(abstract) We studied mechanisms of vegetation change in fens subject
	to succession from open water to floating mats and finally herbaceous
	rich-fens. Earlier research showed that these systems are characterized by
	transient seed banks. Our main question was whether seedlings of later
	succssional fen stages are already present in earlier stages, remaining
	subordinate in the vegetation until conditions become suitable for them.
	If, however, conditions during succession change in a way that only a
	limited set of species can survive as seedlings during each of the succssional
	stages, no seedling bank will exist. The transient character of the
	seeds would then imply that seeds will not germinate and will subsequently
	die and that seeds that have germinated in the ``wrong'' stage will not become
	established. We hypothesized that: (1) germination and seedling survival
	of fen species are significantly better in the succssional fen stage for which
	these sepecies area characteristics. (2) as a consequence no seedling banks
	occurs in these fens.
	
...
	Germination was higher in the ``own'' stage for all species groups as was
	survival for quaking fen species and rich fen species.
	
...
	Because of the transient seed bank and absence of a seedling bank in these
	fen wetlands, successful establishment of species necessitates a continuous
	dispersal of characteristic species until the environmental conditions permit
	establishment.
	This also implies that species of the whole successional sere should be present
	within dispersal distance.
	(abstract) Many glassland restoration projects on former arable land face
	problems because early successional grassland species establish vigorously
	and persistently but late successional grassland species fail to establish.
	Differences in establishment characteristics of early and late successional
	species might provide an explanation for the failure of many late successional
	species to colonize grasslands on ex-arable land.
	
...
	The poor establishment of late successional species on former arable land
	could therefore not be explained by solely by differences in establishment
	characteristics between early and late successional grassland species.
	Competitive processes between early and late successional species later in the
	life cycle probably play an important role. The results do point out that
	establishment of late successional species can be promoted by creating
	vegetative cover from the start of the restoration effort.
	(abstract) Questions: How do physical microsite conditions of microsites affect
	germination and seedling survival in different succssional stages?
	Do different species germinate in similar microsites in a given successional
	stage?
	
...
	Results: In early successional sites, seedlings of several species were
	positively associated with depressions and presence of rocks, and negatively
	associated with ridges. Patterns were generally consistent among species.
	In later succession, seedlings were not signficantly associated with any
	microsite characteristics. For Alnus viridis, seed density decreased
	with distance from seed sources but seedling density did not.
	
	Conclusions: Because of harsh conditions in early succession, physical
	microsites are important, and most species have similar microsite requirements.
	In later succession, physical microsites characteristics are not as important
	and are more variable. Microsites appear to be more important than seed
	rain in controlling the distribution of Alnus viridis in early succession.
	(summary) 1. Changes in farming practice provide an opportunity to restore
	once extensive forested wetlands on agricultural land. In some parts of the world,
	however, it has proved difficult to restore the full complement of plant species
	through natural regeneration. Similarly, the restoration of forested wetlands
	by replanting has often resulted in ecosystems of low diversity. Better methods
	of restoring these important ecosystems are now required and baldcypress swamps
	provide and opportunity to investigate alternative approaches to the restoration
	of forested wetlands. This study examined the composition of of seed banks of
	farmed fields to determine their value in restoring swamps in the south-eastern
	United States.
	
...
	5. Synthesis and applications. Both restoration ecologists and managers
	of nature conservation areas need to be cognisant of seed bank and dispersal
	characteristics of species ot effectively restore and manage forested wetlands
	In the case of baldcypress swamps, critical components of the vegetation are not
	maintained in seed banks, which may make these floodplain wetlands difficult to
	restore via natural recolonization. Ultimately, the successful restoration of
	abandoned farm fields to forested wetlands may depend on the re-engineerring of
	flood pulsing across landscapes to reconnect dispersal pathways.
	(summary) 1. As an aid for restoration projects, the relative potential for
	plants to immigrate to sites after severe disturbance was investigated and an
	index developed to determine their relative immigration potential. The goal
	was to establish baseline knowledge for the species pool in severely disturbed
	sites prior to restoration. The method was based on the identification of
	potential colonists, inventories of populations in surroundings vegetation
	and autecological information on their maximum fecundity and dispersal by wind,
	water or animals.
	
...
	5. Synthesis and applications: An index of immigration potential provides
	information on the probable initial species pool after severe disturbance,
	against which the effects of local habitat suitability and establishment factors
	can be added to assess probable successional patterns. Its flexibility and
	applicability to varied life forms should make it useful for diagonosing
	recolonization bottlenecks in a wide variety of disturbance and restoration
	situations. It also allows for and assessment of the relative need for
	introducing species during the restoration of severely disturbed environments.
	(abstract) Question: Do species from communities with different flooding
	dynamics differ in seed buoyancy? Is there a trade-off between seed buoyancy
	and seed longevity?
	
...
	Results: Community occurenence along the hydrologic gradient was mirrored by
	seed buoyancy. Seed buoyancy was highest for speices of almost permanentaly
	inundated reed beds and lowest for species for species of rarely
	inundated wet meadows. The seed buoyancy characteristics of species
	of reed beds were best adapted to hydrological dynamic conditions
	mimicked by the treatment moving water and were the most independent of the
	flow rate of the water. A high percentage of the species used had a transient
	seed bank. Together with high in many species, this suggests a trade-off between
	dispersal capacity and seed persistence.
	
	Conclusions: In freshwater wetlands with rather stable water levels, many
	species lack a persistent seed bank and depend on dispersal for colonization
	of new habitats. Seed buoyancy enhances aquatic seed dispersal, and can be of
	great importance in both vegetation dynamics and restoration. In wetlands
	that are inundated for a long period during the year and with a water level
	above soil surface, higher seed buoyancy enhances the possibility for
	hydrochory.
	(abstract) Seed production, composition of seed rain, germination and seedling
	mortality, as well as vegetative growth characteristics of common pioneer
	plant species were studied on the foreland of the retreating Morteratsch glacier
	in the Swiss Alps. The frequency of diaspores trapped in different successional
	stages was related to their dispersal mode and was highly skewed towards a few
	species. Plenty of diaspores well adapted for dispersal by wind area a 
	precondition for the most important pioneer species. Seed from all pioneer
	species investigated had a good germination success, provided that the moisture
	content of the soil was high enough. However, requirement for seedling
	establishment differed among sites of increasing terrain age and among species.
	
...
	The life cycle of this species is characterized in succession by
	(1) the colonization of safe sites by small seeds adapted for wind dispersal,
	(2) horizontal spread by clonal growth, and (3) the persisitence through
	phenotypic morphorogical plasticity and clonal growth are thus complementary
	mechanishms in plant succession on recently deglaciated terrian.
dlnorm()
		(対数正規分布) にするとコケることがあるな
		(slice sampler が動かないとかで).
		回避わざとしては
		(ばかばかしいけど)
log.beta2[j] ~ dnorm(0.0, Tau.noninformative) beta2[j] <- exp(log.beta2[j]) # もしくは log(beta2[j]) <- log.beta2[j]なぜかこれだと問題おこらない. どうもこの
dlnorm()
		だの
		dgamma()
		だのといった「正の値しかとらない確率分布」
		からの sampling は得意ではないみたいだねえ.
	
	
	James S. Clark, Mike Dietze, Sukhendu Chakraborty, Pankaj K. Agarwal, Ines Ibanez, Shannon LaDeau, Mike Wolosin.
	2007.
	Resolving the biodiversity paradox.
	Ecology Letters (OnlineEarly Articles).
	doi:10.1111/j.1461-0248.2007.01041.x
		いやはや,
		この御大的 abstract って
		……
	The paradox of biodiversity involves three elements,
	(i) mathematical models predict that species must differ in specific ways
	in order to coexist as stable ecological communities,
	(ii) such differences are difficult to identify,
	yet (iii) there is widespread evidence of stability in natural communities.
	Debate has centered on two views. The first explanation involves tradeoffs
	along a small number of axes, including `colonization-competition',
	resource competition (light, water, nitrogen for plants, including
	`successional niche'), and life history (e.g. high-light growth vs. low-light
	survival and few large vs. many small seeds).
	The second view is neutrality, which assumes that species differences do not
	contribute to dynamics.
	Clark et al. (2004) presented a third explanations,
	that coexistence is inherently high dimensional, but still depends on species
	differences.
	We demonstrte that neither traditional low-dimensional tradeoffs nor
	neutrality can resolve the biodiversity paradox, in part by showing that
	they do not property interpret stochasticity in statistical and theoretical
	models. Unless sample size are small, traditional data modelling assures that
	species will appear different in a few dimensions, but those differences will
	rarely predict coexistence when parameter estimates are plugged into
	theoretical models.
	Contrary to standard interpretations, neutral models do not imply
	...
		う,
		おもしろすぎてつい長々と写経してしまった.
		ここで紹介されてる森林動態の階層ベイズの詳細は
		Clark et al. (2004)
		に書かれている.