Understanding the relationship between climatic niches and dispersal through the lens of bat wing morphology

2020 ◽  
Vol 312 (4) ◽  
pp. 239-247
Author(s):  
L. H. Varzinczak
Mammal Review ◽  
2021 ◽  
Author(s):  
Matt Crane ◽  
Inês Silva ◽  
Matthew J. Grainger ◽  
George A. Gale
Keyword(s):  

2014 ◽  
Vol 92 (2) ◽  
pp. 141-147 ◽  
Author(s):  
M.M. Marinello ◽  
E. Bernard

Wing morphology has a direct influence on the flight manoeuvrability, agility, and speed of bats. Studies addressing the relationship between bat wing morphology and ecology are biased towards Old World species and few of them have addressed the ecologically rich Amazonian bat fauna. We quantitatively and qualitatively characterized the wing shape of 51 bat species found in the Brazilian Amazonia by measuring their aspect ratio (AR) and relative wing load (RWL). We found a high variability in wing shape: AR varied from 5.0862 (pygmy round-eared bat, Lophostoma brasiliense (Peters, 1866)) to 8.2774 (brown dog-faced bat, Molossus (Cynomops) paranus (Thomas, 1901)), while RWL varied from 20.0459 (spectral bat, Vampyrum spectrum (L., 1758)) to 55.3931 (Pallas’s mastiff, Molossus molossus (Pallas, 1766)). Insectivores had the largest variability, whereas frugivores and nectarivores had intermediate values with lower variability, indicating a higher flexibility in the use of space and resources. Our predictions on flight patterns are supported by capture and behavioural data from the literature, both of which point to the use of wing shape as a good proxy for habitat use and food partitioning among species. Our data are useful for integrative studies in ecology, physiology, behaviour, and evolution, and can contribute to a better understanding of the ecological interactions of Neotropical bat species.


Author(s):  
Jian Chen ◽  
Daniel K. Riskin ◽  
Tatjana Y. Hubel ◽  
David Willis ◽  
Arnold Song ◽  
...  

Bat wing morphology is considered in relation to flight performance and flight behaviour to clarify the functional basis for eco-morphological correlations in flying animals. Bivariate correlations are presented between wing dimensions and body mass for a range of bat families and feeding classes, and principal-components analysis is used to measure overall size, wing size and wing shape. The principal components representing wing size and wing shape (as opposed to overall size) are interpreted as being equivalent to wing loading and to aspect ratio. Relative length and area of the hand-wing or wingtip are determined independently of wing size, and are used to derive a wingtip shape index, which measures the degree of roundedness or pointedness of the wingtip. The optimal wing form for bats adapted for different modes of flight is predicted by means of mechanical and aerodynamic models. We identify and model aspects of performance likely to influence flight adaptation significantly; these include selective pressures for economic forward flight (low energy per unit time or per unit distance (equal to cost of transport)), for flight at high or low speeds, for hovering, and for turning. "Turning performance is measured by two quantities: manoeuvrability, referring to the minimum space required for a turn at a given speed; and agility, relating to the rate at which a turn can be initiated. High flight speed correlates with high wing loading, good manoeuvrability is favoured by low wing loading, and turning agility should be associated with fast flight and with high wing loading. Other factors influencing wing adaptations, such as migration, flying with a foetus or young or carrying loads in flight (all of which favour large wing area), flight in cluttered environments (short wings) and modes of landing, are identified. The mechanical predictions are cast into a size-independent principal-components form, and are related to the morphology and the observed flight behaviour of different species and families of bats. In this way we provide a broadly based functional interpretation of the selective forces that influence wing morphology in bats. Measured flight speeds in bats permit testing of these predictions. Comparison of open-field free-flight speeds with morphology confirms that speed correlates with mass, wing loading and wingtip proportions as expected; there is no direct relation between speed and aspect ratio. Some adaptive trends in bat wing morphology are clear from this analysis. Insectivores hunt in a range of different ways, which are reflected in their morphology. Bats hawking high-flying insects have small, pointed wings which give good agility, high flight speeds and low cost of transport. Bats hunting for insects among vegetation, and perhaps gleaning, have very short and rounded wingtips, and often relatively short, broad wings, giving good manoeuvrability at low flight speeds. Many insectivorous species forage by ‘ flycatching ’ (perching while seeking prey) and have somewhat similar morphology to gleaners. Insectivorous species foraging in more open habitats usually have slightly longer wings, and hence lower cost of transport. Piscivores forage over open stretches of water, and have very long wings giving low flight power and cost of transport, and unusually long, rounded tips for control and stability in flight. Carnivores must carry heavy loads, and thus have relatively large wing areas; their foraging strategies consist of perching, hunting and gleaning, and wing structure is similar to that of insectivorous species with similar behaviour. Perching and hovering nectarivores both have a relatively small wing area: this surprising result may result from environmental pressure for a short wingspan or from the advantage of high speed during commuting flights; the large wingtips of these bats are valuable for lift generation in slow flight. The relation between flight morphology (as an indicator of flight behaviour) and echolocation is considered. It is demonstrated that adaptive trends in wing adaptations are predictably and closely paralleled by echolocation call structure, owing to the joint constraints of flying and locating food in different ways. Pressures on flight morphology depend also on size, with most aspects of performance favouring smaller animals. Power rises rapidly as mass increases; in smaller bats the available energy margin is greater than in larger species, and they may have a more generalized repertoire of flight behaviour. Trophic pressures related to feeding strategy and behaviour are also important, and may restrict the size ranges of different feeding classes: insectivores and primary nectarivores must be relatively small, carnivores and frugivores somewhat larger. The relation of these results to bat community ecology is considered, as our predictions may be tested through comparisons between comparable, sympatric species. Our mechanical predictions apply to all bats and to all kinds of bat communities, but other factors (for example echolocation) may also contribute to specialization in feeding or behaviour, and species separation may not be determined solely by wing morphology or flight behaviour. None the less, we believe that our approach, of identifying functional correlates of bat flight behaviour and identifying these with morphological adaptations, clarifies the eco-morphological relationships of bats.


Author(s):  
Dominique G. Maucieri ◽  
Austin James Ashbaugh ◽  
Jessica M. Theodor

Sexual dimorphism can lead to differences in foraging style among conspecifics due to morphological differences. Within bats, maneuverability and speed of flight are influenced by wing shape and size, which may differ between sexes. Female bats gain about 30% of their body mass during pregnancy, affecting their agility and flight efficiency. To fill the same foraging niche as males, pregnant female bats would require wing size and/or shape modifications to maintain maneuverability. We investigated sexual dimorphism in bat wing morphology and how it varies among foraging guilds. Wing photos of male and female adult bats (19 species) in Canada, Belize, and Dominica were analyzed using 2D geometric morphometrics, wing loading, and aspect ratios. Nonpregnant female bats had higher wing loading than males, suggesting they are less maneuverable than males. Additionally, mass increases during pregnancy may not permit female bats to forage as male conspecifics do. Wing shape differed minimally among foraging guilds with only frugivores differing significantly, from all other guilds. Further studies should investigate how female bats forage during their reproductive cycle and determine how frugivore wings differ and whether there are individual differences in wing shape that are not consistent among bat species.


Genome ◽  
2016 ◽  
Vol 59 (9) ◽  
pp. 751-761 ◽  
Author(s):  
Kong-Wah Sing ◽  
Hui Dong ◽  
Wen-Zhi Wang ◽  
John-James Wilson

During 30 years of unprecedented urbanization, plant diversity in Shenzhen, a young megacity in southern China, has increased dramatically. Although strongly associated with plant diversity, butterfly diversity generally declines with urbanization, but this has not been investigated in Shenzhen. Considering the speed of urbanization in Shenzhen and the large number of city parks, we investigated butterfly diversity in Shenzhen parks. We measured butterfly species richness in four microhabitats (groves, hedges, flowerbeds, and unmanaged areas) across 10 parks and examined the relationship with three park variables: park age, park size, and distance from the central business district. Butterflies were identified based on wing morphology and DNA barcoding. We collected 1933 butterflies belonging to 74 species from six families; 20% of the species were considered rare. Butterfly species richness showed weak negative correlations with park age and distance from the central business district, but the positive correlation with park size was statistically significant (p = 0.001). Among microhabitat types, highest species richness was recorded in unmanaged areas. Our findings are consistent with others in suggesting that to promote urban butterfly diversity it is necessary to make parks as large as possible and to set aside areas for limited management. In comparison to neighbouring cities, Shenzhen parks have high butterfly diversity.


2020 ◽  
Author(s):  
Matt Crane ◽  
Inês Silva ◽  
Matthew J. Grainger ◽  
George A. Gale

AbstractSpecies’ life history traits have a wide variety of applications in ecological and conservation research, particularly when assessing threats. The development and growth of global species trait databases are critical for improving trait-based analyses; however, it is vital to understand the gaps and biases of available data. Bats are an extremely diverse and widely distributed mammalian order, with many species facing local declines and extinction. We conducted a literature review for bat wing morphology, specifically wing loading and aspect ratio, to identify issues with data reporting and ambiguity. We collected data on field methodology, trait terminology, and data reporting and quality. We found several issues regarding semantic ambiguity in trait definitions and data reporting. Globally we found that bat wing morphology trait coverage was low. Only six bat families had over 40% trait coverage, and of those none consisted of more than 11 total species. We found similar biases in trait coverage across IUCN Redlist categories with threatened species having lower coverage. Geographically, North America, Europe, and the Indomalayan regions showed higher overall trait coverage, while both the Afrotropical and Neotropical ecoregions showed poor trait coverage. The underlying biases and gaps with bat wing morphology data have implications for researchers conducting global trait-based assessments. Implementing imputation techniques may address missing data, but only for smaller regional subsets with substantial trait coverage. However, due to the low overall trait coverage, increasing species representation in the database should be prioritized. We suggest adopting an Ecological Trait Standard vocabulary to reduce semantic ambiguity in bat wing morphology traits to improve data compilation and clarity. Additionally, we advocate that researchers adopt an Open Science approach to facilitate the growth of a bat wing morphology trait database.


2014 ◽  
Vol 281 (1791) ◽  
pp. 20141257 ◽  
Author(s):  
Brian C. Weeks ◽  
Santiago Claramunt

Different models of speciation predict contrasting patterns in the relationship between the dispersal ability of lineages and their diversification rates. This relationship is expected to be negative in isolation-limited models and positive in founder-event models. In addition, the combination of negative and positive effects of dispersal on speciation can result in higher diversification rates at intermediate levels of dispersal ability. Using molecular phylogenies to estimate diversification rates, and wing morphology to estimate dispersal ability, we analysed the influence of dispersal on diversification in the avifauna of Australasian archipelagoes. Contrary to expectations given the fragmented nature of island systems, the relationship between dispersal ability and diversification rate was monotonically negative. While multiple mechanisms could generate this pattern, they all share a phase of range expansion that is decoupled from speciation.


1967 ◽  
Vol 31 ◽  
pp. 239-251 ◽  
Author(s):  
F. J. Kerr

A review is given of information on the galactic-centre region obtained from recent observations of the 21-cm line from neutral hydrogen, the 18-cm group of OH lines, a hydrogen recombination line at 6 cm wavelength, and the continuum emission from ionized hydrogen.Both inward and outward motions are important in this region, in addition to rotation. Several types of observation indicate the presence of material in features inclined to the galactic plane. The relationship between the H and OH concentrations is not yet clear, but a rough picture of the central region can be proposed.


Paleobiology ◽  
1980 ◽  
Vol 6 (02) ◽  
pp. 146-160 ◽  
Author(s):  
William A. Oliver

The Mesozoic-Cenozoic coral Order Scleractinia has been suggested to have originated or evolved (1) by direct descent from the Paleozoic Order Rugosa or (2) by the development of a skeleton in members of one of the anemone groups that probably have existed throughout Phanerozoic time. In spite of much work on the subject, advocates of the direct descent hypothesis have failed to find convincing evidence of this relationship. Critical points are:(1) Rugosan septal insertion is serial; Scleractinian insertion is cyclic; no intermediate stages have been demonstrated. Apparent intermediates are Scleractinia having bilateral cyclic insertion or teratological Rugosa.(2) There is convincing evidence that the skeletons of many Rugosa were calcitic and none are known to be or to have been aragonitic. In contrast, the skeletons of all living Scleractinia are aragonitic and there is evidence that fossil Scleractinia were aragonitic also. The mineralogic difference is almost certainly due to intrinsic biologic factors.(3) No early Triassic corals of either group are known. This fact is not compelling (by itself) but is important in connection with points 1 and 2, because, given direct descent, both changes took place during this only stage in the history of the two groups in which there are no known corals.


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