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A coupled field-scale aquifer pumping and water infiltration test was conducted at the Idaho National Engineering and Environmental Laboratory in order to evaluate subsurface water and contaminant transport processes in a heterogeneous flow system. The test included an aquifer pumping test to determine the storage properties of the aquifer and the state of confinement of the aquifer (approximately) 190 m below land surface, and a vadose zone infiltration test to determine vertical moisture and radioactive tracer migration rates. Pump test results indicated that the Snake River Plain Aquifer was locally unconfined with a transmissivity ranging from 5.57 x 10(5) to 9.29 x 10(4) m2/day. Moisture monitoring with neutron probes indicated that infiltrating water was initially transported vertically through the upper basalt layer of the vadose zone, primarily through fractures and rubble zones, at an average rate of 5 m/day (based on vertical distance traveled and first arrival of water at the monitoring points). Analysis of breakthrough curves for a conservative tracer allowed estimation of the arrival of the peak concentration and yielded an average velocity of 1 m/day. The migration velocities from the neutron probe and tracer tests are in good agreement given the scale of the test and difference in analysis techniques. None of the data sets showed a correlation between migration velocity (arrival time) and distance from the point source, but they strongly indicate preferential flow through discrete fractures. Upon reaching the first continuous sedimentary interbed layer in the basalt formation, water flow was diverted laterally along the interbed surface where it spread outward in primarily three areas corresponding to topographic lows on the interbed surface, and slowly infiltrated into the interbed. The nonpredictable movement of water and tracer through specific fractures underlying the site suggests that a priori prediction of transmissive fractures in this media

Using structured interviews and surveys of practicing audit partners, this study examines their perceptions with regard to mandatory partner rotation and cooling-off periods, and how recently enacted, more stringent rules, may negatively impact auditors' quality of life to the detriment of audit quality. Results suggest rotation, in general, increases partners' workloads and the likelihood of relocation. Additionally, results suggest that in response to accelerated rotation (and an extended cooling-off period), partners would rather learn a new industry than relocate. Importantly, partners perceive audit quality suffers from retraining, but not from relocating. Thus these results suggest an indirect, negative impact, and unintended consequence, of accelerated rotation/extended cooling-off periods on audit quality. Data Availability: The survey instrument is available upon request. Individual audit partner responses are confidential.

The reality confronting ecosystem managers today is one of heterogeneous, rapidly transforming landscapes, particularly in the areas more affected by urban and agricultural development. A landscape management framework that incorporates all systems, across the spectrum of degrees of alteration, provides a fuller set of options for how and when to intervene, uses limited resources more effectively, and increases the chances of achieving management goals. That many ecosystems have departed so substantially from their historical trajectory that they defy conventional restoration is not in dispute. Acknowledging novel ecosystems need not constitute a threat to existing policy and management approaches. Rather, the development of an integrated approach to management interventions can provide options that are in tune with the current reality of rapid ecosystem change.

The Crystal-Wonder Cave System developed in the Western Escarpment of the southern Cumberland Plateau in the Interior Low Plateau karst region of south-central Tennessee, USA is a global hotspot of cave-limited biodiversity. We combined historical literature, museum accessions, and database occurrences with new observations from bio-inventory efforts conducted between 2005 and 2022 to compile an updated list of troglobiotic and stygobiotic biodiversity for the Crystal-Wonder Cave System. The list of cave-limited fauna includes 31 species (23 troglobionts and 8 stygobionts) with 28 and 18 species documented from the Crystal and Wonder caves, respectively, which represents five phyla, ten classes, nineteen orders, and twenty-six families (six arachnids, three springtails, two diplurans, three millipedes, six insects, three terrestrial snails, one flatworm, five crustaceans, and two vertebrates, respectively). The Crystal-Wonder Cave System is the type locality for six species—Anillinus longiceps, Pseudanophthalmus humeralis, P. intermedius, Ptomaphagus hatchi, Tolus appalachius, and Chitrella archeri. The carabid beetle Anillinus longiceps is endemic to the Crystal-Wonder Cave System. Sixteen species are of conservation concern, including twelve taxa with NatureServe conservation ranks of G1–G3. The exceptional diversity of the Crystal-Wonder Cave System has been associated with several factors, including a high dispersal potential of cave fauna associated with expansive karst exposures along the Western Escarpment of the southern Cumberland Plateau, a high surface productivity, and a favorable climate throughout the Pleistocene.

The expression of chloroplast and mitochondrial genes depends on nucleus-encoded proteins, some of which control processing, stability, and/or translation of organellar RNAs. To test the specificity of one such RNA stability factor, we used two known Chlamydomonas reinhardtii nonphotosynthetic mutants carrying mutations in the Mcd1 nuclear gene (mcd1-1 and mcd1-2). We previously reported that these mutants fail to accumulate the chloroplast petD mRNA and its product, subunit IV of the cytochrome b₆/f complex, which is essential for photosynthesis. Such mutants are generally presumed to be gene specific but are not tested rigorously. Here, we have used microarray analysis to assess changes in chloroplast, mitochondrial, and nuclear RNAs, and since few other RNAs were significantly altered in these mutants, conclude that Mcd1 is indeed specifically required for petD mRNA accumulation. In addition, a new unlinked nuclear mutation was discovered in mcd1-2, which greatly reduced chloroplast atpA mRNA accumulation. Genetic analyses showed failure to complement mda1-ncc1, where atpA-containing transcripts are similarly affected (D. Drapier, J. Girard-Bascou, D.B. Stern, F.-A. Wollman [2002] Plant J 31: 687-697), and we have named this putative new allele mda1-2. We conclude that DNA microarrays are efficient and useful for characterizing the specificity of organellar RNA accumulation mutants.

The 5' untranslated regions (UTR) of chloroplast mRNAs often contain regulatory sequences that control RNA stability and/or translation. The petD chloroplast mRNA in Chlamydomonas reinhardtii has three such essential regulatory elements in its 362-nt long 5' UTR. To further analyze these elements, we compared 5' UTR sequences from four Chlamydomonas species (C. reinhardtii, C. incerta, C. moewusii and C. eugametos) and five independent strains of C. reinhardtii. Overall, these petD 5' UTRs have relatively low sequence conservation across these species. In contrast, sequences of the three regulatory elements and their relative positions appear partially conserved. Functionality of the 5' UTRs was tested in C. reinhardtii chloroplasts using beta-glucuronidase reporter genes, and the nearly identical C. incerta petD functioned for mRNA stability and translation in C. reinhardtii chloroplasts while the more divergent C. eugametos petD did not. This identified what may be key features in these elements. We conclude that these petD regulatory elements, and possibly the corresponding trans-acting factors, function via mechanisms highly specific and surprisingly sensitive to minor sequence changes. This provides a new and broader perspective of these important regulatory sequences that affect photosynthesis in these algae.

The Sarbanes-Oxley Act of 2002 (SOX) shortened the maximum allowable period an audit partner may serve on a US publicly traded company's audit engagement from seven years to five years and lengthened the minimal allowable cooling-off period from two years to five years. Since adoption of the revisions, concerns have been raised about the potential erosion of client-specific and industry knowledge resulting from mandatory audit partner rotation and the resulting potential negative impact on audit quality and financial reporting quality. In this article, the authors report the results of a survey of audit partners subject to the rotation rules. Consistent with the results of other studies that suggest certain SOX mandates may have had a disproportionately negative impact on smaller audit firms, accelerated rotation may have more negative impacts on smaller firms with fewer resources. Regulators may want to consider changes to the current rotation requirements in order to address these issues.

Genetic factors may play an important role in individual susceptibility to infection. Hitherto this problem has been investigated by attempting to relate the distribution of genetic polymorphisms in populations to present or past infection, or by analysing specific infections by classical twin studies or group comparisons. There is reasonable evidence that the common red-cell polymorphisms involving haemoglobin, enzymes or membrane have been maintained by relative resistance to malaria. Blood-group heterogeneity, including secretor status, may reflect varying susceptibility to bacterial, virus and yeast infection. There is increasing evidence that the HLA-DR system may be involved in modifying the clinical course of bacterial, virus and parasitic infection. So far no specific resistance or susceptibility loci similar to those found in murine models have been found in man. DNA analysis, particularly involving restriction fragment length polymorphism associations with candidate genes, offers a valuable new approach to this problem.

The genetic and acquired disorders of human haemoglobin provide a diverse group of naturally occurring models for analysing the regulation of protein synthesis. They include structural haemoglobin variants, thalassaemias, which are conditions in which there is a reduced rate of globin chain production, and hereditary persistence of foetal haemoglobin (HPFH) in which there is an inherited abnormality in the switch from foetal to adult haemoglobin synthesis. The thalassaemias result from a diverse series of cis acting lesions of the globin genes which include deletions, insertions, frame shift mutations, and point mutations involving transcription, messenger RNA processing, initiation, termination, poly A addition and globin chain stability. Many forms of HPFH are due to deletions of the β-like gene cluster; it has been suggested that they may involve regions of the cluster which are involved in the regulation of the foetal to adult globin chain switch. So far, however, no regions of this type have been identified with certainty. The varieties of HPFH not associated with major gene deletions, or those caused by genetic determinants that are not linked to the globin gene clusters, and some of the acquired forms of α thalassaemia associated with mental retardation or leukaemia, may be more useful models for studying the regulation of the globin genes, particularly their developmental control.