590 Tiere (Zoologie)
Refine
Year of publication
- 2020 (356)
- 2021 (329)
- 2017 (297)
- 2022 (294)
- 2012 (258)
- 2018 (257)
- 2013 (237)
- 2014 (231)
- 2019 (231)
- 2023 (230)
- 2011 (217)
- 2015 (216)
- 2009 (206)
- 2008 (199)
- 2016 (192)
- 2024 (161)
- 2006 (152)
- 2007 (149)
- 2010 (142)
- 2005 (135)
- 2004 (111)
- 1995 (105)
- 2001 (100)
- 2003 (91)
- 1998 (86)
- 1999 (81)
- 1996 (77)
- 1997 (74)
- 1993 (73)
- 1994 (70)
- 2002 (69)
- 2000 (65)
- 1992 (63)
- 1991 (56)
- 1989 (45)
- 1988 (42)
- 1986 (39)
- 1881 (34)
- 1990 (27)
- 1981 (20)
- 1985 (20)
- 1987 (18)
- 1914 (16)
- 1911 (14)
- 1984 (14)
- 1884 (13)
- 1904 (13)
- 1926 (13)
- 1982 (13)
- 1913 (11)
- 1923 (11)
- 1886 (10)
- 1930 (10)
- 1979 (10)
- 1980 (10)
- 1983 (10)
- 1894 (9)
- 1896 (9)
- 1908 (9)
- 1891 (8)
- 1893 (8)
- 1898 (8)
- 1900 (8)
- 1907 (8)
- 1859 (7)
- 1861 (7)
- 1873 (7)
- 1885 (7)
- 1887 (7)
- 1888 (7)
- 1889 (7)
- 1892 (7)
- 1901 (7)
- 1933 (7)
- 1936 (7)
- 1937 (7)
- 1965 (7)
- 1968 (7)
- 1970 (7)
- 1977 (7)
- 1858 (6)
- 1868 (6)
- 1897 (6)
- 1903 (6)
- 1912 (6)
- 1915 (6)
- 1918 (6)
- 1927 (6)
- 1931 (6)
- 1934 (6)
- 1940 (6)
- 1971 (6)
- 1972 (6)
- 1973 (6)
- 1976 (6)
- 1848 (5)
- 1857 (5)
- 1862 (5)
- 1866 (5)
- 1878 (5)
- 1879 (5)
- 1890 (5)
- 1895 (5)
- 1906 (5)
- 1909 (5)
- 1916 (5)
- 1919 (5)
- 1921 (5)
- 1928 (5)
- 1935 (5)
- 1938 (5)
- 1975 (5)
- 1844 (4)
- 1865 (4)
- 1870 (4)
- 1872 (4)
- 1876 (4)
- 1883 (4)
- 1899 (4)
- 1902 (4)
- 1910 (4)
- 1917 (4)
- 1924 (4)
- 1929 (4)
- 1939 (4)
- 1952 (4)
- 1966 (4)
- 1974 (4)
- 1978 (4)
- 1842 (3)
- 1845 (3)
- 1855 (3)
- 1905 (3)
- 1922 (3)
- 1949 (3)
- 1953 (3)
- 1957 (3)
- 1962 (3)
- 1967 (3)
- 1969 (3)
- 1752 (2)
- 1817 (2)
- 1822 (2)
- 1836 (2)
- 1841 (2)
- 1853 (2)
- 1854 (2)
- 1867 (2)
- 1869 (2)
- 1874 (2)
- 1875 (2)
- 1877 (2)
- 1880 (2)
- 1925 (2)
- 1932 (2)
- 1941 (2)
- 1942 (2)
- 1947 (2)
- 1948 (2)
- 1956 (2)
- 1958 (2)
- 1959 (2)
- 1960 (2)
- 1963 (2)
- 1964 (2)
- 1705 (1)
- 1740 (1)
- 1748 (1)
- 1787 (1)
- 1791 (1)
- 1794 (1)
- 1801 (1)
- 1802 (1)
- 1803 (1)
- 1804 (1)
- 1810 (1)
- 1815 (1)
- 1816 (1)
- 1823 (1)
- 1824 (1)
- 1829 (1)
- 1830 (1)
- 1832 (1)
- 1835 (1)
- 1837 (1)
- 1840 (1)
- 1849 (1)
- 1850 (1)
- 1856 (1)
- 1860 (1)
- 1863 (1)
- 1864 (1)
- 1871 (1)
- 1882 (1)
- 1920 (1)
- 1951 (1)
- 1954 (1)
- 1955 (1)
- 1961 (1)
Document Type
- Article (3838)
- Part of Periodical (2378)
- Book (107)
- Review (82)
- Doctoral Thesis (71)
- Periodical (20)
- Preprint (20)
- Contribution to a Periodical (14)
- Report (8)
- Diploma Thesis (7)
Language
- English (4145)
- German (1975)
- French (220)
- Spanish (78)
- Multiple languages (52)
- Italian (27)
- Latin (23)
- dut (17)
- Portuguese (10)
- Danish (5)
Is part of the Bibliography
- no (6563)
Keywords
- taxonomy (721)
- new species (437)
- morphology (162)
- distribution (121)
- biodiversity (86)
- Odonata (84)
- systematics (84)
- phylogeny (64)
- Taxonomy (63)
- new records (59)
Institute
- Extern (331)
- Biowissenschaften (249)
- Institut für Ökologie, Evolution und Diversität (160)
- Senckenbergische Naturforschende Gesellschaft (143)
- Biodiversität und Klima Forschungszentrum (BiK-F) (79)
- Medizin (50)
- Präsidium (24)
- Biochemie und Chemie (10)
- Geowissenschaften (7)
- Exzellenzcluster Makromolekulare Komplexe (4)
- MPI für Hirnforschung (4)
- Ernst Strüngmann Institut (3)
- Frankfurt Institute for Advanced Studies (FIAS) (3)
- Biochemie, Chemie und Pharmazie (2)
- Geographie (2)
- Geowissenschaften / Geographie (2)
- Zentrum für Biomolekulare Magnetische Resonanz (BMRZ) (2)
- Fachübergreifend (1)
- Informatik (1)
- Institut für Bienenkunde (1)
- Institut für Wirtschaft, Arbeit, und Kultur (IWAK) (1)
- Institut für sozial-ökologische Forschung (ISOE) (1)
- Kulturwissenschaften (1)
- MPI für Biophysik (1)
- MPI für empirische Ästhetik (1)
- Physik (1)
- Psychologie (1)
- Universität des 3. Lebensalters e.V. (1)
- Universitätsbibliothek (1)
- Zentrum für Interdisziplinäre Afrikaforschung (ZIAF) (1)
The genus Lissocnemis Kohl, 1907 of the subfamily Ctenocerinae is recorded from Korea for the first time. The diagnosis and characteristics of the genus, description of a new species, L. koreana Kim & Shimizu sp. nov. and redescription of another species, L. brevipennis hitherto known from Southeast Asia and Japan, are presented. The biogeographical distribution of the genus is discussed. Cryptosalius Turner, 1917 (type species: Pseudagenia rava Bingham, 1896; in part) and Dinagenia Banks, 1934 (type species: D. apollo Banks, 1934) are synonymized with Lissocnemis and the following new combinations are made: Lissocnemis tonkinensis (Turner, 1920) comb. nov. (= Cryptosalius tonkinensis Turner, 1920); Lissocnemis apollo (Banks, 1934) comb. nov. (= Dinagenia apollo Banks, 1934); and Lissocnemis satyrus (Banks, 1938) comb. nov. (= Dinagenia satyrus Banks, 1938). Lastly, L. satyrus (Banks, 1938) and L. nigricoxis Haupt, 1941 are rendered to be junior synonyms of L. apollo (Banks, 1934) comb. nov.
Due to the fragility of the ophiuroid (brittle star) skeleton, the bulk of the group’s fossil record consists of dissociated ossicles preserved as microfossils. In spite of their great potential as basis for taxonomic and phylogenetic studies, however, ophiuroid ossicles from the Paleozoic have received very little attention so far. Here, we provide an exhaustive taxonomic assessment of such fossils retrieved from sieving residues from the Silurian of Gotland, Sweden. This material was used in a previous study to describe two key taxa that allowed constraining the origin of the extant ophiuroid clade. The remaining taxa belonging to that same lineage are described in the present paper. The evidence at hand suggests that the stem of the extant ophiuroid clade was formed by two genera, Ophiopetagno and Ophiolofsson gen. nov., including six and five species, respectively, and spanning at least the upper Llandovery through upper Ludlow. We conclude that Ophiopetagno and Ophiolofsson represent sister genera that coexisted through most of the Silurian in the shallow tropical seas of Gotland. They underwent repeated body size reductions in correlation with environmental perturbations, with Ophiopetagno paicei eventually giving rise to Muldaster haakei; the first member of the living Ophiuroidea. Herein, we also introduce two new clades, Ankhurida clade nov. and Ophiovalida clade nov., and the following eight new species: Ophiolofsson joelmciveri gen. et sp. nov., O. obituary gen. et sp. nov., O. immolation gen. et sp. nov., O. archspire gen. et sp. nov., O. hendersonorum gen. et sp. nov., Ophiopetagno bonzo sp. nov., O. kansas sp. nov., O. doro sp. nov.; and two probably new species in open nomenclature: Ophiopetagno sp. 1, and Ophiopetagno sp. 2.
Highlights
• A proteomic analysis of the mandibular glands of Shinisaurius crocodilurus and Corucia zebrata, was performed.
• Scanning electron microscopy of S. crocodilurus' teeth revealed a sharp ridge on the anterior surface, but no grooves.
• Scanning electron microscopy of C. zebrata teeth showed a flattened crown with a pointed cusp.
• Proteomic analysis of gland extracts of S. crocodilurus and C. zebrata showed absence of venom-derived peptides or proteins.
• Our results strongly support the non-venomous character of both S. crocodilurus and C. zebrata.
Abstract
Based on its phylogenetic relationship to monitor lizards (Varanidae), Gila monsters (Heloderma spp.), and the earless monitor Lanthanotus borneesis, the Chinese crocodile lizard, Shinisaurus crocodilurus, has been assigned to the Toxicofera clade, which comprises venomous reptiles. However, no data about composition and biological activities of its oral secretion have been reported. In the present study, a proteomic analysis of the mandibular gland of S. crocodilurus and, for comparison, of the herbivorous Solomon Island skink Corucia zebrata, was performed. Scanning electron microscopy (SEM) of the teeth from S. crocodilurus revealed a sharp ridge on the anterior surface, but no grooves, whereas those of C. zebrata possess a flattened crown with a pointed cusp. Proteomic analysis of their gland extracts provided no evidence of venom-derived peptides or proteins, strongly supporting the non-venomous character of these lizards. Data are available via ProteomeXchange with identifier PXD039424.
Highlights
• Proteomic analyses of submandibular gland extracts of two alligator lizards of the Anguidae family are reported.
• A conserved set of putative toxins was found in the submandibular gland extracts of Abronia lythrochila and A. graminea.
• Toxins evolved in oral secretions of paleo- and neoanguimorpha over more than 100 million years of Anguimorpha cladogenesis.
• Electron microscopy of pleurodont teeth of A. lythrochila showed no sign of groove, external opening or striations.
• Assessing the role toxins play in the ecology of extant anguimorph lizards deserves functional studies in natural prey.
Abstract
A useful approach to deepen our knowledge about the origin and evolution of venom systems in Reptilia has been exploring the vast biodiversity of this clade of vertebrates in search of orally produced proteins with toxic actions, as well as their corresponding delivery systems. The occurrence of toxins in anguimorph lizards has been demonstrated experimentally or inferred from reports of the toxic effects of the oral secretions of taxa within the Varanidae and Helodermatidae families. In the present study, we have focused on two alligator lizards of the Anguidae family, the Mexican alligator lizard, Abronia graminea, and the red-lipped arboreal alligator lizard, A. lythrochila. In addition, the fine morphology of teeth of the latter species is described. The presence of a conserved set of proteins, including B-type natriuretic peptides, cysteine-rich secretory proteins, group III phospholipase A2, and kallikrein, in submandibular gland extracts was demonstrated for both Abronia species. These proteins belong to toxin families found in oral gland secretions of venomous reptile species. This finding, along with previous demonstration of toxin-producing taxa in both paleo- and neoanguimorpha clades, provides further support for the existence of a handful of conserved toxin families in oral secretions across the 100+ million years of Anguimorpha cladogenesis.
Among the 44 genera of predatory stink bugs (Asopinae) described for the Old World, there is a notable lack of recent studies. In this research, we aim to fill this gap by investigating the taxonomic history and morphology of species of Cantheconidea. As results, we present the redescription of the genus and validate three species: C. humeralis, C. javana and C. mitis comb. nov. A lectotype for C. mitis is designated and comments on the type material are given. Additionally, we transfer four species from Cantheconidea to the genus Eocanthecona: E. acuta comb. nov., E. variabilis comb. nov., E. gaugleri comb. nov. and E. insularis comb. nov. To accommodate the unique characteristics of Cantheconidea cyanacantha, we describe a new genus, Cantheconesia Brugnera & Roca-Cusachs gen. nov., and transfer the species, resulting in Cantheconesia cyanacantha gen. et comb. nov. Our study provides detailed redescriptions of species and accompanying images to support taxonomic decisions and presents new distribution records.
A comprehensive checklist and host plants of Aphididae (Aphidomorpha: Hemiptera) from Pakistan
(2024)
The family Aphididae (Hemiptera) represents one of the most diverse groups of sap-sucking insect pests referred to as aphids or plant-lice, with 366 species reported in Pakistan, associated with wide array of agricultural and horticultural crops, including fruit and forest trees, weeds, grasses, shrubs, and vines. This work aims to provide an updated checklist of aphids and their associated host plants documented across various regions of Pakistan. The checklist consolidates information from various published literature sources, including annotated checklists, regional distribution data, and host plant records from Pakistan. In this study, we present an annotated checklist of 366 aphid species, belonging to 134 genera and 11 subfamilies, associated with a total of 359 host plant species stretched over 84 families in Pakistan.
Samples of Crustacea and Annelida (Polychaeta, Sipuncula, and Hirudinea) were collected in the Bering Sea and the northwestern Pacific Ocean during scientific cruise SO-249 BERING in 2016. Biological samples were collected from 32 locations by the team on-board RV Sonne using a chain bag dredge at depths ranging between 330–5,070 m, and preserved in 96% ethanol. Specimens were morphologically identified to the lowest taxonomic level possible using a Leica M60 stereomicroscope. The generated data here comprise taxonomic information as well as annotated bathymetric and biogeographic information from a total of 78 samples (26 Crustacea, 47 Polychaeta, 4 Sipuncula, and 1 Hirudinea). The dataset was prepared following Darwin Core Biodiversity standards for FAIR data sharing based on Ocean Biodiversity Information System (OBIS) and Global Biodiversity Facility (GBIF) guidelines. The standardised digitised data were then mobilised to both OBIS and GBIF under CC BY 4.0 licence to publicly share and adopt the data. As records of these important marine taxa from bathyal and abyssal depths are sparse, especially from the deep Bering Sea, the herein generated and digitised data aid in filling existing knowledge gaps on their diversity and distribution in that region. As part of the “Biogeography of the NW Pacific deep-sea fauna and their possible future invasions into the Arctic Ocean” (BENEFICIAL) project, this dataset thus not only increases our knowledge in re-assessing and uncovering the deep-sea diversity of these taxa, but also serves policy and management sectors by providing first-hand data for global report assessments.
The monophyly of Theraphosinae is supported by both morphological and molecular phylogenies. However, intergeneric relationships often show polytomies and branches with low support. A previous phylogenetic study proposed an intergeneric relationship for the subfamily based on molecular data and divided it into three tribes: Grammostolini, Hapalopini and Theraphosini. However, not all genera of Theraphosinae were sampled, and some relationships were inferred based on morphological similarities. Regarding the Hapalopini from Brazil, the relationships of some genera are still uncertain, such as Kochiana, Catanduba, and Munduruku. In this paper, we describe four new species of Hapalopini from Brazil: Cyriocosmus paresi sp. nov., Hapalopus akroa sp. nov., H. guidonae sp. nov., and K. fukushimae sp. nov. In addition, we propose an updated diagnosis for these three genera and for the species K. brunnipes and M. bicoloratum.
Ophioderma teres (Lyman, 1860), an ophiuroid previously believed to have a wide distribution in the eastern Pacific, has been found to have an unclear taxonomic identity. While considered a well-known species, recent studies have revealed that O. teres lacks a holotype and has vague boundaries with its congeners Ophioderma teres unicolor H.L. Clark, 1940 and Ophioderma sodipallaresi Caso, 1986, as well as with two additional new morphotypes detected in Mexico and Nicaragua, causing continuous misidentifications. This study utilized an integrative taxonomy approach based on morphologic, morphometric, and molecular evidence to clarify the taxonomic status of O. teres, O. sodipallaresi, O. teres unicolor, and the two new morphotypes. Data integration led to the following results: 1) the neotype designation and redescription of O. teres; 2) the proposal of O. sodipallaresi as a junior synonym of O. teres; 3) the status change of O. unicolor stat. nov. from subspecies to species, and 4) the description of the morphotypes as the new species Ophioderma aija sp. nov. and Ophioderma bichi sp. nov. An identification key to the eastern Pacific species of Ophioderma was also developed. This work contributes to the knowledge of Ophioderma in the region, increasing the number of described species and providing resources for their accurate identification.