This catalogue includes all valid family-group (six subtribes), genus-group (55 genera, 33 subgenera), and species-group names (1009 species and subspecies) of Sepidiini darkling beetles (Coleoptera: Tenebrionidae: Pimeliinae), and their available synonyms. For each name, the author, year, and page number of the description are provided, with additional information (e.g., type species for genus-group names, author of synonymies for invalid taxa, notes) depending on the taxon rank. Verified distributional records (loci typici and data acquired from revisionary publications) for all the species are gathered. Distribution of the subtribes is illustrated and discussed. Several new nomenclatural acts are included. The generic names Koch, 1958 [= Fåhraeus, 1870] and Koch, 1955 [= Kirby, 1819] are new synonyms (valid names in square brackets). The following new combinations are proposed: (Ancey, 1883), (Koch, 1952), (Koch, 1952), (Koch, 1953), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Guérin-Méneville, 1844), (Koch, 1952), (Haag-Rutenberg, 1875), (Haag-Rutenberg, 1871), (Haag-Rutenberg, 1875), (Koch, 1952), (Koch, 1952), (Gerstaecker, 1854), (Fairmaire, 1888), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Péringuey, 1899), (Haag-Rutenberg, 1871), (Koch, 1952), (Koch, 1952), (Haag-Rutenberg, 1871), (Péringuey, 1899), (Gebien, 1910), (Péringuey, 1899), (Koch, 1952), (Koch, 1952), (Haag-Rutenberg, 1871), (Koch, 1952), (Koch, 1952), (Haag-Rutenberg, 1875), (Koch, 1952), (Haag-Rutenberg, 1875), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Haag-Rutenberg, 1871), (Koch, 1952), (Péringuey, 1908), (Haag-Rutenberg, 1879), (Haag-Rutenberg, 1871), (Koch, 1952), (Haag-Rutenberg, 1871), (Koch, 1960), (Haag-Rutenberg, 1871), (Koch, 1954), (Koch 1954), (Koch, 1952), (Koch, 1952), (Haag-Rutenberg, 1871), (Haag-Rutenberg, 1871), (Koch, 1952), (Koch, 1952), (Péringuey, 1899), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Haag-Rutenberg, 1871), (Péringuey, 1899), (Koch, 1952), (Koch, 1952), (Olivier, 1795), (Koch, 1953), (Peringey, 1899), (Haag-Rutenberg, 1871), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Péringuey, 1899), (Péringuey, 1908), (Koch, 1952), (Fairmaire, 1888), (Haag-Rutenberg, 1871), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Haag-Rutenberg, 1871), (Thunberg, 1787), (Koch, 1952), (Koch, 1952), (Solier, 1843), (Billberg, 1815), (Koch, 1952), (Haag-Rutenberg, 1871), (Koch, 1952), (Péringuey, 1892), (Koch, 1952), (Fairmaire, 1888), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Péringuey, 1899), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Harold, 1878), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Harold, 1878), (Koch, 1952), (Gerstaecker, 1854), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Haag-Rutenberg, 1871), (Koch, 1952), (Péringuey, 1899), (Gebien, 1910), (Koch, 1952), (Péringuey, 1899), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Koch, 1952), (Haag-Rutenberg, 1871), (Erichson, 1843), (Haag-Rutenberg, 1871), (Koch, 1952), (Haag-Rutenberg, 1879), (Haag-Rutenberg, 1871), (Koch, 1952), (Péringuey, 1899), (Péringuey, 1899), (Péringuey, 1899), (Koch, 1952), (Péringuey, 1899), (Koch, 1952), (Koch, 1953), (Haag-Rutenberg, 1875), (Gridelli, 1939), and (Pierre, 1979). The type species [placed in square brackets] of the following genus-group taxa are designated for the first time, Fåhraeus, 1870 [ Fåhraeus, 1870], Péringuey, 1899 [ Péringuey, 1899], and Péringuey, 1899 [ Haag-Rutenberg, 1871]. A lectotype is designated for Koch, 1955 in order to fix its taxonomic status. Kamiński is introduced here as a replacement name for Marwick, 1935 [ Smith, 1817] (Mollusca: Pteriidae) to avoid homonymy with Solier, 1843 (Coleoptera: Tenebrionidae).

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527536PMC
http://dx.doi.org/10.3897/zookeys.844.34241DOI Listing

Publication Analysis

Top Keywords

koch 1952
316
1952 koch
184
koch
88
0
79
haag-rutenberg 1871
76
péringuey 1899
60
1952 haag-rutenberg
56
1871 koch
52
1952 péringuey
40
1899 koch
28

Similar Publications

Objective: Neutrophils play an important role in regulating immune and inflammatory responses in patients with rheumatoid arthritis (RA). We assessed whether baricitinib, a JAK1/JAK2 inhibitor, could reduce neutrophil activation and whether a neutrophil activation score could predict treatment response.

Methods: Markers of neutrophil activation, calprotectin, and neutrophil extracellular traps (NETs) were analyzed using enzyme-linked immunosorbent assay in plasma from patients with RA (n = 271) and healthy controls (n = 39).

View Article and Find Full Text PDF
Article Synopsis
  • The study investigates the pharmacokinetics of oral clavulanic acid in neonates and infants, as existing data on this topic is limited.
  • It analyzes combined data from four datasets using a one-compartment model to determine dosing regimens and exposure levels based on age and body weight.
  • Findings indicate that an amoxicillin/clavulanic acid ratio of 4:1 is optimal, with significant differences in exposure levels based on varying threshold concentrations, laying groundwork for future research.
View Article and Find Full Text PDF

Chikungunya virus is an Alphavirus, it belongs to the family Togaviridae and is transmitted by mosquitoes. It was first described during an outbreak in Southern Tanzania in 1952. It generally causes a febrile syndrome, accompanied by joint pain and arthritis, which is often debilitating and may persist for months or years.

View Article and Find Full Text PDF

Background: There is a lack of evidence on oral amoxicillin pharmacokinetics and exposure in neonates with possible serious bacterial infection (pSBI). We aimed to describe amoxicillin disposition following oral and intravenous administration and to provide dosing recommendations for preterm and term neonates treated for pSBI.

Methods: In this pooled-population pharmacokinetic study, 3 datasets were combined for nonlinear mixed-effects modeling.

View Article and Find Full Text PDF

Pathogenetic mechanisms and therapeutic approaches of acute-to-chronic liver failure.

Am J Physiol Cell Physiol

July 2023

Department of Internal Medicine B, Faculty of Medicine, University of Münster, Münster, Germany.

Liver cirrhosis is the end stage of all chronic liver diseases and contributes significantly to overall mortality of 2% globally. The age-standardized mortality from liver cirrhosis in Europe is between 10 and 20% and can be explained by not only the development of liver cancer but also the acute deterioration in the patient's overall condition. The development of complications including accumulation of fluid in the abdomen (ascites), bleeding in the gastrointestinal tract (variceal bleeding), bacterial infections, or a decrease in brain function (hepatic encephalopathy) define an acute decompensation that requires therapy and often leads to acute-on-chronic liver failure (ACLF) by different precipitating events.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!