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Journal articles on the topic 'Moor ecology'

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1

Whitehead, Siân C., and David Baines. "Moorland vegetation responses following prescribed burning on blanket peat." International Journal of Wildland Fire 27, no. 10 (2018): 658. http://dx.doi.org/10.1071/wf18019.

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Moorlands provide several key ecosystem services, as well as supporting shooting of red grouse (Lagopus lagopus scotica Latham). Prescribed burning of heather is an integral aspect of grouse-moor management but is sometimes presented as ecologically damaging. However, a long-term burning experiment at Moor House National Nature Reserve, North Pennines, northern England, showed that more frequent burning actually increased the cover of peat-building species such as Sphagnum mosses and cotton grass (Eriophorum vaginatum L.). Here we compare those findings with data from another deep-peat site in the North Pennines, but one that is actively managed as a grouse moor. We describe post-fire vegetation change using aerial images to construct a time-series of burns. Comparable with the Moor House study, we found highest levels of Sphagnum and Eriophorum cover on fires last burned within 3–10 years, whereas heather (Calluna vulgaris L.) cover, that of other mosses, and overall vegetation height all increased in a linear manner over time since burning. These results from an actively managed grouse moor subject to prescribed burning demonstrate that the cover and species richness of Sphagnum, a key peat-forming group, correlated with reduced dominance of tall heather, can benefit from a post-burn period of up to 10 years.
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2

Roberts, John Lawton, and Neil Bowman. "Diet and ecology of Short-eared OwlsAsio flammeusbreeding on heather moor." Bird Study 33, no. 1 (March 1986): 12–17. http://dx.doi.org/10.1080/00063658609476885.

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3

Niewold, F. J. J., and H. Nijland. "Die Chancen des westeuropäischen Moor- und Heidebirkhuhns." Zeitschrift für Jagdwissenschaft 33, no. 4 (December 1987): 227–41. http://dx.doi.org/10.1007/bf02241447.

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4

MCDOUGALL, PETER. "The feral goats of Kielderhead Moor." Journal of Zoology 176, no. 2 (August 20, 2009): 215–46. http://dx.doi.org/10.1111/j.1469-7998.1975.tb03194.x.

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5

Widaswari, Kadek Wiwik, Ni Luh Watiniasih, and I. B. Made Suaskara. "DIVERSITY OF INSECT THAT INTERACT WITH BALI CATTLE (Bos sondaicus) IN THE MOOR AREA AND OUTSKIRT OF FOREST." Jurnal Biologi Udayana 20, no. 2 (December 31, 2016): 83. http://dx.doi.org/10.24843/jbiounud.2016.v20.i02.p07.

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This study aimed to determine the types of insects that interact with bali cattle in the moor area in Kepuhvillage, District of Mendoyo, Jembrana and in the outskirts of the forest at Keladian village, Rendang, Karangasem.Samples of flying insects was taken using modified insect nets, whereas insects that patch on the surface of bodycattle were collected manualy. Collected insects were identified at the Laboratory of Ecology, Department of Biology,Udayana University. The data collected were analyzed descriptively. The results showed that the more species ofinsects (7 species) were associated with bali cattle in the outskirt of forest compared to in moor area (3 species).The temperature at the outskirt of forest was lower (average 27.6° during the day) with the average of 86.0%,compared to the average temperature of 36.0° and 65.3% of humidity during the day.
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6

Babik, W., W. Branicki, M. Sandera, S. Litvinchuk, L. J. Borkin, J. T. Irwin, and J. Rafiński. "Mitochondrial phylogeography of the moor frog, Rana arvalis." Molecular Ecology 13, no. 6 (March 4, 2004): 1469–80. http://dx.doi.org/10.1111/j.1365-294x.2004.02157.x.

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7

KNOPP, T., M. HEIMOVIRTA, H. KOKKO, and J. MERILÄ. "Do male moor frogs (Rana arvalis) lek with kin?" Molecular Ecology 17, no. 10 (April 18, 2008): 2522–30. http://dx.doi.org/10.1111/j.1365-294x.2008.03748.x.

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8

Stoddart, D. M., and Raymond Hewson. "Mountain hare, Lepus timidus, bags and moor management." Journal of Zoology 204, no. 4 (August 20, 2009): 563–65. http://dx.doi.org/10.1111/j.1469-7998.1984.tb02388.x.

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9

Stewart, Alan J. A., and Art N. Lance. "Effects of Moor-Draining on the Hydrology and Vegetation of Northern Pennine Blanket Bog." Journal of Applied Ecology 28, no. 3 (December 1991): 1105. http://dx.doi.org/10.2307/2404228.

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10

Baines, David, and Michael Richardson. "Hen harriers on a Scottish grouse moor: multiple factors predict breeding density and productivity." Journal of Applied Ecology 50, no. 6 (August 30, 2013): 1397–405. http://dx.doi.org/10.1111/1365-2664.12154.

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11

Berman, D. I., N. A. Bulakhova, E. N. Meshcheryakova, and S. V. Shekhovtsov. "Overwintering and cold tolerance in the Moor Frog (Rana arvalis) across its range." Canadian Journal of Zoology 98, no. 11 (November 2020): 705–14. http://dx.doi.org/10.1139/cjz-2019-0179.

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Only two species of boreal Holarctic frogs (genus Rana Linnaeus, 1758) can survive freezing and overwinter on land; they are found in the subarctic and cold regions of North America (Wood Frog, Rana sylvatica LeConte, 1825) and Eurasia (Moor Frog, Rana arvalis Nilsson, 1842) and are an example of an unusual adaptive strategy of overwintering. Freeze tolerance (down to –16 °C) of R. sylvatica has been thoroughly studied; however, little is known about cold resistance of R. arvalis in cold regions. We found that R. arvalis from European Russia and from West Siberia tolerate freezing down to –12 or –16 °C, whereas frogs from the Danish population survived freezing only to –4 °C (Y. Voituron et al. 2009b; J. Comp. Physiol. B, 179: 223–230). All of these populations, according to mitochondrial DNA markers, are closely related. We suggest that the observed differences in cold tolerance (–4 °C vs. –12 or –16 °C) could be caused either by adaptations to climatic factors or by differences in experimental protocols. The northeastern boundary of the geographic range of R. arvalis in Yakutia coincides with the transitional area between discontinuous and continuous permafrost; beyond this area, winter soil temperature sharply declines. The lower lethal temperature and overwintering ecology of R. arvalis in Siberia are similar to those of the North American R. sylvatica.
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12

Pahkala, Maarit, Anssi Laurila, Lars Olof Björn, and Juha Merilä. "Effects of ultraviolet-B radiation and pH on early development of the moor frog Rana arvalis." Journal of Applied Ecology 38, no. 3 (June 2001): 628–36. http://dx.doi.org/10.1046/j.1365-2664.2001.00623.x.

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13

Chikhlyaev, Igor V., and Alexander B. Ruchin. "An Overview of the Helminths of Moor Frog Rana arvalis Nilsson, 1842 (Amphibia: Anura) in the Volga Basin." Diversity 13, no. 2 (February 4, 2021): 61. http://dx.doi.org/10.3390/d13020061.

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This is the first review of the helminth fauna of the moor frog Rana arvalis Nilsson, 1842 from the Volga river basin (Russia). The article summarizes the authors’ and literature data on the helminthic fauna of this species. The method of complete helminthological dissection was used. Thirthy-eight helminth species were recorded from three classes: Cestoda (1), Trematoda (28), and Chromadorea (9). Nine helminth species are new to the moor frog in Russia: trematodes Gorgodera varsoviensis Sinitzin, 1905, Strigea falconis Szidat, 1928, larvae, Neodiplostomum spathoides Dubois, 1937, larvae, Tylodelphys excavata (Rudolphi, 1803), larvae, Pharyngostomum cordatum (Diesing, 1850), larvae, Astiotrema monticelli Stossich, 1904, larvae and Encyclometra colubrimurorum (Rudolphi, 1819), larvae, nematodes Strongyloides spiralis Grabda-Kazubska, 1978 and Icosiella neglecta (Diesing, 1851). The cestode Spirometra erinacei (Rudolphi, 1918), larvae were observed of this amphibian species in the Volga basin for the first time. The nematodes Rhabdias bufonis, Oswaldocruzia filiformis, Cosmocerca ornata and the trematode Haplometra cylindracea form the core of the helminth fauna of the moor frog. Information on species of helminths includes systematic position, localization, areas of detection, type and scheme of life cycle, geographical distribution, and degree of specificity to host amphibians.
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14

Simmons, I. G., and J. B. Innes. "Late Quaternary Vegetational History of the North York Moors. X. Investigations on East Bilsdale Moor." Journal of Biogeography 15, no. 2 (March 1988): 299. http://dx.doi.org/10.2307/2845415.

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15

Grant, S. A., L. Torvell, H. K. Smith, D. E. Suckling, T. D. A. Forbes, and J. Hodgson. "Comparative Studies of Diet Selection by Sheep and Cattle: Blanket Bog and Heather Moor." Journal of Ecology 75, no. 4 (December 1987): 947. http://dx.doi.org/10.2307/2260306.

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16

Whitehead, Sian, Hannah Weald, and David Baines. "Post-burning responses by vegetation on blanket bog peatland sites on a Scottish grouse moor." Ecological Indicators 123 (April 2021): 107336. http://dx.doi.org/10.1016/j.ecolind.2021.107336.

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17

Kirkham, F. W., J. O. Mountford, and R. J. Wilkins. "The Effects of Nitrogen, Potassium and Phosphorus Addition on the Vegetation of a Somerset Peat Moor Under Cutting Management." Journal of Applied Ecology 33, no. 5 (October 1996): 1013. http://dx.doi.org/10.2307/2404682.

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18

PILKINGTON, MICHAEL G., SIMON J. M. CAPORN, JACKY A. CARROLL, NEIL CRESSWELL, GARETH K. PHOENIX, JOHN A. LEE, BRIDGET A. EMMETT, and TIM SPARKS. "Impacts of burning and increased nitrogen deposition on nitrogen pools and leaching in an upland moor." Journal of Ecology 95, no. 6 (November 2007): 1195–207. http://dx.doi.org/10.1111/j.1365-2745.2007.01292.x.

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19

Uller, Tobias, Jörgen Sagvik, and Mats Olsson. "Pre-hatching exposure to water mold reduces size at metamorphosis in the moor frog." Oecologia 160, no. 1 (February 3, 2009): 9–14. http://dx.doi.org/10.1007/s00442-009-1280-6.

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20

Matsumura, Shuichi. "Postconflict affiliative contacts between former opponents among wild moor macaques (Macaca maurus)." American Journal of Primatology 38, no. 3 (1996): 211–19. http://dx.doi.org/10.1002/(sici)1098-2345(1996)38:3<211::aid-ajp2>3.0.co;2-1.

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21

Francksen, Richard M., Mark J. Whittingham, Sonja C. Ludwig, and David Baines. "Winter diet of Common Buzzards Buteo buteo on a Scottish grouse moor." Bird Study 63, no. 4 (October 1, 2016): 525–32. http://dx.doi.org/10.1080/00063657.2016.1238868.

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22

TAIRA, Makoto. "Biomass and species composition of crustacean plankton in the pools of Ozegahara Moor." Japanese Journal of Limnology (Rikusuigaku Zasshi) 61, no. 3 (2000): 233–39. http://dx.doi.org/10.3739/rikusui.61.233.

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23

Merilä, Juha, Fredrik Söderman, Robert O'Hara, Katja Räsänen, and Anssi Laurila. "Local Adaptation and Genetics of Acid-Stress Tolerance in the Moor Frog, Rana arvalis." Conservation Genetics 5, no. 4 (August 2004): 513–27. http://dx.doi.org/10.1023/b:coge.0000041026.71104.0a.

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24

Grishin, A. M., A. I. Filkov, E. L. Loboda, V. V. Reyno, A. V. Kozlov, V. T. Kuznetsov, D. P. Kasymov, S. M. Andreyuk, A. I. Ivanov, and N. D. Stolyarchuk. "A field experiment on grass fire effects on wooden constructions and peat layer ignition." International Journal of Wildland Fire 23, no. 3 (2014): 445. http://dx.doi.org/10.1071/wf12069.

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This paper investigates the cause of ignition of wooden shields during surface fire fronts. For this purpose an experiment was conducted in which a zone 50m in length and 10m in width was chosen as the experimental site. Wooden shields (made of spruce boards) and samples of high-moor and valley peat were placed in this zone. In the experiment it was ascertained that to ensure safety during the surface fire in absence of firebrands and embers it was necessary to clear a perimeter around the zone not less than 5m in width, and remove cleared fuels. To reduce the risk of fence ignition, it was necessary to make the fences permeable. It was found that grass fires turn into peat fires if there is a conductor of combustion above the layer of peat.
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25

Pearce-Higgins, James W., and D. W. Yalden. "Golden PloverPluvialis apricariabreeding success on a moor managed for shooting Red GrouseLagopus lagopus." Bird Study 50, no. 2 (July 2003): 170–77. http://dx.doi.org/10.1080/00063650309461309.

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26

Igaune, Kristne, Indriis Krams, Tatjana Krama, and Jadviga Bobkova. "White storks Ciconia ciconia eavesdrop on mating calls of moor frogs Rana arvalis." Journal of Avian Biology 39, no. 2 (January 24, 2008): 229–32. http://dx.doi.org/10.1111/j.2008.0908-8857.04180.x.

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27

Kirkham, F. W., and M. Kent. "Soil Seed Bank Composition in Relation to the Above-Ground Vegetation in Fertilized and Unfertilized Hay Meadows on a Somerset Peat Moor." Journal of Applied Ecology 34, no. 4 (August 1997): 889. http://dx.doi.org/10.2307/2405280.

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28

Shu, Longfei, Jie Qiu, and Katja Räsänen. "De novo oviduct transcriptome of the moor frog Rana arvalis: a quest for maternal effect candidate genes." PeerJ 6 (August 16, 2018): e5452. http://dx.doi.org/10.7717/peerj.5452.

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Maternal effects can substantially affect ecological and evolutionary processes in natural populations. However, as they often are environmentally induced, establishing their genetic basis is challenging. One important, but largely neglected, source of maternal effects are egg coats (i.e., the maternally derived extracellular matrix that surrounds the embryo). In the moor frog, the gelatinous egg coats (i.e., egg jelly) are produced in the mother’s oviduct and consist primarily of highly glycosylated mucin type O-glycans. These O-glycans affect jelly water balance and, subsequently, contribute to adaptive divergence in embryonic acid tolerance. To identify candidate genes for maternal effects, we conducted RNAseq transcriptomics on oviduct samples from seven R. arvalis females, representing the full range of within and among population variation in embryonic acid stress tolerance across our study populations. De novo sequencing of these oviduct transcriptomes detected 124,071 unigenes and functional annotation analyses identified a total of 57,839 unigenes, of which several identified genes likely code for variation in egg jelly coats. These belonged to two main groups: mucin type core protein genes and five different types of glycosylation genes. We further predict 26,711 gene-linked microsatellite (simple sequence repeats) and 231,274 single nucleotide polymorphisms. Our study provides the first set of genomic resources for R. arvalis, an emerging model system for the study of ecology and evolution in natural populations, and gives insight into the genetic architecture of egg coat mediated maternal effects.
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29

Kampichler, Christian, and Ralph Platen. "Ground beetle occurrence and moor degradation: modelling a bioindication system by automated decision-tree induction and fuzzy logic." Ecological Indicators 4, no. 2 (June 2004): 99–109. http://dx.doi.org/10.1016/j.ecolind.2004.01.001.

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30

Stier-Jarmer, M., D. Frisch, C. Oberhauser, G. Immich, M. Kirschneck, and A. Schuh. "Effects of single moor baths on physiological stress response and psychological state: a pilot study." International Journal of Biometeorology 61, no. 11 (June 20, 2017): 1957–64. http://dx.doi.org/10.1007/s00484-017-1385-2.

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31

Miyoshi, Norio, and Norimichi Yano. "Late Pleistocene and Holocene vegetational history of the Ohnuma moor in the Chugoku mountains, western Japan." Review of Palaeobotany and Palynology 46, no. 3-4 (January 1986): 355–76. http://dx.doi.org/10.1016/0034-6667(86)90022-9.

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32

French, D. D. "Some effects of changing soil chemistry on decomposition of plant litters and cellulose on a Scottish moor." Oecologia 75, no. 4 (May 1988): 608–18. http://dx.doi.org/10.1007/bf00776427.

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33

Francksen, Richard M., Mark J. Whittingham, Sonja C. Ludwig, Staffan Roos, and David Baines. "Numerical and functional responses of Common BuzzardsButeo buteoto prey abundance on a Scottish grouse moor." Ibis 159, no. 3 (March 27, 2017): 541–53. http://dx.doi.org/10.1111/ibi.12471.

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34

Arens, Paul, Theo van der Sluis, Wendy P. C. van’t Westende, Ben Vosman, Claire C. Vos, and Marinus J. M. Smulders. "Genetic population differentiation and connectivity among fragmented Moor frog (Rana arvalis) populations in The Netherlands." Landscape Ecology 22, no. 10 (August 28, 2007): 1489–500. http://dx.doi.org/10.1007/s10980-007-9132-4.

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35

Simmons, I. G., and J. B. Innes. "Late Quaternary Vegetational History of the North York Moors. VIII. Correlation of Flandrian II Litho- and Pollen Stratigraphy at North Gill, Glaisdale Moor." Journal of Biogeography 15, no. 2 (March 1988): 249. http://dx.doi.org/10.2307/2845413.

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36

TAIRA, Makoto. "Relationship between Amount of Seston and Species Composition of Crustacean Plankters in the Pools of High Moor." Japanese Journal of Limnology (Rikusuigaku Zasshi) 56, no. 3 (1995): 233–36. http://dx.doi.org/10.3739/rikusui.56.233.

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37

Pontoppidan, M. B., and G. Nachman. "Effects of within-patch heterogeneity on connectivity in pond-breeding amphibians studied by means of an individual-based model." Web Ecology 13, no. 1 (June 12, 2013): 21–29. http://dx.doi.org/10.5194/we-13-21-2013.

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Abstract. The metapopulation framework presumes the habitat of a local population to be continuous and homogenous, and patch area is often used as a proxy for population size. Many populations of pond-breeding amphibians are assumed to follow metapopulation dynamics, and connectivity is mostly measured between breeding ponds. However, the habitat of pond-breeding amphibians is not only defined by the pond but, typically, consists of a breeding pond surrounded by clusters of disjoint summer-habitat patches interspersed with an agricultural/semi-urban matrix. We hypothesise that the internal structure of a habitat patch may change connectivity in two ways: (i) by affecting animal movements and thereby emigration and immigration probabilities; and (ii) by affecting habitat quality and population size. To test our hypotheses, we apply a spatially explicit individual-based model of Moor frog dispersal. We find that the realised connectivity depends on internal structure of both the target and the source patch as well as on how habitat quality is affected by patch structure. Although fragmentation is generally thought to have negative effects on connectivity, our results suggest that, depending on patch structure and habitat quality, positive effects on connectivity may occur.
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38

Usio, N., H. Nakajima, R. Kamiyama, I. Wakana, S. Hiruta, and N. Takamura. "Predicting the distribution of invasive crayfish (Pacifastacus leniusculus) in a Kusiro Moor marsh (Japan) using classification and regression trees." Ecological Research 21, no. 2 (October 26, 2005): 271–77. http://dx.doi.org/10.1007/s11284-005-0120-3.

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39

Knopp, Theresa, José M. Cano, Pierre-André Crochet, and Juha Merilä. "Contrasting Levels of Variation in Neutral and Quantitative Genetic Loci on Island Populations of Moor Frogs (Rana arvalis)." Conservation Genetics 8, no. 1 (June 3, 2006): 45–56. http://dx.doi.org/10.1007/s10592-006-9147-4.

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40

Räsänen, Katja, Anssi Laurila, and Juha Merilä. "GEOGRAPHIC VARIATION IN ACID STRESS TOLERANCE OF THE MOOR FROG, RANA ARVALIS. I. LOCAL ADAPTATION." Evolution 57, no. 2 (2003): 352. http://dx.doi.org/10.1554/0014-3820(2003)057[0352:gviast]2.0.co;2.

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41

SäNEN, Katja Rä, Anssi Laurila, and Juha Merilä. "GEOGRAPHIC VARIATION IN ACID STRESS TOLERANCE OF THE MOOR FROG, RANA ARVALIS. I. LOCAL ADAPTATION." Evolution 57, no. 2 (February 2003): 352–62. http://dx.doi.org/10.1111/j.0014-3820.2003.tb00269.x.

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42

Whitfield, D. Philip, David R. A. McLeod, Jeff Watson, Alan H. Fielding, and Paul F. Haworth. "The association of grouse moor in Scotland with the illegal use of poisons to control predators." Biological Conservation 114, no. 2 (December 2003): 157–63. http://dx.doi.org/10.1016/s0006-3207(03)00019-3.

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43

Okamoto, Kyoko, Shuichi Matsumura, and Kunio Watanabe. "Life history and demography of wild moor macaques (Macaca maurus): Summary of ten years of observations." American Journal of Primatology 52, no. 1 (2000): 1–11. http://dx.doi.org/10.1002/1098-2345(200009)52:1<1::aid-ajp1>3.0.co;2-f.

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44

Wright, P. M. "Distribution, site occupancy and breeding success of the MerlinFalco columbariuson Barden Moor and Fell, North Yorkshire." Bird Study 44, no. 2 (July 1997): 182–93. http://dx.doi.org/10.1080/00063659709461054.

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45

Jenkins, D., and A. Watson. "Bird numbers in relation to grazing on a grouse moor from 1957–61 to 1988–98." Bird Study 48, no. 1 (March 2001): 18–22. http://dx.doi.org/10.1080/00063650109461199.

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46

Vanselow-Algan, M., S. R. Schmidt, M. Greven, C. Fiencke, L. Kutzbach, and E. M. Pfeiffer. "High methane emissions dominated annual greenhouse gas balances 30 years after bog rewetting." Biogeosciences 12, no. 14 (July 28, 2015): 4361–71. http://dx.doi.org/10.5194/bg-12-4361-2015.

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Abstract. Natural peatlands are important carbon sinks and sources of methane (CH4). In contrast, drained peatlands turn from a carbon sink to a carbon source and potentially emit nitrous oxide (N2O). Rewetting of peatlands thus potentially implies climate change mitigation. However, data about the time span that is needed for the re-establishment of the carbon sink function by restoration are scarce. We therefore investigated the annual greenhouse gas (GHG) balances of three differently vegetated sites of a bog ecosystem 30 years after rewetting. All three vegetation communities turned out to be sources of carbon dioxide (CO2) ranging between 0.6 ± 1.43 t CO2 ha−2 yr−1 (Sphagnum-dominated vegetation) and 3.09 ± 3.86 t CO2 ha−2 yr−1 (vegetation dominated by heath). While accounting for the different global warming potential (GWP) of CO2, CH4 and N2O, the annual GHG balance was calculated. Emissions ranged between 25 and 53 t CO2-eq ha−1 yr−1 and were dominated by large emissions of CH4 (22–51 t CO2-eq ha−1 yr−1), with highest rates found at purple moor grass (Molinia caerulea) stands. These are to our knowledge the highest CH4 emissions so far reported for bog ecosystems in temperate Europe. As the restored area was subject to large fluctuations in the water table, we assume that the high CH4 emission rates were caused by a combination of both the temporal inundation of the easily decomposable plant litter of purple moor grass and the plant-mediated transport through its tissues. In addition, as a result of the land use history, mixed soil material due to peat extraction and refilling can serve as an explanation. With regards to the long time span passed since rewetting, we note that the initial increase in CH4 emissions due to rewetting as described in the literature is not inevitably limited to a short-term period.
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47

O'Dowd, Dennis J., and P. S. Lake. "Red crabs in rain forest, Christmas Island: removal and fate of fruits and seeds." Journal of Tropical Ecology 7, no. 1 (February 1991): 113–22. http://dx.doi.org/10.1017/s0266467400005162.

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ABSTRACTThe red land crab (Gecarcoidea nalalis) is the major collector of fruits and seeds from the rain forest Moor on Christmas Island, Indian Ocean. At three sites, they rapidly removed fruits and seeds of 17 species tested (usually within 12 h after placement) and most were taken to crab burrows. Direct observations of seed predation, and application of estimated chelar forces of red crabs indicated that seeds of many species, especially those with thin seed coats, are likely to be killed through handling. However, removal of some resistant seeds to burrows may be favourable for seedling establishment when canopy gaps occur. Fruit removal rates by crabs were positively related to nitrogen concentration in fruit tissues but negatively correlated with condensed tannins. These observations suggest that seed predation by land crabs may affect the success of colonization and the relative abundance of plants on oceanic islands.
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Kumano, Shigeru, Masashi Ihira, Yasuo Maeda, Misako Yamauchi, Eiji Matsumoto, and Isao Matsuda. "Holocene sedimentary history of some coastal plains in Hokkaido, Japan IV. Diatom assemblages in the sediments from Kushiro moor (2)." Ecological Research 5, no. 2 (August 1990): 221–35. http://dx.doi.org/10.1007/bf02346993.

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Ries, C., J. Spaethe, M. Sztatecsny, C. Strondl, and W. Hödl. "Turning blue and ultraviolet: sex-specific colour change during the mating season in the Balkan moor frog." Journal of Zoology 276, no. 3 (May 27, 2008): 229–36. http://dx.doi.org/10.1111/j.1469-7998.2008.00456.x.

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50

Albani, Alessandro, Claudio De Liberato, Isra Wahid, Federica Berrilli, Erin Phelps Riley, Giusy Cardeti, Putu Oka Ngakan, and Monica Carosi. "Preliminary Assessment of Gastrointestinal Parasites in Two Wild Groups of Endangered Moor Macaques (Macaca maura) from Sulawesi." International Journal of Primatology 40, no. 6 (December 2019): 671–86. http://dx.doi.org/10.1007/s10764-019-00114-w.

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