Oxygen isotope fractionation in three freshwater ostracod species from early Holocene lacustrine tufa in northern Estonia

We quantified differences in oxygen isotope fractionation among three biostratigraphically important subfossil ostracod species (Metacypris cordata, Pseudocandona rostrata and Candonopsis kingsleii) from an early Holocene freshwater tufa layer in northern Estonia. Estimated mean δ¹⁸O values are −10.05‰ for M. cordata, −9.34‰ for C. kingsleii and −8.75‰ for P. rostrata. All three species exhibit positive offset from the weighted mean annual δ¹⁸O of contemporary precipitation (−10.7‰ in δ¹⁸O_V-PDB) and from the mean δ¹⁸O value of authigenic tufa carbonate (−10.64‰) in the ostracod-bearing layer. Assuming that the known oxygen isotope fractionation in P. rostrata (+2.5‰) and M. cordata (+1.5‰) has remained constant over time, the theoretical δ¹⁸O_V-SMOW of the early Holocene lake water was calculated to have been between −11.52 and −11.92‰, slightly less negative than the local Ordovician groundwater (−11.7 to −12.2‰). δ¹⁸O values of the tufa carbonate differ by +0.6 to +1.0‰ from the calculated theoretical isotope composition (δ¹⁸O_V-PDB) of lake water, indicating that the tufa also did not precipitate in isotopic equilibrium with ambient waters. Results show that the greater the δ¹⁸O offset from the calculated, theoretical isotope composition of lake water for an ostracod species, the lower is its preferred mean July temperature. Both our data and earlier published results on δ¹⁸O values in Holocene lacustrine carbonates and ostracods from north-eastern Europe, display pronounced decreases in δ¹⁸O with an increase in latitude of the study site. This suggests that temperature-dependent, and therefore latitude-dependent isotopic composition of meteoric waters controlled the δ¹⁸O values in lacustrine tufa and ostracods throughout the Holocene.     

Using variations in the stable carbon isotope composition of macrophyte remains to quantify nutrient dynamics in lakes

The apparent isotope enrichment factor ε_macrophyte of submerged plants (ε_{macrophyte–DIC} = δ¹³C_macrophyte − δ¹³C_DIC) is indicative of dissolved inorganic carbon (DIC) supply in neutral to alkaline waters and is related to variations in aquatic productivity (Papadimitriou et al. in Limnol Oceanogr 50:1084–1095, 2005). This paper aims to evaluate the usage of ε_macrophyte inferred from isotopic analyses of submerged plant fossils in addition to analyses of lake carbonate as a palaeolimnological proxy for former HCO₃ ⁻ concentrations. Stable carbon isotopic analysis of modern Potamogeton pectinatus leaves and its host water DIC from the Tibetan Plateau and Central Yakutia (Russia) yielded values between −23.3 and +0.4‰ and between +14.0 and +6.5‰, respectively. Values of ε _{Potamogeton–DIC} (range −15.4 to +1.1‰) from these lakes are significantly correlated with host water HCO₃ ⁻ concentration (range 78–2,200 mg/l) (r = −0.86; P < 0.001), thus allowing for the development of a transfer function. Palaeo-ε _{Potamogeton–ostracods} values from Luanhaizi Lake on the NE Tibetan Plateau, as inferred from the stable carbon isotope measurement of fossil Potamogeton pectinatus seeds (range −24 to +2.8‰) and ostracods (range −7.8 to +7.5%) range between −14.8 and 1.6‰. Phases of assumed disequilibrium between δ¹³C_DIC and δ¹³C_ostracods known to occur in charophyte swards (as indicated by the deposition of charophyte fossils) were excluded from the analysis of palaeo-ε. The application of the ε _{Potamogeton–DIC}-HCO₃ ⁻ transfer function yielded a median palaeo-HCO₃ ⁻ -concentration of 290 mg/l. Variations in the dissolved organic carbon supply compare well with aquatic plant productivity changes and lake level variability as inferred from a multiproxy study of the same record including analyses of plant macrofossils, ostracods, carbonate and organic content.     

Carbon isotopes of marl and lake sediment organic matter reflect terrestrial landscape change during the late Glacial and early Holocene (16,800 to 5,540 cal yr B.P.): a multiproxy study of lacustrine sediments at Lough Inchiquin,western Ireland

A 7.6-m lake sediment core from a marl lake, Lough Inchiquin, records variation in landscape evolution from 16,800 cal yrs B.P. to 5,540 cal yrs B.P. We observe significant variations (up to 12‰) in δ ¹³C_org and δ ¹³C_calcite values that are interpreted to reflect secular changes in lake water δ ¹³C_DIC values that result from a regional landscape transition from barren limestone bedrock to a forested ecosystem. Lake water δ ¹³C_DIC values are therefore influenced by two isotopically distinct sources of carbon: terrestrial organic material (−27.1 to −31.2‰VPDB) via oxidized soil organic matter and weathered limestone bedrock (+3.4‰VPDB). Isotope excursions in lacustrine sediment records are forced not only by changes in productivity but also by changes in the terrestrial environment. This has profound implications for the interpretation of paleoclimate records derived from lacustrine sediment and suggests that selection of appropriate lakes can provide records of terrestrial change where other related records are not available.     

Holocene Environmental Changes of Lake Geneva (Lac Léman) from Stable Isotopes (δ13C, δ18O) and Trace Element Records of Ostracod and Gastropod Carbonates

Stable isotopes and trace-element contents of ostracod (Candona neglecta) valves mostly from the Holocene portion of two assembled cores from Petit Lac (Lake Geneva, Switzerland-France) were analysed in order to depict the geochemical record of post-glacial environmental changes of this lake. Additional stable isotope and trace element data from the gastropod Bithynia tentaculata (shells and opercula) from some intervals of these cores, as well as previous data from bulk carbonate from the lower part of the studied intervals were also considered. Mg/Ca and Sr/Ca molar ratios for the Holocene lake water have been estimated from evaluations of the partitioning coefficients for Mg and Sr for C. neglecta and B. tentaculata taking into account the modern-lake water composition. This study shows an overall gentle trend to higher δ¹⁸O values in C. neglecta valves from the Boreal interval (mean −8.44‰) to the upper part of the core (mean −8.11‰). This trend is superimposed to higher frequency oscillations of stable isotope values and trace element ratios, especially through the upper Older Atlantic and the Subboreal. The overall isotopic oxygen trend includes several shifts in δ¹⁸O of about 1‰. These shifts are interpreted as major regional-global climate changes that have also been observed in other coeval δ¹⁸O and pollen records which reflect the Holocene climate variability in other European basins. Especially well-defined peaks in some episodes like Older Atlantic (~8200 yr BP), Younger Atlantic – Subboreal transition (~5600 yr BP) and early Subatlantic (~ 2500 yr BP) correspond to well-recognized events in globally-distributed records. Some of these shifts are correlated with pulses in the lake-level curve of the Lake Geneva. An erratum to this article is available at .     

西北干旱地区大气降水δ18O的特征及水汽来源

In order to reveal the characteristics and climatic controls on the stable isotopic composition of precipitation over Arid Northwestern China, eight stations have been selected from Chinese Network of Isotopes in Precipitation (CHNIP). During the year 2005 and 2006, monthly precipitation samples have been collected and analyzed for the composition of δD and δ18O. The established local meteoric water line δD=7.42 δ18O+1.38, based on the 95 ob-tained monthly composite samples, could be treated as isotopic input function across the region. The deviations of slope and intercept from the Global Meteoric Water Line indicated the specific regional meteorological conditions. The monthly δ18O values were characterized by a positive correlation with surface air temperature (δ18O (‰) =0.33 T (℃)-13.12). The amount effect visualized during summer period (δ18O (‰) = -0.04P (mm)-3.44) though not appeared at a whole yearly-scale. Spatial distributions of δ18O have properly portrayed the atmospheric circulation background in each month over Arid Northwestern China. The quan-titative simulation of δ18O, which involved a Rayleigh fractionation and a kinetic fractionation, demonstrated that the latter one was the dominating function of condensation of raindrops. Furthermore, the raindrop suffered a re-evaporation during falling processes, and the pre-cipitation vapor might have been mixed with a quantity of local recycled water vapor. Multiple linear regression equations and a δ18O-T relation have been gained by using meteorological parameters and δ18O data to evaluate physical controls on the long-term data. The estab-lished δ18O-T relation, which has been based on the present-day precipitation, could be considered as a first step of quantitatively reconstructing the historical environmental climate.     

Variations in the oxygen-isotope composition of ancient Lake Superior between 10,600 and 8,800 cal BP

Variations in the oxygen-isotope composition of paleo-water bodies in the Lake Superior Basin provide information about the timing and pathways of glacial meltwater inflow into and within the Lake Superior Basin. Here, the oxygen-isotope compositions of Lake Superior have been determined using ostracodes from four sediment cores from across the Basin (Duluth, Caribou and Ile Parisienne sub-basins, Thunder Bay trough). The δ¹⁸O values indicate that lake water (Lake Minong) at ~10,600–10,400 cal [~9,400–9,250] BP was dominated by glacial meltwater derived from Lake Agassiz and the Laurentide Ice Sheet (LIS). From that time to ~9,000 cal [~8,100] BP, a period associated with formation of thick varves across the Lake Superior Basin, the δ¹⁸O values of Lake Minong decreased even further (−24 to −28‰), symptomatic of an increasing influx of glacial meltwater. Its supply was reduced between ~9,000 and ~8,900 cal [~8,100–8,000] BP, and lake water δ¹⁸O values grew higher by several per mil during this period. Between ~8,900 and ~8,800 cal [~8,000–7,950] BP, there was a return to δ¹⁸O values as low as −29‰ in some parts of the Lake Superior Basin, indicating a renewed influx of glacial meltwater before its final termination at ~8,800–8,700 cal [~7,950–7,900] BP. The sub-basins in the Lake Superior Basin generally displayed very similar patterns of lake water δ¹⁸O values, typical of a well-mixed system. The final stage of glacial meltwater input, however, was largely expressed near its input (Thunder Bay trough) and recognizable in dampened form mainly in the Duluth sub-basin to the west. Water in the easternmost Ile Parisienne sub-basin was enriched in ¹⁸O relative to the rest of the lake, particularly after ~10,000 cal [~8,900] BP, probably because of a strong influence of local precipitation/runoff, and perhaps also enhanced evaporation. By ~9,200 cal [~8,250] BP, lake water δ¹⁸O values in the Ile Parisienne sub-basin were similar to the adjacent Lake Huron Basin, suggesting a strong hydraulic connection between the two water bodies, and common responses to southern Ontario’s shift to warmer and dry climatic conditions after ~9,000 cal [~8,100] BP.     

A multiple stable isotope record of Late Quaternary limnological changes and chironomid paleoecology from northeastern Iceland

We present results from multiple stable isotope analyses (δ¹⁸O of chironomid larval head capsules, chironomid adult thoraxes and other insect remains and δD, δ¹³C, δ¹⁵N of total organic matter—TOM) of a lake sediment core (04-SVID-03) taken from Stora Vidarvatn in northeastern Iceland to reconstruct past environmental, limnological and δ¹⁸O of past lake water changes during the Holocene. Core 04-SVID-03 represents a ∼12,000 cal. yrs BP to present record. Large magnitude changes in δ¹⁸O occurred during the Holocene at the site. Downcore shifts in δ¹⁸O of chironomids did not correlate with measurements of the δ¹³C and δ¹⁵N of chironomid head capsules, implying that the δ¹⁸O changes were not primarily driven by changes in chironomid diet during the Holocene. The δD of TOM provided a proxy of relative lake-water δD changes at the site and also showed large magnitude changes during the record. This approach was supported by analyses of a modern training set where δD_TOM analyses were conducted using surface sediments from a suite of freshwater lakes over a large latitudinal gradient. The magnitude of changes in both the δ¹⁸O and δD and the relatively negative δ¹⁸O values throughout much of the core suggest that the proxies represent more paleoenvironmental information than solely temperature. Additional possible influences on lake-water isotopic composition are discussed, including changes in the seasonality of precipitation, in the patterns of air masses supplying precipitation to Iceland and in the dominant mode of the North Atlantic Oscillation.     

Biomarker and compound-specific δ<Superscript>13</Superscript>C evidence for changing environmental conditions and carbon limitation at Lake Koucha,eastern Tibetan Plateau

A sediment core from Lake Koucha (eastern Tibetan Plateau) was investigated using organic biomarkers and their stable carbon isotope signatures. The correlation between TOC content, total amount of aquatic macrophyte-derived n-alkanes (e.g. nC₂₃) and δ¹³C values of TOC and nC₂₃ indicates that Lake Koucha was macrophyte-dominated before 8 cal ka BP. Shortly after the lake turned from a saline to a freshwater system at 7.2 cal ka BP, a variety of algal and bacterial markers such as hopanoids and isoprenoids emerged, of which phytane, pentamethylicosene (PMI), moretene and diploptene are particularly abundant. Phytane and PMI show different isotopic signals (≈−18 and ≈−28‰, respectively), which indicates that they originated from different sources. Phytane may have been derived from cyanobacteria, while methanogenic archaea may be the source of PMI. The isotopic depletion of diploptene and moretene (≈−60‰) indicates the presence of methanotrophs. After 6.1 cal ka BP, the saturated C₂₀ highly branched isoprenoid (HBI) became the dominant constituent of the aliphatic hydrocarbon fraction. Such dominance has rarely been reported in lacustrine environments, and indicates a strong presence of algae (most likely diatoms) or cyanobacteria. At 4.7 cal ka BP, the appearance of an unsaturated C₂₅ HBI, which is a specific biomarker for diatoms, was noted. Furthermore, the level of nC₁₇-alkane was observed to increase in abundance in the uppermost two samples. These results suggest that the lake was phytoplankton-dominated during the last 6.1 ka. Relatively low biomarker concentrations and δ¹³C values at 6.0, 3.1 and 1.8 cal ka BP indicate the occurrence of cool periods, which is in agreement with inferences from other locations on the Tibetan Plateau. The δ¹³C values of nC₂₃ range from −23.5 to −12.6‰, with high values at the peak of macrophyte abundance at ca. 11 cal ka BP and at the phytoplankton maximum between ca 6.1 and 2.8 cal ka BP. Thus, aquatic macrophyte-derived mid-chain n-alkanes have been found to be excellent indicators of carbon-limiting conditions, which lead to the assimilation of isotopically-enriched carbon species. The limitation of carbon sources could be a localized phenomenon occurring in dense plant stands (as in the older section of the core), or it may be induced by high primary productivity (as in the younger section). Since the δ¹³C value of the inorganic carbon source may vary, the offset between the δ¹³C values of nC₂₃ and TIC could serve as a more precise proxy for carbon-limiting conditions in lacustrine environments, which could in turn be interpreted with respect to lacustrine paleo-productivity.     

Late Holocene storm-trajectory changes inferred from the oxygen isotope composition of lake diatoms,south Alaska

The oxygen isotope ratios of diatoms (δ¹⁸O_diatom), and the oxygen and hydrogen isotope ratios of lake water (δW) of lakes in south Alaska provide insight into past changes in atmospheric circulation. Lake water was collected from 31 lakes along an elevation transect and diatoms were isolated from lake sediment from one lake (Mica Lake) in south Alaska. In general, δW values from coastal lakes overlap the global meteoric water line (GMWL). δW values from interior lakes do not lie on the GMWL; they fall on a local evaporation line trajectory suggesting source isotopes are depleted with respect to maritime lakes. Sediment cores were recovered from 58 m depth in Mica Lake (60.96° N, 148.15° W; 100 m asl), an evaporation-insensitive lake in the western Prince William Sound. Thirteen calibrated ¹⁴C ages on terrestrial macrofossil samples were used to construct an age-depth model for core MC-2, which spans 9910 cal years. Diatoms from 46, 0.5-cm-thick samples were isolated and analyzed for their oxygen isotope ratios. The analyses employed a newly designed, stepwise fluorination technique, which uses a CO₂ laser-ablation system, coupled to a mass spectrometer, and has an external reproducibility of ±0.2‰. δ¹⁸O_diatom values from Mica Lake sediment range between 25.2 and 29.8‰. δ¹⁸O_diatom values are relatively uniform between 9.6 and 2.6 ka, but exhibit a four-fold increase in variability since 2.6 ka. High-resolution sampling and analyses of the top 100 cm of our lake cores suggest large climate variability during the last 2000 years. The 20th century shows a +4.0‰ increase of δ¹⁸O_diatom values. Shifts of δ¹⁸O_diatom values are likely not related to changes in diatom taxa or dissolution effects. Late Holocene excursions to lower δ¹⁸O_diatom values suggest a reduction of south-to-north storm trajectories delivered by meridional flow, which likely corresponds to prolonged intervals when the Aleutian Low pressure system weakened. Comparisons with isotope records of precipitation (δP) from the region support the storm-track hypothesis, and add to evidence for variability in North Pacific atmospheric circulation during the Holocene.

Bias of ostracod stable isotope data caused by drying of sieve residues from water

Stable isotope analysis of ostracod shells is used routinely for palaeoenvironmental studies of ostracod-bearing records. Sample treatment usually involves the disaggregation of sediments and sieving; before the sieving residues were washed with water onto petri dishes and oven-dried. In our study, we compared δ¹⁸O and δ¹³C values of shells that were oven-dried from water and from ethanol alternatively. Large isotopic differences of up to 3‰ were determined for δ¹⁸O values, whereas differences in δ¹³C values were less pronounced with differences of up to 1.6‰. Stable isotope values of shells dried from water were lower for both oxygen and carbon as a result of calcite crystals precipitated on the shell surfaces during the drying process. Therefore, ostracod shells for stable isotope analysis should not be prepared by drying from water. Instead, shells should be dried from ethanol to obtain reliable stable isotope data; likewise freeze-drying is expected to provide trustworthy results.     

Lake Sediment Core Records of Sulphur Accumulation and Sulphur Isotopic Composition in Central Ontario, Canada Lakes

Stable isotopic compositions and concentrations of total sedimentary sulphur (S) were determined in cores from 6 lakes in the acid-sensitive Muskoka-Haliburton region of south-central Ontario. The isotopic composition of S in deep sediment (> ~ 20 cm) was approximately constant in all lakes, and indicated a pre-industrial δ ³⁴S value between +4.0 and +5.3‰, which is similar to current bulk deposition. Similarly, total S concentrations in deep sediment were relatively low (1.9–5 mg S g⁻¹ dwt) and approximately constant with depth within cores. All lakes exhibited up-core increases in total S and decreases in δ ³⁴S at a depth corresponding to the beginning of industrialization in the Great Lakes region ( ~ 1900), resulting in a generally reciprocal depth pattern between total S concentration and δ ³⁴S ratios. While initial shifts in total S and δ ³⁴S were likely due to enhanced SO₄ reduction of newly available anthropogenic SO₄, both the magnitude and pattern of up-core S enrichment and shifts in δ ³⁴S varied greatly among lakes, and did not match changes in S deposition post 1900. Differences between lakes in total S and δ ³⁴S were not related to any single hydrologic (e.g., residence time) or physical (e.g., catchment-area-to-lake area ratio) lake characteristic. This work indicates that sediment cores do not provide consistent records of changes in post-industrial S deposition in this region, likely due to redox-related mobility of S in upper sediment.     

Fossil chironomid δ<Superscript>13</Superscript>C as a proxy for past methanogenic contribution to benthic food webs in lakes?

We used a series of experiments to determine whether stable carbon isotope analysis of modern and fossil larval head capsules of chironomids allowed identification of their dietary carbon source. Our main focus was to assess whether carbon from naturally ¹³C-depleted methane-oxidizing bacteria (MOB) can be traced in chironomid cuticles using stable carbon isotope analysis. We first showed that a minimum sample weight of ~20 μg was required for our equipment to determine head capsule δ¹³C with a standard deviation of 0.5‰. Such a small minimum sample weight allows taxon-specific δ¹³C analyses at a precision sufficient to differentiate whether head capsules consist mainly of carbon derived from MOB or from other food sources commonly encountered in lake ecosystems. We then tested the effect of different chemical pre-treatments that are commonly used for sediment processing on δ¹³C measurements on head capsules. Processing with 10% KOH (2 h), 10% HCl (2 h), or 40% HF (18 h) showed no detectable effect on δ¹³C, whereas a combination of boiling, accelerated solvent extraction and heavy chemical oxidation resulted in a small (0.2‰) but statistically significant decrease in δ¹³C values. Using culturing experiments with MOB grown on ¹³C-labelled methane, we demonstrated that methanogenic carbon is transferred not only into the larval tissue, but also into chironomid head capsules. Taxon-specific δ¹³C of fossil chironomid head capsules from different lake sediments was analyzed. δ¹³C of head capsules generally ranged from −28 to −25.8‰, but in some instances we observed δ¹³C values as low as −36.9 to −31.5‰, suggesting that carbon from MOB is traceable in fossil and subfossil chironomid remains. We demonstrate that stable carbon isotope analyses of fossil chironomid head capsules can give insights into dietary links and carbon cycling in benthic food webs in the past and that the method has the potential to reconstruct the importance of MOB in the palaeo-diet of chironomid larvae and, indirectly, to infer past changes in methane flux at the sediment water interface in lakes.     

Sedimentary facies and climate control on formation of vivianite and siderite microconcretions in sediments of Lake Baikal, Siberia

Authigenic vivianite and siderite microconcretions were found, respectively, in hemipelagic and deltaic facies of 600-m-long BDP-98 sediment section from Lake Baikal. Textural investigations of these microconcretions show that they are typically <1 mm in size, irregular in shape and composed of aggregated crystallites. Dissimilar orientation of vivianite and siderite crystallites suggests formation at different depths in the sediment; up to tens of centimeters for vivianite and tens of meters for siderite. Chemical analyses of both the vivianite and the siderite indicate cation composition characterized by minor amounts of Mn, Ca and Mn apart from the dominating Fe. Rather limited and distinctive carbon isotopic composition of the siderite, with δ ¹³C_VPDB values between about +13 and +16‰, implies formation of the mineral in the methanogenic zone of diagenesis. Isotopic composition of oxygen in the siderite (δ ¹⁸O_VPDB values between about −10 and -11‰ ) is consistent with crystallization temperature at about 10–30°C and water δ ¹⁸O_SMOW values between about −10 and -16‰ . The distribution of the authigenic minerals in the section suggests changes in both sedimentary facies and climate, where vivianite formation was controlled by hemipelagic depositional conditions during the Pliocene and Quaternary, whereas siderite reflects impact of deltaic conditions during the Miocene.     

Evolution of the palaeolake at Ruszkówek (central Poland) during the Eemian Interglacial based on isotope,cladoceran and diatom data

We present isotope, cladoceran and diatom results from investigations of Eemian sediments of the palaeolake at Ruszkówek, central Poland. Our analyses of the 15-m-thick sediments indicate that sandy silts occur on the bottom, followed by calcareous gyttja, interbedded with lake marl. The upper part of the sequence contains peat and peaty sands. Values of δ¹⁸O change from −9.4‰ to −3.3‰ and δ¹³C values oscillate between −3.2‰ and +7.0‰. Nine isotope zones (Is) were defined and characterized using stable isotope analysis of carbonates. Fifteen species of subfossil Cladocera were found and six faunal zones were distinguished (Cladocera zones). One hundred and twenty-three diatom taxa, representing 31 genera were identified, enabling us to discern six Diatom Assemblage Zones. The isotope, cladoceran, and diatom data correlate well with pollen data that define seven phases of evolution of the palaeolake at Ruszkówek. The palaeolake began during the final phase of the Wartanian (Late Saalian Glaciation). During the early Eemian, the palaeolake reached its maximum depth. During the Early Vistulian glaciation, the palaeolake declined. Changes in the cladoceran and diatom communities indicate initial oligotrophic conditions in the lake, then an increase to mesotrophy, and finally eutrophic conditions.     

Sediment lithology and stable isotope composition of organic matter in a core from a cirque in the Krkonoše Mountains,Czech Republic

This study presents detailed lithostratigraphy and stable carbon and nitrogen isotopic variations in a 520-cm-long sediment core from a cirque basin in the Labsky důl Valley, Krkonoše Mountains, Czech Republic. Detailed study of the core reveals five major periods of sedimentation during the last 7600 years: silt and sand deposition during ~7.6–5.1 ka cal BP, Sphagnum peat accumulation during ~5.1–4.0 ka cal BP, sandy silt and sand during ~4.0–2.8 ka cal BP, raised peat bog during ~2.8–2.0 ka cal BP (Sphagnum peat), and sedimentation of sandy silt since ~2.0 ka cal BP. The δ¹³C values of the organic matter in the core vary in the range typical for C3 plants, from −24.35 to −27.68‰, whereas the δ¹⁵N values vary from −2.65 to +4.35‰. Core sections having ash contents ≥70% have δ¹⁵N > 1‰ and δ¹³C < −26‰, whereas those having ≤70% ash content have δ¹⁵N < 1‰ and δ¹³C > −26‰. Strong linear correlations are observed between δ¹³C and δ¹⁵N values as well as between C:N ratios and δ¹⁵N values in the horizons with ash content >10%, primarily for sand and silt horizons. On the other hand, poor correlations between δ¹³C and C:N ratio, as well as δ¹⁵N and C:N ratio, were observed in Sphagnum peat layers (45–125 and 185–265 cm). We conclude that the primary stable isotope variations are not preserved in the layers where significant correlation between δ¹⁵N and C:N ratio is observed. The relatively small δ¹³C variation in the uppermost Sphagnum peat layer suggests stable temperature during ~2.8–2.0 ka cal BP.     

Stable Isotopes (O, H, and S) in the Muteh Gold Deposit, Golpaygan Area, Iran

The Muteh gold district with nine gold deposits is located in the Sanandaj-Sirjan metamorphic zone. Gold mineralization occurs in a pre-Permian complex which mainly consists of green schists, meta-volcanics, and gneiss rocks. Shear zones are the host of gold mineralization. Gold paragenesis minerals include pyrite, chalcopyrite, pyrrhotite, and secondary minerals. Pyrites occur as pre-, syn-, and post-metamorphism minerals. To determine the source of the ore-bearing fluids, fifty samples were selected for petrographical and stable isotope studies. The mean values of 12.4‰, and −42‰ for δ¹⁸O and δD isotopes, respectively, and a mean value of 7.75‰ of calculated fractionation factors for δ¹⁸O H₂O, from quartz veins indicate that metamorphic host rocks are the most important source for the fluids and gold mineralization. Three generations of pyrite can be distinguished showing a wide range of δ³⁴S. Gold mineralization is closely associated with intense hydrothermal alteration along the ductile shear zones. The characteristics of the gold mineralization in the study area are similar to those of orogenic gold deposits elsewhere. An erratum to this article can be found at     

西江河口段溶解无机碳稳定同位素组成的时空变化

For researching the spatio-temporal variation of the stable isotopic composition of the riverine dissolved inorganic carbon（DIC）,we had carried out a survey throughout the hydrologic year during which theδ^13CDIC of the surface water and its physicochemical parameter were examined along the Xijiang River Inner Estuarine waterway from September 2006 to June 2007.There was a striking seasonal variation on the averageδ^13CDIC,as the averageδ^13CDIC in summer（-13.91‰）or autumn（-13.09‰）was much less than those in spring（-11.71‰）or winter（-12.26‰）.The riverineδ13C DIC was controlled by decomposed condition of the riverine organic matter linking the seasonal variation of the physicochemical parameter in the surface water according to the correlation analysis which indicated notable relations betweenδ^13CDIC and water temperature（p=0.000;r=-0.569）or betweenδ^13CDIC and oxide-reduction potential（p=0.000;r=0.646）.The striking positive correlation between δ^13CDIC and the sampling distance happened in the summer rainy season,while striking negative correlation happened in the spring dry season,indicating that river-sea interaction influenced water physicochemical parameters and controlled the riverine DIC property in the survey waterway.In view of the riverineδ^13CDIC decreasing for the decomposition of the terrestrial organic matter in the rainy season in summer and increasing for the briny invaded zone extending in the spring dry season along the waterway from the Makou gauging station to the Modaomen outlet,theδ^13CDIC spatio-temporal variation was closely related to the geographical environment of the Xijiang drainage basin.     

Water isotopic and hydrochemical evolution of a lake chain in the northern Great Plains and its paleoclimatic implications

Oxygen isotopes and geochemistry from lake sediments are commonly used as proxies of past hydrologic and climatic conditions, but the importance of present-day hydrologic processes in controlling these proxies are sometimes not well established and understood. Here we use present-day hydrochemical data from 13 lakes in a hydrologically connected lake chain in the northern Great Plains (NGP) to investigate isotopic and solute evolution along a hydrologic gradient. The ¹⁸O and ²H of water from the chain of lakes, when plotted in ²H - ¹⁸O space, form a line with a slope of 5.9, indicating that these waters fall on an evaporation trend. However, 10 of the 13 lakes are isotopically similar (¹⁸O = –6 ± 1 VSMOW) and show no correlation with salinity (which ranges from 1 to 65). The lack of correlation implies that the isotopic composition of various source waters rather than in-lake evaporation is the main control of the ¹⁸O of the lakes. Groundwater, an important input in the water budget of this chain of lakes, has a lower ¹⁸O value (–16.7 in 1998) than that of mean annual precipitation (–11) owing to selective recharge from snow melt. For the lakes in this chain with salinity < 15, the water Mg/Ca ratios are strongly correlated with salinity, whereas Sr/Ca is not. The poor correlation between Sr/Ca and salinity results from uptake of Sr by endogenic aragonite. These new results indicate that ¹⁸O records may not be interpreted simply in term of climate in the NGP, and that local hydrology needs to be adequately investigated before a meaningful interpretation of sedimentary records can be reached.     

Elemental (C,N, H and P) and stable isotope (δ<Superscript>15</Superscript>N and δ<Superscript>13</Superscript>C) signatures in sediments from Zeekoevlei,South Africa: a record of human intervention in the lake

We used elemental carbon, nitrogen, phosphorus and hydrogen ratios (C/N, N/P and H/C) with total organic carbon (TOC) and total phosphorus (TP) as well as stable carbon and nitrogen isotopes (δ¹³C and δ¹⁵N) to investigate the source and depositional conditions of organic matter in sediments from Zeekoevlei, the largest freshwater lake in South Africa. Typical C/N (10–12), H/C ratios (≥1.7) and δ¹³C_organic values (−22 to −19‰) together with the increase in TOC concentration indicate elevated primary productivity in lower middle (18–22 cm) and top (0–8 cm) sections of the sediment cores. Seepage of nutrients from a nearby waste water treatment plant, rapid urbanization and heavily fertilized farming in the catchments are responsible for the increased productivity. Consistent with this, measured δ¹⁵N_organic values (∼11‰) indicate increased raw sewage input towards the top-section of the core. Although cyanobacterial blooms are evident from the low δ¹⁵N values (∼3‰) in mid-section of the core, they did not outnumber the phytoplankton population. Low N/P ratio (∼0) and high TP (100–2,200 mg l⁻¹) support cyanobacterial growth under N limited condition, and insignificant input of macrophytes towards the organic matter pool. Dredging in 1983, caused sub-aerial exposure of the suspended and surface sediments, and affected organic matter preservation in the upper mid-section (12–14 cm) of the core.