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{"references": ["A. M. Mathai, The concept of correlation and misinterpretations. International\nJournal of Mathematical and Statistical Sciences, 1998, 7: 157-167.", "R. A. Fisher, Distribution of the values of the correlation coefficient in\nsamples from an indefinitely large population. Biometrika, 1915, 10: 507-\n521.", "A. Winterbottom, A note on the derivation of Fisher-s transformation of\nthe correlation coefficient. The American Statistician, 1979, 33: 142-143.", "H. Hotelling, New light on the correlation coefficient and its transforms.\nJournal of Royal Statistical Society, Ser. B., 1953, 15: 193-232.", "A. K. Gayen, The frequency distribution of the product-moment correlation\ncoefficient in random samples of any size drawn from non-normal\nuniverses. Biometrika, 1951, 38: 219-247.", "D. L. Hawkins, Using U statistics to derive the asymptotic distribution\nof Fisher-s Z statistic. The American Statistician, 1989, 43: 235-237.", "S. Konishi, An approximation to the distribution of the sample correlation\ncoefficient. Biometrika, 1978, 65: 654-656.", "H.-T. Ha and S. B. Provost, A viable alternative to resorting to statistical\ntables. Communications in Statistics-Simulation and Computation, 2007,\n36: 1135-1151."]} Given a bivariate normal sample of correlated variables, (Xi, Yi), i = 1, . . . , n, an alternative estimator of Pearson's correlation coefficient is obtained in terms of the ranges, |Xi − Yi|. An approximate confidence interval for ρX,Y is then derived, and a simulation study reveals that the resulting coverage probabilities are in close agreement with the set confidence levels. As well, a new approximant is provided for the density function of R, the sample correlation coefficient. A mixture involving the proposed approximate density of R, denoted by hR(r), and a density function determined from a known approximation due to R. A. Fisher is shown to accurately approximate the distribution of R. Finally, nearly exact density approximants are obtained on adjusting hR(r) by a 7th degree polynomial.

The former genera Oncocnemis Lederer, Apharetra Grote, Hemistilbia Barnes and Benjamin, Adita Grote, Lepipolys Guenée, Homoncocnemis Hampson, and Homohadena Grote are synonymized under Sympistis Hübner. The following are transferred from Oxycnemis Grote to Sympistis: Sympistis franclemonti (Blanchard), comb. n. [Oxycnemis franclemonti Blanchard] and Sympistis subsimplex (Dyar) comb. n. [Oxycnemis subsimplex Dyar]. Two species are transferred to Unciella gen. n. as Unciella primula (Barnes and McDunnough) comb. n. [Oncocnemis primula Barnes and McDunnough] and Unciella flagrantis (Smith) comb. n. [Oncocnemis flagrantis Smith], which along with Leucocnemis Hampson are transferred to tribe Triocnemidini in the Psaphidinae. Supralathosea Barnes and Benjamin is transferred to Psaphidinae: Psaphidini and Catabena pronuba Barnes and McDunnough is transferred to Supralathosea comb. n.. In addition, Cerapoda Smith syn. n. and Prochloridea Barnes and McDunnough syn. n. (Prochloridea is presently in Hodges “unassociated genera”) are synonymized under Rhizagrotis Smith in the Xyleninae. Copanarta sexpunctata Barnes and McDunnough rev. comb. is transferred from Stylopoda to Copanarta. Oncocnemis simplicia Smith syn. n. is synonymized under Homohadena deserta Smith, Oncocnemis mus Troubridge and Crabo syn. n. under Oncocnemis tenuifascia Smith, and Oncocnemis sala Mustelin syn. n. under Oncocnemis aqualis Grote. The following are elevated to species rank: Sympistis deserticola (McDunnough) stat. n., comb. n. [Oncocnemis riparia deserticola McDunnough], Sympistis pallidior (Barnes) stat. n., comb. n. [Oncocnemis figurata pallidior Barnes] and Sympistis pallida (Barnes) stat. n., comb. n. [Oncocnemis homogena pallida Barnes]. The following 50 species are described as new: Sympistis acheron Troubridge, Sympistis amenthes Troubridge, Sympistis amun Troubridge, Sympistis anubis Troubridge, Sympistis anweileri Troubridge and Lafontaine, Sympistis apep Troubridge, Sympistis apis Troubridge, Sympistis babi Troubridge, Sympistis baloghi Troubridge, Sympistis bes Troubridge, Sympistis buchis Troubridge, Sympistis buto Troubridge, Sympistis cherti Troubridge, Sympistis chons Troubridge, Sympistis cleopatra Troubridge, Sympistis cocytus Troubridge, Sympistis collaris Troubridge, Sympistis dischorda Troubridge, Sympistis disfigurata Troubridge, Sympistis doris Dimock and Troubridge, Sympistis hapi Troubridge, Sympistis hathor Troubridge, Sympistis horus Troubridge, Sympistis incubus Troubridge, Sympistis insanina Troubridge, Sympistis isis Troubridge, Sympistis jenniferae Troubridge, Sympistis jocelynae Troubridge, Sympistis khem Troubridge, Sympistis khepri Troubridge, Sympistis knudsoni Troubridge, Sympistis lachrymosa Troubridge, Sympistis min Troubridge, Sympistis mut Troubridge, Sympistis nenun Troubridge, Sympistis opleri Troubridge, Sympistis osiris Troubridge, Sympistis pachet Troubridge, Sympistis ptah Troubridge, Sympistis ra Troubridge, Sympistis richersi Troubridge, Sympistis sakhmet Troubridge, Sympistis septu Troubridge, Sympistis sesmu Troubridge, Sympistis seth Troubridge, Sympistis shait Troubridge, Sympistis shirleyae Troubridge, Sympistis sobek Troubridge, Sympistis sokar Troubridge, and Sympistis serapis Troubridge. Color illustrations are provided for adults of all nearctic Sympistis species. Alphabetical and phylogenetic checklists of North American Oncocnemidinae are also provided, including species formerly placed there, but here transferred to other subfamilies.

We present in this paper a useful strategy to solve stochastic partial differential equations (SPDEs) involving stochastic coefficients. Using the Wick-product of higher order and the Wiener-Itˆo chaos expansion, the SPDEs is reformulated as a large system of deterministic partial differential equations. To reduce the computational complexity of this system, we shall use a decomposition-coordination method. To obtain the chaos coefficients in the corresponding deterministic equations, we use a least square formulation. Once this approximation is performed, the statistics of the numerical solution can be easily evaluated.

This deliverable describes the organisation, results and validation phase of the second Gender STI Co-Design Lab (hereafter the Lab) involving participants from America and Europe. The Co-design Lab that took place between October and November 2022 addressed the Gender STI objectives to integrate the gender perspective in bilateral and multilateral agreements between the EU Member States (MS), Associated Countries (AC) and third countries through design thinking methods and participatory techniques. The document describes the methods, participatory steps and tools that have been applied in the Lab to co-design shared solutions and prototypes for common challenges regarding gender inequalities in STI and to support the emergence of an international community of practitioners with similar challenging objectives. More specifically, the deliverable collects in detail “what” was done and how it was done in the Lab, reflects on the “so what” question, as to the sense and purpose of the challenge-based prototypes and their initial outputs, and finally draws some conclusions with a “now what” reflection on what was learnt and suggests possible priorities for future actions.

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This study investigated, in on-reserve First Nations (FN) youth in Ontario, Canada, the following: (a) the intakes of vegetable and fruit, “other” foods and relevant nutrients as compared to current recommendations and national averages, (b) current prevalence rates of overweight and obesity and (c) the relationship between latitude and dietary intakes. Twenty-four-hour diet recalls were collected via the Waterloo Web-Based Eating Behaviour Questionnaire (WEB-Q) (n = 443). Heights and weights of participants were self reported using measured values and Body Mass Index was categorized using the International Obesity Task Force cutoffs. Food group and nutrient intakes were compared to current standards, Southern Ontario Food Behaviour data and the Canadian Community Health Survey, Cycle 2.2, using descriptive statistics. Mean vegetable and fruit, fibre and folate intakes were less than current recommendations. Girls aged 14–18 years had mean intakes of vitamin A below current recommendations for this sub-group; for all sub-groups, mean intakes of vegetables and fruit were below Canadian averages. All sub-groups also had intakes of all nutrients and food groups investigated that were less than those observed in non-FN youth from Southern Ontario, with the exception of “other” foods in boys 12–18 years. Prevalence rates of overweight and obesity were 31.8% and 19.6%, respectively, exceeding rates in the general population. Dietary intakes did not vary consistently by latitude (n = 248), as revealed by ANOVA. This study provided a unique investigation of the dietary intakes of on-reserve FN youth in Ontario and revealed poor intakes of vegetables and fruit and related nutrients and high intakes of “other” foods. Prevalence rates of overweight and obesity exceed those of the general population.

The Mental Health Commission of Canada’s (MHCC) strategy calls for promoting the health and wellbeing of all Canadians and to improve mental health outcomes. Each year, one in every five Canadians experiences one or more mental health problems, creating a significant cost to the health system. Mental health is pivotal to holistic health and wellbeing. This paper presents the key findings of a comprehensive literature review of Canadian research on the relationship between settlement experiences and the mental health and well-being of immigrants and refugees. A scoping review was conducted following a framework provided by Arskey and O’Malley (Int J Soc Res Methodol 8:19–32, 2005). Over two decades of relevant literature on immigrants’ health in Canada was searched. These included English language peer-reviewed publications from relevant online databases Medline, Embase, PsycInfo, Healthstar, ERIC and CINAHL between 1990 and 2015. The findings revealed three important ways in which settlement affects the mental health of immigrants and refugees: through acculturation related stressors, economic uncertainty and ethnic discrimination. The recommendations for public health practice and policy are discussed.

The Neotropical species of the rarely collected genus Bolitogyrus (Coleoptera: Staphylinidae: Staphylininae: Staphylinini) are revised. The genus exhibits an uncommon, disjunct distribution between the Neotropical and Oriental Regions and is of unknown phylogenetic position within Staphylinini. Morphological evolution remarkable for Staphylinini was discovered within Bolitogyrus, including sexually dimorphic modifications of the pronotum that may be involved in male competition for females. rSEM interactive animations were used to establish morphological species boundaries between two highly variable species and are provided to illustrate diagnostic characters of the genitalia in unconventional views. The genus is redescribed based on the world fauna and twenty-eight Neotropical species are considered valid. Of these, nineteen are described as new to science: Bolitogyrus ashei sp. n.; B. apicofasciatus sp. n.; B. brevistellus sp. n.; B. bufo sp. n.; B. cheungi sp. n.; B. cornutus sp. n.; B. divisus sp. n.; B. falini sp. n.; B. gracilis sp. n.; B. inexspectatus sp. n.; B. longistellus sp. n.; B. marquezi sp. n.; B. newtoni sp. n.; B. pseudotortifolius sp. n.; B. pulchrus sp. n.; B. silex sp. n.; B. thomasi sp. n.; B. tortifolius sp. n.; and B. viridescens sp. n. Bolitogyrus sallei (Kraatz), stat. r. is removed from synonymy with B. buphthalmus (Erichson) and the following new synonyms are proposed: Cyrtothorax cyanescens Sharp, 1884, syn. n. = Quedius buphthalmus Erichson, 1840; C. nevermanni Scheerpeltz, 1974, syn. n. = C. costaricensis Wendeler, 1927. A summary of all available bionomic and distributional data, as well as an illustrated identification key to and diagnoses of all Neotropical species are provided.

Background: We wished to compare the nuisance parameters of pediatric vs. adult randomized-trials (RCTs) and determine if the latter can be used in sample size computations of the former.Methods: In this meta-epidemiologic empirical evaluation we examined meta-analyses from the Cochrane Database of Systematic-Reviews, with at least one pediatric-RCT and at least one adult-RCT. Within each meta-analysis of binary efficacy-outcomes, we calculated the pooled-control-group event-rate (CER) across separately all pediatric and adult-trials, using random-effect models and subsequently calculated the control-group event-rate risk-ratio (CER-RR) of the pooled-pediatric-CERs vs. adult-CERs. Within each meta-analysis with continuous outcomes we calculated the pooled-control-group effect standard deviation (CE-SD) across separately all pediatric and adult-trials and subsequently calculated the CE-SD-ratio of the pooled-pediatric-CE-SDs vs. adult-CE-SDs. We then calculated across all meta-analyses the pooled-CER-RRs and pooled-CE-SD-ratios (primary endpoints) and the pooled-magnitude of effect-sizes of CER-RRs and CE-SD-ratios using REMs. A ratio < 1 indicates that pediatric trials have smaller nuisance parameters than adult trials.Results: We analyzed 208 meta-analyses (135 for binary-outcomes, 73 for continuous-outcomes). For binary outcomes, pediatric-RCTs had on average 10% smaller CERs than adult-RCTs (summary-CE-RR: 0.90; 95% CI: 0.83, 0.98). For mortality outcomes the summary-CE-RR was 0.48 (95% CIs: 0.31, 0.74). For continuous outcomes, pediatric-RCTs had on average 26% smaller CE-SDs than adult-RCTs (summary-CE-SD-ratio: 0.74).Conclusions: Clinically relevant differences in nuisance parameters between pediatric and adult trials were detected. These differences have implications for design of future studies. Extrapolation of nuisance parameters for sample-sizes calculations from adult-trials to pediatric-trials should be cautiously done.

The Micropezidae of Madagascar are reviewed, and the endemic genus Paramimegralla Hennig is revised. Twenty species are recognized including two Hybobata species and 18 Paramimegralla species, of which 12 are described as new (P. luteoscapus , brunnea , zinzala, zarpa, verticalis, taeniola, sulcata, campanula, anchivitta, quadrifasciata and longicephala ). Stiltissima Barraclough is synonymized with Paramimegralla Hennig and previous records of Rainieria Rondani from the island are shown to be incorrect. Paramimegralla steineri (Barraclough) and Paramimegralla volcanica (Barraclough) are given as new combinations, Paramimegralla stuckenbergi Barraclough is synonymized with P. nigra Barraclough, and Hybobata Enderlein is resurrected from synonymy with Mimegralla Rondani. All known Malagasy micropezid species are keyed and illustrated and all Paramimegralla species are described or redescribed.