14C Content Research Articles

Improving the method for calculating carbon emissions from waste incineration: confirmed with carbon-14 testing of flue gas

An improved method was developed to calculate direct emissions from seven municipal solid waste incineration plants by adjusting the physical compositions of waste by invoking the proportion of co-incinerated waste and the bottom ash yield. The fossil carbon fractions of the waste components were determined by carbon-14 (14C) testing. Based on the improved method, direct emissions were in the range of 222–610 kg CO2-eq/t waste, corresponding to reductions of 3.4–221 kg CO2-eq/t waste compared with the method without waste composition adjustment. The 14C contents of the flue gas before and after gas cleaning were tested to validate the improved method, and indicated fossil CO2 emissions of 249–446 and 233–405 kg CO2-eq/t waste, respectively. The direct emissions obtained by the improved method were closer to the results of 14C testing, due to more accurate estimations of the actual waste composition. The method was further combined with a life cycle analysis of the waste incineration process, obtaining total carbon emissions in the range from –33.2 to 483 kg CO2-eq/t waste. The findings provide a new means of accurately calculating carbon emissions from waste incineration.Graphical

Bound phenolics extracts of jujube peel relieve cadmium-induced toxicity by reducing lipid accumulation of Caenorhabditis elegans.

To investigate the effect of bound phenolics extracts (BPEs) of jujube peel on relieving cadmium (Cd)-induced toxicity and its mechanism, the behavioral deficits, lipid accumulation, and fatty acid synthesis-related gene expression in Caenorhabditis elegans in Cd exposure group and BPEs improvement groups were determined and compared. The results showed that BPEs significantly improved Cd-induced behavioral deficits in C. elegans, and no significant differences could be found in low-dose (12.5µg/mL) and high-dose (100µg/mL) BPEs improvement groups. The treatment of BPEs effectively improved intestinal injury and lipofuscin and lipid accumulation. Especially, oil red O staining intensity in C. elegans treated with BPEs at 50µg/mL was reduced by 12.60%. BPEs significantly controlled the increase in content of C16:0, C16:1, C18:0, C18:1, and C18:2 induced by Cd by regulating the lipid accumulation in Escherichia coli OP50. Cd exposure induced lipid accumulation in C. elegans by upregulating oleic acid synthesis-related gene expression in E. coli OP50. Furthermore, BPEs treatment significantly downregulated the fatty acid synthesis-related gene expression in C. elegans and E. coli OP50. This research could reveal the mechanism of BPEs of jujube peel in relieving Cd-induced toxicity and provide a theoretical basis for the development of functional foods rich in polyphenols. PRACTICAL APPLICATION: Jujube peel, a by-product of jujube processing, is usually discarded due to its coarse texture. However, jujube peel has been proven to possess abundant polyphenols, polysaccharides, and cyclic adenosine phosphate. In addition, in our previous research, bound phenolics extracts (BPEs) of jujube peel were found to perform better in lowering lipid accumulation than that of free phenolics extracts. This study further investigate the effect of BPEs of jujube peel on relieving Cd-induced toxicity and its mechanism on the base of our previous research. It could realize the comprehensive utilization of by-products of jujube processing.

Feedbacks From Young Permafrost Carbon Remobilization to the Deglacial Methane Rise

AbstractThe abrupt warming events punctuating the Termination 1 (about 11.7–18 ka Before Present, BP) were marked by sharp rises in the concentration of atmospheric methane (CH4). The role of permafrost organic carbon (OC) in these rises is still debated, with studies based on top‐down measurements of radiocarbon (14C) content of CH4 trapped in ice cores suggesting minimum contributions from old and strongly 14C‐depleted permafrost OC. However, organic matter from permafrost can exhibit a continuum of 14C ages (contemporaneous to >50 ky). Here, we investigate the large‐scale permafrost remobilization at the Younger Dryas‐Preboreal transition (ca. 11.6 ka BP) using the sedimentary record deposited at the Lena River paleo‐outlet (Arctic Ocean) to reflect permafrost destabilization in this vast drainage basin. Terrestrial OC was isolated from sediments and characterized geochemically measuring δ13C, Δ14C, and lignin phenol molecular fossils. Results indicate massive remobilization of relatively young (about 2,600 years) permafrost OC from inland Siberia after abrupt warming triggered severe active layer deepening. Methane emissions from this young fraction of permafrost OC contributed to the deglacial CH4 rise. This study stresses that underestimating permafrost complexities may affect our comprehension of the deglacial permafrost OC‐climate feedback and helps understand how modern permafrost systems may react to rapid warming events, including enhanced CH4 emissions that would amplify anthropogenic climate change.

ORIGIN AND AGE OF CARBON IN THE CELLULOSE OF MID-LATITUDE TREE RINGS

ABSTRACT Cellulose of tree rings is often assumed to be predominantly formed by direct assimilation of CO2 by photosynthesis and consequently can be used to reconstruct past atmospheric 14C concentrations at annual resolution. Yet little is known about the extent and the age of stored carbon from previous years used in addition to the direct assimilation in tree rings. Here, we studied 14C in earlywood and latewood cellulose of four different species (oak, pine, larch and spruce), which are commonly used for radiocarbon calibration and dating. These trees were still growing during the radiocarbon bomb peak period (1958–1972). We compared cellulose 14C measured in tree-ring subdivisions with the atmospheric 14C corresponding to the time of ring formation. We observed that cellulose 14C carried up to about 50% of the atmospheric 14C signal from the previous 1–2 years only in the earlywood of oak, whereas in conifers it was up to 20% in the earlywood and in the case of spruce also in the latewood. The bias in using the full ring of trees growing in a temperate oceanic climate to estimate atmospheric 14C concentration might be minimal considering that earlywood has a low mass contribution and that the variability in atmospheric 14C over a few years is usually less than 3‰.

Plasma ceramides as biomarkers for microvascular disease and clinical outcomes in diabetes and myocardial infarction

BackgroundCeramides have recently been identified as novel biomarkers associated with diabetes mellitus (DM) and major adverse cardiac and cerebrovascular events (MACCE). This study aims to explore their utility in diagnosing microvascular disease.MethodsThis study prospectively enrolled 309 patients from 2018 to 2020 into three groups: healthy controls (Group 1, N = 51), DM patients without acute myocardial infarction (AMI) (Group 2, N = 150), and DM patients with AMI (Group 3, N = 108). We assessed outcomes using stress perfusion cardiac magnetic resonance (CMR) imaging for coronary microvascular disease (CMD) (Outcome 1), retinography for retinal microvascular disease (RMD) (Outcome 2), both CMD and RMD (Outcome 3), and absence of microvascular disease (w/o MD) (outcome 4). We evaluated the classification performance of ceramides using receiver operating characteristic (ROC) analysis and multiple logistic regression. 11-ceramide panel previously identified by our research group as related to macrovascular disease were used.ResultsAverage glycated hemoglobin (HbA1c) values were 5.1% in Group 1, 8.3% in Group 2, and 7.6% in Group 3. Within the cohort, CMD was present in 59.5% of patients, RMD in 25.8%, both CMD and RMD in 18.8%, and w/o MD in 38.5%. The AUC values for the reference ceramide ratios were as follows: CMD at 0.66 (p = 0.012), RMD at 0.61 (p = 0.248), CMD & RMD at 0.64 (p = 0.282), and w/o MD at 0.67 (p = 0.010). In contrast, the AUC values using 11-ceramide panel showed significant improvement in the outcomes prediction: CMD at 0.81 (p = 0.001), RMD at 0.73 (p = 0.010), CMD & RMD at 0.73 (p = 0.04), and w/o MD at 0.83 (p = 0.010). Additionally, the plasma concentration of C14.0 was notably higher in the w/o MD group (p < 0.001).ConclusionsPlasma ceramides serve as potential predictors for health status and microvascular disease phenotypes in diabetic patients.

Traveling Light: Arctic Coastal Erosion Releases Mostly Matrix Free, Unprotected Organic Carbon

AbstractThe Arctic rapidly warms and sea ice retreats, a large fraction of organic carbon (OC), currently stored in coastal permafrost will be released into the marine system. Once reintroduced into the active carbon cycle, this material will either be decomposed or buried on the shelf depending on its hydrodynamic and chemical properties. Currently, carbon estimates are based on bulk measurements, which does not take the hydrodynamic pathway of different fractions into account. Therefore, eight coastal permafrost locations have been sampled along the Canadian Beaufort Sea Coast, hydrodynamically fractionated and analyzed for their C, N, 13C and 14C content. We found that the matrix‐free fraction (low density &lt;1.8 g/cm3, and high‐density &gt;1.8 g/cm3; &lt;38 μm) account for 77%–98% of the OC. By using a coastal classification combined with field data, our results showed that short coastal segments can become key players in delivering matrix‐free, easily degradable OC to the marine system.

Strontium isotopes in the atmosphere, geosphere and hydrosphere: Developing a systematic “fingerprinting” framework of rocks and water in sedimentary basins in eastern Australia

Understanding the connection between aquifers, aquitards, and groundwater-dependant ecosystems remains a key challenge when developing a conceptual hydrogeological model. The aim of this study was to develop a systematic strontium isotope (87Sr/86Sr) fingerprinting framework of rocks and water within the sedimentary Surat and Clarence-Moreton basins (SCM basins) in eastern Australia – an area of extensive coal seam gas development and high potential for aquifer and groundwater-surface water connectivity. To do this, new groundwater samples (n = 298) were collected, analyzed and integrated with published data (n = 154) from the basins' major sedimentary, volcanic and alluvial aquifers, including the major coal seam gas target, the Walloon Coal Measures. Samples were also analyzed from rainfall (n = 2) and surface water (n = 40). In addition, rock core samples (n = 39) from exploration and stratigraphic wells were analyzed to determine the range of Sr isotope composition from host rocks. The analyses of cores demonstrate a distinct and systematic contrast in 87Sr/86Sr between different hydrogeological units. This confirms that all major hydrogeological units have a narrow range with unique 87Sr/86Sr population characteristics that are useful for guiding conceptual model development. Comparison with selected hydrochemical and groundwater age tracers (14C and 36Cl) suggests only limited changes of 87Sr/86Sr from recharge beds to the deeper parts of the basins or with a decrease in natural 14C and 36Cl tracer content along flow paths. Stream sampling during baseflow conditions confirms that 87Sr/86Sr in surface waters are similar to those of the underlying bedrock formations. We demonstrated that 87Sr/86Sr analyses of rocks and water provide a powerful hydrostratigraphic and chemostratigraphic fingerprinting framework in the SCM basins, enabling reliable assessments of plausible aquifer and groundwater-surface water interconnectivity pathways. Applied in other complex multi-aquifer sedimentary basins in Australia, and globally, a similar approach can help to constrain conceptual hydrogeological models and facilitate improved water resource management.

Radioactivity concentration of 14C in the air of 14C urea breath test rooms and the resulting internal dose to medical staff

ObjectiveTo monitor the radioactivity concentration of 14C in the air of rooms used to perform 14C urea breath tests, and evaluate the contamination status of 14C released during such tests, and assess the occupational health risk to medical staff working in such areas. Methods14CO2 in air was absorbed from the air and turned into calcium carbonate through a chemical reaction. Then, calcium carbonate was prepared into a suspension in a low-potassium glass vial. The sample was analyzed using a low-background liquid scintillation counter. ResultsThe radioactivity concentrations of 14C in air of the breath-test rooms in hospitals and physical examination institutions range from 1.35 to 18.41 Bq/m3. The annual committed dose for medical staff was estimated to be between 2.01 × 10−2 and 2.74 × 10−1 μSv. ConclusionsOur results reveal a significant increase of 14C radioactivity concentration in the air of breath-test rooms, but the resulting committed dose is much lower than the limits prescribed by the International Commission on Radiological Protection (ICRP). However, the potential risk of long-term exposure to low-dose radiation should be paid more attention.

Suppression of RCAN1 alleviated lipid accumulation and mitochondrial fission in diabetic cardiomyopathy

BackgroundAlthough metabolic disturbance is a characteristic of diabetic cardiomyopathy (DbCM), the detailed pathogenesis of DbCM remains unknown. MethodsWe used a heart transplantation (HTx) cohort to explore the effect of diabetes mellitus on heart failure (HF) progression dependent of myocardium. Microscopic and ultramicroscopic pathology were used to depict the pathological features of human myocardium of DbCM. We performed targeted metabolomics to characterize the metabolic phenotype of human DbCM. Transcriptomics data were analyzed and weighted gene co-expression network analysis was performed to explore the potential upstream regulator for metabolic remodeling of DbCM. In vivo and in vitro experiments were further conducted to demonstrate the therapeutic effects and molecular mechanisms. ResultsDbCM promoted the progression of HF and increased death or HF-rehospitalization after HTx. Lipid accumulation and mitochondrial fission were the obvious pathological features of DbCM myocardium. The concentrations of C14:0-CoA and C16:1-CoA were significantly increased in the myocardium, and they were positively correlated with the accelerated HF progression and RCAN1 expression in DbCM patients. Knockdown of RCAN1 improved cardiac dysfunction, lipid accumulation, and mitochondrial fission in db/db mice. In vitro studies showed that RCAN1 knockdown improved mitochondrial dysfunction in DbCM cardiomyocytes via the RCAN1-p-Drp1 Ser616 axis. ConclusionsDiabetes is associated with faster progression of HF and causes poor prognosis after HTx, accompanied by metabolic remodeling in the myocardium. Accumulation of long chain acyl-CoA in the myocardium is the metabolic hallmark of human DbCM and is associated with more rapid disease progression for DbCM patients. Upregulation of RCAN1 in the myocardium is associated with the metabolic signatures of DbCM and RCAN1 is a potential therapeutic target for DbCM.

Changes in Oceanic Radiocarbon and CFCs Since the 1990s

AbstractAnthropogenic perturbations from fossil fuel burning, nuclear bomb testing, and chlorofluorocarbon (CFC) use have created useful transient tracers of ocean circulation. The atmospheric 14C/C ratio (∆14C) peaked in the early 1960s and has decreased now to pre‐industrial levels, while atmospheric CFC‐11 and CFC‐12 concentrations peaked in the early 1990s and early 2000s, respectively, and have now decreased by 10%–20%. We present the first analysis of a decade of new observations (2007 to 2018–2019) and give a comprehensive overview of the changes in ocean ∆14C and CFC concentration since the WOCE surveys in the 1990s. Surface ocean ∆14C decreased at a nearly constant rate from the 1990–2010s (20‰/decade). In most of the surface ocean ∆14C is higher than in atmospheric CO2 while in the interior ocean, only a few places are found to have increases in ∆14C, indicating that globally, oceanic bomb 14C uptake has stopped and reversed. Decreases in surface ocean CFC‐11 started between the 1990 and 2000s, and CFC‐12 between the 2000–2010s. Strong coherence in model biases of decadal changes in all tracers in the Southern Ocean suggest ventilation of Antarctic Intermediate Water was enhanced from the 1990 to the 2000s, whereas ventilation of Subantarctic Mode Water was enhanced from the 2000 to the 2010s. The decrease in surface tracers globally between the 2000 and 2010s is consistently stronger in observations than in models, indicating a reduction in vertical transport and mixing due to stratification.

Last ice sheet recession and landscape emergence above sea level in east-central Sweden, evaluated using in situ cosmogenic 14C from quartz

Abstract. In situ cosmogenic 14C (in situ 14C) in quartz provides a recently developed tool to date exposure of bedrock surfaces of up to ∼ 25 000 years. From outcrops located in east-central Sweden, we tested the accuracy of in situ 14C dating against (i) a relative sea level (RSL) curve constructed from radiocarbon dating of organic material in isolation basins and (ii) the timing of local deglaciation constructed from a clay varve chronology complemented with traditional radiocarbon dating. Five samples of granitoid bedrock were taken along an elevation transect extending southwestwards from the coast of the Baltic Sea near Forsmark. Because these samples derive from bedrock outcrops positioned below the highest postglacial shoreline, they target the timing of progressive landscape emergence above sea level. In contrast, in situ 14C concentrations in an additional five samples taken from granitoid outcrops above the highest postglacial shoreline, located 100 km west of Forsmark, should reflect local deglaciation ages. The 10 in situ 14C measurements provide robust age constraints that, within uncertainties, compare favourably with the RSL curve and the local deglaciation chronology. These data demonstrate the utility of in situ 14C to accurately date ice sheet deglaciation, and durations of postglacial exposure, in regions where cosmogenic 10Be and 26Al routinely return complex exposure results.

Fatty acid profile, physicochemical composition and carcass traits of young Nellore bulls fed Acacia mearnsii extract

Fatty acid profile, physicochemical composition, and carcass traits of 32 young Nellore bulls were assessed following the supplementation of Acacia mearnsii extract at levels of 0, 10, 30, and 50 g/kg of total dry matter (DM) in a completely randomized experiment with four treatments and eight replicates. Adding 50 g/kg DM of condensed tannins (CT) from Acacia mearnsii in the bulls' diet reduced DM intake, average daily gain, and meat lipid oxidation (P ≤ 0.05). The pH, centesimal composition, collagen, and meat color indexes of the longissimus muscle were not altered by the addition of Acacia mearnsii (P > 0.05). Cooling loss increased (P = 0.049) linearly. Including Acacia mearnsii in diet reduced the Warner-Bratzler shear force (WBSF, P = 0.018) of longissimus muscle of the bulls. The concentration of C16:0, C17:0, C24:0, t9,10,11,16–18:1, c9t11–18:2, C18:2n–6, C20:4n–6, 20:5n–3, 22:5n–3, and 22:6n–3 in the muscle increased due to the addition of Acacia in the diet (P ≤ 0.05), with the highest muscle concentrations caused by the addition of 10 to 30 g Acacia. c9–18:1 and t16–18:1 reduced linearly. ƩSFA, ƩBI, Ʃcis– and ƩMUFA, Ʃn–3, Ʃn–6, and ƩPUFA (P ≤ 0.05) quadratically increased at higher concentrations of addition of Acacia, above 30 g/kg DM. It is recommended to include Acacia mearnsii extract up to 30 g/kg total DM in diets for young bulls as it improves CLA, PUFA and TI and reduces lipid oxidation. Acacia mearnsii extract as source of CT at 50 g/kg DM negatively impacted the young bulls performance.

Variations in the Solar Modulation Parameter Over the Last 9.5 Thousand Years and the Tilt of the Geomagnetic Dipole

Background: Calculations of the solar modulation parameter (Φ) over the past millennia typically use the relationship between the production rate of cosmogenic isotopes, the earth's dipole moment, and the magnitude of Φ. The cosmogenic isotopes 14C and 10Be are typically used in these studies. When studying solar modulation, the cyclic change in dipole tilt is usually not taken into account, which affects estimates of past solar activity. Methods: Tree rings are a reliable basis for obtaining a radiocarbon time scale (IntCal13). However, determining the concentration of 14C in tree rings is a difficult and controversial task. The time scale derived from the 10Be production rate simulation (GICC05) is less reliable. Nevertheless, there is a way to combine the accuracy of the radiocarbon time scale with the reliability of estimates of the 10Be production rate. This method is the synchronization of the radiocarbon and beryllium-10 series. We have selected the most relevant methods for calculating the solar modulation parameter Φ for the Holocene. When calculating Φ, 10Be data synchronized with 14C data were used. The latest data on the earth's dipole moment were considered. Empirical Mode Decomposition (EMD) was used in the analysis of Φ. Results: It has been shown that the first two decomposition modes are oscillating components with periods of 710 and 208 years, the amplitudes of which increase with time, reaching a maximum of 2500 BP. From contemplation, it follows that the 710-year oscillations are apparently caused by fluctuations in the tilt of the earth's dipole. After excluding the EMD component associated with the 710-year cyclicity, a corrected series was obtained for the solar modulation parameter, free from the influence of changes in the tilt of the magnetic dipole. Conclusion: The rate of formation of cosmogenic radionuclides depends on the intensity of penetration of Galactic Cosmic Rays (GCRs) into the earth's atmosphere. Before reaching earth, GCRs must cross the heliosphere, where they are exposed to solar modulation. Adequate consideration of solar modulation parameters is important for the correct interpretation of the rate of production of cosmogenic isotopes and solar activity.

Aged carbon mineralisation from headwater peatland floodplains in the Peak District, UK

Floodplains are dynamic ecosystems that cycle carbon, which is both delivered from upstream catchment sources and produced in-situ. These systems are being increasingly recognised as key environments of carbon processing, with the capacity for substantial carbon storage, in addition to acting as hotspots of carbon mineralisation. The balance of storage versus mineralisation is dependent on a number of controls including landscape position and environmental conditions. This study focuses on three headwater floodplains downstream of a highly eroded blanket bog peatland in the Peak District, UK. Previous research has shown that aged organic carbon from peatland sources, has been stored in floodplains in this area, and therefore, we aimed to understand whether allochthonous carbon was being mineralised in this context. We examined sediment cores and analysed the radiocarbon (14C) content of soil-respired CO2, using a partitioning approach to scrutinise the depth and age relations of respiration in the individual floodplains, and patterns of age distributions downstream. Aged organic carbon was released from the upper and mid floodplain sites (14C ages of 682 and 232 years BP, respectively), whereas only modern dates were recorded at the lower site. The geomorphic context and sedimentology supported these results, with the stratigraphy suggesting a dominance of allochthonous deposition at the upper sites, but primarily in-situ soil development at the lower site. There were no trends of radiocarbon age with depth in the individual floodplains, suggesting that floodplain sediments were well mixed and that aged organic matter was being processed both at the surface and at depth in the uppermost sites. An isotope mass balance mixing model indicated the dominance of two sources of CO2; recently fixed C3 organic matter (<10 years old) and CO2 produced by methanogenesis. The results indicate that floodplains in a relatively narrow halo around eroding headwater peatlands, could be important sites of aged carbon turnover originally derived from upstream sources. Reworked carbon does not transfer passively through the system and experiences periods of deposition where it can be subject to microbial action. This is an important consideration in other environments where organic carbon has previously been ‘locked up’ (e.g., permafrost regions) but is now under the threat of release due to climate change.

Radiocarbon chronology of Iron Age Jerusalem reveals calibration offsets and architectural developments

Reconstructing the absolute chronology of Jerusalem during the time it served as the Judahite Kingdom's capital is challenging due to its dense, still inhabited urban nature and the plateau shape of the radiocarbon calibration curve during part of this period. We present 103 radiocarbon dates from reliable archaeological contexts in five excavation areas of Iron Age Jerusalem, which tie between archaeology and biblical history. We exploit Jerusalem's rich past, including textual evidence and vast archaeological remains, to overcome difficult problems in radiocarbon dating, including establishing a detailed chronology within the long-calibrated ranges of the Hallstatt Plateau and recognizing short-lived regional offsets in atmospheric 14C concentrations. The key to resolving these problems is to apply stringent field methodologies using microarchaeological methods, leading to densely radiocarbon-dated stratigraphic sequences. Using these sequences, we identify regional offsets in atmospheric 14C concentrations c. 720 BC, and in the historically secure stratigraphic horizon of the Babylonian destruction in 586 BC. The latter is verified by 100 single-ring measurements between 624 to 572 BC. This application of intense 14C dating sheds light on the reconstruction of Jerusalem in the Iron Age. It provides evidence for settlement in the 12th to 10th centuries BC and that westward expansion had already begun by the 9th century BC, with extensive architectural projects undertaken throughout the city in this period. This was followed by significant damage and rejuvenation of the city subsequent to the mid-eight century BC earthquake, after which the city was heavily fortified and continued to flourish until the Babylonian destruction.

Estimation of Groundwater Residence Time Using Radiocarbon and Stable Isotope Ratio in Dissolved Inorganic Carbon and Soil CO2

AbstractEstimation of residence time of groundwater, particularly in regions with inadequate surface waters are very important for formulating sustainable groundwater management policies. We developed a technique for extracting dissolved inorganic carbon (DIC) quantitatively from water for measuring its 14C contents and presented the analytical details here. We also measured stable carbon isotope ratio (δ13C) in soil CO2 and groundwater DIC to correct the groundwater 14C ages. In addition, 14C in soil CO2 were measured for making necessary correction in the initial activity of the recharging water. The corrected 14C contents in the groundwater samples were used to estimate their residence times employing Lumped Parameter Models (LPM), a set of mathematical models to account for the processes that take place during transport from the recharge to the sampling spots. We present a case study focused on the calculation of radiocarbon ages and residence times for a groundwater sample collected from the campus of Physical Research Laboratory in Ahmedabad, Gujarat, India. The study also includes estimations of groundwater residence times using previously measured 14C ages of groundwater samples from Gujarat, India. Various factors controlling the groundwater ages in the LPM and their applicability are discussed.

Comparing MICADAS Gas Source, Direct Carbonate, and Standard Graphite 14C Determinations of Biogenic Carbonate

AbstractNorthern Arizona University, Flagstaff, Arizona, USA, recently installed a MIni CArbon DAting System (MICADAS) with a gas interface system (GIS) for determining the 14C content of CO2 gas released by the acid dissolution of biogenic carbonates. We compare 48 paired graphite, GIS, and direct carbonate 14C determinations of individual mollusk shells and echinoid tests. GIS sample sizes ranged between 0.5 and 1.5 mg and span 0.1 to 45.1 ka BP (n = 42). A reduced major axis regression shows a strong relationship between GIS and graphite percent Modern Carbon (pMC) values (m = 1.011; 95% CI [0.997–1.023], R2 = 0.999) that is superior to the relationship between the direct carbonate and graphite values (m = 0.978; 95% CI [0.959-0.999], R2 = 0.997). Sixty percent of GIS pMC values are within ±0.5 pMC of their graphite counterparts, compared to 26% of direct carbonate pMC values. The precision of GIS analyses is approximately ±70 14C yrs to 6.5 ka BP and decreases to approximately ±130 14C yrs at 12.5 ka BP. This precision is on par with direct carbonate and is approximately five times larger than for graphite. Six Plio-Pleistocene mollusk and echinoid samples yield finite ages when analyzed as direct carbonate but yield non-finite ages when analyzed as graphite or as GIS. Our results show that GIS 14C dating of biogenic carbonates is preferable to direct carbonate 14C dating and is an efficient alternative to standard graphite 14C dating when the precision of graphite 14C dating is not required.

Amphiphilic Compounds as Antihemolytic Agents: Problems and Prospects

In this research the effect of surface-active substances belonging to different classes of amphiphilic compounds (cationic trifluoperazine (TFP), anionic sodium decyl sulfate (C10) and nonionic decyl-β,D-glucopyranoside (DGP)) on the level of damage of human erythrocytes during posthypertonic shock (PHS) and glycerol removal from cells frozen to –196°C was study. All amphiphilic compounds in low concentrations (at which the antihemolytic activity is approximately 45% under the conditions of PHS cells) show the same efficiency when removing glycerol from thawed cells. It was established that among amphiphilic compounds in effective concentrations the maximum antihemolytic (AHmax) activity was shown by DGP (74%) during the removal of glycerol from thawed cells and C10 (74%) under conditions of PHS of erythrocytes, while the AHmax activity indicators of TFP were comparable in both cases. A feature of the effectiveness of C10 under the conditions of deglycerolization of cryopreserved erythrocytes is almost the same AH when used in both concentrations. The method of flow cytometry showed that the amount of annexin-labeled cells depended on the concentration of C10 both in physiological solution and under PHS conditions.

A TIME-INTEGRATED SAMPLER FOR RADIOCARBON ANALYSIS OF AQUATIC METHANE

ABSTRACTFreshwater ecosystems are responsible for a large proportion of global methane emissions to the atmosphere. The radiocarbon (14C) content of this aquatic methane is useful for determining the age and source of this important greenhouse gas. Several methods already exist for the collection of aquatic methane for radiocarbon analysis, but they tend to only sample over short periods of time, which can make them unsuitable for characterizing aquatic methane over longer timespans, and vulnerable to missing short-term events. Here, we describe a new time-integrated method for the collection of aquatic methane that provides samples suitable for radiocarbon analysis, that are representative for periods of up to at least 16 days. We report the results of a suite of tests undertaken to verify the reliability of the method, and the 14C age of aquatic methane from field trials undertaken at sites within Scotland, UK. We believe that this new method provides researchers with a simple approach that is easily deployable and can be used to collect representative time-integrated samples of methane for radiocarbon analysis from a wide range of aquatic environments.

MONITORING OF MODERN CARBON FRACTION IN DISPOSABLE PACKAGING

ABSTRACT Radiocarbon (14C) methodology was used to investigate the presence of biocarbon in different bio-based disposable packaging products. Packaging waste contributes to a municipal solid waste, which is increasing environmental concerns and resulting in the enhancement of EU regulations that aim to reduce packaging waste. The 14C amount in samples reflects how much of the biocarbon has been used. In this study, the concentration of 14C was determined in commonly used types of disposable packaging, such as cups, plates, straws, cutlery, and baking paper. Samples were made of materials such as paper, wheat bran, sugarcane, and wood. The mean concentration of the 14C isotope, measured by the accelerator mass spectrometry (AMS) technique, is greater than 100 pMC in all tested samples, indicating that the samples are modern. The relatively high 14C concentration values in the waterproof layer of the sample indicate that bioplastic, rather than plastic, was used in its production. The highest 14C isotope concentration values were measured for samples that used the oldest biomass (wood and paper), and the lowest for products from current crops (sugarcane and wheat bran), which is consistent with the trend of changes in 14C concentration in the biosphere. The study also addresses the problem of heterogeneity and representativeness of subsamples.