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1.
Fire-derived organic matter (pyrogenic organic matter, or PyOM), despite its apparent long term stability in the environment, has recently been reported to degrade faster than previously thought. Current studies have suggested that the composition and structure of PyOM can provide new insights on the mechanisms by which C and N from pyrolyzed biomaterials are stabilized in soils. To better understand the chemical structure of PyOM produced under typical fire conditions in temperate forests, samples of dual-enriched (13C/15N) Pinus ponderosa wood and the charred material produced at 450 °C were analyzed by solid state nuclear magnetic resonance (ssNMR), electron paramagnetic resonance (EPR), diffuse reflectance Fourier transform infrared (DRIFT) spectroscopy, and both isotopic and elemental composition (C, H, O, and N). Notably, the use of high magnetic field strengths in combination with isotopic enrichment augmented the NMR detection sensitivity, and thus improved the quality of molecular information as compared with previously reported studies of pyrogenic materials. The key molecular groups of pine wood and the corresponding PyOM materials were determined using magic-angle spinning (MAS) 13C, 15N, and 1H NMR. Together with DRIFT and EPR measurements, ssNMR revealed the formation of a free radical-containing disordered blend of nitrogenous aromatics and heat resistant aliphatics in the PyOM due to incomplete combustion of the precursor wood. 13C ssNMR and DRIFT analyses showed the removal of oxygenated aliphatics due to pyrolysis of the precursor wood and the dominant contribution of multiply-bonded and oxygenated aromatic structures in the resulting PyOM. However, the 18O isotopic analyses indicated selective retention of ligneous moieties during charring at 450 °C. 15N ssNMR studies implied that the nitrogenous species in PyOM corresponded to thermally altered rather than heat resistant domains of the pine wood precursor. Our molecular characterization suggests that biomaterials pyrolyzed near 450 °C may degrade in soils faster than those pyrolyzed at higher temperatures and may not represent a stable C sink in terrigenous ecosystems. 相似文献
2.
The microbial recalcitrance of char accumulated after vegetation fires and its transport within a soil column were studied in microcosms using 13C- and 15N-enriched pyrogenic organic material (PyOM). The PyOM from rye grass (Lolium perenne L.) was produced by charring at 350 °C under oxic conditions for 1 and 4 min to examine the impact of the charring degree. After 28 months, 13C recovery decreased to values between 62% and 65%, confirming that this material can be attacked by microorganisms and that the degradation occurs rapidly after accumulation of PyOM at the soil surface. The respective 15N recovery followed the same trend but tended to be higher (between 67% and 80%). Most of the added PyOM isotopic labels were recovered in the particulate organic matter (POM) fraction, containing between 84% and 65% of the added 13C and 15N after the first 2 months, being reduced by half at the end of the experiment. After 1 month, up to 13.8% of the 13C label and 12.4% of the 15N label were detected in the POM-free mineral fractions. This fast association of PyOM with the mineral phase indicates that physical soil properties have to be considered for the elucidation of PyOM stability. Addition of fresh unlabelled grass material as co-substrate resulted in comparable trends as for the pure PyOM but the total recovery of the isotopic labels clearly increased with respect to the amount of mineral-associated PyOM. Between 73% and 82% of the mineral-associated PyOM occurred in the clay separates (<2 μm) for which the highest values were obtained for the experiment with the more intensively charred PyOM and co-substrate addition.In summary, the study demonstrates the degradability of grass-derived PyOM. The addition of fresh plant material as an easily degradable co-substrate promoted the formation of partially decomposed PyOM and subsequently its association with the mineral phase, but did not increase the respective mineralisation rates. Detection of 13C and 15N content at different depths of the microcosm column demonstrated an additional loss of PyOM from top soil by way of mobilisation and transport to deeper horizons. All these processes have to be taken into account in order to obtain a more realistic view about the behaviour of PyOM in environmental systems and for estimation of the C and N sequestration potential. 相似文献
3.
Although rates and mechanisms of early diagenesis have been well studied, the effects of microbial metabolism on the molecular composition of the sedimentary organic matter (SOM) over long periods of time need more investigation. In this study, we characterize the early diagenesis of marine SOM from organic rich sediments of the Ocean Drilling Program site 1082 located off Namibia, in the vicinity of the Benguela coastal upwelling system. We used both Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance spectroscopy (13C NMR) to assess the quantitative partitioning of the organic carbon into major compound classes (aliphatic, aromatic, ester, carboxylic, amide and carbons from carbohydrates). Then, we calculate the SOM composition in the main biomolecules (proteins, carbohydrates, lipids and lignin) on the basis of previous 13C NMR based estimates of the molecular composition of the organic mixtures. Results show that the SOM is still labile at 7 m below the seafloor (mbsf) and composed of about 25% proteins and 15% carbohydrates. With increasing depth, the protein content exponentially decreases to 13% at 367 mbsf, whereas the carbohydrate content decreases linearly to 11%. The lignin and lipid content consistently represent around 10% and 40% of the SOM, respectively, and show an increase with depth, due mostly to selective enrichment as the more labile components are lost by degradation. Thus, these components of the SOM are considered refractory at the depth scale considered. The calculated remineralization rates are extremely slow ranging from 5.6 mol C m−3 ky−1 at the top of the core to 0.2 mol C m−3 ky−1 according to the organic carbon flux to the seafloor. Knowing the labile carbon losses, we propose a method to calculate the initial TOC before the diagenesis took place. 相似文献
4.
Future climatic conditions may coincide with an increased potential for wildfires in grassland and forest ecosystems, whereby charred biomass would be incorporated into soils. Molecular changes in biomass upon charring have been frequently analysed with a focus on black carbon. Aliphatic and aromatic hydrocarbons, known to be liberated during incomplete combustion of biomass have been preferentially analysed in soot particles, whereas determinations of these compounds in charred biomass residues are scarce. We discuss the influence of increasing charring temperature on the aliphatic and aromatic hydrocarbon composition of crop grass combustion residues. Straw from rye, representing C3 grasses and maize, representing C4 grasses, was charred in the presence of limited oxygen at 300, 400 and 500 °C. Typical n-alkane distribution patterns with a strong predominance of long chain odd-numbered n-alkanes maximising at C31 were observed in raw straw. Upon combustion at 300 °C aliphatic hydrocarbons in char were dominated by sterenes, whereas at 400 °C sterenes disappeared and medium chain length n-alkanes, maximising around n-C20, with a balanced odd/even distribution were present. At a charring temperature of 500 °C n-alkane chain length shifted to short chain homologues, maximising at C18 with a pronounced predominance of even homologues. Even numbered, short chain n-alkanes in soils may thus serve as a marker for residues of charred biomass. Aromatic hydrocarbons indicate an onset of aromatization of biomass already at 300 °C, followed by severe aromatization upon incomplete combustion at 400–500 °C. The diagnostic composition of aliphatic and aromatic hydrocarbons from charred biomass affords potential for identifying residues from burned vegetation in recent and fossil soils and sediments. 相似文献
5.
Following surface mining of the Athabasca Oil Sands deposits in northeastern Alberta, Canada, land reclamation entails the reconstruction of soil-like profiles using salvaged soil materials such as peat and mining by-products. The overall objective of this research was to assess soil organic matter (SOM) quality in different reclamation practices as compared to undisturbed soils found in the region. Soil samples (0–10 cm) were taken from 45 plots selected to represent undisturbed reference ecosites and reclamation treatments. Soil OM pools were isolated using a combination of acid hydrolysis and physical separation techniques. Chemical composition of the low density fractions was characterized using ramped cross polarization (RAMP-CP) 13C nuclear magnetic resonance (NMR). Differences between disturbed and undisturbed sites reflected the influence of different botanical inputs (peat vs. forest litter) to SOM composition. Reconstructed soils were characterized by significantly lower alkyl over O-alkyl carbon (ALK/O-ALK) ratios (0.3) than undisturbed sites (0.5). For these reconstructed soils, a significantly higher proportion of soil carbon was present in the sand associated (Heavy sand) pool (49.2 vs. 37.3) and in the acid-unhydrolyzable residue (AUR) fraction (61.3 vs. 54.7). These SOM parameters were significantly related to time since reconstruction, with the AUR (p value = 0.012) and Heavy sand (p value = 0.05) fractions decreasing with time since reconstruction, while the ALK/O-ALK ratio increased (p value = 0.006). These findings suggest that the ALK/O-ALK, AUR, and Heavy sand parameters are suitable indicators for monitoring SOM quality in these reconstructed soils following oil sands mining. 相似文献
6.
《Applied Geochemistry》2006,21(7):1204-1215
Understanding the fate of injected organic matter and the consequences of subsequent redox processes is essential to assess the viability of using reclaimed water in aquifer storage and recovery (ASR). A full-scale field trial was undertaken at Bolivar, South Australia where two ASR cycles injected approximately 3.6 × 105 m3 of reclaimed water into a carbonate aquifer over a 3-a period. Organic C within reclaimed water was predominantly in the dissolved fraction, ranging from 1 to 2 mmol L−1 (10–20 mg L−1), markedly higher than potable supply and stormwater previously reported as source waters for ASR. Between 20% and 24% of the injected dissolved organic C (DOC) was mineralised through reaction with injected O2 and NO3. Furthermore, this was achieved mainly within the first 4 m of aquifer passage. Despite the presence of residual DOC, SO4 reduction was not induced within the bulk of the injected plume. It was only near the ASR well during an extended storage phase where deeply reduced (methanogenic) conditions developed, indicating variable redox zones within the injectant plume. The quality of water recovered from the ASR well indicated that the organic C content of reclaimed water does not restrict its application as a recharge source for ASR. 相似文献
7.
Pyrogenic carbon (PyC), a by-product of recurrent boreal wildfires, is an important component of the global soil C pool, although precise assessment of boreal PyC stock is scarce. The overall objective of this study was to estimate total C stock and PyC stock in forest floors of Eastern Canada boreal forests. We also investigated the environmental conditions controlling the stocks and characterized the composition of the forest floor layers. Forest floor samples were collected from mesic black spruce sites recently affected by fire (3–5 yr) and analyzed using elemental analysis and solid state 13C nuclear magnetic resonance (NMR) spectroscopy. PyC content was further estimated using a molecular mixing model. Total C stock in forest floors averaged 5.7 ± 2.9 kg C/m2 and PyC stock 0.6 ± 0.3 kg C/m2. Total stock varied with position in the landscape, with a greater accumulation of organic material on northern aspects and lower slope positions. In addition, total stock was significantly higher in spruce-dominated forest floors than stands where jack pine was present. The PyC stock was significantly related to the atomic H/C ratio (R2 0.84) of the different organic layers. 13C NMR spectroscopy revealed a large increase in aromatic carbon in the deepest forest floor layer (humified H horizon) at the organic-mineral soil interface. The majority of the PyC stock was located in this horizon and had been formed during past high severity fires rather than during the most recent fire event. 相似文献
8.
《Chemie der Erde / Geochemistry》2015,75(1):65-72
This study was conducted on recent desert samples—including (1) soils, (2) plants, (3) the shell, and (4) organic matter from modern specimens of the land snail Eremina desertorum—which were collected at several altitudes (316–360 m above sea level) from a site in the New Cairo Petrified Forest. The soils and shellE. desertorum were analyzed for carbonate composition and isotopic composition (δ18O, δ13C). The plants and organic matterE. desertorum were analyzed for organic carbon content and δ13C. The soil carbonate, consisting of calcite plus minor dolomite, has δ18O values from −3.19 to −1.78‰ and δ13C values −1.79 to −0.27‰; covariance between the two values accords with arid climatic conditions. The local plants include C3 and C4 types, with the latter being dominant. Each type has distinctive bulk organic carbon δ13C values: −26.51 to −25.36‰ for C3-type, and −13.74 to −12.43‰ for C4-type plants.The carbonate of the shellE. desertorum is composed of aragonite plus minor calcite, with relatively homogenous isotopic compositions (δ18Omean = −0.28 ± 0.22‰; δ13Cmean = −4.46 ± 0.58‰). Most of the δ18O values (based on a model for oxygen isotope fractionation in an aragonite-water system) are consistent with evaporated water signatures. The organic matterE. desertorum varies only slightly in bulk organic carbon δ13C values (−21.78 ± 1.20‰) and these values suggest that the snail consumed more of C3-type than C4-type plants. The overall offset in δ13C values (−17.32‰) observed between shellE. desertorum carbonate and organic matterE. desertorum exceeds the value expected for vegetation input, and implies that 30% of carbon in the shellE. desertorum carbonate comes from the consumption of limestone material. 相似文献
9.
《Quaternary Science Reviews》1999,18(10-11):1185-1203
A 13 m long core from the lake-swamp at Pobochnoye (53°01′30″ N, 51°50′30″ E) in the Buzuluk pine forest in the middle part of the Volga River basin, Russia was studied for pollen, peat stratigraphy, mollusc, δ18O/δ16O and δ13C/δ12C analyses and radiocarbon dating. For the first time the environment history of the east European Russia has been reconstructed for the last 14,000 years; ca 14,000–13,000 BP cold dry steppes spread across the basin of the Samara River. Isotope data indicate that the main climate shift occurred ca 10,000 BP at the Lateglacial–Holocene transition when climate became warmer and forests expanded. Pinus sylvestris L. expanded 10,000 BP. Ca 9,000 BP Ulmus, Quercus and Corylus appeared in the Buzuluk forest followed at ca. 7,000 BP by Alnus, then Tilia and Acer at 6000 BP. Between 6000 and 4500 BP the climatic conditions were optimal for the forest growth in the Samara River basin. 5500–5000 BP the lake became shallower and was transformed into the eutrophic peat swamp. Between 4500–3500 BP climate became drier and hotter and forest less abundant. Between 3500–2400 BP the forest cover again increased. Between 2400–2000 BP the pine forest area has reduced, apparently due to increased dryness, and around 2000 BP the modern environment in the Buzuluk area has been in existence. 相似文献
10.
Ryoshi Ishiwatari Koichi Negishi Hiroyasu Yoshikawa Shuichi Yamamoto 《Organic Geochemistry》2009,40(4):520-530
Temporal changes in paleoproductivity of Lake Biwa (Japan) over the past 32 kyr have been studied by analyzing bulk organic carbon and photosynthetic pigments (chlorins) in the BIW95-5 core. Primary productivity was estimated on the assumption of C/Norg values of 8 for autochthonous organic matter (OM) and 25 for allochthonous OM and using an equation developed for the marine environment. The estimate indicates that primary productivity ranges from 50 to 90 g C m?2 yr?1 in the Holocene, while it is ～60 g C m?2 yr?1 on average in the last glacial. Pheophytin a and pheophorbide a are the major chlorins. A downcore profile of chlorin concentration normalized to autochthonous organic carbon (OC) shows a decreasing trend. Chlorin productivity was corrected by removal of the effect of post-burial chlorin degradation. The temporal profile of chlorin productivity thereby obtained resembles that from autochthonous OC.The difference in primary productivity between the Holocene and the glacial for the lake is markedly smaller than that for Lake Baikal situated in the boreal zone. This difference between the two lakes is probably caused by the difference in their climatic conditions, such as temperature and precipitation. Precipitation at Lake Biwa is relatively large during the glacial and the Holocene because of the continuous influence of the East Asian monsoon. Lake Baikal precipitation is generally small as a result of control by the continental (Siberia) climate regime. In addition, a significant difference in productivity between the glacial and the Holocene for Lake Baikal may be essentially controlled by the hydrodynamic systems in the lake.Lake Biwa terrigenous OM input events occurred at least five times over the period 11–32 kyr BP, suggesting enhanced monsoon activity. Molecular examination of the layer with a large input of terrigenous OM during the Younger Dryas indicates that concentrations of terrigenous biomarkers such as n-C27–C31 alkanes, lignin phenols, cutin acids, ω-hydroxy acids and C29 sterols are high, suggesting that soil OM with peat-like material entered the lake as a result of flooding. An enhanced sedimentation rate in the last 3000 years might have been partially caused by agricultural activity around the lake. 相似文献
11.
《Organic Geochemistry》2012,42(12):1259-1268
Mineralisation rates provide valuable information concerning the overall cycling of soil organic N; however, detailed information regarding the pathways preceding the mineralisation of organic substrates remains elusive. We have adopted a molecular approach to open the ‘black box’ of organic N cycling in soil. Stable isotope probing employing compound-specific isotopic analysis was used to trace the fate of N and C within metabolites central to organic N cycling. In time course experiments, 15N and 13C from two dual-labelled amino acid (AA) substrates (U-13C,15N-glutamate and U-13C,15N-glycine) were followed into AAs biosynthesised de novo. In the majority of cases, highly significant differences (P < 0.01) were revealed in the magnitude and rate of N and C transfer from the AA substrates to products of central metabolic pathways prior to their loss from the AA pool. By applying linear and non-linear regressions, several important parameters were derived, namely rate constants, magnitude of fluxes and measures of biosynthetic proximity, which describe the rate and magnitude of N and C flux through primary metabolic processes. The significant differences in N and C processing demonstrate a decoupling of the N and C cycles at the molecular level, i.e. after 32 days the magnitude of N flux into newly biosynthesised AAs was twofold greater than that of C from both substrates. We anticipate that the parameters derived will have potential for use in developing detailed models of soil organic N and C processing, the construction of which is founded on the connectivity of the processes fundamental to life. 相似文献
12.
Three models were examined to predict C aromaticity (fa) of biochars based on either their elemental composition (C, H, N and O) or fixed C (FC) content. Values of fa from solid state 13C nuclear magnetic resonance (NMR) analysis with Bloch-decay (BD) or direct polarisation (DP) techniques, concentrations of total C, H, N, and organic O, and contents of FC of 60 biochars were either compiled from the literature (dataset 1, n = 52) or generated in this study (dataset 2, n = 8). Models were first calibrated with dataset 1 and then validated with dataset 2. All models were able to fit dataset 1 when atomic H to C ratio (H/C) < 1 (except two ash rich biochars) and to estimate fa of HF treated biochars (H/C < 1). Model 1, which was based on values of H/C only and calibrated with a root mean square of error (RMSE) of 0.04 fa-unit (n = 41), could predict the experimental data with a RMSE = 0.02 fa-unit (n = 6). Model 2, which was based on biochar elemental composition data, showed the most accurate prediction, with a RMSE of 0.03 fa-unit (n = 41) for the calibration data, and of 0.02 fa-unit (n = 6, H/C < 1) for the validation data. Model 3, which was based on contents of FC and C, and modified with a correction factor of 0.96, displayed the highest RMSE (0.06 fa-unit, n = 19) among the three models. Models 1 and 2 did not work properly for samples having either an H/C ratio > 1, high concentrations of carbonate or high inorganic H. These models need to be further tested with a wider range of biochars before they can be recommended for classification of biochar stability. 相似文献
13.
The Sotkavaara Intrusion is a small (2.5 × 1.5 km surface expression) mafic-ultramafic intrusion located in northern Finland, 25 km east-southeast of Rovaniemi. The intrusion was drilled by the Geological Survey of Finland between 2009 and 2012, when low-S, low-grade precious metal mineralisation (<1.1 ppm Pt + Pd + Au) was discovered. Emplaced into the 1.98 Ga eastern Peräpohja Schist Belt, Sotkavaara occurs a few tens of kilometres north of the 2.44 Ga the Penikat, Portimo and Koillismaa intrusions, which together host Europe’s most significant platinum-group element (PGE) mineralisation. The intrusion comprises a volumetrically subordinate Gabbro Unit and volumetrically dominant Pyroxenite Unit, within which layering is poorly-developed. The Pyroxenite Unit is composed predominantly of clinopyroxenite and contains a small number of laterally discontinuous wehrlite, olivine clinopyroxenite and low-Cr clinopyroxenite (<0.1 wt% Cr2O3) layers. Precious metal mineralisation is hosted by low-Cr clinopyroxenite layers and shows systematic Pt, Pd, Au and Cu offsets similar to those in the Munni Munni, Rincón del Tigre, Skaergaard and Great Dyke intrusions. Relative to these global examples, the Sotkavaara Intrusion represents an atypical occurrence, exhibiting poorly-developed modal layering in a small mafic-ultramafic intrusion, alongside moderately heavy δ 34S values (+1.3 to +9.6‰). Despite this, mineralisation can be broadly attributed to similar ore-forming processes, whereby in-situ fractional crystallisation is ultimately responsible for generating small volumes of sulphide melt. Although mineralisation is sub-economic, this occurrence indicates that northern Finland may be prospective for magmatic sulphide deposits in Svecofennian-age mafic-ultramafic intrusions. Globally, Sotkavaara highlights that well-developed modal layering and large magma chambers are not necessarily requirements for forming this type of mineralisation. 相似文献
14.
The textural relationships and geochemistry of feldspars from least-altered to sericite-hematite altered and mineralised ~ 1.595 Ga Roxby Downs Granite (RDG) at Olympic Dam, South Australia, were examined. The sample suite is representative of RDG both distal (> 5 km) and proximal (< 1 km) to the hydrothermal breccias of the Olympic Dam Breccia Complex (ODBC), which host Fe-oxide Cu-Au-(U) mineralisation at Olympic Dam. Microscopic observations and quantitative analyses indicate that a range of feldspar reactions have taken place within the RDG hosting the Olympic Dam deposit. An early phase of igneous plagioclase (~ An27–34) is recognised, along with a more abundant, less-calcic plagioclase (~ An12–20) both displaying rapakivi and anti-rapakivi textures with alkali feldspar. Alkali feldspars (~ Or55Ab43An2) record post-magmatic evolution from cryptoperthite to patch perthite. Subsequent patch perthite is overprinted by highly porous, near end-member albite and K-feldspar, while plagioclase undergoes replacement by albite + sericite ± Ba-rich K-feldspar. In sericite-hematite altered and mineralised RDG along the margin of the ODBC, sericite replaces all plagioclase, whereas red-stained, Fe-rich K-feldspar persists. Sulphide-uranium-rare earth element mineralisation is observed in association with hydrothermal feldspars, and increases in abundance with proximity to the orebody. Petrographic observations and whole-rock geochemistry illustrate the transformation of plagioclase and alkali feldspar from igneous to hydrothermal processes, and indicate that hydrothermal albite and K-feldspar formed within the RDG without the need for an external source of alkalis. Feldspar geothermometry indicates a minimum crystallisation temperature of 765 °C at 2.2 kbar for alkali feldspar (pressure estimate obtained using plagioclase-amphibole geobarometry) followed by a range of lower temperature transformations. Late-stage magma mixing/contamination is postulated from supportive temperature and pressure estimates along with feldspar and mafic mineral relationships. 相似文献
15.
In mine soil, quantification of soil organic carbon (OC) derived recently from biomass decomposition is complicated by the presence of fossil (geogenic) C derived from coal, oil shale, or similar material in the overburden. The only reliable method for such measurement is 14C analysis (i.e. radiocarbon dating) using instrumentation such as accelerator mass spectrometry, which is too expensive for routine laboratory analysis. We tested two previously used and two new methods for recent C quantification and compared them with 14C AMS radiocarbon dating as a reference using a set of soil samples (n = 14) from Sokolov, Czech Republic: (i) 13C isotope ratio composition, (ii) cross polarization magic angle spinning 13C nuclear magnetic resonance (CPMAS 13C NMR) spectroscopy, (iii) near infrared spectroscopy (NIRS) coupled with partial least squares regression and (iv) Rock–Eval pyrolysis. Conventional methods for OC determination (dry combustion, wet dichromate oxidation, loss-on-ignition) were also compared to quantify any bias connected with their use. All the methods provided acceptable recent carbon estimates in the presence of mostly aliphatic fossil C from kerogen. However, the most accurate predictions were obtained with two approaches using Rock–Eval pyrolysis parameters as predictors, namely (i) S2 curve components and (ii) oxygen index (OI). The S2 curve approach is based on the lower thermal stability of recent vs. fossil organic matter. The OI approach corresponded well with 13C NMR spectra, which showed that samples rich in recent C were richer in carboxyl C and O-alkyl C. These two methods showed the greatest potential as routine methods for recent C quantification. 相似文献
16.
《Chemie der Erde / Geochemistry》2014,74(4):681-690
This study presents isotope geochemical analyses conducted on water column samples and core sediments collected from the Swan Lake Basin. Water analyses include the dissolved methane (CH4) content and the ratio of carbon-13 to carbon-12 (δ13C) in dissolved inorganic carbon (DIC). The core sediments – sandy muds containing inorganic calcite, organic matter, and opal phases ± ostracods – were examined by X-ray diffraction, dated by radiocarbon (14C), analyzed for wt% organic carbon, wt% organic nitrogen, wt% organic matter, wt% calcite, δ13C of bulk-sediment insoluble organic matter (kerogen), 18O:16O ratio (δ18O) and δ13C of bulk and ostracod calcite. Of particular significance is the large enrichment in carbon-13 (δ13C = +4.5 to +20.4‰ V-PDB) in the calcite of these sediments. The 13C-enriched calcite is primarily formed from DIC in the water column of the lake as a result of the following combined processes: (i) the incorporation of 13C enriched residual carbon dioxide (CO2) after partial reduction to CH4 in the sediments and its migration into the water column-DIC pool; (ii) the preferential assimilation of 12C by phytoplankton during photosynthesis; (iii) the removal of 13C-depleted CH4 by ebullition and of organic matter by sedimentation and burial. The 13C enrichment was low between 3624 and 2470 yr BP; high between 2470 and 1299 yr BP; and moderate since 1299 yr BP. Low 13C enrichment was formed under low water-column carbon levels while higher ones were formed under elevated rates of biomass and calcite deposition. These associations seem to imply that biological productivity is the main reason for carbon-13 enrichments. 相似文献
17.
Reimo Kindler Anja Miltner Martin Thullner Hans-Hermann Richnow Matthias Kästner 《Organic Geochemistry》2009,40(1):29-37
Soil organic matter (SOM) is a major pool of the global C cycle and determines soil fertility. The stability of SOM strongly depends on the molecular precursors and structures. Plant residues have been regarded as the dominant precursors, but recent results showed a major contribution of microbial biomass. The fate of microbial biomass constituents has not yet been explored; therefore, we investigated the fate of fatty acids (FA) from 13C labeled Gram-negative bacteria (Escherichia coli) in a model soil study [Kindler, R., Miltner, A., Richnow, H.H., Kästner, M., 2006. Fate of gram negative bacterial biomass in soil—mineralization and contribution to SOM. Soil Biology & Biochemistry 38, 2860–2870]. After 224 days of incubation, the label in the total fatty acids (t-FA) in the soil decreased to 24% and in the phospholipid fatty acids (PLFA) of living microbes to 11% of the initially added amount. Since the bulk C decreased only to 44% in this period, the turnover of FA is clearly higher indicating that other compounds must have a lower turnover. The 13C label in the t-FA reached a stable level after 50 days but the label of the PLFA of the living microbial biomass declined until the end of the experiment. The isotopic enrichment of individual PLFA shows that the biomass derived C was spread across the microbial food web. Modelling of the C fluxes in this experiment indicated that microbial biomass is continuously mineralized after cell death and recycled by other organisms down to the 10% level, whereas the majority of biomass derived residual bulk C (～33%) was stabilized in the non-living SOM pool. 相似文献
18.
Black carbon decomposition under varying water regimes 总被引：1，自引：0，他引：1
The stability of biomass-derived black carbon (BC) or biochar as a slow cycling pool in the global C cycle is an important property and is likely governed by environmental conditions. This study investigated the effects of water regimes (saturated, unsaturated and alternating saturated–unsaturated conditions) and differences in BC materials, produced by carbonizing corn residues and oak wood at two temperatures (350 °C and 600 °C) on BC degradation at 30 °C over 1 year in a full factorial experiment. Effects of water regime on C loss and potential cation exchange capacity (CECp at pH 7) significantly depended on biomass type. Corn BC was both mineralized (16% C loss for the first year) and was oxidized [1000 mmole(+) kg?1 C] significantly faster under unsaturated conditions than under other water regimes, whereas oak BC mineralized most rapidly (12%) under alternating saturated–unsaturated conditions with similar oxidation, irrespective of water regime. Over 1 year of saturated incubation, the O/C ratio values did not significantly (P > 0.05) increase even though BC was mineralized by 9% and CECp increased by 170 mmole(+) kg?1 C, in contrast to unsaturated and alternating saturated–unsaturated conditions. While mineralization and oxidation significantly decreased at higher charring temperature for corn, no difference was observed for oak (P > 0.05). Unsaturated and alternating conditions increased carboxylic and OH functional groups, while they decreased aliphatic groups. The pH increased by about one unit for corn BC, but decreased by 0.2 units for oak BC, indicating strong mineral dissolution of corn BC. Carbon loss strongly correlated with changes in O/C values of both corn BC and oak BC, indicating that oxidation of BC was most likely the major mechanism controlling its stability. However, under saturated conditions, additional mechanisms may govern BC degradation and require further investigation. 相似文献
19.
《Ore Geology Reviews》2010,37(4):350-362
The mineralisation potential of Palaeoproterozoic strata from the central Gawler Craton, South Australia, is poorly known. This study defines the timing of Zn-rich skarn formation within Palaeoproterozoic calcsilicate and highlights this as a new mineralisation style for the Gawler Craton. Sulphides within the garnet–diopside skarn in the No. 17 Bore Prospect are predominantly in the form of sphalerite, associated with galena, minor chalcopyrite, pyrrhotite and pyrite. Sulphide is present in disseminated form and as a coarse-grained sulphide within a sericite-rich cavity-fill. Mineralisation is inferred to have formed at 1710 ± 16 Ma through a Sm–Nd isochron from garnet and diopside aliquots. A weakly mineralised and altered granite immediately below the calcsilicate skarn crystallised at 1729 ± 13 Ma (LA-ICPMS U–Pb zircon), within error of the skarn mineralisation. The skarn is interpreted to have formed through the initiation of fluid circulation as a result of high-level granite emplacement within the Palaeoproterozoic strata. Exploration for skarn Zn–Pb deposits such as the No. 17 Bore Prospect is assisted by their geophysical properties. 相似文献
20.
Shailesh Agrawal Prasanta Sanyal Anindya Sarkar Manoj Kumar Jaiswal Koushik Dutta 《Quaternary Research》2012,77(1):159-170
Oxygen and carbon isotope ratios of soil carbonate and carbon isotope ratios of soil organic matter (SOM) separated from three cores, Kalpi, IITK and Firozpur, of the Ganga Plain, India are used to reconstruct past rainfall variations and their effect on ambient vegetation. The δ18O values of soil carbonate (δ18OSC) analyzed from the cores range from ? 8.2 to ? 4.1‰. Using these variations in δ18OSC values we are able, for the first time, to show periodic change in rainfall amount between 100 and 18 ka with three peaks of higher monsoon at about 100, 40 and 25 ka. The estimation of rainfall variations using δ18O value of rainwater-amount effect suggests maximum decrease in rainfall intensity (~ 20%) during the last glacial maximum. The δ13C values of soil carbonate (δ13CSC) and SOM (δ13CSOM) range from ? 6.3 to + 1.6‰ and ? 28.9 to ? 19.4‰, respectively, implying varying proportions of C3 and C4 vegetations over the Ganga Plain during the last 100 ka. The comparison between monsoonal rainfall and atmospheric CO2 with vegetation for the time period 84 to 18 ka indicate that relative abundances of C3 and C4 vegetations were mainly driven by variations in monsoonal rainfall. 相似文献