade-old California mussel shells (Mytilus californianus) in the context of an instrumental seawater record of the same length. We further compared modern shells to shells from 1000 to 1340 years BP and from the 1960s to the present and show declines in the δ13C of modern shells that have no historical precedent. Our finding of decline in another shelled mollusk (limpet) and our extensive environmental data show that these δ13C declines are unexplained by changes to the coastal food web, upwelling regime, or local circulation. Our observed decline in shell δ13C parallels other signs of rapid changes to the nearshore carbon cycle in the Pacific, including a decline in pH that is an order of magnitude greater than predicted by an equilibrium response to rising atmospheric CO2, the presence of low pH water throughout the region, and a record of a similarly steep decline in δ13C in algae in the Gulf of Alaska. These unprecedented changes and the lack of a clear causal variable underscores the need for better quantifying carbon dynamics in nearshore environments

Tropical land carbon cycle responses to 2015/16 El Niño as recorded by atmospheric greenhouse gas and remote sensing data

The outstanding tropical land climate characteristic over the past decades is rapid warming, with no significant large-scale precipitation trends. This warming is expected to continue but the effects on tropical vegetation are unknown. El Niño-related heat peaks may provide a test bed for a future hotter world. Here we analyse tropical land carbon cycle responses to the 2015/16 El Niño heat and drought anomalies using an atmospheric transport inversion. Based on the global atmospheric CO₂ and fossil fuel emission records, we find no obvious signs of anomalously large carbon release compared with earlier El Niño events, suggesting resilience of tropical vegetation. We find roughly equal net carbon release anomalies from Amazonia and tropical Africa, approximately 0.5 PgC each, and smaller carbon release anomalies from tropical East Asia and southern Africa. Atmospheric CO anomalies reveal substantial fire carbon release from tropical East Asia peaking in October 2015 while fires contribute only a minor amount to the Amazonian carbon flux anomaly. Anomalously large Amazonian carbon flux release is consistent with downregulation of primary productivity during peak negative near-surface water anomaly (October 2015 to March 2016) as diagnosed by solar-induced fluorescence. Finally, we find an unexpected anomalous positive flux to the atmosphere from tropical Africa early in 2016, coincident with substantial CO release