Isotopes in Environmental and Health Studies 

About: Isotopes in Environmental and Health Studies is an academic journal published by Taylor & Francis. The journal publishes majorly in the area(s): Stable isotope ratio & Groundwater. It has an ISSN identifier of 1025-6016. Over the lifetime, 3390 publications have been published receiving 21107 citations.

Comparative equilibration and online technique for determination of non-exchangeable hydrogen of keratins for use in animal migration studies.

Abstract: Stable hydrogen-isotope ratios (δD) of keratin provide a novel means for tracking geographical movements of birds and other species. Here we describe a rapid, low cost, analytical approach to facilitate online continuous-flow isotope-ratio mass spectrometry (CF-IRMS) δD analyses of keratins (120-160 samples per day) through the use of calibrated keratin working standards and "comparative equilibration" to correct for the effects of moisture on exchangeable hydrogen. It is anticipated that this analytical approach and CF-IRMS will greatly aid in providing cost effective and directly comparable δD results on keratins and feathers among various laboratories and researchers involved in animal migration studies.

Fertilizer nitrogen isotope signatures

Abstract: There has been considerable recent interest in the potential application of nitrogen isotope analysis in discriminating between organically and conventionally grown crops. A prerequisite of this approach is that there is a difference in the nitrogen isotope compositions of the fertilizers used in organic and conventional agriculture. We report new measurements of δ15N values for synthetic nitrogen fertilizers and present a compilation of the new data with existing literature nitrogen isotope data. Nitrogen isotope values for fertilizers that may be permitted in organic cultivation systems are also reported (manures, composts, bloodmeal, bonemeal, hoof and horn, fishmeal and seaweed based fertilizers). The δ15N values of the synthetic fertilizers in the compiled dataset fall within a narrow range close to 0‰ with 80% of samples lying between−2 and 2‰ and 98.5% of the data having δ15N values of less than 4‰ (mean=0.2‰ n=153). The fertilizers that may be permitted in organic systems have a higher mean δ15N ...

Deuterium excess in precipitation of Alpine regions - moisture recycling.

Abstract: The paper evaluates long-term seasonal variations of the deuterium excess (d-excess = delta(2)H - 8. delta(18)O) in precipitation of stations located north and south of the main ridge of the Austrian Alps. It demonstrates that sub-cloud evaporation during precipitation and continental moisture recycling are local, respectively, regional processes controlling these variations. In general, sub-cloud evaporation decreases and moisture recycling increases the d-excess. Therefore, evaluation of d-excess variations in terms of moisture recycling, the main aim of this paper, includes determination of the effect of sub-cloud evaporation. Since sub-cloud evaporation is governed by saturation deficit and distance between cloud base and the ground, its effect on the d-excess is expected to be lower at mountain than at lowland/valley stations. To determine quantitatively this difference, we examined long-term seasonal d-excess variations measured at three selected mountain and adjoining valley stations. The altitude differences between mountain and valley stations ranged from 470 to 1665 m. Adapting the 'falling water drop' model by Stewart [J. Geophys. Res., 80(9), 1133-1146 (1975).], we estimated that the long-term average of sub-cloud evaporation at the selected mountain stations (altitudes between about 1600 and 2250 m.a.s.l.) is less than 1 % of the precipitation and causes a decrease of the d-excess of less than 2 per thousand. For the selected valley stations, the corresponding evaporated fraction is at maximum 7 % and the difference in d-excess ranges up to 8 per thousand. The estimated d-excess differences have been used to correct the measured long-term d-excess values at the selected stations. Finally, the corresponding fraction of water vapour has been estimated that recycled by evaporation of surface water including soil water from the ground. For the two mountain stations Patscherkofel and Feuerkogel, which are located north of the main ridge of the Alps, the maximum seasonal change of the corrected d-excess (July/August) has been estimated to be between 5 and 6 per thousand, and the corresponding recycled fraction between 2.5-3 % of the local precipitation. It has been found that the estimated recycled fractions are in good agreement with values derived from other approaches.

Stable isotope deltas: Tiny, yet robust signatures in nature

Abstract: Although most of them are relatively small, stable isotope deltas of naturally occurring substances are robust and enable workers in anthropology, atmospheric sciences, biology, chemistry, environmental sciences, food and drug authentication, forensic science, geochemistry, geology, oceanography, and paleoclimatology to study a variety of topics. Two fundamental processes explain the stable isotope deltas measured in most terrestrial systems: isotopic fractionation and isotope mixing. Isotopic fractionation is the result of equilibrium or kinetic physicochemical processes that fractionate isotopes because of small differences in physical or chemical properties of molecular species having different isotopes. It is shown that the mixing of radioactive and stable isotope end members can be modelled to provide information on many natural processes, including 14C abundances in the modern atmosphere and the stable hydrogen and oxygen isotopic compositions of the oceans during glacial and interglacial times. The...

Isotope effects in the evaporation of water: a status report of the Craig–Gordon model

Abstract: The Craig-Gordon model (C-G model) [H. Craig, L.I. Gordon. Deuterium and oxygen 18 variations in the ocean and the marine atmosphere. In Stable Isotopes in Oceanographic Studies and Paleotemperatures, E. Tongiorgi (Ed.), pp. 9-130, Laboratorio di Geologia Nucleare, Pisa (1965).] has been synonymous with the isotope effects associated with the evaporation of water from surface waters, soils, and vegetations, which in turn constitutes a critical component of the global water cycle. On the occasion of the four decades of its successful applications to isotope geochemistry and hydrology, an attempt is made to: (a) examine its physical background within the framework of modern evaporation models, (b) evaluate our current knowledge of the environmental parameters of the C-G model, and (c) comment on a general strategy for the use of these parameters in field applications. Despite its simplistic representation of evaporation processes at the water-air interface, the C-G model appears to be adequate to provide the isotopic composition of the evaporation flux. This is largely due to its nature for representing isotopic compositions (a ratio of two fluxes of different isotopic water molecules) under the same environmental conditions. Among many environmental parameters that are included in the C-G model, accurate description and calculations are still problematic of the kinetic isotope effects that occur in a diffusion-dominated thin layer of air next to the water-air interface. In field applications, it is of importance to accurately evaluate several environmental parameters, particularly the relative humidity and isotopic compositions of the 'free-atmosphere', for a system under investigation over a given time-scale of interest (e.g., hourly to daily to seasonally). With a growing interest in the studies of water cycles of different spatial and temporal scales, including paleoclimate and water resource studies, the importance and utility of the C-G model is also likely to grow in the future.