Similar-sized Birds Research Articles

A field study of auditory sensitivity of the Atlantic puffin, Fratercula arctica.

Hearing is vital for birds as they rely on acoustic communication with parents, mates, chicks and conspecifics. Amphibious seabirds face many ecological pressures, having to sense cues in air and underwater. Natural noise conditions have helped shape this sensory modality but anthropogenic noise is increasingly impacting seabirds. Surprisingly little is known about their hearing, despite their imperiled status. Understanding sound sensitivity is vital when we seek to manage the impacts of man-made noise. We measured the auditory sensitivity of nine wild Atlantic puffins, Fratercula arctica, in a capture-and-release setting in an effort to define their audiogram and compare these data with the hearing of other birds and natural rookery noise. Auditory sensitivity was tested using auditory evoked potential (AEP) methods. Responses were detected from 0.5 to 6 kHz. Mean thresholds were below 40 dB re.20 µPa from 0.75 to 3 kHz, indicating that these were the most sensitive auditory frequencies, similar to other seabirds. Thresholds in the 'middle' frequency range 1-2.5 kHz were often down to 10-20 dBre.20 µPa. The lowest thresholds were typically at 2.5 kHz. These are the first in-air auditory sensitivity data from multiple wild-caught individuals of a deep-diving alcid seabird. The audiogram was comparable to that of other birds of similar size, thereby indicating that puffins have fully functioning aerial hearing despite the constraints of their deep-diving, amphibious lifestyles. There was some variation in thresholds, yet animals generally had sensitive ears, suggesting aerial hearing is an important sensory modality for this taxon.

Parrot Genomes and the Evolution of Heightened Longevity and Cognition

Parrots are one of the most distinct and intriguing groups of birds, with highly expanded brains [1], highly developed cognitive [2] and vocal communication [3] skills, and a long lifespan compared to other similar-sized birds [4]. Yet the genetic basis of these traits remains largely unidentified. To address this question, we have generated a high-coverage, annotated assembly of the genome of the blue-fronted Amazon (Amazona aestiva) and carried out extensive comparative analyses with 30 other avian species, including 4 additional parrots. We identified several genomic features unique to parrots, including parrot-specific novel genes and parrot-specific modifications to coding and regulatory sequences of existing genes. We also discovered genomic features under strong selection in parrots and other long-lived birds, including genes previously associated with lifespan determination as well as several hundred new candidate genes. These genes support a range of cellular functions, including telomerase activity; DNA damage repair; control of cell proliferation, cancer, and immunity; and anti-oxidative mechanisms. We also identified brain-expressed, parrot-specific paralogs with known functions in neural development or vocal-learning brain circuits. Intriguingly, parrot-specific changes in conserved regulatory sequences were overwhelmingly associated with genes that are linked to cognitive abilities and have undergone similar selection in the human lineage, suggesting convergent evolution. These findings bring novel insights into the genetics and evolution of longevity and cognition, as well as provide novel targets for exploring the mechanistic basis of these traits.

Morphospaces of functionally analogous traits show ecological separation between birds and pterosaurs.

Birds originated and radiated in the presence of another group of flying vertebrates, the pterosaurs. Opinion is divided as to whether birds competitively displaced pterosaurs from small-body size niches or whether the two groups coexisted with little competition. Previous studies of Mesozoic birds and pterosaurs compared measurements of homologous limb bones to test these hypotheses. However, these characters probably reflect differing ancestries rather than ecologies. Here, competition and ecological separation were tested for using multivariate analyses of functionally equivalent morphological characters. As well as using characters from the fore- and hindlimbs, these analyses also included measurements of the lower jaw. The results of this study indicate that pterosaurs had relatively longer jaws, shorter metatarsals and shorter brachial regions compared with birds of similar size. Contrary to the results of previous studies, the distal wing was not important for separating the two clades in morphospace owing to the inclusion of the primary feathers in this unit. The differences found here indicate ecological separation based on differences in size, locomotory features and feeding adaptations. Thus, instead of one group displacing the other, birds and pterosaurs appear to have adopted distinctive ecological strategies throughout their period of coexistence.

Reproductive investment in moa: a K-selected life-history strategy?

The exaggerated K-selected life-history strategy of moa has been suggested as an important factor causing their rapid extinction. Classically, this strategy is characterized by few, large offspring and low fecundity rates. Assuming clutches with one or two eggs as derived from the fossil record, we tested if eggs of moa were larger than the average of similar-sized birds, and estimated their unknown annual breeding frequencies. Therefore, we established allometries on body mass and different reproductive traits (i.e. egg mass, clutch mass and annual clutch mass). These were derived for r-selected (r-model) and for K-selected (K-model) bird species. In agreement with our initial expectations, moa had egg to body mass relations seen in “average” extant K-selected birds. While the K-model pointed to a clutch size of one or two eggs for moa corroborating fossil data and a K-selected life-history, the r-model predicted two to three times larger sizes. Under clutch sizes between one and two eggs and an annual clutch mass as observed in other similar-sized flightless island birds (e.g. rails, ratites), the annual clutch mass allometry suggested one to three clutches per year for moa. Even when assuming less than one brood per year (K-model predicts 0.5 clutches per year); annual clutch masses were still consistent with the K-model. Further studies are needed to clarify whether or not the reproductive strategy of flightless island birds and/or of the birds underlying the K-model fits better to the moa strategy. The approach presented herein, illustrates that combining biological and paleontological data can assist in the reconstruction of species traits, which are insufficiently or not preserved in fossils, but are necessary to understand the evolution of traits.

Inexplicable Inefficiency of Avian Molt? Insights from an Opportunistically Breeding Arid-Zone Species, Lichenostomus penicillatus

The majority of bird species studied to date have molt schedules that are not concurrent with other energy demanding life history stages, an outcome assumed to arise from energetic trade-offs. Empirical studies reveal that molt is one of the most energetically demanding and perplexingly inefficient growth processes measured. Furthermore, small birds, which have the highest mass-specific basal metabolic rates (BMRm), have the highest costs of molt per gram of feathers produced. However, many small passerines, including white-plumed honeyeaters (WPHE; Lichenostomus penicillatus), breed in response to resource availability at any time of year, and do so without interrupting their annual molt. We examined the energetic cost of molt in WPHE by quantifying weekly changes in minimum resting metabolic rate (RMRmin) during a natural-molt period in 7 wild-caught birds. We also measured the energetic cost of feather replacement in a second group of WPHEs that we forced to replace an additional 25% of their plumage at the start of their natural molt period. Energy expenditure during natural molt revealed an energy conversion efficiency of just 6.9% (±0.57) close to values reported for similar-sized birds from more predictable north-temperate environments. Maximum increases in RMRmin during the molt of WPHE, at 82% (±5.59) above individual pre-molt levels, were some of the highest yet reported. Yet RMRmin maxima during molt were not coincident with the peak period of feather replacement in naturally molting or plucked birds. Given the tight relationship between molt efficiency and mass-specific metabolic rate in all species studied to date, regardless of life-history pattern (Efficiency (%) = 35.720•10−0.494BMRm; r2 = 0.944; p = <0.0001), there appears to be concomitant physiological costs entrained in the molt period that is not directly due to feather replacement. Despite these high total expenditures, the protracted molt period of WPHE significantly reduces these added costs on a daily basis.

Refinement of Biomarker Pentosidine Methodology for use on Aging Birds

There is no reliable method for determining age for most species of long-lived birds. Recent success using the skin chemical pentosidine as a biomarker has shown promise as an aging tool for birds. Pentosidine levels have been determined only from the breast tissue of carcasses, and we sought to refine the procedure with respect to biopsy size and location for safe and effective use on living birds. We compared pentosidine concentrations in 4 skin-size samples (4, 6, 8, and 20-mm diameter biopsies) from the breast of black vulture (Coragyps atratus) carcasses. We also compared pentosidine levels from breast and patagial tissue to document potential differences among collection sites of deceased vultures (with unknown ages) and monk parakeets (Myiopsitta monachus; with actual, minimal, and unknown ages). Pentosidine concentrations (pmol pentosidine/mg collagen) were similar among the 4 sizes of vulture breast skin (P = 0.82). Pentosidine concentrations for the breast (0 = 8.9, SE = 0.55, n = 28) and patagium (0 = 8.9, SE = 0.51, n = 28) of vultures were similar, but in parakeets, pentosidine was higher in the breast (0 = 15.9, SE = 1.30, n = 105) than the patagium (0 = 11.5, SE = 1.10, n = 105). We made pentosidine-based age estimates for vultures and parakeets using a general age curve for wild birds. We also made vulture age estimates using plumage characteristics and a cormorant (Phalacrocorax auritus) age curve. Vulture pentosidine-based age estimates appear to correspond to plumage-based age estimates. Pentosidine-based age estimates for 88% of the known-aged parakeets (n = 17) were within 6 months of actual ages. Even though known ages were not available for all birds, we found a positive trend in pentosidine versus age for both species. We suggest that 6-mm diameter skin samples from the patagium of living vultures and other similar-sized birds will provide sufficient tissue for reliable age estimation and will not impair flight ability.

Comparative Morphology of Northern Populations of Breeding Cooper's Hawks

Abstract. Few studies at a broad geographical scale have characterized intraspecific variation in morphology of woodland hawks in the genus Accipiter. From 1999 to 2007 we investigated morphological variation in large samples of live Cooper's Hawks (A. cooperii) nesting in four study areas: coniferous woodland around Victoria, British Columbia, Canada, isolated deciduous woodlands in short-grass prairies of northwestern North Dakota, towns and rural deciduous woodlands along the border of North Dakota and Minnesota, and urban and rural mixed deciduous and coniferous landscapes of Wisconsin. These sites span 2660 km across the northern part of the species' breeding range. We measured body mass (i.e., size), wing chord, tail length, tarsus diameter, hallux length, and culmen length of breeding adults, finding significant and clinal variation in body mass (or size). The smallest and most similar-sized birds occurred in British Columbia and western North Dakota, larger birds along the border between North Dak...

Senescence rates are determined by ranking on the fast–slow life‐history continuum

Comparative analyses of survival senescence by using life tables have identified generalizations including the observation that mammals senesce faster than similar-sized birds. These generalizations have been challenged because of limitations of life-table approaches and the growing appreciation that senescence is more than an increasing probability of death. Without using life tables, we examine senescence rates in annual individual fitness using 20 individual-based data sets of terrestrial vertebrates with contrasting life histories and body size. We find that senescence is widespread in the wild and equally likely to occur in survival and reproduction. Additionally, mammals senesce faster than birds because they have a faster life history for a given body size. By allowing us to disentangle the effects of two major fitness components our methods allow an assessment of the robustness of the prevalent life-table approach. Focusing on one aspect of life history - survival or recruitment - can provide reliable information on overall senescence.

RADIONUCLIDES IN MARINE FISHES AND BIRDS FROM AMCHITKA AND KISKA ISLANDS IN THE ALEUTIANS: ESTABLISHING A BASELINE

Amchitka Island (51degrees N lat, 179 degrees E long) was the site of three underground nuclear tests from 1965-1971. There have been no substantive studies of radionuclides in marine fishes and birds in the area since the mid-1970's. In this study, levels of 60Co, 52Eu, 90Sr, 99Tc, 129I, 137Cs, and the actinides (241Am, 238Pu, 239,240Pu, 234U, 235U, 236U, and 238U) were studied in ten marine fish species (including Pacific Cod Gadus macrocephalus and Pacific Halibut Hippoglossus stenolepis) and five marine bird species (including Glaucous-winged Gulls Larus glaucescens, Tufted Puffins Fratercula cirrhata, and Common Eider Ducks Somateria mollissima) from Amchitka. The same species were collected at a reference site, Kiska Island (52 degrees N lat; 177 degrees E long), about 130 km west of Amchitka. Each sample was a composite of edible muscle from five or more individual fish or birds of similar size (+/-15%) from the same sampling station. The null hypotheses of no differences among species or between Amchitka and Kiska were tested. Most analytic results were below the minimum detectable activity (MDA), even when 1,000 g sizes and 72 h counting times were used. The only radionuclides detected above the MDA were 137Cs, 241Am, 239,240Pu, 234U, 235U, and 238U. There were significant differences in 137Cs as a function of species, but not location, for top predatory fishes. Of the fishes, eight of ten species had 137Cs values above the MDA for some samples; only one bird, Glaucous-winged Gull, had 137Cs values above the MDA. The highest concentrations of 137Cs were in Dolly Varden [Salvelinus malma, 0.780 (Bq kg(-1) wet weight)] and Pacific Cod (0.602 Bq kg(-1)). In aggregate for any actinides, 73 of 234 (31%) composites for fish were above the MDA, compared to only 3 of 98 (3%) for birds. 234U and 238U, radionuclides that are primarily natural in origin, were routinely detected in these biological samples, but there were no significant differences in mean concentrations between Amchitka and Kiska. The concentrations of all radionuclides examined at Amchitka are similar to those of other uncontaminated Northern Hemisphere sites, and are lower than those reported for fishes and birds from the Irish Sea in the vicinity of the Sellafield nuclear reprocessing facility, an area with known contamination.

Circadian metabolic and thermoregulatory patterns of red-billed woodhoopoes (Phoeniculus purpureus): the influence of huddling

Circadian rhythms of metabolic rate and body temperature were measured in groups of huddling and solitary red-billed woodhoopoes (Phoeniculus purpureus) as a function of ambient temperature. Basal metabolic rates were 30-60% lower than those of similar-sized birds of other species. As a consequence, circadian amplitudes of Tb and VO2 fluctuation between the rest and activity phases of non-huddling birds were also larger than expected. Circadian rhythms of metabolism save huddling and non-huddling woodhoopoes 19-34% of their potential daily energy expenditure. Birds huddling in groups conserved 12-29% of the daily energy expenditure of non-huddling birds at ambient temperatures of 20°C and below. However, at 30°C huddling birds used c. 12% more energy than non-huddling birds. The various avenues of energy conservation employed by woodhoopoes are suggested to be beneficial in: a) augmenting the proximate benefits of cooperative breeding; and b) optimizing fitness in the drought-prone sub-Saharan savannahs which are heavily influenced by the El Niño Southern Oscillations.

Differences in Population Density and Energy Use between Birds and Mammals: A Macroecological Perspective

1. Data from 364 mammal and 564 bird species were used to compare these two taxa in the patterns of variation in population density and energy use as a function of body mass. 2. This study demonstrates previously unappreciated quantitative differences between mammals and birds. Over a wide range of sizes, population densities and rates of energy use are at least one order of magnitude higher in mammals than in birds of similar size. The highest population densities are found in species that weigh about 100 g in mammals and 30 g in birds. 3. Comparisons between mammals and birds from the same dietary category indicate that mammals maintain higher densities and use more energy than birds. Insectivorous mammals and birds maintain the lowest densities. 4. Flying mammals and birds reach lower densities and use more energy than non-flying forms. 5. These findings reveal relationships between the morphology, physiology and behaviour of individual organisms and the ecological performance of these endothermic vertebrates in populations, communities and ecosystems: relationships that have not previously been appreciated.

Field Metabolism and Water Requirements of Spinifex Pigeons (Geophaps-Plumifera) in Western-Australia

Spinifex pigeons (Geophaps plumifera) are one of the few avian species that have evolved the capacity to reside in the hot and dry regions of central and north-western Australia. Previous investigation has revealed that their basal metabolic rate (BMR) equals only 68% of allometric prediction. In this study, we addressed the hypothesis that these birds have a reduced field metabolic rate (FMR) and water influx as a result of their lowered BMR. We measured the FMR and water flux of free-living spinifex pigeons by means of the doubly labelled water method. Although body mass of free-living male and female pigeons differed significantly, with males weighing on average 90.8 +/- 7.7 g (+/- s.d.) and females 80.2 +/- 5.6 g, FMR was statistically indistinguishable between sexes. For sexes combined, FMR averaged 139.9 mL CO2 h-1, or 73.5 kJ day-1, a value 38.7% of allometric expectation. These data support the hypothesis that spinifex pigeons have a markedly reduced FMR, probably, in part, the result of a depressed BMR compared with other birds of similar size. Our phylogenetic analysis of the BMR of pigeons lacked sufficient data to determine whether a reduced BMR in Australian pigeons was the consequence of ecological adaptation or phylogenetic constraint. Water influx ranged from 2.5 to 39.0 mL day-1 and averaged 18.4 mL day-1. Of the total water intake, 83.5% came from drinking; their food, seeds, supplied about 4%. Maintenance metabolism, energy allocated to basal plus thermoregulatory metabolism, accounted for about 67% of the average FMR, indicating that the activity requires relatively low energy expenditure in these birds.

Proximate, caloric, nitrogen and mineral composition of bodies of some tropical bats

Proximate (live mass, water, lipid, ash, non-fat organic), caloric, nitrogen, and mineral (sodium, potassium, calcium, magnesium, and iron) concentrations and total body content of individuals of 24 species of Neotropical and Paleotropical bats were determined. Mass-related, concentration patterns were found for all measured variables, except iron. Concentrations increase with size for nitrogen, calcium, and magnesium but are concave, opening upward, for sodium and potassium. These last two elements reach minimal concentrations in bats weighing about 22 and 28 g dry mass, respectively. Total body content of nitrogen and minerals was compared with amounts in similar-sized birds and tetrapodal mammals.

Field Metabolism of Tree Swallows during the Breeding Season

Abstract I used doubly labeled water to study the field metabolic rate (FMR) of Tree Swallows (Tachycineta bicolor) on Kent Island, New Brunswick, Canada, during the breeding season. I tested the hypothesis that aerially foraging species have higher energy requirements than other species. For incubating female swallows, carbon dioxide production averaged 201.4 ± 15.8 ml CO2/h. While feeding 5 young, male and female swallows expired CO2 at a rate of 211.6 ± 23.3 and 231.0 ± 26.4 ml CO2/h, respectively. During this period males worked at similar levels to females, but the power consumption of females that fed young was significantly higher than incubating females. For both parents together, the mean number of visits to the nest/h was correlated with CO2 production: ml CO2/h = 201.6 + 2.49 (visits/h). On Kent Island, Tree Swallows had a higher FMR than Savannah Sparrows (Passerculus sandwichensis), suggesting that aerial-foraging birds have a higher FMR than ground-foraging species. For 7 species of hirundines, energy expenditure was associated positively with body mass; log(kJ/d) = 1.34 + 0.53 log(body mass, g). This relationship differed from one for species which use alternative foraging modes (ground foraging and flycatching, n = 11), log(kJ/d) = 0.89 + 0.75 log(body mass, g). Aerial foragers expend from 16-38% more energy/day than do other birds of similar size that spend less time flying.

ADAPTATION, CONSTRAINT, AND COMPROMISE IN AVIAN POSTNATAL DEVELOPMENT

Summary1. This paper discusses factors that influence the evolution of growth rate and determine its variation among species of birds. Growth rate is related to evolutionary fitness through the use of time, energy, and nutrients. In addition, balances between factors favouring rapid growth and those favouring slow growth may be investigated directly by experiment and by comparative observation.2. David Lack (1968) proposed that the growth rate of the young is the optimum balance between selection for rapid growth to reduce the vulnerable period of development and selection for slow growth to reduce the energy requirements of the young.3. To test Lack's hypothesis, the growth rates of birds, estimated by fitting sigmoid equations to curves relating weight to age, were surveyed widely from the literature. Among all species examined, growth rate was inversely related to adult weight. Among birds of similar size, most variation in growth rate was related to the degree of maturity of the neonate. Altricial chicks, which depend upon their parents for food and warmth, grow more rapidly than precocial chicks, which are self‐sufficient shortly after hatching. Lack's hypothesis, which predicts a direct relationship between growth rate and mortality rate, was not supported.4. I propose that the key to understanding variation in growth rate among birds lies in the balance between rate of cell proliferation or cell growth, on one hand, and acquisition of mature function, on the other. This idea is consistent with principles of cellular and developmental biology. It is supported by comparisons of (a) the neonates of different species, (b) the individual over the course of the developmental period, and (c) tissues whose use is acquired at different stages of development, wherein more mature individuals or tissues grow more slowly than those with less developed function.5. Species of birds that are classified as semi‐precocial develop precocially but grow rapidly. Although these seemingly violate the general rule relating growth rate to precocity, a closer inspection of their development reveals that they too support the rule. In the Common Tern, the legs, which are the key organ in precocial development, grow at the expected slow rate. The body as a whole grows rapidly because the growth increment of the legs is small and their growth is completed quickly.6. Growth rates of precocial birds do not decrease abruptly at hatching. This points more to gradual tissue differentiation than to the pattern of procurement and allocation of energy as the primary control for growth rate.7. Precocious development is favoured when the chicks are capable of self‐feeding or when food supplies are distant from the next site and travelling time between one and the other is long. Precocity of the neonates frees both parents to feed at a distant food source.8. Some species having diets with low levels of protein or other nutrients may grow slowly in order to match nutrient requirements to their availability in the diet. This pattern is indicated especially among the Procellariiformes, which feed an oily diet to their young, and also among tropical fruit‐eating birds.9. Some tropical, pelagically‐feeding sea‐birds that rear only one offspring at a time may not be able to procure food sufficient to support rapid chick growth. Alternative explanations for slow growth among these species include difficulty in obtaining essential nutrients and more precocious development of activity than in related species having more rapid growth.

A comparison of flight energetics in hirundines and other birds

1. 1. Metabolism during flight was estimated for Delichon urbica and Hirundo rustica using the D 2O 18 technique. These estimates were compared with data from the literature for hirundines and other groups of birds. 2. 2. Metabolism during flight in hirundines and swifts lies in the range 0.035-0.069 kcal · g −1· h −1 (2.9 – 5.7 × S.M.R.), which is 49.3%–72.6% lower than other birds of similar size. 3. 3. The relatively low cost of flight in hirundines and swifts is discussed in relation to the aerial feeding habit. Features of the morphology and flight behaviour of aerial feeders are discussed.