999 resultados para Calculated from stable oxygen isotopes
Resumo:
There is increasing evidence that the preceding Holocene climate was as unstable as the last glacial period, although variations occurred at much lower amplitudes. However, low-latitude climate records that confirm this variability are sparse. Here we present a radiocarbon-dated Holocene marine record from the tropical western Atlantic. Aragonite dissolution derived from the degree of preservation of the pteropod Limacina inflata records changes in the corrosiveness of the bottom water at the core site due to the changing influence of northern versus southern water masses. The delta18O difference between the shallow-living planktonic foraminifera Globigerinoides sacculifer and the deep-living Globorotalia tumida is used as proxy for changes in the vertical stratification of the surface water, hence the trade wind strength at this latitude. We compared our data to high-latitude records of the North Atlantic region. A good agreement is found between the aragonite dissolution and the strength in the Island-Scotland Overflow Water, which contributes significantly to the North Atlantic Deep Water. This suggests that large-scale variations in the Atlantic thermohaline circulation occurred throughout the Holocene. Concurrently, the comparison of our Delta delta18O with the GISP2 glaciochemical records points to global Holocene atmospheric reorganizations seen in both the tropics and high northern latitudes.
Resumo:
We investigate aragonitic skeletons of the Caribbean sclerosponge Ceratoporella nicholsoni from Jamaica, 20 m below sea level (mbsl), and Pedro Bank, 125 mbsl. We use d18O and Sr/Ca ratios as temperature proxies to reconstruct the Caribbean mixed layer and thermocline temperature history since 1400 A.D. with a decadal time resolution. Our age models are based on U/Th dating and locating of the radiocarbon bomb spike. The modern temperature difference between the two sites is used to tentatively calibrate the C. nicholsoni Sr/Ca thermometer. The resulting calibration points to a temperature sensitivity of Sr/Ca in C. nicholsoni aragonite of about -0.1 mmol/mol/K. Our Sr/Ca records reveal a pronounced warming from the early 19th to the late 20th century, both at 20 and 125 mbsl. Two temperature minima in the shallow water record during the late 17th and early 19th century correspond to the Maunder and Dalton sunspot minima, respectively. Another major cooling occurred in the late 16th century and is not correlatable with a sunspot minimum. The temperature contrast between the two sites decreased from the 14th century to a minimum in the late 17th century and subsequently increased to modern values in the early 19th century. This is interpreted as a long-term deepening and subsequent shoaling of the Caribbean thermocline. The major trends of the Sr/Ca records are reproduced in both specimens but hardly reflected in the d18O records.
Resumo:
Ocean Drilling Program (ODP) Leg 164 recovered a number of large solid gas hydrate from Sites 994, 996, and 997 on the Blake Ridge. Sites 994 and 997 samples, either nodular or thick massive pieces, were subjected to laboratory analysis and measurements to determine the structure, molecular and isotopic composition, thermal conductivity, and equilibrium dissociation conditions. X-ray computed tomography (CT) imagery, X-ray diffraction, nuclear magnetic resonance (NMR), and Raman spectroscopy have revealed that the gas hydrates recovered from the Blake Ridge are nearly 100% methane gas hydrate of Structure I, cubic with a lattice constant of a = 11.95 ± 0.05 angström, and a molar ratio of water to gas (hydration number) of 6.2. The d18O of water is 2.67 per mil to 3.51 per mil SMOW, which is 3.5-4.0 heavier than the ambient interstitial waters. The d13C and dD of methane are -66 per mil to -70 per mil and -201 per mil to -206 per mil, respectively, suggesting that the methane was generated through bacterial CO2 reduction. Thermal conductivity values of the Blake Ridge hydrates range from 0.3 to 0.5 W/(m K). Equilibrium dissociation experiments indicate that the three-phase equilibrium for the specimen is 3.27 MPa at 274.7 K. This is almost identical to that of synthetic pure methane hydrate in freshwater.