Traits influencing the hatching performance of Japanese quail eggs

1. Japanese quail eggs from moderately heavier sires showed superior fertility; while fertile eggs from moderately heavier dams hatched slightly better than the eggs from lighter dams.

2. Higher rates of fertility and hatchability of Japanese quail eggs were observed from parents of 10 to 19 weeks of age, with peak fertility and hatchability at 14 and 12 weeks of age, respectively.

3. Sex ratios of 1:2 to 1:5 gave comparable fertility and hatchability results.

4. The hatching performance of quail eggs from cage and deep litter reared breeders was comparable.

5. Fertility and hatchability were directly proportional to the egg weight.

6. Quail egg shell colour, tints and blotches were found to influence hatching performance.

7. Storing quail eggs at 16 ± 2°C and 75 ± 5% relative humidity for more than 4 d reduced hatchability.

8. Hatchability of eggs stored at room temperature was improved if they were sealed in polyethylene bags.

9. Provision of light during the first 14 d of incubation resulted in a photo‐acceleration of about 3.2 h.     

The influence of sample size on the choice of method and interpretation of incubation experiments

1. An equation relating batch size to between‐treatment differences has been adapted for hatchability studies and its implications for research considered.

2. Very large egg batches are required to detect small improvements in the hatchability of good hatching strains.

3. Small‐scale laboratory studies on hatchability are best confined to strains and species of low hatchability in which larger between‐treatment differences may be expected.

4. The results of hatchability studies should always be subjected to tests of statistical significance.

5. There is a strong case for studying continuous variates in the laboratory before proceeding to large‐scale hatchability studies.     

Genetic inferences from inter‐strain crossing for hatchability and fertility in white leghorns

1. Heritability estimates for hatchability of fertilised eggs were obtained from four White Leghorn strains and their crosses.

2. Based on the variance of the full‐sib family means, the heritability estimates for pure‐bred, cross‐bred and for the combined data were 0.lb186 ± 0.lb105, 0.lb065 + 0.lb021 and 0.lb088 + 0.lb005, respectively: the results showed absence of non‐additive genetic variance for hatchability.

3. Fertility was influenced more by sire strain than by the dam while hatchability was primarily influenced by the dam strain.

4. The sire x dam interaction effect was significant for fertility but not for hatchability.

5. Fertility was influenced by crossing two divergent strains.     

Increasing hatchability of turkey eggs by injecting eggs with pyridoxine

1. In field trials, eggs from two flocks of Large White turkey hens were injected with about 0.2 ml saline solution containing 600 μg of pyridoxine hydrochloride in order to examine its effect on hatchability.

2. Also, in an aseptic laboratory trial, eggs from Large White turkey hens were injected with 0.2 ml of saline solution and 0.2 ml of saline solution containing 600 μg of pyridoxine hydrocholoride.

3. In field trials, hatchability of pyridoxine‐injected eggs was 4.6% higher (P<0.05) than the control (non‐injected) eggs.

4. In the aseptic laboratory trial, hatchability of pyridoxine‐injected eggs was 4.2% higher (P<0.05) than saline‐injected and control (non‐injected) eggs.     

Influence of pre‐incubation treatment on hatching results of broiler breeder eggs produced at 37 and 59 weeks of age

1. The influence of temperature in the nest box, temperature during storage, storage time and pre‐setting temperature on the hatchability of broiler breeder eggs produced by birds of 37 and 59 weeks of age was examined.

2. All treatments that can be characterised as being less optimal for embryo survival than the control treatment affected the hatchability of fertile eggs more in the case of eggs produced by older birds.

3. A higher temperature in the nest box, longer storage periods, higher storage temperature, especially at longer storage periods, and higher pre‐setting temperature significantly reduced the hatchability of fertile eggs from the older birds.

4. For the younger birds, a significant reduction of hatchability was found only for the longest storage period.     

Rate of decline in hatchability with preincubation storage of chicken eggs depends on genetic strain

1. The effect of preincubation storage of chicken eggs on hatchability was studied in an Australorp subline (ASS) that had shown a steady decrease of hatchability compared with the original selection line (AS) since its derivation 10 generations ago. The AS line was also included in the study.

2. Eggs were collected over 21 d and the collected eggs were stored at 10° to 12°C and relative humidity of 70 to 80% until they were set together on d 21. Fertility and hatchability of fertile eggs were calculated for each d of collection to study their relationships with age of eggs (length of storage).

3. The hatchability of fertile eggs was considerably different between the two lines in the average over 21 d and, more importantly, in the pattern of decline with length of storage.

4. In the first 3 to 4 d of storage, hatchability was very similar between the lines. However, it decreased linearly at a rate of 1.9% per day of storage over the 21‐d period in the ASS line (average 65.9%), whereas in the AS line (average 78.6%), it stayed at around 84% up to 12 d of storage, when it started to decline at a similar rate as in the ASS line.

5. Fertility was 2.6% higher in the AS line than in the ASS line, but in each line showed no significant trend with age of eggs.     

The relationship between hatching egg weight and subsequent performance of broiler chickens

Small eggs constitute a high proportion of the eggs laid by pullets. The literature shows that chick hatching weight is strongly correlated with egg weight, but evidence on the influence of egg weight on hatchability and subsequent performance of chicks is less certain.

The aim of this experiment was to determine the profit returned at 12 weeks by broiler chickens hatched from eggs ranging in weight from 44 g. to 58 g. at one gram intervals and to determine how competitive and separate rearing might modify the relationship.

A total of 6000 eggs were collected during 10 days from a 28‐week‐old, broiler breeding flock and graded into the above mentioned egg weight classes. From these, a total of 3480 day‐old broilers were housed. Each egg weight class was equally represented and balanced for sex.

Hatchability and fertility showed no consistent trend with egg weight for eggs above 46 g., but below the 47 g. level there was a trend of declining fertility and hatchability.

A strong positive relationship was found between the weight of the chick at 1 day of age and egg weight for both males and females with no significant difference overall in body weight between the two sexes.

Body weight to 12 weeks was found to be strongly related to egg weight, in a linear fashion, though this influence declined with age.

There was a greater influence of egg weight on body weight at all ages in the separate rearing treatment compared with competitive rearing but this was not significant after 10 weeks.

Egg weight had an important bearing on body weight and profit at 12 weeks, but no effect on food conversion or mortality.

The increased profit over food costs per 100 day‐old chicks was found to be 52.75 cents for the separately reared birds respectively for each 3 g. increase in egg weight.     

Cooling of broiler hatching eggs during incubation

1. Broiler hatching eggs were cooled to 22°C for periods of 8 or 24 h on day 16 of incubation. Cooling had no significant effects on hatchability or chick quality compared with controls.

2. Cooling to 22°C for 24 h on days 14, 15, 16, 17 or 18 yielded similar results but cooling on day 13 increased late embryonic mortality.

3. When eggs were cooled to 22°C on day 16 of incubation there were no major differences in hatchability up to 48 h of cooling but chick quality deteriorated rapidly after 30 h and the limit for embryonic survival at this temperature was about 72 h.

4. There were no significant differences when eggs were cooled on day 16 and held for 24 h at 21.1, 23.9 or 26.7°C but hatchability and late deaths were significantly affected by cooling to 18.3°C.     

Microbial spoilage of ostrich (struthio catnelus) eggs

1. The incidence of microbial spoilage was investigated in three batches of ostrich eggs, one from Africa and two from Europe.

2. 18% to 21% of eggs in each batch were contaminated with bacteria and fungi, with the latter being found more often in eggs which contained more advanced embryos.

3. Although infertility and prolonged storage reduced hatchability, the high inci dence of microbial contamination in ostrich eggs is deemed to be a significant problem.

4. Improving nest hygiene is considered to be the simplest way to reduce microbial spoilage.     

Factors affecting the hatchability of eggs from broiler breeders

1. Four experiments were carried out on eggs from broiler breeding flocks between 26 and 60 weeks of age. The effects of storage and incubation conditions on hatchability were tested.

2. Collecting eggs hourly rather than five hours after lay slightly reduced hatchability (P<0.10). Pre‐storage fumigation of almost un‐contaminated eggs had no effect on hatchability even after storage for 8 d. Storing eggs in unsealed polythene bags did not affect hatchability of eggs stored for 5 or 8 d.

3. Eggs stored for 2 d hatched better when held at 18 °C than at 15 °C (P<0.05). Eggs stored for 8 d at 15 °C hatched better than eggs stored for 8 d at 18 °C (P< 0.01). Best hatchability was in eggs stored in unsealed polythene bags at a room temperature of 15 °C. When older eggs were allowed 30 to 40 min more in the setter for each day of storage, the decline in hatchability was 0.5 to 0.6 percentage units per day in storage as compared with a decline of 1.2 percentage units per day when eggs of different storage times, up to 8 d, were set simultaneously.

4. Those eggs which showed a weight loss during incubation of near average for their relative humidity (RH) treatment tended to hatch better than others except under conditions of very low RH (0.36), when best hatchability was associated with lower than average weight loss.

5. In eggs from a young flock (28 to 44 weeks of age) hatchability of fertile eggs was depressed by 1 percentage unit with an increase in RH of 0.17, and by 1 percentage unit with each decrease of 0.06 in RH from a control RH of 0.53. In eggs from the same flock between 48 and 60 weeks of age hatchability was depressed by 1 percentage unit with each 0.037 increase in RH from 0.44 to 0.70.

6. Eggs from a young flock (34–49 weeks) hatched significantly better when maintained at 0.82 rather than at 0.66 (P<0.05) or 0.95 (P<0.10) RH during the hatching period from 19 to 21 d of incubation. Eggs from an older flock (51–61 weeks) hatched better at 0.82 and at 0.‐92 than at 0.72 RH during the same period, but the differences were not significant.     

Effect of egg composition on hatchability and on growth and slaughter characteristics of meat-type chicks

1.?Using the so-called TOBEC (Total Body Electrical Conductivity) method, which allows the determination of egg composition in vivo, correlations between egg composition, hatchability and hatched chicks’ development were studied.

2.?A total of 1500 hen eggs (Ross-308) were measured by TOBEC, and eggs with extremely high (10%, n = 150), extremely low (10%, n = 150) and average (10%, n = 150) electrical conductivity values were chosen for further investigation.

3.?During the incubation period, it was observed that eggs with high electrical conductivity had a significantly higher mortality than eggs with low electrical conductivity.

4.?It was observed that both the increase in electrical conductivity at the same egg weight, and the increase in egg weight at the same electrical conductivity resulted in an increase in the hatching weight.

5.?It was found that the dry matter, protein and fat content of the chicks hatched from eggs with low electrical conductivity was higher at hatching than that of the chicks hatched from eggs with high electrical conductivity.

6.?At 42 d of age the liveweight of cocks and pullets hatched from eggs with low electrical conductivity was 3·2 and 8·2% higher than the liveweight of cocks and pullets hatched from eggs with high electrical conductivity.

7.?Because of the higher liveweight at slaughter, there was a significant superiority of the chicks hatched from eggs with low electrical conductivity in the case of the examined carcase traits at slaughter.

8.?Similar tendencies were found also in the ratios of carcase variables to liveweight, but the between group differences were not statistically significant in this case.

9.?Based on the results it was concluded that TOBEC seems to be a useful method for separating eggs with different composition.

10.?This could be a good starting point for further in vivo investigations in order to clarify the effect of egg composition on hatchability and further development.     

Effect of oiling on internal quality of eggs stored at 28 and 12°G

1. The effects of spraying linseed oil on naturally clean eggs, subsequently stored for 24 d at 28 °C were studied.

2. Oiling slowed the decline in albumen height (Haugh units) to that which occurred in unoiled eggs stored at 12 °C.

3. Oiling slowed the increase in albumen pH equally at 28 and 12 °C.

4. Oiling markedly decreased the weight loss of eggs stored at either temperature.

5. Oiling and temperature of storage were without effect on the whipping volumes of either albumen or unseparated albumen and yolk.     

Compensation for seasonal changes in eggshell conductance and hatchability of goose eggs by dynamic control of egg water loss

1. The water loss for optimal hatchability of goose eggs was 12% of initial egg mass.

2. Mass specific eggshell water vapour conductance, G_sp, increased by approximately 50% over about 13 weeks during the winter breeding cycle. A similar increase occurred over 8 weeks during summer.

3. Constant setting of humidity in goose incubators and changes in mean G_sp may cause sub‐optimal egg water loss which increases late mortality.

4. Mean G_sp was measured for every batch from each flock. Humidity was changed accordingly in order to reach optimal water loss. A significant improvement of 6% in hatchability and of 8% in Class‐A goslings was noted during 14 successive weeks compared with the previous 11 weeks.

5. Dynamic humidity control for optimising water loss according to mean batch G_sp thus increases hatchability.     

Egg discolouration effects of including screw‐press cottonseed meal in laying hen diets and their prevention

The egg discolouration effects of including a screw‐press cottonseed meal (CSM), containing 68.2 g residual lipid/kg, 290 mg cyclopropenoid fatty acids (CPFA)/kg and 1226 mg free gossypol/kg, in laying hen diets at 300 g/kg were examined.

2. Discolouration prevention methods included treating the meal with ferrous sulphate heptahydrate (FSH), in solution or as crystals, at a 4:1 weight ratio of iron to free gossypol (experiment 1), and reducing its residual lipid (CSL) content to 4.2 g/kg by hexane extraction (experiment 2).

3. In freshly laid eggs, no discolouration was observed when hens were fed a CSM‐based diet containing 250 mg free gossypol/kg and 87 mg CPFA/kg in experiment 1, but slightly brown yolks were produced in experiment 2.

4. Storage of the eggs at 22°C led to yolk mottling, an effect believed to be the initial stages of the brown yolk discolouration.

5. Storage of the eggs at 5°C resulted in enhancement of the brown yolk discolouration, apricot discolouration on surfaces of most yolks and pink albumen discolouration. These effects were prevented when the CSM was extracted with hexane. Apricot yolk and pink albumen discolourations were also produced when hens were fed a non‐CSM diet containing crude CSL at 20.5 g/kg.

6. Dietary CSL increased egg fat saturation, altering the ratios of stearic to oleic, palmitic to palmitoleic and heptadecanoic to hepta‐decenoic fatty acids.

7. Treatment of CSM with FSH reduced the slight brown yolk discolouration in fresh eggs (experiment 2) and the yolk mottling in warm‐stored eggs. Both in solution and as crystals, FSH prevented the enhancement of brown yolk discolouration in cold‐stored eggs, leaving most eggs with apricot yolk and pink albumen discolourations.

8. Treatment of CSM and CSL with FSH reduced the CPFA‐related effects on yolk fat saturation, and the colour and pH changes in cold‐stored eggs.

9. Exposure of yolks to ammonia vapour provided a useful test to predict the development of the gossypol‐related brown discolouration in stored eggs.     

Storage of hatching eggs: The effect on total incubation period

1. A time‐lapse photographic technique has been developed which enables routine recording of the hatching times of up to 192 chicken embryos.

2. Storage of eggs for 14 d caused a delay of 134 h in the mean total incubation period.

3. Female embryos hatched about 3 h earlier than males in the non‐stored eggs but there was no difference between the sexes in eggs stored for 14 d.

4. Rate of weight loss during incubation was similar in both non‐stored and stored eggs: there was no relationship between weight loss at 19 d incubation and total incubation period.

5. Hatchability of fertile eggs was 19.5% lower in eggs stored for 14 d and proportionately more embryos died between 4 d and 18 d incubation than in the non‐stored eggs.     

The bacterial flora of unhatched eggs

1. The methods of bacteriological examination of hatchery waste eggs were compared.

2. Using one of these methods a survey was conducted on eggs which had failed to hatch from commercial hatcheries.

3. An assessment of the level of contamination in the eggs examined indicated an average level of contamination of 12.7%.

4. The contaminating flora was composed mainly of Micrococcus sp. and Enterobacteriaceae, with Streptococcus sp., Staphylococcus sp., Bacillus sp. and Pseudomonas sp. present at lower levels.

5. Various interrelationships between contamination and hatchability are discussed.     

Defective egg production in a population of dwarf white leghorns 1

1. The incidence of defective eggs during the first 60 weeks of age increased with time due to significant increases in broken and membranous eggs in a population of dwarf White Leghorn hens.

2. The production of double‐yolked eggs/100 hen d, high during the initial weeks of lay, rapidly declined and disappeared by 30 weeks of age.

3. The frequencies of broken, membranous and soft‐shelled eggs were significantly correlated with each other and with the frequency of multiple daily ovulations indicating a common aetiology for these defective egg types.

4. Double‐yolked eggs were produced by the heavier, earlier‐maturing pullets in the population.

5. Normal egg production in dwarf White Leghorns may be enhanced by reducing the incidence of defective eggs.     

Comparisons of egg quality traits,egg weight loss and hatchability between striped and normal duck eggs

1. The egg quality of striped and normal duck eggs was compared to determine why striped eggs show decreased hatchability. A total of 430 eggs, obtained from a Pekin duck breeder flock aged 50–65 wks, were used in three experiments. The eggs were weighed and assigned randomly to measure egg quality traits, egg weight (EW) loss and hatchability during incubation.

2. There were no significant differences between egg types in terms of egg shape index, eggshell strength and thickness, albumen height, Haugh unit, yolk colour, weight of the eggshell with or without membranes, calcium, phosphorus, copper and manganese contents in the eggshell (with the inner and outer membranes or without the inner membrane), albumen weight, dry matter of albumen, crude protein (CP) of thick albumen and pH of the thick albumen.

3. The weight of eggshells with membranes, weight of thick albumen and CP of thin albumen in striped eggs were lower than those in normal eggs.

4. The thin albumen in striped eggs was heavier than that in normal eggs. The pH of the thin albumin in striped egg was significantly higher than that in normal eggs.

5. There were no significant differences in EW loss during incubation or duckling weight between striped and normal eggs. However, the hatchability of striped eggs was lower.

6. The lower weight of the eggshell inner membrane and thick albumen, lower CP content and higher pH in the thin albumen of striped eggs might contribute to lower hatchability.     

Effect of incubation temperature on the gross pathology of turkey embryos

1. Turkey eggs were incubated at 36.5, 37.5 and 38.5°C. The age of mortality, the incidence of malpositions and the incidence of morphological abnormalities were recorded from all unhatched eggs.

2. Eggs incubated at 36.5°C hatched later than eggs incubated at 37.5°C but did not differ in age of mortality or incidence of malpositions and abnormalities.

3. Eggs incubated at 38.5°C hatched significantly less well than eggs incubated at 37.5°C and showed significant differences in time of embryo mortality. Overheated embryos had a mortality peak between 15 and 20 d of incubation and an increased mortality after 24 d of incubation.

4. Overheated eggs were characterised by a high incidence of embryos with head in small end, with excess albumen, ruptured yolk sacs, oedematous heads, eye cataracts and swollen down‐plumules.