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Articoli di riviste sul tema "Rwenzori mountains national park"

Autore: Grafiati

Pubblicato: 7 giugno 2025

Ultima modifica: 2 agosto 2025

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1

Sarah, Namayengo. "Dynamics of land use and land cover changes and their effect on carbon stocks of Rwenzori Mountains National Park." Journal of Biodiversity and Environmental Sciences (JBES) 25, no. 2 (2024): 111–25. https://doi.org/10.5281/zenodo.15378775.

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This study characterized the extent of land use land cover changes in Rwenzori Mountains National Park (RMNP) and determined the effect of observed land use land cover changes on the park’s carbon stocks. Landsat 5 images were obtained of 1990; Landsat 7 of 2000 and 2010 and Landsat 8 of 2020 for Rwenzori Mountains National Park and analyzed using GIS tools in ArcGIS 10.5 using supervised classification. The Landsat scenes were obtained from path and row (171, 060) and (172, 060). The effect of land use land cover changes on the park’s carbon stocks was determined by estimating the

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2

Sarah, Namayengo. "Dynamics of land use and land cover changes and their effect on carbon stocks of Rwenzori Mountains National Park." Journal of Biodiversity and Environmental Sciences (JBES) 25, no. 2 (2024): 111–25. https://doi.org/10.5281/zenodo.15379093.

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This study characterized the extent of land use land cover changes in Rwenzori Mountains National Park (RMNP) and determined the effect of observed land use land cover changes on the park’s carbon stocks. Landsat 5 images were obtained of 1990; Landsat 7 of 2000 and 2010 and Landsat 8 of 2020 for Rwenzori Mountains National Park and analyzed using GIS tools in ArcGIS 10.5 using supervised classification. The Landsat scenes were obtained from path and row (171, 060) and (172, 060). The effect of land use land cover changes on the park’s carbon stocks was determined by estimating the

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3

Wesche, Karsten. "The Rwenzori Mountains National Park, Uganda." Mountain Research and Development 20, no. 1 (2000): 102–3. http://dx.doi.org/10.1659/0276-4741(2000)020[0102:trmnpu]2.0.co;2.

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4

Hamilton, Alan. "The Rwenzori Mountains National Park,Uganda." African Journal of Ecology 38, no. 4 (2000): 376–78. http://dx.doi.org/10.1046/j.1365-2028.2000.00222-3.x.

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5

KATAEV, BORIS M. "A review of the Afrotropical genus Kenyacus (Coleoptera: Carabidae: Harpalini) from the Rwenzori Mountains, with description of seven new species." Zootaxa 4679, no. 3 (2019): 463–98. http://dx.doi.org/10.11646/zootaxa.4679.3.3.

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A taxonomic review of the Afrotropical genus Kenyacus Alluaud, 1917 from the Rwenzori Mountains is given. Tropicoritus Alluaud, 1917 is treated as a new synonym of Kenyacus. Seven new species are described from the eastern part of the Rwenzori Mountains National Park (Uganda): K. gusarovi sp. n., K. parvus sp. n., K. berndi sp. n., K. trechoides sp. n., K. angustatus sp. n., K. similis sp. n. and K. pusillus sp. n. Two species previously known from the Rwenzori Mountains, K. ruwenzorii (Alluaud, 1917) and K. ruwenzoricus Basilewsky, 1955, are re-described, and a key to all described species of

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6

Rich, Alicia M., Michael D. Wasserman, Kevin D. Hunt, and Frederika A. Kaestle. "Chimpanzee (Pan troglodytes schweinfurthii) Population Spans Multiple Protected Areas in the Albertine Rift." Folia Primatologica 91, no. 6 (2020): 595–609. http://dx.doi.org/10.1159/000508073.

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We used mitochondrial DNA to examine gene flow in a region of western Uganda that has received little attention regarding chimpanzee population dynamics. The area is critical to gene flow between isolated Democratic Republic of Congo populations and the rest of East Africa. None of the chimpanzees in each of the 4 protected areas under consideration (Toro-Semliki Wildlife Reserve, Semuliki National Park, Rwenzori Mountains National Park and Itwara Central Forest Reserve) are fully habituated. Therefore, it is not clear whether one or more populations have historically used this fragmented land

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7

Moore, Peter D. "The Rwenzori Mountains National Park, Uganda.. H. Osmaston, J. Tukahirwa, C. Basalirwa &; J. Nyakaana (eds) (1998)." Journal of Ecology 88, no. 2 (2000): 368–69. http://dx.doi.org/10.1046/j.1365-2745.2000.00447-4.x.

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8

Jagger, Pamela, Samuel Sellers, Noah Kittner, Ipsita Das, and Glenn K. Bush. "Looking for Medium-term Conservation and Development Impacts of Community Management Agreements in Uganda's Rwenzori Mountains National Park." Ecological Economics 152 (October 2018): 199–206. http://dx.doi.org/10.1016/j.ecolecon.2018.06.006.

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9

Iacopino, Simone, Carlo Piazzi, Julius Opio, et al. "Tourist Agroforestry Landscape from the Perception of Local Communities: A Case Study of Rwenzori, Uganda." Land 11, no. 5 (2022): 650. http://dx.doi.org/10.3390/land11050650.

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The Bakonjo have long practiced an agroforestry system of cultivation on the Ugandan slopes of the Rwenzori Mountain range. All terrain above 1600–2200 m has been strictly protected for many years because it is part of a national park. As a trade-off, the landscapes outside the park have been largely deforested. In the meantime, tourist numbers have increased. In Ruboni, a village of 1200 people, the closest to the eastern gate of the park, we interviewed a random sample of 51 residents aged >14 to understand how they perceived the landscape, park and tourism. Cultivated features were not e

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10

Muhumuza, Moses, Martie Sanders, and Kevin Balkwill. "A theoretical framework for investigating ecological problems associated with biodiversity conservation in national parks: A case of the Rwenzori Mountains National Park, Uganda." Open Journal of Ecology 03, no. 02 (2013): 196–204. http://dx.doi.org/10.4236/oje.2013.32023.

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11

Panizzo, V. N., A. W. Mackay, I. Ssemmanda, R. Taylor, N. Rose, and M. J. Leng. "A 140-year record of recent changes in aquatic productivity in a remote, tropical alpine lake in the Rwenzori Mountain National Park, Uganda." Journal of Paleolimnology 40, no. 1 (2007): 325–38. http://dx.doi.org/10.1007/s10933-007-9163-5.

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12

Steinicke, Ernst, and Kabann I. B. Kabananukye. "National parks and social tensions – Case study Ugandan Rwenzori National Park." eco.mont (Journal on Protected Mountain Areas Research) 6, no. 2 (2014): 29–36. http://dx.doi.org/10.1553/ecomont-6-2s29.

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13

Claudiu, Iușan, and Filipoiu Timoftei. "INVOLVING VOLUNTEERS IN PARTICIPATORY CONSERVATION OF BIODIVERSITY IN RODNA MOUNTAINS NATIONAL PARK (ROMANIA)." Scientific Bulletin Series D : Mining, Mineral Processing, Non-Ferrous Metallurgy, Geology and Environmental Engineering 31, no. 1 (2017): 41–49. http://dx.doi.org/10.37193/sbsd.2017.1.05.

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The Rodna Mountains National Park is a protected areas established in 1990 as a national park with 47.000 ha, being one of the biodiversity hot spot at Carpathian level. The Rodna Mountains National Park Administration implemented in the period 2004-2017 more than 26 projects in partnership with 35 institutions (universities, NGOs, museums, county councils, mayors, ministries, national and international agencies, administrations and custodians of protected areas etc.). The total budget accessed was 4.403.500 euros in partnership with other stakeholders through more than 15 funding sources. Ove

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14

PETERSEN, MATTHEW J., CHARLES R. PARKER, and ERNEST BERNARD. "The crane flies (Diptera: Tipuloidea) of Great Smoky Mountains National Park." Zootaxa 1013, no. 1 (2005): 1. http://dx.doi.org/10.11646/zootaxa.1013.1.1.

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The list of crane flies (Diptera: Ptychopteridae, Tipuloidea, Trichoceridae) known from Great Smoky Mountains National Park is updated. Sampling in association with the All Taxa Biodiversity Inventory of Great Smoky Mountains National Park resulted in the addition of 107 new Park records, bringing the current list to 250 species. This species assemblage is much richer than those of surrounding areas, although similar in composition. Total richness is estimated to be between 450 and 500 species for Great Smoky Mountains National Park.

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15

Pogue, Michael G. "of Great Smoky Mountains National Park." Zootaxa 2499 (December 31, 2010): 1–20. https://doi.org/10.5281/zenodo.195780.

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16

Din, N. A., and S. K. Eltringham. "BREEDING OF THE PINK-BACKED PELICAN PELECANUS RUFESCENS IN RWENZORI NATIONAL PARK, UGANDA." Ibis 116, no. 4 (2008): 477–93. http://dx.doi.org/10.1111/j.1474-919x.1974.tb07647.x.

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17

Barden, Lawrence S., and Margaret Lynn Brown. "Great Smoky Mountains National Park, 1900-2000." Ecology 82, no. 12 (2001): 3563. http://dx.doi.org/10.2307/2680175.

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18

Barden, Lawrence S. "Great Smoky Mountains National Park, 1900–2000." Ecology 82, no. 12 (2001): 3563–64. http://dx.doi.org/10.1890/0012-9658(2001)082[3563:gsmnp]2.0.co;2.

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19

Hillman, Jesse C. "Conservation in Bale Mountains National Park, Ethiopia." Oryx 20, no. 2 (1986): 89–94. http://dx.doi.org/10.1017/s0030605300026314.

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Ethiopia does not often receive publicity for its wildlife conservation work, but there have been a commendable number of achievements over the last 15 years or so. For the last two years the author has been carrying out ecological studies to formulate management plans in the Bale Mountains area, which is in the process of being established as a national park. As a result of the developments and protection already afforded, numbers of the endemic mountain nyala have increased considerably.

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20

Butynski, Thomas M., and Jan Kalina. "Three new mountain national parks for Uganda." Oryx 27, no. 4 (1993): 214–24. http://dx.doi.org/10.1017/s003060530002812x.

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For many years the Fauna and Flora Preservation Society has supported efforts to conserve forests in the Albertine Rift Afromontane Region of east-central Africa. The biodiversity of these forests is especially high but most have been destroyed or badly degraded. There are a large number of local, national and international initiatives to conserve at least some of the forests that remain. In 1991 Uganda created the Rwenzori Mountains, Mgahinga Gorilla, and Bwindi-Impenetrable National Parks, thus protecting all three of its Albertine Rift montane forests. This paper presents a synopsis of the

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21

Glasgow, Benny. "Gall Inducing and Gall Associated Arthropods and Plant Hosts in Great Smoky Mountains National Park." Journal of North Carolina Academy of Science 136-137, no. 1 (2020): 21–31. http://dx.doi.org/10.7572/jncas-d-22-00004.1.

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Abstract Gall inducing and gall associated arthropods were surveyed in Great Smoky Mountains National Park from 2017 until 2021, to find species presence, diversity, and distribution. Survey results identified 36 species or genera and 11 are new reports for Great Smoky Mountains National Park. Notes on host plants, arthropods, and associated species interactions of galls are presented.

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22

Linzey, Donald W. "Mammals of Great Smoky Mountains National Park: 2016 Revision." Southeastern Naturalist 15, no. m8 (2016): 1–93. https://doi.org/10.5281/zenodo.13446814.

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(Uploaded by Plazi for the Bat Literature Project) The 1288-km2 Great Smoky Mountains National Park (the Park) is one of the largest protected temperate forest ecosystems east of the Rocky Mountains. Because of its global ecological importance, the Park was designated an International Biosphere Reserve in 1976 and a World Heritage Site in 1983. The Park's rich biodiversity is the result of a deeply dissected landscape ranging in elevation from 259 m (850 ft) to 2026 m (6643 ft), high primary productivity, and diverse plant communities. These conditions, and the occurrence of several species at

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Linzey, Donald W. "Mammals of Great Smoky Mountains National Park: 2016 Revision." Southeastern Naturalist 15, no. m8 (2016): 1–93. https://doi.org/10.5281/zenodo.13446814.

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Abstract (sommario):

(Uploaded by Plazi for the Bat Literature Project) The 1288-km2 Great Smoky Mountains National Park (the Park) is one of the largest protected temperate forest ecosystems east of the Rocky Mountains. Because of its global ecological importance, the Park was designated an International Biosphere Reserve in 1976 and a World Heritage Site in 1983. The Park's rich biodiversity is the result of a deeply dissected landscape ranging in elevation from 259 m (850 ft) to 2026 m (6643 ft), high primary productivity, and diverse plant communities. These conditions, and the occurrence of several species at

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24

Linzey, Donald W. "Mammals of Great Smoky Mountains National Park: 2016 Revision." Southeastern Naturalist 15, no. m8 (2016): 1–93. https://doi.org/10.5281/zenodo.13446814.

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Abstract (sommario):

(Uploaded by Plazi for the Bat Literature Project) The 1288-km2 Great Smoky Mountains National Park (the Park) is one of the largest protected temperate forest ecosystems east of the Rocky Mountains. Because of its global ecological importance, the Park was designated an International Biosphere Reserve in 1976 and a World Heritage Site in 1983. The Park's rich biodiversity is the result of a deeply dissected landscape ranging in elevation from 259 m (850 ft) to 2026 m (6643 ft), high primary productivity, and diverse plant communities. These conditions, and the occurrence of several species at

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25

Linzey, Donald W. "Mammals of Great Smoky Mountains National Park: 2016 Revision." Southeastern Naturalist 15, no. m8 (2016): 1–93. https://doi.org/10.5281/zenodo.13446814.

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Abstract (sommario):

(Uploaded by Plazi for the Bat Literature Project) The 1288-km2 Great Smoky Mountains National Park (the Park) is one of the largest protected temperate forest ecosystems east of the Rocky Mountains. Because of its global ecological importance, the Park was designated an International Biosphere Reserve in 1976 and a World Heritage Site in 1983. The Park's rich biodiversity is the result of a deeply dissected landscape ranging in elevation from 259 m (850 ft) to 2026 m (6643 ft), high primary productivity, and diverse plant communities. These conditions, and the occurrence of several species at

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Linzey, Donald W. "Mammals of Great Smoky Mountains National Park: 2016 Revision." Southeastern Naturalist 15, no. m8 (2016): 1–93. https://doi.org/10.5281/zenodo.13446814.

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Abstract (sommario):

(Uploaded by Plazi for the Bat Literature Project) The 1288-km2 Great Smoky Mountains National Park (the Park) is one of the largest protected temperate forest ecosystems east of the Rocky Mountains. Because of its global ecological importance, the Park was designated an International Biosphere Reserve in 1976 and a World Heritage Site in 1983. The Park's rich biodiversity is the result of a deeply dissected landscape ranging in elevation from 259 m (850 ft) to 2026 m (6643 ft), high primary productivity, and diverse plant communities. These conditions, and the occurrence of several species at

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27

Marian, J. ŁUSZCZAK, and SZAFRANIEC Stanisław. "Materiały do poznania rozmieszczenia kózkowatych (Coleoptera, Cerambycidae) Beskidu Zachodniego – gatunki nieczęste, częste i pospolite / Contribution to the knowledge of the distribution of longhorn beetles (Coleoptera and Cerambycidae) in the Western Beskid Mountains – infrequent, frequent and common species." Wiadomości Entomologiczne (Entomological News) 40, no. 3 (11A) (2021): 16–34. https://doi.org/10.5281/zenodo.5520589.

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The new chorological data concerning 56 species of the Cerambycidae family are presented from the Western Beskid Mountains (South Poland). The authors compared the species’ composition in the best-studied mezoregions: the Beskid Żywiecki Range (with the Babiogórski National Park), the Gorce Mountains (with Gorczański National Park) and the Beskid Sądecki Range (with Experimental Forestry Facility in Krynica).

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POGUE, MICHAEL G. "The Plusiinae (Lepidoptera: Noctuidae) of Great Smoky Mountains National Park." Zootaxa 1032, no. 1 (2005): 1. http://dx.doi.org/10.11646/zootaxa.1032.1.1.

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Seventeen species of Plusiinae have been found in Great Smoky Mountains National Park, in Tennessee and North Carolina, USA. These species are documented with adult images, description, flight period, abundance, elevation range, Park and general distribution, and larval hosts from the literature. Maps illustrate the known distribution of each species within the Park. Sixteen of the 17 species occur above 4,000 feet in elevation. The most diverse locality in the Park has 14 species.

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THAWARORIT, KITIYA, NARUMON SANGPRADUB, and JOHN C. MORSE. "Five new species of the genus Cheumatopsyche (Trichoptera: Hydropsychidae) from the Phetchabun Mountains, Thailand." Zootaxa 3613, no. 5 (2013): 445–54. http://dx.doi.org/10.11646/zootaxa.3613.5.2.

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Five new species of the genus Cheumatopsyche (Trichoptera: Hydropsychidae) from the Phetchabun Mountains, Thai-land, are described and illustrated. The national parks and wildlife sanctuaries in the Phetchabun Mountains are recognized as areas with a high density of endemic species deserving protection. Four new species of Cheumatopsyche (C. recta, C. diversa, C. triangula, and C. tongto) have been found in Phu Khieo Wildlife Sanctuary, Phu Kradueng National Park and Thung Salaeng Luang National Park; a fifth new species (C. cava) has been found in Phu Kradueng National Park. De-scribing hydro

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NAKAMURA, Michio, Noriko ITOH, and Tetsuya SAKAMAKI. "Site Report: The Mahale Mountains National Park, Tanzania." Primate Research 15, no. 2 (1999): 93–99. http://dx.doi.org/10.2354/psj.15.93.

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Abune, Leykun. "The Simen Mountains National Park World Heritage Site." Mountain Research and Development 23, no. 3 (2003): 238–39. http://dx.doi.org/10.1659/0276-4741(2003)023[0238:tsmnpw]2.0.co;2.

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Purcell, Zoe. "Chimpanzee viewing and regulation: Mahale Mountains National Park." Pan Africa News 9, no. 2 (2002): 17–19. http://dx.doi.org/10.5134/143416.

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Rogowski, Mateusz. "Mountain hiking in the Stołowe Mountains National Park." Turyzm/Tourism 27, no. 2 (2017): 89–97. http://dx.doi.org/10.1515/tour-2017-0017.

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In recent years the Stołowe Mountains National Park has become an increasingly popular destination for the purposes of mountain tourism. Such tourism takes different forms throughout the year, but the most common is hiking. Its continuing popularity results from the close contact with nature it provides, along with the possibility of active leisure pursuits and exploration. The aim of the study is to describe the motivations, preferences and leisure behaviours of hiking tourists who visit the Stołowe Mountains National Park, through survey-based research in 2015 and 2016. The study will highli

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Jenkins, Michael A. "Vegetation Communities of Great Smoky Mountains National Park." Southeastern Naturalist 6, sp2 (2007): 35–56. http://dx.doi.org/10.1656/1528-7092(2007)6[35:vcogsm]2.0.co;2.

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Mokras-Grabowska, Justyna. "Mountain hiking in Tatra National Park." Turyzm/Tourism 26, no. 1 (2016): 71–78. http://dx.doi.org/10.1515/tour-2016-0006.

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Tatra National Park is the most frequently visited national park in Poland. During the peak season (summer), it attracts both ‘fully aware’ tourists, properly prepared for mountain hiking, and ‘casual’ hikers, motivated mainly by the shallow desire to ‘tick off’ the most popular places in the highest Polish mountains. The article describes the specific character of mountain hikers in Tatra National Park during the summer season, with particular attention paid to the motivations and skills involved in active tourism.

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Glasgow, Benny C., and Paula Pierce. "Freshwater Ribbon Worms (Nemertea) from the Great Smoky Mountains National Park." Journal of North Carolina Academy of Science 130, no. 2 (2014): 60–64. http://dx.doi.org/10.7572/2167-5880-130.2.60.

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Abstract Freshwater ribbon worms collected in the Great Smoky Mountains National Park from 9 June 2007 until 28 September 2010 are reported. All six specimens are identified as genus Prostoma. Species identification is not concluded and also no conclusion is made whether any of the specimens are of a new or undescribed species. Some specimen photographs are provided and a discussion is given on specimen characteristics and their possible identification. Ribbon worms are not previously reported in the Great Smoky Mountains National Park.

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POGUE, MICHAEL G. "The Hadeninae (Lepidoptera: Noctuidae) of Great Smoky Mountains National Park, USA." Zootaxa 2380, no. 1 (2010): 1. http://dx.doi.org/10.11646/zootaxa.2380.1.1.

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Fifty-two species of Hadeninae are recorded from Great Smoky Mountains National Park, Tennessee and North Carolina, USA. Of the six hadenine tribes, five are present in the Park. They include 13 species of Orthosiini, one species of Tholerini, ten species of Hadenini, nine species of Leucaniini, and 19 species of Eriopygini. A total of 160 localities were collected across the Park. The three most diverse localities in the Park were Purchase Knob with 44 species, Big Cove Road with 32 species, and Foothills Parkway with 24 species. The most widespread species in the Park was Pseudorthodes vecor

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PARK, JONG-SEOK, CHRISTOPHER E. CARLTON, and MICHAEL L. FERRO. "Diversity and taxonomic review of Leptusa Kraatz (Coleoptera: Staphylinidae: Aleocharinae) from Great Smoky Mountains National Park, U.S.A., with descriptions of four new species." Zootaxa 2662, no. 1 (2010): 1. http://dx.doi.org/10.11646/zootaxa.2662.1.1.

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A taxonomic review of the genus Leptusa Kraatz from Great Smoky Mountains National Park is presented. Ten species are recognized, and four new species are described and illustrated: L. (Adoxopisalia) pseudosmokyiensis Park & Carlton, sp. nov., L. (A.) stocksi Park & Carlton, sp. nov., L. (Dysleptusa) gimmeli Park & Carlton, sp. nov., and L. (Eucryptusa) ferroi Park & Carlton, sp. nov. The previously undescribed female of L. (D.) pusio (Casey) is also reported for the first time. Descriptions, habitus illustrations and line drawings of diagnostic characters of all species occurr

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Zhang, Chao, Yuwei Fan, Minhao Chen, et al. "Identification of Conservation Priority Areas and a Protection Network for the Siberian Musk Deer (Moschus moschiferus L.) in Northeast China." Animals 12, no. 3 (2022): 260. http://dx.doi.org/10.3390/ani12030260.

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Species conservation actions are guided by available information on the biogeography of the protected species. In this study, we integrated the occurrence data of Siberian musk deer (Moschus moschiferus L.) collected from 2019 to 2021 with species distribution models to estimate the species’ potential distribution in Northeast China. We then identified conservation priority areas using a core-area zonation algorithm. In addition, we analyzed core patch fragmentation using FRAGSTATS. Lastly, we identified potential connectivity corridors and constructed a potential protection network based on t

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Zwoliński, Zbigniew, and Jakub Stachowiak. "Geodiversity map of the Tatra National Park for geotourism." Quaestiones Geographicae 31, no. 1 (2012): 99–107. http://dx.doi.org/10.2478/v10117-012-0012-x.

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Geodiversity map of the Tatra National Park for geotourism The paper indicates the relations between geodiversity and geotourism in the Tatra National Park. Geodiversity of the Tatra Mountains is visualized by its geodiversity map, whereas geotouristic attractions are measured by touristic attractions along touristic trails on geodiversity map. Areas of the highest geodiversity cover merely 8.2% of the Tatar National Park area. These are mainly areas close to the Tatra Mountains' main ridge. It is so due to geology, landform energy, slopes, landform fragmentation and geoecological belts. Most

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Şahin, Bülent, and Sophia Barinova. "Environmental Factors Structuring Diatom Diversity of the Protected High Mountain Lakes in the Kaçkar Mountains National Park (Rize, Turkey)." Ecologies 5, no. 2 (2024): 312–41. http://dx.doi.org/10.3390/ecologies5020020.

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The altitude of the habitat is one of the important regulators of species survival. Kaçkar Mountains National Park is located in the Eastern Black Sea region of Turkey. This is the first study on the benthic diatom flora of the high mountain lakes in Kaçkar Mountains National Park, which is situated between 2782 and 3075 m a.s.l. A total of 84 diatom species were identified from benthic communities of 15 habitats in summer (19 July, 28 August) and autumn (10 September) months of 2020. The genus Pinnularia (thirteen species) formed the basis of the taxonomic list, followed by Eunotia (five spec

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42

Tronstad, Lusha, Scott Hotaling, J. Giersch, Debra Finn, Oliver Wilmot, and Mark Anderson. "Characterizing Biodiversity of Alpine Streams in Grand Teton National Park, Wyoming." UW National Parks Service Research Station Annual Reports 38 (January 1, 2015): 89–98. http://dx.doi.org/10.13001/uwnpsrc.2015.4103.

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Abstract (sommario):

The highest rate of climate change is occurring in alpine areas above permanent treeline. The Teton Mountains in northwestern Wyoming are one of these ecosystem and little work has been done on alpine streams in the area. We sampled 6 streams in the Teton Mountains in 2015 at both upper and lower sites. We measured environmental variables (e.g., glacierality index, basic water quality, and temperature), aquatic invertebrate assemblages and microbial diversity. The water sources for sampled streams were glacier-fed, snowmelt and icy-seep. Aquatic invertebrate density (116-11,523 ind/m2) and bio

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43

Sałata, Bogusław, Joanna Romaszewska-Sałata, and Wiesław Mułeszko. "Mycological notes from the Polish Tatra National Park." Acta Mycologica 20, no. 1 (2014): 13–21. http://dx.doi.org/10.5586/am.1984.002.

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Abstract (sommario):

A list of 98 microscopic specimens of parasitic fungi collected in Tatra mountains in 1979-81. Till now they were not published as present in Polish Tatra N.P. Such fungi were collected on new hosts plants or were known from the single localites only.

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44

Shaver, Christine L., Kathy A. Tonnessen, and Tonnie G. Maniero. "Clearing the Air at Great Smoky Mountains National Park." Ecological Applications 4, no. 4 (1994): 690–701. http://dx.doi.org/10.2307/1942000.

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45

Yineger, Haile, Ensermu Kelbessa, Tamrat Bekele, and Ermias Lulekal. "Ethnoveterinary medicinal plants at Bale Mountains National Park, Ethiopia." Journal of Ethnopharmacology 112, no. 1 (2007): 55–70. http://dx.doi.org/10.1016/j.jep.2007.02.001.

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46

ITO, Taiichi. "The Meaning of the Adirondack Mountains National Park Proposal." Journal of the Japanese Institute of Landscape Architecture 58, no. 5 (1994): 41–44. http://dx.doi.org/10.5632/jila.58.5_41.

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47

Linzey, Donald W. "Mammals of Great Smoky Mountains National Park: 2016 Revision." Southeastern Naturalist 15, no. m8 (2016): 1–93. http://dx.doi.org/10.1656/058.015.m801.

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48

Muise, Charles, Keith R. Langdon, Rebecca P. Shiflett, et al. "Checklist of Odonata from Great Smoky Mountains National Park." Southeastern Naturalist 6, sp2 (2007): 207–14. http://dx.doi.org/10.1656/1528-7092(2007)6[207:coofgs]2.0.co;2.

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49

Nelson, Diane R., and Bartels Paul J. "“Smoky Bears”—Tardigrades of Great Smoky Mountains National Park." Southeastern Naturalist 6, sp2 (2007): 229–38. http://dx.doi.org/10.1656/1528-7092(2007)6[229:sbogsm]2.0.co;2.

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50

REEVES, WILL K., PETER H. ADLER, WILLIAM L. GROGAN, and PAUL E. SUPER. "Hematophagous and parasitic Diptera (Insecta) in the Great Smoky Mountains National Park, USA." Zootaxa 483, no. 1 (2004): 1. http://dx.doi.org/10.11646/zootaxa.483.1.1.

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Abstract (sommario):

We present the bionomics, distributions, host associations, and known or potential vector abilities of 112 species of hematophagous Diptera representing 9 families in the Great Smoky Mountains National Park. New Park or state records include the bird blow flies (Calliphoridae) Protocalli-

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