scholarly journals Mechanisms of evolutionary change in structural plumage coloration among bluebirds ( Sialia spp.)

2006 ◽  
Vol 3 (9) ◽  
pp. 527-532 ◽  
Author(s):  
Matthew D Shawkey ◽  
Susan L Balenger ◽  
Geoffrey E Hill ◽  
L. Scott Johnson ◽  
Amber J Keyser ◽  
...  
Keyword(s):  
Outer Cortex ◽  
Sialia Sialis ◽  
Sialia Mexicana ◽  
Transmission Electron ◽  
Spongy Layer ◽  
Eastern Bluebirds ◽  
Evolutionary Changes ◽  
Mountain Bluebirds ◽  
Production Mechanisms ◽  
Dark Blue

Combinations of microstructural and pigmentary components of barbs create the colour displays of feathers. It follows that evolutionary changes in colour displays must reflect changes in the underlying production mechanisms, but rarely have the mechanisms of feather colour evolution been studied. Among bluebirds in the genus Sialia , male rump colour varies among species from dark blue to light blue while breast colour varies from blue to rusty. We use spectrometry, transmission electron microscopy and Fourier analysis to identify the morphology responsible for these divergent colour displays. The morphology of blue rump barbs is similar among the three species, with an outer keratin cortex layer surrounding a medullary ‘spongy layer’ and a basal row of melanin granules. A spongy layer is also present in blue breast barbs of mountain bluebirds Sialia currucoides and in rusty breast barbs of western Sialia mexicana and eastern bluebirds Sialia sialis . In blue barbs melanin is basal to the spongy layer, but is not present in the outer cortex or spongy layer, while in rusty barbs, melanin is present only in the cortex. The placement of melanin in the cortex masks expression of structural blue, creating a rusty display. Such shifts in microstructures and pigments may be widespread mechanisms for the evolutionary changes in the colours of feathers and other reflective structures across colourful organisms.

Anisotropic Membranes as Substrates for Sem

1976 ◽  
Vol 34 ◽  
pp. 444-445
Author(s):  
Thomas P. Turnbull ◽  
W. F. Bowers
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
High Flow ◽  
Polymer Chemistry ◽  
Surface Porosity ◽  
Transmission Electron ◽  
Pore Texture ◽  
Spongy Layer ◽  
Scanning Electron

Until recently the prime purposes of filters have been to produce clear filtrates or to collect particles from solution and then remove the filter medium and examine the particles by transmission electron microscopy. These filters have not had the best characteristics for scanning electron microscopy due to the size of the pores or the surface topography. Advances in polymer chemistry and membrane technology resulted in membranes whose characteristics make them versatile substrates for many scanning electron microscope applications. These polysulphone type membranes are anisotropic, consisting of a very thin (0.1 to 1.5 μm) dense skin of extremely fine, controlled pore texture upon a much thicker (50 to 250μm), spongy layer of the same polymer. Apparent pore diameters can be controlled in the range of 10 to 40 A. The high flow ultrafilters which we are describing have a surface porosity in the range of 15 to 25 angstrom units (0.0015-0.0025μm).

Morphometric analysis of the actions of angiotensin II on renal arterioles and glomeruli

1992 ◽  
Vol 262 (3) ◽  
pp. F367-F372 ◽  
Author(s):  
K. M. Denton ◽  
P. A. Fennessy ◽  
D. Alcorn ◽  
W. P. Anderson
Keyword(s):  
Electron Microscopy ◽  
Angiotensin Ii ◽  
Vascular Resistance ◽  
Morphometric Analysis ◽  
Unit Length ◽  
Average Difference ◽  
Outer Cortex ◽  
Efferent Arteriole ◽  
Transmission Electron ◽  
The Right

To study the effects of angiotensin II on afferent and efferent arteriole diameters and on intraglomerular dimensions, angiotensin II (20 ng.kg-1.min-1) or saline vehicle was infused intravenously for 20 min into anesthetized rabbits pretreated with enalapril. Both kidneys were perfusion fixed (glutaraldehyde), and vascular casts were made of the right kidneys using methacrylate. Morphometric analysis of the left kidneys using transmission electron microscopy revealed no significant effects of angiotensin II within the glomerulus, including the degree of mesangial contraction. The diameters of the afferent and efferent arteriole casts from the right kidneys were measured at 20, 50, and 75 microns from the glomerulus by scanning electron microscopy. In the outer cortex the mean diameters of the afferent and efferent arterioles were 14.1 +/- 0.8 and 9.7 +/- 0.5 microns, respectively, in the angiotensin II-infused rabbits, significantly less than in the control (vehicle) rabbits, 17.0 +/- 0.7 microns (P less than 0.001) and 10.7 +/- 0.4 microns (P less than 0.005), respectively. Calculation of the relative changes in vascular resistance, however, indicated that the effects of angiotensin II on efferent arteriole resistance (average difference 2.4 +/- 1.2 units/microns) were significantly greater per unit length than the effects on afferent arteriole resistance (average difference 0.9 +/- 0.3 units/microns). Thus infused angiotensin II caused greater reduction in afferent arteriolar diameter than in efferent, but the calculated increase in vascular resistance per micron was greater in efferent vessels due to their smaller resting diameter.

Ectoparasitic blow flies (Protocalliphora sp.) and nestling Eastern Bluebirds (Sialia sialis): direct effects and compensatory strategies

2006 ◽  
Vol 84 (7) ◽  
pp. 921-930 ◽  
Author(s):  
Kristina Hannam
Keyword(s):  
Brood Reduction ◽  
Direct Effects ◽  
Negative Effects ◽  
Compensatory Strategies ◽  
Blow Flies ◽  
Sialia Sialis ◽  
Eastern Bluebird ◽  
Eastern Bluebirds ◽  
Nestling Period ◽  
Host Parasite

Variation in environmental factors such as parasitism can have direct effects on an organism’s fitness. Because parasites draw resources directly from their hosts, they are expected to have negative effects; however, several nestling host – parasite systems show no evidence of direct effects. Absence of direct effects may be explained by compensation strategies used by parents or nestlings themselves. In this study evidence for both direct effects and compensatory strategies in a blow fly (genus Protocalliphora Hough, 1899) – Eastern Bluebird (Sialia sialis (L., 1758)) system were examined. Nestlings showed no direct effects of blow flies on survival and on size at fledging; however, parasitized broods were significantly anemic. There was no evidence for compensation by parents in the form of brood reduction and there was no support for compensation by nestlings via a hierarchy of tissue preservation. Nestlings did compensate for parasitism by accelerating growth at the end of the nestling period and delaying fledging.

Annual Productivity and Its Measurement in a Multi-Brooded Passerine, the Eastern Bluebird

The Auk ◽  
1979 ◽  
Vol 96 (3) ◽  
pp. 562-572
Author(s):  
Benedict C. Pinkowski
Keyword(s):  
Success Rate ◽  
Age Groups ◽  
Nesting Success ◽  
Egg Laying ◽  
Success Rates ◽  
Sialia Sialis ◽  
Eastern Bluebird ◽  
Annual Productivity ◽  
Eastern Bluebirds ◽  
Breeding Seasons

Abstract Breeding and demographic parameters are examined for 434 Eastern Bluebirds (Sialia sialis) attempting 324 nests in southeastern Michigan during 1968-1977. Nesting birds spent an average of 10.4 weeks (63.9% of a 16.2-week season) in the study area. Only 154 (35.5%) of the nesting birds remained for entire breeding seasons; these season-long residents averaged 2.14 nests/season and had a higher success rate (68.4%) and presumably greater productivity (5.6 young · pair−1 · season −1) than other birds because site fidelity depends on nesting success. Although two seasonal peaks for egg-laying were observed, only 75 of 357 birds (21.0%) successfully raised two broods. Evidence is presented to suggest that birds observed for only part of a season initiated nests at the same rate while in and not in the study area, so that an average annual productivity value of 5.0 young · pair−1 · season −1 is calculated for all nesting birds from the observed success rate (57.1%) and mean length of stay in the area. Estimated average productivity of yearlings (4.3 young · pair−1 · season −1) was lower than that of adults (5.7 young · pair−1 · season −1) although nesting success rates were similar in the two age groups.

Multiple components of feather microstructure contribute to structural plumage colour diversity in fairy-wrens

2019 ◽  
Vol 128 (3) ◽  
pp. 550-568 ◽  
Author(s):  
Marie Fan ◽  
Liliana D’alba ◽  
Matthew D Shawkey ◽  
Anne Peters ◽  
Kaspar Delhey
Keyword(s):  
Plumage Colour ◽  
Structural Elements ◽  
Closely Related Species ◽  
Microscopic Scale ◽  
Colour Variation ◽  
Multiple Components ◽  
Spongy Layer ◽  
Evolutionary Changes ◽  
Genetic And Environmental Factors ◽  
Feather Microstructure

AbstractClosely related species often differ in coloration. Understanding the mechanistic bases of such differences can reveal whether evolutionary changes in colour are driven by single key mechanisms or changes in multiple pathways. Non-iridescent structural plumage colours in birds are a good model in which to test these questions. These colours result from light absorption by pigments, light scattering by the medullary spongy layer (a nanostructure found within barbs) and contributions from other structural elements. Fairy-wrens (Malurus spp.) are a small clade of closely related birds that display a large diversity of ornamental structural colours. Using spectrometry, electron microscopy and Fourier analysis, we show that 30 structural colours, varying from ultraviolet to blue and purple, share a similar barb morphology. Despite this similarity, we find that at the microscopic scale, variation across multiple structural elements, including the size and density of the keratin cortex, spongy layer and melanin, explains colour diversity. These independent axes of morphological variation together account for sizeable amounts of structural colour variability (R2 = 0.21–0.65). The coexistence of many independent, evolutionarily labile mechanisms that generate colour variation suggests that the diversity of structural colours in this clade could be mediated by many independent genetic and environmental factors.

scholarly journals You Can't Judge a Pigment by its Color: Carotenoid and Melanin Content of Yellow and Brown Feathers in Swallows, Bluebirds, Penguins, and Domestic Chickens

The Condor ◽  
2004 ◽  
Vol 106 (2) ◽  
pp. 390-395 ◽  
Author(s):  
Kevin J. McGraw ◽  
Kazumasa Wakamatsu ◽  
Shosuke Ito ◽  
Paul M. Nolan ◽  
Pierre Jouventin ◽  
...  
Keyword(s):  
High Performance ◽  
Domestic Chick ◽  
Gallus Domesticus ◽  
Hirundo Rustica ◽  
Sialia Sialis ◽  
Aptenodytes Patagonicus ◽  
Eastern Bluebirds ◽  
Eudyptes Chrysolophus ◽  
Barn Swallows ◽  
High Concentrations

Abstract The two main pigment types in bird feathers are the red, orange, and yellow carotenoids and the black, gray, and brown melanins. Reports conflict, however, regarding the potential for melanins to produce yellow colors or for carotenoids to produce brown plumages. We used high-performance liquid chromatography to analyze carotenoids and melanins present in the yellow and brown feathers of five avian species: Eastern Bluebirds (Sialia sialis), Barn Swallows (Hirundo rustica), King Penguins (Aptenodytes patagonicus), Macaroni Penguins (Eudyptes chrysolophus), and neonatal chickens (Gallus domesticus). In none of these species did we detect carotenoid pigments in feathers. Although carotenoids are reportedly contained in the ventral plumage of European Barn Swallows (Hirundo rustica rustica), we instead found high concentrations of both eumelanins and phaeomelanins in North American Barn Swallows (H. r. erythrogaster). We believe we have detected a new form of plumage pigment that gives penguin and domestic- chick feathers their yellow appearance. No Puedes Juzgar un Pigmento por su Color: Contenido de Carotenoide y Melanina de Plumas Amarillas y Marrones en Golondrinas, Azulejos, Pingüinos y Gallinas Domésticas Resumen. Los dos tipos principales de pigmentos que las aves incorporan en sus plumas son carotenoides, para desarrollar plumajes rojo, naranja o amarillo, y melaninas, para adquirir coloración negra, marrón, gris o tonalidades color tierra. Sin embargo, existe información conflictiva sobre la potencial coloración de plumas amarillas basadas en melanina y la presencia de caroteniodes en el plumaje marrón de ciertas especies. En este estudio, usamos cromatografía líquida de alto rendimiento para analizar los tipos y cantidades de carotenoides y melaninas presentes en las plumas amarillas y marrones de cinco especies de aves: el azulejo Sialia sialis y la golondrina Hirundo rustica, los pingüinos Aptenodytes patagonicus y Eudyptes chrysolophus y el plumón natal amarillo de la gallina doméstica Gallus domesticus. En ninguna de estas especies detectamos pigmentos carotenoides en las plumas. A pesar de que los carotenoides han sido encontrados en el plumaje ventral de la golondrina Hirundo rustica rustica, nosotros en cambio encontramos altas concentraciones de eumelaninas y feomelaninas en H. r. erythrogaster y en azulejos que variaron entre individuos y regiones de plumaje. Creemos que hemos detectado una nueva forma de pigmento de plumaje que le da a las plumas de pingüinos y pollos domésticos su apariencia amarilla.

scholarly journals Eastern Bluebirds Eject Brown-Headed Cowbird Eggs

The Condor ◽  
2006 ◽  
Vol 108 (3) ◽  
pp. 741-745 ◽  
Author(s):  
Brian D. Peer ◽  
Lyndon R. Hawkins ◽  
Edwin P. Steinke ◽  
Patricia Blair Bollinger ◽  
Eric K. Bollinger
Keyword(s):  
Selective Pressure ◽  
Molothrus Ater ◽  
Conspecific Brood Parasitism ◽  
Sialia Sialis ◽  
Eastern Bluebird ◽  
Egg Ejection ◽  
Cavity Nesting ◽  
Eastern Bluebirds ◽  
Cowbird Parasitism ◽  
The Relationship

Abstract The relationship between the Brown-headed Cowbird (Molothrus ater) and its cavity-nesting hosts has received little attention because of the assumption that cowbirds rarely parasitize these hosts. We tested the Eastern Bluebird (Sialia sialis), a host that is sometimes heavily parasitized by cowbirds, for egg ejection behavior. Bluebirds ejected 65% of experimentally added cowbird eggs (n  =  20), but ejected no experimentally added conspecific eggs (n  =  66). This suggests that cowbird parasitism, not conspecific brood parasitism, is the selective pressure responsible for egg ejection in this species. This level of rejection may be conservative because bluebirds nest in dark cavities, which may make cowbird eggs difficult to detect by bluebirds.

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