The Nearctic caddisfly genus Hesperophylax Banks (Trichoptera: Limnephilidae)

1985 ◽  
Vol 63 (10) ◽  
pp. 2443-2472 ◽  
Author(s):  
C. R. Parker ◽  
G. B. Wiggins

Seven species of Hesperophylax are recognized: alaskensis (Banks), consimilis (Banks), designatus (Walker), magnus Banks, minutus Ling, occidentalis (Banks), and mexico n.sp. Hesperophylax alaskensis is reestablished as a valid species distinct from occidentalis. Hesperophylax incisus Banks is placed as a junior subjective synonym of designatus. Hesperophylax oreades Saether is placed as a junior subjective synonym of Psychoronia costalis (Banks). Keys are provided for identification of males, females, and larvae. A hypothesis of phylogeny is proposed in which consimilis is the sister group of all other Hesperophylax; magnus and mexico are sister species and together are the closest relatives of occidentalis, designatus, and alaskensis; designatus and alaskensis are sister species. An interpretation of biogeography is offered, suggesting how geological events affected the origin and distribution of Hesperophylax species. Data on food, life cycle, habitat, and distribution are given. All species appear to be univoltine with extended flight periods. Larvae are opportunistic omnivores, but magnus is more predaceous than the other species. Differences in mandibular morphology between consimilis and the other species are not reflected in the food habits of the larvae. Among Trichoptera the species of Hesperophylax are little differentiated morphologically and most species vary within unusually broad limits; most species occur in a wider range of habitat types than do other Trichoptera. Perhaps those factors represent a genetic plasticity selected for generalized adaptability rather than the habitat specialization of other Trichoptera.

2000 ◽  
Vol 13 (3) ◽  
pp. 437 ◽  
Author(s):  
Karen E. Wills ◽  
R. D. B. Whalley ◽  
Jeremy J. Bruhl

The taxonomy ofHomopholis C.E.Hubb. is revised, and anew genus Whalleya K.E.Wills & J.J.Bruhl isdescribed. Relationships among the known species ofHomopholis (H. belsonii C.E.Hubb.,H. proluta F.Muell., and a putative species,H. sp. nov.), and the relationships betweenHomopholis and other genera within the Paniceae were investigated. Morphological and anatomical data forHomopholis and selected species ofDigitaria and Panicum were analysed phenetically and cladistically. The value and contribution ofcharacters to the findings were assessed. In the phenetic analyses, threedistinct clusters of species were formed. The first cluster includedDigitaria coenicola (F.Muell.) Hughes,D. divaricatissima (R.Br.) Hughes andD. papposa (R.Br.) P.Beauv.; the second,Panicum effusum R.Br.,P. queenslandicum Domin var.queenslandicum and P. simileDomin; and the third, H. sp. nov.,H. proluta, H. belsonii andP. subxerophilum Domin. Specimens ofH. belsonii noticeably separated from the other threespecies. For the cladistic analyses, species ofEntolasia and Thyridolepis were used as outgroup taxa. One most parsimonious tree was produced.Homopholis belsonii was well supported as the most basalmember of the ingroup. The three species ofDigitariaformed a well-supported clade.Panicum effusum, P. queenslandicumvar. queenslandicum and P. simileformed a well-supported clade, and were the sister group toEntolasia marginata (R.Br.) Hughes andE. stricta (R.Br.) Hughes.Panicum subxerophilum was in a clade (=Whalleya) with H. sp. nov. andH. proluta, with P. subxerophilumand H. proluta as sister species.


1996 ◽  
Vol 27 (4) ◽  
pp. 441-479 ◽  
Author(s):  
Ole A. Sæther ◽  

AbstractGeneric diagnoses to all stages of the genus Propsilocerus Kieffer, 1923 (= Tokunagayusurika Sasa, 1978, syn. n.) are given. Parsimony analyses of the primitive orthoclads show that either the more plesiomorphic genera of Orthocladiinae form a monophyletic group or Propsilocerus may be more closely related to less plesiomorphic groups. Chasmatonotus Loew forms its likely sister group. The genus is monophyletic in all cladograms. A synapomorphic diagram for Propsilocerus shows P. sinicus sp. n. forming the sister species of the other four species. Keys are given to all stages. Propsilocerus sinicus is described from male and female imagines and as pupa; P. akamusi (Tokunaga) is redescribed in all stages and in all larval instars; P. taihuensis (Wen, Zhou & Rong) comb. n. as male and female; P. paradoxus (Lundström) as male, female and pupa; and P. lacustris Kieffer is described in all stages.


Zootaxa ◽  
2008 ◽  
Vol 1703 (1) ◽  
pp. 25 ◽  
Author(s):  
PIERRE-ANDRÉ CROCHET ◽  
JENS B. RASMUSSEN ◽  
THOMAS WILMS ◽  
PHILIPPE GENIEZ ◽  
JEAN-FRANÇOIS TRAPE ◽  
...  

The systematics and nomenclature of the genus Telescopus in north Africa (the dhara – obtusus – tripolitanus group) have been revised based on examination of the original descriptions and type specimens (when still extant) of all proposed nomina and of more than 100 specimens. Using colour and lepidosis characters, the following taxonomic decisions are proposed: 1. Telescopus tripolitanus (Werner, 1909) is considered a valid species. 2. Tarbophis guidimakaensis Chabanaud, 1916 is a junior subjective synonym of T. tripolitanus. 3. Pseudotarbophis gabesi Domergue, 1955 is a junior subjective synonym of T. tripolitanus. 4. “Pseudotarbophis gabesiensis” Domergue, 1959 is an incorrect subsequent spelling and is thus not an available nomen. 5. Telescopus dhara dhara (Forsskål, 1775), Telescopus dhara obtusus (Reuss, 1834) and Telescopus dhara somalicus (Parker, 1949) are valid, clearly diagnosable, allopatric taxa that we provisionally maintain at subspecific rank. 6. Tarbophis guentheri, Anderson, 1895 is a junior subjective synonym of T. dhara dhara. 7. Telescopus gezirae Broadley 1994 is maintained as a valid species.


1982 ◽  
Vol 60 (5) ◽  
pp. 754-763 ◽  
Author(s):  
Richard Winterbottom

The genus Halidesmus is unique within the Congrogadidae in the possession of three lateral lines. The three species are described, diagnosed, and illustrated, and a key to the species is provided. One of these species, from Kenya, is described as new and is distinguished from the other two species in lacking scales on the cheek and nape, in having 11 suborbital pores, and in the degree of development and form of the lateral lines and associated pores. A tentative hypothesis of relationships is proposed, based primarily on lateral-line structure, relating H. scapularis to Halidesmus polytretus n. sp. as sister species together forming the sister group of H. thomaseni.


Zootaxa ◽  
2020 ◽  
Vol 4801 (2) ◽  
pp. 280-290
Author(s):  
HIDEYUKI CHIBA ◽  
HIROSHI TSUKIYAMA ◽  
JIA-YUAN LIANG ◽  
SHOU-MING WANG ◽  
ZONG-YU SHEN ◽  
...  

Fifteen holotypes of Asian Hesperiidae taxa described by Shu-iti Murayama were examined, and their taxonomic status is discussed. We confirm that five are valid names while the rest are synonyms as indicated partially by previous authors. Valid species-level names are Aeromachus matudai (Murayama), Aeromachus bandaishanus Murayama & Shimonoya, Coladenia pinsbukana (Shimonoya & Murayama), and Sebastonyma suthepiana Murayama & Kimura. Valid subspecies-level name is Ochlodes yuchingkina Murayama & Shimonoya. In order to settle the taxonomic status of Pedesta masuriensis cuneomaculata Murayama, masuriensis and tali were studied morphologically and molecularly. As a result, we consider that masuriensis and tali are two different species and treat cuneomaculata as a junior subjective synonym of tali. 


Zootaxa ◽  
2009 ◽  
Vol 2243 (1) ◽  
pp. 53-56 ◽  
Author(s):  
IVAN MARIN

The palaemonoid family Anchistioididae Borradaile, 1915 includes a single genus Anchistioides Paulson, 1875 with four known valid species: Anchistioides compressus Paulson, 1875 (type species), A. willeyi (Borradaile, 1899), A. australiensis (Balss, 1921) and A. antiguensis (Schmitt, 1924). Borradaile (1915) suggested two more species within the genus Amphipalaemon Nobili, 1901 (a junior synonym of Anchisitioides Paulson), Amphipalaemon gardineri Borradaile, 1915 (= Anchistioides gardineri) and Amphipalaemon cooperi Borradaile, 1915 (= Anchistioides cooperi) which were later synonomyzed with Anchisitioides willeyi by Gordon (1935), who also suggested their conspecificity with Anchistioides australiensis. At the present time, Anchistioides australiensis is a valid species (Bruce, 1971; Chace & Bruce, 1993) based on specific morphological features such as the presence of sharp postorbital tooth, oblique distal lamela of scaphocerite and sharply produced spines on posterodorsal angles of sixth abdominal somite (see Bruce, 1971: fig. 9). The other Indo-Pacific species, Anchistioides compressus and A. willeyi, can be clearly identified by specific form of scaphocerite, the presence of a well marked blunt postorbital tubercle in A. willeyi which is absent in A. compressus (e.g., Bruce, 1971) and the number of ventral rostral teeth (3-4 large ventral rostral teeth present in A. willeyi while up to 8 small ventral rostral teeth in A. compressus (Paulson, 1875; Gordon, 1935)). Anchistioides antiguensis is clearly separated geographically being known only from the tropical Western Atlantic and Caribbean region (Schmitt, 1924; Holthuis, 1951; Wheeler & Brown, 1968; Martinez-Iglesias, 1986; Markham et al, 1990; Ramos-Porto et al, 1998; Cardoso, 2006).


1961 ◽  
Vol 200 (6) ◽  
pp. 1197-1202 ◽  
Author(s):  
Hiroshi Kuida ◽  
Robert P. Gilbert ◽  
Lerner B. Hinshaw ◽  
Joel G. Brunson ◽  
Maurice B. Visscher

Studies were made in 5 monkeys, 7 rabbits, and 33 cats of the effect of gram-negative endotoxin on aortic, pulmonary artery (PAP), and portal venous (PVP) pressures; and on changes in weight of a short segment of intestine. Studies of blood pooling were also made in 12 cats. The responses in these species were compared with those previously observed in the dog. Although variable degrees of hypotension developed at one time or another in all animals following injection of endotoxin, the early precipitous hypotension that characteristically occurs in the dog was observed only in the cat. However, in this species the dramatic fall in pressure could be ascribed to pulmonary vascular constriction and acute right ventricular hypertension and failure, and not to splanchnic pooling. PAP also became elevated in the monkey and the rabbit, but usually was of lesser magnitude and did not appear to explain the development of the relatively late hypotension that occurred in these species. The absence of significant increases in gut weight and the minor increments in PVP in all animals indicate that in none of these species is hepatic vein constriction and splanchnic pooling a significant mechanism in producing early shock as it is in the dog. Pathologic gross and microscopic studies in the monkey and gross examinations in the other species supported this conclusion.


1997 ◽  
Vol 71 (6) ◽  
pp. 1109-1124 ◽  
Author(s):  
Li Guo-Qing ◽  
Mark V. H. Wilson ◽  
Lance Grande

Review of recently collected material of Eohiodon from North America suggests that there are two valid species, E. rosei (Hussakof) and E. woodroffi Wilson. Eohiodon falcatus Grande is identical to E. woodruffi in known skeletal features and nearly all meristic features and is treated as a junior synonym of the latter. The fossil genus Eohiodon Cavender differs from Hiodon Lesueur, which is known from both fossil and extant species, in numerous meristic and osteological features. The caudal skeleton in Eohiodon is nearly identical to that in Hiodon.The traditionally accepted Notopteroidei, containing Lycopteridae, Hiodontidae, and Notopteridae, is a polypheletic group. The Asian fossil family Lycopteridae is not more closely related to Hiodontidae than it is to other taxa in the Osteoglossomorpha, but is sister to all other Osteoglossomorpha. The Hiodontiformes sensu stricto, including only the family Hiodontidae, is the sister-group of the Osteoglossiformes. This family is not more closely related to notopterids than to other taxa in Osteoglossiformes. The Notopteridae are most closely related to the Mormyroidea; together they and the fossil family Ostariostomidae constitute the sister-group of the Osteoglossoidei.Fossil records of Hiodontiformes sensu stricto and Notopteroidei indicate a widespread pre-Neogene biogeographic range of these freshwater teleosts, suggesting that extinction must have been involved in the Cenozoic evolution of these two osteoglossomorph sublineages.


Author(s):  
Lidia Orsi Relini ◽  
Daniela Massi

The presence of Stoloteuthis leucoptera in the Mediterranean is recorded on the basis of three specimens, including an adult male, caught by IKMT and by commercial otter-trawl in the Ligurian Sea. The hypothesis of a recent immigration is discussed.The list of Mediterranean cephalopods (Mangold Wirz, 1963; Torchio, 1968; Bello, 1986; Mangold & Boletzsky, 1987) includes the Sepiolidae of the subfamily Heteroteuthinae, whose members are supposed to be pelagic throughout their life cycle. Mangold Wirz (1963) recognizes in the Mediterranean fauna the unique species Heteroteuthis dispar, the other authors include H. atlantis Voss, which Voss himself (1955) reported at Messina. To this group may now be added Stoloteuthis leucoptera (Verrill, 1878) a species until now recorded in limited Atlantic areas. Verrill (1881) wrote “This species is an exceedingly beautiful one, when living, owing to the elegance and brilliancy of its colours and the gracefulness of its movements. In swimming it moves its fins in a manner analogous to the motion of the wings of a butterfly.”


Zootaxa ◽  
2021 ◽  
Vol 4958 (1) ◽  
pp. 489-502
Author(s):  
FILIPE MICHELS BIANCHI

The Carpocorini are distributed worldwide, and it is one of the most speciose tribes within the Pentatomidae with 127 genera and more than 500 valid species. Recently, Adustonotus Bianchi was described to contain eight species formerly placed within Euschistus Dallas. Among them, Adustonotus grandis (Rolston) and Adustonotus latus (Dallas) are remarkable for their large size. Herein, the phylogenetic position of a new taxon is inferred by a total evidence analysis based on 85 morphological characters and four molecular markers. Adustonotus graziae sp. nov. is described, and is recovered in a polytomic lineage, including A. grandis and A. latus. These species share a solid combination of features that enable them to be separated from the other Adustonotus species (e.g., large size, the humeral angles spatulate and exceptionally produced, and the capsula seminalis shortened). Illustrations of external and internal genitalia, and a distributional map are provided. 


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