The influence of sibling gender on the growth and survival of Great-tailed Grackle nestlings

1990 ◽  
Vol 68 (9) ◽  
pp. 1925-1930 ◽  
Author(s):  
Kevin L. Teather

Growth and survival of Great-tailed Grackle (Quiscalus mexicanus) nestlings were monitored over 3 years to determine if greater food demands of sons influenced nestling success. I predicted that (i) the growth rates of nestlings would be lower in nests containing mostly males, and (ii) the chance of all nestlings in predominantly male broods fledging would be less than that in predominantly female broods. Sibling gender and the overall sex ratio of the brood had little effect on nestling growth. There was no evidence that starvation was more frequent if the oldest nestlings were males rather than females, although there was some evidence that broods of three containing two or three males were less likely to fledge all nestlings than those containing two or three females. Mass at fledging for both males and females was influenced most strongly by hatching sequence and to a lesser extent by egg mass and hatching date.


2009 ◽  
Vol 78 (2) ◽  
pp. 414-426 ◽  
Author(s):  
Marion Nicolaus ◽  
Stephanie P. M. Michler ◽  
Richard Ubels ◽  
Marco van der Velde ◽  
Jan Komdeur ◽  
...  


1971 ◽  
Vol 28 (8) ◽  
pp. 1153-1165 ◽  
Author(s):  
V. S. Kennedy ◽  
D. H. Steele

Monthly samples of winter flounder taken in Long Pond from November 1962 to October 1963 indicated that the flounder moved into deeper water (7–10 m) during the summer and returned to shallow water (1–2 m) from September to June. These movements corresponded to the end of the spawning season and the ripening of the gonads respectively. Spawning occurred from March until early June, most of it in May and early June. Most males were mature at age 6 and most females at age 7. Fifty percent of the males and females were mature at 21 and 25 cm respectively. The growth rates of the males and females were similar until the age of 8, after which the females apparently outgrew the males. Early growth and fecundity were similar to those reported for other areas. No feeding took place in December or January but the flounder fed in March and continued to feed throughout the summer; food intake decreased in the fall. They were omnivorous and the type of food eaten varied with the locality. Polychaetes, plant material, and molluscs were the most common food items throughout the year. Capelin eggs and fish remains were found only during a few months of the year but were eaten in great quantities.



1966 ◽  
Vol 98 (6) ◽  
pp. 639-644 ◽  
Author(s):  
B. C. Smith

AbstractThe weight and size of coccinellid adults varied with species, sex, and feeding. Intraspecies variation in weight was generally similar in the eight species studied. Females were more variable than males in body size. Females of some species were heavier and larger than males, and species can be classified on a basis of difference in the weight and size of the sexes.An increase in the food supply after a period of food scarcity affected the sex ratio, as the minimum food requirement of females was greater than males. Females increased in weight more rapidly than males after feeding. The availability of food in the field affected the weight and size of some species. Adult water content was influenced by feeding but not by sex or the quantity of food given to the larva.Males were more abundant in species with small sexual differences in weight and size. The degree of difference in weight and size between males and females may be used as a criterion to select species that are best adapted to survive when food is scarce.



Copeia ◽  
1992 ◽  
Vol 1992 (4) ◽  
pp. 1098 ◽  
Author(s):  
Alan B. Bolten ◽  
Karen A. Bjorndal ◽  
Janice S. Grumbles ◽  
David W. Owens


1965 ◽  
Vol 97 (5) ◽  
pp. 541-549 ◽  
Author(s):  
E. P. Smereka

AbstractThe life history of Chrysomela crotchi, a univoltine species commonly found on trembling aspen, was studied in northwestern Ontario from 1959 to 1962. The most striking feature of its life history was the longevity of adults, which were capable of overwintering two successive years. Overwintered adults became active and began feeding in late May, and oviposition occurred from early June to late July. The incubation period was approximately 10 days and the three larval instars required approximately one month for development to the adult stage.Females laid more eggs during their second season and the highest number laid was 326. The number of eggs in an egg mass averaged 37.6, and the average interval between the deposition of egg masses was 4 days. Males and females mated more than once, but only one mating was necessary for a female to produce viable eggs throughout the season. Males were capable of fertilizing more than one female and remained potent for more than one season.Parasitism was low, and only two species of larval parasites were reared. Several predator species were observed preying on the immature stages. Predation and overwintering mortality appeared to be the most important control factors.



1987 ◽  
Vol 65 (4) ◽  
pp. 1021-1027 ◽  
Author(s):  
Christian Lydersen ◽  
Ian Gjertz

Samples were taken from 284 ringed seals (Phoca hispida) in the Svalbard area during April–July 1981 and March–April 1982. The age of 283 seals was determined by reading annuli in the cementum of the canine teeth. The mean age of the males was 11.3 years, and of the females, 14.9 years. Females were found to be significantly older than males. The mean length of sexually mature ringed seals was 128.9 cm for both sexes. The mean weight of adult males and females was 53.5 and 61.4 kg, respectively. Females were found to be significantly heavier than males. The sex ratio was 47.8% males and 52.2% females. Studies of microscopic sections of testis and epididymis from ringed seal males showed that 63, 75, and 80% of 5-, 6-, and 7-year-old animals, respectively, were sexually mature. The weights of testis and epididymis, diameters of tubuli, and the size of testis all showed a marked increase in the 5-year age-class. Macroscopic sections of ovaries from ringed seal females showed that 20, 60, and 80% of 3-, 4-, and 5-year-old animals, respectively, were sexually mature. The size of the ovaries showed a marked increase in the 5-year age-class. The ovulation rate of ringed seals from Svalbard was calculated to be 0.91.



Parasitology ◽  
2006 ◽  
Vol 132 (6) ◽  
pp. 757-765 ◽  
Author(s):  
M. C. TINSLEY ◽  
M. E. N. MAJERUS

Whilst most animals invest equally in males and females when they reproduce, a variety of vertically transmitted parasites has evolved the ability to distort the offspring sex ratios of their hosts. One such group of parasites are male-killing bacteria. Here we report the discovery of females of the ladybirdAnisosticta novemdecimpunctatathat produced highly female-biased offspring sex ratios associated with a 50% reduction in egg hatch rate. This trait was maternally transmitted with high efficiency, was antibiotic sensitive and was infectious following experimental haemolymph injection. We identified the cause as a male-killingSpiroplasmabacterium and phylogenetic analysis of rDNA revealed that it belongs to theSpiroplasma ixodetisclade in which other sex ratio distorters lie. We tested the potential for interspecific horizontal transfer by injection from an infectedA. novemdecimpunctataline into uninfected individuals of the two-spot ladybirdAdalia bipunctata. In this novel host, the bacterium was able to establish infection, transmit vertically and kill male embryos.



1994 ◽  
Vol 21 (4) ◽  
pp. 473 ◽  
Author(s):  
AC Robinson ◽  
L Lim ◽  
PD Cantry ◽  
RB Jenkins ◽  
CA MacDonald

A mark-recapture study of Petrogale xanthopus at Middle Gorge in the southern Flinders Ranges revealed that between January 1979 and January 1984 the estimated known-to-be-alive population ranged from 11 to 20. During the main study, individuals living to an estimated age of six years were recorded. Captures of marked animals after completion of the main study revealed both males and females living to at least 10 years old. Births occurred throughout the year but there appeared to be an increase in births following periods of effective rainfall. For the whole study the sex ratio of pouch young did not vary significantly from 1:1. When individuals that gave birth more than once during the study were examined, there was a significant bias towards male young in the later births. It is suggested that this species has a two-phase reproductive strategy with the extra males, produced by older females, sustaining a male-exchange system with nearby colonies.



2018 ◽  
Vol 7 (2) ◽  
pp. 111-115
Author(s):  
Olga Aleksandrovna Sklueva ◽  
Valeriy Vitalyevich Sklyuev ◽  
Rafik Ibragimovich Khakimov

The paper presents some data on the red fox ( Vulpes vulpes , Linnaeus, 1758) sex ratio in the Krasnoarmeysky District of the Samara Region. The results of winter trails traces of mammals show the placement of individual sites of males and females. The authors consider relationship between the population dynamics, sex and age composition and the placement of individual sites. Some aspects of behavioral adaptations and causes of changes in the number of animals in the study area are considered. The influence of a poaching factor on the dynamic indicators of the studied population and the possible danger of the epizootic process is described. A comparative analysis with the previously obtained data on the ratio of males and females in the litter is carried out. The paper indicates possible causes of animals number changes in the study areas. Poaching has a direct impact on the studied population homeostatic state maintaining mechanisms. There is also a forecast of poaching influence on deterioration of epidemiological and epizootic situation in the investigated region. In this paper we give recommendations to minimize possible damage by human activities.



2000 ◽  
Vol 23 (1) ◽  
pp. 97-103 ◽  
Author(s):  
Lincoln S. Rocha ◽  
André Luiz P. Perondini

In sciarid flies, the control of sex determination and of the progeny sex ratio is exercised by the parental females, and is based on differential X-chromosome elimination in the initial stages of embryogenesis. In some species, the females produce unisexual progenies (monogenic females) while in others, the progenies consist of males and females (digenic females). The sex ratio of bisexual progenies is variable, and departs considerably from 1:1. Bradysia matogrossensis shows both monogenic and digenic reproduction. In a recently established laboratory strain of this species, 15% of the females were digenic, 10% produced only females, 13% produced only males, and 62% produced progenies with one predominant sex (33% predominantly of female and 29% predominantly male progenies). These progeny sex ratios were maintained in successive generations. Females from female-skewed progenies yielded female- and male-producing daughters in a 1:1 ratio. In contrast, daughters of females from male-skewed progenies produce bisexual or male-skewed progenies. The X-chromosome of B. matogrossensis shows no inversion or other gross aberration. These results suggest that the control of the progeny sex ratio (or differential X-chromosome elimination) involves more than one locus or, at least, more than one pair of alleles. The data also suggest that, in sciarid flies, monogeny and digeny may share a common control mechanism.



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