Mapping potential motorised sightseeing recreation supply across broad privately-owned landscapes of the Southern United States

The recreational opportunities available across landscapes of the Southern United States can be broad and diverse, and collectively are considered a subset of cultural ecosystem services. In describing the settings of recreational opportunities, a number of methods have been proposed that are based in part on geographic information and that can be facilitated by geographical analyses. Presented here are two expedient and cost-effective methods for assessing the recreation supply potential of large, heavily-roaded areas that are situated mainly with privately-owned land in the Southern United States. One land classification process uses fine-scale aerial imagery and other geospatial data in a process that results in three recreational opportunity setting zones with a focus on motorised sightseeing: foreground, background, and remote areas. Within these zones, land cover was derived and aggregated into three major land cover classes, including forest, agriculture, and bare ground classes. Further, a second process uses fuzzy classification methods, and through this highly suitable recreation settings were identified. Each recreational opportunity zone is further subdivided by public- and privately-owned land. We feel these types of recreation setting models can allow managers and planners to gain an understanding of the passive recreation potential of heavily-roaded privately-owned landscapes typical of the Southern United States.     

Acetate formation and explosive decomposition during ethanol oxidation on Rh

The adsorption and reaction of ethanol with the Rh(110) surface has been studied using a thermal molecular beam system and temperature programmed desorption. On the clean surface, ethanol shows a very simple dehydrogenation, producing hydrogen in the gas phase, adsorbed CO (which is desorbed by heating to 550 K) and carbon. Since in alcohol synthesis reactions it is likely that the surface will be partially oxidised, the reaction with predosed oxygen was also investigated. The reaction pathway then becomes much more complex. The main changes are (i) CH₄ and H₂O evolution during adsorption, and (ii)Acetate formation by oxygen insertion in the molecule. The acetate shows very unusual decomposition kinetics — a surface explosion with a very narrow peak-yielding CO₂ and H₂ in the gas phase and adsorbed C. The acetate is always seen on Rh catalysts which are selective for alcohol synthesis from CO and H₂, and it is proposed that oxidic promoters such as vanadia may act to stabilise this intermediate.     

Measurement of Muscle Exudate Protein Composition as an Indicator of Beef Tenderness

The objective of this study was to determine the relationship between the protein composition of muscle exudates and meat tenderness in beef. Frozen, intact beef strip loins (n = 24) were each divided into 3 equal portions (anterior, middle, and posterior). Steaks were removed from each portion, individually vacuum packaged, thawed at 4 °C, and aged for 0, 7, or 14 d. After the designated aging period, exudate was collected from the packaging and 1 steak from each strip loin portion was utilized for shear force measurements. Muscle exudates were analyzed for protein content (biuret assay) and composition (sodium dodecyl sulfate–polyacrylamide gel electrophoresis). Shear force decreased (P < 0.0001) with aging from 0 to 14 d. The protein concentrations of the muscle exudates were not influenced by the aging period and were not related to the amount of exudate expressed. Electrophoretic analyses of the muscle exudates indicated that with aging the relative abundance of 4 proteins decreased (P < 0.01) and 10 proteins increased (P < 0.05) within the protein profiles of the exudates. The relative abundance of the 167, 97, and 47 kDa proteins in exudates at day 0 were significantly correlated (|r| = 0.57 to 0.77) to shear force at day 14. These data demonstrate that exudate protein composition changes with postmortem aging and beef tenderness.     

Synthesis and Hydrodesulfurization Properties of Noble Metal Phosphides: Ruthenium and Palladium

Silica-supported ruthenium and palladium phosphide catalysts (Ru₂P, RuP, Pd₃P, Pd₅P₂) were investigated for the hydrodesulfurization (HDS) of dibenzothiophene (DBT). The Ru and Pd phosphide catalysts were prepared by temperature-programmed reduction of hypophosphite-based precursors consisting of uncalcined or calcined Ru/SiO₂ or Pd/SiO₂ impregnated with ammonium hyposphosphite (NH₄H₂PO₂). The Ru₂P/SiO₂ and RuP/SiO₂ catalysts prepared from uncalcined precursors had smaller average crystallite sizes, higher CO chemisorption capacities, and higher HDS activities than the catalysts prepared from the calcined precursors, while the effect of preparation method on catalytic properties was less clear for the Pd₃P/SiO₂ and Pd₅P₂/SiO₂ catalysts. Following HDS testing at 673?K, X-ray diffraction analysis revealed that the Pd₅P₂/SiO₂ catalysts decomposed to give Pd₃P on the silica support, while the other phosphides exhibited good stability during the testing period. At temperatures at which high DBT conversion was observed (>598?K), the Ru and Pd phosphide catalysts were less active than sulfided Ru/SiO₂ and Pd/SiO₂ catalysts prepared from the uncalcined metal precursors.     

Alterations in the sarcoplasmic protein fraction of beef muscle with postmortem aging and hydrodynamic pressure processing

Abstract: Capillary electrophoresis (CE) and reversed‐phase high performance liquid chromatography (RP‐HPLC) analyses were utilized to detect differences in the sarcoplasmic protein fractions of beef strip loins subjected to aging and hydrodynamic pressure processing (HDP) treatments. At 48 h postmortem, strip loins (n= 12) were halved and subjected to control or HDP treatments. Following treatment, each half was divided into 3 portions which were aged for 0, 5, and 8 d. After each aging period, steaks were removed for Warner–Bratzler shear force (WBSF) analysis and for the extraction of sarcoplasmic proteins which were analyzed by CE and RP‐HPLC. Aging by HDP interactions were not detected using either separation technique. With CE analysis, no HDP effects were observed; however, the relative peak area of 8 protein peaks ranging in size from 17 to >200 kDa were influenced by postmortem aging. Separation of proteins by RP‐HPLC demonstrated that HDP influenced the relative size of 2 protein peaks while postmortem aging effects were observed in 6 peaks. Alterations in the sarcoplasmic protein fractions detected by both CE and RP‐HPLC were correlated to WBSF measurements. Overall, data demonstrate that HDP has minimal effects on sarcoplasmic proteins and that aging related changes in the water soluble protein fractions of muscle may be useful as indirect indicators of beef tenderness. Practical Application: Using 2 different postmortem tenderization techniques, aging and hydrodynamic pressure processing, this study demonstrates that postmortem changes in the soluble protein fraction of beef may be useful as potential indicators of meat tenderness.     

Method of isolation, rate of postmortem metabolism, and myosin heavy chain isoform composition influence ATPase activity of isolated porcine myofibrils

The objective of this study was to determine the influence of myofibril isolation procedures and myosin heavy chain (MyHC) isoform composition on myofibrillar ATPase activity as related to postmortem muscle metabolism. Myofibrils from the red (RST) and white (WST) portions of semitendinosus muscles were isolated using two different methods (A and B) at 3 min and 24 h postmortem in control (NS) and electrically stimulated (ES) pork carcasses. Comparison of the relative MyHC isoform profiles between the two different myofibril isolation methods and myosin extracts from the RST and WST at 3 min showed that method B myofibrils were more similar to the myosin extract than method A. Myofibrillar ATPase activity remained constant or increased (P<0.01) from 3 min to 24 h postmortem in NS carcasses and decreased (P<0.0001) in ES carcasses. From the RST, method A myofibrils had higher (P<0.0001) ATPase activity compared to method B across sampling time and carcass treatment. In the WST, method A myofibrils had lower (P<0.01) activity at 3 min, were not different at 24 h in NS carcasses, but had higher (P<0.05) activity at 24 h in ES carcasses versus method B myofibrils. Compared to method B, isolation method A biased the isoform profile of myofibril samples more towards faster MyHC (2A and 2X) in the RST and towards MyHC 2X in the WST. Results suggest that the ATPase activity and MyHC isoform profile of isolated myofibril samples are influenced by method of myofibril isolation, postmortem sampling time, and the rate of postmortem metabolism. Thus, differences in MyHC isoform profile and method of myofibril isolation must be taken into account to determine accurately the relationship between myofibrillar ATPase activity and rate of postmortem metabolism.     

Impact of major changes in flow regime on the macroinvertebrate assemblages of four chalk stream sites, 1997–2001

The macroinvertebrate assemblages of three unshaded sites on the River Kennet and one shaded site on the River Lambourn in Berkshire, England, were sampled in summer 1997–2001. Quantitative samples were taken on gravel and on the dominant macrophyte at each site in each year and abundance data were recorded for 57 families of macroinvertebrates. The study commenced during a major drought (1997), but in subsequent years discharge prior to sampling was much higher, culminating in the exceptionally high flows of spring 2001. Both family richness and abundance varied significantly in relation to site, habitat and year. Multidimensional scaling ordination, based on Bray‐Curtis dissimilarities, also displayed significant differences between sites, habitats and years. Differences in composition between the Kennet sites were partly due to longitudinal zonation whilst on the Lambourn, faunal differences resulted from shading and the addition of families from nearby habitats, including marginal vegetation. Major changes took place in family composition and abundance between the drought year of 1997 and 1998, indicating that faunal recovery from drought was rapid. Thereafter, faunal changes between 1998 and 2000 were relatively limited. In 2001, following the prolonged period of exceptionally high discharge, overall family richness peaked on both habitats at the three Kennet sites and family abundance reached peak or second highest values on all four sites and both habitats. Thus, the recent high discharge regimes experienced by these perennial chalk stream sites have had no immediate detrimental consequences for the macroinvertebrate assemblages. Copyright © 2004 John Wiley & Sons, Ltd.     

Bactericidal activity, post antibiotic effect and modified controlled effective regrowth time of meropenem at high concentrations

A PCR method for quantitating the copy number of mutant vs. wild-type alleles in DNA from cell lines is described. The assay can be used to detect a point mutation in any gene that creates or destroys a restriction site. The alleles of interest are amplified by nested PCR and labeled in a second round of PCR. The product is digested with a restriction enzyme specific for that site, resolved on a non-denaturing gel and quantified by phosphor imaging techniques. Cell types with known numbers of wild-type and mutant alleles of c-Harvey-ras are used to validate the assay. The method is then applied to a cell line, homogygous for the mutation, to determine the gene copy number. The applicability of the method to other genes is shown using the matrix metalloproteinase gene, matrilysin. A cell line transfected with a plasmid carrying a mutant, auto-activated form of the gene is compared to its parent cell line. Advantages of this technique compared with Southern analysis are ease of screening a large number of clones or foci and accuracy of quantitation.