Melts of garnet lherzolite: experiments, models and comparison to melts of pyroxenite and carbonated lherzolite

Phase equilibrium experiments on a compositionally modified olivine leucitite from the Tibetan plateau have been carried out from 2.2 to 2.8 GPa and 1,380–1,480 °C. The experiments-produced liquids multiply saturated with spinel and garnet lherzolite phase assemblages (olivine, orthopyroxene, clinopyroxene and spinel ± garnet) under nominally anhydrous conditions. These SiO₂-undersaturated liquids and published experimental data are utilized to develop a predictive model for garnet lherzolite melting of compositionally variable mantle under anhydrous conditions over the pressure range of 1.9–6 GPa. The model estimates the major element compositions of garnet-saturated melts for a range of mantle lherzolite compositions and predicts the conditions of the spinel to garnet lherzolite phase transition for natural peridotite compositions at above-solidus temperatures and pressures. We compare our predicted garnet lherzolite melts to those of pyroxenite and carbonated lherzolite and develop criteria for distinguishing among melts of these different source types. We also use the model in conjunction with a published predictive model for plagioclase and spinel lherzolite to characterize the differences in major element composition for melts in the plagioclase, spinel and garnet facies and develop tests to distinguish between melts of these three lherzolite facies based on major elements. The model is applied to understand the source materials and conditions of melting for high-K lavas erupted in the Tibetan plateau, basanite–nephelinite lavas erupted early in the evolution of Kilauea volcano, Hawaii, as well as younger tholeiitic to alkali lavas from Kilauea.     

The Hydraulic Profiling Tool for Hydrogeologic Investigation of Unconsolidated Formations

The hydraulic profiling tool (HPT) has become one of the basic tools for investigation of soils and unconsolidated formations over the last 10 years. The HPT is advanced into the subsurface using direct push methods. Clean water is injected into the formation from a small screened port on the side of the probe as it is steadily advanced into the subsurface. A downhole pressure sensor detects the pressure required to inject the water into the formation while an up-hole flowmeter monitors the water flow rate. An electrical conductivity (EC) array included in the lower end of the probe provides a simultaneous EC log of the bulk formation. The EC log, HPT pressure, and flow rate are logged and displayed onscreen as the probe is advanced. These logs enable the investigator to evaluate vertical changes in relative formation permeability at high resolution. Pressure dissipation tests may be performed at selected depths in coarse-grained materials to determine the piezometric pressure in saturated formations. This enables the operator to define the piezometric profile and determine the piezometric surface without a well. Post processing of the log in the viewing software provides for calculation of the corrected HPT pressure (Pc) and estimation of hydraulic conductivity (Est. K) within limits (~0.1 to 75 ft/d). In clean, coarse-grained materials the tandem EC log may be used to estimate groundwater specific conductance based on an Archie's Law model. Cross sections of HPT logs provide an efficient means to define hydrostratigraphy. When combined with contaminant logging tools such as the membrane interface probe (MIP) the HPT data may help to define contaminant migration pathways or contaminated low permeability zones that may result in back diffusion. The HPT can be a useful tool for many geoenvironmental investigations in unconsolidated formations.     

Applying the HPT‐GWS for Hydrostratigraphy,Water Quality and Aquifer Recharge Investigations

The primary objective of this study was to evaluate use of the hydraulic profiling tool‐groundwater sampler (HPT‐GWS) log data as an indicator of water quality (level of dissolved ionic species) in an alluvial aquifer. The HPT‐GWS probe is designed for direct push advancement into unconsolidated formations. The system provides both injection pressure logs and electrical conductivity (EC) logs, and groundwater may be sampled at multiple depths as the probe is advanced (profiling). The combination of these three capabilities in one probe has not previously been available. During field work it was observed that when HPT corrected pressure (P_c) indicates a consistent aquifer unit then bulk formation EC can be used as an indicator of water quality. A high correlation coefficient (R ² = 0.93) was observed between groundwater specific conductance and bulk formation EC in the sands and gravels of the alluvial aquifer studied. These results indicate that groundwater specific conductance is exerting a controlling influence on the bulk formation EC of the coarse‐grained unit at this site, and probably many similar sites, consistent with Archie's Law. This simple relationship enables the use of the EC and P_c logs, with targeted water samples and a minimum of core samples, to rapidly assess groundwater quality over extended areas at high vertical resolution. This method was used to identify both a brine impacted zone at the base of the aquifer investigated and a groundwater recharge lens developing below storm water holding ponds in the upper portion of the same aquifer. Sample results for trace level, naturally occurring elements (As, Ba, U) further demonstrate the use of this system to sample for low level groundwater contamination.     

State of water molecules and silanol groups in opal minerals: a near infrared spectroscopic study of opals from Slovakia

Recently, near infrared spectroscopy in combination with double derivative technique has been effectively used by Christy (Vib Spectrosc 54:42–49, 2010) to study and differentiate between free and hydrogen bonded silanol groups on silica gel surface. The method has given some insight into the type of functionalities, their location in silica gel samples, and the way the water molecules bind onto the silanol groups. The important information in this respect comes from the overtones of the OH groups of water molecules hydrogen-bonded to free silanol groups, and hydrogen-bonded silanol groups absorbing in the region 5,500–5,100 cm⁻¹. Chemically, opal minerals are hydrated silica and the same approach was adapted to study the state of water molecules, silanol functionalities, and their locations in opal samples from Slovakia. Twenty opal samples classified into CT and A classes and one quartz sample were used in this work. The samples were crushed using a hydraulic press and powderized. Each sample was then subjected to evacuation process to remove surface-adsorbed water at 200°C, and the near infrared spectrum of each sample was measured using a Perkin Elmer NTS FT-NIR spectrometer equipped with a transflectance accessory and a DTGS detector. The samples were also heated to 750°C to remove the hydrogen-bonded silanol groups on the surface to reveal their locality. Second derivative profiles of the near infrared reflectance spectra were obtained using the instrument’s software and used in the detailed analysis of the samples. The analysis of the near infrared spectra and their second derivative profiles had the aim in finding relationships between the surface chemical structure and the classification of opal samples. The dry opal samples were also tested for their surface adsorption effectivity toward water molecules. The results indicate that the opal samples contain (1) surface-adsorbed water, (2) free and hydrogen-bonded silanol groups on the surface, (3) trapped water molecules in the bulk, and (4) free and hydrogen-bonded silanol groups in the cavity surfaces in the bulk. A part of the water molecules in the bulk of opal minerals are found as free molecules and the rest are found in hydrogen-bonded state to either free or vicinal or geminal silanol groups.     

Towards domestic fair trade? Farm labor, food localism, and the ‘family scale’ farm

Over the past several decades, consumers in the global North have increasingly looked to fair or alternative trading systems as a means to promote ecologically and socially sustainable agricultural production. While fair trade has historically been limited to international commodity networks, US-based agro-food activists have recently turned their attentions towards building a domestic movement, to bring fair trade principles and standards ‘home.’ Through an exploration of this growing movement, we consider the potential for third party certification and labeling to incorporate social justice into US-based agricultural production, with a particular focus on the implications for farm workers. We view current efforts to bring the principles of fair trade to the domestic arena as a reflection of several interrelated developments: a growing need on the part of small and mid-sized farmers to garner price premiums due to the erosion of the organic price premium; a recognition of the failure of organic certification to advance a holistic vision of sustainability; and the strategic embrace of voluntary regulatory mechanisms as an alternative to public regulation and collective bargaining. Initial research suggests that this has led to particular framings of the domestic fair trade concept, which may undermine the movement’s ability to address the social relations of agro-food production. Specifically, prioritization of the ‘family-scale’ farm and an undercurrent of food localism may obscure farm workers’ role in valorizing the US agricultural landscape.

Influence of estuarine hypoxia on feeding and sound production by two sympatric pipefish species (Syngnathidae)

This research utilizes the acoustic behavior of two sympatric pipefish species to assess the impact of hypoxia on feeding. We collected northern, Syngnathus fuscus, and dusky pipefishes, Syngnathus floridae, from the relatively pristine Chincoteague Bay, Virginia, USA and audiovisually recorded behavior in the laboratory of fish held in normoxic (>5 mg/L O(2)) and hypoxic (2 and 1 mg/L O(2)) conditions. Both species produced high frequency ( approximately 0.9-1.4 kHz), short duration (3-22 msec) clicks. Feeding strikes were significantly correlated with both wet weight of ingested food and click production. Thus, sound production serves as an accurate measure of feeding activity. In hypoxic conditions, reduced food intake corresponded with decreased sound production. Significant declines in both behaviors were evident after 1 day and continued as long as hypoxic conditions were maintained. Interspecific differences in sensitivity were detected. Specifically, S. floridae showed a tendency to perform head snaps at the surface. S. fuscus exhibited a breakdown in the coupling of sound production with food intake in 2 mg/L O(2) with clicks produced in other contexts, particularly choking and food expulsion. Reductions in feeding will ultimately impact growth, health, and eventually reproduction as resources are devoted to survival instead of gamete production and courtship. This work suggests acoustic monitoring of field sites with adverse environmental conditions may reflect changes in feeding behavior in addition to population dispersal.     

Depth-dependent sampling to identify short-circuit pathways to public-supply wells in multiple aquifer settings in the United States

Depth-dependent water-quality and borehole flow data were used to determine where and how contamination enters public-supply wells (PSWs) at study sites in different principal aquifers of the United States. At each of three study sites, depth-dependent samples and wellbore flow data were collected from multiple depths in selected PSWs under pumping conditions. The chemistry of these depth-dependent samples, along with samples of the surface discharge from the PSWs, was compared to that of adjacent nested monitoring wells. The results of depth-dependent analyses from sites in Modesto (California), York (Nebraska), and Tampa (Florida) are summarized and compared. Although the exact mechanisms for transport of contaminants to the PSWs varied among these hydrogeologic settings, in all three settings the presence of wells or boreholes or natural preferential flow paths allowed water and contaminants to bypass substantial portions of the aquifer and to reach PSWs or depths in the aquifer more quickly than would have occurred in the absence of these short-circuiting flow paths. The chemistry and flow data from multiple depths was essential to developing an understanding of the dominant flow paths of contaminants to PSW in all three settings. This knowledge contributes to developing effective strategies for monitoring and protection.