Delimitation of the new tribe Parartocarpeae (Moraceae) is supported by a 333-gene phylogeny and resolves tribal level Moraceae taxonomy

Phytotaxa ◽  
2019 ◽  
Vol 388 (4) ◽  
pp. 253 ◽  
Author(s):  
NYREE J.C. ZEREGA ◽  
ELLIOT M. GARDNER

Here we describe the new tribe, Parartocarpeae, within the Moraceae (mulberry family). The tribe comprises two small Malesian genera, Parartocarpus and Hullettia, and brings the total number of Moraceae tribes to seven. Evidence for this new designation comes from a phylogeny based on 333 nuclear genes sequenced using target enrichment via hybridization (hybseq). Morphological characters that set Parartocarpeae apart from other Moraceae tribes include the combination of the following characters: lateral nonamplexicaul stipules, spirally arranged leaves without annulate stipule scars, the presence of a single layer of involucral inflorescence bracts, and the lack of perianth tissue, wherein flowers are embedded in cavities of the receptacle. With the designation of Parartocarpeae, the tribe-level circumscription of Moraceae is now well-supported by phylogenetic methods. Because the phylogenetic markers employed here work well throughout Moraceae, they can facilitate much needed work at the genus level in the family.

2016 ◽  
Vol 47 (1) ◽  
pp. 53-82 ◽  
Author(s):  
Werner P. Strümpher ◽  
Martin H. Villet ◽  
Catherine L. Sole ◽  
Clarke H. Scholtz

Extant genera and subgenera of the Trogidae (Coleoptera: Scarabaeoidea) are reviewed. Contemporary classifications of this family have been based exclusively on morphological characters. The first molecular phylogeny for the family recently provided strong support for the relationships between morphologically defined genera and subgenera. On the basis of morphological, molecular and biogeographical evidence, certain taxonomic changes to the genus-level classification of the family are now proposed. The family is confirmed as consisting of two subfamilies, Omorginae Nikolajev and Troginae MacLeay, the former with two genera,OmorgusErichson andPolynoncusBurmeister, and the latter with two genera,TroxFabricius andPhoberusMacLeaystat. rev.Phoberusis restored to generic rank to include all Afrotropical (including Madagascan endemic) species;Afromorgusis confirmed at subgeneric rank within the genusOmorgus; and the monotypic Madagascan genusMadagatroxsyn. n.is synonymised withPhoberus.The current synonymies ofPseudotroxRobinson (withTrox),ChesasBurmeister,LagopelusBurmeister andMegalotroxPreudhomme de Borre (all withOmorgus) are all accepted to avoid creating speculative synonyms before definitive phylogenetic evidence is available. New combinations resulting from restoringPhoberusto a monophyletic genus are listed in Appendix A.


2000 ◽  
pp. 1-31 ◽  
Author(s):  
Jeffery A. Wilkinson ◽  
Robert C. Drewes

The first comprehensive phylogenetic analysis of the family Rhacophoridae was conducted by Liem (1970) scoring 81 species for 36 morphological characters. Channing (1989), in a reanalysis of Liem’s study, produced a phylogenetic hypothesis different from that of Liem. We compared the two studies and produced a third phylogenetic hypothesis based on the same characters. We also present the synapomorphic characters from Liem that define the major clades and each genus within the family. Finally, we summarize intergeneric relationships within the family as hypothesized by other studies, and the family’s current status as it relates to other ranoid families.


Zootaxa ◽  
2013 ◽  
Vol 3605 (1) ◽  
pp. 1-147 ◽  
Author(s):  
MATTHEW L. GIMMEL

A pre-phylogenetic revision of the family Phalacridae at the genus level is presented. Twenty-eight new generic synonymies are established as follows: Acylomus Sharp 1888 (=Liophalacrus Sharp 1888, syn. nov.; Ganyrus Guillebeau 1894, syn. nov.; Podocesus Guillebeau 1894, syn. nov.; Tinodemus Guillebeau 1894, syn. nov.; Ledorus Guillebeau 1895, syn. nov.; Astenulus Guillebeau 1896, syn. nov.; Afronyrus Švec 2006, syn. nov.), Apallodes Reitter 1873 (=Litolibrus Sharp 1889, syn. nov.; Sphaeropsis Guillebeau 1893, syn. nov.; Gyromorphus Guillebeau 1894, syn. nov.), Augasmus Motschulsky 1858 (=Megischius Guillebeau 1896, syn. nov.; Nematolibrus Sahlberg 1913, syn. nov.), Entomocnemus Guillebeau 1894 (=Stilbomimus Champion 1924, syn. nov.), Grouvelleus Guillebeau 1892 (=Ochrolitoides Champion 1924, syn. nov.; Litotarsus Champion 1925, syn. nov.), Litochrus Erichson 1845 (=Merobrachys Guillebeau 1895, syn. nov.), Litostilbus Guillebeau 1894 (=Pseudolitochrus Liubarsky 1993, syn. nov.), Ochrolitus Sharp 1889 (=Gorginus Guillebeau 1894, syn. nov.), Olibroporus Casey 1890 (=Parasemus Guillebeau 1894, syn. nov.), Olibrosoma Tournier 1889 (=Lichrotus Lyubarsky 1993, syn. nov.), Phaenocephalus Wollaston 1873 (=Phalacratomus Scott 1922, syn. nov.; Heterostilbus Champion 1924, syn. nov.), Phalacrinus Blackburn 1891 (=Sphaerostilbus Champion 1924, syn. nov.), Pseudolibrus Flach 1889 (=Biophytus Guillebeau 1894, syn. nov.; Polyaloxus Guillebeau 1894, syn. nov.), Pycinus Guillebeau 1893 (=Ochrodemus Guillebeau 1893, syn. nov.; Radinus Guillebeau 1893, syn. nov.; Euphalacrus Champion 1925, syn. nov.). Ten new genera and seven new species are described: Antennogasmus, gen. nov. (type species: A. cordatus, sp. nov.), Austroporus, gen. nov. (type species: A. victoriensis (Blackburn)), Malagasmus Gimmel, gen. nov. (type species: M. thalesi, sp. nov.), Malagophytus, gen. nov. (type species: M. steineri, sp. nov.), Neolitochrus, gen. nov. (type species: N. pulchellus (LeConte)), Paracylomus, gen. nov. (type species: P. asiaticus (Champion)), Platyphalacrus, gen. nov. (type species: P. lawrencei, sp. nov.), Ranomafanacrinus, gen. nov. (type species: R. nigrinus, sp. nov.), Steinerlitrus, gen. nov. (type species: S. warreni, sp. nov.), Sveculus, gen. nov. (type species: S. lewisi, sp. nov.). Generic reassignments resulted in 194 new combinations. Nine new names have been established for junior primary and secondary homonyms: Acylomus bicoloratus nom. nov. for Tinodemus bicolor Švec 2002; Acylomus lyubarskyi nom. nov. for Olibrus capriviensis Lyubarsky 1998; Acylomus sveci nom. nov. for Tinodemus reticulatus Švec 2002; Acylomus orientalis nom. nov. for Stilbus similis Švec 1992; Acylomus zdeneki nom. nov. for Afronyrus snizeki Švec 2006; Apallodes championi nom. nov. for Litolibrus ocellatus Champion 1925; Olibrus peringueyi nom. nov. for Olibrus consanguineus Péringuey 1892; Augasmus exquisitus nom. nov. for Litochrus pulchellus Blackburn 1895; Litochrus pronotalis nom. nov. for Augasmus bimaculatus Lyubarsky 1996. A type species is designated for Phalacrinus Blackburn 1891 (P. australis Blackburn 1891). Six new species-group synonymies are established: Acylomus ergoti Casey 1890 (=Tinodemus grouvellei Guillebeau 1894, syn. nov.), Acylomus curvolineatus (Champion 1924) (=Tinodemus meridianus (Švec 1992), syn. nov.; Olibrus stuporatus Lyubarsky 1994, syn. nov.), Xanthocomus attenuatus (Casey, 1890) (=Xanthocomus concinnus (Casey, 1916), syn. nov.; Stilbus thoracicus Casey, 1916, syn. nov.; Stilbus quadrisetosus Casey, 1916, syn. nov.). One name, Olibrus sternalis Casey 1916, is resurrected from synonymy. Lectotypes are designated for 23 nominal species. One genus and two species are excluded from Phalacridae: Sternosternus Guillebeau 1894 (with its type and only species, S. grouvelleiGuillebeau 1894) and Parasemus parvopallidus Lea 1932, both of which belong in Hydrophilidae. All 34 resulting genera in the family Phalacridae are keyed, described, and illustrated. A phylogenetic hypothesis based on analysis of a matrix of 98 morphological characters was created using parsimony. Results of these analyses were not robust enough at deep levels to create a new subfamilial or tribal classification, but nine genus-groups have been hypothesized.


PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e4331 ◽  
Author(s):  
Gustavo Sanchez ◽  
Davin H.E. Setiamarga ◽  
Surangkana Tuanapaya ◽  
Kittichai Tongtherm ◽  
Inger E. Winkelmann ◽  
...  

Comprising more than 800 extant species, the class Cephalopoda (octopuses, squid, cuttlefish, and nautiluses) is a fascinating group of marine conchiferan mollusks. Recently, the first cephalopod genome (of Octopus bimaculoides) was published, providing a genomic framework, which will enable more detailed investigations of cephalopod characteristics, including developmental, morphological, and behavioural traits. Meanwhile, a robust phylogeny of the members of the subclass Coleoidea (octopuses, squid, cuttlefishes) is crucial for comparative and evolutionary studies aiming to investigate the group’s traits and innovations, but such a phylogeny has proven very challenging to obtain. Here, we present the results of phylogenetic inference at the genus level using mitochondrial and nuclear marker sequences available from public databases. Topologies are presented which show support for (1) the monophyly of the two main superorders, Octobrachia and Decabrachia, and (2) some of the interrelationships at the family level. We have mapped morphological characters onto the tree and conducted molecular dating analyses, obtaining congruent results with previous estimates of divergence in major lineages. Our study also identifies unresolved phylogenetic relationships within the cephalopod phylogeny and insufficient taxonomic sampling among squids excluding the Loliginidae in the Decabrachia and within the Order Cirromorphida in the Octobrachia. Genomic and transcriptomic resources should enable resolution of these issues in the relatively near future. We provide our alignment as an open access resource, to allow other researchers to reconstruct phylogenetic trees upon this work in the future.


2011 ◽  
Vol 20 (1) ◽  
pp. 161-173
Author(s):  
A.P. Kassatkina

Resuming published and own data, a revision of classification of Chaetognatha is presented. The family Sagittidae Claus & Grobben, 1905 is given a rank of subclass, Sagittiones, characterised, in particular, by the presence of two pairs of sac-like gelatinous structures or two pairs of fins. Besides the order Aphragmophora Tokioka, 1965, it contains the new order Biphragmosagittiformes ord. nov., which is a unique group of Chaetognatha with an unusual combination of morphological characters: the transverse muscles present in both the trunk and the tail sections of the body; the seminal vesicles simple, without internal complex compartments; the presence of two pairs of lateral fins. The only family assigned to the new order, Biphragmosagittidae fam. nov., contains two genera. Diagnoses of the two new genera, Biphragmosagitta gen. nov. (type species B. tarasovi sp. nov. and B. angusticephala sp. nov.) and Biphragmofastigata gen. nov. (type species B. fastigata sp. nov.), detailed descriptions and pictures of the three new species are presented.


2003 ◽  
Vol 60 (3) ◽  
pp. 533-568 ◽  
Author(s):  
J. C. MANNING ◽  
P. GOLDBLATT ◽  
M. F. FAY

A revised generic synopsis of sub-Saharan Hyacinthaceae is presented, based on a molecular phylogenetic analysis of the family. Generic rank is accorded only to reciprocally monophyletic clades that can be distinguished by recognizable morphological discontinuities, thereby permitting an appropriate generic assignment of species not included in the analysis. Three subfamilies are recognized within the region. Subfamily Ornithogaloideae, characterized by flattened or angular seeds with tightly adhering testa, is considered to include the single genus Ornithogalum, which is expanded to include the genera Albuca, Dipcadi, Galtonia, Neopatersonia and Pseudogaltonia. Recognizing any of these segregates at generic level renders the genus Ornithogalum polyphyletic, while subdivision of Ornithogalum into smaller, morphologically distinguishable segregates in order to preserve the monophyly of each is not possible. Subfamily Urgineoideae, characterized by flattened or winged seeds with brittle, loosely adhering testa, comprises the two mainland African genera Bowiea and Drimia. The latter is well circumscribed by its deciduous, short-lived perianth and includes the previously recognized genera Litanthus, Rhadamanthus, Schizobasis and Tenicroa. The monotypic Madagascan Igidia is provisionally included in the subfamily as a third genus on the basis of its seeds, pending molecular confirmation of its relationships. Subfamily Hyacinthoideae resolves into three clades, distinguished as tribes Hyacintheae (strictly northern hemisphere and not treated further), Massonieae and Pseudoprospereae tribus nov. Full descriptions and a key to their identification are provided for all genera. New combinations reflecting the generic circumscriptions adopted here are made for most African and all Indian and Madagascan species.


2014 ◽  
Vol 46 (1) ◽  
pp. 51-67 ◽  
Author(s):  
Zuzana FERENCOVA ◽  
Paloma CUBAS ◽  
Pradeep Kumar DIVAKAR ◽  
M. Carmen MOLINA ◽  
Ana CRESPO

AbstractThe importance of the anatomy and fine morphology of reproductive structures for the systematics of the family Parmeliaceae is highlighted by the new genus Notoparmelia, described here for Australasian species of Parmelia. These species were known to form a monophyletic lineage but correlated characters for its delimitation were lacking. A major characteristic used here for the circumscription of this genus is the overlooked apothecial anatomy. The proper exciple is reduced to one layer formed exclusively by large hyphae without any clear branching pattern and embedded in an abundant polysaccharide matrix. This feature differs from the rest of Parmeliaceae which have a stratified three-layered proper exciple composed of a thin hyaline layer, intermediate layer and basal cortex-like structure. The anatomy of proper exciple, together with the thickness of spore walls and other morphological characters such as lobe morphology, pseudocyphellae and rhizine type, allow a precise diagnosis of the new genus. The area of distribution is also useful for characterizing this genus. Sixteen new combinations are proposed.


2005 ◽  
Vol 26 (2) ◽  
pp. 139-147 ◽  
Author(s):  
Francisca do Val ◽  
Paulo Nuin

AbstractThe systematics and phylogenetic relationships of the family Leptodactylidae are controversial as is the intrafamilial phylogeny of the leptodactylids. Here we analyze the relationships of the leptodactylid subfamily Hylodinae. This subfamily has been considered to be monophyletic and composed of three genera, Hylodes, Crossodactylus and Megaelosia. In the present study 49 characters were used, based on different studies on Leptodactylidae phylogeny. Maximum parsimony methods with unweighted and successively weighted characters were used to estimate the phylogeny of the Hylodinae. Upon analysis, the data provided further evidence of the monophyletic status of the three genera, with Megaelosia being the basal genus and the other two genera being sister taxa. The analysis with successive weighting results in a more resolved topology of the species subgroups of the genus Hylodes and separates this genus from Crossodactylus and confirms that the hylodines are monophyletic.


2011 ◽  
Vol 98 (8) ◽  
pp. 1356-1365 ◽  
Author(s):  
Eric J. Tepe ◽  
Frank T. Farruggia ◽  
Lynn Bohs

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