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The properties of bird feathers as converse piezoelectric transducers and as receptors of microwave radiation. II. Bird feathers as dielectric receptors of microwave radiation.

The characteristics of bird feathers as receptors of microwave fields were investigated in the 10- to 16-GHz region. Experiments were conducted coupling the specimen (feather) to a length of waveguide which served, together with other microwave components, as a primary detector. Microwave power radiation patterns were measured both in the presence and in the absence of the specimen. Results indicated a substantial increase in the microwave power collected in the forward direction and a decrease of the radiation pattern beam width when the feather was present. Fruthermore, some experiemental evidence indicated the possibility of inducing piezoelectric effects in the specimen by audiofrequency pulse-modulated microwave fields. These results are important in view of (i) the fundamental role that feathers play in the life of birds and (ii) the influence of environmental factors on bird behaviour.

Animals↗

A feather-trap system for the removal of chicken feathers from laboratory sewage.

A simple feather-trap system is described for use on the drain lines of buildings housing poultry for research or other purposes where floors are frequently washed. The trap uses disposable plastic-mesh bags that can efficiently remove almost all feathers from the water, preventing sewer lines from being blocked by compacted feathers. Critical measurements and operational procedures are described.

Animals↗

Psittacine beak and feather disease: a first survey of the distribution of beak and feather disease virus inside the population of captive psittacine birds in Germany.

Psittacine beak and feather disease (PBFD) is the most common viral disease of wild and captive psittacine birds. Here, we designed the first survey to investigate the existence of subclinical infections and the distribution of the causative agent named beak and feather disease virus (BFDV) inside the population of captive psittacine birds in Germany. DNA was isolated from feathers of 146 symptom-free birds from 19 different genera (all psittaformes) taken from 32 independent breeders from all over Germany. The presence of BFDV was analysed by performing polymerase chain reaction assays. Fifty-eight (39.2%) samples were found to be positive for BFDV. As expected, there was no significant predominance of one sex to be infected with BFDV.

Animals↗

Inheritance of the henny feathering trait in the golden Campine chicken: evidence for allelism with the gene that causes henny feathering in the Sebright bantam.

The henny feathering mutation causes roosters to develop female feathering morphology as a result of increased conversion of androgen to estrogen (aromatase activity) in extraglandular tissues, including skin. This trait is maintained in two breeds of chickens: the Sebright Bantam and the Golden Campine. To characterize the inheritance of this trait further, we did breeding studies of the Golden Campine and identified the trait by measuring aromatase activity in biopsied skin. As previously established for the Sebright Bantam, the trait is transmitted in the Campine by an autosomal, incomplete dominant mechanism; heterozygous offspring express half the levels of extraglandular aromatase as do homozygous Campines on average. No reversions to wild-type levels were observed in 555 heterozygous offspring of crosses between homozygous Campines and normals. Compound heterozygotes for the trait were obtained by mating homozygous Sebrights and homozygous Campines. When these compound heterozygote birds were crossed to control birds, all 98 offspring had elevated aromatase activity in skin, suggesting that the traits in Sebright and Campine birds are allelic. Furthermore, the restriction fragment length polymorphism pattern performed on genomic DNA was the same in the Sebright and Campine birds. Thus, the phenotypic, endocrine, and genetic features suggest that the traits in Sebright and Campine birds are the same. The trait in the Campine probably was derived from the Sebright.

Alleles↗

Embryonic morphogenesis: role of fibrous lattice in the development of feathers and feather patterns.

In the morphogenesis of embryonic feather germs the formation of dermal cell groupings is associated with the development of a highly regular pattern of birefringence in the dermis. This birefringence is due to a lattice-like system of collagenous tracts along which dermal cells become progressively aligned and grouped in regularly spaced sites. The experimental results suggest that this fibrous lattice is of major significance in the morphogenesis of feather germs and in their characteristic pattern of distribution.

Animals↗

Effect of the slow (K) or rapid (k+) feathering gene on body and feather growth and fatness according to ambient temperature in a Leghorn x brown egg type cross.

Chicks of both sexes issued from the cross of heterozygous K/k+ cocks for the slow-feathering sex linked K allele with k+ (rapid feathering) hens, were compared from the age of 4 to 10 weeks at two ambient temperatures. In individual cages, 30 male chicks of each genotype (K/k+ and k+/k+) were raised at 21 degrees C, and 60 others, distributed in the same way, were raised at 31 degrees C. 71 K/W females and 69 k+/W females were raised in a floor pen at 31 degrees C till 10 weeks of age. In the males, the body weight, feed consumption and feed efficiency at different ages were influenced only by temperature (lower growth rate and feed intake at 31 degrees C); no significant effects of the genotype at locus K nor genotype x temperature interaction were observed. In females, all at 31 degrees C, the genotype (K/W or k+/W) had no significant effect on growth rate. Plumage weight and weight of abdominal fat (absolute or related to body weight) were measured on half of the males of each group in individual cages, at 10 weeks of age. Moreover, on 36 males and 48 females of the two genotypes, in a group battery at 31 degrees C, the absolute and relative weight of plumage were measured on a sample every two weeks between 4 and 10 weeks. In the first case, no significant effect of genotype appeared. In the second case, an interaction between age and genotype was suggested from plumage weight: its growth, especially in male chicks, appears to be temporarily and unexpectedly faster from 4 to 6 weeks of age for the K/k+ and K/W genotypes.

Adipose Tissue↗

The influence of ev6 on the immune response to avian leukosis virus infection in rapid-feathering progeny of slow- and rapid-feathering dams.

Endogenous virus (EV) locus ev6 encodes only virus envelope glycoprotein. The influence of ev6 on the immune response to contact infection with hatchmates infected with avian leukosis virus (ALV) was compared in replicate hatches. The ALV Subgroup E-resistant, rapid-feathering (RF) female chickens produced by slow-feathering (SF) and RF dams with and without ev6 were exposed at hatch to hatchmates infected with ALV Subgroup A (Strain RPL-40). The RPL-40 viremia, shedding, and virus neutralizing antibodies were measured among pullets from two hatches at 22 wk of age. Although significant (P less than .05) differences between hatches in the immune response to contact infection were noted among ev6+ pullets, significantly fewer ev6+ pullets seroconverted than their ev6- hatchmates. At 22 wk of age, significantly more lymphomas were also found among ev6+ pullets than among ev6- hatchmates. In flocks wherein both parents and progeny were homozygous resistant to Subgroup E virus, there was no deterimental maternal effect on RF progeny from SF dams that carried ev21. These results also confirm that selection for genetic cellular resistance to Subgroup E ALV infection eliminates congenital transmission of EV21.

Animals↗

A question on the locations of the tardy feathering and henny feathering loci in the chicken.

The locus for tardy feathering (t), previously mapped to the long (q) arm of chromosome 1 of the chicken, was tested for genetic linkage with both the NM 7659 t(Z;1) rearrangement break point (RB) and the henny feathering (Hf) locus. The RB is proximal to the centromere on 1q, and Hf has been reported to be on the proximal one-third of the same arm. Independent segregation of all three markers was found in two separate backcrosses.

Animals↗

The properties of bird feathers as converse piezoelectric transducers and as receptors of microwave radiation. I. Bird feathers as converse piezoelectric transducers.

An investigation was made of the properties of bird feathers as piezoelectric transducers in the audiofrequency range and as dielectric receptors of electromagnetic radiation in the microwave region. In the first case, cartridges of the ceramic and magnetic type and an electromagnetic transducer probe were used as detecting devices. Results show piezoelectric resonances in the 1 to 20-kHz region for the calami of feathers.

Animals↗

Hydrolysis time as a factor affecting the nutritive value of feather meal and feather meal-blood meal combinations for growing calves.

The objectives of this research were to determine 1) the effects of hydrolysis time on feather meal (FTH) protein digestion and ruminal escape and 2) whether adding blood meal (BM) to FTH evoked a complementary response in animal performance. A lamb digestion trial was conducted to estimate true protein digestibility of soybean meal (SBM), BM, and FTH hydrolyzed for 10, 12, 15, or 18 min. Ruminal escape was estimated in situ. Two 94-d growth trials were conducted using 60 growing calves (226 kg) per trial to evaluate urea, FTH, BM, and 87.5:12.5, 75:25, and 50:50 combinations (CP percentage basis) of FTH:BM. There were small numerical differences in estimated escape of protein from the rumen and DM and protein digestibilities due to hydrolysis time. True protein digestibility of the 10- and 18-min samples was 5% higher (P less than .05) than for the 12- or 15-min FTH samples. In the growth trial, the slope-ratio technique showed that the most efficiently used protein supplement was 100% BM (protein efficiency = 2.45 +/- .19). No differences (P = .30) in protein efficiency were observed among supplements containing various combinations of FTH:BM. There was a quadratic (P less than .01) response to the level of BM, indicating a complementary effect. The largest complementary effect occurred at the 12.5% level of the BM addition. There were no nutritionally important effects of hydrolysis time between 10 and 18 min. Furthermore, supplements can be formulated more economically using small amounts of BM with FTH without compromising biological efficiency.

Animal Feed↗

The evolutionary origin and diversification of feathers.

Progress on the evolutionary origin and diversification of feathers has been hampered by conceptual problems and by the lack of plesiomorphic feather fossils. Recently, both of these limitations have been overcome by the proposal of the developmental theory of the origin of feathers, and the discovery of primitive feather fossils on nonavian theropod dinosaurs. The conceptual problems of previous theories of the origin of feathers are reviewed, and the alternative developmental theory is presented and discussed. The developmental theory proposes that feathers evolved through a series of evolutionary novelties in developmental mechanisms of the follicle and feather germ. The discovery of primitive and derived fossil feathers on a diversity of coelurosaurian theropod dinosaurs documents that feathers evolved and diversified in nonavian theropods before the origin of birds and before the origin of flight. The morphologies of these primitive feathers are congruent with the predictions of the developmental theory. Alternatives to the theropod origin of feathers are critique and rejected. Hypotheses for the initial function of feathers are reviewed. The aerodynamic theory of feather origins is falsified, but many other functions remain developmentally and phylogenetically plausible. Whatever their function, feathers evolved by selection for a follicle that would grow an emergent tubular appendage. Feathers are inherently tubular structures. The homology of feathers and scales is weakly supported. Feathers are composed of a suite of evolutionary novelties that evolved by the duplication, hierarchical organization, interaction, dissociation, and differentiation of morphological modules. The unique capacity for modular subdivision of the tubular feather follicle and germ has fostered the evolution of numerous innovations that characterize feathers. The evolution of feather keratin and the molecular basis of feather development are also discussed.

Adaptation, Physiological↗

Growth performance, carcass characteristics, nutrient digestibility and fecal odorous compounds in growing-finishing pigs fed diets containing hydrolyzed feather meal.

This study was designed to determine the effects of hydrolyzed feather meal inclusion on growth performance, carcass characteristics, nutrient digestibility and fecal odorous compounds in modern lean growth genotype pigs. Two hundred forty pigs (BW = 23.2 +/- 1.3 kg) were allotted based on BW and sex to a 2 x 6 factorial arrangement of treatments (four pens per treatment; five pigs per pen) in a randomized complete block design. Factors consisted of 1) sex (barrows or gilts) and 2) dietary treatment (0, 2, 4, 6, 8, or 10% hydrolyzed feather meal). Diets were formulated to contain 1.00, 0.90, 0.75, or 0.60% apparent ileal digestible lysine for phases 1 to 4, respectively, with other amino acids provided at an ideal ratio. Available P and ME were kept constant within each phase. No significant interactions between feather meal inclusion and sex were observed for growth performance (P > 0.15). Body weight gain was reduced (P < 0.05) for pigs fed 10% feather meal compared to pigs fed 0, 4, or 8% feather meal. Feed intake of pigs fed 10% feather meal was reduced (P < 0.05) compared to pigs fed 0 or 4% feather meal. Ultrasound backfat measurements tended (P = 0.12) to increase with increasing levels of feather meal. Daily lean gain was less (P < 0.05) in pigs fed 10% feather meal than in pigs fed either 0, 2, 4, or 8% feather meal. Digestibility of N measured on wk 9 decreased quadratically (P < 0.001) with increasing levels of feather meal. Phosphorus digestibility increased in a linear fashion (P < 0.02), however, the improvement in P digestibility with increasing levels of feather meal was more pronounced in barrows compared to gilts (interaction, P < 0.05). Fecal samples obtained from pigs fed 0, 4, or 8% feather meal were analyzed for odorous compounds. Concentrations of butanoic, pentanoic, and 3-methylbutanoic acid were greater (P < 0.05) and concentrations of 3-methylphenol, 4-methylphenol, indole, and decane were less (P < 0.05) in feces from pigs fed feather meal. These results suggest that feather meal can be included in diets for growing-finishing pigs at a rate of 8%. Excretion of N in feces increased but P excretion decreased with increasing levels of feather meal. Odorous compounds in feces can be affected by the inclusion of hydrolyzed feather meal, but the exact impact of these changes on odor perception remains to be elucidated.

Animal Feed↗

Theory of the growth and evolution of feather shape.

We present the first explicit theory of the growth of feather shape, defined as the outline of a pennaceous feather vane. Based on a reanalysis of data from the literature, we propose that the absolute growth rate of the barbs and rachis ridges, not the vertical growth rate, is uniform throughout the follicle. The growth of feathers is simulated with a mathematical model based on six growth parameters: (1) absolute barb and rachis ridge growth rate, (2) angle of helical growth of barb ridges, (3) initial barb ridge number, (4) new barb ridge addition rate, (5) barb ridge diameter, and (6) the angle of barb ramus expansion following emergence from the sheath. The model simulates growth by cell division in the follicle collar and, except for the sixth parameter, does not account for growth by differentiation in cell size and shape during later keratinization. The model can simulate a diversity of feather shapes that correspond closely in shape to real feathers, including various contour feathers, asymmetrical feathers, and even emarginate primaries. Simulations of feather growth under different parameter values demonstrate that each parameter can have substantial, independent effects on feather shape. Many parameters also have complex and redundant effects on feather shape through their influence on the diameter of the follicle, the barb ridge fusion rate, and the internodal distance. Simulated isochrones-the loci, or sets, of feather cells of the same age-have the same oblique chevron-shaped position in the mature feather as fault bars, which are isochronic defects in the barbules created by a disruptions during development. Accurate simulation of fault bar shape and position confirms the uniform absolute growth rate hypothesis and the general realism of the model. The theory defines a six-parameter feather morphospace, and provides many predictions about the developmental determination of feather shape that can be tested with detailed observations and experiments on developing feathers. This theory also provides testable predictions about the changes in developmental mechanisms required to evolve different feather shapes to accomplish various functions.

Animals↗

The spatial pattern and temporal sequence in which feather germs arise in the white Leghorn chick embryo.

Feather germs arise in a specific sequence and spatio-temporal pattern within each of 10 feather areas on the White Leghorn chick embryo. The time of feather germ initiation was determined by histological and gross macroscopic analyses. Protruding feather germs are sequentially visualized in the dorsal, thigh, breast, head, humoral, ventral, wing, eye, and external auditory meatus feather areas, respectively, from stage 31- to stage 39+ [V. Hamburger and H.L. Hamilton (1951) J. Morphol. 88, 49-92]. The rate at which successive feather tracts appear was found to differ for different feather areas and was not simply due to the size of a feather area. Feather germ histogenesis was examined in the dorsal, thigh, breast, ventral, wing, and tail feather areas. The stages of feather germ histogenesis, examined on the wing feather area, are similar to those previously described for the dorsal surface. Gross and histological analyses gave different times and temporal sequences of feather germ visualization. Some feather areas were readily visualized at the time of feather germ initiation, while others showed a lag between the histological appearance of feather germs and their macroscopic visualization. Thus, macroscopic observations do not accurately reflect the pattern of histogenesis.

Animals↗