An illustrated and updated checklist of the Indian Chrysididae is presented, including synonyms and distributional summaries. The list includes 105 species in 20 genera. Six species are described as new: Elampus gladiator Rosa, sp. nov. (Himachal Pradesh, Jammu Kashmir, and Uttar Pradesh), Chrysis aswathiae Rosa, sp. nov. (Tamil Nadu, elegans species group), Chrysis baldocki Rosa, sp. nov. (Tamil Nadu, smaragdula group), Chrysis bernasconii Rosa, sp. nov. (Tamil Nadu, subsinuata group), Chrysis polita Rosa, sp. nov. (West Bengal, Uttaranchal, Myanmar, ignita group), and Chrysis travancoriana Rosa, sp. nov. (Kerala and Tamil Nadu, praecipua group). Six species are newly recorded: Chrysis hecate Mocsáry, 1889; Chrysis jalala Nurse, 1902; Chrysis obscura Smith, 1860; Istiochrysis ziliolii Rosa Xu, 2016; Praestochrysis furcifera (Bingham, 1903); Primeuchroeus siamensis (Bischoff, 1910). Two new synonymies are proposed: Chrysis abuensis Nurse, 1902, syn. nov. of Chrysis wroughtoni du Buysson, 1896b; Chrysis nursei Bingham, 1903 syn. nov. of Chrysis gujaratica Nurse, 1903a. Holopyga (Hedychridium) virescens Mocsáry, 1914 is transferred to the genus Hedychridium Abeille de Perrin, 1878; the name Hedychridium virescens (Mocsáry, 1914) results a secondary homonym of Hedychridium virescens du Buysson, 1908 and it is here replaced with the new name Hedychridium mocsaryi Rosa, nom. nov. Chrysis cotesi du Buysson, 1893, sp. resurr. is here revalidated from the previous synonymy with Chrysis palliditarsis Spinola, 1838. Chrysis bahadur Nurse, 1903a is transferred from the ignita group to the splendidula group, Chrysis bhavanae Bingham, 1903 is transferred from the ignita group to the maculicornis group, and Chrysis thakur is transferred from the smaragdula group to the oculata group. Chrysis nila Bingham, 1903 and Chrysis variipes Mocsáry, 1911 are included in the newly established nila group. Spinolia kashmirae Kimsey in Kimsey Bohart, 1991 is classified as unnecessary replacement name. The name Parnopes oberthuri du Buysson, 1904 is here emendated into Parnopes oberthueri (currently Cephaloparnops oberthueri). Potential erroneous data, misidentifications and dubious distributional records that may exist in the literature are also identified. We examined almost all type specimens, excluding taxa described by Cameron and Smith. We provide a key to Indian genera, including those expected for the country and not yet recorded, and colour images of type and non-type specimens belonging to 82 species.
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http://dx.doi.org/10.11646/zootaxa.4929.1.1 | DOI Listing |
Heliyon
March 2024
Division of Pediatric Endocrinology, Department of Pediatrics, Medical School of Patras, University Hospital, Rio, Greece.
Background And Aims: Osteoprotegerin (OPG) is a tumor necrosis factor receptor superfamily member which increases in chronic inflammation and is associated with altered bone turnover and cardiovascular complications. In this study, we investigated whether OPG increases during acute inflammatory states induced by infections in children and correlated its levels with other biomarkers.
Materials And Methods: This is a prospective study that included 59 patients with documented bacterial infections, 20 with viral infections and 20 healthy controls.
J Diabetes Complications
January 2024
Department of Pediatrics, Division of Endocrinology, Medical School, University of Patras, Patras, Greece.
Aims: In this study we described the clinical and laboratory features of children presented with diabetic ketosis or diabetic ketoacidosis at diagnosis of type 1 diabetes (T1DM) and evaluated its course up to 2 years after initial diagnosis to investigate the progression rate of T1DM in both groups.
Methods: This was a prospective longitudinal cohort study that included 59 children and adolescents presented with either diabetic ketosis (DK) (n = 27) or diabetic ketoacidosis (DKA) (n = 32) at their first diagnosis with T1DM.
Results: Apart from the metabolic state of presentation at diagnosis, differences in the other basic clinical and laboratory features of both DK and DKA were not statistically significant (age, BMI, pre- diagnosis symptomatic period, HbA1c, multiplicity of autoantibodies positivity, fasting insulin, and total IgG levels), except from the C-peptide and IgA levels which were lower in DKA (p < 0.
Information is provided for 143 objectively invalid or unavailable genus-group names used in Chrysididae; 34 are objectively invalid, of which 18 are junior homonyms (five of these are also currently junior subjective synonyms), 18 are junior objective synonyms (two of these are also junior homonyms) of which seven are unjustified emendations, and two are unnecessary replacement names. The remaining 109 names are unavailable; 96 are incorrect subsequent spellings, most of them were originally lapsus calami or misprints, one is hereby deemed to be an incorrect original spelling, eight are nomina nuda, three were originally published as junior synonyms and never adopted before 1961 as valid names of any taxa, and one is a vernacular name previously considered as valid. Gender, type species, taxonomic history and status are given for each name except for incorrect subsequent spellings and unjustified emendations.
View Article and Find Full Text PDFiScience
June 2023
Department of Clinical Science, University of Bergen and Department of Medicine, Haukeland University Hospital, Bergen, Norway.
Autoimmune polyendocrine syndrome type 1 (APS-1) is an autosomal recessive disease characterized by severe and childhood onset organ-specific autoimmunity caused by mutations in the autoimmune regulator () gene. More recently, dominant-negative mutations within the PHD1, PHD2, and SAND domains have been associated with an incompletely penetrant milder phenotype with later onset familial clustering, often masquerading as organ-specific autoimmunity. Patients with immunodeficiencies or autoimmunity where genetic analyses revealed heterozygous mutations were included in the study and the dominant-negative effects of the mutations were functionally assessed .
View Article and Find Full Text PDFMetabolomics
October 2022
Department of Pharmacy, School of Health Sciences, University of Patras, 26504, Rio, Greece.
Introduction: Premature adrenarche (PA) for long time was considered a benign condition but later has been connected to various diseases in childhood and adulthood which remains controversial.
Objective: To investigate the effect of premature adrenarche on the metabolic phenotype, and correlate the clinical and biochemical data with the metabolic profile of children with PA.
Methods: Nuclear magnetic resonance (NMR)-based untargeted and targeted metabolomic approach in combination with multivariate and univariate statistical analysis applied to study the metabolic profiles of children with PA.
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