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Demokratische Skizzen vom Jahre 1848 : mit dem Stahlstich: G. A. Wislicenus / herausgegeben von Gustav Rawald
No full textDie Illustration ist ein gestochenes Frontispiz von Naumburg's Kunstanstalt.Die Rückseite des Titelblatts ist unbedrucktVorlageform der Veröffentlichungsangabe: "Halle, 1849. Verlag des Verfassers und in Commission bei H. W. Schmidt." . - Kolophon: "Halle, Druck von H. W. Schmidt."1 Illustration (Stahlstich
Seiner Hochehrwürden, dem Herrn M. Friedrich Heinrich Starken hochverordneten Superintendenten und Pastori Primario zu Bitterfeld bey dem erfreulichen Antritte dieses Amtes am 1. Januar 1800.
No full textehrfurchtsvoll gewidmet von den sämmtlichen Predigern der Inspection [C. G. Blüthner, Pastor in Alt-Jessnitz. M. A. W. Hofmann, Pastor in Sandersdorf. M. J. G. Köpping, Diaconus in Brena. M. C. G. Martius, Pastor in Niemeck. M. J. A. Mulert, Pastor in Crina. M. F. Ch. Nitzsche, Past. sen. in Roitzsch. J. A. Nitzsche, Past. subst. [in Roitzsch.] G. L. Richter, Pastor in Mühlbeck. W. G. Richter, Pastor in Pouch. M. J. G. Rieck, Pastor in Brena. M. J. Ch. Schmidt, Pastor in Priorau. F. G. Schulz, Diaconus in Bitterfeld. C. A. Schulze, Past. sen. in Rösa. M. C. G. Schulze, Pastor subst. [in Rösa.] C. F. Schulze, Pastor in Sausedlitz. M. J. G. Seyfert, Pastor in Beyersdorf. S. T. Siebold, Pastor in Petersroda. C. A. Wachsmuth, Pastor in Pösigck. J. S. Walther, Pastor in Reuden. M. S. G. Wegner, Pastor in Burgkemnitz. M. C. F. G. Werner, Pastor in Capella]Autopsie nach Exemplar der ULB Sachsen-AnhaltVorlageform des Erscheinungsvermerks: Leipzig, gedruckt in der Sommerschen Buchdruckerey
Bis(arylimido) molybdenum(VI) amidinate and guanidinate complexes; Molecular structures of [(ArN)(2)MoMe{N(Cy)C[N(i-Pr)(2)]N(Cy)}] (Ar=2,6-i-Pr2C6H3; Cy = cyclohexyl) and [(2,6-i-Pr2C6H3N)(2)MoCl2]center dot[NH=C(C6H5)CH(SiMe3)(2)]
No full textThe reaction of [(ArN)(2)MoCl2]. DME (Ar = 2,6-i-Pr6C6H3) (1) with lithium amidinates or guanidinates resulted in molybdenum(VI) complexes [(ArN)(2)-MoCl(N(R-1)C(R-2)N(R-1))] (R-1 = Cy (cyclohexyl), R-2 = Me (2); R-1 = Cy, R-2 = N(i-Pr)(2) (3); R-1 = Cy, R-2 = N(SiMe3)(2) (4); R-1 = SiMe3, R-2 = C6H5 (5)) with five coordinated molybdenum atoms. Methylation of these compounds was exemplified by the reactions of 2 and 3 with MeLi affording the corresponding methylates [(ArN)(2)MoMe(N(R-1)C(R-2)N(R-1))] (R-1 = Cy, R-2 = Me (6); R-1 = Cy, R-2 = N(i-Pr)(2) (7)). The analogous reaction of 1 with bulky [N(SiMe3)C(C6H5)-C(SiMe3)(2)]Li . THF did not give the corresponding metathesis product, but a Schiff base adduct [(ArN)(2)MoCl2]. [NH=C(C6H5)CH(SiMe3)(2)] (8) in low yield. The molecular structures of 7 and 8 are established by the X-ray single crystal structural analysis
Gordius jorriti Schmidt-Rhaesa & Schwarz, 2016, n. sp.
No full textGordius jorriti n. sp. (Figure 2) Holotype. One male from type locality, to be deposited in the PNM. Etymology. The species name “ jorriti ” is chosen after one son of the senior author, Jorrit. Type locality. Northwest Panay Peninsula, Sibaliw Research Station, Buruanga, Aklan, Panay Island, Philippines (11° 49.131' N, 121° 58.246' E), ~ 512 m; primary forest, found in a Barber trap; collected by C. Schwitzke on October 29, 2011. Description. The holotype and only specimen is 345 mm long and measures 0.8 mm in width. It is dark brown in color, and a dark collar is present. The cuticle is generally smooth (Fig. 2 A); high magnification reveals a surface structure including minute bristles and some spine-like structures not exceeding 1 µm (Fig. 2 B). The cloacal opening at the posterior end is not clearly visible, as it is filled with some material (Fig. 2 C). The postcloacal crescent is parabolic (Fig. 2 C), its anterior edge is 11 µm behind the cloacal opening. The two arms of the crescent extend onto the tail lobes, the maximal width of the postcloacal crescent is 290 µm. Anterior to the cloacal opening is a semicircular row of bristles (Fig. 2 C). The region around the cloacal opening is somewhat deeper than the remaining parts, with a kind of ridge present at the row of bristles. Such depressions are probably artifacts after fixation with dehydrating reagents such as ethanol. The maximum width of the row of bristles is 388 µm, it is therefore broader than the postcloacal crescent. The posterior ends of the row are at the level of the anterior part of the postcloacal crescent. The vertex of the row is 83 µm anterior of the cloacal opening. The row contains longer unbranched bristles and shorter branched ones (Fig. 2 D). Up to 6 branches were counted. On the posterior end of the tail lobes, stout bristles are present (Fig. 2 E). Some large artefactual structures (labelled “art” in Fig. 2 C) occur in a few places on the posterior end. Remarks. A row of bristles anterior to the cloaca is present only in two species, Gordius paranensis Camerano, 1892 and Gordius difficilis Smith, 1994. Both species differ in the shape of the postcloacal crescent, which is angled in G. difficilis but round in G. paranensis. While G. difficilis occurs in North America (Schmidt- Rhaesa et al. 2003), G. paranensis is distributed in South America (see De Villalobos et al. 2005, 2009) and in New Zealand (see Schmidt-Rhaesa et al. 2000, Schmidt-Rhaesa 2008). As far as is known, the row of bristles in G. paranensis contains unbranched bristles (Schmidt-Rhaesa et al. 2000, De Villalobos et al. 2009) or a few bristles with two branches (De Villalobos et al. 2005). This is a clear difference from G. jorriti, which has a number of strongly branched bristles. Another difference is the shape of the postcloacal crescent, which distinctly extends onto the tail lobes in G. jorriti, but is arcuate and only slightly extends onto the tail lobes in G. paranensis (Schmidt- Rhaesa et al. 2000, De Villalobos et al. 2005). Therefore, we regard G. jorriti as a distinct species.Published as part of Schmidt-Rhaesa, Andreas & Schwarz, Christian J., 2016, Nematomorpha from the Philippines, with description of two new species, pp. 246-260 in Zootaxa 4158 (2) on page 247, DOI: 10.11646/zootaxa.4158.2.6, http://zenodo.org/record/26690
H. Hiestand, Guide juridique suisse, version française par G. Brosse et C. Schmidt
No full textH. Hiestand, Guide juridique suisse, version française par G. Brosse et C. Schmidt. In: Revue internationale de droit comparé. Vol. 5 N°3, Juillet-septembre 1953. pp. 621-622
Ricardo (David) - Principes de l'économie politique et de l'impôt. Préface de C. Schmidt.
No full textBousquet G.-H. Ricardo (David) - Principes de l'économie politique et de l'impôt. Préface de C. Schmidt.. In: Revue économique, volume 24, n°3, 1973. p. 530
Ricardo (David) - Principes de l'économie politique et de l'impôt. Préface de C. Schmidt.
No full textBousquet G.-H. Ricardo (David) - Principes de l'économie politique et de l'impôt. Préface de C. Schmidt.. In: Revue économique, volume 24, n°3, 1973. p. 530
H. Hiestand, Guide juridique suisse, version française par G. Brosse et C. Schmidt
No full textH. Hiestand, Guide juridique suisse, version française par G. Brosse et C. Schmidt. In: Revue internationale de droit comparé. Vol. 5 N°3, Juillet-septembre 1953. pp. 621-622
Evolution of the G+C content frontier in the rat cytomegalovirus genome
No full textWithin the 230138 bp of the rat cytomegalovirus (RCMV) genome, the G+C content changes abruptly at position 142644, constituting a G+C content frontier. To the left of this point, overall G+C content is 69.2%, and to the right it is only 47.6%. A region of extremely low G+C content (33.8%) is found in the 5 kb immediately to the right of the frontier, in which there are no predicted coding sequences. To the right of position 147501, the G+C content rises and predicted coding sequences reappear. However, these genes are much shorter (average 848bp, 50% G+C) than those in the left two-thirds of the genome (average 1462bp, 70% G+C). Whole genome alignment of several viruses indicates that the initial ultra-low G+C region appeared in the common ancestor of the genera Cytomegalovirus and Muromegalovirus, and that the lowering of G+C in the right third has been a subsequent process in the lineage leading to RCMV. The left two-thirds of RCMV has stop codon occurrences at 67.5% of their expected level, based on a modified Markov chain model of stop codon distribution, and the corresponding figure for the right third is 78%. Therefore, despite heavy mutation pressure, selective constraint has operated in the right third of the RCMV genome to maintain a degree of gene length unusual for such low G+C sequences
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