187,591 research outputs found
Callistomordax kugleri Schoch 2008, SP. NOV.
No full textCALLISTOMORDAX KUGLERI SP. NOV. <p>1985 ‘Metoposaurier-Vorfahr’ Kugler & Bartholomä (1985: 16).</p> <p>1988 ‘oldest undoubted Morales (1988: 23 a). metoposaurid’</p> <p>1993 ‘probably a latiscopid’ Hunt (1993: 90).</p> <p>1998 Almasauridae gen. nov. Schoch & Werneburg sp. nov. (1998: 637).</p> <p>2000 Almasauridae gen. nov. Schoch & Milner (2000: sp. nov. 120, fig. 85).</p> <p> <i>Holotype:</i> SMNS 82035, a nearly complete skeleton. The skull, exposed in dorsal view, has a length of 137 mm (from tip of premaxilla to back rim of postparietal), and the length of the preserved skeleton is 1. 23 m.</p> <p> <i>Type horizon:</i> Top of Untere Graue Mergel (Bed 6 of Schoch, 2002a), Lower Keuper (Erfurt Formation), Longobardian (Upper Ladinian), Middle Triassic.</p> <p> <i>Type locality:</i> Vellberg (Schumann quarry), northern Baden-Württemberg, southern Germany.</p> <p> <i>Referred material:</i> From type locality: SMNS 90516, anterior two-thirds of skeleton with complete skull in dorsal view (153 mm); SMNS 55385, isolated, complete skull (148 mm; Figs 2A, 5); SMNS 90519, isolated left humerus (Fig. 7 D–F); SMNS 90520, parts of skeleton including well-preserved pectoral and pelvic girdle (Fig. 7A, B, H, I) and crushed skull (145 mm); SMNS 90700, articulated skeleton lacking posterior half of tail, but including well-preserved girdles, appendages, and skull (125 mm) in ventral view (Fig. 7C); MHI-K1, a nearly complete postcranial skeleton including one humerus and both hind limbs; MHI-K2, fairly complete, small postcranial skeleton with pectoral girdle; MHI-K3, disarticulated large postcranial skeleton with scapulocoracoid (Fig. 7G), interclavicle, humerus, radius, and ilium; MHI-K4, small skull (95 mm); MHI-K5, slightly disarticulated skull with good snout region (160 mm). From Ummenhofen quarry: SMNS 90506, posterior part of trunk, pelvic elements, and hind limb (Fig. 9). From Kupferzell locality: SMNS 81713, isolated articular; SMNS 84115–84118, 90521, isolated intercentra (Fig. 8C–L); SMNS 84119, atlas (Fig. 8A, B).</p> <p> <i>Stratigraphic range:</i> Albertibank through Untere Graue Mergel, Lower Keuper (Erfurt Formation), Langobardian, Middle Triassic.</p> <p> <i>Etymology:</i> In honour of Werner Kugler, private collector of Crailsheim, who found and prepared the first specimen. His general contributions to our understanding of Lower Keuper vertebrates have been outstanding.</p> <p> <i>Diagnosis:</i> Autapomorphic character states are as follows: (1) frontals co-ossified, with single medial anterior tip and blunt posterior end (Figs 1A, 4B); (2) pterygoid distinct by very broad and flat quadrate ramus combined with a particularly slender and narrow palatine ramus (Figs 1B, 5); (3) subtemporal windows nearly round and wider than the basicranial region (Fig. 1B); (4) anterior palate very short, with vomers and palatines dominated by huge fangs the sockets of which occupy most of the bone surfaces, and minute, obliquely orientated choanae (Figs 1B, 5); (5) palatal and symphyseal fangs laterally compressed and keeled; (6) intercentra forming open crescents with high flanks (except when fused to pleurocentra, then giving a disc-shaped compound bone, see Fig. 8C, D) with pointed upper ends and a massive, anteroposteriorly elongated ventral portion that has a quadrangular outline (Fig. 8C–J); (7) shaft of cleithrum curved in semilunar fashion (Fig. 7H, I).</p> <p> <i>Derived characters shared with other taxa:</i></p> <p> 1. <i>Callistomordax</i> and the Metoposauridae: clavicle extending well posteriorly on interclavicle, with the radial arrangement of the ornament pointing posteromedially.</p> <p> 2. <i>Callistomordax, Rileymillerus</i>, and the Metoposauridae: lacrimal forms small element confined to the anterolateral margin of the orbit [Bolt & Chatterjee, 2000 regarded this as a lateral exposure of the palatine (LEP), in analogy with dissorophoids].</p> <p> 3. <i>Callistomordax</i> and <i>Almasaurus</i>: cultriform process forms a prominent ventral keel, which rises from a ridge on the anterior portion of the basal plate, and terminates shortly posterior to the point where the parasphenoid is framed by posteromedial processes of the vomers; snout narrow, with the nares in the terminal position and located in close proximity.</p> <p> <i>Trigonosternum latum:</i> Schmidt (1931) described and named a partial interclavicle from the Lower Keuper of Kölleda in Thuringia (Germany) as a new genus and species, <i>T. latum</i>, which he referred to the Metoposauridae. Colbert & Imbrie (1956) have argued that the assignment of this fragment to metoposaurids is based on a misinterpretation caused by a wrong orientation of the interclavicle, which is followed here. The type and only specimen is not only indeterminate, but differs from the interclavicle of <i>C. kugleri</i> in ornamentation and overall shape (Werneburg, 1990; Schoch & Milner, 2000).</p>Published as part of <i>Schoch, Rainer R., 2008, A new stereospondyl from the German Middle Triassic, and the origin of the Metoposauridae, pp. 79-113 in Zoological Journal of the Linnean Society 152 (1)</i> on pages 80-84, DOI: 10.1111/j.1096-3642.2007.00363.x, <a href="http://zenodo.org/record/5446990">http://zenodo.org/record/5446990</a>
Plaesiorrhina deussi Schoch 1898
No full textPlaesiorrhina deussi Schoch, 1898 Plaesiorrhina Deussi Schoch, 1898: 101. Two syntypes are deposited in NMPC (ex coll. Nickerl): SYNTYPE (unsexed specimen): ‘Schoch / ex typis / Tschinde [hw, pink label] // TYPUS [p, red label, lack margin] // Coll. Nickerl, Mus. Pragense [p]’. SYNTYPE (unsexed specimen): ‘Schoch / ex typis / 1898 [hw, pink label] // TYPUS [p, red label, black margin] // Coll. Nickerl, Mus. Pragense [p] // Plaesiorrhina / Deussi Schoch / Tschinde [hw]’. Current status. Junior subjective synonym of Pedinorrhina plana (Wiedemann, 1812), see, e.g., HOLM (1994).Published as part of Bezděk, Aleš, Hájek, Jiří & Ascr, Biology Centre, 2010, Catalogue of type specimens of beetles (Coleoptera) deposited in the National Museum, Prague, Czech Republic, pp. 629-655 in Acta Entomologica Musei Nationalis Pragae 50 (2) on pages 643-644, DOI: 10.5281/zenodo.532668
Lomaptera vrazi Schoch 1897
No full textLomaptera vrazi Schoch, 1897 Lomaptera Vrázi Schoch, 1897b: 88. One syntype is deposited in NMPC (ex coll. Nickerl): SYNTYPE (♀): ‘ ♀ [p] // Hattam / Vráz 1896 [hw] // Typus [p, red label] // Vrázi / Schoch typ Hattam [hw] // Mus. Nat. Pragae / Inv. 65790 [p, red labe] // Lomaptera vrazi / Schoch / HOLOTYPE [hw] / J. Rigout det. 1996 [p]’. Current status. Valid species. Remark. Although J. Rigout labelled the specimen as the holotype, SCHOCH (1898) did not distinguish type status of his specimens, and clearly stated that the description was based on a larger number of specimens of both sexes. We thus regard this specimen as a syntype.Published as part of Bezděk, Aleš, Hájek, Jiří & Ascr, Biology Centre, 2010, Catalogue of type specimens of beetles (Coleoptera) deposited in the National Museum, Prague, Czech Republic, pp. 629-655 in Acta Entomologica Musei Nationalis Pragae 50 (2) on page 641, DOI: 10.5281/zenodo.532668
Lomaptera nickerli Schoch 1897
No full textLomaptera nickerli Schoch, 1897 Lomaptera Nickerli Schoch, 1897b: 87. Two syntypes are deposited in NMPC (ex coll. Nickerl): SYNTYPE (J): ‘Hattam / Vráz 1896 [hw] // Typus [p, red label] // Nickerli m. [hw, upper side] / Hattam [hw, under side]’. SYNTYPE (unsexed specimen): ‘Nik [hw, pink label] // Typus / Schoch [hw] // Typus [p, red label] // Coll. Nickerl / Mus. Pragense [p] // nickerli / Schoch Hattam [hw]’. Type condition. The aedeagus of the male syntype is pinned separately. Current status. Valid species.Published as part of Bezděk, Aleš, Hájek, Jiří & Ascr, Biology Centre, 2010, Catalogue of type specimens of beetles (Coleoptera) deposited in the National Museum, Prague, Czech Republic, pp. 629-655 in Acta Entomologica Musei Nationalis Pragae 50 (2) on page 639, DOI: 10.5281/zenodo.532668
Odontothyrea cinnamomea Schoch 1897
No full textOdontothyrea cinnamomea Schoch, 1897 Odontothyrea cinnamomea Schoch, 1897a: 50. One paralectotype is deposited in NMPC (general collection): PARALECTOTYPE (unsexed specimen): ‘Holub [p, blue label] // TYPUS [p, red label, black margin] // Odontothyrea / Schoch [hw] // Odontothyrea / cinnamomea / Schoch Typus! [hw] // Odontothyrea / cinnamomea / Schoch Caff. [hw] // Odontothyrea cinnamomea / Schoch, 1897 / Paralectotypus / det. A. Bezděk & J. Hájek, 2010 [p, red label]’. Current status. Junior subjective synonym of Anoplocheilus (Anoplocheilus) figuratus (Boheman, 1857), see MARAIS & HOLM (1990). Remark. SCHOCH (1897) described this species from an unknown number of specimens. MARAIS & HOLM (1990) designated a lectotype deposited in the collection of Forschungsinstitut und Naturmuseum Senckenberg, Frankfurt am Main, Germany. Because there is no doubt about the authenticity of the specimen housed in NMPC, we have labelled it as a paralectotype.Published as part of Bezděk, Aleš, Hájek, Jiří & Ascr, Biology Centre, 2010, Catalogue of type specimens of beetles (Coleoptera) deposited in the National Museum, Prague, Czech Republic, pp. 629-655 in Acta Entomologica Musei Nationalis Pragae 50 (2) on page 642, DOI: 10.5281/zenodo.532668
Eugene P. Schoch and Senator W. Lee O'Daniel examining business papers
No full text''Inventor of synthetic rubber process visits. L-R: Eugene P. Schoch and Senator W. Lee O'Daniel.''''[They are promoting] state-wide 100,000 synthetic rubber corporation. The enterprise is designed to use the process for rendering acetylene from natural gas, discovered by Dr. Eugene P. Schoch, director, Bureau of Industrial Chemistry, the University of Texas ''. [in] San Antonio Friday for a series of conferences with businessmen in the St. Anthony Hotel.'
Mon voyage à travers l'Inde, I
No full textSchoch Emmanuel. Mon voyage à travers l'Inde, I. In: Le Globe. Revue genevoise de géographie, tome 57, 1918. p. 27
MODULATIONS OF CORTICAL RESPONSES (ERPS)TO PERIPHERALLY PRESENTED EMOTIONAL FACES, WORDS, AND GESTURES BY ATTENTIONAL LOAD
No full textSchoch P, Kißler J. MODULATIONS OF CORTICAL RESPONSES (ERPS)TO PERIPHERALLY PRESENTED EMOTIONAL FACES, WORDS, AND GESTURES BY ATTENTIONAL LOAD. Journal of Cognitive Neuroscience. 2013;(Suppl.):213-213
Concert für das Pianoforte mit Begleitung des Orchesters. Op. 185. Ausgabe für 2 Pianoforte.
No full text2 parts (51, 31 p.) 34 cm.
Second piano part arranged by J. Schoch
A molecular phylogenetic reappraisal of the Hysteriaceae, Mytilinidiaceae and Gloniaceae (Pleosporomycetidae, Dothideomycetes) with keys to world species
No full textAbstractA reappraisal of the phylogenetic integrity of bitunicate ascomycete fungi belonging to or previously affiliated with the Hysteriaceae, Mytilinidiaceae, Gloniaceae and Patellariaceae is presented, based on an analysis of 121 isolates and four nuclear genes, the ribosomal large and small subunits, transcription elongation factor 1 and the second largest RNA polymerase II subunit. A geographically diverse and high density taxon sampling strategy was employed, including multiple isolates/species from the following genera: Anteaglonium (6/4), Encephalographa (1/1), Farlowiella (3/1), Gloniopsis (8/4), Glonium (4/2), Hysterium (12/5), Hysterobrevium (14/3), Hysterographium (2/1), Hysteropatella (2/2), Lophium (4/2), Mytilinidion (13/10), Oedohysterium (5/3), Ostreichnion (2/2), Patellaria (1/1), Psiloglonium (11/3), Quasiconcha (1/1), Rhytidhysteron (8/3), and 24 outgroup taxa. Sequence data indicate that although the Hysteriales are closely related to the Pleosporales, sufficient branch support exists for their separation into separate orders within the Pleosporomycetidae. The Mytilinidiales are more distantly related within the subclass and show a close association with the Gloniaceae. Although there are examples of concordance between morphological and molecular data, these are few. Molecular data instead support the premise of a large number of convergent evolutionary lineages, which do not correspond to previously held assumptions of synapomorphy relating to spore morphology. Thus, within the Hysteriaceae, the genera Gloniopsis, Glonium, Hysterium and Hysterographium are highly polyphyletic. This necessitated the transfer of two species of Hysterium to Oedohysterium gen. nov. (Od. insidens comb. nov. and Od. sinense comb. nov.), the description of a new species, Hysterium barrianum sp. nov., and the transfer of two species of Gloniopsis to Hysterobrevium gen. nov. (Hb. smilacis comb. nov. and Hb. constrictum comb. nov.). While Hysterographium, with the type Hg. fraxini, is removed from the Hysteriaceae, some of its species remain within the family, transferred here to Oedohysterium (Od. pulchrum comb. nov.), Hysterobrevium (Hb. mori comb. nov.) and Gloniopsis (Gp. subrugosa comb. nov.); the latter genus, in addition to the type, Gp. praelonga, with two new species, Gp. arciformis sp. nov. and Gp. kenyensis sp. nov. The genus Glonium is now divided into Anteaglonium (Pleosporales), Glonium (Gloniaceae), and Psiloglonium (Hysteriaceae). The hysterothecium has evolved convergently no less than five times within the Pleosporomycetidae (e.g., Anteaglonium, Farlowiella, Glonium, Hysterographium and the Hysteriaceae). Similarly, thin-walled mytilinidioid (e.g., Ostreichnion) and patellarioid (e.g., Rhytidhysteron) genera, previously in the Mytilinidiaceae and Patellariaceae, respectively, transferred here to the Hysteriaceae, have also evolved at least twice within the subclass. As such, character states traditionally considered to represent synapomorphies among these fungi, whether they relate to spore septation or the ascomata, in fact, represent symplesiomorphies, and most likely have arisen multiple times through convergent evolutionary processes in response to common selective pressures.Taxonomic novelties: New species: Gloniopsis arciformis E.W.A. Boehm, G.K. Mugambi, S.M. Huhndorf & C.L. Schoch, Gp. kenyensis E.W.A. Boehm, G.K. Mugambi, S.M. Huhndorf & C.L. Schoch, Hysterium barrianum E.W.A. Boehm, A.N. Miller, G.K. Mugambi, S.M. Huhndorf & C.L. Schoch. New genera: Hysterobrevium E.W.A. Boehm & C.L. Schoch, Oedohysterium E.W.A. Boehm & C.L. Schoch. New combinations: Gloniopsis subrugosa (Cooke & Ellis) E.W.A. Boehm & C.L. Schoch, Hysterobrevium constrictum (N. Amano) E.W.A. Boehm & C.L. Schoch, Hb. mori (Schwein.) E.W.A. Boehm & C.L. Schoch, Hb. smilacis (Schwein.) E.W.A. Boehm & C.L. Schoch, Oedohysterium insidens (Schwein.) E.W.A. Boehm & C.L. Schoch, Od. pulchrum (Checa, Shoemaker & Umaña) E.W.A. Boehm & C.L. Schoch, Od. sinense (Teng) E.W.A. Boehm & C.L. Schoch, Psiloglonium araucanum (Speg.) E.W.A. Boehm, S. Marincowitz & C.L. Schoch, P. chambianum (Guyot) E.W.A. Boehm & C.L. Schoch, P. colihuae (Lorenzo & Messuti) E.W.A. Boehm & C.L. Schoch, P. ephedrae (Henn.) E.W.A. Boehm & C.L. Schoch, P. hysterinum (Rehm) E.W.A. Boehm & C.L. Schoch, P. pusillum (H. Zogg) E.W.A. Boehm & C.L. Schoch, P. sasicola (N. Amano) E.W.A. Boehm & C.L. Schoch, and P. uspallatense (Speg.) E.W.A. Boehm & C.L. Schoch
- …
