Estimating the extent and change in Broad Habitats in Great Britain.

A stratified random sample of kilometre squares in Great Britain was visited and completely mapped using four areal themes (agriculture and semi-natural vegetation, forestry, physiography and buildings and communications). The maps were digitised and the attribute information recorded to produce an electronic database. Information was summarised by square and then bootstrap re-sampling techniques were used to produce national estimates with statistical confidence intervals. The results for 1998 showed the terrestrial Broad Habitats had a range in extent covering two orders of magnitude from Montane (49000ha) to Improved Grassland (5482000ha). Just under half of Britain is covered by agricultural Broad Habitats, about 12% by woodland and just under 10% by Urban Habitats. The remaining quarter of the land area is covered by semi-natural Broad Habitats. By revisiting the same sample of squares previously visited in 1990, changes in the quantity and quality of the Broad Habitats have been determined. Significant increases in area have occurred in the Broadleaved, Mixed and Yew Woodland and Built Up and Gardens. The largest areal reduction was in Acid Grassland although that was in part balanced by a gain in Fen, Marsh and Swamp. The most significant ecological loss was in the area of Calcareous Grassland. The consequences of having different sample sizes for the different years are discussed.

Changing landscapes, habitats and vegetation diversity across Great Britain.

This paper describes how Countryside Survey 2000 (CS2000) and earlier Countryside Surveys in 1990 and 1984, can be used to develop an integrated view of the changes in land cover, landscape and biodiversity that have taken place at the regional scale in Great Britain. A particular concern is to develop an understanding of how the national patterns of stock and change are distributed across Great Britain, and whether such changes are leading to more or less regional differentiation in our landscapes and biodiversity. A further concern is how the structure of landscape is changing.A description of the major Environmental Zones that make up Great Britain is given. Analysis of the regional patterns of change observed suggests that there has been considerable geographical variation in the gains and losses of the stock of the Biodiversity Action Plan Broad Habitats. Between 1984 and 1990, in the lowlands of the south and west of England and Wales, there were significant increase in the area of the Arable and Horticultural and Broadleaved Woodland Broad Habitats, and a marked loss of Improved Grassland. Over the same period, in the uplands of England and Wales, significant losses of Acid Grassland were observed, with associated gains in Improved Grassland. The Environmental Zones in Scotland were more stable in terms of the changes in stock of Broad Habitats. In addition to the analysis of net changes in stock of the Broad Habitats, the paper provides an analysis of the exchanges of land between major cover categories or each of the Environmental Zones. In contrast to the regionally concentrated changes in habitat stock, more ubiquitous and uniform changes in habitat quality were detected between 1990 and 1998, which continue trends observed for the 1980s. The quality of freshwater habitats increased. However, there were declines in the quality for some terrestrial biotopes, as indicated by the loss of species diversity from agricultural habitats, and the gains in diversity in semi-natural habitats, such as Acid Grasslands, more usually associated with vegetation types that are poor in species. An important driver of qualitative change appears to be widespread nutrient enrichment from nitrogen. However, such processes are probably superimposed upon more local factors, such as changes in the way land is managed for agriculture. The importance of understanding the various drives of change for future countryside policy is emphasized.

Esophageal passage of iodine-131 capsules.

UNLABELLED: The purpose of this study was to determine the orogastric transit time of standard 131I capsules and the incidence of transit delay. METHODS: We studied 58 consecutive subjects receiving outpatient diagnostic and therapeutic 131I dosages. A standard ion chamber survey meter, placed over the left upper quadrant of the abdomen, monitored orogastric transit. Each subject had ample water to subjectively swallow their capsule. Orogastric transit times, volume of water ingested, capsule size, and demographic and historical data were recorded for each subject. RESULTS: Seventeen subjects (29%) had delayed transit, with an orogastric transit time > 90 sec (median 140 sec, range 100-930 sec). Forty-one subjects had normal transit (median 14 sec, range 4-51 sec). We identified delayed transit in 7 of 37 women (19%) and 10 of 21 men (48%) (p = 0.035). Age, capsule size and initial water volume ingested did not differ significantly between subject groups. CONCLUSION: Men were more likely than women to have prolonged orogastric transit of standard 131I capsules. Other than sex, we found no identifiable clinical feature or medical history to predict delayed orogastric transit. A standard survey meter can identify adherent capsules to minimize esophageal radiation exposure.

Determination of halothane-induced sleeping time in the rat: effect of prior administration of centrally active drugs.

A method is described for the determination of halothane-induced sleeping time in the rat. 2 The sleeping time exhibited a diurnal variation which was due, at least in part, to a change in the sensitivity of the central nervous system (CNS) to the anaesthetic. 3 Tolerance to halothane did not develop in rats repeatedly exposed to the anaesthetic over a period of over 48 hours. 4 Repeated sleeping time determinations have been used to follow changes in the sensitivity of the CNS to the anaesthetic occurring with time. 5 A tolerance to halothane was induced by pretreatment of rats with doses of amylobarbitone, pentobarbitone or meprobamate sufficient to keep animals anaesthetized for approximately 12 hours. This tolerance was followed by a period of halothane-hypersensitivity. 6 Halothane-tolerant animals awakened with higher brain halothane concentrations and were also tolerant to intracerebroventricularly administered pentobarbitone. 7 Halothane-hypertensive rats awakened with lower brain halothane concentrations and were also hypersensitivity to intracerebroventricularly administered pentobarbitone. 8 The possibility that the induction of cross-tolerance to halothane may be indicative of a drug's potential to produce dependence is discussed.

Acute tolerance to barbiturate in the rat.

3 experimental approaches to the quantitation of acute barbiturate tolerance have been compared in the rat. There was no difference between the brain hexobarbitone or barbitone concentration found at the time of loss of righting reflex compared with the concentration found on return of the righting reflex following the period of anaesthesia produced by a single i.p. injection of the drug. However, tolerance was induced by a 7 hr infusion of pentobarbitone which kept rats anaesthetized for approximately 8 hr. Such rats awakened with a significantly higher brain pentobarbitone concentration compared with rats awakening after a single i.p. injection. Repeated i.p. injections of pentobarbitone, sufficient to keep animals anaesthetized for 12 hr, also induced a tolerance to pentobarbitone, as indicated by a reduced sleeping time and higher brain barbiturate concentration on awakening following intracerebroventricularly administered pentobarbitone injected 12 hr after the last i.p. injection. The possible relationship between acute cellular tolerance and physical dependence is discussed.

Structure-action relationships of histidine decarboxylase inhibitors.

Substituted phenols were found to be more potent inhibitors of histidine decarboxylase than were the correspondingly-substituted benzoic acids. Regression analysis, though indicating that potent inhibitors of histamine formation are unlikely to be found among simple, substituted phenols, enables tentative conclusions to be drawn regarding the nature of the interaction between these compounds and the enzyme.

High speed holographic digital recorder.

Concepts, feasibility experiments, and key component developments are described for a holographic digital record/reproduce system with the potential for 1.0 Gbit/sec rates and higher. Record rates of 500 Mbits/sec have been demonstrated with a ten-channel acoustooptic modulator array and a mode-locked, cavity-dumped argon-ion laser. Acoustooptic device technology has been advanced notably during the development of mode lockers, cavity dumpers, beam deflectors, and multichannel modulator arrays. The development of high speed multichannel photodetector arrays for the readout subsystem requires special attention. The feasibility of 1.0 Gbits/sec record rates has been demonstrated.