A dinosaur ichnocoenosis from the middle jurassic of Yorkshire,UK

An assemblage of dinosaur tracks from the undersurface of a sandstone bed in the Saltwick Formation (Middle Jurassic) of Yorkshire shows a range of morphological types, preservational variants and behavioral styles. The tracks are combinations of transmitted prints and underprints and include three distinct trackways. One trackway was made by an animal walking on exposed damp sand, another was left by an animal swimming diagonally across a current and being swept down current, while the third may have been made by an animal either running or pushing off with its feet as it drifted down current. Environmental conditions that existed during the formation of the trackways varied between crevasse splay floods and exposed damp sand. The morphology of the swimming tracks is sufficiently distinctive to warrant the erection of a new ichnogenus and ichnospecies—Characichnos tridactylus. Previously described material from Kansas, Wyoming and New Mexico can be attributed to this new ichnogenus, while specimens from Germany and Utah are only provisionally referred to it. This indicates a known range from Triassic to Cretaceous.     

Spatial variation in the magnitude and functional form of density‐dependent processes on the large skipper butterfly Ochlodes sylvanus

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Wood growth response of Calluna vulgaris (L.) Hull to elevated N deposition and drought

Ring diameters and ring number counts were recorded from Calluna stem cross-sections harvested during an N manipulation experiment. The application of dendrochronological methods permitted accurate ageing of shrubs growing in a heathland of known age. Linear regression analyses demonstrated a highly significant association between increasing levels of N input and stem diameter in both watered and droughted plots (droughted in 1997 only). N inputs were identified as the most significant environmental stressor, appearing to speed ageing vis the Calluna growth cycle. Drought sensitivity was noted in the high N treatment plots (120 kg N ha⁻¹ yr⁻¹) with decreased stem diameters. This may have implications in the response of Calluna growth under current climate change scenarios.     

Model erroneously predicts failure for restoration of Lake Apopka,a hypereutrophic,subtropical lake

There are six main species of shellfish of commercial importance within the UK (mussels, flat oysters, cockles, king scallops, Manila clams and lobsters) which can be thought of as ranched to varying degrees. A seventh (Pacific oysters) can be included, since a very small proportion of the production may undergo a period of growth on natural habitats in some areas. An eighth species (Palourdes or native clams) appeared in the statistics for the first time in a number of years in 1998. Seafish, as part of its role in promoting the sustainable management of resources, has examined the current state of the shellfish aquaculture industry in the UK.     

Ligand recognition of serine-cysteine amino acid exchanges in transmembrane domain 5 of alpha2-adrenergic receptors by UK 14,304

Ligand binding of UK 14,304 reveals notable species (i.e., human-rodent) and receptor-subtype differences of alpha2-adrenergic receptors (alpha2-ARs). To study the molecular basis of the selectivity of UK 14,304, we compared a series of conservative serine-cysteine exchange mutants at ligand-accessible positions in transmembrane domain 5 of the human and mouse alpha2A-ARs. UK 14,304 bound with approximately 200-fold higher affinity to the human alpha2A-AR wild-type receptor compared with the human alpha2A-ARSer201 mutant, but only an approximately fivefold difference was seen with the corresponding mouse alpha2A-AR variant. These effects of cysteine-serine exchanges only involved the agonist low-affinity forms of the receptors, as the affinity of [3H]UK 14,304 for the agonist high-affinity receptor populations was not influenced. The apparent affinities of a set of eight structurally diverse alpha2-AR ligands (six agonists and two antagonists) were not influenced significantly by the cysteine-serine exchanges (except for oxymetazoline and yohimbine, with up to nine- and eightfold differences in affinity, respectively). We conclude that position 201 (a) plays a primary role in determining observed subtype/species selectivity of UK 14,304 in competitive antagonist radioligand binding assays and (b) does not determine the subtype selectivity of chlorpromazine.     

REGULATION OF ION TRANSPORT BY P2UPURINOCEPTORS AND α2A ADRENOCEPTORS IN HT29 CELLS

X-ray microanalysis was applied to investigate ion transport mediated by P_2Upurinoceptors and α₂A adrenoceptors as well as their interaction in the regulation of the intracellular elemental concentration in HT29 cells. In response to ATP, HT29 cells showed a decrease of intracellular Cl, Na and an increase in Ca. A similar result was observed with UTP, but UTP appeared to be more potent than ATP. On the other hand, UK14,304, an α₂receptor agonist, was found to be capable of reversing the action of both UTP and ATP on ion secretion, and caused a clear increase in intracellular Na and Cl. Moreover, treatment of cells with UK14,304 before exposure to UTP did not induce a decrease in Cl and Na, suggesting that UK14,304 blocks the action of UTP. The secretory effect of UTP was also blocked by NPPB, a chloride channel blocker, and alloxan. Chelation of extracellular Ca with EGTA abolished ion response to UTP. These results suggest that since inhibition of the intracellular cAMP system and chelation of Ca²⁺can block the nucleotide-induced chloride secretion, the ATP and UTP-induced chloride secretion can be mediated via both cAMP-dependent and Ca²⁺-dependent pathways.     

Characterization and Regional Distribution of α2-Adrenoceptors in Postmortem Human Brain Using the Full Agonist [3H]UK 14304

The full agonist [3H]UK 14304 [5-bromo-6-(2-imidazolin-2-yl-amino)-quinoxaline] was used to characterize alpha 2-adrenoceptors in postmortem human brain. The binding at 25 degrees C was rapid (t1/2, 4.6 min) and reversible (t1/2, 14.1 min), and the KD determined from the kinetic studies was 0.48 nM. In frontal cortex, the rank order of potency of adrenergic drugs competing with [3H]UK 14304 or [3H]clonidine showed the specificity for an alpha 2A-adrenoceptor: UK 14304 approximately equal to yohimbine approximately equal to oxymetazoline approximately equal to clonidine greater than phentolamine approximately equal to (-)-adrenaline greater than idazoxan approximately equal to (-)-noradrenaline greater than phenylephrine greater than (+/-)-adrenaline much greater than corynanthine greater than prazosin much greater than (+/-)-propranolol. GTP induced a threefold decrease in the affinity of [3H]UK 14304, with no alteration in the maximum number of binding sites, suggesting that the radioligand labelled the high-affinity state of the alpha 2-adrenoceptor. In the frontal cortex, analyses of saturation curves indicated the existence of a single population of noninteracting sites for [3H]UK 14304 (KD = 0.35 +/- 0.13 nM; Bmax = 74 +/- 9 fmol/mg of protein). In other brain regions (hypothalamus, hippocampus, cerebellum, brainstem, caudate nucleus, and amygdala) the Bmax ranged from 68 +/- 7 to 28 +/- 4 fmol/mg of protein. No significant changes in the KD values were found in the different regions examined. The binding of [3H]UK 14304 was not affected by age, sex or postmortem delay.(ABSTRACT TRUNCATED AT 250 WORDS)     

The value of blood-based measures of liver function and urate in lung cancer risk prediction: A cohort study and health economic analysis

BackgroundSeveral studies have reported associations between low-cost blood-based measurements and lung cancer but their role in risk prediction is unclear. We examined the value of expanding lung cancer risk models for targeting low-dose computed tomography (LDCT), including blood measurements of liver function and urate.MethodsWe analysed a cohort of 388,199 UK Biobank participants with 1873 events and calculated the c-index and fraction of new information (FNI) for models expanded to include combinations of blood measurements, lung function (forced expiratory volume in 1 s - FEV₁), alcohol status and waist circumference. We calculated the hypothetical cost per lung cancer case detected by LDCT for different scenarios using a threshold of ≥ 1.51 % risk at 6 years.ResultsThe c-index was 0.805 (95 %CI:0.794–0.816) for the model containing conventional predictors. Expanding to include blood measurements increased the c-index to 0.815 (95 %CI: 0.804–0.826;p < 0.0001;FNI:0.06). Expanding to include FEV₁, alcohol status, and waist circumference increased the c-index to 0.811 (95 %CI: 0.800–0.822;p < 0.0001;FNI: 0.04). The c-index for the fully expanded model containing all variables was 0.819 (95 %CI:0.808–0.830;p < 0.0001;FNI:0.09). Model expansion had a greater impact on the c-index and FNI for people with a history of smoking cigarettes relative to the full cohort. Compared with the conventional risk model, the expanded models reduced the number of participants meeting the criteria for LDCT screening by 15–21 %, and lung cancer cases detected by 7–8 %. The additional cost per lung cancer case detected relative to the conventional model was £ 1018 for adding blood tests and £ 9775 for the fully expanded model.ConclusionBlood measurements of liver function and urate made a modest improvement to lung cancer risk prediction compared with a model containing conventional risk factors. There was no evidence that model expansion would improve the cost per lung cancer case detected in UK healthcare settings.     

Copper and molybdenum absorption by rats given ammonium tetrathiomolybdate

Previous studies have shown that the tetrathiomolybdate ion [MoS_4^2?] is a potent antagonist of Cu metabolism. Effects of orally administered MoS_4^2? on the absorption and tissue distribution of ⁶⁴Cu in rats have now been investigated. Four or 12 mg Mo/kg diet, when given as MoS_4^2?, strongly inhibited ⁶⁴Cu absorption and modified the fate of absorbed Cu, decreasing hepatic and renal uptake but increasing plasma retention of ⁶⁴Cu. These effects were not induced by equivalent dietary concentrations of Mo as MoS_4^2? or when S^2? was given as CaS. Clinical and biochemical effects induced by orally administered MoS_4^2? were abolished by increasing dietary concentrations of Cu. Such treatment also inhibited the absorption and tissue retention of ⁹⁹Mo derived from ⁹⁹MoS_4^2?. Intraperitoneal administration of Cu ameliorated clinical effects attributable to MoS_4^2? but neither inhibited ⁹⁹Mo absorption nor the appearance of systemic defects in Cu metabolism. Since the absorption of MoS_4^2? (or its derivatives) from the gastrointestinal tract is inhibited by Cu, it is evident that the site of its action as an antagonist influencing either the absorption or the subsequent metabolic fate of Cu depends upon the ratio Cu/MoS_4^2? in the diet.