Development and metabolism of chicken embryos in the prenatal period under acoustic stimulation

Acoustic influence on the metabolic process in the last days of incubation of embryos of domestic chicken was found. It was shown that the changes that appear under the influence of acoustic signals lead to a decrease in incubation time. As a result of acoustic hyperstimulation, gaseous exchange and growth of the embryo continue to follow a power dependence characteristic of an earlier period of embryogenesis, i.e., the depression typical of these processes in the end of incubation is arrested. In acoustically stimulated embryos, a tendency toward a decrease in the total energy expenses on growth and metabolism is observed in the period from 17 days of incubation up to hatching, but the daily expenses on energetic exchange and growth are higher under acoustic influence than in the control group.     

Embryonic development and functional readiness of the sound-transmitting system of acoustic analyzer in Larus gulls

Morphometric parameters of the developing sound-transmitting system of the peripheral acoustic analyzer have been studied in embryos of the common gull (Larus canus) and black-headed gull (L. ridibundus) beginning from the second half of the incubation period. The results show that structures of the outer ear and the middle-ear columellar complex at the stage corresponding to 77?C79% of the incubation period have not yet completed morphogenesis and cannot perform their functions. At subsequent stages, morphometric characteristics of the columellar complex allow it to participate in sound transmission, but only in the air, while the embryos are still submerged in the amniotic fluid. Beginning from days 23?C24 (88?C92% of the incubation period) in L. canus and days 21?C22 (87?C91%) in L. ridibundus, the embryos perforate the shell membrane, start pulmonary respiration, and develop acoustic signaling. Since that time, the outer and middle ear become involved in continuous transmission of acoustic signal to the inner ear receptors.     

Germ cell cycles during sex inversion in chick embryos]

A study was made of the germ cell cycles of 11 days old embryos injected male or female hormones on the 4 th day of incubation. The cell cycles duration in genetically male 11 days embryos treated with esradiol-benzoate was close to that registered in oogonia of both treated and non-treated female embryos of the same age. The testosterone propionate injection caused an acceleration of the genetically male sex cell proliferation and a decrease of the reproduction rate of the female sex cells. It is proposed that under normal conditions female sex hormones inhibit a hypothethic factor that determines the decrease of cell proliferation during the male embryo development.     

Embryonic developmental plasticity of the chick: increased CO(2) during early stages of incubation changes the developmental trajectories during prenatal and postnatal growth

This study investigated the effect of non-ventilation of the incubator during the first 10 days of incubation on carbon dioxide (CO(2)) concentrations in the incubator and its effects on the embryonic and post-hatch development of the chicken (Gallus gallus). Two different incubation conditions were created, one incubator was kept at standard conditions, with adequate ventilation (V) and a second incubator was non-ventilated (NV) during the first ten days of incubation, allowing the CO(2) to rise. After the first 10 days, both incubations were continued under standard conditions. The experiment was repeated twice with different ages of the breeders (45 and 60 wks) which resulted in different CO(2) levels at ED10 (1.5 and 1%). The CO(2) concentration in the V incubators remained below 0.1% in these first 10 days. The eggs of the NV incubation showed higher pCO(2) levels in the air cell from ED10 until ED14 compared to the eggs of the V group. The NV embryos had significantly higher absolute and relative (to egg weight) body weights from ED10 until ED18, pointing to an accelerated embryonic growth. At internal pipping, the NV chick embryos had higher plasma corticosterone and T(3) levels and higher pCO(2) in the air cell. Chicks incubated under NV conditions hatched 10 h earlier in the first and 15 h earlier in the second experiment and the spread of hatch was narrower. During the post-hatch period, the NV chickens had a higher body weight compared to the V chickens. From these results, it is clear that higher levels of CO(2) during the first ten days of incubation have persistent (epigenetic) effects during the incubation and early post-hatch period.     

Changes in expressions of red blood cell antigens following gamma irradiation of chicken embryos

Red blood cells (RBC) from chicken embryos receiving 450 R of gamma-irradiation on the 6th day of incubation displayed various differences from controls with respect to agglutination properties in the presence of antibodies for three blood group antigens as assayed over a period extending from 12 days of incubation to after hatching. An alloantigen (B21), which normally can be detected prior to 10 days of incubation, showed increased agglutinability following radiation exposure at 6 days. Likewise, an 'embryonic' blood cell antigen, which normally would decrease rapidly after 12 days of incubation, persisted in the blood of irradiated embryos. On the other hand, an alloantigen (B19), which normally appears only after 10 days of incubation, was severely depressed in cases where the embryos received 450 R of gamma-irradiation. The authors propose that in the first two instances gene activation (or induction) for the respective RBC antigens had been accomplished prior to radiation exposure, whereas in the last instance induction had not been accomplished prior to the radiation insult and the gamma-rays had strongly interfered with this process.     

Spontaneous and benzo[a]pyrene-induced micronuclei in the embryos of the black-headed gull (Larus ridibundus L.)

The spontaneous levels of micronuclei in erythrocytes were established in embryos of the black-headed gull of two natural populations. In total 216 blood samples from the same number of individuals were examined. A statistically significant decrease in the number of spontaneous micronucleated erythrocytes was found after 13 days of incubation. We found no statistically significant difference in the spontaneous frequencies of micronucleated erythrocytes in the embryos of the two colonies studied, although they differed in anthropogenic load. Results of analysis of variance indicated that egg incubation time was the only variable significantly (P=0.0001) affecting spontaneous frequency of micronucleated erythrocytes in the embryos of black-headed gulls. We also took 78 eggs of different developmental stages from both colonies and exposed them for a further 24h to a dose of benzo[a]pyrene (30 microg per egg). After exposure to benzo[a]pyrene, the frequency of micronucleated erythrocytes was not increased in the embryos incubated for a total period of 13 days. A statistically significant increase in the number of micronucleated erythrocytes was recorded in the benzo[a]pyrene-treated embryos incubated for a total period of 14 days. Decrease in numbers of spontaneous micronucleated erythrocytes after the 13 day of incubation and increased levels of benzo[a]pyrene-induced micronuclei after the 13 day of incubation were discussed to be caused by changes in spleen and liver function in advanced developmental stages of the embryo.     

Electron microscope study of the developing nerve terminals in the acoustic organs of the chick embryo

Summary The stages of growth of the acoustic pathway (peripheral branch) were studied with the electron microscope in serial sections of the acoustic organs of 3 to 7 day chick embryos.Migration of cells from the acoustic epithelium was found at three days of incubation. These cells are presumably the futur ganglion cells. Fascicles of nerve fibers penetrate the epithelium through gaps of the basement membrane at 4–5 days of incubation. A dilatation develops in the intraepithelial fibers at about six days and thin and long prolongations grow from these dilatations and distribute among the cells. In the course of the next day the fibers embrace the foot of the sensory cell and the prolongations become shortened. Many of these extensions are charged with vesicles. At this stage (seven days) specialized structures (synaptic bars) differentiate in the region of the sensory cell contacting the large nerve ending (calix) or its short extensions. Each cell may show several synaptic bars, and each prolongation may contact with more than one cell.Research sponsored by the Air Force Office of Scientific Research, Office of Aerospace Research, United States Air Force, under AFOSR Grant Nr. 313-67.     

Critical periods during development as assessed by thallium-induced inhibition of growth of embryonic chick tibiae in vitro

In ovo application of thallium sulfate has been shown to produce a characteristic shortening and angulation of the tibia of the embryonic chick. The critical period for susceptibility to thallium-induced inhibition of tibial growth ends at 8 2/3 days of incubation, a time when the growth rate of the embryo declines by 55%. The aim of the present study was to expose tibiae to thallium in vitro to determine whether this response was intrinsic to the tibia. A 4-hour exposure to 400 micrograms thallium was found to be most effective. Growth of tibiae from 8-day-old embryos was inhibited, growth of tibiae from 9-day-old embryos was not, and the response of tibiae isolated from embryos of 8 2/3 days of incubation was intermediate. Therefore, the response of the tibia to thallium represents an intrinsic property and is not secondary to inhibited nerve growth as has been suggested. The critical period and its termination is also an intrinsic property of the tibia. Tibiae were exposed to thallium for 4 hours at various times after the tibiae had been established in vitro. Susceptibility to growth inhibition was shown to decline as tibiae developed beyond the critical period, a decline that could be correlated with a declining growth rate. Emphasis is placed upon critical events during development as a more useful concept than critical periods for explaining susceptibility to teratogens.     

Influence of egg size on embryos and larvae of Fundulus heteroclitus (L.)

Egg size for Fundulus heteroclitus (L.) populations is concordant with the distribution of the two F . heteroclitus subspecies, i.e. F. h. heteroclitus eggs are considerably larger than F. h. macrolepidotus eggs. The influence of egg size on survival of embryos during incubation and survival and growth of newly-hatched larvae was estimated for four populations representing both subspecies along the Atlantic coast of the United States and in Delaware Bay. Survival of embryos was determined for incubation periods of 14, 21 and 28 days. Greatest differences in survival were detected following the longest incubation period where less than 50 per cent of the smaller F. h. macrolepidotus eggs survived while little or no mortality was detected among the larger F. h. heteroclitus eggs . Influence of egg size on larval survival was also greatest among those larvae hatched after 28 days where F. h. macrolepidotus larvae survived without food, for an average of 6 days, while F. h. heteroclitus larvae survived 11–12 days. F. h. heteroclitus larvae were significantly larger at hatching than F. h. macrolepidotus larvae. Larval growth rates were the same (0.4 mm day⁻¹) in both subspecies. As a result, size differences at hatching were still maintained after 42 days of growth. The differences in egg size along with other morphological and reproductive characteristics of F. heteroclitus populations probably represent genetically based adaptations to environmental conditions, of which the length of the spawning season is one of the major components stimulating the coevolution of these traits.     

Effects of temperature during early life history on embryonic and larval development and growth in haddock

The effect of incubation temperature (2, 4, 6, 8 and 10° C) on haddock Melanogrammus aeglefinus development and growth during the embryonic period and in subsequent ontogeny in a common post‐hatch thermal environment (6° C) was investigated. Hatching times were inversely proportional to incubation temperature and ranged from 20·3 days at 2° C to 9·1 days at 10° C. Growth rates were directly proportional to incubation temperature during both the embryonic and larval periods. There was a significant decline in growth rates following hatch in all temperature groups. Compared to the endogenously feeding embryos, growth rates in the exogenous period declined by 4·4‐fold at 4° C to 3·9‐fold at 8° C, indicative of the demarcation between the endogenous and exogenous feeding periods. Yolk utilization varied from 17 days at 2° C to 6 days at 10° C and followed a three‐stage sigmoidal pattern with the initial lag period inversely proportional to incubation temperature. Time to 50% yolk depletion varied inversely with temperature but occurred 1–1·5 days post‐hatch at all temperatures. Additionally, the period between 10 and 90% yolk depletion also decreased with increased temperature. Overall developmental rate was sequential with and directly proportional (2·3‐fold increase) to incubation temperature while the time spent in each developmental stage was inversely proportional to temperature. Larger embryos tended to be produced at lower temperatures but this pattern reversed following hatch, as larvae from higher temperature groups grew more rapidly than those from other temperature groups. Larvae from all temperatures achieved a similar length (c.total length 4·5 mm) upon complete yolk absorption. The study demonstrated the significant impact that temperature has upon developmental and growth rates in both endogenous and exogenous feeding periods. It also illustrated that temperature changes during embryogenesis had significant and persistent effects on growth in subsequent ontogeny.     

Cardiac rhythms in prenatal and perinatal emu embryos

Emu eggs weigh approximately 600 g and have an incubation duration (ID) of approximately 50 days. The egg mass is approximately 10-fold heavier than the chicken egg and the ID is approximately 2.5-fold longer. Daily changes in mean heart rate (MHR) of emu embryos were previously determined, but further measurement was needed to investigate the species-specific behavior of cardiac rhythm for comparison with other species. In the present study, we continuously measured the electrocardiogram of emu embryos while maintaining adequate gas exchange through the eggshell and determined instantaneous heart rate (IHR) during the last 2-7 days of incubation until hatching or death. The MHR over 1-min intervals was calculated from IHR data in order to present continuous developmental patterns of heart rate (HR) in a single graph and 24-h recordings of HR in a single panel, showing the HR trend over a prolonged period. However, neither circadian nor ultradian rhythms of HR were shown in these figures or by power spectrum analysis. The IHR distinctively fluctuated and the fluctuations were mainly comprised of three patterns of irregular HR accelerations in embryos that hatched. Respiratory sinus arrhythmia also occurred in perinatal embryos. During the final stages of the perinatal period, short-term, repeated, large accelerations of IHR appeared, which signaled imminent hatching and has been reported for chick embryos. IHR fluctuations in embryos that failed to hatch tended to become inactive towards death.     

The effects of short- and long-term exposure of chick embryos to neutral red on the frequency of sister-chromatid exchange

The chick embryo was used to study the effects of neutral red (NR) on the frequency of sister-chromatid exchange (SCE) in specific tissues exposed to this mutagen for short and long periods as development proceeded. In short-term trials, aqueous NR at doses of 10, 25 and 100 μg was injected in 3-day and 6-day embryos. In each case, embryos were also treated with 5-bromodeoxyuridine (BrdU) for a 24-h period (two cell cycles) and harvested at 4 days and 7 days, resp. A long-term exposure (about 8 cell cycles) was achieved by exposing embryos to NR from day 3 to day 7 of incubation. At a NR dose of 25 μg, the chronic exposure resulted in a doubling of the rate of SCE (11.4/cell) over that observed in embryos exposed for only 24 h at either days 3–4 (6.0/cell) or days 6–7 (6.0/cell). At 100 μg of NR, the same relationship held with SCE rates of 14.2/cell for the chronic exposure versus rates of 8.0/cell (3–4 days) and 6.9/cell (6–7 days). At 10 μg of NR, no such accumulation of SCE occurred upon long-term treatment.These results show an enhanced SCE response upon growth of embryonic cells in the presence of NR for several days. This may be the result of the persistence of past lesions with the addition of more lesions upon continued exposure to NR.     

Chronic in ovo hypoxia decreases pulmonary arterial contractile reactivity and induces biventricular cardiac enlargement in the chicken embryo

Although chronic prenatal hypoxia is considered a major cause of persistent pulmonary hypertension of the newborn, experimental studies have failed to consistently find pulmonary hypertensive changes after chronic intrauterine hypoxia. We hypothesized that chronic prenatal hypoxia induces changes in the pulmonary vasculature of the chicken embryo. We analyzed pulmonary arterial reactivity and structure and heart morphology of chicken embryos maintained from days 6 to 19 of the 21-day incubation period under normoxic (21% O(2)) or hypoxic (15% O(2)) conditions. Hypoxia increased mortality (0.46 vs. 0.14; P < 0.01) and reduced the body mass of the surviving 19-day embryos (22.4 +/- 0.5 vs. 26.6 +/- 0.7 g; P < 0.01). A decrease in the response of the pulmonary artery to KCl was observed in the 19-day hypoxic embryos. The contractile responses to endothelin-1, the thromboxane A(2) mimetic U-46619, norepinephrine, and electrical-field stimulation were also reduced in a proportion similar to that observed for KCl-induced contractions. In contrast, no hypoxia-induced decrease of response to vasoconstrictors was observed in externally pipped 21-day embryos (incubated under normoxia for the last 2 days). Relaxations induced by ACh, sodium nitroprusside, or forskolin were unaffected by chronic hypoxia in the pulmonary artery, but femoral artery segments of 19-day hypoxic embryos were significantly less sensitive to ACh than arteries of control embryos [pD(2) (= -log EC(50)): 6.51 +/- 0.1 vs. 7.05 +/- 0.1, P < 0.01]. Pulmonary vessel density, percent wall area, and periarterial sympathetic nerve density were not different between control and hypoxic embryos. In contrast, hypoxic hearts showed an increase in right and left ventricular wall area and thickness. We conclude that, in the chicken embryo, chronic moderate hypoxia during incubation transiently reduced pulmonary arterial contractile reactivity, impaired endothelium-dependent relaxation of femoral but not pulmonary arteries, and induced biventricular cardiac hypertrophy.     

Early development and differentiation of the Laysan albatross (Phoebastria immutabilis (Rothschild, 1893): Procellariiformes)

Bird incubation is subdivided into two phases: differentiation (embryonic phase) and growth (fetal phase). Most birds have a relatively short incubation period (20–30 days) with the phase transition occurring midway through the incubation period. The Laysan albatross (Phoebastris immutabilis) is a large pelagic bird with a long incubation period. The purpose of this study was to document the differentiation phase with the aim of ascertaining the impact of a lengthened incubation on embryonic development. Eighty‐two previously collected albatross embryos were examined, measured, and staged. The albatross was found to develop more slowly than smaller birds, with a rate similar to other long‐incubating birds. Legs and wings grow at similar rates but exhibit variation in growth among their anatomical components. While the albatross embryos shared some morphological stages with chickens, they were more similar to ducks and pelicans. Special features of the albatross not shared with the Gallianserae (chickens and ducks) included an alligator‐like curved tail, narial tubes, and a cloacal bulge. Further examination of other larger pelagic birds with long incubation periods are needed to determine the uniqueness of the Laysan albatross embryonic development. Although much embryonic phase growth was documented in the postnatal period, little is known about the later, fetal phase in Laysan albatross. Future studies should involve examination of later (post day 32) fetuses. J. Morphol. 277:1231–1249, 2016. © 2016 Wiley Periodicals, Inc.     

Chick embryo culture using duck egg shell--first successful hatch

The suitability of duck egg shell (DES) for chick embryo culture was investigated. Chick embryos were transferred into DESs with all egg contents after 3 days of normal incubation and cultured. The vessels made of polyethylene cling film were used for shell-less control. Among 35 embryos cultured in DESs, 21 survived until 16 days of incubation (13 days after transfer) and finally 3 newly hatched chicks were obtained at 22 days of incubation. One of them died 4 days later, but remaining two became full-grown cocks showing normal body weight and production of fertile sperms. Among 37 embryos cultured in polyethylene vessels, none survived over the period of 19 days of incubation. It is suggested that DES culture system may be useful for the various experiments using chick embryos.     

The effects of thiourea and cortisone acetate on duodenal length and diameter and on morphogenesis of duodenal villi in chick embryos

Subnormal growth in length and diameter of the duodenum is encountered both in chick embryos injected with thiourea at 11 days of incubation, and in embryos injected with cortisone acetate at 14 days of incubation. Morphogenesis of previllous ridges and villi is retarded in thiourea-treated embryos. Morphogenesis of previllous ridges and villi in cortisone acetate-treated embryos at first seems to be slightly accelerated over that of controls, but the acceleration does not appear to be maintained, and the hormone may actually be inhibitory to normal morphogenesis of villi by 19 days of incubation. The results indicate that normal levels of endogenous thyroxine are necessary for normal growth in length and diameter of the duodenum and for normal morphogenesis of previllous ridges and villi. The possibility that adrenocorticoids may also play a role in the normal development of these parameters is indicated, although the evidence is inconclusive.     

Physiological and Ecological Aspects of Gas Exchange by Sea Turtle Eggs

The sea turtle clutch of about 100 eggs is buried deeply inthe nesting beach.The eggs exchange respiratory gases with thesurrounding beach as their metabolic activity increases throughoutthe 60 day incubation. The O₂ consumption of individual eggsthroughout incubation is less than that of avian eggs of similarmass; however, this difference may be attributed to the differencein incubation temperature and growth rate. The O₂ consumptionof the sea turtle embryo is sufficiently low and the gas conductanceof the shell sufficiently large that only small gas partialpressure gradients occur across the shell. However, the metabolicintensity of the entire clutch is quite large, and since gasmovement through the beach is restricted, increasing gas partialpressure gradients are established between the center and peripheryof the clutch and between the clutch and surrounding beach.The rate of growth and mortality of the embryos is related torespiratory gas exchange, since maximum growth and hatchlingsuccess appear to occur in respiratory environments similarto those observed in natural nests. Embryonic growth slows andmortality increases in environments in which gas exchange isreduced below naturally occurring levels. Gas exchange considerationsmay influence nest construction, clutch size and incubationtime among sea turtles.     

Waiting for a sign: extended incubation postpones larval stage in the beach spawning California Grunion <Emphasis Type="Italic">Leuresthes tenuis</Emphasis> (Ayres)

Unlike most embryos that hatch on a predetermined timetable, California Grunion Leuresthes tenuis can prolong the embryonic period up to three times longer than the time required for hatching readiness. L. tenuis are teleosts that spawn tidally around the highest spring tides of spring and summer, incubating eggs above the water line. Embryos are competent to hatch in 10 days, however they do not hatch until triggered by an environmental cue, agitation in seawater, as the next spring tides rise. This study examined the growth and survival of L. tenuis embryos and larvae that were all fertilized on the same day, then triggered to hatch after different durations of incubation, up to 35 days post fertilization. L. tenuis embryos that survive extended incubation had decreased yolk reserves and did not advance appreciably in morphological development, even when incubation time was extended to its upper limit. After extended incubation, length of hatchlings was significantly longer than hatchlings from the primary incubation time. Regardless of the duration of incubation, larvae provided food ad libitum grew rapidly and were not significantly different in length at three weeks post hatch. Dry mass increased over time and was not significantly different between larval groups within any post-hatch age. Larval growth and survival after one additional tidal cycle of incubation are not adversely affected, but longer incubation significantly decreases embryonic and larval survival. Large reproductive output, environmentally cued hatching, and plasticity in incubation duration enable L. tenuis to reproduce successfully in the unpredictable sandy intertidal ecosystem.     

Teratogenic effects of transplacental transfusion of heterologous antisera simulated in an experimental model using in vitro whole rat embryo culture

The effects of the transplacental transfusion of heterologous rabbit-anti-rat antiserum (RAR antiserum) and subsequent immunological interaction on the development of 9-10 days old rat embryos (stages 8-10 somites) were studied using an in vitro whole rat embryo culture. Transplacental transfusion was simulated by the embryonic intracardiac microinjection of approximately 0.5 microliter RAR antiserum, followed by an incubation period of 24 and 48 hours. All the tested embryos survived the incubation period. Embryos taken from the incubator after 24 hours showed signs of growth retardation and axial non-rotation, a delayed closure of the neural tube and ear vesicle, and a delayed formation of the foregut. They also had a moderate number of areas with local pathogenetic cell degeneration. Embryos taken from the incubator after 48 hours demonstrated signs of growth retardation and incomplete axial rotation. The formation of the foregut and closure of the neural tube was complete, with the exception of one embryo with a persisting open neuroporus posterior. All embryos displayed a considerable number of areas with local pathogenetic cell degeneration. The intracardiac injection technique is an elegant method to test the effects of teratogens administered directly into the embryonic circulation. The results demonstrate that heterologous antisera have teratogenic potential, believed to be due to an immunological reaction, with a particular sensitivity of the neurectoderm in 9-10 day old embryos.