Janzen–Connell hypothesis


The Janzen–Connell hypothesis is a widely accepted explanation for the maintenance of tree species biodiversity in tropical rainforests. It was published independently in the early 1970s by Daniel Janzen and Joseph Connell. According to their hypothesis, host-specific herbivores, pathogens, or other natural enemies make the areas near a parent tree inhospitable for the survival of seedlings. These natural enemies are referred to as 'distance-responsive predators' if they kill seeds or seedlings near the parent tree, or 'density-dependent predators' if they kill seeds or seedlings where they are most abundant. Such predators can prevent any one species from dominating the landscape, because if that species is too common, there will be few safe places for its seedlings to survive. However, because the predators are host-specific, they will not harm other tree species. As a result, if a species becomes very rare, then more predator-free areas will become available, giving that species' seedlings a competitive advantage. This negative feedback allows the tree species to coexist, and can be classified as a stabilizing mechanism.
The Janzen-Connell hypothesis has been called a special case of keystone predation, predator partitioning or the pest pressure hypothesis. The pest pressure hypothesis states that plant diversity is maintained by specialist natural enemies. The Janzen-Connell hypothesis expands on this, by claiming that the natural enemies are not only specialists, but also are distance-responsive or density-responsive.
This mechanism has been proposed as promoting diversity of forests as it promotes survival of a number of different plant species within one localized region. While previously thought to explain the high diversity of tropical forests in particular, subsequent research has demonstrated the applicability of the Janzen–Connell hypothesis in temperate settings as well. The Black Cherry is one such example of a temperate forest species whose growth patterns can still be explained by the Janzen–Connell hypothesis.

History

Daniel Janzen’s hypothesis

Daniel Janzen published his hypothesis in 1970 in The American Naturalist under the article "Herbivores and the Number of Tree Species in Tropical Forests." His hypothesis was based on the observation that in tropical forests, there were few new adult trees in the immediate vicinity of their parent tree. He explained the low density of tropical trees and lack of "bunching" of tree types around parent trees for two reasons: the number of seeds decline with distance from the parent tree and that the adult tree, its seeds, and seedlings are a source of food for host-specific parasites and diseases.
Using his observations, Janzen created a model demonstrating the probability of a seed maturation or a seedling survival as a function of distance from the parent tree.

Joseph Connell hypothesis

Joseph Connell published his hypothesis in 1971 in Dynamics of Populations. Unlike Janzen, Connell proposed experiments that focused on the key prediction that exclusion of host-specific predators would cause a decrease in diversity as tree species with greater establishment or competitive ability formed low-diversity seedling and sapling communities where dominance was concentrated in a few species.
He formed his hypothesis through observations in Queensland, Australia. Along with Jack Greening Tracey and Larry Johnson Webb, he mapped trees in two rainforests and observed that smaller seedlings tended to occur in single-species clumps. Smaller seedlings also exhibited greater mortality, especially when their nearest neighbor was an individual of the same species. This pattern lessened with growth and age until seedlings exhibited similar pattern diversity to adults. To reinforce these observations, Connell ran an experiment showing that adult trees have a deleterious effect on smaller trees of the same species. In another experiment, Connell found that pre-germination predation was greater on seeds near adults of the same species than those near adults of others. Through these observations, Connell suggests that each tree species has host-specific enemies that attack it and any of its offspring which are close to the parent. This emphasizes the importance of the role of predation in preventing trees from forming single-species groves, which is probably the only way in which one species of tree could exclude others by interspecies competition.

Effects on forest dynamics

Disease dynamics and tree density

Plant pathogens follow infectious disease dynamics. The basic reproductive rate of a disease is dependent on three variables such that:
Where β is the transmission rate or infectiousness of the disease, L is the average infection time of the host, and S is the density of the host population. By decreasing any one of the variables, the reproduction rate of the disease decreases. Since seed dispersal is such that the highest density of seeds is around the parent with density decreasing with distance from the parent, the reproduction rate of a disease infecting seeds and seedlings will be highest around the parent and decrease with distance. Thus, seedlings close to the parent are likely to die due to the disease prevalence. However, seedlings farther away are less likely to encounter the disease and therefore will more likely grow into adults.

Herbivory and tree density

Specialist herbivores who consume plant matter can also be thought of as having a "transmission rate" between individuals similarly to a disease. Tree predators are limited by the ease of movement. When individuals are closer together at high density, movement between trees is easier and the predators quickly spread out. However, at low tree density, predators can not find the next individual with as much ease and thus often have low transmission rates leading to less specialist predation.

Problematic aspects

Many studies examining the Janzen–Connell hypothesis have shown supporting patterns with a number of tree species, but despite this there are also problematic aspects of the hypothesis.
  1. The first is that the Janzen–Connell hypothesis explains diversity at a community-wide scale, but most studies have only looked at a single species or a localized region. Most studies do not test the diversity prediction and did not determine the causes for patterns consistent with Janzen–Connell effects. As Wright pointed out, "field measurements only demonstrate that niche differences, Janzen–Connell effects, and negative density dependence occur. Implications for species coexistence and plant diversity remain conjectural."
  2. While these host-specific predators may play keystone species roles as they possibly aid in the prevention of superior tree competitors from monopolizing an area, no study has yet to examine species richness and abundance after removing natural enemies, creating a gap in the supporting research for the hypothesis.
  3. Diversity may be maintained, at least in part, by episodic outbreaks of specialized pests, which may reduce the survivorship, growth, and reproductive success of adults of a species whenever they are particularly aggregated. Thus, specialist predation also impacts adult density, rather than just juveniles which has been the focus of research efforts.
  4. Disease and predation may be just affecting overall density rather than in localized regions around adults alone.
  5. Theoretical work has suggested that distance-responsive predators are less able to promote coexistence than equivalent predators that are not distance-responsive.
  6. Many empirical studies have shown that few natural enemies are host-specific specialists, as the original hypothesis claimed. However, theoretical work has suggested that predators can have broader diets as long as they are more damaging to their primary host than other species.
  7. The responses of density-dependent predators' may not be restricted to a single trophic level, and when multiple trophic levels interact, Janzen-Connell effects may be negated. This is an example of "the enemy of my enemy is my friend" and it has been shown that the potential of host-specific insects to induce negative-density dependence in plant populations can be severely limited when the natural enemies of the seed predators are also density responsive.

    Research testing the hypothesis

Supporting research

There have been over 50 studies designed to test predictions of this hypothesis in tropical and other settings and most show that many tree species exhibit patterns consistent with Janzen–Connell effects. Studies that have supported the Janzen–Connell hypothesis:
Studies questioning the Janzen–Connell hypothesis:
It is tricky to form conclusions regarding the accuracy of the Janzen–Connell hypothesis as it is difficult to falsify. This is because:
It is likely that a number of mechanisms underscore the coexistence of similar species and thus cause biodiversity in ecosystems. It is possible the Janzen–Connell hypothesis is applicable only for some species depending on species characteristics. The hypothesis may also be affected by the kind of predator or pathogen as preliminary research has shown that the hypothesis is true only when host-specific predators have limited mobility with a range less than the seed dispersal range.