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1.
PeerJ ; 12: e16772, 2024.
Article in English | MEDLINE | ID: mdl-38525284

ABSTRACT

Background: Semiaquatic bugs (Hemiptera: Heteroptera: Gerromorpha) are distributed worldwide and play fundamental roles in limnic ecosystems. They are the most successful group of organisms to occupy the air-water interface, are important models to study ecology and evolution, and can be relevant tools in biomonitoring. Veliidae is the second most speciose family of semiaquatic bugs, but its internal classification, including subfamilies and genera, is artificial and based on symplesiomorphies. One of these non-monophyletic entities is Paravelia Breddin, 1898, the largest genus in the subfamily Veliinae. Results: In an effort to better classify the Veliinae, we describe Foveavelia to hold five South American species previously placed in Paravelia. The new genus is characterized by the following combination of features: unusual coarse cuticular punctures throughout the thorax and abdomen; a pair of small, frosty, pubescent areas formed by a very dense layer of short setae on the anterior lobe of the pronotum; fore tibial grasping comb present only in males; middle tibia with a row of elongate dark-brown trichobothria-like setae on the distal third, decreasing in size distally; macropterous specimens with the apical macula of the forewings elongate and constricted at mid-length, reaching the wing apex; and the male proctiger with a pair of anterodorsal projections. Besides the description, a key to the species of Foveavelia is provided, accompanied by illustrations and a species distribution map.


Subject(s)
Heteroptera , Animals , Male , Ecosystem , Ecology , Biological Monitoring , South America
2.
PhytoKeys ; 237: 117-139, 2024.
Article in English | MEDLINE | ID: mdl-38292077

ABSTRACT

Chile's distinctive flora, geographical isolation, and complex topography collectively contribute to a notable endemic species diversity, particularly within central regions identified as critical areas for biodiversity conservation. The cactus genus Eriosyce, as currently circumscribed, encompasses seven sections, with Eriosycesect.Horridocatus presenting a notably complex species group. This study investigates the E.curvispina complex, a member of the Notocacteae tribe common in central Chile, by incorporating new populations and examining phylogenetic relationships using four plastid and one nuclear molecular marker. The phylogenetic analysis of sampled individuals identified nine independent lineages, each warranting recognition at the species rank. Despite minimal morphological differences among taxa, morphological characters were utilized to support and stabilize the DNA-based phylogenetic hypothesis. The results highlight the high taxonomic diversity in these cactus lineages and have implications for the classification of the E.curvispina complex, including new combinations and proposals of conservation status.


ResumenLa flora distintiva de Chile, su aislamiento geográfico y topografía compleja contribuyen colectivamente a una notable diversidad de especies endémicas, particularmente dentro de las regiones centrales identificadas como áreas críticas para la conservación de la biodiversidad. El género de cactus Eriosyce, tal como está circunscrito actualmente, abarca siete secciones, presentando Eriosycesect.Horridocatus un grupo de especies notablemente complejo. Este estudio investiga el complejo E.curvispina, un miembro de la tribu Notocacteae común en Chile central, incorporando nuevas poblaciones y examinando las relaciones filogenéticas utilizando cuatro marcadores moleculares del cloroplasto y uno nuclear. El análisis filogenético de las poblaciones muestreadas identificó nueve linajes independientes, cada uno mereciendo reconocimiento a nivel de especie. A pesar de las mínimas diferencias morfológicas entre los taxones, se utilizaron caracteres morfológicos para apoyar y estabilizar la filogenia basada en ADN. Los resultados resaltan la alta diversidad taxonómica en estos linajes de cactus y tienen implicaciones para la clasificación del complejo E.curvispina, incluyendo nuevas combinaciones y propuestas de estado de conservación.

3.
Zootaxa ; 4946(1): zootaxa.4946.1.1, 2021 Mar 17.
Article in English | MEDLINE | ID: mdl-33757044

ABSTRACT

The Batrachideinae subfamily is a well-defined and taxonomically stable taxon, with a pantropical distribution and an important representation in the Neotropical region. In this study, the characters and distributions of the genera and species are discussed based on a morphological analysis and a key to genera of the American Batrachideinae is also provided. New synonymies are established: Tettigidea Scudder, 1862 = Eotetrix Gorochov, 2012 syn. nov.; Batrachidea mucronata (Saint-Fargeau Serville, 1825) = Tettigidea granulosa Bruner, 1913 syn. nov.; Batrachidea planus (Hancock, 1907) = Batrachidea brevis (Hancock, 1909) syn. nov.; Tettigidea lateralis (Say, 1824) = Tettigidea nicaraguae Bruner, 1895 syn. nov.; Tettigidea lateralis (Say, 1824) = Tettigidea annulipes Bruner, 1910 syn. nov.; Tettigidea cuspidata Scudder, 1875 = Tettigidea corrugata Bruner, 1910 syn. nov.; Tettigidea cuspidata Scudder, 1875 = Tettigidea multicostata Bolívar, 1887 syn. nov.; Tettigidea chapadensis Bruner, 1910 = Tettigidea costalis Bruner, 1910 syn. nov.; Tettigidea chapadensis Bruner, 1910 = Tettigidea hancocki Bruner, 1910 syn. nov.; Tettigidea intermedia Bruner, 1910 = Tettigidea subatera Bruner, 1910 syn. nov.; Tettigidea scudderi Bolívar, 1887 = Tettigidea steinbachi Bruner, 1920 syn. nov. Three species are transferred from the genus Tettigidea to the genus Paxilla Bolívar, 1887: Paxilla mexicana (Hancock, 1915) comb. nov., Paxilla tecta (Morse, 1900) comb. nov., Paxilla nigra (Morse, 1900) comb. nov.; Tettigidea unicornis (Gorochov, 2012) comb. nov. is transferred from the genus Eotetrix Gorochov, 2012 to Tettigidea, and Batrachidea planus (Hancock, 1907) comb. nov. from Tettigidea to Batrachidea Serville, 1838. Five new species groups (lateralis, armata, cuspidata, paratecta and scudderi) are recognized in the genus Tettigidea. Neotype of Tettigidea lateralis lateralis is designated. Keys to the Batrachideinae genera and species of the most diverse American genera (Tettigidea and Paxilla) are also provided.


Subject(s)
Orthoptera , Animal Distribution , Animals
4.
J Phycol ; 57(3): 817-830, 2021 06.
Article in English | MEDLINE | ID: mdl-33565083

ABSTRACT

The recent segregation of 12 genera in the tribe Streblocladieae suggests that the taxonomy of some species belonging to Polysiphonia sensu lato is updated with the transfer and the proposal of new combinations. Accordingly, six new additions to the tribe Streblocladieae on the basis of morphological and molecular analyses are presented as a consequence of this new segregation. These additions include the description of the new species Carradoriella platensis sp. nov., the proposal of the following new combinations Eutrichosiphonia paniculata comb. nov., E. tapinocarpa comb. nov., and the reinstatement of Vertebrata curta, V. decipiens, and V. patersonis. Additionally, our morphological observations identified additional diagnostic features for two genera of the Streblocladieae. Carradoriella has branches with sexual reproductive structures arranged adaxially on branchlets, and the recently described Eutrichosiphonia has rhizoids with multicellular digitate haptera. Our study gives insights in regards to the distribution, the diagnostic features for delimiting genera morphologically, and the molecular evolutionary relationships in the Streblocladieae.


Subject(s)
Rhodophyta , Evolution, Molecular , Phylogeny
5.
Eur J Protistol ; 80: 125662, 2021 Aug.
Article in English | MEDLINE | ID: mdl-32245612

ABSTRACT

I studied a Brazilian population of Holophrya teres (Ehrenberg, 1834) Foissner, Berger and Kohmann, 1994, using live observation, morphometry, silver impregnation, and scanning electron microscopy. This showed a fair similarity with European populations, especially in having a large (about 13 × 5 µm in vivo) micronucleus pyriform in broad-side view and cuneate in narrow-side view. Several new structures were discovered, viz., an internal oral basket, teeth on anterior end of the oral basket rods, and a buccal seal closing the oral basket when not feeding. Based on this knowledge, I provide an improved diagnosis for H. teres, which can be used as template in further species descriptions. Depending on brosse implantation in the somatic ciliature, the genus was split in Holophrya, Hillerophrya nov. gen., Vdacnyophrya nov. gen., and Bardeleophrya nov. gen. Twenty-one Prorodon species were combined with the holophryid genera, using brosse and thick oral basket rods as main markers. This revealed two new species, viz., Holophrya longiarmata nov. spec. and H. agamalievi nov. spec.


Subject(s)
Ciliophora/classification , Ciliophora/ultrastructure , Brazil , Microscopy, Electron, Scanning , Species Specificity , Terminology as Topic
6.
Zootaxa ; 4870(1): zootaxa.4870.1.1, 2020 Nov 05.
Article in English | MEDLINE | ID: mdl-33311339

ABSTRACT

Trichopoda Berthold, 1827 is a tachinid genus belonging to the subfamily Phasiinae and natively distributed in the Americas. Species of Phasiinae are parasitoids of Hemiptera, especially Heteroptera, and are greatly important as biological control agents. Trichopoda is included in the "Trichopoda typica" group sensu Sabrosky, along with the genera Eutrichopoda Townsend, 1908 and Ectophasiopsis Townsend, 1915a. The genus Trichopoda includes several nominal species, many of which have been synonymized, whereas others have been transferred to different genera. Even though the group is morphologically remarkable for its bright colors and feather-like setae on the hind tibia and is important from an agricultural point of view, there have been no revisionary works dealing with its species. Before the present study, 22 valid species were included in Trichopoda, divided into two subgenera: Galactomyia Townsend, 1908 and Trichopoda s. str. In the current study, 25 species of Trichopoda are considered valid, of which twelve are described as new: Trichopoda (Galactomyia) auricauda sp. n., T. (G.) castannea sp. n., T. (G.) curvicercus sp. n., T. (G.) dupuisi sp. n., T. (G.) elongata sp. n., T. (G.) eupilipes sp. n., T. (G.) goiana sp. n., T. (G.) splendida sp. n., T. (G.) tenebrosa sp. n., T. (G.) tschorsnigi sp. n., T. (G.) urucurytuba sp. n. and T. (Trichopoda) sabroskyi sp. n. We also propose two new synonymies: Trichopoda (Galactomyia) giacomellii (Blanchard, 1966) syn. n. of T. (G.) pennipes (Fabricius, 1781) and T. (G.) nigripes Wulp, 1892 syn. n. of T. (G.) pennipes (Fabricius, 1781); the synonymies of T. ciliata (Fabricius, 1805) and T. haitensis Robineau-Desvoidy, 1830 with T. (G.) pennipes (Fabricius, 1781) are confirmed. We resurrect one species, T. (Galactomyia) limbata (Blanchard, 1966), which was previously synonymized under T. giacomellii (= T. pennipes). We also propose two new subgeneric combinations: T. alipes Wulp, 1892 and T. squamipes Wulp, 1892 are moved from the subgenus Galactomyia to the subgenus Trichopoda. The species aurantiaca Townsend, 1891 is considered as unrecognized within the genus Trichopoda, whereas T. mexicana Macquart, 1846 and T. subcilipes Macquart, 1844 are considered incertae sedis within the tribe Gymnosomatini. Three species are removed from the genus Trichopoda and placed in the genus Homogenia Wulp, 1892: Homogenia apicalis (Wiedemann, 1830), comb. n., H. decisa (Walker, 1853), comb. n. and H. luteipennis (Wiedemann, 1830), comb. n. We provide an identification key to Trichopoda species; due to lack of material, T. flava Röder, 1885 was not included in the key. The compositions of the two subgenera of Trichopoda are redefined for the Neotropical species, whereby all species previously placed in the subgenus Trichopoda by Guimarães, with the exception of T. alipes Wulp, 1892, T. indivisa Townsend, 1897 and T. squamipes, are transferred to the subgenus Galactomyia. On the other hand, the subgeneric placement of the Nearctic species stays the same. We also comment on and try to clarify possible misidentifications, notably for use of species in biological control programs. We present photographs of males and females of all examined species, as well as illustrations of almost all male and female terminalia.


Subject(s)
Diptera , Animals , Female , Male
7.
Zootaxa ; 4814(1): zootaxa.4814.1.1, 2020 Jul 14.
Article in English | MEDLINE | ID: mdl-33055727

ABSTRACT

The present paper describes 16 new species and one new genus from French Guiana and numerous taxonomic changes are proposed prior to the publication of a comprehensive guide to the Phasmatodea of French Guiana. The following 16 new species are described and illustrated: Phanocles procerus n. sp., Phanocloidea lobulatipes n. sp., Cladomorphus guianensis n. sp., Hirtuleius gracilis n. sp., Parastratocles rosanti n. sp., Parastratocles fuscomarginatus n. sp., Paraprisopus apterus n. sp., Paraprisopus multicolorus n. sp., Agrostia longicerca n. sp., Isagoras similis n. sp., Paragrostia brulei n. sp., Prexaspes globosicaput n. sp., Prexaspes guianensis n. sp., Dinelytron cahureli n. sp., Prisopus clarus n. sp. and Prisopus conocephalus n. sp.. The new genus Paragrostia n. gen. is established for the newly described Paragrostia brulei n. sp. and Paragrostia flavimaculata (Heleodoro, Mendes Rafael, 2017) n. comb. the latter of which is here transferred from Agrostia Redtenbacher, 1906.                Fifty-six new combinations are proposed with species transferred to other genera: Bacteria pallidenotata Redtenbacher, 1908, is transferred to Phanocloidea Zompro, 2001 (n. comb.); Bacteria maroniensis Chopard, 1911 is transferred to Phanocles Stål, 1875 (n. comb.); Cladomorphus gibbosus (Chopard, 1911) is transferred to Hirtuleius Stål, 1875 (n. comb.); Stratocles soror Redtenbacher, 1906, Parastratocles lugubris (Redtenbacher, 1906) and Parastratocles cryptochloris (Rehn, 1904) are transferred to Brizoides Redtenbacher, 1906 (n. comb.); Stratocles xanthomela (Olivier, 1792), Stratocles forcipatus Bolívar, 1896 and Stratocles tessulatus (Olivier, 1792) are transferred to Parastratocles (n. comb.); Olcyphides cinereus (Olivier, 1792), Perliodes affinis Redtenbacher, 1906, Perliodes nigrogranulosus Redtenbacher, 1906, Perliodes sexmaculatus Redtenbacher, 1906, Isagoras rugicollis (Gray, 1835), Isagoras sauropterus Rehn, 1947, Brizoides viridipes (Rehn, 1905) and Brizoides graminea Redtenbacher, 1906 are transferred to Agrostia Redtenbacher, 1906 (n. comb.); Agrostia flavimaculata Heleodoro, Mendes Rafael, 2017 is transferred to Paragrostia n. gen. (n. comb.); Isagoras affinis Chopard, 1911, Isagoras chocoensis Hebard, 1921, Isagoras metricus Rehn, 1947 and Isagoras schraderi Rehn, 1947 are transferred to Tenerella Redtenbacher, 1906 (n. comb.); Xerosoma glyptomerion Rehn, 1904 is transferred to Isagoras Stål, 1875 (n. comb.); Isagoras venosus (Burmeister, 1838), Paraphasma paulense Rehn, 1918 and Paraphasma quadratum (Bates, 1865) are transferred to Prexaspes Stål, 1875 (n. comb.); Prexaspes (Prexaspes) cneius (Westwood, 1859) is transferred to Tenerella Redtenbacher, 1906 (n. comb.); Prexaspes lateralis (Fabricius, 1775) is transferred to Paraphasma Redtenbacher, 1906 (n. comb.); Isagoras santara (Westwood, 1859) and Prexaspes olivaceus Chopard, 1911 are transferred to Periphloea Redtenbacher, 1906 (n. comb.); Dinelytron agrion Westwood, 1859 is transferred to Paraprisopus Redtenbacher, 1906 (n. comb.); Anarchodes atrophicus (Pallas, 1772) is transferred to Ignacia Rehn, 1904 (n. comb.); Planudes asperus Bellanger Conle, 2013, Planudes brunni Redtenbacher, 1906, Planudes cortex Hebard, 1919, Planudes crenulipes Rehn, 1904, Planudes funestus Redtenbacher, 1906, Planudes melzeri Piza, 1937, Planudes molorchus (Westwood, 1859), Planudes paxillus (Westwood, 1859), Planudes perillus Stål, 1875, Planudes pygmaeus (Redtenbacher, 1906) and Planudes taeniatus Piza, 1944 are transferred to Isagoras Stål, 1875 (n. comb.); Prisopoides atrobrunneus Heleodoro Rafael, 2020, Prisopoides brunnescens Heleodoro Rafael, 2020, Prisopoides caatingaensis Heleodoro Rafael, 2020 and Prisopoides villosipes (Redtenbacher, 1906) are transferred to Prisopus Peletier de Saint Fargeau Serville, 1828 (n. comb.); Melophasma antillarum (Caudell, 1914), Melophasma brachypterum Conle, Hennemann Gutiérrez, 2011, Melophasma colombianum Conle, Hennemann Gutiérrez, 2011 and Melophasma vermiculare Redtenbacher, 1906 are transferred to Paraprisopus Redtenbacher, 1906 (n. comb.); Prexaspes (Elasia) ambiguus (Stoll, 1813), Prexaspes (Elasia) brevipennis (Burmeister, 1838), Prexaspes (Elasia) pholcus (Westwood, 1859), Prexaspes (Elasia) viridipes Redtenbacher, 1906 and Prexaspes (Elasia) vittata (Piza, 1985) are transferred to Prexaspes Stål, 1875 (n. comb.).                Twenty-six new synonymies are established: Perliodes Redtenbacher, 1906 and Chlorophasma Redtenbacher, 1906 are synonymised with Agrostia Redtenbacher, 1906 (n. syn.); Chlorophasma Redtenbacher, 1906 is synonymised with Agrostia Redtenbacher, 1906 (n. syn.); Elasia Redtenbacher, 1906 is synonymised with Prexaspes Stål, 1875 (n. syn.); Prisopoides Heleodoro Rafael, 2020 is synonymised with Prisopus Peletier de Saint Fargeau Serville, 1828 (n. syn.); Melophasma Redtenbacher, 1906 is synonymised with Paraprisopus Redtenbacher, 1906 (n. syn.); Bacteria crassipes Chopard, 1911 is synonymised with Bacteria pallidenotata Redtenbacher, 1908 (n. syn.); Perliodes grisescens Redtenbacher, 1906 and Metriophasma (Metriophasma) pallidum (Chopard, 1911) are synonymised with Agrostia cinerea (Olivier, 1792) (n. syn.); Perliodes nigrogranulosus Redtenbacher, 1906 and Metriophasma (Metriophasma) ocellatum (Piza, 1937) are synonymised with Isagoras rugicollis (Gray, 1835) (n. syn.); Isagoras chopardi Hebard, 1933 is synonymised with Tenerella cneius (Westwood, 1859) (n. syn.); Isagoras proximus Redtenbacher, 1906 is synonymised with Isagoras glyptomerion (Rehn, 1904) (n. syn.); Chlorophasma hyalina Redtenbacher, 1906 is synonymised with Agrostia graminea (Redtenbacher, 1906) (n. syn.); Isagoras nitidus Redtenbacher, 1906 is synonymised with Anisa flavomaculatus (Gray, 1835) (n. syn.); Prexaspes acuticornis (Gray, 1835) is synonymised with Prexaspes servillei (Gray, 1835) (n. syn.); Prexaspes nigromaculatus Chopard, 1911 is synonymised with Periphloea santara (Westwood, 1859) (n. syn.); Prexaspes (Elasia) janus Kirby, 1904 is synonymised with Paraphasma maculatum (Gray, 1835) (n. syn.); Prexaspes dictys (Westwood, 1859) is synonymised with Prexaspes brevipennis (Burmeister, 1838) (n. syn.); Parastratocles aeruginosus Redtenbacher, 1906: 107 is synonymised with Parastratocles forcipatus Bolívar, 1896 (n. syn.); Parastratocles carbonarius (Redtenbacher, 1906: 106) is synonymised with Parastratocles lugubris (Redtenbacher, 1906) (n. syn.); Prisopus spinicollis Burmeister, 1838, Prisopus spiniceps Burmeister, 1838 and Prisopus cornutus Gray, 1835 are synonymised with Prisopus ohrtmanni (Lichtenstein, 1802) (n. syn.); the genus Planudes Stål, 1875 is synonymised with Isagoras Stål, 1875 (n. syn.); Pseudophasma annulipes (Redtenbacher, 1906) is synonymised with Pseudophasma blanchardi (Westwood, 1859) (n. syn.); Ignacia appendiculatum (Kirby, 1904) is synonymised with Anarchodes atrophicus (Pallas, 1772) (n. syn.).                Isagoras obscurum Guérin-Méneville, 1838 is shown to have been erroneously synonymised with Isagoras rugicollis (Gray, 1835) and is here re-established as a valid species (rev. stat.). Pseudophasma castaneum (Bates, 1865) is re-established as a valid species here (rev. stat.).                Paraprisopus Redtenbacher, 1906 and the entire tribe Paraprisopodini are transferred to Pseudophasmatidae: Pseudophasmatinae (n. comb.).                Lectotypes are designated for Perliodes grisescens Redtenbacher, 1906, Isagoras plagiatus Redtenbacher, 1906.Neotypes are designated for Agrostia cinerea (Olivier, 1792), Prexaspes ambiguus (Stoll, 1813), Prisopus horridus (Gray, 1835) and Prisopus sacratus (Olivier, 1792).


Subject(s)
Coleoptera , Heteroptera , Animals , French Guiana , Neoptera
8.
Zootaxa ; 4629(2): zootaxa.4629.2.3, 2019 Jul 05.
Article in English | MEDLINE | ID: mdl-31712520

ABSTRACT

The males of Tropanisopodus tachira Monné Monné, 2007, from Colombia and Paranisopodus granulosus Monné Monné, 2007, from Peru are described for the first time. Anisopodus cochabambaensis Schmid, 2016 is newly recorded for Colombia. Tropanisopodus antonkozlovi sp. nov. is described, and a key to species of Tropanisopodus is provided. Anisopodus acutus Thomson, 1865 is transferred to Paranisopodus Monné Martins, 1976. The female of Paranisopodus heterotarsus Monné Martins, 1976 is described for the first time. Paranisopodus antonkozlovi sp. nov. is described and included in a previous key.


Subject(s)
Coleoptera , Spiders , Animals , Colombia , Female , Male , Peru
9.
Zootaxa ; 4590(4): zootaxa.4590.4.1, 2019 Apr 30.
Article in English | MEDLINE | ID: mdl-31716079

ABSTRACT

On the Hawaiian Islands 22 sciarid species were detected, belonging to the following ten genera: Austrosciara Schmitz Mjöberg, Bradysia Winnertz, Corynoptera Winnertz, Cratyna Winnertz, Epidapus Haliday, Hyperlasion Schmitz, Lycoriella Frey, Phytosciara Frey, Pseudolycoriella Menzel Mohrig and Scatopsciara Edwards. The revision resulted in new combinations for the following five species: Austrosciara hawaiiensis (Hardy) comb. n., Corynoptera prominens (Hardy) comb. n., Cratyna adrostylata (Hardy) comb. n., Cr. longicosta (Hardy) comb. n., and Scatopsciara hoyti (Hardy) comb. n. Eight species were declared as new synonyms: Bradysia bishopi Steffan, 1973 = B. centidens Vilkamaa, Hippa Mohrig, 2012 syn. n.; B. crassicornis (Skuse, 1890) = B. molokaiensis (Grimshaw, 1901) syn. n. and = B. aspercera Mohrig, 2016 syn. n.; B. radicum (Brunetti, 1912) = B. spatitergum (Hardy, 1956) syn. n.; Corynoptera prominens (Hardy, 1956) = C. gladiota Mohrig, 2004 syn. n.; Cosmosciara hartii (Johannsen, 1912) = Plastosciara (Plastosciara) latipons Hardy, 1956 syn. n.; Hyperlasion wasmanni (Schmitz, 1918) = Scythropochroa magnisensoria Hardy, 1956 syn. n.; and Scatopsciara hoyti (Hardy, 1956) = Sc. spiculata Vilkamaa, Hippa Mohrig, 2012 syn. n. These four species are new reports for Hawai'i, three of them are new to science: Epidapus pallidus (Séguy), Pseudolycoriella nigrofemoralis Mohrig, Kauschke Broadley sp. n., Scatopsciara hardyi Mohrig, Kauschke Broadley sp. n. and Sc. steffani Mohrig, Kauschke Broadley sp. n. A lectotype was designated for Bradysia radicum (Brunetti) in order to fix the name. All new and revised species are figured.        The species Bradysia bishopi Steffan, 1973, B. ocellaris (Comstock, 1882), B. radicum (Brunetti, 1912), Cosmosciara hartii (Johannsen, 1912), Pseudolycoriella planiforceps (Steffan, 1971) and Scatopsciara steffani Mohrig, Kauschke Broadley sp. n. are reported from the Galápagos Islands.


Subject(s)
Ceratopogonidae , Diptera , Animals , Ecuador , Fungi , Hawaii , Islands
10.
Zootaxa ; 4605(1): zootaxa.4605.1.1, 2019 May 16.
Article in English | MEDLINE | ID: mdl-31717174

ABSTRACT

In this contribution to the study of gryllacridines or raspy crickets (Orthoptera: Gryllacrididae), a new proposal for classification of this family is provided, dividing it into two subfamilies and ten tribes that includes most of the 114 known genera to date (including the new genera described here). It describes and redefines two subfamilies: Hyperbaeninae n. subf. and Gryllacridinae n. sensu, ten tribes: Phryganogryllacridini n. trib., Capnogryllacridini n. trib., Asarcogryllacridini n. trib., Hyperbaenini n. trib., Paragryllacridini n. trib., Ametrini n. trib., Ametroidini n. trib., Gryllacridini n. sensu., Eremini n. trib. and Progryllacridini n. trib.; ten genera: Claudiagryllacris n. gen., Griffinigryllacris n. gen., Gorochovgryllacris n. gen., Ingrishgryllacris n. gen., Rentzgryllacris n. gen., Willemsegryllacris n. gen., Karnygryllacris n. gen., Brunnergryllacris n. gen., Bianigryllacris n. gen. and Hugelgryllacris n. gen.; seven genera groups: Gryllacrae n. group. (placed under Gryllacridini n. trib. comprising ten genera: Caustogryllacris, Eugryllacris, Gryllacris, Lyperogryllacris, Nesogryllacris, Ocellarnaca, Phlebogryllacris, Prosopogryllacris, Willemsegryllacris n. gen. and Xanthogryllacris), Metriogryllacrae n. group. (under Gryllacridini grouped Metriogryllacris, Homogryllacris, Pseudasarca n. stat. and Furcilarnaca), Anancistrogerae (Anancistrogera, Ancistrogera, Angustogryllacris, Aphanogryllacris, Celebogryllacris), Triaenogryllacrae n. group. (under Gryllacridinae only comprising Triaenogryllacris) the next groups under Ametrini n. trib.: Ametrae n. group. (comprising two genera: Ametrus and Pareremus), Apotrechae n. group. (including three genera: Apotrechus, Apterolarnaca and Bianigryllacris n. gen.) and Apteronomae n. group. (comprising two genera: Ametrosomus and Apteronomus). The status of Dictogryllacris reinst. stat., was restored, previously transferred by Gorochov 2003 as subgenus of Capnogryllacris and to Pseudasarca n. stat. as full genus status is proposed. One genera, one subgenus and one fossil species are synonymized: Xiphogryllacris n. syn. (under Hyalogryllacris) and †Gryllacris brevippennis n. syn. (under †Macrelcana ungeri). The subgenus Glolarnaca n. stat. (included under Zalarnaca), is considered as full genus in Gryllacridinae (Gryllacridini). 57 new combinations are proposed, with particular emphasis on Niphetogryllacris, placing 36 of the 43 existing species of the genus: Pissodogryllacris tesellata n. comb., Willemsegryllacris barnesi n. comb. (previously placed under Gryllacris), Afrogryllacris nigripceps n. comb. (previously placed under in Barombogryllacris), Anancistrogera nigroscutata n. comb., A. cornualis n. comb. and A. genualis n. comb. (included by Karny in Caustogryllacris and by Gorochov in the subgenus Pseudolarnaca, here transfered to Anancistrogera), Hugelgryllacris tchancha n. comb. (before in Psilogryllacris), Diaphanogryllacris annandalei n. comb., D. barkudensis n. comb., D. dravida n. comb., D. gravelyi n. comb., Claudiagryllacris finoti n. comb. C. stigmata n. comb., C. lemur n. comb., C. fryeri n. comb., Stictogrtllacris pungens n. comb., S. madagassa n. comb., S. genufuscata n. comb., S. vosseleri n. comb., S. difficilis n. comb., S. paulani n. comb., Stictogryllacris signoreti n. comb., S. indecisa n. comb., S. conspersa n. comb., S. pittarellii n. comb., S. ametroides n. comb., S. jacobi n. comb., S. kilimandjarica n. comb., S. meruensis n. comb.; S. neglecta n. comb.; S. submutica n. comb., Griffinigryllacris reunionis n. comb., G. adelungi n. comb., G. mauritiana n. comb., Karnygryllacris occipitalis n. comb., K. atriceps n. comb., K. brevipennis n. comb., K. humilis n. comb., K. scurra n. comb., K. triocellata n. comb., K. pittarellii n. comb., K. grylloides n. comb., Brunnergryllacris testaceus n. comb. and B. eximia n. comb (previously placed under Niphetogryllacris), Rentzgryllacris sechellensis n. comb. (before in Prosopogryllacris and the three subspecies are treated as full species), Gorochovgryllacris navicula n. comb. (transferred from Brachybaenus), Bianigryllacris trilobus n. comb., B. bilobus n. comb., B. digitatus n. comb., B. fallax n. comb., B. nigrigeniculatus n. comb., B. parvospinus n. comb., B. quadratus n. comb. and B. transversus n. comb. (previously placed under Apotrechus), Hyalogryllacris orthoxipha n. comb. (previously placed under Xiphogryllacris), Afroneanias glauningi n. comb., A. sphinix n. comb. and Ingrishgryllacris brevifalcatus n. comb. (previously placed under Ametroides and Glomeremus respectively). A key to the identification of the subfamilies and tribes is provided, plus historical background of the major taxonomic works on the group and the few contributions on ecology, morphology, and behavior is also done. It also discusses the status of fossil taxa thought to belong to the family. A preliminary analysis of the zoogeography of the family from the parameters of richness, diversity and distribution patterns of different groups studied, and also, some final comments on what has been achieved in this contribution are give, what is missing to the study of gryllacridines to the future and some problems that still affect the taxonomy to genera and species level. Finally, a check list in which all family taxa are included with the new classification is provided, with some comments on their distribution and taxonomic status if necessary.


Subject(s)
Gryllidae , Orthoptera , Animal Distribution , Animal Structures , Animals , Body Size , Organ Size
11.
Int J Syst Evol Microbiol ; 69(5): 1504-1508, 2019 May.
Article in English | MEDLINE | ID: mdl-30856091

ABSTRACT

Twelve strains of a novel yeast species were isolated from rotting wood, mushrooms and fruit samples in Brazil and French Guiana. Analysis of the sequences of the internal transcribed spacer region and the D1/D2 domains of the large subunit rRNA gene showed that the novel species belongs to the Kurtzmaniella clade. The novel species differed from its closest relative, Candida natalensis, by 12 substitutions in the D1/D2 sequences. The novel species could be distinguished from C. natalensis by its inability to assimilate cellobiose and salicin, and growth at 50 % (w/w) glucose. The name Kurtzmaniella hittingeri f.a., sp. nov. is proposed for the novel species. The type strain of K. hittingeri sp. nov. is CBS 13469T (=UFMG CM-Y272T). The MycoBank number is 827183. We also propose the transfer of Candida fragi, Candida quercitrusa and Candida natalensis to the genus Kurtzmaniella as new combinations.


Subject(s)
Candida/classification , Fruit/microbiology , Phylogeny , Wood/microbiology , Benzyl Alcohols , Brazil , Candida/isolation & purification , Cellobiose , DNA, Fungal/genetics , DNA, Ribosomal Spacer/genetics , French Guiana , Glucosides , Mycological Typing Techniques , Sequence Analysis, DNA
12.
Zootaxa ; 4500(3): 329-340, 2018 Oct 16.
Article in English | MEDLINE | ID: mdl-30486066

ABSTRACT

We examined the type material of 15 species of Naupactus Dejean and related genera (Curculionidae: Entiminae), most of them described by Alphonse Hustache (Museum National d'Histoire Naturelle, Paris) and Carl Boheman (Naturhistoriska Riksmuseet, Stockholm). The information associated with the types was compared with the original descriptions, and large series of specimens were examined in order to analyze the variation of each species throughout its range (sexual dimorphism, other kinds of polymorphism or geographic variation). Based on the results of this study we establish seven new combinations, one new placement and nine new synonymies, we make 21 lectotype designations and provide three new country and state records. Alceis curtus (Boh.), Lanterius leucophaeus (Boh.), L. sparsus (Boh.), L. sellatus (Boh.), Parapantomorus carinirostris (Hust.), Symmathetes signatus (Blanchard) and Teratopactus acerbus (Boh.) are new combinations and T. sulphureoviridis Hust. is a new placement. The following names are senior synonyms of those between parentheses: Lanterius inermis (Hust.) (syn. Macrostylus ocellatus Lanteri); Naupactus auricinctus Boh. (syn. N. ruficornis Boh.); N. bridgesii G.R. Waterhouse (syn. N. angulithorax Hust.); N. condecoratus Boh. (syn. N. bosqi Hust.); N. cyphoides (Heller) (syn. N. calamuchitanensis Hust., N. viridinitens Hust, N. viridulus Hust.); N. peregrinus (Buchanan) (syn. N. brevicrinitus Hust.); and Trichonaupactus densior Hust. (syn. T. rexus Hust.). For each species we provide the following information: synonyms, available data on type specimens (sex, body length, geographic location, kind of type, and repository), complete geographic distribution, pictures of types or specimens compared with types, an explanation about the reasons that justify the nomenclatural acts.


Subject(s)
Coleoptera , Weevils , Animals , Humans , Paris , Population Groups
13.
Zootaxa ; 4486(2): 146-160, 2018 Sep 27.
Article in English | MEDLINE | ID: mdl-30313757

ABSTRACT

Furcidentia Zettel, 1990 (Braconidae: Cheloninae) from the New World has been recently recognised as a genus separate from Pseudophanerotoma Zettel, 1990. Previously known from three species, three additional new species of Furcidentia are described here from the Neotropical region: F. jenningsi sp. nov. (French Guiana), F. llama sp. nov. (Guatemala), and F. tikalensis sp. nov. (Guatemala). The species F. clypeata Zettel (Ecuador) comb. nov., F. pulchra Zettel (Costa Rica) comb. nov., and F. sharkeyi Zettel (Ecuador) comb. nov. are transferred to Furcidentia. Additionally, one new species of Pseudophanerotoma is described: P. austini sp. nov. (Guatemala), while P. paranaensis (Costa Lima) (Brazil) and P. thapsina (Walley) (Texas, USA) are redescribed and are here recorded from French Guiana for the first time, thus considerably expanding their known distribution. Redescriptions include the description of the male of P. thapsina (Walley) for the first time and of the female of P. paranaensis (Costa Lima). Identification keys to the Neotropical genera of Phanerotomini and the species of Furcidentia and Pseudophanerotoma are provided.


Subject(s)
Wasps , Animals , Brazil , Costa Rica , Ecuador , Female , French Guiana , Guatemala , Male , Texas
14.
Zootaxa ; 4482(2): 245-273, 2018 Sep 18.
Article in English | MEDLINE | ID: mdl-30313820

ABSTRACT

Currently with 85 named species, the family Platyrhacidae in America is still poorly studied, particularly regarding Barydesmus Cook, 1896, the most diversified among the American genera. The center of diversification of Barydesmus lies in the northern third of the Andes Mountains, a megadiverse region where surely more species of these large, conspicuous diplopods await description. Here we present a new species, Barydesmus nangaritza sp. nov., easily diagnosable by the shape of the paranota, unique among the American Platyrhacidae. We provide also an updated bibliographical, annotated checklist of the whole family in America, with the aim of encouraging further studies in the group. The checklist includes the following new combinations under the genus Barydesmus: Barydesmus acanthopleurus (Hoffman, 1960) comb. nov., B. acanthosternus (Brölemann, 1900) comb. nov., B. acompus (Chamberlin, 1941) comb. nov., B. aequinoctius (Attems, 1914) comb. nov., B. affinis (Brölemann, 1919) comb. nov., B. andinus (Cook, 1896) comb. nov., B. azulae (Kraus, 1956) comb. nov., B. balsapuertus (Chamberlin, 1941) comb. nov., B. bifasciatus (Silvestri, 1897) comb. nov., B. bombonus (Chamberlin, 1941) comb. nov., B. broelemanni (Attems, 1914) comb. nov., B. brunnior (Chamberlin, 1941) comb. nov., B. celinus (Chamberlin, 1941) comb. nov., B. chuncho (Chamberlin, 1941) comb. nov., B. clathratus (Gervais, 1847) comb. nov., B. comptus Cook, 1896 comb. nov., B. contayus (Chamberlin, 1941) comb. nov., B. dunalii (Gervais, 1847) comb. nov., B. exsul (Cook, 1896) comb. nov., B. festae (Silvestri, 1897) comb. nov., B. fuscatus (Chamberlin, 1941) comb. nov., B. helophorus (Attems, 1899) comb. nov., B. incus (Chamberlin, 1941) comb. nov., B. javarynus (Schubart, 1950) comb. nov., B. leucus (Chamberlin, 1941) comb. nov., B. loretus (Chamberlin, 1941) comb. nov., B. manserichus (Chamberlin, 1941) comb. nov., B. medius (Chamberlin, 1941) comb. nov., B. obscurus (Kraus, 1955) comb. nov., B. orellanus (Chamberlin, 1941) comb. nov., B. pococki (Brölemann, 1911) comb. nov., B. retentus (Chamberlin, 1941) comb. nov., B. riparius (Carl, 1902) comb. nov., B. rufipes (Koch, 1847) comb. nov., B. scaber (Koch, 1847) comb. nov., B. socius (Chamberlin, 1941) comb. nov., B. strenuus (Silvestri, 1897) comb. nov., B. tambonus (Chamberlin, 1952) comb. nov., B. tapichus (Chamberlin, 1941) comb. nov., B. trichotypus (Chamberlin, 1941) comb. nov., B. utoquinius (Chamberlin, 1941) comb. nov. and B. zygethus (Chamberlin, 1941) comb. nov.


Subject(s)
Arthropods , Coleoptera , Animals , Ecuador , Heteroptera , United States
15.
Zootaxa ; 4377(1): 91-109, 2018 Jan 31.
Article in English | MEDLINE | ID: mdl-29690057

ABSTRACT

Two new combinations are proposed in Scatella for Ephydra australis Walker, 1853 and Opomyza guttata Macquart, 1843. Two species are resurrected from synonymy: Scatella lacustris (Meigen, 1830), revised status and Trixoscelis chilensis (Schiner, 1868), revised status (Trixoscelididae). Nine new synonyms are suggested: Scatella insularis Mathis Wirth, 1981 = S. australis (Walker, 1853); S. lutosa nigripes Oldenberg, 1923 = S. obsoleta Loew, 1861; S. septempunctata Malloch, 1933 = S. gratiellae Canzoneri Raffone, 1987 = S. septemfenestrata Lamb, 1912; S. tenuicosta Collin, 1930 = S. lacustris (Meigen, 1830); S. vulgata Cresson, 1931 = S. guttata (Macquart, 1843); Scatophila zlobini Krivosheina, 2009 = S. hirtirostris Sturtevant and Wheeler, 1954; S. grisescens Frey, 1915 = S. mesogramma (Loew, 1869); S. planiceps (Boheman, 1853) = S. quadriguttata (Meigen, 1830).


Subject(s)
Diptera , Animals
16.
Int J Syst Evol Microbiol ; 68(4): 1333-1343, 2018 Apr.
Article in English | MEDLINE | ID: mdl-29498615

ABSTRACT

Six novel yeast species, Starmerella camargoi f.a., sp. nov., Starmerella ilheusensis f.a., sp. nov., Starmerella litoralis f.a., Starmerella opuntiae f.a., sp. nov., sp. nov., Starmerella roubikii f.a., sp. nov. and Starmerella vitae f.a, sp. nov. are proposed to accommodate 19 isolates recovered from ephemeral flowers or bees in Brazil, Costa Rica and Belize. Sequence analysis of the ITS-5.8S region (when available) and the D1/D2 domains of the large subunit of the rRNA gene showed that the six novel yeasts are phylogenetically related to several species of the Starmerella clade. The type strains are Starmerella camargoi f.a., sp. nov. UFMG-CM-Y595T (=CBS 14130T; Mycobank number MB 822640), Starmerella ilheusensis f.a., sp. nov. UFMG-CM-Y596T (=CBS CBS14131T; MB 822641), Starmerella litoralis f.a., sp. nov. UFMG-CM-Y603T (=CBS14104T; MB 822642), Starmerella opuntiae f.a., sp. nov. UFMG-CM-Y286T (=CBS 13466T; MB 822643), Starmerella roubikii f.a., sp. nov. UWOPS 01-191.1 (=CBS 15148; MB 822645) and Starmerella vitae f.a., sp. nov. UWOPS 00-107.2 (=CBS 15147T; MB 822646). In addition, 25 species currently assigned to the genus Candida are reassigned formally to the genus Starmerella.


Subject(s)
Bees/microbiology , Flowers/microbiology , Phylogeny , Saccharomycetales/classification , Animals , Belize , Brazil , Candida/classification , Costa Rica , DNA, Fungal/genetics , DNA, Ribosomal Spacer/genetics , Saccharomycetales/genetics , Saccharomycetales/isolation & purification , Sequence Analysis, DNA
17.
Zootaxa ; 4526(2): 221-231, 2018 Nov 29.
Article in English | MEDLINE | ID: mdl-30651526

ABSTRACT

The genus Camarota is revised with the description of a new species-C. ugandae-and a key to species. The genus Paracamarota Cherian is considered here as a new junior synonym of Camarota. Distinctive morphological characters, such as the dark transverse band on the arista, the "vena spuria" of the wing and the placement of apical scutellar bristles, are interpreted.


Subject(s)
Diptera , Animal Distribution , Animals , Uganda
18.
Antonie Van Leeuwenhoek ; 110(7): 985-994, 2017 Jul.
Article in English | MEDLINE | ID: mdl-28386802

ABSTRACT

During studies of the yeast diversity associated with rotting wood in Brazil and fruits, plants and insects in French Guiana, three strains of a new species were isolated. Analysis of the sequences of the internal transcribed spacer (ITS)-5.8S and D1/D2 domains of the large subunit of the rRNA gene showed that this species belongs to the genus Hyphopichia and its closest relative is Candida homilentoma. These species differ by 44 nucleotide substitutions in D1/D2 sequences. A new species Hyphopichia buzzinii f. a., sp. nov., is proposed to accommodate these isolates. The type strain of Hyphopichia buzzinii sp. nov. is CLIB 1739T (=CBS 14300T = UFMG-CM-Y6121T; MycoBank number is MB 815609). In addition, we isolated 11 strains of C. homilentoma from rotting wood, leaf surfaces, and water bodies in Brazil, and these strains when crossed among one another and with the type strain (CBS 6312T) of this species, produced hat-shaped ascospores typical of the genus Hyphopichia. We describe the teleomorph of C. homilentoma as a new combination, Hyphopichia homilentoma comb. nov. (type strain CBS 6312T; MycoBank number is MB 820009). We also propose to transfer the other six Candida species of the Hyphopichia clade to this genus as new combinations. Hyphopichia homilentoma produced ethanol and xylitol from D-xylose whereas H. buzzinii was only able to convert this pentose to xylitol.


Subject(s)
Candida , DNA, Fungal , Mycological Typing Techniques , Animals , Brazil , Candida/genetics , Candida/metabolism , DNA, Ribosomal Spacer , Phylogeny , Sequence Analysis, DNA
19.
Zookeys ; (720): 23-46, 2017.
Article in English | MEDLINE | ID: mdl-29290723

ABSTRACT

The present study updates previously published biodiversity/faunistics of the flea beetles of Mexico published by the author after examination of 6132 specimens from 8 institutional collections. The following 9 genera were selected as indicators of the effects of known diversity only through examination of museum specimens (i.e., "indoor collecting"): Alagoasa Bechyné; Asphaera Chevrolat; Capraita Bechyné; Disonycha Chevrolat; Kuschelina Bechyné; Omophoita Chevrolat; Prasona Baly; Systena Chevrolat; and Walterianella Bechyné. From the specimens examined in these genera from the 8 collections, there were 394 new records for Mexican states of the 287 new species records representing 47% new records of the species recorded from those states. Total new state records 287 from 80 species. States with most new records: Chiapas (32); Nayarit (27); Sinaloa (24). 80 spp. (47%) with new state records. Systena oberthuri Baly is reported from Mexico for the first time. The current total of Alticinae in Mexico is 90 genera/626 species. The difficulties of the generic boundaries between Systena and Prasona, Alagoasa and Kuschelina; as well as the specific boundaries between A. jacobiana and A. decemguttatus and the specific level pattern variation in Disonycha glabrata and Alagoasa decemguttatus are discussed. Kuschelina semipurpurea, formerly placed in Alagoasa, is placed is considered as a new combination.

20.
Pap. avulsos Zool. ; 54(24): 341-362, 2014.
Article in English | VETINDEX | ID: vti-11457

ABSTRACT

Pseudophygopoda Tavakilian & Peñaherrera-Leiva, 2007 is redescribed. Four new, closely related genera are described. Panamapoda gen. nov., with P. panamensis (Giesbert, 1996); Paraphygopoda gen nov., with Paraphygopoda nappae sp. nov., P. albitarsis (Klug, 1825), P.  viridimicans (Fisher, 1952), and, provisionally, P.  longipennis (Zajciw, 1963); Paramelitta gen. nov., with Paramelitta wappesi sp. nov., and P. aglaia (Newman, 1840); and Phygomelitta gen. nov., with one species, P. triangularis (Fuchs, 1961). All the species are illustrated (including genitalia); and keys to the genera, and their species, are provided.(AU)


Subject(s)
Animals , Species Specificity , Classification , Coleoptera/classification
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