Three phyla—Two type specimens—One shell: History of a snail shell revealed by modern imaging technology

2019 ◽  
Vol 57 (3) ◽  
pp. 527-533
Author(s):  
Thomas Schwaha ◽  
Bernhard Ruthensteiner ◽  
Roland R. Melzer ◽  
Takahiro Asami ◽  
Barna Páll‐Gergely
Zootaxa ◽  
2018 ◽  
Vol 4512 (1) ◽  
pp. 1
Author(s):  
CHRISTINE M. KAISER ◽  
HINRICH KAISER ◽  
MARK O’SHEA

Since its conceptualization in 1854, 29 species of the colubrid genus Stegonotus have been recognized or described, of which 15 (admiraltiensis, batjanensis, borneensis, cucullatus, derooijae, diehli, florensis, guentheri, iridis, heterurus, melanolabiatus, modestus, muelleri, parvus, poechi) are still considered valid today. Original species descriptions for the members of this genus were published in Dutch, English, French, German, and Italian and, perhaps as a consequence of these polyglot origins, there has been a considerable amount of confusion over which species names should be applied to which populations of Stegonotus throughout its range across Borneo, the Philippines, Wallacea, New Guinea, Australia, and associated archipelagos. In addition, the terminology used to notate characteristics in the descriptions of these forms was not uniform and may have added to the taxonomic confusion. In this paper, we trace in detail the history of the type specimens, the species, and the synonyms currently associated with the genus Stegonotus and provide a basic, species-specific listing of their characteristics, derived from our examination of over 1500 museum specimens. Based on our data, we are able to limit the distribution of S. modestus to the islands of Ambon, Buru, and Seram in the central Moluccas of Indonesian Wallacea. We correct the type locality of S. cucullatus to the Manokwari area on the Bird’s Head Peninsula of West Papua, Indonesian New Guinea and designate a neotype for S. parvus, a species likely to be a regional endemic in the Schouten Archipelago of Cenderawasih Bay (formerly Geelvink Bay), Indonesian New Guinea. We unequivocally identify and explain the problematic localities of the type specimens of S. muelleri and Lycodon muelleri, which currently reside in the same specimen jar. We remove L. aruensis and L. lividum from the synonymy of S. modestus and recognize them as S. aruensis n. comb. and S. lividus n. comb., respectively. We remove S. keyensis and Zamenophis australis from the synonymy of S. cucullatus and recognize them as S. keyensis n. comb. and S. australis n. comb., respectively. We further remove S. reticulatus from the synonymy of S. cucullatus, S. dorsalis from the synonymy of S. diehli, and S. sutteri from the synonymy of S. florensis. We designate lectotypes for S. guentheri, S. heterurus, S. lividus, and S. reticulatus. Lastly, we introduce S. poechi, a valid species not mentioned in the scientific literature since its description in 1924. This brings the diversity in the genus Stegonotus to 22 species. We also caution that in a complex group of organisms like Stegonotus any rush to taxonomic judgment on the basis of molecular and incomplete morphological data sets may perpetuate errors and introduce incongruities. Only through the careful work of connecting type material with museum specimens and molecular data can the taxonomy and nomenclature of complex taxa be stabilized. 


2020 ◽  
Vol 14 (2) ◽  
pp. 435-459
Author(s):  
Harold W. Keller ◽  
Relf L. Price ◽  
Billy G. Stone ◽  
Edward D. Forrester

Arcyria versicolor (Trichiales: Trichiaceae) is a distinct myxomycete species described by William Phillips in 1877. The genus Arcyria dates back to Linnaeus in 1753 through the species A. denudata. Arcyria sporangia are brightly colored red, yellow, grey or white, mostly stalked, often in large groups easily seen with the naked eye. Approximately 54 species are known, many are common, and distributed worldwide. Collectors often encounter these colorful species on decaying logs as clusters of many sporangia often covering extensive areas. Arcyria versicolor, collected in the Valles Caldera National Preserve located in the Jemez Mountains of north central New Mexico, is a new record for the state. The nomenclatural history of this species is reviewed and the justification for selection of the species name versicolor is discussed. Arcyria versicolor is accepted as the valid species name and A. vitellina a synonym after examination of type specimens. Environmental parameters for coloration are discussed in general for fruiting bodies of Arcyria and more specifically for nivicolous snowbank species. Transitional stages of plasmodial color to mature fruiting body formation are described for Arcyria versicolor. More than 140 specimens of Arcyria versicolor fruiting bodies were examined with light microscopy and in part illustrated with multifocal computer stacked imaging. Higher magnifications were highlighted using scanning electron microscopy. A more complete and accurate species description is provided for Arcyria versicolor. Differences of fruiting body morphology including habit, color, dehiscence, peridial inner and outer surface features, capillitial ornamentation and size, spore color, size, and ornamentation, and stalk spore-like bodies are described and illustrated. Observation of type specimens from the type locality is illustrated, discussed, and nomenclatural evaluation given for the name selected. Mountain myxomycetes are reviewed based on the observations of T.H. Macbride and his early 1914 paper published in Mycologia. Collection data is presented that compares the dark-spored and light spored nivicolous myxomycetes in the French Alps. The history of renown collectors of nivicolous myxomycetes in western mountains of U.S.A. documents the discovery and study of this special ecological group of myxomycetes. This current paper is the first in a series from an ongoing research project entitled Myxomycetes of New Mexico.


Zootaxa ◽  
2018 ◽  
Vol 4478 (1) ◽  
pp. 1
Author(s):  
JOSÉ IVAN MOJICA ◽  
HENRY D. AGUDELO-ZAMORA

For the first time, the catalog of type specimens of ICN-MHN is presented with high resolution photographs. The catalog lists 87 species in 161 lots and includes 41 holotypes, 3 neotypes, and 117 lots of paratypes. Some doubts remain about type specimens of some species described by Miles and Dahl that were supposedly deposited at ICN-MHN. The history of the collection is reconstructed and valuable specimens once considered lost or destroyed have been rediscovered. The botanical and zoological collections of the ICN can be consulted online (http://www.biovirtual.unal.edu.co). 


2019 ◽  
Vol 110 (3) ◽  
pp. 340-351 ◽  
Author(s):  
Gary S. Taylor ◽  
Francesco Martoni

AbstractThe ‘Eugenia psyllid’ or ‘Lilly pilly psyllid’, widely recognized in Australia and in the USA as Trioza eugeniae Froggatt (Hemiptera: Triozidae), is not T. eugeniae, but rather T. adventicia Tuthill. In this study we assessed morphological comparisons of materials from throughout the native and introduced ranges and re-examined original descriptions of both taxa, together with Froggatt's type specimens of T. eugeniae. Furthermore, through DNA barcoding analyses, we confirmed the validity of both T. adventicia and T. eugeniae as separate species. We re-described both species to include additional characters not previously included and designated a lectotype for T. eugeniae. T. eugeniae has smaller fore wings that are slightly more elongate. These lack infuscation around veins R and R1, vein Rs is relatively longer, meeting the costa closer to the wing apex; with certain veins bearing long, fine divergent setae, a character not previously described. It has consistently three inner and one outer metatibial spurs. The male parameres appear narrowly pyriform with a weak dorsolateral lobe and weakly sclerotized apices. T. adventicia has larger fore wings that are slightly more ovate with dark infuscation around veins R and R1; vein Rs is relatively shorter, meeting the costa further from the wing apex, with veins lacking long, fine divergent setae. The usual configuration of two inner and one outer metatibial spurs, previously used to separate the two species, appears inconsistent. The male parameres appear a little more broadly pyriform with slightly more sclerotized apices. T. eugeniae refers to a distinct species which has a restricted distribution only in its native range in southern subcoastal New South Wales, Australia. T. adventicia refers to a separate species, with a natural distribution in eastern subcoastal Australia, but has been introduced widely in southern Australia, to New Zealand and the USA. This study elucidates a long history of misidentification of T. eugeniae in the nursery industry and in almost 30 years of literature on its biological control in the USA. Regardless, the biological control program, unknowingly, targeted the correct species of psyllid, T. adventicia, in its foreign exploration and importation of the appropriate parasitoid as a biocontrol agent in the USA. Despite being firmly entrenched in both the nursery trade and scientific literature, the name T. eugeniae is misapplied. While the acceptance of the valid name, T. adventicia, might be regarded as both problematic and protracted, this is the correct taxonomical attribution.


Mammalia ◽  
2019 ◽  
Vol 84 (1) ◽  
pp. 74-89 ◽  
Author(s):  
Kees Rookmaaker

Abstract The French pharmacist and explorer Christoph-Augustin Lamare-Picquot (1785–1873) was in South Asia during 1826–1829 to collect ethnographical, anthropological, zoological and botanical specimens. He made an excursion to the Sundarbans (the Ganges-Brahmaputra delta) of Bangladesh, where on 17 November 1828 his team shot a female rhinoceros and caught her young one the next day, just south of Khulna. Both animals were completely hornless. He returned to France in the spring of 1830, where his zoological specimens were assessed by Georges Cuvier, and his other collections relating to ethnography by other scholars. All recommended purchase by the French Government, but circumstances did not allow this. A few animals were described by scientists connected with the Natural History Museum in Paris. After Lamare-Picquot published an account of the hunting expedition in 1835, the rhinoceros was described as a new species Rhinoceros inermis, by René-Primivère Lesson, first in a supplement to Buffon dated 1836, and not, as accepted until now, in restatements dating from 1838 or later. The main part of the zoological collection was bought by the Prussian King Friedrich Wilhelm III in 1836 and integrated in museums in Berlin. Other collections were exhibited as a “Panthéon Indien” in Vienna and Bratislava from 1838, until they were purchased by the Bavarian King Ludwig in 1841, and added to a museum in Munich. The type specimens of R. inermis are still preserved in the Museum für Naturkunde in Berlin. The adult female (ZMB_Mam_1957) was selected as the lectotype.


Phytotaxa ◽  
2017 ◽  
Vol 299 (1) ◽  
pp. 132
Author(s):  
ANDREA D. WOLFE

Hyobanche sanguinea (Orobanchaceae) is a member of a small genus of holoparasitic plants endemic to southern Africa. The description by Linnaeus in 1771 did not include a designated holotype, and no such material has been located in the Linnaean herbaria housed in London or Uppsala. After studying the Linnaean collection of Hyobanche specimens, and researching the history of botany in South Africa, a lectotype is here designated, and an epitype from the Cape Peninsula assigned. In addition, a study of type specimens for H. calvescens, H. glabrata, and H. rubra reveals that the type specimens for H. calvescens and H. glabrata fall within the circumscription of H. rubra, resulting in synonymization of both names.


Paleobiology ◽  
1992 ◽  
Vol 18 (1) ◽  
pp. 50-79 ◽  
Author(s):  
Benjamin J. Greenstein

The class Echinoidea apparently originated during the Ordovician Period and diversified slowly through the Paleozoic Era. The clade then mushroomed in diversity beginning in Late Triassic time and continued expanding into the present. Although this evolutionary history is generally accepted, the taphonomic overprint affecting it has not been explored. To gain a more accurate perception of the evolutionary history of the group, I have compared the diversity history of the family Cidaridae (Echinodermata: Echinoidea) with the preservational style of fossil type species using literature-derived data. The Cidaridae apparently originated in Middle Triassic time and diversified slowly through the Neocomian (Early Cretaceous). Diversity was maintained through the remainder of the Cretaceous and Tertiary Periods, reflecting the diversity history of the subclass. Characterization of the preservational style of type fossil material for the family revealed the following breakdown of preservational states: 60% of species were described on the basis of disarticulated skeletal material, primarily spines; 20% based on intact coronas denuded of spines, apical system, Aristotle's lantern and peristomial plates; 10% based on large coronal fragments; and 10% based on other skeletal elements. This distribution may represent the effect of a disarticulation threshold on the condition of echinoid carcasses before final burial and suggests that preservation of intact specimens may be very unlikely. For cidaroids, previous work has suggested that this threshold is likely to be reached after 7 days of decay.Comparison of the diversity history of the Cidaridae with the preservation data reveals that characteristic patterns of taphonomic overprint have affected the group since its origination in Middle Triassic time, and the nature of that overprint has changed over time: the early diversity history of the group is characterized by occurrences of fragmented fossil material, with spines predominant; further radiation of the group in mid-Jurassic time coincided with an increase in modes of preservation, ranging between exceptionally well-preserved material and disarticulated skeletal elements. Finally, type material is more rarely described from younger stratigraphic intervals (Miocene–Pleistocene) and consists predominantly of disarticulated skeletal elements and coronal fragments larger than an interambulacrum in size. Intact, denuded coronas are noticeably lacking.The number of type species of Cidaridae described in each stratigraphic interval has not been consistent during post-Paleozoic time. Middle Triassic, Malm (Upper Jurassic), Senonian (Upper Cretaceous) and Eocene series yielded significantly (α = .05) higher numbers of type specimens per million years, while the Lias (Lower Jurassic), Dogger (Mid-Jurassic), Lower Cretaceous and Paleocene yielded significantly (α = .05) lower numbers of type specimens per million years. This may be the result of a combination of taxonomic, sampling, and geographical biases.


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