Variation in laying date, clutch size, egg size, and egg composition of yellow-headed blackbirds (Xanthocephalus xanthocephalus): a supplemental feeding experiment

1992 ◽  
Vol 70 (10) ◽  
pp. 1904-1911 ◽  
Author(s):  
Todd W. Arnold

I studied the effects of food availability, habitat quality, and timing of breeding on egg production in yellow-headed blackbirds (Xanthocephalus xanthocephalus). Food availability was experimentally manipulated by providing females on six wetlands with supplemental food; six additional wetlands served as unsupplemented controls. Mean nest initiation dates varied by up to 6 d among wetlands, and supplementally fed blackbirds initiated nests 2 d earlier than controls, on average (although this latter difference was not quite significant; P = 0.07). Clutch size declined with laying date, but was unaffected by wetland location, food supplementation, or interactions between these two factors and laying date. Although egg size did not vary among wetlands or in relation to supplemental feeding, egg composition varied with both of these factors. All egg components except wet and dry shell and dry albumen varied among wetlands, whereas total water, wet yolk, and lean yolk were the only components that varied with food supplementation. Large blackbird eggs contained proportionately more water and albumen, but proportionately less yolk and shell. These patterns were somewhat compensatory, such that proportional protein and energy content did not vary with egg size; however, large eggs contained proportionately less fat than did small eggs. Proportional egg composition varied among wetlands (yolk and energy content), but was not affected by supplemental feeding. In general, egg production by yellow-headed blackbirds was not greatly affected by food availability. This may have been due to any of the following four factors: (1) inaccessibility of food supplements owing to competition between male and female blackbirds, (2) insufficient time for females to respond to food supplements, owing to rapid settlement and nest initiation, (3) a nutritionally inappropriate food supplement (i.e., protein availability may not have been enhanced among fed birds), or (4) superabundance of natural foods such that food availability was not limiting egg production.


1987 ◽  
Vol 65 (5) ◽  
pp. 1270-1274 ◽  
Author(s):  
Wesley M. Hochachka ◽  
David A. Boag

Supplemental food was provided to a breeding population of Black-billed Magpies (Pica pica), starting before and after eggs were laid, to determine if and when natural food was limited. The production of fledgling magpies was increased only when supplemental feeding was begun before laying. Laying date was also advanced when supplemental feeding began before laying, but clutch and egg size were not significantly changed. Because the two feeding treatments were conducted in different years, we cannot conclude whether natural food was limiting before or after egg laying. However, out data suggest that the former may have been the case. An improved design for food supplementation experiments, which can be used to determine the time of food shortage, is suggested.



1988 ◽  
Vol 66 (3) ◽  
pp. 692-695 ◽  
Author(s):  
Wesley M. Hochachka

Viability of hatching birds may be affected by the composition of the eggs from which they come. Egg composition may be influenced by the diet of the female. I examined whether wild Black-billed Magpies (Pica pica) varied the composition of their eggs in response to differences in food supply. Supplemental food was provided on some territories, and the composition of eggs from control and food-supplemented territories was compared. Supplemental feeding had few effects on egg composition. Egg size – water content relationships differed between eggs from food-supplemented and control territories and there was a greater variability in yolk and shell mass within clutches from food-supplemented territories. These results show that food supply to the female can affect the composition of an egg relative both to other eggs in the same clutch and to eggs in other clutches. However, it is not clear whether the observed variation in egg composition would have an effect on the viability of the eggs.



The Auk ◽  
1991 ◽  
Vol 108 (3) ◽  
pp. 532-547 ◽  
Author(s):  
Todd W. Arnold ◽  
Ray T. Alisauskas ◽  
C. Davison Ankney


1989 ◽  
Vol 69 (2) ◽  
pp. 449-458 ◽  
Author(s):  
S. LEESON ◽  
J. D. SUMMERS

In trial 1, eggs from young (28 wk) and old (65 wk) leghorn breeders were categorized into groups with mean weights of 54, 59 or 64 g. Female chicks were cage-reared to 18 wk of age; three rearing treatments involved five replicate cages of nine pullets from each egg size category, while treatment 4 involved a mixed population. The largest eggs contained most yolk fat and protein and albumen protein (P < 0.05). Egg size had no effect on male chick composition (P < 0.05). There was no overall effect of egg size or breeder age on feed intake of pullets, although up to 8 wk of age, pullets from small eggs were consistently smaller than those from large eggs. Egg size and breeder flock age had no effect on pullet weight at 18 wk. Pullets reared as a combination group of small:medium:large (3:3:3, treatment 4) showed a significant (P < 0.05) egg size effect on pullet weight at 18 wk of age. In a second trial, eggs were collected from a 45-wk-old flock of commercial leghorn breeders. Eggs were set according to weight, with mean egg weights of 56.4, 61.1 or 66.8 g. Rearing treatments related to the three egg size categories were represented by 10 replicate groups of nine birds each. A fourth treatment involved 26 groups of three chicks from each of the egg weight treatments. Breeder egg size had a significant effect on pullet weight at 126 d. With this differential maintained through the first 12 wk of lay. Breeder egg size had no effect on egg production (P > 0.05), although mean commercial egg weight and feed intake (P < 0.01) were directly proportional to hatching egg size (P < 0.01). It is concluded that hatching egg size can have a significant effect on life-cycle performance of leghorns, and as such, there may be scope for differential management of pullets hatched from different sizes of egg. Key words: Pullet, egg size, egg composition



1988 ◽  
Vol 66 (7) ◽  
pp. 1527-1536 ◽  
Author(s):  
A. Hailey ◽  
N. S. Loumbourdis

Energetic aspects of female reproduction are described for the tortoises Testudo graeca, Testudo marginata, and Testudo hermanni (three populations of different body size) from northern Greece. Egg width increased with body size in some populations, but smaller individuals produced more elongate eggs, and egg weight was not related to body size. This method for overcoming the constraint of the width of the pelvic canal means that egg width is a poor measure of egg size. Clutch size, clutch mass, and annual egg production varied with body size between populations. Mean relative clutch mass ranged from 4 to 7%, and was highest in the three populations of T. hermanni. All populations laid two or three clutches per year, based on the total number of eggs and large follicles divided by clutch size. Multiple clutches reflect the morphological constraint of packing shelled eggs within the body, rather than energy accumulation during the nesting period. Material for reproduction was stored in growing follicles rather than fat bodies; follicles reached half of their final weight before the animals entered hibernation. Annual reproductive effort as a proportion of body energy content was about 15% in all populations. This is lower than in other reptiles, partly because the carapace accounts for over half of the total ash-free dry weight of the tortoise body.



1989 ◽  
Vol 67 (6) ◽  
pp. 1599-1602 ◽  
Author(s):  
Vital Boulé ◽  
Gerard J. Fitzgerald

Female threespine sticklebacks (Gasterosteus aculeatus) spend only 9–15 days on the spawning grounds, an intertidal salt marsh at Isle Verte, Quebec, during a 2-month breeding season. Individuals average only one spawning. However, in the laboratory they lay clutches of several hundred eggs every 3–5 days for several months. We designed laboratory experiments to determine (i) whether daily temperature fluctuations similar to those encountered in the marsh affect reproduction (number of clutches, number of eggs per clutch, and size of eggs) and (ii) whether the amplitude of the fluctuations encountered by the fish affects reproduction. We compared the reproduction of females held in fluctuating temperatures with that of females kept at 20 °C. Fish kept under fluctuating conditions produced more eggs per clutch but had longer interspawning intervals than those at 20 °C. Total seasonal egg production and egg size did not differ between the two groups. Fish in fluctuating temperatures survived longer and were in better condition than those at 20 °C. We conclude that the amplitude of the fluctuations is less important than mean temperature in determining reproductive performance. Fluctuating temperatures on the spawning grounds are not responsible for the short residency there.



2006 ◽  
Vol 84 (8) ◽  
pp. 1210-1215 ◽  
Author(s):  
Pei-Jen L. Shaner

Food availability often drives consumer population dynamics. However, food availability may also influence capture probability, which if not accounted for may create bias in estimating consumer abundance and confound the effects of food availability on consumer population dynamics. This study compared two commonly used abundance indices (minimum number alive (MNA) and number of animals captured per night per grid) with an abundance estimator based on robust design model as applied to the white-footed mouse ( Peromyscus leucopus (Rafinesque, 1818)) in food supplementation experiments. MNA consistently generated abundance estimates similar to the robust design model, regardless of food supplementation. The number of animals captured per night per grid, however, consistently generated lower abundance estimates compared with MNA and the robust design model. Nevertheless, the correlations between abundance estimates from MNA, number of animals captured, and robust design model were not influenced by food supplementation. This study demonstrated that food supplementation is not likely to create bias among these different measures of abundance. Therefore, there is a great potential for conducting meta-analysis of food supplementation effect on consumer population dynamics (particularly in small mammals) across studies using different abundance indices and estimators.



Ecology ◽  
1997 ◽  
Vol 78 (8) ◽  
pp. 2504-2511 ◽  
Author(s):  
Jeffrey F. Kelly ◽  
Beatrice Van Horne


2010 ◽  
Vol 25 (3) ◽  
pp. 682-690 ◽  
Author(s):  
Garth Herring ◽  
Mark I. Cook ◽  
Dale E. Gawlik ◽  
Erynn M. Call


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