Seasonal temperatures in West Antarctica during the Holocene.

The recovery of long-term climate proxy records with seasonal resolution is rare because of natural smoothing processes, discontinuities and limitations in measurement resolution. Yet insolation forcing, a primary driver of multimillennial-scale climate change, acts through seasonal variations with direct impacts on seasonal climate1. Whether the sensitivity of seasonal climate to insolation matches theoretical predictions has not been assessed over long timescales. Here, we analyse a continuous record of water-isotope ratios from the West Antarctic Ice Sheet Divide ice core to reveal summer and winter temperature changes through the last 11,000 years. Summer temperatures in West Antarctica increased through the early-to-mid-Holocene, reached a peak 4,100 years ago and then decreased to the present. Climate model simulations show that these variations primarily reflect changes in maximum summer insolation, confirming the general connection between seasonal insolation and warming and demonstrating the importance of insolation intensity rather than seasonally integrated insolation or season duration2,3. Winter temperatures varied less overall, consistent with predictions from insolation forcing, but also fluctuated in the early Holocene, probably owing to changes in meridional heat transport. The magnitudes of summer and winter temperature changes constrain the lowering of the West Antarctic Ice Sheet surface since the early Holocene to less than 162 m and probably less than 58 m, consistent with geological constraints elsewhere in West Antarctica4-7.

A 120,000-year long climate record from a NW-Greenland deep ice core at ultra-high resolution.

We report high resolution measurements of the stable isotope ratios of ancient ice (δ18O, δD) from the North Greenland Eemian deep ice core (NEEM, 77.45° N, 51.06° E). The record covers the period 8-130 ky b2k (y before 2000) with a temporal resolution of ≈0.5 and 7 y at the top and the bottom of the core respectively and contains important climate events such as the 8.2 ky event, the last glacial termination and a series of glacial stadials and interstadials. At its bottom part the record contains ice from the Eemian interglacial. Isotope ratios are calibrated on the SMOW/SLAP scale and reported on the GICC05 (Greenland Ice Core Chronology 2005) and AICC2012 (Antarctic Ice Core Chronology 2012) time scales interpolated accordingly. We also provide estimates for measurement precision and accuracy for both δ18O and δD.

The Soil Water Isotope Storage System (SWISS): An integrated soil water vapor sampling and multiport storage system for stable isotope geochemistry.

RATIONALE: Soil water stable isotopes are a powerful tool for tracking interactions among the hydrosphere, geosphere, atmosphere, and biosphere. The challenges associated with creating high-temporal-resolution soil water stable isotope datasets from a diversity of sites have limited the utility of stable isotope geochemistry in addressing a range of complex problems. A device that can enable further development of high-temporal-resolution soil water isotope datasets that are created with minimal soil profile disruption from remote sites would greatly expand the utility of soil water stable isotope analyses. METHODS: We designed a method for sampling and storing soil water vapor for stable isotope analysis that leverages recent advances in soil water sampling strategies. Here, we test the reliability of the storage system by introducing water vapor of known oxygen and hydrogen isotopic composition into the storage system, storing the water vapor for a predetermined amount of time, and then measuring the stable isotope composition of the vapor after the storage period. RESULTS: We demonstrate that water vapor stored in our flasks reliably maintains its isotope composition within overall system uncertainty (±0.5‰ for δ18 O values and ±2.4‰ for δ2 H values) for up to 30 days. CONCLUSIONS: This method has the potential to enable the collection of high-temporal-resolution soil water isotope datasets from remote sites that are not accessed daily in a time- and cost-effective manner. All the components used in the system can be easily controlled using open-source microcontrollers, which will be used in the future to automate sampling routines for remote field deployment. The system is designed to be an open-source tool for use by other researchers.

Enhanced North American carbon uptake associated with El Niño.

Long-term atmospheric CO2 mole fraction and δ13CO2 observations over North America document persistent responses to the El Niño-Southern Oscillation. We estimate these responses corresponded to 0.61 (0.45 to 0.79) PgC year-1 more North American carbon uptake during El Niño than during La Niña between 2007 and 2015, partially offsetting increases of net tropical biosphere-to-atmosphere carbon flux around El Niño. Anomalies in derived North American net ecosystem exchange (NEE) display strong but opposite correlations with surface air temperature between seasons, while their correlation with water availability was more constant throughout the year, such that water availability is the dominant control on annual NEE variability over North America. These results suggest that increased water availability and favorable temperature conditions (warmer spring and cooler summer) caused enhanced carbon uptake over North America near and during El Niño.

Increased water-use efficiency and reduced CO2 uptake by plants during droughts at a continental-scale.

Severe droughts in the Northern Hemisphere cause widespread decline of agricultural yield, reduction of forest carbon uptake, and increased CO2 growth rates in the atmosphere. Plants respond to droughts by partially closing their stomata to limit their evaporative water loss, at the expense of carbon uptake by photosynthesis. This trade-off maximizes their water-use efficiency, as measured for many individual plants under laboratory conditions and field experiments. Here we analyze the 13C/12C stable isotope ratio in atmospheric CO2 (reported as δ13C) to provide new observational evidence of the impact of droughts on the water-use efficiency across areas of millions of km2 and spanning one decade of recent climate variability. We find strong and spatially coherent increases in water-use efficiency along with widespread reductions of net carbon uptake over the Northern Hemisphere during severe droughts that affected Europe, Russia, and the United States in 2001-2011. The impact of those droughts on water-use efficiency and carbon uptake by vegetation is substantially larger than simulated by the land-surface schemes of six state-of-the-art climate models. This suggests that drought induced carbon-climate feedbacks may be too small in these models and improvements to their vegetation dynamics using stable isotope observations can help to improve their drought response.

Upward revision of global fossil fuel methane emissions based on isotope database.

Methane has the second-largest global radiative forcing impact of anthropogenic greenhouse gases after carbon dioxide, but our understanding of the global atmospheric methane budget is incomplete. The global fossil fuel industry (production and usage of natural gas, oil and coal) is thought to contribute 15 to 22 per cent of methane emissions to the total atmospheric methane budget. However, questions remain regarding methane emission trends as a result of fossil fuel industrial activity and the contribution to total methane emissions of sources from the fossil fuel industry and from natural geological seepage, which are often co-located. Here we re-evaluate the global methane budget and the contribution of the fossil fuel industry to methane emissions based on long-term global methane and methane carbon isotope records. We compile the largest isotopic methane source signature database so far, including fossil fuel, microbial and biomass-burning methane emission sources. We find that total fossil fuel methane emissions (fossil fuel industry plus natural geological seepage) are not increasing over time, but are 60 to 110 per cent greater than current estimates owing to large revisions in isotope source signatures. We show that this is consistent with the observed global latitudinal methane gradient. After accounting for natural geological methane seepage, we find that methane emissions from natural gas, oil and coal production and their usage are 20 to 60 per cent greater than inventories. Our findings imply a greater potential for the fossil fuel industry to mitigate anthropogenic climate forcing, but we also find that methane emissions from natural gas as a fraction of production have declined from approximately 8 per cent to approximately 2 per cent over the past three decades.

A 21st-century shift from fossil-fuel to biogenic methane emissions indicated by ¹³CH4.

Between 1999 and 2006, a plateau interrupted the otherwise continuous increase of atmospheric methane concentration [CH4] since preindustrial times. Causes could be sink variability or a temporary reduction in industrial or climate-sensitive sources. We reconstructed the global history of [CH4] and its stable carbon isotopes from ice cores, archived air, and a global network of monitoring stations. A box-model analysis suggests that diminishing thermogenic emissions, probably from the fossil-fuel industry, and/or variations in the hydroxyl CH4 sink caused the [CH4] plateau. Thermogenic emissions did not resume to cause the renewed [CH4] rise after 2006, which contradicts emission inventories. Post-2006 source increases are predominantly biogenic, outside the Arctic, and arguably more consistent with agriculture than wetlands. If so, mitigating CH4 emissions must be balanced with the need for food production.

Demonstration of high-precision continuous measurements of water vapor isotopologues in laboratory and remote field deployments using wavelength-scanned cavity ring-down spectroscopy (WS-CRDS) technology.

This study demonstrates the application of Wavelength-Scanned Cavity Ring-Down Spectroscopy (WS-CRDS) technology which is used to measure the stable isotopic composition of water. This isotopic water analyzer incorporates an evaporator system that allows liquid water as well as water vapor to be measured with high precision. The analyzer can measure H2(18)O, H2(16)O and HD(16)O content of the water sample simultaneously. The results of a laboratory test and two field trials with this analyzer are described. The results of these trials show that the isotopic water analyzer gives precise, accurate measurements with little or no instrument drift for the two most common isotopologues of water. In the laboratory the analyzer has a precision of 0.5 per mil for deltaD and 0.1 per mil for delta(18)O which is similar to the precision obtained by laboratory-based isotope ratio mass spectrometers. In the field, when measuring vapor samples, the analyzer has a precision of 1.0 per mil for deltaD and 0.2 per mil for delta(18)O. These results demonstrate that the isotopic water analyzer is a powerful tool that is appropriate for use in a wide range of applications and environments.

High-precision CO2 isotopologue spectrometer with a difference-frequency-generation laser source.

A precision laser spectrometer for the detection of CO(2) isotopes is reported. The spectrometer measures the fundamental absorption signatures of (13)C and (12)C isotopes in CO(2) at 4.32 microm using a tunable mid-IR laser source based on difference-frequency generation. The spectrometer attains a precision of up to 0.02 per thousand for 150 s of averaging. An overall accuracy of 0.05 per thousand was obtained when sampling various calibrated reference gases.