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P.A. Meyers

Publications and source records attributed to P.A. Meyers.

5 recordsLinked to original sources
USGS2010

A 15 000-year record of climate change in northern New Mexico, USA, inferred from isotopic and elemental contents of bog sediments

Elemental (C, N, Pb) and isotopic ( δ 13 C, δ 15 N) measurements of cored sediment from a small bog in northern New Mexico reveal changes in climate during the Late Pleistocene and Holocene. Abrupt increases in Pb concentration and δ 13 C values ca. 14 420 cal. YBP indicate significant runoff to the shallow lake that existed at that time. Weathering and transport of local volcanic rocks resulted in the delivery of Pb-bearing minerals to the basin, while a 13 C-enriched terrestrial vegetation source increased the δ 13 C values of the sedimentary material. Wet conditions developed over a 300 a period and lasted for a few hundred years. The Younger Dryas period (ca. 12 700–11 500 cal. YBP) caused a reduction in terrestrial productivity reflected in decreasing C/N values, δ 15 N values consistently greater than 0‰ and low organic content. By contrast, aquatic productivity increased during the second half of this period, evidenced by increasing δ 13 C values at the time of highest abundance of algae. Dry conditions ca. 8 000–6 000 cal. YBP were characterised by low organic carbon content and high Pb concentrations, the latter suggesting enhanced erosion and aeolian transport of volcanic rock. The range in δ 13 C, δ 15 N and C/N values in the sedimentary record fall within the range of modern plants, except during the periods of runoff and drought. The sedimentary record provides evidence of natural climate variability in northern New Mexico, including short- (multi-centennial) and long-(millennial) term episodes during the Late Pleistocene and Holocene.

Journal of Quaternary Science↗
USGS1992

Gold deposition by sulfidation of ferrous Fe in the lacustrine sediments of the Pueblo Viejo district (Dominican Republic): The effect of Fe-C-S diagenesis on later hydrothermal mineralization in a Maar-Diatreme complex

The Pueblo Viejo district, located in the Cordillera Central of the Dominican Republic, contains large Au-Ag deposits associated with acid-sulfate alteration within spilites, conglomerates and carbonaceous sedimentary rocks that were deposited in a maar-diatreme complex. Much of the Au mineralization occurs in pyritic, carbonaceous siltstones of the Pueblo Viejo Maar-Diatreme Member of the Cretaceous Los Ranchos Formation. Pyrite is the only Fe-bearing phase in mineralized rock, whereas siderite is the dominant Fe-bearing phase in siltstones distal to mineralization. Disseminated pyrite occurs as framboids, cubes, pyritohedra, concretions and cement. Early framboids occur throughout the district. Au occurs as inclusions in later non-framboid disseminated pyrite (NFDP); an occurrence that is interpreted to be indicative of contemporaneous deposition. Pyrite framboids exhibit a wide range of ??34Scdt-values (-17.5 to +4.8???) and are interpreted to have formed during biogenic reduction of pore-water sulfate. The NFDP yield restricted ??34Scdt-values ( x ?? = -5.2???, s = ??2.4???, n = 43) similar to those obtained from later vein pyrite ( x ?? = -6.4???, s = ??1.5???, n = 12). Alunite and barite have ??34S-values ranging from +18.8 to +21.6???. The interpretation that the NFDP, vein pyrite, alunite and barite, and possibly even the framboidal pyrite share a common source of igneous sulfur is supported by the ??34S data. Siderite occurs as concretions and cement, contains abundant Mg (Fe0.75Mg0.19Mn0.03Ca0.02CO3) and has ??13Cpdb- and ??18Osmow-values ranging from -2.5 to +1.1%. and +14.6 to +19.5???, respectively. These data are consistent with the interpretation that the siderite formed in lacustrine sediments and that the carbonate in the siderite is probably methanogenic, although contributions from oxidation of organic matter during biogenic sulfate reduction, thermal decarboxylation of organic matter, or magmatic vapor cannot be ruled out. Disseminated Au mineralization in the sedimentary rocks formed when a hydrothermal fluid encountered reactive Fe2+ in diagenetic siderite. The ensuing pyrite deposition consumed H2S and destabilized the Au (HS)-2 complex, leading to precipitation of Au. The capacity of the sedimentary rocks to consume H2S and precipitate Au was controlled by the amount of non-pyrite Fe present as siderite. The abundance of siderite was controlled by the extent of pyrite formation during diagenesis. ?? 1992.

Chemical Geology↗
USGS1991

Change in the size of Walker Lake during the past 5000 years

In 1984, a 12-m sediment core (WLC84-8) was taken from the deepest part of Walker Lake. Samples of the core were analysed for diatoms, pollen, carbonate mineralogy, magnesium content, δ 18 O and δ 13 C values of the total inorganic fractin, δ 18 O and δ 13 C values of Limnocythere ceriotuberosa , δ 13 C values of the total organic fraction, grain size, and magnetic susceptibility. The data indicate that Walker Lake became shallow and probably desiccated between ⩾5300-4800 and 2700-2100 yr B.P.. Each of the organic and inorganic proxy indicators of lake size discussed in this paper was useful in determining the presence of the shallow-lake intervals. However, none of the indicators was useful in determining the cause of the shallow-lake intervals. Instead, the types of fish living in Walker Lake prior to 1940 were used to demonstrate that shallow-lake intervals resulted from diversion of the Walker River and not from climatic aridity. Major changes in mineralogy and magnesium content of carbonates and major changes in diatom populations with time were found to be a function of the chemical evolution of Walker Lake combined with changing lake size. The stable isotopes of oxygen and carbon were found to be good indicators of lake volume changes. A lake-level record for Walker Lake constructed from stable-isotope data was found to be similar to a lake-level record constructed using tufa and tree-stump data. Both records indicate relatively high lake levels between 4800−2700 yr B.P., at 1250 yr B.P., and within the last 300 yr. Substantial declines in lake level occurred ∼2000 and ∼1000 yr B.P.

California, Idaho, Nevada, Oregon↗
USGS1988

Sedimentary biomarker and isotopic indicators of the paleoclimatic history of the Walker Lake basin, western Nevada

Walker Lake, a terminal saline lake in western Nevada, has experienced major fluctuations in its water level due to changes in the regional climate during Quaternary times. As part of a paleo-climatological study of western Nevada, we have investigated organic matter δ 13 C and C/N values and lipid biomarker contents of sediments deposited at various periods over the past 150 thousand years of lake history. Surficial sediments from two cross-lake transects contain mostly lake-derived organic matter. Diagenetic losses of organic matter are evident in deeper sediments, and the proportion of aquatic and terrigenous organic materials changes in response to variations in preservational factors. Source identification of organic matter is complicated by the probability that Walker Lake has experienced desiccation at various times in its history which impacts the degree of preservation of organic substances.

Nevada↗