Taxonomy of the Cupressaceae: Subfamilies,Tribes and Genera

Cupressaceae and Taxodiaceae have recently been merged under the earlier name Cupressaceae s.I. by many authors, as the two families are similar in a number of morpho logical characters. Sciadopitys S. et Z., which has often been treated as a morphologically isolated member of the Taxodiaceae, has recently been considered as a monotypic family, Sciadopityaceae. The Cupressaceae s.s. may be reorganized into two subfamilies. The Cu pressoideae is composed of genera with the uppermost cone-scales infertile and can be divided into four tribes: Cnpresseae, including Cupressus, X Cupressocyparis, Charnaecyparis and Fokeinia;Thujopsideae, including Thuja, Thujopsis and Platycladusl Junipereae, including Juniperus and Microbiota; and Tetraclineae, including Calocedrus and Tetraclinis. The Callitroideae is composed of genera with the uppermost cone-scales fertile and can be divided into three tribes: Actinostrobeae, including Actinostrobus, Callitris, Fitzroya and Neocallitropsis; Widdringtoneae, including Pilgerodendron, Diselma and Widdringtonia ; Libocedreae, including Libocedrus, Papuacedrus and Austrocedrus. Five geographical distribution patterns are recognized in the 21 genera of Cupressaceae. (a) One genus, X Cupressocyparis, is a natural hybrid derived from selections in England; (b) Two genera, Cupressus and Juniperus, are distributed in Africa, Europe, Asia and North America; (c) Three genera, Thuja, Chamaecyparis, and Calocedrus, are disjnnctly distributed in Eastem Asia and North America; (d) Five genera, Actinostrobus, Callitris, Libocedrus, Papuacedrus and Widdringtonia, have limited distribution; and (e) The other 10 genera, which are monotypic, are restricted to narrow areas except Plotycladus. Three centers of genera diversity are identified in the Cupressaceae, i. e Eastern Asia with nine genera, southwestern North America with five genera, and Australia and its adjacent islands in the east　with six genera, including New Zealand,. Tasmania, New Caledonia, and New Guinea. Other important areas are western Mediterranean with three genera and Chile and Argentinawith three genera.     

Marine mites (Halacaroidea: Acari): a geographical and ecological survey

Halacarid mites (Acari), with almost 700 species described, inhabit marine and freshwater habitats. The majority of genera are recorded from at least two ocean basins or continents. There is no evidence of endemic genera, in either littoral faunal provinces or in deep-sea regions. Copidognathus, a genus comprising 1/4 of all species described, is found in almost all geographic regions, depths and habitats. Other genera dominate or are restricted to cold waters, to warm waters or to distinct habitats.Corresponding habitats on either side of the boreal Atlantic Ocean harbour congeneric, identical, sibling or morphologically similar species. The fauna in the western Atlantic is less diverse than that in the eastern. Amphiatlantics are restricted to certain genera. Transatlantic distribution is independent of the niche inhabited.Of the marine halacarid species recorded from the boreal western Atlantic, 41% are amphiatlantics, while only one species is recorded from both the Caribbean and the Mediterranean. The Caribbean and the Mediterranean faunas are dominated by genera in which amphiatlantics are unknown.Most of the Black Sea species of the genus Halacarellus also occur in the Baltic, North Sea or North Atlantic, whereas the Copidognathus fauna of the Black Sea is similar to that of the Mediterranean.Halacarids are thought to be an ancient taxon, with most genera probably having been present since the Mesozoic and with several species having an age of at least 50 million years. Evidence for their antiquity is found in the distributional pattern of marine and limnic genera and species, in the lack of endemic genera despite low fecundity and lack of dispersal stages, and in the fact that amphiatlantics are restricted to certain genera without relationships to the niches inhabited.     

Geographical and ecological distribution of marine halacarid genera and species (Acari: Halacaridae)

At the end of 2002, the number of marine halacarid species was 1018, that of genera 51. A single genus, Copidognathus contains 33% of all species (336). Eleven genera are monotypic. Geographical provinces with a large number of species are the tropical western Pacific, temperate northeastern Atlantic, temperate southeastern Pacific, and Mediterranean-Black Sea. Most records of halacarid species are from temperate and tropical areas; 10% of species are known from polar zones. On a generic level, 29 genera are recorded from tropical and temperate but not from polar provinces, five genera are restricted to the tropics, and none to polar regions. The majority (920 species or 90%) of all species live in the upper 200 m. Records of genera with exclusively algivorous or brackish/fresh water species are bound to littoral habitats; all the other genera occur in more than one depth zone. Arenicolous genera, though most abundant in the littoral zone, have representatives in the bathyal. Four marine genera (Copidognathus, Halacarellus, Isobactrus, Lohmannella) have representatives in coastal fresh water, and three genera, Acarothrix, Caspihalacarus and Peregrinacarus, are predominantly inhabitants of diluted brackish and fresh water. None of the free-living halacarid genera of the world's oceans appears to be endemic to one geographical province.     

Tropical and Temperate: Evolutionary History of Páramo Flora

Biogeography of the tropical alpine flora of South and Central America, the páramo flora, has been studied by dividing genera into tropical, temperate, and cosmopolitan chorological flora elements. Published molecular phylogenies of páramo genera are reviewed to summarize knowledge about evolutionary history of the páramo flora and to assess congruence between chorological and phylogenetic approaches. Molecular phylogenies suggest that both the tropical and temperate regions have been important source areas for evolution of the páramo flora. Conclusions derived from chorological patterns regarding origin of genera in páramo are mostly supported by phylogenetic data. Nevertheless, in Chuquiraga, Halenia, Huperzia, and Perezia the chorological scenario is rejected, and in Chusquea-Neurolepis, Elaphoglossum, Gunnera, Halenia, Jamesonia-Eriosorus, and Lasiocephalus independent colonization events from one or several source areas are suggested. Tropical and temperate genera contributed equally to modern species richness of the páramo flora. Among temperate genera, the northern hemisphere genera gave rise to more species in páramo than did genera from the southern hemisphere. So far, no unequivocal evidence has been provided for migration of páramo genera to the temperate zones.     

Physical gills in Elmidae (Coleoptera: Byrrhoidea): Structure and evolutionary pattern of plastron in Stenelmis and related genera

Many species within Elmidae (Coleoptera: Byrrhoidea) have plastrons composed of flattened setae. However, some genera display fine plastrons on the epicuticle, called plastron hairs. In Japanese elmids, members of the genera Stenelmis, Ordobrevia, Nomuraelmis and Leptelmis bear ventral plastron hairs. Based on a maximum likelihood tree including most Japanese genera within Elmidae, we found that these genera are monophyletic and that plastron hairs are a derived character in Elmidae. We also found that the genus Graphelmis bears jigsaw puzzle‐like plastron scales with plastron hair‐like projections, and is sister to the group with plastron hairs.     

Classification, diversity, and distribution of Chilean Asteraceae: implications for biogeography and conservation

This paper provides a synopsis of the Chilean Asteraceae genera according to the most recent classification. Asteraceae is the richest family within the native Chilean flora, with a total of 121 genera and c . 863 species, currently classified in 18 tribes. The genera are distributed along the whole latitudinal gradient in Chile, with a centre of richness at 33°–34° S. Almost one-third of the genera show small to medium-small ranges of distribution, while two-thirds have medium-large to large latitudinal ranges of distribution. Of the 115 mainland genera, 46% have their main distribution in the central Mediterranean zone between 27°–37° S. Also of the mainland genera, 53% occupy both coastal and Andean environments, while 33% can be considered as strictly Andean and 20% as strictly coastal genera. The biogeographical analysis of relationships allows the distinction of several floristic elements and generalized tracks: the most marked floristic element is the Neotropical, followed by the antitropical and the endemic element. The biogeographical analysis provides important insights into the origin and evolution of the Chilean Asteraceae flora. The presence of many localized and endemic taxa has direct conservation implications.     

Seed Dispersal in Páramo Plants: Epizoochorous and Hydrochorous Taxa

Abstract: On the basis of a recent checklist of plant diversity in páramos, diaspores collected from herbaria were studied for adaptations to dispersal on animals and by water. This study shows that the páramo flora has a relatively high percentage of genera with morphological adaptations to epizoochorous and to hydrochorous diaspore dispersal. Genera with hooked and straight appendages are present throughout the páramo belt, while their number decreases in the higher páramo zones. About half of the hydrochorous genera and one-third of the epizoochorous ones can be found throughout all páramo zones. The contribution of holarctic epizoochorous genera to the páramo flora seems to be greater than that of austral-antarctic genera, whereas in hydrochorous genera it is the reverse.     

Seed plant genera endemic to the Caribbean Island biodiversity hotspot: A review and a molecular phylogenetic perspective

The Caribbean Island Biodiversity Hotspot is composed primarily of the Bahamas and Greater and Lesser Antilles. A total of 180 genera (727 spp., ca. 9% of the species endemic to the Antilles) are restricted to this hotspot. Most of these genera are unispecific (51%), a pattern that is also found on other islands of the world. The majority of the endemic genera belong to the “Core Eudicot” clade, and they were published in two time periods (1854–1878 and 1904–1928). There are molecular phylogenies available for 63 of the endemic genera. However, phylogenetic reconstructions of only 21 genera are based on more than one independent DNA region and have well-supported clades and good taxonomic sampling. Six of the endemic genera form part of early-branching groups. We could not infer biogeographical conclusions from the molecular phylogenies of most of the endemic genera (43: 68%). There is an urgent need for (1) additional field studies to learn the conservation status of these genera, (2) effective protection of the habitats where the most endangered genera occur, and (3) additional biological and systematic studies of the least understood genera.     

Geographical and ecological distribution of marine halacarid genera and species (Acari: Halacaridae)

At the end of 2002, the number of marine halacarid species was 1018, that of genera 51. A single genus, Copidognathus contains 33% of all species (336). Eleven genera are monotypic. Geographical provinces with a large number of species are the tropical western Pacific, temperate northeastern Atlantic, temperate southeastern Pacific, and Mediterranean-Black Sea. Most records of halacarid species are from temperate and tropical areas; 10% of species are known from polar zones. On a generic level, 29 genera are recorded from tropical and temperate but not from polar provinces, five genera are restricted to the tropics, and none to polar regions. The majority (920 species or 90%) of all species live in the upper 200 m. Records of genera with exclusively algivorous or brackish/fresh water species are bound to littoral habitats; all the other genera occur in more than one depth zone. Arenicolous genera, though most abundant in the littoral zone, have representatives in the bathyal. Four marine genera (Copidognathus, Halacarellus, Isobactrus, Lohmannella) have representatives in coastal fresh water, and three genera, Acarothrix, Caspihalacarus and Peregrinacarus, are predominantly inhabitants of diluted brackish and fresh water. None of the free-living halacarid genera of the world's oceans appears to be endemic to one geographical province.     

Molecular systematics of peppermint and cleaner shrimps: phylogeny and taxonomy of the genera Lysmata and Exhippolysmata (Crustacea: Caridea: Hippolytidae)

Shrimps from the ecologically diverse genera Lysmata and Exhippolysmata are rare among marine invertebrates because they are protandric simultaneous hermaphrodites: shrimps initially mature and reproduce solely as males, and later in life become functional simultaneous hermaphrodites. Considerable progress on the reproductive ecology of members from these two genera has been achieved during the last decade. However, several outstanding issues of systematic nature remain to be addressed. Here, a molecular phylogeny of these two genera was used to examine the overall evolutionary relationship within and between species and genera, and to answer various questions related to the systematic status of several species. The present phylogenetic analysis, including 53 sequences and 26 species of Lysmata and Exhippolysmata, indicates that semiterrestrial shrimps from the genus Merguia represent the sister group to a second natural clade composed by shrimps from the genera Lysmata and Exhippolysmata. Also, the phylogenetic analysis confirmed that the genus Lysmata is paraphyletic, and includes the genus Exhippolysmata, as noted in a preliminary study. The tree partially supports the separation of species with or without a developed accessory branch into two different genera or subgenera (i.e. Lysmata and Hippolysmata having a well‐developed accessory branch, or not, respectively). The genetic distance between the cleaner shrimps Lysmata amboinensis and Lysmata grabhami was smaller than has been observed between other sister species. On the other hand, the topology of the tree indicates that these two entities are reciprocally monophyletic. Thus, this latter result, together with minor but constant differences in the colour pattern reported for these two entities, indicates that there is no reason to stop treating them as different valid species. This study enabled the long overdue resolution of standing taxonomic questions in shrimps from the genera Lysmata and Exhippolysmata. In the future, this phylogeny will help to reveal the conditions favouring the origins of several behavioural and morphological novelties in these unique shrimps. © 2010 The Linnean Society of London, Zoological Journal of the Linnean Society, 2010, 160 , 254–265.     

Asteropeia and Physena (Caryophyllales): A case study in comparative wood anatomy

Previous analyses ofAsteropeia andPhysena have not compared the wood anatomy of these genera to those of Caryophyllales s.l. Molecular evidence shows that the two genera from a clade that is a sister group of the core Caryophyllales. Synapomorphies of theAsteropeia-Physena clade include small circular alternate pits on vessels, presence of vasicentric tracheids plus fiber-tracheids, presence of abaxial-confluent plus diffuse axial parenchyma, and presence of predominantly uniseriate rays. These features are analyzed with respect to habit and ecology of the two genera. Solitary vessels, present in both genera, are related to the presence of vasicentric tracheids. Autapomorphies in the two genera seem related to adaptations byPhysena as a shrub of moderately dry habitats (e.g., narrower vessel elements, abundant vasicentric tracheids, square to erect cells in rays) as compared to alternate character expressions that seem related to the arboreal habit and humid forest ecology ofAsteropeia. The functional significance of vasicentric tracheids and fiber-tracheids in dicotyledons is briefly reviewed in the light of wood anatomy of the two genera.     

Neotropical ennomine moths: a review of the genera (Lepidoptera: Geometridae)

The classification of the Neotropical genera of the Ennominae is reviewed and 267 genera are recognised to occur in this region. Three new genera are described and three others are reinstated, while 48 generic synonyms are newly established. Other changes established in this work include 14 species synonyms and 237 new or reinstated combinations. External features and genitalia of representative members of the genera are illustrated (753 figures). All the known Neotropical species and subspecies of Ennominae are listed ( c . 3470), plus their synonyms. The tribes to which the genera belong are assessed, with c . 200 of the genera assigned to tribe or other suprageneric grouping.  © 2002 The Linnean Society of London, Zoological Journal of the Linnean Society , 2002, 135 , 121–401.     

柏科分类和分布：亚科,族和属

柏科Cupressaceae和杉科Taxodiaceae有许多相似之处,近年来不少分类学家主张把两科合并成广义的柏科。原杉科中的金松属Sciadopitys与两科其他属的差异较大,被提升为单种科Sciadopity-aceae。本文根据球果可育种鳞的位置把柏科(狭义)分为2亚科,即上部种鳞不可育的柏木亚科Cupres-soideae和上部种鳞可育的澳洲柏亚科Callitroideae。综合其他形态学和解剖学证据,柏木亚科又分4族,即柏木族Cupresseae(包括:柏术属Cupressus、杂交柏属×Cupressocyparis、扁柏属Chamaecyparis和福建柏属Fokeinia)、侧柏族Thujopsideae(包括:崖柏属Thuja、罗汉柏属Thujopsis和侧柏属Platycladus)、圆柏族Junipereae(包括:圆柏属Juniperus和海参威柏属Microbiota)以及香漆柏族Tetraclineae(包括:翠柏属Calocedrus和香漆柏属Tetraclinis)。澳洲柏亚科又分3族,即澳洲柏族Actinostrobeae(包括:西澳柏属Actinostuobus、澳洲柏属Callitris、智利柏属Fitzroya和杉叶柏属Neocallitropsis)、南非柏族Widdring-toneae(包括:白智利柏属Pilgerodendron、塔斯曼柏属Diselma和南非柏属Widdringtonia)以及甜柏族Libocedreae(包括:甜柏属Libocedrus、巴布亚柏属Papuacedrus和南美柏属Austrocedrus)。柏科21个属的地理分布可划分为5种类型,即:(     

Alonella and Dunhevedia (Chydoridae,Cladocera): Morphology of trunk limbs

Summary The legs of some species of genera Alonella and Dunhevedia are described, including the type species of these genera. The structure of the endites and gnathobases is depicted and described in detail. The structure of legs of the studied species is compared with that of species of some other genera, including Eurycercus and Saycia.     

A new genus of Cyrtoscydmini (Coleoptera: Staphylinidae: Scydmaeninae) from Japan

Rutaraphes shikokuensis gen. et sp. nov. is described from Shikoku, Japan. The new taxon belongs to a group of genera characterized by the lateral sutures demarcating the submentum and is most similar to Neuraphes and Scydmoraphes. Morphological structures of Rutaraphes are illustrated and possible affinities with other genera of Cyrtoscydmini are discussed. Keys to identification of Palearctic and Japanese genera of Cyrtoscydmini are given. Including Rutaraphes, 14 genera of Scydmaeninae are currently known to occur in Japan.     

Phylogeny, classification, and biogeography of the cycloteline Therevinae (Insecta: Diptera: Thereavidae)

Twenty-one members of the Laurasian group of Therevinae (Diptera: Therevidae) are compared using 65 adult morphological characters. Cladistic analysis using parsimony on the 17 ingroup and 4 outgroup taxa provides a well-supported hypothesis of relationships among taxa within the Gyclotelini, tribe nov. The Cyclotelini is a monophyletic assemblage of mostly New World genera, including Anolinga , gen. nov. , Breviperna Irwin, Coleiana , gen. nov. , Crebraseta , gen. nov. , Cyclotelus Walker, Mesonana , gen.nov. , and Ozodiceromyia Bigot. In addition, three Old World genera, Ammothereva Lyneborg, Bugulaverpa , gen. nov. , and Procyclotelus Nagatomi & Lyneborg, are included in the tribe. These ten genera are divided into two monophyletic genus-groups, the Brevipema-group and the Cyclotelus-group. Keys are provided for the genera of Cyclotelini. The tribe, the two informal genus-groups, and all genera are diagnosed; five new genera and six new species are proposed. The biogeographical histories of the genera are discussed in terms of their cladistic relationships using methods of cladistic biogeography. Two major vicariant events account for the current distribution of the tribe. The first relates to the Beringian land bridge connecting western North America and eastern Asia. Second, New World cyclotelines were profoundly affected by the Early Eocene breakup of the archipelagic bridge between North and South America, and the distributions support the hypotheses favouring the continental origin of the Greater Antilles.     

Morphology agrees with molecular data: phylogenetic affinities of Euptychiina butterflies (Nymphalidae: Satyrinae)

Euptychiina is the most species‐rich subtribe of Neotropical Satyrinae, with over 450 known species in 47 genera (14 monotypic). Here, we use morphological characters to examine the phylogenetic relationships within Euptychiina. Taxonomic sampling included 105 species representing the majority of the genera, as well as five outgroups. A total of 103 characters were obtained: 45 from wing pattern, 48 from genitalia and 10 from wing venation. The data matrix was analysed using maximum parsimony under both equal and extended implied weights. Euptychiina was recovered as monophyletic with ten monophyletic genera, contrasting previous DNA sequence‐based phylogenies that did not recover the monophyly of the group. In agreement with sequence‐based hypotheses, however, three main clades were recognized: the ‘Megisto clade’ with six monophyletic and three polyphyletic genera, the ‘Taygetis clade’ with nine genera of which three were monophyletic, and the ‘Pareuptyhia clade’ with four monophyletic and two polyphyletic genera. This is the first morphology‐based phylogenetic hypothesis for Euptychiina and the results will be used to complement molecular data in a combined analysis and to provide critical synapomorphies for clades and genera in this taxonomically confused group.