In: AoB PLANTS, 2016, vol. 8, no. 1, p. -
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In: Agronomy for Sustainable Development, 2015, vol. 35, no. 1, p. 145-150
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In: Proceedings of the Royal Society B: Biological Sciences, 2019, vol. 286, no. 1911, p. 20191506
We develop a spatially explicit model of diversification based on palaeohabitat to explore the predictions of four major hypotheses potentially explaining the latitudinal diversity gradient (LDG), namely, the ‘time-area’, ‘tropical niche conservatism’, ‘ecological limits’ and ‘evolutionary speed’ hypotheses. We compare simulation outputs to observed diversity gradients in the...
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In: Oecologia, 2019, vol. 189, no. 1, p. 185–197
Studies on biodiversity–ecosystem functioning (BEF) in highly controlled experiments often yield results incompatible with observations from natural systems: experimental results often reveal positive relationships between diversity and productivity, while for natural systems, zero or even negative relationships have been reported. The discrepancy may arise due to a limited or closed local...
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In: Environmental Management, 2009, vol. 44, no. 1, p. 105-118
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In: Biodiversity & Conservation, 2006, vol. 15, no. 1, p. 275-294
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In: Folia Geobotanica, 2013, vol. 48, no. 3, p. 335-353
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In: Oecologia, 2012, vol. 169, no. 1, p. 269-279
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In: Folia Geobotanica, 1999, vol. 34, no. 1, p. 7-18
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In: BioEnergy Research, 2013, vol. 6, no. 2, p. 533-546
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