104,278 research outputs found
Trichocoelina cochleata Vilkamaa & Menzel 2019, comb. n.
Trichocoelina cochleata (Rübsaamen, 1898) comb. n. Synonym: = haemorrhoidalis (Lundbeck, 1898) [as Sciara]. Literature. Sciara haemorrhoidalis Lundbeck—Lundbeck (1898): 247, pl. 5, fig. 6. Sciara cochleata Rübsaamen— Rübsaamen (1898): 108; text fig. 4, pl. 6, fig. 22; Lundbeck (1900): 312. Lycoria (Neosciara) cochleata (Rübsaa- men) — Lengersdorf (1928 –30): 33, pl. 2, fig. 40. Neosciara cochleata (Rübsaamen) — Lengersdorf (1936): 191; Maschke (1936): 177, 179, 180; Soot-Ryen (1942): 77; Lengersdorf (1951): 26. Bradysia (Hemineurina) cochleata (Rübsaamen) — Frey (1948): 65, 83, pl. 17, fig. 100. Lycoriella cochleata (Rübsaamen) — Steffan (1966): 50, 52; Krivosheina & Mohrig (1986): 157, 161. Lycoriella (Hemineurina) cochleata (Rübsaamen) — Tuomikoski (1960): 75, 76; Stone & Laffoon (1965): 232; Tuomikoski (1967): 47; Gerbachevskaja-Pavluchenko (1986): 30; Menzel & Mohrig (2000): 409, figs 377–379; Coulson & Refseth (2004): 103; Coulson (2008): 161; Coulson (2013): 154; Mohrig et al. (2013): 270; Vilkamaa (2015): 551; Wirta et al. (2016): appendix, unpaginated p. 21 (table S1) and unpaginated p. 39 (cladogram). BIN. BOLD:ABW3844. Verified records. CZECH REPUBLIC, ‘Glatzer Schneeberg, Graphit-Bergwerk Klein Würben bei Mährisch- Altstadt’ [= Králický Sněznik, graphite mine in Malé Vrbno near Staré Mešto], K. Maschke, 16.VII.1935, 3 males, 3 females (in ZFMK); same data but 12.X.1935, 2 males (in ZFMK). Newrecords. FINLAND, Obb (Ostrobothniaborealisborealis), Tornio, Kiviranta, Malaisetrap, 30.VI–4.VII.2008, A. Haarto, 1 male (in MZH); W GREENLAND, Disko Bugt, Quegertasussuk, 68°35’N, 51°05’W, 7.VIII.1991, J. Böcher, 1 male (in ZMUC). NE GREENLAND, Zackenberg, 74°28’N, 20°34’W (UTM8265500:0513778), 44 m, 2–11.VII.2011, T. Roslin & G. Várkonyi, 1 male (in MZH); same locality but UTM 8265758:0513786, 37 m, Malaise trap, 11–20.VII.2011, T. Roslin & G. Várkonyi, 2 males (in MZH, SDEI); same locality but Reseach Station, 74.50°N, 21.00°W, 35 m, 7.VIII.2011, J.B. Mosbacher, 1 male (BOLD Sample ID GRPV2, in DAUH). Discussion. The species was described from Greenland (Rübsaamen, 1898), and redescribed and illustrated by Menzel & Mohrig (2000), with the discussion of the type material. Trichocoelina cochleata is characterized by having a medially impressed gonostylus, with a strongly curved apical part. The antennal scapus and pedicellus as well as the hypopygium and legs are yellow, but the apex of gonostylus has strikingly dark setosity. The gonostylus bears 6–7 rather long and slender gonostylar megasetae, the tegmen is broadly subconical with a sclerotized dorsoapical process. The intergonocoxal lobes of the hypopygium are short. For similar species, see under Trichocoelina aemula sp. n. and T. semusta sp. n.Published as part of Vilkamaa, Pekka & Menzel, Frank, 2019, Re-classification of Lycoriella Frey sensu lato (Diptera, Sciaridae), with description of Trichocoelina gen. n. and twenty new species, pp. 1-67 in Zootaxa 4665 (1) on pages 21-22, DOI: 10.11646/zootaxa.4665.1.1, http://zenodo.org/record/400055
Trichocoelina janetscheki Vilkamaa & Menzel 2019, comb. n.
Trichocoelina janetscheki (Lengersdorf, 1953) comb. n. Figs 10 A, 10 B, 17 D Literature. Neosciara janetscheki Lengersdorf—Lengersdorf (1953): 167, fig. 1; Janetschek (1956): 471. Lycoriella (Hemineurina) janetscheki (Lengersdorf) — Tuomikoski (1959a): 35; Gerbachevskaja-Pavluchenko (1986): 31; Franz (1989): 14; Menzel & Mohrig (2000): 410; Wirta et al. (2016): appendix, unpaginated p. 21 (table S1) and unpaginated p. 39 (cladogram). Material studied. CANADA, Nunavut, Sverdrup Islands, Elles Ringnes Island, Isachsen, 70.79°N, 103.55°W, lemming burrow, 17.VI.1960, J.R. Vockeroth, 4 males (3 in CNC, 1 in MZH); same locality but moss near very small stream, 14.VII.1960, J.F. McAlpine, 2 males (in CNC); Nunavut, Ellesmere Island, Fosheim Peninsula, Hot Weather Creek, 79°58’N, 84°28’W, 2.VII.1990, F. Brodo, 1 male (in MZH); NE Greenland, Mestersvig, 72.24°N, 23,92°W, C. Vibe (in ZMUC); NE GREENLAND, Zackenberg, 74°28’N, 20°34’W (UTM8265500:0513778), 44 m, 2–11.VII.2011, T. Roslin & G. Várkonyi, 1 male (in MZH); same locality but UTM 8265758:0513786, 37 m, Malaise trap, 11–20.VII.2011, T. Roslin & G. Várkonyi, 2 males (in MZH, SDEI); same locality but 74.50°N, 21.00°W, 44 m, 7.VII.2011, T. Roslin & G. Várkonyi, 1 male (BOLD Sample ID GRPV16, in DAUH); same locality but 74.4667°N, 20.5667°W, 48 m, 24.VII.2011, T. Roslin & G. Várkonyi, 3 males (BOLD Sample IDs ZA2012- 50010, ZA2012-50011 and ZA2012-50012, in DAUH); USA, Colorado, Mt. Evans, 14 000 ft, 25.VII.1961, W.R.M. Mason, 1 male (in USNM). Redescription. Male. Head. Face brown, antenna dark brown maxillary palpus pale yellowish. Eye bridge 2–3 facets wide. Face with 15–21 setae. Clypeus with 1–4 setae. Maxillary palpus with 3 segments, 1 st segment as long as or longer than 3 rd segment, 2 nd segment shortest; 1 st segment with 3–9 setae, with dorsal patch of sensilla; surface of antennal flagellomeres smooth, body of 4 th antennal flagellomere 1.95–2.75x as long as wide, the neck shorter than broad, the longest setae shorter than the width of flagellomere. Thorax. Dark brown, setae pale. Anterior pronotum with 5–11 setae. Proepisternum with 7–24 setae. Scutellum with 4 longer and some short and fine setae. Wing. Fumose. Length 2.2–3.1 mm. Width/length 0.35–0.40. Anal lobe weak. Veins distinct. c/w 0.50–0.60. R 1 /R 0.50–0.90. stM shorter than fork of M. r-m longer than bM, bM non-setose, r-m non-setose or with 1–2 setae. Halter yellow. Legs. Yellow, coxal setae pale. Fore tibial organ forming a large patch in shallow depression. Fore tibial spur as long as the tibial width. Abdomen. Pale brown, setae pale, short and fine. Hypopygium (Fig. 10 B). Brown, as abdomen. Intergonocoxal area long, with two short setose lobes. Gonocoxa broad, as long as gonostylus, medial margin basally smoothly curved, with short and fine setosity. Gonostylus (Fig. 10 A) voluminous, apically truncate, impressed; with short setosity, a short apical tooth, and numerous megasetae in the medial impression; megasetae slightly curved or straight, short and slender; with 1 well-differentiated whiplash seta basally at ventromedial margin. Tegmen (Fig. 17 D) longer than broad, laterally straight, apically with a narrow hyalinous acuminate process, weakly sclerotized, aedeagal teeth not detectable in the specimens studied. Aedeagal apodeme long. BIN. BOLD:ACK5495. Discussion. In Fig. 10 A the gonostylus is flattened and distorted to show the arrangement of the megasetae. In its extremely voluminous gonostylus, Trichocoelina janetscheki (Lengersdorf, 1953) resembles most T. incrassata sp. n., for distinguishing characters, see under the latter.Published as part of Vilkamaa, Pekka & Menzel, Frank, 2019, Re-classification of Lycoriella Frey sensu lato (Diptera, Sciaridae), with description of Trichocoelina gen. n. and twenty new species, pp. 1-67 in Zootaxa 4665 (1) on page 33, DOI: 10.11646/zootaxa.4665.1.1, http://zenodo.org/record/400055
Mohrigia hippai Menzel 1995
Mohrigia hippai Menzel, 1995 (Fig. 16) Mohrigia hippai Menzel, 1995: 102 –104; Menzel & Mohrig, 2000: 414 –420. Material examined. China, Tibet. 1 male, Nielamu, Zhangmu, G 318, K5368, 27°57'27''N, 85°58'18''E, 2845 m, 6- VIII-2014, leg. Jun Xu and Mei Qin [SM02488]. Diagnosis. The species is characterized by its broadly clavate gonostylus, with an apical tooth on the dorsal side, and two to three flagellate setae on the apical half; gonocoxite with a wide intercoxal lobe bearing long and dense setae on the ventral side; tegmen longer than wide and apically rounded, parameral apodeme continuously sclerotized forming a central strip on dorsal side; ventral inner side of gonocoxite with long setae; R1 significantly longer than R and extended to the base of the M-fork; eye bridge narrow with perpendicular frontal process and the ommatidia lost at the center (Menzel & Mohrig, 2000). Distribution. China (Tibet— new record; Fig. 16); Nepal (Simbhanjang), Burma (Kambaiti) (Menzel & Martens, 1995; Menzel & Mohrig, 2000). Remarks. This species was first recorded from Nepal and is new to China. The Chinese specimen shares the diagnostic characteristics, but slight differences were found (a broader gonocoxite and a narrower tegmen).Published as part of Xu, Jun, Shi, Kai, Huang, Junhao & Wu, Hong, 2017, Review of the genus Mohrigia Menzel (Diptera, Sciaridae) from China, pp. 71-98 in Zootaxa 4300 (1) on pages 77-78, DOI: 10.11646/zootaxa.4300.1.4, http://zenodo.org/record/83715
History of Germany, from the earliest period to the present time.
The history of Germany, from the earliest period to the present time.Vol.IIIby Wolfgang Menzel. Tr. from the 4th German ed., by Mrs. George Horrock
On the track to biological effects: the 13th Microdosimetry Symposium and the 5th Microbeam Workshop
Wenn aus Rotkohl Blaukraut wird. Mit Kindern der (unbelebten) Natur auf der Spur
Lück G, Menzel P. Wenn aus Rotkohl Blaukraut wird. Mit Kindern der (unbelebten) Natur auf der Spur. Bausteine Kindergarten : Sonderreihe. Aachen: Bergmoser und Höller; 2000
"Outline Map of the Lexington and Danville Railroad: The Central Railroad of Kentucky."
Published in Cincinnati, Ohio, by Klauprech and Menzel
Mononchus zschokkei Menzel 1913, n. sp.
<p> <i>Mononchus</i> <i>zschokkei</i> n. sp.</p> <p> Körpergestalt mäßig schlank, das Vorderende nur wenig verschmälert. Der papillentragende Teil des Kopfendes. unmerklich abgesetzt. Mundhöhle länglich, mit einem dorsalen Zahn, welcher stets im hinteren Drittel der Mundhöhle liegt und nach vorn gerichtet ist (Fig. 1). Kleine Zähnchen oft an der Basis der Mundhöhle vorkommend. Oesophagus nach hinten nur wenig erweitert, stets 1/ <b>4</b> der Gesamtlänge ausmachend. Xervenring vor der Mitte des Oesophagus gelegen. Weibliche Geschlechtsöffnung stets beim Beginn des letzten Körperdrittels liegend. Weibliche Geschlechtsorgane paarig symmetrisch, kurz; 1 bis 2 Eier im Uterus. Schwanz beim Weibchen und Männchen kurz, zugespitzt und nach der Bauchfläche gebogen (Fig. 2). Spicula mäßig schlank, mit centralem Verdickungsstreifen in ihrer distalen Hälfte, schwach gebogen. Accessorisches Stück zweiteilig, die Spicula umfassend, ähnlich wie bei <i>Mononchus</i> <i>hrachyuris</i> Bütschli (<i>vgl</i>. de Man, Onderzoekingen over vrij in de aarde levende Nematoden. Tijdschr. Nederl. Dierk. Ver. Deel 11, 1876, Taf. XIII, Fig. 51). Vor dem After eine Keihe von 21 kegelförmigen Papillen (Fig. 3), Cuticula in dieser Region schräg gestreift.</p> <p>Länge: 2,2—3,2 mm.</p> <p> De Mansche Formel: α = 20-30, β = 4, ɣ = 20—24.</p> <p>Vorkommen: In verschiedenen Gegenden der Schweizer Alpen, von 1500— 3400 m Höhe¹.</p> <p> Yerwandtschaft: <i>Mon</i>. <i>zschokkei</i> zeigt unterden zehn bis jetzt aus Europa bekannten <i>Moìionchus-</i> Arten einzig mit <i>Moii</i>. <i>parvus</i> de Man große Verwandtschaft, er unterscheidet sich von ihm hauptsächlich durch die Lage des dorsalen Zahnes und die Körpergröße. Ferner ist meines Wissens das Männchen von Mon. <i>parvus</i> unbekannt, während es bei <i>Mon</i>. <i>zschokkei</i> ziemlich häufig ist. (Auf 7 ♀ ♀ fallen etwa 2 ♂♂.) Von den aussereuropäischen Arten kämen, wie mir in liebenswürdiger Weise Herr Dr. J. <b>G</b>. de Man (Jerseke) mitteilte, nur <i>Mon</i>. <i> <i>gymnolaimus</i> Cobb, <i>Mon</i>. <i>sunilis</i> Cobb und <i>Mon</i>. <i>rex</i> Cobb in Betracht, bei denen der dorsale Zahn ebenfalls an der Basis der Mundhöhle liegt; doch ist bei diesen 3 Arten der Schwanz lang(γ= 5— 7, und gleicht demjenigen von <i>Mon</i>. <i>macrostoma</i> Bast.</i></p> <p>¹ Herrn cand. phil. W. Sehmassmann, welcher mir das der Beschreibung zugrunde liegende, von ihm neulich im Lünersee Rhätikon) gefundene Männchen überließ, spreche ich meinen herzlichen Dank aus. Ebenso bin ich Herrn Prof. Dr. C. Keller in Zürich für die Überlassung eines bisher undeterminierten, aus den Alpen stammenden Materiales zu großem Danke verpflichtet.</p> <p>Es sei mir gestattet, diese Art meinem verehrten Lehrer, Herrn Prof. Dr. F. Zschokke, zu widmen.</p>Published as part of <i>Menzel, Rich., 1913, Mononchus zschokkei n. sp. und einige wenig bekannte, für die Schweiz neue freilebende Nematoden, pp. 408-413 in Zoologischer Anzeiger 42</i> on pages 408-410, DOI: <a href="http://zenodo.org/record/10797276">10.5281/zenodo.10797276</a>
Measures of internal lumbar load in professional drivers – dependence on posture, anthropometry, age, duration of exposure and type of machine
Introduction
In European and International Standards and Directives, external loads in terms of daily vibration exposure A(8) or vibration dose value VDV are used as predictors of adverse health effects. These values only partly reflect the internal load acting on the lumbar spine. Particularly for shock containing acceleration time histories, a method for the calculation of internal spinal forces on the basis of a Finite-Element-Model (FEM) was developed within the EU VIBRISKS project [1]. The model can be adapted to the anthropometry (ten categories) and the sitting posture (six categories) of the driver. The method has been proposed in a working draft of the Standardisation Committee ISO/TC 108/SC 4/WG 15 [2]. It has already been standardised in the German Standard DIN SPEC 45697 [3]. The risk assessment is based on the daily compressive dose Sed (MPa) and the risk factor R (non-dimensional). Both values are determined by the compressive internal forces, by the daily and lifetime exposure duration and by the age at the start of exposure. For a re-analysis of the Italian part of an epidemiological study performed within the VIBRISKS project, the internal forces, Sed and R were calculated for the 537 participants of the study.
Methods
Typical acceleration time histories for various machine types and working tasks were selected. Impacts due to sitting down or loosing the contact to the seat were eliminated. At the end, 19 checked time histories with a duration of 200 s were available. All signals were shock containing [4]. Beside the calculation of Sed and R factor, r.m.s., r.m.q. and standard deviation of the time histories of the internal forces were assessed in all three axes separately and as a vector sum. Therefore, a modification of the program published on the CD in DIN SPEC 45697 had to be used, because it was necessary to get the interim results of the calculations in terms of internal forces. In the horizontal axes, the daily doses were calculated without relation to the spinal endplate areas. The daily doses for the internal forces acting in anterior and posterior directions were separately computed. In total, 21 different variables were calculated.
Results
The values of the forces, Sed and R factor varied over the lumbar spine levels from T12/L1 to L5/S1. The shapes of the spine-level dependent curves were determined by the posture and the type of machine (example for posture group1 in Fig. 1).
The category of body mass and Body Mass Index (BMI) and the posture - in association with the covariates listed in Table 1 - significantly influenced the maximum R factor (statistical test: ANCOVA). The interaction between the body mass/BMI-category and the posture was not significant (F=1.3, p=0.11). When several machines in identical sitting posture were used, the type of machine showed a significant effect as well (Table 1, last three lines). In these cases, the effect of the yearly exposure duration was not longer calculated due to a lack of variability of the covariate. Instead of that, the last column of Table 1 contains the interaction between the body mass/BMI-category and the type of machine which was significant for all three postures. The p-value was p<0.001 in nearly all cases. The exceptions are indicated with (+) in Table 1.
Similar results were found for the forces and the Sed values.
Conclusions
The results of this study showed that the measures of internal lumbar load in a population of professional drivers according to ISO/WD 2631-5 were significantly influenced by numerous individual and work related factors: anthropometry, age, duration of exposure, posture and type of machine. Measures of internal lumbar load might be well suited as predictors of adverse health effects on the lumbar spine of an individual for a working lifetime.
References
[1] Hinz B, Seidel H, Blüthner R, Menzel G, Hofmann J, Gericke L, Schust M (2007) Whole-body vibration experimental work and biodynamic modelling, Annex 18 to the final report on Task 6.1: Whole-body vibration laboratory studies and biodynamic modelling. VIBRISKS (EC FP5 Project No. QLK4-2002-02650) www.vibrisks.soton.ac.uk
[2] ISO/WD 2631-5. Mechanical vibration and shock – Evaluation of human exposure to vibration – Part 5: Methods for evaluation of vibration containing multiple shocks. DIN, 2011. ISO/TC 108/SC 4/WG 15.
[3] DIN Deutsches Institut für Normung (2012) Mechanische Schwingungen und Stöße – Verfahren zur Bewertung stoßhaltiger Ganzkörper-Vibrationen; mit CD-ROM (Mechanical vibration and shock – Method for evaluation of impulsive whole-body vibration; with CD-ROM), German National Standard, DIN SPEC 45697.
[4] Schust M, Hinz B, Menzel G, Pinto I, Hofmann J, Bovenzi M (2012) Comparison of different methods for detecting multiple shocks in vibration time histories. Paper presented at the 47th United Kingdom Conference on Human Responses to Vibration, held at ISVR, University Southampton, 17 - 19 September 201
BEPU-FSAR : establishing a background for extension of V&V principles to non-thermal-hydraulic codes
Nuclear thermal hydraulic and accident analysis are based in 3 pillar activities, which consists in: Scaling, Coupling and V&V. Each of them are establish technology, whit key documents to describe and widely used. The final goal of this work is to apply the BEPU methodology in all parts of FSAR where analytical techniques are needed and for that the crucial step is the transfer of the BEPU concepts into the other areas. In this sense, the issue is how to adapt to other disciplines the pillar activities presented in the thermal hydraulic area. For that we need to identified which elements can be applied in the other areas, to show that the propose methodology is feasible. For now, this work aims to show that the V&V elements, currently done for thermal-hydraulic codes, can be also done for different codes, which are used to perform different analysis include on a FSAR of a generic plant
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