Population Dynamics of Chewing Lice (Phthiraptera) Infesting Birds (Aves).

In the past 25 years, studies on interactions between chewing lice and their bird hosts have increased notably. This body of work reveals that sampling of live avian hosts, collection of the lice, and the aggregated distributions of louse infestations pose challenges for assessing louse populations. The number of lice on a bird varies among host taxa, often with host size and social system. Host preening behavior limits louse abundance, depending on bill shape. The small communities of lice (typically one-four species) that live on individual birds show species-specific patterns of abundance, with consistently common and rare species, and lower year-to-year population variability than other groups of insects. Most species of lice appear to breed continuously on their hosts, with seasonal patterns of abundance sometimes related to host reproduction and molting. Competition may have led to spatial partitioning of the host by louse species, but seldom contributes to current patterns of abundance.

Interactions between exotic and native lady beetle species stabilize community abundance.

A 23-year time-series of abundance for 13 lady beetle species (Coccinellidae) was used to investigate community stability. The community exhibited persistence in ten habitats, no overall trend in abundance, and low temporal variability quantified as Population variability (PV) = 0.33 on a scale from 0 to 1 that declined to 0.16 in the past 8 years. This high level of stability occurred as exotic lady beetles disrupted populations of the native species. For hypothetical communities of pairs of species (with randomly generated annual abundances in the range for lady beetles), PV increased linearly with the correlation coefficients between individual time series, illustrating a "portfolio effect". PV for the real community and the negative correlation between the abundance of exotics and natives fit this relationship precisely. A gradual decline of natives matched by an equal gradual rise in the abundance of exotics contributed to the negative correlation that stabilized the community. The abundance of the dominant species, an exotic, was negatively correlated with other exotics and most natives, and its stability increased over time, helping to stabilize the community. The community was most stable in habitats where beetle abundance was high (crops, particularly perennial crops) and, unexpectedly, was least stable in habitats with high diversity and stability of vegetation cover (forests). These data are consistent with the hypothesis that competition between exotic and native species, with release from competition for natives in some years, stabilized the abundance of this community. Stability may not last if populations of native species continue declining.

Variability in life history traits of the aphid, Acyrthosiphon pisum (Harris), from sexual and asexual populations.

Many aphid species have shown remarkable adaptability by invading new habitats and agricultural crops, although they are parthenogenetic and might be expected to show limited genetic variation. To determine if the mode of reproduction limits the level of genetic variation in adaptively important traits, we assess variation in 15 life history traits of the pea aphid, Acyrhosiphon pisum (Harris), for five populations sampled along a north-south transect in central North America, and for three traits for three populations from eastern Australia. The traits are developmental times and rates as affected by temperature, body weights as affected by temperature, fecundity, measures of migratory tendency, and photoperiodic responses. The most southerly population from North America is shown to be obligately parthenogenetic, as are the Australian populations, and the four more northerly North American populations are facultatively parthenogenetic with the number of parthenogenetic generations per year increasing from north to south. The broad-sense heritabilities of life history traits varied from 0.36 to 0.71 for nine quantitive traits based on a comparison of within-and between-lineage variances. Using these traits, 7-13 distinct genotypes (i.e. clones) were identified among each of the 18 lines sampled from the North American populations, but the number did not differ significantly among populations. The level of genetic variation differed from trait to trait. For 4 of 12 quantitative traits, the level of variation in the obligately parthenogenetic population from North America was lowest, but significantly lower than all the sexual populations for only 1 trait. The obligately parthenogenetic population had the highest level of genetic variation for two traits, and had intermediate levels for the others. The most northerly population, which was sexual and had relatively few parthenogenetic generations each year, had the lowest level of variation for 5 of 12 traits and the highest level of variation for 2 traits. There was no decline in variability from north to south correlated with the increase in the annual number of parthenogenetic generations. The Australian populations showed no less variation than the North American populations for two of three traits, although the pea aphid was introduced to Australia only 5 years prior to the study, whereas the aphid has been in North America for at least 100 years. The mode of reproduction has not had a substantial impact on the level of genetic variation in life history traits of the pea aphid, but there are population-specific factors that effect the level of variation in certain traits.

Effects of temperature on the development, growth, and survival of larvae and pupae of a north-temperate chrysomelid beetle.

Developoment, growth, and survival of larvae and pupae of the red turnip beetle, Entomoscelis americana Brown, were studied in 10 constant and four alternating temperature regimes (10 to 32.5° C), in field-cages, and in natural populations in Manitoba. This beetle has a northtemperate distribution in North America. Larval and pupal development occurs in spring and normally is completed before the end of June. Growth and development occurred at all constant temperatures tested, but survival was low at the extreme temperatures. Therefore, the threshold and upper limit were near 10 and 32.5° C. The developmental times of the sexes did not differ and decreased with temperature, except possibly at 32.5° C. The average weight of adult females increased with temperature up to 32.5° C and those of males up to 25° C. Considering developmental rate, survival, adult weight, and incidence of malformed adults, the optimum temperature was estimated to be near 27.5° C.Development was accelerated significantly (6 to 9%) in alternating regimes with temperatures differing by 10° C, but not in regimes differing by 5 and 15° C. All alternating regimes increased adult weight, 5 to 17% for females and 2 to 10% for males. Field cage studies confirmed the increase in adult weight, but not the acceleration in development.A three-parameter normal function described accurately the relationship between developmental rate and constant temperature. A computer simulation model based on this equation estimated developmental times in field cages to within one to five days. For natural populations the model overestimated the developmental times by five to 16 days. The discrepancies between model estimates and observed developmental times in natural populations apparently were due to the elevation of larval and pupal body temperatures above air temperatures by behavioral thermoregulation. The elevation of body temperature was estimated to be equivalent to the addition of 5 to 6° C to the maximum daily air temperature. The adaptations and responses of this beetle to the cool spring temperatures of the north-temperate region are discussed.

Variability in migratory tendency within and among natural populations of the pea aphid, Acyrthosiphon pisum.

The migratory tendencies of pea aphids were measured by determining the numbers of winged and non-winged offspring produced by parthenogenetic wingless females after a crowding test. Sources of variability in this measure were investigated. The migratory tendency of an individual clone was found to be stable. Spatial and temporal patterns in migratory tendency were found among nine natural populations. These patterns probably reflect differences in the frequencies of a large number of genetically distinct clones. Hypotheses based on the relative fitness of immigrant and resident clones and the heritability of migratory tendency are offered to account for these results. High migration rates may be required to account for genetic differentiation within and among some parthenogenetic populations of the pea aphid.

Migratory tendency in aging populations of the pea aphid, Acyrthosiphon pisum.

Sweep samples of the aphid, Acyrthosiphon pisum, were collected from six natural populations ranging in age from one to five years. Clones were established in the laboratory from the field-collected adults and tested for their migratory tendency in two subsequent generations by measuring the percentage of winged offspring produced in response to a standard stimulus. The number of aphids in sweep samples and the percentage of winged and wingless aphids were also determined. Tests on the first laboratory generation revealed a decline in migratory tendency with the age of the source population, but no such relationship was detected in tests on the second generation. These results are consistent with an explanation based on maternal age effects and differences in adult age structure among populations of different age. They are not consistent with one based on genetic differences among populations. Older populations also had higher densities and a lower percentage of alate adults. The percentage of larvae with wing buds was positively correlated with population density, but not population age.