Hansjürg Hotz’s research while affiliated with University of Zurich and other places

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Publications (56)


Figure 2. Concentrations (ng/kg, wet weight) of DDT and its decay products in individual organs of an adult female Rana lessonae collected at the Solomeo pond in September 1999.  
Figure 1. Mean concentrations (ng/kg wet weight for animals , ng/L for water) of 16 commonly used OC pesticides and their decay products (above abscissa) and of DDT (below abscissa) in larval and adult water frogs (the parental host species Rana lessonae and the hybridogenetic hybrid Rana esculenta) from an L-E system at the Solomeo breeding pond, and in water of this pond. All animal and water samples were collected in September 2000. Concentrations in animals are based on completely homogenized individuals and may underestimate effective concentrations.  
Concentrations of commonly used OC pesticides and their decay products (ng/kg, wet weight; ND, not detected) in ventral and dorsal skin of three adult water frogs collected at the Solomeo pond in September 1998. a Abbreviations as in table 1.
Bioaccumulation of organochlorine pesticides in frogs of the Rana esculenta complex in central Italy
  • Article
  • Full-text available

January 2013

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575 Reads

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22 Citations

Amphibia-Reptilia

Fagotti

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Lorena Morosi

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Ines Di Rosa

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Hansjürg Hotz

Concentrations of commonly used organochlorine pesticides (OCPs) were determined in tissues of 23 adult and 24 larval water frogs of two coexisting species (Rana lessonae and the hemiclonal hybrid R. esculenta) and in the water of their breeding pond in an agricultural zone in Umbria, central Italy, where increased occurrence of infectious diseases and distinctly oversized tadpoles were recently observed. The concentrations of OCP in tissues of both species were lower than those in the water of their breeding pond, except for DDT, which was more concentrated in adult frogs than in pond water (bioaccumulation factor 7 for R. lessonae, 15 for R. esculenta). Total OCP concentration and adult body weight were positively correlated for both species, which is consistent with bioaccumulation. In accord, adults contained higher OCP concentrations than tadpoles. Oversized tadpoles had higher OCP concentrations than normal tadpoles. Mean OCP concentrations in individual organs were about an order of magnitude higher than those in whole-frog homogenates. They were highest in brain, higher in ventral than in dorsal skin, and moderately high in ovaries; transmission of bioaccumulation loads to the next generation is therefore possible. The observed OCP concentrations appear too low to directly cause mortality in water frogs, but effects of cumulative exposure to low-level pollutants and their synergistic interactions with the effects of other natural and anthropogenic environmental stressors are unknown.

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Figure 1. Map of the collecting localities; numbers correspond to localities in Materials and Methods. At least partial allozyme data are available from each locality. Distribution of Pelophylax ridibundus and P. cf. bedriagae mtDNA in our samples is indicated.  
Table 1 Origin and number (N) of individuals for which allozymes and mtDNA were investigated
Figure 2. Comparison of migration models for allozyme and mtDNA data. Numbers by locality names correspond to those on the map (Figure 1); Paradisos and Toxotai (localities 9 and 10) are close to the Nestos River and the center of the transition zone. The models are described in Material and Methods. The numbers in the box represent model ranks based on Bayes factors calculated with MIGRATE (Beerli and Palczewski 2010); the log marginal likelihood values are tabulated in Supplementary Table 1.
Figure 3. Frequency of alleles more common in western Greece at 5 allozyme loci along a transect from west to east in northeastern Greece and northwestern Turkey. Frequencies of 2 subtypes of P. ridibundus ND3 are also indicted. The lines are based on 3-point running averages.
Figure 4. RAxML tree based on unique mitochondrial ND3 sequences of water frogs across a genetic transition in northern Greece and European Turkey. Tree rooted at midpoint. Sequences are identified by numbers corresponding to the 18 localities with mtDNA data; these are given in Materials and Methods and correspond to those of Figure 1. Number of individuals with a given sequence provided in parentheses if greater than 1.  
Balancing a Cline by Influx of Migrants: A Genetic Transition in Water Frogs of Eastern Greece

November 2012

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272 Reads

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26 Citations

Journal of Heredity

Variation patterns of allozymes and of ND3 haplotypes of mitochondrial DNA reveal a zone of genetic transition among western Palearctic water frogs extending across northeastern Greece and European Turkey. At the western end of the zone, allozymes characteristic of Central European frogs known as Pelophylax ridibundus predominate, whereas at the eastern end, alleles characteristic of western Anatolian water frogs (P. cf. bedriagae) prevail. The ND3 haplotypes reveal 2 major clades, 1 characteristic of Anatolian frogs, the other of European; the European clade itself has distinct eastern and western subclades. Both the 2 major clades and the 2 subclades overlap within the transition zone. Using Bayesian model selection methods, allozyme data suggest considerable immigration into the Nestos River area from eastern and western populations. In contrast, the ND3 data suggest that migration rates are so high among all locations that they form a single panmictic unit; the best model for allozymes is second best for mitochondrial DNA (mtDNA). Nuclear markers (allozymes), which have roughly 4 times as deep a coalescent history as mtDNA data and thus may reflect patterns over a longer time, indicate that eastern and western refugial populations have expanded since deglaciation (in the last 10 000 years) and have met near the Nestos River, whereas the mtDNA with its smaller effective population size has already lost the signal of partitioning into refugia.


RrS1-like Sequences of Water Frogs from Central Europe and Around the Aegean Sea: Chromosomal Organization, Evolution, Possible Function

March 2011

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203 Reads

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15 Citations

Journal of Molecular Evolution

RrS1-like sequences of water frogs (genus Pelophylax) display varied genomic organization, whereas the centromeric hybridization pattern reveals species-specific differences. Using fluorescent in situ hybridization, Pelophylax cf. bedriagae, Pelophylax kurtmuelleri, and Pelophylax ridibundus showed a hybridization signal at centromeres of chromosomes 1–5, but in P. kurtmuelleri the medium-small chromosome labeled was 10 rather than 8. Pelophylax cretensis had almost 16 of 26 centromeres labeled, as did Pelophylax lessonae from Poland when its chromosomes are hybridized with a homologous probe. When StuI-digested genomic DNA was hybridized with RrS1 probe, hybridization ladders for P. ridibundus from Poland have evenly spaced steps (about 100 bp) of uniform intensity from about 200 bp upward. Steps in hybridization ladders from circum-Aegean taxa vary in intensity: larger, odd-numbered steps are often fainter. A strong double band (800/900 bp) in Anatolian P. cf. bedriagae, emphasized by a weak 700 bp band, distinguishes them from P. kurtmuelleri from the Peloponnisos, in which the 900 bp band is almost absent. The ladder in P. cretensis lacks odd-numbered steps. A and B repeats, observed originally within the RrS1 satellite of P. ridibundus, occur also in the circum-Aegean frogs and in P. lessonae, Pelophylax epeiroticus, Pelophylax saharicus, and Pelophylax shqipericus. It is plausible that AB dimers or ABB trimers rather than A or B monomers correspond to functional/evolutionary units. The presence of regions similar to yeast CDEs and mammalian CENP-B boxes suggests a role for RrS1 sequences in centromere organization.


Figure 3: Divergence time (95% credibility intervals) estimated for the following eight comparisons: Western Palaearctic water frogs (WPWF) versus Eastern Palaearctic water frogs (EPWF); Pelophylax saharicus (sah) versus Pelophylax perezi (per); Pelophylax lessonae (les) and Pelophylax bergeri (ber) versus Pelophylax shqipericus (shq); Pelophylax epeiroticus (epe) versus Pelophylax cretensis (cre); P. cretensis (cre) versus MHG1-9; MHG1 (Pelophylax ridibundus Central Europe) versus MHG2 (Pelophylax bedriagae); MHG3 (Cyprus) versus MHG4-9; MHG4-5 (Cilician groups) versus MHG6-9. Four scenarios (CRETE9w, CRETE9n, CRETE5w and CRETE5n) are listed from top to bottom in the box and from left to right in each group of comparisons. All four scenarios assume a mean isolation time for Cyprus of 5.3 ± 0.3 Ma; scenario CRETE9 assumes a mean isolation time of 9.0 Ma for Crete, whereas scenario CRETE5 assumes a mean isolation time of 5.3 Ma; n and w in the scenario names refer to narrow (± 0.3 Ma) and wide (0.5 × mean isolation time) standard deviations around the isolation time of Crete. The grey line indicates the period from the start to the end of the MSC. beast was performed on the basis of 83 concatenated ND2 and ND3 sequences.
Phylogeographic patterns of genetic diversity in eastern Mediterranean water frogs were determined by geological processes and climate change in the Late Cenozoic

November 2010

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660 Reads

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165 Citations

Aim Our aims were to assess the phylogeographic patterns of genetic diversity in eastern Mediterranean water frogs and to estimate divergence times using different geological scenarios. We relate divergence times to past geological events and discuss the relevance of our data for the systematics of eastern Mediterranean water frogs. Location The eastern Mediterranean region. Methods Genetic diversity and divergence were calculated using sequences of two protein‐coding mitochondrial (mt) genes: ND2 (1038 bp, 119 sequences) and ND3 (340 bp, 612 sequences). Divergence times were estimated in a Bayesian framework under four geological scenarios representing alternative possible geological histories for the eastern Mediterranean. We then compared the different scenarios using Bayes factors and additional geological data. Results The extensive genetic diversity in mtDNA divides eastern Mediterranean water frogs into six main haplogroups (MHGs). Three MHGs were identified on the Anatolian mainland; the most widespread MHG with the highest diversity is distributed from western Anatolia to the northern shore of the Caspian Sea, and includes the type locality of Pelophylax ridibundus . The other two Anatolian MHGs are restricted to south‐eastern Turkey, occupying localities west and east of the Amanos mountain range. One of the remaining three MHGs is restricted to Cyprus; the second, to the Levant; and the third was found in the distribution area of European lake frogs ( P. ridibundus group), including the Balkans. Main conclusions Based on geological evidence and estimates of genetic divergence we hypothesize that the water frogs of Cyprus have been isolated from the Anatolian mainland populations since the end of the Messinian salinity crisis (MSC), that is, since c . 5.5–5.3 Ma, while our divergence time estimates indicate that the isolation of Crete from the mainland populations (Peloponnese, Anatolia) probably pre‐dates the MSC. The observed rates of divergence imply a time window of c. 1.6–1.1 million years for diversification of the largest Anatolian MHG; divergence between the two other Anatolian MHGs may have begun about 3.0 Ma, apparently as a result of the uplift of the Amanos Mountains. Our mtDNA data suggest that the Anatolian water frogs and frogs from Cyprus represent several undescribed species.



Fig. 20.1 Gamete production, possible mating combinations and resulting offspring in the L-E system, i.e., mixed populations of Rana lessonae (LL) and R. esculenta (RL), a hemiclonal hybrid between R. ridibunda (RR) and R. lessonae. Reproduced with permission from Vorburger (2001c) 
Fig. 20.3 Proposed mechanism for occasional recombination between otherwise clonally transmitted ridibunda genomes in L-E systems, mediated by viable R. ridibunda females produced by matings among two different, genetically compatible hemiclones of R. esculenta. Reproduced with permission from Vorburger (2001c) 
Masked Damage: Mutational Load in Hemiclonal Water Frogs

September 2009

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183 Reads

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14 Citations

Hemiclonal hybrids of Western Palearctic water frogs of the Rana esculenta complex transmit only one parental genome to their offspring without recombination (hybridogenesis). Such genomes are thus prone to accumulate deleterious mutations. The frog complex is unique among hybridogens in that hemiclonal hybrids occur in both sexes. This provides the opportunity of using experimental crosses to produce offspring possessing two clonal genomes of various origins and thereby study their homozygous and heterozygous effects on fitness. Here we review work that made use of this possibility to assess the evolutionary consequences of clonal inheritance in water frogs. Overall, these studies indicate that clonally transmitted genomes bear a substantial load of fixed deleterious mutations, yet these mutations appear to have minor effects on fitness in the heterozygous state. We also point out potential mechanisms for episodic recombination by which otherwise clonal genomes may be purged of deleterious alleles, and we present evidence for such episodic recombination to occur in natural populations of hybridogenetic frogs. Finally, we provide an outlook on work in progress that exploits the peculiarities of this system to obtain relevant estimates of the frequency of segregating lethal mutations in sexual populations of water frogs.


Figure 1. 
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Evolution of serum albumin intron-1 is shaped by a 5 ‘truncated non-long terminal repeat retrotransposon in western Palearctic water frogs (Neobatrachia)

September 2009

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205 Reads

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51 Citations

Molecular Phylogenetics and Evolution

A 5' truncated non-LTR CR1-like retrotransposon, named RanaCR1, was identified in the serum albumin intron-1 (SAI-1) of at least seven species of western Palearctic water frogs (WPWF). Based on sequence similarity of the carboxy-terminal region (CTR) of ORF2 and/or the highly conserved 3' untranslated region (3' UTR), RanaCR1-like elements occur also in the genome of Xenopus tropicalis and Rana temporaria. Unlike other CR1 elements, RanaCR1 contains a CA microsatellite in its 3' UTR. The low nucleotide diversity of the 3' UTR compared to the CTR and to SAI-1 suggests that this region still plays a role in WPWF, either as a structure-stabilizing element, or within a species-specific transcriptional network. Length variation of water frog SAI-1 sequences is caused by deletions that extend in some cases beyond the 5' or 3' ends of RanaCR1, probably a result of selection for structural and functional stability of the primary transcript. The impact of RanaCR1 on SAI-1 evolution is also indicated by the significant negative correlation between the length of both SAI-1 and RanaCR1 and the percentage GC content of RanaCR1. Both SAI-1 and RanaCR1 sequences support the sister group relationship of R. perezi and R. saharica, which are placed in the phylogenetic tree at a basal position, the sister clade to other water frog taxa. It also supports the monophyly of the R. lessonae group; of Anatolian water frogs (R. cf. bedriagae), which are not conspecific with R. bedriagae, and of the European ridibunda group. Within the ridibunda clade, Greek frogs are clearly separated, supporting the hypothesis that Balkan water frogs represent a distinct species. Frogs from Atyrau (Kazakhstan), the type locality of R. ridibunda, were heterozygous for a ridibunda and a cf. bedriagae specific allele.


Sampling sites of Pelophylax spp. in Flanders (Belgium) and locations of origin of references species, with corresponding geographical coordinates. *Systematic status is uncertain
A cryptic invasion within an invasion and widespread introgression in the European water frog complex: Consequences of uncontrolled commercial trade and weak international legislation

December 2008

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405 Reads

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113 Citations

In Western Europe, many pond owners introduce amphibians for ornamental purposes. Although indigenous amphibians are legally protected in most European countries, retailers are circumventing national and international legislation by selling exotic nonprotected sibling species. We investigated to what extent non-native species of the European water frog complex (genus Pelophylax) have become established in Belgium, using morphological, mitochondrial and nuclear genetic markers. A survey of 87 sampling sites showed the presence of non-native water frogs at 47 locations, mostly Marsh frogs (Pelophylax ridibundus). Surprisingly, at least 19% of all these locations also harboured individuals with mitochondrial haplotypes characteristic of Anatolian water frogs (Pelophylax cf. bedriagae). Nuclear genotyping indicated widespread hybridization and introgression between P. ridibundus and P. cf. bedriagae. In addition, water frogs of Turkish origin obtained through a licensed retailer, also contained P. ridibundus and P. cf. bedriagae, with identical haplotypes to the wild Belgian populations. Although P. ridibundus might have invaded Belgium by natural range expansion from neighbouring countries, our results suggest that its invasion was at least partly enhanced by commercial trade, with origins as far as the Middle East. Also the invasion and rapid spread of Anatolian lineages, masked by their high morphological similarity to P. ridibundus, is likely the result of unregulated commercial trade. We expect that Anatolian frogs will further invade the exotic as well as the native range of P. ridibundus and other Pelophylax species elsewhere in Western and Central Europe, with risks of large-scale hybridization and introgression.


Widespread unidirectional transfer of mitochondrial DNA: A case in western Palaearctic water frogs

June 2008

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163 Reads

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150 Citations

Journal of Evolutionary Biology

Interspecies transfer of mitochondrial (mt) DNA is a common phenomenon in plants, invertebrates and vertebrates, normally linked with hybridization of closely related species in zones of sympatry or parapatry. In central Europe, in an area north of 48 degrees N latitude and between 8 degrees and 22 degrees E longitude, western Palaearctic water frogs show massive unidirectional introgression of mtDNA: 33.7% of 407 Rana ridibunda possessed mtDNA specific for Rana lessonae. By contrast, no R. lessonae with R. ridibunda mtDNA was observed. That R. ridibunda with introgressed mitochondrial genomes were found exclusively within the range of the hybrid Rana esculenta and that most hybrids had lessonae mtDNA (90.4% of 335 individuals investigated) is evidence that R. esculenta serves as a vehicle for transfer of lessonae mtDNA into R. ridibunda. Such introgression has occurred several times independently. The abundance and wide distribution of individuals with introgressed mitochondrial genomes show that R. lessonae mt genomes work successfully in a R. ridibunda chromosomal background despite their high sequence divergence from R. ridibunda mtDNAs (14.2-15.2% in the ND2/ND3 genes). Greater effectiveness of enzymes encoded by R. lessonae mtDNA may be advantageous to individuals of R. ridibunda and probably R. esculenta in the northern parts of their ranges.


Citations (48)


... This set consisted of four loci (supplementary table S1). Two (Cala27 and RlCA18) are amplified only in P. lessonae (Garner et al., 2000); the other two (Res22 and Rrid169A) are amplified only in P. ridibundus (Zeisset, Rowe and Beebee, 2000;Hotz et al., 2001). These four markers are among the most polymorphic loci tested so far and precisely identify ridibundus and lessonae genotypes (Czernicka, 2013). ...

Reference:

Body size variation in hybrids among populations of European water frogs (Pelophylax esculentus complex) with different breeding systems
Microsatellites: A tool for evolutionary genetic studies of western Palearctic water frogs
  • Citing Article
  • January 2001

... GPG species therefore likely are older than FNV genotypes. The two hypotheses have been debated, but no consensus has been reached and, depending on circumstances, either of them may apply (Bierzychudek, 1989;Browne & Wanigasekera, 2000;Kenny, 1996;Parker & Niklasson, 1995;Semlitsch et al., 1997;Van Doninck et al., 2002;Vorburger et al., 2003;Weider, 1993). ...

COMPETITION AMONG TADPOLES OF COEXISTING HEMICLONES OF HYBRIDOGENETIC RANA ESCULENTA: SUPPORT FOR THE FROZEN NICHE VARIATION MODEL
  • Citing Article
  • August 1997

Evolution

... Based on the combined mitochondrial sequences, the time to the most recent common ancestor of the OSC was estimated using the Bayesian Markov chain Monte Carlo (MCMC) approach under a 'relaxed molecular clock' model with a Yule tree prior in BEAST 1.8.4 (Drummond et al. 2012). In this analysis, Rana Linnaeus, 1758 and Odorrana Ye and Huang, 1990 were calibrated at 28.14 ± 1.5 million years ago (Ma) as the primary calibration constraint (Yuan et al. 2018), with Pelophylax bedriagae (Pallas, 1771) and Pelophylax cretensis (Beerli, Hotz, Tunner, Heppich, & Uzzell, 1994) calibrated at 5.25 ± 0.16 Ma as the secondary constraint (Beerli et al. 1996). The calibration nodes used a lognormal prior distribution. ...

GEOLOGICALLY DATED SEA BARRIERS CALIBRATE A PROTEIN CLOCK FOR AEGEAN WATER FROGS
  • Citing Article
  • August 1996

Evolution

... Hybrids between P. epeiroticus and P. kurtmuelleri appear to be sexual, in contrast to asexual (hybridogenetic) hybrids that originate from hybridisation between P. ridibundus (a sister species/phylogenetic lineage of P. kurtmuelleri) with other species (P. lessonae in central Europe, P. perezi in southern France and northeastern Spain and P. bergeri in Italy) (Guerrini et al., 1997;Hotz et al., 1985;Hotz & Uzzell, 1982). However, the presumed sexual mode of reproduction of P. kurtmuelleri × P. epeiroticus hybrids does not correspond to the presence of triploid hybrids that have been identified in western Greece (Kyriakopoulou-Sklavounou & Vasara, 2001;Sofianidou, 1996). ...

Biochemically detected sympatry of two water frog species: Two different cases in the Adriatic Balkans (Amphibia, Ranidae)
  • Citing Article
  • January 1982

... Since the description of P. kurtmuelleri, the taxon was considered the Balkan endemics based on the morphometry (Schneider et al. 1993), bioacoustics (Schneider and Sinsch 1992;Schneider et al. 1993;Lukanov et al. 2015) and supposed inability to induce hybridogenesis in interspecific hybrids (Hotz et al. 1985;Berger et al. 1994;Sinsch and Eblenkamp 1994). On the other hand, P. kurtmuelleri shows only weak morphometrical (Papežík et al. 2021), and genetic differentiation from P. ridibundus in mtDNA (Lymberakis et al. 2007;Hofman et al. 2015;Vucić et al. 2018) as well as nDNA (SAI-1 gene; Kolenda et al. 2017;Papežík et al. 2021). ...

Postzygotic reproductive isolation between Mendelian species of European water frogs
  • Citing Article
  • January 1994

... (7) Pelophylax cretensis (Beerli, Hotz, Tunner, Heppich & Uzzell, 1994 (9) Pelophylax ridibundus from Europe: P. ridibundus ridibundus and P. r. kurtmuelleri; Central Asia: Pelophylax ridibundus cf. ridibundus H-I; and southern Anatolia: P. r. cf. ...

Two new water frog species from the Aegean islands Crete and Karpathos (Amphibia, Salientia, Ranidae)
  • Citing Article
  • January 1994

... Thirteen P. lessonae, 69 P. ridibundus and 83 P. esculentus males and females were collected at 23 sample sites (Supplementary Table 1). Frogs were taxon-determined by phenotypic characters [18,19] (Fig. 1A-C). DNA was extracted from an interdigital forelegs membrane using a commercial Tissue DNA Isolation Kit (Geneaid Biotech, Taipei, Taiwan) following a manufacturer protocol. ...

Sex determination and sex ratios in western Palearctic water frogs: XX and XY female hybrids in the Pannonian Basin?
  • Citing Article
  • January 1988

... Compared to pure clonal reproductive modes such as parthenogenesis or gynogenesis, hybridogenesis combines elements of both clonal and Mendelian inheritance. First detected in Mexican mollies of the genus Poeciliopsis [18], hybridogenesis has also been reported in European water frogs (genus Pelophylax) [19][20][21], Mediterranean stick insects (genus Bacillus) [22], Iberian minnows of the Squalius alburnoides complex [23][24][25], Australian carp gudgeons (genus Hypseleotris) [26], and marine reef shes of the genus Hexagrammos [27,28]. ...

Electrophoretic and Morphological Evidence for Two Forms of Green Frogs (Rana esculenta Complex) in Peninsular Italy (Amphibia, Salientia)
  • Citing Article
  • July 1979

Mitteilungen aus dem Museum für Naturkunde in Berlin Zoologisches Museum und Institut für Spezielle Zoologie (Berlin)

... Pelophylax epeiroticus female and male originated from the localities of Ioannina and Igoumenitsa, respectively, in western Greece; both sexes of P. kurtmuelleri originated from Velipoje, Albania. Experimental crossings were carried out at the Institute of Animal Physiology and Genetics ASCR, Liběchov, Czech Republic based on the protocol described in Berger et al. (1994) and Pruvost et al. (2013). ...

Artificial fertilization of water frogs

Amphibia-Reptilia

... Pelophylax ridibundus, or the Marsh Frog, was described from Guryev in Kazakhstan (Pallas, 1771; (Figure 11). This species occurs over a vast area in Eurasia, from the United Kingdom in the west to the Kamchatka peninsula in the east, and from the outskirts of St. Petersburg (Russia) in the north to Saudi Arabia in the south [22,[95][96][97][98][99][100][101][102][103][104][105][106][107][108][109][110][111]. In mainland Europe, P. ridibundus was repeatedly introduced to Italy [112,113], France [114], Switzerland [115], Belgium [116,117], and Russia [22,118] (Figure 11). ...

Balancing a Cline by Influx of Migrants: A Genetic Transition in Water Frogs of Eastern Greece

Journal of Heredity