178,923 research outputs found
Psychristus (Psychristus) andrewesi JAEGER 1997
No full textPsychristus (Psychristus) andrewesi JAEGER, 1997 Material examined: Nepal: P: Seti /D: Bajhang, 18 km NE Chainpur, Dogaira Khola S Dhalaun, N 29°40'53'', E81°20'44'', 1850 m, riverside #16, 17.VI.2009, A. Kopetz (2♀♀ - cKOP, cJAE); Chordung / Jiri, 2900m, III.1973, J. Martens (1♀ - SMNS); Distr. Karnali, Nähe Pohada, 3010-3400 m, Flussufer, VI.1997, Grill (1 - NME); N slope of Khare Khola, 2200 m, V.- VI.2000, W. Schawaller (1♂ - SMNS). Bhutan: Paro distr., Gedu, 2100 m, VI.1988, C. Holzschuh (1♀ - NME). Thailand: Doi Angkhang, 19°54,157'N 99°02,486'E, 19.- 20.X.2007, U. Scheidt (1♀ - NME). The species was hitherto known from Nepal and the Indian states of Sikkim and West Bengal (JAEGER 1997: 76). Here it is also recorded for Bhutan and Thailand for the first time. For Nepal additional records are provided.Published as part of Jaeger, Bernd, M, Boris & W, David, 2016, New synonyms, and first and interesting records of certain species of the subtribe Stenolophina from the Palaearctic, Oriental and Afrotropical regions (Coleoptera, Carabidae, Harpalini, Stenolophina), pp. 1255-1294 in Linzer biologische Beiträge 48 (2) on page 1284, DOI: 10.5281/zenodo.535499
Bradycellus (Bradycellus) heinzi JAEGER 1990
No full text<i>Bradycellus</i> (<i>Bradycellus</i>) <i>heinzi</i> JAEGER 1990 (Abb. 6, 28-30, 69-71) <p> <i>Bradycellus</i> (s.str.) <i>heinzi</i> JAEGER 1990: 10-13 (loc.typ.: Iran: Azarbaijan: Varid, 1500-1800 m).</p> <p>D i a g n o s e:</p> <p>Mit 4,9-5,8 mm eine grosse Art (Abb. 6) der Untergattung. Ober- und Unterseite dunkel rotbraun bis schwarzbraun, 1. Flügeldeckenintervall, mitunter auch Basis und ein ± ausgedehnter Bereich vor dem Vorderrand des Halsschildes rötlich aufgehellt. Kopf im Verhältnis zum Halsschild von mittlerer Grösse (KB/HB: 0,73-0,78). Augen mässig gewölbt. Halsschild (Abb. 28-30) 1,27-1,32 breiter als lang und 1,28-1,38 breiter als der Kopf. Seiten zu den Vorderwinkeln konvex gerundet verengt, zur Basis gerade oder schwach gerundet verengt, vor den Hinterwinkeln kurz ausgeschweift. Apikalrand annähernd gerade bis schwach konvex, Vorderwinkel nicht vorstehend. Basis in der Mitte konvex, an den Seiten schräg vorgezogen. Hinterecken einen ± scharfen, stumpfen Winkel bildend. Seitenrand relativ schmal, bis zur Mitte der Basalgruben fortgesetzt. Basalgruben schwach bis mässig vertieft und punktiert. Umgebung der Eindrücke ebenfalls ± ausgedehnt punktiert. Apikales Halsschilddrittel vor den Eindrücken mit wenigen feinen Punkten. Medianlinie mässig vertieft und fein punktiert. Flügeldecken, kurz- bis langoval, 1,45-1,56 länger als breit, 1,42-1,51 breiter und nur 2,78-2,99 länger als der Halsschild. Skutellarstreifen beidseitig ausgebildet, mitunter einseitig reduziert. Porenpunkt in der apikalen Hälfte des 3. Intervalls vorhanden. Streifen fein punktiert, Flügel dimorph, makropter oder brachypter. Metepisternen relativ kurz, an der Innennaht nur 1,2- 1,3 länger als an der Basis breit. 6. Sternit in beiden Geschlechtern mit 4 längeren Seten am Apikalrand (JAEGER 1990: 12 gab bei der Beschreibung des Holotypus fälschlicherweise nur 2 Seten an). Medianlobus des Aedoeagus (Abb. 69-71) mit charakteristischer Form und spezifischen Feinstrukturen des Internalsacks.</p> <p> Innerhalb seines Verbreitungsgebietes kann die Art nur mit dem auch aus dem Kaukasus und Iran bekannten <i>B. verbasci</i> verwechselt werden. Von diesem ist er durch den anders geformten Halsschild (Abb. 28-30: <i>B. heinzi</i>, 31-33: <i>B. verbasci</i>), die dunklere, mehr schwarzbraune Färbung und die weiter apikal eingelenkte Seitenrandborste des Halsschildes (Index Halsschildlänge/Distanz Halsschildbasis - Seitenrandborste: <i>B. heinzi</i> 1,30-1,44 und <i>B. verbasci</i> 1,50-1,77) zu unterscheiden. Beide Arten differieren ausserdem im Bau des Medianlobus und dessen Internalsackstrukturen (Abb. 69-71: <i>B. heinzi</i>, 72- 74: <i>B. verbasci</i>).</p> <p>V e r b r e i t u n g:</p> <p>Die Art ist vom Talysch-Gebirge in Südost-Aserbaidschan entlang des Nordabfalls des Elburs-Gebirges und dessen Ausläufern bis nach Tang Rah in der iranischen Provinz Golestan verbreitet.</p> <p>Neben früher revidierten Exemplaren (JAEGER 1990: 10, 2007: 349) konnten zwei weitere Exemplare aus Iran untersucht werden.</p> <p>U n t e r s u c h t e s M a t e r i a l:</p> <p>I r a n: Guilan: Pahlawi 15 km Asalem-Pissason, 220m, VIII. 1975, Mirzayans (1 - HMIM). - Māzanderān: Nowshar, Nāyrank Om, X. 1995, Rex./Badii/Ebrá (1 - HMIM).</p>Published as part of <i>Jaeger, B., 2008, Die westpaläarktischen Arten der Bradycellus-Untergattung Bradycellus ERICHSON 1837 unter besonderer Berücksichtigung des Mittelmeerraumes (Coleoptera, Carabidae), pp. 1509-1577 in Linzer biologische Beiträge 40 (2)</i> on pages 1535-1536, DOI: <a href="http://zenodo.org/record/5431524">10.5281/zenodo.5431524</a>
C. Jaeger, La poursuite pour dettes et la faillite
No full textC. Jaeger, La poursuite pour dettes et la faillite. In: Revue internationale de droit comparé. Vol. 3 N°4, Octobre-décembre 1951. p. 739
C. Jaeger, La poursuite pour dettes et la faillite
No full textC. Jaeger, La poursuite pour dettes et la faillite. In: Revue internationale de droit comparé. Vol. 3 N°4, Octobre-décembre 1951. p. 739
W. Jaeger, Le christianisme ancien et la Paideia grecque, 1980
No full textM. C. W. Jaeger, Le christianisme ancien et la Paideia grecque, 1980. In: Revue des Sciences Religieuses, tome 56, fascicule 2, 1982. p. 140
Alle origini del Terzo Umanesimo. Werner Jaeger su Filologia e storia (Basilea 1914)
No full textIl saggio inquadra storicamente la conferenza su "Filologia e storia" con cui Werner Jaeger inaugurò nel 1914 il suo insegnamento all'università di Basilea. Per molti aspetti si possono rintracciare in questo testo le basi di quel modello culturale che negli anni Trenta assumerà il nome di Terzo Umanesimo. Nella concezione della filologia classica che Jaeger sviluppa e nelle funzioni che le attribuisce si può, inoltre, vedere lo spuntare di una prospettiva classicistica in disaccordo con l'impostazione del suo maestro Wilamowitz
Acupalpus orszuliki W & Jaeger 2017, nov.sp.
No full textAcupalpus (s.str.) orszuliki nov.sp. (Figs 1-6) T y p e m a t e r i a l: Holotype 3: " TURKEY prov. Mardin / Hop Gecidi, Mardin env. / 11.- 14.5.2005 / lgt. Orszulik" (cWR). Paratypes: 1♀, same data as holotype (cORSZ). 13: "TR, Hatay, 15 km WSW / Antakya, Batiayaz, / bottom of Musa Dağ, / ~ 500 m, 6.-23. IV.2014 / pitfall, leg. C. Reuter" (cWR). 13, 1♀: " SYRIA, Homs env. / 10km N Crac de Chev. / Mashta Al Hilv / lgt. Orszulik 25.4.2011 " (cJAEG, cORSZ). E t y m o l o g y: Latinized patronym based on the surname of our estimated colleague Kamil Orszulik (Frýdec-Místek, Czech Republic), who collected the species at first, and whose indefatigable efforts in the field contributed substantial numbers of Carabid beetles, very interesting or new to science. D i a g n o s i s A small Acupalpus species belonging to subgenus Acupalpus with surface reddish brown and with legs yellowish red, antennomeres partly infuscated. D e s c r i p t i o n: General appearance as figured (Fig. 1). Body length 2.9-3.3 mm (mean 3.1, holotype 3.0 mm). Colour: Head dark reddish brown, clypeus, labrum, and mandibles (except apices) somewhat paler, pronotum light red brown with disc often somewhat infuscated, or dark red brown, with margins and epipleura somewhat paler, elytra dark red brown, with first (suture) interval, lateral margins, and epipleura somewhat paler. Legs and first antennomeres reddish yellow, the second one very weakly, the remaining ones distinctly infuscated. Abdomen, mes- and metepisternum dark brown or blackish brown, rest of ventral surface somewhat paler. Head (Figs 1-3): 0.78-0.80 (mean 0.79) times as wide as pronotum, with eyes fairly flat (head 1.33-1.37, mean 1.35 times as wide as head between eyes). Clypeus at apical margin weakly convex, weakly sinuate in front of anterior angle. Antennae moderately long, 2.26-2.52 (mean 2.34) times as long as pronotum and 0.84-0.88 (mean 0.86) times as long as elytra. Pronotum (Figs 1-3) with surface distinctly convex, 1.27-1.36 (mean 1.31) times as wide as long, 1.25-1.28 (mean 1.27) times as wide as head, widest in about end of apical third, lateral seta inserted at about end of apical fifth. Apical margin weakly emarginate, anterior angles narrowly rounded at tips, weakly projecting forward. Sides convex in anterior half, gently convexely narrowed to the widely rounded posterior angles, in one female paratype (Fig. 3), less distinctly and almost rectilinearly narrowed to the posterior angles, which are weakly obtuse-angled, though also widely rounded at tip. Basal margin weakly convex troughout. Lateral edge and lateral furrows narrow, the latter somewhat widened posteriorly and fused with the latero-basal impressions. Latero-basal impressions wide, somewhat obliquely impressed, impressions and area of posterior angles with coarse punctures, between impressions almost smooth, or with some single, smaller punctures, or somewhat wrinkled. Median line or hardly reaching the margins. Anterior and posterior transverse impressions indistinct or only suggested. Elytra (Fig. 1): Laterally behind widely rounded humeri weakly convex, distinctly widened posteriorly, somewhat drop-like, widest somewhat behind middle, 1.48-1.55 (mean 1.52) times as long as wide, 2.66-2.86 (mean 2.72) times as long and 1.34-1.43 (mean 1.38) times as wide as pronotum. Basal bead roundly turning into humerus, without humeral tooth. Elytral striae distinctly impressed and impunctate, scutellar striole long. Intervals comparatively flat, narrowed and somewhat convex at apex. Basal pore puncture at beginning of scutellar striole present, interval 3 in about middle of third quarter with one setiferous pore, adjoining stria 2. Ventral surface: Prosternum medially with about 20 short, erect, scattered setae, prosternal process with some few, short setae, irregularly inserted. Metepisterna elongate, ratio of internal margin/anterior margin (visible parts) about 1.42, strongly narrowed behind. Abdominal segments III-V medially (except obligatory setae) with some single short setae, last sternite in its middle part with about 30-40 scattered short setae, at apical margin on each side with 1 pore puncture bearing a long seta in males and with 2 pore punctures in females. Legs: Normal for Acupalpus species. Males with protarsomeres 2-4 moderately, mesotarsomeres 2-4 weakly dilated, in each case tarsomeres 1-4 with biseriately arranged adhesive scales ventrally. Microsculpture: Distinctly visible only on labrum, clypeus, and scutellum, partly on dorsal surface of mandibles, frons, at sides posterior to eyes, consisting of isodiametric meshes. On vertex of head and disc of pronotum obliterated, on disc of elytra almost so, on lateral parts of pronotum and elytra only slight hints of transverse lines, confused and without forming meshes, in and around basal impressions with isodiametric meshes, weakly engraved and somewhat confused. In females on elytra apically very lightly impressed fine transverse lines visible. Median lobe of aedeagus (Figs 4-6): Relatively short, in its middle part weakly widened, apical lamella short, somewhat button-like produced, rounded at tip (dorsal view), from its middle part towards apex almost rectilinear, apical lamella without capitulum (lateral view). Internal sac without spines, covered with microtrichia solely. I n t r a s p e c i f i c v a r i a b i l i t y: Seedescription. C o m p a r i s o n s a n d R e m a r k s A. orszuliki nov.sp. is considered a member of subgenus Acupalpus by tarsomere 5 with one pair of ventro-lateral setae, antennomere 2 setose, mentum and submentum divided by a distinct suture. Within this subgenus it belongs to a large informal group of species, which are characterized by setose prosternum, immaculate elytra, and the small median lobe of aedoeagus without larger teeth or sclerites. In the Near and Middle East this group is represented by members of the Acupalpus suturalis group, comprising A. suturalis DEJEAN, 1829, A. paludicola REITTER, 1884, A. schnitteri JAEGER, 1999 and A. turcicus JAEGER, 1992, and besides by A. luteatus (DUFTSCHMID, 1812) and A. exiguus DEJEAN, 1829. A. orszuliki nov.sp. differs from most of these species by the strongly reduced microsculpture of head, pronotum and elytra, the different size, and/or construction of the median lobe and its internal sac structure. A. suturalis, which is very similar in its only suggested microsculpture of the superior surface, differs from the new species by the usually darker colour of upper surface, particularly of the pronotum, a different habitus, with elytra longer and subparallel, and humeri more distinct, instead of elytra shortly oval, somewhat drop-like, with less markant humeri; by at average larger body size, 3.0- 4.0 mm, and the construction of the median lobe which is similar, but in A. orszuliki nov.sp. not as strong widened apicad (Figs 5-6), but widest in about apical third (in A. suturalis stronger widened apicad, widest in about apical fourth, see Fig. 7). In general appearance and colour of upper surface A. orszuliki nov.sp. is also similar to smaller specimens of A. oliveirae REITTER, 1884, and to smaller and paler specimens of A. planicollis (SCHAUM, 1857). However, these species occur further west in Balkan Peninsula (A. planicollis) or in NW Africa and the Iberian Peninsula (A. oliveirae), and have, in contrast to A. orszuliki, a distinct microsculpture on surface of head and pronotum, and a larger median lobe of aedoeagus with different shape of the apex. (for A. oliveirae see Figs 3 a-e in JAEGER 1988: 243; for A. planicollis see Fig. 12 in JAEGER 2011a: 202). D i s t r i b u t i o n: Up to now only known from a few specimens from S and SE Turkey close to the Syrian border and from W Syria, close to the Lebanese border. Due to its ability to fly a wider distribution of the species can be expected. H a b i t a t a n d b i o n o m i c n o t e s The specimens from the Hop Gecidi were collected in a wetland with a small creek, together with Diachromus germanus (LINNAEUS, 1758), and Dyschirius and Bembidion species, and interestingly syntopic with A. turcicus). The specimens from Mashta Al Hilv came from the bank of a small brook.Published as part of W, David & Jaeger, Bernd, 2017, Description of Acupalpus orszuliki nov. sp. (Coleoptera, Carabidae, Harpalini, Stenolophina) and faunistic notes on some species previously described, pp. 919-926 in Linzer biologische Beiträge 49 (1) on pages 920-924, DOI: 10.5281/zenodo.540940
Anthracus siamensis Jaeger 2015, nov.sp.
No full text<i>Anthracus siamensis</i> nov.sp. (Figs 21-23, 63-67, 69-73, 80) <p>Type material: Holotype: ♂ (NHMB) labelled "THAI, 26.IV.-6.V.1991 / UMPHANG 500m / 16°04'N 98°53'E / Vit Kubáň leg.", " Thailand' 91/" Thanon Thong Chai " / D. Král & V. Kubáň " and "HOLOTYPE ♂ / Anthracus / siamensis sp. n. / des. B. Jaeger 2015" [red label]. Paratypes: 2♂♂ (NHMB,) with same labels as the holotype. 1♂ labelled "THAI 28/4-6/5.91 / UMPHANG river / 16°07'N 99°00'E / lgt. D.Král 1000m " and " Thailand' 91/" Thanon Thong Chai " / D. Král & V. Kubáň ". 1♂ labelled "THAI 28/4-6/5.91 / UMPHANG 500m / 16 04'N 98°53'E / David Král lgt." and "Thailand' 91/"Thanon Thong Chai" / D. Král & V. Kubáň". 1♂ (MHNG) labelled " THAILAND 7.XI.86 / prov. Chiang Mai / Chiang Mai 320m / P. Schwendinger ". 6♂♂, 1♀ (NHMB, cJAE) labelled " LAOS-C; BOLI KHAM XAI prov. / PAKKADING; ~ 300m; / 18°20'N 104°00'E; / P. Pacholátko leg.: 1.-2.vi.2001 ". 2♂♂ (NHMB, cJAE) labelled " LAOS, 24-29.iv.2001 / Khammouan prov. / 18°07'N 104°29'E, / Ban Khoun Ngeun / - 200m, Vit Kubáň leg." All paratypes additionally with my label " PARATYPE ♂ or ♀ / Anthracus / siamensis sp. n. / des. B. Jaeger 2015 " [red].</p> <p> Additional Material examined: 1♀ with same data as the holotype, and 4♀♀ with same data as the male paratypes from Pakkading. These females probably belong to <i>A. siamensis</i>, but differ externally more or less from the males from the same localities. They were excluded from the type series, because it cannot be ruled out that they belong to another similar species occurring sympatrically in Laos, Thailand or Myanmar.</p> <p>Etymology: The species name refers to the known distribution of the species.</p> <p>Description: General appearance as figured (Fig. 21). Body length 3.2-3.7 mm (HT 3.7 mm); width 1.3-1.4 mm.</p> <p>Shiny, pronotum slightly, elytra moderately iridescent. Head and pronotum either dark brown to dark reddish brown, or paler reddish brown, with clypeus, labrum, and mandibles (inner margins and apices blackish) reddish yellow. Elytra paler than head and pronotum, paler to darker reddish yellow, with each elytron having a large blackish or dark brown central macula, expanding laterally to interval 7 or 8, and leaving base, apex and first interval reddish yellow. Legs and palpi pale yellowish brown, antennae with first two antennomeres yellowish brown, remaining ones moderately infuscated. Ventral surface mainly dark brown or dark reddish brown, with prosternum, epipleura, and sometimes medial part of abdominal sternites moderately paler.</p> <p>Head (Figs 21-23) including eyes 0.78-0.83 times as wide as pronotum, with eyes moderately to distinctly prominent (head 1.61-1.71 times as wide as head between eyes). Labrum almost rectilinear or weakly rounded at apical margin, often somewhat sloped down to the right side. Mandibles medium sized, left mandible rather sharp at apex, not thickened or truncate. Antennae moderately long, 2.42-2.57 times as long as pronotum and 0.87-0.93 times as long as elytra. Microsculpture on clypeus distinct and almost isodiametric, on labrum weakly transverse, on frons with very lightly impressed (sometimes partly obliterated) and on vertex with moderately impressed isodiametric meshes becoming weakly transverse in front of pronotal apical margin.</p> <p>Pronotum (Figs 21-23) 1.30-1.35 times as wide as long, 1.20-1.28 times as wide as head, widest in second quarter, lateral seta inserted a little posterior to beginning of second quarter. Apical margin almost rectangular or weakly emarginated, anterior angles narrowly rounded at tips, not, or weakly to moderately projecting forward. Sides convex in anterior half and rectilinearly narrowed to posterior angles, which are obtuse and weakly to moderately rounded. Basal margin sometimes rectilinear, sometimes weakly arcuate medially, and moderately to markedly oblique laterally. Lateral furrows moderately wide anteriorly, becoming weakly widened at posterior quarter, where they are fused with the baso-lateral impressions. Baso-lateral impressions medium sized, distinctly delimited from the convex pronotal disc and the weakly depressed medial part of base, flattened to basal and lateral margin. Anterior transverse impression almost obsolete. Microsculpture on disc with weakly impressed, moderately to strongly transverse meshes, and at basolateral impressions and lateral furrows with distinct weakly transverse meshes.</p> <p>Elytra (Fig. 21) rather long, 1.53-1.61 times as long as wide, 2.71-2.85 times as long and 1.31-1.38 times as wide as pronotum. Sides weakly widened posteriad, widest at or just posterior to middle. Subapical sinuation weak. Elytral striae distinctly impressed and impunctate, intervals rather flat, becoming weakly narrowed and moderately convex at apex. Microsculpture on scutellum and around basal pore isodiametric, on elytral intervals only with traces of very lightly impressed transverse lines.</p> <p>Metepisterna long and distinctly narrowed posteriad, at inner margin about 1.5 times longer than wide at basal margin. Prosternum medially with 6 and close to apical margin with a row of 9-10 medium long setae (often broken and then insertion points difficult to observe). Prosternal process with 1-2 distinct setae.</p> <p>Protarsomeres 1-4 of males moderately and mesotarsomeres 2-4 weakly dilated. Protarsomere 4 markedly and mesotarsomere 4 moderately bilobed. Protarsomeres and mesotarsomeres 1-4 of males with biseriately arranged adhesive hairs on ventral surface.</p> <p>Median lobe of aedeagus (Figs 63-67, 69-73) moderately large, with external shape as figured. Apical lamella rather short, not markedly narrowed (dorsal aspect), the apex abruptly bent upward (lateral aspect). Internal structures composed of one large apical tooth usually orientated to left side (lateral aspect), 0-3 medium-sized subapical teeth, 1- 3 small teeth in medial portion and 1-2 small and tall teeth somewhat beneath.</p> <p> Comparisons <i>A. siamensis</i> nov.sp. is closely related to <i>A. javaensis</i> nov.sp. and <i>A. skalei</i> JAEGER, 2015 and obviously represents a closely related eastern vicariant of the latter. Both species are very similar in general appearance, microsculpture and body proportions which do not provide reliable differences to distinguish them. However, they differ by constant differences in the arrangement of teeth in the internal sac of the aedeagus (see Figs 62-75, 74-75) and partly also by the darker colour of head and pronotum (only darker specimens of <i>A. siamensis</i>).</p> <p> <i>A. siamensis</i> is also very similar in general habitus to <i>A. hornburgi</i> nov.sp. which occurs in the adjacent areas of Myanmar, and to <i>A. annamensis</i> (BATES) and closely related taxa which occur in Myanmar, Laos and Thailand, at Chiang Mai even sympatrically. <i>A. siamensis</i> differs from <i>A. hornburgi</i> nov.sp. by the aedeagal characters given under this species, and from <i>A. annamensis</i> s.l. (Figs 78-79) by the different external shape of the median lobe of the aedeagus with the peculiar shape of the apex in lateral aspect and the different internal structures with large apical and subapical teeth (in <i>A. annamensis</i> and closely related taxa apex simple without any hook and teeth markedly smaller and with different arrangement). Externally there are often no reliable differences to differentiate <i>A. siamensis</i> from <i>A. hornburgi</i> and <i>A. annamensis</i> (incl. closely related taxa) but darker specimens differ from these taxa by their dark brown head and pronotum.</p> <p> Distribution <i>A. siamensis</i> nov.sp. is so far known from Thailand and Laos (Fig. 80).</p>Published as part of <i>Jaeger, Bernd, 2015, Revision of the maculate species of the Anthracus annamensis group from the East Palaearctic and Oriental Regions. Part 2. A redescription of Anthracus nesophilus (ANDREWES, 1936) and six new species from Nepal, India and SE Asia (Coleoptera, Carabidae, Harpalini, Stenolophina), pp. 1361-1396 in Linzer biologische Beiträge 47 (2)</i> on pages 1374-1376, DOI: <a href="http://zenodo.org/record/5193661">10.5281/zenodo.5193661</a>
- …
