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STATUS OF TILIA MAXIMOWICZIANA (MALVACEAE S.L.) IN RUSSIA
Elena V. Linnik1*, Anatoliy A. Khapugin2,3
Kurilskiy State Nature Reserve, Russia Joint Directorate of the Mordovia State Nature Reserve and National Park «Smolny», Russia
3Tyumen State University, Russia *e-mail: [email protected], [email protected]
Received: 22.10.2019. Revised: 20.12.2019. Accepted: 22.12.2019.
Tilia maximowicziana (Malvaceae) is a plant species endemic to the northern part of the Japanese archipelago and Kunashir Island. In Russia, this species is included in the Red Data Book of the Russian Federation with rarity category 1 (taxon near extinction). In 2014-2019, we conducted field surveys of known Tilia maximowicziana subpopulations in Russia. We found and considered six locations on Kunashir Island. We further estimated mor-phometric traits of individuals and vegetation characteristics. On the basis of obtained data, we conducted regional IUCN estimation of T. maximowicziana for the Russian territory. We found that T. maximowicziana subpopulations inhabited deciduous and mixed forest plant communities, where Sasa sp. plants dominated in the herb layer. We demonstrated that the endemic plant species represented lower values of dBh and tree height, while leaf size (length / width), length of petioles and fruits were within the amplitude of their values known in the main part of the species range. According to IUCN Red List categories, T. maximowicziana has the regional status CR B1ab(iii); C2a(i); D in Russia. The findings of fruit production in a T. maximowicziana subpopulation demonstrated the ability to seed reproduction of this species in northern limit of the natural range. The obtained results allowed us to estimate the global IUCN status of T. maximowicziana, taking into account its subpopulations in the Japanese archipelago.
Key words: endemic, fruit production, IUCN Red List, morphometric traits, plant community, range, threat
Introduction
At present, plant extinction rates are increasing under climatic and anthropogenic influence (Cheaib et al., 2012; Le Roux et al., 2019). It especially concerns endemic plants on small islands, having a restricted range and possibility for dispersal. It increases the extinction risk (Harter et al., 2015), which have been demonstrated in biodiversity hotspots (e.g. Ferreira et al., 2016). Endemic plants are more abundant in tropic and subtropic regions (e.g. Ungricht et al., 2005; Kier et al., 2009), while in temperate zone, endemics are rarer (e.g. Kier et al., 2009; Essl et al., 2013). It is especially true for Russia, where endemic plants are both less represented and less studied.
In Russia, the Far East, Southern Siberia and the Caucasus are biodiversity hotspots (Venevsky & Venevskaia, 2005; Griffin, 1999). The Russian Far East represents 2641 vascular plant species inhabiting an area of229 691 km2. Among the island flora of the Kuril Archipelago, Kunashir Island has the highest species richness - 908 taxa (Pietsch et al., 2003).
The genus Tilia is included in subfamily Tilioide-ae of the family Malvaceae s.l., according to Nyffel-er et al. (2005). There are about 23 species of Tilia worldwide including four species and two hybrids naturally occurring in Europe and Western Asia, four - in North America, and 15 - in Eastern Asia (Pigott,
2002). The natural range of the genus covers temperate regions up to 60-66° N. One of these species is Tilia maximowicziana Shiras. This is a large tree up to 30 m tall with a cylindrical trunk about 1.0-1.5 m in diameter (Pigott, 2012). This species is included in the Red Data Book of the Russian Federation (Bar-dunov & Novikov, 2008) (rarity category 1 - «at-risk of extinction»), being known only on Kunashir Island at the northern limit of its range. The main part of the native range is located in Japan (islands of Hokkaido and Honshu), where the type locality is situated (Shi-rasawa, 1900). According to published data (Alekse-eva, 1983; Kharkevich, 1987; Barkalov & Eremenko, 2003; Bardunov & Novikov, 2008; Volkova et al., 2015), Russian locations of T. maximowicziana are located on the Okhotsk Sea coast up to 43° N. The species usually grows single or in small groups of trees in remotely situated forests.
We have aimed to study the status of Tilia maximowicziana subpopulations known in Russia.
Material and Methods
Study area
The study was confined to Kunashir, the southernmost island of the Kuril Archipelago, including more than 56 islands (Fig. 1). It is located at 43.66666744.500000 N, 145.416667-146.333333 E. The pre-
cipitation ranges between 600 mm and 1300 mm per annum. The climate is oceanic, moderately cold. The summer is cool, rainy with a temperature not higher than +20^ (June). The winter temperature is not lower than -10°C The relief is middle-mountainous, volcanic, represented by three acting volcanoes and mountain massifs connected by low-lying isthmuses. The sea coast is rocky, steep or gently sloping with sand dunes shores.
Site selection
In 2014-2019, we have carried out research and field investigation of T. maximowicziana subpopulations, including our data and literature sourc-
es (Grishchenko et al., 2018) on Kunashir Island (Table 1). These subpopulations were considered to be a representative sample of the T. maximowicziana population on both Kunashir Island and in Russia. In relation to the IUCN Red List categories and criteria the subpopulations are defined as geographically or otherwise distinct groups in the Russian population between which there is little demographic or genetic exchange (IUCN, 2019). However we must note that the subpopulations selected in our study do not fit completely this definition as genetic exchange is highly likely. The term is used here for convenience to mean a portion of the Russian population.
ARCTIC OCEAN
Kunashirskiy Strait пролив Кунаширский
тттш
cP-
ft V
Izmeny Strait пролив Измены
Ш
О
PACIFIC OCEAN
Fig. 1. The locations in which Tilia maximowicziana is located in Russia (Kunashir Island) on map of Asia. Designations: 1 - location A, 2 - location B, 3 - location C, 4 - location D, 5 - location E, 6 - location F.
Table 1. Locations in which we confirmed the occurrence of Tilia maximowicziana on Kunashir Island, Russia, with geographical coordinates, altitude, slope exposure, distance to sea coast, number of mature individuals, and saplings
Locations Description Altitude, m a.s.l. Slope exposure Distance to sea coast, m Number of mature (fruiting) individuals Number of saplings
A. Ivanovskiy cape Left bank of River Krivonozhka 60 NW 340 6 (0) 5
B. Golovnin volcano caldera Right bank of stream Ozernyi 126 NW 400 12 (3) 4
C. Golovnin volcano caldera The top of mud volcano Magnolie-vaya northwest of the stream Ozernyi 140 W 420 1 (0) 2
D. Alekhina cape Upper reaches of the stream Po-granichnyi, left bank 50 NW 1275 8 (0) -
E. Alekhina cape Right bank of stream Alekhina 62 S 1550 1 (0) -
F. Stolbchatyi cape Upper slope part of in 250 m from the mouth of the stream Zmeinyi 90 W 140 3 (1) -
Study design
A complete count of individuals was conducted in each subpopulation within four 100 x 100 m plots. Each plant found was recorded and marked to prevent being counted more than once. Apart of mature individuals, we accounted saplings. Because of inaccessibility of some subpopulations, field population- and habitat-based studies have been carried out in relation to locations A, B, E, F. In them, we estimated width / length of leaves, length of petioles (N = 25 for each parameter), while only in selected subpopulations, the length of bracts (locations B and F, N = 25) and fruits (location F, N = 25) were estimated. For mature individuals, the diameter at breast height (DBH) and tree height were estimated. The Nikon Laser Forestry Pro laser rangefinder was used to determine the tree height and the least distance to the sea coast. The nested quadrate method was used to determine the species composition and projective coverage of species in the plant community associated with the T. maximowicziana subpopulation within four 100 x 100 m plots. Scientific names are standardised according to The Plant List (2013).
IUCN estimation of Tilia maximowicziana
For the definition of the threat status of T. maxi-mowicziana, we used the recently revised evaluation criteria adopted by the IUCN (2012a, 2012b, 2019), focusing on the extent of occurrence (EOO), area of occupancy (AOO), number of locations, and subpopulation size.
Results and Discussion
Locations of Tilia maximowicziana in Russia
Before 2019, four T. maximowicziana locations were reliably known in Russia (Table 1, locations A, C, D, E). These were situated on the west coast of Kunashir Island (Fig. 1). Most of them are located in hard-to-reach areas of the Kurilskiy State Nature Reserve. It is supported by data of some authors (e.g. Volkova et al., 2015). In July 2019, we found two new locations (B and F, Table 1) T. maximowicziana near the Golovnin volcano caldera and Stolbchatyi cape on Kunashir Island, respectively. Noteworthy,
location F is thenorthernmost subpopulation of T. maximowicziana within its total range.
Morphometric traits of Tilia maximowicziana
On the basis of population-based studies on Kunashir Island, morphometric traits of T. maximo-wicziana individuals have been estimated (Table 2). We found about 2-fold excess of DBH and mature tree height between all locations studied. At the same time, the values of these parameters are lower than found in the main range in Japan (Pigott, 2012), where the average tree height and DBH were 30 m and 1.0-1.5 m respectively. It might be explained by the peripheral situation of the studied subpopulations, as deviations from a norm are known in peripheral plant populations (Khapugin & Chugunov, 2015; Vo-lis et al., 1998). At the same time, leaf size, length of petiole, bract and fruit were within the range of known values within the main range (Pigott, 2012).
Characteristics of Tilia maximowicziana habitats
We found that T. maximowicziana inhabits plant communities in deciduous and mixed forests. In deciduous forests, Quercus dentata Thunb. and/or Q. mongolica subsp. crispula (Blume) Menitsky dominated in forest stand, sometimes with participation of Acer pictum Thunb. or Betula ermanii Cham. (Table 3). In location A, a shrub layer was absent, while it was poorly developed in location E. The projective cover of the shrub layer had the highest value in location F (Table 3). The herb layer was represented predominantly by Sasa sp. with participation of Matteuccia struthiopteris (L.) Tod., Dryopteris sp. or Maianthemum dilatatum (Alph. Wood) A.Nelson & J.F.Macbr. Noteworthy, on Ku-nashir Island, T. maximowicziana was associated with other plant species than in the Japanese Archipelago (central part of the species range) (see Pigott, 2012). The similarity concerned to predominance of Sasa sp. in the herb layer, while the forest stand was represented by other tree species. It highlights the need to take into account information on T. maxi-mowicziana habitats on Kunashir Island to obtain complete data on this endemic plant species.
Table 2. Morphometric traits of Tilia maximowicziana individuals in island Kunashir
Locations Average tree height, m DBH, cm Leaf length, cm Leaf width, cm Leaf petiole, cm Bract length, cm Fruit length, cm
Location A 7 ± 0.3 13.5 ± 1.0 12.3 ± 0.5 11.3 ± 0.5 6.3 ± 0.3 - -
Location B 10 ± 0.4 13.2 ± 1.9 9.4 ± 0.8 7.7 ± 0.3 5.0 ± 0.3 8.9 ± 0.3 -
Location C 10 ± 0.0 24.0 ± 0.0 - - - - -
Location E 13 ± 0.0 26.3 ± 0.0 7.7 ± 0.3 8.3 ± 0.3 4.3 ± 0.2 - -
Location F 15 ± 3.9 20.7 ± 6.1 16.3 ± 0.8 16.4 ± 0.8 6.7 ± 0.2 12.4 ± 0.4 1.0 ± 0.03
Table 3. Vegetation characteristics of plant communities with Tilia maximowicziana (projective cover, %)
Species 1 Location A | Location B | Location С | Location E | Location F
Forest stand
Abies sachalinensis (F.Schmidt) Mast. - 5 60 50 -
Acerpictum Thunb. 30 5 10 5 25
Betula ermanii Cham. - 20 30 10 -
Kalopanax septemlobus (Thunb.) Koidz. - 5 - 5 10
Magnolia obovata Thunb. - 10 - 10 -
Picea jezoensis (Siebold & Zucc.) Carrière - 10 - 5 5
Prunus sargentii Rehder - - - - 10
Quercus dentata Thunb. 20 5 - - 20
Quercus mongolica subsp. crispula (Blume) Menitsky 50 40 - 15 30
Shrub layer
Actinidia arguta (Siebold & Zucc.) Planch. ex Miq. - 10 - - 10
Hydrangea paniculata Siebold - 30 10 10 10
Hydrangeapetiolaris Siebold & Zucc. - - - 40 -
Ribes latifolium Jancz. - - - - 10
Sambucus miquelii (Nakai) Kom. - 10 - 10 10
Toxicodendron orientale Greene - - - - 50
Toxicodendron trichocarpum (Miq.) Kuntze - 10 10 - -
Vitis coignetiae Pulliat ex Planch. - 10 - - 10
Herb layer
Aralia cordata Thunb. - - - - 2
Aruncus dioicus (Walter) Fernald - - - - 2
Aconitum kunasirense Nakai - - - - 2
Chloranthus japonicus Siebold - - - - 2
Dryopteris sp. 20 - - 20 10
Hemerocallis esculenta Koidz. - - - - 14
Laportea bulbifera (Siebold & Zucc.) Wedd. - - - - 2
Maianthemum dilatatum (Alph.Wood) A.Nelson & J.F.Macbr. - - - 20 10
Matteuccia struthiopteris (L.) Tod. 20 - - - 15
Petasites japonicus (Siebold & Zucc.) Maxim. - - - - 5
Poa sp. - - - 30 5
Polygonatum odoratum var. maximowiczii (F.Schmidt) Koidz. - - - - 2
Sasa sp. 60 90 90 30 20
Solidago virgaurea subsp. dahurica (Kitag.) Kitag. - - - - 2
Thalictrum sachalinense Lecoyer - - - - 5
Trillium camschatcense Ker Gawl. - - - - 2
IUCN status of Tilia maximowicziana in Russia The extent of occurrence (EOO) of T. maximowicziana was defined as area contained within the shortest continuous imaginary boundary which can be drawn to encompass all the known, inferred or projected sites of present occurrence of a taxon (IUCN, 2019). We found that the EOO was 32.11 km2. The area of occupancy (AOO) was defined as the area within its EOO, which is occupied by a taxon, including areas which could be occupied by this species in future (IUCN, 2019). We found that the AOO was 20 km2. Below we present a detailed description of the IUCN estimation. Criterion B:
AOO: 20.00 km2 calculated with a 2 x 2 km-cell fixed grid by GeoCAT (Bachman et al., 2011).
EOO: 32.11 km2 calculated with minimum convex hull by GeoCAT (Bachman et al., 2011).
a) All subpopulations represent a single location according to definition of IUCN (2019), according to which the term «location» defines a geographically or ecologically distinct area in
which a single threatening event can rapidly affect all individuals of the taxon present.
b) Decline in quality and extent of habitat (iii).
Criterion C:
Population size estimated to 31 mature individuals and (2) no subpopulation estimated to contain more than 50 mature individuals (ii).
Criterion D:
Population size estimated to number fewer than 50 mature individuals.
Thus, in Russia, T. maximowicziana occurs only in six sites close to each other, located on the western coast of Kunashir Island with an AOO of 20 km2. As the species has a low degree of fruiting trees and high vegetative reproduction (Table 1), the elimination of fruiting individuals might be a reason of significant decrease in the effective size of the T. maximowicziana population. The possible decline in habitat quality and in the number of mature individuals support the classification of the species as Critically Endangered at a regional level (Russia) according to the formula CR B1ab(iii); C2a(i); D.
Conservation actions
All subpopulations of Tilia maximowicziana in Russia are under protection in the core and buffer zones of the Kurilsky State Nature Reserve. We suggest the further monitoring and searching of new locations of T. maximowicziana both on Kunashir Island and on other islands of the Kuril Archipelago. Each known subpopulation needs to be investigated in terms of status of population and habitat of the species. Consequently, it seems to be necessary to assess the global IUCN Red List status of T. maximowicziana with involving the estimation of species populations known in Japan. It concerns many plant species in worldwide regions, as regional IUCN estimation is a necessary step and tool to obtain data on the global IUCN status (Khapugin et al., 2017; Kestemont, 2019).
Conclusions
Nowadays, Tilia maximowicziana is represented by six subpopulations in Russia. All these are situated on the Okhotsk Sea coast. Four of these locations (66.7%) are situated 139-403 m away from the sea coast, while two other locations are 1450-2020 m distant from the sea coast , being, thus, the most hard-to-reach forinvestigating. On Kunashir Island, the T. maximowicziana subpopulations inhabit deciduous (dominated by Quercus dentata, Q. mongolica subsp. crispula, and / or Acer pictum and Betula er-manii) or mixed (dominated by Abies sachalinensis (F.Schmidt) Mast. and Betula ermanii) forests, where Sasa sp. dominated in the herb layer. We found that in the northernmost subpopulations, T. maximowicziana individuals had lower values of DBH and tree height, while other studied morphometric traits were consistent with published data concerning the main part of the species' range. According to IUCN Red List categories and criteria, T. maximowicziana has the regional (Russia) status of CR B1ab(iii); C2a(i); D. Data we obtained could be applied to conduct the assessment of global IUCN Red List status of T. maximowicziana taking into account its subpopulations in the Japanese Archipelago. We also recommend maintaining the endemic plant species on the main list of the Red Data Book of the Russian Federation (Bardunov & Novikov, 2008) with rarity category 1 (near extinction in Russia), once it will be re-edited.
References
Alekseeva L.M. 1983. Flora of Kunashir island (vascular
plants). Vladivostok: FESC AS USSR. 72 p. [In Russian] Bachman S., Moat J., Hill A.W., de la Torre J., Scott B. 2011.
Supporting Red List threat assessments with GeoCAT:
geospatial conservation assessment tool. ZooKeys 150: 117-126. DOI: 10.3897/zookeys.150.2109 Bardunov L.V, Novikov VS. (Ed.). 2008. Red Data Book of the Russian Federation (plants and fungi). Moscow: KMK Scientific Press Ltd. 855 p. [In Russian] Barkalov V.Yu., Eremenko N.A. 2003. Flora of the Kurilsky Nature Reserve and Malye Kurily Sanctuary (Sakhalin region). Vladivostok: Dalnauka. 285 p. [In Russian] Cheaib A., Badeau V, Boe J., Chuine I., Delire C., Dufrêne E., François C., Gritti E.S., Legay M., Pagé C., Thuiller W., Viovy N., Leadley P. 2012. Climate change impacts on tree ranges: model intercomparison facilitates understanding and quantification of uncertainty. Ecology Letters 15(6): 533-544. DOI: 10.1111/j.1461-0248.2012.01764.x Essl F., Moser D., Dirnböck T., Dullinger S., Milasowszky N., Winter M., Rabitsch W. 2013. Native, alien, endemic, threatened, and extinct species diversity in European countries. Biological Conservation 164: 90-97. DOI: 10.1016/j.biocon.2013.04.005 Ferreira M.T., Cardoso P., Borges P.A.V, Gabriel R., de Aze-vedo E.B., Reis F., Bastos M., Elias R.B. 2016. Effects of climate change on the distribution of indigenous species in oceanic islands (Azores). Climatic Change 138(3): 603-615. DOI: 10.1007/s10584-016-1754-6 Griffin P.C. 1999. Endangered species diversity 'hot spots' in Russia and centers of endemism. Biodiversity and Conservation 8: 497-511. DOI: 10.1023/A:1008837023242 Grishchenko M.Yu., Miloslavskaya E.S., Chumakova A.V.
2018. Acer tschonoskii Maxim. and some other rare plant species in the Kurilsky State Nature Reserve. In: Sustainable development of Protected Areas. Vol. 5. Sochi: Donskoy Publishing Centre. P. 92-98. [In Russian]
Harter D.E.V, Irl S.D.H., Seo B., Steinbauer M.J., Gillespie R., Triantis K.A., Fernández-Palacios J.-M., Beierkuhnlein C. 2015. Impacts of global climate change on the floras of oceanic islands - Projections, implications and current knowledge. Perspectives in Plant Ecology, Evolution and System-atics 17(2): 160-183. DOI: 10.1016/j.ppees.2015.01.003 IUCN. 2012a. IUCN Red List Categories and Criteria: Version 3.1, 2nd ed. Gland and Cambridge: IUCN. 32 p. IUCN. 2012b. Guidelines for Application of IUCN Red List Criteria at Regional and National Levels: Version 4.0. Gland and Cambridge: IUCN. 41 p. IUCN. 2019. IUCN Standards and Petitions Committee.
2019. Guidelines for Using the IUCN Red List Categories and Criteria. Version 14. Prepared by the Standards and Petitions Committee. Downloadable from http:// www.iucnredlist.org/documents/RedListGuidelines.pdf
Kestemont B. 2019. The bottom-up assessment of threatened species. Nature Conservation Research 4(3): 93-106. DOI: 10.24189/ncr.2019.036 Khapugin A.A., Chugunov G.G. 2015. Two populations of Lunaria rediviva L. (Cruciferae Juss.) at the eastern edge of its range. Wulfenia 22: 83-94. Khapugin A.A., Silaeva T.B., Vargot E.V., Chugunov G.G., Grishutkina G.A., Grishutkin O.G., Pismarkina E.V., Orlova Ju.S. 2017. Estimation of taxa included in the first volume of the Red Data Book of the Republic of Mordovia (Russia) using the IUCN Red List Categories
and Criteria. Nature Conservation Research 2(Suppl.1): 164-189. DOI: 10.24189/ncr.2017.004 [In Russian] Kharkevich S.S. 1987. Vascular plants of Soviet Far East.
Vol. 2. Leningrad: Nauka. 446 p. [In Russian] Kier G., Kreft H., Lee T.M., Jetz W., Ibisch P.L., Nowicki C., Mutke J., Barthlott W. 2009. A global assessment of endemism and species richness across island and mainland regions. Proceedings of the National Academy of Sciences of the United States of America 106(23): 9322-9327. DOI: 10.1073/pnas.0810306106 Le Roux J.J., Hui C., Castillo M.L., Iriondo J.M., Keet J.H., Khapugin A.A., Medail F., Rejmanek M., Theron G., Yannelli F.A., Hirsch H. 2019. Recent Anthropogenic Plant Extinctions Differ in Biodiversity Hotspots and Coldspots. Current Biology 29(17): 2912-2918. DOI: 10.1016/j.cub.2019.07.063 Nyffeler R., Bayer C., Alverson W.S., Yen A., Whitlock B.A., Chase M.W., Baum D.A. 2005. Phylogenetic analysis of the Malvadendrina clade (Malvaceae s.l.) based on plastid DNA sequences. Organisms, Diversity and Evolution 5(2): 109-123. DOI: 10.1016/j. ode.2004.08.001 Pietsch T.W., Bogatov V.V., Amaoka K., Zhuravlev Y.N., Barkalov V.Y., Gage S., Takahashi H., Lelej A.S., Storozhenko S.Y., Minakawa N., Bennett D.J., Anderson T.R., Ohara M., Prozorova L.A., Kuwahara Y., Kholin S.K., Yabe M., Stevenson D.E., MacDonald E.L. 2003. Biodiversity and biogeography of the islands of the Kuril Archipelago. Journal of Biogeography 30(9): 1297-1310. DOI: 10.1046/j.1365-2699.2003.00956.x
Pigott C.D. 2002. A review of chromosome numbers in the genus Tilia (Tiliaceae). Edinburgh Journal of Botany 59(2): 239-246. DOI: 10.1017/S0960428602000057 Pigott D. 2012. Eastern Asian taxa 2: Section Astrophilyra. In: D. Pigott (Ed.): Lime-trees and Basswoods: A Biological Monograph of the Genus Tilia. Cambridge: Cambridge University Press. P. 175-247. doi:10.1017/ CBO9781139033275.012 Shirasawa H. 1900. Die Gattung Tilia in Japan. Bulletin of the College of Agriculture, University of Tokyo 4: 153-162. The Plant List. 2013. Version 1.1. Available from: http://
www.theplantlist.org/ Ungricht S., Rasplus J., Kjellberg F. 2005. Extinction threat evaluation of endemic fig trees of New Caledonia: priority assessment for taxonomy and conservation with herbarium collections. Biodiversity and Conservation 14(1): 205-232. DOI: 10.1007/s10531-005-5049-x Venevsky S., Venevskaia I. 2005. Hierarchical systematic conservation planning at the national level: identifying national biodiversity hotspots using abiotic factors in Russia. Biological Conservation 124(2): 235-251. DOI: 10.1016/j.biocon.2005.01.036 Volis S., Mendlinger S., Olswig-Whittaker L., Safriel U., Orlovsky N. 1998. Phenotypic variation and stress resistance in core and peripheral populations of Hordeum spontaneum. Biodiversity and Conservation 7: 799813. DOI: 10.1023/A:1008844504010 Volkova P.A., Kopylov-Guskov Yu., Zakharchenko D. 2015. Additamenta on distribution and population status of highly endangered plant species on Kunashir Island (Southern Kurils). Wulfenia 22: 265-270.
СТАТУС TILIA MAXIMOWICZIANA (MALVACEAE S.L.) В РОССИИ
Е. В. Линник1*, А. А. Хапугин2,3
Курильский государственный природный заповедник, Россия 2Объединенная дирекция Мордовского государственного природного заповедника имени П.Г. Смидовича и
национального парка «Смольный», Россия 3Тюменский государственный университет, Россия *e-mail: [email protected], [email protected]
Tilia maximowicziana (Malvaceae) - растение-эндемик северной части Японского архипелага и о. Кунашир. В России этот вид включен в федеральную Красную книгу с категорией редкости 1 (находящийся на грани исчезновения). В 2014-2019 гг., были проведены полевые исследования субпопуляций Tilia maximowicziana, известных в России. Обнаружено и рассмотрено шесть местообитаний вида на о. Кунашир. Затем были изучены морфометрические параметры особей и характеристика растительности в этих локалитетах. На основе полученных данных мы провели оценку угрожаемости T. maximowicziana на территории России, согласно методологии МСОП. Нами обнаружено, что в известных местообитаниях T. maximowicziana произрастает в широколиственных и смешанных лесах с доминированием видов рода Sasa в травянистом ярусе. Нами показано, что на о. Кунашир данный эндемик представлен особями с меньшим диаметром ствола на уровне груди и высотой особей, чем в основной части ареала. В то же время значения размера (длина / ширина) листовой пластинки, длины черешка и плодов соответствовали таковым, указанным в основной части ареала вида. Согласно категориям Красного списка МСОП, T. maximowicziana в России имеет статус угрожаемости CR B1ab(iii); C2a(i); D. Находки плодоносящих особей в популяциях T. maximowicziana показали способность вида к семенному размножению в северной части природного ареала. Полученные результаты позволяют провести глобальную оценку угрожаемости T. maximowicziana согласно критериям Красного списка МСОП, принимая во внимание субпопуляции вида на территории Японского архипелага.
Ключевые слова: ареал, Красный список МСОП, морфометрические признаки, плодообразование, растительное сообщество, угроза, эндемик