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Cochlostoma revised: the subgenus Lovcenia Zallot et al., 2015
(Caenogastropoda, Cochlostomatidae)
(2018)
Five species of the subgenus Lovcenia of Cochlostoma (Cochlostomatidae) are recognized, three of which are described as new to science: C. (L.) tropojanum sp. nov., C. (L.) jakschae sp. nov. and C. (L.) lanatum sp. nov. A lectotype is designated for C. (L.) erika (A.J. Wagner, 1906). The shell and the genital tracts are described for all species and the distributional data are summarized.
We describe a new minute species of the genus Pristimantis, P. boucephalus sp. nov., from the Yanachaga-Chemillén National Park, Región Pasco, Peru. The description is based on a freshly collected male specimen found at 2950 m a.s.l. in a cloud forest and four previously unidentified museum specimens consisting of two adult males, one subadult female and a juvenile from the Yanachaga-Chemillén National Park. The new species is mainly characterized by a snout–vent length of 13.4–14.5 mm in adult males (n = 3), and 12.5 mm in the only known subadult female, and is compared morphologically and genetically with other taxonomically and biogeographically relevant species of Pristimantis. The new species is characterized by its small size, disproportionally large head with short snout, absence of a tympanic annulus and membrane, and reddish-copper iris. Phylogenetically it belongs to a speciose clade, an as yet unnamed species group, comprising both montane (Andes, Guiana Shield) and lowland (Amazon) taxa from the northern part of South America. The new species is genetically close to the sympatric P. cruciocularis. Species of Pristimantis occurring in the Cordillera Yanachaga region in the Andes of central Peru are members of six divergent phylogenetic lineages.
The genus Oxidus Cook, 1911 is revised to contain five species, O. avia (Verhoeff, 1937), O. gigas (Attems, 1953), O. gracilis (C.L. Koch, 1847), O. riukiaria (Verhoeff, 1940), and “species inquirenda” O. obtusus (Takakuwa, 1942). A cosmopolitan species, O. gracilis, is widely found in temperate and sub-tropical regions over the world, but other species have limited distribution in restricted regions, e.g., O. gigas in northern Vietnam, O. riukiaria and O. avia in the Ryukyu Islands (Japan). Four species, O. gracilis, O. riukiaria, O. avia and O. gigas, are confirmed as different from each other in gonopod characters, coloration and body size. The status of the last species, O. obtusus, is still doubtful and requires examination of further fresh material. The phylogenetic relationships among species of Oxidus is analyzed using two fragments of the mitochondrial genes COI (Cytochrome c Oxidase subunit I) and 16S rRNA. Three species of Oxidus are clearly separated from each other; O. gigas and O. gracilis form a monophyletic sister group with O. riukiaria. The genus Oxidus is also monophyletic and more closely related to the genus Tylopus Jeekel, 1968 than to the genera Sellanucheza Enghoff, Golovatch & Nguyen, 2004 or Kronopolites Attems, 1914. In addition, an identification key to species of Oxidus is provided.
The molecular phylogeny of Miliusa (Annonaceae) is reconstructed, with 27 (of ca. 50) species included, using a combination of seven plastid markers (rbcL exon, trnL intron, trnL-F spacer, matK exon, ndhF exon, psbA-trnH spacer, and ycf1 exon) constituting ca. 7 kb. In addition, two new species of Miliusa are described from the Malesian area: M. butonensis sp. nov. from Buton Island, Indonesia and M. viridifl ora sp. nov. from Papua New Guinea. The former is included in the molecular phylogenetic analysis. The reconstructed phylogeny corresponds well to the informal morphological grouping proposed earlier. A revised key to 13 Austro-Malesian species of Miliusa is provided.
The lichen-forming genus Pertusaria under its current circumscription is polyphyletic and its phylogenetic affiliations are uncertain. Here we study the species of the genera Pertusaria and Varicellaria which containlecanoric acid as major constituent, have disciform apothecia, strongly amyloid asci, non-amyloid hymenial gel, 1-2-spored asci, and 1- or 2-celled ascospores with thick, 1-layered walls. We infer phylogenetic relationships using maximum likelihood and Bayesian analyses based on four molecular loci (mtSSU, nuLSU rDNA, and the protein-coding, nuclear RPB1 and MCM7 genes). Our results show that the lecanoric acid-containing species form a well-supported, monophyletic group, which is only distantly related to Pertusaria s.str. The phylogenetic position of this clade is unclear, but placement in Pertusaria s.str. is rejected using alternative hypothesis testing. The circumscription of the genus Varicellaria is enlarged to also include species with non-septate ascospores. Seven species are accepted in the genus: Varicellaria culbersonii (Vězda) Schmitt & Lumbsch, comb. nov., Varicellaria hemisphaerica (Flörke) Schmitt & Lumbsch, comb. nov., Varicellaria kasandjeffii (Szatala) Schmitt & Lumbsch, comb. nov., Varicellaria lactea (L.) Schmitt & Lumbsch, comb. nov., Varicellaria philippina (Vain.) Schmitt & Lumbsch, comb. nov., Varicellaria rhodocarpa (Körb.) Th. Fr., and Varicellaria velata (Turner) Schmitt & Lumbsch, comb. nov. A key to the species of Varicellaria is provided.
Die Grabwespen (Sphecidae sensu Bohart & Menke 1976; Sphecidae sensu lato in neueren, phylogenetischen Arbeiten), zu denen nach Day (1984) und späteren Autoren auch die Heterogynaidae zählen, umfassen derzeit 266 Gattungen mit 9559 beschriebene Arten (Pulawski 2006). Zusammen mit den Bienen (= Apiformes nach Michener 2000, bzw. Anthophila nach Engel 2005) bilden die Grabwespen ein gut begründetes Monophylum, das nach Michener (1986) den Namen Apoidea trägt und eine der drei Hauptlinien innerhalb der aculeaten Hymenoptera ist. Die Monophylie der aculeaten Hymenoptera, der Apoidea sowie die der Bienen ist jeweils gut begründet (z.B. Brothers 1975, Königsmann 1978, Lomholdt 1982, Alexander 1992, Brothers & Carpenter 1993). Anders verhält es sich mit den Grabwespen. Neben der phylogenetischen Untersuchung von Brothers & (1993), die die Monophylie der Grabwespen unterstützt, haben andere morphologische als auch molekularsystematische Analysen starken Zweifel an dieser Hypothese aufkommen lassen (z.B. Königsmann 1978, Lomholdt 1982, Alexander 1992, Prentice 1998, Melo 1999, Ohl & Bleidorn 2006).