Spatial distribution of broadleaf weeds within 14 North Carolina soybean fields was characterized by fitting negative binomial distributions to frequency distributions of weed counts in each field. In most cases, the data could be represented by a negative binomial distribution. Estimated values of the parameter K of this distribution were small, often less than one, indicating a high degree of patchiness. The data also indicated that the population as a whole was patchy. Counts of individual species were positively correlated with each other in some fields and total weed count could be represented by a negative binomial for 12 of the 14 fields.

A model of the spatial emergence of an interstellar civilization into a uniform distribution of habitable systems is presented. The process of emigration is modelled as a three-dimensional probabilistic cellular automaton. An algorithm is presented which defines both the daughter colonies of the original seed vertex and all subsequent connected vertices, and the probability of a connection between any two vertices. The automaton is analysed over a wide set of parameters for iterations that represent up to 250 000 years within the model's assumptions. Emigration patterns are characterized and used to evaluate two hypotheses that aim to explain the Fermi Paradox. The first hypothesis states that interstellar emigration takes too long for any civilization to have yet come within a detectable distance, and the second states that large volumes of habitable space may be left uninhabited by an interstellar civilization and Earth is located in one of these voids.

Many small mammals inhabiting vegetation habitats where food resources are scattered have large home ranges with limited overlap. One way that they may effectively defend large territories is to establish dominance over the limited number of sites that provide good protection from predators, since displacement from these sites could have a very high cost to intruders. To examine this hypothesis we studied the fine-scale use of habitat and spatial dispersion of all adult male Mus spretus inhabiting a 1.1 ha grassland study site near Lisbon, Portugal, by radio telemetry, at the start of the breeding season. The location of each of the 10 males was mapped every hour, 24 h/day for up to seven days. Microhabitat characteristics were compared between a random sample of points in the study site and those where mice were found. Individual ranges did not overlap, despite the close proximity of their borders and the occupation of almost all suitable habitat, suggesting that individual dispersion was strongly influenced by the presence of neighbours; mean range size was 343 ± 95 m2. Residents covered less than one-third of their total range over 24 h, though neighbours did not intrude despite the apparent opportunities. Each male territory overlapped the territory of at least two females. Mice were neither nocturnal nor crepuscular, moving around mostly during the morning and evening. They avoided open woodland or pathways, preferring grassland sites with tall vegetation and sites where shrubs, bramble, or dead wood provided additional cover. Most fixes per male (70%) were located in one to four core areas, which represented only a tiny proportion of each range (6.9 ± 0.9%). Although exclusive defence of large complex ranges is likely to be impracticable, defence of core areas seems much more feasible. Our results thus support our hypothesis that mice may be able to maintain large exclusive ranges due to a combination of high predation pressure and a limited number of sites with sufficient ground and overhead cover. This will result in a very high risk to mice entering areas where competitors have priority of access to protected sites.

Spatial dispersion of the nymphs of the jassid, Amrasca biguttula biguttula (Ishida), and the adults of the whitefly, Bemisia tabaci Genn. on F414, a Gossypium hirsutum variety, was systematic in Ludhiana (Punjab). Both the jassid and the whitefly displayed no definite pattern along the height of the plant, though a maximum number of whiteflies were recorded at middle canopy (21–40 cm from bottom). Sample sizes of 10–15 plants, selected in a statistically linear fashion represented populations of jassid nymphs and adult whitefly on all four varieties. Sampling jassid nymphs by visual counting and whitefly by split-cage were the most suitable sampling methods for local cotton growers among the various methods compared.