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Effect of dominance status on sex hormone levels in laboratory and wild-spawning male trout.

We investigated the relationship between male social status and hormone levels in salmonids spawning under laboratory and field conditions. In small groups of rainbow trout (Onchorhynchus mykiss) spawning in the laboratory, dominant males had higher plasma levels of testosterone (T) and 17 alpha, 20 beta-dihydroxy-4-pregnen-3-one (17,20 beta-P) compared with subordinates. Steroid levels increased in subordinate males that became dominant after dominant males were experimentally removed; higher steroid levels in dominant males appears to be a result rather than a cause of their social status. In free-ranging brown trout (Salmo trutta) sampled in the field, we found higher levels of 11-ketotestosterone (11KT) but not T in dominant males. No significant differences in levels of either androgen were found between dominant and subordinate male brook trout (Salvelinus fontinalis) sampled at the same field location. Furthermore, in marked contrast with the laboratory fish, there were no significant differences in plasma 17,20 beta-P between dominant and subordinate males in either species of fish in the wild. The different findings in the laboratory and field may indicate species differences in behavioral endocrinology among brook, brown, and rainbow trout. Alternatively, the greater differential in hormonal profile of dominant and subordinate males in the laboratory may reflect the relative uniformity of the laboratory environment; this simple environment may allow competitively superior males to more completely dominate less competitive tank-mates and to exclude them from female sexual cues. In any case, these results suggest that the relationship between steroid hormones and spawning behavior in male salmonids is likely more complex than suggested by experiments conducted solely on laboratory-held rainbow trout.

Animals↗

A comparison of in situ and laboratory toxicity tests with the estuarine amphipod Eohaustorius estuarius.

Amphipod survival in laboratory and in situ exposures was assessed using the eastern Pacific Haustoriid species Eohaustorius estuarius. Toxicity test results were compared using intact (unhomogenized) and homogenized sediment samples in both field and laboratory exposures. Experiments were conducted in Moss Landing Harbor, California, an impaired waterbody under 303 (d) of the US Clean Water Act. Synoptic laboratory and in situ sediment toxicity tests were conducted at two stations: Sandholdt Bridge (SB), the most contaminated station in the harbor, and at the South Jetty (SJ), a more marine station near the mouth of the harbor. We found that Eohaustorius is amenable to in situ testing. Despite highly variable field salinity regimes (6-32 PSU at SB and 21-34 PSU at SJ), in situ control survival was 87% and 84% at SB and SJ, respectively. Amphipod survival was lower in the in situ exposures relative to the laboratory exposures at both sites. Survival at SB was 30% and 76% in the homogenized in situ and laboratory samples, respectively, and 40% and 64% in the intact (unhomogenized) in situ and laboratory samples, respectively. Neither the homogenized or intact samples from the SJ station were toxic in laboratory experiments, but amphipod survival was only 40% in the intact in situ exposure at this station, possibly due to predation. These experiments suggest that the interaction of contaminants and variable physical parameters such as salinity and temperature may have resulted in lower survival in the in situ exposures. Sediment homogenization prior to in situ deployment may have reduced effects of predators in some samples.

Amphipoda↗

Assessing the Bioaccumulation of Contaminants from Sediments of the Upper Mississippi River Using Field-Collected Oligochaetes and Laboratory-Exposed Lumbriculus variegatus

Concern with the redistribution of contaminants associated with sediment in the upper Mississippi River (UMR) arose after the flood of 1993. This project is designed to evaluate the status of sediments in the UMR and is one article in a series designed to assess the extent of sediment contamination in navigational pools of the river. Companion articles evaluate sediment toxicity and benthic community composition in navigation pools of the river. The objectives of the present study were to: (1) to assess the bioaccumulation of sediment-associated contaminants in the UMR using laboratory exposures with the oligochaete Lumbriculus variegatus, and (2) to compare bioaccumulation in laboratory-exposed oligochaetes to field-collected oligochaetes. Sediment samples and native oligochaetes were collected from 23 navigational pools on the Upper Mississippi River and the Saint Croix River. Contaminant concentrations measured in the L. variegatus after 28-day exposures to sediment in the laboratory were compared to contaminant concentrations in field-collected oligochaetes from the 13 pools where these sediments were collected. Contaminant concentrations were relatively low in sediments and tissues from the pools evaluated. Only polycyclic aromatic hydrocarbons (PAHs) and total polychlorinated biphenyls (PCBs) were frequently measured above detection limits. The majority of the biota-sediment-accumulation factors (BSAFs) for PAHs were within a range of about 1.0 to 2.6, suggesting that the theoretical BSAF value of 1.7 could be used to predict these mean BSAFs with a reasonable degree of certainty. A positive correlation was observed between lipid-normalized concentrations of PAHs detected in laboratory-exposed and field-collected oligochaetes across all sampling locations. Rank correlations for concentrations of individual compounds between laboratory-exposed and field-collected oligochaetes were strongest for benzo(e)pyrene, perylene, benzo(b,k)fluoranthene, and pyrene. About 90% of the paired PAH concentrations in laboratory-exposed and field-collected oligochaetes were within a factor of three of one another indicating laboratory results could be extrapolated to the field with a reasonable degree of certainty.

Journal Article↗

Effects of laboratory versus field exercise on leukocyte subsets and cell adhesion molecule expression in children.

In adults, exercise is a powerful and natural stimulator of immune cells and adhesion molecules. Far less is known about these exercise responses during childhood and whether or not exercise in real-life activities of healthy children might influence immune responses. We compared laboratory exercise (10 x 2 min periods of heavy, constant intensity, cycle ergcometer exercise with 1 min rests between exercise in nine subjects, aged 9-15 years) with field exercise (90 min soccer practice in nine different subjects, aged 9-11 years). Blood was sampled before both protocols, 5 min after the 30 min laboratory protocol, and 10-15 min after the 90 min field protocol. Both field and laboratory exercise protocols led to significant (P<0.05) increases in granulocytes, monocytes, and all lymphocyte subpopulations. The mean (SEM) increases were similar for the two protocols except for the significantly greater increase in laboratory compared with field protocols for natural killer cells [142 (39)% vs 12 (16)%, P<0.001] and monocytes [64 (22)% vs 32 (19)%, P<0.001] Both protocols significantly influenced adhesion molecules (such as CD54) which have not been previously studied in children. However, the adhesion molecule CD8+ CD62L increased to a significantly (P < 0.001) greater extent in the laboratory [101 (25)%] versus field [34 (25)%] protocol. Finally, the density of CD632L on lymphocytes significantly decreased with laboratory exercise but showed no change in the field protocol [-20 (3)% vs -3 (3)%, P<0.001]. The rapid and substantial immune response in both laboratory and field protocols suggests that exercise stimulation of the immune system occurs commonly in the real lives of children and may play a role in their overall immune status.

CD3 Complex↗

CPAP compliance in sleep apnea patients with and without laboratory CPAP titration.

Advances in auto-adjusting positive airway pressure technology for obstructive sleep apnea now permit this treatment to be initiated outside of the sleep laboratory environment, bypassing the need for laboratory-based titration studies. Thus far, little research has addressed how such developments may affect compliance to continuous positive airway pressure (CPAP). We tested the effect of laboratory CPAP exposure and technologist support in a retrospective chart review of 98 veterans with obstructive sleep apnea to determine whether patients who received standard laboratory CPAP titration complied better with CPAP than did patients who received no laboratory CPAP titration. Fifty patients underwent standard technician-attended polysomnography (PSG) with CPAP titration, and 48 patients underwent unattended PSG with no laboratory trial of CPAP (first CPAP exposure was at home). Objective CPAP compliance measures were obtained from CPAP units at follow-up visits. Attended-PSG patients wore CPAP significantly longer per night on average (5.0 hours vs 3.9 hours) and tended to wear CPAP on more nights (76.5% vs 64.2%) compared with unattended-PSG patients. These findings suggest that patients' sleep laboratory experience with CPAP and the support and education provided by sleep technologists are important factors in facilitating CPAP compliance.

Continuous Positive Airway Pressure↗

Veterans Administration Cooperative Studies Project No. 147. Part IX: A comparison of the mechanical properties of several alternative metal ceramic alloys cast in clinical and research laboratories.

Comparison of mechanical properties of five metal ceramic alloys cast in clinical and research laboratories resulted in significant differences. Tested alloys included one Au-Pd (control), one Pd-Ag, and three Ni-Cr. Mechanical properties included strength, elongation, and microhardness. Tensile bars were torch cast simultaneously with restorations in the clinical laboratory and induction cast by using a preformed design in the research laboratory. Mechanical properties of most alloys showed larger variations when cast in the clinical laboratory. In the clinical laboratory the Au-Pd alloy showed significantly higher values for all properties. One Ni-Cr alloy was not significantly affected by environment for all properties. The remaining alloys were significantly affected for some properties by environment. The different laboratories had no greater or lesser effect on the base metals as a group than on the noble metals. Variation in handling, spruing, casting, and specimen size may account for some of the differences between laboratories.

Ceramics↗

Comparison of neuroendocrine measurements under laboratory and naturalistic conditions.

Urinary catecholamines and cortisol were measured in healthy nonsmoking white collar workers (14 male and 15 female managers, 15 male and 14 female clerical workers), aged 30-50 years, during a one-hour period of laboratory-induced stress comprising five tests and a Type A interview, and during a subsequent period of rest in the laboratory. Values were compared with data obtained four months earlier from the same subjects during a normal day at work (4 values) and during a work-free day at home (4 values). No significant group differences were found during rest in the laboratory. However, during laboratory-induced stress, female managers had the highest norepinephrine values, which contributed to significantly (p less than 0.01) higher values in women than in men. Correlations between absolute measurements from laboratory and naturalistic conditions were generally positive and reached significance in most cases. Correlations between reactivity measurements in the laboratory and at work (change from rest to stress and from home to work, respectively) were generally low, whereas correlations between reactivity at different times of the day were relatively high. The data suggest that generalizability of neuroendocrine reactivity from laboratory stress to real-life stress is low. However, in agreement with earlier experimental findings, absolute levels of catecholamine and cortisol excretion were consistent over conditions and time.

Adult↗

The effect of laboratory environment on the morphology of the spleen and the thymus in the yellow-bellied toad, Bombina variegata (L.).

The morphological changes were observed in the spleen and the thymus of the yellow-bellied toad, Bombina variegata, kept under standard laboratory conditions. The mean splenic weights of toads studied soon after capture in July and September were 16.0 mg and 17.7 mg, respectively. In contrast, the mean splenic weights significantly decreased in animals maintained in the laboratory from July till September (to 11.6 mg) and from July till December (to 6.8 mg). In the spleen of toads kept in the laboratory the lymphocyte aggregations were diminished in the white pulp while the amount of connective tissues increased both in the white and in the red pulps. Melano-macrophages were more abundant in the red pulp of toads kept in the laboratory than in freshly collected ones. The thymuses of toads kept in the laboratory were decreased in size and depleted of the majority of their cortical lymphocytes. It is suggested that the morphological changes of the yellow-bellied toad lymphoid organs might be the results of stressful laboratory conditions and lower antigenic stimulation in the laboratory than in nature.

Animals↗

Standardisation of primers and an algorithm for HIV-1 diagnostic PCR evaluated in patients harbouring strains of diverse geographical origin. The Belgian AIDS Reference Laboratories.

Eight Belgian AIDS Reference Laboratories established a multicentre quality control to evaluate the performance of their diagnostic human immunodeficiency virus type 1 (HIV-1) DNA polymerase chain reaction (PCR). A set of Belgian and African HIV-1 seropositive and seronegative patient samples, collected in Belgium, and the British Medical Research Council (MRC) HIV-1 PCR reference reagent kit, containing plasmid HIV-1 DNA at several dilutions in human carrier DNA with appropriate negative controls, were tested by the laboratories. No false positive results were reported. All laboratories were able to detect one to two copies of HIV-1 DNA. Among the 17 Belgian and African HIV-1 seropositives, some laboratories reported up to four indeterminate results, mainly due to failure of the SK38-39, SK68-69 (Ou et al. (1988) Science 239, 295-297) and/or gag881-882 (Simmonds et al. (1990) J. Virol. 64, 864-872) primers and a poorly performing algorithm. Only the H1POL4235-4538 nested pol primer set, developed by one of the laboratories, correctly identified all the tested HIV-1 positive and negative samples. Consequently, the laboratories decided to evaluate these pol primers as a reference primer set and to standardise the testing algorithm. All laboratories achieved a sensitivity and specificity of 100% on testing 10 additional Belgian and African patient samples, when adapting a standardised algorithm based on three HIV-1 primer sets, one of which is the H1POL4235-4538 primer set.

Africa↗

The validation of analytical methods for drug substances and drug products in UK pharmaceutical laboratories.

Results of a survey on method validation of analytical procedures used in the testing of drug substances and finished products, of most major research based pharmaceutical companies with laboratories in the UK, are presented. The results indicate that although method validation shows an essential similarity in different laboratories (in particular, chromatographic assay methods are validated in a similar manner in most laboratories), there is much diversity in the detailed application of validation parameters. Testing procedures for drug substances are broadly similar to finished products. Many laboratories validate methods at clinical trial stage to the same extent and detail as at the marketing authorization application (MAA)/new drug application (NDA) submission stage, however, only a small minority of laboratories apply the same criteria to methodology at pre-clinical trial stage. Extensive details of method validation parameters are included in the summary tables of this survey, together with details of the median response given for the validation of the most extensively applied methods. These median response details could be useful in suggesting a harmonized approach to method validation as applied by UK pharmaceutical laboratories. These guidelines would extend beyond the recommendations made to date by regulatory authorities and pharmacopoeias in that minimum requirements for each method validation parameter, e.g. number of replicates, range and tolerance, could be harmonized, both between laboratories and also in Product Licence submissions.

Chromatography, High Pressure Liquid↗

A comparison of microsatellite polymorphism and heterozygosity among field and laboratory populations of Schistosoma mansoni.

The genetic diversity of a field population (recently collected in Melquiades, Brazil) and two laboratory strains (LE and NMRI) of a human blood fluke, Schistosoma mansoni, were analysed using microsatellite markers. Data from the three groups showed an extreme and consistent discrepancy in the level of polymorphism at all microsatellite loci between the field population and laboratory populations. The numbers of alleles detected in LE and NMRI populations averaged only 14 and 10% of those found in the field population, respectively. Especially apparent was the abundance of rare alleles in the Melquiades population when compared with the laboratory strains. The reduction in allelic diversity in the laboratory strains is most likely due to the founder effect and potential bottlenecks that may have occurred during decades of laboratory maintenance. Surprisingly, a much less drastic difference was found when comparing the average heterozygosity of the field population with the laboratory strains. This apparent anomaly may be explained by observed population substructuring (and a potential resultant Wahlund effect) in the natural population. Our comparison of genetic diversity between laboratory and field populations of S. mansoni emphasizes the need for studies of representative populations in schistosome vaccine development.

Alleles↗

Multicenter evaluation of mycobacteria identification by PCR restriction enzyme analysis in laboratories from Latin America and the Caribbean.

The identification of mycobacterial species in clinical isolates is essential for making patient care decisions. Polymerase chain reaction (PCR) restriction enzyme analysis (PRA) is a simple and rapid identification method, based on amplification of 441 bp of the hsp65 gene and restriction with BstEII and HaeIII. As a contribution to the validation of PRA, a multicenter study was performed in eight laboratories located in Argentina, Brazil, Colombia, Chile, and Guadeloupe. Each laboratory received 18 coded isolates from the collection of the Institute of Tropical Medicine (Antwerp, Belgium), representing duplicates of nine laboratory strains: Mycobacterium terrae CIPT 140320001, Mycobacterium scrofulaceum CIPT 140220031, Mycobacterium flavescens ATCC 14474, Mycobacterium triviale ATCC 23292, Mycobacterium nonchromogenicum ATCC 19530, Mycobacterium chitae ATCC 19627, Mycobacterium abscessus ATCC 19977, Mycobacterium kansasii ATCC 12478, and Mycobacterium peregrinum ATCC 14467. A detailed protocol including amplification, enzymatic digestion, and gel preparation was provided to each laboratory. Two laboratories identified correctly all 18 (100%) isolates, one identified correctly 17 (94.5%), two identified 14 (77.7%), one identified 11 (61%), and two identified 8 (44.4%) isolates. Errors detected in laboratories with more than 77% accuracy were associated with electrophoresis running conditions and an unspecific amplicon produced by a single strain. Lower accuracy was mainly related to inappropriate use of DNA markers and insufficient training in interpretation of patterns. In conclusion, the PRA method was readily implemented in some Latin American and Caribbean laboratories of mycobacteria, but improvements in critical points, as gel running conditions and training in interpretiation of patterns, are needed in order to improve accuracy. In others, improvement in critical points is still necessary.

Bacterial Proteins↗

Antiphospholipid antibody ELISAs: survey on the performance of clinical laboratories assessed by using lyophilized affinity-purified IgG with anticardiolipin and anti-beta2-Glycoprotein I activity.

Lupus anticoagulant (LA) and anticardiolipin (aCL) antibodies are the classical tests used to diagnose the antiphospholipid syndrome (APS). Unfortunately, since these are nonspecific and standardization is lacking, the results of laboratory work-ups upon which diagnosis are made are often misleading. The performance of clinical laboratories in detecting LA using lyophilised affinity purified immunoglobulin has been previously reported. The same material was used to investigate the inter-laboratory variability of aCL and anti-beta(2)-Glycoprotein I (beta(2)-GPI) antibody measurements. Laboratories were asked to test normal plasma spiked with purified IgG or distilled water in order to obtain 3 samples positive for aCL and anti-beta(2)-GPI at different antibody concentration (A, B and C) and 3 samples of normal plasma. Thirty-five laboratories participated and interpreted their test results. All performed an ELISA for IgG aCL antibodies, while 17 also tested samples using IgG anti-beta(2)-GPI antibody ELISA. Sensitivity and specificity were calculated on the basis of the responses provided by each laboratory. Overall, 99/105 samples were correctly interpreted as positive and 97/101 as negative for the presence of IgG aCL, corresponding to a sensitivity and specificity of 94% and 96%, respectively. Likewise, 46/51 samples were correctly defined as positive and 50/51 as negative for the presence of IgG anti-beta(2)-GPI corresponding to a sensitivity and specificity of 90% and 98%, respectively. A wide variability in results pertaining to the positive samples was found for aCL-ELISA (coefficient of variation of 79%, 59%, and 53% for samples A, B, and C, respectively) as well as for abeta(2)-GPI-ELISA (coefficient of variation of 85%, 95%, and 50% for samples A, B, and C, respectively). This was confirmed when the analysis was restricted to those centres using the same commercial kit. Median antibody concentrations reported by centres for positive samples were consistent with the prolongation of coagulation tests assessing lupus anticoagulant (LA). Among these, dRVVT showed a good sensitivity and linear correlation with aCL antibody concentration. In conclusion, on the whole this survey found correct interpretation of positive and negative samples by both ELISAs. Nonetheless the high variability of reported data remains a major problem that only a consensus on the part of laboratories and manufacturers to utilize standard, uniform materials and procedures can hope to overcome.

Antibodies, Anticardiolipin↗

Inter-laboratory comparison of liquid chromatographic techniques and enzyme-linked immunosorbent assay for the determination of surfactants in wastewaters.

Seven laboratories participated in an inter-laboratory comparison exercise within the framework of the PRISTINE, SANDRINE and INEXsPORT European Union Projects. Solid-phase extraction (SPE) methodologies were used for the extraction of target analytes from wastewaters. The analytical strategies were based on liquid chromatography (LC) coupled to mass spectrometric (MS) or to fluorescent (FL) detection in all cases with the exception of one laboratory using a test-tube enzyme-linked immunosorbent assay kit. Samples were spiked with the surfactants nonylphenolpolyglycol ether, coconut diethanolamide, linear alkylbenzene sulfonate, nonylphenolpolyglycol ether sulfate, alkylpolyglycol ether and secondary alkane sulfonate. After enrichment on previously conditioned SPE cartridges, the SPE cartridges were distributed among the participating laboratories without the information about the amount of spiked surfactants. In addition, SPE cartridges loaded with a real-world environmental sample containing a tannery wastewater were also analyzed. The results of the programme showed that SPE followed by LC-MS techniques are reliable for the surfactants determination at submicrogram to microgram per liter levels in wastewaters. Inter-laboratory precision values were calculated as the reproducibility relative standard deviation (RSD(R)) which was determined from the reproducibility standard deviation (sR) and the average concentration at a particular concentration level. When data from all laboratories were pooled, the RSD(R) values ranged from 5.1 to 28.3% for the determination of target analytes. The most accurate result corresponded to that given for linear alkylbenzene sulfonates. Taking into account that different methodologies were used (including non-chromatographic techniques) and the complexity of the samples analyzed, it can be considered that acceptable reproducibility values were obtained in this inter-laboratory study.

Chromatography, Liquid↗

Effect of laboratory procedures and thermocycling on the shear bond strength of resin-metal bonding systems.

STATEMENT OF PROBLEM: During fabrication or repair of removable partial dentures, resin-to-metal or resin-to-denture tooth bonds may be stressed by laboratory procedures. PURPOSE: The purpose of this in vitro study was to evaluate the effect of steam cleaning, boiling, ultrasonic cleaning (laboratory procedures), and thermocycling on shear bond strength of resin bonds to metal and denture teeth. MATERIAL AND METHODS: Resin-metal bonding systems and their specific veneer resins (Rocatec, Sinfony; Rocatec, Visio-Gem, HLC-BOND, Zeta LC and Ducera experimental veneer resin) were tested on a Co-Cr alloy (Wirobond C). The veneer resins were bonded to resin denture teeth. The experimental groups (n=7) were subjected to the following conditions: 24-hour storage of the specimens in air (group I, control group), storage in air and treated with simulated laboratory procedures (2 minutes steam cleaning, 15 minutes ultrasonic cleaning at room temperature, 1 hour boiling in water, group II), storage in air with thermocycling (5000 cycles, 5 degrees to 55 degrees C, group III), storage in air with laboratory procedures followed by thermocycling (group IV), and storage in air with thermocycling followed by laboratory procedures (group V). Shear strength tests (MPa) were performed with a universal testing machine until fracture. After shear bond testing, the failure mode of the resin-metal and resin-denture tooth bonds was assessed. Statistical analysis of the results was carried out with one-way analysis of variance and Bonferroni-Dunn's multiple comparisons post hoc analysis for test groups (alpha=0.05). RESULTS: Except for Ducera/denture tooth specimens (groups III to V: 8.7 +/- 3.4-9.1 +/- 1.7; 10.8 +/- 1.9 MPa control group), the Wirobond C and denture tooth specimens (groups III, IV and V: 1.4 +/- 0.9-11.9 +/- 2.3 MPa), showed significantly lower shear bond strengths than the corresponding control groups (7.5 +/- 2.9-21.0 +/- 3.4 MPa, P<.05). The shear bond strengths of group II of Sinfony/Wirobond C (11.6 +/- 3.3 MPa, P<.0001), Visio-Gem/Wirobond C (7.4 +/- 1.9 MPa, P<0.0001), Ducera/Wirobond C (11.8 +/- 2.9 MPa, P<.0001) and of Zeta/denture tooth (3.9 +/- 1.6 MPa, P=.0005) were significantly decreased by steam, boiling, and ultrasonic procedures compared with the corresponding control groups (21.0 +/- 3.4 MPa; 14.7 +/- 4.0 MPa; 19.1 +/- 2.3 MPa; 7.5 +/- 2.9 MPa, respectively). No significant differences were noted among groups III, IV, and V. Co-Cr specimens subjected to the Rocatec system and bonded with Sinfony and HLC BOND/Zeta specimens showed cohesive failure. Adhesive failure was observed for the experimental veneer resin on the Co-Cr specimens and for all veneer resins on the denture teeth. CONCLUSION: Simulation of laboratory procedures and thermocycling caused a significant drop in shear bond strength of metal-resin and denture tooth-resin bonds for most of the tested veneer resins. Thermocycling before shear testing had the same effect on veneer resin bond strength as the simulated laboratory procedures.

Acrylic Resins↗

Niche-related learning in laboratory paradigms: the case of maze behavior in Norway rats.

The general hypothesis underlying this paper is that behavior in traditional paradigms of laboratory learning is based on niche-related mechanisms. The specific hypothesis is that the behavior of Norway rats in laboratory mazes is based on niche-related mechanisms related to trail following and navigating. I evaluate seven types of evidence for this hypothesis: (a) resemblance of maze behavior to behavior in unconstrained settings; (b) importance of experimenter tuning of apparatus and procedures; (c) overdetermination of laboratory behavior; (d) reverse-engineering of niche-related mechanisms from laboratory data; (e) prediction of laboratory results from ecological data; (f) contribution of specific relative to general mechanisms; and (g) phylogenetic conservation and ecologically-based convergence and divergence of maze mechanisms. I conclude there is strong evidence for the hypothesis that behavior of rats in laboratory mazes is based on niche-related mechanisms. I suggest that a niche-related approach to laboratory learning paradigms has conceptual generality and the potential to facilitate connections with the study of neurophysiology, genetics, and evolution.

Animals↗

Comparison of laboratory uranium sorption data with 'in situ distribution coefficients' at the Koongarra uranium deposit, Northern Australia.

Distribution coefficients derived from laboratory sorption experiments are commonly used to model the migration of long-lived radionuclides in the environment. However, it has been suggested that field measurements in natural systems ('in situ distribution coefficients') may provide a more accurate indication of 'true' partitioning coefficients than laboratory experiments. In this paper, the relationship between field and laboratory sorption data for uranium is evaluated, using data from the Koongarra uranium deposit in Northern Australia. An extensive suite of laboratory sorption measurements and in situ partitioning data for U has been obtained at this site. A valid comparison can only be made when the calculation of field partitioning is based on U in 'accessible' phases (rather than total U in the solid) and U species in true solution (i.e. excluding particles). In this study, accessible U was estimated using a chemical extraction and the results were verified using an isotope exchange technique. A satisfactory correspondence between field and laboratory partitioning data was obtained when the pH values and partial pressures of CO2 in laboratory sorption experiments were similar to those found in the field. Under these conditions, the measured laboratory sorption ratios (Rd) and in-field partitioning values (Pacc) for U at Koongarra were in the range between approximately 1 x 10(3) and 2 x 10(4) ml/g. However, the distribution of U in solid and groundwater phases at Koongarra is extremely heterogeneous. This variability must be taken into account when modelling radionuclide migration at this site.

Adsorption↗

Laboratory reports of opportunistic and other mycobacterial infections and their relationship to notifications of tuberculosis in England and Wales.

SETTING: England and Wales, UK. OBJECTIVE: To investigate: (1) whether misclassification of opportunistic mycobacterial disease had contributed to the failure of tuberculosis notifications to continue declining; (2) whether laboratory reports of Mycobacterium tuberculosis complex infections could be used to validate trends in the tuberculosis notification system. DESIGN: Descriptive epidemiological study using laboratory reports of infections to the Public Health Laboratory Service Communicable Disease Surveillance Centre, Medical Research Council National Surveys of Tuberculosis and tuberculosis notifications to the Office of Population Censuses and Surveys. RESULTS: Compared to 1983, an extra 1% of tuberculosis notifications in 1988 were opportunistic mycobacterial disease inappropriately notified as tuberculosis. On the basis of the expected proportion of microbiologically confirmed tuberculosis infections, laboratory reporting was incomplete: for one laboratory report there were four notifications. CONCLUSION: Misclassification of opportunistic mycobacterial infection was estimated to account for only a small proportion of the excess tuberculosis notifications since 1988. This excess of tuberculosis notifications could be due to artefact, for instance because a greater proportion of cases are being notified. Laboratory reports of tuberculosis infections are of limited use in validating the recent trends in tuberculosis notification rate. At present changes in the level of reporting of laboratory isolates are likely to obscure genuine trends.

Diagnostic Errors↗