When data are limited it is difficult for conservation managers to assess alternative management scenarios and make decisions. The natterjack toad (Bufo calamita) is declining at the edges of its distribution range in Europe and little is known about its current distribution and abundance in Poland. Although different landscape management plans for central Poland exist, it is unclear to what extent they impact this species. Based on these plans, we investigated how four alternative landscape development scenarios would affect the total carrying capacity and population dynamics of the natterjack toad. To facilitate decision-making, we first ranked the scenarios according to their total carrying capacity. We used the software RAMAS GIS to determine the size and location of habitat patches in the landscape. The estimated carrying capacities were very similar for each scenario, and clear ranking was not possible. Only the reforestation scenario showed a marked loss in carrying capacity. We therefore simulated metapopulation dynamics with RAMAS taking into account dynamical processes such as reproduction and dispersal and ranked the scenarios according to the resulting species abundance. In this case, we could clearly rank the development scenarios. We identified road mortality of adults as a key process governing the dynamics and separating the different scenarios. The renaturalisation scenario clearly ranked highest due to its decreased road mortality. Taken together our results suggest that road infrastructure development might be much more important for natterjack toad conservation than changes in the amount of habitat in the semi-natural river valley. We gained these insights by considering both the resulting metapopulation structure and dynamics in the form of a PVA. We conclude that the consideration of dynamic processes in amphibian conservation management may be indispensable for ranking management scenarios.
Citation: Franz KW, Romanowski J, Johst K, Grimm V (2013) Ranking Landscape Development Scenarios Affecting Natterjack Toad (Bufo calamita) Population Dynamics in Central Poland. PLoS ONE 8(5): e64852. https://doi.org/10.1371/journal.pone.0064852
Editor: Christopher Joseph Salice, Texas Tech University, United States of America
Received: January 4, 2013; Accepted: April 18, 2013; Published: May 29, 2013
Copyright: © 2013 Franz et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The authors have no support or funding to report.
Competing interests: The authors have declared that no competing interests exist.
Due to human impact many species are threatened with extinction. The main goals of conservation biology are to identify which species are endangered, which factors drive species to extinction and to develop strategies to prevent extinctions. Because of the scale and speed of species extinctions conservationists require methods that facilitate decision making in the light of scarce data. Important tools often used by policy makers include habitat models  and population viability analysis (PVA) which are used to assess threats and to identify the most suitable management scenarios for a given species . However, it is often challenging to decide which tool is most appropriate for a particular problem and to what extent the ranking of management scenarios depends on the choice of the tool. In this study, we therefore contrast scenario ranking resulting from habitat modelling with that from population dynamic modelling.
We addressed this issue by focusing on the impact of real landscape management scenarios on the Natterjack toad (Bufo calamita Laurenti, 1768) in Poland. This more applied approach allowed us to examine possible conservation implications for amphibian species in general and for natterjack toads in particular. Amphibians belong to the most vulnerable class of vertebrates, with 32% of all known species under threat , . Multiple causes of the decline have been identified, including habitat loss and fragmentation –, climate change  as well as chytrid fungus (Batrachochytrium dendrobatidis) . Natterjack toads have been shown to suffer from all the above mentioned factors (e.g. , ). However, information on the distribution and demography of the natterjack toad in Poland is extremely sparse. Collecting such data, especially for species with cryptic life stages and wide population fluctuations can be very costly and time consuming .
This lack of systematic field studies makes it difficult to assess the population status and prospects of the Natterjack toad. In particular, it is challenging to identify specific threats to population viability and to assess alternative management scenarios for species protection. There are very few conclusive studies on the impact of road-crossing mortality on dynamics of amphibian populations  so we gave special attention to the impact of road mortality on natterjack toad populations. Therefore, we additionally investigated if this problem could be addressed by a modeling approach. Based on the case study of natterjack toad, we show that despite sparse local data, a meaningful ranking of management scenarios is possible by combining landscape information and a population viability analysis, which can be based on demographic parameters extracted from the literature.
Due to increased human pressure, our study region is rapidly undergoing changes in land use and spatial development. The impact of possible landscape development scenarios on biodiversity was addressed by the project VEDI ,  and a multi-stakeholder planning approach was followed. Multiple species were considered using the generic habitat modelling software tool LARCH, which allows the identification of “key patches” (large patches with a stabilising role in habitat networks, ). However, in the multiple species approach single species were represented rather coarsely based on the local experts’ knowledge, and population dynamics were ignored altogether. Therefore, here we augment existing assessments of management scenarios by extending the original expert model approach (LARCH) by a population viability analysis (PVA) of a single species – the natterjack toad, using the software tool RAMAS GIS .
We did not aim to precisely predict current or future population sizes and patch occupancy. Instead our aim was to assess and compare four alternative management scenarios concerning their suitability for natterjack toad protection. We tried to find a solution to the common problem that in the face of rapid landscape changes a decision about landscape development has to be made within limited time and resources. Such a situation might favor the use of simple habitat modelling over the more data demanding PVA. However, we will show that reliable ranking of management scenarios may require consideration of dynamics processes by a PVA instead of focusing on the habitat amount alone. We will show that this is possible even if data on these processes are scarce.
Materials and Methods
The Study Area
The study area is characteristic of the Vistula River and many other central European lowland rivers with the valleys formed during the Pleistocene glacial periods. It covers a 135 km long section of the valley from Warsaw to Włocławek in central Poland with an area of about 1 545 km2 (Figure 1a). The river is only partially transformed by the Włocławek Dam Reservoir located in the lower course of the study area. Segments of the river show a braided pattern with many islands and sandy bars. Flood-control embankments (protective dikes) constructed at distances up to several hundred metres from the main channel limit the inundated area. The area between the dikes is covered by diverse, semi-natural vegetation: permanent meadows, shrubs and riparian forests. Floodplains contain a network of diverse aquatic sites with numerous meanders, former channels and oxbows of various sizes. The study area represents a landscape of low intensity use, with a high nature value and a high level of biodiversity . Management in the valley predominantly involves agriculture: arable lands, gardens and orchards cover 33% of the area, grasslands (mostly meadows of low intensity use) cover 17%, and forests cover 34% . Approximately one third of the study area is protected by 20 small nature reserves, Gostynin-Włocławek landscape park (390 km2), and Kampinos National Park (385 km2). Two areas were included in the NATURA 2000 Network: the Middle Vistula Valley (SPA Pl083) and Kampinos Forest (SPA Pl084 and SAC 158) (Figure 1a).
(A) Study area of the Vistula river valley in central Poland. Optimal habitat for the natterjack toad is marked green and suboptimal habitat is marked brown. Location of the study plots is marked: A – “Brzozówka”, B – “Sadowa”, C – Kępa Kiełpińska”. (B) Metapopulation structure for no change scenario. Sizes and colours of circles indicate sizes of populations (numbers of individuals).
Potential threats and expected or possible management strategies identified for the study area were represented in several scenarios that were developed in consultation with various stakeholders . Detailed maps were prepared for these scenarios, delineating potential changes in vegetation, hydro-technical regulation of the Vistula River, and the network of roads in the study area. For our analysis we considered the following four management scenarios as opposed to the “no change” scenario illustrating present conditions in the study area , . In addition to the general characteristics described below, these scenarios differ regarding the amount of specific habitat and landscape elements relevant for B. calamita as well as several demographic rates used in the model, which are summarised in Table 1 and Tables S1a and S1b.
The objective of this scenario is to increase economic efficiency in transport and energy production. This scenario is characterised by maximal river regulation and the development of infrastructure. Main elements are the construction of two new dams, removal of all trees in the area constrained by the dikes, and development of other infrastructures such as roads, dikes, motorways etc. Construction of new dams and reservoirs in Wyszogród and Płock will cause disturbance of wildlife movement. Flooding the area between the dikes and in the lower and upper course of the river will result in disappearance of several nature reserves in the area and changes in the plant communities (e.g. reduction of willow-poplar alluvial forests). Construction of an intensive road and railway network will form often impassable barriers for dispersal of many animal species.
This scenario is characterised by conversion of low-productivity agricultural fields into forest plantations and natural pine forest succession. The Programme of Rural Areas Development fund is designed for afforestation of areas which are not state property including agricultural areas in Kampinos National Park. Afforestation is planned in areas which are least suited to intensive agriculture (arable lands, meadows, and pastures), while reforestation is planned for wastelands in pine forests, mixed oak-pine forests and willow-poplar alluvial forests. Planned changes are also connected to transformations of forest age classes, e.g., a pine thicket evolves into a stick stand and then into an undefined pine forest. Willow plantations will be limited to the floodplain, which is the natural habitat of willow shrubs.
This scenario presents only moderate changes to present conditions. The main issue addressed here is the abandonment of mowing and grazing practices due to habitat fragmentation and sale of the land to non-farmers. Therefore the main objective is to restore and protect the biodiversity of grasslands by supporting the small-scale farming and traditional grazing through the implementation of agro-environmental programmes. Such programmes will focus on areas of low intensity use of meadows (mown once or twice) and of lowland pastures spread over most of the study area except for the Kampinos National Park. The aim is the preservation of existing grasslands and maintainance of the existing mosaic of grasslands, arable lands, gardens and orchards as a profitable form of land-use for farmers. It is expected to convert ruderal vegetation (by mowing) to more valuable grassland.
This scenario is, from the conservation biologists’ point of view, a “brave vision” for Vistula valley renaturalisation aiming to restore the natural river with minimal anthropogenic impact. Its main elements include the elimination of road impacts by constructing fauna passages on existing roads, removing some of the dikes (where possible), dismantling the present dam at Włocławek, removal of some of the settlements in the river valley, and enhancement of natural succession within the floodplain. Removal of dikes along the river will result in a higher probability of flooding and in a higher risk of grain production leading to a reduction of arable fields. Decreasing the height of the Włocławek dam and protecting the banks against surface erosion will result in changes to the water flow regime in the region, requiring technical modifications of river banks. As a result new islets and sandy areas within the riverbed will be formed; also previously flooded areas will be uncovered. Promotion of meadows, pastures, and natural succession processes in the Vistula valley will result in a reduction of arable lands.
Field observations of breeding amphibians were conducted in three plots (“Brzozówka” −10.5 km2, “Sadowa” −6 km2, “Kępa Kiełpińska” −18 km2) in the eastern part of the study area from April to June in 2005, 2007 and 2008 (Figure 1a). Natterjack toads were present at two study plots: “Kępa Kiełpińska” (one observation in 2005) and “Brzozówka” (22 observations in 2005, 25 in 2007, 21 in 2008). All breeding habitats of natterjack toads were recorded in agricultural areas, mostly low intensity use meadows. The parameterisation of the metapopulation model was based on landscape and vegetation characteristics of these sites and additional data on natterjack toad occurrence in the study area  as well as unpublished data from several zoologists (see Acknowledgments and Tables S1a and S1b).
We used digital maps presenting detailed actual vegetation at a scale of 1∶25000 . At the landscape scale, pond presence is associated with specific meadow and pasture communities. Within these communities, four complexes were identified: (1) wet marsh marigold (Caltha palustris) meadows and (2) rich pastures with Cynosurus as optimal breeding sites, (3) oat-grass (Arrhenatherum) meadows, and (4) complexes of segetal communities on poor habitats as suboptimal breeding sites . However, estimating the potential presence of the species should include not only the breeding habitat but also the availability of wintering habitat in the vicinity –. Juvenile indefinite pine forest, pine thicket and juvenile pine-birch forest (commonly associated with sandy hills in the study area) were defined as natterjack wintering habitats ,  (Table 1).
Only suitable breeding habitats that were located no further than 500 m away from a wintering habitat ,  were selected and defined as separate layers for each scenario in ArcView3.3 and Spatial Analyst 2.0 , . For each layer a single ASCII grid map was created (250 m cell size grids). To obtain the patch structure, maps were analysed in the generic PVA software RAMAS GIS 5.0 , where values were assigned for optimal and suboptimal habitat (1 and 0.5 respectively; ). All cells in the distance of 6.5 cells (cell size 250×250 m) belonged to one patch (within migratory range reported by ). Multiplying habitat suitability value by maximum density of 50 individuals per km2  defined the carrying capacity of each patch which corresponds to the initial conditions of the metapopulation model (Table S1a).
To obtain detailed demographic parameters we conducted a broad review of the existing literature on natterjack toad. To assess the different development scenarios, we determined mean metapopulation abundances and extinction probabilities after 100 years from 1 000 simulation runs.
Within RAMAS GIS, we created an age- and sex-structured stochastic model with seven age classes for both males and females, corresponding to the maximum reproduction age assumed in the model , , . In our model, individuals of both sexes are able to reproduce throughout their adult life starting in the 3rd year of life , , , –. The mating system was set to polygynous with a maximum number of three males per breeding female . The sex ratio (F:M) was set to 1∶1.3; females produce 2.3 new females and three males  with a breeding success of 90% (number of females breeding each year; . It is known that juveniles do not come back to the breeding sites until they reach maturity . Therefore we included density dependence in the form of ceiling carrying capacity only for adult individuals  (Table S1a).
To estimate adult survival rates we used the annual mortality values reported in Germany by Stephan et al.  for medium weather conditions, assuming that breeding males’ survival rates are reduced by 5% to account for the higher vulnerability to predation during mating season . Road infrastructure has been increasingly identified as a direct cause of mortality , , therefore to reflect the differences between scenarios (Table 1), in the infrastructure development scenario we assumed an additional road mortality of 6% affecting all adult individuals during their movement to and from breeding ponds , , . The changes assumed in the renaturalisation scenario (complete elimination of road impact) have the opposite effect on natterjack mortality rates (6% decrease) (Table S1b).
A mean dispersal distance of 2 km was used for the dispersal function , , . A maximum dispersal distance set to 10 km ,  combined with a dispersal proportion of 0.2 of all individuals ,  (Table S1a) allowed us to obtain dispersal rate between patches that were similar to those reported by Marsh and Trenham .
We changed, one after the other, each parameter value by ±20% compared to the standard values and recorded the resulting changes in carrying capacity and metapopulation structure. We choose these large parameter changes to make sure to capture the sensitivity of model predictions to the rather high uncertainty in model parameters. The price for this is that with such large changes, nonlinearities and interactions between parameters can mask differences in sensitivities of individual parameters. In our analyses, though, we saw no indication that this was the case for our model. To test the sensitivity of the scenario ranking, we used the simple outranking method (based on PROMETHEE ; described in detail by Drechsler et al., ). With this method, it is possible to determine how well the different rank orders produced by sensitivity analysis correspond with the single rank order from the original dataset. In this method ranking is done by comparing pairs of values to decide which of the two is preferred. All parameter combinations received equal weights and the preferred action receives one point. Next, the points are summed to obtain a total preference matrix containing sums of preference values for each pair of scenarios. These preference values equal the number of times one scenario ranked higher than the other scenario. Row sums measure how many times a target scenario was preferred compared to other scenarios and column sums indicate how often another scenario was preferred compared to the target scenario. Additionally to the general sensitivity analysis we investigated the impact of road mortality on the ranking of scenarios considering that there is particular uncertainty and potential sensitivity in this parameter.
Metapopulation Structure and Carrying Capacity
Natterjack toad habitats are distributed throughout the study area, with the biggest patches located in the area of the national park (Figure 1a and b). The habitat network is similar for all management scenarios, comprising mainly small habitat patches (Table 2). In the “no change” scenario the carrying capacity cumulated over all patches is estimated at 4 198 adults. In most other scenarios this value is very similar (Figure 2a). Only in the reforestation scenario carrying capacity decreased by about 15% compared to the “no change” scenario (Figure 2a).
(A) Estimated metapopulation carrying capacities of adult individuals for all management scenarios. Estimations were based on habitat suitability and population density. (B) Metapopulation dynamics-based estimations of minimum expected adults’ abundances for all scenarios.
Simulations of metapopulation dynamics revealed pronounced differences in minimum expected adults’ abundance (i.e., the average over all simulation runs of the smallest number of adults occurring within the simulated time period; ; Figure 2b) and final adults’ abundance (including indicator of variability, Figure S1d) among the alternative scenarios. The “no change” scenario predicted a minimum expected abundance of 1002 adult individuals similar to results from the grassland restoration scenario. The reforestation scenario showed noticeably lower values of minimum expected abundance. The renaturalisation scenario resulted in the highest natterjack toad abundance whereas the infrastructure development scenario resulted in an extremely low abundance (Figure 2b).
Sensitivity analysis of scenario ranking based on total carrying capacity (Figure 2a, Table 3) showed that changing the neighbourhood distance by +/−20% resulted in strong differences in metapopulation structure, especially in the number of small populations (Table S2). Changes (+/−20%) in the density affected both the metapopulation structure and the carrying capacity values (Tables S2 and S3). Sums of preference values for each pair of scenarios summed in rows (Sum+) indicated that the grassland restoration scenario was higher ranked in all 12 cases (Table 3). The reforestation scenario was ranked lowest. Infrastructure development was the second best scenario. The summed column values (Sum−) showed that other scenarios were always better than reforestation.
Sensitivity analysis of scenario ranking based on metapopulation dynamics confirmed the robustness of the obtained results (Figure 2b, Table 4). Results from parameter variation provided a preference matrix of metapopulation expected minimum abundance with a column for each scenario and a row for each tested value of the respective parameter (Table S4). The values of the row sums (Sum+) in total the preference matrix indicated that the renaturalisation scenario was preferred 92 out of 93 times (Table 4). The infrastructure development scenario was least preferred. Even though grassland restoration was ranked as the second best scenario, other scenarios were often considered better (1/3 of all cases).
Sensitivity analysis of road mortality demonstrated that a 2% change in mortality resulted in the same scenario ranking as the baseline road mortality of 6% (Figure S1).
Our study provides important conclusions regarding the conservation of the natterjack toad and the benefits of scenario ranking using the PVA approach. Taken together our results emphasise the value of species-specific PVA analyses. As illustrated by road mortality in our study, the metric carrying capacity alone is insufficient especially in situations where proposed management actions influence population dynamics. In the common situation where conservationists are confronted with scarce data, parameterisation of the PVA model for natterjack toad is an important result of our work. Following a detailed protocol , Tables S1a and S1b comprise a compilation of parameter values that can be useful for other scientists as well as for managers. These tables provide the data necessary to conduct similar analyses in other areas with similar environmental conditions.
Ranking the landscape development scenarios based on the total carrying capacity indicated that most of the proposed management scenarios would have a similar impact on natterjack toad as the “no change” scenario. Only the reforestration scenario showed a difference, specifically this scenario had the lowest estimated carrying capacity. Our results support an earlier analysis of the “no change” scenario . Current habitat conditions, mainly the presence of the national park, allow the preservation of the natterjack toad metapopulation in the study area. However, our study suggests a stronger impact of the infrastructure development scenario on the natterjack toad than former multi-species analyses where more pronounced differences among the alternative management scenarios’ effects were demonstrated for aquatic and forest species . However, habitat requirements of the natterjack toad are complex and coupling breeding habitat with wintering habitat resulted in reduced quantitative differences in carrying capacity. Instead of using existing pond locations as breeding habitat we used habitat in which pond presence is most likely. As mapping of breeding ponds would be possible only for present conditions, this approach allowed us to obtain metapopulation structure for all scenarios.
Ranking of the development scenarios based on metapopulation dynamics resulted in distinct differences among the scenarios. The infrastructure development scenario was the worst option for the conservation of the natterjack toad, and the best option was the renaturalisation scenario (Figure 2). The strong impact of roads on local toad population dynamics most likely explains why the infrastructure development scenario obtained the lowest score. The renaturalisation scenario was the best management option for natterjack toad conservation as eliminating this negative effect of roads (e.g. by providing animal passages) resulted in a high increase in the minimum expected abundance (Table S4). The similarity of the metapopulation dynamics between the grassland restoration and “no change” scenario was most likely caused by the highest resemblance of the management practices in those two scenarios.
Road infrastructure seen as a linear barrier would result in more fragmented metapopulation structure but would not lead to pronounced decrease in habitat availability per se. For amphibians, the most direct influence of roads in the landscape is the increase in mortality . Given their specific breeding behaviour, all pond-breeding amphibians, including natterjack toads, have a high mortality risk due to road crossing , . In both of these road-kill studies, natterjack toads were the most common species found among all amphibian and vertebrate species collected. The road-kill hotspots are usually located in suitable habitat patches on local roads with high traffic intensity ,  and many parts of our study area match such a description. The traffic intensity in the Vistula valley exceeds those of the studies mentioned above, reaching to 8000 vehicles per day on minor roads while the major roads reached 32000 vehicles per day in 2004. For several roads in the area the amount of vehicles per day was projected to double by 2010  and in years 2005–2010 increased on average by 22%. Therefore we might expect the amphibian mortalities to be even higher than the values assumed in this study. The analysis of uncertainty in road mortality showed that the scenario ranking did not change as long as there was at least a 2% change in mortality in the infrastructure development and renaturalisation scenarios (Figure S1).
Due to the uncertainty in the estimated road mortality, we do not expect that the PVA carried out in this study will enable accurate predictions of population viability. However, considering the dynamic effects of road mortality on population survival enables us to draw broader conclusions than simply that road mortality has a negative effect on population viability. Despite sparse local data, quantification of these effects and subsequent ranking of landscape development scenarios with different proportions of roadkill mortality is possible.
Considering changes in carrying capacities seems to be a straightforward way to assess changes in available habitat after landscape modifications. However, conservation decisions based upon habitat availability alone can be misleading because they do not include the consequences of demographic and stochastic processes such as dispersal, extinction of small populations, or strategies of habitat use. In particular for amphibians, estimates of carrying capacities provide only poor rankings of management scenarios because of the associated inability to include road mortality in a way that reflects specific habitat use.
Based on our findings we encourage conservation biologists and managers to: combine PVA and habitat modelling; choose appropriate tools that reflect the impact of planned landscape changes; rank and compare the impact of alternative management scenarios produced by PVA; and use real landscape data especially when the species is vulnerable to extinction due to habitat modifications.
Results from sensitivity analysis of road mortality. Final adults’ abundances and standard deviations are shown for road mortality. Values increased in the infrastructure development scenario and decreased in the renaturalisation scenario by (A) 1%, (B) 2%, (C) 3%, (D) 6% - base level in this study and (E) 9%.
(A) Parameterisation summary based on the ODD protocol and new protocol for PVA. (B) Parameters of the metapopulation model.
Results from sensitivity analysis of predicted metapopulation structure.
Results from sensitivity analysis of predicted carrying capacity.
We would like to thank M. Franz, E. McLean, and two anonymous reviewers for their useful comments on the previous version of this manuscript. A. Olszewski, K. Karpowicz, A. Derecka, K. Wróbel, A. Karaś provided additional field observations of the occurrence of natterjack toad in the study area.
Conceived and designed the experiments: KF JR VG KJ. Performed the experiments: KF. Analyzed the data: KF. Contributed reagents/materials/analysis tools: KF JR VG. Wrote the paper: KF JR VG KJ.
- 1. Brainerd S, Kastdalen L, Seiler A (2007) habitat modelling - a tool for managing landscape. Sunnerstra, Sweden.
- 2. Beissinger S, McCullough D, editors (2002) Population viability analysis. Chicago: University of Chicago Press.
- 3. Houlahan JE, Findlay CS, Schmidt BR, Meyer AH, Kuzmin SL (2000) Quantitative evidence for global amphibian population declines. Nature 404: 752–755.
- 4. Stuart SN, Chanson JS, Cox NA, Young BE, Rodrigues ASL, et al. (2004) Status and trends of amphibian declines and extinctions worldwide. Science 306: 1783–1786.
- 5. Beebee TJC, Griffiths RA (2005) The amphibian decline crisis: A watershed for conservation biology? BiolConserv 125: 271–285.
- 6. Cushman SA (2006) Effects of habitat loss and fragmentation on amphibians: A review and prospectus. BiolConserv 128: 231–240.
- 7. Gardner TA, Barlow J, Peres CA (2007) Paradox, presumption and pitfalls in conservation biology: The importance of habitat change for amphibians and reptiles. BiolConserv 138: 166–179.
- 8. Araújo MB, Thuiller W, Pearson RG (2006) Climate warming and the decline of amphibians and reptiles in Europe. J Biogeogr 33: 1712–1728.
- 9. Pounds JA, Bustamante MR, Coloma LA, Consuegra JA, Fogden MPL, et al. (2006) Widespread amphibian extinctions from epidemic disease driven by global warming. Nature 439: 161–167.
- 10. Sillero N (2008) Amphibian mortality levels on Spanish country roads: descriptive and spatial analysis. Amphibia-Reptilia 29: 337–347.
- 11. Schmidt BR (2004) Declining amphibian populations: the pitfalls of count data in the study of diversity, distributions, dynamics, and demography. Herpetol J 14: 167–174.
- 12. Elżanowski A, Ciesiołkiewicz J, Kaczor M, Radwańska J, Urban R (2008) Amphibian road mortality in Europe: a meta-analysis with new data from Poland. Eur J Wildl Res 55: 33–43.
- 13. Van der Sluis T, editor (2005) Evaluation of ecological consequences of development scenarios for the Vistula river valley Vistula Econet Development and Implementation VEDI. Warsaw, Wageningen, Utrecht: Centre for Ecological Research Polish Academy of Sciences.
- 14. Van der Sluis T, Romanowski J, Bouwma IM, Matuszkiewicz J (2007) Comparison of scenarios for the Vistula river, Poland. Landscape ecological applications in man-influenced areas linking man and nature systems. Dordrecht, The Netherlands: Springer. 417–433. Available: http://0-dx.doi.org.unicat.bangor.ac.uk/10.1007/1-4020-5488-2.
- 15. Verboom J, Foppen R, Chardon P, Opdam P, Luttikhuizen P (2001) Introducing the key patch approach for habitat networks with persistent populations: an example for marshland birds. BiolConserv 100: 89–101.
- 16. Akçakaya HR (2005) RAMAS GIS: Linking Spatial Data with Population Viability Analysis (version 5). Setauket, New York: Applied Biomathematics.
- 17. Romanowski J (2007) Vistula River Valley as the ecological corridor for mammals. Pol J Ecol 55: 805–819.
- 18. Sikora AB (2009) Zwierzęta ginące na drodze wojewódzkiej nr 579 w Kampinoskim Parku Narodowym i jego otulinie oraz propozycja działań ochronnych Warszawa: SGGW.
- 19. Matuszkiewicz J, Solon J (1998) Characteristics of spatial diversification of vegetation types and identification of specific habitats and ecosystems of the Vistula valley.
- 20. Głowaciński Z, Rafiński J (2003) Atlas of the Amphibians and Reptiles of Poland Status - Distribution - Conservation. Warszawa-Kraków.
- 21. Huste A, Clobert J, Miaud C (2006) The movements and breeding site fidelity of the natterjack toad (Bufo calamita) in an urban park near Paris (France) with management recommendations. Amphibia-Reptilia 27: 561–568.
- 22. Miaud C, Sanuy D (2005) Terrestrial habitat preferences of the natterjack toad during and after the breeding season in a landscape of intensive agricultural activity. Amphibia-Reptilia 26: 359–366.
- 23. Semlitsch RD, Bodie JR (2003) Biological criteria for buffer zones around wetlands and riparian habitats for amphibians and reptiles. ConservBiol 17: 1219–1228.
- 24. Stephan T, Ulbrich K, Grosse W-R, Meyer F (2001) Modelling the extinction risk of isolated populations of natterjack toad Bufo calamita. Web Ecol 2: 47–56.
- 25. Andrzejewski R (n.d.) Amphibians and Reptiles of the Kampinos National Park. Kampinoski Park Narodowy. Vol. 1 pp. 617–620.
- 26. Klekowski R (1949) Przyczynek do znajomości Ropuchy paskówki Bufo calamita Laurenti 1768. Acta Zoologica et Oecologica Universitatis Lodziensis 13.
- 27. Beebee TJC (1979) Review of Scientific-Information Pertaining to the Natterjack Toad Bufo-Calamita Throughout Its Geographical Range. BiolConserv 16: 107–134.
- 28. Miaud C, Sanuy D, Avrillier JN (2000) Terrestrial movements of the natterjack toad Bufo calamita (Amphibia, Anura) in a semi-arid, agricultural landscape. Amphibia-Reptilia 21: 357–369.
- 29. ArcView (2002). Redlands, California: Environmental Systems Research Institute Inc.
- 30. Spatial Analyst (2002). Redlands, California: Environmental Systems Research Institute Inc.
- 31. Sinsch U (1992) Structure and Dynamic of A Natterjack Toad Metapopulation (Bufo-Calamita). Oecologia 90: 489–499.
- 32. Beebee TJC, Denton JS, Buckley J (1996) Factors affecting population densities of adult natterjack toads Bufo calamita in Britain. JApplEcol 33: 263–268.
- 33. Buckley J, Beebee TJC (2004) Monitoring the conservation status of an endangered amphibian: the natterjack toad Bufo calamita in Britain. Anim Conserv 7: 221–228.
- 34. Leskovar C, Oromi N, Sanuy D, Sinsch U (2006) Demographic life history traits of reproductive natterjack toads (Bufo calamita) vary between northern and southern latitudes. Amphibia-Reptilia 27: 365–375.
- 35. Denton JS, Hitchings SP, Beebee TJC, Gent A (1997) A recovery program for the natterjack toad (Bufo calamita) in Britain. ConservBiol 11: 1329–1338.
- 36. Sinsch U (1997) Postmetamorphic dispersal and recruitment of first breeders in a Bufo calamita metapopulation. Oecologia 112: 42–47.
- 37. Arak A (1983) Sexual Selection by Male Male Competition in Natterjack Toad Choruses. Nature 306: 261–262.
- 38. Arak A (1988) Female Mate Selection in the Natterjack Toad - Active Choice Or Passive Attraction. Behav Ecol Sociobiol 22: 317–327.
- 39. Fahrig L, Rytwinski T (2009) Effects of Roads on Animal Abundance: An Empirical Review and Synthesis. Available: http://dlc.dlib.indiana.edu/archive/00005369/. Accessed 21 July 2010.
- 40. Ascensão F, Mira A (2005) Spatial patterns of road kills: a case study in Southern Portugal. Available: http://www.escholarship.org/uc/item/8r07z6nf.
- 41. Orłowski G (2007) Spatial distribution and seasonal pattern in road mortality of the common toad Bufo bufo in an agricultural landscape of south-western Poland. Amphibia-Reptilia 28: 25–31.
- 42. Marsh DM, Trenham PC (2001) Metapopulation dynamics and amphibian conservation. ConservBiol 15: 40–49.
- 43. Smith MA, Green DM (2005) Dispersal and the metapopulation paradigm in amphibian ecology and conservation: are all amphibian populations metapopulations? Ecography 28: 110–128.
- 44. Bowne DR, Bowers MA (2004) Interpatch movements in spatially structured populations: a literature review. Landscape Ecol 19: 1–20.
- 45. Brans JP, Vincke P (1985) A Preference Ranking Organisation Method: (The PROMETHEE Method for Multiple Criteria Decision-Making). Manage Sci 31: 647–656.
- 46. Drechsler M, Frank K, Hanski I, O’Hara RB, Wissel C (2003) Ranking metapopulation extinction risk: from patterns in data to conservation management decisions. Ecol Appl 13: 990–998
- 47. McCarthy MA, Thompson C (2001) Expected minimum population size as a measure of threat. Anim Conserv 4: 351–355
- 48. Pe’er G, Matsinos Y, Johst K, Franz KW, Turlure C, et al.. (2013) A Protocol for Better Design, Application, and Communication of Population Viability Analyses. Conserv Biol. (in press).
- 49. Mazerolle MJ, Huot M, Gravel M (2005) Behavior of amphibians on the road in response to car traffic. Herpetologica 61: 380–388.
- 50. SISKOM (2004) Generalny Pomiar Ruchu. Available: http://www.siskom.waw.pl/nauka-gpr.htm. Accessed 30 September 2011.