Sex determination in the Lesser Flamingo (Phoenicopterus minor) using morphological measurements

Morphological measurements and blood samples were taken from 154 Lesser Flamingos Phoenicopterus minor, including adults (>3 years old), immature sub-adults (2–3 years old) and first-year juvenile birds of both sexes, captured at Lake Bogoria, Kenya (0°11'–20' N, 036°06' E) during 2001 and 2002. PCR amplification of the CHD-Z and CHD-W genes using DNA extracted from the blood samples was used to determine the sex of each bird. There were significant differences in mass and tarsus length among the three age groups, indicating that Lesser Flamingos continue to grow in skeletal size and mass between fledging and the attainment of adult plumage at 3–4 years of age. On average, males were significantly larger than females in all age groups, although there was substantial overlap between the sexes in all morphological measurements. The element with the least amount of overlap was head-and-bill length. Discriminant functions utilising head-and-bill length that correctly predict the sex of juvenile and immature birds with approximately 93% accuracy are presented. By adding total tarsus length, the sex of wild adult Lesser Flamingos is correctly predicted with approximately 98% accuracy. The same discriminant function developed for wild adult birds predicted the sex of 19 captive adult Lesser Flamingos of known sex with 100% accuracy.     

Sexing greater flamingos by weight and linear measurements

The sex of 59 adult Greater Flamingos (Phoenicopterus ruber roseus L.) was determined by laparoscopic exam of the gonads. Concomitant body weight (kg) and linear measurements (mm) of the culmen (bill), tarsus, middle toe, and wing were taken and compared for males vs. females. Although an overlap between sexes existed in all measurements, males on average were larger than females. Student's t-test indicated significant sexual differences for all five measurements. Thus, weights and linear measurements—especially tarsus, middle toe, and wing length—appear to be a useful parameter in determining an individual's sex in lieu of laparoscopic, feather pulp, blood chromosome, or fecal steroid analysis.     

Avian forensics: predicting body fat and body mass from wing remains

We describe the development of a method to predict percent body fat of killed birds from the percent fat in the most distal wing tissue, which is often left uneaten by aerial predators. When combined with a measure of body structural size, such as tarsus, culmen or keel length, percent wing fat can be used to predict fresh body mass at the time of death. These techniques may prove useful in field studies of mass-dependent predation risk.     

Die Nahrungsprobleme des Zwergflamingos. Rätselhafte Massensterben an den Salzseen

The Lesser Flamingo is well adapted to the extreme conditions for survival at saline‐alkaline waters in Africa and India. It's preferred food is the cyanobacterium Arthrospira fusiformis, which is able to exhibit mass developments in these waters. During the last two decades, an increasing deficite of healthy food of the Flamingos have been reported. Situation reports from the main distribution areas of the Lesser Flamingos show the negative influence of anthropogenic degradation of the habitats of these birds and their food.     

树麻雀表型的环境适应进化

树麻雀(Passer montanus)分布范围广、海拔梯度大,也是人类活动的伴随物种。对中国837个样本的10个形态特征与温度、日照、海拔和风速等4个主要环境因子进行相关分析,结果显示:树麻雀的体重、嘴裂、翅长、尾长、跗跖长、脑骨宽、眼间距与日照因子显著相关(P0.05),体重、体长、翅长、尾长、跗跖长与海拔因子显著相关(P0.05),体重、嘴峰、翅长、脑骨长与温度因子显著相关(P0.05),表明树麻雀的形态指标易随环境因子的变化而变化。通过控制经度和海拔两个变量,对形态指标与纬度的偏相关分析表明,体重、翅长、脑骨长和脑骨宽与纬度呈显著正相关(P0.05),体表突出部分嘴峰、嘴裂与纬度呈显著负相关(P0.05),即随着纬度的升高,树麻雀身体逐渐变大,符合贝格曼规律;体表突出部分嘴峰和嘴裂随纬度升高变短,符合阿伦规律。飞行能力与海拔因子呈极显著正相关(n=92,r=0.217,P=0.038),表明树麻雀在高海拔地区具有更强的飞行能力,这也许是它成为广布种的重要原因。     

4.—A FIELD-NATURALISTS PEREGRINATIONS

Geldenhuys, J. N. 1983. Morphological variation in wing-moulting South African Shelducks. Ostrich 54:19-25. Male and female South African Shelducks Tadorna cana lose 25,6 and 28,2% of their pre-moult weight during the flightless period. Juveniles (3–5 months old) do not take part in the wing-moult aggregation. Subadults (15–17 months old) cannot be distinguished from older birds in wing-moulting populations on the basis of the bursa of Fabricius, penis structure, colour of the wing feathers, foot colour and the size of the culmen and tarsus. It is suggested that the catabolism of body tissue during wing-moult has little effect on the survival of the species.     

Growth of nestling Barn Owls Tyto alba in central Mali

Data on growth of 276 young Barn Owls were analysed with respect to the effects of year and month of hatching, hatch order and brood order. Growth characteristics considered were weight; lengths of culmen, tarsus, central tail feathers and quill of third outermost primary; standard wing length; and wing span. For weight the growth constant K was 0151 and time t ₁₀- t ₉₀ was 32-2 days. Least-squares analyses showed that gain in weight and culmen and tarsus length were affected by month of hatching with young hatched in the middle part of the breeding season showing the most rapid growth. Hatch order affected gain in weight. Differences in growth rates of all these characters were not, however, reflected in differences in weight or length at fledging except for the effects of brood on weight with second broods fledging at significantly lighter weights than first ones. Predictive equations for character against age are provided for all linear measurements. All characters examined attained apparent asymptotes before fledging except tail and standard wing length.     

Body size variation in Audouin's Gull Larus audouinii; a density-dependent effect?

A significant decrease in the body size of Audouin's Gulls Larus audouinii breeding at the Chafarinas Islands is reported. The decrease in linear measurements in the current breeding population ranged from 2.5% to 5.6% in males and from 0.61% to 4.4% in females. This was detected when assessing the reliability of a sex-discriminating function derived for the same colony 13 years earlier. When applied to the current population, this function failed to predict the sex of a large proportion of males (44%). The relative decrease in mean size was significantly greater in males than in females for culmen, nalospi and tarsus lengths, while for bill depth at culmen, wing length and body mass the relative decrease was similar in both sexes. Since the extent of differences depended on sex, these differences cannot be attributed to a systematic between-observer bias. Mean body size reduction might be either the result of a greater proportion of small breeding birds in the current population, because of increased availability of nesting sites (competition relaxation hypothesis), or an outcome of environmental factors affecting growth parameters (environmental constraint hypothesis). According to the first hypothesis, the changes observed would be associated with higher variability values. Conversely, if the second is true, the degree of variability should be similar. Since there are no significant differences in the degree of variability shown in the two data sets, our results support the second hypothesis. The environmental constraint acting via growth parameters is probably related to the increase in the number of Audouin's Gull breeding pairs while food availability was depleted. Our data suggest that changes in the duration of the growth period, rather than in the growth rates themselves, are involved in the body size differences found.     

MINUTES OF THE ANNUAL GENERAL MEETING OF THE SOUTH AFRICAN ORNITHOLOGICAL SOCIETY,HELD AT CAPE TOWN, 26 JUNE 1959

Brown, C. J. 1989. Plumages and measurements of the Bearded Vulture in southern Africa. Ostrich 60: 165–171.

Four different age classes of the southern African Bearded Vulture Gypaetus barbatus are recognized and their plumages described: juvenile (3–24 months old), immature (24–45 months), subadult (45–60 months) and adult (60+ months). There was no significant difference in size between adult male and female birds. Adults were larger than juvenile birds in bill width, beard length, wingspan and mass, and had a higher aspect ratio and wing loading, while juvenile birds were larger than adults in the length of their outer rectrices, tail area, wing breadth and wing area. These features are considered to be adaptive to young birds inexperienced in flying. Immature and subadult birds were intermediate in size between juveniles and adults. Bearded Vultures differ from other large raptors in two sets of physical characteristics, (a) those adapted to cold, mountainous habitat, e.g. feathered head and face, unusually long wings, a high aspect ratio and a particularly long tail, and (b) those adapted to their diet of mainly bones, e.g. wide gape, beard and relatively long talons for carrying food.     

Sexual size dimorphism and positive assortative mating in red-backed shrike Lanius collurio: an adaptive value?

During field studies in 1997–1999 in South Bohemia (Czech Republic), we found significant differences in size between the sexes in a local breeding population of red-backed shrike Lanius collurio. Males were significantly larger than females for wing length and tarsus length, but had smaller body mass than females. However, there was considerable overlap in the ranges of these parameters between the sexes. Interestingly, pairs were formed at random with respect to wing length and tarsus length, but assortative mating was significant for body mass/body condition. Among tested variables, only male wing length correlated significantly with nestling body mass at day 7. However, clutch size and the number of fledglings strongly depended on differences in tarsus length between mates, but not on body size of mates. Individual improvements in foraging skills and/or courtship feeding rates are proposed as possible explanations for these findings.     

Gender determination by body weight and linear measurements in American and Chilean flamingos,previously surgically sexed: Within-sex comparison to greater flamingo measurements

Gender was determined by laparoscopic visualization of the gonads for 38 adult American flamingos (Phoenicopterus ruber ruber L.) and 36 adult Chilean flamingos (P. chilensis L.). Concomitant body weight (kg) and linear measurements (mm) of the culmen (bill), tarsus (tarsometatarsus), middle toe, and wing were taken. Statistical comparisons of body weight and linear measurements for male vs. female were made for each species. Also, the same-sex statistical comparisons were made between these two species, and between each of these two species and with data for greater flamingos (P. r. roseas L.) from a previous publication. As previously published for greater flamingos, an overlap between sexes existed in all measurements with males on average larger than females for both American and Chilean flamingos. However, Students' t-test indicated a significant sexual difference for all measurements between males and females of each species except for culmen length in Chilean flamingos. Students' t-test also indicated a significant difference when species were compared (Chilean vs. greater, and American vs. Chilean) and subspecies (American vs. greater) were compared for most of the 5 measurements. Thus, despite limitations imposed by between-sex overlap, weights and linear measurements, especially tarsus, middle toe, and wing length, appear to be useful in determining an individual's gender when species or subspecies identification is considered.     

The effect of egg size on post-hatching development in the Razorbill: an experimental study

A recent experimental study reported that Thick-billed Murre Uria lomvia chicks that hatched from large eggs grew their wing feathers more quickly than did small-egg chicks. There is little evidence of this (or any other) egg-size effect on post-hatching development in other birds. Thick-billed Murres are marine birds of the family Alcidae that employ the unique "intermediate" developmental strategy: chicks go to sea after 15-30 days at the nest site, at <30% of adult mass, accompanied by their male parent. Rapid feather growth during the brief nestling period is critical to enable chicks to make the transition from life at the nest site to life at sea quickly and safely. At the Gannet Islands, Labrador, Canada, in 1996 and 1997, I tested whether egg size has the same effect on wing-feather growth in the Razorbill Alca torda , another of the intermediate auks. To control for underlying correlations between egg size and other parental attributes, eggs were switched randomly among pairs. As in other birds, egg size strongly predicted hatchling mass, and to less extent hatchling size (tarsus length), but had no effect on the rate at which nestlings gained mass. However, egg size had the same effect on wing growth in Razorbills as in Thick-billed Murres: the wings of large-egg chicks began rapid, linear growth sooner, indicating that early development of wing feathers was enhanced in large-egg chicks. Differences in wing length established in this manner persisted through the nestling period. Egg-size effects on feather growth have not been detected in experimental studies on other birds, suggesting that effects of the magnitude seen in Razorbills and Thick-billed Murres might reflect evolutionary priorities in the post-hatching development of intermediate auks.     

Growth of nestling Hamerkops Scopus umbretta in central Mali

Data on growth of nestling Hamerkops Scopus umbretta were analysed with respect to year and season of hatching and to hatch sequence. Quantitative growth characters included weight, culmen, tarsus, tail, third outermost primary quill, standard wing-length and wing span. The growth constant K of weight was 0·179 and time t₁₀–t₉₀ was 21·8 days. Least-squares analyses showed differences in weight gain, culmen-length and tarsus-length related to year and month but not to sequence of hatching. Predictive equations for character against age are provided for all linear measurements. Characters which attained apparent asymptotes before fledging were weight and culmen and tarsus-length whilst other characters varied between 80 and 90% of reported adult size. Qualitative indications of growth discussed are crest development, colouration and the disappearance of the egg-tooth. The rainy and post-rains seasons appear to offer the Hamerkop the best chances of successful breeding and maximum growth rates.     

Morphometric variability on a microgeographical scale in two inshore seabirds

The range of morphometric variation among two inshore seabirds, the Kerguelen cormorant Phalacrocorax atriceps verrucosus and the gentoo penguin Pygoscelis papua was investigated on the Kerguelen and Crozet archipelagos. Four measurements (weight, culmen, flipper and body length for gentoos; weight, culmen, wing and tarsus length for cormorants) were compared in the same seven localities on Kerguelen. In addition, culmen and wing length were compared in four localities on Crozet for gentoo penguins. The two species exhibited similar trends in variation within Kerguelen although the range of variation was greater in cormorants. Compared to the largest cormorants and gentoo of Kerguelen, the smallest stocks were 60 and 36% of the weights, respectively. There is little evidence elsewhere of similar broad morphometric variability in seabirds on a microgeographical scale. The variation observed did not follow a regular cline and appeared to be less related to physical factors (sea temperatures) than to the local biological factors during the breeding season.     

Growth of nestling Hamerkops Scopus umbretta in central Mali

Data on growth of nestling Hamerkops Scopus umbretto were analysed with respect to year and season of hatching and to hatch sequence. Quantitative growth characters included weight, culmen, tarsus, tail, third outermost primary quill, standard wing-length and wing span. The growth constant K of weight was 0.179 and time t₁₀-t₉₀ was 21.8 days. Least-squares analyses showed differences in weight gain, culmenlength and tarsus-length related to year and month but not to sequence of hatching. Predictive equations for character against age are provided for all linear measurements. Characters which attained apparent asymptotes before fledging were weight and culmen and tarsus-length whilst other characters varied between 80 and 90% of reported adult size. Qualitative indications of growth discussed are crest development, colouration and the disappearance of the egg-tooth. The rainy and post-rains seasons appear to offer the Hamerkop the best chances of successful breeding and maximum growth rates.     

Morphometry, diet and habitat in the kingfishers (Aves: Alcedinidae)

Factor analysis of the linear dimensions of 92 species of kingfisher indicated that morphological differences were associated with four diet categories (aquatic, littoral, terrestrial and fossorial animals). Analysis of covariance confirmed the significance of these differences for culmen, tarsus and tail length but not for wing length. Habitat factors resulted in some significant differences but these were less easy to interpret. One case of intraspecific variation showed similar trends for culmen length.     

Genetic and environmental effects on morphology and fluctuating asymmetry in nestling barn swallows

A barn swallow Hirundo rustica partial cross‐fostering experiment with simultaneous brood size manipulation was conducted in two years with contrasting weather conditions, to estimate heritable variation in tarsus, tail and wing size and fluctuating asymmetry. Environmental stress had contrasting effects depending on trait type. Significant heritabilities for tarsus, tail and wing size were found only in enlarged broods irrespective of year effects, while tarsus asymmetry was significantly heritable in the year with benign weather conditions irrespective of brood size manipulation effects. Tail, wing and composite (multicharacter) asymmetry were never significantly heritable. The environment with the higher heritability generally had higher additive genetic variance and lower environmental variance, irrespective of trait type. Heritability was larger for trait size than for trait asymmetry. Patterns of genetic variation in nestlings do not necessarily translate to the juvenile or adult stage, as indicated by lack of correlation between nestling and fledgling traits.     

When Bergmann's rule fails: evidences of environmental selection pressures shaping phenotypic diversification in a widespread seabird

Organisms tend to exhibit phenotypes that can be shaped by climate, commonly demonstrating clinal variations along latitudinal gradients. In vertebrates, air temperature plays a major role in shaping body size in both ectothermic and endothermic animals. However, additional small‐scale environmental factors can also act as selection pressures in the marine ecosystem (e.g. primary productivity), evidencing multi‐scale processes acting on marine organisms. In this study, we tested Bergmann's rule in a widely distributed seabird, the brown booby Sula leucogaster, in addition to evaluating the relationship of sea surface temperature and chlorophyll α with phenotypes. We used traits from a morphometric dataset (culmen, wing chord, and tarsus length) and body mass of 276 brown boobies distributed on six breeding sites along a latitudinal gradient in the South Atlantic Ocean (0–27°S). We found significant differentiation among colonies, but phenotypic similarities were observed between colonies located at the extremes of the latitudinal gradient. As the colony nearest to the Equator, Saint Peter and Saint Paul archipelago, had the largest and heaviest individuals, the model containing only air temperature explained < 5% of the allometric variation, providing no substantial support for Bergmann's rule. However, when we added the interaction of chlorophyll α and sea surface temperature the deviance explained rose to over 80%. Primary productivity and sea surface temperature do not follow a latitudinal gradient in the ocean and, therefore, the role of small‐scale oceanographic processes in shaping body size and the importance of considering additional environmental variables when testing Bergmann's rule in marine organisms are evident.     

Genetic and environmental components of growth in nestling blue tits (Parus caeruleus)

We investigated the effect of brood‐size mediated food availability on the genetic and environmental components of nestling growth in the blue tit (Parus caeruleus), using a cross‐fostering technique. We found genetic variation for body size at most nestling ages, and for duration of mass increase, but not of tarsus growth. Hence, nestling growth in our study population seems to have the potential to evolve further. Furthermore, significant genotype–environment interactions indicated heritable variation in reaction norms of growth rates and growth periods, i.e. that our study population had a heritable plasticity in the growth response to environmental conditions. The decreasing phenotypic variance with nestling age indicated compensatory growth in all body traits. Furthermore, the period of weight increase was longer for nestlings growing up in enlarged broods, while there was no difference to reduced broods in the period of tarsus growth. At fledging, birds in enlarged broods had shorter tarsi and lower weights than birds in reduced broods, but there was no difference in wing length or body condition between the two experimental groups. The observed flexibility in nestling growth suggests that growing nestlings are able to respond adaptively to food constraint by protecting the growth of ecologically important traits.     

Variation in the magnitude of sexual size dimorphism in nestling Coal Tits (Periparus ater)

The magnitude of sexual size dimorphism can be affected by sex differences in environmental sensitivity early in ontogeny that result in differential growth rates of male and female nestlings. Here, the larger sex might either be more sensitive because of higher food demands or less sensitive due to greater competitive ability. When environmental conditions deteriorate during the breeding season, this “environmental stress” hypothesis predicts differential seasonal declines in the performance of male and female offspring. Based on a sample of molecularly sexed Coal Tit (Periparus ater) nestlings from 2 years, we investigated sexual size dimorphism in body mass, condition (i.e. size-corrected mass), tarsus and wing length and whether its magnitude changed from early to late broods. Male offspring were heavier, larger (in terms of tarsus and wing length) and had higher size-corrected mass than their female nest mates (the same was evident in adult breeders). In 2002 (the year with the longer effective breeding season), body mass and condition declined with progressing hatching date and this effect was significantly more pronounced in male than in female nestlings. There was also a seasonal decline in male wing length, while female wing length remained relatively constant, which resulted in males having shorter wings than females in late broods. Tarsus length was unaffected by time of breeding, except that the difference between males and females was relatively smaller in late (i.e. second) broods in 2002. While these results are in accordance with the idea of an increased environmental sensitivity of the larger males, confounding effects of sex-differential hatching order cannot be ruled out. Dedicated to Doris Winkel.