Acta Herpetologica 16(2): 89-98, 2021 ISSN 1827-9635 (print) © Firenze University Press ISSN 1827-9643 (online) www.fupress.com/ah DOI: 10.36253/a_h-10402 So close so different: what makes the difference? Dario Ottonello1,7,*, Stefania D’Angelo2, Fabrizio Oneto3,6, Stefano Malavasi1, Marco Alberto Luca Zuffi4, Filippo Spadola5 1 Department of Environmental Sciences, Informatics and Statistics, Cà Foscari University of Venice, Via Torino 155, 30172 Venezia Mestre, Italy 2 WWF Italia, via Po 25/c, 00195 Roma, Italy 3 Centro Studi Bionaturalistici srl, Corso Europa 26, 16132 Genova, Italy 4 Museum of Natural History, University of Pisa, via Roma 79, 56011 Calci (Pisa), Italy 5 Department of Veterinary Sciences, University of Messina, Polo Universitario SS. Annunziata, 98128 Messina, Italy 6 Università di Genova, Corso Europa 26, 16132 Genova, Italy 7 ARPAL Ligurian Environmental Protection Agency, Via Bombrini 8, 16149 Genova, Italy *Corresponding author. E-mail: dario.ottonello@arpal.liguria.it Submitted on: 2021, 31st January; Revised on: 2021, 5th May; Accepted on: 2021, 22nd May Editor: Emilio Sperone Abstract. The introduction of alien fish species in wetland ecosystems could have a great impact on freshwater com- munities and ecological processes. Despite fish introduction has been noticed as one of the principal cause of fresh- water extinctions, ecosystem processes alteration, and change in aquatic community assemblage, very few data about impact on freshwater reptiles are available. As study model we used two neighbour sub-populations of the endangered Sicilian pond turtle, Emys trinacris, inhabiting two small, close each other and very similar lakes, except for the pres- ence of allocthonous fish, Cyprinus carpio and Gambusia hoolbroki in one of the two. The multi-year study allowed highlighting significant differences in abundance, growth and reproductive output between the two freshwater tur- tle sub-populations, suggesting their influence on phenotypic plasticity of the studied population. These results are discussed in the light of previous evidence about the impact of these alien species on abundance and assemblage of the invertebrate community with an evident impact on niche width, diet composition and therefore energy intake by Emys trinacris. These data may provide important information to address management strategies and conservation actions of small wetland areas inhabited by pond turtles, pointing out a threats never highlighted up to now. Keywords. Emys trinacris, phenotypic plasticity, Cyprinus carpio, Gambusia hoolbroki, alien fishes impact. INTRODUCTION Phenotypic plasticity is an evolutionary adaptation to environmental variation often used to explain the intraspecific difference observed within various taxa, that could be influenced by local variation in abiotic and biotic factors associated with habitat type (Lubcke and Wilson, 2007). Nowadays, the introduction of alien spe- cies is one of the main stressor of freshwater ecosystem biodiversity (Genovesi, 2007), and it could have a great impact on freshwater communities causing cascading impacts on food webs and complex interactions among species (Ricciardi and MacIsaac, 2011). In the last dec- ades, many species of fishes have been deliberately intro- duced worldwide to provide food or sport leisure, but also released from aquaria, bait buckets, and water gar- dens, as contaminants of fish intended for stocking, or in ballast water (Strayer, 2010). Despite fish introduction has been noticed as one of the principal cause of fresh- water extinctions (Dextrase and Mandrak, 2006), eco- system processes alteration (Pitcher and Hart, 1995) and change in aquatic community assemblage (Parkos et al., 90 D. Ottonello et alii 2003), very few data about impact on freshwater reptiles are available. Within this group, freshwater turtles are known to vary in different natural history traits among conspecific populations both over broad geographic area (Lovich et al., 1998; Joos et al., 2017) as well as among adjacent sites (Tucker at al., 1998). They usually follow a growth pat- tern that involves rapid growth from hatching to sexual maturity, followed by little or no growth once matu- rity is attained (e.g., Wilbur, 1975; Bury, 1979). Growth can be influenced both by different ecological factors, such as hatching size, food availability and habitat suit- ability (Mahmoud, 1969; Bury, 1979). Moreover, dif- ferent growth patterns can lead to the same size (Bury, 1979; Andrews, 1982) or to different size at the maturity (Stearns and Koella, 1986). These differences can have also a direct impact on reproductive output in a taxon where clutch size often increases with maternal body size (Zuffi et al., 2004). In particular, Ottonello et al. (2017a) showed how the presence of two alien fishes, Cyprinus carpio Linnaeus, 1758 and Gambusia holbrooki Girard, 1859, can alter the abundance and the assemblage of the invertebrate com- munity with a considerable impact on niche width and diet composition of an endangered turtle. Local food availability and quality may indeed play a key role to regulate feeding strategy with consequences on growth, reproductive output and population density (Dunham and Gibbons, 1990; Parmenter and Avery, 1990). For these reasons we have aimed at investigating if the pres- ence of alien fishes can have an impact at local scale on a population of an endangered turtle using as case study two neighbour wild sub-populations under similar cli- matic and environmental conditions. As model species we selected Emys trinacris Fritz et al., 2005, the only native freshwater turtle of Sicily, a large island off the coast of Italy. The Sicilian pond turtle lives in wetlands and slow- moving water bodies (e.g., lagoons, deltas, inland waters and mountain lakes) with soft bottoms and abundant aquatic vegetation, especially on the banks, from the sea level up to 1036 m a.s.l. (Marrone et al., 2016). Howev- er, the presence of the species at about 1250 m a.s.l. was recently observed (F. Marrone and R. Scardino, pers. obs.). In view of the low number of sicilian indigenous fish (Zerunian, 2004) and the absence of specialized aquatic vertebrate predators (Aa. Vv., 2008), it is likely to assume that Emys trinacris is one of the top aquatic predators in many of these environments in Sicily, with an opportunistic and generalist pattern oriented mainly towards aquatic invertebrates (Ottonello et al., 2017a). Because of the introduction of non-native fish spe- cies, that are now the most represented non-indigenous taxon occurring in Sicily (Marrone and Naselli-Flores, 2015), new dynamics that can significantly alter and threaten the structure of the native biota have been established (Naselli-Flores and Barone, 2012) and top predators are likely to be valuable indicators of eco- system health (Landres et al., 1988). Although some data and experimental studies highlighted the poorly competitive abilities of the genus Emys against some alien species, like Trachemys scripta (Cadi and Joly, 2003, 2004) and Micropterus salmoides Lacepède, 1802 (Lacomba and Sancho, 2004; Ayres and Cordero, 2007), robust evidence of interactions in the wild is still lack- ing (but see Polo-Cavia et al., 2010; Lambert et al., 2019). Moreover, Rakausas et al. (2016), studying the predator-prey interactions between a recent invader in Lituania, the Chinese sleeper (Perccottus glenii Dybows- ki, 1877) and the European pond turtle stated that this fish does not directly contribute to the decline of E. orbicularis because hatchlings turtles are resistant to P. glenii predation and, adults of E. orbicularis consumed juvenile P. glenii, but no data about indirect impacts (e.g., trophic resource competition) have been evaluated. Therefore, we assumed that Sicilian pond turtles in a habitat without alien fishes would have access to wider food availability than would individuals in a habitat with introduced alien fishes. We therefore hypothesized that this would affect their rates of energy intake and we predicted that turtles in a fish-less habitat would: (1) exhibit different patterns of growth, (2) have higher annual reproductive output, and (3) have higher abun- dance. To test this hypothesis in the wild, we compared the parameters of two Emys trinacris sub-populations inhabiting a fish-inhabited and a fish-less lakes during a multi-year study. The evidence of the negative impact of the presence of introduced fish fauna can provide additional information to further understand the effect of alien species on native fauna as well as promote ade- quate management plans. MATERIALS AND METHODS Study area The Nature Reserve of the “Lake Preola and Gorghi Ton- di” is a protected area of south-western Sicily, established in 1998 and currently managed by the Italian Association for the World Wildlife Fund. The Nature Reserve (medium point at 37°36’36.78”N 12°39’8.19”E) has a surface of 335 hectares and is surrounded by a homogeneous agricultural landscape (vine- yards and olive groves). The Nature Reserve protects four dis- tinct wetlands (Pantano Murana, Lake Preola, Gorghi Alto- Medio and Gorgo Basso), originating in a karstic depression. The basins do not have tributaries and the groundwater table is 91So close so different: what makes the difference? located in the calcarenites and is fed by local meteoric recharge (Cusimano et al., 2006). Lake Preola is the widest water body of the area, with a surface of 33 ha approximately, filled with a thin layer of water occasionally deeper than two meters. The ‘‘Gorghi’’ are lake environments in a mature euthrophic status, with an average surface area of approximately 3 ha for the lake Gorgo Basso (altitude: 6 m a.s.l) and 5 ha for the lake Gorghi Alto-Medio (altitude: 3 m a.s.l.), and a maximum depth of 12 m. They are set on sink-holes and they are therefore immedi- ately deep and surrounded by riparian helophytes [Phragmites australis (Cav.) Trin. ex Steud., Typha latifolia L. and Cladium mariscus (L.) Pohl], with some peripherals areas with a maxi- mum depth of about 2 m. Comparison of water chemistry and benthic samples showed no significant difference between the two lakes and both showed high concentration of lead and arse- nic (Bellante et al., 2015; Arpa Sicilia, 2016). The Gorghi Alto-Medio is situated only 200 m away from the Gorgo Basso, but it is separated by an asphalt road and with a slight difference in elevation. Despite their proximity the two sites can be considered inhabited by two distinct sub-popu- lations of Emys trinacris. Indeed, although no genetic data are available, capture-recapture data showed a very low migration rate between these lakes confirming what observed over the last fourteen years (D’Angelo, unpubl. data), when for instance only five individuals migrated between the two sites, three from the Gorgo Basso to the Gorghi Alto-Medio and two conversely. Different non-indigenous species are reported for this ter- ritory, like the invasive Red swamp crayfish Procambarus clarkii Girard, 1852 (D’Angelo and Lo Valvo, 2003), and Eastern mos- quitofish Gambusia holbrooki and Wild common carp Cyprinus carpio (Ottonello et al., 2017a). Red swamp crayfish is wide- spread in all the basins without significant difference in abun- dance and distribution (Maccarone et al., 2016), while fishes are limited only to the Gorghi Alto-Medio (Ottonello et al., 2017a). In the latter, fish presence affects the food web and the assemblage and abundance of the potential preys of Emys trina- cris (Table 1; Ottonello et al. 2017a), in accordance with avail- able results on the negative impacts that allocthonous species produce on local invertebrates communities (Cyprinus carpio: Parkos et al., 2003; as well as Gambusia holbrooki: Pyke, 2008). Sampling Individuals were captured by six fyke nets and 30 baited funnel traps in Gorgo Basso and Gorghi Alto-Medio located 50 m apart of each other. Fieldwork was carried out from 2014 to 2016 with 10 sampling occasions during the active season (March-October). Date of capture, sex, age (adult/juvenile), straight carapace length (SCL, sliding callipers to the nearest 0.1 mm), width (CW), height (CH) and body mass (BM, digi- tal balance ± 1 g) were recorded on each capture according to a standardized procedure, and only individuals with evident sexual characters were considered as adults (Zuffi and Gari- boldi, 1995). All captured turtles were individually marked by unique notch on their carapace (Servan et al., 1986) as a part of a long-term study on the ecology of the species (Ottonello et al., 2017b). Abundance The abundance of turtles in each site was measured indi- rectly by means of the Catch Per Unit Effort (CPUE) method. CPUE was calculated for each wetland and sampling occasion with effort measured as trap-day, and the number of traps on a site multiplied by the number of days set. Because animals were released after each capture we considered, within the same sam- pling occasion, only the first event for each individual to avoid pseudoreplication (Hurlbert, 1984). We used only data collected in 2015 and 2016 because the sampling was not carried out in Gorghi Alto-Medio in 2014. This method, usually applied in fisheries management (Maunder et al., 2006), can be used also for chelonians to infer the relative abundance and compare dif- ferent groups (Selman et al., 2014). Size and growth Data and sites differences (Gorgo Basso vs Gorghi Alto- Medio) in size and body mass of turtles were firstly checked for normality with Shapiro-Wilk normality test and then analysed using a Student’s t test. Females and males were analysed sepa- rately due to their difference in size and mass (Ottonello et al., 2017b). Recaptured animals were excluded from the analysis to avoid pseudoreplication. Population structure was analysed using a graphical approach by dividing SCL data in size classes of 10 mm. Individual variation in growth was assessed by the Table 1. Comparative descriptive data of the two studied sites. Gorgo Basso Gorghi Alto- Medio Surface (ha) 3.1 4.9 Open deep water (ha) 2.1 4.4 Shallow water dominated by helophytes (ha) 1.0 0.5 Maximum Depth (m) 11 12 Fish Absent Gambusia holbroki Cyprinus carpio Invertebrate alien species Procambarus clarckii Procambarus clarckii Temperature (°C)1 27.9 26.6 Dissolved Oxygen (%sat)1 66.4 77.5 Chlorophyll alfa (μg/L)1 0.11 1.36 Total phosphorus (μg/L)1 6.9 13.3 Total nitrate (mg/L)1 2.21 0.87 N° of invetebrate sampled2 346 103 N° of invertebrate taxa sampled 2 9 6 Food Niche Breadth of E. trinacris2 1.36 0.97 Average number of prey per faecal sample of E. trinacris2 15 1 1 Arpa Sicilia 2016; 2 Ottonello et al. 2017a. 92 D. Ottonello et alii mean of the Relative Growth Rate (RGR) equation modified from Brody (1945) by Cox et al. (1991): 𝑅𝑅𝑅𝑅𝑅𝑅 = 𝑙𝑙𝑙𝑙𝑆𝑆𝑆𝑆𝑆𝑆! − ln𝑆𝑆𝑆𝑆𝑆𝑆" 𝑡𝑡! − 𝑡𝑡" where SCL1 represents straight carapace length at first capture, SCL2 represents straight carapace length at last recapture, and t2 – t1 represents the time interval in months between the two measurements. Juveniles at first and last capture were used in both groups (males and females), based on the assumption that early growth trajectories of the sexes do not differ (Dunham and Gibbons, 1990). Moreover, we considered only growing individuals (class 1, 2, 3) excluding aged (class 4) animals (see Olivier, 2002 for class definition), to avoid the possible bias due the presence or dominance of no or slow growing old animals in the two areas (Bury, 1979). RGR analyses assume that growth is exponential, but this assumption is rarely valid (Cox et al., 1991). However, the regression between RGR and SCL1 gives an estimate of growth rate at a specific carapace length, allowing direct comparison of growth rates both among individuals with different carapace lengths and among individuals with similar carapace lengths (Cox et al. 1991). We tested the effect of the site (Gorgo Bas- so vs Gorghi Alto-Medio) on the RGR using the Analysis of covariance (ANCOVA), separately for males and females. RGR has been identified as the dependent variable, SCL1 as the inde- pendent variable and the site as the categorical variable. The growth has been modelled for each site (Gorgo Bas- so and Gorghi Alto-Medio) using the von Bertalanffy Growth Model (VBGM), as previously used to estimate size-age relation in different species of chelonians (Lovich et al., 1990; Litzgus and Brooks, 1998; Çiçek et al., 2016). The general von Berta- lanffy equation is: SCL = a ∙ (1-be-kt) where SCL is straight carapace length, a is asymptotic cara- pace length, b is a parameter related to length at hatching, e is the base of the natural logarithm, k is the intrinsic growth fac- tor, and t is age in years. Since this is a non-linear model for the parameter estimation, non-linear statistic was used, by the estimation of parameters and their confidence interval (95%) with non-linear least-square regression method using the FSA package (Ogle, 2012) in R. The function “predict” was used to estimate the age at sexual maturity assuming the SCL of the smallest gravid female and of the smallest male showing sec- ondary sex characteristics for each site. The age of individuals was estimated with the count of plastral growth rings (Keller et al., 1998), a reliable method for young European pond turtles as showed by Çiçek et al. (2016) in a comparative study with skeletochronology. The maximum number of growth rings that was possible to count was nine, after which the plastron abra- sion does not allow a reliable estimate of the age of individuals. Because no wild new born of Sicilian pond turtle were captured, we used data of hatchlings from a local breeding centre – where eggs are incubated naturally – for the estimate of parameter b. Juveniles were used in both groups (males and females), based on the assumption that early growth trajectories of the sexes do not differ (Dunham and Gibbons, 1990). Reproductive biology The presence of oviductal eggs was verified by palpation of the inguinal region (Zuffi et al., 1999) directly at the capture site. Gravid females were transferred temporarily to the veteri- nary clinic of the University of Messina for X-ray examinations. In our experiment the exposure was made at 50 mA, 50 kV, 0.1 min, similar to that used by Zuffi et al. (1999) for Emys orbicu- laris (Linnaeus, 1758). As these latter authors, we presumed the absence of significant injuries at the gonadal level in our sam- pled females and in hatchlings (Hinton et al., 1997), although we recommended suspending this type of analysis within this population in next years as a precautionary measure. All indi- viduals were released at the point of capture after the end of the procedures. The size of the eggs has been recorded directly from the radiographic images. Due to the possibility that the eggs were not placed parallel on the radiographic plane we considered only the minimum diameter (Dmin, ± 0.1 mm) in subsequent statistical analyses. The non-parametric Mann-Whitney U test was used to check any difference in the number of eggs between the two sites (Gorgo Basso vs Gorghi Alto-Medio). We tested the effect of the site on the number of eggs using the Analysis of covariance (ANCOVA) to avoid the “size effect”. The num- ber of eggs has been identified as the dependent variable, SCL as the independent covariate and the site as the categorical vari- able. The data collected in different years were treated unique- ly to increase the accuracy of the statistical sample since a no significant inter-annual variability is known for the congeneric Emys orbicularis (Zuffi and Foschi, 2015). Only those females with oviductal eggs were considered certainly sexually mature. The reproductive phenology was considered as a whole, merg- ing data of the two groups. All above analyses were carried out with R 3.2.5 (R Devel- opment Core Team, 2015). RESULTS Abundance A total of 1405 captures of 579 different turtles (493 in the Gorgo Basso, 86 in the Gorghi Alto-Medio) were made in 2015 and 2016. A strong site fidelity was con- firmed as only two individuals were captured in both sites, and this happened only once during all sampling occasions. The sub-population of the Gorgo Basso was more abundant and reached a significant higher CPUE than the sub-population of the Gorghi Alto-Medio (Mann-Whitney U test = 42, N1 = N2 = 6, P < 0.01), respectively with an average of 3.02 and 0.80 turtles/ trap/day. 93So close so different: what makes the difference? Size and growth The sub-population of the Gorgo Basso was char- acterized by a dominance of turtles (72%) with an SCL between 110 and 129.9 mm while the sub-population of Gorghi Alto-Medio is characterized by a dominance of turtles (76%) with an SCL between 100 and 119.9 mm (Fig. 1). Females and males of Gorgo Basso were heavier (t-testfemales= 8.73, df = 45.17, P < 0.001; t-testmales= -9.60, df = 68.20, P < 0.001) and bigger than individuals of Gorghi Alto-Medio, both in terms of carapace length (t-testfemales= 9.61, df= 41.89, P < 0.001; t-testmales= 10.09, df= 66.31, P < 0.001), width (t-testfemales= 5.50, df= 35.37, P < 0.001; t-testmales= 7.67, df= 77.63, P < 0.001), and height (t-testfemales= 4.22, df= 28.13, P < 0.001; t-testmales= 6.48, df= 65.89, P < 0.001) (Table 2). We used data on 79 males (61 from Gorgo Basso and 18 from Gorghi Alto-Medio) and 41 females (27 from Gorgo Basso and 14 from Gorghi Alto-Medio) to estimate relative growth rate (RGR). Individual varia- tion in growth rate was high (range 0.0 – 0.0176), but with no significant difference between the sexes (t-test = -0.59, P = 0.5564). Considering independently the two sites, the models showed for both sexes (models 1 and 3, Table 3) that the interaction between the inde- pendent variable (SCL) and the categorical variable (site) was not significant, indicating that the slopes of Fig. 1. Structure of sub-populations of Emys trinacris inhabiting the Gorgo Basso (a) and the Gorghi Alto-Medio (b). Table 2. Mean values of biometric measurements for Emys trinacris in the two studied sites. SCL = straight carapace length; CW = cara- pace width; CH = carapace height; BM = body mass; n = number of individuals; S.E. = Standard Error. Biometric measurement GT Basso GT Alto-Medio SCL (mm) Adult females Mean 131.5(n =144) 116.5 (n = 21) S.E. 0.7 0,05 Min 110.0 4,42 Max 150.9 5,5 SCL (mm) Adult males Mean 120.1 (n = 291) 111.1 (n = 45) S.E. 0.4 0.9 Min 101.3 99.7 Max 141.1 124.9 CW (mm) Adult females Mean 101.7 (n = 116) 93.7 (n = 21) S.E. 0.8 1.3 Min 77.6 84.0 Max 121.3 102.0 CW (mm) Adult males Mean 94.0 (n = 282) 87.6 (n = 45) S.E. 0.4 0.7 Min 69.4 71.4 Max 112.0 101.5 PH (mm) Adult females Mean 50.9 (n = 124) 47.0 (n = 21) S.E. 0.4 0.8 Min 38.0 40.2 Max 62.6 55.0 PH (mm) Adult males Mean 42.6 (n = 271) 39.9 (n = 45) S.E. 0.2 0.4 Min 25.4 34.6 Max 53.5 46.3 BM (g) Adult females Mean 401.1 (n = 144) 294.7 (n = 21) S.E. 7.7 12.8 Min 217.0 221 Max 658.0 422 BM (g) Adult males Mean 281.2 (n = 290) 223.2 (n = 45) S.E. 3.4 5.7 Min 143.0 154.0 Max 453.0 310.0 94 D. Ottonello et alii the regressions were homogeneous. Therefore, in both sites, the growth rate is reduced progressively as the individual grows. The other models (models 2 and 4, Table 3) showed that the categorical variable (site) has a significant effect on the dependent variable (RGR), due to the significant difference of the intercept regres- sion lines between the two sites. These models showed that individuals, despite having a growth rates that is inversely related to size, display a different growth rate: turtles from the Gorgo Basso are bigger than those of Gorghi Alto-Medio. The von Bertalanffy growth mod- els showed that the Sicilian pond turtle of Lake Preola and Gorghi Tondi Nature Reserve appeared to mature sexually at approximately six years for males of Gorgo Basso (SCLmin = 102.8 mm) and of Gorghi Alto-Medio (SCLmin = 99.5 mm) and between seven and eight years for females of both sites, with a SCLmin of 112.1 mm and 106.2 mm respectively. Allometry and reproductive biology A total of 312 captures of 178 different females (152 in the Gorgo Basso and 26 in the Gorghi Alto-Medio) was made between 2014 and 2016. We collected 28 indi- viduals with detectable eggs, 21 from the Gorgo Basso and seven from the Gorghi Alto-Medio. Reproductive females were found between May and July, with a peak in the first half of June (Fig. 2). In this period, the per- centage of reproductive females collected over two-weeks interval ranged from 20% to 58.3%. We noticed also a double egg deposition of a female (SCL = 132.2 mm) captured on 10 June 2015 with four shelled eggs and on 7 July 2015 with five shelled eggs. The average clutch size was 4.14 ± 0.23 (range 2 – 7, n = 28), with a positive correlation with the mother carapace length (F-statistic = 39.19, df = 27, P < 0.001) and a significant difference between the sites (Mann- Whitney U Test = 132.5, N1 = 21, N2 = 7, P < 0.01). The difference in the clutch size between the sites was signifi- cantly independent of the size of the females (Table 4). The average clutch size was 4.57 ± 1.07 (range 2 – 7, n = 21) for the sub-population of the Gorgo Basso and 2.86 ± 0.69 (range 2 – 4, n = 7) for the sub-population of the Gorghi Alto-Medio. The average minimum diameter (Dmin) was 19.46 ± 1.21 mm (range 16.0 – 21.5 mm, n = 89), with a not sig- nificant difference (t-test = 0.15, df = 24.23, P = 0.8843) between females of Gorgo Basso (Dmin = 19.47 ± 0.94, n = 69) and those of Gorghi Alto-Medio (Dmin = 19.42 ± 1.40, n = 20). The average minimum diameter (Dmin) was positively correlated with the carapace length of the females (rPearson = 0.70; t-test = 4.45, df = 21, P < 0.001), since the increase of the size allows a greater pelvic aperture width (rPearson = 0.89; t-test= 8.75, df = 21, P < 0.001), that is a mechanical limiting factor for egg size in turtles. Table 3. Site effect on growth rate. RGR (relative growth rate) = dependent variable, SCL1 (first capture straight carapace length) = independent variable, Site = categorical variable. F d.f. P M al e Model 1 (interaction test) SCL1 20.03 1 < 0.001 Site 13.17 1 < 0.001 SCL1 × Site 1.50 1 0.22 Model 2 (no interaction) SCL1 19.89 1 < 0.001 Site 13.08 1 < 0.001 Fe m al e Model 3 (interaction test) SCL1 14.39 1 < 0.001 Site 19.84 1 < 0.001 SCL1 × Site 0.69 1 0.41 Model 4 (no interaction) SCL1 14.51 1 < 0.001 Site 20.00 1 < 0.001 Fig. 2. Number of females of Emys trinacris with and without shelled eggs in the oviduct determined by inguinal palpation. Table 4. Site effect on number of eggs per female. Number of eggs = dependent variable, SCL (straight carapace length) = independent variable, Site = categorical variable. F d.f. P Model 5.11 5 < 0.05 SCL 0.81 1 0.38 Site 0.48 2 0.63 SCL × Site 0.55 2 0.59 95So close so different: what makes the difference? DISCUSSION The growth of the Sicilian pond turtles in the Lake Preola and Gorghi Tondi Nature Reserve followed the general pattern described for other freshwater turtles: juveniles display a fast growth until sexual maturity, fol- lowed by a slowdown during ageing and at much larger size (Bury, 1979). The population studied seems to fall in the general rule noticed for the genus Emys (Zuffi et al., 2011) and for many others Emydidae (Iverson et al., 1993) as a typical southern ecotype with an advance in age at maturity at a smaller body size with respect to the northernmost populations, although regional fluctuations of temperature and precipitation are better predictors of body size than latitudinal temperature clines, especially in females of Emys orbicularis (Joos et al., 2017). Moreover, the average clutch size is lower than that of similar sized population of the related Emys orbicu- laris in Italy (Zuffi et al., 1999; Zuffi et al., 2015), while no substantial variation in the nesting period and in the clutch frequency was noticed. Despite these natural history traits, if we analysed separately the two sub-populations, a significant differ- ence is noticeable: turtles in the Gorgo Basso reached higher body size, produced more eggs per clutch and had higher density than individuals in the Gorghi Alto- Medio. Excluding both the presence of environmental and genetic effects due to the proximity and similar- ity of the sites, all these elements suggest the that phe- notypic plasticity, driven by a stressor, may explain the observed difference. Furthermore, this hypothesis is supported by the different size at maturity reached in the two wetlands, following the pattern “five” described by Stearns and Koella (1986), where animals, that are forced to grow slowly by an inhibiting factor, mature at a same age, but a smaller size with respect to unstressed con-specific. This type of response is not uncommon in freshwater turtles at a local scale, such as noticed by Gibbons et al. (1981) for females of Trachemys scripta (Thunberg in Schoepff, 1792), while at a larger scale it can take over an adaptive process involving environ- mental and genetic components (Bernardo, 1993). Indeed, turtles for the most part used energ y resources, depending on age or period of year, for growth, maintenance of baseline metabolism and repro- duction (Kuchling, 1999). In particular, during the juvenile stage of chelonians, almost all resources are dedicated to rapid growth to reach a body size and a strength of the shell that make them less susceptible to predation (Kuchling, 1999) and this is regulated mainly by the temperature and by the availability and qual- ity of trophic resources (Kuchling, 1999) as well as by local factors related to the presence of contaminants that can alter the metabolic processes (Burger et al., 1998). Censi et al. (2013) speculated that smaller body mass of Emys trinacris living in Lake Preola and Gorghi Tondi Nature Reserve with respect to another Sicilian site can be associated to the supposed reduction of food disposal induced by lanthanide pollution of aquatic environment that influences the growth of aquatic micro-organisms, but no differences was observed within our study sites (D’Angelo, unpubl. data). In the same way, there are no substantial differences in the concentration of lead in the sediment - an inhibitor of growth in turtles (Burger et al. 1998) - between the two wetlands (Arpa Sicilia, 2016). Therefore, the differences found could be explained in the light of the alteration of abundance and assem- blage of the invertebrate community induced by the presence of alien fishes (Ottonello et al., 2017a) pos- sibly exacerbated by the ubiquitous presence of Pro- cambarus clarkii. In our opinion these differences in prey availability can definitely alter the energy intake by turtles affecting both the growth of individuals in the two sites, as already observed in other American Emydidae (Cagle, 1946; MacCulloch and Secoy, 1983; Dunham and Gibbons, 1990) and in Chelydra serpen- tina Linnaeus, 1758 (Brown et al., 1994) as well as the abundance (Congdon et al., 1986; Galbraith et al., 1988). These differences are likely to impact both the genetic variability of the population because males of Emys mate preferably with larger females (Poschadel et al., 2006), as well as the reproductive output, with females of the Gorgo Basso that laid twice as many eggs of the Gorghi Alto-Medio. These observations are concordant with the optimal egg size theory, according to which the major variation in the reproductive output due to different environmental conditions is in clutch size rather than in egg size, which has been optimized by natural selection (Brockelman, 1975). In our opinion, these results highlighted how the introduction of non-native fish species can affect the ecology of the Sicilian pond turtle, also focusing on a often overlooked aspect, the problem of the interactions between alien fishes and turtles, on which data are lack- ing, in contrast to the more studied competition with non-native freshwater turtles (Cadi and Joly, 2003; 2004). Although further analyses are needed to confirm our finding with other wild populations, we believe that our data may provide important information for the man- agement strategy of the Nature Reserve and for other similar areas and cases, in order to improve the conser- vation status of Emys trinacris and the quality of habitat in which it lives. 96 D. Ottonello et alii ACKNOWLEDGEMENTS We are grateful to Nino Castelli, Michela Girib- aldo, Maurizio Marchese, Nicola Napolitano, Gian- piero Pace for their help during field surveys and with Manuel Morici for his help during x-ray laboratory analysis. Capture and handling permits were released by the Ministero dell’Ambiente e della Tutela del Territorio e del Mare (DPN/2012/0003156 on 9.X.2012). D.O. was partially supported by Societas Europaea Herpetologica Grant in Herpetology 2014. REFERENCES Andreone, F., Corti, C., Ficetola, G.F., Razzetti, E., Roma- no, A., Sindaco, R. (2013): Liste rosse italiane, http: // www.iucn.it/scheda.php?id=1350576451. [Accessed 1 June 2017] Andrews, R.M. (1982): Patterns of growth in reptiles. In: Biology of the Reptilia, vol. 13, p. 273–320. Gans C., Pough F.H., Eds, Academic Press, London. Arpa Sicilia (2016): Monitoraggio Gorgo Basso 2015 - Classificazione dello stato ecologico e dello stato chimico in base al DM n. 260/2010. http: //www. arpa.sicilia.it/wp-content/uploads/2016/05/Relazione- GORGO-BASSO-TP-2015.pdf. [Accessed 1 June 2017] Aa. Vv. (2008): Atlante della Biodiversità della Sicilia: Vertebrati terrestri. Studi e Ricerche, 6, Arpa Sicilia, Palermo. Ayres, C., Cordero, A. (2007): Site tenacity in European pond turtle (Emys orbicularis) hatchlings in North- western Spain. Amphibia-Reptilia 28: 144-147. Bellante, A., Maccarrone, V., Buscaino, G., Buffa, G., Filiciotto, F., Traina, A., Del Core, M., Mazzola, S., Sprovieri, M. (2015): Trace element concentrations in red swamp crayfish (Procambarus clarkii) and surface sediments in Lake Preola and Gorghi Tondi natural reserve, SW Sicily. Environ. Monit. Assess. 187: 1–18. Bernardo, J. (1993): Determinants of maturation in ani- mals. Trends Ecol. Evol. 8: 166–173. Brockelman, W.Y. (1975): Competition, the fitness of off- spring, and optimal clutch size. Am. Nat. 109: 677– 699. Brody, S. (1945): Bioenergetics and growth. Reinhold Publishing Corp, New York. Brown, G.P., Bishop, C.A., Brooks, R.J. (1994): Growth rate, reproductive output, and temperature selection of snapping turtles in habitats of different productivi- ties. J. Herpetol. 28: 405–410. Burger, J., Carruth-Hinchey, C., Ondroff, J., McMahon, M., Gibbons, J.W., Gochfeld, M. (1998): Effects of lead on behaviour, growth, and survival of hatchling slider turtles. J. Toxicol. Environ. Health 55: 495–502 Bury, R.B. (1979): Population ecology of freshwater tur- tles. In: Harless M, Morlock H (eds) Turtles perspec- tives and research. John Wiley, New York p. 571–602. Cadi, A., Joly, P. (2003): Competition for basking places between the endangered European pond turtle (Emys orbicularis galloitalica) and the introduced red-eared slider (Trachemys scripta elegans). Can. J. Zool. 81: 1392–1398. Cadi, A., Joly, P. (2004) Impact of the introduction of the read-eared slider (Trachemys scripta elegans) on sur- vival rates of the European pond turtle (Emys orbicu- laris). Biodivers. Conserv. 13: 1511–1518. Cagle, F.R. (1946): The Growth of the Slider Turtle: Pseudemys scripta elegans. Miscellaneous Publications of the Museum of Zoology, University of Michigan. Censi, P., Randazzo, L.A., D’Angelo, S., Saiano, F., Zud- das, P., Mazzola, S., Cuttitta, A. (2013): Relationship between lanthanide contents in aquatic turtles and environmental exposures. Chemosphere 91: 1130– 1135. Çiçek, K., Kumaş, M., Ayaz, D., Varol Tok, C. (2016): A skeletochronological study of age, growth and lon- gevity in two freshwater turtles, Emys orbicularis and Mauremys rivulata, from Mediterranean Turkey (Rep- tilia: Testudines). Zool. Middle East 62: 29–38. Congdon, J.D., Greene, J.L., Gibbons, J.W. (1986): Bio- mass of freshwater turtles: a geographic comparison. Am. Midl. Nat. 115: 165–173. Cox, W.A., Hazelrig, J.B., Turner, M.E., Angus, R.A., Marion, K.R. (1991): A model for growth in the musk turtle, Sternotherus minor, in a North Florida spring. Copeia 1991: 954–968. Cusimano, G., Hauser, S., Vassallo, M. (2006): Hydrogeo- chemistry of a wetland of south-western Sicily (Italy). E-Water. http: //www.ewa-online.eu/tl_files/_media/ content/documents_pdf/Publications/E-Water/docu- ments/43_2006_04.pdf. [Accessed 1 June 2017] D’Angelo, S., Lo Valvo, M. (2003): On the presence of the red swamp crayfish Procambarus clarkii in Sicily. Nat- uralista siciliano 27: 325–327. Dextrase, A.J., Mandrak, N.E. (2006): Impact of alien invasive species on freshwater fauna at risk in Canada. Biol. Invasions 8: 13–24. Dunham, A.E., Gibbons, J.W. (1990): Growth of the slider turtle. In: Gibbons, JW (ed) Life History and Ecology of the Slider Turtle. Smithsonian Inst. Press, Washing- ton, p. 135–145. Fritz, U., Fattizzo, T., Guicking, D., Tripepi, S., Pennisi, M.G., Lenk, P., Joger, U., Wink, M. (2005): A new cryptic species of pond turtle from southern Italy, the 97So close so different: what makes the difference? hottest spot in the range of the genus Emys. Zool. Scr. 34: 351–371. Galbraith, D.A., Bishop, C.A., Brooks, R.J., Simser, W.L., Lampman, K. (1988): Factors affecting the density of population of common snapping turtles (Chelydra ser- pentina serpentina). Can. J. Zool. 66: 1233–1240. Genovesi, P. (2007): Towards a European strategy to halt biological invasions in inland waters. In: Biological invaders in inland waters: profiles, distribution, and threats, Invading nature, pp. 627-638. Gherardi, F., Ed., Springer, Dordrecht, The Netherland. Gibbons, J.W., Semlitsc, R.D., Greene, J.L., Schubauers, J.P. (1981): Variation in age and size at maturity of the slid- er turtle (Pseudemys scripta). Am. Nat. 117: 841–845. Hinton, T.G., Fledderman, P.D., Lovich, J.E., Congdon, J.D., Gibbons, J.W. (1997): Radiographic determina- tion of fecundity: is the technique safe for developing turtle embryos? Chelon. Conserv. Biol. 2: 409–414. Hurlbert, S.H. (1984): Pseudoreplication and the design of ecological field experiments. Ecol. Monogr. 54: 187–211. Iverson, J.B., Balgooyen, C.P., Byrd, K.K., Lyddan, K.K. (1993): Latidudinal variation in egg and clutch size in turtles. Can. J. Zool. 71: 2448–2461. Joos, J., Kirchner, M., Vamberger, M., Kaviani, M., Rahimibashar, M. R., Fritz, U., Müller, J. (2017): Cli- mate and patterns of body size variation in the Euro- pean pond turtle, Emys orbicularis. Biol. J. Linn. Soc. 122: 351–365. Keller, C., Andreu, A.C., Ramo, C. (1998): Aspects of the population structure of Emys orbicularis his- panica from southern Spain. In: Fritz, U. et al. (eds), Proceedings of the EMYS Symposium Dresden 96. Mertensiella 10: 147–158. Kuchling, G. (1999): The Reproductive Biology of the Chelonia. Zoophysiology. Springer-Verlag Berlin Hei- delberg. Lacomba, I.A., Sancho, V.A. (2004): Advances in the action plan for Emys orbicularis in the Valencia region, Spain. Biologia 59: 173-176. Landres, P.B., Verner, J., Thomas, J.W., (1988): Ecological uses of vertebrate indicators species. A critique. Con- serv. Biol. 2: 316–328. Lambert, M.R., McKenzie, J.M., Screen, R.M., Clause, A.G., Johnson, B.B., Mount, G.G., Shaffer, H.B., Pau- ly, G.B. (2019): Experimental removal of introduced slider turtles offers new insight into competition with a native, threatened turtle. PeerJ 7: e7444. Litzgus, J.D., Brooks, R.J. (1998): Growth in a cold envi- ronment: body size and sexual maturity in a northern population of spotted turtles, Clemmys guttata. Can. J. Zool. 76: 773–782. Lovich, J.E., Ernst, C.H., McBreen, J.F. (1990): Growth, maturity, and sexual dimorphism in the wood turtle, Clemmys insculpta. Can. J. Zool. 68: 672–677. Lovich, J.E., Ernst, C.H., Zappalorti, R.T., Herman D.W. (1998): Geographic variation in growth and sexual size dimorphism of Bog Turtles (Clemmys muhlenber- gii). Am. Midl. Nat. 139: 69–78. Lubcke, G.M., Wilson, D. S. (2007): Variation in shell morphology of the western pond turtle (Actinemys marmorata Barid and Girard) from threee aquatic habitats in Northern California. J. Herpetol. 4: 107– 114. Maccarrone, V., Filiciotto, F., Buffa, G., Stefano, V.D., Quinci, E.M., Vincenzi, G.d., Mazzola, S., Buscaino, G. (2016): An Invasive Species in a Protected Area of Southern Italy: the Structure, Dynamics and Spa- tial Distribution of the Crayfish Procambarus clarkii. Turkish J. Fish. Aquat. Sci. 16: 401–412. MacCulloch, R.D., Secoy, D.M. (1983): Demography, growth, and food of western painted turtles, Chryse- mys picta bellii (Gray), from southern Saskatchewan. Can. J. Zool. 61: 1499–1509. Mahmoud, I.Y. (1969): Comparative ecology of the kinos- ternid turtles of Oklahoma. Southwestern Naturalist 14: 31–66. Marrone, F., Naselli-Flores, L. (2015): A review on the animal xenodiversity in Sicilian inland waters (Italy). Adv. Oceanogr. Limnol 6: 2–12. Marrone, F., Sacco, F., Arizza, V., Arculeo, M. (2016): Amendment of the type locality of the endemic Sicil- ian pond turtle Emys trinacris Fritz et al. 2005, with some notes on the highest altitude reached by the species (Testudines, Emydidae). Acta Herpetol. 11: 59–61. Maunder, M.N., Sibert, J.R., Fonteneau, A., Hampton, J., Kleiber, P., Harley, S.J. (2006): Interpreting catch per unit effort data to assess the status of individual stocks and communities. ICES J. Mar. Sci. 63: 1373– 1385. Ogle, D.H. (2012): FSA: Fisheries Stock Analysis. R pack- age version 0.2-8. Naselli-Flores, L., Barone, R. (2012): Phytoplankton dynamics in permanent and temporary Mediterrane- an waters: is the game hard to play because of hydro- logical disturbance? Hydrobiologia 698: 147–159. Ottonello, D., D’Angelo, S., Oneto, F., Malavasi, S., Zuffi, M.A.L. (2017a): Feeding ecology of the Sicilian pond turtle Emys trinacris (Testudines, Emydidae) influ- enced by seasons and invasive aliens species. Ecol. Res. 32: 71–80. Ottonello, D., Oneto, F., Malavasi, S., Zuffi, M.A.L., D’Angelo, S. (2017b): Preliminary data on the popu- 98 D. Ottonello et alii lation of the Sicilian pond turtle, Emys trinacris Fritz et al., 2005 (Emydidae) inhabiting the Gorgo Tondo Basso in the “Lago Preola e Gorghi Tondi” Nature Reserve, Sicily, Italy. Acta zool. Bulgar., Supplement 10: 121–128. Parmenter, R.R., Avery, H.W. (1990): The feeding ecology of the slider turtle. In: Gibbons, J.W. (ed) Life History and ecology of the slider turtle. Sithsonian Institution Press, Whashington DC Parkos, J.J., Santucci, V.J., Wahl, D.H. (2003): Effects of adult common carp (Cyprinus carpio) on multiple trophic levels in shallow mesocosms. Can. J. Fish. Aquat. Sci. 60: 182–192. Pitcher, T.J., Hart, P.J.B. (1995): The impact of species changes in African lakes. Chapman and Hall, London. Polo-Cavia, N., López, P., Martín, J. (2010): Competi- tive interactions during basking between native and invasive freshwater turtle species. Biol. Invasions 12: 2141–2152. Poschadel, J.R., Meyer-Lucht, Y., Plath M. (2006): Response to chemical cues from conspecifics reflects male mating preference for large females and avoid- ance of large competitors in the European pond tur- tle, Emys orbicularis. Behaviour 143: 569–587. Pyke, G.H. (2008): Plague minnow or mosquitofish? A review of the biology and impacts of introduced Gam- busia species. Annu. Rev. Ecol. Evol. Syst. 39: 171–191. Ricciardi, A., MacIsaac, H.J. (2011): Impact of biological invasions on freshwater ecosystems, pp. 211-224. In: Fifty Years of Invasion Ecology: The Legacy of Charles Elton, pp. 211-224. Richardson, D.M., Ed., Blackwell Publishing Ltd, Oxford, UK. Selman, W., Baccigalopi, B., Baccigalopi, C. (2014): Dis- tribution and abundance of Diamondback terrapins (Malaclemys terrapin) in Southwestern Louisiana. Chelon. Conserv. Biol. 13: 131–139. Servan, J., Baron, J., Bels, R., Bour, V., Lancon, M., Renon, G. (1986). Le marquage des tortues d’eau douce: application a la cistude d’Europe Emys orbicu- laris (Reptilia, Chelonii). Bull. Soc. Herp. Fr. 37: 9–17. Spadola, F., Insacco, G. (2009): Endoscopy of cloaca in 51 Emys trinacris (Fritz et al., 2005): morphological and diagnostic study. Acta Herpetol. 4: 73–81. Stearns, S.C., Koella, J.C. (1986): The evolution of pheno- typic plasticity in li-history traits: prediction of reac- tion norms for age and size at maturity. Evolution 40: 893–319. Strayer, D.L. (2010): Aliens species in fresh waters: eco- logical effects, interactions with other stressors, and prospects for the future. Freshw. Biol. 55: 152–174. Tucker, J.K., Janzen F.J., Paukstis, G.L. (1998): Variation in carapace morphology and reproduction in the Red- Eared Slider Trachemys scripta elegans. J. Herpetol. 32: 294-298. Wilbur, H.M. (1975): The Evolutionary and Mathematical Demography of the Turtle Chrysemys picta. Ecology 56: 64–77. Zerunian, S. (2004): Pesci delle acque interne d’Italia. Quad Cons. Natura 20, Min Ambiente, Ist. Naz. Fau- na Selvatica, Rome. Zuffi, M.A.L., Citi, S., Foschi, E., Marsiglia, F., Martelli, E. (2015): Into a box interiors: clutch size variation and resource allocation in the European pond turtle. Acta Herpetol. 10: 39–45. Zuffi, M.A.L., Di Benedetto, F., Foschi, E. (2004): The reproductive strategies in neighbouring populations of the European pond turtle, Emys orbicularis, in central Italy. Ital. J. Zool. Suppl. 2: 101–104. Zuffi, M.A.L., Di Cerbo, A., Fritz, U. (2011): Emys orbicu- laris (Linnaeus, 1758). In: Fauna d‘Italia, Reptilia, pp. 153-163. Corti, C., Capula, M., Luiselli, L., Razzetti, E., Sindaco, R., Eds, Edizioni Calderini, Bologna. Zuffi, M.A.L., Gariboldi, A. (1995): Sexual dimorphism in Italian populations of the European pond terrapin, Emys orbicularis. In: Scientia Herpetologica, pp. 124– 129. Llorente, G.A., Montori, A., Santos, X., Carretero, M.A., Eds, Associacion Herpetologica Espanola, Bar- celona. Zuffi, M.A.L., Foschi, E. (2015): Reproductive patterns of European pond turtles differ between sites: a small scale scenario. Amphibia-Reptilia 36: 339–349. Zuffi, M.A.L., Odetti, F., Meozzi, P. (1999): Body size and cluth size in the European pond turtle, Emys orbicula- ris, from central Italy. J. Zool. 247: 139–143. 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