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Register a new userHumans: the hyper-dense species
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Humans, like all organisms, are subject to fundamental biophysical laws. Van Valen predicted that, because of zero-sum dynamics, all populations of all species in a given environment flux the same amount of energy on average. Damuths energetic equivalence rule supported Van Valens conjecture by showing a trade off between few big animals per area with high individual metabolic rates compared to abundant small species with low energy requirements. We use established metabolic scaling theory to compare variation in densities and individual energy use in human societies to other land mammals. We show that hunter-gatherers occurred at lower densities than a mammal of our size. Most modern humans, in contrast, concentrate in large cities at densities that are up to four orders of magnitude greater than hunter-gatherers yet cities consume up to two orders of magnitude greater energy per capita. Today, cities across the globe flux greater energy than net primary productivity on a per area basis. This is possible through enormous fluxes of energy and materials across urban boundaries to sustain hyper-dense, modern humans. The metabolic rift with nature created by hyper-dense cities supported by fossil fuel energy poses formidable challenges for establishing a sustainable relationship on a rapidly urbanizing, yet finite planet.
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The analysis of eight molecular datasets involving human and teleost examples along with morphological samples from several groups of Neotropical electric fish (Order: Gymnotiformes) were used in this thesis to test the dynamics of both intraspecific variation and interspecific diversity. In terms of investigating molecular interspecific diversity among humans, two experimental exercises were performed. A cladistic exchange experiment tested for the extent of discontinuity and interbreeding between H. sapiens and neanderthal populations. As part of the same question, another experimental exercise tested the amount of molecular variance resulting from simulations which treated neanderthals as being either a local population of modern humans or as a distinct subspecies. Finally, comparisons of hominid populations over time with fish species helped to define what constitutes taxonomically relevant differences between morphological populations as expressed among both trait size ranges and through growth patterns that begin during ontogeny. Compared to the subdivision found within selected teleost species, H. sapiens molecular data exhibited little variation and discontinuity between geographical regions. Results of the two experimental exercises concluded that neanderthals exhibit taxonomic distance from modern H. sapiens. However, this distance was not so great as to exclude the possibility of interbreeding between the two subspecific groups. Finally, a series of characters were analyzed among species of Neotropical electric fish. These analyses were compared with hominid examples to determine what constituted taxonomically relevant differences between populations as expressed among specific morphometric traits that develop during the juvenile phase.
Most primates live in social groups which survival and stability depend on individuals abilities to create strong social relationships with other group members. The existence of those groups requires to identify individuals and to assign to each of them a social status. Individual recognition can be achieved through vocalizations but also through faces. In humans, an efficient system for the processing of own species faces exists. This specialization is achieved through experience with faces of conspecifics during development and leads to the loss of ability to process faces from other primate species. We hypothesize that a similar mechanism exists in social primates. We investigated face processing in one Old World species (genus Macaca) and in one New World species (genus Cebus). Our results show the same advantage for own species face recognition for all tested subjects. This work suggests in all species tested the existence of a common trait inherited from the primate ancestor: an efficient system to identify individual faces of own species only.
Cyclic dominance is frequently believed to be a mechanism that maintains diversity of competing species. But this delicate balance could also be fragile if some of the members is weakened because an extinction of a species will involve the annihilation of its predator hence leaving only a single species alive. To check this expectation we here introduce a fourth species which chases exclusively a single member of the basic model composed by three cyclically dominant species. Interestingly, the coexistence is not necessarily broken and we have detected three consecutive phase transitions as we vary only the invasion strength of the fourth pestilent species. The resulting phases are analyzed by different techniques including the study of the Hamming distance density profiles. Some of our observations strengthen previous findings about cyclically dominant system, but they also offer new revelations and counter-intuitive phenomenon, like supporting pestilent species may result in its extinction, hence enriching our understanding about these very simple but still surprisingly complex systems.
Niche and neutral theory are two prevailing, yet much debated, ideas in ecology proposed to explain the patterns of biodiversity. Whereas niche theory emphasizes selective differences between species and interspecific interactions in shaping the community, neutral theory supposes functional equivalence between species and points to stochasticity as the primary driver of ecological dynamics. In this work, we draw a bridge between these two opposing theories. Starting from a Lotka-Volterra (LV) model with demographic noise and random symmetric interactions, we analytically derive the stationary population statistics and species abundance distribution (SAD). Using these results, we demonstrate that the model can exhibit three classes of SADs commonly found in niche and neutral theories and found conditions that allow an ecosystem to transition between these various regimes. Thus, we reconcile how neutral-like statistics may arise from a diverse community with niche differentiation.
We investigate the problem of the predominance and survival of weak species in the context of the simplest generalization of the spatial stochastic rock-paper-scissors model to four species by considering models in which one, two, or three species have a reduced predation probability. We show, using lattice based spatial stochastic simulations with random initial conditions, that if only one of the four species has its probability reduced then the most abundant species is the prey of the weakest (assuming that the simulations are large enough for coexistence to prevail). Also, among the remaining cases, we present examples in which weak and strong species have similar average abundances and others in which either of them dominates -- the most abundant species being always a prey of a weak species with which it maintains a unidirectional predator-prey interaction. However, in contrast to the three-species model, we find no systematic difference in the global performance of weak and strong species, and we conjecture that the same result will hold if the number of species is further increased. We also determine the probability of single species survival and coexistence as a function of the lattice size, discussing its dependence on initial conditions and on the change to the dynamics of the model which results from the extinction of one of the species.
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