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1

Elliott-Fisk, Deborah L. "Timberline." Ecology 66, no. 6 (1985): 1989–90. http://dx.doi.org/10.2307/2937401.

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2

Whitesides, Clayton J. "The original review of alpine timberline in North America: Rexford Daubenmire’s 1954 publication, ‘Alpine Timberlines in the Americas and Their Interpretation’." Progress in Physical Geography: Earth and Environment 44, no. 2 (2020): 285–91. http://dx.doi.org/10.1177/0309133320909592.

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Rexford Daubenmire’s 1954 seminal review of alpine timberline in North America remains a valuable classic for timberline scholars. His article was published at a formative time for timberline studies and, as such, has affected the direction of timberline research for nearly 70 years. Daubenmire’s definition of timberline, his review of climatological theories controlling timberline, and his additions to altitudinal variations of timberline across latitudes remain at the forefront of timberline research.
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3

He, Wen, Chongchong Ye, Jian Sun, Junnan Xiong, Jinniu Wang, and Tiancai Zhou. "Dynamics and Drivers of the Alpine Timberline on Gongga Mountain of Tibetan Plateau-Adopted from the Otsu Method on Google Earth Engine." Remote Sensing 12, no. 16 (2020): 2651. http://dx.doi.org/10.3390/rs12162651.

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The alpine timberline, an ecosystem ecotone, indicates climatic change and is tending to shift toward higher altitudes because of an increase in global warming. However, spatiotemporal variations of the alpine timberline are not consistent on a global scale. The abundant and highest alpine timberline, located on the Tibetan Plateau, is less subject to human activity and disturbance. Although many studies have investigated the alpine timberline on the Tibetan Plateau, large-scale monitoring of spatial-temporal dynamics and driving mechanisms of the alpine timberline remain uncertain and inaccur
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4

Sakio, Hitoshi, and Takehiro Masuzawa. "Advancing Timberline on Mt. Fuji between 1978 and 2018." Plants 9, no. 11 (2020): 1537. http://dx.doi.org/10.3390/plants9111537.

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Climate change is a major cause of changes in alpine and polar vegetation, particularly at the edges of distributions. In temperate regions, these changes are expected to occur at the timberline of alpine zones. On Mt. Fuji, the highest mountain in Japan, the timberline is located 2400–2500 m above sea level. Over a 40-year period (1978–2018), we researched changes in the timberline vegetation of Mt. Fuji. A permanent belt transect extending from the upper timberline to subalpine zones was set up in August 1978. Tree diameters and heights were recorded at the establishment of the transect and
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5

List, Cara. "Tales From Timberline: The 2011 Acquisitions Institute at Timberline Lodge." Collection Management 36, no. 4 (2011): 246–52. http://dx.doi.org/10.1080/01462679.2011.605831.

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6

Mihăilă, Dumitru, Petruț-Ionel Bistricean, and Vasilică-Dănuț Horodnic. "Drivers of Timberline Dynamics in Rodna Montains, Northern Carpathians, Romania, over the Last 131 Years." Sustainability 13, no. 4 (2021): 2089. http://dx.doi.org/10.3390/su13042089.

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Currently, there is little information regarding the recent spatiotemporal dynamics of upper timberline in the Carpathian Mountains. We reconstructed the temporal (1887–2018) and spatial dynamics of upper timberline in the Rodna Mountains (Eastern Carpathians) based on seven sets of maps and aerial photographs and explained its variability in relation to three main drivers: air temperature, land morphometry and anthropogenic pressure. The impact of natural drivers (temperature, morphometry) on timberline position was evaluated using a high-resolution digital elevation model, local and regional
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7

Ma, Xinping, Hongying Bai, Chenhui Deng, and Tao Wu. "Sensitivity of Vegetation on Alpine and Subalpine Timberline in Qinling Mountains to Temperature Change." Forests 10, no. 12 (2019): 1105. http://dx.doi.org/10.3390/f10121105.

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Alpine timberline is a great place for monitoring climate change. The study of alpine and subalpine timberline in Qinling Mountains has led to early warning that reveals the response and adaptation of terrestrial vegetation ecosystem to climate change. Based on the remote sensing image classification method, the typical timberline area in Qinling Mountains was determined. Temperature and normalized difference vegetation index (NDVI) data were extracted from the typical timberline area based on spatial interpolation and NDVI data. The relationship between NDVI and temperature change and the cri
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8

Whitesides, Clayton J. "Henry Gannett." Progress in Physical Geography: Earth and Environment 42, no. 3 (2018): 406–12. http://dx.doi.org/10.1177/0309133318776503.

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Although Henry Gannett is best known as “the father of American map-making,” he made noteworthy contributions to timberline research in the late 1800s. Gannett’s studies attempted to identify a standard isotherm for alpine timberline in the USA, explained the mass elevation effect on timberline altitude in the Rocky Mountains, and recognized the importance of geology and geomorphology as controlling factors. Despite these contributions, Gannett’s timberline work remains in obscurity. As technology enhances our ability to find and cite older literature, the contributions of Gannett, and other u
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9

Beaudoin, Alwynne B. "Using Picea/Pinus Ratios from the Wilcox Pass Core, Jasper National Park, Alberta, to Investigate Holocene Timberline Fluctuations." Géographie physique et Quaternaire 40, no. 2 (2007): 145–52. http://dx.doi.org/10.7202/032634ar.

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ABSTRACT Holocene timberline fluctuations are investigated using Picea/Pinus ratios from the tephra and radiocarbon-dated Wilcox Pass Core (52°14'N, 117°13'W). Timberline elevations are calibrated by comparing Picea/Pinus ratios from the core with modern ratios obtained in surface samples of a transect from alpine vegetation in Wilcox Pass into subalpine forest in adjacent Sunwapta Pass. Ratios higher than present ratios from the site imply higher-than-present timberline elevation. The Picea/Pinus ratios imply higher-than-present timberline between ca. 6540-1480 yr BP, with a minimum about 421
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10

Li, Pei Xiao, Hong Ying Bai, and Hong He. "Study on Response of Alpine Timberline in Taibai Mountain to Climate Changes." Applied Mechanics and Materials 675-677 (October 2014): 1111–19. http://dx.doi.org/10.4028/www.scientific.net/amm.675-677.1111.

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This article based on RS/GIS technology analyzed the spatio-temporal changes of mountain timberline in Taibai Mountain Nature Reserve from 1988 to 2009 which is aimed at reveal the response to climate changes. The study results shown:As the temperatures rise, timberline the overall position was on the move in recent 22 years; in the aspect of vegetation ,the rising line for the top of Larix chinensis forest invasion in shrub meadow vegetation areas proved the rising of timberline in Taibai Mountain Nature Reserve.
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11

Tinner, Willy, and Brigitta Ammann. "Timberline Paleoecology in the Alps." PAGES news 9, no. 3 (2001): 9–11. http://dx.doi.org/10.22498/pages.9.3.9.

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12

Mouw, James R. "Papers from the Timberline Institute." Library Collections, Acquisitions, and Technical Services 28, no. 4 (2004): 459. http://dx.doi.org/10.1016/j.lcats.2004.09.001.

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13

Mouw, James R. "Papers from the Timberline Institute." Library Collections, Acquisitions, & Technical Services 28, no. 4 (2004): 459. http://dx.doi.org/10.1080/14649055.2004.10766017.

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14

Pakharkova, Nina, Irina Borisova, Ruslan Sharafutdinov, and Vladimir Gavrikov. "Photosynthetic Pigments in Siberian Pine and Fir under Climate Warming and Shift of the Timberline." Forests 11, no. 1 (2020): 63. http://dx.doi.org/10.3390/f11010063.

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Research Highlights: For the first time, the Pinus sibirica Du Tour and Abies sibirica L. conifer forest at the West Sayan ridge timberline has been explored to reveal which species is likely to react to climate change and a shift of the timberline. Such a shift may modify the ecological functions of the forests. Background and Objectives: Long-term climate change has become obvious in the mountains of southern Siberia. Specifically, a half-century rise in annual mean temperatures has been observed, while precipitation remains unchanged. Trees growing at the timberline are likely to strongly r
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15

Stuyck, Claire M., Paul B. Leonard, Gerald V. Frost, Michelle L. S. Lake, and Jeffrey D. Walters. "Update on the Status and Breeding Phenology of the Timberline Sparrow (Spizella breweri taverneri) in Alaska." Western Birds 52, no. 3 (2021): 252–60. http://dx.doi.org/10.21199/wb52.3.5.

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In July 2020 we located 10 singing Timberline Sparrows [Spizella (breweri) taverneri] in the region of Gold Hill, Nutzotin Mountains, east-central Alaska. All birds were on southeast-facing slopes in the ecotone between subalpine scrub and alpine tundra, to which habitat breeding Timberline Sparrows seem narrowly confined. The population’s estimated density of 0.77 birds/km2 was similar to that at the time of its discovery in 1994. We located the first active nest of the Timberline Sparrow reported for Alaska, ~0.3 m above the ground in a shrubby resin birch (Betula glandulosa). An observation
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16

Shankman, David, and Stephen F. Arno. "Timberline: Mountain and Arctic Forest Frontiers." Arctic and Alpine Research 18, no. 1 (1986): 123. http://dx.doi.org/10.2307/1551220.

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17

Czajka, Barbara, Adam Łajczak, Ryszard J. Kaczka, and Paweł Nicia. "Timberline in the Carpathians: An overview." Geographia Polonica 88, no. 2 (2015): 7–34. http://dx.doi.org/10.7163/gpol.0013.

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18

Maruta, E. "Winter water relations of timberline larch (." Trees 11, no. 2 (1996): 119. http://dx.doi.org/10.1007/s004680050067.

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19

Takahashi, Koichi, Tatsuru Hirosawa, and Ryohei Morishima. "How the timberline formed: altitudinal changes in stand structure and dynamics around the timberline in central Japan." Annals of Botany 109, no. 6 (2012): 1165–74. http://dx.doi.org/10.1093/aob/mcs043.

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20

Baitsar, A. "Timberline in the Ukrainian Carpathians and its preservation." Visnyk of the Lviv University. Series Geography 1, no. 40 (2012): 101–6. http://dx.doi.org/10.30970/vgg.2012.40.2032.

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The article describes the process of formation and main stages of the Tourism Chair of the Ivan Timberline (TL) is a compound and dynamic organism, which is situated on the boundary of the forest zone and the highland. The study embraces regions of the Ukrainian Carpathians: Chornohora, Svydovets, Gorgany, Polonyna Borzava, Polonyna Krasna, Beskydy. In the Carpathians, nine types of TL are determined: thermal, orographical, wind, avalanche biotic, peat-swamp, gregot, talus and anthropogenic. Key words: Timberline (TL), polonynas, highland.
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21

Moir, William H., and Laurie S. Huckaby. "Displacement Ecology of Trees near Upper Timberline." Bears: Their Biology and Management 9 (1994): 35. http://dx.doi.org/10.2307/3872682.

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22

Wirth, Andrea A. "The 2012 Acquisitions Institute at Timberline Lodge." Collection Management 38, no. 1 (2013): 67–74. http://dx.doi.org/10.1080/01462679.2012.735214.

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23

Hogarth, Margaret. "The 2013 Acquisitions Institute at Timberline Lodge." Collection Management 38, no. 4 (2013): 250–66. http://dx.doi.org/10.1080/01462679.2013.838528.

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24

Cooper, Peggy, and Deborah Babbitt. "Second Annual Acquisitions Institute at Timberline Lodge." Serials Review 28, no. 1 (2002): 67–73. http://dx.doi.org/10.1080/00987913.2002.10764713.

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25

Blake, Julie C. "The 2002 Acquisitions Institute at Timberline Lodge." Serials Review 28, no. 4 (2002): 328–34. http://dx.doi.org/10.1080/00987913.2002.10764768.

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26

DeShazo, Kristina. "The 2009 Acquisitions Institute at Timberline Lodge." Serials Review 35, no. 4 (2009): 296–98. http://dx.doi.org/10.1080/00987913.2009.10765260.

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27

Havranek, W. M., G. Wieser, and M. Bodner. "Ozone fumigation of Norway spruce at timberline." Annales des Sciences Forestières 46, Supplement (1989): 581s—585s. http://dx.doi.org/10.1051/forest:198905art0132.

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28

Renvall, Pertti, Tarja Renvall, and Tuomo Niemelä. "Basidiomycetes at the timberline in Lapland 1. Introduction." Karstenia 31, no. 1 (1991): 1–12. http://dx.doi.org/10.29203/ka.1991.281.

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29

Liu, Hongyan, Zhiyao Tang, Junhu Dai, Yuanxin Tang, and Haiting Cui. "Larch Timberline and its Development in North China." Mountain Research and Development 22, no. 4 (2002): 359–67. http://dx.doi.org/10.1659/0276-4741(2002)022[0359:ltaidi]2.0.co;2.

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30

Garcia-Ruiz, Jose M., Bernardo Alvera, Gabriel Del Barrio, and Juan Puigdefabregas. "Geomorphic Processes above Timberline in the Spanish Pyrenees." Mountain Research and Development 10, no. 3 (1990): 201. http://dx.doi.org/10.2307/3673600.

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31

Mayr, Stefan, Peter Schmid, Barbara Beikircher, Feng Feng, and Eric Badel. "Die hard: timberline conifers survive annual winter embolism." New Phytologist 226, no. 1 (2019): 13–20. http://dx.doi.org/10.1111/nph.16304.

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32

Czajka, Barbara, Adam Łajczak, and Ryszard J. Kaczka. "Geographical characteristics of the timberline in the Carpathians." Geographia Polonica 88, no. 2 (2015): 35–54. http://dx.doi.org/10.7163/gpol.0014.

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33

Yang, Teng, Pamela Weisenhorn, Jack A. Gilbert, et al. "Carbon constrains fungal endophyte assemblages along the timberline." Environmental Microbiology 18, no. 8 (2016): 2455–69. http://dx.doi.org/10.1111/1462-2920.13153.

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34

Timonen, Mauri, Kari Mielikäinen, and Samuli Helama. "Timberline tree-ring statistics examined through chronology stripping." Forestry Studies 56, no. 1 (2012): 5–15. http://dx.doi.org/10.2478/v10132-012-0001-9.

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Abstract Tree-ring data is commonly used in forest science and dendrochronology. As the collected datasets represent restricted populations of theoretical infinite sample size, an interesting question deals with the sample selection that is carried out during the fieldwork and through the data analyses. This paper considers the latter issue, by statistically examining a recently completed Scots pine dataset of timberline tree-rings from Lapland (northern Finland). Following the detrending of individual ring-width series, the composition of the data was restricted using a pre-determined criteri
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35

Urbanska, Krystyna M. "Biodiversity assessment in ecological restoration above the timberline." Biodiversity and Conservation 4, no. 7 (1995): 679–95. http://dx.doi.org/10.1007/bf00158862.

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36

Turunen, Minna, and Kirsi Latola. "UV-B radiation and acclimation in timberline plants." Environmental Pollution 137, no. 3 (2005): 390–403. http://dx.doi.org/10.1016/j.envpol.2005.01.030.

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37

Sakio, Hitoshi, and Takehiro Masuzawa. "Ecological studies on the timberline of Mt. Fuji." Botanical Magazine Tokyo 100, no. 4 (1987): 349–63. http://dx.doi.org/10.1007/bf02488854.

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38

Masuzawa, Takehiro. "Ecological studies on the timberline of Mt. Fuji." Botanical Magazine Tokyo 98, no. 1 (1985): 15–28. http://dx.doi.org/10.1007/bf02488903.

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39

Sakio, Hitoshi, and Takehiro Masuzawa. "Ecological studies on the timberline of Mt. Fuji." Botanical Magazine Tokyo 105, no. 1 (1992): 47–52. http://dx.doi.org/10.1007/bf02489402.

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40

Davis, Susan, Column Editor, and Mary F. Miller. "Report of the First Acquisitions Institute at Timberline Lodge." Serials Review 26, no. 4 (2000): 64–71. http://dx.doi.org/10.1016/s0098-7913(00)00114-3.

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41

Hansen-Bristow, Katherine. "Influence of increasing elevation on growth characteristics at timberline." Canadian Journal of Botany 64, no. 11 (1986): 2517–23. http://dx.doi.org/10.1139/b86-334.

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Significant differences in growing-season air and soil temperatures were found with increasing elevation in the upper montane and forest–alpine tundra ecotone. Temperature inversions in topographic depressions were frequent, especially during the growing season. Variability in bud flush timing with elevation was best accounted for by soil temperatures; however, air temperature recorded within a mat conifer also correlated well with bud flush timing. Significant differences in shoot elongation, needle length, and cuticular thickness were found with differences in climate and elevational changes
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42

Miller, Mary F. "Report of the First Acquisitions Institute at Timberline Lodge." Serials Review 26, no. 4 (2000): 64–71. http://dx.doi.org/10.1080/00987913.2000.10764628.

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43

Han, Fang, Yonghui Yao, Shibao Dai, et al. "Mass elevation effect and its forcing on timberline altitude." Journal of Geographical Sciences 22, no. 4 (2012): 609–16. http://dx.doi.org/10.1007/s11442-012-0950-1.

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44

Hiller, B., A. Müterthies, F. L. Holtmeier, and G. Broll. "Investigations on spatial heterogeneity of humus forms and natural regeneration of Larch (<i>Larix decidua Mill</i>.) and Swiss Stone Pine (<i>Pinus cembra L.</i>) in an alpine timberline ecotone (Upper Engadine, Central Alps, Switzerland)." Geographica Helvetica 57, no. 2 (2002): 81–90. http://dx.doi.org/10.5194/gh-57-81-2002.

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Abstract. The north-west facing study area in the Upper Engadine (Central Alps, Switzerland) encompasses the whole timberline ecotone between 2200 m and 2400 m a.s.l.. By dendroecological methods, clear differences concerning quantity and age structure of the natural regeneration of the main tree species Swiss stone pine (Pinus cembra L.) and larch (Larix decidua Mill.) at different sites could be detected.The differing site conditions, closely linked to the microtopography, determine distribution and age structure of natural tree regeneration, as well as humus forms. On exposed sites characte
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45

Luckman, B. H., and M. S. Kearney. "Reconstruction of Holocene Changes in Alpine Vegetation and Climate in the Maligne Range, Jasper National Park, Alberta." Quaternary Research 26, no. 2 (1986): 244–61. http://dx.doi.org/10.1016/0033-5894(86)90108-0.

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Pollen, macrofossil (logs and needles), and oxygen-isotope data from tree rings are presented for three alpine bog sites in the Maligne Range of the Canadian Rockies. Organic sedimentation at the Watchtower site began prior to ca. 9500 14C yr B.P. and by 8770 yr B.P. timberlines were at least 100 m above present levels. The two pollen records are dominated by Pinus and subsequent changes in timberlines are inferred from pollen-ratio data (Abies/Pinus) and from macrofossils. The recovered records indicate two periods of high Hypsithermal timberlines ca. 8800-7500 and 7200-5200 yr B.P. separated
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46

Bolliger, Janine. "Schweizer Wälder und Klimaveränderungen: Vergleich von Simulationen quantitativer Vegetationsmodelle | Swiss forests and climate change: comparison of simulated quantitative vegetation models." Schweizerische Zeitschrift fur Forstwesen 153, no. 5 (2002): 167–75. http://dx.doi.org/10.3188/szf.2002.0167.

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Using simulation models various climate change scenarios are described and the possible consequences to forests in Switzerland are discussed. Consequences to be reckoned with range from less acute to serious, e.g., with displacement of species and timberline and, in the long term, with desertification of already dry areas.
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47

Olson-Rutz, K. M., C. B. Marlow, K. Hansen, L. C. Gagnon, and R. J. Rossi. "Packhorse Grazing Behavior and Immediate Impact on a Timberline Meadow." Journal of Range Management 49, no. 6 (1996): 546. http://dx.doi.org/10.2307/4002297.

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48

Hadley, J. L., and W. K. Smith. "Wind Erosion of Leaf Surface Wax in Alpine Timberline Conifers." Arctic and Alpine Research 21, no. 4 (1989): 392. http://dx.doi.org/10.2307/1551648.

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49

Rawal, Ranbeer S., and Uppeandra Dhar. "Sensitivity of Timberline Flora in Kumaun Himalaya, India: Conservation Implications." Arctic and Alpine Research 29, no. 1 (1997): 112. http://dx.doi.org/10.2307/1551841.

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50

Scuderi, Louis A. "Late-Holocene upper timberline variation in the southern Sierra Nevada." Nature 325, no. 6101 (1987): 242–44. http://dx.doi.org/10.1038/325242a0.

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