Annotated type catalogue of the Bulimulidae (Mollusca,Gastropoda, Orthalicoidea) in the Natural History Museum,London

The type status is described of 404 taxa classified within the family Bulimulidae (superfamily Orthalicoidea) and kept in the London museum. Lectotypes are designated for Bulimus aurifluus Pfeiffer, 1857; Otostomus bartletti H. Adams, 1867; Helix cactorum d’Orbigny, 1835; Bulimus caliginosus Reeve, 1849; Bulimus chemnitzioides Forbes, 1850; Bulimus cinereus Reeve, 1849; Helix cora d’Orbigny, 1835; Bulimus fallax Pfeiffer, 1853; Bulimus felix Pfeiffer, 1862; Bulimus fontainii d’Orbigny, 1838; Bulimus fourmiersi d’Orbigny, 1837; Bulimus (Mesembrinus) gealei H. Adams, 1867; Bulimus gruneri Pfeiffer, 1846; Bulimus humboldtii Reeve, 1849; Helix hygrohylaea d’Orbigny, 1835; Bulimus jussieui Pfeiffer, 1846; Bulimulus (Drymaeus) binominis lascellianus E.A. Smith, 1895; Helix lichnorum d’Orbigny, 1835; Bulimulus (Drymaeus) lucidus da Costa, 1898; Bulimus luridus Pfeiffer, 1863; Bulimus meleagris Pfeiffer, 1853; Bulimus monachus Pfeiffer, 1857; Bulimus montagnei d’Orbigny, 1837; Helix montivaga d’Orbigny, 1835; Bulimus muliebris Reeve, 1849; Bulimus nigrofasciatus Pfeiffer in Philippi 1846; Bulimus nitelinus Reeve, 1849; Helix oreades d’Orbigny, 1835; Helix polymorpha d’Orbigny, 1835; Bulimus praetextus Reeve, 1849; Bulinus proteus Broderip, 1832; Bulimus rusticellus Morelet, 1860; Helix sporadica d’Orbigny, 1835; Bulimus sulphureus Pfeiffer, 1857; Helix thamnoica var. marmorata d’Orbigny, 1835; Bulinus translucens Broderip in Broderip and Sowerby I 1832; Helix trichoda d’Orbigny, 1835; Bulinus ustulatus Sowerby I, 1833; Bulimus voithianus Pfeiffer, 1847; Bulimus yungasensis d’Orbigny, 1837.The type status of the following taxa is changed to lectotype in accordance with Art. 74.6 ICZN: Bulimulus (Drymaeus) caucaensis da Costa, 1898; Drymaeus exoticus da Costa, 1901; Bulimulus (Drymaeus) hidalgoi da Costa, 1898; Bulimulus (Drymaeus) interruptus Preston, 1909; Bulimulus (Drymaeus) inusitatus Fulton, 1900; Bulimulus latecolumellaris Preston, 1909; Bulimus (Otostomus) napo Angas, 1878; Drymaeus notabilis da Costa, 1906; Drymaeus notatus da Costa, 1906; Bulimulus (Drymaeus) nubilus Preston, 1903; Drymaeus obliquistriatus da Costa, 1901; Bulimus (Drymaeus) ochrocheilus E.A. Smith, 1877; Bulimus (Drymaeus) orthostoma E.A. Smith, 1877; Drymaeus expansus perenensis da Costa, 1901; Bulimulus pergracilis Rolle, 1904; Bulimulus (Drymaeus) plicatoliratus da Costa, 1898; Drymaeus prestoni da Costa, 1906; Drymaeus punctatus da Costa, 1907; Bulimus (Leptomerus) sanctaeluciae E.A. Smith, 1889; Bulimulus (Drymaeus) selli Preston, 1909; Drymaeus subventricosus da Costa, 1901; Bulimulus (Drymaeus) tigrinus da Costa, 1898; Drymaeus volsus Fulton, 1907; Drymaeus wintlei Finch, 1929; Bulimus zhorquinensis Angas, 1879; Bulimulus (Drymaeus) ziczac da Costa, 1898.The following junior subjective synonyms are established: Bulimus antioquensis Pfeiffer, 1855 = Bulimus baranguillanus Pfeiffer, 1853; Drymaeus bellus da Costa, 1906 = Drymaeus blandi Pilsbry, 1897; Bulimus hachensis Reeve 1850 = Bulimus gruneri Pfeiffer, 1846 = Bulimus columbianus Lea, 1838; Bulimus (Otostomus) lamas Higgins 1868 = Bulimus trujillensis Philippi, 1867; Bulimulus (Drymaeus) binominis lascellianus E.A. Smith, 1895 = Bulimulus (Drymaeus) binominis E.A. Smith, 1895; Drymaeus multispira da Costa, 1904 = Helix torallyi d’Orbigny, 1835; Bulimulus (Drymaeus) plicatoliratus Da Costa, 1898 = Bulimus convexus Pfeiffer, 1855; Bulimus sugillatus Pfeiffer, 1857 = Bulimus rivasii d’Orbigny, 1837; Bulimus meridionalis Reeve 1848 [June] = Bulimus voithianus Pfeiffer, 1847.New combinations are: Bostryx montagnei (d’Orbigny, 1837); Bostryx obliquiportus (da Costa, 1901); Bulimulus heloicus (d’Orbigny, 1835); Drymaeus (Drymaeus) lusorius (Pfeiffer, 1855); Drymaeus (Drymaeus) trigonostomus (Jonas, 1844); Drymaeus (Drymaeus) wintlei Finch, 1929; Drymaeus (Mesembrinus) conicus da Costa, 1907; Kuschelenia (Kuschelenia) culminea culminea (d’Orbigny, 1835); Kuschelenia (Kuschelenia) culmineus edwardsi (Morelet, 1863); Kuschelenia (K.) gayi (Pfeiffer, 1857); Kuschelenia (Kuschelenia) tupacii (d’Orbigny, 1835); Kuschelenia (Vermiculatus) anthisanensis (Pfeiffer, 1853); Kuschelenia (Vermiculatus) aquilus (Reeve, 1848); Kuschelenia (Vermiculatus) bicolor (Sowerby I, 1835); Kuschelenia (Vermiculatus) caliginosus (Reeve, 1849); Kuschelenia (Vermiculatus) cotopaxiensis (Pfeiffer, 1853); Kuschelenia (Vermiculatus) filaris (Pfeiffer, 1853); Kuschelenia (Vermiculatus) ochracea (Morelet, 1863); Kuschelenia (Vermiculatus) petiti (Pfeiffer, 1846); Kuschelenia (Vermiculatus) purpuratus (Reeve, 1849); Kuschelenia (Vermiculatus) quechuarum (Crawford, 1939); Naesiotus cinereus (Reeve, 1849); Naesiotus dentritis (Morelet, 1863); Naesiotus fontainii (d’Orbigny, 1838); Naesiotus orbignyi (Pfeiffer, 1846); Protoglyptus pilosus (Guppy, 1871); Protoglyptus sanctaeluciae (E.A. Smith, 1889).Type material of the following taxa is figured herein for the first time: Bulimus cinereus Reeve, 1849; Bulimus coriaceus Pfeiffer, 1857; Bulimulus laxostylus Rolle, 1904; Bulimus pliculatus Pfeiffer, 1857; Bulimus simpliculus Pfeiffer, 1855.     

Annotated type catalogue of the Bothriembryontidae and Odontostomidae (Mollusca, Gastropoda, Orthalicoidea) in the Natural History Museum, London

The type status is described for specimens of 84 taxa classified within the families Bothriembryontidae and Odontostomidae (superfamily Orthalicoidea) and kept in the Natural History Museum, London. Lectotypes are designated for Bulimus (Liparus) brazieri Angas, 1871; Bulimus broderipii Sowerby I, 1832; Bulimus fuligineus Pfeiffer, 1853; Helix guarani d'Orbigny, 1835; Bulimus (Tomigerus) ramagei E.A. Smith, 1890; Helix rhodinostoma d'Orbigny, 1835; Bulimus (Bulimulus) ridleyi E.A. Smith, 1890. The type status of the following taxa is changed to lectotype in accordance with Art. 74.6 ICZN: Placostylus (Euplacostylus) cylindricus Fulton, 1907; Bulimus pyrostomus Pfeiffer, 1860; Bulimus turneri Pfeiffer, 1860. The following taxon is synonymised: Bulimus oblitus Reeve, 1848 = Bahiensis neglectus (Pfeiffer, 1847).     

Planorbidae, Lymnaeidae and Physidae of Ecuador (Mollusca: Basommatophora)

In the course of a trip to Ecuador I had the opportunity of collecting topotypic specimens of the following nominal species of pulmonate molluscs: Biomphalaria cousini Paraense, 1966; Planorbis equatorius Cousin, 1887; P. canonicus Cousin, 1887; Lymnaea cousini Jousseaume, 1887 and P. boetzkesi Miller, 1879. Additional findings were: Helisoma trivolvis (Say, 1817), Biomphalaria peregrina (Orbigny 1835), Drepanotrema anatinum (Orbigny, 1835), D. kermatoides (Orbigny, 1835), D. lucidum (Pfeiffer, 1839), D. surinamense (Clessin, 1884), Lymnaea columella Say, 1817 and Physa acuta Draparnaud, 1805. P. boetzkesi and P. canonicus are considered junior synonyms of Gyraulus hindsianus (Dunker, 1848) and Biomphalaria peregrina (Orbigny, 1835), respectively.     

Annotated type catalogue of the Amphibulimidae (Mollusca, Gastropoda, Orthalicoidea) in the Natural History Museum, London

The type status is described of 39 taxa classified within the family Amphibulimidae (superfamily Orthalicoidea) and kept in the London museum. One taxon, Bulimus elaeodes Pfeiffer, 1853, is removed to the Strophocheilidae. Lectotypes are designated for Bulimus adoptus Reeve, 1849; Bulimus (Eurytus) eros Angas, 1878; Helix onca d'Orbigny, 1835; Amphibulima pardalina Guppy, 1868. The type status of the following taxon is changed to lectotype in accordance with Art. 74.6 ICZN: Strophocheilus (Dryptus) jubeus Fulton, 1908.As general introduction to this and following papers on Orthalicoid types in the Natural History Museum, a brief history of the London collection is given and several examples of handwriting from different authors are presented.     

Taxonomic revision of the Elephant Pupinid snail genus Pollicaria Gould, 1856 (Prosobranchia,Pupinidae)

The status of species currently assigned to the Southeast Asian Elephant Pupinid snail genus Pollicaria Gould, 1856 is reassessed. Shell, radular and reproductive morphology are investigated and analysed with reference to karyotype patterns previously reported and to distribution patterns among the species. Six previously described species are recognised: Pollicaria gravida (Benson, 1856), Pollicaria myersii (Haines, 1855), Pollicaria mouhoti (Pfeiffer, 1862), Pollicaria elephas (Morgan, 1885), Pollicaria crossei (Dautzenberg & d’Hamonville, 1887) and Pollicaria rochebruni (Mabille, 1887). A new subspecies, Pollicaria mouhoti monochroma ssp. n.,is proposed and a dichotomous key to species is provided.     

A new species of Monoplacophora, redescription of the genera Veleropilina and Rokopella, and new information on three species of the class

Vema levinae Warén, sp. n. is described from a submarine volcano off western Mexico. The type species of Rokopella and Veleropilina are redescribed, the usage of the names is discussed and Rokopella and Veleropilina are recognized as valid genera in Neopilinidae. Rokopella euglypta (Dautzenberg & Fischer, 1897) is redescribed from shells and a single live specimen taken from seamounts south of the Azores, from a depth of 1200–1600 m. Tectura reticulata Seguenza, 1876 (Gastropoda, 'Acmaeidae', southern Italy, Upper Pliocene/Lower Pleistocene) is considered to have been based on the monoplacophoran species previously known as Neopilina zografi from the Mediterranean, and is classified in the genus Veleropilina. Veleropilina zografi (Dautzenberg & Fischer, 1896) is redescribed based on shells from several seamounts south of the Azores. It is considered distinct from Rokopella euglypta and classified in the genus Veleropilina. An undescribed species of Veleropilina from a seamount off southern Baja California is reported, figured and discussed but not formally described.     

Annotated type catalogue of the Megaspiridae,Orthalicidae, and Simpulopsidae (Mollusca,Gastropoda, Orthalicoidea) in the Natural History Museum,London

The type status is described for 65 taxa of the Orthalicoidea, classified within the families Megaspiridae (14), Orthalicidae (30), and Simpulopsidae (20); one taxon is considered a nomen inquirendum. Lectotypes are designated for the following taxa: Helix brephoides d’Orbigny, 1835; Simpulopsis cumingi Pfeiffer, 1861; Bulimulus (Protoglyptus) dejectus Fulton, 1907; Bulimus iris Pfeiffer, 1853. The type status of Bulimus salteri Sowerby III, 1890, and Strophocheilus (Eurytus) subirroratus da Costa, 1898 is now changed to lectotype according Art. 74.6 ICZN. The taxa Bulimus loxostomus Pfeiffer, 1853, Bulimus marmatensis Pfeiffer, 1855, Bulimus meobambensis Pfeiffer, 1855, and Orthalicus powissianus var. niveus Preston 1909 are now figured for the first time. The following taxa are now considered junior subjective synonyms: Bulimus marmatensis Pfeiffer, 1855 = Helix (Cochlogena) citrinovitrea Moricand, 1836; Vermiculatus Breure, 1978 = Bocourtia Rochebrune, 1882. New combinations are: Kuschelenia (Bocourtia) Rochebrune, 1882; Kuschelenia (Bocourtia) aequatoria (Pfeiffer, 1853); Kuschelenia (Bocourtia) anthisanensis (Pfeiffer, 1853); Kuschelenia (Bocourtia) aquila (Reeve, 1848); Kuschelenia (Bocourtia) badia (Sowerby I, 1835); Kuschelenia (Bocourtia) bicolor (Sowerby I, 1835); Kuschelenia (Bocourtia) caliginosa (Reeve, 1849); Kuschelenia (Bocourtia) coagulata (Reeve, 1849); Kuschelenia (Bocourtia) cotopaxiensis (Pfeiffer, 1853); Kuschelenia (Bocourtia) filaris (Pfeiffer, 1853); Kara indentata (da Costa, 1901); Clathrorthalicus magnificus (Pfeiffer, 1848); Simpulopsis (Eudioptus) marmartensis (Pfeiffer, 1855); Kuschelenia (Bocourtia) nucina (Reeve, 1850); Kuschelenia (Bocourtia) ochracea (Morelet, 1863); Kuschelenia (Bocourtia) peaki (Breure, 1978); Kuschelenia (Bocourtia) petiti (Pfeiffer, 1846); Clathrorthalicus phoebus (Pfeiffer, 1863); Kuschelenia (Bocourtia) polymorpha (d’Orbigny, 1835); Scholvienia porphyria (Pfeiffer, 1847); Kuschelenia (Bocourtia) purpurata (Reeve, 1849); Kuschelenia (Bocourtia) quechuarum Crawford, 1939; Quechua salteri (Sowerby III, 1890); Kuschelenia (Bocourtia) subfasciata Pfeiffer, 1853; Clathrorthalicus victor (Pfeiffer, 1854). In an addedum a lectotype is being designated for Bulimulus (Drymaeus) interruptus var. pallidus Preston, 1909. An index is included to all taxa mentioned in this paper and the preceding ones in this series (Breure and Ablett 2011, 2012, 2014).     

A revision of Afrotropical Agabus Leach (Coleoptera, Dytiscidae), and the evolution of tropicoalpine super specialists

Abstract. The thirteen species of Agabus Leach, 1817, of the Afrotropical Region are revised and classified into four species groups: the dibasic ambulator -group endemic to Ethiopia, ragazzii -group with five species in Ethiopia, raffrayi -group with five species in East and South Africa, and A.discicollis Ancey, 1882, endemic to Ethiopia, is placed in the Nearctic cordatus -group. Agabus perssoni sp.n. and Agabus galamensis sp.n. are described from the highlands of Ethiopia. Agabus ruwenzoricus Guignot, 1936, stat.n. is given specific rank. Agabus ferrugatus Régimbart, 1905, is synonymized with Agabus ragazzii Régimbart, 1887, and Agabus limbicollis Régimbart, 1905, is synonymized with Agabus raffrayi Sharp, 1882, syn.n. Lectotypes are designated for the following nominal species: Agabus discicollis Ancey, 1882, Agabus raffrayi Sharp, 1882, Agabus limbicollis Régimbart, 1905, Agabus pallidus Omer-Cooper, 1931, Agabus ruwenzoricus Guignot, 1936, Agabus sjostedti Régimbart, 1908, Agabus dytiscoides Régimbart, 1908, Agabus ragazzii Régimbart, 1887, Agabus ferrugatus Régimbart, 1905, and Gaurodytes abessinicus Zimmermann, 1928. Reconstructed phylogenies are presented for the raffrayi -and ragazzii -groups. The following adaptations to tropicoalpine habitats are suggested: (1) body and especially pronotum narrow, (2) head broad anteriorly, (3) hindwing small, and (4) hind leg long and slender. Biogeography and evolution of the studied species are discussed. Four different invasions of Holarctic lineages to the East African mountains are suggested. Recurrent periods of cold and dry climate are considered the chief driving force in the evolution of high altitude super specialists.     

A Review Of Two De Koninck Retzioid Brachiopod Species, And Description Of A New Genus From The Carboniferous Of Europe

A new neoretziid brachiopod genus, Coveenia , from the Lower Carboniferous of western Europe is erected; the type species is Coveenia ulothrix (de Koninck, 1843), and C. buchiana (de Koninck, 1843, sensu 1887) and C. tilsleia sp. nov. are included, diagnosed and described. Neotypes are selected and illustrated for C. ulothrix C. buchiana .     

New taxa of terrestrial molluscs from Turkey (Gastropoda, Pristilomatidae, Enidae, Hygromiidae, Helicidae)

This paper reports on results of several collecting trips of the authors in Turkey. In the course of this research, a long-lasting question was addressed. It could be proven that the nominal species Bulimus frivaldskyi L. Pfeiffer, 1847 is closely related to Meijeriella canaliculata Bank, 1985, and thus this species is shifted from the genus Ena Turton, 1831, to the genus Meijeriella Bank, 1985. Meijeriella canaliculata Bank, 1985, could be recorded from Turkey for the first time. The nomenclatural situation of the species Euchondrus septemdentatus (Roth, 1839) vs. its replacement name Euchondrus borealis (Mousson, 1874) is discussed. A new arrangement of the species formely comprised in the genus Zebrina Held, 1837 is presented, and the genera Rhabdoena Kobelt & Moellendorff, 1902, and Leucomastus A. Wagner, 1927 are re-established. The following species and subspecies new to science could be described: Vitrea gosteliisp. n. (Pristilomatidae), Turanena demirsoyisp. n., Euchondrus paucidentatussp. n., Rhabdoena gosteliisp. n. (all Enidae), Metafruticicola kizildagensissp. n. (Hygromiidae), and Assyriella thospitis menkhorstissp. n. (Helicidae). For several other species, new distribution records are listed.     

A review of the leaf-beetle genus Chrysolina Motschulsky (Coleoptera, Chrysomelidae) from Russia and European countries of the former USSR. III. Remarks on the systematics and distribution of the species

Chrysolina didymata (Scriba, 1791) is repeatedly recorded from Ukraine (Kamianets-Podilskyi), Ch. cuprina (Duftschmid, 1825) is recorded from the South Urals (Bashkiria) for the second time, Ch. oirota Lopatin, 1990 is recorded from Russia (W. Altai), Ch. staphylaea sharpi (Fowler, 1890) is recorded from Russia (the Kandalaksha Bay coast) for the first time. The presence of Ch. roddi in Lipetsk Province (the Galichia Gora Nature Reserve) is confirmed after the finding of three males. The host plant of this species is found to be Seseli intermedia. Chrysolina daghestanica (Reitter, 1912) is synonymized with Ch. cuprina (Duftschmid, 1825); Ch. dudkoi ivanovskiana Mikhailov, 2000 is synonymized with Ch. dudkoi dudkoi Mikhailov, 2000; Ch. tolli kodarensis is synonymized with Ch. cavigera pirka Takizawa, 1970. The infrasubspecific rank of the variety Ch. hyrcana var. cyanescens Jacobson, 1894 is confirmed. The neotype of Ch. sahlbergii (Ménétriés, 1832) is designated. The systematic position of Ch. arctoalpina Mikhailov, 2006, Ch. kholsunica Mikhailov, 2001, Ch. kuznetzowi (Jacobson, 1897), Ch. soiota khakassa Mikhailov, 2002, Ch. cuprina dilecta Bechyné, 1952, Ch. poretzkyi (Jacobson, 1897), Ch. seriepunctata (Weise, 1887), and Ch. ambulans (Faldermann, 1835) is discussed. The authorship and date of the original publication of one name are improved, namely: Chrysomela discipennis Ménétriés, 1848.     

A review of the microgastropod genus Systenostoma Bavay & Dautzenberg, 1908 and a new subterranean species from China (Gastropoda,Pulmonata, Hypselostomatidae)

A review of the microgastropod genus Systenostoma is provided. Thai and Malaysian species are transferred to a new genus, Angustopila (type species: Systenostoma tamlod Panha & Burch, 1999). A new subterranean Angustopila species is described here. Conchologically, the new species is most similar to the cave-dwelling, Thai A. tamlod (Panha & Burch, 1999). One Thai species (Systenostoma edentata) is transferred to the genus Hypselostoma. Vietnamese members remain in the genus Tonkinospira (nomen novum) for Systenostoma Bavay & Dautzenberg, 1908 (non Systenostoma Marsson, 1887). A comprehensive map of former Systenostoma species is presented. SEM and NanoCT images, including a video of A. huoyani sp. n. internal shell morphology, provide novel perspectives of the shells of Angustopila and of the scarcely known Vietnamese Tonkinospira species. The biology of these snails is not yet known but collection localities suggest a troglophilic ecology.     

Virulence and site of infection of the fungus,Hirsutella thompsonii,to the honey bee ectoparasitic mite,Varroa destructor

The Varroa mite, Varroa destructor, is recognized as the most serious pest of both managed and feral Western honey bee (Apis mellifera) in the world. The mite has developed resistance to fluvalinate, an acaricide used to control it in beehives, and fluvalinate residues have been found in the beeswax, necessitating an urgent need to find alternative control measures to suppress this pest. Accordingly, we investigated the possibility of using the fungus, Hirsutella thompsonii, as a biocontrol agent of the Varroa mite. Among the 9 isolates of H. thompsonii obtained from the University of Florida and the USDA, only the 3 USDA isolates (ARSEF 257, 1947 and 3323) were infectious to the Varroa mite in laboratory tests. The mite became infected when it was allowed to walk on a sporulating H. thompsonii culture for 5 min. Scanning electron micrographs revealed that the membranous arolium of the mite leg sucker is the focus of infection where the fungal conidia adhered and germinated. The infected mites died from mycosis, with the lethal times to kill 50% (LT(50)s) dependent on the fungal isolates. Thus, the LT(50)s were 52.7, 77.2, and 96.7h for isolates 3323, 257, and 1947, respectively. Passage of H. thompsonii through Varroa mite three times significantly reduced the LT(50)s of isolates 257 and 1947 (P<0.05) but not the LT(50) of isolate 3323.The fungus did not infect the honey bee in larval, prepupal, pupal, and adult stages under our laboratory rearing conditions. Our encouraging results suggest that some isolates of H. thompsonii have the potential to be developed as a biocontrol agent for V. destructor. However, fungal infectivity against the mites under beehive conditions needs to be studied before any conclusion can be made.     

The systematic status of some land snails mistakenly assigned to the New Zealand fauna

Abstract

Helix regularis, Laoma (Phrixgnathus) lucida var. elevata, L. elegans, and Lagochilus studeri, described from “New Zealand” or “Whangarei”, have proved to be referable to extralimital species, and should therefore be deleted from the New Zealand fauna. Helix regularis Pfeiffer, 1855 is shown to be a species of Coneuplecta Moellendorff, 1893 (Helicarionidae) closely related to or synonymous with Nanina microconus Mousson, 1865, for which a neotype is selected. Laoma (Phrixgnathus) lucida var. elevata Suter, 1896 is based on juveniles of Euconulus fulvus (Müller, 1774); Laoma elegans Suter, 1896 is Strobilops labyrinthica (Say, 1817); and Lagochilus studeri Suter, 1896 is Amnicola limosa (Say, 1817). The last three are all common in eastern North America.     

Ultrastructure of spermatozoa in Orthalicidae (Mollusca,Gastropoda, Stylommatophora) and its systematic implications

Sperm morphology of orthalicid gastropods Clessinia pagoda, Spixia tucumanensis, Plagiodontes daedaleus (Odontostominae) and Drymaeus hygrohylaeus, D. poecilus, Bostryx stelzneri (Bulimulinae) are examined and described for the first time using transmission electron microscopy. Spermatozoa show the general characteristic of Pulmonata: an acrosomal vesicle, sperm nucleus helical, mitochondrial derivative forming a continuous sheath with paracrystalline material and coarse fibers associated with axonemal doublets. Features in the acrosomal complex and shape of the nucleus distinguish orthalicid sperms from other stylommatophoran. The acrosomal pedestal is traversed by fine striations in all species examined except in S. tucumanensis. The structure and thickness of the perinuclear sheath with a single or double layer of electron-dense material ensheathing the nuclear apex is characteristic of the group. The presence of a subnuclear ring in Drymaeus, Bostryx and Clessinia species is also reported. A data matrix of eleven species per 34 characters (16 sperm plus 18 anatomical and shell characters) from orthalicids plus other stylommatophoran and systellommatophoran representative species was constructed. Three cladistic analyses (sperm-based, anatomical-based and a combined sperm + anatomical-based) were performed to test the phylogenetic potential of sperm ultrastructure in orthalicid systematics and understand how sperm characters affect the topology and resolution of the obtained trees. Stylommatophora resulted in a monophyletic clade in the sperm-based and in the combined-character analysis. Orthalicidae is monophyletic only in the combined-character cladogram. Within Orthalicidae, Odontostominae is recovered as a monophyletic clade in all analyses, while Bulimulinae is paraphyletic in all trees except in the combined phylogeny. The present study and cladistic analyses performed support the hypothesis that characters on sperm ultrastructure are informative for stylommatophoran systematic and phylogenetic approaches, providing synapomorphies at familiar, subfamiliar and generic level.     

An annotated catalogue of the types of Chrysididae (Hymenoptera) at the Swedish Museum of Natural History,Stockholm, with brief historical notes

A critical and annotated catalogue of 72 types of Chrysididae (Hymenoptera) belonging to 53 species and subspecies housed in the Swedish Museum of Natural History is given. The lectotypes of Chrysis diversa Dahlbom, 1845, Chrysis soror Dahlbom, 1854, Chrysura sulcata Dahlbom, 1845 and Holopyga amoenula Dahlbom, 1845 are designated. The previous lectotype of Chrysis diversa Dahlbom, 1845 is set aside. Five new synonymies are proposed: Chrysis elegans var. smaragdula Trautmann, 1926 (currently Chrysis elegans ssp. interrogata Linsenmaier, 1959 repl. name for smaragdula Trautmann, nec Fabricius, 1775), syn. n. of Chrysis confluens (Dahlbom, 1845); Chrysis eximia Mocsáry, 1889, syn. n. of Chrysis poecila Mocsáry, 1889; Chrysis pyrrhina Dahlbom, 1845, syn. n. of Chrysis erythromelas Dahlbom, 1845; Chrysis separata Trautmann, 1926, syn. n. of Chrysis lateralis Dahlbom, 1845; Chrysis sicula Abeille de Perrin, 1877, syn. n. of Chrysis erythromelas Dahlbom, 1845. Chrysis serena Radoszkowski, 1891 is the first available name for Chrysis pyrrhina sensu auctorum. Chrysis erythromelas Dahlbom, 1845 is revaluated as valid species. The neotype of Chrysis inaequalis Dahlbom, 1845 is designated in the Linsenmaier collection (NMLS). Illustrations of 34 types are given.