310 research outputs found

    Socio-Economic Instability and the Scaling of Energy Use with Population Size

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    The size of the human population is relevant to the development of a sustainable world, yet the forces setting growth or declines in the human population are poorly understood. Generally, population growth rates depend on whether new individuals compete for the same energy (leading to Malthusian or density-dependent growth) or help to generate new energy (leading to exponential and super-exponential growth). It has been hypothesized that exponential and super-exponential growth in humans has resulted from carrying capacity, which is in part determined by energy availability, keeping pace with or exceeding the rate of population growth. We evaluated the relationship between energy use and population size for countries with long records of both and the world as a whole to assess whether energy yields are consistent with the idea of an increasing carrying capacity. We find that on average energy use has indeed kept pace with population size over long time periods. We also show, however, that the energy-population scaling exponent plummets during, and its temporal variability increases preceding, periods of social, political, technological, and environmental change. We suggest that efforts to increase the reliability of future energy yields may be essential for stabilizing both population growth and the global socio-economic system

    Vegetation dynamics and plant constraints: separating generalities and specifics

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    Vegetation dynamics is a stochastic process of species replacement after disturbance. It occurs because individual species are limited by general constraints and trade-offs. As these constraints and trade-offs are becoming better known, we understand more about the relationships between disturbance dynamics, species pools, and vegetation dynamics. This paper provides a summary of recent work on plant scaling and ecological trade-offs, and explores its implications for vegetation dynamics. Those aspects of succession that are predictable . given the local species complement . can be understood as consequences of these general patterns and constraints. Several are explored in this paper. The inherently stochastic nature of the process derives from the disturbance dynamics that forces it, from the sampling processes that are responsible for selecting potential invaders, and from the chance processes involved in species interactions. The dynamics of species that invade established communities is the least understood but potentially the most crucial aspect of vegetation dynamics. The relation of community invasion to gap creation and to scaling constraints is briefly discussed

    Senescence and Sexual Selection in a Pelagic Copepod

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    The ecology of senescence in marine zooplankton is not well known. Here we demonstrate senescence effects in the marine copepod Oithona davisae and show how sex and sexual selection accelerate the rate of ageing in the males. We show that adult mortality increases and male mating capacity and female fertility decrease with age and that the deterioration in reproductive performance is faster for males. Males have a limited mating capacity because they can fertilize < 2 females day−1 and their reproductive life span is 10 days on average. High female encounter rates in nature (>10 day−1), a rapid age-dependent decline in female fertility, and a high mortality cost of mating in males are conducive to the development of male choosiness. In our experiments males in fact show a preference for mating with young females that are 3 times more fertile than 30-day old females. We argue that this may lead to severe male-male competition for young virgin females and a trade-off that favours investment in mate finding over maintenance. In nature, mate finding leads to a further elevated mortality of males, because these swim rapidly in their search for attractive partners, further relaxing fitness benefits of maintenance investments. We show that females have a short reproductive period compared to their average longevity but virgin females stay fertile for most of their life. We interpret this as an adaptation to a shortage of males, because a long life increases the chance of fertilization and/or of finding a high quality partner. The very long post reproductive life that many females experience is thus a secondary effect of such an adaptation
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