Population Interactions and the Determinants of Population Size

Abstract The flux of individuals within populations is dependent upon six controlling processes: the intrinsic rate of increase of the plant, intraspecific competition for resources, interspecific competition, natural enemies, mutualisms and refuge effects such as the immigration of seeds from other populations. Although population interactions are generally believed to play a major role in determining the flux of individuals within populations, little attempt has been made to quantify the strength of these interactions and their role in the dynamics of populations. In this paper we examine the role of competition, herbivory and mutualistic interactions in determining the dynamics of a range of annual plant species. Firstly, it is shown that the dynamics of three weed species ( Bromus sterilis, Galium aparine, Papaver rhoeas ) in an experimental community in an arable cropping system of winter wheat are determined primarily by the rapid population growth of B. sterilis . Interactions between the species play a minor part in the dynamics of the system. Secondly, it is shown that current levels of grazing by overwintering populations of brent geese have a minor impact on the abundance of Salicornia europaea , but that increased grazing has the potential to reduce abundance and increase the instability of S. europaea populations. This is a consequence of the aggregative response of the geese, which results in an increasing proportion of the seeds of S. europaea being eaten as plant density increases. Thirdly, it is shown that there is a complex interaction between root pathogenic and arbuscular mycorrhizal fungi in natural field populations of Vulpia ciliata and that the benefit of mycorrhizal fungi to the plant is in providing protection against pathogens.     

Dynamics of Competition in Populations of Carrot (Daucus carota)

Populations of carrot (Daucus carota) were raised over a widerange of densities (79–5763 plants m^-2) to examine thedynamics of competition in terms of yield–density relationshipsand size variability, and to investigate the effects of nutrientsupply on competition. While the relationship between shootyield and density was asymptotic, the relationship between rootand total yield and density tended to be parabolic. For a giventime and density series the relationship between yield per unitarea and density could best be described by the model: y=w_mD_(1+aD)^b wherey is the yield per unit area,D is density,w_m, a andb arefitted parameters. The parametersw_m anda increased over timebut nutrient availability affected onlyw_m. An extension of thebasic yield-density model is proposed to describe the dynamicsof the yield–density relationship over time: y=kD_{[1+cexp(-rt)]{1+}     

Shared Lipid Phosphate Carrier in the Biosynthesis of Teichoic Acid and Peptidoglycan

THE pathways for the formation of several bacterial wall polymers have been thoroughly investigated. In some cases it has been shown that the biosynthesis involves the participation of lipid intermediates that are concerned with the transfer and transport through the membrane, of sugar residues and related components from intracellular nucleotide precursors to polymer chains in the wall. All these membrane lipids so far isolated and identified have been shown to be the C₅₅ polyisöprenol, undecaprenol, although it has not yet been demonstrated that they are the same isomer. Thus poly-isoprenols have been demonstrated to participate in the synthesis of O-antigen¹, peptidoglycan^{2, 3} and mannan⁴.     

Region‐wide temporal and spatial variation in Caribbean reef architecture: is coral cover the whole story?

The architectural complexity of coral reefs is largely generated by reef‐building corals, yet the effects of current regional‐scale declines in coral cover on reef complexity are poorly understood. In particular, both the extent to which declines in coral cover lead to declines in complexity and the length of time it takes for reefs to collapse following coral mortality are unknown. Here we assess the extent of temporal and spatial covariation between coral cover and reef architectural complexity using a Caribbean‐wide dataset of temporally replicated estimates spanning four decades. Both coral cover and architectural complexity have declined rapidly over time, with little evidence of a time‐lag. However, annual rates of change in coral cover and complexity do not covary, and levels of complexity vary greatly among reefs with similar coral cover. These findings suggest that the stressors influencing Caribbean reefs are sufficiently severe and widespread to produce similar regional‐scale declines in coral cover and reef complexity, even though reef architectural complexity is not a direct function of coral cover at local scales. Given that architectural complexity is not a simple function of coral cover, it is important that conservation monitoring and restoration give due consideration to both architecture and coral cover. This will help ensure that the ecosystem services supported by architectural complexity, such as nutrient recycling, dissipation of wave energy, fish production and diversity, are maintained and enhanced.     

A Model for Growth and Self-thinning in Even-aged Monocultures of Plants

A theoretical model is derived from simple postulates to describethe rates of growth and mortality of plants in populations ofdifferent densities. The growth rate is described by a modificationof the logistic growth differential equation in which the increasein weight of an individual plant depends on its area, s_i ratherthan on its weight. The effective area for growth of a plantis reduced by an empirical function, f(s_i) with two terms: oneterm expresses the constraint imposed upon the increasing totalarea of plants by the limited physical area of the plot; theother term allows for a competitive advantage or disadvantagefor plants of varying sizes. Depending on the value of the parametercontrolling the relative competitive advantage term, intrinsicvariability between plants can be amplified or suppressed. Anindividual plant dies if the f(s_i) results in a negative growthrate for that plant. Computer simulations of the growth andsurvival of plants at different population densities were run.The results exhibit characteristics that appear realistic uponcomparison with published data: a survival of the fittest occurringduring thinning; a line of slope close to –3/2 boundingthe graphs of log weight versus log density; and the occurrenceof bimodality, associated with subsequent mortality, on frequencydistribution of log weight. computer logistic model, growth differential equation, density-effect, competition, mortality, self-thinning     

Yield-density Relationships: the Influence of Resource Availability on Growth and Self-thinning in Populations of Vulpia fasciculata

Monocultures of Vulpia fasciculata were grown over a wide rangeof densities to investigate the influence of crowding and nutrientsupply on growth and self-thinning. For a given time and densityseries the relationship between mean yield per plant (w) andthe density of survivors (N) could be described by the equation w= w_m (1+aN)^–b. where w_m is the yield of an isolated plant, a is the area requiredto achieve a yield of w_m and b describes the effectiveness withwhich resources are taken up from the area. All three parametersincreased with time. Adding nutrients changed not only the rate at which the effectsof crowding occurred but also the intensity of crowding since w_m = C(a^b)^D. where C and D are constants. The addition of nutrients resultedin an increase in the value of C. Such an increase means thata larger weight can be supported by a given area because theresources within that area are greater. During the early phases of growth, populations of V. fasciculataconformed to the –3/2 power law, w = cN^–3/2, butonly at very high densities with a plentiful supply of nutrients.However, once the maximum standing crop had been reached thetrajectory of the thinning line switched to a slope of justless than –1 when weight was ploted against density onlogarithmic scales. The intercept of the –3/2 thinningline was considerably higher (log c = 5.74) than those for mosttrees and forbs but was similar to those of a number of othergrasses. Vulpia fasciculata, dune fescue, yield-density models, self-thinning, density-dependence, nutrient supply