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Atmospheric aerosols strongly influence the global climate by their light absorption (e.g., black carbon, BC, brown carbon, BrC) and scattering (e.g., sulfate) properties. This study presents simultaneous measurements of ambient aerosol light absorption properties and chemical composition from three large-footprint South Asian receptor sites during the South Asian Pollution Experiment (SAPOEX) in December-March 2018. The BC mass absorption cross-section (BC-MAC678) values increased from 3.5 ± 1.3 at the Bhola Climate Observatory-Bangladesh (i.e., located at exit outflow of Indo-Gangetic Plain) to 6.4 ± 1.3 at the two regional receptor observatories at Maldives Climate Observatory-Hanimaadhoo (MCOH) and Maldives Climate Observatory-Gan (MCOG). This likely reflects a coating-enhancement effect due to ageing of the aerosols during long-range transport. At the same time, the BrC-MAC365 decreased by a factor of three from the IGP exit to the equatorial Indian Ocean, likely due to photochemical bleaching of organic chromophores. The high chlorine-to-sodium ratio at the near-source-region BCOB suggests a significant contribution of chorine from anthropogenic activities. This particulate Cl- has the potential to convert into Cl-radicals that can affect the oxidation capacity of the polluted air. Moreover, Cl- is shown to be near-fully consumed during the long-range transport. The results of this synoptic study over the large South Asian scale have significance for understanding the ageing effect of the optical and chemical properties of aerosols as the pollution from the Indo-Gangetic Plain disperses over regional scales. [ABSTRACT FROM AUTHOR]

Nitrous oxide (N2O) is a strong greenhouse gas and stratospheric ozone‐depleting substance. Around 20% of global emissions stem from the ocean, but current estimates and future projections are uncertain due to poor spatial coverage over large areas and limited understanding of drivers of N2O dynamics. Here, we focus on the extensive and particularly data‐lean Arctic Ocean shelves north of Siberia that experience rapid warming and increasing input of land‐derived nitrogen with permafrost thaw. We combine water column N2O measurements from two expeditions with on‐board incubation of intact sediment cores to assess N2O dynamics and the impact of land‐derived nitrogen. Elevated nitrogen concentrations in water column and sediments were observed near large river mouths. Concentrations of N2O were only weakly correlated with dissolved nitrogen and turbidity, reflecting particulate matter from rivers and coastal erosion, and correlations varied between river plumes. Surface water N2O concentrations were on average close to equilibrium with the atmosphere, but varied widely (N2O saturation 38%–180%), indicating strong local N2O sources and sinks. Water column N2O profiles and low sediment‐water N2O fluxes do not support strong sedimentary sources or sinks. We suggest that N2O dynamics in the region are influenced by water column N2O consumption under aerobic conditions or in anoxic microsites of particles, and possibly also by water column N2O production. Changes in biogeochemical and physical conditions will likely alter N2O dynamics in the Siberian Arctic Ocean over the coming decades, in addition to reduced N2O solubility in a warmer ocean. Plain Language Summary: Nitrous oxide (N2O) is a strong greenhouse gas and can reduce the stratospheric ozone layer. Around 20% of global N2O emissions come from the ocean. These estimates are uncertain due to scarce data from large areas and a limited understanding of controls on N2O production and consumption. Here, we focus on the shallow but large continental shelves of the Arctic Ocean north of Siberia. This area is rapidly warming, and receives land‐derived nitrogen from rivers and coastal erosion that is expected to increase with permafrost thaw. We analyzed N2O concentrations in the water column during two expeditions, and performed incubations with intact sediment cores to measure N2O release from sediment to water. Our data show that concentrations of dissolved nitrogen in the water and of total nitrogen in sediments increase toward large river mouths. Concentrations of N2O were weakly correlated with a range of parameters including dissolved inorganic nitrogen and turbidity, with high variability among river plumes. On average, water‐air N2O fluxes were low, but strong N2O sources and sinks were observed locally. An increase in water temperature could substantially reduce N2O solubility in the ocean water, and add to biogeochemical and physical changes that could alter N2O production itself. Key Points: We studied N2O dynamics on the vast Siberian Arctic Ocean shelves that experience strong warming and nitrogen input from land permafrostN2O was variably influenced by dissolved nitrogen and turbidity from land, and likely consumed in the water columnSurface water N2O was on average in equilibrium with the atmosphere, but strong local sources and sinks were observed [ABSTRACT FROM AUTHOR]

A method has been developed for the direct determination of the stable chlorine isotope composition ([delta][sup.37]Cl) of organochlorines that eliminates sample preparation, achieves precision comparable to earlier techniques while improving the sensitivity, and makes use of benchtop gas chromatography--quadrupole mass spectrometry instruments (GCqMS). The method is based on the use of multiple injections (n = 8-10) of the sample, bracketed by a molecularly identical isotopic standard with known [delta][sup.37]Cl, determined using off-line thermal ionization mass spectrometry (TIMS). Mass traces of two isotopologues differing by one chlorine isotope were used to calculate [delta][sup.37]Cl values. Optimization of mass spectrometry and peak integration parameters as well as method validation was achieved using tetrachloroethene (PCE), p,p'-dichlorodiphenyl-trichloroethane (DDT), and pentachlorophenol (PCP), spanning a [delta][sup.37]Cl range of -5.5 to +3.2%0 vs SMOC. Injecting 1.6-1100 pmol resulted in standard deviations (1[sigma]) of 0.6-1.3[per thousand], and the [delta][sup.37]Cl results agreed with values independently measured with TIMS. The method was tested by determining the Rayleigh fractionation during evaporation of pure liquid PCE, resulting in a chlorine isotopic enrichment factor of [[epsilon].sub.Cl] = -1.1 [+ or -] 0.4[per thousand]%0. Furthermore, position-specific [delta][sup.37]Cl analysis based on analysis of DDT mass fragments was evaluated. The GCqMS-[delta][sup.37]Cl method offers a simplified yet sensitive approach for compound-specific chlorine isotope analysis. 10.1021/ac902445f

Improved sensitivity in the analysis of stable chlorine isotopes of organochlorines ([[delta].sup.37]C1-OC1) has been established using sealed tube combustion in conjunction with thermal ionization mass spectrometry (TIMS). TIMS of chlorine isotopes was performed on

According to ecological theory, two species cannot occupy the same niche. Using nitrogen isotope analyses (δ15N) of amino acids, we tested the extent to which two sympatric deposit‐feeding amphipods, Monoporeia affinis and Pontoporeia femorata, partition their trophic resources. We found that trophic position (TP) and resynthesis index (∑V; a proxy for degradation status of ingested material prior to assimilation by the consumer) differ between species. The surface‐feeding M. affinis had higher TP and intermediate ∑V, both pointing to a large contribution of metazoans in its diet. P. femorata, which feeds in the subsurface layers, had lower TP and a bimodal distribution of the ∑V values, supporting previous experimental evidence of a larger feeding niche. We also evaluated whether TP and ∑V values have consequences for amphipod fecundity and embryo viability and found that embryo viability in M. affinis was negatively linked to TP. Our results indicate that the amino acid‐δ15N data paired with information about reproductive status are useful for detecting differences in the trophic ecology of sympatric amphipods. [ABSTRACT FROM AUTHOR]

Pleistocene ice complex permafrost deposits contain roughly a quarter of the organic carbon (OC) stored in permafrost (PF) terrain. When permafrost thaws, its OC is remobilized into the (aquatic) environment where it is available for degradation, transport or burial. Aquatic or coastal environments contain sedimentary reservoirs that can serve as archives of past climatic change. As permafrost thaw is increasing throughout the Arctic, these reservoirs are important locations to assess the fate of remobilized permafrost OC. We here present compound-specific deuterium (δ2H) analysis on leaf waxes as a tool to distinguish between OC released from thawing Pleistocene permafrost (ice complex deposits; ICD) and from thawing Holocene permafrost (from near-surface soils). Bulk geochemistry (%OC; δ13C; %total nitrogen, TN) was analyzed as well as the concentrations and δ2H signatures of long-chain n-alkanes (C21 to C33) and mid-to long-chain n-alkanoic acids (C16 to C30) extracted from both ICD-PF samples (n = 9) and modern vegetation and Ohorizon (topsoil-PF) samples (n = 9) from across the northeast Siberian Arctic. Results show that these topsoil-PF samples have higher %OC, higher OC= TN values and more depleted δ13C-OC values than ICD-PF samples, suggesting that these former samples trace a fresher soil and/or vegetation source. Whereas the two investigated sources differ on the bulk geochemical level, they are, however, virtually indistinguishable when using leaf wax concentrations and ratios. However, on the molecular isotope level, leaf wax biomarker δ2H values are statistically different between topsoil PF and ICD PF. For example, the mean δ2H value of C29 n-alkane was -246±13% (mean ± SD) for topsoil PF and -280±12% for ICD PF. With a dynamic isotopic range (difference between two sources) of 34 to 50 %; the isotopic fingerprints of individual, abundant, biomarker molecules from leaf waxes can thus serve as endmembers to distinguish between these two sources. We tested this molecular δ2H tracer along with another source-distinguishing approach, dual-carbon (δ13C-Δ14C) isotope composition of bulk OC, for a surface sediment transect in the Laptev Sea. Results show that general offshore patterns along the shelf-slope transect are similar, but the source apportionment between the approaches vary, which may highlight the advantages of either. This study indicates that the application of δ2H leaf wax values has potential to serve as a complementary quantitative measure of the source and differential fate of OC thawed out from different permafrost compartments. [ABSTRACT FROM AUTHOR]

Rationale The environmental occurrence of chlorinated acetic acids (CAAs) has been extensively studied, but the sources and transport are still not yet fully understood. A promising approach for source apportionment and process studies is the isotopic characterization of target compounds. We present the first on-line stable chlorine isotope analysis of CAAs by use of gas chromatography/quadrupole mass spectrometry (GC/qMS). Methods Following approved procedures for concentration analysis, CAAs extracted into MTBE were methylated to GC-amenable methyl esters (mCAAs). These mCAAs were then analyzed by GC/qMS for their stable chlorine isotope composition using a sample/standard-bracketing approach (CAA standards in the range δ37Cl −6.3 to −0.2 ‰, Standard Mean Ocean Chloride). Results Cross-calibration of the herein presented method with off-line reference methods (thermal ionization and continuous-flow GC isotope ratio mass spectrometry; TI-MS and CF-GC/IRMS, respectively) shows good agreement between the methods (regression slope for GC/qMS vs reference method data sets: 0.92 ± 0.29). Sample amounts as small as 10 pmol Cl can herewith be analyzed with a precision of 0.1 to 0.4 ‰. Conclusions This method should be useful for environmental studies of CAAs at ambient concentrations in precipitations (<0.06 to 100 nmol L-1), surface waters (<0.2 to 5 nmol L-1) and soil (<0.6 to 2000 nmol kg-1 dry soil) where conventional off-line methods cannot be applied. Copyright © 2015 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

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 contributes to ozone loss processes. Studies of stable isotope composition may reduce uncertainties in the atmospheric CH3Br budget, but require well-constrained isotope fingerprints of the source end members. Here we report the first measurements of stable bromine isotopes (δ81Br) in CH3Br from abiotic plant emissions. Incubations of both KBr-fortified pectin, a ubiquitous cell-stabilizing macromolecule, and of a natural halophyte (Salicornia fruticosa), yielded an enrichment factor (ε) of −2.00±0.23‰ (1σ, n =8) for pectin and −1.82±0.02‰ (1σ, n =4) for Salicornia (the relative amount of the heavier 81Br was decreased in CH3Br compared to the substrate salt). For short incubations, and up to 10% consumption of the salt substrate, this isotope effect was similar for temperatures from 30 up to 300°C. For longer incubations of up to 90h at 180°C the δ81Br values increased from −2‰ to 0‰ for pectin and to −1‰ for Salicornia. These δ81Br source signatures of CH3Br formation from plant matter combine with similar data for carbon isotopes to facilitate multidimensional isotope diagnostics of the CH3Br budget. [ABSTRACT FROM AUTHOR]

A system was developed for collecting from the ambient atmosphere the methyl halides CH3Cl and CH3Br in quantities sufficient for chlorine and bromine isotope analysis. The construction and operation of the novel cryogenic collection system (cryosampler) and sample purification system developed for this task are described. This study demonstrates the capability of the cryosampler by quantifying the CH3Cl and CH3Br collected from atmospheric samples and the nonfractionating bromine isotope fingerprint of CH3Br from synthetic air samples of controlled composition. An optimized cryosampler operation time of 4 h at a flow rate of 15 L min−1 is applied to yield the nearly 40 ng required for subsequent δ81Br-CH3Br analyses. The sample purification system is designed around a packed column gas chromatography-quadropole-mass spectrometry (GCqMS) system with three additional cryotraps and backflushing capacity. The system's suitability was tested by observing both the mass recovery and the lack of Δ81Br isotope fractionation induced during sample purification under varying flow rates and loading scenarios. To demonstrate that the entire system samples and dependably delivers CH3Br to the isotope analysis system without inducing isotope fractionation, diluted synthetic air mixtures prepared from standard gases were processed through the entire system, yielding a Δ81Br-CH3Br of +0.03‰ ± 0.10‰ relative to their starting composition. Finally, the combined cryosampler-purification and analysis system was applied to demonstrate the first-ever δ81Br-CH3Br in the ambient atmosphere with two samples collected in the autumn of 2011, yielding −0.08‰ ± 0.43‰ and +1.75‰ ± 0.13‰ versus standard mean ocean bromide for samples collected at a suburban Stockholm, Sweden, site. [ABSTRACT FROM AUTHOR]

Tropospheric methyl bromide (CH3Br) is the largest source of bromine to the stratosphere and plays an important role in ozone depletion. Here, the first stable bromine isotope composition (δ81Br) of atmospheric CH3Br is presented. The δ81Br of higher concentration Stockholm samples and free air subarctic Abisko samples suggest a source/background value of −0.04±0.28‰ ranging up to +1.75±0.12‰. The Stockholm δ81Br versus concentration relationship corresponds to an apparent isotope enrichment factor of −4.7±3.7‰, representing the combined reaction sink. This study demonstrates the scientific potential of atmospheric δ81Br measurements, which in the future may be combined with other isotope systems in a top-down inverse approach to further understand key source and sink processes of methyl bromide. [ABSTRACT FROM AUTHOR]

Compound-specific chlorine isotope analysis (CSIA–Cl) is promising as a novel and powerful method for monitoring in situ degradation of organochlorines in the environment and for source fingerprinting purposes. In order to apply CSIA–Cl in field studies of polychlorinated biphenyls (PCBs), the chlorine isotopic composition (δ37Cl) of individual PCB congeners in source materials must be known. In the present study, we determined δ37Cl of 18 congeners isolated from three widely produced technical mixtures. All congeners provided δ37Cl ranging between −1.9‰ and −3.5‰. Although the comparable products Aroclor 1242 (−2.0‰ to −2.5‰) and Clophen A30 (−1.9‰ to −3.0‰) were synthesized by different industries, they provided similar δ37Cl for the same type of congeners. On the contrary, the more chlorinated congeners present in Aroclor 1254 (−2.1 to −3.5‰) were more 37Cl depleted compared to Aroclor 1242 manufactured by the same company. Overall, δ37Cl of PCB congeners decreased by −0.26 ‰ for each additional chlorine atom. [Copyright &y& Elsevier]

Compound-specific chlorine-isotope analysis (CSIA-Cl) of 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane (p,p′-DDT) and 1,1-dichloro-2,2-bis(p-chlorophenyl)ethene (p,p′-DDE) in blubber from Baltic Grey seal (Halichoerus grypus) was performed in order to investigate if a kinetic isotope effect (KIE) could be observed concomitant to environmental degradation of DDT. The δ37Cl of p,p′-DDT and p,p′-DDE were −0.69±0.21‰ and −2.98±0.57‰ (1σ, n =3), respectively. Both samples were enriched relative to the hypothesized initial isotope composition (−4.34‰), thus indicating a composite KIE associated with the degradation mechanisms pertaining to DDT. An isotope fractionation factor for degradation of dichloromethane, from the literature, was adapted and modified for use in the calculation of DDT degradation. A subsequent simplified Rayleigh distillation model of the DDT chlorine-isotope composition yielded an estimated fraction (f) of 7±2% of released DDT presently remaining as undegraded compound in the environment. The consistency between the result of the Rayleigh model (f ∼7%) and the use of the DDT/(DDT+DDE) ratio as a measure of DDT degradation (∼10% undegraded DDT) suggests that the KIE of DDT degradation may be significant, and that the novel approach of CSIA-Cl may be a valuable tool for degradation/persistence studies of lipophilic organochlorines in the environment. [Copyright &y& Elsevier]

Polychlorinated dibenzo-p-dioxins (PCDDs) of high concentrations in a ball clay deposit from the Mississippi Embayment were found to be consistent with a natural abiotic and non-pyrogenic origin by investigation with bulk radiocarbon analysis, compound-specific chlorine isotope analysis (CSIA-δ37Cl) of octachlorodibenzo-p-dioxin (OCDD), and black carbon (BC) analysis. The conventional radiocarbon date of total organic carbon from a depth of approximately 10 m in three parallel cores ranged from 14 700 years to >48 000 years, indicating that the strata with elevated levels of PCDDs have remained isolated from recent anthropogenic input in these >40 Ma old clay sediments. The CSIA-δ37Cl of OCDD yielded a δ37Cl of -0.2‰, which is significantly higher than the postulated range for biotic chlorination by chloroperoxidase enzymes, -11 to -10‰, and falls within the known range for abiotic organochlorines, -6 to +3‰. The absence of correlations between concentrations of PCDDs and corresponding pyrogenic black carbon (BC), together with estimations of BC sorptive loadings and the absence of polychlorinated dibenzofurans (PCDFs), suggest that vegetation fires did not form these ball-clay PCDDs. Results from this study indicate that the high levels of the toxic and carcinogenic PCDDs found in kaolinite-bearing clays may result from natural abiotic formation via in situ surface-promoted reactions on the clay mineral, including a so-far unknown organic precursor, rather than being the result of anthropogenic contamination. [ABSTRACT FROM AUTHOR]

Black carbon (BC) aerosols affect climate, especially in high aerosol loading regions such as South Asia. A key uncertainty for the climate effects of BC is the evolution of light‐absorbing properties in the atmosphere. Here, we present a year‐round comparison of the mass absorption cross section (MAC; 678 nm) of BC in air (PM10) and rain, for samples collected at the Maldives Climate Observatory at Hanimaadhoo. We develop a filter‐loading correction scheme for estimating BC absorption on filters used in high‐volume samplers. The year‐round average MAC678 of BC in the rain is almost twice (13.3 ± 4.2 m2/g) compared to the PM10 aerosol (7.2 ± 2.6 m2/g). A possible explanation is the elevated ratio of organic carbon (OC) to BC observed in rain particulate matter (9.4 ± 6.3) compared to in the aerosols (OC/BC 2.6 ± 1.4 and water‐insoluble organic carbon/BC 1.2 ± 0.8), indicating a coating‐enhancement effect. In addition to BC, we also investigated the MAC365 of water‐soluble brown carbon in PM10 (0.4 ± 0.4 m2/g, at 365 nm). In contrast to BC, MAC365brown carbon relates to air mass history, showing higher values for samples from air originating over the South Asian landmass. Furthermore, calculated washout ratios are much lower for BC compared to OC and inorganic ions such as sulfate, implying a longer atmospheric lifetime for BC. The wet deposition flux for BC during the high loading winter was 3 times higher than during the wet summer, despite much less precipitation in the winter. Key Points: Year‐round black carbon mass absorption cross sections were simultaneously constrained for rainwater and aerosolsThe mass absorption cross section of black carbon in rainwater was twice as large as in PM10 aerosolsThe washout ratio for black carbon is an order of magnitude lower than, for example, organic and sulfate, suggesting greater atmospheric longevity [ABSTRACT FROM AUTHOR]

Methyl chloride and methyl bromide (CH 3 Cl and CH 3 Br) 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 CH 3 Cl and CH 3 Br 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 CH 3 Br emissions from breadbaking likely peaked circa 1990 at approximately 200 tonnes per year (about 0.3% of industrial production), prior to restrictions on the dough conditioner potassium bromate. In contrast, CH 3 Cl emissions from breadbaking may be of similar magnitude as acknowledged present-day CH 3 Cl 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. [ABSTRACT FROM AUTHOR]

A key challenge in climate change research is apportioning the greenhouse gas methane (CH 4 ) between various natural and anthropogenic sources. Isotopic source fingerprinting of CH 4 releases, particularly with radiocarbon analysis, is a promising approach. Here, we establish an analytical protocol for preparing CH 4 from seawater and other aqueous matrices for high-precision natural abundance radiocarbon measurement. Methane is stripped from water in the optionally field-operated system (STRIPS), followed by shore-based purification and conversion to carbon dioxide (CO 2 ) in the CH 4 Isotope Preparation System (CHIPS) to allow Accelerator Mass Spectrometry analysis. The blank (±1σ) of the combined STRIPS and CHIPS is low (0.67 ± 0.12 μg C), allowing natural sample sizes down to 10 μg C-CH 4 (i.e., 30 L samples of 40 nM CH 4 ). The full-system yield is >90% for both CH 4 -spiked seawater and ambient samples from CH 4 hotspots in the Baltic Sea and the Arctic Ocean. Furthermore, the radiocarbon isotope signal of CH 4 remains constant through the multistage processing in the STRIPS and the CHIPS. The developed method thus allows for in-field sampling and sample size reduction followed by precise and CH 4 -specific radiocarbon analysis. This enables powerful source apportionment of CH 4 emitted from aquatic systems from the tropics to the polar regions.

South Asian air is among the most polluted in the world, causing premature death of millions and asserting a strong perturbation of the regional climate. A central component is carbon monoxide (CO), which is a key modulator of the oxidizing capacity of the atmosphere and a potent indirect greenhouse gas. While CO concentrations are declining elsewhere, South Asia exhibits an increasing trend for unresolved reasons. In this paper, we use dual-isotope (δ 13 C and δ 18 O) fingerprinting of CO intercepted in the South Asian outflow to constrain the relative contributions from primary and secondary CO sources. Results show that combustion-derived primary sources dominate the wintertime continental CO fingerprint ( f primary ∼ 79 ± 4%), significantly higher than the global estimate ( f primary ∼ 55 ± 5%). Satellite-based inventory estimates match isotope-constrained f primary -CO, suggesting observational convergence in source characterization and a prospect for model-observation reconciliation. This "ground-truthing" emphasizes the pressing need to mitigate incomplete combustion activities for climate/air quality benefits in South Asia.

Light-absorbing organic aerosols, known as brown carbon (BrC), counteract the overall cooling effect of aerosols on Earth's climate. The spatial and temporal dynamics of their light-absorbing properties are poorly constrained and unaccounted for in climate models, because of limited ambient observations. We combine carbon isotope forensics (δ 13 C) with measurements of light absorption in a conceptual aging model to constrain the loss of light absorptivity (i.e., bleaching) of water-soluble BrC (WS-BrC) aerosols in one of the world's largest BrC emission regions-South Asia. On this regional scale, we find that atmospheric photochemical oxidation reduces the light absorption of WS-BrC by ~84% during transport over 6000 km in the Indo-Gangetic Plain, with an ambient first-order bleaching rate of 0.20 ± 0.05 day -1 during over-ocean transit across Bay of Bengal to an Indian Ocean receptor site. This study facilitates dynamic parameterization of WS-BrC absorption properties, thereby constraining BrC climate impact over South Asia.

Wintertime East Asia is plagued by severe haze episodes, characterized by large contributions of carbonaceous aerosols. However, the sources and atmospheric transformations of these major components are poorly constrained, hindering development of efficient mitigation strategies and detailed modelling of effects. Here we present dual carbon isotope (δ 13 C and Δ 14 C) signatures for black carbon (BC), organic carbon (OC) and water-soluble organic carbon (WSOC) aerosols collected in urban (Beijing and BC for Shanghai) and regional receptors (e.g., Korea Climate Observatory at Gosan) during January 2014. Fossil sources (>50%) dominate BC at all sites with most stemming from coal combustion, except for Shanghai, where liquid fossil source is largest. During source-to-receptor transport, the δ 13 C fingerprint becomes enriched for WSOC but depleted for water-insoluble OC (WIOC). This reveals that the atmospheric processing of these two major pools are fundamentally different. The photochemical aging (e.g., photodissociation, photooxidation) during formation and transport can release CO 2 /CO or short-chain VOCs with lighter carbon, whereas the remaining WSOC becomes increasingly enriched in δ 13 C. On the other hand, several processes, e.g., secondary formation, rearrangement reaction in the particle phase, and photooxidation can influence WIOC. Taken together, this study highlights high fossil contributions for all carbonaceous aerosol sub-compartments in East Asia, and suggests different transformation pathways for different classes of carbonaceous aerosols.

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., (Copyright © 2011 John Wiley & Sons, Ltd.)