The star-forming content of the W3 giant molecular cloud

We have surveyed a ∼0.9 square degree area of the W3 giant molecular cloud (GMC) and star-forming region in the 850-μm continuum, using the Submillimetre Common-User Bolometer Array on the James Clerk Maxwell Telescope. A complete sample of 316 dense clumps were detected with a mass range from around 13 to  2500 M_⊙  . Part of the W3 GMC is subject to an interaction with the H  ii region and fast stellar winds generated by the nearby W4 OB association. We find that the fraction of total gas mass in dense, 850-μm traced structures is significantly altered by this interaction, being around 5–13 per cent in the undisturbed cloud but ∼25–37 per cent in the feedback-affected region. The mass distribution in the detected clump sample depends somewhat on assumptions of dust temperature and is not a simple, single power law but contains significant structure at intermediate masses. This structure is likely to be due to crowding of sources near or below the spatial resolution of the observations. There is little evidence of any difference between the index of the high-mass end of the clump mass function in the compressed region and in the unaffected cloud. The consequences of these results are discussed in terms of current models of triggered star formation.     

The relationship between dissolved hydrogen and nitrogen fixation in ocean waters

Fixed nitrogen is a key nutrient involved in regulating global marine productivity and hence the global oceanic carbon cycle. Oceanic nitrogen (N₂) fixation is estimated to supply 8×10¹² moles N y^?1 to the ocean, approximately equal to current riverine and the atmospheric inputs of fixed N, and between 50 and 100% of current estimates of oceanic denitrification. However, the spatial and temporal variability of N₂ fixation remains uncertain, mostly because of the normal low resolution sampling for diazotroph distribution and fixation rates. It is well established that N₂ fixation, mediated by the enzyme nitrogenase, is a source of hydrogen (H₂), but the extent to which it leads to supersaturation of H₂ in oceanic waters is unresolved. Here, we present simultaneous measurements of upper ocean dissolved H₂ concentration (nmol L^?1), and rates of N₂ fixation (μmol N m^?3 d^?1), determined using ¹⁵N₂ tracer techniques (at 7 or 15 m), on a transect from Fiji to Hawaii. We find a significant correlation (r=0.98) between dissolved H₂ and rates of N₂ fixation, with the greatest supersaturation of H₂ and highest rates of N₂ fixation being observed in the subtropical gyres at the southern (～18°S) and northern (18°N) reaches of the transect. The lowest H₂ saturation and N₂ fixation were observed in the equatorial region between 8°S and 14°N. We propose that an empirical relationship between H₂ supersaturations and N₂ fixation measurements could be used to guide sampling for ¹⁵N fixation measurements or to aid the spatial interpolation of such measurements.     

Ammonia-water ice laboratory studies relevant to outer Solar System surfaces

Although water- and ammonia-ices have been observed or postulated as important components of the icy surfaces of planetary satellites in the outer Solar System, significant gaps exist in our knowledge of the spectra and behavior of such mixtures under astrophysical conditions. To that end, we have completed low-temperature spectroscopic studies (1-20 μm) of water-ammonia mixtures, with an emphasis on features in the near-IR, a region which is accessible to ground-based observations. The influences of composition, formation temperature, thermal- and radiation-processing, and phase (crystalline or amorphous) of the components were examined. Spectra of both pure NH₃ and H₂O-NH₃ icy mixtures with ratios from 0.7 to 57 were measured at temperatures from 10 to 120 K. Conditions for the formation and thermal stability of the ammonia hemihydrate (2NH₃⋅H₂O) and the ammonia monohydrate (NH₃⋅H₂O) have been examined. Band positions of NH₃ in different H₂O-ices and major band positions of the hydrates were measured. We report spectral shifts that depend on concentration and temperature. The radiation-induced amorphization of the hemihydrate was observed and the radiation destruction of NH₃ in H₂O-ices was measured. Implications of these results for the formation, stability, and detection of ammonia on outer satellite surfaces are discussed.     

The formation and stability of carbonic acid on outer Solar System bodies

The radiation chemistry, thermal stability, and vapor pressure of solid-phase carbonic acid (H₂CO₃) have been studied with mid-infrared spectroscopy. A new procedure for measuring this molecule’s radiation stability has been used to obtain intrinsic IR band strengths and half-lives for radiolytic destruction. We report, for the first time, measurements of carbonic acid’s vapor pressure (0.290-2.33 × 10⁻¹¹ bar for 240-255 K) and its enthalpy of sublimation (71 ± 9 kJ mol⁻¹). We also report the first observation of a chemical reaction involving solid-phase carbonic acid. Possible applications of these findings are discussed, with an emphasis on the outer Solar System icy surfaces.     

Nitrate contamination in irrigation groundwater,Isfahan, Iran

Groundwater is one of the major sources of water in Isfahan. Efficient management of these resources requires a good understanding of its status. This paper focuses on the hydrochemistry and also it wants to assess the nitrate concentration in irrigation groundwater of Isfahan suburb. All the groundwater samples are grouped into three categories, including Na-Cl + Ca-Cl (63 %), Na-SO₄ + Ca-SO₄ (23 %) and Ca-HCO₃ (14 %). According to the EC and SAR, the most dominant classes are C3S1, C4S2 and C4S3. 55 % of samples indicate very high salinity and medium to very high alkalinity that is not suitable for irrigation. 84 % of the groundwater samples show nitrate contents higher than HAV (13 mg l^?), while more than 25 % exceeded the maximum contamination level (44.27 mg l^?) according to EPA regulations. The horizontal and vertical distribution patterns of nitrate in groundwater samples show a surficial origin for nitrate contamination. The high nitrate content can be attributed to the agricultural activities along with domestic sewage and industrial wastewaters in populated area. Based on results, using high nitrate groundwater for irrigation can minimize the requirement for inorganic fertilizers and reduce the cost of cultivation and nitrate contamination.     

Vanadium and niobium behavior in rutile as a function of oxygen fugacity: evidence from natural samples

Vanadium occurs in multiple valence states in nature, whereas Nb is exclusively pentavalent. Both are compatible in rutile, but the relationship of V–Nb partitioning and dependence on oxygen fugacity (expressed as fO₂) has not yet been systematically investigated. We acquired trace-element concentrations on rutile grains (n = 86) in nine eclogitic samples from the Dabie-Sulu orogenic belt by laser ablation inductively coupled plasma mass spectrometry (LA–ICP–MS) and combined them with published results in order to assess the direct and indirect effects of oxygen fugacity on the partitioning of V and Nb into rutile. A well-defined negative correlation between Nb (7–1,200 ppm) and V concentrations (50–3,200 ppm) was found, documenting a competitive relationship in the rutile crystal that does not appear to be controlled by bulk rock or mineral compositions. Based on the published relationship of ^RtD_V and V valence with ?QFM, we suggest that the priority order of V incorporation into rutile is V⁴⁺ > V³⁺ > V⁵⁺. The inferred Nb–V competitive relationship in rutile from the Dabie-Sulu orogenic belt could be explained by decreasing fO₂ due to dehydration reactions involving loss of oxidizing fluids during continental subduction: The increased proportion of V³⁺ (expressed as V³⁺/∑V) and attendant decrease in ^RtD_V is suggested to lead to an increase in rutile lattice sites available for Nb⁵⁺. A similar effect may be observed under more oxidizing conditions. When V⁵⁺/∑V increases, ^RtD_V shows a dramatic decline and Nb concentration increases considerably. This is possibly documented by rutile in highly metasomatized and oxidized MARID-type (MARID: mica–amphibole–rutile–ilmenite–diopside) mantle xenoliths from the Kaapvaal craton, which also show a negative V–Nb covariation. In addition, their Nb/Ta covaries with V concentrations: For V concentrations <1,250 ppm, Nb/Ta ranges between 35 and 45, whereas for V > 1,250 ppm, Nb/Ta is considerably lower (5–15). This relationship is mainly controlled by a change in Nb concentrations, suggesting that the indirect dependence of ^RtD_Nb on fO₂, which is not mirrored in ^RtD_Ta, can exert considerable influence on rutile Nb–Ta fractionation.     

Spatial interpolation of snow water equivalency using surface observations and remotely sensed images of snow‐covered area

As demand for water continues to escalate in the western Unites States, so does the need for accurate monitoring of the snowpack in mountainous areas. In this study, we describe a simple methodology for generating gridded‐estimates of snow water equivalency (SWE) using both surface observations of SWE and remotely sensed estimates of snow‐covered area (SCA). Multiple regression was used to quantify the relationship between physiographic variables (elevation, slope, aspect, clear‐sky solar radiation, etc.) and SWE as measured at a number of sites in a mountainous basin in south‐central Idaho (Big Wood River Basin). The elevation of the snowline, obtained from the SCA estimates, was used to constrain the predicted SWE values. The results from the analysis are encouraging and compare well to those found in previous studies, which often utilized more sophisticated spatial interpolation techniques. Cross‐validation results indicate that the spatial interpolation method produces accurate SWE estimates [mean R² = 0·82, mean mean absolute error (MAE) = 4·34 cm, mean root mean squared error (RMSE) = 5·29 cm]. The basin examined in this study is typical of many mid‐elevation mountainous basins throughout the western United States, in terms of the distribution of topographic variables, as well as the number and characteristics of sites at which the necessary ground data are available. Thus, there is high potential for this methodology to be successfully applied to other mountainous basins. Copyright © 2010 John Wiley & Sons, Ltd.