Direct data on the ore potential of acid magmas of the Uzel’ginskoe ore field (Southern Urals,Russia)

Doklady Earth Sciences -     

Seasonal and Annual Fluxes of Nutrients and Organic Matter from Large Rivers to the Arctic Ocean and Surrounding Seas

River inputs of nutrients and organic matter impact the biogeochemistry of arctic estuaries and the Arctic Ocean as a whole, yet there is considerable uncertainty about the magnitude of fluvial fluxes at the pan-Arctic scale. Samples from the six largest arctic rivers, with a combined watershed area of 11.3?×?10⁶?km², have revealed strong seasonal variations in constituent concentrations and fluxes within rivers as well as large differences among the rivers. Specifically, we investigate fluxes of dissolved organic carbon, dissolved organic nitrogen, total dissolved phosphorus, dissolved inorganic nitrogen, nitrate, and silica. This is the first time that seasonal and annual constituent fluxes have been determined using consistent sampling and analytical methods at the pan-Arctic scale and consequently provide the best available estimates for constituent flux from land to the Arctic Ocean and surrounding seas. Given the large inputs of river water to the relatively small Arctic Ocean and the dramatic impacts that climate change is having in the Arctic, it is particularly urgent that we establish the contemporary river fluxes so that we will be able to detect future changes and evaluate the impact of the changes on the biogeochemistry of the receiving coastal and ocean systems.     

Open-Source Software Implementation and Validation of the Split-Window Method for Automated Land Surface Temperature Retrieval from Landsat 8 Data

Izvestiya, Atmospheric and Oceanic Physics - An open software implementation of the algorithm for retrieving the land surface temperature (LST) from Landsat 8 remote sensing satellite data is...     

Multi-Elemental Analysis of ATHO-G Rhyolitic Glass (MPI-DING Reference Material) by Femtosecond and Nanosecond LA-ICP-MS: Evidence for Significant Heterogeneity of B,V, Zn,Mo, Sn,Sb, Cs,W, Pt and Pb at the Millimetre Scale

This paper reports on the application of variants of LA-ICP-MS – including infrared femtosecond laser ablation (fs-LA) inductively coupled plasma-quadrupole mass spectrometry (ICP-QMS) and nanosecond laser ablation (ns-LA) coupled with single-collector sector-field (SF-) ICP-MS – to the in situ determination of trace elements in different splits of the reference material (RM) ATHO-G (MPI-DING). Analyses of the materials performed by fs- and ns-LA-ICP-MS demonstrated the efficiency of the techniques with typical accuracy at a level of ≤ ± 20%. One ‘anomalous’ split, however, displayed a significant discrepancy from the reference concentrations for B, V, Zn, Mo, Sn, Sb, Cs, W and Pb. Three- to six-fold enrichment of V, Mo, Cs and Pt relative to the reference contents in this split is likely to have been due to direct contact of the silicate melt with Pt crucible walls and ceramics. Boron, Zn, Sn, Sb, W and Pb depletion relative to the reference concentrations is probably due to siderophile element adsorption by the Pt walls and/or related to the formation of volatile-depleted compositional cords during the preparation process. Our results imply that additional precautions should be taken against volatile/siderophile element heterogeneity in marginal/surface layers (≤ 10 mm) during the preparation of RMs by the fusion technique.     

Ten guiding principles for the delineation of priority habitat for endangered small cetaceans

The adoption of endangered species laws in various nations has intensified efforts to better understand, and protect, at-risk species or populations, and their habitats. In many countries, delineating a portion of a species' habitat as particularly worthy of protection has become a mantra of these laws. Unfortunately, the laws themselves often provide scientists and managers with few, if any, guidelines for how to define such habitat. Conservationists and scientists may view protecting part of the habitat of an endangered species as an ineffectual compromise, while managers may be under pressure to allow a range of human activities within the species' habitat. In the case of small cetaceans, establishing boundaries for such areas can also be complicated by their mobility, the fluid nature of their environment, and the often ephemeral nature of their habitat features. The convergence of multiple human impacts in coastal waters around the world is impacting many small cetaceans (and other species) that rely on these areas for feeding, reproducing, and resting. The ten guiding principles presented here provide a means to characterize the habitat needs of small, at-risk cetaceans, and serve as a basis for the delineation of ‘priority habitat’ boundaries. This conceptual approach should facilitate a constructive discourse between scientists and managers engaged in efforts to recover endangered species. The degree to which the recovery of an at-risk species can be reconciled with sustainable economic activity will depend in part on how well these principles are incorporated into the delineation of priority habitat.     

会徽——地质学会的文化表达

会徽是一种行业标识、一段历史烙印、一个学术品牌,它作为一种信息载体,以简单、形象、易识别的图像表达了学术团体的学术宗旨和使命,同时彰显了学术团体的工作目标、学术精神等科学文化内涵。笔者等以中国地质学会会徽为分析案例,通过与东西方几个代表性国家地质学会的文化宗旨与会徽内涵的比较,探讨会徽在学会科学文化建设中的作用。     

Speciation and solubility of heavy metals in contaminated soil using X-ray microfluorescence, EXAFS spectroscopy, chemical extraction, and thermodynamic modeling

Synchrotron-based X-ray radiation microfluorescence (μ-SXRF) and micro-focused and powder extended X-ray absorption fine structure (EXAFS) spectroscopy measurements, combined with desorption experiments and thermodynamic calculations, were used to evaluate the solubility of metal contaminants (Zn, Cu, Pb) and determine the nature and fractional amount of Zn species in a near-neutral pH (6.5-7.0) truck-farming soil contaminated by sewage irrigation for one hundred years. Zn is the most abundant metal contaminant in the soil (1103 mg/kg), followed by Pb (535 mg/kg) and Cu (290 mg/kg). The extractability of Zn, Pb, and Cu with citrate, S,S-ethylenediaminedisuccinic acid (EDDS), and ethylenediaminetetraacetic acid (EDTA) was measured as a function of time (24 h, 72 h, 144 h), and also as a function of the number of applications of the chelant (5 applications each with 24 h of contact time). Fifty-three percent of the Zn was extracted after 144 h with citrate, 51% with EDDS and 46% with EDTA, compared to 69, 87, and 61% for Cu, and 24, 40, and 34% for Pb. Renewing the extracting solution removed more of the metals. Seventy-nine, 65, and 57% of the Zn was removed after five cycles with citrate, EDDS and EDTA, respectively, compared to 88, 100, and 72% for Cu, and 91, 65, and 47% for Pb. Application to the untreated soil of μ-SXRF, laterally resolved μ-EXAFS combined with principal component analysis, and bulk averaging powder EXAFS with linear least-squares combination fit of the data, identified five Zn species: Zn-sorbed ferrihydrite, Zn phosphate, Zn-containing trioctahedral phyllosilicate (modeled by the Zn kerolite, Si₄(Mg_1.65Zn_1.35)O₁₀(OH)₂ · nH₂O), willemite (Zn₂SiO₄), and gahnite (ZnAl₂O₄), in proportions of ∼30, 28, 24, 11, and less than 10%, respectively (precision: 10% of total Zn). In contrast to Cu and Pb, the same fractional amount of Zn was extracted after 24 h contact time with the three chelants (40-43% of the initial content), suggesting that one of the three predominant Zn species was highly soluble under the extraction conditions. Comparison of EXAFS data before and after chemical treatment revealed that the Zn phosphate component was entirely and selectively dissolved in the first 24 h of contact time. Preferential dissolution of the Zn phosphate component is supported by thermodynamic calculations. Despite the long-term contamination of this soil, about 79% of Zn, 91% of Pb, and 100% of Cu can be solubilized in the laboratory on a time scale of a few days by chemical complexants. According to metal speciation results and thermodynamic calculations, the lower extraction level measured for Zn is due to the Zn phyllosilicate component, which is less soluble than Zn phosphate and Zn ferrihydrite.