Open Access
Translator Disclaimer
27 October 2021 Phenotypic Plasticity and the Endless Forms of Freshwater Gastropod Shells
Nathan V. Whelan
Author Affiliations +
Abstract

Freshwater gastropod shells display a striking amount of variation. Shell characters are the foundation of most freshwater gastropod taxonomy and the basis for identifying most species. However, intraspecific shell variation is common, and the mechanisms that give rise to this variation are often unclear. One source of shell variation is phenotypic plasticity, in which one genotype gives rise to multiple phenotypes as a response to environmental cues. This phenomenon is often invoked as an explanation for intraspecific shell variation in gastropods, but its existence has not been confirmed experimentally or otherwise in many gastropod lineages. I review the evidence for phenotypic plasticity in freshwater gastropods, and I discuss areas of research needed for a better understanding of intraspecific shell variation. Phenotypic plasticity is well documented in the superorder Hygrophila, but evidence in other freshwater gastropod groups is limited or nonexistent because of the scarcity of common garden experiments for those groups. Despite statements to the contrary, studies that show correlations of shell traits with environmental factors, population genetic analyses, and phylogenetic inference fail to provide evidence of phenotypic plasticity. Researchers must be careful not to postulate about phenotypic plasticity without evidence. I argue that phenotypic plasticity should not be the default hypothesis for explaining intraspecific shell variation in freshwater gastropods and that more common garden experiments are needed to test its existence. Genomic studies of mantle gene expression and transgenerational epigenetic studies also will increase our understanding of gastropod shell variation.

INTRODUCTION

Shells are the most prominent feature of freshwater gastropods (snails and limpets). They protect the animals, form the basis of most taxonomy and species identification, and are linked inextricably to many aspects of gastropod biology (Brusca and Brusca 2003). Gastropods have arguably the greatest diversity of shell forms of any shell-bearing molluscan group. Adult shells of freshwater species range in size from less than 3 mm to more than 16 cm (Thompson 1977; Burch and Tottenham 1980; Hayes et al. 2012), and they can be dome shaped, coiled, extremely ornamented, or without distinguishing features (Figs. 13). Intraspecific shell variation is also common and extensive. For example, shell coiling can be dextral or sinistral (Figs. 2, 3), and both forms can be present in the same population (Fig. 3A, B; Freeman and Lundelius 1982; Asami et al. 2008; Tiemann and Cummings 2008; Abe and Kuroda 2019). Many other types of shell variation occur among and within populations of the same species (e.g., Whelan et al. 2012; Zuykov et al. 2012).

For most freshwater gastropod groups, our current knowledge of shell variation does not extend past superficial documentation of shell forms, and the genetic and environmental mechanisms that influence shell shape are largely unknown. Gastropod shells are hypothesized to be under strong selection from predators (Vermeij 1974, 1982; Vermeij and Covich 1978), an idea that has been corroborated experimentally for many marine gastropods (Palmer 1979; Vermeij 2015). However, less evidence is available for freshwater groups. Stream flow also is hypothesized to influence shell shape (Statzner 2008), but the advantages conferred by different shapes to slower or faster flows are unclear. Genomic and proteomic tools have been used to study the genetic basis of shell shape in only a few lineages (reviewed by Kocot et al. 2016; Song et al. 2019), and difficulties associated with captive rearing of many lineages hinder experimental studies on shell variation. Our poor knowledge of the causes of shell variation may have led to overdescription of gastropod taxa (Burch 1982; Graf 2001), and species hypotheses in most groups have yet to be tested with molecular data.

Figure 1.

Artist rendering of a dextral freshwater snail shell with example shell features and measurements. Abbreviations: Be, beads (small, round protrusions); Ca, carinae (horizontal ribs); Co, costae (vertical ribs); Su, suture (connection point between two whorls); SH, shell or spire height; SW, shell width (usually measured at widest points across body whorl); AW, aperture width (usually measured across widest points); AH, aperture height (usually measured from contact point of the top aperture lip with shell body across to the widest point on anterior aperture lip). This figure does not include spines (see Fig. 3F), tubercles, lirae, or other uncommon types of ornamentation.

img-z2-1_87.jpg

One source of shell variation is phenotypic plasticity, when a single genotype gives rise to multiple phenotypes through developmental responses to biotic or abiotic environmental factors such as presence of predators, stream flow, and Ca2+ limitation (Bradshaw 1965; West-Eberhard 1989). This phenomenon is often invoked to explain shell variation in freshwater gastropods. The term also has been used in the gastropod literature simply to describe intraspecific shell variation, but it must be distinguished from heritable genetic variation that causes variation (Table 1). The extent to which phenotypic plasticity contributes to shell shape is well studied in a few lineages such as Potamopyrgus antipodarum and Ampullaceana balthica (see Patterns and Causes of Shell Variation). However, the extent to which shell variation can be attributed to phenotypic plasticity is poorly understood in most freshwater groups.

Understanding the basis of shell variation in gastropods is important to many research areas, including ecological interactions, systematics, and conservation. For example, misinterpreting phenotypic shell morphs as distinct species could alter fundamentally how we interpret ecological interactions between those morphs. Uncritically dismissing shell variation between two distinct species as phenotypic plasticity would lead to erroneous taxonomic conclusions and underestimation of biodiversity. Conversely, describing ecomorphs that result from phenotypic plasticity as distinct species would lead to overestimation of biodiversity. Such erroneous taxonomic conclusions could lead to inappropriate conservation actions because species-level taxonomy typically informs delineation of management units (Margules and Pressey 2000).

I review the evidence for phenotypic plasticity in freshwater gastropods. I discuss the types of evidence needed to attribute shell variation to phenotypic plasticity, and I assess whether the evidence supports phenotypic plasticity as a common cause of shell variation across freshwater gastropods. I focus on freshwater gastropods because phenotypic plasticity may be more common in freshwater lineages than in marine lineages, even though the reasons for this pattern are unclear (Bourdeau et al. 2015). My goals are to review what is known about phenotypic plasticity, clarify confusion about the evidence for phenotypic plasticity that has permeated some freshwater gastropod literature, and identify research that is needed to better understand the basis of shell variation in freshwater gastropods.

WHAT KIND OF EVIDENCE IS NECESSARY TO ATTRIBUTE SHELL VARIATION TO PHENOTYPIC PLASTICITY?

Testing for phenotypic plasticity requires careful experimental design (Table 1). The most powerful approach for testing the cause of intraspecific shell variation is a common garden experiment. Common garden experiments are designed specifically to evaluate phenotypic plasticity by growing individuals from different populations in a common environment and measuring the expression of traits of interest (de Villemereuil et al. 2016). Examples of shell traits measured in common garden experiments include size (e.g., Krist 2002; Hoverman et al. 2005), shape (e.g., Kistner and Dybdahl 2013), shell thickness (e.g., Hoverman et al. 2005), crush resistance (e.g., Lakowitz et al. 2008), and presence–absence of discrete characters (e.g., Whelan et al. 2012; see Fig. 1). Shell variation observed in the absence of environmental variation can then be attributed to specific stimuli or genetic variation. A disadvantage of common garden experiments is that they require the ability to breed and grow offspring of the study species to a size at which shell traits of interest are expressed and measurable. In part for this reason, common garden studies are far less common than claims about phenotypic plasticity causing shell variation (see subsequent; Table 2).

Figure 2.

A sample of Hygrophila shell morphologies. Shells are from the Auburn Museum of Natural History (AUMNH) unless otherwise noted. (A) Physella sp. (AUMNH 905). (B) Ampullaceana balthica (photo by J. Trausel and F. Slieker; Langeveld et al. 2020; licensed under  http://creativecommons.org/licenses/by/4.0/). (C) Galba humilis (University of Michigan Museum of Natural History, UMMNH 75881). (D) Ladislavella humilis (Chicago Academy of Sciences, CHAS MAL23622). (E) Helisoma anceps (AUMNH 8010). F) Anisus complanatus (AUMNH 5412). Scale bars, 1 cm.

img-z3-1_87.jpg

Reciprocal transplant experiments also can be used to make inferences about phenotypic plasticity. In this approach, individuals from two or more populations or environments are transplanted into the other environment, and shell traits are measured in the new environment. A disadvantage of this approach is that transplanted individuals may have lower survival than native individuals, which would make possible inferences about adaptation but potentially obscure patterns of phenotypic plasticity (de Villemereuil et al. 2016). Transplant experiments also run the risk of inadvertent release of nonnative individuals, which must be avoided. Transplant experiments are uncommon for freshwater gastropods (Tables 1 and 2).

Genomic approaches such as sequencing genes involved in shell shape or other traits have been used in other organisms to determine whether intraspecific variation is genetically controlled or caused by phenotypic plasticity (e.g., McCairns and Bernatchez 2010; Flamarique et al. 2013; Chang and Yan 2019). This approach is difficult, particularly for polygenic traits, and I am aware of no such studies in freshwater snails.

Other approaches for examining intraspecific shell variation cannot provide solid evidence about phenotypic plasticity. Many studies on freshwater gastropods show correlations or clinal variation between shell traits and environmental factors or geography (Table 2). These patterns can appear to provide compelling evidence for phenotypic plasticity. However, clinal variation can have an underlying genetic basis (e.g., Ma et al. 2010; McKechnie et al. 2010; Paaby et al. 2010; Machado et al. 2016; Koch et al. 2021). Consequently, correlations or clinal variation by themselves cannot provide unequivocal evidence about whether genetic differences, phenotypic plasticity, or both, contribute to shell variation.

Figure 3.

A sample of Caenogastropoda shell morphologies. Shells are from University of Michigan Museum of Natural History (UMMNH) unless otherwise noted. (A) Dextral Campeloma regulare (photo by N. Whelan). (B) Sinistral Campeloma regulare (photo by N. Whelan). (C) Tarebia granifera (iBOL 2016). (D) Smooth Io fluvialis (UMMNH 49486). (E) Spined Io fluvialis (UMMNH 132421). (F) Semisulcospira libertina (UMMNH 153930). (G) Smooth Leptoxis ampla (photo by N. Whelan). (H) Carinate Leptoxis ampla (photo by N. Whelan). (I) Smooth Potamopyrgus anitopodarum (photo by K. Mahlfeld, D. Roscoe, F. Climo; Ueda 2020). (J) Spined P. antipodarum (photo by M. Bowie; Ueda 2020). (I, J) Licensed under  http://creativecommons.org/licenses/by-nc/4.0/. Scale bars, 1 cm unless otherwise noted.

img-z4-1_87.jpg

Population genetic analyses in combination with morphological analyses are a powerful tool for understanding spatial genetic patterns, gene flow, and conservation needs of freshwater gastropods (Table 2). However, they cannot provide evidence for phenotypic plasticity because such studies use noncoding loci (e.g., microsatellites) or loci not involved with shell shape (e.g., allozymes, genome-wide single-nucleotide polymorphisms). Population genetic analyses could provide evidence that shell variation is not the result of phenotypic plasticity if shell shape and genetic variation are highly correlated (e.g., Whelan et al. 2019), but other lines of evidence are needed to be conclusive because genome-wide genetic variation may not indicate differences in genes involved with shell variation.

Table 1.

Study types used to examine shell variation in freshwater gastropods.

img-z4-7_87.gif

Table 2.

Summary of studies evaluating phenotypic plasticity in freshwater gastropod shells. All studies refer to intraspecific variation unless otherwise noted.

img-z5-2_87.gif

continued.

img-z6-2_87.gif

continued.

img-z7-2_87.gif

continued.

img-z8-2_87.gif

continued.

img-z9-2_87.gif

Examining shell traits in a phylogenetic context is also common for freshwater gastropods (Tables 1 and 2), but phylogenetic studies without sequencing genes involved with shell morphology cannot provide information about whether phenotypic plasticity causes shell variation. That is, closely related individuals could have differences in the genes controlling shell traits, but be identical with respect to genes used to infer a phylogeny (e.g., mitochondrial genes). The one exception would be if genes involved in shell variation are used for phylogenetic tree inference, but this has not been done for freshwater snails. By contrast, phylogenetic results showing that two entities are distinct species could be used as evidence that observed shell variation is not caused by phenotypic plasticity because variation in genes controlling shell shape can be assumed to have accumulated since the species diverged.

Finally, evidence of plasticity in one group of freshwater snails is not suitable evidence that phenotypic plasticity controls shell traits in other groups. “Freshwater gastropods” is a polyphyletic group. Freshwater habitats have likely been invaded by gastropods at least 30 times (Strong et al. 2008), and all freshwater gastropods have not shared an ancestor for at least 350 million yr (Zapata et al. 2014). This means that factors that control shell traits likely vary widely among disparate lineages. Even within a lineage (e.g., family or genus), the existence of phenotypic plasticity in one species does not necessarily support its existence in other members of the lineage.

PATTERNS AND CAUSES OF SHELL VARIATION

Superorder Hygrophila

Phenotypic plasticity is unusually well studied in the superorder Hygrophila (Table 2). Hygrophila gastropods lack an operculum, and many have a thin and transparent shell (Fig. 2). Historically, these gastropods were considered pulmonates, but molecular phylogenetic analyses determined Pulmonata to be polyphyletic (Jörger et al. 2010). Nevertheless, the term Pulmonata, or pulmonate, is still in use (e.g., Goeppner et al. 2020). Many Hygrophila are reared easily in captivity, which makes common garden experiments and other experimental approaches feasible.

Lymnaeidae.—Phenotypic plasticity is perhaps better documented for Ampullaceana balthica (=Radix balthica; Fig. 2B) than for any other freshwater snail (Table 2). In common garden experiments, A. balthica shell shape was strongly influenced by the presence of predators (Brönmark et al. 2011, 2012), and shell shape varied such that crush resistance to specific predators was maximized in the presence of the specific predator (e.g., crayfish vs. fish; Lakowitz et al. 2008). Brönmark et al. (2012) showed that production of predator-resistant shells carried a fitness trade-off in which higher crush resistance was associated with reduced growth and fecundity. Mantle pigmentation in A. balthica, which can be seen through the shell, is also influenced by predatory fish and UV light (Ahlgren et al. 2013). Shell shape of A. balthica also displays phenotypic plasticity in response to flow, with individuals having proportionally larger apertures in the presence of higher flow (Lam and Calow 1988; Wullschleger and Jokela 2002). Furthermore, some responses to flow by A. balthica appear to be epigenetic because shell shape of subsequent generations can be influenced by stimuli experienced by parents before egg laying (Wullschleger and Jokela 2002).

Both Galba humilis (Fig. 2C) and Ladislavella elodes (Fig. 2D) display shell-shape variation that is associated with abiotic environmental factors, such as substrate composition, watershed drainage area, and pH (Ross et al. 2014). This variation was revealed only by geometric morphometrics, and the variation is subtle and likely not readily perceptible to the human eye. Ross et al. (2014) acknowledged that the causes of variation in these two species are unclear because shape variation is correlated only with environmental factors.

Some lymnaeid species display rare shell abnormalities such as detachment between whorls and bulges on the external shell surface. The causes of such abnormalities are unknown, but they are unlikely to be caused by phenotypic plasticity in every case (Zuykov et al. 2012). The growth of abnormal spires may be similar to intraspecific chirality dimorphisms (i.e., dextral or sinistral) where a small percentage of individuals will have shell chirality opposite of what is common for the species (Freeman and Lundelius 1982; Asami et al. 2008; Abe and Kuroda 2019). Chirality dimorphisms are not well studied in most species, but multiple studies on Peregriana peregra (=Lymnaea peregra) and Ampullaceana balthica indicate that chirality is heritable (Freeman and Lundelius 1982; Asami et al. 2008) and probably controlled by a single gene (Abe and Kuroda 2019).

Planorbidae.—Juvenile Planorbella trivolvis (=Helisoma trivolvis) grew thicker or wider shells depending on whether individuals were exposed to predatory crayfish or waterbugs, respectively (Hoverman et al. 2005; Hoverman and Relyea 2007; Tamburi et al. 2018). Sexually mature P. trivolvis can initiate production of thicker shells when exposed to predators, but previously deposited shell is not modified, emphasizing the developmental aspect of phenotypic plasticity (Hoverman and Relyea 2007). In one of the few common garden experiments that included multiple freshwater snail species, Hoverman et al. (2014) showed that P. trivolvis, P. campanulata, and Helisoma anceps (Fig. 1F) all expressed predator-induced phenotypic plasticity in shell shape or thickness, but phenotypic responses varied by species: H. anceps developed a lower spire and thicker shell in the presence of crayfish and water bugs; P. campanulata developed a lower spire and wider shells in the presence of water bugs, but was unresponsive to crayfish; and P. trivolvis responded differently to each predator, developing a wider shell in response to water bugs but a thicker shell in response to crayfish.

Intraspecific variation in shell spire shape of planorbids is at least sometimes genetically controlled. Some planorbid lineages comprise individuals that grow abnormal, corkscrew-like spires (Zuykov et al. 2012; Clewing et al. 2015), which is heritable and genetically controlled in at least two species, Anisus leucostoma (Fig. 2F; Boettger 1949) and Biomphalaria glabrata (Richards 1971). Clewing et al. (2015) hypothesized that corkscrew-like spires in Gyraulus were ecomorphs caused by phenotypic plasticity, but no experiments were done that could corroborate their hypothesis.

Phenotypic plasticity was invoked to explain interspecific shell-shape variation between the limpets Ferrissia californica (=Ferressia fragilis) and Ferressia rivularis (Dillon and Herman 2009). This conclusion was based on shell shape differences between wild populations that were not present when offspring of each population were raised in a common garden, and the result was the basis for synonymization of F. californica and F. rivularis (Dillon and Herman 2009). However, Walther et al. (2010) demonstrated that F. californica is a valid species and that Dillon and Herman (2009) examined only F. rivularis sensu stricto. Thus, the shell variation documented by Dillon and Herman (2009) was a result of intraspecific phenotypic plasticity within F. rivularis. This example emphasizes the importance of accurate taxonomy and species identification for studying shell variation.

Physidae.—Common garden experiments showed that both genetic differences and phenotypic plasticity affect intraspecific shell variation in at least some physids (Fig. 2A). The genealogy of Physella heterostropha (=Physa heterostropha) individuals influences the degree to which phenotypic plasticity modifies shell shape (DeWitt 1998), and genetic variation in P. virgata influences shell shape more than thermal environment (Britton and McMahon 2004). Furthermore, P. virgata has faster growth rates in the presence of predators, but faster growth has the cost of delayed reproduction (Crowl and Covich 1990). Physella virgata also responds similarly to molluscivorous and nonmolluscivorous fish: it grows thicker shells even in the presence of a nonmolluscivorous fish, which results in decreased fecundity (Langerhans and DeWitt 2002). This demonstrates that phenotypic plasticity can sometimes result in reduced fitness, but provides no offsetting benefit if environmental cues are too general (i.e., any fish vs. a fish predator).

Physella acuta shell shape can vary with abiotic environmental factors, such as pH and substrate composition, but it is unclear to what extent this variation is genetically controlled or a result of phenotypic plasticity (Ross et al. 2014). Both plasticity and genetic background affected shell shape and crush resistance of P. acuta in response to predators (Goeppner et al. 2020; Tariel et al. 2020). Interestingly, common garden experiments showed that the presence of predators also can have transgenerational effects as shell shape appeared to be partly influenced by predator cues experienced by parents and grandparents (Goeppner et al. 2020; Tariel et al. 2020). Dillon and Jacquemin (2015) showed that shell variation between P. acuta and P. carolinae was genetically controlled, indicating that the two species should not be synonymized despite their ability to hybridize.

Subclass Caenogastropoda

Tateidae.—Environmental correlates of shell variation are better demonstrated for the minute and highly invasive Potamopyrgus antipodarum (Fig. 3I, J) than for any other non-Hygrophila freshwater gastropod. Potamopyrgus antipodarum has larger and more slender shells and larger apertures in riverine environments compared with individuals in lakes, both within and beyond its native range (Verhaegen et al. 2018a). Invasive P. antipodarum and native Pyrgulopsis robusta in the Snake River drainage, USA, both have larger apertures in riverine environments compared with individuals in lakes, suggesting convergent environmental adaptation (Kistner and Dybdahl 2014). In its native range, P. antipodarum shells are larger at more downstream-riverine locations, and shell size increases with depth in lakes (Haase 2003; Vergara et al. 2016). The selective advantages of such shell variation are unclear because larger apertures do not convey resistance to dislodgement (Verhaegen et al. 2019), and environmental correlations do not inform the causes of shell variation.

Spines on P. antipodarum shells are more common in lakes than in rivers (Fig. 1J; Holomuzki and Biggs 2006; Verhaegen et al. 2018b), and spine prevalence appears to increase with lake depth (Vergara et al. 2016). The presence of parasites also was associated with larger shells (Levri et al. 2005), but whether parasites induce larger size or simply infect larger individuals has not been determined. Individuals with parasites also are less likely to have spines, but again, whether parasites influenced shell morphology is unclear (Levri et al. 2005). Spines may provide predator defense, but they incur the cost of increased drag (Holomuzki and Biggs 2006). These relationships suggest that flow and predators influence spine development in opposite ways, but spines also are associated with genetic variation (Verhaegen et al. 2018b), casting doubt that phenotypic plasticity alone determines spine development in P. antipodarum.

I am aware of only two studies on P. antipodarum that were common garden or transplant experiments. Negovetic and Jokela (2001) demonstrated through transplantation to different wild habitats that shell shape was influenced by both genetics and environmentally induced plasticity, but shell size was influenced only by phenotypic plasticity. Their findings were corroborated by the common garden experiments of Kistner and Dybdahl (2013). No study has examined spine development in a common garden experiment. Clearly, shell morphology of P. antipodarum is correlated with environmental factors, but data on the mechanisms underlying shell variation are either equivocal (Haase 2003; Levri et al. 2005; Holomuzki and Biggs 2006; Kistner and Dybdahl 2014; Vergara et al. 2016) or suggest an interplay between genetics and phenotypic plasticity (Negovetic and Jokela 2001; Kistner and Dybdahl 2013; Verhaegen et al. 2018a, 2018b).

Hydrobiidae.—Using geometric morphometrics, Albarrán-Melzér et al. (2020) showed that Pyrgophorus coronatus grew slightly wider at lower temperatures, but the differences were exceedingly small and probably not readily perceptible to the human eye. However, small differences may be meaningful to snails, and shell width may affect thermoregulation (Albarrán-Mélzer et al. 2020). Shell variation in Pyrgulopsis robusta is correlated with environmental factors, but the cause of this variation is unknown (Kistner and Dybdahl 2014).

Ampullariidae.—A common garden experiment with Pomacea canaliculata showed that interpopulation shell-shape variation was genetically controlled (Estebenet and Martín 2003). By contrast, another common garden experiment confirmed phenotypic plasticity in P. canaliculata; shells grew larger, but were thinner, at higher temperatures, likely due to reduced shell deposition per unit area as the active edge of the mantle moved forward faster (Tamburi et al. 2018). Another common garden experiment revealed sex-specific phenotypic plasticity in P. canaliculata in which shell height was reduced in females in the presence of a turtle predator, but not in males (Guo et al. 2009). However, both male and female P. canaliculata grew shells with greater crush resistance and smaller opercula when exposed to a turtle predator (Guo et al. 2009).

Viviparidae.—In the only common garden study conducted with Viviparidae, Cipangopaludina chinensis (=Bellamya chinensis) produced offspring with greater shell organic content and slightly larger shells in the presence of a crayfish predator (Prezant et al. 2006). Studies of more obvious traits provide no unequivocal evidence for phenotypic plasticity in the family. Cipangopaludina japonica and Heterogen longispira are indistinguishable on mitochondrial gene trees, but are distinguished easily by shell-suture depth, size of the body whorl, and aperture shape (Hirano et al. 2015). This variation was hypothesized to be the result of phenotypic plasticity within a single species, but the possibility of undiscovered genetic variation sufficient to support the existence of two species was acknowledged (Hirano et al. 2015). Like some Hygrophila, Campeloma spp. can display intraspecific differences in chirality (Fig. 3A, B; Tiemann and Cummings 2008, and references therein), but the underlying causes of this variation are unknown. Furthermore, Campeloma decisum shell shape varies with abiotic environmental factors, but the cause of this variation is also unknown (Ross et al. 2014).

Superfamily Cerithioidea

Thiaridae and Semisulcospiridae.—Common garden experiments have shown that temperature induced small shell-shape differences in the thiarid Tarebia granifera (Fig. 3C) in its invasive range, but the degree of shell-shape variation was lower than in a sympatric, native snail Pyrgophorus coronatus (see Tateidae; Albarrán-Mélzer et al. 2020). Common garden experiments also showed that phenotypic plasticity results in coloration and small shape differences in the thiarid Melanoides tuberculata (Van Bocxlaer et al. 2015). Studies on the semisulcospirid Semisulcospira reiniana suggested a larger environmental effect than genetic effect on shell shape, but estimates of heritability were confounded by an experimental design that failed to account for paternal shell shape (Urabe 1998, 2000). Thus, environmental influence on the shell shape of S. reiniana may be overstated.

Pleuroceridae.—The Pleuroceridae exhibits extensive shell variation within recognized species. For example, the seminal study of Adams (1915) documented striking clinal variation in the genus Io (Fig. 3D, E). Many studies have invoked phenotypic plasticity as a cause of shell variation in Pleuroceridae (e.g., Minton et al. 2008; Dillon 2011, 2014; Minton et al. 2011; Dunithan et al. 2012; Dillon et al. 2013). However, the evidence presented in these studies is limited to correlations with environmental factors or examination of allozyme variation unrelated to shell traits, and none provide unequivocal evidence of phenotypic plasticity. Other studies have documented shell variation in Lithasia geniculata, Elimia spp., and Pleurocera acuta that is correlated with environmental factors or stream position, but have not proposed a cause for this variation (Minton et al. 2007, 2018; Dillon and Robinson 2011; Ross et al. 2014; Cazenave and Zanatta 2016).

Only three common garden experiments have been done on the family, and only one showed evidence of phenotypic plasticity. In the latter study, Elimia livescens grew a slightly narrower (<1.0 mm difference) shell in the presence of a predator cue, but this effect was observed in individuals from only one of three populations studied (Krist 2002). Two studies on Leptoxis ampla, including a common garden experiment, showed that the presence of carinae and other intraspecific shell variation are genetically controlled (Fig. 3G, H; Whelan et al. 2012, 2019). Common garden rearing of all currently recognized, extant Leptoxis species indicated that interspecific shell variation is under genetic control and not a result of phenotypic plasticity (Whelan et al. 2015), supporting the validity of each species.

Despite claims to the contrary, evidence does not support the existence of widespread phenotypic plasticity in pleurocerids. Considering the attention devoted to describing shell variation in the Pleuroceridae, it is curious that little research has attempted to examine the causes or adaptive significance of that variation. For example, no studies have examined the potential adaptive significance or cause of the extensive variation documented by Adams (1915) in Io, and Io fluvialis is currently the only species recognized in the genus (Johnson et al. 2013; MolluscaBase 2021). An impediment to study of the Pleuroceridae is that its taxonomy is in need of revision (Graf 2001; Johnson et al. 2013). This issue complicates the study of shell variation because uncertainty persists about whether shell differences are intra- or interspecific.

Other Freshwater Gastropod Groups

No conclusive evidence exists that shell variation in other gastropod groups is a result of phenotypic plasticity. Freshwater Neritidae in the genus Theodoxus have variable shell coloration and shape (Zettler et al. 2004; Sands et al. 2020), and Heller (1979) suggested that the different shell coloration provides differential protection from predators and UV radiation in specific environments. However, these studies were descriptive or designed to test selective advantages of shell coloration, not underlying causes of variation. Thus, unsubstantiated claims by some authors that morphological variation in Theodoxus is a result of phenotypic plasticity (Zettler et al. 2004; Glöer and Pešić 2015; Sands et al. 2020) should be approached with caution. Morphological variation in Valvatidae is understudied, but some individuals of Valvata lewisi grow abnormal, corkscrew-like shells (Baker 1931; Clarke 1973; Burch and Tottenham 1980; Hinchliffe et al. 2019). The cause and distribution of corkscrew-like individuals of V. lewisi need more research as no common garden experiments have been done, and genetic data are equivocal (Hinchliffe et al. 2019).

GENERAL PATTERNS OF PHENOTYPIC PLASTICITY AND SOURCES OF CONFUSION

Most documented examples of phenotypic plasticity in freshwater gastropods are for the Hygrophila, and phenotypic plasticity appears to be widespread in this group. Most other groups have not been studied well enough to determine the extent of phenotypic plasticity and whether this cause of shell variation is rare or merely poorly documented. Yet, phenotypic plasticity is often stated, or implied, to be common throughout freshwater gastropods (e.g., Urabe 2000; Glaubrecht and Köhler 2004; Minton et al. 2008, 2011; Dillon 2011, 2014; Dunithan et al. 2012; Dillon et al. 2013; Clewing et al. 2015). Such statements appear to stem from untested assumptions and confusion about the types of studies that can confirm phenotypic plasticity. Confusion about the causes of shell variation also appears to stem from using the term “phenotypic plasticity” to mean any type of intraspecific shell variation (e.g., Glaubrecht and Köhler 2004; Glöer and Pešić 2015; Marković et al. 2019; Sands et al. 2020). Researchers must consider what types of evidence are necessary to confirm phenotypic plasticity (Table 1) before invoking it uncritically to explain shell variation.

Importantly, none of the studies discussed in the previous section provided evidence that phenotypic plasticity is the cause of shell variation used to diagnose two putative species. At least two studies on freshwater gastropods showed that interspecific variation is genetically controlled and heritable, thus supporting the distinctiveness of those taxa (Dillon and Jacquemin 2015; Whelan et al. 2015). When phenotypic plasticity is clearly documented as a cause of shell variation between two putative species, synonymy may be warranted, especially if coupled with supporting evidence such as phylogenetic analyses. However, several studies have proposed taxonomic revisions based on unproven claims of phenotypic plasticity as a cause of shell variation (e.g., Dillon and Herman 2009; Dillon 2011, 2014; Dillon et al. 2013), which should be avoided.

Confusion in the literature also exists about the degree to which shells vary due to phenotypic plasticity. In many cases, phenotypic plasticity has a small effect on shell shape (e.g., a slightly wider aperture or thicker shell). This variation may not be perceptible to the human eye, but in some cases, it has demonstrated fitness benefits (e.g., Lakowitz et al. 2008; Hoverman et al. 2014; Albarrán-Melzér et al. 2020). Variation in larger, more conspicuous shell traits such as spines, carinae, etc., also have been attributed to phenotypic plasticity, but almost always without evidence and often based only on speculation about fitness benefits (e.g., Minton et al. 2008; Dillon 2011; Dunithan et al. 2012). Currently, there is no evidence that phenotypic plasticity is the cause of shell ornamentation and the potential fitness benefits of ornamentation are mostly unknown, but few studies have examined these traits.

Much of the confusion about phenotypic plasticity in freshwater gastropods seems to come down to expectations and generalizations. That is, to what extent should we expect phenotypic plasticity to cause shell variation? In Planorbidae, where phenotypic plasticity is well documented in multiple species, the prevalence of phenotypic plasticity may be high. In P. antipodarum, an interplay between genetics and plasticity appears to influence shell shape (Verhaegen et al. 2018a). Clearly, some authors expect phenotypic plasticity to be common in pleurocerids, but phenotypic plasticity has been documented in only one pleurocerid species. Thus, data do not support broad generalizations, and phenotypic plasticity must be evaluated on a case-by-case basis to better understand its prevalence in freshwater gastropods.

FUTURE DIRECTIONS

The greatest research needs for advancing our understanding of phenotypic plasticity in freshwater gastropods are studies with broader taxonomic focus. Although model systems are useful, what makes a system easy to study (e.g., ease of raising in captivity) does not necessarily make the system general enough to explain a phenomenon in disparate lineages. In freshwater gastropods, generalizations are not possible currently because most studies have been conducted with easily studied systems (e.g., Hygrophila). We lack common garden experiments for most groups, and difficulties with raising many groups in captivity are an obstacle. For example, at least some species of pleurocerids can be raised in captivity, but their captive culture needs are more exacting than those of Hygrophila (e.g., larger tanks with flow), and it may take 3–6 mo or longer after hatching before traits of interest are expressed and measurable (Whelan et al. 2012, 2015). Research is needed to develop cost-effective captive-propagation methods for many freshwater gastropods. Such research would improve our ability to study morphological variation and also would be useful for conservation efforts.

Comparative studies among freshwater gastropod lineages also should be pursued, particularly those that examine the potential adaptive value of shell variation. Predation is an important factor in gastropod evolution, and research examining the value of shell traits in predator defense would be fruitful for better understanding phenotypic plasticity. Experimental studies also are needed to examine how shell traits influence fitness relative to flow and stream size (e.g., rivers vs. lakes or tributaries vs. mainstem) and other abiotic variables. Trade-offs between traits such as shell thickness, size, and ornamentation also are of interest. Such studies have the potential to reveal broad patterns and processes that contribute to evolution of shell traits. Phylogenetic comparative analyses should be a major component of comparative studies because they would reveal broad evolutionary patterns of phenotypic plasticity in freshwater gastropods.

Genomic tools also should be used to advance understanding of phenotypic plasticity. By examining mantle tissue, the tissue responsible for shell growth, RNA-sequencing experiments could identify genes involved in biomineralization and reveal how differential expression contributes to phenotypic plasticity. Coupling common garden experiments with gene expression studies will be fruitful. Genomic tools also could be used in a comparative framework to examine sequence differences of biomineralization genes among closely related species or populations. Such studies would allow researchers to determine whether morphological variation is caused by genetic differences without having to do common garden experiments. Thus, genomic data may make studying phenotypic plasticity in difficult-to-propagate species more cost-effective. Evidence of transgenerational effects of predators on shell morphology in Physella acuta (Goeppner et al. 2020; Tariel et al. 2020) suggests epigenetic studies also are needed.

Finally, future studies must be precise in how they use the term phenotypic plasticity. The term should not be used to describe morphological variation when the underlying cause is unknown. Authors also should be precise when referring to shell traits. Terms such as “robustly shelled” and “fusiform” are subjective and vague; traits such as these require quantification by geometric morphometrics or other methods so that they are repeatable by other researchers.

CONCLUSION

Even in the genomic era, shells will continue to be a focus of malacologists. Given the limited number of lineages that have been studied with genetic or common garden experiments, phenotypic plasticity cannot be invoked based on its documentation in other groups. In other words, phenotypic plasticity should not be a default hypothesis for explaining difference in shell morphology. I argue that a high bar should be set when concluding that morphological variation is a result of phenotypic plasticity, and that bar requires common garden experiments or direct studies of genes that control shell shape. By adopting this standard, researchers can avoid past mistakes and clarify misconceptions about the causes of shell variation in freshwater gastropods.

ACKNOWLEDGMENTS

I thank Nicholas Gladstone (Auburn University) and Ashantye' Williams (U.S. Fish and Wildlife Service) for feedback on this article and help with Figure 1. Discussions with Paul Johnson, Jeff Garner (Alabama Department of Conservation and Natural Resources), and Ellen Strong (National Museum of Natural History) also contributed to my interest in this topic. Paul Johnson and Michael Buntin (Alabama Department of Conservation and Natural Resources) kindly shared Campeloma shells for photographing. Jonathan Armbruster (Auburn University) and Melissa Callahan (Auburn University) provided access to Auburn University Museum of Natural History. Two anonymous reviewers and editor Wendell Haag provided feedback that improved this article. The findings and conclusions in this article are those of the author and do not necessarily represent the views of the U.S. Fish and Wildlife Service.

LITERATURE CITED

1.

Abe, M., and R. Kuroda. 2019. The development of CRISPR for a mollusc establishes the formin Lsdia1 as the long-sought gene for snail dextral/ sinistral coiling. Development 146:dev175976. Google Scholar

2.

Adams, C. C. 1915. The variation and ecological distribution of the snails in the genus Io. Memoirs of the National Academy of Sciences 12:1–92, plates 91–60. Google Scholar

3.

Ahlgren, J., X. Yang, L.-A. Hansson, and C. Brönmark. 2013. Camouflaged or tanned: Plasticity in freshwater snail pigmentation. Biology Letters 9:201330464. Google Scholar

4.

Albarrán-Mélzer, N. C., L. J. R. Ruix, H. A. Benítez, and M. E. Lagos. 2020. Can temperature shift morphological changes of invasive species? A morphometeric approach on the shells of two tropical freshwater snail species. Hydrobiologia 847:151–160. Google Scholar

5.

Asami, T., E. Gittenberger, and G. Falkner. 2008. Whole-body enantiomorphy and maternal inheritance of chiral reversal in the pond snail Lymnaea stagnalis. Journal of Heredity 99:552–557. Google Scholar

6.

Baker, F. C. 1931. Description of a new variety of Valvata lewisi Currier. Nautilus 44:119–121. Google Scholar

7.

Becker, M., S. Zielske, and M. Haase. 2016. Conflict of mitochondrial phylogeny and morphology-based classification in a pair of freshwater gastropods (Caenogastropoda, Truncatelloidea, Tateidae) from New Caledonia. ZooKeys 603:17–32. Google Scholar

8.

Boettger, V. C. R. 1949. Über das Auftreten einer erheblichen Schalenabweichung bei einer Posthornschnecke. Abhandlungen der Braunschweigischen Wissenschaftlichen Gesellschaft Band 1:1–7. Google Scholar

9.

Bourdeau, P. E., R. K. Butlin, C. Brönmark, T. C. Edgell, J. T. Hoverman, and J. Hollander. 2015. What can aquatic gastropods tell us about phenotypic plasticity? A review and meta-analysis. Heredity 115:312–321. Google Scholar

10.

Bradshaw, A. D. 1965. Evolutionary significance of phenotypic plasticity in plants. Advances in Genetics 13:115–155. Google Scholar

11.

Britton, D. K., and R. F. McMahon. 2004. Environmentally and genetically induced shell-shape variation in the freshwater pond snail Physa (Physella) virgata (Gould, 1855). American Malacological Bulletin 19:93–100. Google Scholar

12.

Brönmark, C., T. Lakowitz, and J. Hollander. 2011. Predator-induced morphological plasticity across local populations of a freshwater snail. Journal of Molluscan Studies 6:e21773. Google Scholar

13.

Brönmark, C., T. Lakowitz, P. A. Nilsson, J. Ahlgren, C. Lennartsdotter, and J. Hollander. 2012. Costs of inducible defence along a resource gradient. PLoS ONE 7:e30467. Google Scholar

14.

Brusca, R. C., and G. J. Brusca. 2003. Invertebrates, 2nd ed. Sinauer Associates, Inc., Sunderland, Massachusetts. 936 pp. Google Scholar

15.

Burch, J. B. 1982. North American freshwater snails, identification keys, generic synonymy, supplemental notes, glossary, references, index. Walkerana 1:217–365. Google Scholar

16.

Burch, J. B., and J. Tottenham. 1980. North American freshwater snails, species list, ranges, and illustrations. Walkerana 1:1–215. Google Scholar

17.

Cazenave, K. R., and D. T. Zanatta. 2016. Environmental drivers of shell shape in a freshwater gastropod from small and large lakes. Freshwater Science 35:948–957. Google Scholar

18.

Chang, C.-H., and H. Y. Yan. 2019. Plasticity of opsin gene expression in the adult red shiner (Cyprinella lutrensis) in response to turbid habitats. PLoS ONE 14:e0215376. Google Scholar

19.

Clarke, A. H., Jr. 1973. The freshwater mollusks of the Canadian Interior Basin. Malacologia 13:1–509. Google Scholar

20.

Clewing, C., F. Riedel, T. Wilke, and C. Albrecht. 2015. Ecophenotypic plasticity leads to extraordinary gastropod shells found on the “Roof of the World.” Ecology and Evolution 5:2966–2979. Google Scholar

21.

Crowl, T. A., and A. P. Covich. 1990. Predator-induced life-history shifts in a freshwater snail. Science 247:949–951. Google Scholar

22.

de Villemereuil, P., O. E. Gaggiotti, M. Mouterde, and I. Till-Bottraud. 2016. Common garden experiments in the genomic era: New perspectives and opportunities. Heredity 116:249–254. Google Scholar

23.

DeWitt, T. J. 1998. Costs and limits of phenotypic plasticity: Tests with predator-induced morphology and life history in a freshwater snail. Journal of Evolutionary Biology 11:465–480. Google Scholar

24.

Dillon, R. T. 2011. Robust shell phenotype is a local response to stream size in the genus Pleurocera (Rafinesque, 1818). Malacologia 53:265–277. Google Scholar

25.

Dillon, R. T. 2014. Cryptic phenotypic plasticity in populations of the North American freshwater gastropod, Pleurocera semicarinata. Zoological Studies 53:31. Google Scholar

26.

Dillon, R. T., and J. J. Herman. 2009. Genetics, shell morphology, and life history of the freshwater pulmonate limpets Ferrissia rivularis and Ferressia fragilis. Journal of Freshwater Ecology 24:261–271. Google Scholar

27.

Dillon, R. T., and S. J. Jacquemin. 2015. The heritability of shell morphometrics in the freshwater pulmonate gastropod Physa. PLoS ONE 14:e012962. Google Scholar

28.

Dillon, R. T., S. Jacquemin, and M. Pryon. 2013. Cryptic phenotypic plasticity in populations of the freshwater prosobranch snail, Pleurocera canaliculata. Hydrobiologia 709:117–127. Google Scholar

29.

Dillon, R. T., and J. D. Robinson. 2011. The opposite of speciation: Genetic relationships among the populations of Pleurocera (Gastropoda: Pleuroceridae) in central Georgia. American Malacological Bulletin 29:159–168. Google Scholar

30.

Dunithan, A., S. Jacquemin, and M. Pyron. 2012. Morphology of Elimia livescens (Mollusca: Pleuroceridae) in Indiana, U.S.A. covaries with environmental variation. American Malacological Bulletin 30:127–133. Google Scholar

31.

Dupoy, J., D. Rousseau, G. Dussart, M. V. Liaud, and H. Nassi. 1993. Correspondence analysis of shell morphology in the African freshwater snail Biomphalaria pfeifferi (Kraus 1848) (Pulmonata: Gastropoda). Biological Journal of the Linnean Society 50:329–338. Google Scholar

32.

Estebenet, A. L., and P. R. Martín. 2003. Shell interpopulation variation and its origin in Pomacea canaliculata (Gastropoda: Ampullariidea) from southern Pampas, Argentina. Journal of Molluscan Studies 69:301–310. Google Scholar

33.

Flamarique, I. N., C. L. Cheng, C. Bergstrom, T. E. and Reimchen. 2013. Pronounced heritable variation and limited phenotypic plasticity in visual pigments and opsin expression of threespine stickleback photoreceptors. Journal of Experimental Biology 216:656–667. Google Scholar

34.

Freeman, G., and J. W. Lundelius. 1982. The developmental genetics of dextrality and sinistrality in the gastropod Lymnaea peregra. Roux's Archives of Developmental Biology 191:69–83. Google Scholar

35.

Glaubrecht, M., and F. Köhler. 2004. Radiating in a river: Systematics, molecular genetics and morphological differentiation of viviparous freshwater gastropods endemic to the Kaek River, central Thailand (Cerithioidea, Pachychilidae). Biological Journal of the Linnean Society 82:275–311. Google Scholar

36.

Glöer, P., and V. Pešić. 2015. The morphological plasticity of Theodoxus fluviatilus (Linnaeus, 1758) (Mollusca: Gastropoda: Neritidae). Ecologica Montenegrina 2:88–92. Google Scholar

37.

Goeppner, S. R., M. E. Roberts, L. E. Beaty, and B. Luttbeg. 2020. Freshwater snail responses to fish predation integrate phenotypic plasticity and local adaption. Aquatic Ecology 54:309–322. Google Scholar

38.

Graf, D. L. 2001. The cleansing of the Augean stables, or a lexicon of the nominal species of the Pleuroceridae (Gastropoda: Prosobranchia) of recent North America, north of Mexico. Walkerana 12:1–124. Google Scholar

39.

Guo, J., C. Zhang, J. Zhang, and B. Zhao. 2009. Sex differences in the morphological defenses of an invasive snail: Dimorphism and predator-induced plasticity. Freshwater Science 38:582–590. Google Scholar

40.

Haase, M. 2003. Clinal variation in shell morphology of the freshwater gastropod Potamopyrgus antipodarum along two hill-country streams in New Zealand. Journal of the Royal Society of New Zealand 33:549–560. Google Scholar

41.

Hayes, K. A., R. H. Cowie, S. C. Thiengo, and E. E. Strong. 2012. Comparing apples with apples: Clarifying the identities of two highly invasive Neotropical Ampullariidae (Caenogastropoda). Zoological Journal of the Linnean Society 166:723–753. Google Scholar

42.

Heller, J. 1979. Visual versus non-visual selection of shell color in an Israeli freshwater snail. Oecologia 44:98–104. Google Scholar

43.

Hinchliffe, R. P., C. Tebby, and T. P. Cobb. 2019. First recorded co-occurrence of Valvata lewisi Currier, 1869 and Valvata lewisi ontariensis Baker, 1931 (Gastropoda: Valvatidae) from Alberta, Canada, with notes on morphometric and genetic variability. Canadian Field-Naturalist 133:189–192. Google Scholar

44.

Hirano, T., T. Saito, and S. Chiba. 2015. Phylogeny of freshwater viviparid snails in Japan. Journal of Molluscan Studies 81:435–441. Google Scholar

45.

Hirano, T., T. Saito, Y. Tsunamoto, J. Koseki, B. Ye, V. T. Do, O. Miura, Y. Suyama, and S. Chiba. 2019. Enigmatic incongruence between mtDNA and nDNA revealed by multi-locus phylogenomic analyses in freshwater snails. Scientific Reports 9:6223. Google Scholar

46.

Holomuzki, J. R., and B. J. F. Biggs. 2006. Habitat-specific variation and performance trade-offs in shell armature of New Zealand Mudsnails. Ecology 87:1038–1047. Google Scholar

47.

Hoverman, J. T., J. R. Auld, and R. A. Relyea. 2005. Putting prey back together again: Integrating predator-induced behavior, morphology, and life history. Oecologia 144:481–491. Google Scholar

48.

Hoverman, J. T., R. D. Cothran, and R. A. Relyea. 2014. Generalist versus specialist strategies of plasticity: Snail responses to predators with different foraging modes. Freshwater Biology 59:1101–1112. Google Scholar

49.

Hoverman, J. T., and R. A. Relyea. 2007. How flexible is phenotypic plasticity? Developmental windows for trait induction and reversal. Ecology 88:693–705. Google Scholar

50.

(iBOL) The International Barcode of Life Consortium. 2016. International Barcode of Life Project. Occurrence Dataset  https://doi.org/10.15468/inygc6 accessed via GBIF.org. Available at  https://www.gbif.org/occurrence/2632910498 (accessed November 12, 2020). Google Scholar

51.

Johnson, P. D., A. E. Bogan, K. M. Brown, N. M. Burkhead, J. R. Cordeiro, J. T. Garner, P. D. Hartfield, D. A. W. Lepitzki, G. L. Mackie, E. Pip, T. A. Tarpley, J. S. Tiemann, N. V. Whelan, and E. E. Strong. 2013. Conservation status of freshwater gastropods of Canada and the United States. Fisheries 38:247–282. Google Scholar

52.

Jörger, K. M., I. Söger, Y. Kano, H. Fukuda, T. Knebelsberger, and M. Schrödl. 2010. On the origin of Acochlidia and other enigmatic euthyneuran gastropods, with implications for the systematics of Heterobranchia. BMC Evolutionary Biology 10:323. Google Scholar

53.

Kistner, E. J., and M. F. Dybdahl. 2013. Adaptive responses and invasion: The role of plasticity and evolution in snail shell morphology. Ecology and Evolution 3:424–436. Google Scholar

54.

Kistner, E. J., and M. F. Dybdahl. 2014. Parallel variation among populations in the shell morphology between sympatric native and invasive snails. Biological Invasions 16:2615–2626. Google Scholar

55.

Koch, E. L., H. E. Morales, J. Larsson, A. M. Westram, R. Faria, A. R. Lemmon, E. M. Lemmon, K. Johannesson, and R. K. Butlin. 2021. Genetic variation for adaptive traits is associated with polymorphic inversions in Littorina saxatilis. Evolution Letters 5:196–213. Google Scholar

56.

Kocot, K. M., F. Aguilera, C. McDougall, D. J. Jackson, and J. H. Degnan. 2016. Sea shell diversity and rapidly evolving secretomes: Insights into the evolution of biomineralization. Frontiers in Zoology 13:23. Google Scholar

57.

Krist, A. C. 2002. Crayfish induce a defensive shell shape in a freshwater snail. Invertebrate Biology 121:235–242. Google Scholar

58.

Lakowitz, T., C. Brönmark, and P. Nyström. 2008. Tuning in to multiple predators: Conflicting demands for shell morphology in a freshwater snail. Freshwater Biology 53:2184–2191. Google Scholar

59.

Lam, P. K. S., and P. Calow. 1988. Differences in the shell shape of Lymnaea peregra (Müller) (Gastropoda: Pulmonata) from lotic and lentic habitats; environmental or genetic variance? Journal of Molluscan Studies 54:197–207. Google Scholar

60.

Langerhans, R. B., and T. J. DeWitt. 2002. Plasticity constrained: Overgeneralized induction cues cause maladaptive phenotypes. Evolutionary Ecology Research 4:857–870. Google Scholar

61.

Langeveld B., J. Creuwels, F. Slieker, and H. van der Es. 2020. Natural History Museum Rotterdam - Specimens. Version 1.17. Natural History Museum Rotterdam. Occurrence dataset  https://doi.org/10.15468/kwqaay. Available at  https://www.gbif.org/occurrence/2570084645 (accessed November 3, 2020). Google Scholar

62.

Levri, E. P., J. Dillard, and T. Martin. 2005. Trematode infection correlates with shell shape and defence morphology in a freshwater snail. Parasitology 130:699–708. Google Scholar

63.

Ma, X.-F., D. Hall, K. R. St. Onge, S. Jansson, and P. K. Ingvarsson. 2010. Genetic differentiation, clinal variation and phenotypic associations with growth cessation across the Populus tremula photoperiodic pathway. Genetics 186:1033–1044. Google Scholar

64.

Machado, H. E., A. O., Bergland, K. R. O'Brien, E. L. Behrman, P. S. Schmidt, and D. A. Petrov. 2016. Comparative population genomics of latitudinal variation in Drosophila simulans and Drosophila melanogaster. Molecular Ecology 25:723–740. Google Scholar

65.

Margules, C. R., and R. L. Pressey. 2000. Systematic conservation planning. Nature 405:243–253. Google Scholar

66.

Marković, V., V. Vujić, M. Ilić, J. Tomović, V. Nikolić, and Karan-Žnidaršić. 2019. Operculum shape variation in Theodoxus Montfort, 1810 (Gastropoda: Neritidae). Zootaxa 4560:563–575. Google Scholar

67.

McCairns, R. J. S., and L. Bernatchez. 2010. Adaptive divergence between freshwater and marine sticklebacks: Insights into the role of phenotypic plasticity from an integrated analysis of candidate gene expression. Evolution 64:1029–1047. Google Scholar

68.

McKechnie, S. W., M. J. Blacket, S. V. Song, L. Rako, X. Carroll, T. K. Johnson, L. T. Jensen, S. F. Lee, C. W. Wee, and A. A. Hoffmann. 2010. A clinally varying promoter polymorphism associated with adaptive variation in wing size in Drosophila. Molecular Ecology 19:775–784. Google Scholar

69.

Minton, R. L., K. C. Hart, R. Fiorillo, and C. Brown. 2018. Correlates of snail shell variation along a unidirectional freshwater gradient in Lithasia geniculata (Haldeman, 1840) (Caenogastropoda: Pleuroceridae) from the Duck River, Tennessee, USA. Folia Malacologica 26:95–102. Google Scholar

70.

Minton, R. L., E. M. Lewis, B. Netherland, and D. M. Hayes. 2011. Large differences over small distances: Plasticity in the shell of Elimia potosiensis (Gastropoda: Pleuroceridae). International Journal of Biology 3:23–32. Google Scholar

71.

Minton, R. L., A. P. Norwood, and D. M. Hayes. 2008. Quantifying phenotypic gradients in freshwater snails: A case study in Lithasia (Gastropoda: Pleuroceridae). Hydrobiologia 605:173–182. Google Scholar

72.

Minton, R. L., S. A. Reese, K. Swanger, K. E. Perez, and D. M. Hayes. 2007. Changes in shell morphology of Elimia comalensis (Gastropoda: Pleuroceridae) from the Edwards Plateau, Texas. Southwestern Naturalist 52:475–481. Google Scholar

73.

MolluscaBase, editors. 2021. MolluscaBase. Available at  http://www.molluscabase.org (accessed March 1, 2021). Google Scholar

74.

Negovetic, S., and J. Jokela. 2001. Life-history variation, phenotypic plasticity, and subpopulation structure in a freshwater snail. Ecology 82:2805–2815. Google Scholar

75.

Ó Foighil, D., J. Li, T. Lee, P. D. Johnson, R. Evans, and J. B. Burch. 2011. Conservation genetics of a critically endangered limpet genus and rediscovery of an extinct species. PLoS ONE 6:e204496. Google Scholar

76.

Paaby, A. B., M. J. Blacket, A. A. Hoffmann, and P. S. Schmidt. 2010. Identification of a candidate adaptive polymorphism for Drosophila life history by parallel independent clines on two continents. Molecular Ecology 19:760–774. Google Scholar

77.

Palmer, A. R. 1979. Fish predation and the evolution of gastropod shell sculpture: Experimental and geographic evidence. Evolution 33:697–713. Google Scholar

78.

Prezant, R. S., E. J. Chapman, and A. McDougall. 2006. In utero predator-induced responses in the viviparid snail Bellayma chinensis. Canadian Journal of Zoology 84:600–608. Google Scholar

79.

Richards, C. S. 1971. Biomphalaria glabrata genetics: Spire formation as a sublethal character. Journal of Invertebrate Pathology 17:53–58. Google Scholar

80.

Ross, B., S. J. Jacquemin, and M. Pyron. 2014. Does variation in morphology correspond with variation in habitat use in freshwater gastropods? Hydrobiologia 736:179–188. Google Scholar

81.

Sands, A. F., P. Glöer, M. E. Gürlek, C. Albrecht, and T. A. Neubauer. 2020. A revision of the extant species of Theodoxus (Gastropoda, Neritidae) in Asia, with the description of three new species. Zoosystematics and Evolution 96:25–66. Google Scholar

82.

Song, X., Z. Liu, L. Wang, and L. Song. 2019. Recent advances of shell matrix proteins and cellular orchestration in marine molluscan shell biomineralization. Frontiers in Marine Science 6:41. Google Scholar

83.

Statzner, B. 2008. How views about flow adaptations of benthic stream invertebrates changed over the last century. International Review of Hydrobiology 93:593–605. Google Scholar

84.

Strong, E. E., O. Gargominy, W. Ponder, F. and P. Bouchet. 2008. Global diversity of gastropods (Gastropoda; Mollusca) in freshwater. Hydrobiologia 595:149–166. Google Scholar

85.

Strong, E. E., and N. V. Whelan. 2019. Assessing the diversity of Western North American Juga (Semisulcospiridae, Gastropoda). Molecular Phylogenetics and Evolution 136:87–103. Google Scholar

86.

Tamburi, N. E., M. E. Seuffert, and P. R. Martín. 2018. Temperature-induced plasticity in morphology and relative shell weight in the invasive apple snail Pomacea canaliculata. Journal of Thermal Biology 74:331–336. Google Scholar

87.

Tariel, J., S. Plénet, and E. Luquet. 2020. Transgenerational plasticity of inducible defences: Combined effects of grand-parental, parental and current environments. Ecology and Evolution 10:2367–2376. Google Scholar

88.

Thompson, F. G. 1977. The hydrobiid snail genus Marstonia. Bulletin of the Florida State Museum, Biological Sciences 21:113–158. Google Scholar

89.

Tiemann, J. S., and K. S. Cummings. 2008. Sinistral Campeloma decisum (Say, 1817) (Gastropoda: Viviparidae) from the Fox River, Illinois. Nautilus 122:259–260. Google Scholar

90.

Ueda, K. 2020. iNaturalist Research-grade Observations. iNaturalist.org. Occurrence dataset  https://doi.org/10.15468/ab3s5x accessed via GBIF.org. Available at  https://www.gbif.org/occurrence/1802694769 (assessed November 12, 2020). Google Scholar

91.

Urabe, M. 1998. Contributions of genetic and environmental factors to shell shape variation in the lotic snail Semisulcospira reiniana (Prosobranchia: Pleuroceridae). Journal of Molluscan Studies 64:329–343. Google Scholar

92.

Urabe, M. 2000. Phenotypic modulation by the substratum of shell structure in Semisulcospira reiniana (Prosobranchia: Pleuroceridae). Journal of Molluscan Studies 66:53–59. Google Scholar

93.

Van Bocxlaer, B., C. Clewing, J.-P.M. Etimosundja, A. Kankonda, O. W. Ndeo, and C. Albrecht. 2015. Recurrent camouflaged invasions and dispersal of an Asian freshwater gastropod in tropical Africa. BMC Evolutionary Biology 15:33. Google Scholar

94.

Vergara, D., J. A. Fuentes, K. S. Stoy, and C. M. Lively. 2016. Evaluating shell variation across different populations of a freshwater snail. Molluscan Research 37:120–132. Google Scholar

95.

Verhaegen, G., H. Herzog, K. Korsch, G. Kerth, M. Brede, and M. Haase. 2019. Testing the adaptive value of gastropod shell morphology to flow: A multidisciplinary approach based on morphometrics, computational fluid dynamics and a flow tank experiment. Zoological Letters 5:5. Google Scholar

96.

Verhaegen, G., K. E. McElroy, L. Bankers, M. Neiman, and M. Haase. 2018a. Adaptive phenotypic plasticity in a clonal invader. Ecology and Evolution 8:4465–4483. Google Scholar

97.

Verhaegen, G., M. Neiman, and M. Haase. 2018b. Ecomorphology of a generalist freshwater gastropod: Complex relations of shell morphology, habitat, and fecundity. Organisms Diversity & Evolution 18:425–441. Google Scholar

98.

Vermeij, G. J. 1974. Marine faunal dominance and molluscan shell form. Evolution 28:656–664. Google Scholar

99.

Vermeij, G. J. 1982. Unsuccessful predation and evolution. American Naturalist 120:701–720. Google Scholar

100.

Vermeij, G. J. 2015. Gastropod skeletal defences: Land, freshwater, and sea compared. Vita Malacologica 13:1–25. Google Scholar

101.

Vermeij, G. J., and A. P. Covich. 1978. Coevolution of freshwater gastropods and their predators. American Naturalist 112:833–843. Google Scholar

102.

Walther, A. C., J. B. Burch, and D. Ó Foighil. 2010. Molecular phylogenetic revision of the freshwater limpet genus Ferrissia (Planorbidae: Ancylinae) in North America yields two species: Ferrissia (Ferrissia) rivularis and Ferrissia (Kincaidilla) fragilis. Malacologia 53:25–45. Google Scholar

103.

West-Eberhard, M. J. 1989. Phenotypic plasticity and the origins of diversity. Annual Review of Ecology and Systematics 20:249–278. Google Scholar

104.

Whelan, N. V., M. P. Galaska, B. N. Sipley, J. M. Weber, P. D. Johnson, K. M. Halanych, and B. S. Helms. 2019. Riverscape genetic variation, migration patterns, and morphological variation of the threatened Round Rocksnail, Leptoxis ampla. Molecular Ecology 28:1593–1610. Google Scholar

105.

Whelan, N. V., P. D. Johnson, and P. M. Harris. 2012. Presence or absence of carinae in closely related populations of Leptoxis ampla (Anthony, 1855) (Gastropoda: Cerithioidea: Pleuroceridae) is not the result of ecophenotypic plasticity. Journal of Molluscan Studies 78:231–233. Google Scholar

106.

Whelan, N. V., P. D. Johnson, and P. M. Harris. 2015. Life-history traits and shell morphology in the genus Leptoxis Rafinesque, 1819 (Gastropoda: Cerithioidea: Pleuroceridae). Journal of Molluscan Studies 81:85–95. Google Scholar

107.

Wullschleger, E. B., and J. Jokela. 2002. Morphological plasticity and divergence in life-history traits between two closely related freshwater snails, Lymnaea ovata and Lymnaea peregra. Journal of Molluscan Studies 68:1–5. Google Scholar

108.

Zapata, F., N. G. Wilson, M. Howison, S. C. S. Andrade, K. M. Jörger, M. Schrödl, F. E. Goetz, G. Giribet, and C. W. Dunn. 2014. Phylogenomic analyses of deep gastropod relationships reject Orthogastropoda. Proceedings of the Royal Society B 281:20141739. Google Scholar

109.

Zettler, M. L., J. Frankowski, R. Bochert, and M. Röhner. 2004. Morphological and ecological features of Theodoxus fluviatilis (Linnaeus, 1758) from Baltic brackish water and German freshwater populations. Journal of Conchology 38:305–316. Google Scholar

110.

Zuykov, M., M. Vinarski, E. Pelletier, S. Demers, and D. A. T. Harper. 2012. Shell malformations in seven species of pond snail (Gastropoda, Lymnaeidae): Analysis of large museum collections. Zoosystematics and Evolution 88:365–368. Google Scholar
© Freshwater Mollusk Conservation Society 2021
Nathan V. Whelan "Phenotypic Plasticity and the Endless Forms of Freshwater Gastropod Shells," Freshwater Mollusk Biology and Conservation 24(2), 87-103, (27 October 2021). https://doi.org/10.31931/fmbc-d-20-00015
Published: 27 October 2021
JOURNAL ARTICLE
17 PAGES


Share
SHARE
KEYWORDS
biomineralization
Common garden
ecomorph
morphology
review
RIGHTS & PERMISSIONS
Get copyright permission
Back to Top