Decrease in respiratory rate in a wolf spider,Pardosa astrigera (L. Koch), under starvation

Summary Effects of starvation on the suryival period and the respiratory rate in adults of a wolf spider,Pardosa astrigera (L. Koch), were investigated. The spiders used were divided into four groups: well-fed, starved and two limited food groups; in the latter two, each spider was supplied with one leafhopper every second or third day. Adult males and females ofP. astrigera could survive for a long time; 28.8±2.7 days and 54.4±18.9 days, respectively, without any food. The longevities shown here were 73.8% for males and 78.6% for females of those of well-fed spiders, indicating thatP. astrigera adults have a strong tolerance to starvation. The respiratory rate of well-fed adults showed no tendency to increase or decrease with their aging; the mean respiratory rates were 4.86×10⁻⁴ mg CO₂/mg f.w. (fresh body weight)/hr for males and 3.80×10⁻⁴ mg CO₂/mg f.w./hr for females. The respiratory rates of starved spiders increased during the first two days of starvation but decreased markedly from the third to the twelfth day, and thereafter retained an almost constant level for each sex. The mean respiratory rates after the twelfth day of starvation were 2.49×10⁻⁴ mg CO₂/mg f.w./hr for males and 2.76×10⁻⁴ mg CO₂/mg f.w./hr for females; these values were respectively 48.4% and 63.0% of those prior to starvation. The fresh body weight of starved spiders decreased linearly with time but the rate was small. The respiratory rates of the limited food groups tended to decline with time and thereby their weight losses were minimized. The decrease in the respiratory rate under starvation was considered not to be due to spider exhaustion or senescence but due to an intrinsic change in behaviour and/or metabolism, because when the spiders were supplied with ample food for five days after starvation, the respiratory rate and the body weight rapidly recovered to near the levels prior to starvation. It is suggested that starved spiders use a higher ratio of fat as catabolic substrate than normally fed or satiated ones. Feeding strategies of poikilo-therm predators are discussed. This work was partially supported by the Nippon Life Insurance Foundation Research Fund and Grant-in-Aid (No. 56480039) from the Ministry of Education, Science and Culture, Japan.     

Prey capture tactics of spiders: An analysis based on a simulation model for spider's growth

Summary The prey capture tactics of spiders was analyzed, considering the energy gained by the capture of prey and that required for it. For the purpose of it, a growth model of spiders was constructed, expressing the flow rate of prey biomass to the spider's body by differential equations. Solving these equations under the differing values of three parameters, growth curves of spiders was obtained. These three parameters are the amount of prey biomass supplied daily to spiders,x ₀, the rate of prey capture of spiders, α, and a coefficient of the respiration rate required for the capture of prey,k. When the value ofk increased, spiders could grow only at high value ofx ₀. These results suggest that habitats with small prey biomass are preferred by spiders adopting a sit-and-wait tactics for prey capture, which requires small values ofk. Wolf spiders are one of these spiders showing that tactics. On the other hand, web-builders which require large amount of energy for spinning webs (namely, take large value ofk), are able to grow only in the habitats with large prey biomass. Each species of spiders are considered to locate in a certain point between both extremes of these tactics for the capture of prey.     

Relationship between surplus energy and body weight in fish populations

Summary This paper theoretically analyses the relationship between surplus energy, which is available for either somatic growth or reproduction, and body weight. From the data of metabolism and growth of the biwamasu,Oncorhynchus rhodurus, obtained by Miura et al., a Bernoulli's differential equation is induced to represent the relationship between body weight and the sum of surplus energy and active metabolic rate. Solving this equation gives the amount of surplus energy,f(W_x), as follows:f(W_x) = (αW _x ^1−γ +β^1−γ)^1/(1−γ)−W_x, in which α, β and γ are constants andW _x is body weight at agex. The function is applied to ten fish populations and consequently it is found to be useful for a wider age range and a wider variety of fishes than the conventional function.     

Variability in food consumption rate of natural populations in the spider,Nephila clavata

Summary Mean daily food consumption and total lifetime food consumption of the spider,Nephila clavata, were estimated in natural populations. Daily food consumption in the late adult stage was 27–150 mg wet weight, which was nearly equivalent or slightly larger than that in other large web-building spiders. Considerable variation in food consumption was found among habitats or years. The largest variation among habitats in the same year was 7 and 5 fold for daily and lifetime consumption, respectively, while that among years in the same habitat was 3.5 and 2.5 for daily and lifetime consumption, respectively. Feeding conditions evaluated from the food consumption per body weight of spiders declined during the period from mid-July to mid-September in almost all the populations, which suggested that they faced to severe food limitation in this period.     

Intraspecies competition in a field population ofGregopimpla himalayensis (Hymenoptera: Ichneumonidae) parasitic onMalacosoma neustria testacea (Lepidoptera: Lasiocampidae)

Summary Intraspecies competition in a field population ofGregopimpla himalayensis (Hym.: Ichneumonidae) parasitic on the prepupae ofMalacosoma neustria testacea (Lep.: Lasiocampidae) was investigated. The parasite oviposits the sufficient number of progeny (5 individuals/0.1 g dry weight of host) to exhaust a single host in a single attack. However, at the intensity less than 22–26 individuals/0.1 g d.w. of host, all individuals can emerge, i.e. density-dependent mortality does not occur. Within this range of intensity, survival of parasite larvae is guaranteed by diminution in body size and decreasing sex ratio. In contrast, total biomass of parasites showed a peak at 5 individuals/0.1 g d.w. of host at which a single host is exhausted. Above the intensity of 22–26, extraordinary minute individuals appeared and they died before maturation. If intraspecies competition play a role in regulation ofG. himalayensis population in the field, the process is usually not through density-dependent mortality but through decreasing reproductive rate caused by decrease in the sex ratio, adult longevity and fecundity. Contribution Ser. 2, No. 275. Entomological Laboratory, Faculty of Agriculture, Kyushu University.     

Nutritional contribution to females of14C-labeled male secretions transferred during mating inMenida scotti (Heteroptera: Pentatomidae)

Menida scotti (Puton) males have been shown to transfer secretions from their bulbus ejaculatorius and reservoir of ectodermal accessory gland to females by mating during hibernation. In the present study, the major components of the secretions were found to be proteins and lipids. To specify the female organ incorporating the male secretions, a radiotracer experiment in which the male secretions were labeled by [¹⁴C]valine was conducted in nine tissues of females collected in the fall and spring of the hibernation period. Relatively high radioactivities were detected in the haemolymph and the residual carcass (head, legs, air-sacs, exoskeleton, etc.) in the fall females, and in CO₂ gas evolved and carcasses in the spring females. The radioactivities in the fat body were significantly higher in the fall mating females than in the spring mating females, and vice versa in the ovary. The radioactivities in six fractions (lipids, proteins, glycogen, sugars, free amino acids and the residues) were also assayed in the five organs of females that had a relatively high radioactivity. The highest radioactivity was detected in the protein fraction of the haemolymph in fall and spring females. There were significant differences in the radioactivities incorporated into the lipid fractions of the carcass between fall and spring females.     

Theoretical studies on the role of food exploitation for the competition of scaamble type

Summary A model was made to clarify the basic processes of competition to occur among larvae by the exploitation as defined byBakker (1969). It was found that this model is applicable to the experimental results on the food exploitation amongDroshophila larvae obtained byBakker (1961). In the model the preimaginal stage is divided into two periods;T _f which is the time that a group of larvae spends in exhausting the food after hatching, andT _s which is the duration of the starvation period afterT _f .T _f and thenW _l (larval body weight) just after the end ofT _f are decided byF _s (amount of food supplied per larva at larval hatching) andF _c (amount of food consumed per larva).T _f affects on the onset ofT _s as well asR _l (rate of decrease in the individual body weight duringT _s ).W _a (weight of emerging adults) is gotten by a subtraction ofR _l fromW _l just after the end ofT _f ,R _e is affected directly by these components ofW _l andR _l . As a result,W _a andR _e are expressed by functions ofF _s . This model confirmed that the food exploitation lead to the competition of scramble type. Finally it was suggested that there exist some strategies which prevent ill-effects owing to the food exploitation.     

The ingestion in wolf spiders I. Capacity of gut ofLycosa pseudoannulata

Summary An wolf spider,Lycosa pseudoannulata, collected from the field were reared in test tubes supplied with fruit flies as the food, and the number and weight of fruit flies killed per unit time and the weight of residuum of killed flies were recorded. When the cumulative number of flies killed by a spider was plotted against time after the beginning of food supply, the angle of the curve obtained decreased gradually until a constant value. In this time, it seems that the gut of spider had saturated with food and the increase rate of number of flies killed reflects the rate of food disappeared from gut by assimilation and egestion. The amount of ingestion was obtained by subtracting the weight of residuum and the gain of live weight of the spider from the weight of killed flies. After the gut has saturated, the amount of food remained in the gut is considered to be equal to the capacity of gut, which is an essential factor in the study of predation. The amount of food disappearance from gut was also estimated. There was a linear relationship between the log body weight of spiders and the log capacity of gut. The linear relationship was also seen between the log total amount of ingestion and the log total amount of food disappeared from gut.     

Atmospheric lifetime of carbon dioxide

The yearly carbon dioxide (CO₂) released by animal and plant respiration is in balance with photosynthetic carbon fixation. However, human activities (fuel burning) add about 10% above this equilibrium amount. The excess CO₂ of anthropogenic origin is absorbed in about equal parts by the atmosphere and the surface layer of the oceans. The deep ocean is potentially a large reservoir for CO₂ storage, but the exchange rate between ocean layers is slow (thousands of years). The present concentration of atmospheric CO₂ is 350 ppmv. During the last interglacial period it hovered near 270 ppmv. The range during the Riss and Wurm ice ages was about 180 to 240 ppmv.     

Counter-Examples about Lower- and Upper-Bounded Population Growth

ABSTRACT

For a unimodal growth function f having its maximum at a critical state x _c , the interval bounding the population size asymptotically is usually presented as being equal to [f ^○2(x _c ), f(x _c )]. This interval however does not represent the maximum range within which the population size can vary, even asymptotically. The actual invariant interval containing the population size is equal to: [min(x*, f ^○2(x _c )), f(x _c )], where x* denotes the non-zero fixed point, assumed to be unique, of the iteration of f.     

The genetic heterogeneity of deer mouse populations ( Peromyscus maniculatus ) in an insular landscape

A survey of the genetic variability in deer mouse populations was performed using specimens collected from six different islands on a lake covering approximately 50 km². Random amplified polymorphic DNA (RAPD) was used to measure the extent of the genetic differences in this insular system. An analysis of molecular variance (AMOVA) revealed that populations are clearly separated at this microgeographic scale (F _st = 0.13863; P < 0.001). The homogeneity of molecular variance test (HOMOVA) indicated that within-population levels vary greatly (B _p = 0.76831; P < 0.001). The within-population molecular variance was found to be mainly correlated with the accessibility of the islands, computed as the inverse of the geographic distance separating an island from the lakeshore (r = 0.916; P < 0.003). Received: March 5, 1999 / Accepted: July 16, 1999     

A distance measure of spatial pattern in a biological population

Summary Suppose thatn individuals locate independently and randomly on a segment of line of finite length (habitat). Let the theoretical and observed ranges of the sites of the individuals on the segment be μ _n-1 andr _n-1, respectively. Then, the degree of dispersion of the individual sites is measured by the ratio, T _n =n _n-1/μ _n-1, as follows: A random spatial pattern forI _r−1 =1 An aggregated spatial pattern for 0≤I _r <1 A uniform spatial pattern for (n+1)/(n−1)≥I _r >1. Another method was derived. Let the probability that an observed range is less thanr _n−1 beI _p , under the hypothesis of a Beta distribution. Then indicates A random spatial pattern forI _p =1/2 An aggregated spatial pattern forI _p <1/2 A uniform spatial pattern forI _p >1/2. The first index can be used for comparing populations having the same number of individuals, whereas the second one can be used for comparing populations with different numbers of individuals.     

A probabilistic interpretation of the United Nations’ 1995–2005 population projections

I develop probabilistic interpretations for the United Nations’ 10-year population forecasts by comparing 1995 projections for 212 countries to the population sizes reported for 2005. Errors in the estimation of the intrinsic rate of increase, presumably caused by erroneous assumptions about birth, death and/or immigration rates, appear to be more consequential than errors based on inaccurate estimation of the starting, or ‘jump-off’, population size. For only about 20% of the countries did the ‘actual’ 2005 population size fall between the United Nations’ low- and high-variant projections. I propose prediction intervals for country-specific population sizes 10 years in the future of the form [ N_i^￠ (t+10) / k ,  k ·N_i^￠ (t+10) ],[ N_i^{\prime} (t+10) / k , \, k \cdot N_i^{\prime} (t+10) ], where N _i ′(t + 10) is the medium-variant prediction for year t + 10 made in year t, and k is a number that varies with starting population size. Based on the 1995–2005 United Nations’ data, values of k giving 95% coverage range from 1.11 for countries with a population on the order of 10⁹, to 1.45 for countries with a population of 10⁵.     

The spatial distribution pattern of the brown planthopperNilaparvata lugens St?l (Homoptera: Delphacidae) in west Java, Indonesia

Summary Spatial distribution pattern of the brown planthopper (BPH) was analyzed at 9 experimental fields in the northern part of West Java during two consecutive rice cropping seasons, i.e., wet and dry seasons. The population of each developmental stage and wing form of BPH at each location showed consistent departure from the random (Poisson) distribution, the variances of the densities in most cases exceeding their means. Namely, the distribution pattern of BPH per hill of rice plant was found to have a general tendency to be aggregated or contagious and to fit fairly well to the negative binomial model. The tendency for aggregation was further confirmed by both the β-values of -m regression being larger than unity and theC _A -values being larger than zero for each developmental stage. Although significant variations in the distribution pattern as measured by β- orC _A -value were observed between different developmental stages, between wing forms and among locations, the degree of aggregation for a given developmental stage at each experimental field remained fairly stable throughout the crop period, despite wide temporal changes in population density. Possible factors to explain these characteristics of the spatial distribution pattern of the BPH in West Java were discussed with reference to the process generating it.     

Relationship between female body size and demographic parameters inBactrocera Malaysian A (Diptera: Tephritidae)

Summary The effect of body size, as measured by the head width, of the femaleBactrocera sp. Malaysian A (kept separately in sexual pairs) on the demographic parameters was investigated in the laboratory under ambient conditions of 28–30°C, 78–85% RH and natural photoperiod. Body size was shown to influence significantly all the demographic parameters. The expectation of life of females at eclosion from pupae was respectively for head widths of 1.6, 1.8, 1.9, 2.0 and 2.1 mm: 76.2, 73.4, 73.8, 102.4 and 115.2 days. The mean number of eggs laid per female in its life time was respectively: 86.4±48.7, 181.8±56.1, 229.7±72.6, 364.3±69.4 and 477.5±109.3 which was significantly different from one another (F=3.73,P<0.05) especially the two smaller sizes from the two larger sizes. The regression line for total eggs laid (Y) against head width (X) wasY=785.2X−1208.7 (R ²=0.35,P<0.001). The net reproductive rate (R ₀) was respectively 15.8, 34.0, 43.5, 66.9 and 88.8 eggs, while the intrinsic rate of increase (r) was respectivley 0.0435, 0.0538, 0.0670, 0.0665 and 0.0711. The results confirm that for mass rearing purposes, larger females which produce more offspring are to be preferred.     

Active female courtship behavior and male nutritional contribution to female fecundity in Bruchidius dorsalis (Fahraeus) (Coleoptera: Bruchidae)

Mating behavior and the male's contribution to female fecundity were studied in the bean weevil Bruchidius dorsalis (Fahraeus) (Coleoptera: Bruchidae) in comparison with two other species, Callosobruchus chinensis (which infests stored beans) and Kytorhinus sharpianus (which feeds on wild legumes). Only females of B. dorsalis showed multiple mating and characteristic precopulatory behavior that appeared to solicit the male's nutritious secretion. In contrast, all females of the other two species did not copulate multiply and did not show such precopulatory behavior. In B. dorsalis, the decrement of male body weight just after copulation indicated that seminal fluid weighing as much as approximately 7% of the male's body weight was transferred to the female. Fecundity was more than eight times higher in females that had copulated ten times than in females that had copulated only once, indicating that males paid most of the nutritional cost of egg production. These facts suggest that the sex role is reversed in B. dorsalis. Received: May 22, 1998 / Accepted: July 19, 1999     

Effects of grouping and fighting on the reproductive tracts of male white-footed mice (Peromyscus leucopus)

Adult, male white-footed mice (Peromyscus leucopus) were subjected to a variety of social situations ranging from isolation during the 20 day experimental period to constant contact with both females and other adult males. Contacts included grouping (three or four males per cage) and exposure to fighters (once daily for 20 minutes). The following measurements were recorded: weights of the body, testes, epididymides, vesicular glands, vesicular gland tissue (wet and dry), seminal fluid of the vesicular gland, adrenal glands, and baculum; spermatozoan reserves of the testes and epididymides. Grouping significantly affected both the weight and spermatozoan reserves of the testes and epididymides, as well as both the tissue and seminal fluid weight of the vesicular glands. The results suggested a graded effect of all treatments on the reproductive tract. In order of magnitude of the associated response, from none to greatest, the treatments may be ranked as follows: pairing with females, isolating, handling, fighting, and grouping. All reproductive parameters measured showed this general ranking, suggesting that the response to the various treatments was similar and differed only quantitatively. The results further suggested decreased secretion of LH and testosterone, although measurements of testosterone did not substantiate this conclusion. The lack of significant effects of grouping on adrenal gland weights strengthened the argument that adrenal involvement is not a necessary adjunct to the suppression of the reproductive tract in groupedPeromyscus, but the adrenal may be involved if contacts between males result in overt fighting.     

Body Image and Quality of Life in a Group of African American Women

African American (AA) women’s preference for a larger body size and underestimation of their body weight may affect the relationship between their body weight and weight-related quality of life (QOL). We wanted to examine the relationship between weight-related QOL and body mass index (BMI) in a sample of overweight AA women. Thirty-three overweight AA women completed a clinic visit to measure height, weight, and complete surveys including the Impact of Weight on Quality of Life-Lite (IWQOL-Lite) and the Stunkard Figure Rating Scale. BMI was calculated using measured height and weight. Correlations and linear regression models were estimated using SAS v 9.1. In this sample, the mean total quality of life score was 78.00 ± 17.68 on a 100 point scale. There was a modest correlation between BMI and total weight-related QOL (r = −0.034, p = 0.053). Body image dissatisfaction was the strongest predictor of total quality of life score (p = 0.04). African American women’s unique cultural perception of body image may play a key role in weight-related QOL.     

The Leverage of Demographic Dynamics on Carbon Dioxide Emissions: Does Age Structure Matter?

This article provides a methodological contribution to the study of the effect of changes in population age structure on carbon dioxide (CO₂) emissions. First, I propose a generalization of the IPAT equation to a multisector economy with an age-structured population and discuss the insights that can be obtained in the context of stable population theory. Second, I suggest a statistical model of household consumption as a function of household size and age structure to quantitatively evaluate the extent of economies of scale in consumption of energy-intensive goods, and to estimate age-specific profiles of consumption of energy-intensive goods and of CO₂ emissions. Third, I offer an illustration of the methodologies using data for the United States. The analysis shows that per-capita CO₂ emissions increase with age until the individual is in his or her 60s, and then emissions tend to decrease. Holding everything else constant, the expected change in U.S. population age distribution during the next four decades is likely to have a small, but noticeable, positive impact on CO₂ emissions.     

Population fluctuation and persistence of one-host–two-parasitoid systems depending on resource distribution: from parasitizing behavior to population dynamics

Population dynamics and variability were examined in one-host–two-parasitoid experimental systems with different resource distributions: resource-clumped and resource-sparse conditions. The system consists of a seed beetle host, Callosobruchus chinensis, and two parasitoid wasps, Anisopteromalus calandrae (Pteromalidae) and Heterospilus prosopidis (Braconidae). In the resource-clumped condition, suitable hosts for parasitism (the late fourth-instar larvae and pupae) were clumped in 1 large resource patch, but they were scattered evenly among 16 small patches in the resource-sparse condition. Population censuses were conducted at 10-day intervals in long-term cultures, renewing 10 g of azuki beans (Vigna angularis). In both resource conditions, the first period was a single-species system of C. chinensis only, and A. calandrae was added in the second period. The one-host–one-parasitoid system with C. chinensis and A. calandrae showed stable population dynamics with small fluctuations. After addition of H. prosopidis in the third period, two of three replicates persisted to day 800 in each resource condition, although one replicate in each went to extinction at an immediate outbreak of the H. prosopidis population after the introduction. Population variabilities of C. chinensis and H. prosopidis were significantly higher and the mean population size of A. calandrae was significantly smaller in the resource-sparse condition than that in the resource-clumped one. A short-term experiment on parasitism efficiencies revealed that H. prosopidis parasitized significantly more at a low host density in the resource-sparse condition than in the resource-clumped one. Mutual interference of H. prosopidis was weak enough at low parasitoid densities but became abruptly stronger with high densities. Providing fresh hosts in a mixture of already parasitized ones, host-searching behaviors of a parasitoid were recorded by video for 3 h and were compared between the two wasp species. H. prosopidis could parasitize fresh hosts more efficiently than A. calandrae through frequent long-distance walks (walking to distant beans at one bout or outside a clump of beans with hosts and back soon on a distant bean of the clump) after reencounters with parasitized hosts. Considering all the experimental results, populations were judged to be more fragile and more likely to go to extinction in the resource-sparse condition than in the resource-clumped one. A higher attacking efficiency of H. prosopidis destabilized population dynamics more in the resource-sparse condition. Received: December 23, 1998 / Accepted: January 20, 1999