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1.
Critics of the Endangered Species Act have asserted that is protects an inordinate number of subspecies and populations, in addition to full species, and that the scientific rationale for listing decisions is absent or weak. We reviewed all U.S. plants and animals proposed for listing or added to the endangered species list from 1985 through 1991 to determine the relative proportion of species, subspecies, and populations, and their rarity at time of listing. Approximately 80% of the taxa added to the list were full species, 18% were subspecies, and 2% were distinct populations segments of more widespread vertebrate species. The proportion of subspecies and populations was considerably higher among birds and mammals than among other groups. The median populations size at time of listing for vertebrate animals was 1075 individuals; for invertebrate animals it was 999. The median population size of a plant at time of listing was less than 120 individuals. Earlier listing of declining species could significantly improve the likelihood of successful recovery, and it would provide land managers and private citizens with more options for protecting vanishing plants and animals at less social or economic cost. 相似文献
2.
3.
Magnuson ML Kelty CA Urbansky ET Owens JH Kelty KC Speth TF 《Journal of environmental monitoring : JEM》2002,4(1):102-108
Analytical chemistry is an important tier of environmental protection and has been traditionally linked to compliance and/or exposure monitoring activities for environmental contaminants. The adoption of the risk management paradigm has led to special challenges for analytical chemistry applied to environmental risk analysis. Namely, methods developed for regulated contaminants may not be appropriate and/or applicable to risk management scenarios. This paper contains examples of analytical chemistry applied to risk management challenges broken down by the analytical approach and analyte for some selected work in our laboratory. Specific techniques discussed include stable association complex electrospray mass spectrometry (cESI-MS), gas chromatography-mass spectrometry (GC-MS), split-flow thin cell (SPLITT) fractionation and matrix-assisted laser desorption time of flight mass spectrometry (MALDI-ToF-MS). Specific analytes include haloacetic acids (HAA9), perchlorate, bromate, triazine degradation products, metal-contaminated colloids and Cryptosporidium parvum oocysts. 相似文献
4.
In the aquatic environment, the accumulation of chemicalcontaminants by sediments poses a potential threat to endemiclife forms and drinking water resources. Trace metals such asCd, Cu, Cr, Ni, Pb, and toxic organic compounds, are among awide variety of contaminants having an affinity for sediments.In this study, experiments were performed simulating sedimentresuspension in the lower Housatonic River, Connecticut, using aParticle Entrainment Simulator. Analyses of grain sizedistributions, porosities and total organic contents of thesediments suggested that these parameters influence theredistribution and entrainment of settleable solids in the watercolumn. These findings were established by evaluating the impactof one parameter on sediment resuspension as a function ofstream flow with the other two characteristics being heldconstant. Total suspended solids and volatile suspended solidsresuspension concentration ranged from 3.2 to 20648.3 mg L-1,and 1.5 to 1823.8 mg L-1, respectively, with subsequentincreases in flow rates from 9 to 6 dynes cm-2. The resuspension concentrations were augmentedby sediment porosity (22.0 to 57.5%), percent finer grain-size distributions at 0.1 mm, and total organic content (2.7 g kg-1 to 29.0 g kg-1). Using K
p values, and the dissolvedcontaminant levels of various trace metals, the particulatecontaminant levels of the metals were determined under variousoscillation rates. As sediment resuspension increased withincreased stream flow, there was an overall general increasefrom 0.02 to 33.6 g L-1 in the particulatecontaminant levels of Cd, Cu, Cr, Ni and Pb. 相似文献
5.
Keith E. Schilling Robert D. Libra 《Journal of the American Water Resources Association》2003,39(4):851-860
ABSTRACT: Historical trends in annual discharge characteristics were evaluated for 11 gauging stations located throughout Iowa. Discharge records from nine eight‐digit hydrologic unit code (HUC‐8) watersheds were examined for the period 1940 to 2000, whereas data for two larger river systems (Cedar and Des Moines Rivers) were examined for a longer period of record (1903 to 2000). In nearly all watersheds evaluated, annual base flow, annual minimum flow, and the annual base flow percentage significantly increased over time. Some rivers also exhibited increasing trends in total annual discharge, whereas only the Maquoketa River had significantly decreased annual maximum flows. Regression of stream discharge versus precipitation indicated that more precipitation is being routed into streams as base flow than as storm flow in the second half of the 20th Century. Reasons for the observed stream flow trends are hypothesized to include improved conservation practices, greater artificial drainage, increasing row crop production, and channel incision. Each of these reasons is consistent with the observed trends, and all are likely responsible to some degree in most watersheds. 相似文献
6.
Impact of Land Use on Soluble Organic Nitrogen in Soil 总被引:5,自引:0,他引:5
Victoria B. Willett James J. Green Andrew J. Macdonald John A. Baddeley Georg Cadisch Steven M. J. Francis Keith W. T. Goulding Gary Saunders Elizabeth A. Stockdale Christine A. Watson David L. Jones 《Water, Air, & Soil Pollution: Focus》2004,4(6):53-60
Although it has been hypothesized that soluble organic nitrogen (SON) plays a central role in regulating productivity in some terrestrial ecosystems, the factors controlling the size of the SON pool in soil remain poorly understood. Therefore our principal aim in this work was to assess the impact of seven different land use systems (rough and managed grassland, deciduous and coniferous woodland, heathland, wetland and tilled land) on the size of the SON and inorganic N (NO
3
–
, NH
4
+
) pools in the surface soil layer (0–15 cm). After extraction with deionised water, we found that in most cases the size of the water extractable organic N (WEON) pool was similar in size to the inorganic N pool. In contrast, the KCl extractable organic N (KClEON) pool constituted the dominant form of soluble N in soils under all land uses, perhaps indicating that significant amounts were held on the soil exchange phase. In contrast to inorganic N, which varied significantly with land use, the size of the KClEON and WEON pool was similar for all land uses with the exception of KClEON in tilled land, where significantly lower amounts were observed. We conclude that SON constitutes an important soil N pool in a broad range of land uses, and that its role in microbial N assimilation, plant nutrition and ecosystem responses to atmospheric N deposition warrants further attention.
SAFRD, University of Newcastle, Newcastle-upon-Tyne, NE1 7RU, U.K. 相似文献
7.
David S. Reay Keith A. Smith Anthony C. Edwards 《Water, Air, & Soil Pollution: Focus》2004,4(2-3):437-451
Dissolved nitrous oxide (N2O), nitrate (NO3 -), and ammonium (NH4 +) concentrations in an agricultural field drain were intensively measured over the period of field nitrogen (N) fertilisation and for several weeks thereafter. Supersaturations of dissolved N2O were observed in field drain waters throughout the study. On entry to an open drainage ditch, concentrations of dissolved N2O rapidly decreased and a total N2O-N emission via this pathway of 13.2 g over the period of study (45 days) was calculated. This compared with a predicted emission of the order of 300 g, based on measured losses of NO3 - and NH4 + in the field drainage water, and the default IPCC emission factor of 0.01 kg N2O-N per kg Nentering rivers and estuaries. In contrast to widespread evidence of a clear relationship between the amount of N applied to agricultural land and subsequent direct N2O emission from the soil surface, the relationship between the amount of N2O in soil drainage waters and the amount of N applied was poor. We conclude that the complexity, both spatially and temporally, of the processes ultimately responsible for the amount of N2O in agricultural drainage waters make a straightforward relationship between N2O concentration and N application rate unlikely in all but the simplest of systems. 相似文献
8.
Page T Haygarth PM Beven KJ Joynes A Butler T Keeler C Freer J Owens PN Wood GA 《Journal of environmental quality》2005,34(6):2263-2277
A measure of soil P status in agricultural soils is generally required for assisting with prediction of potential P loss from agricultural catchments and assessing risk for water quality. The objectives of this paper are twofold: (i) investigating the soil P status, distribution, and variability, both spatially and with soil depth, of two different first-order catchments; and (ii) determining variation in soil P concentration in relation to catchment topography (quantified as the "topographic index") and critical source areas (CSAs). The soil P measurements showed large spatial variability, not only between fields and land uses, but also within individual fields and in part was thought to be strongly influenced by areas where cattle tended to congregate and areas where manure was most commonly spread. Topographic index alone was not related to the distribution of soil P, and does not seem to provide an adequate indicator for CSAs in the study catchments. However, CSAs may be used in conjunction with soil P data for help in determining a more "effective" catchment soil P status. The difficulties in defining CSAs a priori, particularly for modeling and prediction purposes, however, suggest that other more "integrated" measures of catchment soil P status, such as baseflow P concentrations or streambed sediment P concentrations, might be more useful. Since observed soil P distribution is variable and is also difficult to relate to nationally available soil P data, any assessment of soil P status for determining risk of P loss is uncertain and problematic, given other catchment physicochemical characteristics and the sampling strategy employed. 相似文献
9.
Jennifer E. Kay Stephanie K. Kampf Rebecca N. Handcock Keith A. Cherkauer Alan R. Gillespie Stephen J. Burges 《Journal of the American Water Resources Association》2005,41(5):1161-1175
Emitted thermal infrared radiation (TIR, λ= 8 to 14 μm) can be used to measure surface water temperatures (top approximately 100 μm). This study evaluates the accuracy of stream (50 to 500 m wide) and lake (300 to 5,000 m wide) radiant temperatures (15 to 22°C) derived from airborne (MASTER, 5 to 15 m) and satellite (ASTER 90 m, Landsat ETM+ 60 m) TIR images. Applied atmospheric compensations changed water temperatures by ?0.2 to +2.0°C. Atmospheric compensation depended primarily on atmospheric water vapor and temperature, sensor viewing geometry, and water temperature. Agreement between multiple TIR bands (MASTER ‐ 10 bands, ASTER ‐ 5 bands) provided an independent check on recovered temperatures. Compensations improved agreement between image and in situ surface temperatures (from 2.0 to 1.1°C average deviation); however, compensations did not improve agreement between river image temperatures and loggers installed at the stream bed (from 0.6 to 1.6°C average deviation). Analysis of field temperatures suggests that vertical thermal stratification may have caused a systematic difference between instream gage temperatures and corrected image temperatures. As a result, agreement between image temperatures and instream temperatures did not imply that accurate TIR temperatures were recovered. Based on these analyses, practical accuracies for corrected TIR lake and stream surface temperatures are around 1°C. 相似文献
10.
"二噁英"是指具有相似化学结构和生物特征的一族化合物,分别属于三大类别:多氯代二苯并二噁英(PC-DDs),多氯代二苯并呋喃(PCDFs)以及多氯联苯(PCBs).PCDDs和PCDFs无商业目的性生产,而是在大量的人类活动中产生的.自然过程也可以产生PCDDs和PCDFs.在过去的十年里,环境立法机构和企业一起致力于减少二噁英的排放. 相似文献