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This paper offers an explanation of each of the 44 scientific names given by Leopold Krüger (1861-1942) to odonate taxa together with that for the names of all the genera into which they are sorted now. But prior to that there is some information about the life and work of this scientist, and in the final part his preferences in odonatological nomenclature are compared with those in the names created by F.M. Brauer and F. Ris and some impressions of his studies on Neuroptera are presented and considerations about his aspirations in his work are given.
An explanation is presented for each of the 135 scientific names given to Odonata by F. M. Brauer (fossils and synonyms included), in addition the names of the actual genera in which Brauer’s species are now classified are explained. Prior to that part biographical information is given and Brauer’s merits in enlightening the taxonomy of dragonflies are analysed. Conclusions are drawn as to his preferences in odonatological nomenclature and finally the difficulties are discussed, which Brauer had to face in his taxonomic work.
We present an updated, subjective list of the extant, non-marine ostracod genera and species of the world, with their distributions in the major zoogeographical regions, as well as a list of the genera in their present hierarchical taxonomic positions. The list includes all taxa described and taxonomic alterations made up to 1 July 2018. Taxonomic changes include 17 new combinations, 5 new names, 1 emended specific name and 11 new synonymies (1 tribe, 4 genera, 6 species). Taking into account the recognized synonymies, there are presently 2330 subjective species of non-marine ostracods in 270 genera. The most diverse family in non-marine habitats is the Cyprididae, comprising 43.2% of all species, followed by the Candonidae (29.0%), Entocytheridae (9.1%) and the Limnocytheridae (7.0%). An additional 13 families comprise the remaining 11.8% of described species. The Palaearctic zoogeographical region has the greatest number of described species (799), followed by the Afrotropical region with 453 species and the Nearctic region with 439 species. The Australasian and Neotropical regions each have 328 and 333 recorded species, respectively, while the Oriental region has 271. The vast majority of non-marine ostracods (89.8%) are endemic to one zoogeographical region, while only six species are found in six or more regions. We also present an additional list with 'uncertain species', which have neither been redescribed nor re-assessed since 1912, and which are excluded from the main list; a list of taxonomic changes presented in the present paper; a table with the number of species and % per family; and a table with numbers of new species described in the 20-year period between 1998 and 2017 per zoogeographical region. Two figures visualize the total number of species and endemic species per zoogeographical region, and the numbers of new species descriptions per decade for all families and the three largest families since 1770, respectively.
The Odonata collection deposited at the Museum of Comparative Zoology (MCZ) includes specimens of 634 taxa labeled as types. Fifteen of these have been incorrectly labeled as types (pseudotypes) and eight are apparently lost, leaving a total of 611 types currently deposited at MCZ. From these, 489 represent primary namebearing types (syntype/s, holotype, lectotype and neotype), 21 are probable primary types, and 101 are secondary types (paratype/s, paralectotype/s).
A new classification of Ophiuroidea, considering family rank and above, is presented. The new family and superfamily taxa in O’Hara et al. (2017) were proposed to ensure a better readability of the new phylogeny but are unavailable under the provisions of the ICZN. Here, the morphological diagnoses to all 33 families and five superfamilies are provided. Ten new families, Ophiosphalmidae fam. nov., Ophiomusaidae fam. nov., Ophiocamacidae fam. nov., Ophiopteridae fam. nov., Clarkcomidae fam. nov., Ophiopezidae fam. nov., Ophiernidae fam. nov., Amphilimnidae fam. nov., Ophiothamnidae fam. nov. and Ophiopholidae fam. nov., are described. The family Ophiobyrsidae Matsumoto, 1915, not yet discovered in the previous publication, is added, based on new molecular data. A new phylogenetic reconstruction is presented. Definitions of difficult-to-apply morphological characters are given.
Improving nomenclatural consistency: a decade of experience in the World Register of Marine Species
(2017)
The World Register of Marine species (WoRMS) has been established for a decade. The early history of the database involved compilation of existing global and regional species registers. This aggregation, combined with changes to data types and the changing needs of WoRMS users, has resulted in an evolution of data-entry consistency over time. With the task of aggregating the accepted species names for all marine species approaching completion, our focus has shifted to improving the consistency and quality of data held while keeping pace with the addition of > 2000 new marine species described annually. This paper defines priorities and longer-term aims that promote standardisation within and interoperability among biodiversity databases, provides editors with further information on how to input nomenclatural data in a standardised way and clarifies for users of WoRMS how and why names are represented as they are. We 1) explain the categories of names included; 2) list standard reasons used to explain why a name is considered ‘unaccepted’ or ‘uncertain’; 3) present and explain the more difficult situations encountered; 4) describe categories of sources and notes linked to a taxon; and 5) recommend how type material, type locality and environmental information should be entered.
Tineobius (Tineobius) tamaricis Ribes & Fusu sp. nov. is newly described from Parapodia sinaica (Frauenfeld, 1859) (Lepidoptera, Gelechiidae) galls from Catalonia in Spain. This is the first record of the so far Palaeotropical genus Tineobius Ashmead, 1896 in the Palaearctic region. Basic biological data and a DNA barcode are provided for the new species. Parapodia sinaica (the host of T. tamaricis sp. nov.) is reported for the first time to form galls on Tamarix canariensis (Willd). A checklist of described world Tineobius species is provided, with nine species formally transferred to Tineobius from Anastatoidea Gahan, 1927 and thirteen species newly assigned to T. (Tineobius). Metapelma seyrigi (Risbec, 1952) is transferred to Tineobius and the replacement name Tineobius (Tineobius) madagascariensis nom. nov. is proposed, as the name is preoccupied by Tineobius (Tineobius) seyrigi (Ferrière, 1938) comb. nov.; Tineobius (Tineobius) albopalpalis (Brues, 1907) comb. nov. is transferred from Charitopus Förster, 1856 (a genus in Encyrtidae). One species is transferred from Anastatoidea to Eupelmus Dalman, 1820 as Eupelmus (Episolindelia) ambatomangae (Risbec, 1958) comb. nov.
Taxonomic supplement (2001 to 2015) to the catalogue of New Zealand Carabidae (Insecta: Coleoptera)
(2016)
A supplement to the “Carabidae (Insecta: Coleoptera): catalogue” published by Larochelle and Larivière (2001; Fauna of New Zealand 43), is provided. A total of 99 genera and 547 species and subspecies belonging to 21 tribes and 8 subfamilies of Carabidae (including Cicindelini and Rhysodini), is recorded for New Zealand. Endemism is high, with 93% of the species and subspecies as well as 62% of the genera recorded from this country only. Changes to the 2001 catalogue are documented. The synonymy and type locality of taxa described between 2001 and 2015 are also provided.
Molecular phylogenetic analysis has demonstrated that the genus Gallinula is not monophyletic and comprises four major lineages. A review of the nomenclature of Gallinula shows that generic names are available for three lineages but that a fourth is as yet unnamed. A new monotypic genus, Paragallinula gen. nov., is described for Lesser Moorhen (Gallinula angulata Sundevall, 1850).
Debate exists regarding the number of species of the moon jellyfish (genus Aurelia), a common member of the planktonic community of the coastal shelf seas around the world. Three Aurelia congeners (A. aurita, A. labiata and A. limbata) are currently considered to exist but recent genetic analyses suggested that this is an oversimplification. We analyzed the morphological characteristics of scyphistomae, morphological characteristics of ephyrae and differences in the time span of the strobilation process of Aurelia congeners from 17, 7 and 6 different source populations, respectively, of known species. Morphological characteristics of scyphistomae were similar among the 17 populations but those of ephyrae, such as the shape and form of lappets, were effective discriminators in the 6 cases examined. We recommend identifying species based on differences in 1) the morphological characteristics of scyphistomae and ephyrae (and not only medusae), 2) the genetics of individuals, and 3) the geographical occurrence of the population. This study adds to the growing body of knowledge on scyphozoan scyphistomae and ephyrae, stages of the metagenic life cycle of scyphozoans that have received relatively little study compared to medusae.