Climate change in lowland Central America during the late deglacial and early Holocene

The transition from arid glacial to moist early Holocene conditions represented a profound change in northern lowland Neotropical climate. Here we report a detailed record of changes in moisture availability during the latter part of this transition (～11 250 to 7500 cal. yr BP) inferred from sediment cores retrieved in Lake Petén Itzá, northern Guatemala. Pollen assemblages demonstrate that a mesic forest had been largely established by ～11 250 cal. yr BP, but sediment properties indicate that lake level was more than 35 m below modern stage. From 11 250 to 10 350 cal. yr BP, during the Preboreal period, lithologic changes in sediments from deep‐water cores (>50 m below modern water level) indicate several wet–dry cycles that suggest distinct changes in effective moisture. Four dry events (designated PBE1‐4) occurred centred at 11 200, 10 900, 10 700 and 10 400 cal. yr BP and correlate with similar variability observed in the Cariaco Basin titanium record and glacial meltwater pulses into the Gulf of Mexico. After 10 350 cal. yr BP, multiple sediment proxies suggest a shift to a more persistently moist early Holocene climate. Comparison of results from Lake Petén Itzá with other records from the circum‐Caribbean demonstrates a coherent climate response during the entire span of our record. Furthermore, lowland Neotropical climate during the late deglacial and early Holocene period appears to be tightly linked to climate change in the high‐latitude North Atlantic. We speculate that the observed changes in lowland Neotropical precipitation were related to the intensity of the annual cycle and associated displacements in the mean latitudinal position of the Intertropical Convergence Zone and Azores–Bermuda high‐pressure system. This mechanism operated on millennial‐to‐submillennial timescales and may have responded to changes in solar radiation, glacial meltwater, North Atlantic sea ice, and the Atlantic meridional overturning circulation (MOC). Copyright © 2005 John Wiley & Sons, Ltd.     

Enceladus' south polar sea

Recent observations of the south pole of Saturn's moon Enceladus by the Cassini spacecraft have revealed an active world, powered by internal heat. In this paper, we propose that localized subsurface melting on Enceladus has produced an internal south polar sea. Evidence for this localized sea comes from the shape of Enceladus, which does not match a differentiated body at its current orbital position. We show that melting induced by the observed heat flow at the south pole produces a large enough pit to match the shape of Enceladus with a differentiated rock and ice interior. Numerical modeling of melting and ice flow shows that the sea produced beneath the south pole is stable against inflow of ductile ice from its surroundings for the duration of the heating. The shape modification due to melting also produces a negative degree-two gravity anomaly, which can reorient the spin axis of Enceladus in order to place the sea at the pole.     

Solute geochemical mass-balances and mineral weathering rates in small watersheds II: Biomass nutrient uptake,more equations in more unknowns,and land use/land cover effects

Paired watersheds are used to develop a deciduous nutrient uptake stoichiometry. The watersheds are those of the House Rock Run and the Brubaker Run located in the Pennsylvania Appalachian Piedmont, USA. These two watersheds are nearly identical with respect to bedrock, regolith, climate, geomorphology, morphometry, baseflow hydrology, and type and successional stage of forest vegetation. They only differ by the percentage of deciduous forest cover, with House Rock Run having 59% and Brubaker Run having 76%. From differences in their stream chemistries the biomass nutrient uptake stoichiometry of K_1.0Mg_1.0Ca_1.4 was determined. This stoichiometry applies to an aggrading deciduous biomass and differs from those previously used which were derived from net primary production (NPP) data. The difference may reflect that macronutrients in plant tissue may also originate from atmospheric inputs and/or decomposing biomass. Although this stoichiometry may not be applied to all deciduous forest-covered watersheds, it is likely an improvement over a stoichiometry determined from NPP data.     

The Effects of Road Salt on Stream Water Chemistry in Two Small Forested Watersheds,Catoctin Mountain,Maryland, USA

The Hauver Branch and Hunting Creek watersheds in Catoctin Mountain, Maryland, USA, are small rural watersheds that receive road salt during the winter. Base cation evidence of road salt application in stream water disappears by approximately September for Hauver Branch, but never disappears for Hunting Creek. The fraction of the precipitation-corrected watershed fluxes of both Mg²⁺ and Ca²⁺ attributable to cation exchange associated with road salt Na⁺ inputs are 14 and 19 % for Hauver Branch and Hunting Creek, respectively. The percentage of divalent cations in stream waters resulting from road salt application is calculated using the watershed chemical weathering Na⁺/SiO₂ molar ratio. Calculation of a representative chemical weathering Na⁺/SiO₂ molar ratio may be problematic with spatially variable bedrock, and/or inputs from water softeners, septic systems, and wastewater treatment plants. Therefore, investigations of small forested rural watersheds offer insights into road salt dynamics that may be lost at larger scales and/or with increased urbanization. The quantities of road salt application to the Hauver Branch and Hunting Creek watersheds are 3.3 and 11 t km^?2 year^?1, respectively. The per-lane-length-normalized road salt application rates for the Hauver Branch and Hunting Creek watersheds are 10 and 22 t lane^?1 km^?1 year^?1, respectively. These per-lane-length-normalized road salt application rates are relatively large compared to more urbanized watersheds located north of the study site where the application rates are reported by municipalities. These findings may indicate that road and highway administrations may underestimate their rates of road salt application.     

变泥质岩的深熔作用与具铈（Ce）负异常熔体的成因

对美国加州南Sierra Nevada岩基中一个典型的中生代变质表壳岩及其混合岩带进行了详细的野外观察和元素地球化学研究。研究发现:在持久(约为150Ma)的花岗岩侵位作用下,早白垩世变泥质岩发生达角闪岩相的中高级变质作用和部分熔融,导致Isabella混合岩的形成;浅色体具有和变泥质岩及混合岩近平行的REE分布模式,但浅色体的LREE含量相对较低;和变泥质岩相似,混合岩中的浅色体具有显著的Ce负异常。野外观测、岩相观察及元素地球化学特征表明,浅色体显著的Ce负异常是继承了原岩的Ce负异常特征,而不是由于副矿物(磷灰石、独居石或锆石)的差异溶解或结晶分异作用造成的。早白垩世变泥质岩(浅色体的原岩)主要由泥质及沙质海相沉积物组成,局部夹基性火山灰和火山碎屑,形成于与大陆岛弧密切相关的浅海环境。原岩的Ce负异常反映了较还原的浅海沉积环境。具有Ce负异常浅色体的产出表明,如果俯冲带上的沉积岩在俯冲过程中发生部分熔融作用并且所产生的熔体参与大洋型岛弧岩浆作用,最终可以导致具有Ce异常的基性岩浆生成。     

A radical pathway for organic phosphorylation during schreibersite corrosion with implications for the origin of life

Phosphorylated compounds (e.g., DNA, RNA, phospholipids, and many coenzymes) are critical to biochemistry. Thus, their origin is of prime interest to origin of life studies. The corrosion of the meteoritic mineral schreibersite ((Fe, Ni)₃P) may have significantly contributed to the origin of phosphorylated biomolecules. Corrosion of synthetic schreibersite in a variety of solutions was analyzed by nuclear magnetic resonance spectroscopy, mass spectrometry, and electron paramagnetic resonance spectroscopy. These methods suggest a free-radical reaction pathway for the corrosion of schreibersite to form phosphite radicals () in aqueous solution. These radicals can form activated polyphosphates and can phosphorylate organic compounds such as acetate to form phosphonates and organophosphates (3% total yield). Phosphonates (O₃P-C) are found in the organic P inventory of the carbonaceous meteorite Murchison. While phosphonates are rare in biochemistry, the ubiquity of corroding iron meteorites on the early Earth could have provided a source of organic phosphorous compounds for the origin of life, and may have led to the role of organophosphates as a product of early evolution.     

Estimating carbon sequestration in the piedmont ecoregion of the United States from 1971 to 2010

Human activities have diverse and profound impacts on ecosystem carbon cycles. The Piedmont ecoregion in the eastern United States has undergone significant land use and land cover change in the past few decades. The purpose of this study was to use newly available land use and land cover change data to quantify carbon changes within the ecoregion. Land use and land cover change data (60-m spatial resolution) derived from sequential remotely sensed Landsat imagery were used to generate 960-m resolution land cover change maps for the Piedmont ecoregion. These maps were used in the Integrated Biosphere Simulator (IBIS) to simulate ecosystem carbon stock and flux changes from 1971 to 2010. Results show that land use change, especially urbanization and forest harvest had significant impacts on carbon sources and sinks. From 1971 to 2010, forest ecosystems sequestered 0.25 Mg C ha?1 yr?1, while agricultural ecosystems sequestered 0.03 Mg C ha?1 yr?1. The total ecosystem C stock increased from 2271 Tg C in 1971 to 2402 Tg C in 2010, with an annual average increase of 3.3 Tg C yr?1. Terrestrial lands in the Piedmont ecoregion were estimated to be weak net carbon sink during the study period. The major factors contributing to the carbon sink were forest growth and afforestation; the major factors contributing to terrestrial emissions were human induced land cover change, especially urbanization and forest harvest. An additional amount of carbon continues to be stored in harvested wood products. If this pool were included the carbon sink would be stronger.     

Time scales of DNAPL migration in sandy aquifers examined via numerical simulation

The time required for dense nonaqueous phase liquid (DNAPL) to cease migrating following release to the subsurface is a valuable component of a site conceptual model. This study uses numerical simulation to investigate the migration of six different DNAPLs in sandy aquifers. The most influential parameters governing migration cessation time are the density and viscosity of the DNAPL and the mean hydraulic conductivity of the aquifer. Releases of between 1 and 40 drums of chlorinated solvent DNAPLs, characterized by relatively high density and low viscosity, require on the order of months to a few years to cease migrating in a heterogeneous medium sand aquifer having an average hydraulic conductivity of 7.4 x 10(-3) cm/s. In contrast to this, the release of 20 drums of coal tar (rho(D)= 1061 kg/m(3), micro(D)= 0.161 Pa.s) requires more than 100 years to cease migrating in the same aquifer. Altering the mean hydraulic conductivity of the aquifer results in a proportional change in cessation times. Parameters that exhibit relatively little influence on migration time scales are the DNAPL-water interfacial tension, release volume, source capillary pressure, mean aquifer porosity, and ambient ground water hydraulic gradient. This study also demonstrates that low-density DNAPLs (e.g., coal tar) give rise to greater amounts of lateral spreading and greater amounts of pooling on capillary barriers than high-density DNAPLs such as trichloroethylene or tetrachloroethylene.     

Topical Collection: Climate-change research by early-career hydrogeologists

Scientific outreach, international networking, collaboration and adequate courses are needed in both developed and developing countries to enable early-career hydrogeologists to promote long-term multidisciplinary approaches to cope with climate-change issues and emphasize the importance of groundwater in a global strategy for adaptation. One such collaboration has involved the Early Career Hydrogeologists’ Network of the International Association of Hydrogeologists (ECHN-IAH) and the UNESCO International Hydrological Programme’s (IHP) Groundwater Resources Assessment under the Pressures of Humanity and Climate Changes (GRAPHIC) project. This collaboration seeks to foster the education and involvement of the future generation of water leaders in the debate over groundwater and climate change.