441 research outputs found

    The relationship between species detection probability and local extinction probability.

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    In community-level ecological studies, generally not all species present in sampled areas are detected. Many authors have proposed the use of estimation methods that allow detection probabilities that are <1 and that are heterogeneous among species. These methods can also be used to estimate community-dynamic parameters such as species local extinction probability and turnover rates (Nichols et al. Ecol Appl 8:1213–1225; Conserv Biol 12:1390–1398). Here, we present an ad hoc approach to estimating community-level vital rates in the presence of joint heterogeneity of detection probabilities and vital rates. The method consists of partitioning the number of species into two groups using the detection frequencies and then estimating vital rates (e.g., local extinction probabilities) for each group. Estimators from each group are combined in a weighted estimator of vital rates that accounts for the effect of heterogeneity. Using data from the North American Breeding Bird Survey, we computed such estimates and tested the hypothesis that detection probabilities and local extinction probabilities were negatively related. Our analyses support the hypothesis that species detection probability covaries negatively with local probability of extinction and turnover rates. A simulation study was conducted to assess the performance of vital parameter estimators as well as other estimators relevant to questions about heterogeneity, such as coefficient of variation of detection probabilities and proportion of species in each group. Both the weighted estimator suggested in this paper and the original unweighted estimator for local extinction probability performed fairly well and provided no basis for preferring one to the other

    Extended chiral algebras and the emergence of SU(2) quantum numbers in the Coulomb gas

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    We study a set of chiral symmetries contained in degenerate operators beyond the `minimal' sector of the c(p,q) models. For the operators h_{(2j+2)q-1,1}=h_{1,(2j+2)p-1} at conformal weight [ (j+1)p-1 ][ (j+1)q -1 ], for every 2j \in N, we find 2j+1 chiral operators which have quantum numbers of a spin j representation of SU(2). We give a free-field construction of these operators which makes this structure explicit and allows their OPEs to be calculated directly without any use of screening charges. The first non-trivial chiral field in this series, at j=1/2, is a fermionic or para-fermionic doublet. The three chiral bosonic fields, at j=1, generate a closed W-algebra and we calculate the vacuum character of these triplet models.Comment: 23 pages Late

    Extended multiplet structure in Logarithmic Conformal Field Theories

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    We use the process of quantum hamiltonian reduction of SU(2)_k, at rational level k, to study explicitly the correlators of the h_{1,s} fields in the c_{p,q} models. We find from direct calculation of the correlators that we have the possibility of extra, chiral and non-chiral, multiplet structure in the h_{1,s} operators beyond the `minimal' sector. At the level of the vacuum null vector h_{1,2p-1}=(p-1)(q-1) we find that there can be two extra non-chiral fermionic fields. The extra indicial structure present here permeates throughout the entire theory. In particular we find we have a chiral triplet of fields at h_{1,4p-1}=(2p-1)(2q-1). We conjecture that this triplet algebra may produce a rational extended c_{p,q} model. We also find a doublet of fields at h_{1,3p-1}=(\f{3p}{2}-1)(\f{3q}{2}-1). These are chiral fermionic operators if p and q are not both odd and otherwise parafermionic.Comment: 24 pages LATEX. Minor corrections and extra reference

    Extended chiral algebras in the SU(2)_0 WZNW model

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    We investigate the W-algebras generated by the integer dimension chiral primary operators of the SU(2)_0 WZNW model. These have a form almost identical to that found in the c=-2 model but have, in addition, an extended Kac-Moody structure. Moreover on Hamiltonian reduction these SU(2)_0 W-algebras exactly reduce to those found in c=-2. We explicitly find the free field representations for the chiral j=2 and j=3 operators which have respectively a fermionic doublet and bosonic triplet nature. The correlation functions of these operators accounts for the rational solutions of the Knizhnik-Zamolodchikov equation that we find. We explicitly compute the full algebra of the j=2 operators and find that the associativity of the algebra is only guaranteed if certain null vectors decouple from the theory. We conjecture that these algebras may produce a quasi-rational conformal field theory.Comment: 18 pages LATEX. Minor corrections. Full j=2 algebra adde

    Two-Point Functions and Boundary States in Boundary Logarithmic Conformal Field Theories

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    Our main aim in this thesis is to address the results and prospects of boundary logarithmic conformal field theories: theories with boundaries that contain the above Jordan cell structure. We have investigated c_{p,q} boundary theory in search of logarithmic theories and have found logarithmic solutions of two-point functions in the context of the Coulomb gas picture. Other two-point functions have also been studied in the free boson construction of BCFT with SU(2)_k symmetry. In addition, we have analyzed and obtained the boundary Ishibashi state for a rank-2 Jordan cell structure [hep-th/0103064]. We have also examined the (generalised) Ishibashi state construction and the symplectic fermion construction at c=-2 for boundary states in the context of the c=-2 triplet model. The differences between two constructions are interpreted, resolved and extended beyond each case.Comment: Ph.D. Thesis (University of Oxford), 96 pages, the layout is modified from the origina

    Dietary inflammatory potential, oxidative balance score, and risk of breast cancer: Findings from the Sister Study

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    Diet, inflammation, and oxidative stress may be important in breast carcinogenesis, but evidence on the role of the inflammatory and prooxidative potential of dietary patterns is limited. Energy adjusted-Dietary Inflammatory Index (E-DII™) and dietary oxidative balance score (D-OBS) were calculated for 43 563 Sister Study cohort participants who completed a Block 1998 food frequency questionnaire at enrollment in 2003–2009 and satisfied eligibility criteria. D-OBS was validated using measured F2-isoprostanes and metabolites. High E-DII score and low D-OBS represent a more proinflammatory and prooxidant diet, respectively, and associations of quartiles of each index with breast cancer (BC) risk were estimated using multivariable Cox proportional hazards regression. There were 2619 BCs diagnosed at least 1 year after enrollment (mean follow-up 8.4 years). There was no overall association between E-DII and BC risk, whereas there was a suggestive inverse association for the highest vs lowest quartile of D-OBS (HR 0.92 [95% CI, 0.81-1.03]). The highest quartile of E-DII was associated with risk of triple-negative BC (HR 1.53 [95% CI, 0.99-2.35]). When the two indices were combined, a proinflammatory/prooxidant diet (highest tertile of E-DII and lowest tertile of D-OBS) was associated with increased risk for all BC (HR 1.13 [95% CI, 1.00-1.27]) and for triple-negative BC (1.72 [95% CI, 1.10-2.70]), compared to an antiinflammatory/antioxidant diet (lowest tertile of E-DII and highest tertile of D-OBS). Diets with increased inflammatory potential and reduced oxidative balance were positively associated with overall and triple-negative BC

    Gestational diabetes and risk of breast cancer before age 55 years

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    Background: The history of gestational diabetes mellitus (GDM) has been associated with breast cancer risk in some studies, particularly in young women, but results of cohort studies are conflicting. Methods: We pooled data from 257 290 young (age <55 years) women from five cohorts. We used multivariable Cox proportional-hazards regression to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for the association between GDM history and risk of breast cancer, overall and by oestrogen receptor (ER) status, before age 55 years, adjusted for established breast cancer risk factors. Results: Five percent of women reported a history of GDM and 6842 women reported an incident breast-cancer diagnosis (median follow-up = 16 years; maximum = 24 years). Compared with parous women without GDM, women with a history of GDM were not at increased risk of young-onset breast cancer overall (HR = 0.90; 95% CI: 0.78, 1.03) or by ER status (HR = 0.96; 95% CI: 0.79, 1.16 for ER-positive; HR = 1.07; 95% CI: 0.78, 1.47 for ER-negative). Compared with nulliparous women, parous women with a history of GDM had a lower risk of breast cancer overall (HR = 0.79; 95% CI: 0.68, 0.91) and of ER-positive (HR = 0.82; 95% CI: 0.66, 1.02) but not ER-negative (HR = 1.09; 95% CI: 0.76, 1.54) invasive breast cancer. These results were consistent with the HRs comparing parous women without GDM to nulliparous women. Conclusions: Results of this analysis do not support the hypothesis that GDM is a risk factor for breast cancer in young women. Our findings suggest that the well-established protective effect of parity on risk of ER-positive breast cancer persists even for pregnancies complicated by GDM

    Genetic variants in anti-MĂĽllerian hormone-related genes and breast cancer risk: results from the AMBER consortium

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    Purpose: Circulating anti-Müllerian hormone (AMH) levels are positively associated with time to menopause and breast cancer risk. We examined breast cancer associations with single nucleotide polymorphisms (SNPs) in the AMH gene or its receptor genes, ACVR1 and AMHR2, among African American women. Methods: In the AMBER consortium, we tested 65 candidate SNPs, and 1130 total variants, in or near AMH, ACVR1, and AMHR2 and breast cancer risk. Overall, 3649 cases and 4230 controls contributed to analyses. Odds ratios (OR) and 95% confidence intervals (CI) for breast cancer were calculated using multivariable logistic regression. Results: After correction for multiple comparisons (false-discovery rate of 5%), there were no statistically significant associations with breast cancer risk. Without correction for multiple testing, four candidate SNPs in ACVR1 and one near AMH were associated with breast cancer risk. In ACVR1, rs13395576[C] was associated with lower breast cancer risk overall (OR 0.84; 95% CI 0.72, 0.97) and for ER+ disease (OR 0.75; CI 0.62, 0.89) (p < 0.05). Rs1220110[A] and rs1220134[T] each had ORs of 0.89–0.90 for postmenopausal and ER+ breast cancer (p ≤ 0.03). Conversely, rs1682130[T] was associated with higher risk of ER+ breast cancer (OR 1.17; 95% CI 1.04, 1.32). Near AMH, rs6510652[T] had ORs of 0.85–0.90 for breast cancer overall and after menopause (p ≤ 0.02). Conclusions: The present results, from a large study of African American women, provide limited support for an association between AMH-related polymorphisms and breast cancer risk and require replication in other studies
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