198,258 research outputs found
Les chevaux de pur sang du célèbre Cirque Renz
Mit Unterstützung von Zirkusdirektor Franz Renz und erstem Stallmeister Emil Ackerman
Disputatio medica inauguralis de hypercatharsi
quam ... pro summis in medicina honoribus & privilegiis doctoralibus legitime consequendis publico philiatrorum examini submittit Benedictus Renz, Ulmensis. Ad diem Octobr. anni M DC XCIIDruckjahr nach dem Datum der DissertationDatum auf Titelblatt hs. ergänzt: Ad diem 17 Octobr.Enth. 50 ThesenDiss. med. Basel, 169
Ophrys sphegodes subsp. aesculapii (Renz) Soo 1970
(f) Subsp.aesculapii (Renz) Soö, Acta Bot. Acad. Sei. Hung. 16: 383 (1970): Perianth-segments pale olive-green. Labellum 10-14 x 12-18 mm, entire, without basal protuberances, blackish- brown, shortly velutinous, with wide, glabrous yellowish margin; speculum H-shaped, glabrous. Greece.Published as part of D. M. Moore (ed.), 1980, CCIII Orchidaceae, pp. 325-350 in Flora Europaea, Vol 5: Alismataceae to Orchidaceae, Camebridge :Cambridge University Press on page 347, DOI: 10.5281/zenodo.21552
Wilhelm Qualitz : Cirque Ernst Renz, Berlin, vers 1880-1881
Chez Ullstein & C ie (Berlin), 1897‟M. Qualitzˮ apparaît dans les programmes des pantomimes et des entrées clownesques du cirque Olympique d’Ernts Renz des années 1840 aux années 1870. Il a le profil du Popanz berlinois, gourmet, replet, qui complète la palette des comiques de la maison. Dans une traduction de Katrin Wolf, un extrait du livre de Alwill Raeder sur le Cirque Renz précise : « En Allemagne c’est le Popanz costaud qui fait office de joyeux compagnon dans les anciens spectacles de cirque. Qualitz, un des préférés des Berlinois, parce qu’il était berlinois, endossait un rôle de comique plutôt patriarcal, pépère, mais très drôle dans ses facéties fines, avec une échelle, ou quand il parodiait un baigneur frileux. Quand le nouveau clown se joint à l’ancien Popanz, il l’interpelle : ‟Eh Cousin, tu y arrives encore ?ˮ » Depuis, le clown a acquis une domination absolue sur le comique au cirque et devient gymnaste, musicien virtuose et dresseur de créatures à quatre ou deux pattes. L’‟Aujustˮ de Belling annonce le début d’une nouvelle ère du clown. Cet August allemand réussit à conquérir toutes les pistes du monde, à y être apprécié et en même temps à témoigner de la force créative du cirque Renz.téléchargeabl
Ophrys lutea subsp. melena Renz 1928
(c) Subsp. melena Renz, Feddes Repert. 25: 264 (1928): Labellum 9-12 mm, the lobes subequal or the middle lobe smaller, with marginal zone 1 -2 mm wide with blackish-purple hairs, blackish-purple (except the marginal zone and speculum); speculum 2 -lobed, wide in relation to labellum. • Greece. Subspp. (b) and (c) are perhaps of hybrid origin.Published as part of D. M. Moore (ed.), 1980, CCIII Orchidaceae, pp. 325-350 in Flora Europaea, Vol 5: Alismataceae to Orchidaceae, Camebridge :Cambridge University Press on page 346, DOI: 10.5281/zenodo.21552
Himmel, Hölle
Benz M. Himmel, Hölle. In: Renz T, Hanauska M, Herweg M, eds. Literarische Orte in deutschsprachigen Erzählungen des Mittelalters. Ein Handbuch. Berlin ; Boston: De Gruyter; 2018: 271-285
The definition of the human mind and the numerical difference between subjects (2p11-2p13s)
Bradyidius parabyssalis Markhaseva & Renz 2021, sp. nov.
<i>Bradyidius parabyssalis</i> sp. nov. <p>(Figs 5–6)</p> <p> <b>Holotype</b>. Adult female, dissected, body length 3.25 mm. SMF 37264/1-3 (slides) and 37265 (vial) (Senckenberg). Collected above the sea bed at Sta. 533, in the Argentine Basin, 36° 00.20’ S 49° 01.96’ W, on 15 July 2009 by the DIVA 3 expedition, Meteor cruise ME 79–1, at a depth of 4602 m.</p> <p> <b>Paratype</b>. One adult female, partly dissected, body length 3.10 mm (poor condition). ZIN, 91150. Collected above the sea bed at Sta. 676, Meteor Seamount 31° 44.58’ N 28° 12.26’ W, on 20 August 2009 by the DIVA 3 expedition, Meteor cruise ME 79–1, at a depth of 2560 m.</p> <p> <b>Additional material</b>. One female (specimen 1), from the Pacific Ocean, body length 3.10 mm, collected above the sea bed in the Kurile-Kamchatka Trench, at Sta. 7–10 on 17 August 2012, 43°01.82’ N 152°58.55’ E, by the KuramBio 1 expedition, Sonne cruise SO 223, at a depth of 5223 m; 2 females (specimens 2 & 3), damaged, not measured, collected above the sea bed in the Kurile-Kamchatka Trench, at Sta. 12–4 on 31 August 2012, 39°42.78’ N 147°09.55’ E, by the KuramBio 1 expedition, Sonne cruise SO 223, at a depth of 5224 m.</p> <p> <b>Description.</b> Female. Body length 3.10–3.25 mm. Prosome 3.7 times as long as urosome. Rostrum (Fig. 5A–D) two-pointed, divergent, excavation between points with two tubercles. General body view including the posterior corners length (Fig. 5E–F) as in <i>B. abyssalis</i> <b>sp. nov.</b> Genital double-somite symmetrical, in its anterior half with lateral swellings in dorsal view and dorsal swelling in lateral view (Fig. 5E–J). Spermathecae visible in holotype only and narrow-elongate and rounded in distal part (Fig. 5E–F). Caudal rami with 1 lateral seta, 1 ventral seta, and 4 terminal setae (Fig. 5E–F).</p> <p> Antennule (Fig. 5K–L) totally retained in holotype only. Ancestral segment I retained in all specimens possesses 3 setae, the distal seta is the longest, proximal are shorter and nearly equal in length. Antennule of holotype reaching pedigerous somite 5, of 24 articulating segments setal numbers at the segments II–XXVIII as in <i>B. abyssalis</i> <b>sp. nov.</b></p> <p> Antenna (Fig. 6A), as in <i>B. abyssalis</i> <b>sp. nov.</b></p> <p> Mandible (Fig. 6B–D), as in <i>B. abyssalis</i> <b>sp. nov.,</b> except for middle basal seta is longer.</p> <p> Maxillule (Fig. 5M), maxilla and maxilliped as in <i>B. abyssalis</i> <b>sp. nov.</b></p> <p> Legs. P1–P4 (Fig.5N, 6E–G) as in <i>B. abyssalis</i> <b>sp. nov.,</b> except for P4 coxa with lateral spinules.</p> <p>P5 absent.</p> <p> <b>Type locality</b>. 36° 00.20’ S 49° 01.96’ W.</p> <p> <b>Etymology.</b> The species name “ <i>parabyssalis</i> ” refers to the close similarity of the species to the above described species “ <i>abyssalis</i> ”.</p> <p> <b>Remarks.</b> The species <i>Bradyidius parabyssalis</i> <b>sp. nov.</b> and <i>B. abyssalis</i> <b>sp. nov.</b> share the general habitus and the main morphological features of oral parts and swimming legs. <i>B. parabyssalis</i> <b>sp. nov.</b> differs from <i>B. abyssalis</i> <b>sp. nov.</b> in the following characters: 1) body size over 3.00 mm (vs 2.45–2.90 mm in <i>B. abyssalis</i> <b>sp. nov.</b>); 2) two tubercles present in excavation between rostral points (vs tubercles between rostral points absent in <i>B. abyssalis</i> <b>sp. nov.</b>); 3) antennule ancestral segment I with 3 setae and proximal setae about twice shorter than the distal seta (vs antennule ancestral segment I usually with 2 setae and proximal seta much more than twice shorter than distal seta in <i>B. abyssalis</i> <b>sp. nov.</b>); 4) mandible basal middle seta is well developed (vs this seta is vestigial in <i>B. abyssalis</i> <b>sp. nov.</b>), and 5) P4 coxa with lateral spinules (vs lateral spinules absent in <i>B. abyssalis</i> <b>sp. nov.</b>).</p> <p> The combination of the following characters distinguish <i>B. parabyssalis</i> <b>sp. nov.</b> and <i>B. abyssalis</i> <b>sp. nov.</b> from other species of the genus: 1) the species are the only known representatives of <i>Bradyidius</i>, that possess 3 setae at the basis of the mandible (vs a single seta present in <i>B</i>. <i>hirsutus</i> and 2 setae in the other congeners); 2) both new species possess a long lateral spine on the P1 exopod segment 1 reaching, or exceeding the base of lateral spine at the exopod segment 2 and reaching, or exceeding the base of the second medial seta on the exopod segment 3 (this character is shared with <i>B</i>. <i>luluae</i> and <i>B</i>. <i>spinifer</i>, vs in the other congeners if this spine reaching, or exceeding the base of lateral spine at the exopod segment 2, then it is not reaching the base of the first medial seta on the exopod segment 3), and 3) both new species share the short posterior corners of the prosome, not reaching the middle length of the genital double-somite (this character is shared with <i>B</i>. <i>curtus</i> vs posterior corners of prosome reaching or exceeding the middle length, the posterior third, or posterior border of the genital double-somite in the other congeners) (Bradford, 1969, 1976; Grice, 1972; Markhaseva, 1996 and personal data herein).</p>Published as part of <i>Markhaseva, Elena L. & Renz, Jasmin, 2021, Description of three new species of Bradyidius (Copepoda: Calanoida), the new aetideids from the deep Pacific Ocean, with notes on the genera Bradyidius and Aetideopsis, pp. 343-369 in Zootaxa 5004 (2)</i> on pages 351-354, DOI: 10.11646/zootaxa.5004.2.5, <a href="http://zenodo.org/record/5757521">http://zenodo.org/record/5757521</a>
Byrathis penicillatus Markhaseva & Renz, 2011, sp. nov.
<i>Byrathis penicillatus</i> sp. nov. <p>(Figs 5–9)</p> <p> <b>Holotype.</b> Partly dissected adult female, body length 4.05 mm. ZMH Reg. no. K–42157. Collected on 15 March 2005 by the DIVA –II expedition above the sea bed at abyssal depths (5058 m).</p> <p> <b>Paratypes</b>, 1 partly dissected adult female, body length 3.95 mm. ZMH Reg. no. K–42158. Collected on 15 March 2005 by the DIVA –II expedition above the sea bed at abyssal depths (5050 m) in the South Atlantic (00º08.5’S 02º30.2’W); 1 partly dissected adult female, body length 3.35 mm. ZIN –91103. Collected 23 July 2009 by the DIVA –III expedition in the South Atlantic (26º35’S 35º14’W), above the sea bed at abyssal depths (4482– 4489 m). Additional material: 4 females, body length 3.20–4.90 mm, collected in the South Atlantic from the equator to about 36ºS at depths from 4601 to 5395 m.</p> <p> <b>Type locality.</b> South Atlantic (00º01.2’S, 02º28.7’W).</p> <p> <b>Description.</b> Female. Body length 3.35–4.90 mm. Prosome 3.7–4.1 times as long as urosome. Rostrum as a triangular plate with 2 filaments (Fig. 5 C–D). Cephalosome and pedigerous somite 1 and pedigerous somites 4 and 5 partly separate; posterior corners sharply triangular in dorsal and lateral view (Fig. 5 A–B, E–G). Urosome of 4 somites. Caudal rami with 4 terminal setae, 1 ventral seta and 1 small dorsolateral seta (Fig.5 E–F).</p> <p>Antennule (Fig. 6 A–C) extending to distal margin of pedigerous somites 4–5, of 24 articulating segments; armature as follows: I–3 s, II– IV–6 s + 1ae, V–2 s + 1ae, VI–2 s, VII–2 s + 1ae, VIII–1 s+1?, IX–2 s + 1ae, X– XI–4 s + 1ae, XII–1?, XIII–1?, XIV–2s + 1ae, XV–1?, XVI–2s + 1ae, XVII–1?, XVIII–2?, XIX–1?, XX–2?, XXI–1s + 1ae, XXII–1?, XXIII–1s, XXIV–1s + 1?, XXV–2s, XXVI–2s, XXVII–XXVIII–4s + 1ae, (setation on Fig. 6 A–C is given for segments II–IV, VI, VII, IX–XI, XIV, XVI and XXIII after the holotype and supplemented from the paratypes).</p> <p>Antenna (Fig. 6 D), coxa with 1 seta, basis with 2 setae; exopod of 7 free segments with 1, 1-1-1-1, 1, 1, 1, 1, and 3 setae, seta on proximal exopod segment rudimentary, following complex segment with 3 rudimentary setae, partly fused with first short segment bearing long seta; first endopodal segment with 2 setae, second with 8 + 7 setae.</p> <p>Mandible (Fig. 6 E–G), gnathobase with crest, number of teeth on cutting edge of holotype difficult to follow, paratype bearing 4 large and 3 small teeth near dorsal seta, lateral tooth situated apart from the remaining teeth; basis with 3 setae; exopod 5-segmented with 1, 1, 1, 1, and 2 setae; endopod segment 1 with 2 setae, segment 2 with 9 setae and distal rows of small surface spinules.</p> <p>Maxillule (Fig. 6 H–I), praecoxal arthrite with 9 terminal, 4 posterior, and 1 anterior setae; coxal endite with 2 setae; coxal epipodite with 9 setae; proximal basal endite with 3 setae, distal basal endite with 3 setae; endopod with 9 setae; exopod with 8 setae.</p> <p>Maxilla (Fig. 7 A–C), praecoxal endite (previously considered as proximal praecoxal endite) with 4 setae and a short attenuation; coxal endite (previously considered as distal praecoxal endite) with 3 setae; basal endites (previously considered as coxal endites) with 3 setae each, 1 seta on the proximal basal endite very short, 1 seta on distal basal endite very strong, spine-like, enditic-like lobe of proximal endopodal segment (previously considered as proximal basal endite) with 4 setae, 1 is thicker and 1 is sensory; all endites with a patch of long spinules at the base of the setae; endopod with 3 worm-like and 5 brush-like sensory setae: 2 setae shorter with large brushes, 3 setae longer with smaller brushes.</p> <p>Maxilliped (Fig. 7 D), syncoxa with 1 seta and a row of spinules on proximal praecoxal endite, 2 setae (1 sensory in distal part) and a patch of spinules on the middle endite and 2 sclerotized and 1 large brush-like seta on the distal praecoxal endite; coxal endite with 3 setae. Basis with 3 setae, proximal row of long spinules extended to the proximal basal seta and row of small spinules extended from the proximal to the distal-most basal seta. Endopod 6- segmented with 2, 4, 4, 3, 3+1, and 4 setae.</p> <p>Swimming legs. P1 (Fig. 8 A), coxa with anterior row of spinules along the distal margin; basis with medial distal seta strongly curved with setules; endopod 1-segmented with lateral lobe, its lateral margin with spinules; exopod segments 1 to 3 with 1 lateral spine each, spine of segment 1 reaching base of following spine; spine of exopod segment 2 not reaching the base of distal-most spine. P2–P4 (Fig. 8 B–D), coxa with 1 seta; basis without seta; endopod 2-segmented in P2, second segment on posterior surface with patch of long spinules; exopods 3-segmented. Endopods 3-segmented in P3–P4, segment 2 with a patch of long spinules on the posterior surface, segment 3 posterior surface densely spinulate, although with shorter spinules. Posterior surface of P4 coxa, basis and exopod densely spinulate.</p> <p>P5 (Fig. 7 E) 3-segmented, coxa and basis of equal length; coxa and basis with a patch of minor spinules distolaterally; exopod ornamented with surface spinules, 4 distal spines, medial terminal spine is curved, about 1.7 times longer than lateral terminal spine.</p> <p> <b>Etymology.</b> The species name “ <i>penicillatus</i> ” refers to a large brush-like sensory seta on the syncoxa of the maxilliped.</p> <p> <b>Remarks.</b> <i>B. penicillatus</i> <b>sp. nov.</b> is more closely related to its most geographically distant congener <i>B. laptevorum</i> (Fig. 9) and shares with this species the following distinguishing characters: i) maxilla distal basal endite (previously considered as distal coxal endite) and enditic-like lobe of proximal endopodal segment (previously considered as proximal basal endite), each with 1 very strong, spine-like setal element (<i>vs.</i> these setal elements are neither strong nor spine-like in congeners); ii) each maxilla endite with a patch of long surface spinules (<i>vs.</i> surface spinule patch is absent in the other species of the genus); iii) medial praecoxal endite of maxilliped syncoxa with a patch of spinules (<i>vs.</i> no spinule patch in congeners).</p> <p> <i>B. penicillatus</i> <b>sp. nov.</b> differs from <i>B. laptevorum</i> in: i) large brush-like sensory seta on distal praecoxal endite (<i>vs.</i> poorly developed brush in <i>B. laptevorum</i>); ii) maxilliped basis with a patch of long spinules proximally (<i>vs.</i></p> <p> spinules absent in <i>B. laptevorum</i>), and iii) P5 medial terminal spine curved, about 1.7 times longer than lateral terminal spine (<i>vs.</i> straight spine, nearly twice as long as lateral terminal spine in <i>B. laptevorum</i>). Maxilla endopod of single known specimen of <i>B. laptevorum</i> is described as bearing 1 worm-like sensory seta (<i>vs.</i> 3 brush-like setae in <i>B. penicillatus</i> <b>sp. nov.</b>), but this character should be re-examined for the species when new specimens of <i>B. laptevorum</i> are obtained.</p>Published as part of <i>Markhaseva, Elena L. & Renz, Jasmin, 2011, Two new Byrathis species (Copepoda: Calanoida) from the deep South Atlantic and Southern Ocean and first description of an adult male, pp. 49-68 in Zootaxa 2889</i> on pages 56-61, DOI: <a href="http://zenodo.org/record/201061">10.5281/zenodo.201061</a>
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