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Communication

Assessment of the Conservation Value of Abandoned Land on Gogland Island, Baltic Sea

1
Department of Applied Ecology, Faculty of Biology, Saint Petersburg State University, Universitetskaya n. 7/9, Saint Petersburg 199034, Russia
2
Nizhne-Svirsky Nature Reserve, Lodeynoye Pole, ul. Praviy bereg r. Svir, d. 1, 187715, Russia
3
Main Botanical Garden of the Russian Academy of Science Named after N. V. Tsitsin RAS, St. Botanicheskaya 4, Moscow 127276, Russia
*
Author to whom correspondence should be addressed.
Land 2023, 12(10), 1946; https://doi.org/10.3390/land12101946
Submission received: 11 September 2023 / Revised: 15 October 2023 / Accepted: 17 October 2023 / Published: 20 October 2023

Abstract

:
Gogland Island, located in the Gulf of Finland in the Baltic Sea, was densely populated in the past but has been nearly abandoned since the Second World War. The self-restoration of wildlife takes place there. Recent research on the island aimed to evaluate the conservation value of this process. It was expected that the island would demonstrate a standard for the perfect state of protected areas of the boreal zone of Europe. The island has been overgrown with forests; open areas occupy insignificant parts and tend to shrink. Picturesque landscapes have been formed, but the conservation value of these areas are questionable as the biodiversity is rather low there. They contain “empty forest” that is partly impassable. The island demonstrates that to achieve the maximum effect for biodiversity conservation, the abandonment of land without any management would be insufficient. The fate of the island partly supports the concept of Pleistocene rewilding: a mosaic of forests and meadows, maintained by ungulates, should be considered a normal state of environments.

1. Introduction

The establishment of protected areas where anthropogenic activities are either restricted or prohibited is one of the most effective measures for environmental protection [1,2]. However, in Europe, these areas are being created in places that have long been subjected to anthropogenic pressures; felling, grazing, the extermination of wild animals, and other human activities have progressed in these locations over several thousands of years. Perceptions about the normal state of the environment have shifted over time [3,4,5]. Therefore, it is no longer clear how to manage protected wildlife areas: either to strive to eliminate all human activities or somehow influence the areas to improve their state. To answer this question, it is important to assess areas that have existed for a long time under extremely weak anthropogenic impacts. Gogland Island located in the Gulf of Finland in the Baltic Sea is one such area. It has been nearly abandoned since the Second World War, although the nearest mainland is densely populated and suffers from strong anthropogenic pressure. The island was (and still is) not a protected area officially, but in fact, it was strongly protected. Access to the island was limited for a long time because it is located close to the state border zone and has military significance. In the 1990s, several changes were made in this regard, and since then, the island has been visited by various researchers. In particular, the Russian Geographical Society has been carrying out expeditions to the island for several years, in which we took part. Our research aimed to characterize the habitats and biodiversity of the island and to reveal the objects representing special value in terms of environment conservation. It was expected that the island would demonstrate a standard for the perfect state of protected areas of the boreal zone of Europe.

2. Materials and Methods

2.1. Study Area

Gogland Island has the shape of an elongated oval that is 11 km long and 1.5–3 km wide. The distance to the mainland is 44 km in the north and 55 km in the south. There are several smaller islands at a distance of 10–18 km around it. Before World War II, Gogland belonged to Finland and was densely populated; the population was approximately 1000 people. They lived in several settlements and were mainly engaged in fishing, seal hunting, and sea transport. Part of the island was used for agriculture. To arrange farmlands, a system of dams and ditches was created in the central part of the island. In the 1920s, the island became a recreational place; restaurants and hotels were built and their number increased. The number of visitors reached up to 10,000 per summer [6]. After the Second World War, the island was annexed to Russia, the local population was evicted, and economic activity was essentially stopped [7]. The presence of humans on the island has been insignificant; several military posts, a weather station, and two lighthouses occupy a small portion of the island.

2.2. Methodology

To assess the state of the island, we used the approaches developed during the design and survey of the protected areas [8,9]. To determine the nature conservation value of an area, the research focused on the variety of habitats and the objects demonstrating the following: high biodiversity, concentrations of animals, a presence of threatened species (listed in the regional red data books or classified as threatened in the IUCN Red List), uniqueness, and aesthetic value. Particular attention was paid to the registration of vertebrates or traces of their occurrence because these animals are good indicators of the state of the environment. Since they require a relatively large space, their presence reflects ecosystems that include other animals and plants.
To collect this information, the following methods were used:
  • Literature search: We gathered publications on Gogland Island by examining the Russian Science Citation Index [10] and Scopus databases [11], as well as by searching in the libraries of the Russian Academy of Sciences and St. Petersburg State University.
  • Survey of the island: We walked around the island along the coastline and crossed it lengthwise, i.e., from north to south, and in several places from east to west or vice versa, and observed the inland water bodies. A schematic map of the habitats was composed by combining the observation results with aerial pictures. Moreover, we focused on the animal species that had not been sufficiently studied by other researchers. We registered bats during the nighttime with the assistance of an ultrasonic detector (Patterson D 200) and photographed them. To identify bat species, we used sound records [12]. To study the carnivorous mammals, we installed camera traps (Bushnell Nature View). To attract the animals, we used fish as bait (Crucian carp Carassius carassius caught on-site). Our surveys were performed during four expeditions: September 2015, August 2018, June 2021, and September 2022.

3. Results

3.1. Habitats

The island was almost completely overgrown with trees. Most of the forests were composed of pines (Pinus sylvestris) and spruce (Picea abies), and fallen tree trunks were numerous. In some places, windblows occupied an area of several hectares. Such areas were practically impassable because they were comprised of a continuous layer of fallen trunks and dense thickets of young trees. Open areas occupied an insignificant part of the island. Arboreal vegetation was scarce only in rocky areas, where there was no continuous soil cover (Figure 1 and Figure 2). In some places, signs of forest fires were evident, but even these plots were covered by dense thickets of small trees. There were several meadows near the meteorological station and the military posts, as well as on the sites of abandoned villages. However, the overgrowth of arboreal vegetation still progressed there. Relatively stable meadows were found only near houses.

3.2. Biodiversity

During the re-exploration of the island by biologists in the period of 1990–2000, 663 species of vascular plants [13,14], 178 species of mosses [15], and 385 species of lichens [16] were recorded. This list of local flora and fauna has been minimally supplemented [17], the process of which is gradually continuing. The number of known species is higher on the nearest mainland. Relevant estimates were not made for all taxa, but it is known that there are at least 824 species of higher plants [18] and 722 species of lichens [19]. At the same time, six species of vascular plants and several species of mosses not registered on the mainland were recorded on the island [14,17].
As for the animals, most of the data concern vertebrates (the invertebrates are understudied and comparing the island with the mainland in this respect is problematic). There are three species of amphibians (the toad Bufo bufo, common frog Rana temporaria, and common newt Lissotriton vulgaris) and three species of reptiles (the common viper Vipera berus, grass snake Natrix natrix, and common lizard Zootoca vivipara) [20]. Such numbers are slightly higher on the nearest mainland, where six other species of reptiles and amphibians occur.
During the studies performed in the 2000s, 113 bird species were registered [21]. We also observed some of them and added one (the grey heron Ardea cinerea) (Table 1). The total number of bird species for the area around the island is two times larger [22].
Seven mammal species were recorded on the island in the 2000s: red fox Vulpes vulpes, raccoon dog Nyctereutes procyonoides, European mink Mustela lutreola, mountain hare Lepus timidus, red squirrel Sciurus vulgaris, common shrew Sorex araneus, and yellow-necked mouse Apodemus flavicollis [23]. We added four species of bats to them: Daubenton’s bat Myotis daubentoni, pond bat Myotis dasycneme, Nathusius’s pipistrelle Pipistrellus nathusii, and northern bat Eptesicus nilssonii. Two species of seals were registered on the island, ringed seal Pusa hispida and grey seal Halichoerus grypus, but they only visit it in small numbers. The number of mammal species is 4–5 times higher on the nearest mainland [24].
In the past, ungulates existing on the island were reported. Feral goats and sheep were included in the list of local fauna. Their number was estimated as 100–200 in the 2000s. Moreover, the arrival of white-tailed deer Odocoileus virginianus, which are bred on the nearest mainland (Finland), was recorded. The other visitor was the Eurasian lynx Lynx lynx [23]. However, both had not settled on the island. During our survey, we did not find any traces of ungulates or other large mammals over most of the island, with only a small number of goats and sheep kept at the lighthouses.

3.3. Concentration of Animals

The island is located within a zone of the North Atlantic bird flyway. Numerous birds fly over the island during spring and autumn. Some birds linger there for some time under certain circumstances (during storms) [21], but the particular role of the island as a migratory stopover has not been noted. It is likely that the flyway of bats also passes there. Our bat surveys took place in August–September, which is a season of bat migrations.

3.4. Threatened Species

Several dozen plant species occurring on the island are listed in the local red data books [25]. However, they are not threatened on a global scale. The island is at the edge of their range, which is mostly located outside of Russia. Regarding animals, the most remarkable species is the European mink, which is a critically endangered species (it has almost disappeared over most of its native range because of competition with an invasive species of American mink, Neovison vison) [26]. It had been observed on the island in 2003 [23], but no other information about this was obtained afterwards. We found the scat of minks on two occasions in 2018 and 2021. However, the registration of minks using camera traps failed (foxes and raccoon dogs were photographed). Several other vertebrate species (bats and some birds) are listed in the regional red data books, but most of them are classified in the “Least Concern” category in the IUCN Red List. One of the local species, the velvet scoter, is considered vulnerable on a global scale [27], and three species are considered near-threatened: the pond bat [28], Eurasian oystercatcher [29], and northern lapwing [30]. The northern lapwing was observed once in 2004 [21], but its stable existence on the island is hardly probable because of the lack of open areas. Islands often serve as a refuge for pinnipeds, which are threatened animals, but in this case, they were extremely small in number [31]. They prefer small islands without trees.

3.5. Uniqueness and Aesthetic Value

There were many picturesque objects on the island, including rocks at the seashore, steep (up to 50–70 m) hills, grottoes, streams, lakes surrounded by rocks, and trees on rocks. The common pine and spruce often acquire unusual forms when they grow on stones. A unique object was a “stone river”, which is a plot without vegetation covered with rounded boulders, similar to a river bottom; there were several such rivers. Several “seids”, i.e., large stones on supports, were found on the island (Figure 3). The entire island, when viewed from the sea or from above, is perceived as an aesthetically valuable object.

4. Discussion

Gogland Island demonstrates that open areas in the Baltic region can disappear without anthropogenic activities. The area of plots on the island without forests is insignificant and is predicted to decrease. Fires, windblows, and other natural processes can barely resist complete afforestation. The conservation value of this process provokes doubts. The island can hardly be considered a standard for the perfect state of wildlife. Among the criteria used to assess the value of the studied area, aesthetics was almost the only criterion that was clearly expressed. The island corresponds well to the characteristics of the “empty forest” [32] or “empty landscape” [33]: it seems to be in a good state but is defaunated. (Although the analysis of these “empty” lands concerned the tropics, the situation in a boreal zone seems to be similar). The biodiversity on the island is relatively high only for some plant taxa, but it is rather low as a whole. This is only partly explained by the small area and distance from the mainland and is probably related to “excessive” afforestation. The visits by lynx and deer showed that other ungulates or carnivorous mammals can reach the island by either walking on ice or swimming (e.g., elks, wild boars, or wolves), but they cannot settle there. This means that there is no favorable environment for them. Dense forest with numerous fallen tree trunks is unsuitable, not only for humans but for large mammals as well. They need a larger portion of open areas. The same is true for several bird species. Any bird species could easily visit the island, but some “common” species from the mainland are absent there (e.g., several grouses and waders) as they need either open areas or a combination of open areas with forests. With the exception of the European mink, the list of local species is rather trivial. Meanwhile, the local mink population is very small and it may be on the edge of extinction. Usually, the minks inhabiting the island can easily be recorded as they are used to feeding at the coastline, but in our case, they were well observed only once 20 years ago. It is perhaps the case that the transformation of the island is not favorable for this species.
Afforestation on Gogland Island shows that to achieve the maximum effect for biodiversity conservation, the abandonment of land without any management could be insufficient. In a boreal environment, some activity to keep a number of open areas is desirable. Open areas could be maintained by ungulates, but in this case, a small number of feral goats and sheep turned out to be insufficient to resist afforestation; they have decreased in number and disappeared over the last few decades. To maintain a significant portion of open areas, the ungulates should be larger and/or more numerous.
The case of wildlife restoration on Gogland Island is interesting with respect to assessing the normal state of vegetation in Europe. Since the Neolithic period, forest area has been continuously decreasing there [4,34]. This means that the overgrowth of open spaces and settlements with forests is a return to the original or normal state. However, overgrowing forests can be undesirable as open spaces can also be valuable habitats with high biological productivity. The overgrowth of grasslands with arboreal vegetation is often viewed as a negative process as it reduces ecosystem services and exterminates endemic ecosystems [35]. Protests against “the tyranny of trees” have occurred [36]. A “war” against forests and swamps of the boreal zone was declared with the concept of a Pleistocene park [37]. According to this concept, modern taiga and tundra represent an abnormal dominance of arboreal vegetation and mosses, which originated because of the extermination of large herbivores at the turn of the Holocene–Pleistocene period. In the past, tundra-steppe covered most of the northern part of Eurasia; its existence was supported by a large population of herbivores, and because of their extermination, shrubs, mosses, lichens, and trees expanded instead of grasses. This means that to restore the norm, it is necessary to introduce various ungulates (bison, horses, yaks, etc.), which could facilitate a reverse transformation. Experiments on such a transformation have been conducted in Pleistocene Park, a protected area in Yakutia. They have demonstrated that introduced ungulates survive, but because of their low abundance, no significant transformation of habitats has taken place to date [38]. The question of the possibility and feasibility of “returning to the Pleistocene” remains open. At the moment, such rewilding is a dream of several enthusiasts, which seems to be unrealistic. However, at least a partial return to the “Pleistocene” is a promising perspective. The fate of Gogland Island testifies rather in favor of this concept as it demonstrates well the opposite extreme: without large ungulates, an area becomes covered in an impassable mass of trees. This means that a norm for the environment should be assessed based not only on historic data but on prehistoric data as well.

5. Conclusions

Gogland Island demonstrates that in a boreal environment, the abandonment of land can result in total afforestation, which, in turn, results in a decline in biodiversity. In spite of the strong level of protection, the island hardly became a standard for the perfect state of a wildlife area. To achieve the maximum effect for biodiversity conservation, the abandonment of land without any management could be insufficient; human interventions might be appropriate aiming to maintain a number of open areas and the enrichment of fauna. A mosaic of forests and meadows inhabited by various animals would likely be more beneficial than a total overgrowth of forests. Otherwise, defaunated habitats could materialize (“the empty forests” or “empty landscapes”). The fate of the island partly supports the concept of Pleistocene rewilding: the baselines for nature conservation should be sought in the remote past, when large herbivores were much more numerous than now.

Author Contributions

Conceptualization, I.P., A.I. and E.A.; methodology, I.P., A.I. and E.A.; software, I.P., A.I. and E.A.; validation, I.P., A.I. and E.A.; formal analysis, I.P., A.I. and E.A.; investigation, I.P., A.I. and E.A.; resources, I.P., A.I. and E.A.; data curation, I.P., A.I. and E.A.; writing—original draft preparation, I.P.; writing—review and editing, I.P.; visualization, I.P., A.I. and E.A.; supervision, I.P.; project administration, I.P., A.I. and E.A.; funding acquisition, E.A. All authors have read and agreed to the published version of the manuscript.

Funding

The work by Evgeny Abakumov was supported by the Russian Science Foundation, project No. 23-16-20003, dated 20 April 2023, and the Saint Petersburg Scientific Foundation, agreement No. 23-16-20003, dated 5 May 2023.

Data Availability Statement

The data are contained within the article.

Acknowledgments

The authors thank the Russian Geographical Society for organizing the expeditions to Gogland Island. Anton Iurmanov acknowledges Tsitsin Main Botanical Garden Unique Scientific Installation “Fund Greenhouse” for their assistance in the analysis of data.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Gaston, K.J.; Jackson, S.F.; Cantú-Salazar, L.; Cruz-Piñón, G. The ecological performance of protected areas. Annu. Rev. Ecol. Evol. Syst. 2008, 39, 93–113. [Google Scholar] [CrossRef]
  2. Watson, J.E.M.; Darling, E.S.; Venter, O.; Maron, M.; Walston, J.; Possingham, H.P.; Dudley, N.; Hockings, M.; Barnes, M.; Brooks, T.M. Bolder science needed now for protected areas. Conserv. Biol. 2016, 30, 243–248. [Google Scholar] [CrossRef] [PubMed]
  3. Papworth, S.K.; Rist, J.; Coad, L.; Milner-Gulland, E.J. Evidence for shifting baseline syndrome in conservation. Conserv. Lett. 2009, 2, 93–100. [Google Scholar] [CrossRef]
  4. Holmgren, M.; Scheffer, M. To Tree or Not to Tree: Cultural Views from Ancient Romans to Modern Ecologists. Ecosystems 2017, 20, 62–68. [Google Scholar] [CrossRef]
  5. Soga, M.; Gaston, K.J. Shifting baseline syndrome: Causes, consequences, and implications. Front. Ecol. Environ. 2018, 16, 222–230. [Google Scholar] [CrossRef]
  6. Röyhkä, K. Suursaari; Johnny Kniga: Helsinki, Finland, 2009; pp. 1–150. [Google Scholar]
  7. Gaginskaya, A.R.; Noskov, G.A. History of Gogland. In Gogland Island. Results of the Survey of the Natural Complexes; Gaginskaya, A.R., Noskov, G.A., Eds.; Tuscarora: Saint Petersburg, Russia, 2006; pp. 7–8, (In Russian with English abstract). [Google Scholar]
  8. Kovalyov, D.N.; Noskov, G.A.; Noskova, M.G.; Popov, I.Y.; Rymkevich, T.A. Concept of formation of regional systems of protected areas (by the example of St Petersburg and Leningradskaya oblast). Biosfera 2012, 4, 427–462, (In Russian with English abstract). [Google Scholar]
  9. Aksenov, D.; Dobrynin, D.; Filonenko, I.; Esipova, E.; Kirillov, A.; Kobyakov, K.; Koltsov, D.; Popov, I.; Tokarev, P. Methods for delineation of the high conservation value. In Atlas of High Conservation Value Areas, and Analysis of Gaps and Representativeness of the Protected area Network in Northwest Russia Arkhangelsk, Vologda, Leningrad, and Murmansk Regions, Republic of Karelia, and City of St. Petersburg; Kobyakov, K., Jakovlev, J., Eds.; Edita Prima Oy: Helsinki, Finland, 2013; pp. 63–125. [Google Scholar]
  10. RSCI. Russian Science Citation Index. 2023. Available online: https://www.elibrary.ru/org (accessed on 4 January 2023).
  11. Scopus. 2023. Available online: https://www.www.scopus.com (accessed on 4 January 2023).
  12. Barataud, M. Acoustic Ecology of European Bats; Biotope: Paris, France, 2015. [Google Scholar]
  13. Glazkova, E.A. On some rare plant species from the islands of eastern Gulf of Finland. Bot. J. 1996, 81, 111–114, (In Russian with English abstract). [Google Scholar]
  14. Glazkova, E.A. Vascular plants. In Gogland Island. Results of the Survey of the Natural Complexes; Gaginskaya, A.R., Noskov, G.A., Eds.; Tuscarora: Saint Petersburg, Russia, 2006; pp. 15–19, (In Russian with English abstract). [Google Scholar]
  15. Noskova, M.G.; Kurbatova, E.L. Bryophytes. In Gogland Island. Results of the Survey of the Natural Complexes; Gaginskaya, A.R., Noskov, G.A., Eds.; Tuscarora: Saint Petersburg, Russia, 2006; pp. 20–21, (In Russian with English abstract). [Google Scholar]
  16. Alexeeva, N.M. Lichens. In Gogland Island. Results of the Survey of the Natural Complexes; Gaginskaya, A.R., Noskov, G.A., Eds.; Tuscarora: Saint Petersburg, Russia, 2006; p. 21, (In Russian with English abstract). [Google Scholar]
  17. Potemkin, A.D.; Kurbatova, L.E.; Kotkova, V.M. Liverworts from Hogland Island (Baltic Sea, Gulf of Finland) new and less known for the Leningrad Region and Russia. Bot. J. 2008, 93, 466–471, (In Russian with English abstract). [Google Scholar]
  18. Flora of Leningradskaya Oblast. 2023. Available online: https://www.inaturalist.org/projects/leningrad-oblast-flora?tab=species (accessed on 4 January 2023). (In Russian).
  19. Zavarzin, A.A.; Katenina, O.A.; Kotlov, Y.V.; Sokolova, S.V. Lichens of St Peterstburg and Leningradskaya oblast. In Biodiversity of Leningradkaya Oblast; Saint-Petersburg State University: Saint-Petersburg, Russia, 1999; pp. 208–260. (In Russian) [Google Scholar]
  20. Gaginskaya, A.R. Amphibians and reptiles. In Gogland Island. Results of the Survey of the Natural Complexes; Gaginskaya, A.R., Noskov, G.A., Eds.; Tuscarora: Saint Petersburg, Russia, 2006; pp. 25–26, (In Russian with English abstract). [Google Scholar]
  21. Antipin, M.A.; Gaginskaya, A.R. Birds. In Gogland Island. Results of the Survey of the Natural Complexes; Gaginskaya, A.R., Noskov, G.A., Eds.; Tuscarora: Saint Petersburg, Russia, 2006; pp. 26–27, (In Russian with English abstract). [Google Scholar]
  22. Malchevsky, A.S.; Pukinsky, Y.B. Birds of Leningradskaya oblast. Russ. J. Ornithol. 2021, 30, 3713–3797. (In Russian) [Google Scholar]
  23. Gaginskaya, A.R. Mammals. In Gogland Island. Results of the Survey of the Natural Complexes; Gaginskaya, A.R., Noskov, G.A., Eds.; Tuscarora: Saint Petersburg, Russia, 2006; pp. 27–29, (In Russian with English abstract). [Google Scholar]
  24. Ayrapetianz, A.E.; Fokin, I.M.; Strelkov, P.P. Mammals. In Environment of Leningradskaya Oblast; Leninzdat: Leningrad, Russia, 1987; pp. 1–143. (In Russian) [Google Scholar]
  25. Red Data Book of Russian Federation; VNII Ecologica: Moscow, Russia, 2021. (In Russian)
  26. Maran, T.; Skumatov, D.; Gomez, A.; Podra, M.; Abramov, A.V.; Dinets, V. Mustela lutreola. In The IUCN Red List of Threatened Species; International Union for Conservation of Nature: Grann, Switzerland, 2016. [Google Scholar] [CrossRef]
  27. BirdLife International. Melanitta fusca. In The IUCN Red List of Threatened Species; International Union for Conservation of Nature: Grann, Switzerland, 2020. [Google Scholar] [CrossRef]
  28. Piraccini, R. Myotis dasycneme. In The IUCN Red List of Threatened Species; International Union for Conservation of Nature: Grann, Switzerland, 2016. [Google Scholar] [CrossRef]
  29. BirdLife International. Haematopus ostralegus. In The IUCN Red List of Threatened Species; International Union for Conservation of Nature: Grann, Switzerland, 2019. [Google Scholar] [CrossRef]
  30. BirdLife International. Vanellus vanellus (amended version of 2016 assessment). In The IUCN Red List of Threatened Species; International Union for Conservation of Nature: Grann, Switzerland, 2017; p. E.T22693949A111044786. [Google Scholar] [CrossRef]
  31. Loseva, A.V.; Sagitov, R.A. New data on distribution of spring and autumn haul-out sites of the Baltic ringed seals (Pusa hispida botnica) in the Gulf of Finland. Vestn. SPbGU 2015, 1, 15–40, (In Russian with English abstract). [Google Scholar]
  32. Redford, K.H. The empty forest. Biosciences 1992, 42, 412–422. [Google Scholar] [CrossRef]
  33. Pires, M.M.; Galetti, M. Beyond the “empty forest”: The defaunation syndromes of Neotropical forests in the Anthropocene. Glob. Ecol. Conserv. 2023, 41, e02362. [Google Scholar] [CrossRef]
  34. Kaplan, J.O.; Krumhardt, K.M.; Zimmermann, N. The prehistoric and preindustrial deforestation of Europe. Quat. Sci. Rev. 2009, 28, 3016–3034. [Google Scholar] [CrossRef]
  35. Brandt, J.S.; Haynes, M.A.; Kuemmerle, T.; Waller, D.M.; Radeloff, V.C. Regime shift on the roof of the world: Alpine meadows converting to shrublands in the southern Himalayas. Biol. Conserv. 2013, 158, 116–127. [Google Scholar] [CrossRef]
  36. Veldman, J.W.; Overbeck, G.E.; Negreiros, D.; Mahy, G.; Le Stradic, S.; Fernandes, G.W.; Durigan, G.; Buisson, E.; Putz, F.E.; Bond, W.J. Tyranny of trees in grassy biomes. Science 2015, 347, 484–485. [Google Scholar] [CrossRef] [PubMed]
  37. Zimov, S.A. Pleistocene park: Return of the mammoth’s ecosystem. Science 2005, 308, 796–798. [Google Scholar] [CrossRef] [PubMed]
  38. Popov, I. The current state of Pleistocene Park, Russia (An experiment in the restoration of megafauna in a boreal environment). Holocene 2020, 30, 1471–1473. [Google Scholar] [CrossRef]
Figure 1. A scheme of habitats on Gogland Island.
Figure 1. A scheme of habitats on Gogland Island.
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Figure 2. Habitats of Gogland Island: spruce forests (a), pine forests (b), broad-leaved forests (c), and rocks (d).
Figure 2. Habitats of Gogland Island: spruce forests (a), pine forests (b), broad-leaved forests (c), and rocks (d).
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Figure 3. Sights of Gogland Island: “creeping spruce” (a), “dwarf pines” (b), “stone river” (c), and “seid” (d).
Figure 3. Sights of Gogland Island: “creeping spruce” (a), “dwarf pines” (b), “stone river” (c), and “seid” (d).
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Table 1. Species of birds recorded on Gogland Island.
Table 1. Species of birds recorded on Gogland Island.
No.Species IUCN
Category
No.SpeciesIUCN
Category
1Arctic loon Gavia arcticaLC38Northern lapwing Vanellus vanellusLC
2Red-throated loon Gavia stellataLC39Arctic jaeger Stercorarius parasiticusLC
3Great crested grebe Podiceps cristatusLC40Mew gull Larus canus LC
4Mute swan Cygnus olorLC41European herring gull Larus argentatusLC
5Whooper swan Cygnus cygnusLC42Lesser black-backed gull Larus fuscusLC
6Tundra swan Cygnus columbianus LC43Great black-backed gull Larus marinusLC
7Greylag goose Anser anserLC44Black-headed gull Larus ridibundusLC
8Greater white-fronted goose Anser albifronsLC45Arctic tern Sterna paradisaeaLC
9Barnacle goose Branta leucopsisLC46Common tern Sterna hirundo LC
10Brent goose Branta berniclaLC47Razorbill Alca tordaLC
11Mallard Anas platyrhynchos LC48Common woodpigeon Columba palumbus LC
12Common teal Anas creccaLC49Stock dove Columba oenasLC
13Common eider Somateria mollissimaNT50Common cuckoo Cuculus canorus LC
14Tufted duck Aythya fuligulaLC51European nightjar Caprimulgus europaeusLC
15Velvet scoter Melanitta fuscaVU52Common swift Apus apusLC
16Common goldeneye Bucephala clangulaLC53Eurasian wryneck Jynx torquillaLC
17Red-breasted merganser Mergus serrator LC54Black woodpecker Dryocopus martius LC
18Goosander Mergus merganserLC55Great spotted woodpecker Dendrocopos majorLC
19Grey heron Ardea cinereaLC56White-backed woodpecker Dendrocopos leucotosLC
20White-tailed sea-eagle Haliaeetus albicillaLC57Three-toed woodpecker Picoides tridactylusLC
21Greater spotted eagle Clanga clangaVU58Eurasian skylark Alauda arvensisLC
22Northern goshawk Accipiter gentilis LC59Barn swallow Hirundo rusticaLC
23Eurasian sparrowhawk Accipiter nisusLC60Western yellow wagtail Motacilla flava LC
24Eurasian buzzard Buteo buteo LC61White wagtail Motacilla alba LC
25Rough-legged buzzard Buteo lagopusLC62Tree pipit Anthus trivialisLC
26Eurasian hobby Falco subbuteoLC63Meadow pipit Anthus pratensisLC
27Peregrine falcon Falco peregrinus LC64Rock pipit Anthus petrosusLC
28Western capercaillie Tetrao urogallus LC65Red-backed shrike Lanius collurioLC
29Common crane Grus grus LC66Northern wren Troglodytes troglodytesLC
30Corncrake Crex crexLC67Dunnock Prunella modularisLC
31Common ringed plover Charadrius hiaticulaLC68European robin Erithacus rubeculaLC
32Eurasian oystercatcher Haematopus ostralegusNT69Thrush nightingale Luscinia luscinia LC
33Green sandpiper Tringa ochropusLC70Common redstart Phoenicurus phoenicurus LC
34Common greenshank Tringa nebulariaLC71Whinchat Saxicola rubetraLC
35Common sandpiper Actitis hypoleucosLC72Northern wheatear Oenanthe oenantheLC
36Eurasian woodcock Scolopax rusticola LC73Eurasian blackbird Turdus merula LC
37Jack snipe Lymnocryptes minimusLC74Fieldfare Turdus pilarisLC
75Redwing Turdus iliacusNT95Great tit Parus majorLC
76Song thrush Turdus philomelos LC96Eurasian blue tit Cyanistes caeruleus LC
77Mistle thrush Turdus viscivorusLC97Eurasian treecreeper Certhia familiarisLC
78Marsh warbler Acrocephalus palustrisLC98Yellowhammer Emberiza citrinellaLC
79Common grasshopper warbler Locustella naeviaLC99Reed bunting Emberiza schoeniclusLC
80Garden warbler Sylvia borinLC100Common chaffinch Fringilla coelebs LC
81Eurasian blackcap Sylvia atricapilla LC101Brambling Fringilla montifringillaLC
82Common whitethroat Curruca communisLC102European greenfinch Chloris chlorisLC
83Icterine warbler Hippolais icterinaLC103Eurasian siskin Spinus spinusLC
84Willow warbler Phylloscopus trochilusLC104Common rosefinch Carpodacus erythrinusLC
85Greenish warbler Phylloscopus trochiloidesLC105Red crossbill Loxia curvirostraLC
86Common chiffchaff Phylloscopus collybitaLC106Eurasian bullfinch Pyrrhula pyrrhula LC
87Wood warbler Phylloscopus sibilatrixLC107House sparrow Passer domesticus LC
88Goldcrest Regulus regulusLC108Common starling Sturnus vulgaris LC
89Spotted flycatcher Muscicapa striata LC109Eurasian golden oriole Oriolus oriolusLC
90European pied flycatcher Ficedula hypoleucaLC110Siberian jay Perisoreus infaustusLC
91Red-breasted flycatcher Ficedula parva LC111Northern nutcracker Nucifraga caryocatactes LC
92Long-tailed tit Aegithalos caudatusLC112Eurasian magpie Pica picaLC
93Willow tit Poecile montanus LC113Carrion crow Corvus coroneLC
94Coal tit Periparus ater LC114Common raven Corvus coraxLC
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MDPI and ACS Style

Popov, I.; Iurmanov, A.; Abakumov, E. Assessment of the Conservation Value of Abandoned Land on Gogland Island, Baltic Sea. Land 2023, 12, 1946. https://doi.org/10.3390/land12101946

AMA Style

Popov I, Iurmanov A, Abakumov E. Assessment of the Conservation Value of Abandoned Land on Gogland Island, Baltic Sea. Land. 2023; 12(10):1946. https://doi.org/10.3390/land12101946

Chicago/Turabian Style

Popov, Igor, Anton Iurmanov, and Evgeny Abakumov. 2023. "Assessment of the Conservation Value of Abandoned Land on Gogland Island, Baltic Sea" Land 12, no. 10: 1946. https://doi.org/10.3390/land12101946

APA Style

Popov, I., Iurmanov, A., & Abakumov, E. (2023). Assessment of the Conservation Value of Abandoned Land on Gogland Island, Baltic Sea. Land, 12(10), 1946. https://doi.org/10.3390/land12101946

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