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The Central Arctic Ocean’s (CAO) current and future role in the exchange of climate-forcing trace gases with the atmosphere is highly uncertain, in particular the effect of sea ice on the exchange. There are no previously reported direct air-sea methane (CH4) flux estimates from the CAO. We present direct measurements of the air-sea flux of CH4 and carbon dioxide (CO2), as well as air-ice fluxes of CO2 in the summertime CAO North of 82.5 N from the Synoptic Arctic Survey (SAS) expedition carried out on the Swedish icebreaker Oden in 2021. Measurements of air-sea CH4 and CO2 flux were made using floating chambers deployed in leads accessed from sea ice and from the side of Oden. Fluxes and dissolved gas concentrations from surface water were used to determine gas transfer velocities that exhibited a weaker wind speed dependence than existing parameterisations, with a median gas transfer rate in sea-ice leads 2.5 cm hr−1. Average observed CO2 air-sea flux were −7.6 mmol m−2 day−1, and the average air-snow flux −1.1 mmol m−2 day−1. Extrapolating these fluxes and the corresponding sea ice concentrations gives an August and September flux for the CAO of −1.75 mmol m−2 day−1 and a corresponding annual CAO uptake of 126.6 Tg yr−1. Average observed air-sea CH4 flux of 3.5 μmol m−2 day−1, accounting for sea ice concentration, equates to a CAO flux of 0.35 μmol m−2 day−1, or 9.2 Gg yr−1, lower than previous estimates and implying that the CAO is a very small, << 1 %, contributor to the flux of CH4 to the atmosphere from the Arctic.

Lakes and reservoirs contribute to regional carbon budgets via significant emissions of climate forcing trace gases. Here, for improved modelling, we use 8 years of floating chamber measurements from three small, shallow subarctic lakes (2010–2017, n=1306 ) to separate the contribution of physical and biogeochemical processes to the turbulence-driven, diffusion-limited flux of methane ( CH4 ) on daily to multi-year timescales. Correlative data include surface water concentration measurements (2009–2017, n=606 ), total water column storage (2010–2017, n=237 ), and in situ meteorological observations. We used the last to compute near-surface turbulence based on similarity scaling and then applied the surface renewal model to compute gas transfer velocities. Chamber fluxes averaged 6.9±0.3 mg CH4 m −2 d −1 and gas transfer velocities ( k600 ) averaged 4.0±0.1 cm h −1 . Chamber-derived gas transfer velocities tracked the power-law wind speed relation of the model. Coefficients for the model and dissipation rates depended on shear production of turbulence, atmospheric stability, and exposure to wind. Fluxes increased with wind speed until daily average values exceeded 6.5 m s −1 , at which point emissions were suppressed due to rapid water column degassing reducing the water–air concentration gradient. Arrhenius-type temperature functions of the CH4 flux ( E a ′ = 0.90 ± 0.14 eV) were robust ( R2≥0.93 , p ) and also applied to the surface CH4 concentration ( E a ′ = 0.88 ± 0.09 eV). These results imply that emissions were strongly coupled to production and supply to the water column. Spectral analysis indicated that on timescales shorter than a month, emissions were driven by wind shear whereas on longer timescales variations in water temperature governed the flux. Long-term monitoring efforts are essential to identify distinct functional relations that govern flux variability on timescales of weather and climate change.

Characterizing methane sources in the Arctic remains challenging due to the remoteness, heterogeneity and variety of such emissions. In situ campaigns provide valuable datasets to reduce these uncertainties. Here we analyse data from the summer 2014 SWERUS-C3 campaign in the eastern Arctic Ocean, off the shore of Siberia and Alaska. Total concentrations of methane, as well as relative concentrations of 12CH4 and 13CH4, were measured continuously during this campaign for 35 d in July and August. Using a chemistry-transport model, we link observed concentrations and isotopic ratios to regional emissions and hemispheric transport structures. A simple inversion system helped constrain source signatures from wetlands in Siberia and Alaska, and oceanic sources, as well as the isotopic composition of lower-stratosphere air masses. The variation in the signature of lower-stratosphere air masses, due to strongly fractionating chemical reactions in the stratosphere, was suggested to explain a large share of the observed variability in isotopic ratios. These results point towards necessary efforts to better simulate large-scale transport and chemistry patterns to make relevant use of isotopic data in remote areas. It is also found that constant and homogeneous source signatures for each type of emission in a given region (mostly wetlands and oil and gas industry in our case at high latitudes) are not compatible with the strong synoptic isotopic signal observed in the Arctic. A regional gradient in source signatures is highlighted between Siberian and Alaskan wetlands, the latter having lighter signatures (more depleted in 13C). Finally, our results suggest that marine emissions of methane from Arctic continental-shelf sources are dominated by thermogenic-origin methane, with a secondary biogenic source as well.

Recent efforts have brought together bottom-up quantification approaches (inventories and process-based models) and top-down approaches using regional observations of methane atmospheric concentrations through inverse modelling to better estimate the northern high-latitude methane sources. Nevertheless, for both approaches, the relatively small number of available observations in northern high-latitude regions leaves gaps in our understanding of the drivers and distributions of the different types of regional methane sources. Observations of methane isotope ratios, performed with instruments that are becoming increasingly affordable and accurate, could bring new insights on the contributions of methane sources and sinks. Here, we present the source signal that could be observed from methane isotopic 13CH4 measurements if high-resolution observations were available and thus what requirements should be fulfilled in future instrument deployments in terms of accuracy in order to constrain different emission categories. This theoretical study uses the regional chemistry-transport model CHIMERE driven by different scenarios of isotopic signatures for each regional methane source mix. It is found that if the current network of methane monitoring sites were equipped with instruments measuring the isotopic signal continuously, only sites that are significantly influenced by emission sources could differentiate regional emissions with a reasonable level of confidence. For example, wetland emissions require daily accuracies lower than 0.2 ‰ for most of the sites. Detecting East Siberian Arctic Shelf (ESAS) emissions requires accuracies lower than 0.05 ‰ at coastal Russian sites (even lower for other sites). Freshwater emissions would be detectable with an uncertainty lower than 0.1 ‰ for most continental sites. Except Yakutsk, Siberian sites require stringent uncertainty (lower than 0.05 ‰) to detect anthropogenic emissions from oil and gas or coal production. Remote sites such as Zeppelin, Summit, or Alert require a daily uncertainty below 0.05 ‰ to detect any regional sources. These limits vary with the hypothesis on isotopic signatures assigned to the different sources.

Northern lakes are important sources of the climate forcing trace gases methane (CH4) and carbon dioxide (CO2). A substantial portion of lakes' annual emissions can take place immediately after ice melt in spring. The drivers of these fluxes are neither well constrained nor fully understood. We present a detailed carbon gas budget for three subarctic lakes, using 6 years of eddy covariance and 9 years of manual flux measurements. We combine measurements of temperature, dissolved oxygen, and CH4 stable isotopologues to quantify functional relationships between carbon gas production and conversion, energy inputs, and the redox regime. Spring emissions were regulated by the availability of oxygen in winter, rather than temperature as during ice‐free conditions. Under‐ice storage increased predictably with ice‐cover duration, and CH4 accumulation rates (25 ± 2 mg CH4‐C·m−2·day−1) exceeded summer emissions (19 ± 1 mg CH4‐C·m−2·day−1). The seasonally ice‐covered lakes emitted 26–59% of the annual CH4 flux and 15–30% of the annual CO2 flux at ice‐off. Reduced spring emissions were associated with winter snowmelt events, which can transport water downstream and oxygenate the water column. Stable isotopes indicate that 64–96% of accumulated CH4 escaped oxidation, implying that a considerable portion of the dissolved gases produced over winter may evade to the atmosphere.

Record-high air temperatures were observed over Greenland in the summer of 2019 and melting of the northern Greenland Ice Sheet was particularly extensive. Here we show, through direct measurements, that near surface ocean temperatures in Sherard Osborn Fjord, northern Greenland, reached 4 °C in August 2019, while in the neighboring Petermann Fjord, they never exceeded 0 °C. We show that this disparity in temperature between the two fjords occurred because thick multi-year sea ice at the entrance of Sherard Osborn Fjord trapped the surface waters inside the fjord, which led to the formation of a warm and fresh surface layer. These results suggest that the presence of multi-year sea ice increases the sensitivity of Greenland fjords abutting the Arctic Ocean to climate warming, with potential consequences for the long-term stability of the northern sector of the Greenland Ice Sheet. Much higher surface temperatures in a north Greenland fjord, compared to a neighbouring fjord, during high air temperatures in 2019 can be explained by a sea ice dam at the fjord entrance that trapped a buoyant surface layer, suggests an analysis of hydrographic observations.

The processes controlling advance and retreat of outlet glaciers in fjords draining the Greenland Ice Sheet remain poorly known, undermining assessments of their dynamics and associated sea-level rise in a warming climate. Mass loss of the Greenland Ice Sheet has increased six-fold over the last four decades, with discharge and melt from outlet glaciers comprising key components of this loss. Here we acquired oceanographic data and multibeam bathymetry in the previously uncharted Sherard Osborn Fjord in northwest Greenland where Ryder Glacier drains into the Arctic Ocean. Our data show that warmer subsurface water of Atlantic origin enters the fjord, but Ryder Glacier’s floating tongue at its present location is partly protected from the inflow by a bathymetric sill located in the innermost fjord. This reduces under-ice melting of the glacier, providing insight into Ryder Glacier’s dynamics and its vulnerability to inflow of Atlantic warmer water. A bathymetric sill in Sherard Osborn Fjord, northwest Greenland shields Ryder Glacier from melting by warm Atlantic water found at the bottom of the fjord, according to high-resolution bathymetric mapping and oceanographic data.

The continental shelves of the Arctic Ocean and surrounding seas contain large stocks of organic matter (OM) and methane (CH4), representing a potential ecosystem feedback to climate change not included in international climate agreements. We performed a structured expert assessment with 25 permafrost researchers to combine quantitative estimates of the stocks and sensitivity of organic carbon in the subsea permafrost domain (i.e. unglaciated portions of the continental shelves exposed during the last glacial period). Experts estimated that the subsea permafrost domain contains ∼560 gigatons carbon (GtC; 170–740, 90% confidence interval) in OM and 45 GtC (10–110) in CH4. Current fluxes of CH4 and carbon dioxide (CO2) to the water column were estimated at 18 (2–34) and 38 (13–110) megatons C yr−1, respectively. Under Representative Concentration Pathway (RCP) RCP8.5, the subsea permafrost domain could release 43 Gt CO2-equivalent (CO2e) by 2100 (14–110) and 190 Gt CO2e by 2300 (45–590), with ∼30% fewer emissions under RCP2.6. The range of uncertainty demonstrates a serious knowledge gap but provides initial estimates of the magnitude and timing of the subsea permafrost climate feedback.

Methane (CH4) strongly contributes to observed global warming. As natural CH4 emissions mainly originate from wet ecosystems, it is important to unravel how climate change may affect these emissions. This is especially true for ebullition (bubble flux from sediments), a pathway that has long been underestimated but generally dominates emissions. Here we show a remarkably strong relationship between CH4 ebullition and temperature across a wide range of freshwater ecosystems on different continents using multi-seasonal CH4 ebullition data from the literature. As these temperature–ebullition relationships may have been affected by seasonal variation in organic matter availability, we also conducted a controlled year-round mesocosm experiment. Here 4 °C warming led to 51% higher total annual CH4 ebullition, while diffusion was not affected. Our combined findings suggest that global warming will strongly enhance freshwater CH4 emissions through a disproportional increase in ebullition (6–20% per 1 °C increase), contributing to global warming., The impacts of climate change on natural methane (CH4) emissions via ebullition are unclear. Here, using published and experimental multi-seasonal CH4 ebullition data, the authors find a strong relationship between CH4 ebullition and temperature across a wide range of freshwater ecosystems globally.

The recent paper in Geosciences, “Understanding the Permafrost−Hydrate System and Associated Methane Releases in the East Siberian Arctic Shelf” by Shakhova, Semiletov, and Chuvilin, (henceforth “S2019”), contains a number of false statements about our 2016 paper, “Methane fluxes from the sea to the atmosphere across the Siberian shelf seas”, (henceforth “T2016”). S2019 use three paragraphs of section 5 of their paper to claim methodological errors and issues in T2016. Notably they claim that in T2016, we systematically removed data outliers including data with high methane concentrations; this claim is false. While we appreciate that flawed methodologies can be a problem in any area of science, in this case, the claims made in S2019 are simply false. In this comment, we detail the incorrect claims made in S2019 regarding T2016, and then discuss some additional problematic aspects of S2019.

Lakes and reservoirs are important emitters of climate forcing trace gases. Various environmental drivers of the flux, such as temperature and wind speed, have been identified, but their relative importance remains poorly understood. Here we use an extensive field dataset to disentangle physical and biogeochemical controls on the turbulence-driven diffusive flux of methane (CH4) on daily to multi-year timescales. We compare 8 years of floating chamber fluxes from three small, shallow subarctic lakes (2010–2017, n = 1306) with fluxes computed using 9 years of surface water concentration measurements (2009–2017, n = 606) and a small-eddy surface renewal model informed by in situ meteorological observations. Chamber fluxes averaged 6.9 ± 0.3 mg m−2 d−1 and gas transfer velocities (k600) from the chamber-calibrated surface renewal model averaged 4.0 ± 0.1 cm h−1. We find robust (R2 ≥ 0.93, p

At its inception, the periodic table sorted elements by weight, so it may be surprising that the heaviest natural element on Earth remains controversial, or at best, nebulous. In the strange, perhaps-unfinished search for this weightiest nucleus, the only definitive conclusion is that it lies somewhere beyond uranium.

The Laptev and East Siberian Seas have been proposed as a substantial source of methane (CH4) to the atmosphere. During summer 2014, we made unique high-resolution simultaneous measurements of CH4 ...

Of all the things humans can bestow names upon, new chemical elements are about the rarest. Our group of periodic table experts attempts to read the tea leaves and predict the names for elements 113, 115, 117 and 118.

In anticipation of the IPCC's Sixth Assessment Report we look back at our evolving understanding of atmospheric CH4. Though sources, sinks, and atmospheric burden are now well known, apportionment between the myriad sources and sinks, and forecasting natural emissions, remains a challenge.

A new book by Peter Wothers delves into the tumultuous history of naming (and symbolizing) the elements.

Despite their modest 4 % magnitude compared to global emissions, Arctic methane sources are key elements in closing the global atmospheric methane budget, due to high uncertainties in their quantification and to their strong climate sensitivity. Recent efforts brought together bottom-up quantification approaches (inventories, process-based models) and regional observations of methane concentrations through inverse modelling to better estimate the Arctic methane sources, but the relatively small number of available observations in Arctic regions leaves gaps in fully understanding the drivers and distributions of the different types of methane sources present in the Arctic. Observations of methane isotope ratios could bring new insights on methane processes with increasingly affordable and accurate instruments. Here, we present the source signal that could be observed from methane isotopic measurements if high-resolution observations were available, and thus what requirements should be fulfilled in future instrument deployments in terms of accuracy in order to constrain different emission categories. This theoretical study uses the regional chemistry-transport model CHIMERE driven by different scenarios of isotopic signatures for each regional methane source mix. It is found that if the current network of methane monitoring sites is equipped with instruments measuring the isotopic signal continuously, only sites that are significantly influenced by emission sources could differentiate regional emissions from the background with a reasonable level of confidence. Nevertheless, we show that the detection of individual Arctic sources requires daily accuracies of

Strong correlations between seasonal energy input and methane (CH4) bubbling (ebullition) in northern lakes suggest that energy proxies might provide a constraint on the magnitude of future CH4 emi ...

Measurements from the SWERUS-C3 and ISSS-08 Arctic expeditions were used to calibrate and validate a new physical-biogeochemical model developed to quantify key carbon cycling processes on the East Siberian Arctic Shelf (ESAS). The model was used in a series of experimental simulations with the specific aim to investigate the pathways of terrestrial dissolved and particulate organic carbon (DOCter and POCter) supplied to the shelf. Rivers supply on average 8.5 Tg C yr−1 dissolved inorganic carbon (DIC), and further 8.5 and 1.1 Tg C yr−1 DOCter and POCter respectively. Based on observed and simulated DOC concentrations and stable isotope values (δ13CDOC) in shelf waters, we estimate that only some 20 % of the riverine DOCter is labile. According to our model results, an additional supply of approximately 14 Tg C yr−1 eroded labile POCter is however required to describe the observed stable isotope values of DIC (δ13CDIC). Degradation of riverine DOCter and POCter results in a 1.8 Tg C yr−1 reduction in the uptake of atmospheric CO2, while degradation of eroded POCter results in an additional 10 Tg C yr−1 reduction. Our calculations indicate nevertheless that the ESAS is an overall small net sink for atmospheric CO2 (1.7 Tg C yr−1). The external carbon sources are largely compensated by a net export from the shelf to the Arctic Ocean (31 Tg C yr−1), and to a smaller degree by a permanent burial in the sediments (2.7 Tg C yr−1).

Alasdair Skelton and Brett F. Thornton examine the twisting path through the several discoveries of ytterbium, from the eighteenth century to the present.

From grand challenges of nineteenth century chemistry to powerful technology in small packages, Brett F. Thornton and Shawn C. Burdette explain why neodymium is the twin element discovered twice by ...

Although the modern periodic table barely resembles the one constructed by Dmitri Mendeleev, every chemistry student learns that the placement of missing elements in the open slots of Mendeleev’s t ...

Emission of methane (CH4) from surface waters is often dominated by ebullition (bubbling), a transport mode with high-spatiotemporal variability. Based on new and extensive CH4 ebullition data, we ...

Methyl bromide (CH3Br) emitted from plants constitutes a natural source of bromine to the atmosphere, and is a component in the currently unbalanced global CH3Br budget. In the stratosphere, CH3Br ...

The global methane (CH4) budget is becoming an increasingly important component for managing realistic pathways to mitigate climate change. This relevance, due to a shorter atmospheric lifetime and a stronger warming potential than carbon dioxide, is challenged by the still unexplained changes of atmospheric CH4 over the past decade. Emissions and concentrations of CH4 are continuing to increase, making CH4 the second most important human-induced greenhouse gas after carbon dioxide. Two major difficulties in reducing uncertainties come from the large variety of diffusive CH4 sources that overlap geographically, and from the destruction of CH4 by the very short-lived hydroxyl radical (OH). To address these difficulties, we have established a consortium of multi-disciplinary scientists under the umbrella of the Global Carbon Project to synthesize and stimulate research on the methane cycle, and producing regular (similar to biennial) updates of the global methane budget. This consortium includes atmospheric physicists and chemists, biogeochemists of surface and marine emissions, and socio-economists who study anthropogenic emissions. Following Kirschke et al. (2013), we propose here the first version of a living review paper that integrates results of top-down studies (exploiting atmospheric observations within an atmospheric inverse-modelling framework) and bottom-up models, inventories and data-driven approaches (including process-based models for estimating land surface emissions and atmospheric chemistry, and inventories for anthropogenic emissions, data-driven extrapolations). For the 2003-2012 decade, global methane emissions are estimated by top-down inversions at 558 TgCH(4) yr(-1), range 540-568. About 60% of global emissions are anthropogenic (range 50-65 %). Since 2010, the bottom-up global emission inventories have been closer to methane emissions in the most carbon-intensive Representative Concentrations Pathway (RCP8.5) and higher than all other RCP scenarios. Bottom-up approaches suggest larger global emissions (736 TgCH(4) yr(-1), range 596-884) mostly because of larger natural emissions from individual sources such as inland waters, natural wetlands and geological sources. Considering the atmospheric constraints on the top-down budget, it is likely that some of the individual emissions reported by the bottom-up approaches are overestimated, leading to too large global emissions. Latitudinal data from top-down emissions indicate a predominance of tropical emissions (similar to 64% of the global budget, amp;lt;30 degrees N) as compared to mid (similar to 32 %, 30-60 degrees N) and high northern latitudes (similar to 4 %, 60-90 degrees N). Top-down inversions consistently infer lower emissions in China (similar to 58 TgCH(4) yr(-1), range 51-72, -14 %) and higher emissions in Africa (86 TgCH(4) yr(-1), range 73-108, + 19 %) than bottom-up values used as prior estimates. Overall, uncertainties for anthropogenic emissions appear smaller than those from natural sources, and the uncertainties on source categories appear larger for top-down inversions than for bottom-up inventories and models. The most important source of uncertainty on the methane budget is attributable to emissions from wetland and other inland waters. We show that the wetland extent could contribute 30-40% on the estimated range for wetland emissions. Other priorities for improving the methane budget include the following: (i) the development of process-based models for inland-water emissions, (ii) the intensification of methane observations at local scale (flux measurements) to constrain bottom-up land surface models, and at regional scale (surface networks and satellites) to constrain top-down inversions, (iii) improvements in the estimation of atmospheric loss by OH, and (iv) improvements of the transport models integrated in top-down inversions. The data presented here can be downloaded from the Carbon Dioxide Information Analysis Center (http://doi.org/10.3334/CDIAC/GLOBAL_METHANE_BUDGET_2016_V1.1) and the Global Carbon Project. Funding Agencies|Swiss National Science Foundation; NASA [NNX14AF93G, NNX14AO73G]; National Environmental Science Program - Earth Systems and Climate Change Hub; European Commission [283576, 633080]; ESA Climate Change Initiative Greenhouse Gases Phase 2 project; US Department of Energy, BER [DE-AC02-05CH11231]; FAO member countries; Environment Research and Technology Development Fund of the Ministry of the Environment, Japan [2-1502]; ERC [322998]; NERC [NE/J00748X/1]; Swedish Research Council VR; Research Council of Norway [244074]; NSF [1243232, 1243220]; National Science and Engineering Research Council of Canada (NSERC); Chinas QianRen Program; CSIRO Australia; Australian Bureau of Meteorology; Australian Institute of Marine Science; Australian Antarctic Division; NOAA USA; Meteorological Service of Canada; National Aeronautic and Space Administration (NASA) [NAG5-12669, NNX07AE89G, NNX11AF17G, NNX07AE87G, NNX07AF09G, NNX11AF15G, NNX11AF16G]; Department of Energy and Climate Change (DECC, UK) [GA01081]; Commonwealth Scientific and Industrial Research Organization (CSIRO Australia); Bureau of Meteorology (Australia); Joint DECC/Defra Met Office Hadley Centre Climate Programme [GA01101]

Lanthanum is the first lanthanide — or the last. Or it’s not a lanthanide at all. In any case, Brett Thornton and Shawn Burdette are sure that it’s an element that might or might not be in group three of the periodic table.

Methane emissions from lakes are widely thought to be highly irregular and difficult to quantify with anything other than numerous distributed measurement stations and long-term sampling campaigns. In spite of this, a large majority of the study sites north of 50 degrees N have been measured over surprisingly short time periods of only one to a few days. Using long-term data from three intensively studied small subarctic lakes, we recommend that measurements of diffusive methane flux and ebullition should be made over at least 11 and 39days scattered throughout the ice-free season using depth-stratified sampling at 3 and 11 or more locations, respectively. We further show that low temporal and spatial resolutions are unlikely to cause overestimates. Therefore, we argue that most sites measured previously are likely underestimated in terms of emission potential. Avoiding these biases seen in much of the contemporary data is crucial to further constrain large-scale methane emissions from northern lakes and ponds. Funding Agencies|Swedish Research Council [2007-4547]; Nordic Center of Excellence DEFROST under Nordic Top-Level Research Initiative

Methyl bromide is the most important natural bromine contributor to stratospheric ozone depletion, yet there are still large uncertainties regarding quantification of its sources and sinks. The stable bromine isotope composition of CH(3)Br is potentially a powerful tool to apportion its sources and to study both its transport and its reactive fate. A novel compound-specific method to measure (81)Br/(79)Br isotope ratios in CH(3)Br using gas chromatography hyphenated with inductively coupled plasma multiple-collector mass spectrometry (GC/MCICPMS) was developed. Sample amounts of >40 ng could be measured with a precision of 0.1‰ (1σ, n = 3). The method results are reproducible over the long term as shown with 36 analyses acquired over 3 months, yielding a standard deviation (1σ) better than 0.4‰. This new method demonstrates for the first time Br isotope ratio determination in gaseous brominated samples. It is three orders of magnitude more sensitive than previously existing isotope ratio mass spectrometry methods for Br isotope determination of other organobromines, thus allowing applications towards ambient atmospheric samples.

Shawn C. Burdette and Brett F. Thornton examine hafnium’s emergence from ores containing a seemingly identical element to become both a chemical oddity and an essential material for producing nuclear energy.

Methyl chloride and methyl bromide (CH3Cl and CH3Br) are the largest natural sources of chlorine and bromine, respectively, to the stratosphere, where they contribute to ozone depletion. We report the anthropogenic production of CH3Cl and CH3Br during breadbaking, and suggest this production is an abiotic process involving the methyl ester functional groups in pectin and lignin structural polymers of plant cells. Wide variations in baking styles allow only rough estimates of this flux of methyl halides on a global basis. A simple model suggests that CH3Br emissions from breadbaking likely peaked circa 1990 at approximately 200tonnes per year (about 0.3% of industrial production), prior to restrictions on the dough conditioner potassium bromate. In contrast, CH3Cl emissions from breadbaking may be of similar magnitude as acknowledged present-day CH3Cl industrial emissions. Because the mechanisms involve functional groups and compounds widely found in plant materials, this type of methyl halide production may occur in other cooking techniques as well.

A century ago this month, Frederick Soddy described and named isotopes in the pages of Nature. Brett F. Thornton and Shawn C. Burdette discuss how chemists have viewed and used isotopes since then — either as chemically identical or chemically distinct species as the need required and technology allowed.