Spatial variations in δ13C and δ15N values of primary consumers in a coastal lagoon

Seasonal variations in bulk tissue, fatty acid and monosaccharide δ13C values of leaves from mesotrophic grassland plant communities under different grazing managements

We examine patterns of intra-otolith variation in δ13C values of fossil Aplodinotus grunniens (freshwater drum) otoliths recovered from an archeological site in northeast Tennessee. We find three repeatable patterns: an initial increase early in ontogeny followed by relatively stable δ13C values as the fish ages, an initial strong covariation between seasonal δ18O and δ13C values, and a decrease with age in the magnitude of seasonal change in δ13C values. These last two observations are illustrated by seasonal least-squares linear regressions between δ13C and δ18O values that tend to progressively decrease in r2 value and slope with fish age. These patterns are evaluated by using a mass balance model in which otolith δ13C values are derived from dissolved inorganic carbon of ambient water mixing with carbon derived from metabolic processes. The proportion of metabolically derived carbon is found to be the dominant factor controlling intra-otolith variation in δ13C values. Thus, the difference between maximum and minimum δ13C values from a single otolith (δ13Cmax–min) is postulated to reflect the total change in metabolic rate over the lifetime of a fish. δ13Cmax–min values significantly and negatively covary with average δ18O(CaCO3) values, suggesting either a higher total change in metabolic rate over the lifetime of a fish in cooler climates characterized by shorter growing seasons, or a decrease in summer/winter precipitation ratio. A proxy for metabolic rate preserved in otoliths would facilitate the understanding of evolutionary history in physiological traits of fishes and improve our understanding of bioenergetics.

The Qinling Mountains, serving as a natural geographical and climatic boundary in China, require comprehensive climatic records to elucidate the trends in climate changes across the country. While stable isotopes in tree rings are widely employed to indicate historical environmental changes, investigations into tree ring isotopes in the Qinling Mountains, particularly within the widespread broad-leaf oaks, remain limited. In this study, we investigated both intra- and inter-annual variations in the δ13C values of tree rings and their correlations with climatic signals over the past two decades for Quercus aliena var. acuteserrata, a dominant species among oak trees on the main peak of the Qinling Mountains. Our results reveal that responses to climate differ among altitudes and individual trees, with trees at higher altitudes exhibiting higher sensitivity to extreme climate, which is low temperatures and rainfall fluctuations during the growth period in intra-annual δ13C variations. Furthermore, the positive correlations are observed between temperature during growing season and both tree growth and the inter-annual δ13C variations. However, the climate signal appears to be hampered by oak-specific factors, such as intense competition among individuals and the age of trees. Therefore, we suggest a more rigorous selection of sampling and propose further investigations into isotopic fractionation processes in oaks for future studies.

Variability in δ13C values between individual Daphnia ephippia: Implications for palaeo-studies

This study aimed to: (1) investigate intra-sample variability in the stable isotope composition (δ13C and δ18O values) measured in several individual mollusc shells; and (2) determine the optimum number of individual mollusc shells required to obtain stable isotope values representative of the mean climate signal for a sediment sample. Seven hundred and six gastropod shells were analysed, representing eight species. These eight species were most abundant and consistently present in the sediment sequence of the Paddenluch outcrop, Brandenburg, northeast Germany. Significant differences between minimum and maximum δ13C and δ18O values of the shells were recorded within all sediment samples and for all analysed species. Within the sediment samples, the greatest mean variability in both δ13C and δ18O values was found for Hippeutis complanatus, 5.84 and 5.23 ‰, respectively. The greatest intra-specific variability in C and O isotope values within individual sediment samples, however, was 10.2 and 6.8 ‰, respectively. Significant differences between minimum and maximum δ13C and δ18O values of individual mollusc shells within the same sediment sample are probably the result of population isotope variability, variations in species life span, thickness of the sediment sample, sediment accumulation rate, and environmental fluctuations during the time span when the sediment was deposited. Shells were randomly selected to determine the optimum number of shells necessary to obtain stable isotope values that are representative of the mean climate signal, from a 1-cm sample of sediment. For each layer of the Paddenluch sediment sequence, 15 or more shells (N ≥ 15) was the required sample size to provide representative isotope values and yield a reliable mean isotope value. Sample sizes with fewer shells displayed more variable mean δ13C and δ18O values. Stable isotope composition of the analyzed molluscs was species-specific, with differences in mean δ13C and δ18O values of 2.5 and 3 ‰, respectively. This illustrates the need to use mono-specific samples throughout a sediment sequence to generate reliable data.

The stable carbon isotope composition, expressed as δ13C values, of chitinous resting stages of planktivorous invertebrates can provide information on past changes in carbon cycling in lakes. For example, the δ13C values of cladoceran ephippia and bryozoan statoblasts have been used to estimate the past contribution of methane-derived carbon to lake food webs and variations in the δ13C value of planktonic algae. Limited information, however, is available concerning seasonal variations in δ13C values of these organisms and their resting stages. We measured the seasonal variation in δ13C values of Daphnia (Branchiopoda: Cladocera: Daphniidae) and their floating ephippia over a 2-year period in small, dimictic Lake Gerzensee, Switzerland. Floating ephippia of Ceriodaphnia (Branchiopoda: Cladocera: Daphniidae) and statoblasts of Plumatella (Phylactolaemata: Plumatellida: Plumatellidae) were analysed during parts of this period. Furthermore, δ13C values of remains from all three organism groups were analysed in a 62-cm-long sediment core. Throughout the year, Daphnia δ13C values tracked the δ13C values of particulate organic matter (POM), but were more negative than POM, indicating that Daphnia also utilize a relatively 13C-depleted carbon source. Daphnia ephippia δ13C values did not show any pronounced seasonal variation, suggesting that they are produced batch-wise in autumn and/or spring and float for several months. In contrast, δ13C values of Ceriodaphnia ephippia and Plumatella statoblasts followed variations in δ13CPOM values, Ceriodaphnia values being the most negative of the resting stages. Average cladoceran ephippia δ13C values in the flotsam agreed well with ephippia values from Gerzensee surface sediments. In contrast, average Plumatella statoblast δ13C values from the flotsam were 4‰ more negative than in the surface sediments. In the sediment core, δ13C values of the two cladocerans remained low (mean −39.0 and −41.9‰) throughout the record. In contrast, Plumatella had distinctly less negative δ13C values (mean −32.0‰). Our results indicate that in Gerzensee, Daphnia and Ceriodaphnia strongly relied on a 13C-depleted food source throughout the past 150 years, most likely methane-oxidising bacteria, whereas this food source was not a major contribution to the diet of bryozoans.

We used the stable isotopes of carbon and nitrogen to examine the food webs of three small flood-plain lakes (billabongs) in south-eastern Australia. With few exceptions, stable carbon isotope analysis could not be used to discriminate among the conspicuous potential sources of fringing, emergent or floating vegetation or benthic detritus. These primary sources showed little spatial or temporal variation in δ13C values, with means ranging from-28.5 to-26.8‰ in spring and-29.1 to-25.4‰ in late summer. Submerged vegetation had similar δ13C values to the above sources in spring but showed greater spatial variation and were less 13C-depleted, considerably so in some species, in late summer. Epiphytes and algae were 13C-depleted in spring compared with the other primary sources but became more 13C-enriched in late summer. Mean δ13C values for primary and secondary consumers were not only far more variable (-37.4 to-22.7‰) but in general were more negative than the potential food sources, particularly in spring. Using the combined information from stable carbon and nitrogen isotope analysis, we could narrow down the list of potential primary sources driving food webs in these billabongs. The freshwater crayfish (Cherax) was one of the few taxa that appeared to obtain its biomass carbon from detrital material. Gastropods and leptocerid caddis larvae on emergent or submerged vegetation obtained a mixture of carbon from epiphytes and macrophytes; in both taxa, epiphytes contributed more to biomass carbon than did the macrophytes. However, other common grazers and collector/gatherers sampled from macrophytes, e.g. baetid mayflies, chironomid larvae and atyid shrimps, were often too 13C-depleted even to have derived their biomass carbon solely from epiphytes. Many other primary consumers, including zooplankton, and mussels (Velesunio), and most of the secondary consumers, including water mites (Hydracarina), phantom midge larvae (Chaoborus) and fish, were also 13C-depleted. The enormous biomass of littoral and fringing vegetation could contribute to metazoan food webs in these billabongs only if an additional highly 13C-depleted source was consumed simultaneously. Methane released from billabong sediments could provide such a 13C-depleted carbon source that is re-introduced into metazoan food webs via the consumption of methanotrophic bacteria. Alternatively, food webs in these water bodies are largely driven by an unknown and inconspicuous 13C-depleted primary producer, such as planktonic Chlorophyta.

Carbon and nitrogen sources in tropical coastal lagoon food webs under variable hydrological conditions

Migratory birds travel vast distances and the timing of migratory flights can affect survival and the ability to reproduce. For Neotropical migrant songbirds, early spring departure from wintering sites, early arrival to the breeding grounds and higher reproductive success have been related to the use of suitable habitats and environmental conditions during the non-breeding season. However, how migratory strategies are shaped by winter habitat choice is largely unknown due to the general inability to track birds from specific wintering habitats to stopovers or breeding destinations. We assessed how winter habitat (native forest vs. shade-grown coffee plantations) relates to spring departure date and migration pace in Swainson's Thrush Catharus ustulatus. We also determined the effect of departure date and total migration duration on the arrival date of birds detected near or within their breeding range. We used a novel application of Motus radiotelemetry arrays to track individuals from their wintering grounds in the Andes of South America along their migratory journey to North America. We found variation in migratory strategies between habitats, with birds wintering in native forest departing later than birds in coffee. We present isotopic evidence for native forest being of higher quality than shade-coffee for Swainson's Thrush and hypothesize that moister conditions in forest, as shown by stable isotope (δ13 C) analysis of thrush whole blood, provides favourable pre-migratory conditions allowing birds to delay departure from wintering grounds. Habitat, between-site and -year variation in departure date, suggests that birds made facultative adjustments to winter habitat quality and environmental conditions. Independent of habitat, birds that departed later migrated faster and this pattern was maintained along the migration route (n=44). Migrating earlier and slower or later and faster was unlikely to result in significant differences in arrival time to breeding destinations. Our findings reveal underappreciated complexity in migratory decisions by long-distance migrants that contrast with the current paradigm of earlier departures and arrival from optimal habitats. The next step is to understand the relative fitness benefits of early versus late schedules or whether each strategy is an equally good response to experienced conditions.

Nitrogen and carbon stable isotopic compositions (δ15N and δ13C) of consumers have been used for physiological and food web studies. Previous studies have shown δ15N and δ13C values are affected by several biological and environmental factors during starvation, but the generality of the effect of starvation on δ15N and δ13C values has not yet been tested. Here, we performed a meta-analysis to evaluate the effects of starvation on δ15N and δ13C values of consumers, and the underlying factors that may explain the observed variation. The δ15N and δ13C values were calculated as the differences between the final δ15N and δ13C values of consumers (post-starvation) and the pre-starvation values on each experiment. Our meta-analysis showed a large variation in the δ15N and δ13C values of consumers (δ15N range: –0.82 to 4.30‰; mean: 0.47‰ and δ13C range: –1.92 to 2.62‰; mean: 0.01‰). The δ15N values of most consumers increased along the length of the starvation period and were influenced by nitrogen excretion and thermoregulation types, probably because differences in nitrogen metabolism and thermoregulation affect nitrogen processing and excretion rates. None of our predictor variables accounted for the variation in δ13C values, which showed both increases and decreases due to fasting. Our findings suggest that starvation results in changes in consumer δ15N values which are mainly explained by the length of the fasting period and by nitrogen and energy metabolism, but the underlying mechanisms of the starvation effects on δ13C values seem to be more complex than previously thought.

The ∼3.5 Ga Dresser Formation from the North Pole Dome of the Pilbara Craton (Western Australia) contains some of the oldest evidence for life on Earth. Here, we present a detailed study of microstructure-specific carbon isotopic composition of organic matter (OM) preserved in Dresser Formation bedded cherts and hydrothermal chert vein using in situ Secondary-Ion Mass Spectrometry (SIMS). The OM in these rocks occurs mainly as clots that, together with minor fine OM layers and laminae, are considered primary textures formed prior to host rock lithification. Other than rare OM-rich stylolites, no evidence was found for later OM migration beyond the micrometer scale. Average δ13C(OM) values in specific microstructural types range between −33.6‰ and −25.7‰. No correlation is seen between measured δ13C values and H/C ratios in the studied OM microstructures. This lack of correlation and the low metamorphic grade of the rocks studied argue against significant modification of OM isotopic composition by later metamorphic alteration. It is thus concluded that the range of δ13C values found in the samples represents primary OM isotopic variability. Within some individual samples variable δ13C(OM) values are correlated with specific microstructural types. This observation is not consistent with solely abiotic OM formation via Fisher-Tropsch type reactions. When compared with associated δ13C(ankerite) values, average δ13C(OM) values indicate C isotopic fractionation [Δ13C(Ank–OM)] of 25–33‰, which translates to dissolved CO2–OM isotopic fractionation [Δ13C(CO2–OM)] of 20–30‰. This range of Δ13C(CO2–OM) is consistent with enzymatic C fixation via the Calvin cycle utilized by photoautotrophs and the reductive acetyl-CoA pathway utilized by chemolithoautotrophs. Photosynthetic OM formation is supported by the relatively shallow water depth inferred for the Dresser environment and the restricted occurrence of stromatolites to shallow water deposits in this unit, whereas chemolithosynthesis is supported by the abundance of OM in sub-seafloor hydrothermal chert veins. The range of δ13C(OM) values observed in the samples may therefore represent the remains of different organisms utilizing different C-fixation pathways. Other biologic effects, such as the growth rate and density of microbial communities, and further heterotrophic overprinting of the autotrophic biomass may have also contributed to the observed range of δ13C(OM) values.

ABSTRACTDissolved inorganic carbon (DIC) in ocean water is a major sink of fossil fuel derived CO2. Carbon isotopes in DIC serve as tracers for oceanic water masses, biogeochemical processes, and air-sea gas exchange. We present a timeseries of surface DIC δ13C and Δ14C values from 2011 to 2022 from Newport Beach, California. This is a continuation of previous timeseries (Hinger et al. 2010; Santos et al. 2011) that together provide an 18-year record. These data show that DIC Δ14C values have declined by 42‰ and that DIC δ13C values have declined by 0.4‰ since 2004. By 2020, DIC Δ14C values were within analytical error of nearby clean atmospheric CO2 Δ14C values. These long-term trends are likely the result of significant fossil fuel derived CO2 in surface DIC from air-sea gas exchange. Seasonally, Δ14C values varied by 3.4‰ between 2011 and 2022, where seasonal δ13C values varied by 0.7‰. The seasonal variation in Δ14C values is likely driven by variations in upwelling, surface eddies, and mixed layer depth. The variation in δ13C values appears to be driven by isotopic fractionation from marine primary producers. The DIC δ13C and Δ14C values record the influence of the drought that began in 2012, and a major upwelling event in 2016.

Dacryoconarids are extinct marine zooplankton known from abundant, globally distributed calcite microfossils in the Devonian, but their shell stable isotope composition has not been previously explored. Devonian stable isotope stratigraphy is currently limited to less common invertebrates or bulk rock analyses of uncertain provenance. As with Cenozoic planktonic foraminifera, isotopic analysis of dacryoconarid shells could facilitate higher-resolution, geographically widespread stable isotope records of paleoenvironmental change, including marine hypoxia events, climate changes, and biocrises. We explored the use of Dacryoconarid isotope stratigraphy as a viable method in interpreting paleoenvironments. We applied an established method for determining stable isotope ratios (δ(13) C, δ(18) O values) of small carbonate microfossils to very well-preserved dacryoconarid shells. We analyzed individual calcite shells representing five common genera using a Kiel carbonate device coupled to a MAT 253 isotope ratio mass spectrometer. Calcite shell δ(13) C and δ(18) O values were compared by taxonomic group, rock unit, and locality. Single dacryoconarid calcite shells are suitable for stable isotope analysis using a Kiel-IRMS setup. The dacryoconarid shell δ(13) C values (-4.7 to 2.3‰) and δ(18) O values (-10.3 to -4.8‰) were consistent across taxa, independent of shell size or part, but varied systematically through time. Lower fossil δ(18) O values were associated with warmer water temperature and more variable δ(13) C values were associated with major bioevents. Dacryoconarid δ(13) C and δ(18) O values differed from bulk rock carbonate values. Dacryoconarid individual microfossil δ(13) C and δ(18) O values are highly sensitive to paleoenvironmental changes, thus providing a promising avenue for stable isotope chemostratigraphy to better resolve regional to global paleoceanographic changes throughout the upper Silurian to the upper Devonian. Our results warrant further exploration of dacryoconarid stable isotope proxy sensitivity, the isotopic contrast among dacryoconarids, other taxa, and bulk rock, as well as other potential dacryoconarid proxies (Mg/Ca, Sr/Ca, (87) Sr/(86) Sr, microlaser and ion microprobe isotope techniques, and clumped isotopes) for stratigraphic research.

Stable oxygen and carbon isotope systematics of exquisitely preserved Turonian foraminifera from Tanzania — Understanding isotopic signatures in fossils

This study examines the distribution of soil organic carbon and carbon-isotopes with depth and among particle size fractions in 2 forest soil profiles of contrasting texture from Cape York Peninsula, Queensland, Australia. The profile on sand has a comparatively low inventory of carbon (557 mg/cm2 from 0–100 cm) and exhibits comparatively small variations in d13C value. In contrast, the clay-rich profile has a much larger inventory of soil organic carbon (1725 mg/cm2 from 0–100 cm) and large variations in d13C value occur both with depth in the profile and between different particle size fractions. The considerable differences in carbon inventories and d13C values between the sites appear to be largely due to soil textural differences. In the absence of fine minerals the trend in d13C value with decreasing particle size is to similar or lower d13C values, due to an increase in the relative abundance of low d13C compounds in the residue left by microbial decomposition. In the presence of fine minerals, the trend is to higher d13C values due to the stabilisation of the products of microbial decomposition by the fine minerals. Thus, the bulk d13C value of soil organic carbon appears to be determined as much by the abundance of fine minerals in a soil profile as by isotope fractionation effects accompanying degradation. It is further postulated that an initial rapid rise in d13C value in the upper soil layers is due to an increase in the relative importance of higher 13C, root-derived carbon immediately below the soil surface.