Drapeable unit arcs fit in the unit 30° sector

2017 ◽  
Vol 17 (4) ◽  
Author(s):  
Yevgenya Movshovich ◽  
John E. Wetzel

AbstractWe show that a 30° circular sector of unit radius contains an isometric copy of every drapeable unit arc, and we describe the family of drapeable exit arcs of unit length in the sector. The conjecture that this sector is a cover for the family of all unit arcs remains unresolved.

Author(s):  
N. A. Sereda

The article examines crank-rocker mechanisms. Such mechanisms are used in transport and technological machines. The article is devoted to the search for a new family of crank-rocker mechanisms. A mathematical model of a new family of crank-rocker mechanisms is obtained. In this family, the maximum transmission angle reaches 90 when the crank angle is 75. Thus, the new family of crank-rocker mechanisms differs from the known families by the position of the mechanism in which the maximum of the transmission angle function takes place. It is shown that, with a certain ratio of link lengths, the new family corresponds to the known families KKM-5 and KKM-7. The area of existence of a new family of crank-rocker mechanisms is established. This area is bounded by the arc of the circle of the unit radius and the curve. The mentioned curve is based on a joint solution of a mathematical model of a new family of mechanisms and the famous Kolchin straight line. The dependence for the minimum transmission angle is obtained. A formula for determining the angle of the rocker arm span is proposed. A graphical interpretation of the mentioned dependencies and formulas is constructed. The scope of existence of a new family of crank-rocker mechanisms and graphical interpretations are used in determining the geometric parameters of mechanisms. These mechanisms are part of a new family of mechanisms.


Author(s):  
Matthias Jakob ◽  
A. C. Offord

SynopsisThis is a study of the family of power series where Σ αnZn has unit radius of convergence and the εn are independent random variables taking the values ±1 with equal probability. It is shown that ifthen almost all these power series take every complex value infinitely often in the unit disk.


2000 ◽  
Vol 30 (9) ◽  
pp. 1443-1452 ◽  
Author(s):  
Alena Jonsson ◽  
Gösta Eriksson ◽  
Zhi-hong Ye ◽  
Francis C Yeh

Stored seeds from 30 open-pollinated families that had been field tested for 28 years provided a retrospective opportunity to assess the efficiency of early testing in Scots pine (Pinus sylvestris L.). Seedlings height at the end of first (HGP1), second (HGP2) and third growth period (HGP3), and in the third growth period, leader length (LEADER3), basal stem diameter (DIA3), number of stem units (NSU3), mean stem unit length (MSUL3), aboveground fresh weight (AGFWT3), stem dry weight (STDWT3), and shoot and needle dry weight (SHNDWT3) were studied under wide and dense spacing. Families differed at the 1 or 0.1% level of probability. Differences between spacing were significant at the 0.01% level of probability for all traits measured in the third growth period. Families interacted significantly with spacing for HGP2, HGP3, LEADER3, AGFWT3, SHNDWT3 and MSUL3. Interactions were due to rank changes and the interaction component of variance varied from 26 to 96% of the family variance. Estimates of hi2over wide and dense spacing ranged between 0.23 ± 0.11 (HGP2) and 0.51 ± 0.14 (NSU3). Spacing did not alter the variance structure, hi2for each trait under wide or dense spacing were similar. However, spacing affected the phytotron-field genetic correlations. The average of 80 genetic correlation estimates was 0.52 under wide spacing and 0.29 under dense spacing. Averaged over eight field traits, the efficiency of indirect juvenile selection for the field traits indirect-direct selection percentage ranged from -15% for NSU3 under dense spacing to 99% for HGP3 under wide spacing.


1988 ◽  
Vol 62 (03) ◽  
pp. 419-423 ◽  
Author(s):  
Baba Senowbari-Daryan ◽  
George D. Stanley

Two Upper Triassic sphinctozoan sponges of the family Sebargasiidae were recovered from silicified residues collected in Hells Canyon, Oregon. These sponges areAmblysiphonellacf.A. steinmanni(Haas), known from the Tethys region, andColospongia whalenin. sp., an endemic species. The latter sponge was placed in the superfamily Porata by Seilacher (1962). The presence of well-preserved cribrate plates in this sponge, in addition to pores of the chamber walls, is a unique condition never before reported in any porate sphinctozoans. Aporate counterparts known primarily from the Triassic Alps have similar cribrate plates but lack the pores in the chamber walls. The sponges from Hells Canyon are associated with abundant bivalves and corals of marked Tethyan affinities and come from a displaced terrane known as the Wallowa Terrane. It was a tropical island arc, suspected to have paleogeographic relationships with Wrangellia; however, these sponges have not yet been found in any other Cordilleran terrane.


Author(s):  
L.E. Murr

Ledges in grain boundaries can be identified by their characteristic contrast features (straight, black-white lines) distinct from those of lattice dislocations, for example1,2 [see Fig. 1(a) and (b)]. Simple contrast rules as pointed out by Murr and Venkatesh2, can be established so that ledges may be recognized with come confidence, and the number of ledges per unit length of grain boundary (referred to as the ledge density, m) measured by direct observations in the transmission electron microscope. Such measurements can then give rise to quantitative data which can be used to provide evidence for the influence of ledges on the physical and mechanical properties of materials.It has been shown that ledge density can be systematically altered in some metals by thermo-mechanical treatment3,4.


Author(s):  
S.B. Andrews ◽  
R.D. Leapman ◽  
P.E. Gallant ◽  
T.S. Reese

As part of a study on protein interactions involved in microtubule (MT)-based transport, we used the VG HB501 field-emission STEM to obtain low-dose dark-field mass maps of isolated, taxol-stabilized MTs and correlated these micrographs with detailed stereo images from replicas of the same MTs. This approach promises to be useful for determining how protein motors interact with MTs. MTs prepared from bovine and squid brain tubulin were purified and free from microtubule-associated proteins (MAPs). These MTs (0.1-1 mg/ml tubulin) were adsorbed to 3-nm evaporated carbon films supported over Formvar nets on 600-m copper grids. Following adsorption, the grids were washed twice in buffer and then in either distilled water or in isotonic or hypotonic ammonium acetate, blotted, and plunge-frozen in ethane/propane cryogen (ca. -185 C). After cryotransfer into the STEM, specimens were freeze-dried and recooled to ca.-160 C for low-dose (<3000 e/nm2) dark-field mapping. The molecular weights per unit length of MT were determined relative to tobacco mosaic virus standards from elastic scattering intensities. Parallel grids were freeze-dried and rotary shadowed with Pt/C at 14°.


Author(s):  
E. S. Boatman ◽  
G. E. Kenny

Information concerning the morphology and replication of organism of the family Mycoplasmataceae remains, despite over 70 years of study, highly controversial. Due to their small size observations by light microscopy have not been rewarding. Furthermore, not only are these organisms extremely pleomorphic but their morphology also changes according to growth phase. This study deals with the morphological aspects of M. pneumoniae strain 3546 in relation to growth, interaction with HeLa cells and possible mechanisms of replication.The organisms were grown aerobically at 37°C in a soy peptone yeast dialysate medium supplemented with 12% gamma-globulin free horse serum. The medium was buffered at pH 7.3 with TES [N-tris (hyroxymethyl) methyl-2-aminoethane sulfonic acid] at 10mM concentration. The inoculum, an actively growing culture, was filtered through a 0.5 μm polycarbonate “nuclepore” filter to prevent transfer of all but the smallest aggregates. Growth was assessed at specific periods by colony counts and 800 ml samples of organisms were fixed in situ with 2.5% glutaraldehyde for 3 hrs. at 4°C. Washed cells for sectioning were post-fixed in 0.8% OSO4 in veronal-acetate buffer pH 6.1 for 1 hr. at 21°C. HeLa cells were infected with a filtered inoculum of M. pneumoniae and incubated for 9 days in Leighton tubes with coverslips. The cells were then removed and processed for electron microscopy.


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