白毫早茶园3种害虫与其捕食性天敌的数量、时间和空间关系

为了合理利用和保护天敌进行卵形短须螨、双斑长跗萤叶甲和假眼小绿叶蝉的综合防治,用灰色系统分析方法和生态位分析法对合肥地区白毫早茶园3种主要害虫与其捕食性天敌在数量、时间、空间等方面关系进行分析,利用害虫与天敌关系密切指数之和综合评判9种天敌与3种害虫关系密切的前四位天敌。2015年卵形短须螨的前四位天敌是鳞纹肖蛸(5.3079)、三突花蟹蛛(5.1716)、锥腹肖蛸(4.8367)和草间小黑蛛(4.7869);2016年前四位天敌依次是三突花蟹蛛(5.3975)、鳞纹肖蛸(4.9414)、茶色新圆蛛(4.8757)、锥腹肖蛸(4.6815)。对两年结果综合分析,卵形短须螨的前四位天敌依次是三突花蟹蛛(10.5691)、鳞纹肖蛸(10.2493)、茶色新圆蛛(9.6353)和锥腹肖蛸(9.5182)。2015年双斑长跗萤叶甲的前四位天敌依次是锥腹肖蛸(5.6926)、异色瓢虫(5.6976)、八斑球腹蛛(5.5101)和斜纹猫蛛(5.4552);2016年依次是茶色新圆蛛(5.2909)、锥腹肖蛸(5.2710)、鳞纹肖蛸(5.1063)和斜纹猫蛛(5.0703)。对两年结果综合评判,双...     

Taxonomic review of the genus Lymantria (Lepidoptera: Erebidae: Lymantriinae) in Korea

A taxonomic review of the Korean Lymantria Hübner, 1819 was conducted. A total of nine species of five subgenera with two unrecorded species are listed: Lymantria (Porthetria) dispar Linnaeus 1758, L. (P.) xylina Swinhoe 1903, L. (Lymantria) monacha (Linnaeus 1758), L. (L.) minomonis Matsumura 1933 (new to Korea), L. (L.) similis monachoides Schintlimeister 2004 (new to Korea), L. (L.) lucescens (Butler 1881), L. (Nyctria) mathura Moore 1865, L. (Collentria) fumida Butler 1877, and L. (Spinotria) bantaizana Matsumura 1933. Lymantria (Lymantria) minomonis and L. (L.) similis monachoides are newly added to the Korean fauna. Lymantria (L.) minomonis was found only on Bogildo Island of Jeollanam‐do in the southern part of Korea, and L. (L.) similis monachoides was collected in central Korea. Lymantria (Porthetria) xylina and L. (Collentria) fumida were not examined in this study, and it is considered that the previous records were due to misidentification or they are only distributed in the northern part of the Korean Peninsula. We provide diagnoses of two unrecorded species and adult habitus and genitalia photos of the Korean Lymantria species.     

Further study on the phylogeny,taxonomy and distribution of the genus Veturius Kaup in Central and South America (Coleoptera: Passalidae)

This study provides data on the phylogeny, taxonomy and distribution of 14 known and five new species of the Neotropical genus Veturius Kaup (Proculini), belonging to various subgenera and species groups: V. (Veturius) latissimus n. sp. (Colombia, Central Andes) and V. (V.) calimanus n. sp. (Pacific slope of the Occidental Cordillera) are separated from V. (V.) caquetaensis Boucher, 1988, which seems restricted to the Amazonian slope of the Oriental Cordillera (Caquetá, Putumayo); V. (V.) sinuatomarginatus Luederwaldt, 1941 (Costa Rica), n. syn. of V. sinuatocollis Kuwert, 1890; V. sinuatocollis aculeatus Luederwaldt, 1941 (syntype from Costa Rica); V. (V.) aspina Kuwert, 1898 (located in Occidente of Ecuador, Guayaquil); V. (V.) yahua Boucher, 2006 (located in Occidente of Ecuador, Pichincha and SW Colombia, Nariño); V. (V.) guntheri Kuwert, 1898 (located in Peru, SE Puno and Colombia, W Putumayo); V. (V.) cephalotes (Le Peletier & Serville, 1825) (citation from Guyana); V. (V.) sinuatus (Eschscholtz, 1829) (previous synonymy); V. (V.) libericornis Kuwert, 1891 (located in Peru, Cuzco); V. (V.) lepidus Fonseca, 1999 (revision; located in Colombia, Amazonas, Putumayo and Peru, Loreto); V. (V.) transversus (Dalman, 1817) [syntype; previous synonymy of V. trituberculatus (Eschscholtz, 1829) with V. assimilis (Weber, 1801) and located in Brazil, Mato Grosso]; V. (V.) sinuosus (Drapiez, 1820) (corrected reference for Colombia); V. (Publius) crassus (Smith, 1852) (new syntype); V. (P.) danieli Boucher, 2006 (holotype deposit); V. (P.) vazdemelloi Boucher, n. sp. (Andes of Ecuador, Azuay); V. (Ouayana) unicornis Gravely, 1918 (located in Colombia, E Vaupés); V. (O.) costaianus Boucher, n. sp. (Venezuela, Amazonas, NW Pacaraima Massif); Ticoisthmus Boucher, n. subg., for the species group of V. (O.) laevior (Kaup, 1868), of southern Central America; and V. (T.) brachypterus Boucher, n. sp. (Costa Rica, Sierra Talamanca). Ticoisthmus is considered the sister group of Ouayana. It belongs to the Meso-American low mountain dispersion pattern and demonstrates, especially in the genus Veturius, but also more generally in the Neotropical passalids, the hot-spot characteristics, with diversity and endemism, of the narrow land between the Depression of Nicaragua and the Isthmus of Panama.     

Phylogeny and classification of Aedini (Diptera: Culicidae), based on morphological characters of all life stages

Higher‐level relationships within Aedini, the largest tribe of Culicidae, are explored using morphological characters of eggs, fourth‐instar larvae, pupae, and adult females and males. In total, 172 characters were examined for 119 exemplar species representing the existing 12 genera and 56 subgenera recognized within the tribe. The data for immature and adult stages were analysed separately and in combination using equal (EW) and implied weighting (IW). Since the classification of Aedini is based mainly on adult morphology, we first tested whether adult data alone would support the existing classification. Overall, the results of these analyses did not reflect the generic classification of the tribe. The tribe as a whole was portrayed as a polyphyletic assemblage of Aedes and Ochlerotatus within which eight (EW) or seven (IW) other genera were embedded. Strict consensus trees (SCTs) derived from analyses of the immature stages data were almost completely unresolved. Combining the adult and immature stages data resulted in fewer most parsimonious cladograms (MPCs) and a more resolved SCT than was found when either of the two data subsets was analysed separately. However, the recovered relationships were still unsatisfactory. Except for the additional recovery of Armigeres as a monophyletic genus, the groups recovered in the EW analysis of the combined data were those found in the EW analysis of adult data. The IW analysis of the total data yielded eight MPCs consisting of three sets of two mutually exclusive topologies that occurred in all possible combinations. We carefully studied the different hypotheses of character transformation responsible for each of the alternative patterns of relationship but were unable to select one of the eight MPCs as a preferred cladogram. Overall, the relationships within the SCT of the eight MPCs were a significant improvement over those found by equal weighting. Aedini and all existing genera except Ochlerotatus and Aedes were recovered as monophyletic. Ochlerotatus formed a polyphyletic assemblage basal to Aedes. This group included Haemagogus and Psorophora, and also Opifex in a sister‐group relationship with Oc. (Not.) chathamicus. Aedes was polyphyletic relative to seven other genera, Armigeres, Ayurakitia, Eretmapodites, Heizmannia, Udaya, Verrallina and Zeugnomyia. With the exception of Ae. (Aedimorphus), Oc. (Finlaya), Oc. (Ochlerotatus) and Oc. (Protomacleaya), all subgenera with two or more species included in the analysis were recovered as monophyletic. Rather than leave the generic classification of Aedini in its current chaotic state, we decided a reasonable and conservative compromise classification would be to recognize as genera those groups that are ‘weighting independent’, i.e. those that are common to the results of both the EW and IW analyses of the total data. The SCT of these combined analyses resulted in a topology of 29 clades, each comprising between two and nine taxa, and 30 taxa (including Mansonia) in an unresolved basal polytomy. In addition to ten genera (Armigeres, Ayurakitia, Eretmapodites, Haemagogus, Heizmannia, Opifex, Psorophora, Udaya, Verrallina and Zeugnomyia), generic status is proposed for the following: (i) 32 existing subgenera of Aedes and Ochlerotatus, including nine monobasic subgenera within the basal polytomy, i.e. Ae. (Belkinius), Ae. (Fredwardsius), Ae. (Indusius), Ae. (Isoaedes), Ae. (Leptosomatomyia), Oc. (Abraedes), Oc. (Aztecaedes), Oc. (Gymnometopa) and Oc. (Kompia); (ii) three small subgenera within the basal polytomy that are undoubtedly monophyletic, i.e. Ae. (Huaedes), Ae. (Skusea) and Oc. (Levua), and (iii) another 20 subgenera that fall within the resolved part of the SCT, i.e. Ae. (Aedes), Ae. (Alanstonea), Ae. (Albuginosus), Ae. (Bothaella), Ae. (Christophersiomyia), Ae. (Diceromyia), Ae. (Edwardsaedes), Ae. (Lorrainea), Ae. (Neomelaniconion), Ae. (Paraedes), Ae. (Pseudarmigeres), Ae. (Scutomyia), Ae. (Stegomyia), Oc. (Geoskusea), Oc. (Halaedes), Oc. (Howardina), Oc. (Kenknightia), Oc. (Mucidus), Oc. (Rhinoskusea) and Oc. (Zavortinkius). A clade consisting of Oc. (Fin.) kochi, Oc. (Fin.) poicilius and relatives is raised to generic rank as Finlaya, and Downsiomyia Vargas is reinstated from synonymy with Finlaya as the generic name for the clade comprising Oc. (Fin.) leonis, Oc. (Fin.) niveus and their relatives. Three other species of Finlaya?Oc. (Fin.) chrysolineatus, Oc. (Fin.) geniculatus and Oc. (Fin.) macfarlanei? fall within the basal polytomy and are treated as Oc. (Finlaya) incertae sedis. Ochlerotatus (Ochlerotatus) is divided into three lineages, two of which, Oc. (Och.) atropalpus and Oc. (Och.) muelleri, are part of the basal polytomy. The remaining seven taxa of Oc. (Ochlerotatus) analysed, including the type species, form a reasonably well‐supported group that is regarded as Ochlerotatus s.s. Ochlerotatus (Rusticoidus) is retained as a subgenus within Ochlerotatus s.s. Ochlerotatus (Nothoskusea) is recognized as a subgenus of Opifex based on two unique features that support their sister‐group relationship. A new genus, Tanakaius gen. nov. , is proposed for Oc. (Fin.) togoi and the related species Oc. (Fin.) savoryi. The taxonomic status and generic placement of all currently valid species of Aedini are listed in an appendix. © 2004 The Linnean Society of London, Zoological Journal of the Linnean Society, 2004, 142 , 289?368.     

Phylogenetic systematics of the Empis (Coptophlebia) hyalea-group (Insecta: Diptera: Empididae)

Six clades are inferred from a phylogenetic analysis including 42 species belonging to the Empis (Coptophlebia) hyalea‐group. These clades are named as follows: E. (C.) acris, E. (C.) aspina, E. (C.) atratata, E. (C.) hyalea, E. (C.) jacobsoni and E. (C.) nahaeoensis. The presence of two dorsal more or less developed epandrial projections is considered autapomorphic for the E. (C.) hyalea‐group in addition to two characters previously found to support the monophyly of this group (presence of an unsclerotized zone in the middle of labella and epandrium unpaired). Amongst the cladistically analysed species, 24 are newly described [ E. ( C. ) acris , E. ( C. ) aspina , E. ( C. ) cameronensis , E. ( C. ) duplex , E. ( C. ) incurva , E. ( C. ) inferiseta , E. ( C. ) kuaensis , E. ( C. ) lachaisei , E. ( C. ) lamellalta , E. ( C. ) lata , E. ( C. ) loici , E. ( C. ) longiseta , E. ( C. ) mengyangensis , E. ( C. ) menglunensis , E. ( C. ) missai , E. ( C. ) nimbaensis , E. ( C. ) padangensis , E. ( C. ) parvula , E. ( C. ) projecta , E. ( C. ) pseudonahaeoensis , E. ( C. ) submetallica , E. ( C. ) urumae , E. ( C. ) vitisalutatoris and E. ( C. ) woitapensis ], five are reviewed [E. (C.) hyalea Melander, E. (C.) jacobsoni De Meijere, E. (C.) ostentator Melander, E. (C.) sinensis Melander and E. (C.) thiasotes Melander] and 13 were recently described in two previous papers. Two additional species, E. (C.) abbrevinervis De Meijere and E. (C.) multipennata Melander, are also reviewed but not included in the cladistic analysis since they are only known from the female. A lectotype is designated for E. (C.) jacobsoni. A key is provided to the six clades of the E. (C.) hyalea‐group as well as to species of each clade. A catalogue of the E. (C.) hyalea‐group, including 72 species, is given. The taxonomic status of 25 additional species mainly described by Bezzi and Brunetti, from the Oriental and Australasian regions, is discussed. The E. (C.) hyalea‐group is firstly recorded from the Palaearctic Region and Australia. Finally, the distribution and the habitats of the species compared with their phylogeny suggest a possible relationship between the diversification of the group and forest fragmentations during the Quaternary. © 2005 The Linnean Society of London, Zoological Journal of the Linnean Society, 2005, 145 , 339–391.     

Species diversity and abundance of small mammals in Nechisar National Park,Ethiopia

Species diversity and abundance of small mammals were studied in Nechisar National Park, Ethiopia, during August 2008 – March 2009. Twenty species of rodents and four species of insectivores were recorded from the study area. Mastomys natalensis (17.37%), Arvicanthis dembeensis (17.09%), Mastomys erythroleucus (8.90%), Stenocephalemys albipes (8.76%), Arvicanthis niloticus (8.19%), Acomys cahirinus (7.34%), Lemniscomys striatus (6.92%), Gerbilliscus nigricauda (6.21%), Grammomys dolichurus (3.67%), Gerbilliscus robusta (2.12%), Mus proconodon (1.98%), Mus mahomet (1.41), Dendromus melanotis (1.27%), Arvicanthis abyssinicus (1.13%), Mus musculus (0.99%), Praomys fumatus (0.85%), Xerus erythropus (0.85%), Lemniscomys barbarus (0.71%), Mus tenellus (0.71%) and Otomys typus (0.28%) were the rodents and their respective relative abundance in the study area. Crocidura olivieri (1.55%), Crocidura fumosa (0.85%), Crocidura bicolor (0.57%) and Elephantulus rufescens (0.28%) were the insectivores recorded with their respective relative abundance. Mastomys natalensis was the most abundant and O. typus and E. rufescens were the least (two each). Diversity of small mammals ranged from 2.299 to 2.625 with an average of 2.412. The highest small mammal diversity was in grasslands and the lowest was in Lake Chamo shore. Small mammal density varied from 5 to 43 ha^?1 and biomass varied from 244 to 2559 g ha^?1 with significant changes in relation to seasons and habitats.     

Even more new taxa from South and East Anatolia I

A total of 25 items are listed. 16 are new taxa described from South and East Anatolia:Papaver (1),Heldreichia (1),Astragalus (1),Lotus (1),Onobrychis (3),Sempervivum (2),Hellenocarum (1),Cirsium (2),Campanula (1),Omphalodes (1),Allium (1) andPuccinellia (1). Nine other species belonging to the generaDiplotaxis, Beta, Acacia, Lupinus, Cirsium, Limonium, Calamagrostis andPuccinellia, are new records for the Flora of Turkey area. Two combinations are made, one inPapaver (p. 113), the other inHellenocarum (p. 122).     

New records of freshwater rotifers (Rotifera) from Indian waters

This study adds 25 rotifer species to the fauna of India viz.Cyrtonia tuba (Ehrb.)Epiphanes macrourus (Barrois & Daday),Liliferotrocha subtilis (Rodewald),Microcodides chleana (Gosse),Brachionus dimidiatus (Bryce),Keratella ticinensis Carlin,Notholca labis (Gosse),Platyias leloupi (Gillard),Euchlanis incisa Carlin,Mytilina bisulcata (Lucks),Wolga spinifera (Western),Lecane (Lecane)althausi Rudescu,L. (L.)doryssa Harring,L. (L.)elongata Harring & Myers,L. (Monostyla)bifurca (Bryce)L. (M.)lamellata thalera (Harring & Myers),L. (Hemimonostyla)blachei Berzins,Cephalodella giganthea Remane,Monommata arndti Remane,Trichocerca (Trichocerca)pusilla (Lauterborn),Testudinella emarginula (Stenroos),Ptygura melicerta Ehrb,P. tacita Edmondson,Filinia cornuta (Weisse),Collotheca mutabilis (Hudson),C. ornata (Ehrb.) andC. trilobata (Collins).B. dimidiatus andP. leloupi are new records from Delhi Region.     

Incidence of keratinophilic fungi from selected soils of Kerala state (India)

One hundred and fifty-eight soil samples were collected from various areas of four districts of Kerala and screened for prevalence of keratinophilic fungi and related dermatophytes. From the positive samples (60.75%), a total of eight genera with 15 species were isolated viz., Arthroderma simii (0.63%), Chrysosporium indicum (20.25%), C. keratinophilum (6.96%), C. lobatum (1.26%), C. pannicola (1.26%), C. tropicum (5.06%), Chrysosporium state of Arthroderma cuniculi (1.26%), Chrysosporium state of Ctenomyces serratus (2.53%), Gymnascella hyalinospora (1.26%), Malbranchea aurantiaca (0.63%) M. fulva (1.26%), Microsporum gypseum complex (12.65%), Pseudogymnoascus roseus (1.26%), Trichophyton mentragrophytes (1.26%), and T. terrestre (3.16%).This revised version was published online in October 2005 with corrections to the Cover Date.     

Pollination ofOphrys (Orchidaceae) in Cyprus

In the southern part of Cyprus the pollinator —Ophrys (Orchidaceae) relationships and its specifity have been investigated from the end of February until the middle of March 1986. 12Ophrys spp. were found. To date, only a single pollinator reference has been reported from this island. We found the following pollinators:Melecta tuberculata (Ophrys kotschyi),Eucera dimidiata (Ophrys flavomarginata),Eucera gaullei (Ophrys umbilicata),Eucera paulusi (Ophrys bornmuelleri),Anthophora erschowi (Ophrys elegans),Andrena torda (Ophrys sicula =O. lutea subsp.minor),Andrena cinereophila (Ophrys fusca, small-flowered),Andrena flavipes (Ophrys israelitica),Andrena morio (Ophrys iricolor andOphrys transhyrcana),Andrena bimaculata (Ophrys sphegodes aggr., probably formerly confused withO. transhyrcana). Most interestingly, it could be verified thatO. flavomarginata/O. umbilicata, O. bornmuelleri/O. levantina andO. transhyrcana/O. sphegodes aggr. (possiblyO. sintenisii) are different biospecies. This is a result of genetic isolation due to varying pollinators, and of differences in flower morphology.     

Pericarp structure and phylogeny of theLamiaceae-Verbenaceae-complex

Pericarp structure was investigated in 158 species of the familiesLamiaceae andVerbenaceae. Data from 221 out of 262 genera ofLamiaceae s.l. and a few ofVerbenaceae s.str. were collected in a table. A cladistic analysis was performed on the basis of pericarp characters only. The abandonment of subfam.Pogostemonoideae as a taxonomic unit is considered. Examples of groups given additional support by similarities in pericarp characters are: (1) the gynobasic-styled labiates (subfamiliesPogostemonoideae, Lamioideae, Nepetoideae); (2) aLamioideae-Pogostemonoideae-group; (3)Nepetoideae; (4) aWestringia-Hemigenia-Hemiandra-Microcorys group (in subfam.Chloranthoideae); (5) aLepechinia-Chaunostoma-group (inNepetoideae); (6) aPrunella-Cleonia-group (inNepetoideae).     

Phylogeny and classification of tribe Aedini (Diptera: Culicidae)

The phylogeny and classification of tribe Aedini are delineated based on a cladistic analysis of 336 characters from eggs, fourth‐instar larvae, pupae, adult females and males, and immature stage habitat coded for 270 exemplar species, including an outgroup of four species from different non‐aedine genera. Analyses of the data set with all multistate characters treated as unordered under implied weights, implemented by TNT version 1.1, with values of the concavity constant K ranging from 7 to 12 each produced a single most parsimonious cladogram (MPC). The MPCs obtained with K values of 7–9 were identical, and that for K = 10 differed only in small changes in the relationships within one subclade. Because values of K < 7 and > 10 produced large changes in the relationships among the taxa, the stability of relationships exemplified by the MPC obtained from the K = 9 analysis is used to interpret the phylogeny and classification of Aedini. Clade support was assessed using parsimony jackknife and symmetric resampling. Overall, the results reinforce the patterns of relationships obtained previously despite differences in the taxa and characters included in the analyses. With two exceptions, all of the groups represented by two or more species were once again recovered as monophyletic taxa. Thus, the monophyly of the following genera and subgenera is corroborated: Aedes, Albuginosus, Armigeres (and its two subgenera), Ayurakitia, Bothaella, Bruceharrisonius, Christophersiomyia, Collessius (and its two subgenera), Dahliana, Danielsia, Dobrotworskyius, Downsiomyia, Edwardsaedes, Finlaya, Georgecraigius (and its two subgenera), Eretmapodites, Geoskusea, Gilesius, Haemagogus (and its two subgenera), Heizmannia (and subgenus Heizmannia), Hopkinsius (and its two subgenera), Howardina, Hulecoeteomyia, Jarnellius, Kenknightia, Lorrainea, Macleaya, Mucidus (and its two subgenera), Neomelaniconion, Ochlerotatus (subgenera Chrysoconops, Culicelsa, Gilesia, Pholeomyia, Protoculex, Rusticoidus and Pseudoskusea), Opifex, Paraedes, Patmarksia, Phagomyia, Pseudarmigeres, Rhinoskusea, Psorophora (and its three subgenera), Rampamyia, Scutomyia, Stegomyia, Tanakaius, Udaya, Vansomerenis, Verrallina (and subgenera Harbachius and Neomacleaya), Zavortinkius and Zeugnomyia. In addition, the monophyly of Tewarius, newly added to the data set, is confirmed. Heizmannia (Mattinglyia) and Verrallina (Verrallina) were found to be paraphyletic with respect to Heizmannia (Heizmannia) and Verrallina (Neomacleaya), respectively. The analyses were repeated with the 14 characters derived from length measurements treated as ordered. Although somewhat different patterns of relationships among the genera and subgenera were found, all were recovered as monophyletic taxa with the sole exception of Dendroskusea stat. nov. Fifteen additional genera, three of which are new, and 12 additional subgenera, 11 of which are new, are proposed for monophyletic clades, and a few lineages represented by a single species, based on tree topology, the principle of equivalent rank, branch support and the number and nature of the characters that support the branches. Acartomyia stat. nov. , Aedimorphus stat. nov. , Cancraedes stat. nov. , Cornetius stat. nov. , Geoskusea stat. nov. , Levua stat. nov. , Lewnielsenius stat. nov. , Rhinoskusea stat. nov. and Sallumia stat. nov., which were previously recognized as subgenera of various genera, are elevated to generic status. Catageiomyia stat. nov. and Polyleptiomyia stat. nov. are resurrected from synonymy with Aedimorphus, and Catatassomyia stat. nov. and Dendroskusea stat. nov. are resurrected from synonymy with Diceromyia. Bifidistylus gen. nov. (type species: Aedes lamborni Edwards) and Elpeytonius gen. nov. (type species: Ochlerotatus apicoannulatus Edwards) are described as new for species previously included in Aedes (Aedimorphus), and Petermattinglyius gen. nov. (type species: Aedes iyengari Edwards) and Pe. (Aglaonotus) subgen. nov. (type species: Aedes whartoni Mattingly) are described as new for species previously included in Aedes (Diceromyia). Four additional subgenera are recognized for species of Ochlerotatus, including Oc. (Culicada) stat. nov. (type species: Culex canadensis Theobald), Oc. (Juppius) subgen. nov. (type species: Grabhamia caballa Theobald), Oc. (Lepidokeneon) subgen. nov. (type species: Aedes spilotus Marks) and Oc. (Woodius) subgen. nov. (type species: Aedes intrudens Dyar), and seven are proposed for species of Stegomyia: St. (Actinothrix) subgen. nov. (type species: Stegomyia edwardsi Barraud), St. (Bohartius) subgen. nov. (type species: Aedes pandani Stone), St. (Heteraspidion) subgen. nov. (type species: Stegomyia annandalei Theobald), St. (Huangmyia) subgen. nov. (type species: Stegomyia mediopunctata Theobald), St. (Mukwaya) subgen. nov. (type species: Stegomyia simpsoni Theobald), St. (Xyele) subgen. nov. (type species: Stegomyia desmotes Giles) and St. (Zoromorphus) subgen. nov. (type species: Aedes futunae Belkin). Due to the unavailability of specimens for study, many species of Stegomyia are without subgeneric placement. As is usual with generic‐level groups of Aedini, the newly recognized genera and subgenera are polythetic taxa that are diagnosed by unique combinations of characters. The analysis corroborates the previous observation that ‘Oc. (Protomacleaya)’ is a polyphyletic assemblage of species.     

Aerobiology of Vigo, North-Western Spain: atmospheric pollen spectrum and annual dynamics of the most important taxa, and their clinical importance for allergy

Vigo is a city located in the northwest of the Iberian Peninsula. Influenced by the Atlantic climate, it is surrounded by a Eurosiberian-type vegetation, modified by the introduction of forestry and ornamental species. Different ruderal vegetation types, resulting from human influence, grow in the area. The study of the pollen content of the air of Vigo started in 1989, with a Cour trap. Average results for the period 1989–1995 are presented in this paper, together with the lowest and highest values found. The representativeness of the mean values is analysed by calculating the coefficient of variation of the data series. Most pollen types in the atmosphere of Vigo are from tree species (54.2%); an important proportion comes from herb species (43.9%) and very few (1.8%) correspond to shrub species. A total of 73 different pollen types have been identified. The most abundant, listed in decreasing order of mean annual values for the period, are:Pinus (25.1%), Poaceae (21.1%), Urticaceae (14.6%),Quercus (8.5%),Castanea (3.7%),Betula (3.6%),Eucalyptus (3.4%),Plantago (3.2%),Alnus (2.1%), Cupressaceae (2.1%), Oleaceae (1.6%;Olea 1.3%),Platanus (1.3%),Rumex (1.3%), Chenopodiaceae/Amaranthaceae (1.0%), Ericaceae (0.8%), Asteraceae (0.6%;Artemisia 0.1% andTaraxacum type 0.2%) andMercurialis (0.5%). A pollen calendar showing the annual dynamics of all these pollen types is presented in this paper. A parallel study of the clinical importance of respiratory allergies in Vigo was also conducted. From a sample of 2750 patients, 87.2% suffered from rhinoconjunctivitis, 26.0% of these due to pollen, and 78.3% from asthma, 17.2% due to pollen. The pollen types responsible for these allergies, listed in decreasing order, are: Poaceae (78%),Parietaria (12%),Chenopodium (11%),Plantago (9%), Oak (4%),Artemisia (3%),Pinus (3%),Eucalyptus (3%),Olea (2%),Platanus (2%),Castanea (2%),Taraxacum (2%),Rumex (2%),Betula (1%),Cupressus (1%) andMercurialis (1%).     

Clock Gene Expression Levels and Relationship With Clinical and Pathological Features in Colorectal Cancer Patients

The clock gene machinery controls cellular metabolism, proliferation, and key functions, such as DNA damage recognition and repair. Dysfunction of the circadian clock is involved in tumorigenesis, and altered expression of some clock genes has been found in cancer patients. The aim of this study was to evaluate the expression levels of core clock genes in colorectal cancer (CRC). Quantitative real-time polymerase chain reaction (qPCR) was used to examine ARNTL1, CLOCK, PER1, PER2, PER3, CRY1, CRY2, Timeless (TIM), TIPIN, and CSNK1Ε expression levels in the tumor tissue and matched apparently healthy mucosa of CRC patients. In the tumor tissue of CRC patients, compared to their matched healthy mucosa, expression levels of ARNTL1 (p?=?.002), PER1 (p?=?.002), PER2 (p?=?.011), PER3 (p?=?.003), and CRY2 (p?=?.012) were lower, whereas the expression level of TIM (p?=?.044) was higher. No significant difference was observed in the expression levels of CLOCK (p?=?.778), CRY1 (p?=?.600), CSNK1Ε (p?=?.903), and TIPIN (p?=?.136). As to the clinical and pathological features, a significant association was found between low CRY1 expression levels in tumor mucosa and age (p?=?.026), and female sex (p?=?.005), whereas high CRY1 expression levels in tumor mucosa were associated with cancer location in the distal colon (p?=?.015). Moreover, high TIM mRNA levels in the tumor mucosa were prevalent whenever proximal lymph nodes were involved (p?= .013) and associated with TNM stages III–IV (p?=?.005) and microsatellite instability (p?=?.015). Significantly poorer survival rates were evidenced for CRC patients with lower expression in the tumor tissue of PER1 (p?=?.010), PER3 (p?= .010), and CSNKIE (p?=?.024). In conclusion, abnormal expression levels of core clock genes in CRC tissue may be related to the process of tumorigenesis and exert an influence on host/tumor interactions. (Author correspondence: g.mazzoccoli@tin.it)     

Reassessment of type specimens of Cordyceps and its allies described by Dr. Yosio Kobayasi preserved in the mycological herbarium of the National Museum of Nature and Science (TNS). Part 1: the genus Torrubiella

Nineteen holotype specimens of the genus Torrubiella described by Dr. Yosio Kobayasi and Mr. Daisuke Shimizu were relocated and accession numbers (TNS-F number) were given. A new scientific name, Torrubiella plana Hiroki Sato, Ban, Masuya & Hosoya nom. nov. (TNS-F-12061), was proposed for T. minutissima Kobaysi & Shimizu (homonym of T. minutissima Lagarde). The other 18 species follow: T. alboglobosa (TNS-F-12067), T. aurantia (TNS-F-12069), T. corniformis (TNS-F-12064), T. ellipsoidea (TNS-F-12055), T. formosana (TNS-F-12059), T. fusiformis (TNS-F-234548), T. globosostipitata (TNS-F-12057), T. longissima (TNS-F-12071), T. mammillata (TNS-F-12060), T. miyagiana (TNS-F-12062), T. neofusiformis (TNS-F-12058), T. oblonga (TNS-F-12070), T. ooaniensis (TNS-F-12063), T. pallida (TNS-F-12789), T. rosea (TNS-F-12065), T. ryogamimontana (TNS-F-12058), T. ryukyuensis (TNS-F-11932), and T. superficialis (TNS-F-12072).     

Cryptosporidium spp. in pet birds: genetic diversity and potential public health significance

To characterize the prevalence and assess the zoonotic transmission burden of Cryptosporidium species/genotypes in pet birds in Henan, China, 434 fecal samples were acquired from 14 families of birds in pet shops. The overall prevalence of Cryptopsoridium was 8.1% (35/434) by the Sheather’s sugar flotation technique. The Cryptosporidium-positive samples were analyzed by DNA sequence analysis of the small subunit (SSU) rRNA gene. Three Cryptosporidium species and two genotypes were identified, including C. baileyi (18/35 or 51.4%) in five red-billed leiothrixes (Leiothrix lutea), four white Java sparrows (Padda oryzivora), four common mynas (Acridotheres tristis), two zebra finches (Taeniopygia guttata), a crested Lark (Galerida cristata), a Gouldian finch (Chloebia gouldiae), and a black-billed magpie (Pica pica); Cryptosporidium meleagridis (3/35 or 8.6%) in a Bohemian waxwing (Bombycilla garrulus), a Rufous turtle dove (Streptopelia orientalis), and a fan-tailed pigeon (Columba livia); Cryptosporidium galli (5/35 or 14.3%) in four Bohemian waxwings (Bombycilla garrulus) and a silver-eared Mesia (Leiothrix argentauris); Cryptosporidium avian genotype III (3/35 or 8.6%) in two cockatiels (Nymphicus hollandicus) and a red-billed blue magpie (Urocissa erythrorhyncha); and Cryptosporidium avian genotype V (6/35 or 17.1%) in six cockatiels (Nymphicus hollandicus). Among the pet birds, 12 species represented new hosts for Cryptosporidum infections. The presence of C. meleagridis raises questions on potential zoonotic transmission of cryptosporidiosis from pet birds to humans.     

A critical review of Antarctic Conoidea (Neogastropoda)

ABSTRACT

The Antarctic Conoidean fauna is critically reviewed based on published data and specimens in the collections of the USNM, IORAS and MNHN. Forty-two species and subspecies of the superfamily Conoidea are recorded as occurring within the Antarctic Convergence (excluding the fauna of the Kerguelen Islands) and are attributed to 14 genera and seven families. These include the new taxa: Antarctospira n. gen. (type species—Leucosyrinx badenpowelli Dell, 1990); Drilliola antarctica n. sp.; Pleurotomella (Pleutoromella) tippetti n. sp.; Pleurotomella (Anomalotomella) petiti n. sp.; Xanthodaphne pastorinoi n. sp. Aforia watsoni is introduced as a new name for Pleurotoma (Surcula) lepta Watson, 1881, non Pleurotoma lepta Edwards, 1861. A lectotype is designated for Conorbella antarctica (Strebel, 1908). New combinations are also proposed. Antarctospira badenpowelli (Dell, 1990), n. comb. (previously assigned to Leucosyrinx); Antarctospira principalis (Thiele, 1912), n. comb. (previously assigned to Typhlomangelia); Antarctospira mawsoni (Powell, 1958), n. comb. (previously assigned to Leucosyrinx); Typhlodaphne paratenoceras (Powell, 1951), n. comb. (previously assigned to Leucosyrinx); Belalora weirichi (Engl, 2008), n. comb. (previously assigned to Oenopota); Pleurotomella (Anomalotomella) innocentia (Dell, 1990), n. comb. (previously assigned to Typhlodaphne); Pleurotomella (Anomalotomella) nipri (Numanami, 1996), n. comb. (previously assigned to Typhlodaphne); Xanthodaphne raineri (Engl, 2008), n. comb. (previously assigned to Pleurotomella); Aforia hedleyi (Dell, 1990), n. comb. (previously assigned to Pontiothauma). The majority of Antarctic conoidean taxa have hypodermic marginal teeth. Although there is a similar relative abundance of conoideans in Antarctic waters to that seen in other well-studied faunas, the low number of conoideans is indicative of the general impoverishment of the gastropod fauna in the region. Fourteen percent (2 of 14) of conoidean genera that occur within the Antarctic Convergence are endemic to Antarctic waters, as are 82% (34 of 42) of the species. Most taxa have very broad bathymetric ranges, some extending from bathyal to hadal depths. The greatest species diversity was at bathyal depths.     

Contribution to the knowledge of the Ichneumonidae (Hymenoptera) fauna of Turkey

This study is based upon material of the family Ichneumonidae collected from Erzurum and Tunceli provinces of Turkey between 2011 and 2012. 64 species in 49 genera of the family Ichneumonidae were recorded. Among them, Alloplasta tomentosa (Gravenhorst, 1829), Lissonota (Lissonota) accusator (Fabricius, 1793), Dusona nidulator (Fabricius, 1804), Olesicampe fulviventris (Gmelin, 1790), Olesicampe proterva (Brischke, 1880), Olesicampe radiella (Thomson, 1885), Aptesis nigrocincta (Gravenhorst, 1815), Cryptus moschator (Fabricius, 1787), Pleolophus brachypterus (Gravenhorst, 1815), Hadrodactylus flavofacialis Horstmann, 2000, Lagarotis semicaligata (Gravenhorst, 1820), Coelichneumon (Coelichneumon) consimilis (Wesmael, 1845), Hoplismenus axillatorius (Thunberg, 1822) and Eridolius pictus (Gravenhorst, 1829) are new to the Turkish fauna. A short zoogeographic characterisation is given for each species.     

Mycological flora of cigarettes

Hundred strains of fungi were isolated from 48 packets of Greek cigarettes. They were:Aspergillus (28 strains),Penicillium (22),Mucor (18),Alternaria (14),Cladosporium (1),Streptomyces (4),Candida (11) andGeotrichum (2). From 55 packets of cigarettes manufactured outside of Greece other 100 strains of fungi were isolated and identified asAspergillus (35),Penicillium (23),Mucor (10),Alternaria (13),Cladosporium (5),Streptomyces (4),Candida (3),Geotrichum (1),Cephalosporium (2) andScopulariopsis (4).Results of the present study are discussed in relation to the mycological flora of the air in Athens and to the coli-aerogenes bacteria of cigarettes.

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Résumé Les auteurs ont isolé 100 souches de champignons à partir de 48 paquets de cigarettes préparées en Grèce. Ces souches étaient identifiées commeAspergillus (28 souches),Penicillium (22),Mucor (18),Alternaria (14),Cladosporium (1),Streptomyces (4),Candida (11) etGeotrichum (2). D'autre part on a isolé 100 souches de champignons à partir de 55 paquets de cigarettes préparées à l'étranger (surtout aux Etats-Unis et en Angleterre). Ces souches étaientAspergillus (35),Penicillium (23),Mucor (10),Alternaria (13),Cladosporium (5),Streptomyces (4),Candida (3),Geotrichum (1),Cephalosporium (2) etScopulariopsis (4).Les résultats sont discutés en relation avec la flore mycosique de l'air à Athènes et les bactéries coliformes rétrouvées dans les cigarettes préparées en Grèce.