From forest to farmland: diversity of geometrid moths along two habitat gradients on Borneo

By Jan Beck, C. Schulze, K. Linsenmair, K. Fiedler. Journal of Tropical Ecology, 2002

184 citations recorded by the source corpus.

Subfields: Ecological Modeling, Ecology, Evolution, Behavior and Systematics, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/5cb7ad40c5783c4096e1f0524061f87e8cdbb03a

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecological Modeling

In Ecology, Evolution, Behavior and Systematics

In Nature and Landscape Conservation

Citations in the corpus

Attraction to light - from how far do moths (Lepidoptera) return to weak artificial sources of light? (2012, background): “Various studies (Beck et al., 2002; Schulze & Fiedler, 2003) indicate clear differences in the samples of insects caught by light traps located in different forest strata (20–40 m height).”
BIODIVERSITY INDICATOR GROUPS OF TROPICAL LAND‐USE SYSTEMS: COMPARING PLANTS, BIRDS, AND INSECTS (2004, methodology): “Secondary forests and agroforestry systems may help to maintain a certain portion of diversity (e.g., Lawton et al. 1998, Schulze 2000, Beck et al. 2002), but not of all taxonomic groups.”
Faunal composition of geometrid moths changes with altitude in an Andean montane rain forest (2003, background): “Geometrids are a relatively habitat-specific group of herbivorous insects and thus very suitable for ecological studies (for tropical geometrids: Intachat et al., 1997; Kitching et al., 2000; Beck et al., 2002).”
Beta diversity of geometrid moths (Lepidoptera: Geometridae) in an Andean montane rainforest (2003, background): “Geometrid moths are well known in taxonomic terms (Scoble, 1999) and have served as model organisms for environmental changes in a range of studies, mainly in South-east Asia (e.g. Intachat et al., 1997; Beck et al., 2002).”
Changes of dung beetle communities from rainforests towards agroforestry systems and annual cultures in Sulawesi (Indonesia) (2005, background): “insect diversity related to forest disturbance (e.g., Holloway et al. 1992; Hill et al. 1995; Lawton et al. 1998; Intachat et al. 1999; Schulze 2000; Brühl et al. 2001; Beck et al. 2002) and conversion of forests or forest plantations to agricultural habitats (Holloway 1987; Wolda 1987) has been als”
Disturbance effects on diversity of epiphytes and moths in a montane forest in Ecuador (2008, background): “Previous studies however, found no evidence of a true geometrid canopy fauna (Intachat & Holloway, 2000; Beck et al., 2002; Brehm, 2007), whereas tropical arctiid moths are significantly more abundant and diverse in the canopy than in the understorey (Schulze, Linsenmair, & Fiedler, 2001; Brehm, 200”
Diversity and community composition of butterflies and odonates in an ENSO-induced fire affected habitat mosaic: a case study from East Kalimantan, Indonesia (2004, unknown): “MDS does not have stringent model assumptions, such as correspondence analysis, which assumes a unimodal response, and any similarity measure can be used for ordination (Beck et al. 2002).”
Determinants of diversity in afrotropical herbivorous insects (Lepidoptera: Geometridae): plant diversity, vegetation structure or abiotic factors? (2009, background): “The hypothesized link between geometrid moth and plant assemblages (Lewinsohn & Roslin, 2008) is corroborated by observations from Southeast Asia, where the alpha diversity of geometrid moths has been positively correlated with the overall species density of vascular plants, and particularly with th”
Macro‐moth families differ in their attraction to light: implications for light‐trap monitoring programmes (2014, unknown): “…actinic), showed marked differences in moth assemblages between undergrowth and canopy at local sites, providing indirect evidence of low attraction radii as species were not drawn towards the different habitats over vertical distances as small as 30–45 m (Beck et al., 2002; Beck & Schulze, 2003).”
The persistence and conservation of Borneo’s mammals in lowland rain forests managed for timber: observations, overviews and opportunities (2007, background): “Other groups of Bornean invertebrates affected by logging include butterflies (Cleary 2004), beetles (Chung et al. 2000), and geometrid moths ( Beck et al. 2002 ).”
Southeast Asian biodiversity: an impending disaster. (2004, background): “Recent studies reveal a trend of declining species richness and population density with increasing forest disturbance through logging activities, agriculture or urbanization across a range of Southeast Asian taxa, including termites [27], dung beetles [28], ants [29], bees [30], butterflies [31], mo”
Diversity and composition of Arctiidae moth ensembles along a successional gradient in the Ecuadorian Andes (2005, background): “Fisher’s alpha has also been extensively used in many other arthropod and especially moth studies, thus facilitating comparisons between studies (e.g. Wolda, 1983, 1987; Thomas & Thomas, 1994; Beck et al., 2002; Brehm et al., 2003b).”
Global dung beetle response to tropical forest modification and fragmentation: A quantitative literature review and meta-analysis (2007, methodology): “We defined land-use categories with the original published definitions and ordered them in a qualitative gradient of increasing habitat modification relative to intact forest (Glor et al., 2001, Beck et al., 2002 and Jones et al., 2003).”
Montane Andean rain forests are a global diversity hotspot of geometrid moths (2005, unknown): “500 20–630 500 (4585) 143 Beck et al. (2002); area,”
Unique elevational diversity patterns of geometrid moths in an Andean montane rainforest (2003, background): “Rahbeck (1997) and Körner (2000) emphasised the importance of decreasing area at high altitudes, and Holloway (1987) discussed a higher diversity of moths in montane Papua New Guinea compared to Borneo, as a consequence of greater land area situated above 2000 m.”