Functional integration for enrolment constrains evolutionary variation of phacopid trilobites despite developmental modularity

Modularity and integration are variational properties expressed at various levels of the biological hierarchy. Mismatches among these levels, for example developmental modules that are integrated in a functional unit, could be informative of how evolutionary processes and trade‐offs have shaped organismal morphologies as well as clade diversification. In the present study, we explored the full, integrated and modular spaces of two developmental modules in phacopid trilobites, the cephalon and the pygidium, and highlight some differences among them. Such contrasts reveal firstly that evolutionary processes operating in the modular spaces are stronger in the cephalon, probably due to a complex regime of selection related to the numerous functions ensured by this module. Secondly, we demonstrate that the same pattern of covariation is shared among species, which also differentiate along this common functional integration. This common pattern might be the result of stabilizing selection acting on the enrolment and implying a coordinate variation between the cephalon and the pygidium in a certain direction of the morphospace. Finally, we noticed that Austerops legrandi differs slightly from other species in that its integration is partly restructured in the way the two modules interact. Such a divergence can result from the involvement of the cephalon in several vital functions that may have constrained the response of the features involved in enrolment and reorganized the covariation of the pygidium with the cephalon. Therefore, it is possible that important evolutionary trade‐offs between enrolment and other functions on the cephalon might have partly shaped the diversification of trilobites.     

Drosophila wing modularity revisited through a quantitative genetic approach

To predict the response of complex morphological structures to selection it is necessary to know how the covariation among its different parts is organized. Two key features of covariation are modularity and integration. The Drosophila wing is currently considered a fully integrated structure. Here, we study the patterns of integration of the Drosophila wing and test the hypothesis of the wing being divided into two modules along the proximo‐distal axis, as suggested by developmental, biomechanical, and evolutionary evidence. To achieve these goals we perform a multilevel analysis of covariation combining the techniques of geometric morphometrics and quantitative genetics. Our results indicate that the Drosophila wing is indeed organized into two main modules, the wing base and the wing blade. The patterns of integration and modularity were highly concordant at the phenotypic, genetic, environmental, and developmental levels. Besides, we found that modularity at the developmental level was considerably higher than modularity at other levels, suggesting that in the Drosophila wing direct developmental interactions are major contributors to total phenotypic shape variation. We propose that the precise time at which covariance‐generating developmental processes occur and/or the magnitude of variation that they produce favor proximo‐distal, rather than anterior‐posterior, modularity in the Drosophila wing.     

Structural coloration signals condition, parental investment, and circulating hormone levels in Eastern bluebirds (Sialia sialis)

Many of the brilliant plumage coloration displays of birds function as signals to conspecifics. One species in which the function of plumage ornaments has been assessed is the Eastern bluebird (Sialia sialis). Studies of a population breeding in Alabama (USA) have established that plumage ornaments signal quality, parental investment, and competitive ability in both sexes. Here we tested the additional hypotheses that (1) Eastern bluebird plumage ornamentation signals nest defense behavior in heterospecific competitive interactions and (2) individual variation in plumage ornamentation reflects underlying differences in circulating hormone levels. We also tested the potential for plumage ornaments to signal individual quality and parental investment in a population breeding in Oklahoma (USA). We found that Eastern bluebirds with more ornamented plumage are in better condition, initiate breeding earlier in the season, produce larger clutches, have higher circulating levels of the stress hormone corticosterone, and more ornamented males have lower circulating androgen levels. Plumage coloration was not related to nest defense behavior. Thus, plumage ornamentation may be used by both sexes to assess the physiological condition and parental investment of prospective mates. Experimental manipulations of circulating hormone levels during molt are needed to define the role of hormones in plumage ornamentation.     

Developmental integration in a complex morphological structure: how distinct are the modules in the mouse mandible?

The mouse mandible has long served as a model system for studying the development and evolution of complex morphological structures. We used the methods of geometric morphometrics to reassess the hypothesis that the mandible consists of two separate modules: an anterior part bearing the teeth and a posterior part with muscle attachment surfaces and articulating with the skull. The analyses particularly focused on covariation of fluctuating asymmetry, because such covariation is due exclusively to direct interactions between the developmental processes that produce the traits of interest, whereas variation of traits among individuals also reflects other factors. The patterns of fluctuating asymmetry and individual variation were only partly consistent, indicating that developmental processes contribute differentially to variation at different levels. The results were in agreement with the hypothesis that the anterior and posterior parts of the mandible are separate develop-mental modules. Comparison of all alternative partitions of the landmarks into two contiguous subsets confirmed the hypothesis for the location of the boundary between modules but also underscored that the separation between them is not complete. Modularity is therefore manifest as the relative independence of parts within the framework of overall integration of the mandible as a whole-it is a matter of degrees, not all or nothing.     

The "eyespot module" and eyespots as modules: development, evolution, and integration of a complex phenotype

Organisms are inherently modular, yet modules also evolve in response to selection for functional integration or functional specialization of traits. For serially repeated homologous traits, there is a clear expectation that selection on the function of individual traits will reduce the integration between traits and subdivide a single ancestral module. The eyespots on butterfly wings are one example of serially repeated morphological traits that share a common developmental mechanism but are subject to natural and sexual selection for divergent functions. Here, I test two hypotheses about the organization of the eyespot pattern into independent dorsal-ventral and anterior-posterior modules, using a graphical modeling technique to examine patterns of eyespot covariation among and within wing surfaces in the butterfly Bicyclus anynana. Although there is a hierarchical and complex pattern of integration among eyespots, the results show a surprising mismatch between patterns of eyespot integration and the developmental and evolutionary eyespot units identified in previous empirical studies. These results are discussed in light of the relationships between developmental, functional, and evolutionary modules, and they suggest that developmental sources of independent trait variation are often masked by developmental sources of trait integration.     

Morphometric integration and modularity in configurations of landmarks: tools for evaluating a priori hypotheses

SUMMARY Identifying the modular components of a configuration of landmarks is an important task of morphometric analyses in evolutionary developmental biology. Modules are integrated internally by many interactions among their component parts, but are linked to one another only by few or weak interactions. Accordingly, traits within modules are tightly correlated with each other, but relatively independent of traits in other modules. Hypotheses concerning the boundaries of modules in a landmark configuration can therefore be tested by comparing the strength of covariation among alternative partitions of the configuration into subsets of landmarks. If a subdivision coincides with the true boundaries between modules, the correlations among subsets should be minimal. This article introduces Escoufier's RV coefficient and the multi-set RV coefficient as measures of the correlation between two or more subsets of landmarks. These measures can be compared between alternative partitions of the configuration into subsets. Because developmental interactions are tissue bound, it is sensible to require that modules should be spatially contiguous. I propose a criterion for spatial contiguity for sets of landmarks using an adjacency graph. The new methods are demonstrated with data on shape of the wing in Drosophila melanogaster and the mandible of the house mouse.     

Inferring developmental modularity from morphological integration: analysis of individual variation and asymmetry in bumblebee wings

Organisms are built from distinct modules, which are internally coherent but flexible in their relationships among one another. We examined morphological variation within and between two candidate modules: the fore- and hindwings of bumblebees (Hymenoptera: Apidae: Bombus empatiens). We used the techniques of geometric morphometrics (Procrustes superimposition) to analyze the variation of landmark configurations in fore- and hindwings. Regression was used to correct for size-related shape variation (allometry). Principal component analysis revealed patterns of variation that were remarkably similar for individual variation and fluctuating asymmetry (FA). Because covariation of FA among parts must be due to direct transmission of the developmental perturbations causing FA, this agreement of patterns suggests that much of individual variation is also due to direct developmental interactions within each developing wing. Moreover, partial least squares analysis indicated that the patterns of shape covariation between fore- and hindwings were nearly the same as the patterns of within-wing variation. Shape covariation of FA was only found in bees that had been reared under elevated CO(2) concentration but not in bees from the control treatment, suggesting that the mechanisms of developmental interactions between fore- and hindwings are related to gas exchange. We conclude that the fore- and hindwings are developmental modules that maintain internal coherence through direct developmental interactions and are connected to each other only by relatively few links that use the system of interactions within modules.     

SEXUAL DICHROMATISM IN BIRDS: IMPORTANCE OF NEST PREDATION AND NEST LOCATION FOR FEMALES VERSUS MALES

Examinations of variation in plumage dichromatism in birds have focused on male plumage brightness and largely neglected variation in female plumage brightness. Nest predation previously was concluded to constrain male brightness and thereby reduce dimorphism in ground-nesting birds based on an incorrect assumption that nest predation is greater for ground nests. Correlations of plumage brightness and dichromatism with nest predation have never been tested directly and we do so here with data for warblers (Parulinae) and finches (Carduelinae). We show that male plumage brightness varies among nest heights, but in a pattern that is not correlated with nest predation. Female plumage brightness also varies among nest heights, but in a pattern that differs from males, and one in which variation in female plumage brightness was negatively correlated with nest predation. These results suggest that nest predation may place greater constraints on female than male plumage brightness, at least in taxa where only females incubate eggs and brood young. These results also show that female plumage patterns vary at least partly independently of male patterns and emphasize the need to include consideration of both female and male plumage variation in tests of plumage dimorphism. Plumage dimorphism differs between ground and off-ground nesters as previously described and, if anything, the relationship between plumage dimorphism and nest predation was positive rather than negative as previously argued.     

Morphological integration and serial homology: A case study of the cranium and anterior vertebrae in salamanders

Serial homology or the repetition of equivalent developmental units and their derivatives is a phenomenon encountered in a variety of organisms, with the vertebrate axial skeleton as one of the most notable examples. Serially homologous structures can be viewed as an appropriate model system for studying morphological integration and modularity, due to the strong impact of development on their covariation. Here, we explored the pattern of morphological integration of the cranium and the first three serially homologous structures (atlas, first, and second trunk vertebrae) in salamandrid salamanders, using micro-CT scanning and three-dimensional geometric morphometrics. We explored the integration between structures at static and evolutionary levels. Effects of allometry on patterns of modularity were also taken into account. At the static level (within species), we analyzed inter-individual variation in shape to detect functional modules and intra-individual variation to detect developmental modules. Significant integration (based on inter-individual variation) among all structures was detected and allometry is shown to be an important integrating factor. The pattern of intra-individual, asymmetric variation indicates statistically significant developmental integration between the cranium and the atlas and between the first two trunk vertebrae. At the evolutionary level (among species), the cranium, atlas, and trunk vertebrae separate as different modules. Our results show that morphological integration at the evolutionary level coincides with morphological and functional differentiation of the axial skeleton, allowing the more or less independent evolutionary changes of the cranial skeleton and the vertebral column, regardless of the relatively strong integration at the static level. The observed patterns of morphological integration differ across levels, indicating different impacts of developmental and phylogenetic constraints and functional demands.     

The Role of the Plumage in Heat Transfer Processes of Birds

The plumage of birds provides a critical thermal buffer betweenthe animal and its environment. Rates of energy expenditureare strongly influenced by the thermal properties of the environmentor the microclimates the animal occupies. Current data suggestthat the addition of solar radiation is equivalent to threeto four-fold changes in wind speed and that solar heat gaincan be extremely sensitive to changes in wind speed. Dry heat transfer through the plumage occurs by three avenues1) conduction and free convection through air 2) conductionalong the solid elements of the plumage and 3) radiation. Overall,about 95% of the total heat flow is evenly divided between thefirst two avenues. Radiative heat transfer accounts for onlyabout 5% of total heat flow. Plumage color, as well as the microstructureand micro-optical properties of plumage elements, when combinedwith environmental properties (e.g., wind speed), determinethe radiative heat loads that birds acquire from solar radiation.Although plumage color or reflectivity determines the fractionof incident solar radiation that is absorbed by the plumageand generates heat, the fraction of this heat that contributesto the thermal load on the animal can vary greatly. In a fibrouscoat such as a plumage, there is some variable penetration intothe coat, with absorption over a range of coat depths. Factorssuch as feather micro-optics and structure are critical determinantsof radiation penetration into avian coats. Significant differencesin solar heat loads can also result from behavioral adjustmentsin plumage thickness.     

Modularity in Development and Why It Matters to Evo-Devo

The concept of modularity is fundamental to research in bothevolutionary and developmental biology, though workers in eachfield use the idea in different ways. Although readily and intuitivelyrecognized, modularity is difficult to define precisely. Mostdefinitions of modularity are operational and implicit, particularlyin developmental biology. Examination of several proposed definitionspoints to some general characteristics of developmental modules,for example their internal integration, and suggests the importanceof devising a definition applicable at different levels of thebiological hierarchy. Modules, like homologs, must be definedwith respect to a specified level of the hierarchy, and a generaldefinition should support both analyses of the evolving causalrelationships between levels, and studies of the interconnectionsbetween modules of the same type. The designation of a developmentalstructure, process, or function as a "module" is a testablehypothesis; this hypothesis is confirmed in the case of thedorsal marginal zone of the amphibian gastrula, which acts asa morphogenetic module. Discussions of developmental modularitycan provide a meeting place for developmental and evolutionarybiologists by helping us articulate key questions at the intersectionof the two fields, and design experiments to begin answeringthem.     

Plumage coloration can be perceived as a multiple condition‐dependent signal by Great Tits Parus major

The evolution of multiple signals can be explained because they enhance the perception of a general message by recipients. Plumage coloration frequently acts as a condition‐dependent signal, so that species displaying different colour patches have the potential to transmit information on condition through a multiple signalling system. The Great Tit Parus major exhibits plumage colour patches generated by the main types of colour production, some of which, particularly those based on melanins and carotenoids, are known to be related to body condition. However, the colour expressions of all of the different colour types have never been investigated simultaneously to determine whether they function as multiple signals of condition. In addition, visual perception models have never been applied to a multiple signalling system in a wild population of birds. Here I present information that links body condition with the colour expression of almost all of the different plumage patches of male Great Tits captured during the winter. Birds in better condition had greater reflectance values at short wavelengths in all plumage patches, and this was especially so in the white (i.e. structural) colour of the cheeks. Plumage colour characteristics were calculated by means of avian visual models, suggesting that Great Tits have the capacity to perceive information contained in the plumage coloration of conspecifics. These results show that short‐wavelength reflectance has great potential to transmit biologically significant information on the body condition of birds, even in achromatic plumage patches.     

Colourful male European Serins Serinus serinus are more careful with their plumage

Ornamental traits typically advertise individual condition and can be costly to maintain. Plumage maintenance behaviour can increase plumage quality and positively influence female mate preference. We investigated this prediction by performing female mate‐choice trials and measuring male plumage maintenance behaviour in the European Serin Serinus serinus. More colourful males spent more time in plumage maintenance than less colourful males, but this was not correlated with body condition or ectoparasite load. Females preferred more colourful males, although this was not influenced by male plumage maintenance. Our findings highlight the fact that investment in plumage maintenance depends on individual coloration and this may reinforce the honesty of ornamental plumage and convey positive information for mate choice.     

A female melanin ornament signals offspring fluctuating asymmetry in the barn owl

Sexual selection theory predicts that males advertise quality by displaying extravagant ornaments. By contrast, whether phenotypic variation in females has a signalling function remains an open question. Here, to our knowledge, we provide the first evidence that a female plumage trait can signal fluctuating asymmetry in the offspring. We experimentally demonstrate in wild barn owls (Tyto alba) that the extent to which females display black spots on their plumage does not only signal offspring parasite resistance as shown in a previous study but also developmental homeostasis in the offspring. A greater number of spotted females produced offspring that had more symmetrical feathers during the period of growth. Males, that pair non-randomly with respect to female plumage spottiness therefore appear to gain substantial benefits by mating with heavily spotted females. Genetic variation in plumage spottiness is nevertheless maintained as the covariation between offspring body mass and mother plumage spottiness varies annually depending on environmental conditions.     

PLUMAGE CHANGES IN THE MALE MACCOA DUCK

Clark, A. 1974. Plumage changes in the male Maccoa Duck. Ostrich 45: 251–254.

Maccoa Duck Oxyura mi ccoo counts made at various waters in the Transvaal and Orange Free State, South Africa, in which the numbers are separated according to plumage, are presented and discussed in the light of the work done by Siegfried (1968, 1970) on this species. Males invariably outnumber females and the indications are that Transvaal birds move out of the area during winter when most males are in non-breeding plumage. There is little difference in the pattern of plumage changes between Transvaal and Cape birds.     

Modules, kinds, and homology

Developmental modules are best conceptualized as homeostatic property cluster natural kinds. As is true in other fields of biology, an individual may instantiate properties of various natural kinds. Through their dissociability, developmental modules can be recruited to function as evolutionary modules. The proper analogy to developmental modules, atoms, or biological species depends on the scope over which specific developmental modules allow generalizations. The nature of the relationship between developmental modules, evolutionary modules, and taxic (phylogenetic) homology are explored. Similarity of gene expression patterns and developmental pathways as captured by biological homology may support hypotheses of taxic homology, but not the other way around.     

Continuous, age-related plumage variation in male Kirtland's Warblers

ABSTRACT.   The ability to age individual birds visually in the field based on plumage variation could provide important demographic and biogeographical information. We describe an approach to infer ages from a distribution of plumage scores of free-ranging male Kirtland's Warblers ( Dendroica kirtlandii ). We assigned ages to males using a scoring scheme (0–12 points) based on variation in plumage coloration, brightness, and contrast on three dorsal and three ventral body regions presumed to be age-related. The distribution of total additive plumage scores for 875 breeding males was normally distributed, indicating no distinct age classes. Thus, we developed provisional plumage-age classes of second year (SY) and after second-year (ASY), and compared them to the total plumage scores of a smaller subsample of known age ( N = 92) and minimum age ( N = 143) males. Plumage scores of known-age male Kirtland's Warblers increased nonlinearly with age ( r _s= 0.67), but with some overlap. The median plumage score for SY males (median = 5.0) was significantly lower than for third-year (TY) males (median = 7.0) and after third-year (3 year and older) males (median = 8.0), indicating that the plumage of male Kirtland's Warblers becomes more distinctive and brighter with age. Linear discriminant function analysis differentiated ASY male Kirtland's Warbler from SY males with 78.3% accuracy. Investigators could use the distribution of plumage scores and approximate age structures to document changes in male age structure during colonization, use, and abandonment of habitats by Kirtland's Warblers or other species that occupy early successional habitats. Aging free-ranging birds based on a plumage scoring scheme may be especially critical for demographic studies of less-studied species where it is unlikely that a banding program will be initiated, but where plumage-age inferences or management decisions must be made.     

Size,plumage, moult and supposed hybrids of African Goshawks (Accipiter tachiro/toussenelii group) in DR Congo

Parapatric A. tachiro sparsimfasciatus and A. toussenelii canescens are in a size cline from large east African to small west African birds. While their plumage colour is different, the pattern of spotting (juvenile) and barring (adult) of the breast feathers is similar. No general hybridisation is found in the contact region in Kivu: the plumage of some aberrant individuals can be due to great age or to individual variation. One supposed hybrid was obtained far from the contact region. I consider them as paraspecies. Based on direct evidence and on annual moult I conclude that the breeding period is prolonged in both taxa in equatorial DR Congo, and that it is seasonal in tachiro sparsimfasciatus in southern DR Congo. In the latter population, the postjuvenile moult starts probably just before the age of one year but it lasts many months, leaving the juvenile upper tail coverts in place for one more year. Plumage characteristics are related to habitat. The female of the woodland sparsimfasciatus is cryptically coloured, with individual variation, possibly helpful for 'image avoidance'. The male is even more variable in colour, in part age related: a 'sepia' morph is described for the first adult plumage. Older birds are grey with reddish flanks, becoming darker with age. The adult evergreen forest canescens shows enforcement of colourful advertising plumage and loss of sexual plumage dimorphism. The first adult is advertised by the late moult of the barred juvenile flank feathers in both sexes. Its juvenile is peculiar; it lacks breast spots, suggesting image avoidance, but possibly also character displacement or mimicry.     

A Young Manakin Knows His Place: Evidence for an Age‐Graded Dominance Hierarchy Among Long‐Tailed Manakins

In lek‐breeding systems where many males gather at display sites, males benefit from the establishment of dominance hierarchies to reduce intrasexual aggression and the associated risk of injuries. Long‐tailed manakins (Chiroxiphia linearis) exhibit an exploded lek‐breeding system wherein the two top‐ranking males at each display site team up to perform elaborate coordinated courtship displays for females. Young males undergo delayed plumage maturation whereby they acquire distinct pre‐definitive plumage patterns each year until they attain definitive plumage in their fifth year. This unique characteristic is thought to have evolved as a status‐signalling mechanism to aid in the establishment of an age‐graded dominance hierarchy in which older males are dominant to younger males. Previous research has shown evidence for such a dominance hierarchy among alpha and beta males; however, the presence of this hierarchy among males of other age classes has never been quantified. In this study, we investigated the presence of an age‐graded dominance hierarchy by determining whether older males direct more aggressive behaviours towards younger males. We also investigated whether status signalling is less clear within age classes than between age classes, by determining whether males within the same age class exhibit more aggression towards each other. We found that older males performed aggressive behaviours towards younger males much more frequently than younger males performed aggressive behaviours towards older males. We also found that some aggressive interactions occurred between males within the same age class more frequently than between males from different age classes. Our study provides some evidence for an age‐graded dominance hierarchy among male long‐tailed manakins of all age classes and also provides some support for the status‐signalling hypothesis. However, further research is needed to conclusively establish the presence of a linear dominance hierarchy among younger male manakins. This research may help us better understand the evolution of complex hierarchical systems in animals.