ON THE DEFINITIONS AND FUNCTIONS OF DOMINANCE AND TERRITORIALITY

1. Dominance/subordinance is a relationship between two individuals in which one defers to the other in contest situations. Each such relationship represents an adaptive compromise for each individual in which the benefits and costs of giving in or not giving in are compared. Familiar associates in groups or neighbours on nearby territories may develop relatively stable dominant-subordinate relationships based on individual recognition. Although the aggressive aspects of dominance are usually emphasized, the less conspicuous actions of the subordinate individual are actually more important in maintaining a stable relationship. 2. In evolutionary terms, dominance essentially equals priority of access to resources in short supply. Usually the subordinate, who would probably lose in combat anyway, is better off to bide its time until better able to compete at another time or another place. Both individuals save time, energy, and the risk of injury by recognizing and abiding by an established dominant-subordinate relationship. 3. Dominance can be either absolute or predictably reversible in different locations or at different times. Of the various forms of dominance behaviour, rank hierarchies and territoriality represent the two extremes of absolute and relative dominance, respectively. A dominance hierarchy is the sum total of the adaptive compromises made between individuals in an aggregation or organized group. Many animals seem to be capable of both absolute and relative dominance, and within species-specific limits the balance may shift toward one or the other. High density, or a decrease in available resources, favours a shift from relative to absolute dominance. Some species may exhibit both simultaneously. Social mammals may have intra-group hierarchies and reciprocal territoriality between groups, while the males of lek species may exhibit ‘polarized territoriality’ by defending small individual territories, with the most dominant males holding the central territories where most of the mating takes place. 4. Territoriality is a form of space-related dominance. Most biologists agree that its most important function is to provide the territory holder with an assured supply of critical resources. Territoriality is selected for only when the individual's genetic fitness is increased because its increased access to resources outweighs the time, energy, and injury costs of territorial behaviour. 5. Territoriality was first defined narrowly as an area from which conspecifics are excluded by overt defence or advertisement. The definition has been variously expanded to include all more or less exclusive areas without regard to possible defence, and finally to include all areas in which the owner is dominant. I define territory as a fixed portion of an individual's or group's range in which it has priority of access to one or more critical resources over others who have priority elsewhere or at another time. This priority of access must be achieved through social interaction. 6. My definition excludes dominance over individual space and moving resources, and includes areas of exclusive use maintained by mutual avoidance. It differs from most other definitions in its explicit recognition of time as a territorial parameter and its rejection of exclusivity and overt defence as necessary components of territorial behaviour. There is an indivisible continuum of degrees of trespass onto territories, and functionally it is priority of access to resources that is important rather than exclusive occupancy. 7. There is a similarly indivisible continuum in the intensity of behaviour needed to achieve priority of access to resources. Deciding whether or not an exclusive area is defended leads to the pointless exercise of trying to decide which cues indicating the owner's presence are conspicuous enough to merit being called defence. Concentrating on overt defence emphasizes the aggressive aspects of territorial behaviour rather than the equally or more important submissive aspects such as passive avoidance.     

THE INFLUENCE OF MATING SYSTEM AND OVERLAPPING GENERATIONS ON EFFECTIVE POPULATION SIZE

The effective population size (N_e) depends strongly on mating system and generation time. These two factors interact such that, under many circumstances, N_e is close to N/2, where N is the number of adults. This is shown to be the case for both simple and highly polygynous mating systems. The random union of gametes (RUG) and monogamy are two simple systems previously used in estimating N_e, and here a third, lottery polygyny, is added. Lottery polygyny, in which all males compete equally for females, results in a lower N_e than either RUG or monogamy! Given nonoverlapping generations the reduction is 33% for autosomal loci and 25% for sex-linked loci. The highly polygynous mating systems, harem polygyny and dominance polygyny, can give very low values of N_e/N when the generation time (T) is short. However, as T is lengthened, N_e approaches N/2. The influence of a biased sex ratio depends on the mating system and, in general, is not symmetrical. Biases can occur because of sex differences in either survival or recruitment of adults, and the potential for a sex-ratio bias to change N_e is much reduced given a survival bias. The number of juveniles present also has some influence: as the maturation time is lengthened, N_e increases.     

GENETIC LOAD AND THE MATING SYSTEM IN HOMOSPOROUS FERNS

The mutational genetic load was calculated assuming mutation-selection-inbreeding equilibrium and applied to homosporous ferns. Diploid species with past inbreeding should have a low genetic load while outcrossers should have a high genetic load. These predictions are consistent with the bimodal pattern of genetic load found in 18 diploid homosporous fern species. The prediction that tetraploids should have a low genetic load is also consistent with estimates of genetic load in several species.     

SONG MIMICRY AND SPECIES STATUS OF THE GREEN WIDOWFINCH VIDUA CODRINGTONI

Summary

Payne, R. B., Payne, L. L. &; Nhlane, M. E. D. 1992. Song mimicry and species status of the Green Widowfinch Vidua codringtoni. Ostrich 63:86-97.

The Green Widowfinch Vidua codringtoni mimics the songs of the Redthroated Twinspot Hypargos niveoguttatus, its apparent foster species, in Zimbabwe, Zambia and Mala?i. Of 38 male Green Widowfinches, 37 mimicked the twinspot; one mimicked a firefinch and not the twinspot. A wild-captured juvenile developed mimicry of twinspot song after six months and retained its mimicry through the next year. Male Green Widowfinches have glossy breeding plumage (green to blue), black wings, white bill and bright orange feet, a colour combination unlike other widowfinches in their range in southern Africa. Females are marginally distinguishable from other widowfinch species. Green Widowfinches occur together locally with Black V. funerea nigerrima, Purple V. purpurascens and Steelblue V. chalybeata Widowfinches and do not interbreed with them. The four species of widowfinches in southern Africa each have distributional ranges within the limits of their foster species.     

MATING SYSTEM AND GENETIC STRUCTURE OF THE DISTYLOUS TROPICAL TREE PSYCHOTRIA FAXLUCENS (RUBIACEAE)

The population genetics and mating system of the understory tropical rain forest tree Psychotria faxlucens were studied at two plots in Los Tuxtlas, Veracruz, México, on the Gulf of México coast. This species is distylous and is pollinated by moths, mainly small hawkmoths. The seeds are dispersed by gravity and by frugivorous birds. Controlled pollinations indicate that the trees are self-incompatible and that intramorph pollinations have lower compatibilities than intermorph pollinations. The pollen: ovule ratio is high, suggesting obligate xenogamy. Using electrophoretic allozyme methods we found that eight out of 20 loci were polymorphic (P = 0.400), the observed heterozygosity (H) was 0.198, and the mean expected heterozygosity (H) was 0.495, both relatively high values compared with that reported for tropical trees. The genetic differentiation between the two plots is low, as shown by the heterogeneity in allele frequencies and the F_st (mean F_st seedlings = 0.031, mean F_st adults = 0.026), although for some loci the plot differentiation is statistically significant. The studied populations are near Hardy-Weinberg proportions, both for seedlings (mean F = 0.128) and adults (mean F = 0.075). From the fixation rate, an indirect estimate of the outcrossing rate at equilibrium gave a mean of t = 0.898 for plot 1 and 0.685 for plot 2. Direct single loci and multiloci outcrossing rate estimates were generally not statistically different from 1.0.     

THE COMPARATIVE AND DEVELOPMENTAL MORPHOLOGY OF THE ROOT SYSTEM OF SELAGINELLA SELAGINOIDES (L.) LINK

All of the roots of Selaginella selaginoides are attached laterally to the base of the shoot, which has monopolar growth as is characteristic of Selaginella. The first three roots are produced by meristematic activity in the cortex of the hypocotyl as in several other species of Selaginella. The fourth root is produced in the same way as the first three, except that not all of the cortical cells which become meristematic mature into root tissue. Some of the meristematic tissue remains undifferentiated and continues to produce additional roots. Potentially an unlimited number of roots could be produced, but no plant was found to have more than eight. There is some secondary growth in the cortex of the basal swelling on the hypocotyl, but no secondary vascular tissue is produced and no cambium of any sort is ever organized. On the basis of comparisons with other living species of Selaginella. the centralized root system of S. selaginoides is interpreted as having been modified from a noncentralized type of root system by the persistence of the juvenile mode of root production.     

POLLEN MORPHOLOGY AND THE RELATIONSHIPS OF CIRCAEASTER,OF KINGDONIA,AND OF SARGENTODOXA TO THE RANUNCULALES

The pollen of three monotypic genera, Circaeaster, Kingdonia, and Sargentodoxa has been examined by light and scanning electron microscopy and in the case of the last genus, also by transmission electron microscopy. The type of tectum found in Circaeaster and Kingdonia, derivations of a compound layer of striae, has a restricted distribution in the Order Ranunculales. Of 64 genera examined in this order only six had species with a similar tectum. They include Achlys, Epimedium, Jeffersonia, and Vancouveria of the Berberidaceae s.l., the controversial Hydrastis, and Trollius of the Ranunculaceae. Circaeaster and Kingdonia have been considered as related since both have rare and primitive vegetative characteristics, the most notable being open dichotomous leaf venation. They are probably best treated as a ditypic family, Circaeasteraceae. The pollen of Sargentodoxa, especially the structure of the exine, closely resembles that of the Lardizabalaceae. However, the fruits of Sargentodoxa have been considered to be distinct from those of the Lardizabalaceae, suggesting that it be treated as a separate, but closely allied, family.     

THE MORPHOLOGY AND RELATIONSHIPS OF RHODEA,TELANGIUM, TELANGIOPSIS,AND HETERANGIUM

This study deals with four form or organ genera from the Upper Mississippian (Chester Series) of the Illinois Basin, and provides evidence that they were produced by a single natural genus with gymnospermous affinity. The plant remains—compressions, impressions, petrifactions, and specimens that combine compression or impression with petrifaction—allow examination of both external morphology and internal anatomy. The specimens include foliage corresponding to Rhodea, stems and petioles corresponding to Heterangium, and synangiate fructifications corresponding to either Telangium or Telangiopsis. The stems and foliage are considered parts of the same plant because of the identity of the anatomical and cuticular features of petioles attached to stem and those petioles with attached foliage. The fertile material is regarded as part of the same plant because: (1) The anatomy of axes of the fertile specimens is like that of the sterile specimens. (2) A single specimen may contain both sterile Rhodea-type axes and fertile regions. (3) Axes bearing synangia have the same size and patterns of divisions as the sterile foliage. Features that indicate lyginopterid affinities include: (1) Equal forking of the petiole. (2) Presence of fiber bands in the outer cortex and sclerotic nests in the inner part of the cortex. (3) Crowded circular bordered pits on the lateral walls of the metaxylem tracheids. (4) The presence of a small amount of secondary xylem. A variety of structural details of the stem and petiole suggest the genus Heterangium. The phyletic position of the plant that produced Rhodea, Telangium, Telangiopsis, and Heterangium is reviewed in light of such discoveries as the presence of a planated frond that lacks a lamina and the presence of both monolete and trilete microspores in a single synangium.     

植物交酸系统的进化、资源分配对策与遗传多样性

影响植物自交率进化的选择力量主要体现在两个方面：当外来花粉量不足时,自交可以提高植物的结实率,即雌性适合度（繁殖保障）;而如果进行自交的花粉比异交花粉更易获得使胚珠受精的机会,那么自交也可以提高植物的雄性适合度（自动选择优势）。但是,鉴别什么时候是繁殖保障、什么时候是自动选择优势导致了自交的进化却是极其困难的。花粉贴现降低了自交植物通过异交花粉途径获得的适合度,即减弱了自动选择优势,而近交衰退既减少了自动选择优势也减少了繁残给自交者带来的利益。具有不同交配系统的植物种群将具有不同的资源分配对策。理论研究已经说明,自交率增加将减少植物对雄性功能的资源分配比例,但将使繁殖分配加大,而且在一定条件下交配系统在改变甚至可以导致植物生活史发生剧烈变化,即从多年生变为一年生。文献中支持自交减少植物雄性投入的证据有很多,但是对繁殖分配与自交率的关系目前还没有系统的研究,资源分配理论可以解释植物繁育系统的多样性,尤其是能够3说明为什么大多数植物都是雌雄同体的,自交对植物种群遗传结构的影响是减少种群内的遗传变异,增加种群间的遗传分化,长期以来人们一直猜测,自交者可能会丢掉一些长期进化的潜能,目前这个假说得到了一些支持。