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.     

Survival of faecal streptococci in raw and pasteurised egg products

1. The ability of Streptococcus faecalis and Streptococcus faecium strains to survive in egg albumen and liquid whole egg before and after laboratory pasteurisation was studied.

2. Pasteurisation of egg albumen caused a decrease in viable cells of less than 10‐fold, while pasteurisation of whole egg caused decreases of more than 100‐fold in only two of the eight strains studied. After growth in whole egg, some strains were more resistant to pasteurisation in whole egg.

3. Strep, faecalis multiplied in raw and pasteurised whole egg but not in egg albumen.

4. Strep, faecium multiplied in raw and pasteurised whole egg only after an initial decline in viability which was not shown by cells adapted to whole egg. Together with storage temperature this affected the number of viable cells after a storage period of 5 d.

5. In raw and pasteurised egg albumen Strep, faecium strains lost viability; this was maximal at 37 °C and more cells survived as the storage temperature decreased.     

The choline and sulphur amino acid requirements of broiler chickens fed on semi‐purified diets

1. Growth and food conversion efficiency of broilers were reduced at low dietary choline concentrations. These effects were accentuated by low dietary total sulphur amino acids (TSAA).

2. Increased mortality, perosis and other pathological changes involving a number of tissues were observed in birds fed on a low‐choline diet.

3. Methionine replaced part of the dietary requirement for choline at low dietary choline concentrations.

4. High dietary concentrations of choline (> 1 750 mg/kg) increased the requirement for dietary TSAA.

5. Increasing the dietary choline while maintaining the TSAA at an inadequate level may decrease performance.     

The incidence of bruising in broiler flocks

1. The amount of down‐grading due to bruising in 55 flocks of broilers was investigated.

4. Bruising was classified as light or bad bruising and it is suggested that this division represents two distinct types of bruises with different causes.

3. The incidence of bruising was greater in female flocks than in male although the bruising in the former tended to be less severe.

4. The relationships between incidence of bruising and several variables associated with the flock and the environment were examined using regression analysis. The factors shown to have a significant influence on the incidence of bruising were: the age and mean weight of the flock, and the temperature and humidity on the day of processing.     

An age-related coagulation disorder associated with experimental infection with infectious bursal disease virus

Specific-pathogen-free White Leghorn chickens were inoculated with a field strain of infectious bursal disease virus. One group (A) was inoculated at 17 days after the chicks were hatched, and the other groups (C and E) were inoculated at posthatch day 42. Blood samples were obtained for determination of clotting times (whole blood recalcification, prothrombin, and activated partial thromboplastin times), virus-neutralizing antibody, and total hemolytic complement. There were significant increases in clotting times for groups C and E at 3 and 5 days after they were inoculated. There were no significant increases in clotting times at 3 days after inoculation in the group A chickens (inoculated at 17 days after hatching). There were no significant decreases in total complement activity in any of these chickens (groups A, C, and E). This study indicates that the mortality and clinical symptoms observed in chickens experimentally infected with infectious bursal disease virus may be associated with a clotting abnormality because it was noted only in chickens that developed severe clinical disease (inoculated at 42 days after hatching) and was not noted in chickens that remained clinically normal (inoculated at 17 days).     

Determination of extractable and non-extractable radioactivity from prairie soils treated with carboxyl- and ring-labelled [14C]2,4-D

Ring- and carboxyl-labelled [¹⁴C]2,4-D were incubated under laboratory conditions, at the 2 g/g level, in a heavy clay, sandy loam, and clay loam at 85% of field capacity and 20 1C. The soils were extracted at regular intervals for 35 days with aqaeous acidic acetonitrile, and analysed for [¹⁴C]2,4-D and possible radioactive degradation products. Following solvent extraction, a portion of the soil residues were combusted in oxygen to determine unextracted radioactivity as [¹⁴C]carbon dioxide. The remaining soil residues were then treated with aqueous sodium hydroxide, and the radioactivity associated with the fulvic and humic soil components determined. In all soils there was a rapid decrease in the amounts of extractable radioacitivity, with only 5% of that applied being recoverable after 35 days. All recoverable radioactivity was attributable to [¹⁴C]2,4-D, and no [¹⁴C]-containing degradation products were observed. This loss of extractable radioactivity was accompanied by an increase in non-extractable radioactivity. Approximately 15% of the applied radioactivity, derived from carboxyl-labelled [¹⁴C]2,4-D, and 30% from the ring-labelled [¹⁴C]2,4-D was associated with the soil in a non-extractable form, after 35 days of incubation. After 35 days, less than 5% of the radioactivity from the carboxyl-labelled herbicide, and less than 10% of the ringlabelled material, was associated with the fulvic components derived from the three soils. Less than 5% of the applied radioactivities were identifiable with any of the humic acid components. It was considered that during the incubation [¹⁴C]2,4-D did not become bound or conjugated to soil components, and that non-extractable radioactivity associated with the three soil types resulted from incorporation of radioactive degradation products, such as [¹⁴C]carbon dioxide, into soil organic matter.     

The use of separate root and shoot tests in the screening of herbicides for strawberries

The tolerance of strawberries to herbicides was tested by applications to the roots of plants growing in sand and by foliage applications to plants grown in compost, and compared with tolerance in the field. Dimefuron was safe as a foliar application but much more toxic than simazine when applied in sand or in the field. Metamitron caused slight injury as a foliar spray; in sand and in the field it was intermediate in toxicity between simazine and lenacil. At normal rates propachlor was safe as a foliar spray and much safer than lenacil when applied in sand. High rates had no adverse effect in the field. Ethofumesate and pendimethalin caused some temporary stunting when applied to foliage, but were less toxic than lenacil when applied to roots in sand. Field applications of both herbicides at 1–1.5 kg/ha were safe. Foliage sprays of bentazone, oxadiazon and oxyfluorfen severely damaged the sprayed leaves, but these herbicides were less active than lenacil when applied to the roots. In the field they caused severe leaf damage, but by the end of the growing season the plants had recovered. The experiments demonstrated the value of separate root and shoot activity tests for indicating which herbicides merit further field testing.     

Translocation of 14C-glyphosate in johnsongrass (Sorghum halepense L. Pers.) as affected by growth stage and rhizome length

Studies were conducted in the green house on ¹⁴C-methyllabelled glyphosate translocation in johnsongrass as affected by rhizome length and growth stage. The amount of ¹⁴C measured by the liquid scintillation technique in the rhizomes (2-8%) increased with rhizome length (10, 20 or 30 cm) and tended to increase with growth stage (15-30 cm tall, 45-60 cm tall, or at seedhead), but the amount of ¹⁴C per g fresh rhizome weight was almost similar in all cases. Of the total amount applied per plant (0·2 μCi) about 1/3 or less remained on the treated leaf area, while another 1/3 was a absorbed into the treated leaves. Autoradiographs showed that the ¹⁴C label moved to all plant parts, basipetally and acropetally. Migration du glyphosate ¹⁴ C chez le sorgho d'Alep (Sorghum halepense L. Pers.) en relation avec le stage de croissance et la longueur du rhizome Des recherches ont été effectuées en serru sur la migration du glyphosate marqué au ¹⁴C sur le méthyle, chez le sorgho d'Alep, en relation avec la longueur du rhizome et le stade de croissance. La quantité de ¹⁴C mesurée par la technique de scintillation liquide dans les rhizomes (2 à 8%) s'est accrue avec la longueur du rhizome (10, 20 ou 30 cm) et elle a eu tendance à augmenter avec le stade de croissance (Hauteur 15-30 cm, hauteur 45-60 cm ou épiaison), mais la quantité de ¹⁴C par gramme de poids frais de rhizome est restée Presque identique dans tous les cas. Environ 1/3, ou moins, de la quantitéà la surface des feuilles traitées par plante (0,2 μCi), est restéà la surface des feuilles traitées cependant qu'un autre 1/3 a été absorbé dans less feuilles traitées Les autoradiographies ont montré que le ¹⁴C marqueur a migré dans toutes les parties de la plante, dans le sens basipète et dans le sens acropète. Translokation von ¹⁴C-Glyphosat in Johnsongras (Sorghum halepense L. Pers.) in Abhängigkeit vom Wachstumsstadium der Pflanzen und der Rhizomlänge Im Gewächshaus wurden Versuche über die Translokation von ¹⁴C-Glyphosat in Johnsongras (Sorghum halepense L. Pers.) in Abhängigkeit vom Wachstumsstadium der Pflanzen und der Rhizomlänge durchgeführt. An den Rhizomen stieg der Gehalt von ¹⁴C(2–8%), gemessen mit der Flüssig-Szintillationstechnik, mit zunehmender Rhizomlänge (10, 20 oder 30 cm) an und nahm tendenziell auch mit fortschreitendem Pflanzenwachstum zu (15–30 cm und 45–60 cm Sprosslänge oder nach dem Rispenschieben); jedoch blieb die Menge pro g Rhizomfrischgewicht beinahe konstant. Von der insgesamt ausgebrachten Menge pro Pflanze (0.2 μCi) blieben bis zu 1/3 auf der behandelten Blättern absorbiert wurde. Die Autoradiographie zeigte, dass der ¹⁴C markierte Teil in alle Pflanzenteile sowohl basipetal wie auch akropetal transportiert wurde.