30 research outputs found
On Kentrodoris and Jorunna (Gastropoda Opisthobranchia)
As 15 espĂ©cies anteriormente descritas como Kentrodoris ou Jorunna sĂŁo revistas. O resultado Ă© que 6 espĂ©cies sĂŁo vĂĄlidas, 3 jĂĄ tinham sido removidas para outros gĂȘneros, uma Ă© sinĂŽnimo, e 5 nĂŁo podem com certeza ser colocadas no presente grupo. Por outro lado, descriçÔes pormenorizadas de 3 materiais, identificados com outras espĂ©cies, revelam tratar-se de 3 espĂ©cies novas, Jorunna alisonae, J. malcolmi e /. zania. AlĂ©m disso, 2 espĂ©cies novas sĂŁo descritas, J. luisae e J. lemchei. Awuka spazzola revelou-se como Jorunna. A distinção entre Kentrodoris e Jorunna no Tratado de GrassĂ© (Odhner, 1968: 871) baseia-se ainda nas diagnoses de Bergh (1876). Bergh tinha, nas suas espĂ©cies, confundido a papila penial inerme e o estilete da glĂąndula vestibular, e descrito o gĂȘnero Kentrodoris com estilete penial e glĂąndula vestibular inerme. Em Doris johnstoni (= tomentosa) Alder Hancock (1845) haviam acertadamente reconhecido a papila penial inerme e o estilete da glĂąndula vestibular. Para esta espĂ©cie Bergh criou o gĂȘnero Jorunna (1876). O meu estudo de 9 espĂ©cies, como tambĂ©m boas descriçÔes de 2 espĂ©cies ulteriores, mostram que todas as 10 espĂ©cies suficientemente conhecidas tĂȘm estilete na glĂąndula vestibular e a papila penial inerme. A Ășnica espĂ©cie com duto masculino cuticularizado Ă© Kendrodoris rubescens. Todas as outras espĂ©cies pertencem a Jorunna
On some Opisthobranchs from Cananéia, Brazil
Dez espĂ©cies de CananĂ©ia e uma de Ubatuba foram colecionadas. Duas das espĂ©cies sĂŁo novas para a ciĂȘncia: Coryphella verta e Catriona oba. Elysia serca Ă© comparada com E. clena Marcus (1970, p. 49). Os gĂȘneros Cuthona, Trinchesia, e Catriona sĂŁo discutidos
Gastropods
82 p. : ill. ; 24 cm.Includes bibliographical references (p. 69-82)
Slugs from Brazil
21 p. : ill. ; 24 cm.Includes bibliographical references (p. 17-21)
Gastropods
33 p. : ill. ; 24 cm.Includes bibliographical references (p. 29-33)
Author Correction: A consensus-based transparency checklist.
An amendment to this paper has been published and can be accessed via a link at the top of the paper
A consensus-based transparency checklist
We present a consensus-based checklist to improve and document the transparency of research reports in social and behavioural research. An accompanying online application allows users to complete the form and generate a report that they can submit with their manuscript or post to a public repository
Subcortical volumes across the lifespan: Data from 18,605 healthy individuals aged 3â90 years
Age has a major effect on brain volume. However, the normative studies available are constrained by small sample sizes, restricted age coverage and significant methodological variability. These limitations introduce inconsistencies and may obscure or distort the lifespan trajectories of brain morphometry. In response, we capitalized on the resources of the Enhancing Neuroimaging Genetics through MetaâAnalysis (ENIGMA) Consortium to examine ageârelated trajectories inferred from crossâsectional measures of the ventricles, the basal ganglia (caudate, putamen, pallidum, and nucleus accumbens), the thalamus, hippocampus and amygdala using magnetic resonance imaging data obtained from 18,605 individuals aged 3â90âyears. All subcortical structure volumes were at their maximum value early in life. The volume of the basal ganglia showed a monotonic negative association with age thereafter; there was no significant association between age and the volumes of the thalamus, amygdala and the hippocampus (with some degree of decline in thalamus) until the sixth decade of life after which they also showed a steep negative association with age. The lateral ventricles showed continuous enlargement throughout the lifespan. Age was positively associated with interâindividual variability in the hippocampus and amygdala and the lateral ventricles. These results were robust to potential confounders and could be used to examine the functional significance of deviations from typical ageârelated morphometric patterns
Cortical thickness across the lifespan: Data from 17,075 healthy individuals aged 3-90 years
Delineating the association of age and cortical thickness in healthy individuals is critical given the association of cortical thickness with cognition and behavior. Previous research has shown that robust estimates of the association between age and brain morphometry require largeâscale studies. In response, we used crossâsectional data from 17,075 individuals aged 3â90âyears from the Enhancing Neuroimaging Genetics through MetaâAnalysis (ENIGMA) Consortium to infer ageârelated changes in cortical thickness. We used fractional polynomial (FP) regression to quantify the association between age and cortical thickness, and we computed normalized growth centiles using the parametric Lambda, Mu, and Sigma method. Interindividual variability was estimated using metaâanalysis and oneâway analysis of variance. For most regions, their highest cortical thickness value was observed in childhood. Age and cortical thickness showed a negative association; the slope was steeper up to the third decade of life and more gradual thereafter; notable exceptions to this general pattern were entorhinal, temporopolar, and anterior cingulate cortices. Interindividual variability was largest in temporal and frontal regions across the lifespan. Age and its FP combinations explained up to 59% variance in cortical thickness. These results may form the basis of further investigation on normative deviation in cortical thickness and its significance for behavioral and cognitive outcomes