scholarly journals Origin and percolation times of Milandre Cave drip water determined by tritium time series and beryllium-7 data from Switzerland

2020 ◽  
Vol 222 ◽  
pp. 106346
Author(s):  
Stéphane Affolter ◽  
Philipp Steinmann ◽  
Franziska Aemisegger ◽  
Roland Purtschert ◽  
Markus Leuenberger
2020 ◽  
Vol 47 (5) ◽  
Author(s):  
Shelby A. Ellis ◽  
Kim M. Cobb ◽  
Jessica W. Moerman ◽  
Judson W. Partin ◽  
A. Landry Bennett ◽  
...  

2013 ◽  
Vol 9 (1) ◽  
pp. 377-391 ◽  
Author(s):  
T. Kluge ◽  
H. P. Affek ◽  
T. Marx ◽  
W. Aeschbach-Hertig ◽  
D. F. C. Riechelmann ◽  
...  

Abstract. The geochemical signature of many speleothems used for reconstruction of past continental climates is affected by kinetic isotope fractionation. This limits quantitative paleoclimate reconstruction and, in cases where the kinetic fractionation varies with time, also affects relative paleoclimate interpretations. In carbonate archive research, clumped isotope thermometry is typically used as proxy for absolute temperatures. In the case of speleothems, however, clumped isotopes provide a sensitive indicator for disequilibrium effects. The extent of kinetic fractionation co-varies in Δ47 and δ18O so that it can be used to account for disequilibrium in δ18O and to extract the past drip-water composition. Here we apply this approach to stalagmites from Bunker Cave (Germany) and calculate drip-water δ18Ow values for the Eemian, MIS3, and the Holocene, relying on independent temperature estimates and accounting for disequilibrium. Applying the co-variation method to modern calcite precipitates yields drip-water δ18Ow values in agreement with modern cave drip-water δ18Ow of −7.9 ± 0.3‰, despite large and variable disequilibrium effects in both calcite δ18Oc and Δ47. Reconstructed paleo-drip-water δ18Ow values are lower during colder periods (e.g., MIS3: −8.6 ± 0.4‰ and the early Holocene at 11 ka: −9.7 ± 0.2‰) and show higher values during warmer climatic periods (e.g., the Eemian: −7.6 ± 0.2‰ and the Holocene Climatic Optimum: −7.2 ± 0.3‰). This new approach offers a unique possibility for quantitative climate reconstruction including the assessment of past hydrological conditions while accounting for disequilibrium effects.


2019 ◽  
Vol 651 ◽  
pp. 2175-2186 ◽  
Author(s):  
Carol V. Tadros ◽  
Pauline C. Treble ◽  
Andy Baker ◽  
Stuart Hankin ◽  
Regina Roach

2019 ◽  
Vol 7 (2) ◽  
pp. 33 ◽  
Author(s):  
Eric Marques ◽  
Gislaine Silva ◽  
João Dias ◽  
Eduardo Gross ◽  
Moara Costa ◽  
...  

Restricted contact with the external environment has allowed the development of microbial communities adapted to the oligotrophy of caves. However, nutrients can be transported to caves by drip water and affect the microbial communities inside the cave. To evaluate the influence of aromatic compounds carried by drip water on the microbial community, two limestone caves were selected in Brazil. Drip-water-saturated and unsaturated sediment, and dripping water itself, were collected from each cave and bacterial 16S rDNA amplicon sequencing and denaturing gradient gel electrophoresis (DGGE) of naphthalene dioxygenase (ndo) genes were performed. Energy-dispersive X-ray spectroscopy (EDX) and atomic absorption spectroscopy (AAS) were performed to evaluate inorganic nutrients, and GC was performed to estimate aromatic compounds in the samples. The high frequency of Sphingomonadaceae in drip water samples indicates the presence of aromatic hydrocarbon-degrading bacteria. This finding was consistent with the detection of naphthalene and acenaphthene and the presence of ndo genes in drip-water-related samples. The aromatic compounds, aromatic hydrocarbon-degrading bacteria and 16S rDNA sequencing indicate that aromatic compounds may be one of the sources of energy and carbon to the system and the drip-water-associated bacterial community contains several potentially aromatic hydrocarbon-degrading bacteria. To the best of our knowledge, this is the first work to present compelling evidence for the presence of aromatic hydrocarbon-degrading bacteria in cave drip water.


Radiocarbon ◽  
2010 ◽  
Vol 52 (4) ◽  
pp. 1529-1544 ◽  
Author(s):  
J Fohlmeister ◽  
A Schröder-Ritzrau ◽  
C Spötl ◽  
S Frisia ◽  
R Miorandi ◽  
...  

14C and δ13C values of C-containing species in cave drip waters are mainly controlled by the C isotope composition of karst rock and soil air, as well as by soil carbon dynamics, in particular the amount of soil CO2 in the unsaturated soil zone and the process of calcite dissolution. Here, we investigate soil carbon dynamics by analyzing the 14C activity and δ13C values of C dissolved in cave drip water. Monthly over a 2-yr period, we collected drip water from 2 drip sites, one fast and one relatively slow, within the shallow Grotta di Ernesto Cave (NE Italy). The 14C data reveal a pronounced annual cycle. In contrast, the δ13C values do not show an annual pattern and only small interannual variability compared to the δ13C values of soil waters. The annual 14C drip-water cycle is a function of drip-rate variability, soil moisture, and ultimately hydrology.


2010 ◽  
Vol 394 (3-4) ◽  
pp. 396-406 ◽  
Author(s):  
T. Kluge ◽  
D.F.C. Riechelmann ◽  
M. Wieser ◽  
C. Spötl ◽  
J. Sültenfuß ◽  
...  
Keyword(s):  

2015 ◽  
Vol 166 ◽  
pp. 15-28 ◽  
Author(s):  
Helen Rutlidge ◽  
Martin S. Andersen ◽  
Andy Baker ◽  
Khorshed J. Chinu ◽  
Mark O. Cuthbert ◽  
...  

2021 ◽  
Author(s):  
Xia Wu ◽  
Moucheng Pan ◽  
Meiliang Zhang ◽  
Jianhua Cao

Abstract The hydrogeochemistry of cave drip water is an important environmental index in cave systems, and drip water monitoring may be an essential solution for paleoclimate reconstructions. We measured the hydrogeochemical properties of the seasonal and perennial drip water and CO2 concentrations from 2015 to 2019 in Liangfeng Cave, Guilin, Southwest China. This study identified the difference in the regional environmental records in perennial and seasonal drip water. By comparing the regional climate data recorded by the drip water, the results showed the perennial drip water recorded regional climate information throughout the year, while the seasonal drip water only recorded the high precipitation periods. The precipitation during the 2015 dry season was abnormally high, which not sure what index is higher than the values in other rainy seasons. This indicates that hydrogeochemistry only represents changes in precipitation and not the alternation of dry and rainy seasons during this period.


2021 ◽  
Vol 9 ◽  
Author(s):  
Barbara E. Wortham ◽  
Isabel P. Montañez ◽  
Kimberly Bowman ◽  
Daphne Kuta ◽  
Nora Soto Contreras ◽  
...  

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.


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