Rediagnosis of the squat lobster genus Gastroptychus Caullery, 1896, with a new genus Sternostylus and a new family Sternostylidae (Crustacea: Decapoda: Anomura: Chirostyloidea)

Zootaxa ◽  
2018 ◽  
Vol 4524 (1) ◽  
pp. 77 ◽  
Author(s):  
KEIJI BABA ◽  
SHANE T. AHYONG ◽  
KAREEN E. SCHNABEL

The chirostyloidean squat lobster genus Gastroptychus Caullery, 1896 is revised and is split into two genera: Gastroptychus sensu stricto (type species, Ptychogaster spinifer A. Milne-Edwards, 1880) and Sternostylus new genus (type species, Ptychogaster formosus Filhol, 1884). Gastroptychus sensu stricto, is restricted to nine species with a sternal plastron, at sternite 3, abruptly demarcated from the preceding sternites (excavated sternum) by a distinct step forming a well-defined transverse or concave anterior margin at the articulation with maxillipeds 3, the maxillipeds 3 widely separated, with the distal parts accommodated in the excavated sternum between the left and right maxillipeds 3 when folded, and the P2–4 dactyli with the terminal spine demarcated by a suture. Sternostylus new genus, represented by 12 species, has the sternite 3 anteriorly bluntly produced medially and steeply sloping anterodorsally to the anterior sternite, with a pair of spines directly behind the anterior margin, the left and right maxillipeds 3 adjacent, and the P2–4 dactyli ending in an indistinctly demarcated corneous spine. The above-mentioned characters of Gastroptychus are consistent with Chirostylidae sensu stricto. Published molecular phylogenies indicate, however, that Sternostylus is the sister group to all the other Chirostylidae, and is designated the type genus of a new family, Sternostylidae. 

Phytotaxa ◽  
2014 ◽  
Vol 181 (4) ◽  
pp. 238 ◽  
Author(s):  
Maarten J.M. Christenhusz ◽  
Samuel F. Brockington ◽  
Pascal-Antoine Christin ◽  
Rowan F. Sage

Molecular studies have shown that Molluginaceae in the traditional sense is polyphyletic. Several genera have already been separated into various families (e.g. Caryophyllaceae, Limeaceae, Lophiocarpaceae, Microteaceae), but recent studies have shown that Macarthuria and Hypertelis also make Molluginaceae polyphyletic if they remain to be included in this family. Hypertelis is biphyletic, with its type species found to belong to Molluginaceae sensu stricto, but the remainder of the genus is to be placed elsewhere. Therefore a new genus, Kewa, is proposed for the rest of Hypertelis, and two new family names are coined: Kewaceae and Macarthuriaceae, which are here morphologically characterized.


2021 ◽  
Author(s):  
Stephen D. Cairns ◽  
Ralf T. S. Cordeiro ◽  
Yu Xu ◽  
Zifeng Zhan ◽  
Philip Alderslade

Golden corals (chrysogorgiids sensu lato) are conspicuous components in deep-sea gorgonian assemblages. Although common, their taxonomy still conflicts with evolutionary histories, mostly due to low character availability and poor taxonomic knowledge. This is the case for the genus Pleurogorgia, which has been frequently reported in ROV surveys, dominating hard-bottoms throughout the Indo-Pacific. Herein, molecular phylogenetic reconstructions based on mitochondrial and nuclear datasets, and examination of new and old type material led us to suggest new systematic arrangements for some of the genera. We create a new genus, Ramuligorgia, to accommodate Pleurogorgia militaris, redescribing it as Ramuligorgia militaris comb. nov. within the family Chrysogorgiidae sensu stricto. Additionally, we describe Aurogorgia tasmaniensis gen. nov. et sp. nov., including it and the type species, Pleurogorgia plana, within Pleurogorgiidae fam. nov.


2020 ◽  
Vol 51 (3) ◽  
pp. 444-471 ◽  
Author(s):  
Lauri Kaila ◽  
Kari Nupponen ◽  
Pavel Yu. Gorbunov ◽  
Marko Mutanen ◽  
Maria Heikkilä

Ustyurtiidae Kaila, Heikkilä & Nupponen, a new family of Urodoidea is introduced. The family is based on the genus Ustyurtia Kaila, Heikkilä & Nupponen, gen. n. The genus includes the type species U. zygophyllivora Kaila, Heikkilä & Nupponen, sp. n. and U. charynica Kaila, Heikkilä & Nupponen, sp. n., both from Kazakhstan. These two species, in particular the immature stages, have morphological attributes apomorphic of Urodoidea. The close affinity is also supported by DNA data based on several markers. We consider this new family warranted due to its sister group position to the remaining Urodoidea and a number of significant morphological differences in wing venation, male genitalia and the structure of the cocoon, apomorphic for Ustyurtiidae on the basis of an earlier published phylogeny. All other recognized genera of Urodoidea belong to the family Urodidae. The closest relatives and phylogenetic position of Urodoidea are not firmly established, but Urodoidea and Schreckensteinioidea have morphological similarities which, in the light of genetic analyses appear synapomorphic and possibly uniting these groups, rather than homoplasious as assumed earlier. The affinities of these superfamilies are discussed.


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.


2007 ◽  
Vol 44 (10) ◽  
pp. 1479-1501 ◽  
Author(s):  
John Pojeta Jr. ◽  
Christopher A Stott

The new Ordovician palaeotaxodont family Nucularcidae and the new genus Nucularca are described. Included in Nucularca are four previously described species that have taxodont dentition: N. cingulata (Ulrich) (the type species), N. pectunculoides (Hall), N. lorrainensis (Foerste), and N. gorensis (Foerste). All four species are of Late Ordovician (Cincinnatian Katian) age and occur in eastern Canada and the northeastern USA. Ctenodonta borealis Foerste is regarded as a subjective synonym of Nucularca lorrainensis. No new species names are proposed. The Nucularcidae includes the genera Nucularca and Sthenodonta Pojeta and Gilbert-Tomlinson (1977). Sthenodonta occurs in central Australia in rocks of Middle Ordovician (Darriwilian) age. The 12 family group names previously proposed for Ordovician palaeotaxodonts having taxodont dentition are reviewed and evaluated in the Appendix.


1956 ◽  
Vol 34 (4) ◽  
pp. 675-687 ◽  
Author(s):  
Roy F. Cain

Phaeotrichum hystricinum Cain and Barr is described from specimens collected in Ontario, Vermont, New York, and Michigan and is made the type species of a new genus. It has been found on porcupine dung from numerous localities. The black, shining, superficial ascocarps are covered with scattered straight black appendages. The clavate stalked asci are in irregular fascicles, eight spored, and with a firm wall which is evanescent at maturity. The ascospores are two-celled, thick-walled, deeply constricted, and readily separating at the transverse septum. There is a large conspicuous germ pore at each end of the ascospore. P. circinatum Cain is described from specimens collected on lemming dung in Northern Ungava, Quebec. This species is distinguished from the former by means of the appendages, which are stouter and curved at the apex. These two species are closely related and very similar to the ostiolate Trichodelitschia bisporula (Crouan) Munk. The new genus is made the type of a new family of cleistocarpous Ascoloculares, with a discussion on the evolution, in many Ascomycete taxa, of cleistocarps adapted either to the utilization of special agencies, rather than air currents, for carrying the ascospores or to delayed dispersal.


Zootaxa ◽  
2009 ◽  
Vol 2052 (1) ◽  
pp. 1-31 ◽  
Author(s):  
CHRISTIANA KLINGENBERG ◽  
C. ROBERTO F. BRANDÃO

Based on the morphology of workers, gynes and males, we revise the taxonomy of nominal taxa traditionally included by authors in the fungus-growing ant genus Mycetophylax. Our results indicate that Mycetophylax Emery (Myrmicocrypta brittoni Wheeler, 1907, type species, by designation of Emery, 1913; junior synonym of Cyphomyrmex conformis Mayr, 1884 by Kempf, 1962) includes M. conformis, M. simplex (Emery, 1888), and M. morschi (Emery, 1888) new combination (formerly in Cyphomyrmex), with several synonymies. Mycetophylax bruchi (Santschi, 1916) does not belong to the same genus and is diagnosed, in addition to other characters, by a psammophore arising at the anterior margin of the clypeus. For this species we are resurrecting from synonymy Paramycetophylax Kusnezov, 1956 (Mycetophylax bruchi as type species, by original designation, with M. cristulatus as its new synonym). Myrmicocrypta emeryi Forel, 1907 is the only attine in which females lack the median clypeal seta and have the antennal insertion areas very much enlarged and anteriorly produced, with the psammophore setae arising from the middle of the clypeus and not at its anterior margin as in Paramycetophylax. Notwithstanding its inclusion in Mycetophylax by recent authors, it is here recognized as belonging to a hitherto undescribed, thus far monotypic genus, Kalathomyrmex new genus (Myrmicocrypta emeryi as its type species, here designated). We redescribe workers, gynes and males of all species in the


2010 ◽  
Vol 60 (2) ◽  
pp. 460-468 ◽  
Author(s):  
Miao Miao ◽  
Yangang Wang ◽  
Weibo Song ◽  
John C. Clamp ◽  
Khaled A. S. Al-Rasheid

Recently, an undescribed marine ciliate was isolated from China. Investigation of its morphology and infraciliature revealed it as an undescribed species representing a new genus, Eurystomatella n. gen., the type of the new family Eurystomatellidae n. fam. The new family is defined by close-set, apically positioned oral membranelles and a dominant buccal field that is surrounded by an almost completely circular paroral membrane. The new genus is defined by having a small oral membranelle 1 (M1), bipartite M2 and well-developed M3, a body surface faintly sculptured with a silverline system in a quadrangular, reticulate pattern and a cytostome located at the anterior third of a large buccal field. The type species of the new genus, Eurystomatella sinica n. sp., is a morphologically unique form that is defined mainly by the combination of a conspicuously flattened body, several caudal cilia, extremely long cilia associated with the buccal apparatus and a contractile vacuole located subcaudally. According to phylogenetic analyses of small-subunit (SSU) rRNA gene sequences, Eurystomatella clusters with the genus Cyclidium, as a sister group to the family Pleuronematidae. The great divergence in both buccal and somatic ciliature between Eurystomatella and all other known scuticociliates supports the establishment of a new family for Eurystomatella.


Zootaxa ◽  
2009 ◽  
Vol 2096 (1) ◽  
pp. 287-298 ◽  
Author(s):  
ELKE WILLEN ◽  
JANINE DITTMAR

A new species of the new genus Keraia gen. nov. from the Guinea Basin is described in the present paper. The new taxon belongs to the Pseudomesochrinae Willen, 1996, which until now has contained only the genus Pseudomesochra T. Scott, 1902. Both genera are prevalent in the deep sea. Whereas Pseudomesochra reaches quite high individual and species numbers in the investigated samples of the DIVA 1, DIVA 2 and ANDEEP deep-sea expeditions, Keraia is found only occasionally and as single specimens. Keraia is characterised among others by a modified antenna exopodite and the shape of P1. Pseudomesochra on the other hand can still be identified as a monophylum by specialised setation on the P1 endopodite and the lack of the inner setae of the first segment of swimming leg exopodites. Other species of Keraia gen. nov. are K. longiseta (Vasconcelos, George & Santos 2008) and the type species K. tamara (Smirnov, 1946). The available records implicate a widespread occurrence of Keraia gen. nov. from the northern to the southern Atlantic, and even reaching both northern and southern polar regions. Up to now all individuals that have been found occur exclusively at deep-sea sites and in very low abundances.


Zootaxa ◽  
2008 ◽  
Vol 1730 (1) ◽  
pp. 1 ◽  
Author(s):  
GARY A. P. GIBSON

Leptoomus janzeni, n. gen. and n. sp., is described from 5 females and 2 males in 7 pieces of Baltic amber. An enlarged acropleuron forming the entire mesopleuron places the taxon within Eupelmidae, Tanaostigmatidae or Encyrtidae (Chalcidoidea), but it has a unique combination of features that differentiates it from extant members of these families. Its structural features are compared with those that characterize the three families and it is postulated to be the sister group of Tanaostigmatidae sensu stricto + (Cynipencyrtus + Encyrtidae) based on relative structure of its pronotum, prepectus and mesothoracic spiracle, and retention of two other putative symplesiomorphies, the presence of complete furrowlike notauli and a protibial apical spicule. Conflicting character states indicate other possible relationships, including a sistergroup relationship with Cynipencyrtus + Encyrtidae based on transverse-triangular axillae and a flagellum having only seven funicular segments, or with Tanaostigmatidae s. s. based on presence of an externally visible prepectal pouch, or possibly forming a monophyletic group with Tanaostigmatidae s. s. + Cynipencyrtus based on combined acropleuralmetacoxal structure. Several features support the monophyly of Tanaostigmatidae s. s., that is excluding Cynipencyrtus and Leptoomus, but these two genera are both classified in Tanaostigmatidae sensu lato until relationships are resolved more conclusively. Features possessed by different members of Neanastatinae (Eupelmidae) suggest that this subfamily may be closely related to Tanaostigmatidae s. l. + Encyrtidae, but possible relationships of Tanaostigmatidae s. s. are also discussed if its enlarged acropleuron and other skeletomusculature features associated with jumping are convergent to similar features in the other taxa.


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