Feral horse demography and population growth in the Kaimanawa Ranges, New Zealand

2004 ◽  
Vol 31 (2) ◽  
pp. 119 ◽  
Author(s):  
Wayne L. Linklater ◽  
Elissa Z. Cameron ◽  
Ed O. Minot ◽  
Kevin J. Stafford

Although feral horses are a common management problem in numerous countries, detailed and long-term demographic studies are rare. We measured the age and sex structure, and pregnancy, birth and death rates in a population of 413 feral horses in New Zealand during 1994–98 and used them to construct a model simulating population growth. Survivorship increased with age (0–1 years old = 86.8%, 1–2 = 92.3%, 2–4 = 92.4%, ≥�4 years old = females 94%, males 97% per annum). Birth sex ratio parity, a slight female bias in the adult sex ratio (92 males per 100 females) and higher adult male survivorship indicated lower average survivorship for young males than females that was not detectable in mortality statistics. Pregnancy and foaling rates for mares ≥�2 years old averaged 79 and 49%, respectively. Foaling rates increased as mares matured (2–3-year-old mares = 1.9%, 3–4 = 20.0%, 4–5 = 42.1%, ≥�5 = 61.5% per annum). Young mares had higher rates of foetal and neonatal mortality (95% of pregnancies failed and/or were lost as neonatal foals in 2–3-year-old mares, 70.6% in 3–4, 43.2% in 4–5, and 31% in mares ≥�5 years old). Population growth was 9.6% per annum (9.5–9.8, 95% CI) without human-induced mortalities (i.e. r = 0.092). Our model, standardised aerial counts, and historical estimates of annual reproduction suggest that the historical sequence of counts since 1979 has overestimated growth by ~50% probably because of improvements in count effort and technique.

2020 ◽  
Vol 89 (12) ◽  
pp. 2909-2921
Author(s):  
Charlotte E. Regan ◽  
Sarah A. Medill ◽  
Jocelyn Poissant ◽  
Philip D. McLoughlin

1989 ◽  
Vol 67 (5) ◽  
pp. 1279-1284 ◽  
Author(s):  
J. Servan ◽  
P. Zaborski ◽  
M. Dorizzi ◽  
C. Pieau

Adult sex ratio in the turtle Emys orbicularis was determined in populations from seven ponds in Brenne (Indre, France). In all populations, the sex ratio was biased toward females. Among 290 captured animals, the male:female ratio was close to 0.5. Among different demographic factors that could affect the adult sex ratio, the most influential was probably the sex ratio of hatchlings. In Emys orbicularis, a ZZ male/ZW female system of genotypic sex determination has been postulated. Moreover, gonad differentiation is dependent on temperature and sex-reversed individuals can occur. To evaluate the importance of sex reversal among adult females, the blood of 78 animals was typed for the serologically detectable H-Y antigen, used as a tool to identify sexual genotype. In 73 of them, the H-Y phenotype was positive, conforming with female genotype, but in the other 5 females, it was negative (as in genotypic males), revealing that the sexual phenotype of these animals had been inverted. As the percentage of these sex-reversed genotypic males is low, the influence of temperature would appear not to be the sole cause of the observed unbalanced sex ratio. The female bias can be partly explained by the interaction of temperature with the ZZ/ZW system of genotypic sex determination. Indeed, in this system, sexual inversion under the influence of an epigenetic factor increases the ratio of genotypic females (ZW and WW) in the progeny.


The Auk ◽  
1987 ◽  
Vol 104 (2) ◽  
pp. 234-241 ◽  
Author(s):  
John R. Probst ◽  
Jack P. Hayes

Abstract We compared pairing success of male Kirtland's Warblers (Dendroica kirtlandii) in different habitats to test the hypothesis that a lower proportion of males in marginal habitat are mated. Fewer than 60% of the males in marginal habitat were paired, but 95% of the males in suitable habitat were paired. We estimated the overall pairing success of the known breeding population at 85%. We could not estimate the number of females because the adult sex ratio is unknown, and an unknown proportion of Kirtland's Warblers are polygynous. The Kirtland's Warbler population was fairly constant from 1971 to 1983, despite markedly improved nest success resulting from cowbird control measures. If there are more males than females, or if many females fail to breed or must accept mated males or marginal habitat, population growth could be impeded. We combined reduced pairing success with an estimate of fledgling mortality, and revised the estimated number of fall immatures to between 369 and 471 birds-about 36% lower than the uncorrected estimate. Lower annual productivity of a static population implies higher annual survivorship of adults, yearlings, or both.


2017 ◽  
Vol 114 (27) ◽  
pp. E5474-E5481 ◽  
Author(s):  
Luke J. Eberhart-Phillips ◽  
Clemens Küpper ◽  
Tom E. X. Miller ◽  
Medardo Cruz-López ◽  
Kathryn H. Maher ◽  
...  

Adult sex ratio (ASR) is a central concept in population biology and a key factor in sexual selection, but why do most demographic models ignore sex biases? Vital rates often vary between the sexes and across life history, but their relative contributions to ASR variation remain poorly understood—an essential step to evaluate sex ratio theories in the wild and inform conservation. Here, we combine structured two-sex population models with individual-based mark–recapture data from an intensively monitored polygamous population of snowy plovers. We show that a strongly male-biased ASR (0.63) is primarily driven by sex-specific survival of juveniles rather than adults or dependent offspring. This finding provides empirical support for theories of unbiased sex allocation when sex differences in survival arise after the period of parental investment. Importantly, a conventional model ignoring sex biases significantly overestimated population viability. We suggest that sex-specific population models are essential to understand the population dynamics of sexual organisms: reproduction and population growth are most sensitive to perturbations in survival of the limiting sex. Overall, our study suggests that sex-biased early survival may contribute toward mating system evolution and population persistence, with implications for both sexual selection theory and biodiversity conservation.


2012 ◽  
Vol 15 (5) ◽  
pp. 466-471 ◽  
Author(s):  
M. de L. Brooke ◽  
T. P. Flower ◽  
E. M. Campbell ◽  
M. C. Mainwaring ◽  
S. Davies ◽  
...  

1991 ◽  
Vol 69 (1) ◽  
pp. 208-212 ◽  
Author(s):  
Dan L. Johnson ◽  
Heather C. Proctor

The effect of predator presence on the adult sex ratio of a spider mite (Panonychus ulmi) was examined in a field experiment. Phytoseiid predators (chiefly Typhlodromus occidentalis) were removed from 32 trees harboring P. ulmi populations, and allowed to remain at natural levels on 32 other trees. Both total population density and proportion of males in the prey population were significantly higher in predator-free trees. Mechanisms that could explain the increase in the proportion of males are examined. The most probable is that greater male activity results in a higher encounter rate between predator and prey, and that subsequent higher male mortality when predators are present exaggerates the female-biased sex ratio. The theoretical effects of sex-biased predation on diplo-diploid and haplo-diploid organisms are discussed.


2015 ◽  
Vol 2 (1) ◽  
pp. 140402 ◽  
Author(s):  
Ryan Schacht ◽  
Monique Borgerhoff Mulder

Characterizations of coy females and ardent males are rooted in models of sexual selection that are increasingly outdated. Evolutionary feedbacks can strongly influence the sex roles and subsequent patterns of sex differentiated investment in mating effort, with a key component being the adult sex ratio (ASR). Using data from eight Makushi communities of southern Guyana, characterized by varying ASRs contingent on migration, we show that even within a single ethnic group, male mating effort varies in predictable ways with the ASR. At male-biased sex ratios, men's and women's investment in mating effort are indistinguishable; only when men are in the minority are they more inclined towards short-term, low investment relationships than women. Our results support the behavioural ecological tenet that reproductive strategies are predictable and contingent on varying situational factors.


2018 ◽  
Vol 285 (1891) ◽  
pp. 20181251 ◽  
Author(s):  
Andrea E. Wishart ◽  
Cory T. Williams ◽  
Andrew G. McAdam ◽  
Stan Boutin ◽  
Ben Dantzer ◽  
...  

Fisher's principle explains that population sex ratio in sexually reproducing organisms is maintained at 1 : 1 owing to negative frequency-dependent selection, such that individuals of the rare sex realize greater reproductive opportunity than individuals of the more common sex until equilibrium is reached. If biasing offspring sex ratio towards the rare sex is adaptive, individuals that do so should have more grandoffspring. In a wild population of North American red squirrels ( Tamiasciurus hudsonicus ) that experiences fluctuations in resource abundance and population density, we show that overall across 26 years, the secondary sex ratio was 1 : 1; however, stretches of years during which adult sex ratio was biased did not yield offspring sex ratios biased towards the rare sex. Females that had litters biased towards the rare sex did not have more grandoffspring. Critically, the adult sex ratio was not temporally autocorrelated across years, thus the population sex ratio experienced by parents was independent of the population sex ratio experienced by their offspring at their primiparity. Expected fitness benefits of biasing offspring sex ratio may be masked or negated by fluctuating environments across years, which limit the predictive value of the current sex ratio.


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