scholarly journals Cribrilinid bryozoans from Pleistocene Mediterranean deep-waters, with the description of new species

2020 ◽  
pp. 1-23
Author(s):  
Antonietta Rosso ◽  
Emanuela Di Martino ◽  
Andrew N. Ostrovsky

Abstract Cribrilinid bryozoans originating from Pleistocene deep-water sediments from two localities near Messina (Sicily, Italy)—Capo Milazzo (Gelasian) and Scoppo (Calabrian)—were examined. Five cribrilinid species were found, three in each locality and time interval, with only one species shared. Three species, Cribrilaria profunda n. sp., Glabrilaria transversocarinata n. sp., and Figularia spectabilis n. sp., are new to science. Of the two remaining species, Figularia figularis was already known from local fossil associations, whereas Glabrilaria pedunculata, a present-day Mediterranean species, is recorded for the first time as a fossil. New combinations are suggested for two species previously assigned to Puellina, Cribrilaria saldanhai (Harmelin, 2001) n. comb. and Cribrilaria mikelae (Harmelin, 2006) n. comb. The diagnosis of the genus Figularia was amended to include an erect growth morphology in addition to the encrusting form, and the occurrence of ooecia formed by the distal kenozooid. Following a literature revision of all species currently assigned to Figularia, the new combinations Vitrimurella capitifera (Canu and Bassler, 1929) n. comb. and Hayamiellina quaylei (Powell, 1967a) n. comb. are suggested, and problematic species are listed and briefly discussed. UUID: http://zoobank.org/b7b36152-bf7b-4e00-b6ec-2614b2a58f1b

2016 ◽  
Vol 90 (5) ◽  
pp. 815-853 ◽  
Author(s):  
Susannah M. Porter ◽  
Leigh Anne Riedman

AbstractThe ca. 780–740 Ma Chuar Group, Grand Canyon, Arizona, provides an exceptional record of life during the diversification of crown-group eukaryotes, just prior to the first Cryogenian glaciation. We document in detail the assemblage of organic-walled microfossils preserved in fine-grained siliciclastics throughout the unit. In contrast with earlier studies, we primarily used SEM to document fossil morphologies, augmented by transmitted light microscopy, FIB-SEM, and TEM. This resulted in the discovery of new species and the recognition of broad-ranging, intraspecific biological and taphonomic variation in other species. Twenty-two species and five unnamed morphotypes are described, including three new species:Kaibabia gemmulella,Microlepidopalla mira, andVolleyballia dehlerae; two new combinations:Galerosphaera walcottiiandLanulatisphaera laufeldii; and 17 previously described forms. The possible colonial green algaPalaeastrum dyptocranumButterfield in Butterfield, Knoll, and Swett, 1994 and the index fossilCerebrosphaera globosa(Ogurtsova and Sergeev, 1989) Sergeev and Schopf, 2010 (=C. buickiiButterfield, 1994) are described for the first time from Chuar rocks.Lanulatisphaera laufeldii, a locally abundant and globally widespread species characterized by submicrometer filamentous processes that form a reticulate network, may be a useful marker for the time interval just before the appearance of vase-shaped microfossils (VSMs) ca. 740 Ma.Organic-walled microfossil assemblages decline in diversity upsection, coincident with the appearance of VSMs and intermittent euxinia within the basin. Whether this pattern is due to preservational bias related to greater water depth or the higher TOC of upper Chuar rocks or instead reflects biotic turnover related to the spread of euxinic water masses in the basin is unknown.


1976 ◽  
Vol 7 (4) ◽  
pp. 241-251 ◽  
Author(s):  
Ebbe Schmidt Nielsen ◽  
Ole Karsholt

AbstractNotes are given on the identity and synonymy of five species of Lepidoptera described by Linnaeus, twenty-eight by Fabricius and two by Ström. Each species dealt with is treated under the apparent valid combination; for each species reference is given to the original description. Twenty-four new species-group name synonyms are introduced and nine new combinations are established: Nemaxera betulinella (Fabr.), Argyresthia arcella (Fabr.), Depressaria depressana (Fabr.), Chrysoesthia drurella (Fabr.), Brachmia blandella (Fabr.), Acleris laterana (Fabr.), Pseudohermenias abietana (Fabr.), Epinotia abbreviana (Fab.) and Acrobasis repandana (Fabr.). During the work two neotypes, twenty-seven lectotypes and two paralectotypes have been designated and are here cited for the first time.


2019 ◽  
Vol 64 (2) ◽  
pp. 345-366
Author(s):  
Mikhail P. Zhurbenko ◽  
Ochirbat Enkhtuya ◽  
Samiya Javkhlan

AbstractA first synopsis of lichenicolous fungi of Mongolia based on new collections and literature data is provided, including 114 species. Five new species are described: Capronia cogtii (on Vahliella leucophaea), Echinothecium hypogymniae (on Hypogymnia bitteri), Feltgeniomyces mongolicus (on H. bitteri), Phacopsis vulpicidae (on Vulpicida juniperina) and Roselliniella javkhlanae (on Rinodina turfacea var. ecrustacea). Two new combinations are proposed: Endococcus hafellneri (≡ Stigmidium hafellneri) and Sphaerellothecium taimyricum (≡ Sphaerellothecium thamnoliae var. taimyricum). Unidentified specimens of Acremonium (on Mycoblastus sanguinarioides), Cercidospora (on Rhizoplaca chrysoleuca s.lat.), Didymocyrtis (on Rhizoplaca chrysoleuca s.lat.), Lichenochora (on Physcia alnophila), Lichenostigma (on species of Xanthoparmelia), Phoma (on Vulpicida juniperina) and a leotialean fungus (on Cetraria laevigata) are characterized and discussed. Taxonomic notes are provided for Cercidospora macrospora s.lat., Didymocyrtis cf. melanelixiae, Minutoexcipula cf. beaglei, Nesolechia cetrariicola, Sphaerellothecium cf. parmeliae and Stigmidium cf. psorae. Sphaeropezia intermedia is newly reported for Eurasia. Didymocyrtis grumantiana is newly reported for Asia. Additionally, 71 species of lichenicolous fungi and five species of lichenicolous lichens are documented in Mongolia for the first time. Allocetraria is reported as a new host genus for Abrothallus peyritschii, Vulpicida for Arthonia triebeliae, and Anamylopsora for Muellerella pygmaea.


Zootaxa ◽  
2009 ◽  
Vol 2318 (1) ◽  
pp. 552-565 ◽  
Author(s):  
PIERFILIPPO CERRETTI ◽  
THOMAS PAPE

A cladistic analysis of the genus Melanophora Meigen, 1803 (type-species: Musca grossificationis Linnaeus, 1758 [= Musca roralis Linnaeus, 1758]) is presented and the generic delimitation is critically redefined. The nominal genus-group taxon Bequaertiana Curran, 1929 (type-species: Bequaertiana argyriventris Curran, 1929) is synonymised with Melanophora Meigen syn. nov. The following new combinations are proposed: Melanophora argyriventris (Curran, 1929) comb. nov. and Melanophora basilewskyi (Peris, 1957) comb. nov. Melanophora chia sp. nov. from SW Sardinia is described, illustrated and compared with the other known species of the genus. The male of Melanophora asetosa Kugler, 1978 is described for the first time. Melanophora basilewskyi (Peris, 1957) is recorded from Kenya for the first time.


Zootaxa ◽  
2019 ◽  
Vol 4630 (1) ◽  
pp. 1-619 ◽  
Author(s):  
MASSIMO OLMI ◽  
ROBERT S. COPELAND ◽  
SIMON VAN NOORT

An updated revision of Afrotropical Dryinidae is presented. Nine subfamilies, 23 genera and 430 species (including 60 new species) are treated. Six new species-level synonymies and three new combinations are proposed. Descriptions, geographic distribution, known hosts, natural enemies and type material of each species are presented, together with illustrations of the main morphological characters and keys to the subfamilies, genera and species. A complete list of references concerning the Afrotropical Dryinidae and their hosts is provided. The following new species are described: Anteon ambrense, sp. nov. (Madagascar), Anteon beankanum, sp. nov. (Madagascar), Anteon elongatum, sp. nov. (Madagascar), Anteon hoekense, sp. nov. (South Africa), Anteon mabibiense, sp. nov. (South Africa), Anteon majunganum, sp. nov. (Madagascar), Anteon malagasy, sp. nov. (Madagascar), Anteon musmani, sp. nov. (Kenya), Anteon nigropictum, sp. nov. (South Africa), Anteon nimbense, sp. nov. (Guinea), Anteon pseudohova, sp. nov. (Madagascar), Anteon sakalavense, sp. nov. (Madagascar), Anteon tulearense, sp. nov. (Kenya, Madagascar), Aphelopus sequeirai, sp. nov. (Kenya), Apoaphelopus fisheri, sp. nov. (Madagascar), Apoaphelopus wallacei, sp. nov. (Kenya), Bocchus forestalis, sp. nov. (Madagascar), Bocchus granulatus, sp. nov. (South Africa), Bocchus harinhalai, sp. nov. (Madagascar), Bocchus nigroflavus, sp. nov. (Madagascar), Bocchus parkeri, sp. nov. (Madagascar), Bocchus ruvidus, sp. nov. (Madagascar), Conganteon hawleyi, sp. nov. (Kenya), Conganteon sensitivum, sp. nov. (Madagascar), Crovettia afra, sp. nov. (Kenya, Madagascar), Deinodryinus ambrensis, sp. nov. (Madagascar), Deinodryinus granulatus, sp. nov. (South Africa), Deinodryinus nigropictus, sp. nov. (South Africa), Deinodryinus piceus, sp. nov. (Madagascar), Dryinus bellicosus, sp. nov. (Madagascar), Dryinus dentatiforceps, sp. nov. (South Africa), Dryinus erenianus, sp. nov. (Ivory Coast), Dryinus milleri, sp. nov. (Kenya), Dryinus mobotensis, sp. nov. (Madagascar), Dryinus nigrithorax, sp. nov. (Ivory Coast), Dryinus teres, sp. nov. (Madagascar), Dryinus tulearensis, sp. nov. (Madagascar), Dryinus whittleorum, sp. nov. (Kenya), Gonatopus avontuurensis, sp. nov. (South Africa), Gonatopus bellicosus, sp. nov. (Madagascar), Gonatopus comorensis, sp. nov. (Union of the Comoros), Gonatopus costalis, sp. nov. (South Africa), Gonatopus flavotestaceus, sp. nov. (Madagascar), Gonatopus gumovskyi, sp. nov. (Democratic Republic of the Congo), Gonatopus hantamensis, sp. nov. (South Africa), Gonatopus harinhalai, sp. nov. (Madagascar), Gonatopus karooensis, sp. nov. (South Africa), Gonatopus koebergensis, sp. nov. (South Africa), Gonatopus marojejyanus, sp. nov. (Madagascar), Gonatopus minutus, sp. nov. (Madagascar), Gonatopus nigropictus, sp. nov. (South Africa), Gonatopus ranomafanensis, sp. nov. (Madagascar), Gonatopus robertsoni, sp. nov. (South Africa), Gonatopus rugithorax, sp. nov. (South Africa), Gonatopus scholtzi, sp. nov. (South Africa), Gonatopus wikstrandae, sp. nov. (Kenya), Lonchodryinus madagascolus, sp. nov. (Madagascar), Madecadryinus ranomafanensis, sp. nov. (Madagascar), Neodryinus bimaculatus, sp. nov. (Madagascar), Neodryinus keleboensis, sp. nov. (Democratic Republic of the Congo). The ♀ of Deinodryinus danielssoni Olmi, 1998, is described for the first time. The following new synonymies are presented: Anteon fiorii Olmi, 1984 (=A. proteicolum Olmi, 2006, syn. nov.); Anteon madagascolum (Benoit, 1954) (=Anteon brooksi Olmi, 2003, syn. nov.); Anteon zairense Benoit, 1951 (=A. terminale Olmi, 2007, syn. nov.); Aphelopus incisus Olmi, 1984 (=A. himyarita Olmi & van Harten, 2006, syn. nov.); Bocchus watshami Olmi, 1987 (=Bocchus simoni Olmi, 2005, syn. nov.); Dryinus ugandanus Olmi, 1984 (=Dryinus constantiae Olmi, 2006, syn. nov.). The following new combinations are presented: Dryinus luweli (Benoit, 1951) new comb. in place of Lestodryinus luweli Benoit, 1951; Gonatopus africanus (Benoit, 1951) new comb. in place of Aphelopus africanus Benoit, 1951; Gonatopus ghanensis (Olmi, 1987) new comb. in place of Pseudogonatopus ghanensis Olmi, 1987. Gynander specimens of Deinodryinus rusticus Olmi, 2004 and Deinodryinus steineri Olmi, 1994 are described (first gynander specimens of Dryinidae from the Afrotropical region). The authors provide well-illustrated identification keys to all species of Afrotropical Dryinidae. Online Lucid Phoenix and Lucid matrix interactive keys are provided at http://www.waspweb.org. 


Zootaxa ◽  
2019 ◽  
Vol 4652 (1) ◽  
pp. 165-173
Author(s):  
RAM KESHARI DUWAL ◽  
MICHAEL D. SCHWARTZ ◽  
TOMOHIDE YASUNAGA

The genus Rubrocuneocoris Schuh is recognized from Vietnam for the first time, with a new species, R. vietnamensis n. sp.  The new species is described and documented with images of the habitus and male genitalic structures. Male and female genitalic structures are described for R. albescens Yasunaga. Species of Rubrocuneocoris described from Taiwan are herein transferred to Atractotomoidea Yasunaga and the following new combinations are accordingly proposed: Atractotomoidea falcis (Lin 2006) n. comb., A. maculosus (Lin 2006) n. comb., A. nodus (Lin 2006) n. comb., and A. trifidus (Lin 2006) n. comb. A revised checklist of Rubrocuneocoris is presented. 


Zootaxa ◽  
2019 ◽  
Vol 4677 (1) ◽  
pp. 1-68 ◽  
Author(s):  
OLEKSIY BIDZILYA ◽  
OLE KARSHOLT ◽  
VASILIY KRAVCHENKO ◽  
JAN ŠUMPICH

One hundred forty-six species of Gelechiidae including 36 new records are reported from Israel. Anarsia balioneura Meyrick, 1921 and Polyhymno chionarcha Meyrick, 1913 are recorded for the first time in the Palaearctic region. Two new species are described: Metzneria freidbergi sp. nov., and Scrobipalpa aravensis sp. nov. Six new synonyms are established: Stygmatoptera Hartig, 1936 syn. nov. of Polyhymno Chambers, 1874; Eulamprotes Bradley, 1971 syn. nov. of Oxypteryx Rebel, 1911; Polyhymno abaiella Amsel, 1974 syn. nov. of Polyhymno chionarcha, Meyrick, 1913; Gelechia haifella Amsel, 1935 syn. nov. of Athrips rancidella (Herrich-Schäffer, 1854); Sophronia catharurga Meyrick, 1923 and Sophronia parahumerella Amsel, 1935 syn. nov. of Pseudosophronia exustellus (Zeller, 1847). The following new combinations are proposed: Anacampsis karmeliella (Amsel, 1935) comb. nov., Stomopteryx tesserapunctella (Amsel, 1935) comb. nov., Aproaerema languidella (Amsel, 1936) comb. nov., Aproaerema telaviviella (Amsel, 1935) comb. nov., Acompsia (Telephila) ballotellus (Amsel, 1935) comb. nov., Polyhymno dumonti (Hartig, 1936) comb. nov., Oxypteryx atrella (Denis & Schiffermüller, 1775) comb. nov., Oxypteryx immaculatella (Douglas, 1850) comb. nov. and Chrysoesthia amseli (Bidzilya, 2008) comb. nov. A lectotype is designated for Lita rhamnifoliae Amsel & Hering, 1931.The genitalia of both sexes of Sophronia sagittans Meyrick, 1923, Anacampsis karmeliella (Amsel, 1935), Stomopteryx tesserapunctella Amsel, 1935 as well as male genitalia of Stomopteryx lacteolella Caradja, 1924, Aproaerema telaviviella (Amsel, 1935), Acompsia ballotellus (Amsel, 1935), Polyhymno dumonti (Hartig, 1936) and Chrysoesthia amseli (Bidzilya, 2008) are illustrated and described for the first time. New or additional host plants are recorded for Metzneria aspretella Lederer, 1869, M. agraphella (Ragonot, 1895), M. ehikeella Gozmány, 1954 and Scrobipalpa suaedivorella (Chrétien, 1915). Photographs of the type specimens of most taxa described from Israel and Palestine are presented. The following species are removed from the list of Gelechiidae of Israel: Nothris sulcella Staudinger, 1879, N. skyvai Karsholt & Šumpich, 2015, Anarsia spartiella Schrank, 1802, Megacraspedus cerussatellus Rebel, 1930, Oxypteryx atrella (Denis & Schiffermüller, 1775), Isophrictis anthemidella (Wocke, 1871), Metzneria metzneriella (Stainton, 1851), Scrobipalpa otregata Povolný, 1972, Scrobipalpa nitentella (Fuchs, 1902), Scrobipalpa remota Povolný, 1972, Scrobipalpa salinella (Zeller, 1847) and Ephysteris diminutella (Zeller, 1847). Moreover, Stomopteryx remissella (Zeller, 1847) is recorded as new to the Altai Mountains of Russia, Anarsia balioneura Meyrick, 1921 is new to Cyprus and Libya, Polyhymno dumonti (Hartig, 1936) is new to Libya and Sudan, Scrobipalpa superstes is new to Greece, Stenolechia gemmella (Linnaeus, 1758) is new to Jordan and Polyhymno chionarcha is new to Saudi Arabia. 


Zootaxa ◽  
2012 ◽  
Vol 3413 (1) ◽  
pp. 44 ◽  
Author(s):  
TOMOHIDE YASUNAGA ◽  
RAM KESHARI DUWAL ◽  
MICHAEL D. SCHWARTZ

The mirine plant bug genus Neolygus Knight is reported from Nepal and North India for the first time, thus representing the first confident distributional record of this genus from the Himalayas. A new species, Neolygus machanensis, is described from Nepal. Two known members, N. bui Lu & Zheng and N. keltoni (Lu & Zheng), newly recognized as occurring in Nepal and/or North India, are diagnosed. Habitus images of live individuals and illustrations of the male genitalia are provided for all treated species. A checklist of the Old World species, and discussion of the systematic position and zoogeography of Neolygus are included. Neolygus partitus (Walker, 1873) [Capsus], N. mjohjangsanicus (Josifov, 1992) [Lygocoris], and Neolygus zebei (Günther, 1997) [Lygocoris] are proposed as new combinations.


Zootaxa ◽  
2017 ◽  
Vol 4300 (1) ◽  
pp. 71
Author(s):  
JUN XU ◽  
KAI SHI ◽  
JUNHAO HUANG ◽  
HONG WU

The genus Mohrigia Menzel, 1995 from China is reviewed and 20 species are recognized. Among them, nine new species, M. angusta sp. nov., M. cylindrata sp. nov., M. inflata sp. nov., M. globulosa sp. nov., M. notolobos sp. nov., M. ovoidea sp. nov., M. scrobiculata sp. nov., M. subrhynchophysa sp. nov., M. truncatula sp. nov., are described with detailed illustrations, and one described species, M. hippai Menzel, 1995 is reported for the first time from China. Lycoriella longirostris Yang, Zhang & Yang, 1995 is recognized as new synonym of M. megalocornuta (Mohrig & Menzel, 1992). In addition, M. rhynchophysa (Yang, Zhang & Yang, 1993) and M. orthacantha (Yang, Zhang & Yang, 1993) are new combinations. The geographical distribution of the 20 Chinese species is provided, as well as a key to the 21 species of Mohrigia. 


Zootaxa ◽  
2018 ◽  
Vol 4407 (3) ◽  
pp. 383
Author(s):  
VLADIMIR V. DUBATOLOV ◽  
ANTON V. VOLYNKIN ◽  
YASUNORI KISHIDA

The Prabhasa Moore, 1878 genus-group is reviewed. The male and female genitalia of Prabhasa venosa Moore, 1878, the type species of the genus, are described and illustrated for the first time. Two new genera, Macohasa Dubatolov, Volynkin & Kishida, gen. nov. and Chinasa Dubatolov, Volynkin & Kishida, gen. nov. and two new species, Macohasa cernyi Dubatolov, Volynkin & Kishida, sp. nov. and Chinasa sapa Dubatolov, Volynkin & Kishida, sp. nov. are described for Prabhasa venosa sensu authors. Seven new combinations are established: Zadadra plumbeomicans (Hampson, 1894), comb. nov., Zadadra monastyrskyi (Dubatolov, 2012), comb. nov., Macohasa orientalis (Hampson, 1905), comb. nov., Macohasa tetraspila (Černý, 2009), comb. nov., Macohasa dimorpha (Hampson, 1918), comb. nov., Chinasa costalis costalis (Moore, 1878), comb. nov. and Chinasa costalis bicoloriceps (Strand, 1916), comb. nov. 


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