Effectiveness of second mating for two incompatible types of the citrus red mite,Panonychus citri (McGregor)

Summary Two types of the citrus red mite,Panonychus citri (M.) occur in some pear orchards in the intermediate latitudal areas in Japan during a certain period of the year (Takafuji andMorimoto, 1983): one is a diapausing type (DP) and the other a non-diapausing type (C). These two types are incompatible: no adult females are produced from the crosses between them (Takafuji andFujimoto, 1985). In the present study, females of each type were doubly crossed, first with a male of the other type, and then with a male of the same type, to examine the effectiveness of the second mating. In the females of the DP type, the second mating with a male of the same type was almost totally ineffective. In contrast, for the females of the C type the effectiveness of the second mating depended on the durations of the first and second matings: the famles produced female offspring only when the duration of the first copulation with a male of the DP type was brief and the second copulation with a male of the C type lasted relatively long. The results suggested that if the two types coexist, the intercrossing between them will favour the C type over the DP type.     

A model of the species rank-abundance relation for a community in an open habitat

Summary A mathematical model is proposed to describe the relationship between the abundance and the rank of species in order from the most abundant to the least in a community in an open habitat. This model is derived as a corollary of a species-area equation (Kobayashi, 1975) which could be expected in the case where the individuals of each species are uniformly distributed over a habitat area. Numerical simulation reveals that a rank-abundance curve for a universe results in different species-area or species-individual curves according to the spatial distribution of individuals, and that the relative abundance of each species in a sample varies with sample size unless the spatial distribution of individuals is uniform. A species-individual curve obtained bySanders’s (1968) rarefaction method agrees with that observed actually only for the spatially uniform distribution. Change in the pattern of rank-abundance curve with species diversity and with sample size is discussed in relation to the present model.     

Maternal age as a source of variation in the ability of an aphid to produce dispersing forms

Summary Apterous parthenogentic females of the pea aphid,Acyrthosiphon pisum (Harris), begin to produce alate offspring soon after they have been subjected to crowding. Females which were born early in their own parent's reproductive period respond most strongly to crowding, producing much larger numbers of alatae than their late-born sisters. In contrast, the early-born daughters of most alate females do not produce winged offspring after being crowded. Some of their later-born sisters may produce a few winged individuals, resembling in this respect the late-born daughters of the apterous females. Control of the production of alatae thus begins in the grandparental generation. Risk-spreading by means of differential dispersal becomes a less uncertain venture when local populations can modify their responses to environmental changes by utilizing past as well as present signals from their surroundings.     

Extraordinary effects of fertilization status on the reproduction of an arrhenotokous and sub-social spider mite (Acari: Tetranychidae)

Summary Experimental observations on the arrenotokous reproductive patterns of two spider mite species (Acari: Tetranychidae), the long-seta form ofSchizotetranychus celarius (Banks) andTetranychus urticae Koch, revealed that reproduction of unfertilized females of the former is very differnt from that of the latter. Unfertilized females ofS. celarius, which has a subsocial life, laid a few eggs and then became inactive. In contrast, the fecundity of unfertilizedT. urticae females was only slightly reduced as compared with fertilized females. Mother-son matings may thus sometimes occur in naturalS. celarius populations. A two-year field survey revealed that, in the absence of males, overwintering females ofS. celarius occasionally remain unfertilized until early spring. Furthermore, nest foundation observed in late spring indicated that most of the season's first nests were founded by single females. These two sets of observations strongly suggest that motherson mating takes places in nature, corresponding to the reproductive trait seen in the experiment. Mother-son mating inevitably increases the relatedness between nest members. The estimated father's relatedness to its offspring is extraordinarily high under such condition. The possibility that kin-selection in the long seta-form ofS. celarius led to subsociality, especially paternal care, is suggested. This study was supported in part by Grant-in-Aid No. 61540468 from the Ministry of Education, Science and Culture, Japan.     

Anopheles subpictus Grassi: Observations on survivorship and population size using mark-release-recapture and dissection methods

Summary A mark-release-recapture experiment to estimate population survivorship and absolute size was performed with wild-caughtAn. subpictus adults at the village of Khano-Harni, Lahore District, Punjab Province, Pakistan during September 1978, the end of the monsoon rainy season, when temporal population abundance was maximized. Daily survival rate estimated from the recapture sequence of marked adults was low, males=0.192 and females=0.343. Survivorship for females estimated by several vertical age-grading procedures ranged from 0.347 to 0.628. Both stage- and age-specific life tables were calculated from vertical age-grading data determined by the dilatation method. Female and male population size was estimated byBailey’s modification of theLincoln Index and was found to average 4478.4 and 6106.8, respectively. The bionomics, survivorship and population size ofAn. subpictus in the Lahore are indicated that this species was probably not important in the transmission of human malaria.     

Relationships of latitude, altitude, and body size to litter size and mean annual production of offspring inPeromyscus

Summary Litter size was positively correlated with latitude and altitude but not with production of offspring or with body size inPeromyscus. Increased litter size in northern populations probably reflects shortening the breeding season by climate and not a greater mortality rate at northern latitudes compared to southern latitudes. Production of offspring was negatively correlated with body size but not with latitude, altitude, or litter size. This is probably due to larger species living longer and taking longer to mature.     

Parental care and EGG size in salamanders: An examination of the safe harbor hypothesis

Summary The safe harbor hypothesis includes the suggestion that parental care causes the embryonic stage to be the safest harbor, and, therefore, egg size will increase in populations with parental care to decrease the duration of subsequent, higher risk stages. Neither the safe habor hypothesis nor r and K theory seem adequate to explain the correlation between egg size and the presence/absence of parental care among salamanders, a group in which there is a further correlation between the larval (hatchling) habitat and egg size/parental care. Pond-breeding salamanders generally have small eggs and lack parental care, and stream-breeding salamanders generally have large eggs and parental care. I argue that the fundamental difference in the food available to hatchling salamanders between lentic (plankton-rich) and lotic (plankton-poor) environments selects for relatively lower parental investment in the lentic environment. From the standpoint of parental fitness, small (more numerous) hatchlings have a greater payoff where the available food is mall and dense (zooplankton in lentic environments), and large hatchlings are selectively advantageous where the food is of large size and less dense (benthic invertebrates in lotic environments). Selection for larger hatchlings in lotic environments results in longer embryonic periods and,ceteris paribus, greater total embryonic mortality. Embryo hiding and guarding have evolved among lotic-breeding salamanders as compensatory mechanisms to reduce the rate of embryonic mortality. In this view, parental care is a consequence of selection for larger egg size and not an umbrella that allows egg size to increase, contrary to the safe harbor hypothesis. The relationship between variance in parental investment and food available to offspring, developed here for salamanders, may be of general significance. YosiakiIt?, a critic of r and K theory, independently arrived at a similar conclusion from a broader data base.     

A sequential estimation technique for capture-recapture censuses

A simple technique of sequential estimation was proposed for capture-recapture census by thePetersen method. In theory this technique makes it possible to secure automatically a required precision level for the population estimate to be obtained, irrespective of the population size. Some problems about its practical application were discussed.     

Anopheles culicifacies giles: Adult ecological parameters measured in rural punjab province, pakistan using capture-mark-release-recapture and dissection methods, with comparative observations onAn. stephensi liston andAn. subpictus grassi

Summary Dispersal, immigration and emigration rates, horizontal and vertical survivorship and absolute population size were estimated for micropopulations ofAn. culicifacies, An. stephensi andAn. subpictus at a series of cattle sheds in rural Punjab Province, Pakistan, during November 1979 and May 1980 using capture-mark-release-recapture and dissection methods. Dispersal was temperature-related, with populations more vagile during May. Mean dispersal distance per individual was low for all species. More than 70% of all recaptures were taken at the point of release and the longest detected flight was 1250 meters. Horizontal survivorship was greater during November and was always less than vertical survivorship calculated from dissection agegrading data. Survivorship during the nulliparous period was greater than survivorship throughout total life, indicating the survivorship curve may be slightly sigmoid. Daily population sizes of endemic and immigrating females and males were calculated usingBailey's (1952) modification of the Lincoln Index, with the daily captures adjusted for immigration which was highest in May. Daily additions to the indoor resting population exclusive of immigrants were estimated using the method ofManly andParr (1968). The relationship of the present findings to malaria transmission and genetic control were discussed.     

Inconstancy of Taylor'sb: Simulated sampling with different quadrat sizes and spatial distributions

Summary Taylor's power law,s ² =am ^b , provides a precise summary of the relationship between sample variance (s ² ) and sample mean (m) for many organisms. The coefficientb has been interpreted as an index of aggregation, with a characteristic value for a given species in a particular environment, and has been thought to be independent of the sample unit. Simulation studies were conducted that demonstrate that the value ofb may vary with the size of the sample unit in quadrat sampling, and this relationship, in turn, depends on the underlying spatial distribution of the population. For example, simulated populations with hierarchical aggregation on a large scale produced values ofb that increased with the size of the sample unit. In contrast, for a simulated population with randomly distributed clusters of individuals, the value ofb eventually decreased with increasing quadrat size, as sample counts became more uniform. A single value ofTaylor'sb, determined with a particular sample unit, provides neither a fixed index of aggregation nor a complete picture of a species' spatial distribution. Rather, it describes a consistent relationship between sample variance and sample mean over a range of densities, on a spatial scale related to the size of the sample unit. This relationship may reflect, but not uniquely define, density-dependent population and behavioral processes governing the spatial distribution of the organism. Interpretation ofTaylor'sb for a particular organism should be qualified by reference to the sample unit, and comparisons should not be made between cases in which different sample units were used. Whenever possible, a range of sample units should be used to provide information about the pattern of distribution of a population on various spatial scales.     

A sequential estimation technique for capture-recapture censuses

Summary A simple technique of sequential estimation was proposed for capture-recapture census by thePetersen method. In theory this technique makes it possible to secure automatically a required precision level for the population estimate to be obtained, irrespective of the population size. Some problems about its practical application were discussed. This study was supported by science research fund from the Ministry of Education.     

Genetic variation of density responses in relation to wing polymorphism in the oriental chinch bug,Cavelerius saccharivorus Okajima (Heteroptera: Lygaeidae)

Summary Responses to nymphal density in the determination of wing form were compared between the offspring from brachypter x brachypter crosses and those from macropter x macropter crosses of the oriental chinch bug,Cavelerius saccharivorus. In the offspring from crosses between macropters, there was a strong tendency for macropters to increase to a rather high level with increasing nymphal density in both sexes. In contrast to this, in the offspring from crosses between brachypters, the appearance rate of macropters attained a maximum value in moderately crowded conditions and conversely decreased to a lower level in more crowded conditions in both sexes. Thus density response patterns concerning the determination of wing form were quite different between the offspring from different crosses in the wing form, indicating that there is a genetic basis underlying wing polymorphism in this species. As for the body size of emerged adults, macropters tended to be larger than brachypters in the same crowded condition. Moreover, the rate of decrease of body size with nymphal density was lower in the offspring from crosses between macropters than in the offspring from crosses between brachypters. This indicated that the former offspring are more tolerant of nymphal crowding than the latter. The difference in such a tolerance against nymphal crowding between the offspring from different crosses was considered to be related to the difference in the appearance of macropters in the crowded conditions between them.     

Group predatory behavior by the assassin bugAgriosphodrus dohrniSignoret (Hemiptera: Reduviidae)

Summary Nymphs ofAgriosphodrus dohrni Signoret (Reduviidae) have a strong gregariousness and show group predatory behavior. This study was conducted to clarify adaptive significance of group predation of this species, including laboratory observations and 6-year field surveys. In the laboratory, observations on both solitary and group attacking against armyworms were made at varying prey size classes to compare the capture success rate by solitary predators with that by groups. The efficiency in capturing the prey was significantly higher in group attacking at any prey size class compared. Data obtained from the field surveys indicated the tnedency for searching nymphs to feed in group and to increase the number of predators feeding per prey item with increasing prey size. Average sizes of prey captured were also larger in group feeding throughout the nymphal stage. In particular, it was remarkable that, when prey were “creeping” types, the upper size limit of prey eaten was dramatically increased.     

Investigation into the edge effect by use of capture-recapture data in a vole population

Summary A substantial explication of the edge effect has been attempted by use of capture-recapture data for a vole population (Microtus montebelli), gathered intwo plots of 100×100 m or less during 12 days, cheked twice daily, in August 1970; the sample was quite sufficient for the aim. The edge effect as guessed by increased catch per trap is usually suspected to ensue from range-settlers in the outside boundary strip of a plot and immigrants. But by a theoretical analysis I could attain a tentative conclusion that no increased catch per trap will occur unless any invasion takes place. Then it follows that, apart from the effect of invasion, the role of the adjoining outside settlers in the edge effect is essentially required to be studied in the light of knowledge on the truth of size and shift in home range. The variation in range behavior for 183 adult voles, captured 6 times or more, could be grouped into eight types, of which the range-conservative type possessed 52% of the sample and the group of the type was justly utilized for giving averages of range size. Besides, it was seen from the observed frequency of types that a considerable number of immigrants onto the census plot were induced perhaps being allured by trap baits, but the majority of them proved to be assigned to the voles that have their ranges inside the assessment line ofDice; the rest referable to effective immigrants was only a few (7%). I could perceive no reason such as disproves the idea ofDice’s additional boundary strip. Viewed from maps of ingress shift of ranges, the effect of ingress must have been greater in the outer trap rows than in the inner within the plot, so that it might well be called edge effect in general; such effect, however, is seen gradually diminishing toward the center, and hence it is almost unlikely that one should find any clear-cut intra-plot assessment lines demarcating such an inner square as quite free from edge effects. Averages of observed range length and width (ORL and ORW), as reliable measures for the true range size, were determined from the above group of specimens; as a result, the remarkable concept of elliptic range shape was established by regarding ORL as long axis and ORW as short one, and, directly from these averages, the mean range sizes worked out at 0.04 for females and 0.09 for males in acreage which proved to be surprisingly well agreeable with those of isotope-revealed ranges for voles given byGodfrey (1954) andAmbrose (1969). The catchability for marked voles ( ) was estimated by the maximum likelihood method by use ofJolly’s formulae (1965), but that for unmarked ones ( ) was made by the regression census formula; as a result it was shown that the population was clearly of π>p type and that the trap-experience that voles underwent one month or more ago can make them retain as high catchability as π. Contribution from JIBP-PT No. 110, carried out by the grant from the expenditure of Education Department to the specific study on “Dynamics of Biosphere”.     

A note on key factor analysis

Summary Various aspects of a model for key factor analysis (Manly, 1977a) are discussed. Equations for estimating the parameters of the model are given. The jackknife method is suggested for obtaining standard errors for estimators. The case of circular populations (where the adults in one generation produce all the individuals alive at the start of the next, generation) is considered. A computer program is described. Varley et al.’s (1973) data on the winter moth is used for illustrative purposes.     

Effects of host age and host availability on developmental period, adult size, sex ratio, longevity and fecundity inLariophagus distinguendusF?rster (Hymenoptera: Pteromalidae)

Summary The effects of host age on parasitoid reproductive capacity are studied using the pteromalid parasitoidLariophagus distinguendus F?rster and its bruchid hosts,Callosobruchus chinensis (L.) andC. maculatus (F.). A series of experiments were performed to investigate relationships between age and size of host parasitized and the developmental period of pre-imaginal progeny, sex ratio, female size, longevity, fecundity and oviposition rate. There was no effect of host size on preimaginal parasitoid developmental period. Sex ratio varied from less than 5% females from young (small) hosts to 60% females from mature (large) hosts. Adult size, female longevity, fecundity, and oviposition rate were also positively related to host age. Females provided mature hosts lived longer than those provided either young hosts or no hosts, possibly because of an increased ability to host-feed from the larger hosts. The implications of these findings to parasitoid population reproductive capacity and host-parasitoid synchrony are discussed.     

A mathematical model for the survivorship curve

Summary A mathematical function describing the various kinds of survivorship curve is formulated with the useful parameter, environmental capacity. Three types of the survivorship curve illlustrated byDeevey can be obtained from changing the value of this function. When a cohort is large and the competition occurs in the scramble type, this function shows the third type ofDeevy's and this to the first type in the case of low density and the contest type of competition. But the second type would rather be obtained by the action of density independent agencies. Contribution from the Entomological Laboratory, Kyoto Univeristy. No. 400.     

Sampling techniques and the use of Tang's procedure in insect population dynamics studies

Summary Some calculations were performed usingTang's method as an aid in planning experiments for studying the population dynamics of the Jeffrey pine beetle. The population dynamics studies were aimed at detecting the importance of specific effects, e. g., tree diameter, tree height. TheTang procedure is a method of estimating the sample size required to detect effects of a given magnitude with analysis of variance tests. Using this procedure some sample calculations were performed which indicated the sample size needed, and the efficacy of different strategies of improving the results, e. g., increasing the number of trees sampled versus increasing the area of the tree sampled. The statistical parameters used in the calculations were estimated from some preliminary sampling data. Use of this procedure is recommended in insect population studies as a method of optimally planning experiments, and as a method of making precise conclusions about the significance of specific effects. This study was supported by Contracts 68-03-0273 and 68-03-2442 with the U. S. Environmental Protection Agency, Corvallis Environmental Research Laboratory, Corvallis, Oregon. This paper has been reviewed by the Corvallis Environmental Research Laboratory and approved for publication. Approval does not signify that the contents necessarily reflect the views and policies of the U. S. Environmental Protection Agency, nor does mention of trade names or commercial products constitute endorsement or recommendation for use.     

Variation in offspring size within a population of the web-building spiderAgelena limbata

Within a population of the web-building spiderAgelena limbata, the weight of the first instar nymphs ranged from 1.187 to 6.559 mg. Both intraclutch and interclutch variation were recorded. The mean weights were different among clutches and the coefficients of variation within a clutch ranged from 3.3 to 29.2%. Variation in the nymphal weight was certainly derived from variation in the egg weight because there was a high correlation between the two weights. Factors affecting interclutch variation in nymphal weight were examined by multiple regression analysis. Nymphal weight was positively correlated with the body size and food conditions of female parents, and negatively correlated with the clutch size. Among these three factors, the food conditions of female parents had the largest apparent effect on the interclutch variation. The results suggest that females with larger body size and more food produce larger offspring, and that there is a trade-off between offspring size and clutch size. Heavier nymphs had larger body size (carapace width) and may have larger energy reserves. Heavier nymphs survived experimental starvation for a significantly longer period.