Prodromus of a fern flora for Bolivia. VI. Psilotaceae

Phytotaxa ◽  
2017 ◽  
Vol 327 (1) ◽  
pp. 95
Author(s):  
MICHAEL KESSLER ◽  
ALAN R. SMITH

We provide a synopsis to the family Psilotaceae in Bolivia, consisting of the single species Psilotum nudum.

2021 ◽  
Vol 20 (7) ◽  
pp. 911-927
Author(s):  
Lucia Muggia ◽  
Yu Quan ◽  
Cécile Gueidan ◽  
Abdullah M. S. Al-Hatmi ◽  
Martin Grube ◽  
...  

AbstractLichen thalli provide a long-lived and stable habitat for colonization by a wide range of microorganisms. Increased interest in these lichen-associated microbial communities has revealed an impressive diversity of fungi, including several novel lineages which still await formal taxonomic recognition. Among these, members of the Eurotiomycetes and Dothideomycetes usually occur asymptomatically in the lichen thalli, even if they share ancestry with fungi that may be parasitic on their host. Mycelia of the isolates are characterized by melanized cell walls and the fungi display exclusively asexual propagation. Their taxonomic placement requires, therefore, the use of DNA sequence data. Here, we consider recently published sequence data from lichen-associated fungi and characterize and formally describe two new, individually monophyletic lineages at family, genus, and species levels. The Pleostigmataceae fam. nov. and Melanina gen. nov. both comprise rock-inhabiting fungi that associate with epilithic, crust-forming lichens in subalpine habitats. The phylogenetic placement and the monophyly of Pleostigmataceae lack statistical support, but the family was resolved as sister to the order Verrucariales. This family comprises the species Pleostigma alpinum sp. nov., P. frigidum sp. nov., P. jungermannicola, and P. lichenophilum sp. nov. The placement of the genus Melanina is supported as a lineage within the Chaetothyriales. To date, this genus comprises the single species M. gunde-cimermaniae sp. nov. and forms a sister group to a large lineage including Herpotrichiellaceae, Chaetothyriaceae, Cyphellophoraceae, and Trichomeriaceae. The new phylogenetic analysis of the subclass Chaetothyiomycetidae provides new insight into genus and family level delimitation and classification of this ecologically diverse group of fungi.


Zootaxa ◽  
2011 ◽  
Vol 2825 (1) ◽  
pp. 1 ◽  
Author(s):  
MICHEL ROUX ◽  
PHILIP LAMBERT

Two new species of deep-sea stalked crinoids belonging to the family Hyocrinidae were collected in the northeastern Pacific. The descriptions contain detailed information on character variations and ontogeny. The five specimens of Gephyrocrinus messingi n. sp. lived at depths ranging from 1,777 m to 2,110 m off British Columbia and California. This new species is the first record of the genus Gephyrocrinus in the Pacific Ocean, which was previously known from only a single species, G. grimaldii, from the northeastern Atlantic at the same depth range. The two species illustrate opposing phenotypes within the same genus. Fifty-eight specimens of the second new species, Ptilocrinus clarki n. sp., were dredged off British Columbia close to the type-locality of P. pinnatus, the type species of the genus Ptilocrinus, but at shallower depths ranging from 1,178 to 1,986 m. This exceptional collection provides significant data on intraspecific variation in the main morphological characters, especially arm pattern. The ontogeny of stalk articulations and the main traits of adoral plate differentiation are described in detail. A complementary investigation on P. pinnatus was conducted using specimens collected by the “Albatross” expedition at a depth of 2,906 m. Despite similarities in external morphology, tegmen and cover plates, the two ptilocrinid species display significant differences in pinnule architecture, aboral cup and stalk articulations. From comparison with Gephyrocrinus messingi n. sp. and Ptilocrinus clarki n. sp., G. grimaldii and P. pinnatus are interpreted as the result of heterochronic development by paedomorphy after ecological or geographic isolation. Pinnule architecture in the two new species suggests first steps in an evolutionary trend toward a rigid box which protects gonad inflation in the proximal part of the pinnule. These new data on Ptilocrinus and Gephyrocrinus create problems in the current taxonomy of the family Hyocrinidae. The main derived characters, especially in pinnule and arm pattern, are used to propose new hypotheses for hyocrinid phylogeny.


2016 ◽  
Vol 15 (4) ◽  
pp. 11-22
Author(s):  
H M Ashashree ◽  
H A Sayeswara ◽  
K L Naik ◽  
N Kumara Swamy ◽  
Nafeesa Begum

Fresh water wetlands are fragile ecosystems, which are fast deterioring and shrinking due to manmade activities. The fish composition of Huchharayanakere of Shikaripura was studied for a period of twelve months from January to December 2015. The icthyo-faunal diversity of this pond confirmed the occurrence of 13 species of fishes belonging to 5 families. The family Cyprinidae represented by 9 species. Families Anabantidae, Bagridae, Clupeidae and Notopteridae were represented by only a single species. Simultaneously the physico-chemical condition of the water body revealed that water quality is suitable for fish culture. The study of fish fauna of an aquatic body is useful for planning of fisheries development. The pond needs proper management and utilization of this fish wealth and sustainable steps to monitor and conserve the fish health. The present study revealed that Huchharayanakere of Shikaripura harbors wide varieties of fish with economic importance in local and global trade. The study will provide future strategies for development and fish conservation.


Zootaxa ◽  
2012 ◽  
Vol 3271 (1) ◽  
pp. 1 ◽  
Author(s):  
CONRAD J. HOSKIN

In Australia the frog family Microhylidae is largely restricted to tropical rainforests of the Wet Tropics region in the north-east of the country, but in that region the family is diverse. Only one species, Cophixalus ornatus, is widespread in the WetTropics but there has been suspicion that it may comprise multiple species. A recent study (Hoskin et al. 2011) assessedgenetic and phenotypic variation across the range of C. ornatus, finding three deeply divergent genetic lineages that differin mating call and some aspects of morphology. Two of these lineages abutt in the central Wet Tropics and in that areahybridization was found to be very limited despite sympatry at high densities. Based on multiple lines of data, Hoskin etal. (2011) concluded that the three genetic lineages represent biological species. The taxonomy of these three lineages isresolved here. I describe two new species, Cophixalus australis sp. nov. and Cophixalus hinchinbrookensis sp. nov., andredescribe C. ornatus. The three species are not distinguishable based on any single morphological or call trait and arebest identified by genetics or locality. The distributions of the three species are largely allopatric. Cophixalus ornatus isfound in rainforest in the northern Wet Tropics, C. australis sp. nov. occurs in rainforest and adjacent wet sclerophyllforests in the central and southern Wet Tropics, and C. hinchinbrookensis sp. nov. inhabits rainforest and montane heathon Hinchinbrook Island. All three species are common. Cophixalus australis sp. nov. contains three genetic subgroupsthat are considered a single species based on phenotypic similarity and high levels of hybridization at contact zones. Thedescription of Cophixalus australis sp. nov. and Cophixalus hinchinbrookensis sp. nov. brings the number of Australian Cophixalus species to 18, 15 of which are restricted to the Wet Tropics region.


Zootaxa ◽  
2019 ◽  
Vol 4657 (2) ◽  
pp. 352-360
Author(s):  
WILLIAM A. SHEAR ◽  
PAUL E. MAREK

Urochordeumatidae Silvestri, 1909 includes a single species, Urochordeuma bumpusi Silvestri, 1909, with U. porona Chamberlin, 1941 as a new junior subjective synonym. The family Urochordeumatidae is removed from the superfamily Caseyoidea and transferred to the superfamily Striarioidea. The species is known only from four counties in Washington State in the North Cascades: Pierce, King, Thurston and Whatcom. The occurrence of U. bumpusi from Whatcom County is a significant range extension. 


Zootaxa ◽  
2007 ◽  
Vol 1494 (1) ◽  
pp. 1-44 ◽  
Author(s):  
JAMES DARWIN THOMAS ◽  
KRISTINE N. KLEBBA

Six new amphipod species in the genus Leucothoe from the tropical western Atlantic Ocean are described and illustrated. Extensive field collecting and specialized underwater collecting techniques have documented 43 new invertebrate host records for these new taxa. Four of these new species inhabit interior canals of sponges; Leucothoe barana n.sp., Leucothoe garifunae n.sp., Leucothoe saron n.sp., and Leucothoe ubouhu n.sp. A remarkable new species, Leucothoe flammosa n.sp., nestles in the gills of seven species of bivalve mollusks. A single species, Leucothoe wuriti n.sp., appears restricted to the branchial chamber of two species of solitary ascidians. Detailed illustrations and scanning electron microscopy enables comparison of ultrastructure details. More precise taxonomic character morphologies are also presented thus allowing improved taxonomic precision within the family Leucothoidae.


2020 ◽  
Vol 34 (2) ◽  
pp. 113 ◽  
Author(s):  
Rafael Robles ◽  
Peter C. Dworschak ◽  
Darryl L. Felder ◽  
Gary C. B. Poore ◽  
Fernando L. Mantelatto

The axiidean families Callianassidae and Ctenochelidae, sometimes treated together as Callianassoidea, are shown to represent a monophyletic taxon. It comprises 265 accepted species in 74 genera, twice this number of species if fossil taxa are included. The higher taxonomy of the group has proved difficult and fluid. In a molecular phylogenetic approach, we inferred evolutionary relationships from a maximum-likelihood (ML) and Bayesian analysis of four genes, mitochondrial 16S rRNA and 12S rRNA along with nuclear histone H3 and 18S rRNA. Our sample consisted of 298 specimens representing 123 species plus two species each of Axiidae and Callianideidae serving as outgroups. This number represented about half of all known species, but included 26 species undescribed or not confidently identified, 9% of all known. In a parallel morphological approach, the published descriptions of all species were examined and detailed observations made on about two-thirds of the known fauna in museum collections. A DELTA (Description Language for Taxonomy), database of 135 characters was made for 195 putative species, 18 of which were undescribed. A PAUP analysis found small clades coincident with the terminal clades found in the molecular treatment. Bayesian analysis of a total-evidence dataset combined elements of both molecular and morphological analyses. Clades were interpreted as seven families and 53 genera. Seventeen new genera are required to reflect the molecular and morphological phylograms. Relationships between the families and genera inferred from the two analyses differed between the two strategies in spite of retrospective searches for morphological features supporting intermediate clades. The family Ctenochelidae was recovered in both analyses but the monophyly of Paragourretia was not supported by molecular data. The hitherto well recognised family Eucalliacidae was found to be polyphyletic in the molecular analysis, but the family and its genera were well defined by morphological synapomorphies. The phylogram for Callianassidae suggested the isolation of several species from the genera to which they had traditionally been assigned and necessitated 12 new generic names. The same was true for Callichiridae, with stronger ML than Bayesian support, and five new genera are proposed. Morphological data did not reliably reflect generic relationships inferred from the molecular analysis though they did diagnose terminal taxa treated as genera. We conclude that discrepancies between molecular and morphological analyses are due at least in part to missing sequences for key species, but no less to our inability to recognise unambiguously informative morphological synapomorphies. The ML analysis revealed the presence of at least 10 complexes wherein 2–4 cryptic species masquerade under single species names.


2009 ◽  
Vol 34 (3) ◽  
pp. 443-454 ◽  
Author(s):  
Dietmar Quandt ◽  
Sanna Huttunen ◽  
Ray Tangney ◽  
Michael Stech

Although the Lembophyllaceae has undergone considerable revision during the last century, the generic and familial level relationships of this pleurocarpous moss family are still poorly understood. To address this problem, a generic revision of the Lembophyllaceae based on molecular data was undertaken. We analyzed two plastid markers, the trnL-trnF and the psbT-psbH region in combination with the ITS2 of nuclear ribosomal DNA. The molecular data reveal that the current circumscription of the family is too narrow and that several genera previously placed in the Lembophyllaceae should be reincluded. The family includes: Bestia, Camptochaete, Dolichomitra, Dolichomitriopsis, Fallaciella, Fifea, Isothecium, Lembophyllum, Looseria stat. nov., Pilotrichella, Rigodium, Tripterocladium, and Weymouthia. Looseria contains a single species: Looseria orbiculata comb. nov. Acrocladium is excluded and provisionally accommodated in the Lepyrodontaceae. Generic limits supported by the molecular data support a return to the early twentieth century family concept of Brotherus. The analyses indicate that the segregate genus Orthostichella is distinct from its parent genus Pilotrichella, probably at the family level. Whereas Pilotrichella is resolved within the Lembophyllaceae, Orthostichella clusters with Porotrichum and Porothamnium forming a clade (OPP-clade) sister to the remaining Neckeraceae and Lembophyllaceae. Hence, the Neckeraceae is paraphyletic. Recognition of the OPP-clade as a new family is desirable but awaits the results of detailed ongoing morphological studies.


Author(s):  
Michael F Braby

This is the first complete field guide to all butterfly species on Australia’s mainland and its remote islands. Written by one of Australia's leading lepidopterists, it is stunningly illustrated with colour photographs of each of the 416 currently identified species. There is also a distribution map for each species on the Australian mainland. It covers the five major family groups: Hesperiidae, Paplionidae, Pieridae, Nymphalidae and Lycaenidae, as well as the family Riodinidae, which has but a single species in Australia. The introduction covers adult structure, classification, distribution and habitats, and life cycle and behaviour. This is followed by accounts of each of the 416 species, giving common name, scientific name, and other names (if any), as well as details of behaviour, habitat, status, and larval food plants. Accompanying each species is a distribution map, and photographs of the upperside and underside of both male and female specimens. The book also contains a checklist of all species, a list of entomological contacts, a glossary, a bibliography, an index of common names and an index of scientific names.


2019 ◽  
Vol 187 (2) ◽  
pp. 378-412 ◽  
Author(s):  
Fabiana Criste Massariol ◽  
Daniela Maeda Takiya ◽  
Frederico Falcão Salles

AbstractOligoneuriidae is a Pantropical family of Ephemeroptera, with 68 species described in 12 genera. Three subfamilies are recognized: Chromarcyinae, with a single species from East Asia; Colocrurinae, with two fossil species from Brazil; and Oligoneuriinae, with the remaining species distributed in the Neotropical, Nearctic, Afrotropical and Palaearctic regions. Phylogenetic and biogeographical analyses were performed for the family based on 2762 characters [73 morphological and 2689 molecular (COI, 16S, 18S and 28S)]. Four major groups were recovered in all analyses (parsimony, maximum likelihood and Bayesian inference), and they were assigned to tribal level, namely Oligoneuriini, Homoeoneuriini trib. nov., Oligoneuriellini trib. nov. and Elassoneuriini trib. nov. In addition, Yawari and Madeconeuria were elevated to genus level. According to Statistical Dispersal-Vicariance (S-DIVA), Dispersal Extinction Cladogenesis (DEC) and divergence time estimation analyses, Oligoneuriidae originated ~150 Mya in the Gondwanan supercontinent, but was probably restricted to the currently delimited Neotropical region. The initial divergence of Oligoneuriidae involved a range expansion to Oriental and Afrotropical areas, sometime between 150 and 118 Mya. At ~118 Mya, the family started its diversification, reaching the Nearctic through dispersal from the Neotropical region and the Palaearctic and Madagascar from the Afrotropical region.


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