2002
DOI: 10.1038/nature00809
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Density-dependent mortality and the latitudinal gradient in species diversity

Abstract: Ecologists have long postulated that density-dependent mortality maintains high tree diversity in the tropics. If species experience greater mortality when abundant, then more rare species can persist. Agents of density-dependent mortality (such as host-specific predators, and pathogens) may be more prevalent or have stronger effects in tropical forests, because they are not limited by climatic factors. If so, decreasing density-dependent mortality with increasing latitude could partially explain the observed … Show more

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Cited by 304 publications
(241 citation statements)
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“…Janzen-Connell effects (i.e., patterns of negative density dependence related to natural enemies; Janzen 1970, Connell 1971 are one likely explanation in this and other systems (e.g., Hille Ris Lambers et al 2002, Comita et al 2010, Martin and Canham 2010, Metz et al 2010. Negative-density effects may contribute to the maintenance of species diversity by leading to higher mortality rates in conspecific seedlings.…”
Section: Discussionmentioning
confidence: 99%
“…Janzen-Connell effects (i.e., patterns of negative density dependence related to natural enemies; Janzen 1970, Connell 1971 are one likely explanation in this and other systems (e.g., Hille Ris Lambers et al 2002, Comita et al 2010, Martin and Canham 2010, Metz et al 2010. Negative-density effects may contribute to the maintenance of species diversity by leading to higher mortality rates in conspecific seedlings.…”
Section: Discussionmentioning
confidence: 99%
“…The effects of CNDD are proposed to be a powerful mechanism of species coexistence, particularly in diverse tropical forests (Janzen 1970;Connell 1971;Mangan et al 2010) and, more recently, broadly across North American forests (Packer and Clay 2000;Nakashizuka 2001;HilleRisLambers et al 2002;McCarthy-Neumann and Kobe 2010;Johnson et al 2012). However, while CNDD is thought to occur via the accumulation of species-specific pathogens and predators, our model generates these effects via hosts' impacts on partner communities that include cheaters.…”
Section: Discussionmentioning
confidence: 99%
“…Interannual variation has long been used to analyze climate regulation of tree growth (Graumlich 1991, Clark et al 2003a, Stevens et al 2006) and fecundity (McKone et al 1998, Schauber et al 2002, Hampe 2005, Mutke et al 2005. But dynamics of tree populations are highly dependent on recruitment (e.g., Clark et al 1998, Houle 1998, Hubbell et al 1999, Brown and Wu 2005, Stephenson and van Mantgem 2005, Matthes and Larson 2006, which has been studied primarily at fine spatial scales, involving biotic interactions and microsite variation (Beckage et al 2000, Connell and Green 2000, Harms et al 2000, Hille Ris Lambers et al 2002, Wright et al 2005, rather than variation in time. Experiments involving atmospheric effects on recruitment are expensive and, thus, rare (but see DeLucia et al 1999, Ko¨rner 2004, Mohan et al 2007).…”
Section: Introductionmentioning
confidence: 99%
“…We analyzed dynamic responses to climatic variability at the recruitment stage, for dominant tree species growing in five representative communities of the Southern Appalachians. To understand dynamics, more than a decade of spatiotemporal data on each stage, from seed production, through the seed bank, to germination were assimilated in population dynamic models that allowed us to evaluate how environmental influences, light availability, and seed density affected recruitment success (e.g., Kobe et al 1995, Beckage et al 2000, Harms et al 2000, Hille Ris Lambers et al 2002, Hille Ris Lambers and Clark 2003 and, thus, might interact with climate change.…”
Section: Introductionmentioning
confidence: 99%