The Bombycoidea: Phylogeny and higher classification (Lepidoptera: Glossata)

1994 ◽  
Vol 25 (1) ◽  
pp. 63-88 ◽  
Author(s):  
Joel Minet

AbstractThis paper is chiefly aimed at reassessing the limits of four bombycoid families, namely the Eupterotidae, Saturniidae, Lemoniidae, and Brahmaeidae. An incompletely resolved cladogram is proposed for the whole 'bombycoid complex' (Mimallonoidea + Lasiocampoidea + Bombycoidea). Within the Bombycoidea, the primary dichotomy is considered to lie between the Eupterotidae + Bombycidae s.lat. + Endromidae + Mirinidae + Saturniidae, and the Carthaeidae + Lemoniidae + Brahmaeidae + Sphingidae. Sharing at least nine synapomorphies, the Lemoniidae and Brahmaeidae are regarded as reliable sister groups, and the Lemoniidae + Brahmaeidae are proposed as a sister group to the Sphingidae. Another newly proposed clade groups together the Endromidae, Mirinidae and Saturniidae. At family level, the Hibrildidae are synonymized with the Eupterotidae (syn. n.), for which the most significant autapomorphy lies in a previously unnoticed particularity of the female hind leg (distitarsus typically provided with a midventral row of spines). Sexual dimorphism in leg structure also leads to a redefinition of the Saturniidae, a family which must include, with subfamily rank (stat. rev.), the 'Oxytenidae' and 'Cercophanidae' of modern authors. A pair of distal, tooth-like structures on the fourth tarsomere of the female fore leg can thus be ascribed to the ground plan of the Saturniidae, along with a few other convincing autapomorphies. On the other hand, the 'Apatelodidae' are only tentatively placed in the 'Bombycidae sensu lato', a group provisionally resurrected insofar as the Apatelodidae sensu auct. prove to be diphyletic. As a matter of fact, the 'apatelodid' subfamily Epiinae is synonymized with the Bombycinae (syn. n.) in consideration of a rather large number of synapomorphies. When more extensively studied, the morphology of the eighth sternum of the male abdomen might lead to a slightly different, more restricted, concept of the Bombycidae (Le. excluding 'true' Apatelodidae). Often regarded as incertae sedis, the African genera Sabalia Walker and Spiramiopsis Hampson are definitely assigned to the Lemoniidae and Brahmaeidae respectively. Autapomorphies of these two families are recorded and discussed, as are those found to characterize the Sphingidae. Three subfamilies are tentatively recognized within the latter (Smerinthinae stat. rev., Sphinginae, Macroglossinae), five within the Eupterotidae (Hibrildinae, Tissanginae, Janinae, Panacelinae, Eupterotinae), and four within the Bombycidae s.lat. (Apatelodinae, Phiditiinae subfam. n., Prismostictinae [= Oberthueriinae, syn. rev.], Bombycinae). Three of these subfamilies are considered in a new sense, viz. the Panacelinae, Apatelodinae, and Bombycinae. Although the phylogeny of the Saturniidae is not fully taken into account in the present study, the composition of three saturniid subfamilies is critically examined (Oxyteninae, Cercophaninae, Ludiinae), and the Oxyteninae are viewed as the most 'primitive' member of the family.

1988 ◽  
Vol 66 (12) ◽  
pp. 2797-2810 ◽  
Author(s):  
François Chapleau ◽  
Allen Keast

This article presents the phylogenetic conclusions of an osteological study of species belonging to the subfamilies (Soleinae and Achirinae) of the dextral flatfish family Soleidae (Pieuronectiformes; Soleoidei). A cladistic analysis of the data revealed that the subfamilies, but not the family, are monophyletic. The Soleinae were found to be more closely related to the other soleoid family, the Cynoglossidae, than to the Achirinae. If we accept the principle that only monophyletic groups are to be admitted into Linnean classification, it is suggested that the two subfamilies be raised to the family level. The anatomical data led to the proposal (with caution) that the sister group of the achirid–soleid–cynoglossid lineage is the pleuronectid subfamily Samarinae. Consequently, it is suggested that the suborder Soleoidei be eliminated by incorporating its three families into the Pleuronectoidei which becomes monophyletic. Also, it is proposed that the Pleuronectid subfamilies (Pleuronectinae, Poecilopsettinae, Paralichthodinae, Rhombosoleinae, Samarinae) be raised to the family level. However, since the monophyletic status of these taxa is dubious (except for the Samarinae) any hypothesis including them must await a proper cladistic analysis of their intra- and inter-relationships.


Zootaxa ◽  
2006 ◽  
Vol 1180 (1) ◽  
pp. 1 ◽  
Author(s):  
BRADLEY J. SINCLAIR ◽  
JEFFREY M. CUMMING

A cladistic analysis of the Empidoidea and basal lineages of the Cyclorrhapha, based on morphological characters, confirms the monophyly of both groups as well as that of the                    Eremoneura. The resulting final trees are used to revise the classification of the Empidoidea to include the following five families: Empididae, Hybotidae, Atelestidae (including Nemedininae n. subfam.), Brachystomatidae rev. stat. (comprising the subfamilies Brachystomatinae, Ceratomerinae and Trichopezinae), and Dolichopodidae s.lat. The family Microphoridae is not recognized, and the Microphorinae and Parathalassiinae are assigned to the Dolichopodidae s.lat. The Dolichopodidae s.str. includes 15 subfamilies that were previously recognized within the family. Within the Empidoidea we found support for Atelestidae as the sister group to the Hybotidae and for the monophyly of Parathalassiinae + Dolichopodidae s.str. The Empididae remains poorly defined and the genera Homalocnemis Philippi, Iteaphila Zetterstedt, Anthepiscopus Becker, and Oreogeton Schiner are classified as incertae sedis within the                   Empidoidea. In addition, the following higher taxa are proposed: Symballophthalmini n. tribe, Bicellariini n. tribe, Oedaleinae rev. stat., and Trichininae rev. stat., which are all assigned to the Hybotidae. The genus Sematopoda Collin is tentatively assigned to Trichopezinae, and Xanthodromia Saigusa is transferred from Hemerodromiinae to Brachystomatinae.        All morphological characters are extensively discussed and illustrated, including details of the antennae, mouthparts, internal thoracic structures, wings, and male and female terminalia. In addition, a key to families and unplaced genus groups of the Empidoidea is provided. Feeding habits are also discussed in terms of the empidoid ground plan condition.


2014 ◽  
Vol 58 (1) ◽  
pp. 13-22
Author(s):  
Roman Wituła ◽  
Edyta Hetmaniok ◽  
Damian Słota

Abstract In the paper we present the selected properties of composition relation of the convergent and divergent permutations connected with commutation. We note that a permutation on ℕ is called the convergent permutation if for each convergent series ∑an of real terms, the p-rearranged series ∑ap(n) is also convergent. All the other permutations on ℕ are called the divergent permutations. We have proven, among others, that, for many permutations p on ℕ, the family of divergent permutations q on ℕ commuting with p possesses cardinality of the continuum. For example, the permutations p on ℕ having finite order possess this property. On the other hand, an example of a convergent permutation which commutes only with some convergent permutations is also presented.


2016 ◽  
Vol 3 (01) ◽  
Author(s):  
Shlesha Singh ◽  
Mrinalini Pandey

Organizations are these days realizing the importance of women in the workforce and to tap that talent, organizations are now-a-days putting extra efforts. Workplaces were designed keeping men in mind and which has been intercepting women from continuing the competitive jobs and career along with the family responsibilities. On the other hand, there are various workplace barriers which are adding to the other problems. Women face several barriers at the workplace like sexual harassment, glass ceiling and gender stereotype.


1895 ◽  
Vol 2 (12) ◽  
pp. 529-539 ◽  
Author(s):  
H. A. Nicholson ◽  
J. E. Marr

Since the remarkable paper by Professor Lapworth “On an Improved Classification of the Rhabdophora” was published in the Geological Magazine for 1873, a great deal of fresh information has been gathered as to these interesting fossils; but the classification given in that paper, though to some extent confessedly artificial, is still generally adhered to. Observations made by the authors in recent years lead them to suppose that that classification will in the future undergo considerable modification; but in the present state of our knowledge it serves a purpose so useful, that it is not our intention to propose any immediate change in it. Our object, on the other hand, is to bring forward certain conclusions which we have independently reached, and which will, we believe, enhance the value of Graptolites to the stratigraphical geologist, and lead to results important to the biologist. Our conclusions are based upon an examination of a large number of forms generally referred to the family Dichograptidæ; but, as we propose very briefly to indicate, they affect the relationships of Graptolites belonging to other families also.


Zootaxa ◽  
2021 ◽  
Vol 5051 (1) ◽  
pp. 346-386
Author(s):  
SÜPHAN KARAYTUĞ ◽  
SERDAR SAK ◽  
ALP ALPER ◽  
SERDAR SÖNMEZ

An attempt was made to test if Lourinia armata (Claus, 1866)—as it is currently diagnosed—represents a species complex. Detailed examination and comparisons of several specimens collected from different localities suggest that L. armata indeed represents a complex of four closely related morphospecies that can be differentiated from one another by only detailed observations. One of the four species is identified as Lourinia aff. armata and the other three species are described as new to science and named as Lourinia wellsi sp. nov., L. gocmeni sp. nov., and L. aldabraensis sp. nov. Detailed review of previous species records indicates that the genus Lourinia Wilson, 1924 is distributed worldwide. Ceyloniella nicobarica Sewell, 1940, originally described from Nicobar Island and previously considered a junior subjective synonym of L. armata is reinstated as Lourinia nicobarica (Sewell, 1940) comb. nov. on the basis of the unique paddle-shaped caudal ramus seta V. It is postulated that almost all of these records are unreliable in terms of representing true Lourinia aff. armata described herein. On the other hand, the comparative evaluation of the illustrations and descriptions in the published literature indicates the presence of several new species waiting to be discovered in the genus Lourinia.                 It has been determined that, according to updated modern keys, the recent inclusion of the monotypic genus Archeolourinia Corgosinho & Schizas, 2013 in the Louriniidae is not justified since Archeolourinia shermani Corgosinho & Schizas, 2013 does not belong to this family but should be assigned to the Canthocamptidae. On the other hand, it has been argued that the exact phylogenetic position of the Louriniidae still remains problematic since none of the diagnostic characters supports the monophyly of the family within the Oligoarthra. It has also been argued that the close relationship between Louriniidae and Canthocamptidae is supported since both families share the homologous sexual dimorphism (apophysis) on P3 endopod. The most important characteristic that can possibly be used to define Louriniidae is the reduction of maxilliped.  


1985 ◽  
Vol 16 (1) ◽  
pp. 27-67 ◽  
Author(s):  
Henrik Enghoff

AbstractThe family Nemasomatidae is redefined to include onty genera with all sterna secondarily free from pleurotergites. Comments are given on the included genera, viz., Antrokoreana, Basoncopus gen. n. (type-species B. filiformis sp. n.) (Kazakhstan), Dasynemasoma, Thalassisobates, Sinostemmiulus, Nemasoma, and Orinisobates. Isobates coiffaiti Demange, 1961 is synonymized with Thalassisobates littoralis (Silvestri, 1903). Orinisobates is revised and shown to include O. soror sp. n. (Kuril Islands), O. microthylax sp. n. (Kamchatka and Siberia), O. gracilis (Verhoeff, 1933) (NW China), O. sibiricus (Gulicka, 1963) (Altai region, Kazakhstan), O. kasakstanus (Lohmander, 1933) (Kazahkstan), O. nigrior (Chamberlin, 1943) (eastern United States), O. utus (Chamberlin, 1912) (northwestern United States), and O. expressus (Chamberlin, 1941) (northwestern United States and adjacent Canada). Mimolene oregona Chambertin, 1941 and M. sectile Loomis & Schmitt, 1971 are synonymized with O. expressus. A possible case of parthenogenesis in O. microthylax is recorded. Evidence is presented for the following sister-group relationships: Antrokoreana + (Basoncopus + (Dasynemasoma + (Thalassisobates + (Sinostemmiulus + (Orinisobates + Nemasoma))))). The position of Basoncopus is uncertain, and O. soror may belong in a separate genus and constitute the sister-group of Orinisohates + Nemasoma. If soror does belong in Orinisobates, it is the sister-group of all its congeners. The American species of Orinisobates are shown probably to constitute a monophyietic group. The family is suggested to have originated in the eastern Palearctic region, Orinisobates having invaded North America via the Bering Bridge. Doubtful species and species erroneously assoiciated with the Nemasomatidae are listed. The genera Okeanobates and Yosidaiulus are excluded from the family and referred to Okeanobatidae stat. n. in superfamily Blaniuloidea. The genera Trichonemasoma, Telsonemasoma, and Chelojulus are also excluded from the Nemasomatidae and relegated to Julida incertae sedis.


2003 ◽  
Vol 81 (12) ◽  
pp. 1285-1292 ◽  
Author(s):  
Takefumi Hattori ◽  
Akira Ohta ◽  
Masayuki Itaya ◽  
Mikio Shimada

We have investigated growth of ectomycorrhizal (ECM) fungi (i.e., 55 strains of 32 species in 15 genera) on saturated (palmitate), monounsaturated (oleate), diunsaturated (linoleate), triunsaturated (linolenate) fatty acids, and the triacylglyceride of oleate (triolein) lipid to elucidate an ability to utilize the fatty acids and lipid as a carbon source for growth. Relative utilization ratios (URs, %) based on mycelial growth on glucose suggest that ECM fungi belonging to the family Thelephoraceae have an ability to utilize palmitate. On the other hand, ECM fungi in the genus Laccaria can utilize at least either palmitate or oleate. Furthermore, Hygropharus russula grows on palmitate, oleate, and slightly on triolein. Lactarius chrysorrheus grows only on palmitate. These fatty-acid- and lipid-utilizing fungi may be promising as model fungi for further elucidation of the metabolic ability to utilize the fatty acids and lipid as a carbon source. On the contrary, the fungi in the genus Suillus were shown to scarcely utilize the fatty acids and lipid. Furthermore, most ECM fungi did not grow on either linoleate or linolenate.Key words: carbon source, ectomycorrhizal fungi, fatty acid, lipid, mycelial growth.


2021 ◽  
Author(s):  
Fermanto Lianto ◽  
Lilianny Sigit Arifin ◽  
Y. Basuki Dwisusanto ◽  
Rudy Trisno

Abstract Sharing a corridor space in a rusunawa could form patterns of adaptation and exemplify the phenomenon of territorial mastery. This research aims to understand the form of this mastery as perceived by the occupants using the Grounded Theory method. The results show a theory of territorial mastery that can be developed from the findings in the field is a new theory of territorial characteristics, based on hard and soft territory. The hard territory is territorial control that is tangible or intangible, fixed or unchanged, and firm, whose existence is clear in a space that can be seen, occupied or controlled and maintained, and recognized by other residents. On the other hand, the soft territory is territorial control that is tangible and intangible, and which allows for flexible and soft shifts because it is an expression of the family and cultural emotions of guyub, so that mastery of the soft territory occurs not only because of tolerance, but also because of the prioritization of the feeling of kinship in living under one roof, and the harmonization of guyub relationships amongst people in a community


2020 ◽  
Vol 2 (1) ◽  
pp. 65
Author(s):  
Syaiful Marwan ◽  
Himyar Pasrizal

Every family member has different needs from one another. Children are the most important members of the family, especially in completing their needs. Each child has different basic needs. In the case of gender, sometimes boys are often prioritized over girls. But on the other hand girls also have many needs related to their nature as women. This various cases cause different need compliance that requires parents’ consideration. Therefore, parents need to accommodate their children needs which have gender diversity. In managing these children's needs, parents' creativity and understanding of their children are needed.


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