Influence of climate factors on spatial distribution of Texas cattle breeds

This paper investigates the spatial distribution of cattle breeders in Texas to quantify how climate factors influence cattle breed selection. A multivariate probit model is employed to examine the county-level binary choices of Bos taurus, Bos indicus and composite breeds derived from cattle breed association membership data. The estimation results suggest that summer heat stress is a significant factor for breed selection: positive for Bos indicus and negative for Bos taurus and composite breeds, with the average marginal effects on breed membership probability being 9.7 %, ?26.5 % and ?7.9 %, respectively. The intensity of the summer heat impacts can lead to noteworthy changes in spatial distributions of Texas cattle breeds in the event of climate change.     

The High-Resolution Coronal Imager (Hi-C)

The High-Resolution Coronal Imager (Hi-C) was flown on a NASA sounding rocket on 11 July 2012. The goal of the Hi-C mission was to obtain high-resolution (≈?0.3?–?0.4′′), high-cadence (≈?5 seconds) images of a solar active region to investigate the dynamics of solar coronal structures at small spatial scales. The instrument consists of a normal-incidence telescope with the optics coated with multilayers to reflect a narrow wavelength range around 19.3 nm (including the Fe xii 19.5-nm spectral line) and a 4096×4096 camera with a plate scale of 0.1′′?pixel^?1. The target of the Hi-C rocket flight was Active Region 11520. Hi-C obtained 37 full-frame images and 86 partial-frame images during the rocket flight. Analysis of the Hi-C data indicates the corona is structured on scales smaller than currently resolved by existing satellite missions.     

Heterogeneous distributions of CO2 may be more important for dissolution and karstification in coastal eogenetic limestone than mixing dissolution

Mixing dissolution, a process whereby mixtures of two waters with different chemical compositions drive undersaturation with respect to carbonate minerals, is commonly considered to form cavernous macroporosity (e.g. flank margin caves and banana holes) in eogenetic karst aquifers. On small islands, macroporosity commonly originates when focused dissolution forms globular chambers lacking entrances to the surface, suggesting that dissolution processes are decoupled from surface hydrology. Mixing dissolution has been thought to be the primary dissolution process because meteoric water would equilibrate rapidly with calcium carbonate as it infiltrates through matrix porosity and because pCO₂ was assumed to be homogeneously distributed within the phreatic zone. Here, we report data from two abandoned well fields in an eogenetic karst aquifer on San Salvador Island, Bahamas, that demonstrate pCO₂ in the phreatic zone is distributed heterogeneously. The pCO₂ varied from less than log ?2.0 to more than log ?1.0 atm over distances of less than 30 m, generating dissolution in the subsurface where water flows from regions of low to high pCO₂ and cementation where water flows from regions of high to low pCO_2. Using simple geochemical models, we show dissolution caused by heterogeneously distributed pCO₂ can dissolve 2.5 to 10 times more calcite than the maximum amount possible by mixing of freshwater and seawater. Dissolution resulting from spatial variability in pCO₂ forms isolated, globular chambers lacking initial entrances to the surface, a morphology that is characteristic of flank margin caves and banana holes, both of which have entrances that form by erosion or collapse after cave formation. Our results indicate that heterogeneous pCO₂, rather than mixing dissolution, may be the dominant mechanism for observed spatial distribution of dissolution, cementation and macroporosity generation in eogenetic karst aquifers and for landscape development in these settings. Copyright © 2015 John Wiley & Sons, Ltd.     

Water in the upper martian surface at mid- and low-latitudes: presence, state, and consequences

Sublimation of water ice is more effective than evaporation of sorption water at the same temperature. Therefore, water in the form of ice must, over geologic time-scales, have left the upper martian surface (m-scale) at mid- and low-latitudes, leaving sorption water as a possible physical form of stable subsurface water. Adsorption water is “liquid-like” at these temperatures (in the sense of a 2D-liquid). This property is the reason for the specific importance of physisorbed water under martian conditions. It is shown that unfrozen adsorption water can cause numerous physical, chemical, and possibly also biological processes in the upper martian surface and may be responsible for a number of its properties.     

Sub-micron scale distributions of trace elements in zircon

Sub-micron scale zoning of Ti concentrations and correlations between concentrations of Ti and other trace elements (P, Ce, and Y) and cathodoluminescent (CL) banding is observed in natural zircons. Ion images were made using the Caltech Microanalysis Center’s CAMECA NanoSIMS 50L with an O⁻ primary beam focused to ~300 nm on the sample surface. The high spatial resolution of this technique allows for interrogation of chemical variations at or below the scale of CL banding in natural zircons. Images produced in this manner display two types of correlations among Ti, P, Ce, and Y (which appears to be a proxy for CL intensity): strong (correlation coefficients >0.8) and subtle (correlation coefficients ~0.15–0.4). Strongly correlated images, which display Ti variations of ca. a factor of 3 between adjacent CL bands and overall elevated trace element concentrations in CL-dark bands, were found within an oscillatory-zoned, trace element enriched sector of a CL sector-zoned zircon. Three possible causes for such correlations include: temperature-dependent equilibrium partitioning, trace element partitioning limited by diffusion in the host melt and surface-controlled, non-equilibrium growth. Comparison of our data with the expected results of these processes suggests that: (1) Ti partitioning in zircon is dependent upon non-equilibrium effects in addition to temperature and/or (2) the incorporation of elements that co-vary with Ti in zircon (e.g., Y, P and Ce) is also temperature-dependent. Sub-micron scale, high-Ti regions are also found within Proterozoic Adirondack and >4 Ga Jack Hills zircons as well as trace element enrichments (including Ti) along cracks within Jack Hills zircons.     

Verification of tropical cyclone deposits with oxygen isotope analyses of coeval ostracod valves

Reconstruction of prehistoric tropical cyclone (TC) activity often relies on the identification of distinctive overwash deposits (tempestites) in coastal lagoon sediments. Similar sediment deposits, however, can result from high-energy events other than TCs. In this study we assessed the utility of using the geochemistry of ostracod valves, specifically their stable oxygen isotope composition (δ¹⁸O), as a potential validation variable that could reduce the chances of misidentifying an overwash deposit as having been generated by a TC, when in fact it formed from another high-energy depositional process (type 1 error). We applied this technique to a sediment core recovered from Laguna Alejandro, Dominican Republic, which had already been analyzed for other sedimentary TC proxies. Negative δ¹⁸O anomalies identified in the ostracod valve stable isotope record are associated with TC deposits and are most easily explained by large influxes of ¹⁸O-depleted meteoric waters typical of intense tropical storms. There is potential for this technique to be used to identify TC landfalls that are not represented by overwash deposits. We, however, propose a more conservative approach and suggest this technique be used to validate the origin of a storm deposit and reduce the odds of a type 1 error.     

Palaeoecology, facies and stratigraphy of shallow marine macrofauna from the Upper Oligocene (Palaeogene) of the southern Pre-North Sea Basin of Astrup (NW Germany)

The 22 meter thick marine carbonate Upper Oligocene series of Astrup (NW Germany) is correlated with the Chattian type section of Doberg. It indicates a more constrained palaeogeographical and biostratigraphical position ranging from the biozones of Chlamys (C.) decussata (upper Chattian A) to Chlamys (C.) semistriatus (lower Chattian C). The macrofauna can be subdivided into three main benthic communities: A. the ?coarse gravel spondylid beach fauna?? of the shore zone with ?pebble beach facies?? dominated by sessile brachiopods, large balanids, spondylids, oysters or small regular echinoids. Borings are common in pebbles; B. the ?glauconite fine gravel brachiopod-bryozoan littoral fauna?? of the shallow subtidal zone where a terebratulid/lithothamnid dominated fauna/flora is present. The rhodophyceans were most possibly anker stones and substrates for cirripeds and serpulids; C. the ?glauconite carbonate sand phytal fauna?? of the shallow subtidal zone with a rich benthic mollusc dominated fauna. Indirect evidence for seagrass and macroalgae occurs on the attachment negatives of balanids and oysters, and also on Cibicides foraminifera or bryozoans like Cellepora. The facies types along the Wiehengebirge Island and Teutoburger Wald Peninsula coasts of the southern Pre-North Sea Basin differ with respect to their benthic communities to that of the siliciclastic Leipziger and the Rhenish Bay facies.     

Isotopic and elemental fractionation of solar wind implanted in the Genesis concentrator target characterized and quantified by noble gases

Abstract– We report concentrations and isotopic compositions of He, Ne, and Ar measured with high spatial resolution along a radial traverse of a silicon carbide (SiC) quadrant of the Genesis mission concentrator target. The Ne isotopic composition maps instrumental fractionation as a function of radial position in the target: the maximum observed isotopic fractionation is approximately 33‰ per mass unit between the center and periphery. The Ne fluence is enhanced by a factor of 43 at the target center and decreases to 5.5 times at the periphery relative to the bulk solar wind fluence. Neon isotopic profiles measured along all four arms of the “gold cross” mount which held the quadrants in the concentrator target demonstrate that the concentrator target was symmetrically irradiated during operation as designed. We used implantation experiments of Ne into SiC and gold to quantify backscatter loss and isotopic fractionation and compared measurements with numerical simulations from the code “stopping and range of ions in matter.” The ²⁰Ne fluence curve as a function of radial distance on the target may be used to construct concentration factors relative to bulk solar wind for accurate corrections for solar wind fluences of other light elements to be measured in the concentrator target. The Ne isotopic composition as a function of the radial distance in the SiC quadrant provides a correction for the instrumental mass‐dependent isotopic fractionation by the concentrator and can be used to correct measured solar wind oxygen and nitrogen isotopic compositions to obtain bulk solar wind isotopic compositions.     

Uranium-lead isotope systematics of Mars inferred from the basaltic shergottite QUE 94201

Uranium-lead ratios (commonly represented as ²³⁸U/²⁰⁴Pb = μ) calculated for the sources of martian basalts preserve a record of petrogenetic processes that were active during early planetary differentiation and formation of martian geochemical reservoirs. To better define the range of μ values represented by the source regions of martian basalts, we completed U-Pb elemental and isotopic analyses on whole rock, mineral and leachate fractions from the martian meteorite Queen Alexandra Range 94201 (QUE 94201). The whole rock and silicate mineral fractions have unradiogenic Pb isotopic compositions that define a narrow range (²⁰⁶Pb/²⁰⁴Pb = 11.16-11.61). In contrast, the Pb isotopic compositions of weak HCl leachates are more variable and radiogenic. The intersection of the QUE 94201 data array with terrestrial Pb in ²⁰⁶Pb/²⁰⁴Pb-²⁰⁷Pb/²⁰⁴Pb-²⁰⁸Pb/²⁰⁴Pb compositional space is consistent with varying amounts of terrestrial contamination in these fractions. We calculate that only 1-7% contamination is present in the purified silicate mineral and whole rock fractions, whereas the HCl leachates contain up to 86% terrestrial Pb. This terrestrial Pb contamination generated a ²⁰⁶Pb-²⁰⁷Pb array in the QUE fractions that appears to represent an ancient age, which contrasts with a much younger crystallization age of 327 ± 10 Ma derived from Rb-Sr and Sm-Nd isochrons (Borg L. E., Nyquist L. E., Taylor L. A., Wiesmann H. and Shih C. -Y. (1997) Constraints on Martian differentiation processes from Rb-Sr and Sm-Nd isotopic analyses of the basaltic shergottite QUE 94201. Geochim. Cosmochim. Acta61, 4915-4931). Despite the contamination, and accepting 327 ± 10 Ma as the crystallization age, we use the U-Pb data to determine the initial ²⁰⁶Pb/²⁰⁴Pb of QUE 94201 to be 11.086 ± 0.008 and to calculate the μ value of its mantle source to be 1.82 ± 0.01. The μ value calculated for the QUE 94201 source is the lowest determined for any martian basalt source, and, when compared to the highest values determined for martian basalt sources, indicates that μ values in martian source reservoirs vary by at least a factor of two. Additionally, the range of source μ values indicates that the μ value of bulk silicate Mars is approximately three. The amount of variation in the μ values of the mantle sources (μ ∼ 2-4) is greater than can be explained by igneous processes involving silicate phases alone. We suggest the possibility that a small amount of sulfide crystallization may generate greater extents of U-Pb fractionation during formation of the mantle sources of martian basalts.