Terrestrial and marine biomarker estimates of organic matter sources and distributions in surface sediments from the East China Sea shelf

Revealing of the sources and distributions of sedimentary organic matter in the East China Sea (ECS) is important for understanding its carbon cycle, which has significant temporal and spatial variability due to the influences of recent climate changes and anthropogenic activities. In this study, we report the contents of both terrestrial and marine biomarkers including ∑C₂₇+C₂₉+C₃₁n-alkanes (38.6-580 ng/g), C₃₇ alkenones (5.6-124.6 ng/g), brassicasterol (98-913 ng/g) and dinosterol (125-1521 ng/g) from the surface sediments in the Changjiang River Estuary (CRE) and shelf areas of the ECS. Several indices based on biomarker contents and ratios are calculated to assess the spatial distributions of both terrestrial and marine organic matter in the ECS surface sediments, and these results are compared with organic matter distribution patterns revealed by the δ¹³C (−20.1‰ to −22.7‰) and C/N ratio (5-7.5) of total organic matter. The contents of terrestrial biomarkers in the ECS surface sediments decrease seaward, controlled mostly by Changjiang River (CR) inputs and surface currents; while higher contents of the two marine biomarkers (brassicasterol and dinosterol) occur in upwelling areas outside the CRE and in the Zhejiang-Fujian coastal zone, controlled mostly by marine productivity. Four proxies, f_Terr(δ¹³C) (the fraction of terrestrial organic matter in TOC estimated by TOC δ¹³C), odd-alkanes (∑C₂₇+C₂₉+C₃₁n-alkanes), 1/P_mar-aq ((C₂₃+C₂₅+C₂₉+C₃₁)/(C₂₃+C₂₅) n-alkanes) and TMBR (terrestrial and marine biomarker ratio) (C₂₇+C₂₉₊C₃₁n-alkanes)/((C₂₇+C₂₉+C₃₁) n-alkanes+(brassicasterol+dinosterol+alkenones)), reveal a consistent pattern showing the relative contribution of terrestrial organic matter (TOM) is higher in the CRE and along the Zhejiang-Fujian coastline, controlled mostly by CR inputs and currents, but the TOM contribution decreases seaward, as the influences of the CR discharge decrease.     

Organic sources and carbon sequestration in Holocene shelf sediments from the western Arctic Ocean

To quantify changes in organic carbon inputs and preservation, sediments from the Northern Chukchi Sea spanning the last 9000 years of the Holocene period were collected during the HOTRAX expedition and analyzed. The multi-proxy approach included molecular organic markers, bulk carbon and isotope measurements plus more recent approaches to terrestrial carbon estimation (the BIT index of Branched and Isoprenoid Tetraethers). The upper 1100 cm of the core, corresponding to the last 7.4 ka, showed a relatively stable total organic carbon content of 1.13-1.38% which decreased below 1100 cm to 0.6%. C:N ratios ranged from 8.4 to 10.83 over the Holocene time period examined. The distribution of n-alcohols and n-alkanes revealed major contributions from long-chain n-alcohols and n-alkanes while minimal contributions were seen from short-chain n-alkanes. The majority of the total fatty acids was comprised of saturated and monounsaturated fatty acids with short-chain and long-chain saturated fatty acids present in similar concentrations throughout most of the core and monounsaturated fatty acids decreasing down-core. Total sterol concentrations showed considerable inputs from marine sterols, C₂₈Δ^5,22, C₂₈Δ^5,24(28) and dinosterol, as well as C₂₉Δ⁵, typically considered a terrestrial marker. The BIT indices for core sediments ranged from 0.021 to 0.216 with minor changes seen in older sequences. Overall, organic biomarkers indicate marine sources as the more dominant input of organic matter with lower but continual contributions from terrestrial sources at this location during the Holocene. The remarkable consistency among multiple molecular organic markers of both marine and terrestrial origin over the Holocene period encompassed by the core suggests that sinking material or surface sediments were heavily influenced by bottom currents or other mixing processes prior to their deposition.     

Influence of aquatic plants on the hydrogen isotope composition of sedimentary long-chain n-alkanes in the Lake Qinghai region,Qinghai-Tibet Plateau

The hydrogen isotopic composition(δD) of leaf wax long-chain n-alkanes(C27, C29, and C31) from lacustrine sediments has been widely applied to reconstruct terrestrial paleoclimatic and paleohydrological changes. However, few studies have addressed whether the aquatic-derived n-alkanes can affect the δD values of lake sedimentary long-chain n-alkanes, which are usually regarded as a recorder of the terrestrial hydrological signals. Here we systematically investigated δD values of long-chain n-alkanes from modern aquatic plants, both near-shore and off-shore surface sediments, surrounding terrestrial plant litters, as well as river water and lake water in Lake Qinghai and its satellite lakes on the northeastern Qinghai-Tibet Plateau. Our data showed that(i) δD values of long-chain n-alkanes from aquatic plants varied from-184‰ to-132‰ for n-C27, from-183‰ to-138‰ for n-C29, and from-189‰ to-130‰ for n-C31, respectively, with no significant differences among the three n-alkanes homologues;(ii) δD values of long-chain n-alkanes from aquatic plants were generally more positive than those from surrounding terrestrial plants, possibly because that they recorded the D-enrichment of lake water in this semi-arid region;(iii) δD values of long-chain n-alkanes from surface sediments showed significant differences among the three n-alkanes homologues, due to the larger aquatic input of n-C27 to the sedimentary lipid pool than that of n-C31, and(iv) n-C27 δD values of near-shore aquatic plants and near-shore sediments are more negative than those from off-shore as a result of lower δD values of near-shore lake water. Our findings indicate that in this region(i) the offset between sedimentary n-C27 and n-C31 δD values(ΔδDC27-C31) could potentially be used to evaluate if sedimentary long-chain n-alkanes are derived from a single source;(ii) while δD values of n-C27 may be influenced by lake water hydrological changes, sedimentary n-C31 is derived predominantly from terrestrial plants and thus its δD can serve as a relatively reliable indicator for terrestrial paleoclimatic and paleohydrological reconstructions.     

Aliphatic hydrocarbon concentrations in short sediment cores from the southern Okinawa Trough: Implications for lipid deposition in a complex environment

Seven short sediment cores from the southern Okinawa Trough were collected and analyzed for the aliphatic hydrocarbon concentrations by capillary gas chromatography to explore the deposition of hydrocarbons to this area. For all cores studied, ratios of Σhydrocarbons/TOC, (nC₂₇+nC₂₉+nC₃₁)/TOC, terrigenous/aquatic, and diploptene/ΣC_25–33n-alkanes fluctuated around a mean value with coefficients of variation ranging from 9.0% to 19.7%, 4.9% to 20.0%, 27.3% to 129%, and 3.8% to 163%, respectively. For the nC₃₁/(nC₂₇+nC₂₉+nC₃₁) ratio, only station 21 showed fluctuation. Moreover, the carbon preference indexes in the C₂₅–C₃₃n-alkane range also exhibited fluctuating values with coefficients of variation of 1.9–14.4%. These results indicate that concentrations of hydrocarbon inputs to the sampling sites vary with time; this may result from complex current flow and sediment transport, leading to variable lipid deposition. In addition, significant correlation between diploptene (hop-22(29)-ene) and higher plant n-alkanes was found for cores 21, 42 and 46, indicating that diploptene was predominantly from higher plant sources. However, no correlation between diploptene and higher plant n-alkanes was found for cores 20, 36, 43 and 44; autochthonous sources of diploptene in these cores were quite probable.     

Compositional characteristics of <Emphasis Type="Italic">n</Emphasis>-alkanes of the glaciers over the Tibetan Plateau and their environmental and climatic significances

We report on the concentration and compositional features of n-alkanes of natural and anthropogenic origins in the snow samples collected from the Qiyi glacier in the Qilian Mountains, the Yuzhufeng glacier in eastern Kunlun Mountains, the Xiaodongkemadi glacier in the Tanggula Mountains, and the Gurenhekou glacier in the Nyainqêntanglha Range. The results indicate a decrease in the total n-alkane concentration (T-HCs) from the northeast to the south over the Tibetan Plateau. The T-HCs in these studied areas were close to those in the Belukha and Sofiyskiy glacier, Russian Alati Mountains and the Dasuopu glacier in the Himalaya but were much higher than those in the Greenland ice sheet, suggesting that the mountain glaciers in the Asian continent may receive a higher loading of n-alkanes than the Greenland ice core. Moreover, the compositional characteristics of n-alkanes indicated that the n-alkanes in the studied areas were probably originated from the plant waxes as well as the fossil-fuel combustion exhaust, whereas the contribution from the lower organisms was small. In addition, the plant wax (C_n(wax)) and anthropogenic (non-C_n(wax)) contributions revealed that fast industrialization may have significant effects on the organic pollutant composition in glacier over the Tibetan Plateau and its circumference environment. Particularly, except for the Yuzhufeng glacier, the ΣnC₂₁ ⁻/ΣnC₂₂ ⁺ and (nC₁₅+nC₁₇+nC₁₉)/(nC₂₇+nC₂₉+nC₃₁) ratio decreased from the Qiyi glacier to the Gurenhekou glacier over the Tibetan Plateau, while the carbon preference index (CPI) values increased. These results indicate a decrease in terrigenous input while an increase in marine input from the northeast to the south over the Tibetan Plateau. These two ratios can be used as the climatic and environmental change indicators.     

Hydrogen isotopic compositions, distributions and source signals of individual n-alkanes for some typical crude oils in Lunnan Oilfield, Tarim Basin, NW China

Petroleum mainly comprises carbon and hydrogen elements. The stable carbon isotopic analysis for whole oil was undertaken as early as the 1930s. After decades, the stable carbon isotopic analytical methods have been developed from analysis for whole oil and oil fractions (e.g., saturated, aromatic and polar frac-tions) into compound-specific isotopic analysis with the emergence of the newly developed GC-C-IRMS analytical technique. Especially, by using com-pound-specific isotopic analytical…     

The molecular and isotopic effects of hydrothermal alteration of organic matter in the Paleoproterozoic McArthur River Pb/Zn/Ag ore deposit

The molecular distribution and compound specific stable carbon and hydrogen isotope ratios were measured on solvent extractable hydrocarbons from the Late Paleoproterozoic McArthur River, or “Here's Your Chance” (HYC) Pb/Zn/Ag ore deposit in the Northern Territory of Australia. Five samples were collected from the McArthur River mine on a northeast–southwest transect in order to sample a gradient of hydrothermal alteration. One sample was taken from the unmineralized W-Fold Shale unit immediately below the HYC ore deposit. δD of n-alkanes, branched alkanes and bulk aromatic fractions were measured, and δ¹³C of n-alkanes, polynuclear aromatic hydrocarbons (PAHs) and bulk kerogen were measured to assess the isotopic effects of a varying degree of hydrothermal alteration on different components of HYC organic matter (OM). Relative to n-alkanes in Barney Creek Formation sediments that did not undergo mineralization, HYC n-alkanes are enriched in deuterium (D) by 50–60‰. This is likely to be a result of equilibrium hydrogen exchange during ore genesis with a highly D-enriched fluid that originated in an evaporitic basin. Trends with distance along the sample transect are ambiguous, but from the northernmost to southernmost point, n-alkanes are less D-enriched, and PAHs are less abundant and less ¹³C-enriched. This could be due to decreasing hydrothermal alteration effects, decreasing delivery of highly altered OM by the mineralizing fluid, or both. The carbon isotopic composition of HYC PAHs is inconsistent with a Barney Creek Fm source, but consistent with an origin in the underlying Wollogorang Formation. PAHs are ¹³C-depleted relative to n-alkanes, reflecting a kerogen source that was ¹³C-depleted compared to n-alkanes, typical for Precambrian sediments. PAHs are more ¹³C-depleted with increasing molecular weight and aromaticity, strengthening the case for a negative isotopic effect associated with aromatization in ancient sediments. Together, these data are consistent with a an ore deposition model in which fluids originated in an evaporitic deposit lower in the basin and interacted with metals and OM in the Tawallah Group at temperatures above 250 °C and a depth of ~ 6 km before ascending along a flower structure associated with the Emu Fault and cooling to 200 ± 20 °C before reaching Barney Creek sediments.     

Catchment environmental change over the 20th Century recorded by sedimentary leaf wax n-alkane δ~(13)C off the Pearl River estuary

The compound-specific stable carbon isotope compositions(δ~(13)C) of leaf wax n-alkanes from two short sediment cores recovered off the Pearl River estuary(PRE) were analyzed to check for their capability of indicating decadal scale catchment environmental change. Sedimentary long-chain n-alkanes exhibited an odd-over-even predominance, with a maximum at n-C_(29) or n-C_(31), indicating their leaf wax origin was from vascular plants. The δ~(13)C values of C_(29) and C_(31) n-alkane in all the sediment samples were in the range of -28.8‰ to -31.2‰, consistent with the C_3 plant-dominated vegetation in the Pearl River catchments. The time series of δ~(13)C records from the two cores were comparable and displayed a decreasing trend from the early 20 th century to the end of the 1970s, followed by a reversal in that change leading to continued increase for ca. 15 years. After being corrected for the effect of atmospheric CO_2 rise and δ~(13)C_(atm) decline, the δ~(13)C_(29) records largely retained their raw changing pattern; the post-1980 increase being more conspicuous. The slightly decreasing trend in corrected δ~(13)C records before around 1980 may have been caused by an increase in precipitation, whereas the subsequent increase of δ~(13)C is likely associated with the observed dry climate and/or intensive anthropogenic deforestation. Our results thus demonstrate that leaf wax n-alkanes buried in the sediments off the PRE may well reflect change in the regional climate and/or human activity in the river catchments over the past century.     

Distribution and sources of aliphatic and polycyclic aromatic hydrocarbons in suspended particulate matter in water from two Brazilian estuarine systems

The levels of selected organic markers, including 17 polycyclic aromatic hydrocarbons (PAHs), 16 of which are classified as priority pollutants by the US-EPA and perylene, aliphatic hydrocarbons (total and linear alkanes) and petroleum biomarkers (hopanes and steranes), were measured in suspended particulate matter (SPM) of the Mundaú-Manguaba estuarine-lagoon system (MMELS) in northeastern Brazil and the Paraíba do Sul River (PSR) estuary in southeastern Brazil, both of which are affected by sugarcane agriculture and urbanization. A total of 33 surface water samples of SPM were collected (22 from the MMELS and 11 from the PSR). The ∑16PAH ranged from 221 to 1243 ng g⁻¹ in the MMELS and from 228 to 1814 ng g⁻¹ in the PSR. Hopane and sterane concentrations in the PSR were higher than in the MMELS due to the input from petrogenic sources in PSR. The contributions of higher plants were also observed by n-alkane analyses. The PAH isomeric ratios indicated that the SPM from MMELS showed characteristics of combustion from biomass or petroleum and PSR was associated to petrogenic input, either from combustion or from unburned petroleum. Three sampling sites located near to the sugarcane plant and mouth of the rivers showed higher PAH concentrations and may largely be considered as highly contaminated. However, levels of n-alkanes and petroleum biomarkers in both study areas were relatively low.     

Characterization of the negative carbon isotope shift in segment C2, its global implications as a harbinger of OAE1a

Lower Cretaceous C-isotope records show intermittent negative/positive spikes, and consistent patterns of coeval chemostratigraphic curves thus document shifts that signal simultaneous responses of temporal changes in the global carbon reservoir. The standard pattern registered by the δ ¹³C_org and δ ¹³C_carb in Lower Aptian sediments includes distinct isotope segments C1 to C8 (Menegatti et al., 1998). In the El Pui section, Organyà Basin, Spain, C-isotope segment C2 is the longest interval preceding segments C3–C6 associated with oceanic anoxic event 1a (OAE 1a), and reveals a distinct negative shift of ~1.8‰ to ~2.23‰ defining the C-isotope pattern within that interval. Total inorganic carbon (TIC), total organic carbon (TOC), δ ¹³C_org, microfacies, n-alkanes show no difference before, during, or after the negative inflection. The biomarkers indicate that organic matter (OM) mainly originates from algal/microbial sources because short-chain length homologues (≤nC₁₉) dominate. nC₂₀ through nC₂₅ indicate some contribution from aquatic vegetation, but little from higher plants (>nC₂₅), as also suggested by the terrestrial/aquatic ratio of n-alkanes or (TAR) = [(nC₂₇+nC₂₉+nC₃₁)/(nC₁₅+nC₁₇+nC₁₉)] (averages 0.085). We suggest that conjoint pulses of contemporaneous LIPs (Ontong Java) and massive explosive volcanism in northeast Asia, the Songliao Basin (SB-V), best conform to plausible causes of the negative intra-C2 carbon isotopic excursion (CIE) at that time. Because of its apparent common occurrence the intra-C2 inflection could be a useful marker harbinger to the more pronounced CIE C3, the hallmark of OAE1a.     

Identification and quantification of mixed sources of oil spills based on distributions and isotope profiles of long-chain n-alkanes

Combined with quantitative determination of concentration and isotopic composition of petroleum hydrocarbons, weathering simulation experiments on artificially mixed oils and their two end-member oils are performed for identification and quantification of mixed sources. The >C₁₈n-alkanes show no appreciable losses during a short-term weathering process. An approach based on distribution of long-chain n-alkanes (>C₁₈) is suggested for estimating the contribution proportion of each source in mixed oils. Stable carbon isotope profile of individual n-alkanes is a powerful tool to differentiate sources of oil spills, but unavailable to accurately allocate each contribution due to a relatively large analytical error.     

Distribution and significance of C~_(40) alkanes in the extracts of Cretaceous source rocks from the Songliao Basin

Source rock extracts and crude oils from the Songliao Basin were analyzed by high-temperature gas chromatography (HTGC), gas chromatography-mass spectrometry (HTGC-MS) and gas chromatography-isotope ratio-mass spectrometry (GC-IRMS), for high molecular-weight alkanes. The distributions of n-alkanes in the Nenjiang Formation extracts are in the C14―C63 range; a bimodal distribution occurs in the C-21 and C21―40 regions. The C30―C37 n-alkanes are accompanied by C29―C35 hopanes, whereas the high molecular-weight C45―C47 n-alkanes co-occur with abundant isoalkanes, alkylcyclohexanes and alkylcyclopentanes. The high δ 13C values of the n-alkanes and the microscopic maceral compositions indicate a highly diversified organic source input for the Nenjiang Formation source rocks, ranging from aquatic plants, blue alge-bacteria, to land plant material. In contrast, n-alkanes in the rock extracts of the Qingshankou Formation are characterized by a single modal distribution, with relatively low abundances of C29―C35 hopanes, but high molecular-weight isoalkanes, alkylcyclohexanes and alkylcyclopentanes. The relatively low δ 13C values of C22―C44 n-alkanes and organic material compositions indicate that the source rocks in the Qingshankou Formation contain dominantly type I algal organic matter. The relative abundance of C 40 compounds in source rocks changes little at low maturity stage, but decreases drastically at higher maturity levels, with a concurrent reduction in the odd/even carbon predominance. In crude oils, in contrast, the relative abundance of C 40 compounds appears to relate closely with the oil source and oil viscosity.     

Geochemical characteristics of light hydrocarbons in cracking gases from chloroform bitumen A,crude oil and its fractions

The composition characteristics of light hydrocarbons from crude oil, chloroform bitumen A, saturated hydrocarbon fraction, aromatic hydrocarbon fraction, and asphaltene fraction during cracking have been studied systematically. The results revealed that the content of n-alkanes, branched alkanes and cycloalkanes in light hydrocarbons from the samples gradually decreased as the simulation temperature increased, and finally almost depleted completely, while the abundance of methane, benzene and its homologues increased obviously and became the main products. The ratios of benzene/ n-hexane and toluene/n-heptane can be used as measures for oil cracking levels. Variation characteristics of maturity parameters of light hydrocarbons, for example, iC₄/nC₄, iC₅/nC₅, isoheptane value, 2,2-DMC₄/nC₆, and 2-MC₆+3-MC₆/nC₇ for different samples with increasing pyrolysis temperature, are consistent with those in petroleum reservoirs, indicating that these parameters may be efficient maturity index.     

The spatial distribution of sedimentary compounds and their environmental implications in surface sediments of Lake Khar Nuur (Mongolian Altai)

Lake sediments are valuable natural archives to reconstruct paleoclimate and paleoenvironmental changes which consist of inorganic and organic sediment compounds of allochthonous origin from the catchment and of autochthonous production in the lake. However, for robust paleo-reconstructions it is important to develop a better understanding about sedimentation processes, the origin of inorganic and organic sediment compounds and their distribution within the lake. In this context, modern process studies provide important insights, although environmental and anthropological changes can affect the spatial distribution of sediment compounds through time. Therefore, in this study the spatial distribution of grain size and geochemical proxies in 52 surface sediment samples from Lake Khar Nuur, a small high-altitude lake in the Mongolian Altai with a small and anthropogenically used hydrological catchment, is investigated. The results show a distinct sediment focussing in the two deep basins of the lake, which therefore act as accumulation zones. In those accumulation zones, total organic carbon (TOC), total nitrogen (N) and their isotopic composition (δ¹³C_TOC, δ¹⁵N) as well as n-alkanes indicate that organic sediment compounds are a mixture of both allochthonous and autochthonous origin. While the recent catchment vegetation consists of grasses/herbs and the shrub Betula nana (L.) with distinct differences in their n-alkane homologue patterns, those differences are not reflected in the sediment surface samples which rather indicates that grass-derived n-alkanes become preferentially incorporated in the lake. Extensive anthropogenic activity such as grazing and housing in the southern part of the catchment causes soil erosion which is well reflected by high TOC, N and sulphur (S) contents and ¹⁵N depleted δ¹⁵N values at the central southern shore, i.e. increased allochthonous sediment input by anthropogenically-induced soil erosion. Overall, the surface sediments of Lake Khar Nuur origin from allochthonous and autochthonous sources and are focussed in the accumulation zones of the lake, while their distribution is both environmentally and anthropogenically driven.     

Carbon isotopic characteristics and their genetic relationships for individual lipids in plants and sediments from a marsh sedimentary environment

The carbon isotopic compositions of individual lip-ids can provide the genetic information about sedi-mentary lipids so that it has extensively applied pros-pects in geochemically studied field[1―8]. However, this applied research relies heavily on the accumula-tion of studied data in the genetic relationships between carbon isotopic compositions of individual lipids and their biological precursors in different sedi-mentary environments. Recently, the useful δ 13C data of individual lipids f…     

Chromatographic separation of diasteriomeric isoprenoids for the identification of fossil oil contamination

In aliphatic hydrocarbon fractions of crude oils eight acyclic isoprenoid alkanes were separated from accompanying n-alkanes and iso-alkanes by high-performance glasscapillary gas chromatography. Four of these: 2,6,10-trimethyltetradecane (V), norpristane (IV), pristane (III), and phytane (II) could be resolved further to reveal a doublet produced by the different diastereoisomers.In these doublets the front peak represents stereoisomers formed during maturation of crude oil while the rear peak indicates the respective hydrocarbons carrying the original biogenic precursor configuration. This appearance of doublets demonstrates the loss of stereospecificity in hydrocarbons derived from phytol (I). By using the front peaks as diagenetic ‘maturity markers’ attributable to fossil fuels, hydrocarbon mixtures extracted from sea water samples contaminated with fossil oil could be investigated in detail. The quantitative relationship between recent biogenic and fossil fuel hydrocarbons could be determined in extracts in the lower boiling point range.     

Detection of aliphatic hydrocarbons derived by recent “bio-conversion” from fossil fuel oil in North Sea waters

The higher boiling point range of saturated aliphatic hydrocarbon fractions extracted from North Sea water have been re-investigated in detail with improved high resolution glass capillary columns suitable for high temperature gas-chromatography. The resulting chromatograms reveal hydrocarbon patterns, most of which have the same common feature: a smooth distribution of the long-chain n-alkanes combined with a lack of the branched alkanes normally expected for fossil fuel oil. Instead, two homologous series of iso- and anteiso-alkanes could be detected. Since this finding is always associated with traces of present or past fossil fuel oil contamination of the upper water column, these environmental n-, iso and anteisoalkanes are considered to be recently ‘bio-converted’ from fossil fuel oil hydrocarbons. They form a third group beside recent biogenic and fossil petrogenic hydrocarbons in the marine environment. Oil pollution records of the marine environment will have to take into account this group of microbial hydrocarbons.     

Molecular structure of kerogens from source rocks of the Tarim Basin: A study by Py-GC-MS and methylation-Py-GC-MS

Kerogen is the organic matter in sediments that isneither soluble in common organic solvents nor in hy-drous alkaline solvents[1]. It is the most important or-ganic matter on the earth and regarded as the majorsource of natural gas and petroleum. Being the mac-romolecule, kerogen is not readily to be contaminatedby other organic matter. It is the most reliable indige-nous organic matter in sediments[2]. The structure of kerogen is one of the key sub-jects of organic geochemical studies in…     

Relationships between surface-active organic substances, chlorophyll a and nutrients in the northern Adriatic Sea

Surface-active organic substances (SAS), nutrients, chlorophyll a (Chl a), dissolved oxygen (O₂), salinity (S) and temperature (T) were measured approximately monthly in the northern Adriatic Sea (NA) during two years. Results were elaborated for two stations of different trophic status. Exhaustive statistical examinations of measured variables were performed to contribute to better understanding of the processes and interdependence of the measured parameters. The results of those analyses allowed the region to be described based on several groups of data relevant for particular processes. Chl a appear to be independent parameter; orthosilicate, nitrite and ammonium represent the parameter group most relevant for regeneration processes; the second group includes nutrients dominant in freshwater inputs (orthophosphate and nitrate), while in the third group are parameters related to primary production processes (T, O₂, organic phosphorus and SAS). Probably due to time lags between nutrient uptake and phytoplankton growth as well as between cells growth/division and SAS release, both, the correlation between nutrients and Chl a and the correlation between Chl a and SAS were not statistically significant. Although significantly higher nutrient and Chl a concentrations were found in the mesotrophic western part of the region in comparison to the oligotrophic eastern part, the SAS concentration differences were less marked. It is assumed that more OM is produced, but also at the same time remineralized, at the mesotrophic western part, leading to higher concentrations of regenerated nutrients there. Presence of different phytoplankton taxa and/or fractions (micro and nano) at the two stations may have also contributed to minimize the difference in SAS contents. Higher SAS acidities were noticed in the mesotrophic than in the oligotrophic part.     

太湖冬季有色可溶性有机物吸收荧光特性及遥感算法

基于2006年和2007年1月两次太湖采样,对50个点位的有色可溶性有机物(CDOM)光谱吸收、荧光、溶解性有机碳(DOE)浓度及遥感反射率进行测定与分析,探讨冬季太湖CDOM的吸收荧光特性及空间分布,建立CDOM吸收系数的遥感反演算法.结果表明,太湖冬季CDOM在355nm处吸收系数a(355)变化范围和均值分别为1...