Is there a future for biomonitoring of elemental air pollution? A review focused on a larger-scaled health-related (epidemiological) context.

The present paper focuses on biomonitoring of elemental atmospheric pollution, which is reviewed in terms of larger-scaled biomonitoring surveys in an epidemiological context. Based on the literature information, today's availability of solar-powered small air filter samplers and fibrous ion exchange materials is regarded as adequate or an even better alternative for biomonitor transplant materials used in small-scaled set-ups, but biomonitors remain valuable in larger-scaled set-ups and in unforeseen releases and accidental situations. In the latter case, in-situ biomonitoring is seen as the only option for a retrospective study: biomoniors are there before one even knows that they are needed. For biomonitoring, nuclear analytical techniques are discussed as key techniques, especially because of the necessary multi-element assessments in both source recognition and single-element interpretation. To live up to the demands in an epidemiological context, larger-scaled in-situ biomonitoring asks for large numbers of samples, and consequently, for large total sample masses, this all to ensure representation of both local situations and survey area characteristics. Possibly, this point should direct studies into new "easy-to-sample" biomonitor organisms, of which high masses and numbers may be obtained in field work, rather than continue with biomonitors such as lichens. This also means that both sample handling and processing are of key importance in these studies. To avoid problems in comparability of analytical general procedures in milling, homogenization and digestion of samples of large masses, the paper proposes to involve only few but high-quality laboratories in the total element assessment routines. In this respect, facilities that can handle large sample masses in the assessment of element concentrations are to be preferred. This all highlights the involvement of large-sample-volume nuclear facilities, which, however, should be upgraded and automated in their operation to ensure the necessary sample throughput in larger-scaled biomonitoring.

Cell-membrane damage and element leaching in transplanted Parmelia sulcata lichen related to ambient SO2, temperature, and precipitation.

Measurements were performed in lichen (Parmelia sulcata) transplants, to gain insight into the lichen vitality as possibly affected by both element deposition or lichen element content and further ambient atmospheric conditions (temperature, precipitation, SO2 levels). The electrical conductivity of rinsing solutions was used to assess cell-membrane damage in Parmelia sulcata in an experiment, which ran from August 2001 until August 2002. Element contents of the solutions and lichens were determined by inductively coupled plasma-optical emission spectrometry and by k0-instrumental neutron activation analysis, respectively. Factor analysis (MCATTFA) was used to determine grouping of elements of similar origin and/ or behavior. All in all, the data indicate that, apartfrom lichen Na and Cl levels, and for temperature and precipitation, no clear relationships with conductivity could be observed. Conductivity was mostly related to released Na, Cl, K, Mg, and Cs. On the basis of concentrations, Na, Cl, and K could be considered as largely determining the conductivity. The data suggest a different origin for K than that for Na and Cl: the latter two are most probably due to effects from sea salt sprays. Parmelia sulcata was sensitive enough to reflect appreciable ambient rises in air SO2 and resistant enough to recover afterward. MCATTFA on selected elements (K, Sc, Cu, V, As, and Sb) indicated the absence of any comparability between K and V, As and Sb, suggesting differences in origin and/or chemico-physical occurrence. Generally speaking, the present data suggest that the comparability of lichen vitality in large geographical areas may be limited and governed by the area's variability in temperature and precipitation rather than by variability in metal deposition rates. The leaching data on all elements and element groups, however, strongly suggest that wet deposition may also severely affect lichen elemental levels. This latter observation means that comparing outcomes for time or spatial series of lichen samples should be accompanied by a comparably careful monitoring of (preceding) ambient conditions.

Accumulation and elimination of lanthanum by duckweed (Lemna minor L.) as influenced by organism growth and lanthanum sorption to glass.

Lanthanide emissions to the environment increase as a result of the growing industrial applications of these elements. However, robust data to evaluate the environmental fate of lanthanides are scarce. This article describes the accumulation and elimination of lanthanum (La) by common duckweed (Lemna minor L.). Speciation modeling was performed to assure that solubility products were not exceeded. It also showed that La was predominantly associated with ethylenediaminetetraacetic acid (EDTA). Lanthanum concentrations in plants and medium and the amounts sorbed to glass vessels were quantified by using the radioisotope 140La. The amount of La adsorbed on the glass reached values of 25% of the total La present. A model was formulated to describe La uptake in exponentially growing duckweed in the presence of an adsorptive surface. Growth-induced dilution appeared more efficient in lowering plant La concentrations than actual elimination. An elimination study revealed two compartments, of which the smallest eliminated 50 times faster than the bigger compartment, which eliminated mainly by growth dilution. The average bioconcentration factor was 2,000 L/kg fresh weight and 30,000 L/kg dry weight, comparable with those of other higher plants. At the applied concentration of 10 nM, no effects were observed on duckweed growth. However, the high bioconcentration factor warrants monitoring of lanthanide emissions.

Three kinetically different inorganic phosphate entities in bovine casein micelles revealed by isotopic exchange method and compartmental analysis.

Much controversy exists concerning the way calcium phosphate is linked to milk phosphoproteins including caseins. Homoionic exchange of inorganic phosphate between micellar calcium phosphates (MCP) of casein micelles and solute phosphates in cows' milk was investigated using H(32)PO(4)(2-) as radiotracer. Compartmental analysis and modelling revealed the presence of three MCP-related inorganic phosphate compartments each representing a separate phosphate entity. The relative phosphate quantities per compartment, i.e. the quantities of kinetically identical phosphate ions per MCP-ion cluster, and their mean residence times are 2:1:1 and 818, 0.24 and 23 h, respectively. Hence each MCP-ion cluster comprises four inorganic phosphate ions divided over three intra-MCP binding sites each characterised by a mean residence time for homomolecular phosphate exchange at solution/MCP interface.