Systematics and phylogeny of Vasseuromys (Mammalia,Rodentia, Gliridae) with a description of a new species from the late Miocene of eastern Europe

Vasseuromys is a species‐rich genus of small‐ to medium‐sized glirids spanning the latest Oligocene to late Miocene of Europe and western Asia. Despite extensive discoveries over the past 50 years, little phylogenetic work has been done on Vasseuromys. This study presents the first phylogenetic analysis of the genus that includes all the described species and a new taxon Vasseuromys tectus sp. nov. from the late Miocene of eastern Europe, providing the first insights into the evolutionary relationships within the clade. Results suggest that the genus is clearly paraphyletic. Two strongly supported genus‐level clades are recognized within ‘Vasseuromys’: a restricted Vasseuromys clade (containing the three species, V. pannonicus, V. rugosus and V. tectus) and the Glirulus clade that includes ‘Vasseuromys’ duplex. The remaining ‘Vasseuromys’ species are found to constitute a set of paraphyletic taxa, with the polyphyletic ‘Ramys’ nested within it. The genus Gliruloides is synonymized with Glirulus. Vasseuromys tectus sp. nov. is the most derived member of the genus in having a greater number of cheek teeth ridges including constantly present anterotrope, centrotrope, second prototrope on M1–2, third metatrope on M2, two to three posterotropids on p4 and strong ectolophids on lower molars. The results of the study confirm a European origin for Vasseuromys while suggesting that the late Miocene species of the genus dispersed from the east in the early Turolian.     

Talking Pleasures,Writing Dialects. Outlining Research on Schmecka

This text is written in English so that it may reach an international academic audience. However, if all academic research comes to be outlined in English we are to lose a lot. Here, we argue this by presenting the case of schmecka. Drawing on fieldwork done in the Austrian region of Vorarlberg, we suggest that the word schmecka differs from the factual ‘flavour perception’ investigated in physiology; from the culturally informed ‘sensory experiences’ explored by anthropologists and even from the sociological ‘tasting in practice’. For one, schmecka is shared between modest good food and assembled eaters; two, it draws together the English ‘tasting’ and ‘smelling’; and three, it has positive overtones. This means that using schmecka is not just judicious when writing about ‘others’, here the people of Vorarlberg. It also, more interestingly, allows ‘us’ to write in another way: one that foregrounds valuing rather than facting.     

The odontode explosion: The origin of tooth‐like structures in vertebrates

Essentially we show recent data to shed new light on the thorny controversy of how teeth arose in evolution. Essentially we show (a) how teeth can form equally from any epithelium, be it endoderm, ectoderm or a combination of the two and (b) that the gene expression programs of oral versus pharyngeal teeth are remarkably similar. Classic theories suggest that (i) skin denticles evolved first and odontode‐inductive surface ectoderm merged inside the oral cavity to form teeth (the ‘outside‐in’ hypothesis) or that (ii) patterned odontodes evolved first from endoderm deep inside the pharyngeal cavity (the ‘inside‐out’ hypothesis). We propose a new perspective that views odontodes as structures sharing a deep molecular homology, united by sets of co‐expressed genes defining a competent thickened epithelium and a collaborative neural crest‐derived ectomesenchyme. Simply put, odontodes develop ‘inside and out’, wherever and whenever these co‐expressed gene sets signal to one another. Our perspective complements the classic theories and highlights an agenda for specific experimental manipulations in model and non‐model organisms.     

A new species of the sclerorhynchid sawfish Borodinopristis from the Campanian (Upper Cretaceous) of North Carolina,USA

Elasmobranch fossils recovered from Campanian marine exposures at Elizabethtown, Bladen County, NC, include species from at least seven genera of sharks and four genera of batoids. Of particular interest is the recovery of multiple isolated rostral spines from a new sclerorhynchid sawfish, Borodinopristis shannoni, sp. nov. Species of Borodinopristis are known from oral teeth and/or rostral spines (‘rostral teeth’ for some authors). In species known from the latter, the spines differ from those of other sclerorhynchids by the presence of one or more ‘collared’ barbs on the posterior margin of the crown. Unlike the previously described B. schwimmeri, the rostral spines of the new species have well-developed hooked barbs with collars (curved, connected crests) extending asymmetrically onto the dorsal and ventral surfaces of the spine, as well as small, rudimentary barbs. Also unlike B. schwimmeri, the anterior margin of the spine is strongly convex and there is no enamelled collar at the base of the crown. The new species also occurs in the Upper Cretaceous of the Gulf Coastal Plain.     

Characterization of the orchid bee Euglossa viridissima (Apidae: Euglossini) and a novel cryptic sibling species,by morphological,chemical, and genetic characters

In orchid bees, males signal their availability as mates by fanning ‘perfumes’, i.e. blends of volatiles that are collected from environmental sources and stored in hind leg pouches. The chemical composition of such perfumes in males with either two or three mandibular teeth has previously led to the discovery of two sympatric, cryptic lineages within Euglossa viridissima Friese on the Yucatan peninsula, Mexico. Here, we combine chemical, morphological, and genetic data for an integrated characterization of the two lineages. The lectotype of E. viridissima Friese in the Museum of Natural History in Vienna has two mandibular teeth, and the species name viridissima must thus be assigned to the predominantly bidentate lineage, whereas the completely tridentate lineage is described as a novel species, Euglossa dilemma sp. nov. Bembé & Eltz. Chemical profiling and microsatellite genotyping revealed that E. viridissima males can occasionally (～10% of individuals) express a third mandibular tooth, but this tooth is not positioned centrally on the mandible as in E. dilemma, but is displaced towards the tip. Thus, males of the two lineages can be unambiguously diagnosed by mandibular characters alone. Based on 889 bp of CO1 sequence data, we confirm that E. viridissima and E. dilemma constitute a monophyletic group within the genus Euglossa. However, CO1 alone failed to separate these two lineages due to the lack of parsimony‐informative sites. Both species occur in broad sympatry across Central America, but the orchid bees recently introduced to Florida have three mandibular teeth in males, i.e. belong to E. dilemma. © 2011 The Linnean Society of London, Zoological Journal of the Linnean Society, 2011, 163 , 1064–1076.     

The phylogenetic relationships of sauropod dinosaurs

A data-matrix of 205 osteological characters for 26 sauropod taxa is subjected to cladistic analysis. Two most parsimonious trees are produced, differing only in the relationships between Euhelopus, Omeisaurus and Mamenchisaurus. The monophyly of the Euhelopodidae (including Shunosaurus) is supported by seven synapomorphies. The Cetiosauridae (Patagosaurus, Cetiosaurus and Haplocanthosaurus) is paraphyletic with respect to the Neosauropoda. The latter clade divides into two major radiations–the ‘Brachiosauria’ (Camarasaurus, brachiosaurids and titanosauroids), and the Diplodocoidea (nemegtosaurids, dicraeosaurids, diplodocids and Rebbachisaurus). Further evidence for the inclusion of Opisthocoelwaudia in the Titanosauroidea is presented. Phuwiangosaurus, a problematic sauropod from Thailand, may represent one of the most plesiomorphic titanosauroids. ‘Peg’-like teeth have evolved at least twice within the Sauropoda. The postspinal lamina, on the neural spines of middle and caudal dorsal vertebrae, represents a neomorph rather than a fusion of pre-existing structures. Forked chevrons may have evolved convergently in the Euhelopodidae and the diplodocid-dicraeosaurid clade, or they may have been acquired early in sauropod evolution and subsequently lost in the ‘Brachiosauria’. The strengths and weaknesses of the data-matrix and tree topologies are explored using bootstrapping, decay analysis and randomization tests. Several nodes are only poorly supported, but this seems to reflect the large proportion of missing data in the matrix (～46%), rather than an abnormally high level of homoplasy. The results of the randomization tests indicate that the ‘data-matrix’ probably contains a strong phylogenetic ‘signal’. The relationships of some forms, such as Haplocanthosaurus, are influenced by the inclusion or exclusion of certain taxa with unusual combinations of character states. Such a result suggests that there are dangers inherent in the view that ‘higher’ level sauropod phylogeny can be accurately reconstructed using only a small number of well-known taxa.     

CYTOGENETICS OF RUBUS. II. CYTOLOGICAL STUDIES OF THE VARIETIES ‘YOUNG,’ ‘BOYSEN,’ AND RELATED FORMS

Thompson , Maxine M. (U. California, Davis.) Cytogenetics of Rubus. II. Cytological studies of the varieties ‘Young,’ ‘Boysen’ and related forms. Amer. Jour. Bot. 48(8): 667–673. Illus. 1961.—Chromosome numbers are given for the trailing blackberry varieties, ‘Young’ (2n = 49), ‘Boysen’ (2n = 49), ‘Nectar’ (2n = 49) and for related forms which include the parents of ‘Young,’ ‘Phenomenal’ (2n = 42) and ‘Mayes’ (2n = 56), and 3 cytologically resynthesized ‘Young’ plants (2n = 49) as a basis for interpreting the postulated origin of ‘Young.’ Cytological evidence substantiated the conclusion that ‘Young’ is a hybrid between ‘Phenomenal’ and ‘Mayes.’ Contributions to the understanding of genomic relationships in Rubus are offered from detailed analyses of meiosis in ‘Phenomenal,’ ‘Mayes,’ ‘Young,’ and ‘Boysen.’ ‘Phenomenal’ and ‘Mayes’ both had a very regular meiosis. ‘Young,’ as well as ‘Boysen,’ showed a greater degree of chromosome association than either parent of ‘Young.’ Meiotic behavior in ‘Boysen’ presented a close parallel to that of ‘Young’ which, correlated with morphological similarities and the same 2n chromosome number, suggests a similar origin. The mode of reproduction in ‘Young’ and ‘Boysen’ was found to be sexual on the basis of morphological variation in the open-pollinated (selfed) progeny, the varying aneuploid somatic chromosome numbers in these progeny (2n = 32–54) and aneuploid chromosome numbers in hybrids having either variety as one parent. The productiveness of ‘Young’ and ‘Boysen’ in commercial plantings and their successful utilization in breeding programs indicate a high fertility regardless of their having an odd multiple of the basic number. It is concluded that the production of balanced euploid gametes is not necessarily a criterion of fertility, at least not at this high level of ploidy.     

The turtles of the Purbeck Limestone Group of Dorset, southern England

The turtles from the Purbeck Limestone are revised and it is concluded that there are four shell‐based cryptodire species present, namely Pleurosternon bullockii, ‘Glyptops’typocardium comb. nov., Helochelydra anglica comb. nov.,Hylaeochelys latiscutata. There is also one skull‐based species, Dorsetochelys delairi, which may prove to be the skull of ‘Glyptops’, Hylaeochelys or an unknown shell‐type. All other taxa are junior synonyms except ‘Chelone’obovata Owen, 1842 and Tretosternon punctatum Owen, 1842 which are nomina dubia, the material being unfigured and either lost or incorrectly associated. Other taxonomic conclusions are that (1) because Tretosternon is a nomen dubium, the next senior name for this Purbeck–Wealden genus is Helochelydra Nopcsa, 1928; (2) ‘Pleurosternon’typocardium and ‘Glyptops’ruetimeyeri are synonymous, the senior combination being ‘Glyptops’typocardium; (3) the Purbeck ‘Tretosternon’ material is combined with the holotype and only specimen of Platychelys? anglica as Helochelydra anglica comb. nov.; (4) Hylaeochelys emarginata and H. sollasi are junior synonyms of Hylaeochelys latiscutata; (5) one of Owen's ‘lost’ syntypes of ‘Tretosternon punctatum’ has been recognised and is a plastron of Hylaeochelys latiscutata.     

Eocene Pachynolophinae (Perissodactyla,Palaeotheriidae) from China,and their palaeobiogeographical implications

The Eocene perissodactyl family Palaeotheriidae has traditionally been considered to be a nearly endemic European group within Equoidea, but a few palaeotheres have been reported from Asia. Here, I reanalyse a maxilla containing M1–3 from the Lunan Basin, Yunnan Province, China. This element was initially assigned to a new tapiromorph species, Lophialetes yunnanensis, but is here placed in a new genus Lophiohippus within Pachynolophinae based mainly on the absence of mesostyles, the strongly oblique metalophs, the strong development of lophodonty, parastyles overlapping metastyles of preceding teeth and situated mesial to the paracone, and the fact that M3 is longer than wide and has a large and buccally deflected metastyle. Lophiohippus differs from European Anchilophus and Paranchilophus in that the parastyles are situated mesial or even slightly lingual, rather than mesiobuccal, to the paracones, and M3 is markedly relatively larger than M1. I further reanalyse Qianohippus magicus from the Shinao Basin of Guizhou Province, China, in which the complete dentition is known. Qianohippus is characterized by a molariform P2 and non‐molariform P3–4; a relatively high degree of lophodonty; the absence of mesostyles; an angular bending in the protoloph on P3‐M3 and the metaloph on M1–3 at the paraconule and metaconule, respectively; and weakly developed ‘metastylid’ on the lower cheek teeth. A cladistic analysis supports a close relationship between Lophiohippus yunnanensis and Paranchilophus, and suggests that Qianohippus is closely related to some derived pachynolophs. The appearance of the pachynolophins Lophiohippus and Qianohippus in China supports the existence of a biogeographical connection between Europe and Asia in the Middle‐Late Eocene, and the dispersal route was probably along the Tethyan microcontinents in the south.     

New information on cranial and dental features of the Triassic archosauriform reptile Euparkeria capensis

The course of the nasolacrimal duct, interdental plate morphology, and most details of tooth and denticle morphology have not previously been described in non–archosauriform reptilkes. Here I describe these details in the Triassic archosauriform Euparkeria capensis. The nasolacrimal canal opens orbitally via a pair of foramina between the lacrimal and prefrontal. The canal arches over the antorbital fenestra, as in archosaurs. The term ‘interdental unit’ is introduced for the unit composed of an interdental septum and its accompanying interdental plate. There is no demarcation between interdental plate and septum in E. capensis. The interdental units are heavily pitted on exposed surfaces. Like teeth, they are implanted in the dental groove and are separate from the surrounding bone and from each other. They are well positioned to serve as spacers between teeth, and to resist sagittal forces on teeth during prey capture. The teeth of E. capensis are labiolingually compressed, except for the nearly conical premaxillary teeth and mesialmost dentary tooth. Lateral teeth are serrated on mesial and distal keels. The denticles are low, rounded, and separated by grooves, and are slightly larger on the distal keel. Tooth morphology suggests carnivorous habits for Euparkeria.     

A new agenda for blue agave landraces: food,energy and tequila

Agave tequilana Weber (Rigidae, Agavaceae), blue agave, is a native Mexican plant that has been associated with tequila since the 17th century. The tequila industry has matured over time and now has a geographical indication (Denominación de Origen; DOT). The tequila industry has grown substantially in the last 15 years (19.82% annual increase between 1995 and 2008), resulting in an increase in agave production and associated residue (leaves) and bagasse that can be used for second‐generation biofuels. At a time when the biofuel industry is undergoing unprecedented changes, with diversified demand and predictions of increased competitiveness, this paper presents a review of agave landraces that have been affected by tequila production but may be beneficial for a biofuel industry. Conventional botanical studies have revealed domestication syndromes in races related to blue agave (‘azul listado’, ‘sigüín’ and ‘pata de mula’) specifically for production of fructans in the plant core as would be expected in mezcal agaves (including those used for tequila). Some others, such as the ‘moraleño’ and ‘bermejo’ cultivars (Sisalanae) show domestication syndrome only in the fibers, while others, such as ‘chato,’A. americana L. subtilis (Americanae) show domestication syndrome in fructans and fibers and ‘zopilote,’A. rhodacantha (Rigidae) a relatively low domestication syndrome. No specimens of the cultivars named ‘mano larga’, ‘mano anchaque’ and ‘cucharo’ were found in the Tequila Region of Origin (Western Mexico). The genetic resources from landraces ignored by the tequila industry may be valuable for both ethanol production and conservation.     

Neoselachian sharks from the Callovian–Oxfordian (Jurassic) of Ogrodzieniec,Zawiercie Region,southern Poland

Abstract: Callovian and Oxfordian strata in Ogrodzieniec near Zawiercie, southern Poland, have yielded two shark tooth assemblages that collectively include 14 neoselachian taxa. A previously unrecognised member of the Orectolobiformes, Akaimia altucuspis gen. et sp. nov., is described and characterised by a dentition remarkably similar to modern wobbegong sharks (Orectolobidae) by convergence. The assemblages also include the first anterior teeth ever found of the palaeospinacid ‘Synechodus’prorogatus Kriwet, in addition to teeth from two other palaeospinacids, Sphenodus spp., four different orectolobiforms, two hexanchids and Protospinax spp. These shark tooth assemblages contribute to the poorly known Callovian and Oxfordian neoselachian faunas and indicate that the diversity was higher than previously appreciated, particularly within the Orectolobiformes.     

Turiasauria-like teeth from the Upper Jurassic of the Lusitanian Basin,Portugal

Turiasauria is a clade of eusauropods with a wide stratigraphic range that could extend from the Bathonian to the lower Aptian including Turiasaurus, Losillasaurus, Zby and putatively, Galveosaurus, Atlasaurus and isolated remains from Middle Jurassic-to-Lower Cretaceous. Some are characterised by the presence of heart-shaped teeth. Several tooth occurrences from the Portuguese Upper Jurassic with this type of morphology (SI: 1.1–1.8) are reported and discussed. If this morphology is regarded as synapomorphic of Turiasauria, the teeth will be tentatively related to this clade. From a sample of 43 teeth, three main morphotypes are described. Three hypotheses might explain the morphological variation: (1) the range of tooth morphologies indicates variation in the jaw, (2) the range of tooth morphologies indicates taxonomic variation or (3) a combination of both. The general wear pattern in morphotypes I and II starts with a distal facet, then the appearance of mesial/apical facet and finally a ‘V’-shaped facet. In morphotype III, the wear begins with a mesial facet. The variability observed for Portuguese Upper Jurassic specimens is congruent with the morphological variability along the tooth row shown by other sauropods with spatulate/spoon-shaped teeth and it is considered the most parsimonious hypothesis to explain it.     

Male-like females, mimicry and transvestism in butterflies (Lepidoptera: Papilionidae)

Abstract. When a butterfly species has a polymorphic female, with one of the forms closely resembling the male, it is customary to suppose that this form is ancestral, and that the ‘odd’ forms have arisen later. R. I. Vane-Wright, on the other hand, has suggested that in some species the male-like form may be a ‘transvestite’ female, the ancestral form of the female having been strikingly unlike the male. As later-derived forms are usually, but not always, genetically dominant to ancestral forms, we can make some choice between these hypotheses by discovering the dominance relations of the male-like and the ‘odd’ forms of the female. In the mimetic Papilio aegeus the male-like form is shown to be recessive to the ‘odd’ (mimetic) form, as has essentially been the case in all other butterflies so far investigated. Papilio phorcas is now shown to be the exception: the ‘odd’ (non-mimetic) form is recessive to the male-like form. We conclude that usually the male-like form is ancestral, but that P.phorcas may be an authentic example of ‘transvestism’, or the ‘transfer’ of male epigamic colour to the female of the species. The yellow, male-like pattern of the mimetic Papilio dardanus may be dominant or recessive to the mimetic forms according to the genetic background: largely recessive in Madagascar, and southern and western Africa, dominant to most forms in Ethiopia, and probably dominant to one mimetic form but recessive to the others in Kenya. All female dardanus patterns, both mimetic and yellow, are strongly dominant to both female phorcas patterns in P. dardanus × P. phorcas hybrids (P. ‘nandina’). The simplest explanation of this situation is that the male-like pattern of dardanus is ancestral, and that dominance has become locally reversed in Ethiopia. The dominance relations, and the sex- or autosomal-linkage of two forms can be determined without pedigree-breeding, simply by observing a few offspring each from a large number of wild-caught females.     

Male aggression,limited female choice and the ontogeny of mating behaviour in the flesh fly Sarcophaga crassipalpis

Previous work has shown that male flesh flies (Sarcophaga crassipalpis Macquart) exhibit an ontogeny of behaviour from eclosion through sexual maturity that includes extensive changes in the expression of aggressive, non‐aggressive interactive and non‐interactive behaviours. To determine how the presence of a female flesh fly influences the manifestation of these behaviours, male flesh flies of different ages post‐eclosion are paired with same‐age females and their behaviours are monitored in a simple arena during a 50‐min observation period. All flies are socially isolated until pairing. Although the levels of expression of aggressive and non‐aggressive interactive behaviours are depressed relative to previous findings in male‐opponent pairs, the ontogeny of aggression still occurs as indicated by a significant increase, with age, in the agonistic behaviour ‘hold’. Similar to male‐opponent pairs and individual males, the performance by males of the non‐interactive behaviours ‘walking’ and ‘standing’ diminishes, whereas ‘upside‐down’ increases with age. By contrast, ‘grooming’ shows a significant age‐related decline. No courtship behaviours are observed in the males, although the aggressive behaviour ‘hold’ is a significant transition to mating. Females show no obvious courtship or rejection behaviours, although the significant increase in ‘upside‐down’ with age could possibly be a behavioural gateway to mating. The results of this study indicate that extensive age‐related changes encompassing the entire behavioural repertoire are intrinsic to male flesh flies and persist under a variety of different social contexts.     

Towards a phylogeny and evolution of Acochlidia (Mollusca: Gastropoda: Opisthobranchia)

The Acochlidia are unique among opisthobranch gastropods in combining extremely high morphological and ecological diversity with modest species diversity. The phylogeny of acochlidians has never been addressed by cladistic means, as their evolution has remained unknown. This study gives a first overview on more than 150 biological and morphological characters that are potentially useful for phylogenetic analysis. Based on 107 characters, a parsimony analysis (PAUP) was performed for all 27 valid acochlidian species together with 11 (plus two) outgroup taxa. The resulting strict consensus tree shows a moderate overall resolution, with at least some bootstrap support for most resolved nodes. The Acochlidia are clearly monophyletic, and originate from an unresolved basal opisthobranch level. The Acochlidia split into the Hedylopsacea (Tantulum (Hedylopsis (Pseudunela (Strubellia (‘Acochlidium’, ‘Palliohedyle’))))) and Microhedylacea (Asperspina (Pontohedyle, ‘Parhedyle’, ‘Microhedyle’, (Ganitus, Paraganitus))). The formerly enigmatic Ganitidae, resembling sacoglossan opisthobranchs by having dagger‐like rachidian radular teeth, are likely to be highly derived microhedylids. The paraphyly of some of the traditionally recognized family level taxa induced a preliminary reclassification. From the phylogenetic hypothesis obtained, we conclude that the acochlidian ancestor was marine mesopsammic. The colonization of limnic systems occurred twice, independently: first in the Caribbean (with the development of the small interstitial Tantulum elegans), and second in the Indo‐Pacific, with a radiation of large‐sized benthic acochlidian species. The evolution of extraordinary reproductive features, such as hypodermic impregnation by a complex copulative aparatus in hedylopsaceans, cutaneous insemination via spermatophores in microhedylaceans, and gonochorism in Microhedylidae s.l. (including Ganitidae), is discussed. © 2010 The Linnean Society of London, Zoological Journal of the Linnean Society, 2010, 158 , 124–154.     

Mouthpart evolution in adults of the basal, 'symphytan', hymenopteran lineages

We review feeding biology and mouthpart structure generally among adults of the basal hymenopteran, or ‘symphytan’, lineages (sawflies, woodwasps, horntails and their relatives). These insects feed on a wide range of materials: floral and extrafloral nectar, pollen, plant (floral and leaf) tissues, plant (angiosperm) sap, the juice of ripe fruit, die spermatial fluid of rust fungi, sternorrhynchan bug honeydew, and insect tissues. Adults show feeding‐related mouthpart specialization either for consuming pollen (the Xyelidae only) or for consuming ‘concealed’ floral nectar (several families). Seven functional types of elongated proboscis or ‘concealed‐nectar extraction apparatus (GNEA)’ have previously been recognized among Hymenoptera. We identify an additional type, which appears to be unique among Hy‐menoptera and has probably evolved direcdy from unspecialized mouthparts (labiomaxillary complex). In total, three types of CNEA are known to occur in ‘Symphyta’. Type 1 occurs in Pamphiliidae, Megalodontesidae, Argidae, Pergidae, Tenthredinidae, Cimbicidae and Cephidae. Type 5 occurs in Pergidae (in two unidentified species of Euryinae). Type 8 occurs in Tenthredinidae (in the genus Nipponorhynchus Takeuchi). CNEA of some type or other has arisen at least twice within the family Tenthredinidae and at least twice widiin die pergid subfamily Euryinae. Evolutionary parallelism in CNEA structure has occurred between the basal, ‘symphytan’, hymenopteran lineages and die Apocrita, a phenomenon hitherto not mentioned in the literature. Within the ‘Symphyta’, possession of Type 1 CNEA appears to be a ground plan feature of each of the following taxa: the pergid genus Eurys Newman, the megalodontesid genus Megalodontes Latreille (the only extant representative of the Megalodontesidae) and the tenthredinid genus Cuneala Zirngiebl, while possession of Type 8 appears to be a ground plan feature of die tenthredinid genus Mpponorhynchus Takeuchi. However, in general among ‘Symphyta’, possession of CNEA is characteristic of only small and taxonomically subordinate groups, suggesting that CNEA has evolved independendy many times within the basal hymenopteran lineages rather than being inherited from a common ancestor early in the evolutionary history of the Hymenoptera. In other words, ecological expediency radier than phylogenetic history mainly accounts for its distribution pattern within the basal lineages. The results of a morphological survey of ‘Symphyta’ indicate that the habit of exploiting ‘concealed nectar’, by means of CNEA, is fairly     

Chronological implications of the nothrotheriid ‘Xyophorus’ (Mammalia,Xenarthra) from the Collón Curá Formation (Miocene of Patagonia,Argentina)

The specimen described herein and assigned to ‘Xyophorus’ sp. (Mammalia, Xenarthra, Tardigrada) was collected in the locality Cerro Zeballos, northwestern Chubut Province, Argentina. The fossiliferous sediments bearing the specimen are correlated with Collón Curá Formation. The specimen has the features described for other members of ‘Xyophorus’ (e.g. shape and size of the molariforms, relationship between diastema length, m1 and m2 length) and has a Diastema Length/Tooth Row Length index (DL/TRL index) of ca. 14, between that of ‘X.’ villarroeli (12.07) from the Mauri Formation, Bolivia (ca. 10.3 Ma) and that of ‘X.’ bondesioi (16.45) from Arroyo Chasicó Formation, Argentina (ca. 10–8.7 Ma). The relationship between DL/TRL index and age of the bearing sediments, would suggest a Tortonian age (late Miocene) for the deposits of Collón Curá Formation at Cerro Zeballos, which results in a ‘younger age’ compared to the middle Miocene age traditionally accepted for the Collón Curá Formation bearing the Colloncuran fauna sensu stricto. Although no absolute ages for Cerro Zeballos are available yet, the geographic proximity of Cerro Zeballos to Cushamen River (with levels dated at ca. 11.2 Ma) supports the tentative Tortonian age indicated by the presence of ‘Xyophorus’ sp.     

Craniological differentiation between European wildcats (Felis silvestris silvestris), African wildcats (F. s. lybica) and Asian wildcats (F. s. ornata): implications for their evolution and conservation

Intraspecific diversification of the wildcat (Felis silvestris), including the European wildcat (F. s. silvestris), the Asian wildcat (F. s. ornata) and the African wildcat (F. s. lybica), was examined based on 39 cranial morphology variables. The samples of free‐ranging cats originated from Britain, Europe, Central Asia and southern Africa, consisting of both nominal wildcat specimens (referred to henceforth as ‘wildcats’) and nominal non‐wildcat specimens (‘non‐wildcats’) based on museum labels. The skull morphology of ‘wildcats’ from Britain and Europe is clearly different from that of ‘wildcats’ of Central Asia and southern Africa. The latter are characterized especially by their proportionately larger cheek teeth. On the basis of principal component, discriminant function and canonical variate analyses, the skull morphology of British ‘non‐wildcats’ is less distinct than is that of British ‘wildcats’ from the skull morphologies of ‘wildcats’ of Central Asia and southern Africa. On the other hand, the skull morphology of southern African ‘non‐wildcats’ is as distinct from those of ‘wildcats’ of Britain and Europe as is that of southern African ‘wildcats’. We suggest that the evolution of the modern wildcat probably consisted of at least three different distribution expansions punctuated by two differentiation events: the exodus from Europe during the late Pleistocene, coinciding with the emergence of the steppe wildcat lineage (phenotype of Asian–African wildcat), followed by its rapid range expansion in the Old World. The second differentiation event was the emergence of the domestic cat followed by its subsequent colonization of the entire world with human assistance. Considering the recent evolutionary history of, and morphological divergence in, the wildcat, preventing hybridization between the European wildcat and the domestic cat is a high conservation priority. © 2004 The Linnean Society of London, Biological Journal of the Linnean Society, 2004, 83 , 47–63.