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24 - Edge effects on tree dendrometrics, abiotics, and mouse lemur densities in western dry forests in Madagascar

from Part V - Cheirogaleidae: conservation biogeography

Published online by Cambridge University Press:  05 March 2016

Shawn M. Lehman
Affiliation:
University of Toronto, Canada
Shawn M. Lehman
Affiliation:
University of Toronto
Ute Radespiel
Affiliation:
University of Veterinary Medicine Hannover, Foundation
Elke Zimmermann
Affiliation:
University of Veterinary Medicine Hannover, Foundation
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Summary

Introduction

Anthropogenic disturbance of forests leads to fragmentation and habitat loss, which strongly influence genetic diversity, extirpations, and extinction of many species (e.g., Fahrig and Merriam, 1994; Gibson et al., 2013; Radespiel and Bruford, 2014). One of the most significant consequences of fragmentation and habitat loss is an increase in the amount of edge effects and edge habitat (Chen et al., 1992). Edge effects represent the penetration, to varying depths and intensities, of biotic and abiotic conditions from the surrounding environment (matrix) into the forest interior (Malcolm, 1994). Murcia (1995) described three ecological consequences of edge effects: (1) abiotic effects, (2) direct biological effects, and (3) indirect biological effects. Abiotic effects occur as the result of the penetration of environmental factors, such as temperature and light levels, from the matrix into the forest interior. Direct biological effects are changes in the abundance and distribution of organisms due to physical conditions near the forest edge. For example, Laurance et al. (1997) documented that wind damage led to a drastic drop in tree biomass within 100 m of the forest edge in South America. Indirect biological effects involve changes in species interactions (e.g., herbivory, frugivory), such that species that avoid the edge may be doing so due to the scarcity of preferred food items in these stochastic habitats (Mills, 1995). The combination of these three ecological processes results in dynamic, multidimensional edge habitats that differ from the matrix and forest interior. Although edge effects have been shown to alter forest structure and animal communities (e.g., Lovejoy et al., 1986; Laurance and Yensen, 1991; Laurance et al., 1997), they have rarely been studied directly in regards to primate ecology and biogeography.

Edge effects are particularly relevant to ecological and biogeographic studies in Madagascar. Madagascar has an unrivaled level of plant endemicity and diversity: of the estimated 12,000 species of plants in Madagascar, 81% are endemic to this country (e.g., Phillipson, 1994, 1996; Du Puy et al., 1999). This plant diversity is remarkable given that much of the original forest cover has been lost to human perturbations, such as slash-and-burn agriculture, logging, mining, and associated erosion (Green and Sussman, 1990; Du Puy and Moat, 1998).

Type
Chapter
Information
The Dwarf and Mouse Lemurs of Madagascar
Biology, Behavior and Conservation Biogeography of the Cheirogaleidae
, pp. 462 - 476
Publisher: Cambridge University Press
Print publication year: 2016

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References

Bloesch, U. 1999. Fire as a tool in the management of a savanna/dry forest reserve in Madagascar. Applied Vegetation Science 2(1):117–124.Google Scholar
Brenneman, RA, Johnson, SE, Bailey, CA, et al. 2012. Population genetics and abundance of the Endangered grey-headed lemur Eulemur cinereiceps in south-east Madagascar: assessing risks for fragmented and continuous populations. Oryx 46(02):298–307.Google Scholar
Brown, KA, Johnson, SE, Parks, KE, et al. 2013. Use of provisioning ecosystem services drives loss of functional traits across land use intensification gradients in tropical forests in Madagascar. Biological Conservation 161:118–127.Google Scholar
Buckland, S, Plumptre, A, Thomas, L, Rexstad, E. 2010. Design and analysis of line transect surveys for primates. International Journal of Primatology 31(5):833–847.Google Scholar
Burke, RJ, Lehman, S. 2014. Edge effects on morphometrics and body mass in two sympatric species of mouse lemurs in Madagascar. Folia Primatologica 85:277–291.Google Scholar
Chen, J, Franklin, JF, Spies, TA. 1992. Vegetation responses to edge environments in old-growth Douglas-fir forests. Ecological Applications 2(4):387–396.Google Scholar
Chen, J, Franklin, JF, Spies, TA. 1995. Growing-season microclimatic gradients from clearcut edges into old-growth Douglas-fir forests. Ecological Applications 5:74–86.Google Scholar
Crowley, BE, McGoogan, KC, Lehman, SM. 2012. Edge effects on foliar stable isotope values in a Madagascan tropical dry forest. PLoS ONE 7(9):e44538.Google Scholar
Debinski, DM. 2006. Forest fragmentation and matrix effects: the matrix does matter. Journal of Biogeography 33(10):1791–1792.Google Scholar
Didham, RK, Lawton, JH. 1999. Edge structure determines the magnitude of changes in microclimate and vegetation structure in tropical forest fragments. Biotropica 31(1):17–30.Google Scholar
Donovan, TM, Jones, PW, Annand, EM, Thompson, FR. 1997. Variation in local-scale edge effects: mechanisms and landscape context. Ecology 78(7):2064–2075.Google Scholar
Puy, D Du, Moat, J. 1998. Vegetation mapping and classification in Madagascar (using GIS): implications and recommendations for the conservation of biodiversity. In Huxley, CR, Lock, JM, Cutler, DF (eds.), Chorology, Taxonomy & Ecology of the Floras of Africa and Madagascar (pp. 97–117). Royal Botanic Gardens, Kew.
Puy, D Du, Cribb, P, Bosser, J, Hermans, J, Hermans, C. 1999. The Orchids of Madagascar. Royal Botanic Gardens, Kew.
Puy, DJ Du, Moat, J. 1996. A refined classification of the primary vegetation of Madagascar based on the underlying geology: using GIS to map its distribution and to assess its conservation status. In Lourenço, WR (ed.), Proceedings of the International Symposium on the Biogeography of Madagascar (pp. 205–218). Editions de l'ORSTOM, Paris.
Elmqvist, T, Pyykönen, M, Tengö, M, et al. 2007. Patterns of loss and regeneration of tropical dry forest in Madagascar: the social institutional context. PLoS ONE 2(5):e402.Google Scholar
Esseen, P-A, Renhorn, K-E. 1998. Edge effects on an epiphytic lichen in fragmented forests. Conservation Biology 12(6):1307–1317.Google Scholar
Ewers, RM, Thorpe, S, Didham, RK. 2007. Synergistic interactions between edge and area effects in a heavily fragmented landscape. Ecology 88(1):96–106.Google Scholar
Fahrig, L, Merriam, G. 1994. Conservation of fragmented populations. Conservation Biology 8(1):50–59.Google Scholar
FAO. 2003. The State of the World's Forests. Food and Agricultural Organization, United Nations, Rome.
Fernandez, C, Acosta, FJ, Abella, G, Lopez, F, Diaz, M. 2002. Complex edge effect fields as additive processes in patches of ecological systems. Ecological Modeling 149:273–283.Google Scholar
Fletcher, RJ. 2005. Multiple edge effects and their implications in fragmented landscapes. Journal of Animal Ecology 74(2):342–352.Google Scholar
Fortin, M-J, Dale, MRT. 2005. Spatial Analysis: A Guide for Ecologists. Cambridge University Press, Cambridge.
Ganzhorn, JU, Malcolmber, A, Adrianantoanina, O, Goodman, SM. 1997. Habitat characteristics and lemur species richness in Madagascar. Biotropica 29(3):331–343.Google Scholar
Ganzhorn, JU, Wright, PC, Ratsimbazafy, HJ. 1999. Primate communities: Madagascar. In Fleagle, JG, Janson, CH, Reed, K (eds.), Primate Communities (pp. 75–89). Cambridge University Press, Cambridge.
Gascon, C, Lovejoy, TE, Bierregaard, RO, et al. 1999. Matrix habitat and species richness in tropical forest remnants. Biological Conservation 91:223–229.Google Scholar
Gehlhausen, SM, Schwartz, MW, Augspurger, CK. 2000. Vegetation and microclimatic edge effects in two mixed-mesophytic forest fragments. Plant Ecology 147:21–35.Google Scholar
Gibson, L, Lynam, AJ, Bradshaw, CJA, et al. 2013. Near-complete extinction of native small mammal fauna 25 years after forest fragmentation. Science 341(6153):1508–1510.Google Scholar
Green, GM, Sussman, RW. 1990. Deforestation history of the eastern rain forests of Madagascar from satellite images. Science 248(4952):212–215.Google Scholar
Harper, KA, Macdonald, SE, Burton, P, et al. 2005. Edge influence on forest structure and composition in fragmented landscapes. Conservation Biology 19(3):1–15.Google Scholar
Irwin, MT. 2008. Diademed sifaka (Propithecus diadema) ranging and habitat use in continuous and fragmented forest: higher density but lower viability in fragments?Biotropica 40(2):231–240.Google Scholar
Jenkins, RKB, Brady, LD, Bisoac, M, Rabearivony, J, Griffiths, RA. 2003. Forest disturbance and river proximity influence chameleon abundance in Madagascar. Biological Conservation 109:407–415.Google Scholar
Laurance, WF, Yensen, E. 1991. Predicting the impacts of edge effects in fragmented habitats. Biological Conservation 57(2):205–219.Google Scholar
Laurance, WF, Laurance, SG, Ferreira, LV, et al. 1997. Biomass collapse in Amazonian forest fragments. Science 278:1117–1118.Google Scholar
Lehman, SM. 2007. Spatial variations in Eulemur fulvus rufus and Lepilemur mustelinus densities in Madagascar. Folia Primatologica 78(1):46–55.Google Scholar
Lehman, SM. 2013. Effects of altitude on the conservation biogeography of lemurs in south east Madagascar. In Gursky, S, Krzton, A, Grows, N (eds.), High Altitude Primates (pp. 3–22). Springer Press, New York.
Lehman, SM, Rajaonson, A, Day, S. 2006a. Lemur responses to edge effects in the Vohibola III Classified Forest, Madagascar. American Journal of Primatology 68(3):293–299.Google Scholar
Lehman, SM, Rajoanson, A, Day, S. 2006b. Edge effects and their influence on lemur distribution and density in southeast Madagascar. American Journal of Physical Anthropology 129(2):232–241.Google Scholar
Lehman, SM, Rajoanson, A, Day, S. 2006c. Edge effects on the density of Cheirogaleus major. International Journal of Primatology 27(6):1569–1588.Google Scholar
Lehtinen, RM, Ramanamanjato, J-B, Raveloarison, JG. 2003. Edge effects and extinction proneness in a herpetofauna from Madagascar. Biodiversity & Conservation 12(7):1357–1370.Google Scholar
Lovejoy, TE, Bierregaard, RO, Rylands, AB, et al. 1986. Edge and other effects of isolation on Amazon forest fragments. In Soulé, ME (ed.), Conservation Biology: the Science of Scarcity and Diversity (pp. 257–285). Sinauer Associates, Sunderland, MA.
Lowry, PP, Schatz, GE, Phillipson, PB. 1997. The classification of natural and anthropogenic vegetation in Madagascar. In Goodman, SM, Patterson, BD (eds.), Natural Change and Human Impact in Madagascar (pp. 93–123). Smithsonian Institution Press, Washington, DC.
Malcolm, JR. 1994. Edge effects in central Amazonian forest fragments. Ecology 75(8):2438–2445.Google Scholar
Malcolm, JR. 2001. Extending models of edge effects to diverse landscape configurations, with a test case from the Neotropics. In Bierregaard, RO, Gascon, C, Lovejoy, TE, Mesquita, RM (eds.), Lessons from Amazonia: The Ecology and Conservation of a Fragmented Forest (pp. 346–357). Yale University Press, New Haven.
McGoogan, K. 2011. Edge effects on Coquerel's sifaka (Propithecus coquereli) in northwest Madagascar. Unpublished PhD, University of Toronto.
Mesquita, RM, Delamônica, P, Laurance, WF. 1999. Effect of surrounding vegetation on edge-related tree mortality in Amazonian forest fragments. Biological Conservation 91(2–3):129–134.Google Scholar
Mills, LS. 1995. Edge effects and isolation: red-backed voles on forest remnants. Conservation Biology 9(2):395–403.Google Scholar
Murcia, C. 1995. Edge effects in fragmented forests: implications for conservation. Trends in Ecology and Evolution 10(2):58–62.Google Scholar
Nascimento, HE, Andrade, AC, Camargo, JL, et al. 2006. Effects of the surrounding matrix on tree recruitment in Amazonian forest fragments. Conservation Biology 20(3):853–860.Google Scholar
Peres, CA, Dolman, PM. 2000. Density compensation in neotropical primate communities: evidence from 56 hunted and nonhunted Amazonian forests of varying productivity. Oecologia 122(2):175–189.Google Scholar
Phillipson, PB. 1994. Madagascar. In Davis, D, Heywood, VH, Hamilton, AC (eds.), Centres of Plant Diversity (pp. 271–281). WWF and IUCN, Gland.
Phillipson, PB. 1996. Endemism and non-endemism in the flora of south-west Madagascar. In Lourenço, WR (ed.), Biogeography of Madagascar (pp. 125–136). ORSTROM, Paris.
Quéméré, E, Louis, E, Ribéron, A, Chikhi, L, Crouau-Roy, B. 2010. Non-invasive conservation genetics of the critically endangered golden-crowned sifaka (Propithecus tattersalli): high diversity and significant genetic differentiation over a small range. Conservation Genetics 11(3):675–687.Google Scholar
Radespiel, U, Bruford, MW. 2014. Fragmentation genetics of rainforest animals: insights from recent studies. Conservation Genetics 15(2):245–260.Google Scholar
Radespiel, U, Raveloson, H. 2001. Preliminary study on the lemur communities at three sites of dry deciduous forest in the Réserve Naturelle d'Ankarafantsika. Lemur News 6:22.Google Scholar
Rakotondravony, R, Radespiel, U. 2009. Varying patterns of coexistence of two mouse lemur species (Microcebus ravelobensis and M. murinus) in a heterogeneous landscape. American Journal of Primatology 71(11):928–938.Google Scholar
Ramanamanjato, JB. 2001. Fragmentation effects on reptile and amphibian diversity in the littoral forest of southeastern Madagascar. In Rheinwald, G (ed.), Isolated Vertebrate Communities in the Tropics (pp. 299–310). Museum Alexander Koenig, Bonn.
Ramanamanjato, JB, Ganzhorn, JU. 2001. Effects of forest fragmentation, introduced Rattus rattus and the role of exotic tree plantations and secondary vegetation for the conservation of an endemic rodent and a small lemur in littoral forests of southeastern Madagascar. Animal Conservation 4(2):175–183.Google Scholar
Randrianambinina, B, Rakotondravony, D, Radespiel, U, Zimmermann, E. 2003. Seasonal changes in general activity, body mass and reproduction of two small nocturnal primates: a comparison of the golden brown mouse lemur (Microcebus ravelobensis) in Northwestern Madagascar and the brown mouse lemur (Microcebus rufus) in Eastern Madagascar. Primates 44(4):321–331.Google Scholar
Ratsimbazafy, J. 2002. On the brink of extinction and the process of recovery: responses of black-and-white ruffed lemurs (Varecia variegata variegata) to disturbance in Manombo Forest, Madagascar. Unpublished PhD dissertation, Stony Brook University, Stony Brook, NY.
Rendigs, A, Radespiel, U, Wrogemann, D, Zimmermann, E. 2003. Relationship between microhabitat structure and distribution of mouse lemurs (Microcebus spp.) in Northwestern Madagascar. International Journal of Primatology 24(1):47–64.Google Scholar
Ries, L, Sisk, TD. 2004. A predictive model of edge effects. Ecology 85(11):2917–2926.Google Scholar
Schatz, GE. 2001. Generic Tree Flora of Madagascar. Royal Botanic Gardens and Missouri Botanical Garden Press, Kew and St. Louis.
Schwitzer, C, Mittermeier, RA, Johnson, SE, et al. 2014. Averting lemur extinctions amid Madagascar's political crisis. Science 343(6173):842–843.Google Scholar
Schwitzer, N, Randriatahina, GH, Kaumanns, W, Hoffmeister, D, Schwitzer, C. 2007. Habitat utilization of blue-eyed black lemurs, Eulemur macaco flavifrons (Gray, 1867), in primary and altered forest fragments. Primate Conservation 22:79–87.Google Scholar
Watson, JEM, Whittaker, RJ, Dawson, TP. 2004. Habitat structure and proximity to forest edge affect the abundance and distribution of forest-dependent birds in tropical coastal forests of southeastern Madagascar. Biological Conservation 120(3):311–327.Google Scholar
Whitesides, GH, Oates, JF, Green, SM, Kluberdanz, RP. 1988. Estimating primate densities from transects in a West African rain forest: a comparison of techniques. Journal of Animal Ecology 57:345–367.Google Scholar

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