Geology ReportsSearch

USGS · 70015007

U-series ages of solitary corals from the California coast by mass spectrometry

Abstract

The purpose of this study is to evaluate the feasibility of dating fossil solitary corals from Pleistocene marine strandlines outside tropical latitudes using the recently developed high sensitivity, high-precision U-series technique based on thermal-ionization mass-spectrometry (TIMS). The TIMS technique is much more efficient than conventional a spectrometry and, as a result, multiple samples of an individual coral skeleton, or different specimens from the same bed can be analyzed. Detached and well-rounded fossil specimens of the solitary coral Balanophyllia elegans were collected from relict littoral deposits on emergent marine terraces along the California coast at Cayucos terrace (elevation 8 m, previously dated at 124 and 117 Ky by α counting), Shell Beach terrace (elevation about 25 m, previously undated), Nestor terrace, San Diego (elevation 23 m, previously dated at 131 to 109 Ky ), Bird Rock terrace, San Diego ( elevation 8 m, previously dated at 81 Ky ). Attached living specimens were collected from the intertidal zone on the modern terrace at Moss Beach. Concentrations of 232 Th in both living and fossil specimens are much higher than in reef-building corals (12 to 624 pmol/g vs. 0.1 to 1.6 pmol/g, respectively). However, because 230 Th/ 232 Th in Balanophyllia elegans are very low (2.22 × 10 −3 to 4.33 × 10 −4 ), the high 232 Th concentrations have negligible effect on the 230 Th- 234 U dates. The high 232 Th concentration in the living specimen (33.1 pmol/g) indicates that a significant amount of 232 Th is incorporated in the aragonitic skeleton during growth, or attached to clay-sized silicates trapped in the skeletal material. The calculated initial 234 U activities in the fossil specimens of Balanophyllia elegans are higher than the 234 U activity in modern seawater or in the modern specimen. The higher initial activities could possibly reflect the influx of 234 U-enriched continental water into Pleistocene coastal waters, or it could reflect minor diagenetic alteration, a persistent and fundamental problem in dating all corals. Samples from a compound specimen from the Cayucos terrace were subjected to different preparation procedures. Samples prepared by a standard acid washing procedure yielded 230 Th- 234 U ages of 125, 123, and 122 Ky, whereas samples prepared by an abbreviated procedure without acid washing yield significantly lower ages of 113 and 112 Ky. Two other specimens from the same bed yielded 230 Th- 234 U ages of 118 and 115 Ky. Also, two specimens from a stratigraphically higher bed yielded ages of 120 and 117 Ky, and three specimens from a lower bed yield ages of 115, 113, and 101 Ky. Nine of the twelve ages of the treated samples from the Cayucos terrace range from 125 to 113 Ky. However, the ages do not follow the stratigraphie order. Two possible interpretations are ( 1 ) the age of the terrace deposit is 125 Ky and all younger ages reflect variable diagenetic alteration or (2) the age of the terrace is 125 to 113 Ky and the ages reflect sediment reworking over a period of 12 Ky. Three specimens from a single bed on the Shell Beach terrace yield ages of 126, 122, and 121 Ky, similar to the older ages from Cayucos. The ages of solitary corals from the Cayucos and Shell Beach terraces are similar to ages of reef-building corals from terraces at numerous tropical localities. These are correlated with the last interglacial sea-level highstand, which probably stood 2 to 10 m above present sea level. The youngest ages and present elevations of the Cayucos and Shell Beach terraces yield tectonic uplift rates of 0.01 and 0.15 m/Ky, respectively, assuming the original elevation of each terrace was 7 m. Four specimens from the basal gravel on the Nestor terrace yielded ages of 145, 143, 137, and 133 Ky. The three oldest ages, however, are older than that associated with the last interglacial. The possible explanations for these older ages are ( 1 ) diagenic alteration or ( 2 ) the Nestor terrace deposits reflect in some way a poorly documented early phase of the last interglacial sea level high stand.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Martin Stein, G.J. Wasserburg, K. R. Lajoie, J.-H. Chen. 1991. U-series ages of solitary corals from the California coast by mass spectrometry. https://doi.org/10.1016/0016-7037(91)90069-h

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related USGS reports

Organic and isotopic indicators for sorting of sedimentary organic matter along a marginal submarine canyon

Submarine canyons are incised features of many continental margins that can have significant influence on the hydrodynamic distribution of sediments and organic matter eroded and deposited from the continents. Baltimore Canyon, on the mid-Atlantic margin of the United States, contains a complex set of sedimentary processes that simultaneously create unique benthic habitats and control the deposition of organic matter. Along the canyon axis, loci of net erosion, net deposition, and intense winnowing each host diverse faunal assemblages and varying mixtures of sedimentary organic matter derived both from production in the overlying water column and from mobilized sediments. Bioavailable components of this deposited organic matter sustain benthic communities, while recalcitrant components can contribute to long-term carbon burial in the deep sea. However, commonly employed bulk geochemical analyses provide little information about the relative bioavailability or depositional history of sedimentary organic matter. Here we employ a range of organic and isotopic analyses to explore in more detail how canyon-specific sediment dynamics determine the sorting of organic matter from shelf to open ocean. In combination with bulk geochemical characteristics, we subjected surface sediments from water depths of ∼200–1200 m in Baltimore Canyon to a sequential extraction procedure, isolating nonpolar and polar lipid classes, an acid-soluble fraction, and an acid-insoluble fraction. Each class was analyzed for carbon and nitrogen quantities and stable isotope ratios, and radiocarbon content where possible, along with compound-specific carbon and nitrogen isotope analysis of individual amino acids in the acid-hydrolysed fraction. We find different organic matter sources and depositional history recorded in the properties of younger, bioavailable organic matter components (polar lipids, amino acids) in comparison to the older, more recalcitrant components (nonpolar lipids, acid-insoluble fraction). These differences in source and bioavailability of organic matter vary along the canyon, correlating with grain size and erosion/deposition dynamics, and may help shape the benthic faunal assemblages. Additionally, our results suggest that determining the relative concentrations of acid-soluble and acid-insoluble organic matter may provide an easily accessible method to improve our understanding of the nutritional quality of sediments for benthic fauna than more commonly used bulk carbon or nitrogen concentrations.

Delaware, New Jersey

Bayesian calibration of the 40K decay scheme with implications for 40K-based geochronology

The K/Ar and 40 Ar/ 39 Ar geochronometers are based on the naturally occurring radionuclide 40 K. Their precision and accuracy are limited by uncertainties on the 40 K decay constants and, in the case of the 40 Ar/ 39 Ar geochronometer, the isotopic composition of neutron fluence monitors. To address these limitations, we introduce a Bayesian calibration of the 40 K decay scheme. We formulate robust priors for all model parameters including partial 40 K decay constants, 238 U and 235 U decay constants, and age offset parameters to account for phenomena that can perturb apparent U-Pb and 40 Ar/ 39 Ar ages. We then harness a set of complementary 40 Ar/ 39 Ar, 238 U/ 206 Pb, and 235 U/ 207 Pb data from well- characterized geological samples with ages from 1.919 ka to 2000 Ma to derive Bayesian estimates of the 40 K decay constants. Posterior values for the partial 40 K decay constants are λ β - "> λ β - = (4.9252 ± "> ± 0.0054) × "> × 10 −10 yr −1 , λ β + "> λ β + = (5.6658 ± "> ± 0.1543) × "> × 10 −15 yr −1 , λ EC ∗ "> λ EC0 = (5.7404 ± "> ± 0.0053) × "> × 10 −11 yr −1 , and λ EC 0 "> λ EC0 = (4.9060 ± "> ± 0.2942) × "> × 10 −13 yr −1 (uncertainties reported at the 68 % (1 σ "> σ ) credible interval). These combine to a total 40 K decay constant λ tot "> λ tot = (5.5042 ± "> ± 0.0054) × "> × 10 −10 yr −1 . Model estimates of the 238 U and 235 U decay constants are statistically indistinguishable from those reported by Jaffey et al. (1971) . Posterior values of the 40 K decay constants and the 40 Ar*/ 40 K isotopic composition of Fish Canyon sanidine (FCs) define a K/Ar FCs age of 28.183 ± "> ± 0.017 Ma (1 σ "> σ ). Significantly, Bayesian calibrated 40 Ar/ 39 Ar ages align with astronomically tuned ages throughout the Cenozoic and with 238 U/ 206 Pb and 235 U/ 207 Pb ages in the Mesozoic, Paleozoic, and Proterozoic, as well as having comparable precision to the 238 U/ 206 Pb method. Thus, Bayesian calibration of the 40 K decay scheme and the K/Ar age of FCs reconciles the 40 Ar/ 39 Ar, U-Pb, and astronomical chronometers.

Geochimica et Cosmochimica Acta

Characterizing sulfur redox state and geochemical implications in deep-time using mineral chemistry network analysis

Sulfur (S) is a central element in global biogeochemical cycling and Earth’s redox evolution. Minerals that contain S are an important record of local environmental conditions at the time of their formation based on chemical speciation and redox. However, the oxidation state of S for hundreds of different S-containing minerals and thousands of S-containing mineral localities is unknown, largely sulfides and sulfosalts, and the redox state alone does not fully capture mineral chemistry diversity, thus limiting understanding of S redox evolution. Here, we use mineral chemistry network analysis and the weighted Mineral Element Electronegativity Coefficient of Variation (wMEE CV ) metric to investigate the element interactions and localities of S-containing minerals from the Mineral Evolution Database (MED) to infer the redox state of S in minerals where the redox state is unknown (S U ). Louvain community detection of the S mineral chemistry redox network reveals that there are three main network communities that are separated by redox state. The S 6+ community includes minerals that contain the S 6+ redox state and a small number of S 4+ and S 2+ minerals, the S 2− community includes S 2− -containing minerals, and the S U community includes minerals in which the redox state of S is unknown. The wMEE CV values of the S U community closely overlap with the wMEE CV values of the S 2− community, and do not overlap with the wMEE CV values of the S 6+ community, indicating the S U community minerals contain predominately reduced S. Assuming that S U community minerals contain reduced S, as supported by their network chemical associations and wMEE CV values, then reduced S-containing minerals make up approximately 81 % of S-containing mineral localities in the S mineral chemistry network, even though the majority of all mineral localities (S-containing and non-S-containing) are oxygen (O)-containing minerals. Additionally, reduced S-containing minerals make up the majority (∼75 %) of all non-O containing mineral localities in the MED, representing the importance of reduced S as an electron source and substrate in the evolution of microbial metabolic networks. The range wMEE CV values of S 6+ community minerals expands through time due primarily to formation of chemically diverse sulfate minerals, coinciding with crustal oxidation from the late Proterozoic to Phanerozoic and the expansion of the marine sulfate reservoir. The intersection of shared constituent elements among reduced and oxidized S in the mineral chemistry network represents redox convergence of weathered S in the geosphere that was crucial in the formation of natural resource deposits and the evolution of biogeochemical cycles.

Geochimica et Cosmochimica Acta