
Citation: | Peiqi LIU, Feng LI, Huidong SONG, Qiang WANG, Yuwen SONG, Yusen LIU, Zhengji PIAO. 2010: A survey to the distribution of the Scaly-sided Merganser (Mergus squamatus) in Changbai Mountain range (China side). Avian Research, 1(2): 148-155. DOI: 10.5122/cbirds.2010.0008 |
In 2008 and 2009, we made continuous and repeated breeding surveys of the Scaly-sided Merganser (Mergus squamatus) in the Changbai Mountain range (China side), using a combination of rubber-boat drifting and walking. Each survey consisted of a census of breeding pairs in the spring and broods in the summer. A total of 1553 km in length of 17 river stretches were surveyed in four different river systems of the Yalujiang, Songhuajiang, Tumenjiang and Mudanjiang rivers. A total of 1354 individuals of the Scaly-sided Merganser were recorded during the both surveys. The breeding density for all the stretches surveyed over both years averaged 0.26 ±0.30 pairs per km; the population density in the spring averaged 0.75 ±0.88 individuals per km. According to our survey results, we estimated that the breeding population in the Changbai Mountain range was about 170 breeding pairs of the Scaly-sided Merganser. Three major breeding sites of this bird were found in the Changbai Mountain range in these surveys.
The brood parasitic Common Cuckoos (hereafter "Cuckoo"; Cuculus canorus) lay eggs into nests of other bird species, and the Cuckoo chick evicts all nest contents, eggs or nestlings, after hatching, typically causing the failure of all host offspring. This represents a high cost of parasitism for the hosts (Davies, 2000; Kilner, 2006). However, future prospects of the cuckoo eggs depend on host egg recognition and their decision on egg discrimination. Hosts may possess the ability to recognize and reject the parasite egg (Davies and Brooke, 1989; Moksnes et al., 1991; Hauber and Sherman, 2001), so natural selection favors the development of mimetic foreign eggs (Davies, 2000). Mimicry of the parasites' eggs in relation to host eggs may reach high levels in some populations (Moksnes and Røskaft, 1995; Igic et al., 2012).
Acrocephalus warblers are favored hosts of the cuckoo in the Palearctic (Johnsgard, 1997; Payne, 2005; Leisler and Schulze-Hagen, 2011). In East-Central Europe the Great Reed Warbler (Acrocephalus arundinaceus) is a frequently used host (e.g. Moksnes et al., 1993; Moskát and Honza, 2000, 2002; Trnka and Prokop, 2011). In Hungary, parasitism rate reaches an unusually high level (41–68%; Moskát et al., 2008b), instead of the typical 1–10% (Davies, 2000). In this area mimicry of the Cuckoo eggs in relation to host eggs often shows a high degree (Southern, 1954; Moskát and Honza, 2002; Cherry et al., 2007a). As the size of a Cuckoo egg is similar to the size of a Great Reed Warbler egg (e.g., Hargitai et al., 2010), the recognition of a Cuckoo egg sometimes needs special caution for the human observer (but the result is almost 100%; C. Moskát, unpubl.). However, the recognition of the Cuckoo eggs seems to be more difficult for Great Reed Warblers than for human observers: they accepted 66% of the Cuckoo eggs, and rejected the rest by egg ejection (12%), nest desertion (20%) and egg burial (2%) (Moskát and Honza, 2002). The typically good, sometimes perfect mimicry of the Cuckoo eggs are regarded as the result of the coevolutionary process between hosts and brood parasites (Brooke and Davies, 1988; see for reviews in Davies, 2000, 2011; Krüger, 2007). Cuckoo hosts discriminate against poorly matching parasitic eggs (Davies and Brooke, 1988; Moskát and Honza, 2002; Cherry et al., 2007a; Yang et al., 2010; Vikan et al., 2011). Consequently, parasite egg mimicry is expected to be increasing over time (Takasu, 1998).
In Japan, Common Cuckoos also parasitize a closelyrelated Acrocephalus species, the Oriental Reed Warbler (Acrocephalus orientalis), which previously was not separated from the Great Reed Warbler, but regarded as one of its subspecies (A. arundinaceus orientalis). Oriental Reed Warblers are also parasitized in a relatively high frequency (8–22%; Lotem et al., 1995), but lower than Great Reed Warblers in Hungary (see above). The Japanese population of Oriental Reed Warblers at Nagano City also showed antiparasite defenses against Cuckoo eggs, where different studies revealed 62% (Lotem et al., 1995) or 45% rejection rates towards Cuckoo eggs (Nakamura et al., 1998).
Rejection of parasite eggs by hosts is an important indicator of host adaptations to cuckoo parasitism (Davies and Brooke, 1989; Moksnes et al., 1991; Lovászi and Moskát, 2004; Stokke et al., 2005), as well as to other brood parasites (e.g., Davies 2000; Begum et al. 2011; de la Colina et al., 2012). Most of previous studies used model Cuckoo eggs in experimental parasitism, for studying egg rejection behavior of hosts (reviews in Davies, 2000; Kilner, 2006; Krüger, 2007). Much fewer studies have revealed egg discrimination of hosts against naturally parasitized Cuckoo eggs, typically in Acrocephalus warblers (e.g., Davies and Brooke, 1988; Lotem et al., 1992; Moksnes et al., 1993; Moskát and Honza, 2002; Cherry et al., 2007a; Honza et al., 2011). As vision of many bird species covers a wider range of reflectance spectra (300–700 nm) than that of humans (Bennett and Cuthill, 1994), UV-VIS spectrophotometers have proved to be most useful to evaluate egg mimicry (Cherry et al., 2007a).
As both the Japanese and the Hungarian populations of the above-mentioned Acrocephalus hosts show moderately developed antiparasite defenses, it may be a reflection of that both the host and brood parasite populations have been in contact with each other. Although the two populations of the two studied warblers may be different in their evolutionary history, including their coevolution with the Cuckoo, this case offers a unique situation for the comparison of egg mimicry and antiparasite defense in two distant areas. Hostbrood parasite coevolution might take several alternative directions regarding egg appearances in time and space (Dawkins and Krebs, 1979; Rothstein, 1990), while still maintaining the adaptive value of egg coloration (Underwood and Sealy, 2002; Kilner, 2006). Although brood parasitism is a dominant selective agent forcing the development of Cuckoo egg characteristics (Stokke et al., 2002; Kilner, 2006), we have no previous knowledge if hosts and brood parasites follow the same scenario in their coevolution at two distant sites. However, modeling coevolution has revealed several alternative potential pathways for Cuckoos and their hosts (Takasu, 1998, 2003; Barabás et al., 2004; Røskaft et al., 2006; Takasu and Moskát, 2011).
In this paper, we compared main characteristics of Cuckoo parasitism on two relatively large-sized Acrocephalus species in Japan and Hungary. We analyzed spectrophotometric data by visual models taking into account the sensitivity to different wavelengths of the four cone types in the avian retina (Endler and Milke, 2005). This method let us incorporate the effects of avian perceptual properties as it has recently been applied and recommended for the comparison of color attributes of Cuckoo and host eggs (e.g., Cassey et al., 2008; Avilés, 2008; Langmore et al., 2009; Antonov et al., 2010; Stoddard and Stevens, 2010; Vikan et al., 2011). Following the idea of the arms race hypothesis (Dawkins and Krebs, 1979; Davies, 2000; Krüger, 2007) applied for the coevolution between the Cuckoo and its hosts, we predicted that Cuckoos developed adaptations to host rejection by developing mimetic eggs in both areas. We also examined host responses to Cuckoo parasitism in the two distant areas, and predicted higher similarities between accepted eggs and lower similarities between eggs which were rejected. Finally, we predicted that the Cuckoo egg mimicry and host egg rejection behavior are similar in the two areas, indicating a similar level of coevolutionary adaptations.
The study was carried out at two sites: (1) Nobeyama highlands (35°57'N, 138°28'E), ca. 120 km south of Nagano city, central Japan. In this area Oriental Reed Warblers breed in small patches of reeds (Phragmites australis and Miscanthus sacchariflorus) along small (1–2 m wide) streams, and reed patches are surrounded by wooded vegetation composed primarily of maple trees (Acer ginnala) and willow bushes (Salix integra). The study was conducted during May–July 2004. (For more details of the habitat, see Muñoz et al., 2007). (2) In the surroundings of Apaj (47°07'N, 19°06'E), ca. 50 km south of Budapest in the Hungarian Great Plains, central Hungary. Here Great Reed Warblers breed in 2–4 m wide stripes of reed (Phragmites australis) growing along both sides of small (5–10 m wide) channels. Lines of trees (hybrid poplars, Populus alba, Salix cinerea, Elaeagnus angustifolia) and bushes typically follow the channels, although treeless sections also occur. (For more details of the habitat, see Moskát and Honza, 2000, 2002). Only those nests containing one Cuckoo egg and at least one host egg, and if the hosts' response to parasitism was known, were used for analyses.
We systematically searched for nests in parts of the study area ca. twice per week. Nests in the egg laying stage were controlled daily. Nests parasitized by a Cuckoo were controlled for six consecutive days to observe host reactions, and used to categorize host responses to parasitism. This 6-day (or 5-day) long period for monitoring hosts' reactions is typically used in studies of natural Cuckoo parasitism (e.g., Lotem et al., 1995; Moskát and Honza, 2002) and experiments with model Cuckoo eggs (e.g., Moksnes et al., 1991; Bártol et al., 2002). Host responses were categorized as acceptance or rejection of the Cuckoo egg. The term rejections included egg ejections and nest desertions (see more details on the method of nest monitoring in Moskát and Honza, 2002).
Eggs were photographed using digital cameras (Olympus E-20 and Nikon CoolPix 995) on Kodak grey card with Kodak control color patches. We measured reflectance spectra (300–700 nm) from the eggshells by spectrophotometers type Ocean Optics USB 2000, which interval covers the range of the vision of small passerines (e.g., Bennett and Cuthill, 1994; Endler and Milke, 2005). All eggs were measured in a clutch, although not all clutches were measured by spectrophotometer, so sample sizes slightly differ for host responses and egg characteristics. We measured reflectances at eight points on the eggshell, i.e., two measurements at four zones of the eggs, dividing the eggshell surface into four equally long parts along the long axis (see for more details on measuring reflectances from eggs in Takasu et al., 2009). A conceptually similar method, when the eggshell surface is divided into segments along the long axis, was developed by Cherry and Bennett (2001).
For the evaluation of chromatic difference (∆TC) among Cuckoo and host eggs we applied the perceptual models developed for avian vision (Kelber et al., 2003; Endler and Milke, 2005). These models provide a useful way for the quantification of color difference between eggs as birds can see, with respects to the spectral sensitivities of the avian single cone photoreceptors in the retina (Vorobyev and Osorio, 1998). In birds the four single photoreceptors are sensitive to certain parts of the whole spectra within 300 and 700 nm, called ultraviolet, short-wavelength, medium-wavelength and long-wavelength (Hart et al., 2000). In comparison of color differences between Common Cuckoo and host eggs these models have already been useful (e.g., Avilés, 2008; Cassey et al., 2008; Antonov et al., 2010; Vikan et al., 2011), and also for other brood parasite-host relationships (Langmore et al., 2009; Spottiswoode and Stevens, 2010). We used the "woodland canopy-filtered green light" (also called "green leaves"; Endler, 1993) and "open nest" (Avilés, 2008) ambient light conditions for ambient irradiance in the perceptual models, as Acrocephalus warblers typically breed in open nests in the reeds, in the shade of long reed leaves. We also calculated achromatic contrast (∆TQ) expressing brightness differences between Cuckoo and host eggs. Chromatic and achromatic differences are expressed in just noticeable difference thresholds (JNDs), where a value above the JND = 1 threshold suggests that the cuckoo egg can be discriminated from the host eggs, but a value below this threshold suggests that the parasitic egg is undistinguishable (Osorio and Vorobyev, 1996, see for more details in Avilés, 2008 and Igic et al., 2012). For visual modeling we used Avicol version 4 (Gomez, 2010).
In the present study we focused on the importance of chromatic and achromatic components of eggshell characteristics in coevolution between brood parasites and their hosts, but spottiness may also have some relevance (Polaciková and Grim, 2010). However, the fiber optic probe of our spectrophotometer only allows samples from larger spots, only > 2 mm in diameter, which is not suitable for speckles or lines. Experimental studies on the Hungarian Great Reed Warbler population has shown that small spots may be important in egg recognition (Moskát et al., 2008a), but the role of larger spots is not so clear (Moskát et al., 2008c).
We used generalized linear models to test the dependent variable (acceptance versus rejection), involving intercept, country as independent fixed factor, chromatic difference (∆TC), and achromatic difference (∆TQ) as covariates. We also involved the interaction terms chromatic difference×country and achromatic difference ×country. Data were analyzed with SPSS version 17.0 (SPSS, Inc.). We applied the Levene's test for testing homogeneity of variances prior to parametric tests.
Some of the Cuckoo eggs found in Hungary showed a good mimicry to host eggs, while in general mimicry was lower in Japan (Fig. 1). Although the main characteristics of host eggs were similar in Japan and Hungary, Cuckoos in Japan often showed red markings, sometimes with the special line pattern (Fig. 1). Visual modeling on spectrophotometer measurements revealed that chromatic difference between Cuckoo and host eggs was lower in Hungary than in Japan, whereas the achromatic difference showed the opposite trend (Fig. 2; open nest ambient light conditions, Mann-Whitney U-tests were significant for both the chromatic and achromatic cases: U = 100.00, p = 0.049). The values of chromatic difference did not differ significantly from the just noticeable difference threshold (JND = 1) (ones-sample t-test, t17 = 0.910, p = 0.375) in Hungary, which means that Cuckoo eggs are more difficult to recognize in Hungary than in Japan, where chromatic difference exceeded the threshold significantly (t17 = 2.948, p = 0.009). However, the achromatic difference between parasite and host eggs did not differ from the threshold in Japan (two-sample t-test, t17 = 0.867, p = 0.398), but it was significantly different in Hungary (t17 = 3.244, p = 0.005). We found similar results when the green ambient light conditions was used for calculation (Hungary: chromatic contrast: t17 = 0.505, p = 0.620, achromatic contrast: t17 = 3.246, p = 0.005; Japan: chromatic contrast: t17 = 2.461, p = 0.025, achromatic contrast: t17 = 0.887, p = 0.388).
We observed host reactions toward Cuckoo eggs in 37 nests. Rejection rates against single Cuckoo eggs were similar at the two sites (7/19 in Hungary and 7/18 in Japan; Fig. 3; χ12 = 0.02, p = 0.898). Parasitism rate was higher in Hungary than in Japan (28/46 nests, i.e., 61% parasitism rate in Hungary and 22/57 nests, i.e., 39% in Japan in 2004), however, the difference was not statistically significant (χ12 = 1.73; p = 0.188).
Generalized linear models on egg characteristics of the two Acrocephalus species revealed no direct effect of chromatic and achromatic difference between host and parasite eggs on the rejection of Cuckoo eggs. However, we revealed significant effects of country and the term of interaction between country and achromatic distance (∆TQ) in the generalized linear model, while achromatic distance without the interaction term proved not to be significant (country: χ2 = 3.90, p = 0.048; ∆TC: χ2 = 0.24, p = 0.628; ∆TQ: χ2 = 3.31, p = 0.069; country×∆TC: χ2 = 0.41, p = 0.524; country×∆TQ: χ2 = 5.90, p = 0.015; intercept: χ2 = 0.04, p = 0.853).
Regarding eggshell colors, our analyses revealed a higher similarity of Cuckoo eggs with respect to host eggs in Hungary than in Japan. It is an important indicator of coevolutionary adaptations, as mimicry of Cuckoo eggs is expected to increase over time during Cuckoo parasitism (see review by Davies, 2000). Although exact time when Cuckoo parasitism started is not known, neither for the Great Reed Warbler in Hungary, nor the Oriental Reed Warbler in Japan, circumstantial evidence suggests that the history of these coevolutionary interactions reflects a longer history in the Western Palearctic than in the Eastern Palearctic. Recent Cuckoo parasitism is estimated for more than 110 years in Hungary, since parasitized Great Reed Warbler clutches with Cuckoo eggs were already collected ca. 110 years ago and stored in museums (C. Moskát unpubl.). Cuckoo parasitism started ca. 50 years ago in the Nobeyama district, but probably it started earlier in other parts of Japan (Nakamura, 1990). In Hungary, Cuckoos have developed almost perfect mimicry regarding background and spot colors and spottiness of eggs, but not in egg shape (Bán et al., 2011). On the one hand, high interclutch variation of hosts makes it more difficult for the Cuckoo to match the host eggs even when Cuckoo eggs show perfect mimesis to one type of Great Reed Warbler eggs (Moskát and Honza, 2002). On the other hand Cuckoos selecting actively for proper nests may increase their success of matching (Cherry et al., 2007b; see also Avilés et al., 2006).
Cuckoo eggs in the Hungarian study area are found to be polymorphic (Moskát and Honza, 2002), therefore, even cuckoo eggs showing poor mimesis to host eggs can be found in the area. For example, one poorly mimetic egg type, the so-called Garden Warbler (Sylvia borin)-type Cuckoo egg was also found in the study area, which seems to be a generalist Cuckoo egg-type in central Europe (Lovászi and Moskát, 2004). This egg type has also been reported from the Czech Republic (Edvardsen et al., 2001; Honza et al., 2001). Interestingly, the Garden Warbler-type Cuckoo egg morph found in Hungary had a high similarity with Garden Warbler eggs from Germany, but this egg morph is different from Garden Warbler eggs in Hungary (C. Moskát, unpubl.). In the 1920s a system of flood relief and irrigation channels was established in Hungary, offering a preferable habitat with narrow reed beds along both sides of the channels. This habitat offered the open water surface-reed edge for birds, which is favored by Great Reed Warblers (Báldi and Kisbenedek, 2000). Although in the Hungarian Great Plains wetland habitats dominated originally, they were lost gradually. However, extensive work to control rivers' flood during the second half of the 19th century made numerous dead branches, especially suitable habitats for the Great Reed Warbler (Molnár, 1944). We therefore suppose that Cuckoos started to parasitize this warbler extensively in the dead branches, and, later, in the channels depending on the availability of trees used for vantage points by nest searching Cuckoos (Moskát and Honza, 2000). The possible origin of recent Cuckoo parasitism on the Great Reed Warbler was the parasitism on several Acrocephalus species, including the Great Reed Warbler, Reed Warbler (A. scirpaceus), Sedge Warbler (A. schoenobaenus) and Marsh Warbler (A. palustris), because parasitized clutches of these species can be found from the first half of the 20th century in Hungarian bird egg collections (C. Moskát, unpubl.). However, recent parasitism on these three smaller Acrocephalus species seems to be scarce (C. Moskát, unpubl.).
In Japan the different Cuckoo gentes are less separated than in Europe (Higuchi, 1998; Nakamura et al., 1998). The Bunting-type Cuckoo eggs seem to be the ancient form, and probably Cuckoos of several host species radiated from this gens (c.f. Nakamura et al., 1998; Takasu et al., 2009). Although the Siberian Meadow Bunting (Emberiza cioides) used to be the most Common Cuckoo host in the first half of the 20th century (Nakamura et al., 1998), it is presently almost abandoned by Cuckoos. This host species developed high level egg discrimination ability, and, consequently, Cuckoos expanded the number of their hosts. Many Cuckoo eggs exhibit small lines as pigments on the eggshell (Nakamura et al., 1998; Takasu et al., 2009), which is not typical for European Cuckoos. In our study area at Nobeyama, in central Japan, four host species are frequently parasitized by Cuckoos: Black-faced Buntings (E. spodocephala), Bull-headed Shrikes (Lanius bucephalus), Azure-winged Magpies (Cyanopica cyana) and Oriental Reed Warblers. Cuckoo eggs parasitizing these four host species seem to be similar, but some early separation was revealed by a recent spectrophotometer study (Takasu et al., 2009). The bunting-type Cuckoo egg morph matches well the eggs of Bull-headed Shrikes, but it is non-mimetic for the Azure-winged Magpie and Oriental Reed Warbler. So the Japan Cuckoo-host relationship is a sympatric multihost system, as Cuckoos parasitize several host species at the same location. Although these hosts prefer different habitats, the imperfect isolation of these host populations from each other slows down adaptational mechanisms (sensu Møller et al., 2011). The presence of lines as egg markings on Cuckoo eggs in Japan is unique when compared either to Cuckoo eggs in Hungary, or any of the studied Acrocephalus hosts (Fig. 1). This special marking on Cuckoo eggs may also reduce mimicry between Oriental Reed Warbler and Cuckoo eggs. Contrary, in the Hungarian Great Plane Cuckoos parasitize only one dominant host species, the Great Reed Warbler. There is another frequently used host species in Hungary, the Robin (Erithacus rubecula), which shows a strong separation from Great Reed Warblers by habitat, as Robins occur in the woodlands of hilly areas (Fuisz and de Kort, 2007).
Rejection rates in the two Acrocephalus Warbler populations proved to be highly similar, despite the differences in Cuckoo egg mimicry. This finding suggests that coevolutionary mechanisms, i.e., hosts' antiparasite defences, and Cuckoos' counter-adaptations to hosts by mimetic eggs may have different speed. Thus coevolutionary interactions are probably less synchronized than predicted by the arms race model (Dawkins and Krebs 1979; Davies 2000; Krüger 2007). This might be due to hosts' immigration from nearby, highly productive, probably unparasitized or less parasitized source populations in a metapopulation structure (Barabás et al., 2004). Immigration of hosts with less developed antiparasite defense might result in reduced egg discrimination ability in the Hungarian study area. This process might explain the similar level of egg rejection in Japan and Hungary, even though, the Hungarian Cuckoo-Great Reed Warbler system is more developed, as indicated by the higher level of mimesis of Cuckoo eggs here.
A previous study on the Oriental Reed Warbler in Nagano district, Japan (ca. 120 km away from our study www.chinesebirds.net site in Nobeyama district) revealed an even higher rejection rate than our study revealed (62% vs 39%) towards natural Cuckoo eggs between 1989 and 1991 (Lotem et al., 1995). The population in Nagano district started to be parasitized only 30 years ago, so it is likely that some parts of egg discrimination is the result of a former interaction with the Cuckoo, or due to gene flow from other areas (Lotem et al., 1995).
Our results revealed similar efficiency in egg rejection behavior of the two Acrocephalus studied hosts, which can be regarded as one of the most important indicators of hosts' evolutionary adaptation to brood parasitism. On the other hand, we also revealed better mimicry of Cuckoo eggs to host eggs in Hungary than in Japan. The origin of Cuckoo parasitism on the Great Reed Warbler in Hungary differs from that of the Oriental Reed Warbler in Japan. While Cuckoos might have radiated from the Bunting Cuckoo-gens in Japan, in Hungary the Great Reed Warbler-Cuckoo gens probably originated from the Acrocephalus group. It is a surprising result that Japanese Cuckoos show low level mimicry to Oriental Reed Warbler eggs, although this warbler species possess a moderate egg rejection ability. Theoretically, in such type of systems better parasite egg mimicry is expected, as simulation models have revealed (Takasu, 2003). There are two possible explanations for this interesting result. At one hand there is a multihost system in central Japan, which might slow down separation of Cuckoos into distinct gentes (c.f. Higuchi, 1998; Nakamura et al., 1998). Takasu (2003) showed by simulation models, if the host population is polymorphic regarding egg morphs, this might prevent Cuckoos to develop a better mimicry.
Host aggression against the Cuckoo may also be evolved during sympatry with the brood parasite, and typically coevolves with egg rejection ability (Røskaft et al., 2002). As hosts breed in similar habitats in our two study sites, we think that host defense plays the most important role in Cuckoo-host coevolutions in these cases. In Hungary Great Reed Warblers show high aggression against the Cuckoo (85% attack, n = 40; Bártol et al., 2002), but Oriental Reed Warblers attacked Cuckoos at a lower frequency (38%; Andou et al., 2005). However, sample size in the Japanese study was low (n = 8).
We conclude that despite of the dissimilar features of Cuckoo-Warbler coevolution in Japan and Hungary, including possible different origins of parasitism and levels of parasitic pressure, Cuckoos showed adaptations to host eggs at varying degrees of egg mimicry, and hosts developed egg discrimination behavior against Cuckoo eggs. Hosts' egg discrimination proved to be very similar in the two host-brood parasite systems, although the pattern of egg mimicry is clearly different. Our results suggest that Cuckoos and Warblers followed different pathways of coevolution in the two distant areas, and they seem to be at different stages in the arms race.
The authors are thankful to Tibor Kisbenedek, László Bagó, István Bártol and Kinga Iglói for their assistance in the field work. For discussions we thank Maria Altamirano, Michael I. Cherry, Marcel Honza, Rita Hargitai, Branislav Igic and many other colleagues. We thank two anonymous reviewers and the guest editors for helpful comments on our manuscript. The study was supported by the bilateral project of the Japan Society for the Promotion of Science (JSPS) and the Hungarian Academy of Sciences to F.T. and C.M. 2003-2005, and by the Hungarian Scientific Research Fund (OTKA; grant No. T35015, 48397 and 83217) to C.M. The Duna-Ipoly and Kiskunság National Parks provided permissions for research.
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