The distribution of meteoric <Superscript>36</Superscript>Cl/Cl in the United States: a comparison of models

The natural distribution of ³⁶Cl/Cl in groundwater across the continental United States has recently been reported by Davis et al. (2003). In this paper, the large-scale processes and atmospheric sources of ³⁶Cl and chloride responsible for controlling the observed ³⁶Cl/Cl distribution are discussed.The dominant process that affects ³⁶Cl/Cl in meteoric groundwater at the continental scale is the fallout of stable chloride from the atmosphere, which is mainly derived from oceanic sources. Atmospheric circulation transports marine chloride to the continental interior, where distance from the coast, topography, and wind patterns define the chloride distribution. The only major deviation from this pattern is observed in northern Utah and southern Idaho where it is inferred that a continental source of chloride exists in the Bonneville Salt Flats, Utah.In contrast to previous studies, the atmospheric flux of ³⁶Cl to the land surface was found to be approximately constant over the United States, without a strong correlation between local ³⁶Cl fallout and annual precipitation. However, the correlation between these variables was significantly improved (R ²=0.15 to R ²=0.55) when data from the southeastern USA, which presumably have lower than average atmospheric ³⁶Cl concentrations, were excluded. The total mean flux of ³⁶Cl over the continental United States and total global mean flux of ³⁶Cl are calculated to be 30.5±7.0 and 19.6±4.5 atoms m^–2 s^–1, respectively.The ³⁶Cl/Cl distribution calculated by Bentley et al. (1986) underestimates the magnitude and variability observed for the measured ³⁶Cl/Cl distribution across the continental United States. The model proposed by Hainsworth (1994) provides the best overall fit to the observed ³⁶Cl/Cl distribution in this study. A process-oriented model by Phillips (2000) generally overestimates ³⁶Cl/Cl in most parts of the country and has several significant local departures from the empirical data.

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Resumen Davis et al. (2003) han informado de la distribución natural de la proporción ³⁶Cl/Cl en las aguas subterráneas de la parte continental de los Estados Unidos de América [EUA]. En este artículo, se discute cuáles son los procesos a gran escala y las fuentes atmosféricas del ³⁶Cl y del cloruro que dan lugar a la distribución observada de ³⁶Cl/Cl.El proceso dominante que afecta a la relación ³⁶Cl/Cl en las aguas subterráneas de origen meteórico a escala continental es el aporte de cloruro estable desde la atmósfera, que procede principalmente de los océanos. La circulación atmosférica transporta el cloruro marino hacia el interior, donde la distancia a la costa, topografía y corrientes del viento definen la distribución del cloruro. La única desviación principal de este esquema tiene lugar al norte de Utah y en el sur de Idaho, donde se deduce que existe una fuente continental de cloruro en los Rellanos Salados de Bonneville (Salt Flats).En contraste con estudios previos (Knies et al. 1994; Phillips 2000), se ha descubierto que el flujo atmosférico de ³⁶Cl hacia la superficie terrestre es aproximadamente constante en todos los estados, sin deducirse una correlación fuerte entre el aporte de ³⁶Cl y la precipitación anual. Sin embargo, la correlación entre estas variables se ve mejorada de forma significativa, con coeficientes de regresión comprendidos entre 0,15 y 0,55, cuando se excluyen los datos recogidos en el sudeste de los EUA, que tienen concentraciones de ³⁶Cl atmosférico presuntamente inferiores a la media. El flujo medio total de ³⁶Cl calculado en la zona continental de los Estados Unidos vale 30,5±7,0 átomos por metro cuadrado y segundo, mientras que el flujo total global de ³⁶Cl es de 19,6±4,5 átomos por metro cuadrado y segundo.La distribución de ³⁶Cl/Cl calculada por Bentley et al. (1986) infravalora la magnitud y variabilidad observada en los valores medidos a lo largo de los Estados Unidos. El modelo propuesto por Hainsworth (1994) proporciona el mejor ajuste conjunto a la distribución observada de ³⁶Cl/Cl en este estudio. El modelo orientado a procesos de Phillips (2000) sobreestima por lo general la distribución de ³⁶Cl/Cl en la mayoría del país y difiere significativamente de algunos valores locales empíricos.

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Résumé La distribution naturelle du rapport ³⁶Cl/Cl dans les eaux souterraines des États-Unis a été récemment présentée par Davis et al. (2003). Dans ce travail, les processus à grande échelle et les sources atmosphériques de ³⁶Cl et de chlorure responsables du contrôle de la distribution observée du rapport ³⁶Cl/Cl sont discutés. Le processus dominant qui affecte le rapport ³⁶Cl/Cl dans les eaux souterraines dorigine météorique à léchelle continentale est lapport atmosphérique de chlorure stable, qui provient pour lessentiel de sources océaniques. La circulation atmosphérique transporte des chlorures marins vers lintérieur des continents, où la distribution de chlorure est définie par la distance à la côte, la topographie et les régimes des vents. La seule exception majeure à ce schéma est observée dans le nord de lUtah et le sud de lIdaho où lon suppose quil existe une source continentale de chlorure dans les bas-fonds salés de Bonneville. Au contraire de précédentes études (Knies et al. 1994; Phillips 2000), on trouve que le flux atmosphérique de ³⁶Cl vers le sol est approximativement constant sur lensemble des États-Unis, sans forte corrélation entre la retombée locale de ³⁶Cl et les précipitations annuelles. Cependant, la corrélation entre ces variables devient significative (R ²=0.15 à 0.55) lorsquon supprime les données du sud-est des États-Unis, dont on pense quelles présentent des concentrations en ³⁶Cl atmosphérique inférieures à la moyenne. Le flux total moyen de ³⁶Cl sur les États-Unis continentaux et le flux moyen global de ³⁶Cl sont respectivement évalués à 30.5 ± 7.0 et 19.6 ± 4.5 atomes.m^–2.s^–1. La distribution du rapport ³⁶Cl/Cl calculée par Bentley et al. (1986) sous-estime lordre de grandeur et la variabilité observés pour la distribution mesurée du rapport ³⁶Cl/Cl sur les États-Unis continentaux. Le modèle proposé par Hainsworth (1994) fournit le meilleur ajustement densemble à la distribution du rapport ³⁶Cl/Cl observée dans cette étude. Un modèle orienté vers les processus proposé par Phillips (2000) surestime dans lensemble le rapport ³⁶Cl/Cl dans la plupart des régions du pays et présente plusieurs désaccords locaux avec les données empiriques.

     

Stable Isotope Ratios: Hurricane Olivia

The oxygen and hydrogen isotopic compositions of rains from HurricaneOlivia (1994) in the eastern Pacific were measured. The rains werecollected on 24 and 25 September during airplane flights conducted at anelevation of 3 km. Hurricane Olivia peaked in intensity to a category-4storm between the two dates. Isotope ratios of rains from HurricaneOlivia were markedly lower ( ¹⁸O = –13.9to –28.8) than that of rain collected from a thunderstormat an elevation of 2.3 km outside the influence of Olivia (¹⁸O = –3.8). A distinct decrease in isotoperatios from the first day to the next ( ¹⁸O =–18.4 to –21.9) in Hurricane Olivia wasattributed to decreased updraft velocities and outflow aloft. Thisshifted the isotopic water mass balance so that fewer hydrometeors werelifted and more ice descended to flight level. A decrease in the averagedeuterium excess from the first day to the next (d = 15.5 to 7.1)was attributed to an increase in the relative humidity of the watervapor `source' area. We hypothesize that the `source' region for therain was in the boundary layer near the storm center and that becausethe hurricane was at peak intensity prior to the second day the relative humidity was higher.     

Quaternary depositional patterns and sea-level fluctuations, northeastern North Carolina

A detailed record of late Quaternary sea-level oscillations is preserved within the upper 45 m of deposits along an eight km transect across Croatan Sound, a drowned tributary of the Roanoke/Albemarle drainage system, northeastern North Carolina. Drill-hole and seismic data reveal nine relatively complete sequences filling an antecedent valley comprised of discontinuous middle and early Pleistocene deposits. On interfluves, lithologically similar marine deposits of different sequences occur stacked in vertical succession and separated by ravinement surfaces. Within the paleo-drainage, marine deposits are separated by fluvial and/or estuarine sediments deposited during periods of lowered sea level. Foraminiferal and molluscan fossil assemblages indicate that marine facies were deposited in a shallow-marine embayment with open connection to shelf waters. Each sequence modifies or truncates portions of the preceding sequence or sequences. Sequence boundaries are the product of a combination of fluvial, estuarine, and marine erosional processes. Stratigraphic and age analyses constrain the ages of sequences to late Marine Isotope Stage (MIS) 6 and younger (∼ 140 ka to present), indicating multiple sea-level oscillations during this interval. Elevations of highstand deposits associated with late MIS 5 and MIS 3 imply that sea level was either similar to present during those times, or that the region may have been influenced by glacio-isostatic uplift and subsidence.     

Discussion of: Ortega-Flores et al. (2018) Provenance analysis of Oligocene sandstone from the Cerro Pelón area,southern Gulf of Mexico.https://doi.org/10.1080/00206814.2018.1476922

ABSTRACT

We discuss the 2018 publication that reports petrographic, heavy mineral data, mineral chemistry, and zircon geochronology for Oligocene sandstones in the Cerro Pelón area in southern Mexico Sureste basin. As the title of their paper says, the goal of their study is to establish the source (s) of the voluminous Cenozoic section in this region, reaching several kilometres in thickness and important as a petroleum system. These authors conclude that Oligocene sandstones of La Laja Formation were mostly sourced from eclogite- to greenschist-facies metasedimentary, metaigneous, and ultramafic rocks of the Guatemala suture complex. Minor contributions from the Chiapas Massif Complex, exposed directly to the south ~60 km of the Cerro Pelón area, were also suggested by the authors. They thus conclude that the Palaeogene stratigraphic record in southeastern Mexico was mostly controlled by the development of the Caribbean–North America plate boundary rather than by orogenic processes at the Pacific margin of North America. Presently, we do not agree with the conclusions of Ortega Flores and colleagues who studied the Cerro Pelón section, thus some discussion is required. Serpentinite bearing Nanchital Conglomerate is well exposed in the Cerro Pelón area, and high- to low-grade metamorphic rocks experienced an uplift in the vicinity of the Cerro Pelón area at the time of deposition of the La Laja Formation. We believe the data are better explained by multiple local sources in southern and eastern Oaxaca as well as sources to the south and southwest, which include the Cenozoic coastal batholith, the Grenvillean/Guichicovi basement complexes, the Chiapas Massif, the Mazatlán schist and other units in the Cuicateco Belt, as well as the Mesozoic cover of these areas (Todos Santos Formation, Cretaceous carbonate rocks, and Paleogene strata such as the Soyaló and Bosque Formations).     

Non-equilibrium alcohol flooding model for immiscible phase remediation: 1. Equation development

The equations for a compositional model for simulation of a two-phase, three-component system with inter-phase mass transfer are developed. Emphasis is placed on development of inter-phase mass transfer equations for incorporation of rate-limited inter-phase mass transfer. Due to the nature of the three-component systems considered, a single-film model may be inadequate and a two-film model must be utilized. A two-film model accounts for the simultaneous transfer of components in both directions across phase interfaces. The effect of interaction between components on diffusion is considered using a general form of Fick's Law. A Hand Plot representation of ternary phase behavior is chosen since it allows for straightforward calculation of miscibility of bulk phases under conditions of local non-equilibrium. The developed set of equations form the basis for a numerical model to simulate the enhanced removal of non-aqueous phase liquids (NAPLs) from porous media using single-component alcohol floods.     

Line-Driven Instability

Line-driven winds are subject to a strong radiation-hydrodynamic instability. We discuss the linear stability analysis and numerical simulations of the fully developed wind structure. The latter show sequences of strong reverse shocks, and two different families of clouds which mutually collide. Possible applications are the X-ray emission from O stars and the formation of dense clouds in broad absorption line quasars. This revised version was published online in July 2006 with corrections to the Cover Date.     

Development of longitudinal profiles of alluvial channels in response to base-level lowering

Degradation of alluvial channels in cohesive sediments was studied in 15 m and 20 m long flumes with a slope of 0°01 cm/cm. Degradation was initiated by lowering base level to a fixed position, and the development of the longitudinal profile of the channel is analysed through a model formulated as a heat (diffusion) equation. It is based on the equation of sediment continuity, combined with an assumption regarding sediment transport, namely that sediment discharge is linearly proportional to the channel slope. In accordance with the boundary and initial conditions imposed by the experimental setup and procedure, the basic equation is amenable to an analytical solution, which defines bed elevation at any distance and time, as a function of the amount of base-level lowering and a ‘diffusion’ coefficient. Additional problems arising from bank erosion and channel armouring are also treated successfully within the framework of the same model. The results show that in homogeneous alluvial sediments, not subject to armouring, the ultimate result of base-level lowering by a certain amount is degradation all along the channel by the same amount. The main impact of erosion is felt in the early stages after initiation of the process, and mainly near the mouth. The rate of degradation at any station along the channel reaches a peak and then slowly decreases with time, and the peak rate is attenuated with distance from the outlet. The model permits the prediction of intermediate stages of profile development at any distance from the outlet and at different times.     

A general mixing equation with applications to Icelandic basalts

The mixing equation applied by Vollmer [1] to Pb and Sr isotope ratios is shown to be a general equation applicable to consideration of element and isotope ratios. The mixing equation is hyperbolic and has the form:Ax + Bxy + Cy + D = 0where the coefficients are dependent on the type of plot considered: i.e. ratio-ratio, ratio-element, or element-element. Careful use of this equation permits testing whether mixing is a viable process, places constraints on end member compositions, allows distinction between mixing of sources and mixing of magmas, and should allow distinction between recent mixing and long-term evolution of sources.The available chemical data for postglacial basalts from Iceland and along the Reykjanes Ridge are not consistent with either mixing of magmas or simple mixing of an enriched ocean island source with a depleted ocean ridge source. If the available analyses for basalts are representative of the source regions, the data are consistent with at least two models neither of which can be properly tested with the available data.(1) There are two separate mixing trends: one beneath Iceland with the alkali basalt source and a depleted Iceland source as end members; the second along the Reykjanes Ridge with a heterogeneous ocean ridge basalt source and a source similar to that for intermediate basalts on Iceland as end members. The depleted Iceland source and the depleted ocean ridge source are not the same.(2) The chemistry of the basalts is not determined by mixing. Instead the basalts are derived from a multiplicity of sources with a similar history which have been isolated for hundreds of millions of years.     

Organochlorine residues,eggshell thickness,and nest success in barn owls from the Chesapeake Bay

Eggs of barn owls (Tyto alba) were collected from 18 nests in offshore duck blinds on the Maryland side of the lower Potomac River estuary in 1972 and 1973 and analyzed for organochlorine residues. DDE was found in 100% of the clutches, PCBs in 89%, and dieldrin in 78%. Eggshell thickness was inversely correlated with concentrations of DDE, DDD, and dieldrin residues. Six of the 18 clutches had mean DDE residues above 5 ppm, and eggshell thickness in these six clutches was significantly less (P<0.001) than in the other 12 clutches. The owls produced 1.7 young per active nest in 1973. This rate is slightly below the reproductive rate needed to maintain a stable population. An estimated 15% of the population carried concentrations of organochlorine residues that may have been detrimental to their reproduction. Passerine birds, taken extensively as food by a small proportion of the population, are believed to have been the source of elevated concentrations of organochlorines in these barn owls.     

Strontium isotope geochemistry of a low potassium olivine tholeiite and two basalt-pyroxene andesite magma series from the Medicine Lake Highland,California

Three contemporaneous yet mineralogically and chemically distinct lava series which range in composition from olivine basalt through basaltic andesite through two-pyroxene andesite, have been analyzed for their strontium isotopic composition. The Mammoth-Modoc lavas produce a mantle isochron which suggests derivation from a source approximately 243 m.y. old. The Medicine Lake shield-forming extrusives produce a minimum mantle isochron; the age of this source is likely greater than 760 m.y. old. Encompassing the entire time span of eruption for the two basalt-andesite series are a number of low potassium high alumina olivine tholeiite lavas which, when analyzed as a coherent group, produce a zero age. Lavas related to these three magma series have been extruded during the last 10⁵ years and cover a limited geographic area. The isotope data suggest a model with substantial heterogeneity in the subcontinental lithosphere and asthenosphere, at least beneath the Medicine Lake Highland portion of the southern Cascade petrographic province.Contribution No. 126