The shedding of mesoscale anticyclonic eddies from the Alaskan Stream and westward transport of warm water

The south-flowing waters of the Kamchatka and Oyashio Currents and west-flowing waters of the Alaskan Stream are key components of the western sub-Arctic Pacific circulation. We use CTD data, Argo buoys, WOCE surface drifters, and satellite-derived sea-level observations to investigate the structure and interannual changes in this system that arise from interactions among anticyclonic eddies and the mean flow. Variability in the temperature of the upstream Oyashio and Kamchatka Currents is evident by warming in mesothermal layer in 1994–2005 compared to 1990–1991. A major fraction of the water in these currents is derived directly from the Alaskan Stream. The stream also sheds large anticyclonic (Aleutian) eddies, averaging approximately 300 km in diameter with a volume transport significant in comparison with that of the Kamchatka Current itself. These eddies enclose pools of relatively warm and saline water whose temperature is typically 4 °C warmer and salinity is 0.4 greater than that of cold-core Kamchatka eddies in the same density range. Aleutian eddies drift at approximately 1.2 km d⁻¹ and retain their distinctive warm and salty characteristics for at least 2 years. Selected westward pathways during 1990–2004 are identified. If the shorter northern route is followed, Aleutian eddies remain close to the stream and persist sufficiently long to carry warm and saline water directly to the Kamchatka Current. This was observed during 1994–1997 with substantial warming of the waters in the Kamchatka Current and upstream Oyashio. If the eddies take a more southern route they detach from the stream but can still contribute significant quantities of warm and saline water to the upstream Oyashio, as in 2004–2005. However, the eddies following this southern route may dissipate before reaching the western boundary current region.     

The effect of Ca-Tschermaks component on trace element partitioning between clinopyroxene and silicate melt

We have studied the influence of Ca-Tschermaks (Calcium Tschermaks or CaTs) content of clinopyroxene on the partitioning of trace elements between this phase and silicate melt at fixed temperature and pressure. Ion probe analyses of experiments carried out in the system Na₂O–CaO–MgO–Al₂O₃–SiO₂, at 0.1 MPa and 1218°C, produced crystal-melt partition coefficients (D) of 36 trace elements (Li, Cl, Sc, Ti, V, Cr, Fe, Co, Ge, Sr, Y, Zr, Nb, Mo, Ru, Rh, In, Sn, Sb, Ba, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Hf, Ta and W), for clinopyroxene compositions between 10 and 32 mol% CaTs. Partition coefficients for 2+ to 5+ cations show, for each charge, a near parabolic dependence of log D on ionic radius of the substituting cation, for partitioning into both the M1 and M2 sites of clinopyroxene. Fitting the results to the elastic strain model of Blundy and Wood [Blundy, J.D., Wood, B.J., 1994. Prediction of crystal-melt partition coefficients from elastic moduli. Nature 372, 452–454] we obtain results for the strain-free partition coefficients of theoretical cations (D₀), with site radius r₀, and for the site's Young's Modulus (E).

In agreement with earlier data our results show that increasing ^ivAl concentration in cpx is matched by increasing D, E_M1, E_M2 and D₀ for tri-, tetra- and pentavalent cations. The degree of fractionation between chemically similar elements (i.e. Ta/Nb, Zr/Hf) also increases. In contrast, D values for mono-, di- and hexavalent cations decrease with increasing ^ivAl in the cpx. The large suite of trace elements used has allowed us to study the effects of cation charge on D₀, r₀ and E. We have found that D₀ and r₀ decrease with increasing cation charge, e.g. r₀=0.66 Å for 4+ cations and 0.59 Å for 5+ cations substituting into M1. Values of E_M1 and E_M2 increase with cation charge as well as with increasing ^ivAl content. The increase in E_M2 is linear and close to the trend set by Hazen and Finger [Hazen, R.M., Finger, L.W., 1979. Bulk modulus-volume relationship for cation–anion polyhedra. J. Geophys. Res. 84 (10) 6723–6728] for oxides. E_M1 values are much higher and do not fit the trend predicted by the Hazen and Finger relationship.     

Effect of heat treatment on tourmaline from Brazil

The crystal-chemical behaviour of tourmaline from Araçuaí, Minas Gerais state, Brazil, when subjected to heating in air atmosphere has been studied by several techniques, including EMPA, UV–Vis, TGA, and Mössbauer spectroscopy. The tourmaline samples are typically intermediate members of the elbaite-schorl series. The origin of colour and of its change after treatment has been discussed in terms of local disorder, presence of metal transition elements, oxidation of ferrous iron at the octahedral site, and simultaneous trap of the excess electron. These findings may be used to enhance the colour in tourmaline crystals or generate wanted colour changes.     

The agricultural utility of lithic-mulch gardens: Past and present

The mulching of agricultural fields and gardens with stones, pebbles, volcanic ash and similar lithic materials is a variant agricultural strategy uniquely suited to the constraints of a dryland environment. While the agricultural literature contains reports on limited experiments with stone or gravel mulch, data regarding the employment of lithic mulch are lacking. This paper works to bridge this gap by comparing empirical data collected from prehistoric pebble-mulch gardens in the Galisteo Basin (New Mexico) to contemporary agricultural experiments with lithic mulch. Such past-present and experimental-real world comparisons allow us to more fully address the effectiveness of lithic mulching as an agricultural strategy. It is affirmed that lithic mulch is applied to garden plots, especially during periods of drought, in order to reduce soil erosion from wind and water, increase soil temperature to extend the growing season, increase water infiltration, and reduce the evaporative loss of water from wind and sun. The cumulative effect of this soil and water conserving technique is an increase in crop biomass and crop yield.     

AMRVAC and relativistic hydrodynamic simulations for gamma-ray burst afterglow phases

We apply a novel adaptive mesh refinement (AMR) code, AMRVAC (Adaptive Mesh Refinement version of the Versatile Advection Code), to numerically investigate the various evolutionary phases in the interaction of a relativistic shell with its surrounding cold interstellar medium (ISM). We do this for both 1D isotropic and full 2D jet-like fireball models. This is relevant for gamma-ray bursts (GRBs), and we demonstrate that, thanks to the AMR strategy, we resolve the internal structure of the shocked shell–ISM matter, which will leave its imprint on the GRB afterglow. We determine the deceleration from an initial Lorentz factor  γ= 100  up to the almost Newtonian     phase of the flow. We present axisymmetric 2D shell evolutions, with the 2D extent characterized by their initial opening angle. In such jet-like GRB models, we discuss the differences with the 1D isotropic GRB equivalents. These are mainly due to thermally induced sideways expansions of both the shocked shell and shocked ISM regions. We found that the propagating 2D ultrarelativistic shell does not accrete all the surrounding medium located within its initial opening angle. Part of this ISM matter gets pushed away laterally and forms a wide bow-shock configuration with swirling flow patterns trailing the thin shell. The resulting shell deceleration is quite different from that found in isotropic GRB models. As long as the lateral shell expansion is merely due to ballistic spreading of the shell, isotropic and 2D models agree perfectly. As thermally induced expansions eventually lead to significantly higher lateral speeds, the 2D shell interacts with comparably more ISM matter and decelerates earlier than its isotropic counterpart.     

Multimodel analysis on the response of the AMOC under an increase of radiative forcing and its symmetrical reversal

Climate Dynamics - The response of the Atlantic meridional overturning circulation (AMOC) to an increase of radiative forcing (ramp-up) and a subsequent reversal of radiative forcing (ramp-down) is...     

Bromine cycle in subduction zones through in situ Br monitoring in diamond anvil cells

The geochemical partitioning of bromine between hydrous haplogranitic melts, initially enriched with respect to Br and aqueous fluids, has been continuously monitored in situ during decompression. Experiments were carried out in diamond anvil cells from 890 °C to room temperature and from 1.7 GPa to room pressure, typically from high P, T conditions corresponding to total miscibility (presence of a supercritical fluid). Br contents were measured in aqueous fluids, hydrous melts and supercritical fluids. Partition coefficients of bromine were characterized at pressure and temperature between fluids, hydrous melts and/or glasses, as appropriate: D^Br_fluid/melt = (Br)_fluid/(Br)_melt, ranges from 2.18 to 9.2 ± 0.5 for conditions within the ranges 0.66-1.7 GPa, 590-890 °C; and D^Br_fluid/glass = (Br)_fluid/(Br)_glass ranges from 60 to 375 at room conditions. The results suggest that because high pressure melts and fluids are capable of accepting high concentrations of bromine, this element may be efficiently removed from the slab to the mantle source of arc magmas. We show that Br may be highly concentrated in subduction zone magmas and strongly enriched in subduction-related volcanic gases, because its mobility is strongly correlated with that of water during magma degassing. Furthermore, our experimental results suggest that a non negligible part of Br present in the subducted slab may remain in the down-going slab, being transported toward the transition zone. This indicates that the Br cycle in subduction zones is in fact divided in two related but independent parts: (1) a shallower one where recycled Br may leave the slab with a water and silica-bearing “fluid” leading to enriched arc magmas that return Br to the atmosphere. (2) A deeper cycle where Br may be recycled back to the mantle maybe to the transition zone, where it may be present in high pressure water-rich metasomatic fluids.     

Density-Stratified Flow Events in Great Salt Lake,Utah, USA: Implications for Mercury and Salinity Cycling

Density stratification in saline and hypersaline water bodies from throughout the world can have large impacts on the internal cycling and loading of salinity, nutrients, and trace elements. High temporal resolution hydroacoustic and physical/chemical data were collected at two sites in Great Salt Lake (GSL), a saline lake in the western USA, to understand how density stratification may influence salinity and mercury (Hg) distributions. The first study site was in a causeway breach where saline water from GSL exchanges with less saline water from a flow restricted bay. Near-surface-specific conductance values measured in water at the breach displayed a good relationship with both flow and wind direction. No diurnal variations in the concentration of dissolved (<0.45 μm) methylmercury (MeHg) were observed during the 24-h sampling period; however, the highest proportion of particulate Hg_total and MeHg loadings was observed during periods of elevated salinity. The second study site was located on the bottom of GSL where movement of a high-salinity water layer, referred to as the deep brine layer (DBL), is restricted to a naturally occurring 1.5-km-wide “spillway” structure. During selected time periods in April/May, 2012, wind-induced flow reversals in a railroad causeway breach, separating Gunnison and Gilbert Bays, were coupled with high-velocity flow pulses (up to 55 cm/s) in the DBL at the spillway site. These flow pulses were likely driven by a pressure response of highly saline water from Gunnison Bay flowing into the north basin of Gilbert Bay. Short-term flow reversal events measured at the railroad causeway breach have the ability to move measurable amounts of salt and Hg from Gunnison Bay into the DBL. Future disturbance to the steady state conditions currently imposed by the railroad causeway infrastructure could result in changes to the existing chemical balance between Gunnison and Gilbert Bays. Monitoring instruments were installed at six additional sites in the DBL during October 2012 to assess impacts from any future modifications to the railroad causeway.