Low-Permeation Fuel Fill and Vent Tube

2021 ◽  
Author(s):  
Keyword(s):  
1991 ◽  
Vol 290 (1) ◽  
pp. 66-78 ◽  
Author(s):  
Franco Renosto ◽  
Robert L. Martin ◽  
Jeffrey L. Borrell ◽  
Douglas C. Nelson ◽  
Irwin H. Segel

1961 ◽  
Vol 42 (5) ◽  
pp. 311-313
Author(s):  
F. B. Gomm

This article describes a modified collection unit for the standard Weather Bureau-type rain gage. The described unit, consisting of a polyethylene bottle, rubber stopper, vent tube and adapter funnel, replaces the metal collection tube of the standard gage. In a laboratory test, evaporation from the modified system was not great enough in a 30-day period to measure with a standard measuring tube. Field tests showed the described unit superior to the standard collection unit and equal to the standard unit with a 0.20-inch oil film in the reduction of evaporation. The described unit, which eliminates recharging with oil or antifreeze after each reading, has been in field use for two years without damage from freezing.


2013 ◽  
Vol 46 (4) ◽  
pp. 1236-1239 ◽  
Author(s):  
S. Pangelis ◽  
S. R. Olsen ◽  
J. Scherschligt ◽  
J. B. Leão ◽  
S. A. Pullen ◽  
...  

A combined solution is presented for minimizing the safety hazards associated with closed cycle cryostats described by Swainson & Cranswick [J. Appl. Cryst.(2010),43, 206–210]. The initial solution is to install a vent tube with one open end deep inside the sample space and a pressure relief valve at the top. This solution works for either a cryogen or a cryogen-free (closed cycle) system. The second approach, which can be combined with the first and is applicable to cryogen-free cryostats, involves electrically interlocking the closed cycle refrigerator compressor to the sample space, so that the system cannot be cooled in the presence of a leak path to air.


2020 ◽  
Author(s):  
Tjorven Hinzke ◽  
Manuel Kleiner ◽  
Mareike Meister ◽  
Rabea Schlüter ◽  
Christian Hentschker ◽  
...  

AbstractThe hydrothermal vent tube worm Riftia pachyptila lives in intimate symbiosis with intracellular sulfur-oxidizing gammaproteobacteria. Although the symbiont population consists of a single 16S rRNA phylotype, bacteria in the same host animal exhibit a remarkable degree of metabolic diversity: They simultaneously utilize two carbon fixation pathways and various energy sources and electron acceptors. Whether these multiple metabolic routes are employed in the same symbiont cells, or rather in distinct symbiont subpopulations, was unclear. As Riftia symbionts vary considerably in cell size and shape, we enriched individual symbiont cell sizes by density gradient centrifugation in order to test whether symbiont cells of different sizes show different metabolic profiles. Metaproteomic analysis and statistical evaluation using clustering and random forests, supported by microscopy and flow cytometry, strongly suggest that Riftia symbiont cells of different sizes represent metabolically dissimilar stages of a physiological differentiation process: Small symbionts actively divide and may establish cellular symbiont-host interaction, as indicated by highest abundance of the cell division key protein FtsZ and highly abundant chaperones and porins in this initial phase. Large symbionts, on the other hand, apparently do not divide, but still replicate DNA, leading to DNA endoreduplication. Highest abundance of enzymes for CO2 fixation, carbon storage and biosynthesis in large symbionts indicates that in this late differentiation stage the symbiont’s metabolism is efficiently geared towards the production of organic material. We propose that this division of labor between smaller and larger symbionts benefits the productivity of the symbiosis as a whole.


Zootaxa ◽  
2007 ◽  
Vol 1435 (1) ◽  
pp. 1 ◽  
Author(s):  
M. FLORENCIA VERA CANDIOTI ◽  
FRANCISCO BRUSQUETTI ◽  
FLAVIA NETTO

In this paper we characterize the morphology of Leptodactylus elenae tadpoles (L. fuscus group) from central Paraguay, considering external morphology, oral disc, buccopharyngeal cavity, skeleton and musculature (N = 17; Gosner Stage 36–37; Central, Paraguay). Specimens were fixed with 10% formaline and were prepared according to a classic staining protocol. These larvae show external traits similar to those of other taxa within the group, such as an ovoid and depressed body, left spiracle, ventromedial vent tube, and marginal papillae interrupted in a wide rostral gap. Distinctive features are the rounded snout, the distally wide and rounded tail, the labial tooth formula 2(2)/3(1), lateral constrictions absent, and the large internal marginal papillae, intercalated every two or four small external marginal papillae. Inside the buccopharyngeal cavity, traits shared with related species are the prenarial ridge, the transversal nares, two pairs of infralabial papillae, the medial ones joined at their bases, four lingual papillae, and dorsal and ventral vela with secretory epithelium. Skeletal configuration is constant within the genus, with common character states such as the quadripartite suprarostral cartilage, quadratoorbital commissure and larval crista parotica present, larval otic process absent, ceratobranchials fused to the hypobranchial plates, anterior branchial process, and basihyal absent. Leptodactylus elenae and other L. fuscus group species resemble taxa from the L. pentadactylus group, due to the configuration of the branchial process, the articular process of the palatoquadrate, the suspensorium, and the trabecular horns; this can be observed in the chondrocranium and hyobranchial skeleton morphospaces for 22 species of the genus. Finally, muscular features are also maintained at intra-genus level, with common traits such as m. mandibulolabialis superior absent, mm. diaphragmatopraecordialis, interhyoideus posterior and hyoangularis medialis present, m. subarcualis rectus I with 3 slips, and m. subarcualis rectus II–IV inserted on ceratobranchial III. Further analyses on intraspecific variation and descriptions of related larvae are needed to improve the knowledge about this diverse genus.


Science ◽  
1981 ◽  
Vol 213 (4505) ◽  
pp. 344-346 ◽  
Author(s):  
J. B. WITTENBERG ◽  
R. J. MORRIS ◽  
Q. H. GIBSON ◽  
M. L. JONES

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