309,311 research outputs found
Feyrliches Danck-Gedächtnuss der sel. Reformation der Kirchen zu Bern, oder, Jubel-Predigt uber die Wort: Psal. CXXVI. 3.4
No full textgehalten, und auff Begehren in Truck gegeben von Daniel Wetzel ... den 7. Januarii 1728.S. 43 fälschlicherweise als 33 bezeichne
Der König, oder, Das Abentheuer : ein Lustspiel in drey Aufzügen
No full textvon Friedrich Wilhelm Wetzel ; aufgeführt auf der Schaubühne zu Augsburg unter der Direktion Herrn Schopf des ältere
L' hospice du Grimsel
No full textdessiné d'après nature par J. J. Wetzel ; gravé par F. HegiDritter ZustandAus Vues de l'Oberland bernoisAus der Sammlung von Heinrich Appenzeller (1854-1921) Exemplar der Zentralbibliothek Zürich, Graphische Sammlung und Fotoarchi
Interlachen
No full textdessiné d'après nature par J. J. Wetzel ; gravé par F. HegiDritter ZustandAus Vues de l'Oberland bernoisAus der Sammlung von Heinrich Appenzeller (1854-1921) Exemplar der Zentralbibliothek Zürich, Graphische Sammlung und FotoarchivAus dem Nachlass Dr. R. von Schulthess Exemplar der Zentralbibliothek Zürich, Graphische Sammlung und Fotoarchi
Achnanthidium peetersianum C. E. Wetzel, Juttner & Ector
No full textAchnanthidium peetersianum C.E.Wetzel, Jüttner & Ector in Wetzel et al. (2019: 345) (Figs 144–165) Morphometric features:— 7.6–12.3 µm long; 2.0–2.7 µm wide; 29–34 striae in 10 µm; striae mainly composed of 3–5 areolae. Taxonomical remarks:— Our population is in agreement with the type species, besides it has slightly narrower valves when compared to the French population (2.8–3.3 μm, Wetzel et al. 2019). This species has narrow valves with subcapitate to small capitate apices, similar to A. macrocephalum (Hustedt) Round & Bukhtiyarova (1996: 349), although the latter taxon presents broadly capitate apices. Despite being difficult to separate, a reevaluation of A. macrocephalum type material was recently published in the same study as A. peetersianum (Wetzel et al. 2019). Using SEM micrographs, the authors showed that A. peetersianum presented predominantly rounded areolae and had a higher density per stria, while A. macrocephalum striae are composed of 1–2 elongated areolae of different lengths. Moreover, the axial area of the rapheless valve of the latter taxon is expanded, widening towards the central area. Recently, Yu et al. (2019) described two small species that resemble ours: A. subtilissimum P.Yu, Q. -M.You & Q.-X.Wang (in Yu et al. 2019: 161) and A. limosua P.Yu, Q. -M.You & Q.-X.Wang (in Yu et al. 2019: 158). The first species is likely a synonym of A. macrocephalum, and the second presents visibly larger valves (3.2–4.0 µm) than A. peetersianum. Achnanthidium indistinctum also bears several similarities with A. peetersianum. They can be distinguished in girdle view by the apparently thickened striae in the first taxon, which is not visible in our specimens (see Figs 158, 159). Concerning the valve view, A. indistinctum presents rostrate apices and an almost nonexistent central area that never forms a fascia. On the other hand, A. peetersianum exhibits subcapitate to capitate apices and a small rounded central area that rarely forms a fascia. Notably, SEM analysis can also help separate both taxa due to the distal raphe ends straight in A. indistinctum and bent in our specimens. Despite the slightly narrower valves in the latter taxon (1.8–2.2 µm, Van de Vijver & Kopalová 2014), the metric features of these two species overlap. Achnanthidium reimeri (Camburn) Ponader & Potapova (2007: 235) has a similar valve outline with our population, however, it presents longer and wider valves and a rhomboid central area on the rapheless valve (Ponader & Potapova 2007). Distribution and ecological information:— Recently described from Le Sauvigny River in France, it was one of the most well-distributed species found in this study (40 % of occurrence). It is plausible that this taxon was previously identified in Brazilian publications as A. macrocephalum. In this study, A. peetersianum occurred in all of the sampled habitats. Its ecological preference was for slightly acidic (pH optimum of 6.6–6.7), electrolytic-poor (optimum of 28.2–49 μS∙ cm-1) and oligo- to mesotrophic waters (TP optimum of 14.9–27.1 μg∙L- 1, TN optimum of 374.4–519.4 μg∙L- 1). We also observed this species in enriched waters (TP> 50 μg∙L- 1).Published as part of Costa, Lívia F., Wetzel, Carlos E., Maquardt, Gisele C., Zanon, Jaques E., Ector, Luc & Bicudo, Denise C., 2022, Taxonomy and ecology of Achnanthidium (Bacillariophyta, Achnanthidiaceae) from southeastern Brazil with the description of six new species, pp. 187-223 in Phytotaxa 575 (3) on pages 204-205, DOI: 10.11646/phytotaxa.575.3.1, http://zenodo.org/record/743124
Bicudoa amazonica C. E. Wetzel, Lange-Bertalot & Ector 2012, sp. nov.
No full textBicudoa amazonica C.E. Wetzel, Lange-Bertalot & Ector sp. nov. Diagnosis microscopio photonico: Frustula aspectu cinguli fere rectangulata. Valvae late ellipticae, lineari-ellipticae ad lineares apicibus cuneatis denique curte rostratis. Valvae dorsiventrales quia ad axem apicalem leviter ad levissime asymmetricae margine una semper convexa altera modice concava in mediis partibus quoad specimina media et maiora. Longitudo 40–120 μ m, latitudo 17–20 μ m. Area axialis (id est sternum) angustissima plerumque excentrica sita. Areae angustae marginales prope limbos adsunt. Alterae areae absunt. Systema raphidea nulla. Striae transapicales, sicut in Eunotia, subparallelae saepe plusminusve irregulariter sitae inter se, sub apices transientes distincte radiantes, 10–12 in 10 μ m, sub apices modice densius sitae usque ad 16 in 10 μ m. Interstriae comparate latiores. Areolae vix aspectabiles quia circiter 75–80 in 10 μ m. Structura chromatophorum incognita. Diagnosis microscopio electronico: Aspectus externus: Frontes valvarum fere planae cum foraminibus areolarum uniseriatis omnino comparate minimis circularibus (hic apertis) diameter circiter 0.1 μ m. Series foraminum curte interruptae sterno angustissimo et latius interruptae ad iuncturam inter frontem et limbum valvae ubi series apicalis spinarum verrucosa num est tum series continuantes in limbis. Campi porellorum absunt. Aspectus internus: Superficies interna perforata areolis circularibus crateriformibus apertis. Depressiones transapicales id est alveoli vacant. Systema raphidea ut in familia Eunotiaceae sive ut in familia Bacillariaceae nulla. Etiam rimoportulae et porelli apicales ut in familia Fragilariaceae et alteris familiis diatomearum araphidearum vacant. Cingulum frustulorum: cingulum utraeque valvae 3–10 copulis apertis vel clausis constans. Omnes copulae preditae multis areolis uniseriatis transapicaliter (vel quodammodo pervalvariter ita ut in Eunotia nec in familia Fragilariaceae vel alteris familiis araphideis). Light microscopy observations: —Valves isopolar, moderately dorsiventral, broadly linear with slightly constricted center in large specimens; cuneate to sub-rostrate ends (Figs 7–13). Dorsal margins consistently convex. Ventral margins variable, either less concave in small valves or nearly straight to concave in mediumsized and large specimens. Length 40–120 µm, width 17–20 µm. Axial area or sternum extremely narrow, sometimes displaced toward ventral side of valve (Fig. 8) or centrally positioned (Fig. 9). Narrow lateral area located close to the valve margins, visible in both valves and girdle view. Raphe system, helictoglossae and rimoportulae lacking. Transapical striae subparallel often irregularly spaced, 10–12 in 10 µm, becoming radiate toward the ends where they are more densely spaced (up to 16 in 10 µm) (Fig. 12). Costae comparatively much wider. Areolae observable in LM. Plastids unknown. Frustules rectangular in girdle view (Fig. 14). Cells forming band-like colonies (no more than 4 joined cells observed). Scanning electron microscope observations: —In external view, valve face slightly curved with a shallow longitudinal depression near the valve center (Fig. 21). Striae uniseriate situated both on valve face and mantle, interrupted by lateral area developing on the junction between valve face and mantle (Figs 22–25). Areolae small, circular with foramina ca. 0.1 µm in diameter (Fig. 22). Each foramen lies in a shallow depression visible in oblique view (Figs 23–25). Valve face showing wart-like growths and siliceous thickenings, which allow the connection between contiguous valves (Fig. 25). Sternum narrow, sometimes displaced toward the ventral side of the valve. Apical pore fields absent. The cingulum is composed of 3–10 open copulae that are perforated by pervalvar multiporoid striae arranged in discernible rows (Fig. 27). Girdle band areolae density 75–80 in 10 µm. A small linear depression is present near the apex at the junction between valve face and mantle. In both external and internal view, rimoportulae are always absent. Internally, but never in external view, one raphe slit vestige is present in some specimens (Figs 28, 30–31), but in most cases it is completely lacking (Figs 28 and 32). Type: — BRAZIL. Amazonas: Rio Negro basin, Alto Rio Negro, 0° 30' 43'' S, 64°49'45''W, 11 March 2005; Wetzel C. E. & Ector L., sample n° 265; Holotype here designated SP –400.480, depicted here in Fig. 8, deposited at the ' Herbário Científico do Estado Maria Eneyda P. Kauffmann Fidalgo'(SP), São Paulo, Brazil. Sample from feces of an adult specimen of the freshwater turtle Podocnemis erythrocephala Spix (1824). Isotypes: slide BR –4167 (Meise) and slide BM –101392 (London). Etymology: —The new genus is dedicated to Prof. Dr. Carlos Eduardo de Mattos Bicudo at the 'Instituto de Botânica de São Paulo' for his pioneering work on freshwater microalgae in Brazil and for the relevant role on the formation of Brazilian phycologists; ' amazonica' refers to the type locality. Additional material examined: — BRAZIL. Amazonas: Rio Negro basin, Alto Rio Negro, 03 March 2005; Wetzel C . E. & Ector L., phytoplankton, sample n° 82; SP–400.297; BRAZIL. Amazonas: Rio Negro basin, Alto Rio Negro, 04 March 2005; Wetzel C . E. & Ector L., periphytic biofilm growing on submerged Arecaceae palm tree, sample n° 104; SP–400.319; BRAZIL. Amazonas: Rio Negro basin, Alto Rio Negro, 04 March 2005; Wetzel C . E. & Ector L., phytoplankton, sample n° 106; SP–400.321; BRAZIL. Amazonas: Rio Negro basin, Alto Rio Negro, 04 March 2005; Wetzel C . E. & Ector L., periphytic biofilm growing on a submerged trunk, sample n° 116; SP–400.331; BRAZIL. Amazonas: Rio Negro basin, Alto Rio Negro, 04 March 2005; Wetzel C . E. & Ector L., phytoplankton, sample n° 117; SP–400.332; BRAZIL. Amazonas: Rio Negro basin, Alto Rio Negro, 11 March 2005; Wetzel C . E. & Ector L., phytoplankton, sample n° 260; SP–400.475; BRAZIL. Amazonas: Rio Negro basin, Alto Rio Negro, 11 March 2005; Wetzel C . E. & Ector L., phytoplankton, sample n° 261; SP–400.476.Published as part of Wetzel, Carlos E., Lange-Bertalot, Horst, Morales, Eduardo A., Bicudo, Denise De C., Hoffmann, Lucien & Ector, Luc, 2012, Bicudoa amazonica gen. nov. et sp. nov. (Bacillariophyta) - a new freshwater diatom from the Amazon basin with a complete raphe loss in the Eunotioid lineage, pp. 1-18 in Phytotaxa 75 (1) on pages 7-9, DOI: 10.11646/phytotaxa.75.1.1, http://zenodo.org/record/506663
Vue de Zurich, prise du Zurichhorn
No full textdessiné d'après nature par J. Wetzel ; gravé par F. HegiAus "Voyage pittoresque aux Lacs de Zurich, Zoug, Lowertz, Egeri et Wallenstadt", 181
Vue du lac de Zurich prise du Bastion de la katze à Zurich
No full textdessiné d'après nature par I. Wetzel ; gravé par F. HegiDruckmotiv verwendet in: "Voyage pittoresque aux Lacs de Zurich, Zoug, Lowertz, Egeri et Wallenstadt"Weitere Versionen der Druckgrafik (koloriert) siehe unter gleichlautendem Titel, ebenfalls von Wetzel und Hegi, 181
Zoug vers le Righi
No full textZug von der Platzwehre aus[Wetzel, J.J.]Nach dem grösseren Blatt von Johann Jakob Wetzel und Franz HegiAus der Sammlung des Kunst-Antiquariats Hermann Koller, Zug Exemplar der Zentralbibliothek Zürich, Graphische Sammlung und Fotoarchi
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