A new genus of ichthyosaur from the Late Triassic Pardonet Formation of British Columbia: bridging the Triassic Jurassic gap

2001 ◽  
Vol 38 (6) ◽  
pp. 983-1002 ◽  
Author(s):  
Elizabeth L Nicholls ◽  
Makoto Manabe

Both the genus Shastasaurus and the family Shastasauridae have long been hard to define due to the fragmentary nature of the type specimens. Consequently, recent interpretations of the genus have been based almost entirely on Shastasaurus neoscapularis from the Late Triassic Pardonet Formation of British Columbia. Two new specimens of this taxon, from Pink Mountain, British Columbia, demonstrate that it does not belong in the genus Shastasaurus. This paper describes the new specimens, and refers the species to Metashastasaurus gen nov. Post-cranially, the skeleton of Metashastasaurus resembles that of shastasaurids, differing primarily only in the shape of the scapula and fibula. However, the skull has a unique combination of characters, including large diamond-shaped frontals that enter the supratemporal fenestrae, and very narrow posterior extensions of the nasals, which contact the postfrontals. It also differs from the skull of Shastasaurus in the presence of both a parietal ridge and postparietal shelf. This is a combination of derived characters previously known only in Jurassic forms. The front limb has four proximal carpals and four digits, indicating that previous reconstructions were based on incomplete material. Shastasaurus pacificus Merriam 1895, the type species of the genus Shastasaurus, must be considered a nomen dubium, making the genus Shastasaurus invalid. Until this problem is clarified, the use of the generic name Shastasaurus should be restricted to Merriam's type specimens, of which only Shastasaurus alexandrae and Shastasaurus osmonti are based on adequate material.

2018 ◽  
Vol 2018 ◽  
pp. 1-12 ◽  
Author(s):  
Richard S. Kelly ◽  
Andrew J. Ross ◽  
Robert A. Coram

Species previously attributed to Necrotauliidae are revised from the Late Triassic and Early Jurassic of England based on examination of type specimens and non-type material. The necrotauliids have been considered as a basal family of caddisflies (Trichoptera) or as a paraphyletic assemblage of stem-amphiesmenopterans. Herein a new genus, Austaulius, is erected which includes all Lilstock Formation∖Lower Lias material from England; the previously described species are synonymized with A. furcatus and a new species, A. haustrum, is described from the Dorset Coast, the holotype of which preserves synapomorphic traits of the Trichoptera not previously described suggesting that the family is trichopteran. The type genus remains Necrotaulius and type species N. parvulus (Geinitz, 1884) from the type locality of Dobbertin, Germany. One species of Necrotaulius is represented in the UK, N. parvulus, which is found in the Upper Lias.


1988 ◽  
Vol 62 (2) ◽  
pp. 218-233 ◽  
Author(s):  
John Mark Malinky

Concepts of the family Hyolithidae Nicholson fide Fisher and the genera Hyolithes Eichwald and Orthotheca Novak have been expanded through time to encompass a variety of morphologically dissimilar shells. The Hyolithidae is here considered to include only those hyolithid species which have a rounded (convex) dorsum; slopes on the dorsum are inflated, and the venter may be flat or slightly inflated. Hyolithes encompasses species which possess a low dorsum and a prominent longitudinal sulcus along each edge of the dorsum; the ligula is short and the apertural rim is flared. The emended concept of Orthotheca includes only those species of orthothecid hyoliths which have a subtriangular transverse outline and longitudinal lirae covering the shell on both dorsum and venter.Eighteen species of Hyolithes and one species of Orthotheca from the Appalachian region and Western Interior were reexamined in light of more modern taxonomic concepts and standards of quality for type material. Reexamination of type specimens of H. similis Walcott from the Lower Cambrian of Newfoundland, H. whitei Resser from the Lower Cambrian of Nevada, H. billingsi Walcott from the Lower Cambrian of Nevada, H. gallatinensis Resser from the Upper Cambrian of Wyoming, and H. partitus Resser from the Middle Cambrian of Alabama indicates that none of these species represents Hyolithes. Hyolithes similis is here included under the new genus Similotheca, in the new family Similothecidae. Hyolithes whitei is designated as the type species of the new genus Nevadotheca, to which H. billingsi may also belong. Hyolithes gallatinensis is referred to Burithes Missarzhevsky with question, and H. partitus may represent Joachimilites Marek. The type or types of H. attenuatus Walcott, H. cecrops Walcott, H. comptus Howell, H. cowanensis Resser, H. curticei Resser, H. idahoensis Resser, H. prolixus Resser, H. resseri Howell, H. shaleri Walcott, H. terranovicus Walcott, and H. wanneri Resser and Howell lack shells and/or other taxonomically important features such as a complete aperture, rendering the diagnoses of these species incomplete. Their names should only be used for the type specimens until better preserved topotypes become available for study. Morphology of the types of H.? corrugatus Walcott and “Orthotheca” sola Resser does not support placement in the Hyolitha; the affinities of these species are uncertain.


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.


Zootaxa ◽  
2021 ◽  
Vol 4958 (1) ◽  
pp. 702-712
Author(s):  
MARCOS ROCA-CUSACHS ◽  
MERCEDES PARIS ◽  
ALMA MOHAGAN ◽  
SUNGHOON JUNG

A new species of Urostylididae from the Philippine islands (Mindanao) is herein described. This new species, similar to Urolabida bipunctata Stål, 1871, differs from the latter in the shape of the external male genitalia. Urolabida bipunctata and the new species, Urolabida graziae Roca-Cusachs, sp. nov., are extremely similar in external appearance, and fit into the (incomplete) description of genus Urolabida Westwood, 1837. The examination and comparison with the type specimens of other Urostylididae species, especially the male genital capsule, clearly separates this two species from Urolabida tenera Westwood, 1837, the type species of the genus Urolabida, however the taxonomy of this group is not resolved and needs a deep revision, therefore we refrain from description of a new genus-group taxon here. Additionally, images of the type specimens of Urolabida tenera, Urostylis histrionica Westwood, 1837, and Urostylis punctigera Westwood, 1837, are provided and discussion on the current systematics and classification of the family, and particularly of genus Urolabida are also given. 


Phytotaxa ◽  
2021 ◽  
Vol 482 (3) ◽  
pp. 291-292
Author(s):  
UMAKANT BHOOPATI DESHMUKH

The generic name Udaria Gupta (1996:103) was established by Gupta (1996) with two fossil fungi species Udaria singhii Gupta (1996:103) and U. saxenae Gupta (1996:104) from Lower Tertiary sediments of Himachal Pradesh, India. Later on, Singh et al. (2018) described the new genus of liverworts, Udaria Singh, Majumdar & Singh (2018: 1537)   with the single species Udaria lamellicaulis Singh, Majumdar & Singh (2018: 1537) to the family Lophocoleaceae Vanden Berghen (1956: 208) from Arunachal Pradesh and Sikkim in Eastern Himalaya, India. After a thorough scrutiny of literature and type specimens, it was found that the liverwort genus name, Udaria Singh, Majumdar & Singh (2018: 1537) is illegitimate as it is a later homonym of the fossil fungi genus Udaria Gupta (1996:103). Therefore, a new replacement name Pandea U. B. Deshmukh is proposed with a new combination for the type species here in accordance with article 53.1 of Shenzhen Code (Turland et al. 2018).


Phytotaxa ◽  
2021 ◽  
Vol 513 (2) ◽  
pp. 118-128
Author(s):  
WEN-LI LI ◽  
DAN-FENG BAO ◽  
NING-GUO LIU ◽  
KEVIN D. HYDE ◽  
JIAN-KUI LIU

A novel hyphomycetous genus collected from submerged wood in a freshwater stream in Thailand is introduced. The fungus is similar to Tetraplosphaeriaceae species in having subglobose conidial body and elongated setose appendages arising from conidial body. However, its unique combination of macronematous conidiophores and conidia composed with several columns of cells differs it from other genera in Tetraplosphaeriaceae. The phylogenetic analysis based on a combined LSU, ITS and SSU sequence data indicated that our two strains formed a distinct lineage in the family and they cannot be assigned to any existing genera. Therefore, we introduce a new genus Aquatisphaeria to accommodate the new taxa with A. thailandica as the type species. The detailed description, illustration and comparison with related taxa are provided.


Zootaxa ◽  
2012 ◽  
Vol 3595 (1) ◽  
pp. 1 ◽  
Author(s):  
RONALD M. CLOUSE

The taxonomy of the Southeast Asian mite harvestman family Stylocellidae is updated in light of new molecular and mor-phometric phylogenies, examinations of type specimens, and a new species from Thailand. A new genus, Giribetia gen.nov., is erected, and Fangensis insulanus Schwendinger & Giribet, 2005, recombined in it as Giribetia insulana newcomb. All species in the genus Stylocellus have been recombined in Miopsalis and Leptopsalis, except for the type species,S. sumatranus Westwood, 1874, and a new species, S. lornei, sp. nov., described here. The new recombinations of formerStylocellus species are as follows: Leptopsalis pangrango (Shear, 1993), new comb., Leptopsalis sedgwicki (Shear, 1979),new comb., Leptopsalis laevichelis (Roewer, 1942), new comb., Miopsalis globosa (Schwendinger & Giribet, 2004), newcomb., Miopsalis kinabalu (Shear, 1993), new comb., Miopsalis leakeyi (Shear, 1993), new comb., Miopsalis mulu(Shear, 1993), new comb., and Miopsalis pocockii (Hansen & Sørensen, 1904), new comb. “Stylocellus” spinifronsRoewer, 1942 is now designated as nomen dubium, as the sole type specimen has been found to be a juvenile. Two newsubfamilies are proposed, each with two genera: Fangensinae subfam. nov., containing Fangensis and Giribetia, and Lep-topsalinae subfam. nov., containing Leptopsalis and Miopsalis. The subfamily sensu strictu Stylocellinae contains the remaining two genera: Stylocellus and Meghalaya


Zootaxa ◽  
2017 ◽  
Vol 4362 (4) ◽  
pp. 517
Author(s):  
FRANCISCO LIMEIRA-DE-OLIVEIRA ◽  
DAYSE W. A. MARQUES ◽  
GENIANA A. REIS ◽  
JOSÉ A. RAFAEL

A new genus and five new species of odiniids (Odiniidae: Traginopinae) are described from the Brazilian Amazon and Cerrado biomes: Inpauema mirador gen. nov. et sp. nov. (type species), I. catarinae sp. nov., I. gaimarii sp. nov., I. raimundoluizi sp. nov., and I. xavieri sp. nov. The genus is being characterized by a unique combination of diagnostic characters: body predominantly dark brown to black, with silvery-gray pruinose spots on inner margin of eyes, longitudinally along middle of lunule and face, on notopleuron and mesopleuron; postcranium concave from dorsal view; one pair of stout proclinate ocellar setae; postocellar setae absent; lunule shorter than frons; gena lacking upturned seta; antennae separated by a maximum distance of 2X the diameter of a single antennal socket and gonocoxal apodemes directed upward, forming an arch. A key to separate Helgreelia Gaimari, 2007 from Inpauema gen. nov. and for the new species is provided. 


Zootaxa ◽  
2018 ◽  
Vol 4540 (1) ◽  
pp. 7
Author(s):  
BEVERLY S. GERDEMAN ◽  
RUFINO C. GARCIA ◽  
ANDREW HERCZAK ◽  
HANS KLOMPEN

The generic classification of millipede associated Heterozerconidae in the Oriental region is revised. The genus Allozercon Vitzthum is re-diagnosed and Asioheterozercon Fain is designated as an subjective junior synonym of Allozercon. Philippinozercon gen. nov., with the type species P. makilingensis sp. nov., is described for all instars. This genus may be endemic for the Philippines, but is quite widespread in that country. All immature instars are described, making this the second species of Heterozerconidae known for all instars. The morphology of the immatures is compared with that of immatures of the temperate species Narceoheterozercon ohioensis and unnamed species from Brazil and Thailand. All immatures were collected from millipede frass and litter, never from millipedes. Adults are associated with millipedes in the family Trigoniulidae (Spirobolida). 


2020 ◽  
Vol 6 ◽  
pp. 583-594 ◽  
Author(s):  
Yuri M. Marusik ◽  
Alexander A. Fomichev

A new genus, Platnickgen. n., with three new species, P. shablyaisp. n. (♂, type species), P. astanasp. n. (♀) and P. sangloksp. n. (♀), are described from Tajikistan. The male of the type species has a unique pair of longitudinal ventral postgastral scuta. Females have such scuta also, but they are much shorter. The new genus is placed in Liocranidae Simon, 1897. A discussion on the subfamilies of Liocranidae and comments on the family-group names are provided.


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