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Abstract South American summer monsoon (SASM) strength tracks insolation on orbital timescales, linking global climate and continental hydrology. However, whether local water availability also responds to global climate forcings is unclear. Here, we present water balance records from Lake Junín, an Andean lake within the SASM domain. Local water balance and SASM strength is inferred from triple oxygen isotopes of lake carbonates during two interglacial periods (Marine Isotope Stage (MIS) 15, 621–563 ka; the Holocene, 11.7–0 ka). We find SASM strength and water balance both follow the precession‐pacing of local summer insolation, with the driest conditions occurring at Lake Junín under weakened SASM conditions (and vice versa). Further, the largest variations occurred during MIS 15, when insolation was more variable than the Holocene. These results suggest that global climate influences South American hydrology on both the local and continental scales, with implications for tropical water resources, the atmospheric greenhouse effect, and ecosystem dynamics. 

In humid, continental Michigan, we identified pedogenic carbonate in a soil profile developed on glacial drift sediments, as rinds, rhizoliths, and filaments (at depths >50 cm). Given that the climate setting is unusual for pedogenic carbonate, we investigated its formation with environmental monitoring and isotope analyses of carbonate (δ13C, δ18O, Δ47, and 14C) and waters (δ18O and δ2H). We found covariation in δ13C and Δ47 amongst the carbonate types (rhizoliths, rinds, filaments, bulk soil, and detrital clasts), and 14C ages of rinds that predate plausible formation ages. The δ13C and Δ47 values of the bulk carbonate and some of the pedogenic morphologies are not fully compatible with pedogenic formation in the modern environment. The δ18O data from precipitation and river waters and from carbonates are not uniquely identifying; they are compatible with the soil carbonate being pedogenic, detrital, or a mix. We conclude that the soil carbonate is likely a physical mix of pedogenic and detrital carbonate. Pedogenic carbonate is forming in this humid setting, likely because seasonal cycles in soil respiration and temperature cause cycles of dissolution and re-precipitation of detrital and pedogenic carbonate. The pedogenic carbonate may be a transient feature as carbonate-rich till undergoes post-glacial chemical weathering.