Canid Paleoichnology: Taxonomic Review and Producers of Canipeda from the Late Pleistocene of Argentina

This contribution reviews the worldwide record of canid and canid-like (creodont and hyaenid) fossil footprints, the taxonomy of this type of footprints, and reports a new record of canid footprints from the late Pleistocene Pehuen Co site of southern Buenos Aires province, Argentina. On the basis of the comparison of proposed ichnogenera and features of modern canid and felid footprints, a set of ichnogeneric and ichnospecific taxobases are proposed. The ichnotaxonomic review includes Bestiopeda Vialov, 1965; Canipeda Panin and Avram, 1962; Felipeda Panin and Avram, 1962; Pehuencoichnum Aramayo and Manera de Bianco, 1987b Aramayo, S. A., and T. Manera de Bianco. 1987b. Hallazgo de una icnofauna continental (Pleistoceno tardío) en la localidad de Pehuén Co, Provincia de Buenos Aires, Argentina. Parte II: Carnivora, Artiodactyla y Aves. IV Congreso Latinoamericano de Paleontología Actas 1:532–47. [Google Scholar]; Creodontipus Santamaría et al. 1989–1990; Tetrastoibopus Sarjeant and Langston, 1994; and Quiritipes Sarjeant et al. 2002. A key to discriminate these ichnotaxa is also proposed and the diagnosis of Canipeda emended. The new findings of canid footprints from Pehuen Co are indistinguishable from Pehuencoichnum gracilis Aramayo and Manera de Bianco, 1987b, and this ichnospecies is synonymized under Canipeda gracilis (Vialov, 1965). An emended diagnosis for C. gracilis is proposed. The most likely producer of C. gracilis from Pehuen Co is a medium-sized fox similar to the extant representatives of Lycalopex.     

Rediscovery of the Tagragra Tracksite (Maastrichtian,Agadir, Morocco): Agadirichnus elegans Ambroggi and Lapparent 1954 is Pterosaurian Ichnotaxon

ABSTRACT

Discovered in 1954 by Ambroggi and Lapparent, the Tagragra tracksite (Maastrichtian, Agadir, Morocco) yielded tracks of theropod dinosaurs, birds and enigmatic forms tentatively attributed to Lacertilia under the name Agadirichnus elegans. The original specimens are today considered to be lost, and the status of A. elegans has been questioned, even though these footprints can retrospectively be referred to pterodactyloid pterosaur tracks. In order to discuss the status of these foot prints, the historical site has been actively sought and recently rediscovered by one of us (MdD). New material confirms the presence of pterodactyloid footprints, with two morphotypes, in two different facies, respectively associated with bird and theropod tracks. Morphotype I is tentatively conferred to Pteraichnus Stokes 1957 Stokes, W. L. 1957. Pterodactyl tracks from the Morrison Formation. Journal of Palaeontology, 31:952–4.[Web of Science ®] , [Google Scholar], which extends the stratigraphical distribution of this ichnotaxon to the Maastrichtian. Morphotype II corresponds to the original ichnospecies A. elegans Ambroggi and Lapparent 1954 Ambroggi, R., and A. F. de Lapparent 1954. Les empreintes de pas fossiles du Maestrichtien d'Agadir. Notes du Service Géologique du Maroc, 10:43–6. [Google Scholar], which is here reassessed as a valid ichnotaxon, with the designation of a neotype. Thus, A. elegans Ambroggi and Lapparent 1954 Ambroggi, R., and A. F. de Lapparent 1954. Les empreintes de pas fossiles du Maestrichtien d'Agadir. Notes du Service Géologique du Maroc, 10:43–6. [Google Scholar] is historically the first pterosaurian ichnotaxon ever described.     

Review of the genus Catomus Allard, 1876 (Coleoptera: Tenebrionidae) in Iran

Five species of the genus Catomus Allard, 1876 Allard, E. (1876): Révision des Helopines vrais de Lacordaire. L'Abeille. Journal d'Entomologie, 14, 1–80. [Google Scholar] are known from Iran. Catomus fragilis (Ménétriés, 1848) is recorded from Iran for the first time. Lectotypes of C. persicus Allard, 1876 Allard, E. (1876): Révision des Helopines vrais de Lacordaire. L'Abeille. Journal d'Entomologie, 14, 1–80. [Google Scholar] (type species of the genus) and C. semiruber Allard, 1876 Allard, E. (1876): Révision des Helopines vrais de Lacordaire. L'Abeille. Journal d'Entomologie, 14, 1–80. [Google Scholar] are designated. These species are also redescribed and figured. A key to the species of Catomus in the Iranian fauna is given.     

New Important Iguanodontid and Theropod Trackways of the Tracksite Obernkirchen in the Berriasian of NW Germany and Megatracksite Concept of Central Europe

This article examines the high-resolution track horizon stratigraphy at the outcrop Obernkirchen. Massive sandstones, products of marine sand bar and fluviatile environments are present at the tracksite. Recently two track beds were examined in the outcrop. One new track slab of the lower track bed is described exposing well-preserved quadrupedal iguanodontid tracktypes of Iguanodontipus Sarjeant, Delair, and Lockley, 1998 Sarjeant, W. A. S., Delair, J. B. and Lockley, M. G. 1998. The footprints of Iguanodon: a history and taxonomic study. Ichnos, 6: 183–202. [Taylor & Francis Online] , [Google Scholar], and bipedal theropod tracks Megalosauropus Kaever and Lapparent, 1974 Kaever, M. and Lapparent, A. F. de. 1974. Les traces des pas le Dinosaures du Jurassique des Barkhausen (Basse Saxe, Allemagne). Bulletin de la Societé Geologique Français, 16: 516–525.  [Google Scholar]. The ichnogenus Iguanodontipus is discussed and the diagnosis extended. The tracksite Obernkirchen belongs to a megatracksite of the ancient coastline of the marginal marine Hercynic Basin of the Lower Cretaceous of Europe, including the four well-known sites Obernkirchen, Bad Rehburg, Münchehagen, and Bückeburg of Northwest Germany. Three different tracktypes of huge sauropods, theropods, and ornithopods are abundant at basal Lower Cretaceous siliciclastic coastlines in different regions in Spain, Portugal, England, Germany, and Switzerland. Dinosaur tracks are also present in carbonate platform environments of northern Italy and Istria.     

Integrative taxonomy of the cave-dwelling mysids of the genus Hemimysis

The genus Hemimysis (Malacostraca: Mysida: Mysidae) encompasses near-bottom, demersal and cave-dwelling mysids living in the marine, brackish and freshwater habitats around the European coast, from the Caspian Sea to the Scandinavian Peninsula. We conducted cladistic analysis of 52 morphological characters of all nine species and three subspecies of the genus Hemimysis. We also completed a molecular analysis based on three molecular markers of Hemimysis lamornae (Couch, 1856) found in the English Channel, the Mediterranean Sea, and the Black Sea. Both analyses did not support monophyly of Hemimysis lamornae. We thus consider the former subspecies H. lamornae pontica (Czerniavsky, 1882 Chevaldonné, P., &; Lejeusne, C. (2003). Regional warming‐induced species shift in north‐west Mediterranean marine caves. Ecology Letters, 6, 371–379. doi:10.1046/j.1461-0248.2003.00439.x.[Crossref], [Web of Science ®] , [Google Scholar]) and H. lamornae mediterranea Bacescu, 1936 Bacescu, M. (1936). Hemimysis lamornae sbsp. reducta, nov. sbsp. et Hemimysis anomala dans les eaux roumaines de la Mer Noire (avec une etude comparative des forms de Hem. lamornae des autres mers: H. l. typica et H.l. mediterranea, nov. sbsp.). Annales Scientifiques de L’Universite de Jassy, 23, 331–338. [Google Scholar] as valid species. Analysis of mitochondrial cytochrome oxidase subunit I (COI) sequences of H. pontica shows no significant divergence between mysids living in the marine caves of Crimea and Bulgaria. Morphological trends in Hemimysis are discussed, H. pontica Czerniavsky, 1882 Chevaldonné, P., &; Lejeusne, C. (2003). Regional warming‐induced species shift in north‐west Mediterranean marine caves. Ecology Letters, 6, 371–379. doi:10.1046/j.1461-0248.2003.00439.x.[Crossref], [Web of Science ®] , [Google Scholar] is redescribed, and a new key to all 11 species of the genus is given.     

Small Amphibian and Reptile Footprints from the Permian Carapacha Basin,Argentina

This paper contains a taxonomic study of the Permian tetrapod ichnofauna from the Carapacha Basin. Tetrapod traces are analyzed in their environmental context and compared with similar faunas from Europe and North America. This ichnofauna is particularly relevant because of the scarcity of Permian tetrapod tracks from South America and also of Permian tetrapod fossils from Argentina. Ephemeral fluvial and shallow lacustrine deposits compose the sedimentary succession of the basin, which is represented by the Carapacha Formation. Most of the tracks have been collected from the upper member of the formation (Urre-Lauquen Member), mainly from freshwater ephemeral lake deposits as well as from playa-lake mudflats. The deposits of this member have been attributed to the early Late Permian on the basis of a Glossopteris fossil flora. Ichnotaxonomic designations of tetrapod traces are made on the basis of morphologic features that reflect the anatomy of the producer and special attention has been paid to extramorphologic deformations observed in the track assemblage. A total of four footprint ichnotaxa have been recognized, namely Batrachichnus salamandroides (Geinitz, 1861 Geinitz, H. B. 1861. Dyas oder die Zechsteinformation und das Rhotliegende—Die animalischen Überreste der Dyas, 130 ppLeipzig: Wilhelm Engelmann.  [Google Scholar]), Hyloidichnus bifurcatus Gilmore, 1927 Gilmore, C. W. 1927. Fossil footprints from the Grand Canyon: second contribution. Smithsonian Miscellaneous Collection, 80(3): 1–78.  [Google Scholar], cf. Amphisauropus isp. and cf. Varanopus isp. These track taxa are associated with two forms of vertebrate swimming traces (Characichnos isp. and type A swimming trace) and a possible fish trail. Invertebrate trace fossils include abundant arthropod locomotion traces and Scoyenia isp. The ichnofauna is composed of six tetrapod ichnocoenoses that are dominated by tiny amphibian tracks attributed to Temnospondyli (Batrachichnus and type A swimming trace) and Seymouriamorpha (Amphisauropus), and also contain the footprints of small reptiles, mostly Captorhinomorpha and possibly Pelycosauria (Hyloidichnus and Varanopus). Even if the ichnofauna of the Carapacha Basin is slightly younger than typical examples from the literature of the Early Permian “red bed ichnofacies” (Hunt et al., 1995b Hunt, A. P., Lucas, S. G., Lockley, M. G., Haubold, H. and Braddy, S. 1995b. Tetrapod ichnofacies in Early Permian red beds of the American Southwest. Bulletin New Mexico Museum of Natural History and Science, 6: 295–301. Early Permian footprint facies [Google Scholar]), a comparison is made. However, further detailed case studies are needed to formally define this “red bed ichnofacies” and its prospective subdivisions.     

Index 1999

Phylloicus Müller, 1880 Müller, F. 1880. ‘Sobre as casas construídas pelas larvas de insectos Trichopteros da Provincia de Santa Catharina’. Archivos do Museu Nacional, Rio de Janeiro, 3: 99–134. 210–214, plates 8–11 [Google Scholar] and Banyallarga Navás, 1916 Navás, R. P.L. 1916. ‘Neuroptera nova Americana’. Memorie della Pontificia Accademia Romana dei Nuovi Lincei, Serie II, 2: 59–80.  [Google Scholar] are endemic Neotropical genera of Calamoceratidae. Currently, Phylloicus has 55 extant species, 19 of which are recorded from Brazil, and a fossil species from Dominican amber. In this paper, a new species of Phylloicus is described and illustrated from specimens collected in Amazonas State, Brazil. This new species has peculiar hind wing venation, with vein R₄ attached basally to the base of R₂₊₃. Therefore, a modified diagnosis to the genus is presented to include Phylloicus dumasi sp. nov. The new species is somewhat similar to P. paprockii Prather, 2003 Prather, A. L. 2003. ‘A revision of the Neotropical caddisfly genus Phylloicus (Trichoptera: Calamoceratidae)’. Zootaxa, 275: 1–214.  [Google Scholar], but can be distinguished from these and other Phylloicus species by the atypical hind wing venation, uniform colouration, and male genitalia with tergum IX produced posteriorly into two wide lobes.     

Revision of the Clytra subfasciata species group (Coleoptera: Chrysomelidae: Cryptocephalinae: Clytrini)

The Clytra subfasciata species group is proposed, to comprise Clytra subfasciata Lacordaire, 1848 Lacordaire, J. T. (1848): Monographie des coléoptères subpentamères de la famille des phytophages. Tome second. Mémoires de la Société Royale des Sciences de Liége, 5, 1–890 pp. [Google Scholar], C. hajeki Medvedev &; Kantner, 2002 Medvedev, L. N., &; Kantner, F. (2002): Some new and poorly know Clytrinae (Coleoptera, Chrysomelidae) of the Old World. Entomologica Basiliensia, 24, 259–269. [Google Scholar] and C. kadleci sp. n. (Yemen). The species of the group are characterised by the peculiar shape of the aedeagus, with a dorsal plate separated from the rest of aedeagus by a deep narrow slit. Colour photographs of habitus and drawings of genitalia are provided for all three species.

http://www.zoobank.org/urn:lsid:zoobank.org:pub:F6706A76-CD49-4A5A-A109-A6E6C23514A5     

Early Oligocene Mammal Tracks from Southeastern France

Two new sites with mammalian footprints in the early Oligocene of southeastern France are described here. They represent one of the best preserved and more numerous record of tracks and trackways in the world with more than 320 ichnites. Many of those are arranged in trackways and sometimes show pes-manus impressions, a quite rare feature in mammalian ichnology. The ichnotaxonomic study indicates the presence of perissodactyls tracks referred to as Rhinoceripeda voconcense (Demathieu et al., 1984 Demathieu, G., Ginsburg, L., Guérin, C. and Truc, G. 1984. Etude paléontologique, ichnologique et paléoécologique du gisement oligocène de Saignon (bassin d’Apt, Vaucluse). Bulletin du Museum National d’Histoire Naturelle, Paris, 6: 153–183.  [Google Scholar]), artiodactyls footprints referred to as Megapecoripeda velox (Demathieu et al., 1984 Demathieu, G., Ginsburg, L., Guérin, C. and Truc, G. 1984. Etude paléontologique, ichnologique et paléoécologique du gisement oligocène de Saignon (bassin d’Apt, Vaucluse). Bulletin du Museum National d’Histoire Naturelle, Paris, 6: 153–183.  [Google Scholar]) and a carnivore footprint referred to as Bestiopeda sp. Vialov (1966) Vialov, O. S. 1966. Sledy zhiznedeyatelnosti organizmow i ikh paleontologicheskoe znachenie. Naukova Dumka, : 219 (in Russian) [Google Scholar]. They can be attributed to early Rhinocerotids, Lophiomerycids and/or Entelodonts and Mustelid-like carnivore, respectively. This study also aims at homogenizing the ichnotaxonomy used for mammal tracks where several genera were erected without a full review of the literature. All this taken together reveals a rich mammalian ichnofauna at a time period when no other fossils of mammals are known in the area and represents a good opportunity to provide state-of-the-art concerning the worldwide known sites that yielded mammalian footprints.     

EFFICIENT SYNTHESIS OF FUSED ISOTHIAZOLO C-NUCLEOSIDES. III. SYNTHESIS OF 7-SUBSTITUTED ISOTHIAZOLO[4,5-d]PYRIMIDINE C-NUCLEOSIDES*

The Divakar-Reese procedure has been successfully applied for transforming 7-oxo-isothiazolo[4,5-d]pyrimidine C-nucleosides (4a,b, 5a,b, 6a) via 1,2,4-triazol-1-yl intermediates (7a,b, 8a,b) into various 7-substituted C-nucle- osides 15a,b, 16a,b, 17a, 18a, 19a,b, 20a,b; their subsequent deprotection provides novel types of unusual C-glycosides 22b, 23a, 24a,b, 25b, 26b.

C-Nucleosides, possessing on its heterocyclic base other than naturally occuring oxo- or amino substituents, are important model compounds for biological or medicinal studies [2a] Hanessian, S. and Pernet, A. G. 1976. Adv. Carbohydr. Chem. Biochem., 32: 111–188. cf. [Google Scholar], [2b] Mizuno, Y. 1986. The Organic Chemistry of Nucleic Acids Amsterdam: Elsevier.  [Google Scholar], [2c] Huryn, D. M. and Okabe, M. 1992. Chem. Rev., 92: 1745–1768. [Crossref], [Web of Science ®] , [Google Scholar], [2d] Häbich, D. 1991. Chem. in uns. Zeit, 25: 295–307.  [Google Scholar], [2e] Uhlmann, E. and Peyman, A. 1990. Chem. Rev., 90: 543–584. [Crossref], [Web of Science ®] , [Google Scholar], [2f] Thuong, N. T. and Helene, C. 1993. Angew. Chem., 105: 697–723. [Crossref] , [Google Scholar], [2g] 1993. Angew. Chem. Int. Ed. Engl., 33: 666–690.  [Google Scholar], [2h] Yarchoan, R., Mitsuya, H., Zhomas, R. V., Pluda, J. M., Hartman, N. R., Perno, C. F., Marczyk, K. S., Allain, J. P., Johns, D. G. and Broder, S. 1989. Science, 245: 412–414. [Crossref], [PubMed], [Web of Science ®] , [Google Scholar], [2i] Tanaka, H., Baba, M., Hayakawa, H., Sakamaki, T., Miyasaka, T., Ubasawa, M., Takashima, H., Sekiya, E., Nitta, I., Shigeta, S., Walker, R. T., Balzarini, J. and De Clerq, E. 1991. J. Med. Chem., 34: 349–357. [Crossref], [PubMed], [Web of Science ®] , [Google Scholar] [3a] Koyama, G., Maeda, K., Umezawa, H. and Iitaka, Y. 1966. Tetrahedron Lett., : 597–602. Some C-glycosides with antibiotic, antiviral (HIV), and anticancer activities [Google Scholar], [3b] Hori, M., Wakashiro, T., Ito, E., Sawa, T., Takeuchi, T. and Umezawa, H. J. 1968. J. Antibiot., 21A: 264–270. [Chem. Abstr. 1968, 69, 11356j] [Google Scholar], [3c] Farkas, J. and ?orm. 1972. F. Collect. Czech. Chem. Commun., 37: 2798–2803.  [Google Scholar], [3d] Acton, E. M., Ryan, K. J., Henry, D. W. and Goodman, L. 1971. J. Chem. Soc., Chem. Commun., : 986–988.  [Google Scholar], [3e] Nakagawa, Y., Kano, H., Tsukuda, Y. and Koyama, H. 1967. Tetrahedron Lett., : 4105–4109.  [Google Scholar], [3f] Inoue, I. and Kuwaijama, I. 1980. J. Chem. Soc., Chem. Commun., : 251–253.  [Google Scholar], [3g] Buchanan, J. G., Stobie, A. and Wightman, R. H. 1980. ibid., : 916–917. [Crossref] , [Google Scholar], [3h] Hildebrand, S. and Leumann, C. 1996. Angew. Chem., 108: 2100–2102. Angew. Chem. Int. Ed. Engl. 1996, 35, 1968–1970 [Google Scholar]. We want to report on the synthesis of novel 7-substituted isothiazolo = [4,5-d]pyrimidine C-nucleosides. As we could show in previous papers [1] Wamhoff, H., Berressem, R. and Nieger, M. 1994. J. Org. Chem., 59: 1912–1917. Part 2 [Google Scholar], [4] Wamhoff, H., Berressem, R. and Nieger. 1993. M. J. Org. Chem., 58: 5181–5185.  [Google Scholar], there exists a simple approach to the protected C-glycosides 4–6.

     

Cryptic diversity among the achaetous Marionina (Annelida,Clitellata, Enchytraeidae)

This study investigates the diversity and taxonomy of a mainly marine group of species lacking chaetae currently assigned to the genus Marionina. This achaetous group includes four nominal species: M. achaeta (Hagen, 1954 Hagen, G. 1954. Michaelsena achaeta nov. sp., ein neuer mariner Oligochaet aus der Kieler Bucht. Faunistische Mitteilungen aus Norddeutschland, 1: 12–13.  [Google Scholar]), M. achaeta sensu Lasserre, 1964 Lasserre, P. 1964. Notes sur quelques oligochètes Enchytraeidae présents dans les plages du Bassin d’Arcachon. Procés-Verbaux des Séances de la Société Linnéenne de Bordeaux, 101: 87–91.  [Google Scholar], M. nevisensis Righi & Kanner, 1979 Righi, G. and Kanner, E. 1979. Marine Oligochaeta (Tubificidae and Enchytraeidae) from the Caribbean Sea. Studies of the Fauna of Curaçao and other Caribbean Islands, 58: 44–68.  [Google Scholar] and M. arenaria Healy, 1979 Healy, B. 1979a. Marine fauna of County Wexford. 1 – Littoral and brackishwater Oligochaeta. The Irish Naturalists' Journal, 19: 418–422.  [Google Scholar]. As Lasserre's (1964 Lasserre, P. 1964. Notes sur quelques oligochètes Enchytraeidae présents dans les plages du Bassin d’Arcachon. Procés-Verbaux des Séances de la Société Linnéenne de Bordeaux, 101: 87–91.  [Google Scholar]) M. achaeta appears to be morphologically different from its (then) senior homonym M. achaeta (Hagen, 1954 Hagen, G. 1954. Michaelsena achaeta nov. sp., ein neuer mariner Oligochaet aus der Kieler Bucht. Faunistische Mitteilungen aus Norddeutschland, 1: 12–13.  [Google Scholar]), the replacement name M. nothachaeta nom. nov. is proposed for it. We studied the genetic and morphological diversity of achaetous specimens of Marionina collected in Florida, the Great Barrier Reef, New Caledonia, Sweden, England and the Bahamas. The collection localities are almost all supralittoral and often brackish-water habitats. Parts of the mitochondrial genes 12S, 16S, COI and the nuclear genes 18S, 28S and ITS were analysed to assess the genetic variation and phylogeny of the achaetous Marionina species. The molecular data reveal one monophyletic group of 11 separately evolving lineages, and between these lineages, K2P distances in the barcoding gene COI vary between 5.4 and 25.0%. On a morphological basis, the lineages could be assigned to seven different groups (morphotypes), of which only two could be identified as described nominal taxa: M. nevisensis s. lat. (several lineages) and M. nothachaeta. Since the former taxon appears to be a complex of cryptic species around the world and the original type material no longer exists, a neotype from the Caribbean was designated for M. nevisensis s. str. The remaining achaetous lineages represent five morphologically distinct species that are left unnamed, awaiting finer morphological scrutiny and detailed comparisons with new collections of M. achaeta and M. arenaria. Summing up, the group of achaetous Marionina now seems to contain up to 13 different species, seven of which are yet to be formally described and named.     

Carnivore Trackways from the Miocene Site of Salinas de Añana (Alava,Spain)

A fossil tracksite of Lower Miocene age discovered near Salinas de Añana, Alava (Spain), has rendered an exceptionally well-preserved assemblage of vertebrate ichnites. The site shows a high proportion of carnivore tracks (3 out of 5 mammal ichnospecies) and a high number of individual trackways (15), some including over 50 consecutive footprints. The carnivore ichnites are classified as Felipeda lynxi Panin & Avram, 1962 Panin, M. and Avram, B. 1962. Noi urme de vertebrate in Miocenul Subcarpatilor Rominesti. Studii Cercet Geologia, 13: 521–525.  [Google Scholar], Felipeda parvula ichnosp. nov. and Canipeda longigriffa Panin & Avram, 1962 Panin, M. and Avram, B. 1962. Noi urme de vertebrate in Miocenul Subcarpatilor Rominesti. Studii Cercet Geologia, 13: 521–525.  [Google Scholar], and they are attributed to a felid, an undetermined small aeluroid, and a herpestid, respectively. The long trackways allow determination of gaits, which include lateral sequence walks and diagonal sequence trots, and of speed, which ranges from 0.4 to 1.4 m/s. Froude numbers range between 0.1 and 0.8, agreeing with gait interpretations and speed calculations. The felid trackways provide the first known evidence of group traveling in fossil cats. The herpestid footprints show modern-grade adaptations for terrestrial locomotion and digging.     

Nucleoside dimers analogs containing floxuridine and thymidine with unnatural linker groups: synthesis and cancer line studies. Part III

Abstract

Two series of novel fluorinated nucleosides dimers with an unnatural 1,2,3-triazole linkage were synthesized. The obtained molecules were prepared using “click” chemistry approach based on copper(I) catalyzed Huisgen azide–alkyne cycloaddition. It was performed between 3′- and 5′-azido-nucleosides as the azide components, and the 3′-O- and 5′-O-propargyl-nucleosides as the alkyne components. Based on analysis of the ³ Brunton, L. L.; Lazo, J. S.; Parker, K. L. (Eds.), Goodman & Gilman’s the Pharmacological Basis of Therapeutics, 11th ed.; McGraw-Hill, Medical Publishing Division: New York, NY, 2006. [Google Scholar]J_HH, ³ Brunton, L. L.; Lazo, J. S.; Parker, K. L. (Eds.), Goodman & Gilman’s the Pharmacological Basis of Therapeutics, 11th ed.; McGraw-Hill, Medical Publishing Division: New York, NY, 2006. [Google Scholar]J_H1′C2 and ³ Brunton, L. L.; Lazo, J. S.; Parker, K. L. (Eds.), Goodman & Gilman’s the Pharmacological Basis of Therapeutics, 11th ed.; McGraw-Hill, Medical Publishing Division: New York, NY, 2006. [Google Scholar]J_H1′C6 we estimated conformational preferences of sugar part and orientation around glycosidic bond. All described nucleosides dimers analogs were characterized by spectroscopic methods and evaluated for their in vitro cytotoxicity in three human cancer cell lines: cervical (HeLa), oral (KB) and breast (MCF-7).     

Redefinition of the hypotrichous ciliate Uncinata,with descriptions of the morphology and phylogeny of three urostylids (Protista,Ciliophora)

We investigated the morphology, morphogenesis and small subunit rRNA gene-based phylogeny of three marine urostylids, Uncinata gigantea Bullington, 1940 Bullington, W. E. (1940). Some ciliates from Tortugas. Papers from the Tortugas Laboratory, 32, 179–221. [Google Scholar], Holosticha heterofoissneri Hu & Song, 2001 Hu, X., & Song, W. (2001). Morphology and morphogenesis of Holosticha heterofoissneri n. sp. from the Yellow Sea, China (Ciliophora, Hypotrichida). Hydrobiologia, 448, 171–179. doi:10.1023/A:1017553406031.[Crossref], [Web of Science ®] , [Google Scholar], and Holosticha cf. heterofoissneri. The dorsal morphogenesis of Uncinata gigantea shows de novo formation of two groups of anlagen near the marginal rows. Holosticha cf. heterofoissneri demonstrates fragmentation of the first dorsal kinety anlage as in Holosticha heterofoissneri. Our population of H. heterofoissneri corresponds well with previously described populations in terms of its general morphology and ciliary pattern. Uncinata gigantea can be recognized by its large and highly contractile body, yellowish to brownish cell colour, two types of cortical granules, and 20–30 transversely oriented and densely arranged cirri in the left marginal row, which often overlie the buccal vertex. Based on the new data, especially infraciliature, the genus Uncinata is here redefined. Both the morphology and phylogenetic analyses suggest that the genus Uncinata should be classified within the family Urostylidae. In addition, both morphological and morphogenetic data suggest that Holosticha bradburyae Gong et al., 2001 Gong, J., Song, W., Hu, X., Ma, H., & Zhu, M. (2001). Morphology and infraciliature of Holosticha bradburyae n. sp. (Ciliophora, Hypotrichida) from the Yellow Sea, China. Hydrobiologia, 464, 63–69. doi:10.1023/A:1013901621439.[Crossref], [Web of Science ®] , [Google Scholar] should be transferred to Uncinata as U. bradburyae (Gong et al., 2001 Gong, J., Song, W., Hu, X., Ma, H., & Zhu, M. (2001). Morphology and infraciliature of Holosticha bradburyae n. sp. (Ciliophora, Hypotrichida) from the Yellow Sea, China. Hydrobiologia, 464, 63–69. doi:10.1023/A:1013901621439.[Crossref], [Web of Science ®] , [Google Scholar]) comb. nov., due to its possession of a characteristically prominent beak-like, leftwards curved projection and the developmental mode of the dorsal kineties. This assignment is supported by the phylogenetic analyses, which placed Uncinata gigantea in a clade with U. bradburyae (Gong et al., 2001 Gong, J., Song, W., Hu, X., Ma, H., & Zhu, M. (2001). Morphology and infraciliature of Holosticha bradburyae n. sp. (Ciliophora, Hypotrichida) from the Yellow Sea, China. Hydrobiologia, 464, 63–69. doi:10.1023/A:1013901621439.[Crossref], [Web of Science ®] , [Google Scholar]) comb. nov., and revealed only 1.13% (19 bp) difference in their SSU-rDNA gene sequence.     

Qualitative examination of diatom diversity in black fly (Diptera: Simuliidae) gut contents across a mortality gradient after exposure to Bacillus thuringiensis subsp. israelensis de Barjac, 1978

While Bacillus thuringiensis subsp. israelensis de Barjac, 1978 de Barjac, H. (1978), ‘Une Nouvelle Variété de Bacillus thuringiensis Très Toxique Pour les Moustiques: B. thuringiensis var. israelensis Sérotype H14’, Comptes Rendus de l'Académie des Sciences de Paris 286D, 797–800. [Google Scholar] (Bti) is generally effective in reducing Simulium Latreille, 1802 Latreille, P.A. (1802–1803), Histoire Naturelle, Générale et Particulière des Crustacés et des insectes (Vol. 3), Paris: F. Dufart. [Google Scholar] pest levels, impaired toxicity has been identified. Diatoms are typically abundant in Simulium larval gut contents and thought to affect feeding behaviour and/or Bti ingestion. We sought to determine diatom composition in larval Simulium gut contents and periphyton in relation to mortality subsequent in situ Bti application across three stream reaches. Generally, lower larval mortality after Bti exposure was associated with comparatively greater diatom diversity inside gut contents, corresponding with an inverse relationship between periphyton diatom diversity and larval mortality across our study reaches. High profile diatoms inside gut contents were positively correlated with mortality, suggesting microbial morphology may affect Bti efficacy. Diatoms inside live larval guts were most similar to periphyton which indicates that these larvae may have been feeding less on lower quality detrital material and/or exhibiting comparatively greater benthic feeding.     

Buried Tracks: Ichnological Applications of High-Frequency Georadar

Recognition and sampling of traces in unconsolidated sands present a major challenge for ichnologists. This can be partially remedied through the application of high-resolution geophysical techniques, such as ground-penetrating radar (GPR or georadar), which uses electromagnetic impulse for continuous imaging of shallow subsurface. It addition to geological applications, GPR imaging has been used in several studies focused on animal traces as related to conservation of endangered fossorial species (Kinlaw et al., 2007 Kinlaw, A. E., Conyers, L. B. and Zajac, W. 2007. Use of ground penetrating radar to image burrows of the gopher tortoise (Gopherus polyphemus). Herpetological Review, 38: 50–56.  [Google Scholar]; Martin et al., 2011 Martin, A. J., Skaggs, S. A., Vance, R. K. and Greco, V. 2011. Ground-penetrating radar investigation of gopher-tortoise burrows: Refining the characterization of modern vertebrate burrows and associated commensal traces. Geological Society of America Abstracts with Programs, 43: 381 [Google Scholar]), slope and levee stability (Nichol et al., 2003 Nichol, D., Lenham, J. W. and Reynolds, J. M. 2003. Application of ground-penetrating radar to investigate the effects of badger setts on slope stability at St. Asaph Bypass, North Wales. Quarterly Journal of Engineering Geology and Hydrogeology, 36: 143–153.  [Google Scholar]; Di Prinzio et al., 2010 Di Prinzio, M, Bittelli, M., Castellarin, A. and Pisa, P. R. 2010. Application of GPR to the monitoring of river embankments. Journal of Applied Geophysics, 7: 53–61.  [Google Scholar]), and mapping of fossil tracks (Matthews et al., 2006 Matthews, N. A., Noble, T. A. and Breithaupt, B. H. 2006. “The application of photogrammetry, remote sensing and geographic information systems (GIS) to fossil resource management”. In Fossils from Federal Lands, Edited by: Lucas, S. G., Spielmann, J. A., Hester, P. M., Kenworthy, J. P. and Santucci, V. L. Vol. 34, 119–131. New Mexico Museum of Natural History and Science Bulletin.  [Google Scholar]; Aucoin and Hasbargen, 2010 Aucoin, C. D. and Hasbargen, L. 2010. Using GPR, GPS and close-range photography to map and characterize dinosaur tracks in the Connecticut River valley. Geological Society of America Abstracts with Programs, 42: 276 [Google Scholar]) and tracking surfaces (Webb, 2007 Webb, S. 2007. Further research of the Willandra Lakes fossil footprint site, southeastern Australia. Journal of Human Evolution, 52: 711–715. [Crossref], [PubMed], [Web of Science ®] , [Google Scholar]). Few efforts have been dedicated specifically to characterizing burrow and track characteristics (Stott, 1996 Stott, P. 1996. Ground-penetrating radar: a technique for investigating the burrow structure of fossorial vertebrates. Wildlife Research, 22: 519–530.  [Google Scholar]; Sensors & Software Inc., 2010 [compilation on geophysical projects related to animal burrows]; Buynevich and Hasiotis, 2011; Buynevich et al., 2011; Martin et al., 2011) and most of the above studies are published in journals not routinely accessed by ichnologists.     

The genera Stegastopsis Kraatz, 1865 and Orostegastopsis Koch, 1962 with description of O. planioculata sp. n. from Oman (Coleoptera: Tenebrionidae: Tentyriini)

The first Asian member of Orostegastopsis Koch, 1962 Koch, C. (1962): Vierter taxonomischer Beitrag zur Kenntnis der Tenebrioniden Somalias: Über die von Prof. G. Scortecci 1953 und 1957 in der Migiurtinia-Provinz gesammelten Arten. 1. Teil. Atti della Società Italiana di Scienze Naturali, 51, 237–270. [Google Scholar] is described and figured: O. planioculata sp. n., which can be easily distinguished from the two Somalian species O. scorteccii Koch, 1962 Koch, C. (1962): Vierter taxonomischer Beitrag zur Kenntnis der Tenebrioniden Somalias: Über die von Prof. G. Scortecci 1953 und 1957 in der Migiurtinia-Provinz gesammelten Arten. 1. Teil. Atti della Società Italiana di Scienze Naturali, 51, 237–270. [Google Scholar] and O. kaszabi (Bremer, 1985 Bremer, H. J. (1985): Eine neue Stegastopsis-Art (Coleopt., Tenebrionidae, Tentyriini) aus Somalia. Entomologische Blätter, 81, 59–61. [Google Scholar]) comb. nov. by the shallow eyes. According to the shape of the clypeus, Stegastopsis kaszabi Bremer, 1985 Bremer, H. J. (1985): Eine neue Stegastopsis-Art (Coleopt., Tenebrionidae, Tentyriini) aus Somalia. Entomologische Blätter, 81, 59–61. [Google Scholar] is transferred from the genus Stegastopsis Kraatz to the genus Orostegastopsis Koch as was already indicated by Bremer (1985 Bremer, H. J. (1985): Eine neue Stegastopsis-Art (Coleopt., Tenebrionidae, Tentyriini) aus Somalia. Entomologische Blätter, 81, 59–61. [Google Scholar]) who treated Orostegastopsis as a subgenus of Stegastopsis: Orostegastopsis kaszabi (Bremer, 1985 Bremer, H. J. (1985): Eine neue Stegastopsis-Art (Coleopt., Tenebrionidae, Tentyriini) aus Somalia. Entomologische Blätter, 81, 59–61. [Google Scholar]) comb. nov. Keys to the species of Stegastopsis and Orostegastopsis are given.