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).     

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 Orthalicoidea (Mollusca, Gastropoda) in the Royal Belgian Institute of Sciences, Brussels, with descriptions of two new species

The type status is described of 57 taxa from the superfamily Orthalicoidea in the collection of the Brussels museum. Two new species are described: Stenostylus perturbatussp. n., and Suniellus adrianisp. n. New lectotypes are designated for Bulimulus (Naesiotus) amastroides Ancey, 1887; Bulimulus blanfordianus Ancey, 1903; Bulimulus montivagus chacoensis Ancey, 1897; Bulimus coloratus Nyst, 1845; Plecochilus dalmasi Dautzenberg, 1900; Placostylus porphyrostomus elata Dautzenberg, 1923; Bulimulus ephippium Ancey, 1904; Bulimus fulminans Nyst, 1843; Bulimus funckii Nyst, 1843; Orphnus thompsoni lutea Cousin, 1887; Bulimus melanocheilus Nyst, 1845; Orphnus thompsoni nigricans Cousin, 1887; Orphnus thompsoni olivacea Cousin, 1887; Bulimulus pollonerae Ancey, 1897; Orphnus thompsoni zebra Cousin, 1887. New combinations are: Bostryx borellii (Ancey, 1897); Bostryx carandaitiensis (Preston, 1907); Protoglyptus mazei (Crosse, 1874); Kuschelenia (Vermiculatus) sanborni (Haas, 1947). New synonymies are established for the following nominal taxa: Orphnus thompsoni var. lutea Cousin, 1887 = Kara thompsonii (Pfeiffer, 1845); Orphnus thompsoni var. nigricans Cousin, 1887 = Kara thompsonii (Pfeiffer, 1845); Thaumastus nystianus var. nigricans Cousin, 1887 = Drymaeus (Drymaeus) nystianus (Pfeiffer, 1853); Orphnus thompsoni var. olivacea Cousin, 1887 = Kara thompsonii (Pfeiffer, 1845); Orphnus thompsoni var. zebra Cousin, 1887 = Kara thompsonii (Pfeiffer, 1845).     

Annotated type catalogue of the Orthalicoidea (Mollusca,Gastropoda) in the Museum für Naturkunde,Berlin

The type status is described of 96 taxa classified within the superfamily Orthalicoidea and present in the Mollusca collection of the Museum für Naturkunde der Humboldt-Universität zu Berlin. Lectotypes are designated for the following taxa: Orthalicus elegans Rolle, 1895; Bulimus maranhonensis Albers, 1854; Orthalicus nobilis Rolle, 1895; Orthalichus tricinctus Martens, 1893. Orthalicus sphinx tresmariae is introduced as new name for Zebra sphinx turrita Strebel, 1909, not Zebra quagga turrita Strebel, 1909. The following synonyms are established: Zebra crosseifischeri Strebel, 1909 = Orthalicus princeps fischeri Martens, 1893; Orthalicus isabellinus Martens, 1873 = Orthalicus bensoni (Reeve, 1849); Zebra zoniferus naesiotes Strebel, 1909 = Orthalicus undatus (Bruguière, 1789); Porphyrobaphe (Myiorthalicus) dennisoni pallida Strebel, 1909 = Hemibulimus dennisoni (Reeve, 1848); Zebra delphinus pumilio Strebel, 1909 = Orthalicus delphinus (Strebel, 1909); Orthalicus (Laeorthalicus) reginaeformis Strebel, 1909 = Corona perversa (Swainson, 1821); Bulimus (Eurytus) corticosus Sowerby III, 1895 = Plekocheilus (Eurytus) stuebeli Martens, 1885. The taxon Bulimus (Eudioptus) psidii Martens, 1877 is now placed within the family Sagdidae, tentatively in the genus Platysuccinea. Appendices are included with an index to all the types of Orthalicoidea extant (including those listed by Köhler 2007) and a partial list of letters present in the correspondence archives.     

On the osteology and phylogenetic affinities of the Pseudasturidae – Lower Eocene stem-group representatives of parrots (Aves, Psittaciformes)

The osteology of the early Eocene (about 50 mya) avian taxon Pseudasturidae Mayr, 1998 is revised and its phylogenetic affinities are analysed. Members of the Pseudasturidae are known from abundant and excellently preserved skeletal material, both complete skeletons on slabs as well as isolated, three-dimensional bones. Although this taxon is thus among the best represented of all small early Tertiary birds, its systematic affinities were unknown so far. Derived osteological characters which are visible in newly recognized specimens from the Lower Eocene London Clay of England most convincingly support classification of the Pseudasturidae into the Psittaciformes (parrots). Both, in overall morphology and in terms of derived characters, the tarsometatarsus of the Pseudasturidae closely resembles that of the Eocene Quercypsittidae, which were assigned to the Psittaciformes by Mourer-Chauviré (1992 ). The Pseudasturidae are considered to be stem-group representatives of the Psittaciformes and the sister taxon of all other known psittaciform birds. The Eocene taxon lacks the specialized bill morphology of crown-group Psittaciformes of the Psittacidae. Several other osteological differences between the Pseudasturidae and the Psittacidae probably are also functionally correlated with the specialized feeding technique of the latter.  © 2002 The Linnean Society of London, Zoological Journal of the Linnean Society , 2002, 136 , 715–729.     

The Linnaean fish collection in the Linnean Society of London

Linnaeus's personal collection of fishes was part of the material purchased by J. E. Smith in 1783–1784 from Linnaeus's widow and which became the property of the Linnean Society of London in 1828. There are extant 168 dried specimens of fishes, mostly skins mounted on paper in the manner of herbarium specimens. The spirit-preserved material which belonged to Linnaeus was never sent from Sweden.
The history of the collection is recounted, and the sources of the specimens discussed. A catalogue of the collection is presented with discussion of the type status of the specimens and the sources for the typification of each taxon.     

A new stereospondyl from the German Middle Triassic, and the origin of the Metoposauridae

Recent finds of well-preserved temnospondyl skeletons from the Lower Keuper (Ladinian, Middle Triassic) in southern Germany are assigned to a new genus and species, Callistomordax kugleri . This taxon is characterized by the following autapomorphies: (1) wide unpaired frontal; (2) vomerine fangs greatly enlarged to occupy entire width of element; (3) intercentra elongated and massive, anterior face being convex; (4) humerus semilunar with enlarged deltopectoral crest; (5) cleithrum strongly curved and bow-shaped; (6) trunk extremely elongated to reach three times the length of the skull. Callistomordax shares with the Metoposauridae the pattern of dermal ornamentation, the proportion of both posterior skull table and snout, the position of the lacrimal, the morphology of the basicranial region, and the structure of the clavicle and interclavicle. Phylogenetic analysis suggests Callistomordax to be the sister taxon of the Metoposauridae, nested within a grade formed by various trematosaurian taxa. In this assemblage, Lyrocephaliscus and a clade formed by Almasaurus , Rileymillerus , Callistomordax , and the Metoposauridae are sister taxa. In all variants of the cladistic analysis, Callistomordax and the Metoposauridae form immediate sister groups. According to the present findings, neither plagiosaurids nor brachyopoids and rhytidosteids are closely related to this 'trematosaurian' monophylum, although these taxa share a range of homoplasies.  © 2008 The Linnean Society of London, Zoological Journal of the Linnean Society , 2008, 152 , 79–113.     

Genets and 'genet-like' taxa (Carnivora, Viverrinae): phylogenetic analysis, systematics and biogeographic implications

The subfamily Viverrinae is a taxon of uncertain systematic status. This study consists of cladistic analyses based on morphological characters of specimens belonging to the genera Genetta , Osbornictis , Poiana and Prionodon . Two levels of analysis are carried out, one concerning generic relationships (intergeneric analysis) and one dealing with the interrelationships of species within the genus Genetta (intrageneric analysis). In the first analysis, different outgroups were used in order to test the ingroup topology.
With regard to the intergeneric analysis, Osbornictis , Poiana and Prionodon , together with Genetta johnstoni , constitute a monophyletic group (including Nandinia ), which is the sister-group of a clade formed by the other species of genets. Thus, the genus Genetta is regarded as paraphyletic. Prionodon appears to be a derived taxon. The Poiana – Prionodon clade is well supported, especially by ultrastructural hair characters. The cladogram topology in the intrageneric analysis indicates an ecological transition from the rain forest genets to the savanna genets. This supports a rain forest origin of the genus Genetta , a conclusion which may be generalized to the entire study group. © 2002 The Linnean Society of London, Zoological Journal of the Linnean Society , 2002, 134 , 317–334.     

On the validity of the genus Ichthyobronema Gnedina et Savina, 1930 (Nematoda, Spirurida: Quimperiidae)

The author maintains Moravec's (1994) point of view about attachment of valid taxon status to the genus Ichthyobronema Gnedina et Savina, 1930 with type and single species I. hamulatum (Moulton, 1931) Moravec, 1994.     

Phenotypic and genetic differentiation of two major phylogeographical lineages of arctic grayling Thymallus arcticus in the Lena River, and surrounding Arctic drainages

Two phylogeographical lineages of arctic grayling, Thymallus arcticus , in Siberia are extensively characterized based on both molecular genetic (mtDNA control region sequences) and phenotypic (12 meristic characters) data. One lineage, occurring in the delta region of the Lena River as well as all other Arctic draining rivers sampled, corresponds to the subspecific taxon Thymallus arcticus pallasii , whose type locality is the Kolyma River. This taxon is proposed to be a postglacial colonizer of the Lena delta. The second lineage occurs throughout the rest of the Lena basin and is proposed to have survived in a glacial refugium in the middle reaches of the Lena. These lineages form reciprocally monophyletic groups based on mtDNA sequences (net divergence 3.2%), a relationship that is concordant with phenotypic data, and thus reflects distinct taxa. The upper Lena taxon is given the preliminary name of Thymallus arcticus lenensis . Phylogenetic analysis, together with previously published data from North America, reveals that mtDNA sequences from North American populations group within the diverse clade corresponding to T. a. pallasii in Siberia. Despite the relatively close genetic relationship of most North American haplotypes with those in northern Siberia, inferences of fragmentation between the continents are supported, but bidirectional movements between the two continents are seen as likely. Despite inclusion in the clade representing T. a. pallasii in Siberia, the source of the relatively divergent Nahanni refuge haplotypes in North America is not resolved. Otherwise, inferences of postglacial expansion across several thousand kilometres are well supported within North America, but only smaller-scale colonization events among drainages are supported in Siberia.  © 2006 The Linnean Society of London, Biological Journal of the Linnean Society , 2006, 88 , 511–525.     

On the identity of turmeric: the typification of Curcuma longa L. (Zingiberaceae)

Although Curcuma L. (Zingiberaceae) is a conserved name, with C. longa L. as its conserved type, the type of C. longa is still uncertain. Numerous discussions about the identity of the taxon called C. longa by Linnaeus have been followed by various attempts to rename turmeric, suggestions as how to settle the type and proposals to conserve the name from a later author in order to stabilize the situation. Unfortunately, none of the previous proposals can be upheld for reasons which are discussed in this article. A lectotype is selected from extant material examined by Linnaeus and an epitype collected near the type locality is designated here. The identity of C. longa is discussed and a colour plate of the species is included. Synonyms of C. longa and their types are discussed and notes on the variability of C. longa are provided.  © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society , 2008, 157 , 37–46.     

Introvert,mouth cone,and nervous system of Echinoderes capitatus (Kinorhyncha,Cyclorhagida) and implications for the phylogenetic relationships of Kinorhyncha

Summary The introvert, mouth cone, and nervous system of Echinoderes capitatus were examined by transmission and scanning electron microscopy. The introvert bears seven rings of primarily quincunxial sensory scalids, including type 1 and 2 spinoscalids as well as trichoscalids; the latter two types are additionally provided with glandular cells. The mouth cone bears one ring of decamerous sensory oral styles and three rings of quincunxial sensory pharyngeal styles. The intra- to basiepithelial, bilateral nervous system consists of a circumentric nerve ring in the introvert, a terminal and proximal nerve ring in the mouth cone, a ventral chain of ganglia, one in each trunk zonite, and a caudal ganglion. The introvert, the neck, and the trunk zonites are innervated from the forebrain; the mouth cone and the pharyngeal bulb are innervated from the hindbrain. The monophyly of the Kinorhyncha is based upon the following autapomorphic characters: (1) a mouth cone, (2) a neck with 16 placids, (3) a trunk with 11 zonites, (4) scalids of three types: type 1 and type 2 spinoscalids, and trichoscalids, (5) an anteriormost ring of ten type 1 spinoscalids (sensory organs divided into a basal and a terminal part), (6) a posteriormost ring of 14 trichoscalids (glandular sensory organs which are undivided), (7) rings in between the anteriormost and posteriormost are type 2 spinoscalids (glandular sensory organs divided into a basal and a terminal part), (8) a mouth cone with a terminal and a proximal nerve ring, (9) nine sensory oral styles with decamerous symmetry (the dorsal style is missing) and (10) three rings of sensory pharyngeal styles with, from anterior to posterior, ten, five, and five styles with quincunxial arrangement. The following characters are assumed to be autapomorphic for the taxon Nematoda+Gastrotricha+Kinorhyncha+Loricifera+Priapulida: (1) a basiepithelial circumentric brain and (2) a neuropileous nerve ring in a subterminal position. The following characters are assumed to be autapomorphic for the taxon Kinorhyncha+Loricifera+Priapulida: (1) a neuropileous nerve ring in a terminal position, (2) an introvert with scalids, (3) an eversible foregut and (4) tanycytes.The unpublished doctoral thesis of B. Neuhaus [1991 Zur Ultrastruktur, Postembryonalentwicklung und phylogenetischen Verwandtschaft der Kinorhyncha. PhD thesis. University of Götingen, Germany] was finished simultaneously with the completion of this study.     

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.     

Caloplaca awasthii, a new lichen species from India

The warm, dry climate in central India provides suitable conditions for the growth of many crustose lichens, including Caloplaca species. A new species, Caloplaca awasthii Joshi, Y. & Upreti, is described from this region, where it is found growing in rocky areas of Madhya Pradesh (Bedinagar Hills and Bhimbetka) and Rajasthan (Mount Abu). The new taxon belongs to the section Gasparrinia and is characterized by the presence of blastidia, but lacks apothecia and pycnidia. It is a saxicolous species and is similar to C. decipiens (Arnold) Blomb. & Fross., but differs in having blastidia instead of soredia which are present in C. decipiens. Another closely related species, C. fuerteventurae van den Boom & Etayo, belonging to the C. flavescens complex, differs from the new taxon in having numerous apothecia and citriform spores.  © 2007 The Linnean Society of London, Botanical Journal of the Linnean Society , 2007, 155 , 149–152.     

Systematics of Oreobates and the Eleutherodactylus discoidalis species group (Amphibia, Anura), based on two mitochondrial DNA genes and external morphology

We present morphological and molecular (mitochondrial DNA, mtDNA) evidence supporting the validity and monophyly of the genus Oreobates . This genus also includes members of the former Eleutherodactylus discoidalis species group plus Eleutherodactylus heterodactylus . The presence of prominent conical subarticular tubercles and prominent supernumerary tubercles associated with the axis of fingers and toes, the presence of glandular axillary pads, and the absence of vocal sacs are proposed as morphological synapomorphies. Species of this taxon form a well-supported crown clade in a phylogeny including members of the genera Craugastor and Eleutherodactylus s.l. The sister taxon to Oreobates is the Eleutherodactylus martinicensis series; Oreobates does not appear to be closely related to the Eleutherodactylus binotatus series or to members of the Eleutherodactylus dolops and Eleutherodactylus nigrovittatus species groups. The taxonomic status of all species of Oreobates is reassessed. Hylodes philippi and Hylodes verrucosus are removed from the synonymy of Oreobates quixensis . We redescribe Oreobates cruralis on the basis of the holotype and new material from Bolivia and Peru, and restrict its distribution to the humid forests of the lowlands and adjacent foothills of the Andes, from southern Peru to central Bolivia. Oreobates granulosus is rediscovered, redescribed, and resurrected, on the basis of the examination of the holotype and additional material from Peru. Phylogenetic analyses of partial 16S mtDNA are used to test the independence of lineages (species). The 14 species of Oreobates are distributed from southern Ecuador to northern Argentina. © 2008 The Linnean Society of London, Zoological Journal of the Linnean Society , 2008, 152 , 737–773.     

An extinct nestorid parrot (Aves,Psittaciformes, Nestoridae) from the Chatham Islands,New Zealand

We describe an extinct parrot from late Quaternary fossil bone deposits on the Chatham Islands, located c. 800 km east of mainland New Zealand. Mitochondrial DNA analyses and osteological characters confirm that the Chatham Islands parrot was a sister taxon to the New Zealand kaka (Nestor meridionalis Gmelin, 1788). The relatively large femur : humerus length ratio and broad pelvis of the Chatham Islands parrot indicate that it had a more terrestrial habit than the kaka. Stable dietary isotope analyses (δ ¹⁵N and δ ¹³C) of Chatham Islands parrot bones suggest that the species may have been mainly herbivorous, although further analyses are required to confirm this. The presence of Chatham Islands parrot bones in early midden deposits shows that the species persisted into the post‐settlement era, and became extinct possibly as a result of habitat loss, hunting pressure, and rat predation following initial Polynesian settlement of the islands (sometime between the 13^th and 16^th centuries AD). © 2014 The Linnean Society of London