External morphology is commonly used to identify bats as well as to investigate flight and foraging behavior, typically relying on simple length and area measures or ratios. However, geometric morphometrics is increasingly used in the biological sciences to analyse variation in shape and discriminate among species and populations. Here we compare the ability of traditional versus geometric morphometric methods in discriminating between closely related bat species – in this case European horseshoe bats (Rhinolophidae, Chiroptera) – based on morphology of the wing, body and tail. In addition to comparing morphometric methods, we used geometric morphometrics to detect interspecies differences as shape changes. Geometric morphometrics yielded improved species discrimination relative to traditional methods. The predicted shape for the variation along the between group principal components revealed that the largest differences between species lay in the extent to which the wing reaches in the direction of the head. This strong trend in interspecific shape variation is associated with size, which we interpret as an evolutionary allometry pattern.
Citation: Schmieder DA, Benítez HA, Borissov IM, Fruciano C (2015) Bat Species Comparisons Based on External Morphology: A Test of Traditional versus Geometric Morphometric Approaches. PLoS ONE 10(5): e0127043. https://doi.org/10.1371/journal.pone.0127043
Academic Editor: Sharon Swartz, Brown University, UNITED STATES
Received: December 29, 2014; Accepted: April 11, 2015; Published: May 12, 2015
Copyright: © 2015 Schmieder et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All raw files are available from the dryad database (http://datadryad.org/review?doi=doi:10.5061/dryad.705q4).
Funding: The study was funded by grants from the Max Planck Society. Additional funding to DAS was provided by the International Max Planck Research School (IMPRS) for Organismal Biology. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Studies relating bat wing morphology to flight characteristics date back to the beginning of the 20th century [1–4]. Lengths and areas of wings or their parts were typically measured to compare wing morphology among species. Wing loading, the first ratio proposed, is still used for size-independent species comparison . In following decades, further ratios, such as aspect ratio, tip length ratio, tip area ratio and the wingtip shape index were defined [5–7]. Many studies of wing morphology were conducted using these ratios to compare interspecies morphology [5,8–13]. The methods for obtaining raw morphometric variables (e.g. wing area or arm wing area) to construct such ratios often varied among studies, making results difficult to compare (see [5,7,10,11,14–16] for examples). Another problem was the way in which bats were measured. That is, early studies collected measurements on museum specimens [5,7], while later ones relied on wing tracings from live bats [10,12,17,18]. Finally, in recent years, photographs of bats with fully extended wings have been analysed with image programs [19,20]. For a long time, differences in total wing area and shape in relation to flight and foraging performance were emphasized and in most studies the tail was assumed to play a minor role or was not measured independently. Typically, the tail area was included in measurements of the wing area together with the body or parts of the body [5,8,10–13]. However, Schmieder et al. , used two ratios to exclusively capture tail morphology and found differences between two similar species.
Since the 80s a new set of morphometric techniques has been established: geometric morphometrics [21–23]. This set of techniques has gained enormous popularity and has been used across a large number of taxa and questions (for a recent review see ). These methods have become popular because they permit separation of the size and shape components of morphometric variation. The resulting variables are not redundant and these approaches allow visualization of results in terms of shape changes while retaining the geometric properties of objects throughout the analysis . Moreover, geometric morphometrics allows quantifying changes in the position of anatomical structures relative to one another, which sometimes are not captured by linear morphometric techniques. Contrasting this popularity in studies of other taxa, geometric morphometrics has had limited use in studies of external morphology in bats (but see [25,26]). In the present study, we quantitatively compared the ability of traditional and geometric morphometric methods to discriminate among species of bats based on external morphology. If geometric morphometrics proves to be better in capturing differences in bats’ external morphology, this method could be a helpful tool where traditional morphometrics is limited (i.e. when traditional morphometrics cannot be used to discriminate among species or when shape is itself of interest). We quantitatively compared the different methods by using classification rates in discriminant analysis and we focused on bat species that are closely related and known to be very similar in morphology. We, therefore, set out to analyse the differences in morphology of the five European horseshoe bat species (Rhinolophidae, Chiroptera). These species sometimes overlap in size and they are very similar in morphology [5,13,27–29]. The smallest European horseshoe bat is Rhinolophus hipposideros Bechstein, 1800 and the largest is Rhinolophus ferrumequinum Schreber, 1774. The other three species: Rhinolophus blasii Peters, 1866, Rhinolophus euryale Blasius, 1853 and Rhinolophus mehelyi Matschie, 1901 are of intermediate size and sometimes difficult to differentiate. European horseshoe bats do not only overlap in size (especially the intermediate species). In fact, all five species are known to forage in or close to vegetation [30–37] and belong to the same foraging guild—the flutter detecting foragers . In south-eastern Europe all five species occur sympatrically  and can partly overlap in diet (e.g. moths [34,39–41]) and hunting strategies (foraging on the wing, foraging from perches and foraging on the ground) [34,42,43]. The species choose similar summer roosting places like caves (in the Mediterranean regions) or roof spaces and other parts within buildings [30,34,36,37]. Although the phylogenetic relationships of this group are not fully resolved, all phylogenies published to date agree in considering R. mehelyi and R. euryale to be closely-related [44–46]. R. hipposideros seems most distantly related to the other four horseshoe bat species and R. blasii is considered as a sister group of R. ferrumequinum .
Materials and Methods
Capture and handling of bats was in accordance with recommendations of the Canadian Council on Animal Care on bats  and the EUROBATS Resolution  and was licensed by the responsible Bulgarian authorities (MOEWSofia and RIOSV-Ruse, field permit numbers 297/09.03.2011, 465/29.06.2012, 554/20.01.2014). The mentioned field permits authorized us to capture and measure (including taping of bats for making wing pictures) the studied species at the differing capture sites (S1 Table). Officials from the Bulgarian Ministry of Environment and Water (MOEW) inspected our work in accordance with Section 8, Article 23, Paragraph 3 and 4 of the Bulgarian Biodiversity Law. According to Bulgarian laws no further ethical approval by a committee is required for a non-invasive study. These procedures were not part of a routine care or monitoring project. No bats were harmed. After the experiments all bats were released in good health at their respective capture sites.
We caught bats in a harp trap (Faunatech, Victoria, Australia), mist nets (Ecotone, Sopot, Poland) or hand nets at the entrances of caves, in or near abandoned buildings in north-eastern, central and southern Bulgaria (maximal distance between capture sites approx. 260 km, S1 Table) between May and September in 2011, 2012 and 2014. We identified the five European horseshoe bat species using an identification key . Only adult male bats with no wing injuries were used for wing pictures. We analysed pictures of 6 Rhinolophus hipposideros, 7 Rhinolophus blasii, 22 Rhinolophus euryale, 20 Rhinolophus mehelyi and 21 Rhinolophus ferrumequinum.
Wing photographs were taken by fixing each individual with its ventral side held firmly against the board of a copy stand (custom-made, Max-Planck Institute for Ornithology, Seewiesen, Germany). The board of the copy stand was covered with graph paper and transparent self-adhesive cover film pasted on top of it. The wings and tail membrane were carefully extended (starting with the right wing, then the left wing and ending with the tail membrane) with the largest possible stretching of the wing and tail membrane and fixed each time with transparent adhesive tape (width 19 mm) to the board. For the standardization of wing position, we have considered that the upper arm was at a 90° angle to the midline of the body. Before taking pictures, we ensured that the wings and the tail were properly fixed and that no movement of the fixated body parts was possible. In the rare cases where movement of fixated body parts occurred, we readjusted and re-fixated the wing or tail before taking pictures. While fixating the bat, the head was covered with a black cotton cloth to calm the animal down and to reduce attempts of the bat to move. Each individual was fixed two times to reduce measurement error due to fixation. For each fixation, we took several digital photos with a digital camera (12 megapixel, DMC-TZ10, Panasonic, Ōsaka, Japan) mounted on the copy stand at a height of 47 cm. The tape was then carefully removed without injury. From each of the 76 individuals, we chose the three best pictures (one or two per fixation) which were then used in downstream traditional and geometric morphometric analyses. A picture was chosen as best picture if there was no blurriness in the picture, the wings were fixated symmetrically, the wing and tail membranes were fully extended and the head was straight and pointed towards the plate.
For traditional morphometrics, we measured the right wing, tail and body to obtain multiple lengths (hand wing length, arm wing length, wing span) and areas (arm wing area, hand wing area, tail area and wing area) (Fig 1), using an image processing program (Adobe Photoshop, version 13.0.1, Adobe Systems, San Jose, USA). We also digitized 17 landmarks on the right side of each specimen (Fig 2), using tpsDig . From landmark coordinates, we obtained using the program TMorphGen6 of the IMP package , linear distances between the landmarks 1 and 7 (3rd digit), 7 and 9 (5th digit), 5 and 6 (first phalanx of 4th digit) as well as 4 and 5 (second phalanx of 4th digit). For reduction of measurement error in geometric morphometrics, for each bat we subjectively determined and digitized the best two pictures of the best fixation and the best picture of the other fixation. We quantified the measurement error present in the dataset obtained with the above-mentioned experimental design using a Procrustes ANOVA , which showed that measurement error was small relative to the variation among individuals and among species (S2 Table). The resulting coordinates were then averaged—thus further reducing measurement error [54–56]—for each bat after a generalized Procrustes analysis  in MorphoJ . As a preliminary MANCOVA showed that the interaction between species and centroid size was not significant, residuals of a pooled within-group regression of shape on centroid size (accounting for 16.08% of total variance) were obtained to take into account intra-species allometry and these were used in subsequent analyses.
These measures were used for methods 1 and 2.
Comparison of morphometric methods in species discrimination
In this study we compared four morphometric methods for their ability in discriminating bat species based on external morphology.
The first method involved ratios and other measures that are thought to be “size-independent” (i.e. corrected for allometry): tip length ratio, tip area ratio, wing tip shape index, aspect ratio and wing loading  (S3 Table). The second method includes measures from the first method except that wing loading is replaced by relative wing loading (which is less dependent on size) and that the tail-to-wing area ratio is added to the other variables [5,9,16]. In the third method we followed Dietz and colleagues , using residuals of regression on forearm length for each of the length measurements of digits 3 and 5 and also the first and second phalanges of the fourth digit. These three methods represent the traditional morphometric methods most commonly used to analyse external bat morphology of European horseshoe bats. In a fourth and final method we employed geometric morphometrics using the set of landmarks defined above. We used landmarks only on the right wings to maintain consistency with the other methods and because preliminary analyses on a subset of the specimens showed a lower measurement error due to fixation, as compared to a symmetric configuration of landmarks on both sides of the bat.
To compare methods, we used the correct classification rate of discriminant analysis estimated using a leave-one-out cross-validation procedure. We obtained discriminant analyses and correct classification rates both for pairwise comparisons among species and using a single discriminant analysis on all the species at the same time (canonical variate analysis). We obtained discriminant functions and correct classification rates for the pairwise comparisons among species using geometric morphometric data (method 4) in MorphoJ. All the other discriminant functions and correct classification rates were computed in SPSS (Version 21.0, IBM Corp. Armonk, NY). Given that linear discriminant analysis is known to have artefactually high classification rates at increasing number of dimensions , for the geometric morphometric dataset, we also performed discriminant analyses on, respectively, the first two, three, ten, seventeen and twenty-five principal components. The first twenty-five principal components were chosen performing in the R package nFactors  the Anderson's test , as suggested by Mitteroecker and Bookstein  for dimensionality reduction prior to discriminant analyses. The first two, three, ten and seventeen principal components were chosen arbitrarily as lower numbers of principal components.
To test for the presence of a species signal in the raw geometric morphometric data prior to allometric correction, we also performed discriminant analyses on the geometric morphometric dataset obtained from the measurement reduction procedure without subjecting it to the regression-based removal of the allometric component.
Geometric morphometrics—testing and visualizing differences among species
In addition to the comparison of different morphometric methods, we exploited the advantages of geometric morphometrics by further analysing the geometric morphometric dataset and visualizing differences among species as shape changes. All the analyses were performed on the right-side configurations described above. However, to visualize results we reflected the configurations of points obtained as results , thus producing more easily interpretable “bat-like” symmetric displays.
To visualize patterns of variation among species, we used between-group principal component analysis . This method has been suggested to produce ordinations that are preferable to the commonly used scatterplots of canonical variate scores  and is increasingly used in geometric morphometric studies [64,65] as the ordinations do not exaggerate the extent of separation between groups. To better interpret variation along the first between-group principal component (bwgPC1)—which was computed based on data after a pooled within-group regression on centroid size and is therefore already corrected for intra-specific allometry—in terms of evolutionary allometry, we regressed bwgPC1 scores on centroid size. We tested for pairwise differences in mean shape among species using the permutational procedure based on Procrustes distances implemented in MorphoJ (10,000 permutations). Differences between species were visualized through wireframe graphs of each species’ mean shape relative to the grand mean.
Comparison of morphometric methods in species discrimination
There are clear differences in correct classification rates across the four methods (Table 1 and S4 Table). The poorest classification rate was found for method 1  which uses ratios related to the wing, followed by method 2 [5,9,16] which uses ratios related to wing and tail and method 3  which employs linear measurements on the wing. The latter two methods were rather similar in correct classification rates. Method 4 (data obtained through geometric morphometrics) achieved the greatest success as correct classification was achieved with 94.7% accuracy when comparing all the species (canonical variate analysis) and ranged between 84.6% and 100% in the pairwise comparison (Table 1). Consistent across-methods among-species differences in correct classification were found. For instance, R. hipposideros showed consistently high correct classification rates in all methods. Correct classification was higher for geometric morphometrics relative to traditional methods also when the geometric morphometric dataset was subjected to dimensionality reduction (i.e. when discriminant analysis was performed on a subset of principal components; S5 Table).
Discriminant analyses on the geometric morphometric dataset containing allometric variation produced lower correct classification rates when compared to the geometric morphometric dataset obtained after allometric correction. However, correct classification rates in the former case were still higher than the ones obtained using a traditional morphometric dataset.
In fact, the cross-validated correct classification rate for the CVA on the geometric morphometric dataset containing allometric variation was 93.4% (the same percentage of correct classification is obtained both using the full-dimensional space and using the first 25 principal components) and on average 91.63% in pairwise comparisons (range 76.92–100%). This shows that bat species could be discriminated with geometric morphometrics even in the presence of significant allometry.
Geometric morphometrics—testing and visualizing differences among species
The first between-group principal component accounts for most (91.03%) of the shape variation in the dataset. The second principal component accounted for a mere 4.26% percent of total variance. Interestingly, the different species show little overlap in the scatterplot of the first two between-group principal components (bwgPC), and variation along bwgPC1 mirrors inter-specific variation in body size as species with lower scores on bwgPC1 are larger (Fig 3). This is confirmed by the regression of bwgPC1 scores (which are already corrected for intra-specific allometry) on centroid size, which is significant (p<0.0001) and accounts for 83% of the variation in bwgPC1 scores. Predicted shape for the variation along bwgPC1 (Fig 3) revealed that the largest differences between species lay in the extent to which the wing reaches in the direction of the head. Not much variation among species was present along bwgPC2, with the only exception that R. blasii has, on average, lower scores along this axis. Considering the low amount of variance explained by bwgPC2 and the fact that it is constructed, by definition, to be orthogonal to bwgPC1, differences along this direction are difficult to interpret and, possibly, of little biological significance. R. mehelyi and R. euryale showed the largest level of overlap in the scatterplot.
Scatterplot of the scores along the first two between-group principal components. Overlaid, predicted shape changes along the first between-group principal component and average shape of each species. Points in the scatterplot are color-coded as the average shapes. In the plots of average species shape, the grand average shape is depicted in grey.
Permutation tests of difference in average shape were significant across all pairwise comparisons (Table 2). The lowest Procrustes distance was found between R. mehelyi and R. euryale, as suggested by their close position in the scatterplot of the scores on the first two between-group principal components.
A narrative description of the differences of each species average shape relative to the overall average shape is provided in Table 3 and documents extensive variation in arm-wing, hand-wing, body and tail regions.
We compared the ability of four multivariate approaches to discriminate between morphologically similar, closely related species of European horseshoe bats. Landmark-based geometric morphometrics performed best at species discrimination—as measured by its highest levels of correct classification in discriminant analysis. This is not surprising since geometric morphometrics has long been suggested as particularly useful in detecting even relatively small, localized changes in shape , making this approach particularly useful in intraspecific studies . Our results suggest that geometric morphometric analyses are as useful in bats as in other groups.
This approach is not practical for rapid species identification in the field. However, it can be used to find anatomical regions where linear measures for species identification in the field should be taken, e.g. for other bat species where no field identification keys exist. Perhaps most importantly, when external morphology and species discrimination are themselves of interest geometric morphometric methods may be especially helpful.
Using geometric morphometrics, we found interspecific differences in horseshoe bats that were not detected by previously used methods. What is more interesting is that we were able to identify strong trends in interspecific shape variation associated with size. In fact, by taking into account allometric variation using a pooled within-group regression, we removed intraspecific allometric variation but not interspecific size-associated shape changes. We, therefore, conclude that the clear trend observed along the first between-group principal component—which accounts for a very high proportion of total variance—can be interpreted as a pattern of evolutionary allometry. Allometry in bats already has been described for various traits (e.g. [67–71]). The comparison of the elongated fingers of bats compared to other mammals may be the most famous example of allometry in regard to morphology . However, to our knowledge, this is the first study to describe evolutionary allometry of external wing morphology in a detailed way and across a group of closely-related bat species.
When considering the functional implication of the shape variation we documented in horseshoe bats, we speculate that a wing reaching farther toward the head—i.e. moving in the positive direction of bwgPC1 (Fig 3)—might be advantageous for flight in dense vegetation. Incidents when bats touch obstacles while wings are positioned in front (ahead of the body centre) might be easier to cope with and therefore less risky. Furthermore it may be easier for bats to evaluate their ability to fly through a specifically narrow spot as well as increasing their manoeuvrability. Especially R. hipposideros and R. euryale—which have wings reaching farther towards the head—forage regularly in dense vegetation [30,33–35,73,74]. The foraging behaviour of R. blasii is less studied, but it is known to forage close to shrubs and hedges . In contrast, the larger species R. mehelyi and R. ferrumequinum are at the negative extreme of our bwgPC1 (Fig 3 and Table 3) and these species spend more time in less-cluttered habitat foraging above or along vegetation (e.g. pastures, hedges or arable land) [28,34,37]. Furthermore, both species frequently hunt from perches (flycatcher style) [29,34]. We assume that, for this foraging behaviour, wings reaching less far toward the head should be energetically more efficient during flight. These assumptions should be tested in a biomechanics experiment since bats flight performance cannot be predicted from wing shape alone [71,75]. We cannot determine to which extent the foraging performance of the studied bat species in different environments might be influenced by wing shape alone as opposed to body size as we have shown that these co-vary across species. Former studies, however, have reported that smaller species have better flight performance close to or within cluttered environments [8,14,16,76].
An interesting possibility to test in the future is that our results may describe a more general phenomenon, i.e. bats foraging in dense vegetation have wings reaching farther towards the head compared to bats foraging in edge or open space. Norberg  reported that the wings of some bat species show strong convergence with some bird wings, e.g. Mollosid bats have wings similar to the ones of swifts and swallows. Geometric morphometrics is scarcely used to study wing morphology also in birds (but see ). It is, therefore, possible that future geometric morphometric studies on birds will allow further (and more precise) tests of the parallelism across taxa of the relationship between wing shape and its functional significance.
S1 Table. Locality and method of capture for all individuals used in this study.
S2 Table. Procrustes ANOVA on repeated mesures of shape in the geometric morphometric dataset.
SS = sum of squares; MS = mean squares; df = degrees of freedom.
S3 Table. List of all traditional morphometric variables used for the discriminant analysis and description of how the measures were taken and what general functional importance they have for flight performance.
S4 Table. Cross-validated correct classification rates for each pairwise species comparison across different morphometric methods.
Rates are expressed as percentages. Species abbreviations as follows: Rhip = R. hipposideros, Rbla = R. blasii, Reur = R. euryale, Rmeh = R. mehelyi, Rfer = R. ferrumequinum.
S5 Table. Correct cross-validated classification rates (CV rate) for the geometric morphometric dataset after dimensionality reduction when performing discriminant analysis on multiple groups (canonical variate analysis = CVA) and in pairwise comparison.
Species abbreviations as follows: Rhip = R. hipposideros, Rbla = R. blasii, Reur = R. euryale, Rmeh = R. mehelyi, Rfer = R. ferrumequinum.
We thank the Directorate of Rusenski Lom Nature Park & Regional Inspectorate of the Ministry of Environment and Water (RIOSV Ruse) for allowing us to conduct this research project in Bulgaria. Special thanks go to Björn Siemers, Tigga Kingston, Raphaël Arlettaz and Veronika Braunisch for scientific advice as well as to Antonia Hubancheva and Paula Tuttle for help with catching bats and taking wing pictures in 2014. We are also very grateful to Merlin Tuttle for comments and proofreading of the manuscript. We thank Sharon Swartz, Adrien Perrard and one anonymous reviewer for comments to the manuscript. The present work was supported by the International Max Planck Research School (IMPRS) for Organismal Biology. Further thanks go to the Siemers Bat Research Station teams 2011, 2012 and 2014, as well as to the sensory ecology group in Seewiesen for scientific support and the Max-Planck workshop team for technical support.
Conceived and designed the experiments: DAS. Performed the experiments: DAS IMB. Analyzed the data: DAS HAB CF. Contributed reagents/materials/analysis tools: DAS CF. Wrote the paper: DAS HAB IMB CF.
- 1. Banks V. The relation of weight to wing area in the flight of animals. J Malays Branch R Asiat Soc. 1930; 8: 334–360.
- 2. Eisentraut M. A contribution on the mechanics of bat flights. Z Wiss Zool. 1936; 148: 159–188.
- 3. Poole EL. Relative wing ratios of bats and birds. J Mammal. 1936; 17: 412–413.
- 4. Revilliod PA. A propos de l'adaption au vol chez les Microcheiroptères. Verh Naturforsch Ges Basel. 1916; 27: 156–183.
- 5. Norberg UM, Rayner JMV. Ecological morphology and flight in bats (Mammalia, Chiroptera)—Wing adaptations, flight performance, foraging strategy and echolocation. Philos Trans R Soc Lond B Biol Sci. 1987; 316: 337–419.
- 6. Struhsaker T. Morphological factors regulating flight in bats. J Mammal. 1961; 42: 152–159.
- 7. Findley JS, Studier EH, Wilson DE. Morphologic properties of bat wings. J Mammal. 1972; 53: 429–444.
- 8. Aldridge HDJN Rautenbach IL. Morphology, echolocation and resource partitioning in insectivorous bats. J Anim Ecol. 1987; 56: 763–778.
- 9. Norberg UM.Wing design, flight performance, and habitat use in bats. In: Wainwright PC, Reilly SM, editors. Ecological morphology, integrative organismal biology. Chicago: The University of Chicago Press. 1994. pp. 205–239.
- 10. Rhodes MP. Wing morphology and flight behaviour of the golden-tipped bat, Phoniscus papuensis (Dobson) (Chiroptera: Vespertilionidae). Aust J Zool. 1995; 43: 657–663.
- 11. Saunders MB, Barclay RMR. Ecomorphology of insectivorous bats—a test of predictions using two morphologically similar species. Ecology. 1992; 73: 1335–1345.
- 12. Zhang L, Liang B, Parsons S, Wei L, Zhang S. Morphology, echolocation and foraging behaviour in two sympatric sibling species of bat (Tylonycteris pachypus and Tylonycteris robustula) (Chiroptera: Vespertilionidae). J Zool. 2007; 271: 344–351.
- 13. Salsamendi E, Aihartza JR, Goiti U, Almenar D, Garin I. Echolocation calls and morphology in the Mehelyi`s (Rhinolophus mehelyi) and mediterranean (R. euryale) horseshoe bats: implications for resource partitioning. Hystrix It J Mamm. 2006; 16: 149–158.
- 14. Stockwell EF. Morphology and flight manoeuvrability in New World leaf-nosed bats (Chiroptera: Phyllostomidae). J Zool. 2001; 254: 505–514.
- 15. Sevcik M. Does wing morphology reflect different foraging strategies in sibling bat species Plecotus auritus and P. austriacus? Folia Zool. 2003; 52: 121–126.
- 16. Schmieder DA, Zsebők S, Siemers BM. The tail plays a major role in the differing manoeuvrability of two sibling species of mouse-eared bats (Myotis myotis and Myotis blythii). Can J Zool. 2014; 92: 965–977.
- 17. Bowie RCK, Jacobs DS, Taylor PJ. Resource use by two morphologically similar insectivorous bats (Nycteris thebaica and Hipposideros caffer). S Afr J Zool. 1999; 34: 27–33.
- 18. Brigham RM, Francis RL, Hamdorf S. Microhabitat use by two species of Nyctophilus bats: a test of ecomorphology theory. Aust J Zool. 1997; 45: 553–560.
- 19. Mancina CA, Garcia-Rivera L, Miller BW. Wing morphology, echolocation, and resource partitioning in syntopic Cuban mormoopid bats. J Mamm. 2012; 93: 1308–1317. pmid:23043412
- 20. Voigt CC. Bat flight with bad wings: is flight metabolism affected by damaged wings? J Exp Biol. 2013; 216: 1516–1521. pmid:23348945
- 21. Adams DC, Rohlf FJ, Slice DE. Geometric morphometrics: ten years of progress following the 'revolution'. Ital J Zool. 2004; 71: 5–16.
- 22. Adams DC, Rohlf FJ, Slice DE. A field comes of age: geometric morphometrics in the 21st century. Hystrix It J Mamm. 2013; 24: 7–14.
- 23. Rohlf FJ, Marcus LF. A revolution in morphometrics. Trends Ecol Evol. 1993; 8: 129–132. pmid:21236128
- 24. Zelditch ML, Swiderski DL, Sheets HD: Geometric morphometrics for biologists. 1st ed. New York and London: Elsevier Academic Press; 2012.
- 25. de Camargo NF, de Oliveira HFM. Sexual dimorphism in Sturnira lilium (Chiroptera, Phyllostomidae): can pregnancy and pup carrying be responsible for differences in wing shape? PLoS ONE. 2012; 7(11): e49734. pmid:23166759
- 26. Birch JM. Comparing wing shape of bats: The merits of principal-components analysis and relative-warp analysis. J Mamm. 1997; 78: 1187–1198.
- 27. Dietz C, Dietz I, Siemers BM. Wing measurement variations in the five European horseshoe bat species (Chiroptera: Rhinolophidae). J Mamm. 2006; 87: 1241–1251.
- 28. Salsamendi E, Garin I, Arostegui I, Goiti U, Aihartza J. What mechanism of niche segregation allows the coexistence of sympatric sibling rhinolophid bats? Front Zool. 2012; 9(1):30. pmid:23148596
- 29. Dietz C. Aspects of ecomorphology in the five European horseshoe bats (Chiroptera: Rhinolophidae) in the area of sympatry. Dissertation: Eberhard Karls Universität Tübingen. 2007. Available: http://www.fledermaus-dietz.de/publications/publications.html. Accessed 21 October 2014.
- 30. Zahn A, Holzhaider J, Kriner E, Maier A, Kayikcioglu A. Foraging activity of Rhinolophus hipposideros on the island of Herrenchiemsee, Upper Bavaria. Mamm Biol. 2008; 73: 222–229. pmid:18221762
- 31. Bontadina F, Schofield H, Naef-Daenzer B. Radio-tracking reveals that lesser horseshoe bats (Rhinolophus hipposideros) forage in woodland. J Zool. 2002; 258: 281–290.
- 32. Russo D, Jones G, Migliozzi A. Habitat selection by the Mediterranean horseshoe bat, Rhinolophus euryale (Chiroptera: Rhinolophidae) in a rural area of southern Italy and implications for conservation. Biol Conserv. 2002; 107: 71–81.
- 33. Goiti U, Garin I, Almenar D, Salsamendi E, Aihartza J. Foraging by Mediterranean horseshoe bats (Rhinolophus euryale) in relation to prey distribution and edge habitat. J Mamm. 2008; 89: 493–502.
- 34. Dietz C, von Helversen O, Nill D. Bats of Britain, Europe and northwest Africa. 1st ed. London: A and C Black Publishers Ltd; 2009.
- 35. Russo D, Almenar D, Aihartza J, Goiti U, Salsamendi E, Garin I. Habitat selection in sympatric Rhinolophus mehelyi and R. euryale (Mammalia: Chiroptera). J Zool. 2005; 266: 327–332.
- 36. Salsamendi E, Arostegui I, Aihartza J, Almenar D, Goiti U, Garin I. Foraging ecology in Mehely's horseshoe bats: influence of habitat structure and water availability. Acta Chiropt. 2012; 14: 121–132.
- 37. Flanders J, Jones G. Roost use, ranging behavior, and diet of greater horseshoe bats (Rhinolophus ferrumequinum) using a transitional roost. J Mamm. 2009; 90: 888–896. pmid:18433981
- 38. Denzinger A, Schnitzler H-U. Bat guilds, a concept to classify the highly diverse foraging and echolocation behaviors of microchiropteran bats. Front Physiol. 2013; 4: 164. pmid:23840190
- 39. Goiti U, Aihartza JR, Garin I. Diet and prey selection in the Mediterranean horseshoe bat Rhinolophus euryale (Chiroptera, Rhinolophidae) during the pre-breeding season. Mammalia. 2004; 68: 397–402.
- 40. Salsamendi E, Garin I, Almenar D, Goiti U, Napal M, Aihartza J. Diet and prey selection in Mehelyi's horseshoe bat Rhinolophus mehelyi (Chiroptera, Rhinolophidae) in the south-western Iberian Peninsula. Acta Chiropt. 2008; 10: 279–286.
- 41. Ahmim M, Moali A. The diet of four species of horseshoe bat (Chiroptera: Rhinolophidae) in a mountainous region of Algeria: evidence for gleaning. Hystrix It J Mamm. 2013; 24: 174–176.
- 42. Siemers BM, Ivanova T. Ground gleaning in horseshoe bats: comparative evidence from Rhinolophus blasii, R. euryale and R. mehelyi. Behav Ecol Sociobiol. 2004; 56: 464–471.
- 43. Voigt CC, Schuller BM, Greif S, Siemers BM. Perch-hunting in insectivorous Rhinolophus bats is related to high energy costs of manoeuvring flights. J Comp Physiol B. 2010; 79 877–883.
- 44. Bogdanowicz W, Owen RD. Phylogenetic analyses of the bat family Rhinolophidae. J Zoolog Syst Evol Res. 1992; 30: 142–160.
- 45. Jones KE, Purvis A, Maclarnon A, Bininda-Emonds ORP, Simmons NB. A phylogenetic supertree of the bats (Mammalia: Chiroptera). Biol Rev Camb Philos Soc. 2002; 77(2):223–59. pmid:12056748
- 46. Guillén-Servent A, Francis CM, Ricklefs RE. Phylogeny and biogeography of the horseshoe bats. In: Csorba G, Ujhelyi P, Thomas N, editors. Horseshoe bats of the world. Exeter: Pelagic Publishing Ltd; 2003. pp. xii–xxiv.
- 47. Stoffberg S, Jacobs DS, Mackie IJ, Matthee CA. Molecular phylogenetics and historical biogeography of Rhinolophus bats. Mol Phylogenet Evol. 2010; 54: 1–9. pmid:19766726
- 48. Canadian Council On Animal Care. CCAC species-specific recommendations on: Bats: 2003. Available: http://www.ccac.ca/en_/standards/guidelines/additional/recommendations-species. Accessed 21 October 2014.
- 49. Eurobats. Resolution 6.5: Guidelines on ethics for research and field work pratices. 2010. Available: http://eurobats.eaudeweb.ro/en/document/resolution-65-guidelines-ethics-research-and-field-work-pratices. Accessed 21 October 2014.
- 50. Dietz C, von Helversen O. Illustrated identification key to the bats of Europe. 2004. Available: http://www.fledermaus-dietz.de/publications/publications.html. Accessed 21October 2014.
- 51. Rohlf FJ. TpsDig. 2.17 ed. Department of Ecology and Evolution, State University of New York at Stony Brook. 2013. Available: http://life.bio.sunysb.edu/morph/. Accessed 21 October 2014.
- 52. Sheets HD, Zelditch ML. IMP: TMorphGen6- Traditional morphometrics variables generation utility. Dept. of Physics, Canisius College and Dept. of Geology, SUNY at Buffalo, Buffalo NY. 2003 Available: http://www3.canisius.edu/~sheets/morphsoft.html. Accessed 21 October 2014.
- 53. Klingenberg CP, McIntyre GS. Geometric morphometrics of developmental instability: analyzing patterns of fluctuating asymmetry with procrustes methods. Evolution. 1998; 1363–1375.
- 54. Arnqvist G, Mårtensson T. Measurement error in geometric morphometrics: empirical strategies to assess and reduce its impact on measures of shape. Acta Zool Acad Sci H. 1998; 44: 73–96.
- 55. Fruciano C, Tigano C, Ferrito V. Body shape variation and colour change during growth in a protogynous fish. Environ Biol Fishes. 2012; 94: 615–622.
- 56. Fruciano C, Tigano C, Ferrito V. Geographical and morphological variation within and between colour phases in Coris julis (L. 1758), a protogynous marine fish. Biol J Linn Soc. 2011; 104: 148–162.
- 57. Rohlf FJ, Slice D. Extensions of the procrustes method for the optimal superimposition of landmarks. Syst Zool. 1990; 39: 40–59.
- 58. Klingenberg CP. MorphoJ: an integrated software package for geometric morphometrics. Mol Ecol Resour. 2011; 11: 353–357. pmid:21429143
- 59. Mitteroecker P, Bookstein F. Linear discrimination, ordination, and the visualization of selection gradients in modern morphometrics. Evol Biol. 2011; 38: 100–114.
- 60. Raiche G. nFactors: Parallel analysis and non graphical solutions to the Cattell Scree test. 2010. R package version 2.3.3. Available: http://cran.r-project.org/web/packages/nFactors/index.html. Accessed 24 October 2014.
- 61. Anderson TW. Asymptotic theory for principal component analysis. Ann Math Stat. 1963;34: 122–148.
- 62. Fruciano C, Tigano C, Ferrito V. Traditional and geometric morphometrics detect morphological variation of lower pharyngeal jaw in Coris julis (Teleostei, Labridae). Ital J Zool. 2011; 78: 320–327.
- 63. Boulesteix A-L. A note on between-group PCA. Int J Pure Appl Math. 2005; 19: 359–366.
- 64. Fruciano C, Pappalardo AM, Tigano C, Ferrito V. Phylogeographical relationships of Sicilian brown trout and the effects of genetic introgression on morphospace occupation. Biol J Linn Soc. 2014;112: 387–398.
- 65. Franchini P, Fruciano C, Spreitzer ML, Jones JC, Elmer KR, Henning F et al. Genomic architecture of ecologically divergent body shape in a pair of sympatric crater lake cichlid fishes. Mol Ecol. 2014; 23: 1828–1845. pmid:24237636
- 66. Loy A. An introduction to geometric morphometrics and intraspecific variation. In: Marcus L, Corti M, Loy A, Naylor GP, Slice D, editors. Advances in morphometrics. New York: Springer Science and Business Media; 1996. pp. 271–273.
- 67. Jacobs DS, Barclay RMR, Walker MH. The allometry of echolocation call frequencies of insectivorous bats: why do some species deviate from the pattern? Oecologia. 2007; 152: 583–594. pmid:17345101
- 68. Hayssen V, Kunz TH. Allometry of litter mass in bats: Maternal size, wing morphology, and phylogeny. J Mamm. 1996; 77: 476–490.
- 69. Norberg UM. Allometry of bat wings and legs and comparison with bird wings. Philos Trans R Soc Lond B Biol Sci. 1981; 292: 359–398.
- 70. Lupold S, McElligott AG, Hosken DJ. Bat genitalia: allometry, variation and good genes. Biol J Linn Soc. 2004; 83: 497–507.
- 71. Riskin DK, Iriarte-Diaz J, Middleton KM, Breuer KS, Swartz SM. Allometry of inertial power during flight in pteropodid bats. Bat Research News. 2008; 49: 164.
- 72. Swartz SM. Allometric patterning in the limb skeleton of bats: Implications for the mechanics and energetics of powered flight. J Morphol. 1997; 234: 277–294.
- 73. Reiter G (2004) The importance of woodland for Rhinolophus hipposideros (Chiroptera, Rhinolophidae) in Austria. Mammalia. 2004; 68: 403–410.
- 74. Uhrin M, Boldogh S, Bücs S, Paunovic M, Mikova E, Juhász M et al. Revision of the occurrence of Rhinolophus euryale in in the Carpathian region, Central Europe. Vespertilio. 2012; 16: 289–328.
- 75. Swartz SM, Iriarte-Diaz J, Riskin DK, Breuer KS. A bird? A plane? No, it's a bat: an introduction to the biomechanics of bat flight. In: Gunnell GF, Simmons NB, editors. Evolutionary History of Bats. Cambridge Univ Press; 2012. pp. 317–352.
- 76. Aldridge HDJN. Manoeuvrability and ecology in British bats. Myotis. 1985; 23–24: 157–160.
- 77. Brewer ML, Hertel F. Wing morphology and flight behavior of pelecaniform seabirds. J Morphol. 2007; 268: 866–877. pmid:17638303