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Plasma Ca concentration (annual mean) in males Coturnix cotumix coturnix was 10.27 +/- 0.14 mg/100 ml while it was slightly higher (11.85 +/- 0.15 mg/100 ml) among females. Plasma Pi levels (annual mean) in males and females were 5.62 +/- 0.12 mg/100 ml and 6.52 +/- 0.20 mg/100 ml, respectively. While the males did not exhibit marked fluctuation in plasma Ca and Pi levels either in winter or summer, the females did record significant elevation in the levels of both these electrolytes during breeding season. The peak values of plasma Ca (17.66 +/- 0.38 mg/100 ml) and Pi (8.64 +/- 0.22 mg/100 ml) in females were observed during June. Parathyroid gland of the grey quail exhibited hyperactivity (hypertrophy and hyperplasia) during breeding season, however, the activity was more conspicuous among females than in males. The maximum increase in cell and nuclear diameters were observed in females during May-July. The follicles were also filled with AF- and PAS-positive materials during these months. The glands depicted signs of hypoactivity and degeneration during peak winter season (November-December) as evident by decrease in cell and nuclear diameters as well as vacuolation in the chief cells.
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The mechanics of avian take-off are central to hypotheses about flight evolution, but have not been quantified in terms of whole-body movements for any species. In this study, I use a combination of high-speed video analysis and force plate recording to measure the kinematics and mechanics of ground take-off in the European starling Sturnis vulgaris and the European migratory quail Coturnix coturnix. Counter to hypotheses based on the habits and morphology of each species, S. vulgaris and C. coturnix both produce 80-90 % of the velocity of take-off with the hindlimbs. S. vulgaris performs a countermovement jump (peak vertical force four times body weight) followed by wing movement, while C. coturnix performs a squat jump (peak vertical force 7.8 times body weight) with simultaneous wing movement. The wings, while necessary for continuing the movement initiated by the hindlimbs and thereafter supporting the body weight, are not the primary take-off accelerator. Comparison with one other avian species in which take-off kinematics have been recorded (Columba livia) suggests that this could be a common pattern for living birds. Given these data and the fact that running take-offs such as those suggested for an evolving proto-flier are limited to large or highly specialized living taxa, a jumping model of take-off is proposed as a more logical starting point for the evolution of avian powered flight.
A study was conducted to determine the effects to two dietary compounds, biochanin A and ferulic acid, on the reproductive performance of Japanese quail, Coturnix coturnix. These compounds may be present in the diet of wild birds during dry years or at the end of the growing season during normal years. Four treatment groups, each fed a diet supplemented with biochanin A or ferulic acid, and a control group were tested for morphological and behavioral effects before, during and after treatment. Fertility and hatchability data were collected during treatment only. Ferulic acid was shown to inhibit male copulatory behavior during treatment. Biochanin A inhibited male copulatory behavior during and after treatment. Neither drug affected female copulatory behavior though egg-laying was inhibited by the low dose of biochanin A. Ferulic acid significantly reduced the hatchability of eggs. Biochanin A increased the fertility of males and the hatchability of eggs fertilized by them. A correlation between results of this study and natural conditions of reproduction is discussed. It is concluded that both biochanin A and ferulic acid exert inhibiting influences on the reproductive behavior of Coturnix.
The quail, Coturnix coturnix, is small, gentle, hardy, adaptable, easy to house, and economical to maintain. Wetherbee and Jacobs (1960) call it the "Drosophila of the avian laboratory," and yet this charming bird is virtually unknown to the psychological laboratory. Our preliminary investigations show that the pecking operant is readily conditioned and that little or no deprivation is necessary to maintain behavior with food as a reinforcer. Visual and temporal discriminations were very quickly made. Our observations suggest that the social behavior of these birds might be a fruitful area for psychological study. On the basis of our somewhat limited observations, we believe that C. coturnix should prove a useful experimental animal for comparative studies, for basic research in learning, motivation, and perhaps social behavior, and for teaching the analysis of behavior in demonstrations and laboratory courses.
Coturnix kept in a 14L:10D photoperiod from hatch began to lay their first eggs at a mean age of 42.8 days (range 38-55). Approximately 2/3 of Coturnix held from hatch in photoperiods of 6L:16D light were laying at 165 days of age. Mean age at first egg was 112.7 days (range 68-162 days) in 8L:16D and 130.8 days (range 117-158 days) in 6L:18D photoperiod. Coturnix transferred from a non-stimulatory (8L:16D) photoperiod to a stimulatory one (14L:10D or 24L) begun laying in 15-20 days if less than 140 days old, and in about 5 days if greater than 140 days old, when trasferred. Birds which has spontaneously begun to lay in an 8L:16D photoperiod did not stop laying when the photoperiod was reduced to 6L:18D. Those which began laying under 14L:10D photoperiod ceased laying in about 15 days if 89 or fewer days old when switched to 8L:16D, or in about 6 days if 140 or more days old. Those switched from 14L:10D to 6L:18D ceased laying in about 13 days when 76 days old, and 7 days when 89 days old.
The embryogenesis of the proctodeal gland and development of the connective tissue of the associated lamina propria in the dorsal wall of the proctodeum of Common Coturnix (Coturnix c. japonica) were studied on embryos collected at 12-hour intervals from day 7 of incubation through hatching. Gland development began at 9.5 days from ectodermal-derived epithelial buds developing in the craniolateral region of the dorsal proctodeal epithelium. At 11 days, the epithelial buds had become solid convoluted epithelial cords which, by 11.5 days branced to form solid individual glandular units. Lumina of the unit were formed by degeneration and vacuolization of the central cells of these solid units. Squamous epithelial caps, several layers thick, separated the vacuolizing units from the proctodeal cavity at day 13; these caps subsequently thinned, bulged into the proctodeal cavity and, by day 16, began to disappear opening the lumen of the units to the proctodeal cavity. Sequential formation of epithelial buds, by region, was: craniolateral at 9.5 days, craniomedial expansion at 10.5 days followed, beginning at 11 days, by caudal expansion along entire dorsal proctodeal wall. Sequence of appearance of gland-associated connective tissue fibers was: 9.5 days, reticular fibers already present; 11 days, collagen fibers; 11.5 days elastic fibers. Serially reconstructed models of an individual glandular unit at hatching enabled classification of the unit as a simple branched alveolar gland.
Despite extensive knowledge of the neuroepithelial endocrine (NEE) system in the lungs of species of various vertebrate classes, data on avians are limited. The present investigation deals with the light- and electron-microscopical immunocytochemistry and morphology of pulmonary NEE cells in the quail, Coturnix coturnix. Light-microscopically, serotonin immunoreactivity was detected in numerous solitary and clustered NEE cells located in the cilio-mucous epithelium of primary and secondary bronchi in adult as well as in newly hatched quails. Only in newly hatched quails could a small number of bombesin- and somatostatin-like immunoreactive NEE cells be demonstrated. Electron-microscopical morphology revealed that NEE cells contained dense-cored vesicles of a wide range of diameters and electron densities. Nearly all of the NEE cells were seen to rest on the basement membrane of the cilio-mucous epithelium, lacking direct contact with the luminal surface. Nerve varicosities or nerve endings, of both afferent and efferent morphological appearance, were found directly apposed to the basal portion of NEE cells, invaginating between NEE cells or between NEE cells and adjacent epithelial cells. Often, synaptic specializations could be recognized between NEE cells and nerve terminals. Electron-microscopical immunocytochemistry confirmed that the intraepithelial serotonin-containing cells correspond to the cells with NEE characteristics. Moreover, two types of NEE cells could be distinguished in newly hatched quail lungs. Both types showed serotonin immunoreactivity selectively distributed over the dense-cored vesicles, but somatostatin- and bombesin-like immunoreactivities were only noted in one of the NEE cell types and were never seen colocalized. Thus, the avian NEE system too, harbors at least three different bioactive substances and has a morphology comparable to that of mammals, reptiles and amphibians.
By RT-PCR two transcripts for arylalkylamine N-acetyltransferase (AA-NAT; serotonin N-acetyltransferase; EC 2.3.1.87), the key enzyme in melatonin synthesis, were found, for the first time, in the oocytes and blastoderms from freshly laid eggs (323- and 238-bp RT-PCR products), and one (238-bp product) in the pineal gland of Japanese quail (Coturnix coturnix japonica). The two products differed by an intron of 85-bp present in the 323-bp band and absent from the 238-bp band. The identity of the products was confirmed by restriction analysis and sequencing. The ratio of the 323:238-bp bands changed during oogenesis from approximately 17:1 in small 3-mm oocytes to approximately 4:1 in immature vitellogenic oocytes and approximately 1:1 in mature, preovulatory oocytes; it was reversed to approximately 0.2:1 in blastoderms from fertile freshly laid eggs, corresponding to embryo of approximately 40,000 cells. It is proposed that the longer 323-bp product, containing an intron, represents a translationally inactive form of the transcript, stored in maternal RNA. The shorter 238-bp product lacking an intron may represent the mature active AA-NAT mRNA found in the pineal gland and in early embryos, and-to a lower proportion-in older oocytes. These data constitute the first direct proof of an intron sequence in maternal RNA of avian oocyte. It is possible that differential processing of the immature mRNA is part of a transcriptional regulation mechanism of AA-NAT activity. A possible role of extrapineal melatonin in early avian development is discussed.
The hypothalamus of Japanese quail, Coturnix coturnix japonica, has been studied by means of the peroxidase-antiperoxidase immunocytochemical method, with the use of antibodies to synthetic neurotensin (NT). A number of immunoreactive neuronal perikarya occur in the medial preoptic nucleus of the rostral hypothalamus and a few in the accessory part of paraventricular nucleus and dorsal portion of the infundibular nucleus. Some of them correspond to the parvocellular neurons previously identified tentatively as neurosecretory (Mikami et al. 1975, 1976). Large numbers of immunoreactive neuronal fibers are found in the preoptic area, which extend as a remarkable fiber tract from this area to the ventral septal area and to the subfornical organ. A few immunoreactive fibers also extend ventrocaudally to the infundibular nucleus and to the neural lobe.
Neuronal morphology and dendritic architecture of the tuberal and mammillary regions in the hypothalamus of the quail (Coturnix coturnix japonica) were investigated by means of classical neuroanatomical methods (Bodian silver impregnation, Luxol-fast blue, cresyl violet, toluidine blue, rapid Golgi method). The tuberal region is characterized by isodendritic neurons, in particular: a) pyriform and bipolar neurons, occasionally arranged diagonally to the ventricular surface; b) CSF-contacting neurons, located subependymally or more deeply in the periventricular gray, which are especially abundant in the paraventricular organ and in the proximity of the median eminence; c) numerous multipolar neurons, endowed with stout, almost unbranched dendritic processes, occupying generally the medio-lateral areas of the hypothalamus. Some multipolar neurons display somata, pyramidal or ovoidal in shape, almost imperceptibly tapering into three or more dendritic trunks. These relatively straight and long dendrites are rich in dendritic spines. In the mammillary region, Golgi impregnation shows multipolar neurons of medium size, most likely belonging to the lateral mammillary nucleus.
In Japanese quail, Coturnix coturnix japonica the tanycytes of the median eminence absorbed peroxidase injected into the third ventricle. The number of tanycytes showing peroxidase reaction was greater in the posterior median eminence than in the anterior median eminence. Following hypothalamic deafferentation, the tanycyte absorption was augmented both in the posterior and anterior median eminence. These findings suggest that axons of some neurons, which have inhibitory action on the tanycyte absorption, were transected by deafferentation resulting in augmentation of tanycyte absorption. A considerable number of ependymal cells lining the upper portion of the third ventricle and those of the pars nervosa also absorbed peroxidase. In birds with a deafferented hypothalamus, photostimulated ovarian growth was completely inhibited.
Monoamine fluorescence was examined in the ventral hypothalamus of the Japanese quail, Coturnix coturnix japonica after medial basal hypothalamic deafferentation. In sham-operated control birds, numerous yellow-green fluorescent fibers were observed in the median eminence and the nucleus tuberis. In the area of the paraventricular organ, a number of fluorescent fibers and cell bodies were observed. In birds with deafferented hypothalami, fluorescence disappeared both in the median eminence and the nucleus tuberis. In the area of the paraventricular organ, which was within the area of deafferentation, fluorescence of neuronal perikarya did not change, but fluorescent fibers decreased markedly in number. Disappearance of monoamine fluorescence in the median eminence and the nucleus tuberis is discussed in relation to the tanycyte absorptive function and gonadaly development.
Ultrastructural and ultrahistochemical studies were performed on the uterovaginal sperm host glands of the quail (Coturnix coturnix japonica). The proximal parts of the glandular necks are lined by a pseudostratified epithelium, consisting of high columnar ciliated cells and small, irregular shaped, basal cells. The true glandular epithelium is composed only of columnar cells with microvilli on their luminal end. A characteristic luminal feature is a large lipid droplet in the perinuclear region. In the subplasmalemmal region numberous tubular profiles are seen which could represent a cellular resorption system. To evaluate the absorptive capacity of the uterovaginal sperm host glands, tracer studies with HRP, ferritin, lanthanum and ruthenium red were undertaken. Since between 5 min and 3 h after injection no absorption could be found with the techniques mentioned, it is suggested that phagocytosis of spermatozoa by the glandular epithelium is not likely to occur.
Mechanisms inducing drinking after water deprivation, and mechanisms terminating drinking after rehydration, were investigated in the quail, Coturnix coturnix japonica. 1. Water intake was induced after 4 h of water deprivation, and the amount of water drunk increased in proportion to the period of water deprivation. Drinking occurred immediately after deprivation. Drinking occurred immediately after deprived birds were given access to water, and continued for periods proportional to the period of water deprivation. 2. Plasma angiotensin II concentration increased, as did plasma osmolality and Na+ concentration, and blood volume decreased after water deprivation. The increase in plasma angiotensin II concentration and decrease in blood volume occurred soon after the start of water deprivation, whereas plasma osmolality and Na+ concentration did not increase until at least 4 h after the start of water deprivation. 3. These results indicate that extracellular dehydration and angiotensin II are responsible for the significant drinking that follows 4 h of water deprivation, and that cellular dehydration is also involved in the stimulation of drinking that occurs after longer periods of water deprivation. 4. Plasma osmolality and Na+ concentration in birds deprived of water for 48 h quickly returned to normal levels after the birds were allowed access to water. Plasma angiotensin II levels and blood volume also approached the values measured prior to water deprivation. However, the rate and degree of restoration of normal values were reduced, and normal values were not restored even after 1.5 h or rehydration when drinking terminated.(ABSTRACT TRUNCATED AT 250 WORDS)