scholarly journals Mitogenomics of historical type specimens of Australasian turtles: clarification of taxonomic confusion and old mitochondrial introgression

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Christian Kehlmaier ◽  
Xiuwen Zhang ◽  
Arthur Georges ◽  
Patrick D. Campbell ◽  
Scott Thomson ◽  
...  
Zootaxa ◽  
2012 ◽  
Vol 3490 (1) ◽  
pp. 49 ◽  
Author(s):  
JAE-SANG HONG ◽  
BYUNG-MEE CHOI ◽  
AKI KUBO ◽  
MASANORI SATO

There has been a long-standing taxonomic confusion over the name of a giant nereidid worm living in Asian intertidalmud flats. To clear up the confusion, we examined the type specimens of Paraleonnates uschakovi Khlebovich and Wu,1962 described from China as well as Periserrula leucophryna Paik, 1977 described from Korea (Polychaeta: Nereididae),together with additional non-type materials newly collected from Korea, China, Taiwan, and Thailand. Our results con-firmed that Periserrula leucophryna should be reduced to a junior synonym of Paraleonnates uschakovi as previouslynoted, and that this species is widely distributed in Asia, newly recorded from Taiwan and Thailand. We also present newinformation about the arrangement of three kinds of chaetae in the parapodia as a characteristic of this species. We alsocompared this species with Paraleonnates bolus (Hutchings and Reid, 1991) described from Australia and concluded thatthese are different species. Based on our examination, we propose the amended diagnosis of the genus ParaleonnatesKhlebovich and Wu, 1962. Paraleonnates Amoureux, 1985 erected as a monotypic genus for P. guadalupensis Amoureux,1985 was judged as a junior homonym of Paraleonnates Khlebovich and Wu, 1962, and P. guadalupensis is transferred to the genus Leonnates Kinberg, 1865.


2021 ◽  
Vol 97 (1) ◽  
pp. 121-139
Author(s):  
Isabel Cristina Molina-Acevedo ◽  
Izwandy Idris

Marphysa simplex is a name that three species bear within the same genus, but each has a different authority and morphological characteristics. This homonymy condition leads to taxonomic confusion and the finite designation of name-bearing is imperative. The current study focuses on two species identified as M. simplex Crossland, 1903 and M. simplex Treadwell, 1922 and a third one, recently considered a secondary homonymy, M. simplex (Langerhans, 1884), is also assessed. The available type specimens were examined and re-described in detail using updated characters and the original descriptions. Marphysa simplex (Langerhans, 1884) is herein judged as an indeterminable species. Marphysa simplex Crossland, 1903 is confirmed as a junior synonym of M. teretiuscula (Schmarda, 1861a) because the differences are minimal. Moreover, M. teretiuscula has characteristics similar to Group B2 (Sanguinea-group; only compound spinigers), instead of the Teretiuscula-group (compound spinigers in the anterior region, subacicular limbate in all chaetigers). On the other hand, M. simplex Treadwell, 1922 is a junior primary homonym of Crossland’s species replaced by M. fijiensisnom. nov. with the chaetal arrangement similar to Group A (limbate chaetae only). In conclusion, the name M. simplex is now unacceptable. The hypothesis on species group only with limbate chaetae and the redescription on M. teretiuscula is also given.


PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e7090
Author(s):  
Sarah J. Jacobs ◽  
Sarah Herzog ◽  
David C. Tank

Robustly delimited species are of paramount importance, the identification of which relies on our ability to discern boundaries between one species and the next. This is not difficult to do when species are very distinct from one another. However, in recently evolved lineages where putative species may have relatively few diagnostic features (e.g., species complexes composed of very similar species, the boundaries between which are often unclear), defining species boundaries can be more challenging. Hence, the field of species delimitation has widely advocated the use of multiple lines of evidence to delimit species, particularly in species complexes. Excessive taxonomic confusion, often the result of species descriptions that shift through time (e.g., during revisionary work and regional treatments), can further complicate the search for diagnostic features in species complexes. Here, as a first step in robustly delimiting species boundaries, we quantify and describe morphological variation in the Castilleja pilosa species complex. We first infer the morphospace of the species complex and use fuzzy-clustering techniques to explore the morphological variation in the system. Next, we hypothesize the position of type specimens within that morphospace. In so doing, we aim to visualize the impact that regional treatments have had on the conceptualization of taxa through time. We find that there is limited morphological variation among members of this complex, and we determine that the morphological concept of these species have shifted through time and are no longer accurately represented by species descriptions.


Author(s):  
Tatsuya Ide ◽  
Yoshihisa Abe

Abstract In heterogonic gall wasps, the gall structure, phenology, and adult morphology differ between the asexual and sexual generations, even within the same species. Dryophanta japonica Ashmead and Dryophanta mitsukurii Ashmead were described in 1904, but their heterogonic life cycles were uncertain. To match their asexual and sexual generations, we compared the type specimens of both species with specimens of gall wasps reared to demonstrate heterogonic life cycles. This revealed that these two species are the respective asexual and sexual generations of a single heterogonic species. Based on the morphological characteristics, we transferred D. japonica to Cerroneuroterus Melika and Pujade-Villar as Cerroneuroterus japonicus (Ashmead, 1904) comb. nov. and treated the sexual generation as a junior synonym: Dryophanta mitsukurii  Ashmead, 1904  syn. nov. Moreover, we examined the type specimens of other species previously suggested to be synonymous with D. mitsukurii. This showed that Neuroterus vonkuenburgi  Dettmer, 1934  syn. nov. (and N. vonkuenburgi wakayamensis  Monzen, 1954  syn. nov.) is the asexual generation of C. japonicus and that Neuroterus bonihenrici  Dettmer, 1934  syn. nov. is the sexual generation. Judging from the original descriptions, Andricus asakawae  Shinji, 1943  syn. nov., Andricus kanagawae  Shinji, 1943  syn. nov., Andricus asakawae  Shinji, 1944  syn. nov., Andricus kanagawae  Shinji, 1944  syn. nov., and Neoneuroterus kashiyamai  Monzen, 1954  syn. nov. were also regarded as the sexual generation of C. japonicus. Finally, we discussed how matching asexual and sexual generations in heterogonic gall wasps not only avoids taxonomic confusion but also contributes to progress in gall wasp biology.


2021 ◽  
Vol 779 ◽  
pp. 1-70
Author(s):  
Sergio I. Salazar-Vallejo ◽  
Jesús Angel De León-González ◽  
Victor M. Conde-Vela

Nereis falsa de Quatrefages, 1866 has been regarded as a cosmopolitan species, and several species described from different localities have been regarded as junior synonyms of N. falsa. The present study is an attempt to resolve the taxonomic confusion in N. falsa, which seems to contain several distinct species due to previous inappropriate synonymy, widely distributed in the Atlantic and eastern Pacific Oceans. For this purpose, the authors first propose the resurrection of the synonymy of N. falsa with Hediste diversicolor that was concluded during the 19th century but disregarded later. After the fixation of the identity of N. falsa sensu stricto, the authors re-evaluate the proper taxonomic status of species which have previously been confused with N. falsa. Type, topotype and non-type specimens were examined; most species are redescribed, and others are reinstated. Nereis splendida Grube, 1840 is a valid Mediterranean species, and a neotype is proposed; it includes the Mediterranean populations of what is currently regarded as N. falsa. Consequently, N. falsa is transferred to Hediste Malmgren, 1867, and some taxonomic comments are added for the latter genus and a key to species is also included. Nereis callaona Grube & Kröyer in Grube, 1857, N. marginata Grube & Örsted in Grube, 1857 and N. riisei Grube & Örsted in Grube, 1857 are restricted to tropical American shores and are all redescribed. Nereis pelagica lunulata Ehlers, 1901, formerly regarded as a junior synonym of N. falsa by Fauvel (1941), is redescribed and elevated in rank to species level. Nereis lucipeta Ehlers, 1908, formerly regarded as a junior synonym of N. splendida by Ehlers (1913) and of N. falsa by Fauvel (1919), is reinstated. Nereis occidentalis Hartman, 1945 is also redescribed. Furthermore, N. ambigua Treadwell, 1937, formerly regarded as a junior synonym of N. riisei by Monro (1933), deserves to be reinstated. Western Africa specimens recorded as N. falsa are newly described as N. mezianei sp. nov.


Author(s):  
Christine Hanna Lydia Schönberg ◽  
Lydia Beuck

Early descriptions for species of Aka were poor in detail, and the only spicule type that occurs in this genus does not vary much between species, which led to taxonomic confusion. Moreover, the type specimens of five species of Aka are lost, causing considerable problems. Mediterranean specimens of Aka were identified as Aka labyrinthica (Hancock, 1849) by Topsent (1900), even though this species was originally described from the Indo-Pacific. All following publications on Mediterranean Aka accepted Topsent's decision. We assessed this problem with new samples from the Ionian Sea. Our material consisted of only one specimen of Aka, and we had to rely mainly on spicule characters for comparison with other species. We developed a system for species recognition solely based on spicular characters and biometry, involving a combination of the parameters oxea length, width, tip form and angle of curvature. This approach was surprisingly accurate. Forming ratios of the above parameters was less helpful, but can sometimes provide additional information. We identified our sample as Aka infesta (Johnson, 1899), and describe it as a minute-fistulate species with large, multicamerate erosion traces and stout, smooth oxeas. Our data further imply that A. labyrinthica sensu Hancock has not yet been found in the Mediterranean. Aka labyrinthica sensu Topsent is a collection of different species not including A. labyrinthica sensu Hancock.


2018 ◽  
Vol 24 (1) ◽  
Author(s):  
JASWINDER KAUR ◽  
SATYA NARAIN

The floristic exploration and critical examination of specimens collected of family Convolvulaceae from Upper Gangetic Plains of India, resulted in addition of 2 new records for the flora viz. Ipomoea littoralis and Ipomoea capitellata var. multilobata. Detailed description, phenology, ecology, distribution, locality, field number, type specimens examined, illustrations and other relevant notes are provided.


2014 ◽  
Vol 41 (1) ◽  
pp. 113-123 ◽  
Author(s):  
Gary M. Fellers

Rollo Howard Beck (1870–1950) was a professional bird collector who spent most of his career on expeditions to the Channel Islands off southern California, the Galápagos Islands, South America, the South Pacific, and the Caribbean. Some of the expeditions lasted as long as ten years during which time he and his wife, Ida, were often working in primitive conditions on sailing vessels or camps set up on shore. Throughout these expeditions, Beck collected specimens for the California Academy of Sciences, the Museum of Vertebrate Zoology at Berkeley (California), the American Museum of Natural History, and the Walter Rothschild Museum at Tring, England. Beck was one of the premier collectors of his time and his contributions were recognized by having 17 taxa named becki in his honor. Of these taxa, Beck collected 15 of the type specimens.


2018 ◽  
Vol 14 (1) ◽  
pp. 25-34
Author(s):  
M. D. Zerova ◽  
S. A. Simutnik ◽  
V. N. Fursov ◽  
S. I. Klymenko ◽  
I. T. Stetsenko

The list of type specimens of chalcid wasps of four families (Eurytomidae, Torymidae, Ormyridae, Encyrtidae) described by experts of Schmalhausen Institute of Zoology of National Academy of Sciences after 2012 is given. Data of original labels and reference to original description are given for each taxon. The catalogue includes types of 41 nominal taxa: Eurytomidae (15): Nikanoria deserta Zer., N. halimodendrae Zer., N. kazakhstanica Zer., N. leleji Zer., N. mongolica punctata Zer., N. orski Zer., N. pygmaea Zer., N. sugonjaevi Zer., Parabuchophagus rasnitsyni Zer., Eurytoma gleditsiae Zer. et Furs., E. koreana Zer. et Furs., E. trjapitzini Zer. et Klym., Torymidae (5): Idiomacromerus artusis Zer., I. persimilis Zer., Adontomerus centaurei Zer., A. trjapitzini Zer., Torymus leleji Zer. et Furs., Ormyridae (8): Ormyrus askanicus Zer., O. kasparyani Zer., O. nitens Zer., O. novus Zer., O. punctellus Zer., O. qurrayahi Zer., O. spadiceus Zer., O. sugonjaevi Zer., Encyrtidae (13): Rovnosoma gracile Simut., Eocencnemus sugonjaevi Simut., E. vichrenkoi Simut., Eocencyrtus zerovae Simut., Microterys ashkhabadensis mediterraneus Simut., M. hermonicus Simut., M. nevoi Simut., M. pavliceki Simut., M. vichrenkoi Simut., M. wasseri Simut., Encyrtus sugonjaevi Simut., Echthroplexiella talitzkyi Trjapitzin, Copidosoma trjapitzini Simut. The majority of type specimens are deposited in the collection of Schmalhausen Institute of Zoology (Kyiv, Ukraine). The depositories of all other type specimens are indicated.


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