87,102 research outputs found
Données récentes sur la contamination des produits laitiers français par les composés organo-chlorés
No full textRichou-Bac Lucien, Mollet M. F., Restuit Annick, Pantaléon Jean. Données récentes sur la contamination des produits laitiers français par les composés organo-chlorés. In: Bulletin de l'Académie Vétérinaire de France tome 127 n°8-9, 1974. pp. 379-390
Etat actuel de la contamination des produits laitiers par les résidus de pesticides organo-chlorés
No full textRichou-Bac Lucien, Mollet M. F., Pantaléon Jean. Etat actuel de la contamination des produits laitiers par les résidus de pesticides organo-chlorés. In: Bulletin de l'Académie Vétérinaire de France tome 125 n°3, 1972. pp. 131-146
Pollanisus nocturna Mollet & Tarmann 2023, sp. n.
No full text<i>Pollanisus nocturna</i> sp. n. <p> <b>Material examined (Table 12).</b> <b>Holotype</b>. ♁ (943) (Figs 173, 176), <b>Queensland</b>. Road Paluma-Hidden Valley, Mt Zero Taravale, 19°00′40.5″S, 146°03′58.5″E, 817 m, 28.IV.2013, at night, B. Mollet & G. M. Tarmann <i>leg</i>., (BMC).</p> <p> <b>Paratypes</b>. 6 ♁, same data as holotype; <b>Queensland</b>. 1 ♁, Brisbane, North Stradbroke Island, s/e Amity Beehive Road, N, 27°25′58′′S, 153°27′46′′E, 37 m, 14.I.2006, a. L., E. Friedrich <i>leg.</i> (TLMF). <b>New South Wales</b>. 1 ♁ (934) (Figs 174, 177), 50 km SE of Goulburn, Nerriga, 6.XII.2008, lux., A. Kallies & E. D. Edwards <i>leg.</i> (BMC).</p> <p> <b>Paratypes examined, head ratios not included in Table 12. Queensland</b>. 7 ♁, Road Paluma-Hidden Valley, Mt Zero Taravale, 19°00′40.5″S, 146°03′58.5″E, 817 m, 28.IV.2013, at night, B. Mollet & G. M. Tarmann <i>leg</i>., (TLMF), 2 ♁, Qld, Road Paluma-Hidden Valley, 4 km E, (19°00′09.9″S, 146°04′05.9 E, 795 m, 27.IV.2013, at night, Mollet & G. M. Tarmann <i>leg</i>., (TLMF)</p> <p> <b>Discussion and differential diagnosis</b>. The strong difference in head ratios with <i>Pollanisus viridipulverulenta</i> and <i>P. apicalis</i> justifies the description of these specimens as a new species.</p> <p> Although the specimen collected in NSW, Goulburn area, shows a slightly different compound eye feature with compound eye slightly smaller and more globular, its head ratios are very similar to that of the holotype and paratype collected in the Northern and Southern parts of Queensland, and moreover, it was collected at night. New data from this population, localized very far from the <i>P. nocturna</i> <b>sp. n.</b> type locality, are necessary to confirm conspecifity. Therefore this specimen is here only provisionally included in the paratype series.</p> <p> <b>Description</b></p> <p>Female unknown</p> <p>Male holotype. Length of body: 6.9 mm; length of forewing: 8.9 mm; breadth: 3.9 mm; length of hindwing: 6.6 mm; breadth: 3.8 mm; length of antenna: 6.5 mm; distance between compound eyes in frontal view, 0.98 x the breadth of compound eye and 0.65x the height; compound eye black almost circular in lateral view; ocellus slightly ovoid; chaetosemata of triangular shape with a long and very narrow extension occupying all the space between compound eye and ocellus. Antenna. Brown with satin sheen, segments 1 to 31 bipectinate, 32 to 44 biserrate, pectinations of maximum length at segment 12, about 4.8x longer than breadth of shaft in dorsal view. Body. Frons brown, vertex with blue metallic sheen, edging of blue metallic scales bordering the compound eyes; proboscis dark brown, porrect labial palps brown with blue metallic scales; patagia and tegulae covered with bluish green metallic sheen; thorax with strong bluish green metallic sheen dorsally and ventrally; abdomen brown with bluish green metallic sheen dorsally and ventrally except segments 1-2 which are brown without metallic sheen ventrally. Forewing. Upperside brown, with satin sheen, underside light brown with some bluish green metallic scales below costa. Hindwing. Brown,opaque, with narrow slightly translucent area medially, underside with strong shiny blue scales anteriad of medial stem and at anal angle. Legs and coxae. Brown, with strong green metallic sheen on coxa and femur.</p> <p> <b>Genitalia</b> (948) (Fig. 40). Valva with pointed apex, distally straight dorsally, ventral margin straight. Phallus nearly x3.5 longer than broad, cylindrical, slightly upcurved, cornutus as long as phallus.</p> <p> <b>Phenology and bionomics</b>. The first observation of this species in nature was a total surprise. On the evening of 27.iv.2013 BM & GMT drove from the tropical village Paluma, the centre of the Paluma Range National Park, westwards on the road that descends towards Hidden Valley which is already situated in the northern part of the Coane Range that runs parallel to the tropical Paluma Range and is, contrary to the Paluma Range, covered with a sclerophyll <i>Eucalyptus</i> forest, mixed with <i>Casuarina</i> trees (Fig. 180). Four kilometres to the East of the Hidden Valley camping site a small gravel road branched off to the left heading SSW into the Coane Range. After ca 400 metres we found a nice place for a camp, where we also could put up our lights for night collecting. The forest was still damaged from a former bushfire that must have taken place some months before. However, the vegetation had recovered nicely after the rainy season, that had ended some weeks ago. The locality is situated at an elevation of 795 metres with GPS: S 19°00’09.9″, E 146°04’05.9″. The weather was nice with a cloudless sky, a slight easterly wind and an evening temperature at 18.30 of 23°C. We built up our light tower (15 W UV blacklight) (Fig. 181) and started the observations at 18.30, shortly after sunset but already in twilight before getting dark. Already at 18.40 a male of a <i>Pollanisus</i> was observed inside the translucent wall of the light tower running up and down. This was strange, because the mast of the tower was fixed on the ground and there was only a small slit where a specimen could have the chance to come inside. We collected this specimen and much to our surprise it was a male of ‘ <i>P. apicalis’</i>, as we thought. Shortly after this (ca. 18.50) we saw a second male coming on the ground heading for the centre of the light tower by running on the floor into the inner side of the net, and shortly later, at 19.00 a third male did the same. It was already fully dark by that time. However this was a full moon night and the darkness was not complete.</p> <p> The occurrence of <i>Pollanisus apicalis</i> in northern Queensland (around Herberton and Ravenshoe) and from Paluma was not new, as I. F. B. Common had taken a male on 27.VIII.1985 around Paluma, that is deposited in the ANIC in Canberra (Tarmann 2004). However, a night active habit has not been known from the more southern populations and was new to us.</p> <p> On the next evening (28.IV.2013) we came back to the same place but drove further into the forest and found an even better locality with more diverse vegetation at a point that is called Mount Zero crossing, at an elevation of 817 metres, GPS: S 19°00’40.5″, N 146°03’58.5″. We used the same light equipment as the day before, but also an 8 W UV blacklight tube in a small cage that we placed high up on a tree. Exactly at 18.45 the first male of <i>Pollanisus apicalis</i> came quickly running on the floor in small jumps to the light and tried to slip under the mast of the light tower that we had fixed with stones to the floor. Only minutes later more males came running towards the light and three of them managed to come into the inner surface of the tower, in spite of our attempts to prevent this by fixing the mast to the ground. None of them weres observed flying. The males inside the tower ran vertically up and down the light tube. Until 19.05 we had observed 14 males all with the same habit. Then the attraction of the light seemed to stop suddenly and no more specimens came. We tried to find this species next day in daylight. However, not a single specimen was observed.</p> <p>The time of activity of this population,shortly after darkness, must be really very short. We observed the specimens for only 20 minutes! Maybe that this is also the time when the females call for males.</p> <p> Of course we also looked for a potential larval host-plant for this population. We found a small <i>Hibbertia</i> sp. with narrow leaves (like <i>Rosmarinus</i> genus) and <i>H. lepidota</i> R. Br. Ex DC. and also small and somehow ‘spiny’ bush that likes granite ground, which is everywhere here.</p> <p> <b>Etymology</b>. From the Latin <i>nocturna</i>, by reference to the exclusive nocturnal activity.</p> <p> <b>Distribution</b> (Fig. 182)</p>Published as part of <i>Mollet, Bernard & Tarmann, Gerhard M., 2023, Revision of the genus Pollanisus Walker, 1854 (Lepidoptera: Zygaenidae: Procridinae), pp. 1-72 in Zootaxa 5281 (1)</i> on pages 50-54, DOI: 10.11646/zootaxa.5281.1.1, <a href="http://zenodo.org/record/7912043">http://zenodo.org/record/7912043</a>
Geologie der Schafmatt-Schimberg-Kette und ihrer Umgebung (Kt. Luzern) / Geologische Karte des Schafmatt-Schimberggebietes (Kt. Luzern)
No full textHans Mollet; Schweiz. Geol. KommissionAus: Beiträge zur geologischen Karte der Schweiz, N. F., Lief. XLVII, 3Mit Bewilligung der Schweiz. Landestopographie vom 19. VIII. 1920.Ueberdruck aus dem topographischen Atlas der Schweiz. Blätter No. 373 u. 375.Exlibrisstempel: "Geograph. Institut Zürich Eidg. techn. Hochschule" 002611507_0001 Exemplar der ETH-BIB, KS 222: 91Exlibirsstempel: " Gepgraphisches Institut ETH Sonneggstrasse 5 Zürich 6" 005372492_0001 Exemplar der ETH-BIB, KS 222: 9
Contamination de l’environnement et de la faune par des polluants industriels : les diphényles polychlorés (P.C.B.)
No full textRichou-Bac Lucien, Cumont G., Mollet M. F., Pantaléon Jean. Contamination de l’environnement et de la faune par des polluants industriels : les diphenyles polychlorés (P.C.B.). In: Bulletin de l'Académie Vétérinaire de France tome 125 n°6, 1972. pp. 293-303
Pollanisus incertus Tarmann 2004
No full textPollanisus incertus = P. species 5 Published data (Tarmann 2004) and additional localities. Material examined (Table 10), all from Queensland. Holotype: 1 ♁ (Figs 133, 138), 2.5 km N of Kuranda, e. l. on Tetracera nordtiana (Dilleniaceae), 20.X.1985, I. F. B. Common leg. (ANIC). 1 ♁, Kuranda, Top of the range, 19 Butler Drive, 16°48′S 145°38′E (GPS), 335 m, 15/ 30.IV.2005, D. C. F. Rentz leg. (BMC); 1 ♁, same data but, 16/ 31.X.2005, (BMC); 1 ♁, same data but, 1/ 15.V.2007, (ANIC); 2 ♁, Windsor Tableland, 8.V.1984, A. N. Gillison leg. (ANIC); 1 ♁, Carnavon N. P., West Branch, Maranoa River, 24°58°S, 148°01°E, 760 m (GPS), 10.IV.1999, E. D. Edwards leg. (ANIC); 1 ♁ (747) (Figs 135, 140), W. Bramston Beach, Tower acc. road, N Innisfail, 17°21′S, 145°58′E, (lux), A. Kallies leg. (BMC); 1 ♁, Track to Mt Lewis, 16°34′42.4″S, 145°19′28.9″E, 450 m, 22.XI.2011, e. l. on Hibbertia scandens, S. & B. Mollet leg. (BMC); 1 ♁, Road to Mowbray N. P., 2 km E of Julatten, 16°36′16.9″S, 145°21′09.6″E, 388 m, 27.XI.2011, e. l. on H. scandens, S. & B. Mollet leg. (BMC); 1 ♁ (1424) (Figs 137, 142), same data but, 20.IV.2013, B. Mollet & G. M. Tarmann leg., (BMC); 3 ♁, Kuranda N. P., 16°41′51.8″S, 145°31′31.2″E, 432 m, 26.XI.2011, e. l. on H. scandens, S. & B. Mollet leg. (BMC); 1 ♁ (815) (Figs 136, 141), Track in Mt Windsor Tableland N. P., 16°15′51.7′′S, 145°03′50.2″E, 1082 m, 23.XI.2011, e. l. on H. scandens, S. & B. Mollet leg., (BMC); 1 ♁, Road to Lake Morris, 16°58′35.3″S, 145°41′28.4″E, 460 m, 25.XI.2011, e. l. on T. nordtiana, S. & B. Mollet leg., (BMC); 1 ♁, Murray Upper Falls N. P., Car Park day visitors, 18°09′13.9″S, 145°49′00″E, 100 m, 26.IV.2013, (night), B. Mollet & G. M. Tarmann leg., (BMC); 2 ♁, Clohesy River, end of track, 16°58′36.2″S, 145°39′21.5″E, 605 m, 19.IV.2013, (night), B. Mollet & G. M. Tarmann leg., (BMC). 1 ♁ (Figs 134, 139), Kennedy River, 30 km W of ‘ Fairview′, 15°35′S, 144°03′E, 24.XII.1984, at m. v. lamp, G. & A. Daniels leg. (ANIC; Pollanisus species 5 as per Tarmann 2004). Discussion and differential diagnosis. Both occurring in Northern Queensland, the habitus and head ratio of Pollanisus incertus are close to those of P. jirrbal sp. n., but the former differs in its slightly smaller compound eyes and the different larval host-plant. The holotype of P. incertus was obtained from a larvae collected on Tetracera nordtiana (Figs 143–145) (Tarmann 2004). Pollanisus species 5 (sensu Tarmann 2004) shares the same head ratio (Table 10) and the nocturnal activity with P. incertus. and is therefore considered to belong to the same species. Phenology and bionomics. Eggs and larvae (Figs 146–148) were mainly collected on Hibbertia scandens and rarely on Tetracera nordtiana (both Dilleniaceae). These two larval host-plants are often growing together. Most of the imagines (Figs 149, 150) were collected at night with U. V. light. The collected larvae found feeding on T. nordtiana, were easily moved to H. scandens (rearing observation BM). Distribution map (Fig. 151)Published as part of Mollet, Bernard & Tarmann, Gerhard M., 2023, Revision of the genus Pollanisus Walker, 1854 (Lepidoptera: Zygaenidae: Procridinae), pp. 1-72 in Zootaxa 5281 (1) on pages 42-45, DOI: 10.11646/zootaxa.5281.1.1, http://zenodo.org/record/791204
Mollet Music Store, 208 Walnut, Yankton SD, Yankton County
No full text35 mm slide, a Honda CVCC Civic in front of a single-story brick building with a bay door and metal awning, text in the window includes "Mollet Music Band Inst. Repair" and "212"Drawer info: Union - Zieback - Other State, Murals Historic Photos; Yankton Historical Commereal DistrictKodachrome Slide Yankton 208 Walnut 96 F CMT 27 Nov 80C
Diagnostic accuracy of multislice computed tomography coronary angiography is improved at low heart rates
No full textSpatial variation in growth, condition and maturation reaction norms of the Baltic herring, Clupea harengus membras
No full textUnderstanding of spatial patterns in life-history traits can help fisheries management focus on biologically and functionally relevant stock units. In the present study, we examined lifehistory variation in growth, condition and maturation of the Baltic herring Clupea harengus membras among different areas of the Baltic Sea. As expected based on environmental gradients, herring grew faster in southern than in northern areas. The condition factor for young individuals was higher in the north, but higher for older individuals in the south. Probabilistic maturation reaction norms (PMRNs) based on age, length and condition indicated counter-gradient variation: young herring in the northern areas reached the size at which they had a 50% probability of maturing when they were comparatively smaller than the southern specimens. However, the north–south differences in PMRNs were reversed in older age groups. This indicated that maturation of herring in the north was more size dependent (zero PMRN slope) than it was for herring in the south, where maturation was predominantly determined by age (negative PMRN slope). The geographical differentiation in maturation schedules would potentially translated into divergent changes in recruitment in response to changes in density-dependent growth and, hence, also fishing pattern
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