landau silva (33 resultados)

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Paperback. Condición: Brand New. pap/psc edition. 422 pages. 9.25x6.10x1.10 inches. In Stock.

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101 S., 11 Abb., 10 Tab., 23 Taf., Tertiäre Gastropoda der Provinz Malaga. Palaeontos 9. Sprache: Deutsch Gewicht in Gramm: 500.

Hardbound. Condición: Good. Folio, black cloth with gold spine lettering and a blind-stamped emblem on the front board, vi, 422, 230, 33 pp., yellowed paper Text is in Hebrew.

101 S., 3 Abb., 22 Taf., Tertiäre Gastropoda der Provinz Malaga. Palaeontos 17. Sprache: Deutsch Gewicht in Gramm: 1500.

87 S., 17 Abb., 15 Taf., Tertiäre Gastropoda der Provinz Malaga. Palaeontos 11. Sprache: Deutsch Gewicht in Gramm: 500.

In this part of the series, giving a systematic account of the Gastropoda of the Lower Pliocene (Zanclean) deposits of Estepona, province of Málaga, Spain, the Nassariidae are described and discussed. The study area has been expanded to include other major Iberian Pliocene deposits, those of the Mondego basin of central-west Portugal, the Guadalquivir basin of southern Atlantic Spain and the Alt Empordà (Girona), Baix Llobregat (Barcelona) and Baix Ebre (Tarragona), all northern Mediterranean Spain. The faunal composition is compared with that present in the Atlantic, North Sea Basin and Mediterranean Miocene to Recent times. The diversity of Nassariidae in the Iberian assemblages is comparable in number of species and composition to that found in the Italian Pliocene. 60 species are described and discussed, with particular emphasis on protoconch morphology. Ten species are new to science, Nassarius iberoclathratus nov. sp., Nassarius patnuttalli nov nom., Nassarius dinizi nov. sp., Nassarius plioholsaticus nov. sp., Nassarius manuelmolinai nov. sp., Nassarius cotteri nov. sp., Nassarius lusitanicus nov. sp., Nassarius mondegoensis nov. sp., Demoulia zbyszewskii nov. sp. and Cyllenina amaldiformis nov. sp. One further species we consider new, Nassarius sp. indet. an nov sp., but do not name formally due to lack of well-preserved specimens. Several new subjective synonymies are suggested; Nassa olivii Bellardi, 1882 junior synonym of Nassarius semistriatus (Brocchi, 1814); Nassa semistriata var. restitutiana Fontannes, 1873, Nassa semistriata var. cabrierensis Fischer & Tournouer, 1873, Nassa dertonensis Bellardi, 1882, Buccinum (Caesia) inconstans Hoernes & Auinger, 1882, Nassa (Amyclina) dertonensis italicistria Ruggieri, 1949, Nassa (Amyclina) dertonensis neogigas Ruggieri, 1949 and Hinia (Hinia) pseudocostulata Venzo & Pelosio, 1963 junior synonyms of Nassarius striatulus striatulus (Eichwald, 1829); Buccinum cuvierii Payaudeau, 1826 and Nassa atava Bellardi, 1882 junior synonyms of Nassarius corrugatus (Brocchi, 1814); Nassa pinnata Bellardi, 1882, Nassa neglecta Bellardi, 1882 and Nassa catalaunica Almera & Bofill, 1898 junior synonyms of Nassarius elatus (Gould, 1845); Nassa crebricostulata Bellardi, 1882, Nassa subecostata Bellardi, 1882 and Nassa nova Bellardi, 1882 junior synonyms of Nassarius elabratus (Doderlein,1862); Nassa pyrenaica var. compacta Fontannes, 1879, Nassa tersa Bellardi, 1882, Nassa heynemanni von Maltzan, 1884 and Nassa tersa var. abbreviatula Sacco, 1904 junior synonyms of Nassarius pyrenaicus (Fontannes, 1879); Nassa semperi Bellardi, 1882 and Nassa longa Bellardi, 1882 junior synonyms of Nassarius aldrovandii (Bellardi, 1882); Nassa planicostata Bellardi, 1882 junior synonym of Nassarius angulatus (Brocchi, 1814); Nassa (Hima) rozieri Peyrot, 1925 junior synonym of Nassarius serraticosta (Bronn, 1831); Nassa andonae Bellardi, 1882 junior synonym of Nassarius productus (Bellardi, 1882); Buccinum carcassonni De Serres, 1829, Nassa eurosta Fontannes, 1879, Nassa fanconae Bellardi, 1882, Nassa forestii Bellardi, 1882, Nassa interposita Bellardi, 1882, Nassa inaequicostata Bellardi, 1882 and Nassa fallax (Michelotti) in Bellardi, 1882 junior synonyms of Nassarius turritus (Borson, 1820); Eione affinis Cocconi, 1873 junior synonym of Nassarius circumcinctus (A. Adams, 1852); Buccinum lampas Brocchi, 1814, Nassa (Desmoulaea[sic]) conglobata var. subobsoletecostata Sacco, 1904 and Nassa (Desmoulea) conglobata altavillensis Ruggieri et al., 1959 junior synonyms of Demoulia conglobata (Brocchi, 1814); Nassa (Desmoulaea[sic]) conglobata var. subobsoletecostata Sacco, 1904 junior synonym of Demoulia pupa (Brocchi, 1814). The Italian Late Miocene and Pliocene shells identified in the literature as Nassarius tumidus (Eichwald, 1830) are shown not to be conspecific with this Middle Miocene Paratethyan taxon, and are considered a distinct taxon, Nassarius tauroprimus (Sacco, 1904). The fossil and Recent populati.

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A systematic account of the Early Pliocene (late Zanclean to early Piacenzian) gastropod assemblage found on the Island of Cubagua, Venezuela is given. 126 species are recorded belonging to 95 genera. Eleven species are new to science; Calliostoma (Calliostoma) calderense nov. sp., Calliostoma (Elmerlinia) pascaleae nov. sp., Calliostoma (Elmerlinia) macsotayi nov. sp., Modulus vermeiji nov. sp., Crucibulum (Crucibulum) cubaguaense nov. sp., Strombus arayaensis nov. sp., Pseudozonaria fehsei nov. sp., Mammilla arepa nov. sp., Malea beui nov. sp., Neoteron emilyvokesae nov. sp., Prunum carmengutierrezae nov. sp. Several new subjective synonymies are suggested: Turbo crenulatoides Maury, 1917 and Turbo (Marmarastoma) crenulatus venezuelensis Weisbord, 1962 = Turbo (Senectus) castanea Gmelin, 1791; Astralium brevispinum var. basalis Olsson, 1922 = Lithopoma brevispinum (Lamarck, 1822); Cerithium prismaticum Gabb, 1873 = Cerithium dentilabre Gabb, 1873, as first revisers the name Terebralia dentilabris (Gabb, 1873) is chosen; Potamides (Pyrazisinus) bolivarensis Weisbord, 1929 = Cerithium dentilabre Gabb, 1873; Pyrazisinus harrisi Maury, 1902 is a distinct species, Terebralia harrisi (Maury, 1902); Cypraea rugosa Ingram, 1947, junior homonym of C. rugosa Broderip, 1827 = Muracypraea grahami (Ingram, 1947), Cypraea caroniensis Maury, 1925 is removed from synonymy of C. henekeni G. B. Sowerby I, 1850; Xancus praeovoideus riosecanus Hodson, 1931 = Turbinella trinitatis (Maury, 1925); Vasum quirosense Hodson, 1931 = V. haitense (Sowerby, 1850); Solenosteira hasletti Anderson, 1929 and Solenosteira falconensis urumacoensis F. Hodson, 1931 = S. falconensis Weisbord, 1929; Melongena consors taurus Petuch, 1994 = Melongena consors (G. B. Sowerby I, 1850); Marginella venezuelana falconensis F. Hodson, 1927 is removed from the synonymy of Marginella venezuelana lavelana F. Hodson, 1927 and Persicula venezuelana, Persicula falconensis and Persicula lavelana, (F. Hodson in Hodson, Hodson & Harris, 1927) are considered distinct at full specific rank; Mitra (Tiara) woodringi H. E. Vokes, 1938 = Fusimitra sanctifrancisci Maury, 1925; Fusimitra sanctifrancisci and Fusimitra limonensis Olsson, 1922 are considered distinct species; Conomitra weeksi F. Hodson, 1931 = Conomitra lavelana F. Hodson, 1931; Lindoliva spengleri Petuch, 1988 and Lindoliva griffini Petuch, 1988 = Lindoliva diegelae Petuch, 1988; Conus trisculptus Pilsbry & Johnson, 1917 = Conus jaspideus Gmelin, 1791; Clavatula (Fusiturricula) pagodula Rutsch, 1934 and Knefastia altenai Macsotay & Campos Villarroel, 2001 = Fusiturricula springvaleensis (Mansfield, 1925) and Architectonica catanesei Petuch, 1994 = Architectonica nobilis Röding, 1798. Patterns of extinction and local disappeance at subgenus and species level are discussed and compared to those seen in other Tropical American Neogene assemblages. The figures suggest a high degree of generic stability within the Caribbean Neogene prior to the total closure of the Central American Seaway (CAS), but a rapid turnover at specific level. The biogeography of the southern Caribbean is discussed and previous work updated. Our data again distinguish a biogeographic unit centred on the north coast of Venezuela, including the Colombian Pliocene assemblages. This group of assemblages is distinct from those found in the Isthmian region of Tropical America, and in the central Caribbean. This biogeographic unit seems to have been in place since at least the Early Miocene, and whilst showing dramatic changes in faunal composition at specific level over time, altered little at generic level until the total disappearance of the 'paciphile taxa', which occurred in two pulses, the first at the beginning of the Late Pliocene, the second at the end of the Early Pleistocene. The geographic expression of this unit apparently has not altered over time, and does not seem to have been greatly affected by the closure of the CAS responsible for the demise.

221 S., 20 Abb., 23 Taf., Palaeontos 19. Sprache: Deutsch Gewicht in Gramm: 1500.

A systematic account of the middle Miocene late Serravallian gastropod assemblage found in the Karaman Basin of Turkey is given. In this work 437 species are recorded belonging to 252 genera, of which 60 were left in open nomenclature. Four new genera are proposed; Erentoezia nov. gen., Janssenia nov. gen., Europhos nov. gen. and Nisosyrnola nov. gen. Forty-one species are described as new; Homalopoma laleensis nov. sp., Thericium ataturki nov. sp., Tiaracerithium eceae nov. sp., Gibborissoia angulosa nov. sp., Erentoezia akpinarensis nov. sp., Rhombostoma? meesi nov. sp., Rhombostoma? daani nov. sp., Elachisina rolani nov. sp., Elachisina gofasi nov. sp., Tornus karamanensis nov. sp., Solariorbis punctatocarinatus nov. sp., Dermomurex (Trialatella) kilikiensis nov. sp., Ocinebrina perparva nov. sp., Nassarius gilii nov. sp., Nassarius barbarossai nov. sp., Nassarius erunalae nov. sp., Nassarius erentoezae nov. sp., Nassarius pseudoserrulus nov. sp., Nassarius pascaleae nov. sp., Melongena jaapi nov. sp., Polygona vermeiji nov. sp., Vexillum baluki nov. sp., Conomitra karamanensis nov. sp., Scalptia? problematica nov. sp., Tritonoharpa alanbeui nov. sp., Varioconus erunalerentoezae nov. sp., Genota pseudoelisae nov. sp., Clathurella pouweri nov. sp., Pleurotomoides isabelae nov. sp., Bela seyithasanensis nov. sp., Raphitoma spinosissima nov. sp., Raphitoma vandervoorti nov. sp., Cochlespira protomediterranea nov. sp., Clavatula labiolirata nov. sp., Clavatula seyithasanensis nov. sp., Perrona robustocarinifera nov. sp., Chrysallida majae nov. sp., Henrya wareni nov. sp., 'Acteon' problematicus nov. sp., Philine seyithasanensis nov. sp. and Micratys fragilissimus nov. sp. The following taxonomic changes are made: type species are designated for the turritellid genera Oligodia Handmann, 1882 and Helminthia Handmann, 1882. Trochus buchii Dubois de Montpéreux, 1831 is suppressed in favour of the senior subjective synonym Trochus catenularis von Eichwald, 1830, Turritella turris var. badensis Sacco, 1896 is suppressed in favour of the senior subjective synonym Turritella vindobonensis Handmann, 1882, Phorus gratteloupi d'Orbigny, 1852 is suppressed in favour of the senior subjective synonym Trochus conchyliophorus var. italica Grateloup, 1845, Melongena pseudobasilica Strausz, 1966 is suppressed in favour of the senior subjective synonym Melongena hungarica Csepreghy Meznerics, 1950 and Chrysallida interita van der Linden & Eikenboom, 1992 is suppressed in favour of the senior subjective synonym Parthenia (Pyrgisculus) longula Boettger, 1906. Mangilia hörnesi Brusina, 1870 is considered a nomen oblitum. Nassarius schoenni (Hoernes & Auinger, 1882) is considered a nomen protectum and Nassa laevigata Pusch, 1837 a nomen oblitum. Nassa explorata Boettger 1906 is considered a subjective synonym of Naytiopsis hypertropha (Boettger, 1906), which is chosen as the valid name of the species. Galeodes (Galeodes) thraciensis Lebküchner, 1974, is considered a nomen nudum. Raphitoma antonjanseni Marquet, 1998 is corrected to Raphitoma antonjansei. Lectotypes are designated for Conus subraristriatus Pereira da Costa, 1866 and Andonia transsylvanica (Hoernes & Auinger, 1890). The Karaman assemblages all correspond to soft bottom habitats. The fully marine layers at Seyithasan represent sandy bottom habitats, possibly with sea grass communities, deposited probably in the shallow sub-tidal zone. The clayey sediments at Akp?nar correspond to shelf environments, and reflect slightly more open and deeper marine conditions than Seyithasan. Brackish deposits are also present in some localities, which probably represent lagoonal environments. The importance of the assemblage is highlighted, as it is the only rich and diversified middle Miocene assemblage known from the Mediterranean region. The assemblage is compared with those found in the middle Miocene European AtlantoProto-Mediterranean and Paratethyan regions and a very close correlation (72.9%) is.

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