The social cost of greenhouse gases is important in many regulatory impact analyses. However, calculations of the social cost of greenhouse gases are highly complex and periodically revisited. We offer seven recommendations to improve current estimates. These include recommendations to use both country-level and global measures of the social cost of greenhouse gases, to use country-specific values for monetizing climate damages, to represent uncertainties by reporting distributions instead of using only central values, and to conduct a temporal distributional analysis that shows the magnitudes of climate damages across generations. We also provide recommendations for the discount rates that should be used when estimating the social cost of greenhouse gases, and the appropriate discount rates for regulatory impact analyses that include the social cost of greenhouse gases.

An indirect enzyme-linked immunosorbent assay (ELISA) for EPTC was developed that may be useful for predicting enhanced carbamothioate herbicide degradation in adapted soils. A modified radioimmunoassay (RIA) procedure was used to detect antibodies specific for EPTC and establish antibody dilutions for optimum ELISA sensitivity. Antibodies were obtained from a rabbit injected with a butylate-analog protein conjugate. An indirect ELISA subsequently was developed for EPTC with a detection range of 10 to 1280 ng ml−1 in a 1:3 aqueous dilution of a 90:10 (v/v) acetonitrile (ACN):water soil extract. EPTC recovery from soil was > 96%, as determined by conventional gas chromatography. Measurement of low concentrations of residual EPTC with the ELISA was less quantitative than by gas chromatography, but the immunoassay provided a rapid, potentially cost-effective method for screening soils to determine enhanced carbamothioate degradation.

Immunochemical techniques offer many advantages over chromatographic methods used for pesticide trace analysis of substrates such as soil, water, plants, urine, and blood. These advantages include speed of processing samples, high specificity for detecting a pesticide, reduced amount of preparation and cleanup of the sample before analysis, and a dramatic increase in the number of samples that can be analyzed. Immunoassays are based on the principle that antibodies to pesticides can be prepared, in animals, that can recognize and attach with exquisite specificity to certain chemical configurations displayed on the surface of a molecule. Small molecules such as herbicides usually are not immunogenic but can be made so by chemically bonding them to a large immunogenic protein such as bovine serum albumin before injection into an animal. Development of herbicide-specific antibodies and their use in direct and indirect enzyme-linked immunosorbent assays (EIA or ELISA) as well as radioimmunoassays (RIA) are discussed. The principles behind monoclonal antibody production are outlined, and immunoassays using polyclonal and monoclonal antibodies are compared. Specific reference is made to the development and use of indirect ELISA and RIA procedures for trace analysis of 2,4-D and picloram.

The northern Galician rias provide important economic and social services from fisheries, shellfish harvesting and recreational activities. Consequently, these rias have been included in the Nature 2000 Network as a Special Conservation Zone. The aims of this study were to describe the meiofauna spatial structure in terms of diversity and abundance of major taxa, as well as its relationship with the environmental characteristics in the Ria de Foz nature reserve. For this aim, environmental gradients and distribution patterns of intertidal meiobenthic communities at the Ria de Foz nature reserve were studied using multivariate methods. Ria de Foz showed to be a complex transitional habitat with significant changes in its environment along the estuarine gradient. An abundant and rich meiofauna community was reported at Ria de Foz. A total of 21 higher taxa of meiofauna were found. The most common taxa were nematodes, copepods, ostracods and turbellarians. Three clear different meiobenthic communities were defined. These three communities showed a clear spatial distribution pattern along the estuarine gradient. Moreover, a high degree of similarity between distribution patterns of meiobenthic communities and previously studied macrobenthic communities was found. Regarding the role of environmental factors shaping meiobenthic community distribution patterns distance to the river mouth was the environmental variable that best explained meiobenthic community structure and distribution. Therefore, changes on hydrodynamics that affect environmental factors related to the estuarine gradient will change the distribution pattern and diversity of benthic communities. This work provides the first information about meiobenthos diversity and structure in the Ria de Foz nature reserve and should be useful for future management and conservation plans on this and other similar protected areas.

Specific antisera, raised in rabbits, against somatostatin 1-14, somatostatin 1-28, the fragment 1-12 of somatostatin 1-28, and prosomatostatin 20-36 were used for immunohistochemistry and gel filtration of the rat retina.

With all antisera, immunoreactive perikarya could be located in the inner nuclear and ganglion cell layers. In the inner nuclear layer, amacrine cells with processes extending predominantly into the first sublayer of the inner plexiform layer were observed. Some processes extended also to the ganglion cell layer. In addition, somatostatin-immunoreactive interplexiform cells were present in the inner nuclear layer.

In the ganglion cell layer, perikarya were found located in the midperiphery and in the far periphery of the retina. The neurons located in the midperiphery of the retina possessed a round perikaryon from which processes could be followed going into the inner plexiform layer, where they dichotomized in the third and first sublayers. The perikarya in the far periphery of the retina near the ora serrata exhibited an ovoid-shaped cell body from which processes extended horizontally in a bipolar manner in the layer itself.

By use of an [35S]-labeled antisense oligonucleotide probe, in situ hybridization of the rat retina showed the presence of perikarya in the inner nuclear layer and ganglion cell layer containing mRNA encoding for prosomatostatin.

Gel filtration of the retinal extracts followed by radioimmunoassay showed the presence of somatostatin 1-14, the fragment 1-12 of somatostatin 1-28, and prosomatostatin 1-64. However, somatostatin 1-28 was not detected.

The results obtained in this study verify the presence of somatostatin 1-14 in the rat retina located in perikarya and processes in the inner nuclear and ganglion cell layers. The positive in-situ hybridization signals show that the intraneuronal somatostatin immunoreactivity is due to synthesis of the peptide and not uptake in the neurons. The presence of the somatostatin propeptide and fragments of this propeptide, in both intraretinal perikarya and fibers, indicate a posttranslational modification of this neuropeptide in the perikarya and the processes as well.