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Using a data set corresponding to an integrated luminosity of 6.32 fb−1 recorded by the BESIII detector at center-of-mass energies between 4.178 and 4.226 GeV, an amplitude analysis of the decay D+s → π+π0π0 is performed, and the relative fractions and phases of different intermediate processes are determined. The absolute branching fraction of the decay D+s → π+π0π0 is measured to be (0.50 ± 0.04stat ± 0.02syst)%. Theabsolute branching fraction of the intermediate process D+s → f0(980)π+, f0(980) → π0π0 is determined to be (0.28 ± 0.04stat ± 0.04syst)%.
We report an amplitude analysis and branching fraction measurement of 𝐷+
𝑠→𝐾+𝐾−𝜋+ decay using a data sample of 3.19 fb−1 recorded with BESIII detector at a center-of-mass energy of 4.178 GeV. We perform a model-independent partial wave analysis in the low 𝐾+𝐾− mass region to determine the 𝐾+𝐾− S-wave line shape, followed by an amplitude analysis of our very pure high-statistics sample. With the detection efficiency based on the amplitude analysis results, the absolute branching fraction is measured to be ℬ(𝐷+𝑠→𝐾+𝐾−𝜋+)=(5.47±0.08stat±0.13sys)%.
We report an amplitude analysis and branching fraction measurement of D+s→K+K−π+ decay using a data sample of 3.19 fb−1 recorded with BESIII detector at a center-of-mass energy of 4.178 GeV.
We perform a model-independent partial wave analysis in the low K+K− mass region to determine the K+K− S-wave lineshape,
followed by an amplitude analysis of our very pure high-statistics sample.
The amplitude analysis provides an accurate determination of the detection efficiency allowing us to measure the branching fraction B(D+s→K+K−π+)=(5.47±0.08stat±0.13sys)%.
We report an amplitude analysis and branching fraction measurement of D+s→K+K−π+ decay using a data sample of 3.19 fb−1 recorded with BESIII detector at a center-of-mass energy of 4.178 GeV.
We perform a model-independent partial wave analysis in the low K+K− mass region to determine the K+K− S-wave lineshape, followed by an amplitude analysis of our very pure high-statistics sample.
The amplitude analysis provides an accurate determination of the detection efficiency allowing us to measure the branching fraction B(D+s→K+K−π+)=(5.47±0.08stat±0.13sys)%.
We report an amplitude analysis and branching fraction measurement of D+s→K+K−π+ decay using a data sample of 3.19 fb−1 recorded with BESIII detector at a center-of-mass energy of 4.178 GeV.
We perform a model-independent partial wave analysis in the low K+K− mass region to determine the K+K− S-wave lineshape, followed by an amplitude analysis of our very pure high-statistics sample.
The amplitude analysis provides an accurate determination of the detection efficiency allowing us to measure the branching fraction B(D+s→K+K−π+)=(5.47±0.08stat±0.13sys)%.
We report an amplitude analysis and branching fraction measurement of D+s→K+K−π+ decay using a data sample of 3.19 fb−1 recorded with BESIII detector at a center-of-mass energy of 4.178 GeV.
We perform a model-independent partial wave analysis in the low K+K− mass region to determine the K+K− S-wave lineshape, followed by an amplitude analysis of our very pure high-statistics sample.
The amplitude analysis provides an accurate determination of the detection efficiency allowing us to measure the branching fraction B(D+s→K+K−π+)=(5.47±0.08stat±0.13sys)%.
Using 2.93 fb−1 of 𝑒+𝑒− collision data taken at a center-of-mass energy of 3.773 GeV with the BESIII detector, we report the first measurements of the absolute branching fractions of 14 hadronic 𝐷0(+) decays to exclusive final states with an 𝜂, e.g., 𝐷0→𝐾−𝜋+𝜂, 𝐾0𝑆𝜋0𝜂, 𝐾+𝐾−𝜂, 𝐾0𝑆𝐾0𝑆𝜂, 𝐾−𝜋+𝜋0𝜂, 𝐾0𝑆𝜋+𝜋−𝜂, 𝐾0𝑆𝜋0𝜋0𝜂, and 𝜋+𝜋−𝜋0𝜂; 𝐷+→𝐾0𝑆𝜋+𝜂, 𝐾0𝑆𝐾+𝜂, 𝐾−𝜋+𝜋+𝜂, 𝐾0𝑆𝜋+𝜋0𝜂, 𝜋+𝜋+𝜋−𝜂, and 𝜋+𝜋0𝜋0𝜂. Among these decays, the 𝐷0→𝐾−𝜋+𝜂 and 𝐷+→𝐾0 𝑆𝜋+𝜂 decays have the largest branching fractions, which are ℬ(𝐷0→𝐾−𝜋+𝜂) = (1.853±0.025stat±0.031syst)% and ℬ(𝐷+→𝐾0𝑆𝜋+𝜂) = (1.309±0.037stat±0.031syst)%, respectively. The charge-parity asymmetries for the six decays with highest event yields are determined, and no statistically significant charge-parity violation is found.
As insect decline threatens the fauna of Central Europe, “dark taxa” present an obstacle to understanding biodiversity loss. The superfamily Platygastroidea is a dark taxon, with many superficial descriptions requiring examination of type material to characterize and revise species and genera. The Natural History Museum Vienna (Naturhistorisches Museum Wien) is arguably the most important historical collection of Platygastroidea in Central Europe. Type specimens from 85 species in 21 genera and three families are here catalogued and photographically illustrated, including previously undocumented types described by Förster, Kieffer, Nees von Esenbeck, and Ratzeburg. Lectotypes are designated for Anteris bicolor Kieffer, Anteris simulans Kieffer, Hadronotus laticeps Kieffer, Leptacis foersteri Kieffer, Plastogryon investis Kieffer, Plastogryon sagax Kieffer, Prophanurus mayri Kieffer, and Telenomus laeviceps Förster. Trissolcus schimitsheki (Szelényi) syn. nov. is treated as a junior synonym of Trissolcus scutellaris (Thomson) and Telenomus nomas Förster syn. nov. is treated as a junior synonym of Trissolcus semistriatus (Nees). Baeus maculatus (Förster) comb. nov. is transferred from Telenomus. Historical, taxonomic, and curatorial remarks are included, providing an essential foundation for revisionary work on the Platygastroidea of Central Europe and beyond.
Rove beetles (Staphylinidae) are a diverse insect group, especially in the Neotropical region. At the same time, this fauna remains significantly understudied. During our visits to museum collections, we encountered numerous specimens of undescribed species representing the Neotropical genus Neolindus Scheerpeltz, 1933 which was earlier thought to be rare. To address the knowledge gap in the genus, we studied the museum material that resulted in descriptions of 21 new species. Our work involves the redescription of the genus, descriptions of the new species, and an updated identification key to 39 previously described and new species. The newly described species are Neolindus bicornis Guzman, Tokareva & Żyła sp. nov., N. elegans Guzman, Tokareva & Żyła sp. nov., N. longithorax Guzman, Tokareva & Żyła sp. nov., N. luxipenis Guzman, Tokareva & Żyła sp. nov., N. maya Guzman, Tokareva & Żyła sp. nov., N. minutus Guzman, Tokareva & Żyła sp. nov., N. napo Guzman, Tokareva & Żyła sp. nov., N. niger Guzman, Tokareva & Żyła sp. nov., N. ornatus Guzman, Tokareva & Żyła sp. nov., N. parahermani Guzman, Tokareva & Żyła sp. nov., N. paraplectrus Guzman, Tokareva & Żyła sp. nov., N. parasinuatus Guzman, Tokareva & Żyła sp. nov., N. parautriensis Guzman, Tokareva & Żyła sp. nov., N. pseudosensillaris Guzman, Tokareva & Żyła sp. nov., N. sauron Guzman, Tokareva & Żyła sp. nov., N. sibyllae Guzman, Tokareva & Żyła sp. nov., N. triangularis Guzman, Tokareva & Żyła sp. nov., N. tropicalis Guzman, Tokareva & Żyła sp. nov., N. utriensis Guzman, Tokareva & Żyła sp. nov., N. volkeri Guzman, Tokareva & Żyła sp. nov., and N. yotokae Guzman, Tokareva & Żyła sp. nov. This research emphasises the importance of museum collections in advancing taxonomy and enriching biodiversity knowledge. With these contributions, the known number of species of Neolindus reaches 60, thereby enhancing data on the Neotropical rove beetles diversity. Additionally, we provide several new country records for the genus (Guyana, Mexico, Nicaragua, and Suriname), which widen its distribution, and new occurrence records for the described species of Neolindus, N. agilis Herman, 1991; N. apiculus Herman, 1991; N. basisinuatus Herman, 1991; N. campbelli Herman, 1991; N. cuneatus Herman, 1991; N. hermani Asenjo, 2011; N. irmleri Asenjo, 2011; N. lodhii Herman, 1991; N. procarinatus Herman, 1991; N. punctogularis Herman, 1991; and N. retusus Herman, 1991.
The fossil record of the diverse subfamily Passifloroideae (>750 species and 17 genera) is relatively poor. Despite the distinctiveness of its leaves (glandular and often emarginate), most of the fossils from this group have been described from seeds. Fossil seeds have been recovered from Europe, and North and South America. A lack of information on seed morphology for all the genera and tribes of this subfamily has prevented a tribe-level identification of the fossils and a better understanding of their biogeographic patterns. The Passifloroideae is divided into three tribes: Passifloreae with 10 genera, Paropsieae with six genera and the monotypic Jongkindieae. This study provides new descriptions for 15 species from 5 genera from the mostly Afrotropical tribe Paropsieae based on herbarium material, and introduces an online seed database and a key for 100 species of Passifloroideae compiled from literature and direct observations. Our study shows a low morphological diversity among the seeds of Paropsieae in comparison to a much larger diversity within Passifloreae. Some rare morphologies are only present in Passifloreae and can be used to assign seeds to this tribe. Within the Paropsieae, Androsiphonia has seed that are very distinct from those in the other genera in the tribe and also from the rest of the subfamily. The genus Paropsia exhibits two main morphotypes, while the genera Barteria, Paropsiopsis and Smeathmannia have very similar seeds with a highly conserved morphology. These results suggest that living or fossil Paropsieae cannot be identified confidently based solely on seed characters.
Four new species of the Australian genus of Eurybrachidae (Hemiptera, Fulgoromorpha) Olonia Stål, 1862 are described from northern Queensland: O. albomarginata sp. nov., O. aschei sp. nov., O. jackiei sp. nov. and O. lindae sp. nov. Host plants and natural history data are documented and additional new records provided for O. guillaumei Constant, 2018, O. hochae Constant, 2018, O. picea Kirkaldy, 1906, O. rubicunda (Walker, 1851) and O. soulierae Constant, 2018. Trophobiosis is recorded for the first time in the genus, between a female of O. hochae and ants of the genus Camponotus Mayr, 1861 (Hymenoptera, Formicidae), representing the second record of trophobiosis in Australian Eurybrachidae. The male terminalia of the new species are illustrated and photographs of collection and live specimens, distribution maps, biological data and an identification key are provided. The genus Olonia currently contains sixteen species.
Twenty-one species of Mysidae were sampled by three ANDEEP expeditions to the Southern Ocean with epibenthic sledges dragged over the deep-sea floor in the realm of 58–71° S and 00–65° W, depth 774–5190 m. Previously known ranges are significantly extended southward for four species and to greater depth in the same four species plus two other species. Supplementary descriptions are given for Amblyops tattersalli and Dactylamblyops murrayi, and a first description of a (subadult) male for Thalassomysis tattersalli. The definitions of the genera Amphiakrops gen. nov., Chelamblyops gen. nov., Desmocornea gen. nov. and Schizurakrops gen. nov. are mainly based on the structure of the eyes as well as of the antennal peduncle, chelate second thoracic endopod and telson. These structures are also important for the descriptions of Amblyops arianii sp. nov., A. bipapillatus sp. nov., Amblyopsoides fenestragothica sp. nov., A. lepidophthalma sp. nov., Amphiakrops brandtae gen. et sp. nov., Dactylamblyops benthophilus sp. nov., Desmocornea subchelata gen. et sp. nov., Paramblyops petrescui sp. nov., Schizurakrops meesi gen. et sp. nov., Scolamblyops muehlenhardtae sp. nov., Stellamblyops doryphorus sp. nov. and Mysidella antarctica sp. nov. Six previously described taxa are recombined as Amblyopsoides laticauda comb. nov., Amphiakrops bidigitatus comb. nov., A. japonicus comb. nov., Chelamblyops globorostris comb. nov., Meierythrops tattersalli comb. nov. and M. triangulatus comb. nov. One species is revised back to the initial combination as Dactylamblyops japonicus. All except one (Mysidella antarctica sp. nov.) newly described (12), newly recombined (6) or back-combined (1) species belong to the Erythropinae. Keys to the resulting 61 genera and 263 species of Erythropinae and 18 species of Mysidellinae are given at the world-wide scale. Ocular papillae with a terminal pore (sensory pore organ) are recorded in nine ANDEEP species. The organ of Bellonci is identified on the reduced eyes in 16 species, among which D. subchelata gen. et sp. nov. has many ommatidia arranged in a self-contained ribbon which shows a banded rhabdom only in non-adults. Reduction of visual elements together with shrinking of ocular papillae during ontogenetic development suggest that non-adults of D. subchelata and T. tattersalli stay in the photic zone for feeding and growth and then descend only once during their lifetime to the abyss for reproduction.