Glacial runoff characteristics of the Koxkar Glacier,Tuomuer-Khan Tengri Mountain Ranges,China

This paper presents the glacial runoff characteristics of the Koxkar Glacier, China using flow records collected near the snout of the glacier in four consecutive years (2005–2008). The mean annual discharge of the Koxkar Glacier is 102.86 × 10⁶ m³, in which 93.6% occurs in ablation season (May–October). August brings about maximum discharge of about 29.6% to the total streamflow followed by July of some 26.0%. During the study years, total discharge varies little from year to year, whereas the inter-annual variability in monthly discharge is prominent, particularly in the beginning and in the end of the melt season. Seasonal runoff variability shows great monthly variations in discharge with mean coefficient of variation ranging from 0.02 in January to 0.77 in April. The mean diurnal amplitudes are found to be 0.90, 1.86, 4.71, 4.92, 1.17 and 0.43 m³ s⁻¹ for May, June, July, August, September and October, respectively. In the melt season, the maximum runoff is observed during 1800–0200 hours and the minimum occurs during 0700–1000 hours. Delaying effects are prominent in discharge over the ablation period. The time-lag between meltwater generation and its appearance in the streamflow near the snout of the glacier varies between 4.00 and 10.00 h, and time to peak varies between 10.00 and 17.00 h over the entire melt season. The relationship between discharge and temperature on monthly scale (R ² = 0.77) is better than that on daily scale (R ² = 0.55).     

Partition of arsenic in soils sediments and the origin of naturally elevated concentrations in groundwater of the southern pampa region (Argentina)

Excessive arsenic concentrations above the Argentinean and WHO guidelines for drinking water (10 μg L⁻¹) affects shallow aquifers of the southern Pampean Plain (Argentina) hosted in the Pampean and the Post Pampean formations (loess and reworked loess; Plio-Pleistocene–Holocene). Health problems related to high As concentrations in drinking waters are known as Endemic Regional Chronic Hydroarsenicism. Hydrochemistry of shallow groundwaters and soil geochemistry were investigated aiming to (1) understand the partition of As in the solid phase and its relationship with unacceptable As concentrations in waters, (2) identify the provision source of As to groundwaters. Only 5% of the samples had As concentrations <10 μg L⁻¹; in 27% As concentrations ranged from 10 to 50 μg L⁻¹ and in 58% it reached 60–500 μg L⁻¹. The coarse fraction (50–2,000 μm) hosts about 27% of the total As in the solid phase, being positively correlated to Ba (p < 0.01; r ² = 0.93). About 70% is included in the <2 μm fraction and had positive correlations of As–Fe (p < 0.05; r ² = 0.85) and As–Cr (p < 0.05; r ² = 0.68). Soils and sediment sand fractions of vadose zones are the primary sources of As in shallow groundwater while adsorption–desorption processes, codisolution–coprecipitation, and evaporation during the dry seasons raise As concentrations in waters exceeding the guideline value for drinking water.     

Hydrogeochemical processes in the groundwater environment of Heihe River Basin,northwest China

The Heihe River Basin is a typical arid inland river basin for examining stress on groundwater resources in northwest China. The basin is composed of large volumes of unconsolidated Quaternary sediments of widely differing grain size, and during the past half century, rapid socio-economic development has created an increased demand for groundwater resources. Understanding the hydrogeochemical processes of groundwater and water quality is important for sustainable development and effective management of groundwater resources in the Heihe River basin. To this end, a total of 30 representative groundwater samples were collected from different wells to monitor the water chemistry of various ions and its quality for irrigation. Chemical analysis shows that water presents a large spatial variability of chemical facies (SO₄ ²⁻–HCO₃⁻, SO₄ ²⁻–Cl⁻, and Cl⁻–SO₄ ²⁻) as groundwater flow from recharge area to discharge area. The ionic ratio indicates positive correlation between the flowing pairs of parameters: Cl⁻ and Na⁺(r = 0.95), SO₄ ²⁻ and Na⁺ (r = 0.84), HCO₃ ⁻ and Mg²⁺(r = 0.86), and SO₄ ²⁻ and Ca²⁺ (r = 0.91). Dissolution of minerals, such as halite, gypsum, dolomite, silicate, and Mirabilite (Na₂SO₄·10H₂O) in the sediments results in the Cl⁻, SO₄ ²⁻, HCO₃ ⁻, Na⁺, Ca²⁺ and Mg²⁺ content in the groundwater. Other reactions, such as evaporation, ion exchange, and deposition also influence the water composition. The suitability of the groundwater for irrigation was assessed based on the US Salinity Laboratory salinity classification and the Wilcox diagram. The results show that most of the groundwater samples are suitable for irrigation uses barring a few locations in the dessert region in the northern sub-basin.     

The Geochemistry of Supraglacial Streams of Canada Glacier,Taylor Valley (Antarctica), and their Evolution into Proglacial Waters

We have investigated the geochemistry of supraglacial streams on the Canada Glacier, Taylor Valley, Antarctica during the 2001–2002 austral summer. Canada Glacier supraglacial streams represent the link between primary precipitation (i.e. glacier snow) and proglacial Lake Hoare. Canada Glacier supraglacial stream geochemistry is intermediate between glacier snow and proglacial stream geochemistry with average concentrations of 49.1 μeq L⁻¹ Ca2+, 19.9 μeq L⁻¹ SO₄²⁻, and 34.3 μeq L⁻¹ HCO₃⁻. Predominant west to east winds lead to a redistribution of readily soluble salts onto the glacier surface, which is reflected in the geochemistry of the supraglacial streams. Western Canada Glacier supraglacial streams have average SO₄²⁻:HCO₃⁻ equivalent ratios of 1.0, while eastern supraglacial streams average 0.5, suggesting more sulfate salts reach and dissolve in the western supraglacial streams. A graph of HCO₃⁻ versus Ca2+ for western and eastern supraglacial streams had slopes of 0.87 and 0.72, respectively with R2 values of 0.84 and 0.83. Low concentrations of reactive silicate (> 10 μmol L⁻¹) in the supraglacial streams suggested that little to no silicate weathering occurred on the glacier surface with the exception of cryoconite holes (1000 μmol L⁻¹). Therefore, the major geochemical weathering process occurring in the supraglacial streams is believed to be calcite dissolution. Proglacial stream, Anderson Creek, contains higher concentrations of major ions than supraglacial streams containing 5 times the Ca²⁺ and 10 times the SO₄²⁻. Canada Glacier proglacial streams also contain higher concentrations (16.6–30.6 μeq L⁻¹) of reactive silicate than supraglacial streams. This suggests that the controls on glacier meltwater geochemistry switch from calcite and gypsum dissolution to both salt dissolution and silicate mineral weathering as the glacier meltwater evolves. Our chemical mass balance calculations indicate that of the total discharge into Lake Hoare, the final recipient of Canada Glacier meltwater, 81.9% is from direct glacier runoff and 19.1% is from proglacial Andersen Creek. Although during a typical, low melt ablation season Andersen Creek contributes over 40% of the water added to Lake Hoare, its overall chemical importance is diluted by the direct inputs from Canada Glacier during high flow years. Decadal warming events, such as the 2001–2002 austral summer produce supraglacial streams that are a major source of water to Lake Hoare.     

Effects of nitrogen fertilization on soil respiration in temperate grassland in Inner Mongolia,China

Nitrogen addition to soil can play a vital role in influencing the losses of soil carbon by respiration in N-deficient terrestrial ecosystems. The aim of this study was to clarify the effects of different levels of nitrogen fertilization (HN, 200 kg N ha⁻¹ year⁻¹; MN, 100 kg N ha⁻¹ year⁻¹; LN, 50 kg N ha⁻¹ year⁻¹) on soil respiration compared with non-fertilization (CK, 0 kg N ha⁻¹ year⁻¹), from July 2007 to September 2008, in temperate grassland in Inner Mongolia, China. Results showed that N fertilization did not change the seasonal patterns of soil respiration, which were mainly controlled by soil heat-water conditions. However, N fertilization could change the relationships between soil respiration and soil temperature, and water regimes. Soil respiration dependence on soil moisture was increased by N fertilization, and the soil temperature sensitivity was similar in the treatments of HN, LN, and CK treatments (Q ₁₀ varied within 1.70–1.74) but was slightly reduced in MN treatment (Q ₁₀ = 1.63). N fertilization increased soil CO₂ emission in the order MN > HN > LN compared with the CK treatment. The positive effects reached a significant level for HN and MN (P < 0.05) and reached a marginally significant level for LN (P = 0.059 < 0.1) based on the cumulative soil respiration during the 2007 growing season after fertilization (July–September 2007). Furthermore, the differences between the three fertilization treatments and CK reached the very significant level of 0.01 on the basis of the data during the first entire year after fertilization (July 2007–June 2008). The annual total soil respiration was 53, 57, and 24% higher than in the CK plots (465 g m⁻² year⁻¹). However, the positive effects did not reach the significant level for any treatment in the 2008 growing season after the second year fertilization (July–September 2008, P > 0.05). The pairwise differences between the three N-level treatments were not significant in either year (P > 0.05).     

Characteristics of aerosol dust in fresh snow in the Asian dust and non-dust periods at Urumqi glacier no. 1 of eastern Tian Shan,China

Windblown mineral aerosol dust derived from the crustal surface is an important atmospheric component affecting the earth’s radiation budget. Deposition of atmospheric dust was measured in the fresh snow on glacier no. 1 at the headwater of the Urumqi River in eastern Tian Shan, central Asia. An analysis of seasonal variation of concentrations of dust particles in the snow suggests that the number concentration of dust particle is significantly high from April to June, which may be caused by Asian dust storms in the spring. The comparison of mass-size distribution of dust particles from April to August shows an obvious seasonal change trend. The distribution of particles changes from single model (3–21 μm) in the non-dust period before dust events in April, to bi-model (3–21 and 20–80 μm) during the Asian dust period, and to single model (3–21 μm) after July in the non-dust period again. The Ca²⁺ concentration in the fresh snow is also very high from April to June, while NH₄ ⁺ and SO₄ ²⁻, as water-soluble constituents, have concentration changes that are different from each other. Backward trajectory was also employed to examine the transport process of air mass in this region.     

Glacier No. 4 of Sigong River over Mt. Bogda of eastern Tianshan, central Asia: thinning and retreat during the period 1962–2009

RTK-GPS data, aerial photographs and Aster images were used to quantify volume, surface elevation, terminus position and area changes of Glacier No. 4 of Sigong River over Mt. Bogda, Tianshan during the period from 1962 to 2009. Glacier surface elevation of the tongue area decreased by 15 ± 8 m (0.32 ± 0.17 m a⁻¹) and ice volume loss reached 0.014 ± 0.008 km³ (0.013 ± 0.007 km³ w. e.). The glacier terminus retreated at a rate of 8.0 m a⁻¹ and the area decreased by about 0.53 km², accounting for 15.8% of the glacier area in 1962 (3.33 km²). The changes can be primarily attributed to the significant increase in temperature in this region. A comparison with glacier changes by field measurements in other regions of eastern Tianshan showed obvious spatial differences in the magnitude of the changes, owing to a combination of regional climate change and topographical factors.     

National scale evaluation of groundwater chemistry in Korea coastal aquifers: evidences of seawater intrusion

Pollution of groundwater by seawater intrusion poses a threat to sustainable agriculture in the coastal areas of Korea. Therefore, seawater intrusion monitoring stations were installed in eastern, western, and southern coastal areas and have been operated since 1998. In this study, groundwater chemistry data obtained from the seawater intrusion monitoring stations during the period from 2007 to 2009 were analyzed and evaluated. Groundwater was classified into fresh (<1,500 μS/cm), brackish (1,500–3,000 μS/cm), and saline (>3,000 μS/cm) according to EC levels. Among groundwater samples (n = 233), 56, 7, and 37% were classified as the fresh, brackish, and saline, respectively. The major dissolved components of the brackish and saline groundwaters were enriched compared with those of the fresh groundwater. The enrichment of Na⁺ and Cl⁻ was especially noticeable due to seawater intrusion. Thus, the brackish and saline groundwaters were classified as Ca–Cl and Na–Cl types, while the fresh groundwater was classified as Na–HCO₃ and Ca–HCO₃ types. The groundwater included in the Na–Cl types indicated the effects of seawater mixing. Ca²⁺, Mg²⁺, Na⁺, K⁺, SO₄ ²⁻, and Br⁻ showed good correlations with Cl⁻ of over r = 0.624. Of these components, the strong correlations of Mg²⁺, SO₄ ²⁻, and Br⁻ with Cl⁻ (r ≥ 0.823) indicated a distinct mixing between fresh groundwater and seawater. The Ca/Cl and HCO₃/Cl ratios of the groundwaters gradually decreased and approached those of seawater. The Mg/Cl, Na/Cl, K/Cl, SO₄/Cl, and Br/Cl ratios of the groundwaters gradually decreased, and were similar to or lower than those of seawater, indicating that Mg²⁺, Na⁺, K⁺, SO₄ ²⁻, and Br⁻, as well as Cl⁻ in the saline groundwater can be enriched by seawater mixing, while Ca²⁺ and HCO₃ ⁻ are mainly released by weathering processes. The influence of seawater intrusion was evaluated using threshold values of Cl⁻ and Br⁻, which were estimated as 80.5 and 0.54 mg/L, respectively. According to these criteria, 41–50% of the groundwaters were affected by seawater mixing.     

Stable water isotope climate archives in springs from the Olympic Mountains,Washington

The ¹⁸O and ²H (HDO) compositions are summarized for sampled springs (n = 81) within the Elwha watershed (≈692 km²) on the northern Olympic Peninsula. Samples, collected during 2001–2009, of springs (n = 158), precipitation (n = 520), streams (n = 176), and firn (n = 3) assisted the determinations for meteoric composition of recharge waters. The local mean water line (LMWL) is defined as δ²H = 8.2δ¹⁸O − 9.3 for the watershed. Recharge history is surmised from groundwater ages ranging from 5 ± 3 years (apparent ⁸⁵Kr) to 9,490 ± 420 ¹⁴C cal years BP. About 56% of the springs were recharged over the last 1,000 years while 13% of springs were recharged over 5,000 years ago. Spring HDO values fluctuate between −11.8 to −15.6‰ δ¹⁸O and −90.9 to −119.4‰ δ²H. Deuterium excess values predominate around 4–6‰. The HDO proxy records from springs suggest a pronounced paleoclimate shift in air masses near 5,000 year BP on the Peninsula.     

Coastal Phytoplankton Do Not Rest in Winter

The climatology and interannual variability of winter phytoplankton was analyzed at the Long Term Ecological Research Station MareChiara (LTER-MC, Gulf of Naples, Mediterranean Sea) using data collected from 1985 to 2006. Background winter chlorophyll values (0.2–0.5 μg chl a dm⁻³) were associated with the dominance of flagellates, dinoflagellates, and coccolithophores. Winter biomass increases (<5.47 μg chl a dm⁻³) were often recorded until 2000, generally in association with low-salinity surface waters (37.3–37.9). These blooms were most often caused by colonial diatoms such as Chaetoceros spp., Thalassiosira spp., and Leptocylindrus danicus. In recent years, we observed more modest and sporadic winter biomass increases, mainly caused by small flagellates and small non-colonial diatoms. The resulting negative chl a trend over the time series was associated with positive surface salinity and negative nutrient trends. Physical and meteorological conditions apparently exert a strict control on winter blooms, hence significant changes in winter productivity can be foreseen under different climatic scenarios.     

A comparative study on isotopic composition of precipitation in wet tropic and semi-arid stations across southern India

Isotopic composition of monthly composite precipitation samples from Kozhikode (n = 31), a wet tropic station and Hyderabad (n = 25), a semi-arid station across southern India were studied for a period of four years from 2005 to 2008. During the study period, the Kozhikode station recorded an average rainfall of 3500 mm while the Hyderabad station showed an average rainfall of 790 mm. The average stable isotope values in precipitation at the Kozhikode station were δ ¹⁸O = −3.52‰, d-excess = 13.72‰; δ ¹⁸O = −2.94‰, d-excess = 10.57‰; and δ ¹⁸O = −7.53‰, d-excess = 13.79‰, respectively during the pre-monsoon (March–May), monsoon (June–September) and post-monsoon (October–February) seasons. For the Hyderabad station, the average stable isotope values were δ ¹⁸O = −5.88‰, d-excess = 2.34‰; δ ¹⁸O = −4.39‰, d-excess = 9.21‰; and δ ¹⁸O = −8.69‰, d-excess = 14.29‰, respectively for the three seasons. The precipitation at the two stations showed distinctive isotopic signatures. The stable isotopic composition of precipitation at the Hyderabad station showed significant variations from the global trend while the Kozhikode station almost followed the global value. These differences are mainly attributed to the latitudinal differences of the two stations coupled with the differences in climatic conditions.     

Submarine Groundwater Discharge to a High-Energy Surf Zone at Stinson Beach,California, Estimated Using Radium Isotopes

Two 14-day experiments conducted in the dry summer (July 2006) and wet winter (March 2007) seasons, respectively, examined tidal, wave-driven, and seasonal variability of submarine groundwater discharge (SGD) at Stinson Beach, CA, using natural radium tracers. Tide stage, tide range, breaker height, and season each explained a significant degree of radium variability in the surf zone. A mass balance of excess radium in the surf zone was used to estimate SGD for each season, confirming larger discharge rates during the wet season. Our results indicate median groundwater discharge rates of 6 to 8 L min⁻¹ m⁻¹ in July 2006 and 38 to 43 L min⁻¹ m⁻¹ in March 2007. SGD from 200 m of Stinson Beach in March 2007 contributed a flux of phosphate and dissolved inorganic nitrogen approximately equal to that associated with all local creeks and streams within 6 km of the study site at that time.     

Correlative and comparative characterization of main ion concentrations in laterite groundwater in semi-arid northern Burkina Faso

About 24 samples from hand-dug wells and boreholes were used to characterize concentrations of the main inorganic ions in a laterite environment under semi-arid climatic conditions in Tikaré, northern Burkina Faso. It was found that the most represented groundwater anion in groundwater was HCO₃ ⁻ with average levels of 49.1 mg/L in the dry season and 33.5 mg/L in the rainy season. The most represented cation was Ca²⁺ with mean concentrations of 13.7 and 9.5 mg/L, respectively. The main processes, which influence the concentrations of these ions, are evaporation (dry season), local enrichment of recharge water in some elements, ion exchange and fixation by clay minerals (in case of K⁺). The best correlations were found between Ca²⁺ and Mg²⁺ (r = 0.95), Cl⁻ and Na⁺ (r = 0.95), HCO₃ ⁻ and Mg²⁺ (r = 0.89), HCO₃ ⁻ and Ca²⁺ (r = 0.89), and between HCO₃ ⁻ and Na⁺ (r = 0.80). In general, the quality of the groundwater from the different wells sampled for this study was good enough to serve as drinking water. However, there were situations where the quality of water was polluted because of anthropogenic contaminants (mainly NO₃ ⁻, K⁺, Cl⁻) from septic tanks and manure pits located in the vicinity of some sampled wells. In addition, application of fertilizers also represents a potential anthropogenic contamination source with regard to SO₄ ²⁻, Ca²⁺, K⁺, Na⁺, and Mg²⁺. Considering the high concentrations of SO₄ ²⁻, Mg²⁺, Na⁺ and Ca²⁺ found in one borehole, the deeper, fractured aquifers were also likely to be enriched in these elements. In contrast, the shallow aquifers are likely to be contaminated with Cl⁻, NO₃ ⁻ and K⁺. Cl⁻ and K⁺ seem to be locally present in recharge water as shown by their relative higher mean concentrations in the rainy season samples.     

Nitrate pollution of groundwater in Toyserkan,western Iran

A total of 95 groundwater samples were collected from Toyserkan, western Iran to assess the chemical composition and nitrate (NO₃ ⁻) status of groundwater. The most prevalent water type is Ca–HCO₃ followed by water types Ca–Mg–HCO₃. In comparison with the World Health Organization (WHO) drinking water guideline of 50 mg l⁻¹ for NO₃ ⁻, a total of nine wells (9.5%) showed higher concentrations. In 36% of samples (34) NO₃ ⁻ concentration was low (<20 mg l⁻¹), and in 53.7% of samples (51), in the range of 20–50 mg l⁻¹. The samples were classified into four groups based on NO₃ ⁻ and chloride (Cl⁻) concentrations. Of the samples, 40% were classified as group 4 and were relatively high in Cl⁻ and NO₃ ⁻ (Cl⁻ > 47 mg l⁻¹, NO₃ ⁻ > 27 mg l⁻¹). The high correlation between NO₃ ⁻ and Cl⁻ (r = 0.86, p < 0.01) is consistent with a manure source, resulting from the practice of adding salt to animal feed. Pollution of groundwaters appeared to be affected by the application of inorganic fertilizer at greater than agronomic rates, Cl-salt inputs, and irrigation practice.     

High-pressure X-ray diffraction study of ε-FeOOH

An in situ synchrotron X-ray diffraction study was carried out on ε-FeOOH at room temperature up to a pressure of 8.6 GPa using the energy-dispersive method. The linear compressibility was determined to be β _a  = 1.69(3) × 10⁻³ GPa⁻¹, β _b  = 2.86(6) × 10⁻³ GPa⁻¹, and β _c  = 1.73(5) × 10⁻³ GPa⁻¹. The b-axis of the unit cell is more compressible than the a and c axes. The pressure–volume data were fitted to a third-order Birch–Murnaghan equation of state. The best fit was found using a room temperature isothermal bulk modulus of K ₀ = 126(3) GPa and its pressure derivative K′ = 10(1).     

Single-crystal EPR and DFT study of a <Superscript>VI</Superscript>Al–O<Superscript>−</Superscript>–<Superscript>VI</Superscript>Al center in jeremejevite: electronic structure and <Superscript>27</Superscript>Al hyperfine constants

Single-crystal electron paramagnetic resonance (EPR) spectra of a gem-quality jeremejevite, Al₆B₅O₁₅(F, OH)₃, from Cape Cross, Namibia, reveal an S = 1/2 hole center characterized by an ²⁷Al hyperfine structure arising from interaction with two equivalent Al nuclei. Spin-Hamiltonian parameters obtained from single-crystal EPR spectra at 295 K are as follows: g ₁ = 2.02899(1), g ₂ = 2.02011(2), g ₃ = 2.00595(1); A ₁/g _e β _e  = −0.881(1) mT, A ₂/g _e β _e  = −0.951(1) mT, and A ₃/g _e β _e  = −0.972(2) mT, with the orientations of the g ₃- and A ₃-axes almost coaxial and perpendicular to the Al–O–Al plane; and those of the g ₁- and A ₁-axes approximately along the Al–Al and Al–OH directions, respectively. These results suggest that this aluminum-associated hole center represents hole trapping on a hydroxyl oxygen atom linked to two equivalent octahedral Al³⁺ ions, after the removal of the proton (i.e., a ^VIAl–O⁻–^VIAl center). Periodic ab initio UHF and DFT calculations confirmed the experimental ²⁷Al hyperfine coupling constants and directions, supporting the proposed structural model. The ^VIAl–O⁻–^VIAl center in jeremejevite undergoes the onset of thermal decay at 300 °C and is completely bleached at 525 °C. These data obtained from the ^VIAl–O⁻–^VIAl center in jeremejevite provide new insights into analogous centers that have been documented in several other minerals.     

X-ray diffraction study of arsenopyrite at high pressure

The high-pressure X-ray diffraction study of a natural arsenopyrite was investigated up to 28.2 GPa using in situ angle-dispersive X-ray diffraction and a diamond anvil cell at National Synchrotron Light Source, Brookhaven National Laboratory. The 16:3:1 methanol–ethanol–water mixture was used as a pressure-transmitting medium. Pressures were measured using the ruby-fluorescence method. No phase change has been observed up to 28.2 GPa. The isothermal equation of state (EOS) was determined. The values of K ₀, and K′ ₀ refined with a third-order Birch–Murnaghan EOS are K ₀ = 123(9) GPa, and K′ ₀ = 5.2(8). Furthermore, we confirm that the linear compressibilities (β) along a, b and c directions of arsenopyrite is elastically isotropic (β _a  = 6.82 × 10⁻⁴, β _b  = 6.17 × 10⁻⁴ and β _c  = 6.57 × 10⁻⁴ GPa⁻¹).     

Excess heat capacity and entropy of mixing along the chlorapatite–fluorapatite binary join

The heat capacity at constant pressure, C _p, of chlorapatite [Ca₅(PO₄)₃Cl – ClAp], and fluorapatite [Ca₅(PO₄)₃F – FAp], as well as of 12 compositions along the chlorapatite–fluorapatite join have been measured using relaxation calorimetry [heat capacity option of the physical properties measurement system (PPMS)] and differential scanning calorimetry (DSC) in the temperature range 5–764 K. The chlor-fluorapatites were synthesized at 1,375–1,220°C from Ca₃(PO₄)₂ using the CaF₂–CaCl₂ flux method. Most of the chlor-fluorapatite compositions could be measured directly as single crystals using the PPMS such that they were attached to the sample platform of the calorimeter by a crystal face. However, the crystals were too small for the crystal face to be polished. In such cases, where the sample coupling was not optimal, an empirical procedure was developed to smoothly connect the PPMS to the DSC heat capacities around ambient T. The heat capacity of the end-members above 298 K can be represented by the polynomials: C _p^ClAp = 613.21 − 2,313.90T ^−0.5 − 1.87964 × 10⁷ T ⁻² + 2.79925 × 10⁹ T ⁻³ and C _p^FAp = 681.24 − 4,621.73 × T ^−0.5 − 6.38134 × 10⁶ T ⁻² + 7.38088 × 10⁸ T ⁻³ (units, J mol⁻¹ K⁻¹). Their standard third-law entropy, derived from the low-temperature heat capacity measurements, is S° = 400.6 ± 1.6 J mol⁻¹ K⁻¹ for chlorapatite and S° = 383.2 ± 1.5 J mol⁻¹ K⁻¹ for fluorapatite. Positive excess heat capacities of mixing, ΔC _p^ex, occur in the chlorapatite–fluorapatite solid solution around 80 K (and to a lesser degree at 200 K) and are asymmetrically distributed over the join reaching a maximum of 1.3 ± 0.3 J mol⁻¹ K⁻¹ for F-rich compositions. They are significant at these conditions exceeding the 2σ-uncertainty of the data. The excess entropy of mixing, ΔS ^ex, at 298 K reaches positive values of 3–4 J mol⁻¹ K⁻¹ in the F-rich portion of the binary, is, however, not significantly different from zero across the join within its 2σ-uncertainty.     

The Kinetics of the Interaction Between Iron(III)-Ethylenediaminetetraacetate and Peroxynitrite

The kinetics of the formation of the purple-colored species between Fe^III-EDTA and peroxynitrite were studied as a function of pH (10.4–12.3) at 22°C in aqueous solutions using a stopped-flow technique. A purple-colored species was immediately formed upon mixing, which had an absorbance maximum at 520 nm. The increase in absorbance with time could be fit empirically by a power function with two parameters a and b. The power equation determined was absorbance = a*t ^b , where a increased linearly with pH and the concentration of peroxynitrite, while b almost remained constant with a value of ~0.25. The molar extinction coefficient ε_520 nm for the colored species was determined as 13 M⁻¹cm⁻¹, which is much lower than ε_520 nm = 520 M⁻¹ cm⁻¹ for the [Fe^III(EDTA)O₂]³⁻, a purple species observed in the Fe^III–EDTA–H₂O₂ system. The results of kinetics and spectral measurements of the present study are briefly discussed and compared with those of the reaction between Fe(III)-EDTA and hydrogen peroxide.     

Climate change and local adaptation strategies in the middle Inner Mongolia,northern China

According to records of 17 meteorological stations distributed in the study area, climate change of the middle Inner Mongolia in northern China was analyzed in this paper. Based on SPOT VGT data, combined with field investigation, local vegetation change was detected in the last 10 years. The results show that annual mean air temperature obviously rose, while precipitation slightly decreased in fluctuation in the study area during the last 50 years. Air temperature increasing rates are +0.318°C 10 year⁻¹ during 1960-2009 and +0.423°C 10 year⁻¹ during 1980–2009, while precipitation decreasing rates are −2.91 mm 10 year⁻¹ during 1960–2009. There were five different dry or wet periods from the 1960s to the 2000s in order, and the wetter 1990s and the drier 2000s changed dramatically in the study area. Local climate totally tend to warm–dry conditions during the last 50 years. According to coefficient of variation (Cv) of yearly growing-season cumulative NDVI value and yearly NDVI maximum in pixel scale, vegetation had experienced huge temporal and spatial variation during the last 10 years. Recently, frequent droughts and dust storms seriously affected local agriculture and grazing activities, and resulted in heavy economic loss, especially over the drought period of 1999–2001. Faced with those drought disasters accompanied with strong dust storms, the local authorities proposed the enclosing-transferring strategy and made great efforts to adapt overt climate change and improve environment, including making selective emigration, decreasing livestock numbers, fencing grasslands and building forage production bases with irrigation instruments and actively adjusting industry structure. However, some effects and potential problems of this adaptation strategy still need to be comprehensively assessed further in longer time scales and aimed at different sub-regions.