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Urinary bladders and urethrae were collected from six adult and two juvenile female dogs. Five urethral regions and the neck and body of the bladder were sampled. Volume fractions for connective tissue including elastic fibers, smooth and striated muscle, and epithelium were obtained by projecting section images onto an array of points and computing the number of points overlying a tissue constituent per total points overlying the tissue section. Smooth muscle occupied approximately half the volume of the bladder wall, one-third the volume of the vesical neck, and one-fourth the volume of the proximal urethra. Striated muscle was present in the distal half of the urethra, where the total muscle coat occupied about one-third of the urethral wall volume. Smooth muscle was practically absent in the terminal urethra, where the striated urethralis muscle encircles urethra and vagina in common. Epithelial area and lumen perimeter were not significantly different along the length of the urethra except that urethral epithelium was significantly thicker adjacent to the vesical neck. In terms of histological proportions, the vesical neck was intermediate between the body of the bladder and the proximal urethra.

Lumbar and sacral afferent axons in the submucosa of the urinary bladder were recognized by degeneration in seven cats subjected to spinal ganglionectomies. Of 2,935 observed terminating axon profiles, 145 were found degenerating. Lumber afferent axons were 3.7 times more numerous than sacral afferent axons in the submucosa, a reversal of the ratio reported for the muscle coat of the bladder. Sacral afferent axons were evenly distributed to different regions of the bladder, but lumbar afferents were concentrated in the bladder neck. Apparent afferent endings in the submucosa of the urinary bladder were principally free nerve endings. Synaptic vesicles were found in 57% of observed terminating axon profiles. The bladder neck had more terminating axon profiles of all kinds than other regions of the urinary bladder.

Urinary bladders and pelvic urethrae were collected from six adult and two juvenile male dogs. Within two vesical and six urethral sampling regions, volume densities were estimated for smooth and striated muscle, connective tissue and elastic fibers, stratum cavernosum, luminal epithelium, and prostate. The neck had significantly less smooth muscle and more connective tissue than the body of the bladder. In the prostatic urethra, smooth muscle was associated principally with trabeculae surrounding prostate lobules. Smooth muscle was sparse superficially in the prostatic capsule and practically absent in relation to the mid-prostatic urethra. Thus there was no mechanism for active closure of the middle prostatic urethra, and elastic fiber density was correspondingly high in this region. The smooth muscle sphincter needed to maintain urinary continuence and prevent semen reflux was primarily the vesical neck. Caudal to the body of the prostate, striated muscle comprised more than 40% of the urethral wall. Juvenile and adult postprostatic urethrae were similar except for a decreased quantity of stratum cavernosum in the pups.

Cilia in neonatal canine articular chondrocytes were studied using morphometric techniques and transmission electron microscopy. The cilia in chondrocytes were morphologically similar to cilia in a variety of other cell types. A chondrocytic cilium consisted of a basal body and a ciliary shaft. The cylindrical basal body was 0.21 micron (S.D. = 0.01 micron) in diameter, 0.50 micron (S.D. = 0.03 micron) in length and contained nine microtubular triplets. The ciliary shaft was 0.196 micron (S.D. = 0.02 micron) in diameter and 1.76 micron (S.D. = 0.80 micron) in length. The number of microbtubular doublets in the ciliary shaft varied depending on where along the length of the shaft the section was taken. This study demonstrates that on the average the frequency of cilia in neonatal articular chondrocytes, as estimated sterologically, was about one cilium per cell.

Capillary density and capillary orientation in canine spinal cords were estimated by calculating actual lengths, surfaces, and volumes of capillary segments in tissue sections. Transverse, sagittal, and frontal section planes were samples from dorsal, ventral, and lateral funiculi and from dorsal and ventral gray horns of spinal segments C3, T6, and L3 from three dogs. Capillaries were defined as vessels less than 10 micrometer in diameter. Electron microscopy of 104 such vessels revealed no muscle coat but collagen fibrils between endothelium and astrocyte process in 68% of the white matter capillaries and 16% of those in gray matter. Capillary diameter was significantly different among regions in some cases, but consistent patterns of variation were not found. Capillary density was four to five times greater in gray matter than in white matter. Capillary density differed significantly among the same-size dogs, but within dogs, density was similar among segments and within gray matter and white matter regions. In 62% of the transverse sections, capillary orientation was always along the craniocaudal axis of the spinal cord. The craniocaudal orientation was significant in 96% of the white matter sections and 78% of the gray sections, and in 97% of the cervical and thoracic sections but only 73% of the lumbar sagittal and frontal sections. Because capillary orientation is neither isotropic nor regular, unbiased, low-variance estimates of capillary density cannot be expected without resorting to excessive sampling. An efficient method of quantifying spinal capillaries for comparative purposes by counting number of profiles per unit area is recommended.