Growing Short Hair, Long Hair, Grass, and Electric Arcs with Fur and nHair

2014 ◽  
pp. 33-66
Keyword(s):  
2020 ◽  
Vol 98 (Supplement_4) ◽  
pp. 307-307
Author(s):  
Matthew McIntosh ◽  
Alfredo Gonzalez ◽  
Andres Cibils ◽  
Rick Estell ◽  
Shelemia Nyamuryekung’e ◽  
...  

Abstract Raramuri Criollo (RC) are one of 33 known biotypes of heritage Criollo cattle that exist throughout the Americas today. They have been raised by the Tarahumara peoples of the Copper Canyon in Chihuahua, Mexico, for over 400 years and exhibit remarkable rusticity and adaptation to harsh grazing environments. To date, no quantitative phenotypic description of this biotype exists. Our objective was to characterize RC cattle via 26 phenotype traits to provide a preliminary biotype standard. Twenty-eight multiparous RC cows, 4 primiparous heifers, and 4 bulls were selected from a purebred herd of approximately 200 animals at the USDA-ARS Jornada Experimental Range. These 36 animals were selected by a Criollo cattle expert based on body conformation correctness. SAS 9.4 was used to determine means, SEs or frequency of measured traits. Multiparous pregnant and cycling cows averaged 366.8 ± 9.8 kg live body weight, 121.8 ± 0.9 cm withers height, horn widths of 60.3 ± 1.6 cm, horn diameters of 5.7 ± 0.1 cm, chest girths of 183.6 ± 12.0 cm, hip widths of 44.5 ± 0.5 cm, flank girths of 52.2 ± 0.9 cm, body length of 90.0 ± 1.7 cm, neck lengths of 52.0 ± 0.9 cm, and tail lengths of 83.3 ± 1.4 cm. Bulls consistently averaged higher values for all traits and weighed 618.2 ± 9.8 kg with scrotal circumferences of 36.8 ± 0.7 cm. RC cattle exhibited mostly convex nose bridges (89%), open-back horns (49%), black muzzles, hooves, and eyes (62, 69, and 81%, respectively), small ears (78%), oblique eyes (70%), high-set tail heads (86%), short hooves (95%), and short hair (78%). Our preliminary characterization of RC phenotypes will be useful in selecting RC individuals for genotypic evaluation to eventually maintain a distinct purebred registry of this Criollo biotype.


2010 ◽  
Vol 72 (3) ◽  
pp. 293-296 ◽  
Author(s):  
Hojjatollah SHOKRI ◽  
AliReza KHOSRAVI ◽  
MohammadAli RAD ◽  
Shahram JAMSHIDI

1966 ◽  
Vol 20 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Richard H. Tourin

Spectroscopy is a useful means to study the ways in which energy is transferred within and from plasmajets and electric arcs. For this purpose, measurements of spectral intensities and line widths are applied to measure thermodynamic properties of the hot ionized gases. Methods, apparatus, and applications are illustrated by examples from the author's laboratory.


1998 ◽  
Vol 70 (6) ◽  
pp. 1163-1168 ◽  
Author(s):  
C. Delalondre ◽  
Alain Bouvier ◽  
Ange Caruso ◽  
Namane Méchitoua ◽  
O. Simonin ◽  
...  

1991 ◽  
Vol 24 (1) ◽  
pp. 26-35 ◽  
Author(s):  
A D Stokes ◽  
W T Oppenlander
Keyword(s):  

2013 ◽  
Vol 109 (8) ◽  
pp. 2007-2020 ◽  
Author(s):  
Xiaodong Tan ◽  
Maryline Beurg ◽  
Carole Hackney ◽  
Shanthini Mahendrasingam ◽  
Robert Fettiplace

The avian auditory papilla contains two classes of sensory receptor, tall hair cells (THCs) and short hair cells (SHCs), the latter analogous to mammalian outer hair cells with large efferent but sparse afferent innervation. Little is known about the tuning, transduction, or electrical properties of SHCs. To address this problem, we made patch-clamp recordings from hair cells in an isolated chicken basilar papilla preparation at 33°C. We found that SHCs are electrically tuned by a Ca2+-activated K+ current, their resonant frequency varying along the papilla in tandem with that of the THCs, which also exhibit electrical tuning. The tonotopic map for THCs was similar to maps previously described from auditory nerve fiber measurements. SHCs also possess an A-type K+ current, but electrical tuning was observed only at resting potentials positive to −45 mV, where the A current is inactivated. We predict that the resting potential in vivo is approximately −40 mV, depolarized by a standing inward current through mechanotransducer (MT) channels having a resting open probability of ∼0.26. The resting open probability stems from a low endolymphatic Ca2+ concentration (0.24 mM) and a high intracellular mobile Ca2+ buffer concentration, estimated from perforated-patch recordings as equivalent to 0.5 mM BAPTA. The high buffer concentration was confirmed by quantifying parvalbumin-3 and calbindin D-28K with calibrated postembedding immunogold labeling, demonstrating >1 mM calcium-binding sites. Both proteins displayed an apex-to-base gradient matching that in the MT current amplitude, which increased exponentially along the papilla. Stereociliary bundles also labeled heavily with antibodies against the Ca2+ pump isoform PMCA2a.


1974 ◽  
Vol 94 (10) ◽  
pp. 417-424
Author(s):  
A. TAKAHASHI ◽  
K. MIYACHI
Keyword(s):  

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