scholarly journals Algunos aspectos ecológicos y fitogeográficos de las especies de Cyperaceae en el Valle de México. II. Análisis fitogeográfico

2017 ◽  
pp. 29
Author(s):  
Socorro González-E. ◽  
J. Rzedowski

The analysis of the geographic affinities of the members of Cyperaceae belonging to the flora of the V alley of Mexico reveals that, in general terms, neotropical relationships prevail amply over the holarctic ones that were detected, while species with distribution restricted to Mexico amount to about 30% of the total number. With countries as distant as Poland and Liberia there are few species in common, although at the generic level, the similarity exceeds 50%. On a more regional scale, the cyperaceous flora of the Valley shows evident links with that of the Mexican High Plateau, but has relatively little in common with the flora of warmer parts of the country. The results support the idea of Raven and Axelrod, who claim that the family evolved initially in tropical and subtropical areas and later migrated northward and southward.

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.


2021 ◽  
Vol 95 ◽  
Author(s):  
F.B. Drago ◽  
M. Dueñas Díaz ◽  
R. Draghi ◽  
V. Núñez

Abstract An annotated checklist of the cestode parasites of Argentinean wild birds is presented, as the result of a compilation of parasitological papers published between 1900 and April 2021. This review provides data on hosts, geographical distribution, sites of infection, location of material deposited in helminthological collections, references and taxonomic comments. A host/parasite list is also provided. During this period, 38 papers were published that gather information about 34 cestode nominal species and 11 taxa identified at generic level, belonging to three orders, ten families and 35 genera. The highest number of cestode taxa was recorded in the family Hymenolepididae, with 12 nominal species and two taxa identified at generic level, followed by Dilepididae, with eight nominal species and three taxa identified at generic level. Of the 1042 species of birds reported in Argentina, only 29 (2.8%) were reported as hosts of adult cestodes. The families of birds with the highest number of reported taxa were Laridae and Anatidae, with 20 and 14 taxa, respectively.


1992 ◽  
Vol 6 ◽  
pp. 26-26
Author(s):  
James Bergen

Long-term cycles are evident in the stratigraphic distribution(appearances/extinctions) and dominance changes of Mesozoic calcareous nannofossils. These assemblage turnovers correspond to major episodes of biological extinction recognized in inverterbrate genera and families. The identified Mesozoic nannofossil assemblage turnovers are gradual, in contrast to the well-documented and geologically instantaneous terminal Cretaceous event. Such continuity indicates a non-catatrophic cause and suggests that these turnovers are unrelated to the terminal Cretaceous “accident”. Their timing instead corresponds to interpreted sea level trends and paleoceanographic changes in the sections studied.Current evidence is based on a limited number of sections spanning the Pliensbachian to Cenomanian, although published literature and a thorough analysis of the Cenomanian show that these turnovers can be recognized over a wide geographic area. These preliminary conclusions are based on detailed sample analyses of marine sections selected for their nannofossil content. This has eliminated any taxonomic or preservational bias and problems related to compiled literature ranges.Major dominance changes are recorded in the Pliensbachian, Bajocian, Tithonian, and Aptian. The Pliensbachian turnover is evident at the family and ordinal level, whereas the younger dominance changes occur at the generic level. A major diversification during the Pliensbachian resulted in the replacement of the Jurassic Family Crepidolithaceae by the important Jurassic placolith families. The Bajocian and Tithonian turnovers were initiated by dominance changes within the common imbricate placolith family, Ellipsagelosphaeraceae. The Tithonian turnover was most dramatic including: (1) a major diversification near the Jurassic/Cretaceous boundary; (2) the extinction of several genera; and (3) the establishment of a dominant low latitude assemblage (Nannoconus, Conusphaera, Micrantholithus). Species appearances and extinctions characterize the Cretaceous turnovers. There was an increase in species extinctions during the Hauterivian, Aptian, and Cenomanian. The Aptian also includes the extinction of the aforementioned low latitude assemblage and the subsequent diversification and radiation of more cosmopolitan floras, which continued until the end of the Albian. The highest number of nannofossil species extinctions within any Mesozoic stage (except for the terminal Cretaceous) are recorded in the Cenomanian. Although several of these species extinctions are associated with the Cenomanian/Turonian boundary anoxic event, most preceeded this event.


Zootaxa ◽  
2006 ◽  
Vol 1142 (1) ◽  
pp. 51-55 ◽  
Author(s):  
DIETER KOCK ◽  
COLLEEN M. INGRAM ◽  
LAURENCE J. FRABOTTA ◽  
RODNEY L. HONEYCUTT ◽  
HYNEK BURDA

Recently, in an examination of the phylogenetic relationships among the mole-rats of the family Bathyergidae (Mammalia: Rodentia), Ingram et al. (2004) documented molecular evidence for the recognition of the Cryptomys mechowii species group at the generic level and resurrected the name Coetomys Gray, 1864 for this group. Subsequent literature review revealed that Coetomys is not available to this species group, being a junior synonym of Cryptomys Gray, 1864. Here, we describe and diagnose Fukomys genus novum. In addition, we discuss the taxonomic history of this group in an attempt to reduce the nomenclatural confusion that has plagued studies of the Bathyergidae for over a century.


2017 ◽  
Vol 31 (5) ◽  
pp. 566 ◽  
Author(s):  
Michael G. Rix ◽  
Robert J. Raven ◽  
Barbara Y. Main ◽  
Sophie E. Harrison ◽  
Andrew D. Austin ◽  
...  

The Australasian spiny trapdoor spiders of the family Idiopidae (subfamily Arbanitinae) are revised at the generic level, using a multi-locus molecular phylogenetic foundation and comprehensive sampling of all known lineages. We propose a new family- and genus-group classification for the monophyletic Australasian fauna, and recognise 10 genera in four tribes. The Arbanitini Simon includes Arbanitis L. Koch, 1874 (61 species), Blakistonia Hogg, 1902 (one species) and Cantuaria Hogg, 1902 (43 species). The Aganippini Simon includes Bungulla Rix, Main, Raven & Harvey, gen. nov. (two species), Eucanippe Rix, Main, Raven & Harvey, gen. nov. (one species), Eucyrtops Pocock, 1897 (two species), Gaius Rainbow, 1914 (one species) and Idiosoma Ausserer, 1871 (14 species). The Cataxiini Rainbow and Euoplini Rainbow include just Cataxia Rainbow, 1914 (11 species) and Euoplos Rainbow, 1914 (12 species), respectively. Two distinctive new genera of Aganippini are described from Western Australia, and several previously valid genera are recognised as junior synonyms of existing genus-group names, including Misgolas Karsch, 1878 (= Arbanitis; new synonymy), Aganippe O. P.-Cambridge, 1877 (= Idiosoma; new synonymy) and Anidiops Pocock, 1897 (= Idiosoma; new synonymy). Gaius stat. rev. is further removed from synonymy of Anidiops. Other previously hypothesised generic synonyms are supported by both morphology and molecular phylogenetic data from 12 genes, including the synonymy of Neohomogona Main, 1985 and Homogona Rainbow, 1914 with Cataxia, and the synonymy of Albaniana Rainbow & Pulleine, 1918, Armadalia Rainbow & Pulleine, 1918, Bancroftiana Rainbow & Pulleine, 1918 and Tambouriniana Rainbow & Pulleine, 1918 with Euoplos. At the species level, the identifications of Eucy. latior (O. P.-Cambridge, 1877) and I. manstridgei (Pocock, 1897) are clarified, and three new species are described: Bungulla bertmaini Rix, Main, Raven & Harvey, sp. nov., Eucanippe bifida Rix, Main, Raven & Harvey, sp. nov. and Idiosoma galeosomoides Rix, Main, Raven & Harvey, sp. nov., the latter remarkable for its phragmotic abdominal morphology. The Tasmanian species Mygale annulipes C. L. Koch, 1842 is here transferred to the genus Stanwellia Rainbow & Pulleine, 1918 (family Nemesiidae), comb. nov., Arbanitis mestoni Hickman, 1928 is transferred to Cantuaria, comb. nov. and Idiosoma hirsutum Main, 1952 is synonymised with I. sigillatum (O. P.-Cambridge, 1870), new synonymy. In addition to the morphological synopses and an illustrated key to genera, molecular diagnoses are presented for all nominal taxa, along with live habitus and burrow images to assist in field identification. The Australasian idiopid fauna is highly diverse, with numerous new species known from all genera. As a result, this study provides a taxonomic and nomenclatural foundation for future species-level analyses, and a single reference point for the monographic documentation of a remarkable fauna. http://zoobank.org/?lsid=urn:lsid:zoobank.org:pub:BACE065D-1EF9-40C6-9134-AADC9235FAD8


Phytotaxa ◽  
2014 ◽  
Vol 173 (1) ◽  
pp. 91 ◽  
Author(s):  
Xiaolan He ◽  
David Glenny ◽  
Lars Söderström ◽  
Anders Hagborg ◽  
Matt Von Konrat

The family Schistochilaceae Buch (1928: 9) consists of approximately 80 extant species. More than two-thirds of its diversity occurs in temperate to subantarctic South America and Australasia, and nearly one third in the tropical mountain forests of Southeast Asia and the western Pacific Islands. The plants of Schistochilaceae are usually robust and form a prominent component of the ground layer of cool temperate forests or upper montane tropical forests, commonly forests in which Nothofagus is a dominant genus.  The first species of the family, published as Jungermannia appendiculata Hooker (1818: tab. 15), Jungermannia glaucescens Hooker (1818: tab. 39), Jungermannia lamellata Hooker (1818: tab. 49), Jungermannia nobilis Hooker (1818: tab. 11), Jungermannia sphagnoides Schwägrichen (1814: 23) and Jungermannia thouarsii Hooker (1818: tab. 48), were described during 1814–1818. Dumortier established the genus Schistochila Dumortier (1835: 15) to accommodate the above mentioned species except Jungermannia glaucescens and Jungermannia sphagnoides, but he also added one new species, Schistochila pinnatifolia Dumortier (1835: 15) nom. inval. (ICN Art. 38.1(a); no description; McNeill et al. 2012). The definition of Schistochilaceae has remained largely unchanged since it was separated from Scapaniaceae Migula (1904: 479) by Buch (1928) and then later Balantiopsaceae Buch (1955: 23). The presence of magenta rhizoids, winged and complicate-bilobed leaves with smaller dorsal lobes, a shoot calyptra elaborated into a well-developed coelocaule, and a cylindrical sporophyte capsule with straight valves generally defines the family. These features, to a great extent, isolate Schistochilaceae from the rest of the leafy liverworts. Therefore, taxonomic rearrangements or revisions, based on morphological investigations, have mostly been at generic level or below (Grolle 1966, 1968, Hässel 1973, Schuster 1971a, Schuster & Engel 1977, 1985). So far, taxonomic revisions have only been done at regional scales, a study at global scale is under way (Glenny et al., unpublished).


1990 ◽  
Vol 68 (12) ◽  
pp. 2649-2687 ◽  
Author(s):  
F. Rafi ◽  
Diana R. Laubitz

The distribution of the northeastern North Pacific Idoteidae reflects the general eurytopy in the shallow marine environment of the component species. The family is represented by four genera and 20 species in the region between Juan de Fuca Strait, Washington, and Prince William Sound, Alaska. Collections studied from this area contained 16 species of idoteids, of which 3 (Idotea (Pentidotea) recta, Synidotea cornuta, and S. minuta) are new; the new species are fully illustrated and described. The status of nine additional species recorded in the literature from the area is discussed, and four of them are diagnosed and included in the keys. The morphological characters of the four genera were examined in detail and their systematic importance is discussed. All the appendages surveyed showed differences at least at the generic level.


Zootaxa ◽  
2010 ◽  
Vol 2501 (1) ◽  
pp. 37 ◽  
Author(s):  
ROWAN M. EMBERSON

Macrocheles analis Hyatt & Emberson is redescribed and assigned to a new genus, Reductholaspis gen. nov. Longicheles Valle is separated from the genus Geholaspis Berlese and given generic rank, based on a complex of strongly autapomorphic features and a possible synapomorphy with Reductholaspis. The new tribe Geholaspini, including the genera Dissoloncha Falconer, Geholaspis, Longicheles, and Reductholaspis is described and a key to the genera is provided. The genus Macrholaspis Oudemans and the subgenus Nothrholaspis Berlese of Macrocheles Latreille are reinstated at the generic level, based on distinctive synapomorphies of the included species. Scleritholaspis Mašàn is newly synonymised with Nothrholaspis. Lists of included species are provided for each of the genera discussed. Proposed new combinations are: Longicheles bianchii (Valle & Mazzoleni), L. lagrecai (Valle), L. ilvana (Valle & Mazzoleni), L. longisetosus (Balogh), L. longulus (Berlese), L. mandibularis (Berlese), L. ranzii (Valle & Mazzoleni), Reductholaspis analis (Hyatt & Emberson), Nothrholaspis banaticus (Iavorschi), N. caucasicus (Bregetova & Koroleva), N. coenosus (Takaku), N. shennongjianensis (Ma & Liu), N. subcoenosus (Takaku), N. submotus (Falconer), Macrholaspis beieri (Johnston), M. carpathicus (Mašán), M. georgicus (Bregetova), M. morikawai (Ishikawa), M. recki (Bregetova & Koroleva), M. reductus (Petrova), M. similiopacus (Mašán), M. stammeri (Krauss), M. terreus (Canestrini & Fanzago), M. tianschanicus (Bregetova).


2011 ◽  
Vol 20 (2) ◽  
pp. 340-349
Author(s):  
E.P. Nartshuk

Sixteen species are found in the chloropid collection made by A.P. Fedchenko in Turkestan in 1869–1871 and three more species were identified to the generic level only. A new genus, Alajichlorops, and four new species, A. fedchenkoi, Chlorops kirghisicus, Ch. olgafedchenkoae, and Polyodaspis palpata are described. A key for the palaearctic species of the genus Polyodaspis Duda, 1933 is presented.


1973 ◽  
Vol 51 (2) ◽  
pp. 179-186 ◽  
Author(s):  
H.-C. Lim ◽  
V. R. Vickery ◽  
D. K. McE. Kevan

Twelve species of Gryllinae were studied to determine the number, morphology and behavior of their chromosomes. The male diploid numbers ranged from 19 to 31. Gryllus campestris and a population of "G. bimaculatus" from Singapore showed anomalies in chromosome behavior and structure, including breaks, stickiness, C-mitosis, polyploidy, lagging, unequal segregation and non-disjunction in the former and many aberrations and loss of fertility in the latter. One or two B-chromosomes occurred in some individuals of G. veletis, the chromosome number of this species thus varying from 2n ♀ = 29 to 31. In the Gryllinae, karyotypic differences are shown to be more useful than chromosome number at the species level; differences in chromosome number are useful taxonomically at the generic level, when combined with differences in karyotypes.


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