The Modeling and Measurement of Respiratory Carbon Use and Net Carbon Gain of Two Agropyron Bunchgrasses

The rate of photosynthetic carbon fixation and of root and shoot xiv respiratory carbon use was measured in the laboratory and in the field (shoots only) for Agropyron desertorum (Fisch. ex Link) Schult. and Agropyron spicatum (Pursh) Scribn. and Smith. The rate of respiratory carbon use of the root system declined within hours of the shading or defoliation of the shoot system, resulting in as much as 60% reduction in specific rate of root respiration. The mean whole-plant growth efficiency (the ratio of whole-plant net carbon gain to gross photosynthetic carbon fixation) in full irradiance in the laboratory was 0.53 and was reduced both by shading and defoliation. The mean conversion efficiency was o. 70 and o. 73, and the mean maintenance coefficient 20°c was 10.8 and 9.9 mmol C mol C-1 d-1 for A. desertorum and A. spicatum, respectively. These maintenance coefficients are lower than previously reported for fast growing crop plants. The rate of respiratory carbon use and the dynamics of labile carbon compounds were simulated both for intact plants and for plants regrowing following defoliation. The partitioning of assimilates between root and shoot was explicitly modeled to make the separate simulation of root and shoot respiration possible . The simulated daily net mobilization of labile carbon compounds exceeded carbon input from photosynthesis for only the first one-to-two days of regrowth, depending on the severity of the defoliation. The instantaneous rate of respiratory carbon use of the shoot system in the field during short-term light exclusion during the day was higher than the rate at the same temperature during the subsequent night. The Qio of shoot respiration was estimated to be 2.1-2.2. The mean growth efficiency in the field for the shoots only was 0.65 for sunny days. This efficiency was higher than the whole-plant growth efficiency in the laboratory because root respiration was not measured in the field

Temporal and spatial partitioning of the soil water resource between two Agropyron bunchgrasses and Artemisia tridentata

Dynamics of soil water use by two cool-season Agropyron bunchgrasses during the warm season depletion of soil water reserves were monitored for two years in experimental plots in the field. Agropyron desertorum, an introduced, competitive species from Eurasia, extracted more water from the deeper ( \u3e 50 cm) soil layers than the native, less competitive Agropyron spicatum. Agropyron desertorum both extracts this water earlier and to lower soil water potentials than Agropyron spicatum. From the water extraction dynamics of the grasses in monocultures and in their two-way (50:50) mixtures with a shrub they commonly co-occur with, Artemisia tridentata, partitioning of the soil water resource between the grasses and the shrub was inferred. This indicated that Artemisia tridentata and Agropyron desertorum partitioned the soil water resource fairly evenly, while considerable quantities of water in the deeper soil layers under Agropyron spicatum seemed to be available to the shrub without direct competition. The implications of this difference in water resource partitioning for competition of the grasses with Artemisia tridentata are discussed. Predawn and midday xylem pressure potentials were not different between the two grasses in spite of different fluxes through the plants. Agropyron desertorum initiated new adventitious roots in fall and early spring while Agropyron spicatum did so only during spring. Observations from a root observation chamber indicated essentially parallel pattern of lateral root elongation during the depletion phase through top 200 cm of the profile. In both species the number of active tips, and the rate of elongation of active tips, decreased as the soil dried out. Root tips at all depths were inactive by the middle of September. Agropyron desertorum maintained root elongation at 50-110 cm for two weeks longer than A. spicatum

Anxiety with Panic Disorder Linked to Chromosome 9q in Iceland

The results of a genomewide scan for genes conferring susceptibility to anxiety disorders in the Icelandic population are described. The aim of the study was to locate genes that predispose to anxiety by utilizing the extensive genealogical records and the relative homogeneity of the Icelandic population. Participants were recruited in two stages: (1) Initial case-identification by a population screening for anxiety disorders, using the Stamm Screening Questionnaire, was followed by aggregation into extended families, with the help of our genealogy database; and (2) those who fulfilled the diagnostic and family aggregation criteria underwent a more detailed diagnostic workup based on the Composite International Diagnostic Interview. Screening for anxiety in close relatives also identified additional affected members within the families. After genotyping was performed with 976 microsatellite markers, affected-only linkage analysis was done, and allele-sharing LOD scores were calculated using the program Allegro. Linkage analysis of 25 extended families, in each of which at least one affected individual had panic disorder (PD), resulted in a LOD score of 4.18 at D9S271, on chromosome 9q31. The intermarker distance was 4.4 cM on average, whereas it was 1.5 cM in the linked region as additional markers were added to increase the information content. The linkage results may be relevant not only to PD but also to anxiety in general, since our linkage study included patients with other forms of anxiety

To Alfred Deakin

To access publisher version of this article. Please click on the hyperlink in Additional Links fieldTo access full text version of this article. Please click on the hyperlink "View/Open" at the bottom of this pageThe results of a genomewide scan for genes conferring susceptibility to anxiety disorders in the Icelandic population are described. The aim of the study was to locate genes that predispose to anxiety by utilizing the extensive genealogical records and the relative homogeneity of the Icelandic population. Participants were recruited in two stages: (1) Initial case-identification by a population screening for anxiety disorders, using the Stamm Screening Questionnaire, was followed by aggregation into extended families, with the help of our genealogy database; and (2) those who fulfilled the diagnostic and family aggregation criteria underwent a more detailed diagnostic workup based on the Composite International Diagnostic Interview. Screening for anxiety in close relatives also identified additional affected members within the families. After genotyping was performed with 976 microsatellite markers, affected-only linkage analysis was done, and allele-sharing LOD scores were calculated using the program Allegro. Linkage analysis of 25 extended families, in each of which at least one affected individual had panic disorder (PD), resulted in a LOD score of 4.18 at D9S271, on chromosome 9q31. The intermarker distance was 4.4 cM on average, whereas it was 1.5 cM in the linked region as additional markers were added to increase the information content. The linkage results may be relevant not only to PD but also to anxiety in general, since our linkage study included patients with other forms of anxiety

To Sydney Jephcott

To access publisher full text version of this article. Please click on the hyperlink in Additional Links fieldWe mapped a gene predisposing to myocardial infarction to a locus on chromosome 13q12-13. A four-marker single-nucleotide polymorphism (SNP) haplotype in this locus spanning the gene ALOX5AP encoding 5-lipoxygenase activating protein (FLAP) is associated with a two times greater risk of myocardial infarction in Iceland. This haplotype also confers almost two times greater risk of stroke. Another ALOX5AP haplotype is associated with myocardial infarction in individuals from the UK. Stimulated neutrophils from individuals with myocardial infarction produce more leukotriene B4, a key product in the 5-lipoxygenase pathway, than do neutrophils from controls, and this difference is largely attributed to cells from males who carry the at-risk haplotype. We conclude that variants of ALOX5AP are involved in the pathogenesis of both myocardial infarction and stroke by increasing leukotriene production and inflammation in the arterial wall

Energy Partitioning Between Latent And Sensible Heat Flux During The Warm Season At Fluxnet Sites

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A variant associated with nicotine dependence, lung cancer and peripheral arterial disease.

Contains fulltext : 69066.pdf (publisher's version ) (Closed access)Smoking is a leading cause of preventable death, causing about 5 million premature deaths worldwide each year. Evidence for genetic influence on smoking behaviour and nicotine dependence (ND) has prompted a search for susceptibility genes. Furthermore, assessing the impact of sequence variants on smoking-related diseases is important to public health. Smoking is the major risk factor for lung cancer (LC) and is one of the main risk factors for peripheral arterial disease (PAD). Here we identify a common variant in the nicotinic acetylcholine receptor gene cluster on chromosome 15q24 with an effect on smoking quantity, ND and the risk of two smoking-related diseases in populations of European descent. The variant has an effect on the number of cigarettes smoked per day in our sample of smokers. The same variant was associated with ND in a previous genome-wide association study that used low-quantity smokers as controls, and with a similar approach we observe a highly significant association with ND. A comparison of cases of LC and PAD with population controls each showed that the variant confers risk of LC and PAD. The findings provide a case study of a gene-environment interaction, highlighting the role of nicotine addiction in the pathology of other serious diseases