Radiocarbon Content Research Articles

Comparison of 14C Collected by Precipitation and Gas-Strip Methods for Dating Groundwater

AbstractDissolved inorganic carbon (DIC) in groundwater is used to estimate the residence time based on radiocarbon concentration. DIC is usually extracted by a gas-strip or precipitation (SrCO3 or BaCO3) method. In this study, the gas-strip and precipitation methods of DIC were applied to both artificially prepared NaHCO3 solutions and natural groundwater to estimate the certainty of the two methods for 14C dating. 14C values obtained by the gas-strip method for NaHCO3 solutions with distinct salinity, DIC, and 14C concentrations were close to the theoretically predicted 14C value based on the 14C value of NaHCO3 powder. Conversely, the 14C value obtained by the precipitation method always showed higher values than the predicted values. The difference in 14C value between the gas-strip and precipitation methods was assumed to be caused by the contamination of modern carbon in the NaOH solution used in the precipitation method. The contamination of modern carbon derived from the NaOH solution during precipitation was found to range from less than 1 mg/L to about 1 mg/L. The applicability of the precipitation method for groundwater should be considered carefully according to the DIC, 14C concentration of groundwater, and purpose of the study being conducted.

Contamination on AMS Sample Targets by Modern Carbon is Inevitable

AbstractAccelerator mass spectrometry (AMS) measurements of the radiocarbon content in very old samples are often challenging and carry large relative uncertainties due to possible contaminations acquired during the preparation and storage steps. In case of such old samples, the natural surrounding levels of 14C from gases in the atmosphere, which may well be the source of contamination among others, are 2–3 orders of magnitude higher than the samples themselves. Hence, serious efforts are taken during the preparation steps to have the samples pristine until measurements are performed. As samples often have to be temporarily stored until AMS measurements can be performed, storage conditions also become extremely crucial. Here we describe an assessment of this process of contamination in background AMS samples. Samples, both as pressed graphite (on AMS targets) and graphite powder, were stored in various storage conditions (CO2-spiked air) to investigate the extent of contamination. The experiments clearly show that the pressed targets are more vulnerable to contamination than the unpressed graphite. Experiments conducted with enriched CO2-spiked laboratory air also reveal that the contaminating carbon is not only limited to the target surface but also penetrates into the matrix. A combination of measurements on understanding the chemical nature of the graphitization product, combined with long-available knowledge on “adventitious carbon” from the surface science community, brought us to the conclusion that contamination is to a certain extent inevitable. However, it can be minimized, and should be dealt with by sputter-cleaning the samples individually before the actual measurement.

Seasonal Variations of Radiocarbon Content in Plant Leaves in a 14C-Depleted Area

The determination of radiocarbon content in biogenic samples such as tree leaves and short-lived plants is crucial when studying the anthropogenic impact on the ecosystem and for detecting any alteration in stable and radioactive CO 2 . A total of 76 samples of evergreen and deciduous tree leaves as well seasonal plants were collected in winter, spring, and summer. Sampling was carried out from rural villages located in Mount Lebanon Province, Lebanon. Based on the data obtained from a previous study carried out in autumn, which showed that the selected sites are characterized by depletion of 14 C caused by the releases of pollutants and CO 2 from a cement factory in the region, further investigation was carried out in the present work to determine possible significant seasonal variations in Δ 14 C values. Reference samples of identical species were collected in the same period from a clean zone. The conventional 14 C method was used to determine the carbon isotopic ratio. Δ 14 C data are compared to those obtained in autumn. 14 C concentration in the studied sites was significantly lower than in the clean area in all seasons. ANOVA tests showed that there is a significant seasonal variation for deciduous leaves and seasonal plants, while this difference was not significant in evergreen leaves. In addition, no significant variation was recognized for different species in the same season. DOI: 10.2458/azu_rc.57.18350

The nature of organic carbon in density-fractionated sediments in the Sacramento-San Joaquin River Delta (California)

Abstract. Rivers are the primary means by which sediments and carbon are transported from the terrestrial biosphere to the oceans but gaps remain in our understanding of carbon associations from source to sink. Bed sediments from the Sacramento-San Joaquin River Delta (CA) were fractionated according to density and analyzed for sediment mass distribution, elemental (C and N) composition, mineral surface area, and stable carbon and radiocarbon isotope compositions of organic carbon (OC) and fatty acids to evaluate the nature of organic carbon in river sediments. OC was unevenly distributed among density fractions. Mass and OC were in general concentrated in mesodensity (1.6–2.0 and 2.0–2.5 g cm−3) fractions, comprising 84.0 ± 1.3 % of total sediment mass and 80.8 ± 13.3 % of total OC (TOC). Low-density (< 1.6 g cm−3) material, although rich in OC (34.0 ± 2.0 % OC) due to woody debris, constituted only 17.3 ± 12.8 % of TOC. High-density (> 2.5 g cm−3) organic-poor, mineral-rich material made-up 13.7 ± 1.4 % of sediment mass and 2.0 ± 0.9 % of TOC. Stable carbon isotope compositions of sedimentary OC were relatively uniform across bulk and density fractions (δ13C −27.4 ± 0.5 ‰). Radiocarbon content varied from Δ14C values of −382 (radiocarbon age 3800 yr BP) to +94 ‰ (modern) indicating a mix of young and old OC. Fatty acids were used to further constrain the origins of sedimentary OC. Short-chain n-C14–n-C18 fatty acids of algal origin were depleted in 13C (δ13C −37.5 to −35.2 ‰) but were enriched in 14C (Δ14C > 0) compared to long-chain n-C24–n-C28 acids of vascular plant origins with higher δ13C (−33.0 to −31.0 ‰) but variable Δ14C values (−180 and 61 ‰). These data demonstrate the potentially complex source and age distributions found within river sediments and provide insights about sediment and organic matter supply to the Delta.

Dissolved organic carbon in the deep Southern Ocean: Local versus distant controls

AbstractThe global ocean contains a massive reservoir (662 ± 32 Pg C) of dissolved organic carbon (DOC), and its dynamics, particularly in the deepest zones, are only slowly being understood. DOC in the deep ocean is ubiquitously low in concentration (~35 to 48 µmol kg−1) and aged (4000 to 6000 years), persisting for multiple meridional overturning circulations. Deep waters relatively enriched in DOC form in the North Atlantic, migrate to the Southern Ocean to mix with waters from Antarctic shelves and the deep Pacific and Indian Oceans, in turn forming the voluminous waters of the Circumpolar Deep Water. Here we seek evidence for local (autochthonous) versus distant (allochthonous) processes in determining the distribution of DOC in the deep Southern Ocean. Prior analyses on DOC in the deep Southern Ocean have conflicted, describing both conservative and nonconservative traits: the deep DOC field has been reported as uniform in distribution, yet local inputs have been suggested as quantitatively important. We use multiple approaches (multiple linear regression, mass transport, and mass balance calculations) with data from Climate Variability and Predictability Repeat Hydrography sections to evaluate the system. We find that DOC concentrations in the deep Southern Ocean largely reflect the conservative mixing of the several deep waters entering the system from the north. Mass balance suggests that the relatively depleted DOC radiocarbon content in the deep Southern Ocean is a conserved property as well. These analyses advance our understanding of the controls on the DOC reservoir of the Southern Ocean.

Radiocarbon version of 11-year variations in the interplanetary magnetic field since 1250

It is known that the interplanetary magnetic field (IMF), which is controlled by solar activity, modulates the flux of galactic cosmic rays (GCRs). Because GCRs are the only source of the 14C isotope in the atmosphere before the era of atmospheric nuclear tests, the formation rate of this isotope in the atmosphere is one of the few reliable sources of information on solar activity before the initiation of regular telescopic observations. In this study, we solve the inverse problem for the equation of radiocarbon diffusion from the atmosphere into the ocean by calibrating the radiocarbon content in tree rings from 1510 to 1950. We obtain an approximation of 11-year IMF cycles represented by the IDV index from 1872 to 1950. The model extrapolation to the calibration curve for the Korean Peninsula over the time period from 1250 to 1650 makes it possible to calculate the sequence of minima of quasi-11-year cycles since 1250.

Possible contribution of surface temperature variation to the radiocarbon concentration in the Earth’s atmosphere

Data on the cosmogenic isotope (14C) concentration in the Earth’s atmosphere are widely used to reconstruct solar activity in past epochs. However, the concentration of this isotope in the atmosphere (Δ14C) and tree rings can also be affected by climatic factors. The possible effect of the variations in the Earth’s surface temperature on atmospheric 14C in the time interval from 1511 to 1954 is considered in the work. It was shown that the agreement between the Δ14C calculated curves and the experimental curve can be improved if the effect of temperature variations on (a) the radiocarbon exchange rate between the atmosphere and ocean and (b) atmospheric CO2 is taken into account. Further research trends are discussed.

Investigating the influence of regional climate and oceanography on marine radiocarbon reservoir ages in southwest New Zealand

The New Zealand fjords are located at a latitude where distinct oceanic and atmospheric fronts separate carbon reservoirs of varying residence time. The marine radiocarbon reservoir age in this region is likely to deviate from the global average reservoir age over space and time as frontal boundaries migrate north and south. Here we present new estimates of modern radiocarbon reservoir age using the radiocarbon content of bivalve shells collected live before 1950. Multiple measurements from hydrographically distinct sites support the use of a ΔR, defined as the regional offset between measured and modeled marine radiocarbon reservoir age, of 59 ± 35 years for the New Zealand fjords. We also assess the radiocarbon content of bulk surface sediments throughout the fjord region. Sediment with a higher proportion of marine organic carbon has relatively less radiocarbon than more terrestrial sediment, suggesting a short residence time of organic carbon on land before deposition in the fjords. Additionally, we constrain reservoir age variability throughout the Holocene using coeval terrestrial and marine macrofossils. Although our modern results suggest spatial consistency in ΔR throughout the fjords, large deviations from the global average marine radiocarbon reservoir age exist in the paleo record. We find four ancient ΔR values, extending back to ∼10.2 cal kyr BP, to be negative or near zero. A likely cause of younger radiocarbon reservoir ages at select intervals throughout the Holocene is the increased influence of the Southern Hemisphere westerly winds, which cause extreme precipitation in the region that delivers terrestrial carbon, enriched in radiocarbon, to fjord basins. However, bivalve depth habitat may also influence radiocarbon content due to a stratified water column containing distinct carbon pools. This work highlights the need for thorough assessment of local radiocarbon cycling in similar regions of dynamic ocean/atmosphere frontal zones, especially fjords and other semi-restricted estuaries.

Black carbon aerosol dynamics and isotopic composition in Alaska linked with boreal fire emissions and depth of burn in organic soils

AbstractBlack carbon (BC) aerosol emitted by boreal fires has the potential to accelerate losses of snow and ice in many areas of the Arctic, yet the importance of this source relative to fossil fuel BC emissions from lower latitudes remains uncertain. Here we present measurements of the isotopic composition of BC and organic carbon (OC) aerosols collected at two locations in interior Alaska during the summer of 2013, as part of NASA's Carbon in Arctic Reservoirs Vulnerability Experiment. We isolated BC from fine air particulate matter (PM2.5) and measured its radiocarbon (Δ14C) content with accelerator mass spectrometry. We show that fires were the dominant contributor to variability in carbonaceous aerosol mass in interior Alaska during the summer by comparing our measurements with satellite data, measurements from an aerosol network and predicted concentrations from a fire inventory coupled to an atmospheric transport model. The Δ14C of BC from boreal fires was 131 ± 52‰ in the year 2013 when the Δ14C of atmospheric CO2was 23 ± 3‰, corresponding to a mean fuel age of 20 years. Fire‐emitted OC had a similar Δ14C (99 ± 21‰) as BC, but during background (low fire) periods OC (45 to 51‰) was more positive than BC (−354 to −57‰). We also analyzed the carbon and nitrogen elemental and stable isotopic composition of the PM2.5. Fire‐emitted aerosol had an elevated carbon to nitrogen (C/N) ratio (29 ± 2) and δ15N (16 ± 4‰). Aerosol Δ14C and δ13C measurements were consistent with a mean depth of burning in organic soil horizons of 20 cm (and a range of 8 to 47 cm). Our measurements of fire‐emitted BC and PM2.5composition constrain the end‐member of boreal forest fire contributions to aerosol deposition in the Arctic and may ultimately reduce uncertainties related to the impact of a changing boreal fire regime on the climate system.

Multimolecular tracers of terrestrial carbon transfer across the pan‐Arctic: 14C characteristics of sedimentary carbon components and their environmental controls

AbstractDistinguishing the sources, ages, and fate of various terrestrial organic carbon (OC) pools mobilized from heterogeneous Arctic landscapes is key to assessing climatic impacts on the fluvial release of carbon from permafrost. Through molecular 14C measurements, including novel analyses of suberin‐ and/or cutin‐derived diacids (DAs) and hydroxy fatty acids (FAs), we compared the radiocarbon characteristics of a comprehensive suite of terrestrial markers (including plant wax lipids, cutin, suberin, lignin, and hydroxy phenols) in the sedimentary particles from nine major arctic and subarctic rivers in order to establish a benchmark assessment of the mobilization patterns of terrestrial OC pools across the pan‐Arctic. Terrestrial lipids, including suberin‐derived longer‐chain DAs (C24,26,28), plant wax FAs (C24,26,28), and n‐alkanes (C27,29,31), incorporated significant inputs of aged carbon, presumably from deeper soil horizons. Mobilization and translocation of these “old” terrestrial carbon components was dependent on nonlinear processes associated with permafrost distributions. By contrast, shorter‐chain (C16,18) DAs and lignin phenols (as well as hydroxy phenols in rivers outside eastern Eurasian Arctic) were much more enriched in 14C, suggesting incorporation of relatively young carbon supplied by runoff processes from recent vegetation debris and surface layers. Furthermore, the radiocarbon content of terrestrial markers is heavily influenced by specific OC sources and degradation status. Overall, multitracer molecular 14C analysis sheds new light on the mobilization of terrestrial OC from arctic watersheds. Our findings of distinct ages for various terrestrial carbon components may aid in elucidating fate of different terrestrial OC pools in the face of increasing arctic permafrost thaw.

Multiradionuclide evidence for the solar origin of the cosmic-ray events of ᴀᴅ 774/5 and 993/4.

The origin of two large peaks in the atmospheric radiocarbon (14C) concentration at AD 774/5 and 993/4 is still debated. There is consensus, however, that these features can only be explained by an increase in the atmospheric 14C production rate due to an extraterrestrial event. Here we provide evidence that these peaks were most likely produced by extreme solar events, based on several new annually resolved 10Be measurements from both Arctic and Antarctic ice cores. Using ice core 36Cl data in pair with 10Be, we further show that these solar events were characterized by a very hard energy spectrum with high fluxes of solar protons with energy above 100 MeV. These results imply that the larger of the two events (AD 774/5) was at least five times stronger than any instrumentally recorded solar event. Our findings highlight the importance of studying the possibility of severe solar energetic particle events.

Organic matter transfer in Lake Superior's food web: Insights from bulk and molecular stable isotope and radiocarbon analyses

A suite of isotopic methods were combined to provide a comprehensive investigation of organic matter transfer and consumer-resource links in a large lake food web. We applied compound specific isotope analysis (CSIA) of nitrogen within amino acids of organisms, a relatively new method and one not yet widely applied to large lake systems, to determine the trophic positions of several dominant species. Comparison of this CSIA trophic designation to those calculated by traditional bulk stable carbon and nitrogen isotope ratios, as well as gut content analyses, revealed this CSIA method to be the most representative of known trophic links in Lake Superior. Limnocalanus macrurus, an omnivorous copepod, was found to occupy a trophic position higher than would have been predicted based on gut analyses, and one full trophic position above primary consumer Daphnia. Radiocarbon analysis of bulk zooplankton and fish tissue was employed as a modern carbon tracer to elucidate the relative ages of carbon incorporated into, and propagated through, the food web. Comparison of animal tissue, non-living carbon pools (DOC, DIC), and POC radiocarbon content indicate the food web is supported predominately by newly synthesized autochthonous material. The uniquely depleted radiocarbon signature of the benthic amphipod Diporeia, attributed to consumption of aged sedimentary or allochthonous material, was not reflected in its known predators, indicating little overall incorporation of that aged carbon source into the pelagic food web. This multi-method isotopic investigation extends our understanding of food web structure and organic matter flow in this large lake.

Accuracy and precision of <sup>14</sup>C-based source apportionment of organic and elemental carbon in aerosols using the Swiss_4S protocol

Abstract. Aerosol source apportionment remains a critical challenge for understanding the transport and aging of aerosols, as well as for developing successful air pollution mitigation strategies. The contributions of fossil and non-fossil sources to organic carbon (OC) and elemental carbon (EC) in carbonaceous aerosols can be quantified by measuring the radiocarbon (14C) content of each carbon fraction. However, the use of 14C in studying OC and EC has been limited by technical challenges related to the physical separation of the two fractions and small sample sizes. There is no common procedure for OC/EC 14C analysis, and uncertainty studies have largely focused on the precision of yields. Here, we quantified the uncertainty in 14C measurement of aerosols associated with the isolation and analysis of each carbon fraction with the Swiss_4S thermal–optical analysis (TOA) protocol. We used an OC/EC analyzer (Sunset Laboratory Inc., OR, USA) coupled to a vacuum line to separate the two components. Each fraction was thermally desorbed and converted to carbon dioxide (CO2) in pure oxygen (O2). On average, 91 % of the evolving CO2 was then cryogenically trapped on the vacuum line, reduced to filamentous graphite, and measured for its 14C content via accelerator mass spectrometry (AMS). To test the accuracy of our setup, we quantified the total amount of extraneous carbon introduced during the TOA sample processing and graphitization as the sum of modern and fossil (14C-depleted) carbon introduced during the analysis of fossil reference materials (adipic acid for OC and coal for EC) and contemporary standards (oxalic acid for OC and rice char for EC) as a function of sample size. We further tested our methodology by analyzing five ambient airborne particulate matter (PM2.5) samples with a range of OC and EC concentrations and 14C contents in an interlaboratory comparison. The total modern and fossil carbon blanks of our setup were 0.8 ± 0.4 and 0.67 ± 0.34 μg C, respectively, based on multiple measurements of ultra-small samples. The extraction procedure (Swiss_4S protocol and cryo-trapping only) contributed 0.37 ± 0.18 μg of modern carbon and 0.13 ± 0.07 μg of fossil carbon to the total blank of our system, with consistent estimates obtained for the two laboratories. There was no difference in the background correction between the OC and EC fractions. Our setup allowed us to efficiently isolate and trap each carbon fraction with the Swiss_4S protocol and to perform 14C analysis of ultra-small OC and EC samples with high accuracy and low 14C blanks.

Intracavity OptoGalvanic Spectroscopy Not Suitable for Ambient Level Radiocarbon Detection

IntraCavity OptoGalvanic Spectroscopy as a radiocarbon detection technique was first reported by the Murnick group at Rutgers University, Newark, NJ, in 2008. This technique for radiocarbon detection was presented with tremendous potentials for applications in various fields of research. Significantly cheaper, this technique was portrayed as a possible complementary technique to the more expensive and complex accelerator mass spectrometry. Several groups around the world started developing this technique for various radiocarbon related applications. The IntraCavity OptoGalvanic Spectroscopy setup at the University of Groningen was constructed in 2012 in close collaboration with the Murnick group for exploring possible applications in the fields of radiocarbon dating and atmospheric monitoring. In this paper we describe a systematic evaluation of the IntraCavity OptoGalvanic Spectroscopy setup at Groningen for radiocarbon detection. Since the IntraCavity OptoGalvanic Spectroscopy setup was strictly planned for dating and atmospheric monitoring purposes, all the initial experiments were performed with CO2 samples containing contemporary levels and highly depleted levels of radiocarbon. Because of recurring failures in differentiating the two CO2 samples, with the radiocarbon concentration 3 orders of magnitude apart, CO2 samples containing elevated levels of radiocarbon were prepared in-house and experimented with. All results obtained thus far at Groningen are in sharp contrast to the results published by the Murnick group and rather support the results put forward by the Salehpour group at Uppsala University. From our extensive test work, we must conclude that the method is unsuited for ambient level radiocarbon measurements, and even highly enriched CO2 samples yield insignificant signal.

Sedimentation of particulate organic carbon on the Amundsen Shelf, Antarctica

We examined the recent history of sedimentary organic carbon (SOC) accumulation on the western Amundsen Shelf, to help characterize the biological carbon pump in the Amundsen Sea, Antarctica. Vertical sedimentary profiles (in the upper 21-cm) of SOC content, radio- and stable-carbon isotopes were obtained at four locations in the western Amundsen Sea: near the shelf break, inside the polynya near the Dotson Ice Shelf, and at both the periphery and the center of the Amundsen Sea polynya. Profiles were representative not only of various distances from the coast, but also of various summertime sea ice conditions and bottom depths. The SOC content (up to 1.1%) and the radiocarbon content were distinctly higher at the periphery and at the center of the polynya than at the other sites. The SOC and 14C contents were generally consistent with the spatial distribution of primary productivity in the surface water. A linear SOC accumulation rate of about 1.0gCm−2yr−1 was determined from the conventional 14C ages of bulk SOC below the surface mixed layer at the periphery and at the center of the polynya, for the time period of 3.1–4.7kyr before present (BP). This linear SOC accumulation rate was about 20 times greater than the rates determined at the two other sites for the period of 4.6–15.7kyr BP. Note that all values are for uncorrected 14C ages. At the center of the polynya, a sudden change in SOC accumulation rate was observed at about 16cm depth, corresponding to 4.7kyr BP, implying that changes (during this time period) in physical environments greatly affected primary production, SOC burial and/or supply of allochthonous particles to this site. The vertical distribution of 14C content in the sediments implies that aged organic matter, likely associated with resuspended sediments, was also being deposited inside the polynya, in addition to autochthonous biogenic particles. If our estimation of SOC accumulation is extrapolated to the western Amundsen Shelf between 110°W and 120°W, approximately 3×1010gCyr−1 is buried on the shelf, with ~90% of SOC accumulation occurring in the Amundsen Sea polynya.

<sup>14</sup>C in cropland soil of a long-term field trial – experimental variability and implications for estimating carbon turnover

Abstract. Because of their controlled nature, the presence of independent replicates, and their known management history, long-term field experiments are key to the understanding of factors controlling soil carbon. Together with isotope measurements, they provide profound insight into soil carbon dynamics. For soil radiocarbon, an important tracer for understanding these dynamics, experimental variability across replicates is usually not accounted for; hence, a relevant source of uncertainty for quantifying turnover rates is missing. Here, for the first time, radiocarbon measurements of five independent field replicates, and for different layers, of soil from the 66-year-old controlled field experiment ZOFE in Zurich, Switzerland, are used to address this issue. 14C variability was the same across three different treatments and for three different soil layers between the surface and 90 cm depths. On average, experimental variability in 14C content was 12 times the analytical error but still, on a relative basis, smaller than variability in soil carbon concentration. Despite a relative homogeneous variability across the field and along the soil profile, the curved nature of the relationship between radiocarbon content and modelled carbon mean residence time implies that the absolute error of calculated soil carbon turnover time increases with soil depth. In our field experiment findings on topsoil carbon turnover variability would, if applied to subsoil, tend to underweight turnover variability even if experimental variability in the subsoil isotope concentration is the same. Together, experimental variability in radiocarbon is an important component in an overall uncertainty assessment of soil carbon turnover.

The glacial mid‐depth radiocarbon bulge and its implications for the overturning circulation

AbstractPublished reconstructions of radiocarbon in the Atlantic sector of the Southern Ocean indicate that there is a mid‐depth maximum in radiocarbon age during the Last Glacial Maximum (LGM). This is in contrast to the modern ocean where intense mixing between water masses results in a relatively homogenous radiocarbon profile. Ferrari et al. (2014) suggested that the extended Antarctic sea ice cover during the LGM necessitated a shallower boundary between the upper and lower branches of the meridional overturning circulation. This shoaled boundary lay above major topographic features associated with strong diapycnal mixing, isolating dense southern sourced water in the lower branch of the overturning circulation. This isolation would have allowed radiocarbon to decay and thus provides a possible explanation for the mid‐depth radiocarbon age bulge. We test this hypothesis using an idealized, 2‐D, residual‐mean dynamical model of the global overturning circulation. Concentration distributions of a decaying tracer that is advected by the simulated overturning are compared to published radiocarbon data. We find that a 600 km (~5° of latitude) increase in sea ice extent shoals the boundary between the upper and lower branches of the overturning circulation at 45°S by 600 m and shoals the depth of North Atlantic Deep Water convection at 50°N by 2500 m. This change in circulation configuration alone decreases the radiocarbon content in the mid‐depth South Atlantic at 45°S by 40‰, even without an increase in surface radiocarbon age in the source region of deep waters during the LGM.

Influence of contemporary carbon originating from the 2003 Siberian forest fire on organic carbon in PM2.5 in Nagoya, Japan

In May 2003, high concentrations of organic carbon (OC) in PM2.5 were measured in Nagoya, a representative metropolitan area in Japan. To investigate the influence of possible forest fires on PM2.5 in Japan via long-range aerosol transport, the radiocarbon (14C) concentrations of PM2.5 samples from April 2003 to March 2004 were measured. 14C concentrations in total carbon (TC) from May to early June showed higher values than those in other periods. The OC/elemental carbon (EC) ratios from May to early June were also significantly higher than the ones in other periods. In addition, OC concentrations from May to early June were typically high. These results indicate that the abundant OC fraction from May to early June in Nagoya consisted predominantly of contemporary carbon. Furthermore, simulations of diffusion and transport of organic matter (OM) in East Asia showed that abundant OM originating from East Siberia spread over East Asia and Japan in May and early June. Backward air mass trajectories from this time frame indicate that the air mass in Nagoya likely first passed through East Siberia where fire events were prevalent. However, the backward trajectories showed that the air mass after early June did not originate mainly from Siberia, and correspondingly, the 14C and OC concentrations showed lower values than those from May to early June. Therefore, the authors conclude that contemporary carbon originating from the forest fire in East Siberia was transported to Nagoya, where it significantly contributed to the high observed concentrations of both OC and 14C.

Radiocarbon concentration in modern tree rings from Fukushima, Japan

A 30-year-old Japanese cedar (Cryptomeria japonica), collected from Iwaki, Fukushima in 2014, was analyzed for the long-lived radionuclide 14C. Values of Δ14C varied from 211.7‰ in 1984 to 16.9‰ in 2013. The temporal Δ14C variation can be described as an exponential decline, indistinguishable from the general Northern Hemisphere Zone 2 (NH Zone 2) values in the atmosphere, until at least 1994. Values of Δ14C for 1999 and 2004 are slightly depleted compared with NH Zone 2 values, while from 1999 to 2013 the data suggest a clear depletion with a 2–8 ppmV additional CO2 contribution from a 14C-free (i.e. fossil carbon) source. This change coincides with local traffic increases since two nearby expressways were opened in the 1990's. In addition, the small but visible 14C pulse observed in the 2011 tree-ring might be caused by release from the damaged reactors during the Fukushima nuclear accident.

Sinking particle flux in the sea ice zone of the Amundsen Shelf, Antarctica

We have examined the flux, biogenic composition, and isotopic values of sinking particles collected by a time-series sediment trap deployed in the sea ice zone (SIZ) of the Amundsen Sea from January 2011 for 1 year. The major portion of the particle flux occurred during the austral summer in January and February when sea ice concentration was reduced to <60%. Biogenic components, dominated by opal (~78% of the biogenic components), accounted for over 75% of particle flux during this high-flux period. The dominant source of sinking particles shifted from diatoms to soft-tissued organisms, evidenced by high particulate organic carbon (POC) content (>30%) and a low bio-Si/POC ratio (<0.5) during the austral winter. CaCO3 content and its contribution to total particle flux was low (~6%) throughout the study period. Aged POC likely supplied from sediment resuspension accounted for a considerable fraction only from October to December, which was evidenced by a low radiocarbon content and relatively high (30–50%) content of the non-biogenic components. When compared with POC flux inside the Amundsen Sea polynya obtained by the US Amundsen Sea Polynya International Research Expedition (ASPIRE), the POC flux integrated over the austral summer in the SIZ was virtually identical, although the maximum POC flux was approximately half that inside the Amundsen Sea polynya. This comparatively high POC flux integrated over the austral summer in the SIZ may be caused by phytoplankton blooms persisting over a longer periods and more efficient export of organic matter potentially owing to the diatom-dominant plankton community. If this observation is a general phenomenon on the Amundsen Shelf, the role of the SIZ, compared with the polynyas, need to be examined more carefully when trying to characterize the POC export in this region.