Seasonal and spatial changes in the zooplankton community of Kongsfjorden, Svalbard

Seasonal changes in the zooplankton composition of the glacially influenced Kongsfjorden, Svalbard (79°N, 12°E), and its adjacent shelf were studied in 2002. Samples were collected in the spring, summer and autumn in stratified hauls (according to hydrographic characteristics), by means of a 0.180-mm Multi Plankton Sampler. A strong front between the open sea and the fjord waters was observed during the spring, preventing water mass exchange, but was not observed later in the season. The considerable seasonal changes in zooplankton abundance were related to the seasonal variation in hydrographical regime. The total zooplankton abundance during the spring (40–2010 individuals m⁻³) was much lower than in the summer and autumn (410–10 560 individuals m⁻³). The main factors shaping the zooplankton community in the fjord include: the presence of a local front, advection, the flow pattern and the decreasing depth of the basin in the inner fjord. Presumably these factors regulate the gross pattern of zooplankton density and distribution, and override the importance of biological processes. This study increased our understanding of seasonal processes in fjords, particularly with regard to the strong seasonal variability in the Arctic.     

Seasonal and spatial changes of metal concentrations in groundwater outflows from porous sediments in the Gryżyna-Grabin Tunnel Valley in western Poland

Groundwater outflows (springs and seeps) from porous sediments on European lowlands play a significant role in the surface water balance. It is therefore important to document these outflows’ water quality and spatial and temporal changes. The present study focused on changes in iron, manganese, and heavy metals in waters of groundwater outflows in an area of low anthropogenic impact—the Gryżyna-Grabin Tunnel Valley in western Poland. Eleven outflows were studied for a period of 2 years. Most of the samples analyzed revealed low element contents and little variation in time and space. Only values of iron and lead were above World Health Organization limits for drinking water. The concentrations of these elements were also variable in time and space. The seasonal changes in iron content are probably due to natural, temperature- and pH-controlled reactions of shallow groundwater with aquifer sediments. On the other hand, the elevated lead content points to regional water contamination.     

Fractionation of heavy metals in bottom sediments using Tessier procedure

The study presents the results of Cu, Pb, Zn, Mn and Fe determination in the samples of bottom sediments collected from the Oder and Warta rivers. The sequential extraction of metals in the samples of bottom sediments was performed after introducing the modification of the extraction scheme suggested by Tessier et al. (Anal Chem 51(7):844–851, 1979). The extraction times of particular stages were optimised. The fifth stage was altered by introducing the new methods of performing extraction. The samples of bottom sediments submitted the following granulometric analyses: dry, wet and wet with (HMP) dispersing reagent. Seven granulometric fractions with the following grain sizes were isolated: >2.0, 2.0–1.0, 1.0–0.5, 0.5–0.25, 0.25–0.1, 0.1–0.063 and <0.063 mm. The sequential extraction of particular granulometric fractions was performed. The concentration of metals variability was analysed depending on the method of sample preparation for the chemical analysis, granulometric fraction of sediments subjected to the analysis, extraction conditions and the site of samples collection. The lack of linearity between the metal concentration and the size of granulometric fraction was observed. The highest concentrations of metals were observed in fractions >2.0, 2.0–1.0 and 0.1–0.063 and <0.063 mm while the lowest concentrations occurred in fractions 1.0–0.5, 0.5–0.25, and 0.25–0.1 mm. The atomic absorption spectrometry with flame atomisation (F-AAS) was used for the determination of the investigated elements.     

Micrometeorological Measurements in a Street Canyon during the Joint ATREUS-PICADA Experiment

In order to investigate the microclimatic conditions in a street canyon, a physical model was used to conduct the Joint ATREUS-PICADA Experiment (JAPEX) in situ experimental campaign. Four lines of buildings simulated by steel containers were installed to form three parallel street canyons at 1:5 scale, with width/height aspect ratio approximately 0.40. The reference wind and atmospheric conditions were measured, as well as the flow velocity and direction in the street. Preliminary results concern street canyon ventilation and thermal effects on in-canyon airflow, and show that vortical motions appear for reference wind directions perpendicular to the street axis. The presence of adjacent rows of buildings did not appear to significantly influence the flow character within the canyon for the case of a low aspect ratio corresponding to a skimming flow regime. The flow structure was not significantly affected by the thermal effects although some slight interference occurred in the lower part of the canyon. An analysis of horizontal temperature gradients indicated that a thin boundary layer develops near the heated facade. These facts imply that the thermal effects are considerable only very close to the wall.     

Characteristics and Possible Source of a 1479 A.D. Volcanic Ash Layer in a Greenland Ice Core

A microparticle concentration peak in a GISP2 ice core contains volcanic glass shards of rhyolitic composition that correspond in age to the 1479-1480 A.D. Mt. St. Helens Wn eruption. These glass shards are compositionally similar to the Wn tephra and constitute 83% of the total particle population. The shards are very coarse-grained (up to 40 μm diameter), suggesting rapid transport from their source to Greenland. A major sulfate peak in the ice occurs approximately 4 months after deposition of the glass shards. This difference in depositional timing suggests primarily tropospheric transport of the ash and stratospheric transport of the sulfate aerosol. Large-scale climatic perturbations following this eruption were evidently negligible. Glaciochemical seasonal indicators suggest a late-fall to early-winter 1479 A.D. eruption.     

Leaching characteristics of ash from the May 18, 1980, eruption of Mount St. Helens volcano,Washington

Leaching of freshly erupted air-fall ash, unaffected by rain, from the May 18, 1980, eruption of Mount St. Helens volcano, Washington, shows that Ca²⁺, Na⁺, Mg²⁺, SO ₄ ^2? , and Cl^? are the predominant chemical species released on first exposure of the ash to water. Extremely high correlation of Ca with SO₄ and Na with Cl in water leachates suggests the presence of CaSO₄ and NaCl salts on the ash. The amount of water soluble material on ash increases with distance from source and with the weight fraction of small (less than 63 micrometers) ash particles of high-surface area. This suggests that surface reactions such as adsorption are responsible for concentrating the soluble material. CaSO₄, NaCl, and other salts are probably formed as microscopic crystals in the high-temperature core of the eruption column and are then adsorbed by silicate ash particles. The environmentally important elements Zn, Cu, Cd, F. Pb, and Ba are released by a water leach in concentrations which could pose short-term hazards to some forms of aquatic life. However, calculated concentrations are based on a water-to-ash ratio of 4:1 or less, which is probably an underestimation of the regionally operative ratio. A subsequent leach of ash by warm alkaline solution shows dramatic increases, in the amount of dissolved SiO₂, U, and V, which are probably caused by increased dissolution of the glassy component of ash. Glass dissolution by alkaline ground water is a mechanism for providing these three elements to sedimentary traps where they may coaccumulate as uraniferous silica or U-V minerals. Leaching characteristics of ash from Mount St. Helens are comparable to characteristics of ash of similar composition from volcanoes in Guatemala. Ashes from each locality show similar ions predominating for a given leachate and similar fractions of a particular element in the ash removed on contact with the leach solution.     

Use of 234U and 238U isotopes to evaluate contamination of near-surface groundwater with uranium-mill effluent: a case study in south-central Colorado, U.S.A.

The ²³⁴U/²³⁸U alpha activity ratio (AR) was determined in 47 samples of variably uraniferous groundwater from the vicinity of a uranium mill near Cañon City, Colorado. The results illustrate that uranium isotopes can be used to determine the distribution of uranium contamination in groundwater and to indicate processes such as mixing and chemical precipitation that affect uranium concentrations. Highly to moderately contaminated groundwater samples collected from the mill site and land immediately downgradient from the mill site contain more than 100?μg/l of dissolved uranium and typically have AR values in the narrow range of 1.0–1.06. Other samples from the shallow alluvial aquifer farther downgradient from the mill contain 10–100?μg/l uranium and plot along a broad trend of increasing AR (1.06–1.46) with decreasing uranium concentration. The results are consistent with mixing of liquid mill waste (AR≈1.0) with alluvial groundwater of small, but variable, uranium concentrations and AR of 1.3–1.5. In the alluvial aquifer, the spatial distribution of wells with AR values less than 1.3 is consistent with previous estimates of the probable distribution of contamination, based on water chemistry and hydrology. Wells more distant from the area of probable contamination have AR values that are consistently greater than 1.3 and are indicative of little or no contamination. The methodology of this study can be extended usefully to similar sites of uranium mining, milling, or processing provided that local geohydrologic settings promote uranium mobility and that introduced uranium contamination is isotopically distinct from that of local groundwater.     

Landslide databases in the Geological Surveys of Europe

Landslides are one of the most widespread geohazards in Europe, producing significant social and economic impacts. Rapid population growth in urban areas throughout many countries in Europe and extreme climatic scenarios can considerably increase landslide risk in the near future. Variability exists between European countries in both the statutory treatment of landslide risk and the use of official assessment guidelines. This suggests that a European Landslides Directive that provides a common legal framework for dealing with landslides is necessary. With this long-term goal in mind, this work analyzes the landslide databases from the Geological Surveys of Europe focusing on their interoperability and completeness. The same landslide classification could be used for the 849,543 landslide records from the Geological Surveys, from which 36% are slides, 10% are falls, 20% are flows, 11% are complex slides, and 24% either remain unclassified or correspond to another typology. Most of them are mapped with the same symbol at a scale of 1:25,000 or greater, providing the necessary information to elaborate European-scale susceptibility maps for each landslide type. A landslide density map was produced for the available records from the Geological Surveys (LANDEN map) showing, for the first time, 210,544 km² landslide-prone areas and 23,681 administrative areas where the Geological Surveys from Europe have recorded landslides. The comparison of this map with the European landslide susceptibility map (ELSUS 1000 v1) is successful for most of the territory (69.7%) showing certain variability between countries. This comparison also permitted the identification of 0.98 Mkm² (28.9%) of landslide-susceptible areas without records from the Geological Surveys, which have been used to evaluate the landslide database completeness. The estimated completeness of the landslide databases (LDBs) from the Geological Surveys is 17%, varying between 1 and 55%. This variability is due to the different landslide strategies adopted by each country. In some of them, landslide mapping is systematic; others only record damaging landslides, whereas in others, landslide maps are only available for certain regions or local areas. Moreover, in most of the countries, LDBs from the Geological Surveys co-exist with others owned by a variety of public institutions producing LDBs at variable scales and formats. Hence, a greater coordination effort should be made by all the institutions working in landslide mapping to increase data integration and harmonization.     

Assessment of heavy metal contamination levels of street dust in the city of Lublin,E Poland

Heavy metals are constantly emitted into the environment and pose a major threat to human health, particularly in urban areas. The threat is linked to the presence of Cd, Cr, Cu, Ni, Pb, and Zn in street dust, which consists of mineral and organic particles originating from the soil, industrial emitters, motor vehicles, and fuel consumption. The study objective was to determine the level of street dust contamination with trace metals in Lublin and to indicate their potential sources of origin. The analyses were carried out with an energy-dispersive X-ray fluorescence spectrometer. The sampling sites (49) were located within the city streets characterised by varying intensity of motor traffic. The following mean content values and their variation (SD) were determined: Cd: 5.1?±?1.7 mg kg^?1, Cr: 86.4?±?23.3 mg kg^?1, Cu: 81.6?±?69.2 mg kg^?1, Ni: 16.5?±?3.9 mg kg^?1, Pb: 44.1?±?16.4 mg kg^?1, and Zn: 241.1?±?94.6 mg kg^?1. The level of pollution was assessed with several widely used geochemical indices (geoaccumulation index, enrichment factor, pollution index, index of ecological risk, and potential ecological risk index). For most of the indices, the mean (median) values are arranged in the following manner: Zn?>?Cu(or Cd)?>?Pb?>?Ni?>?Cr. In general, street dust in Lublin does not show pollution with Cr, Ni, and Pb. I_geo and EF indices show moderate levels for Cu, Cd, and Zn; their presence in street dust is linked with anthropogenic factors (motor traffic). A significant threat is posed by Cd, and more than half of the samples show considerable pollution with cadmium (median for the index of ecological risk: 151). The spatial pattern of indices and the results of statistical analyses (CA, PCA) indicate three groups of elements: (1) Cr and Ni: natural origin; (2) Pb: mixed origin; and (3) Cd, Cu, and Zn: anthropogenic origin (mainly motor vehicle traffic). Higher content values for metals of anthropogenic origin in street dust indicate that it is a source of pollution of soil and air in the city.