Developmental instability of shelled gastropods is measured as deviations from a perfect equiangular (logarithmic) spiral. We studied six species of gastropods at ‘Evolution Canyons I and II’ in Carmel and the Galilee Mountains, Israel, respectively. The xeric, south-facing, ‘African’ slopes and the mesic, north-facing, ‘European’ slopes have dramatically different microclimates and plant communities. Moreover, ‘Evolution Canyon II’ receives more rainfall than ‘Evolution Canyon I.’
We examined fluctuating asymmetry, rate of whorl expansion, shell height, and number of rotations of the body suture in six species of terrestrial snails from the two ‘Evolution Canyons.’ The xeric ‘African’ slope should be more stressful to land snails than the ‘European’ slope, and ‘Evolution Canyon I’ should be more stressful than ‘Evolution Canyon II.’ Only Eopolita protensa jebusitica showed marginally significant differences in fluctuating helical asymmetry between the two slopes. Contrary to expectations, asymmetry was marginally greater on the ‘European’ slope. Shells of Levantina spiriplana caesareana at ‘Evolution Canyon I,’ were smaller and more asymmetric than those at ‘Evolution Canyon II.’ Moreover, shell height and number of rotations of the suture were greater on the north-facing slopes of both canyons.
Our data is consistent with a trade-off between drought resistance and thermoregulation in snails; Levantina was significantly smaller on the ‘African’ slope, for increasing surface area and thermoregulation, while Eopolita was larger on the ‘African’ slope, for reducing water evaporation. In addition, ‘Evolution Canyon I’ was more stressful than Evolution Canyon II’ for Levantina.
Citation: Raz S, Schwartz NP, Mienis HK, Nevo E, Graham JH (2012) Fluctuating Helical Asymmetry and Morphology of Snails (Gastropoda) in Divergent Microhabitats at ‘Evolution Canyons I and II,’ Israel. PLoS ONE 7(7): e41840. https://doi.org/10.1371/journal.pone.0041840
Editor: Shree Ram Singh, National Cancer Institute, United States of America
Received: May 24, 2012; Accepted: June 25, 2012; Published: July 26, 2012
Copyright: © Raz 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.
Funding: There are no sources of funding to this study.
Competing interests: The authors have declared that no competing interests exist.
Fluctuating asymmetry, a measure of developmental instability , is usually estimated from bilaterally symmetrical traits. Many organisms, however, have other kinds of symmetry (i.e., translatory, radial, dihedral, or helical symmetries). Gastropods, for example, have helical symmetry, which can be the basis for fluctuating helical asymmetry. Previously, Graham, Freeman & Emlen  studied deviations from a perfect equiangular (logarithmic) spiral in three populations of the terrestrial snail Cepaea nemoralis (Helicidae: Gastropoda) in the Ukraine. Others have studied shell deformities in snails  and other mollusks , , . Here we study growth, shell morphology, and fluctuating helical asymmetry of six species of terrestrial pulmonate and prosobranch snails from the opposing slopes of ‘Evolution Canyon I,’ Lower Nahal Oren, Mount Carmel (EC I) and ‘Evolution Canyon II,’ Lower Nahal Keziv, Western Upper Galilee (EC II), in Israel.
The ‘Evolution Canyon’ microsites are model systems for the study of adaptation and speciation. The opposite slopes of these canyons, the abiotically stressed south-facing, ‘African’ slopes and the moderate, north-facing, ‘European’ slopes, diverge biotically and abiotically, providing an opportunity to study developmental instability in a natural experiment. Hundreds of studies have been conducted here in the last 20 years , , , , , .
Four ‘Evolution Canyon’ microsites are distributed across Israel: EC I in the mountains of Carmel, EC II in Galilee, EC III in the Negev, and EC IV in the Golan , . Most of the studies on these canyons were conducted at ‘Evolution Canyons I and II’ (Figure 1). They have demonstrated that the ‘African’ slope is more stressful for many mesic organisms (reviewed in , , , , , ). The microclimatic differences produce strong differentiation of local biodiversity at all developmental levels (base sequences, genes, genomes, populations, species, ecosystems, and biota). The interslope differences at the molecular level (greater mutation frequency and recombination rate on the ‘African’ slope, in different taxa) are accompanied by interslope differences in species richness and abundance (reviewed in , , , , , ).
The xeric ‘African’ slopes are on the right, and the mesic ‘European’ slopes are on the left. A. ‘Evolution Canyon I,’ Lower Nahal Oren, Mount Carmel, Israel. B. ‘Evolution Canyon II,’ Lower Nahal Keziv, western Upper Galilee, Israel.
In 11 of 14 model species at ‘Evolution Canyon I,’ Nevo and colleagues , , , , ,  found significantly greater genetic polymorphism on the ‘African’ slope than on the ‘European’ slope. They also found adaptive changes in other genetic characteristics. Populations of several model species on the more stressful ‘African’ slope had greater rates of mutation, gene conversion, recombination, and DNA repair, as well as greater genome size, more SSRs, SNPs, retrotransposons, transposons, candidate gene diversity, and genome-wide gene expression and regulation.
The coprophilous fungus Sordaria fimicola, for example, has heritable mutation rates 3-fold higher on the ‘African’ slope. Drosophila melanogaster has male recombination rates 4-fold higher on the ‘African’ slope. The filamentous cyanobacterium, Nostoc linckia, has higher haplotype diversity of clock genes KaiABC on the ‘African’ slope, and wild barley, Hordeum spontaneum, shows genetic divergence between the opposing slopes.
In addition to genetic divergence, species richness and abundance differ between the slopes. Pavlíček et al. , for example, showed that different taxonomic groups of terrestrial animals, such as scorpions, reptiles, butterflies (Rhopalocera), darkling beetles (Tenebrionidae), skin beetles (Dermestidae), and grasshoppers (Orthoptera), are more abundant on the ‘African’ slope than on the ‘European’ slope. The opposite trend occurs with springtails (Collembola), soil microfungi, basidiomycetous fungi (Basidiomycetes), mosses (Bryophyta), and trees and shrubs. These taxa have greater species richness on the ‘European’ slope than on the ‘African’ slope.
These results  demonstrate that species richness and abundance vary along a climatic transect of only a few hundred meters (the geology is identical on both slopes), revealing ecological (climatic) selection strong enough to override the mixing effects of migration and stochasticity. The ecological selection caused by higher insolation on the ‘African’ slope leads to greater ecological heterogeneity on that slope, as well as a savanna ecosystem that accommodates more species of heat-dependent taxa.
In a previous study at ‘Evolution Canyon I,’ Raz et al.  studied leaf asymmetry of twelve species of vascular plants growing on the opposing slopes. Two of the species had more asymmetrical leaves on the ‘African’ slope, while one species had more asymmetrical leaves on the ‘European’ slope. Overall, the differences in fluctuating asymmetry between the slopes were negatively correlated with the differences in relative abundance. Species displayed greater fluctuating asymmetry on the slope where they were less abundant, and hence more stressed.
In the current study we explore the fluctuating helical asymmetry of six land-snail species from the opposing slopes of ‘Evolution Canyons I and II.’ Because land snails are susceptible to desiccation, the xeric ‘African’ slope should be more stressful. But unlike plants, land-snails can hide under stones and in cracks. And like plants, they can also become inactive during the dry season. In Israel's Mediterranean region, snails are typically active during rainy days from November to April . Such behavior reduces temperature stress and water loss . Morphology, physiology, and life history can also influence resistance to desiccation . Consequently, some species of land snails can live abundantly in deserts.
Previous research on snails at ‘Evolution Canyon I’ shows that most snails are larger on the ‘European’ slope, but more abundant on the ‘African’ slope , . Rainfall is roughly the same on both slopes, but temperatures on the ‘African’ slope may be more amenable for growth during the rainy winter, when the snails are active. Broza & Nevo  suggested that the size differences between the two slopes might be due to r- and k-selection; snails on the ‘African’ slope put more energy into reproduction, while those on the ‘European’ slope put more energy into competitive ability. Size differences could also reflect Bergmann's ecogeographic rule extended to invertebrates: smaller body size supporting thermal tolerance on the warmer slope.
These results suggest that the interslope differences in insolation, temperature, and humidity at ‘Evolution Canyon’ differentially influence growth, morphology, and developmental instability of snails . Hence, snails should be larger and more symmetrical on the ‘European’ slope than on the ‘African’ slope of ‘Evolution Canyon.’ We recognize, however, that the cool and humid ‘European’ slope could be stressful to land-snails adapted to more xeric and warm climatic conditions. Moreover, one expects this stress to influence snails mostly during the November-to-April rainy and cold season. Species intolerant of prolonged summer drought and heat during the May-to-October period of aestivation should have slower growth and be more developmentally unstable on the ‘African’ slope, while those intolerant of shade and lower winter temperatures should have slower growth and be more developmentally unstable on the ‘European’ slope.
Materials and Methods
‘Evolution Canyon I’ (EC I) (Figure 1) is located at Lower Nahal Oren (32°42′51.09″N; 34°58′26.81″E), a deeply incised valley running from Mount Carmel, Israel, westwards into the Mediterranean Sea. The opposite slopes share identical geological history (Plio-Pleistocene canyon, presumably 3–5 million years old ), geology, soils (terra rossa on Upper Cenomanian limestone), and regional climate, although they differ in topography (dip in opposite directions; the ‘African’ slope dips 35°; the ‘European’ slope dips 25°) and aspect. Interslope distance is 100 m at the valley bottom and 400 m at the top; ‘African’ and ‘European’ slopes are 120 m and 180 m long, respectively (Figure 1). Rainfall at ‘Evolution Canyon I’ is 600 mm per year. The percentage of plant cover varies from 35% on the ‘African’ slope to 150% on the ‘European’ slope . Life-form analysis clearly illustrates the dramatic interslope differences between the hot, xeric, Mediterranean savannoid formation of Ceratonia siliqua–Pistacia lentiscus on the ‘African’ slope and the dense maquis of Quercus calliprinos–Pistacia palaestina on the ‘European’ slope .
‘Evolution Canyon II’ (EC II) is located 38 km northeast of ‘Evolution Canyon I’ at Lower Nahal Keziv, western Upper Galilee (33°02′34.86″N, 35°11′05.74″E). Like ‘Evolution Canyon I,’ ‘Evolution Canyon II’ has a south-facing ‘African’ slope and a north-facing ‘European’ slope that incline 20–40° and 30–40°, respectively. The canyon is narrower and steeper than that at ‘Evolution Canyon I’ (50 m at the bottom and 350 m at the top). It is also further inland from the Mediterranean Sea, and more sheltered, than ‘Evolution Canyon I.’ The underlying rocks are upper Cenomanian limestone, with colluvial and alluvial soils at the bottom and terra rossa on the slopes. Rainfall at ‘Evolution Canyon II’ is 700 mm per year, which is 17% greater than that at ‘Evolution Canyon I.’ The plant communities also vary between the slopes. The number of vascular plant species on the ‘African’ slope (205 species) is substantially greater than on the ‘European’ slope (54 species). The percentage of plant cover varies from 70% on the ‘African’ slope to 100% on the ‘European’ slope . The ‘African’ slope changes from Calicotome villosa and Salvia fruticosa garrigue at the bottom to a dry, Mediterranean, savannoid, open Park Forest of C. siliqua – P. lentiscus association at the top. The ‘European’ slope is covered by a dense forest of Acer obtusifolium and Laurus nobilis, which is very different from the ‘European’ slope of ‘Evolution Canyon I,’ and represents a Mediterranean maquis forest.
We collected shells of six species of shelled gastropods (both juveniles and adults) from north- and south-facing slopes of ‘Evolution Canyon I’ and ‘Evolution Canyon II’ (Table 1). The collections were approved by the Israeli Nature and Park Authority [Permit 2010/38005 and 2010/38006 for Oren Canyon (‘Evolution Canyon I’) and Keziv Canyon (‘Evolution Canyon II’), respectively], so all necessary permits were obtained for the described field studies.
We sampled four land-snail species from the opposing slopes of ‘Evolution Canyon I,’ the pulmonate snails Buliminus labrosus labrosus, Monacha syriaca, Xeropicta vestalis joppensis, and Levantina spiriplana caesareana. Two of these species, L. s. caesareana and B. l. labrosus, were also sampled at ‘Evolution Canyon II.’ In addition, we sampled Pomatias olivieri, a prosobranch snail, and Eopolita p. jebusitica, a pulmonate snail, only at ‘Evolution Canyon II.’ The taxonomy of Buliminus, Monacha, Xeropicta, Pomatias, and Eopolita follows Heller , while Levantina follows Pfeiffer  and Forcart (unpublished work).
We scanned each snail twice on a flatbed scanner, at a resolution of 600 dpi. To support a snail for the scan, we pressed it into a cubic block of clay so that the columella was either parallel or perpendicular to the scan surface, depending upon the species. For replicate scans, and to estimate the measurement error associated with each scan, we repositioned each snail in the clay, from scratch. We also made three replicate sets of measurements per scan, using SigmaScan Pro: Image Analysis Version 5.0.0. Consequently, there were six replicate measurements made on each snail. The main measurement was the radius from apex to curve (the suture) for every 180° of clockwise rotation. All scans were done by Shmuel Raz. All measurements on the images were made by a single observer (Nathan Schwartz).
Different species of snails required different approaches. Those having a relatively depressed, flat shell (Monacha, Xeropicta, Eopolita, and Levantina) could be scanned such that the apex and entire spiral suture were clearly visible (apical view, with columella perpendicular to the scan surface). Measuring the radius from apex to curve of the suture was straightforward. This could not be done with snails having an oblong or globose shell (Pomatias and Buliminus). These species were scanned from the side, in apertural view (columella parallel to the scan surface). We measured the distance from apex to the nearest suture on the left side, and then from that suture to the next one, and so on, repeating the process on the right side.
Fluctuating helical asymmetry
Helical symmetry involves rotation, along with translation along an axis of rotation. The spiral shell approximates an equiangular (logarithmic) spiral. The equation for an equiangular spiral is r = aeθ cot Φ, where r is the radius from apex to curve, a is a constant, e is the base of natural logarithms, θ is the angle made with a reference line passing through the apex, and Φ is the constant angle at which the radius vector cuts the curve. Graham et al.  regressed loge (r+1) on angle θ for each individual snail and used the standard error of the estimate, divided by the mean of the dependent variable (), as an estimate of individual asymmetry (Figure 2).
Measurement error (s2me) inflates estimates of fluctuating asymmetry. It also creates problems when the researcher later corrects for size scaling , , . A preliminary study of Cepaea nemoralis (previously collected in the Ukraine) suggested that the variation among photos within snails within sites accounted for 22.5% of the variation, while variation among replicate measurements accounted for 3.5%. The remaining variation (74.0%) was among individual snails within a site.
Trait-size variation is often a problem in studies of fluctuating asymmetry. Positive size-scaling of asymmetry, for example, is largely due to multiplicative error associated with the active-tissue model of growth , . We found no evidence for positive (or negative) size scaling after averaging all of the replicate measurements and loge transforming r. The averaging of replicates removes most of the additive measurement error and the logarithmic transform eliminates the multiplicative error associated with growth.
Size and growth
As a measure of body size, we measured the height of the shell from the apex to the closest part of the aperture and quantified the rate of expansion of the body whorl as the slope of the regression of loge (r+1) on angle θ. The number of complete rotations of the suture around the apex is also an indicator of size. This is not equivalent to the number of whorls; the number of suture rotations always exceeds the number of whorls.
We used SPSS's GLM Varcomp procedure to estimate the variance components associated with sites, snails within sites, scans of snails within sites, and replicate measures of scans within snails within sites.
We used one-way ANOVA to compare fluctuating asymmetry, shell height, regression coefficient, and number of rotations of the suture between ‘African’ and ‘European’ slopes. Slope is a fixed effect and snail within slope (the average of six replicate measurements) is a random effect. For Levantina and Buliminus, which were sampled at both ‘Evolution Canyons I and II,’ we included canyon as a fixed effect.
Fluctuating helical asymmetry
Variance components associated with slope, individuals, scans, and replications were estimated for B. l. labrosus and L. s. caesareana (Table 2). The among-individual variation represents both genotypic and microenvironmental variation. Measurement error includes variation among scans and among replicate measurements. For Levantina, which we scanned in apical view, most of the variation was due to measurement error (49–57% of the total variation was among scans and 17–30% was among replicate measurements). For Buliminus, which we scanned in apertural view, measurement error was much smaller (4% of the total variation was among scans and 1% was among replicate measurements).
Eopolita p. jebusitica at ‘Evolution Canyon II’ showed marginally significant differences in fluctuating asymmetry between the ‘African’ and ‘European’ slopes (F1, 18 = 4.146, P = 0.057, Figure 3). Shells were more asymmetric on the ‘European’ slope. None of the other species showed significant differences in fluctuating asymmetry between the slopes (F1, 22–93≤1.19, P≥0.215).
Light gray indicates the ‘African’ slope; dark gray indicates the ‘European’ slope.
Levantina s. caesareana had greater fluctuating asymmetry at ‘Evolution Canyon I’ than at ‘Evolution Canyon II’ (F1, 145 = 36.978, P<0.001). Neither the differences between slopes (F1, 145 = 0.031, P>0.850), nor the interaction of slope and canyon (F1, 145 = 0.279, P>0.550) were significant. Buliminus l. labrosus, the only other species collected at both canyons showed no differences in fluctuating asymmetry between them (F1, 158 = 0.813, P>0.350).
Mean shell height is indicative of overall size (Figure 4). There were significant differences in shell height between L. s. caesareana from the two canyon sites (F1, 145 = 150.414, P<0.001) and from ‘African’ and ‘European’ slopes (F1, 145 = 21.117, P<0.001). There was also a significant interaction between canyon site and slope (F1, 145 = 9.338, P<0.005). Shell heights were greater on the ‘European’ slope, though the differences were less extreme at ‘Evolution Canyon II,’ and shell heights were greater at ‘Evolution Canyon II’ than at ‘Evolution Canyon I.’ Xeropicta v. joppensis, in contrast, had greater shell height on the ‘African’ slope (F1, 38 = 19.811, P<0.001).
Light gray indicates the ‘African’ slope; dark gray indicates the ‘European’ slope.
There were significant differences in shell height between B. l. labrosus from the two canyon sites (F1, 158 = 15.916, P<0.001), but not between ‘African’ and ‘European’ slopes (F1, 158 = 0.001, P>0.950). The interaction between canyon site and slope was also insignificant (F1, 158 = 1.280, P>0.250). Shell heights were greater at ‘Evolution Canyon II’ than at ‘Evolution Canyon I.’
The shell heights of M. syriaca, P. olivieri, and E. p. jebusitica did not differ between the two slopes (F1, 18–32≤1.409, P≥0.251).
Expansion of the body whorl
The rate of expansion of the body whorl (i.e., the slope of the regression of loge r+1 on angle θ for each individual) reflects the rate at which the spiral opens up (Figure 5). Only B. l. labrosus showed significant differences between the canyon sites (F1, 158 = 19.560, P<0.001) and marginally significant differences between the two slopes (F1, 158 = 3.682, P = 0.057). The interaction between site and slope was also significant (F1, 158 = 20.870, P<0.001). The body whorl expanded more rapidly on the ‘European’ slope at ‘Evolution Canyon I,’ but the reverse was true at ‘Evolution Canyon II.’ None of the other species displayed differences in the body whorl between the ‘African’ and ‘European’ slopes (F1, 18–93 = 0.765–2.050, P≥0.166).
Number of rotations of the body suture
The mean number of rotations of the body suture (Figure 6) is indicative of age and size. Populations of B. l. labrosus at ‘Evolution Canyon II’ had more suture rotations on the ‘European’ slope than on the ‘African’ slope (F1, 73 = 12.374, P<0.001). Populations of L. s. caesareana had significant differences in the number of suture rotations between the two canyon sites (F1, 145 = 48.126, P<0.001) and between ‘African’ and ‘European’ slopes (F1, 145 = 18.731, P<0.001). The interaction between canyon site and slope was insignificant (F1, 145 = 0.355, P>0.550). The number of rotations of the body suture was greater on the ‘European’ slope.
Light gray indicates the ‘African’ slope; dark gray indicates the ‘European’ slope.
There were significant differences in the numbers of suture rotations between Buliminus from the two canyon sites (F1, 158 = 26.637, P<0.001), and from ‘African’ and ‘European’ slopes (F1, 158 = 7.497, P<0.010). The interaction between canyon site and slope was also significant (F1, 158 = 14.704, P<0.001). The number of suture rotations was greater at ‘Evolution Canyon II’ than at ‘Evolution Canyon I,’ but differences between ‘African’ and ‘European’ slopes were only evident at ‘Evolution Canyon II,’ where snails on the ‘European’ slope had more suture rotations.
In contrast to Buliminus and Levantina, X. v. joppensis had more suture rotations on the ‘African’ slope (F1, 38 = 5.492, P<0.025). None of the other species and populations had different numbers of suture rotations on the two slopes (F1, 18–85 = 0.002–1.833, P≥0.189).
Gastropods are distributed from the arctic to the tropics and can be terrestrial (one-third of species) or aquatic (two-thirds of species) . They are adapted to most of the habitats on Earth and in terrestrial habitats they are subjected to daily and seasonal variation in temperature and water availability. Their success in colonizing different habitats is due to physiological, behavioral, and morphological adaptations to water availability , , , as well as ionic and thermal balance . The shell of a snail is constructed of calcium carbonate, but even in acidic soils one can find various species of shell-less slugs. Interestingly, land-snails also live in deserts, where they must contend with heat and aridity .
Species richness and abundance
Adaptation of land-snails to different regimes of heat and aridity may influence species richness and abundance of snails on the opposing slopes of ‘Evolution Canyon’ , , , , . For example, species richness is greater on the ‘European’ slope of ‘Evolution Canyon I,’ but overall abundance is greater on the ‘African’ slope . The greater species richness on the ‘European’ slope represents the addition of European species of snails and slugs at the southern limits of their adaptive range.
The greater overall abundance of snails on the ‘African’ slopes may reflect a better nutritional environment, less predation from small mammals , abiotic stress or all of these together. Early successional plants on the ‘African’ slope may be more palatable , and plant secondary compounds influence choice of food . If this is true, then the snails that feed on live plants and lichens should show the greatest differences in abundance. The four species that feed on living plants or lichens (L. s. caesareana, B. l. labrosus, M. syriaca, X. v. joppensis) were rare (M. syriaca) or considerably more abundant on the ‘African’ slope, whereas the species that feed on decaying plants (P. olivieri, E. p. jebusitica) or other invertebrates (E. p. jebusitica) were slightly more abundant on the ‘European’ slope.
According to Pavlíček et al. , six of seven species more abundant on the south-facing slope fed on live plants, whereas only one of eleven species that fed exclusively on decaying plants was more abundant on the south-facing slope. Finally, the main predators, such as shrews (Crocidura spp. and Suncus etruscus), may be unwilling to venture out onto the more open south-facing slopes, which lack natural shelters .
Fluctuating helical asymmetry
To the best of our knowledge, the only work on fluctuating helical asymmetry of land-snails was done by Graham et al. , who studied deviations from a perfect equiangular spiral in three populations of the terrestrial land-snail Cepaea nemoralis in the Ukraine. The highest level of asymmetry was found in populations exposed to ammonia emissions and pesticides. Individuals in the population having the greatest helical asymmetry also showed erosion of their periostracum, which was not evident in the other two populations.
Overcrowding and nutritional deprivation can influence shell microstructure, increasing fluctuating helical asymmetry. Chunhabundit et al. , for example, raised maculated top shells, Trochus maculatus, a marine gastropod, under high density and inadequate nutrition. The periostracum was reduced and shell structure was dissolved in the vicinity of the shell apex. The suture lines were less smooth.
As with twelve species of vascular plants at ‘Evolution Canyon I,’ we cannot reject the null hypothesis of no differences in deviations from perfect symmetry between the land-snails from the opposing slopes. In the case of the vascular plants, the leaves were bilaterally symmetrical. For the snails, the shells are helically symmetrical. We suggest that land-snails are better adapted to the ‘African’ slope than we had anticipated. They can hide themselves in different locations, such as under stones and in cracks. Such behavior reduces their temperature and water loss, though Xeropicta aestivates high up on shrubs. In addition, the shells may serve as a CaCO3 ‘door,’ separating land-snails from environmental stress.
Thermoregulation, drought resistance, and body size
There is a trade-off between drought resistance and thermoregulation in snails . Thermoregulation requires water for evaporative cooling. The smaller the snail, the more effective the cooling, but this system nevertheless requires more water. Evaporative cooling is more effective for smaller snails because a smaller body size increases the surface area to volume ratio, which in turn increases both absorption and radiation of heat , . The ecological rule associated with this phenomenon is Bergmann's rule , which predicts larger body size of warm-blooded vertebrates in colder areas. According to Mayr , this is an adaptive response to environmental temperatures. Although Bergmann's rule was intended to describe body-size variation among species, it has been extended to intraspecific variation in body size ,  as well as to ectotherms , but with variable success , . This rule is exemplified by the spiny mouse, Acomys cahirinus, and the broad-toothed field mouse, Apodemus mystacinus, from the opposing slopes of ‘Evolution Canyon.’ Individuals from the ‘African’ slope are smaller  than those from the ‘European’ slope.
Is it possible that Bergmann's rule, which was meant for endothermic species, also holds for land-snails? Are the size differences of the snails between the canyons and the opposing slopes a result of microclimatic differences? We believe that, yes, the larger shells of Levantina s. caesareana at ‘Evolution Canyon II’ (i.e., Keziv Canyon) and on the ‘European’ slopes of both canyons do indeed represent Bergmann's rule on a microscale. Nevertheless, we collected both adults and juveniles, hence size differences may also be due to differences in age structure.
These results are supported by evidence for a correlation between habitat and body size in invertebrates. The body size of insects and spiders, for example, is smaller when the humidity is lower , . Moreover, a correlation was found between shell diameter and climate in the snail Xerocrassa seetzenii, from Israel . The latitudinal gradient of decreasing body size, from north to south, in Israel, accompanied by decreasing rainfall, also occurs in Levantina s. caesareana .
The smaller the individual, however, the more water it loses for cooling. Hence, there is a lower-size threshold for a given individual and environment . Very small animals lose almost 100% of their body mass for cooling . Accordingly, the amount of water in the tissues of X. v. joppensis may be so small that they are selected for larger body size on the ‘African’ slope than on the ‘European’ slope of ‘Evolution Canyon.’
Xeropicta lives for only one year, while Levantina and Buliminus live for several years. During years with reduced rainfall, adult Xeropicta and Monacha may be extremely small, while in a year with extremely high rainfall and numerous nights with heavy dew, they may reach very large size (Mienis, personal observations).
Morphological differences in body size between relatively large snails (Buliminus and Levantina) and somewhat smaller snails (Monacha) from the opposing slopes of ‘Evolution Canyon’ were found in previous studies . Accordingly, five-out-of-seven species were larger on the ‘European’ slope.
The differences in fluctuating helical asymmetry between ‘African’ and ‘European’ slopes were either non-existent or only marginally significant (shell asymmetry of E. p. jebusitica was marginally greater on the north-facing slope), hence we cannot reject the null hypothesis for no differences between the slopes. There were, however, differences between shell asymmetry of L. s. caesareana from the two canyons; asymmetry was greater at the more arid Nahal Oren, ‘Evolution Canyon I.’
The authors are indebted to Cathy Chamberlin-Graham for her help and comments. We thank Maayan Kotzan for helping with the field work.
Conceived and designed the experiments: SR EN JG. Performed the experiments: SR NS. Analyzed the data: SR HM NS JG. Wrote the paper: SR JG. Performed the taxonomy: HM.
- 1. Graham JH, Raz S, Hel-Or H, Nevo E (2010) Fluctuating asymmetry: methods, theory, and applications. Symmetry 2: 466–540.
- 2. Graham JH, Freeman DC, Emlen JM (1993) Developmental stability: a sensitive indicator of populations under stress. In: Environmental Toxicology and Risk Assessment. Landis WG, Hughes JS, Lewis MA, editors. Philadelphia: American Society for Testing and Materials. 136–158.
- 3. Chunhabundit S, Chunhabundit P, Aranyakananda P, Moree N (2001) Dietary effects on shell microstructures of cultured, maculate top shell (Trochidae: Trochus maculatus, Linnaeus, 1758). SPC Trochus Information Bulletin 8: 15–22.
- 4. Alzieu C (1991) Environmental problems caused by TBT in France: assessment, regulations, prospects. Marine Environmental Research 32: 7–17.
- 5. Batley GE, Fuhua C, Brockbank CI, Flegg KJ (1989) Accumulation of Tributyltin by the Sydney Rock Oyster, Saccostrea commercialis. Australian Journal of Marine and Freshwater Research 40: 49–54.
- 6. Alzieu CL, Sanjuan J, Deltreil JP, Borel M (1986) Tin contamination in Arcachon Bay: effects on oyster shell anomalies. Marine Pollution Bulletin 17: 494–498.
- 7. Nevo E (1995) Asian, African and European biota meet at ‘Evolution Canyon’ Israel: local tests of global biodiversity and genetic diversity patterns. Proceedings of the Royal Society B: Biological Sciences 262: 149–155.
- 8. Nevo E (1997) Evolution in action across phylogeny caused by microclimatic stresses at “Evolution Canyon”. Theoretical Population Biology 52: 231–243.
- 9. Nevo E (2001) Evolution of genome–phenome diversity under environmental stress. Proceedings of the National Academy of Sciences 98: 6233–6240.
- 10. Nevo E (2006) “Evolution Canyon”: a microcosm of life's evolution focusing on adaptation and speciation. Israel Journal of Ecology and Evolution 52: 485–506.
- 11. Nevo E (2009) Evolution in action across life at “Evolution Canyons”, Israel. Trends in Evolutionary Biology 1: e3.
- 12. Nevo E (2011) Selection overrules gene flow at ‘Evolution Canyons’, Israel. In: Advance in Genetics Research. Urbano KV, editor. Hauppauge: NY Nova Science Publishers, Inc. 67–89.
- 13. Pavlíček T, Mienis HK, Raz S, Hassid V, Rubenyan A, et al. (2008) Gastropod biodiversity at the ‘Evolution Canyon’ microsite, lower Nahal Oren, Mount Carmel, Israel. Biological Journal of the Linnean Society 93: 147–155.
- 14. Raz S, Graham JH, Hel-Or H, Pavlíček T, Nevo E (2011) Developmental instability of vascular plants in contrasting microclimates at ‘Evolution Canyon’. Biological Journal of the Linnean Society 102: 786–797.
- 15. Broza M, Nevo E (1996) Differentiation of the snail community on the north- and south-facing slopes of lower Nahal Oren (Mount Carmel, Israel). Israel Journal of Zoology 42: 411–424.
- 16. Garrity SD (1984) Some adaptations of gastropods to physical stress on a tropical rocky shore. Ecology 65: 559–574.
- 17. Rankevich D, Lavie B, Nevo E, Belles A, Arad Z (1996) Genetic and physiological adaptations of the prosobranch landsnail Pomatias olivieri to microclimatic stresses on Mount Carmel, Israel. Israel Journal of Zoology 42: 425–441.
- 18. Pavlíček T, Sharon D, Kravchenko V, Saaroni H, Nevo E (2003) Microclimatic interslope differences underlying biodiversity contrasts in “Evolution Canyon”, Mt. Carmel, Israel. Israel Journal of Earth Sciences 52: 1–9.
- 19. Nevo E, Fragman O, Dafni A, Beiles A (1999) Biodiversity and interslope divergence of vascular plants caused by microclimatic differences at “Evolution Canyon”, Lower Nahal Oren, Mount Carmel, Israel. Israel Journal of Plant Sciences 47: 61–62.
- 20. Finkel M, Fragman O, Nevo E (2001) Biodiversity and interslope divergence of vascular plants caused by sharp microclimatic differences at “Evolution Canyon II”, Lower Nahal Keziv, Upper Galilee, Israel. Israel Journal of Plant Sciences 49: 285–296.
- 21. Heller J, Arad Z, Kurts T (2009) Land Snails of the Land of Israel: Natural History and a Field Guide. Sofia, Bulgaria: Pensoft Publishers. 360.
- 22. Pfeiffer KL (1949) Levantina spiriplana. Archiv für Molluskenkunde 77: 1–51.
- 23. Cowart NM, Graham JH (1999) Within-and among-individual variation in fluctuating asymmetry of leaves in the fig (Ficus carica L.). International Journal of Plant Sciences 160: 116–121.
- 24. Graham JH, Shimizu K, Emlen JM, Freeman DC, Merkel J (2003) Growth models and the expected distribution of fluctuating asymmetry. Biological Journal of the Linnean Society 80: 57–65.
- 25. Ponder WF, Lindberg DR (2008) editors (2008) Phylogeny and Evolution of the Mollusca. Berkeley: University of California Press. 488.
- 26. Arad Z (1993) Effect of desiccation on the water economy of terrestrial gastropods of different phylogenetic origins: a prosobranch (Pomatias glaucus) and two pulmonates (Sphincterochila cariosa and Helix engaddensis). Israel Journal of Zoology 39: 95–104.
- 27. Arad Z, Goldenberg S, Heller J (1989) Resistance to desiccation and distribution patterns in the land snail Sphincterochila. Journal of Zoology 218: 353–364.
- 28. Arad Z, Goldenberg S, Heller J (1992) Intraspecific variation in resistance to desiccation and climatic gradients in the distribution of the land snail Xeropicta vestalis. Journal of Zoology 226: 643–656.
- 29. Riddle WA, Russell-Hunter WD (1983) Physiological ecology of land snails and slugs. In: The Mollusca: Ecology. Russell-Hunter WD, editor. London: Academic Press. 431–461.
- 30. Schmidt-Nielsen K, Taylor CR, Shkolnik A (1971) Desert snails: problems of heat, water and food. Journal of Experimental Biology 55: 385–398.
- 31. Warburg MR (1965) On the water economy of some Australian land-snails. Proceedings of the Malacological Society of London 36: 297–305.
- 32. Rankevich D (1997) Genetic variation and resistance to dessication in populations of landsnails on the southern and northern slopes of Nahal Oren. Haifa: Technion - Israel Institute of Technology. 143.
- 33. Yom-Tov Y (1970) The effect of predation on population densities of some desert snails. Ecology 51: 907–911.
- 34. Cates RG, Orians GH (1975) Sucessional status and the palatability of plants to generalized herbivores. Ecology 56: 410–418.
- 35. Hagele BF, Rahier M (2001) Determinants of seasonal feeding of the generalist snail Arianta arbustorum at six sites dominated by Senecioneae. Oecologia 128: 228–236.
- 36. Abramsky Z, Alfia H, Schachak M, Brand S (1990) Predation by rodents and the distribution and abundance of the snail Trochoidea seetzenii in the Central Negev Desert of Israel. Oikos 59: 225–234.
- 37. Schmidt-Nielsen K (1997) Animal physiology: adaptation and environment. Cambridge, UK: Cambridge University Press. 607.
- 38. Bergmann C (1847) Über die Verhältnisse der Wärmeökonomie der Thiere zu ihrer Grösse. Göttinger Studien 3: 595–708.
- 39. Mayr E (1956) Geographical character gradients and climatic adaptation. Evolution 10: 105–108.
- 40. James FC (1970) Geographic size variation in birds and its relationship to climate. Ecology 51: 365–390.
- 41. Huey RB, Stevenson RD (1979) Integrating thermal physiology and ecology of ectotherms: a discussion of approaches. American Zoologist 19: 357–366.
- 42. Ashton KG, Tracy MC, Queiroz A (2000) Is Bergmann's rule valid for mammals? The American Naturalist 156: 390–415.
- 43. Meiri S, Dayan T, Simberloff D (2004) Carnivores, biases and Bergmann's rule. Biological Journal of the Linnean Society 81: 579–588.
- 44. Nevo E, Filippucci GM, Pavlíček T, Gorlova O, Shenbrot G, et al. (1998) Genotypic and phenotypic divergence of rodents (Acomys cahirinus and Apodemus mystacinus) at “Evolution Canyon”: micro- and macroscale parallelism. Acta Theriologica. Suppl 59–34.
- 45. Cloudsley-Thompson JL (1976) Terrestrial environments. In: Environmental Physiology of Animals. Bligh J, Cloudsley-Thompson JL, MacDonald AG, editors. Oxford, UK: Blackwell Scientific Publishers. 96–103.
- 46. Remmert H (1981) Body size of terrestrial arthropods and biomass of their populations in relation to the abiotic parameters of their milieu. Oecologia 50: 12–13.
- 47. Nevo E, Bar-El C, Bar Z, Beiles A (1981) Genetic structure and climatic correlates of desert landsnails. Oecologia 48: 199–208.
- 48. Heller J (1979) Distribution, hybridization and variation in the Israeli landsnail Levantina (Pulmonata: Helicidae). Zoological Journal of the Linnean Society 67: 115–148.
- 49. Schmidt-Nielsen K (1964) Desert Animals: Physiological Problems of Heat and Water. Oxford, UK: Oxford University Press.
- 50. Prange HD (1996) Evaporative cooling in insects. Journal of Insect Physiology 42: 493–499.