6 research outputs found

    An 1800-year oxygen-isotope record of short- and long-term hydroclimate variability in the northern neotropics from a Jamaican marl lake

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    Hydroclimate variability on multi-decadal timescales has been a prominent feature of the circum-Caribbean region over the common era, with marked dry intervals noted in particular for the period 800–950 CE coinciding with the Terminal Classic Period (the so-called Terminal Classic Drought: TCD) in Mesoamerica, and with the Little Ice Age from about 1500 to 1800 CE, linked to complex ocean-atmosphere interactions. Previous compilations of palaeoclimate reconstructions have revealed a clear precipitation dipole between northern and southern Mesoamerica over the common era, which is consistent with meteorological data and modelling experiments. However, patterns of variability elsewhere within the region are less well understood, although palaeoclimate records do point to spatial complexity. Here, we present a ∼sub-decadal-scale lake-sediment hydroclimate reconstruction based on ostracod-shell stable isotopes from Wallywash Great Pond, Jamaica, covering the past ∼1800 years, which fills a spatial gap in records for the region. Variations in δ18O values at this site are a proxy for changes in effective moisture and they reveal a marked wet phase over the Terminal Classic Period (TCP), suggesting that the precipitation dipole over northern and southern Mesoamerica may have an east to west component. This is supported by some previous studies, although additional sites are required from strategic localities within the region to confirm this. The Little Ice Age interval at Wallywash is drier than the TCP, although the signal is less clear than at some sites within the wider region, suggesting that regional complexity in hydroclimate has characterised this interval as well

    Effect of moisture on leaf litter decomposition and its contribution to soil respiration in a temperate forest

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    The degree to which increased soil respiration rates following wetting is caused by plant (autotrophic) versus microbial (heterotrophic) processes, is still largely uninvestigated. Incubation studies suggest microbial processes play a role but it remains unclear whether there is a stimulation of the microbial population as a whole or an increase in the importance of specific substrates that become available with wetting of the soil. We took advantage of an ongoing manipulation of leaf litter <sup>14</sup>C contents at the Oak Ridge Reservation, Oak Ridge, Tennessee, to (1) determine the degree to which an increase in soil respiration rates that accompanied wetting of litter and soil, following a short period of drought, could be explained by heterotrophic contributions; and (2) investigate the potential causes of increased heterotrophic respiration in incubated litter and 0–5 cm mineral soil. The contribution of leaf litter decomposition increased from 6 ± 3 mg C m<sup>−2</sup> hr<sup>−1</sup> during a transient drought, to 63 ± 18 mg C m<sup>−2</sup> hr<sup>−1</sup> immediately after water addition, corresponding to an increase in the contribution to soil respiration from 5 ± 2% to 37 ± 8%. The increased relative contribution was sufficient to explain all of the observed increase in soil respiration for this one wetting event in the late growing season. Temperature (13°C versus 25°C) and moisture (dry versus field capacity) conditions did not change the relative contributions of different decomposition substrates in incubations, suggesting that more slowly cycling C has at least the same sensitivity to decomposition as faster cycling organic C at the temperature and moisture conditions studied

    Testing sealed-tube Graphitization at the NERC Radiocarbon facility, East Kilbride

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    Graphitization of 0.5–1.5 mg C, and of smaller samples to a lesser extent, is routinely done at our Facility by reduction over zinc. The method yields low background, good accuracy but offers a limited throughput, requires dedicated equipment and considerable operator time. Sealed-tube graphitization is faster, easier and cost-efficient producing as many graphites as CO2 can be purified in one day with low background, good accuracy and precision, provided precise measurements of δ13C values can be attained by accelerator mass spectrometry (AMS) to correct for isotope fractionation (Xu et al. 2007). We tested sealed-tube graphitization on 0.1 to 1.0 mg C samples and found that while we were able to obtain low backgrounds of >57,000 ±1000 yr BP for ∼1.7 mg C and 41,230 ± 430 yr BP for ∼0.09 mg C (0.0008 ± 0.0001 and 0.0059 ± 0.0003 Fraction Modern, respectively), results were variable for sample sizes <0.5 mg C. Measurements of FIRI Belfast Cellulose and TIRI Barleymash showed 0.3–0.6% precision and 1% accuracy for most sample sizes. We found better results in our laboratory by introducing the following modifications: (1) shorter inner tube (2 cm long), (2) short flame-seal length (∼7–8 cm) and (3) keeping the inner tube with iron separate from the outer tube containing zinc and titanium hydride during cleaning
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