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In the southwestern United States, California (CA) is one of the most climatically sensitive regions given its low (≤250 mm/year) seasonal precipitation and its inherently variable hydroclimate, subject to large magnitude modulation. To reconstruct past climate change in CA, cave calcite deposits (stalagmites) have been utilized as an archive for environmentally sensitive proxies, such as stable isotope compositions (δ¹⁸O, δ¹³C) and trace element concentrations (e.g., Mg, Ba, Sr). Monitoring the cave and associated surface environments, the chemical evolution of cave drip-water, the calcite precipitated from the drip-water, and the response of these systems to seasonal variability in precipitation and temperature is imperative for interpreting stalagmite proxies. Here we present monitored drip-water and physical parameters at Lilburn Cave, Sequoia Kings Canyon National Park (Southern Sierra Nevada), CA, and measured trace element concentrations (Mg, Sr, Ba, Cu, Fe, Mn) and stable isotopic compositions (δ¹⁸O, δ²H) of drip-water and for calcite (δ¹⁸O) precipitated on glass substrates over a two-year period (November 2018 to February 2021) to better understand how chemical variability at this site is influenced by local and regional precipitation and temperature variability. Despite large variability in surface temperatures and precipitation amount and source region (North Pacific vs. subtropical Pacific), Lilburn Cave exhibits a constant cave environment year-round. At two of the three sites within the cave, drip-water δ¹⁸O and δ²H are influenced seasonally by evaporative enrichment. At a third collection site in the cave, the drip-water δ¹⁸O responds solely to precipitation δ¹⁸O variability. The Mg/Ca, Ba/Ca, and Sr/Ca ratios are seasonally responsive to prior calcite precipitation at all sites but minimally to water-rock interaction. Lastly, we examine the potential of trace metals (e.g., Mn²⁺and Cu²⁺as a geochemical proxy of recharge and find that variability in their concentrations has high potential to denote the onset of the rainy season in the study region. The drip-water composition is recorded in the calcite, demonstrating that stalagmites from Lilburn Cave, and potentially more regionally, could record seasonal variability in weather even during periods of substantially reduced rainfall. 

Abstract Application of novel proxies, such as the stable isotope compositions and noble gas concentrations of fossil drip water trapped as inclusions in stalagmites, have the potential to provide unique constraints on past hydroclimate states and surface temperatures. Geochemical analysis of inclusion waters, however, requires an understanding of the three‐dimensional spatial distribution of dominantly liquid‐ versus air‐filled inclusions in a given stalagmite. Here we couple neutron computed tomography and medium‐ to high‐resolution X‐ray computed tomography to map out the three‐dimensional calcite density and distribution of liquid‐ versus air‐filled inclusions within a Sierra Nevada stalagmite (ML‐1), which formed during the last deglaciation (18.5 to 11.7 ka). Comparison of coupled neutron computed tomography‐X‐ray computed tomography results with a time series of stalagmite calcite fabrics indicates that although highest density calcite contains abundant liquid (fluid)‐filled inclusions, calcite density and fabric overall were secondary controls on the liquid inclusion distribution (LID). Furthermore, a multistatistical evaluation of the stalagmite time series indicates a significant relationship at the multicentury‐ to millennial‐scale between LID and calcite δ¹⁸O and δ¹³C that suggests a potential link between LID and water availability to the cave.