Christoph Häggi

and 8 more

The stable carbon isotope composition (δ13C) of plant components such as plant wax biomarkers is an important tool for reconstructing past vegetation. Plant wax δ13C is mainly controlled by photosynthetic pathways, allowing for the differentiation of C4 tropical grasses and C3 forests. Proxy interpretations are however complicated by additional factors such as aridity, vegetation density, elevation, and the considerable δ13C variability found among C3 plant species. Moreover, studies on plant wax δ13C in tropical soils and plants have focused on Africa, while structurally different South American savannas, shrublands and forests remain understudied. Here, we analyze the δ13C composition of long-chain n-alkanes and fatty acids from tropical South American soils and leaf litter to assess the isotopic variability in each vegetation type and to investigate the influence of climatic features on δ13C. Rainforests and open vegetation types show distinct values, with rainforests having a narrow range of low δ13C values (n-C29 n-alkane: -34.5 +0.9/-0.6 ‰ ; Suess-effect corrected) allowing for the detection of even minor incursions of savanna into rainforests (13C-enriched). While Cerrado savannas and semi-arid Caatinga shrublands grow under distinctly different climates, they can yield indistinct δ13C values for most compounds. Cerrado soils and litter show pronounced isotopic spreads between the n-C33 and n-C29 alkanes, while Caatinga shrublands show consistent values across the two homologues, thereby enabling the differentiation of these vegetation types. The same multi-homologue isotope analysis can be extended to differentiate African shrublands from savannas.

Rachel So

and 4 more

The Great Salt Lake (UT) is a hypersaline terminal lake in the US Great Basin, and the remnant of the late glacial-pluvial Lake Bonneville. During the Holocene, hydroclimate variations have been more subtle in the basin. These variations can be investigated by organic geochemical methods within the sediment core GLAD1-GSL00-1B, cored in 2000 and recently well-dated by radiocarbon for the Holocene section (Bowen et al., 2019) with 11 meters representing 8 ka to present. Sediment samples every 30 cm (~200 years) were extracted and the total lipid extracts were analyzed by HPLC-MS to detect the full suite of microbial membrane lipids, including those responsive to temperature and salinity. Modern samples were also collected to provide local calibration for the archaeol-caldarchaeol ecometric (ACE) salinity proxy, where ACE = archaeol/(archaeol + caldarchaeol). ACE detects the increase in lipids of halophilic archaea, relative to generalists, as salinity increases. From currently analyzed data and calibrations, we find Holocene lake salinity estimates ranged from 239 to 283 psu, suggesting persistent hypersalinity with < 50 psu variability across 8 kyr. For comparison, the modern salinity of the lake ranges from 100 to 160 psu in the southern half, and 240 to 270 psu in the north. From ~7-6 ka, salinity estimates were relatively high at 270 to ~280 psu. Following 6 ka, salinity decreases and reaches its lowest value of 239 psu at 4.8 ka. Afterwards, salinity increases and varies between ~250 to ~270 psu, remaining at 270 psu in the last 1 kyr. This new salinity record is compared to available shoreline reconstructions and regional climate records. The temperature proxy, MBT’5Me,­ as calibrated by BayMBT, suggests mean annual air temperature estimates ranged from 12°C to 24°C (compared to modern mean temperature of 13°C). This indicates a substantial, variable complication from salinity in this consistently hypersaline lake, as recently reported for the MBT’5Me­ proxy.