The biology of the mud-wasp Zeta abdominale (Drury) (Hymenoptera: Eumenidae)

The adult female nesting behaviour and biology of the neotropical mud-wasp Zeta abdominale (Drury) was studied in Jamaica. The cell-building behaviour was generally similar to that of Eumenes, but Zeta closed the apical funnel of the cell by moistening and re-moulding it into a plug. Each nest was built by a solitary female, who often built several small, mostly one-celled nests. Females efficiently used mud in cell-building, and small nests were advantageous, in needing less mud per cell and incurring a lower rate of predation than larger nests. Cellwall construction and provisioning were each completed in < 3 h, but a long pause between these activities, probably for feeding, delayed cell completion to 2.33 ± 1.0 days.
The number of active nesting females during a 10-h cycle was influenced by the time of day and weather. A relatively dense population had about 6.4 females ha^-1, whose age distribution, longevity and fecundity were estimated.     

The effect of size and sex ratio experiences on reproductive competition in Nicrophorus vespilloides burying beetles in the wild

Male parents face a choice: should they invest more in caring for offspring or in attempting to mate with other females? The most profitable course depends on the intensity of competition for mates, which is likely to vary with the population sex ratio. However, the balance of pay‐offs may vary among individual males depending on their competitive prowess or attractiveness. We tested the prediction that sex ratio and size of the resource holding male provide cues regarding the level of mating competition prior to breeding and therefore influence the duration of a male's biparental caring in association with a female. Male burying beetles, Nicrophorus vespilloides were reared, post‐eclosion, in groups that differed in sex ratio. Experimental males were subsequently translocated to the wild, provided with a breeding resource (carcass) and filmed. We found no evidence that sex ratio cues prior to breeding affected future parental care behaviour but males that experienced male‐biased sex ratios took longer to attract wild mating partners. Smaller males attracted a higher proportion of females than did larger males, securing significantly more monogamous breeding associations as a result. Smaller males thus avoided competitive male–male encounters more often than larger males. This has potential benefits for their female partners who avoid both intrasexual competition and direct costs of higher mating frequency associated with competing males.     

Open-cell parasitism shapes maternal investment patterns in the Red Mason bee Osmia rufa

Brood cell parasitism inflicts high fitness costs on solitary,nest-constructing bees. Many of these parasites enter open cellsduring its provisioning, when the mother bee is absent. Therefore,females can reduce the risk of open-cell parasitism by limitingthe time they are away from the nest. However, provisioningefficiency (provisioning time per unit of progeny body mass)decreases due to aging. To limit the increasing risk of open-cellparasitism as the nesting season progresses, female bees couldoptimize their maternal investment strategy by shifting thesex ratio and the body size of offspring during the nestingseason. This prediction was tested in the Red Mason bee Osmiarufa (O. bicornis), a stem- or hole-nesting, polylectic, univoltinemegachilid bee. In O. rufa, the risk of open-cell parasitismwas found to be correlated with cell provisioning time. Additionally,the provisioning efficiency of females declined during the nestingseason to one-fourth of the initial value. However, cell-provisioningtime did not increase correspondingly. Bees dealt with theirdecreasing provisioning efficiency by reducing the amount ofstored larval food, leading to a reduction of offspring sizeand a seasonal shift toward males in the offspring sex ratio.The influence of provisioning efficiency and risk of open-cellparasitism on optimal offspring size was analyzed by means ofa statistical model. The observed maternal investment patternof Red Mason bees is an adaptive strategy to reduce open-cellparasitism.     

The relationship of provision weight to adult weight and sex ratio in the solitary bee, Ceratina calcarata

ABSTRACT.

• 1 The female of the solitary bee Ceratina calcarata (Robertson) (Hymenoptera: Anthophoridae) excavates a tunnel in a pithy twig and then constructs and provisions a linear series of brood cells that make up her nest.
• 2 Adult females are, on the average, 1.3 times heavier than the males, a significant difference (P<0.001). There is no difference between the sexes in the amount of weight gained per unit of larval food.
• 3 Larger females occur because their provision masses are, on the average, 1.3 times heavier than male-producing provision masses, a significant difference (P<0.001).
• 4 Because mothers invest more time and energy in their daughters, Fisher's theory predicts that they should produce more sons. When available resources are fewer in a given year as reflected in lighter provision masses, more males are produced during the year.
• 5 The observed sex ratio did not differ significantly from the expected, calculated as mean female weight/mean male weight and was male-biased.
• 6 Unlike species which nest in pre-formed tunnels, the sex of any brood cell except the innermost is random with respect to that cell's position in the nest and the tunnel's depth and diameter. The innermost position contained offspring with a female biased sex ratio (P<0.005).

     

Description of the larvae of Dicronocephalus wallichi bourgoini Coleoptera: Scarabaeidae: Cetoniinae) with observations on nesting behavior and life cycle of two Dicronocephalus species under laboratory conditions

Larva of the fruit beetle Dicronocephalus wallichi bourgoini Pouillaude 1914 is described and illustrated. The following unique morphological characters within Cetoniinae are discussed: shape of claw, spindle-shaped last antennomera, general body shape. The presence of metathoracic egg-bursters in the first instar larva has been found. Its significance for distinguishing the first instar larvae of Cetoniinae is discussed. The nesting behaviours of D. wallichi bourgoini and D. adamsi(Pascoe 1863) are described. The course of the life cycle of both species under laboratory condition is presented and discussed.     

Sex-Biased Parental Investment in Primates

Parental investment enhances an offspring's chances of survival concomitant with reducing the parent's ability to invest in other offspring. Three main models might explain the conditions under which parental investment is expected to be sex-biased, but accurately testing the models is difficult. At least 7 fundamental issues remain unresolved in the area of parental investment in primates. The central dilemma is trying to gauge how the process improves the survival and reproductive prospects of current progeny at the expense of the survival or fertility of the parent. No single model is likely to be applicable to all primates. Parental investment probably operates in a condition-dependent framework designed to maximize lifetime reproductive success, but whether sex-biased investment occurs in an adaptive fashion remains unresolved.     

Sex ratio and maternal investment in the multivoltine large carpenter bee Xylocopa sulcatipes (Apoideh: Anthophoridae)

Abstract. 1. Females of the multivoltine carpenter bee Xylocopa sulcutipes (Maa) (Hymenoptera: Anthophoridae) usually excavate a straight tunnel in dead twigs and mass provision a linear array of up to ten brood cells with pollen and nectar. An egg is deposited upon each food mass within one cell.
2. Female offspring generally receive a higher provisioning mass (0.180 ± 0.048 g) than males, a significant difference ( P > 0.001). There are, however, male larvae that receive as much food or more as their sisters or female larvae reared in another nest.
3. There is a close positive association between the size of a mother and the weight of provisions for individual daughters, but not for sons.
4. Female offspring are positioned in the innermost brood cells (Gositions 1, 2 and 3). The sex ratio of the outer cells is either significantly male biased (positions 4–6) or skewed towards males (positions 8 and 9). Positions 7 and 10 are in equilibrium.
5. Solitary females produce a significantly female biased sex ratio ( P < 0.01). Sex ratio in social nests is skewed toward females, but not significantly so ( P < 0.2). There is no significant difference between the sex ratio of solitary and social nests ( P = 0.361). The population sex ratio (pooled sex ratio of all broods produced) is significantly female biased ( P = 0.003).
6. Females kept in the laboratory produced female biased sex ratios whilst unmated females produced all-male broods indicating that insemination and ovarian development are not causally related.
7. The expected sex ratio (ESR) under equal investment, calculated as 1/CR (CR = mean male provision weight/mean female provision weight), is 137.5:117.5 (males:females), and differs significantly from that observed, 104:151 (males:females) ( P < 0.001). The 'Local Resource Enhlancement' hypothesis best explains the female biased sex ratio found in X.sulcatipes and its maintenance in the population.     

Predicting the direction of sexual selection

Our current understanding of the operation of sexual selection is predicated on a sex difference in parental investment, which favours one sex becoming limiting and choosy over mates, the other competitive and nonchoosy. This difference is reflected in the operational sex ratio (OSR), the ratio of sexually receptive males to females, considered to be of fundamental importance in predicting the direction of sexual selection. Difficulties in measuring OSR directly have led to the use of the potential reproductive rates (PRR) as a measure of the level of investment in offspring of males and females. Several recent studies have emphasized that other factors, such as variation in mate quality and sex differences in mortality patterns, also influence the direction of sexual selection. However, as yet there has been no attempt to form a comprehensive theory of sex roles. Here we show that neither OSR nor PRR is the most fundamentally important determinant of sex roles, and that they are not interchangeable. Instead, the cost of a single breeding attempt has a strong direct effect on competition and choosiness as well as consistent relationships to both OSR and PRR. Our life history based approach to mate choice also yields simple, testable predictions on lack of choice in either sex and on mutual mate choice.     

The evolution of sex roles in mate searching

Searching for mates is a critical stage in the life cycle of most internally, and many externally, fertilizing species. Males usually invest more in this costly activity than females, but the reasons for this are poorly understood. Previous models have shown that female‐biased parental investment, including anisogamy, does not by itself select for male‐biased mate searching, so it requires additional explanations. Here, we correct and expand upon earlier models, and present two novel hypotheses that might explain the evolution of male‐biased mate searching. The “carry‐over hypothesis” states that females benefit less from searching if the associated costs affect other stages of the life cycle, rather than arising only while searching. It is relevant to the evolution of morphological traits that improve searching efficiency but are also expressed in other contexts. The “mating window hypothesis” states that females benefit less from searching if their life cycle includes intervals during which the exact timing of mating does not matter for the appropriate timing of reproduction (e.g., due to sperm storage or delayed embryo implantation). Such intervals are more likely to exist for females given the general pattern of greater female parental investment. Our models shed new light on classic arguments about sex role evolution.     

Sex allocation within broods: the intrabrood sharing-out hypothesis

Selection is expected to cause parents to adjust the sex oftheir offspring when the environment is predictable during development,and it is expected to affect each sex differently. When severaloffspring compete for limited resources, the environmental conditionsacting on the brood are not a good predictor of the conditionsaffecting individual offspring. There is evidence for some speciesthat, regardless of any bias in brood sex ratio, the sex ofindividual offspring within a brood may be related to its positionin the hatching/birth/weight rank, in ways that might correlatewith the expected share of available resources. Here I proposethat parents may be selected to adjust offspring sex withinthe brood, provided that some depreciable environmental qualityis unequally distributed among siblings in a predictable manner.I call this the "intrabrood sharing-out" hypothesis and presenta graphical model to derive predictions about the relationshipbetween offspring sex and positions within the brood. The modelconsiders that sibling competition not only produces differencesin the mean share of resources among siblings, but it also increasesthe predictability of the share obtained by high-ranking sibsand decreases the predictability of the share for low-rankingones. Consequently, parents should be selected to deal withsuch a distribution by promoting the conditions to make it morepredictable and then adaptively adjust the sex of particularsiblings, especially in high-ranking positions within the brood,rather than to modify the sex ratio of the brood as a whole.     

Sex ratios and sexual selection in socially monogamous zebra finches

An experiment was performed in which adult sex ratios of zebrafinches, Taeniopygyia guttata castanotis, were varied to testpossible effects of adult population sex ratios on sexual selectionintensity and mating system dynamics in species with biparentalcare. The possibility that sex ratio influences the successof social mating patterns (leading to polygyny when males arerare and polyandry when females are rare) was not supported.Results did support the prediction of the differential allocationhypothesis that individuals of the abundant sex would increasetheir relative parental expenditure (PE). Although total (male+ female) PE did not vary between treatments, relative malePE was significantly higher in the male-biased treatment (MBT;sex ratio 64% male) than in the female-biased treatment (FBT; sexratio 36% male). In both treatments, male PE contributions contributedto female reproductive rate. Results also supported the predictionof the differential access hypothesis that individuals of theabundant sex would experience greater intensity of selectionon sexually selected attributes. Male beak color, a sexuallyselected trait, influenced male social parentage in the MBTbut not in the FBT. Finally, broods in the FBT displayed higher hatchingasynchrony and lower hatching success; we believe this was causedby early onset of incubation, a tactic used as a defense againstintraspecific brood parasitism, which was much higher in theFBT. Population sex ratios may be an important factor affectingfemale ability to influence male parental investment patterns.     

Sex differences in parental care: Gametic investment,sexual selection,and social environment

Male and female parents often provide different type and amount of care to their offspring. Three major drivers have been proposed to explain parental sex roles: (1) differential gametic investment by males and females that precipitates into sex difference in care, (2) different intensity of sexual selection acting on males and females, and (3) biased social environment that facilitates the more common sex to provide more care. Here, we provide the most comprehensive assessment of these hypotheses using detailed parental care data from 792 bird species covering 126 families. We found no evidence for the gametic investment hypothesis: neither gamete sizes nor gamete production by males relative to females was related to sex difference in parental care. However, sexual selection correlated with parental sex roles, because the male share in care relative to female decreased with both extra‐pair paternity and frequency of male polygamy. Parental sex roles were also related to social environment, because male parental care increased with male‐biased adult sex ratios (ASRs). Taken together, our results are consistent with recent theories suggesting that gametic investment is not tied to parental sex roles, and highlight the importance of both sexual selection and ASR in influencing parental sex roles.     

Observations on the breeding biology of the Writhed-billed Hornbill (Aceros waldeni) in the Philippines

Summary We report on some aspects of the breeding biology of the critically endangered Writhed-billed Hornbill (Aceros waldeni) on the island of Panay, Philippines. Observations were made at three nests during 1995–1997. Walling-in of the females commenced in the first week of March. One female remained incarcerated for 77 days, two of three broods completed fledging around May 20 (1995, 1997). Details on fledging of the female and her brood and postfledging care by both parents are reported.The food of the males at two nests was ca. 98% fruits and 2% invertebrates. The plants exploited comprised at least 14 species. Over a third of the fruits delivered were figs of a small number of species.Two males had average feeding rates of 0.56 and 0.88 times per hour respectively, and fed 1 to 66 (median 8) items per feeding visit at the nest. The hourly feeding rate increased after hatching, but the composition of the diet did not change noticeably. As a rule, food items were delivered singly and, during one visit, in runs of one, or rarely up to 3, species.In the three weeks following vacation of the nest, the male appeared to be the sole food provider while the female stayed continually with the 3 young (as sentinel?) in the vicinity of the nest.The nest environs were defended by the male against Tarictic Hornbills (Penelopides panini panini). Six vocalisations of the parents are mentioned. One was used in territorial skirmishes with Tarictic Hornbills.With perhaps less than 30 pairs of the Writhed-bill surviving, the future for the species looks bleak. Only drastic conservation measures can prevent the species' demise. Some have been started by the PESCP.This paper is publication No. 11 of the Philippine Endemic Species Conservation Project (PESCP) of the Frankfurt Zoological Society.     

Seasonal variation in sex ratio and sexual egg dimorphism favouring daughters in first clutches of the spotless starling

We investigated possible pre‐hatching mechanisms of sex‐differential investment by females that may contribute to offspring sex‐ratio adjustment enhancing the fitness return from reproductive effort in the spotless starling (Sturnus unicolor). We found a seasonal shift in sex ratio from daughters to sons as the season advances. Furthermore, the probability of breeding at 1‐year old and recruitment into the breeding population in daughters is associated with laying date but not with mass at fledging. The reverse is true for males which rarely bred at 1‐year old. We also found that eggs containing female embryos are significantly heavier than those containing males in spite of the slight sexual dimorphism in favour of males. This suggests maternal control of provisioning, favouring daughters that may balance sibling mortality and competition with their brothers. Our results on seasonal variation in sex ratio and differential egg provisioning are consistent with an adaptive tactic in which mothers increase their reproductive return by enhancing the probability that daughters survive and breed in their first year of life.     

Nesting biology,life cycle,and interactions between females of Manuelia postica,a solitary species of the Xylocopinae (Hymenoptera: Apidae)

Abstract

The Xylocopinae contains four tribes with species which show a range of nesting habits, from solitary to social. The Manueliini is the sister group to all other Xylocopine tribes, with one genus, Manuelia, of three species found mainly in Chile. This is a solitary genus, whose biology is scarcely known for two species, M. gayatina and M. gayi, and so far completely unknown for M. postica. This paper reports on nesting substrates, nest architecture, nesting behaviours, life cycle, and interactions between females at nesting sites, for M. postica. The results indicate that M. postica presents some features which are typical of solitary life, and also some features which are unusual in solitary bees but have been reported in phylogenetically more apical social species. Our findings open interesting questions on the ecological scenarios involved in the evolution of sociality within the Xylocopinae.     

Reproductive biology of female bigeye tuna Thunnus obesus in the western Pacific Ocean

The reproductive biology of female bigeye tuna Thunnus obesus was assessed by examining 888 fish (ranging from 84·9 to 174·4 cm fork length, L_F) caught by Taiwanese offshore longliners in the western Pacific Ocean from November 1997 to November 1998 and November to December 1999 and 258 gonad samples from these fish. The overall sex ratio of the catch during the sampling differed significantly from 0·5, but males were predominant in sizes >140 cm L_F. Reproductive activity (assessed by histology), a gonado‐somatic index, and the size‐frequency distributions of whole oocytes indicated that spawning occurred throughout the year and the major spawning season appeared to be from February to September. The estimated sizes at 50% maturity (L_F50) of females was 102·85 cm (95% c.i .: 90·79–110·21 cm) and the smallest mature female was 99·7 cm L_F. They are multiple spawners and oocytes develop asynchronously. The proportion of mature (0·63) and reproductively active (0·70) females with ovaries containing postovulatory follicles indicated that they spawn almost daily. Batch fecundity for 15 females with the most advanced oocytes (>730 µm) ranged from 0·84 to 8·56 million eggs (mean ± s.d . = 3·06 ± 2·09). The relationships between batch fecundity (F_B, in millions of eggs) and L_F (cm) and round mass (M_R, kg) were (r² = 0·84) and (r² = 0·80), respectively. The parameters estimated in this study are key information for stock assessments of T. obesus in the western Pacific Ocean and will contribute to the conservation and sustainable yield of this species.     

Allocation of parental investment among individual offspring in the European beewolf Philanthus triangulum F. (Hymenoptera: Sphecidae)

Optimal allocation of parental resources is an important life history trait. However, it has been rarely investigated empirically. We tested aspects of optimal allocation theory in a digger wasp, the European beewolf. Investment allocation theory assumes (1) a trade‐off between investment per offspring and offspring number and (2) a convex relationship between investment per offspring and fitness returns. From mis relationship an optimum amount of investment per offspring can be derived and parents are predicted to provide each offspring with this optimum amount of investment. We used the number of bees in a brood cell as a measure of parental investment. Offspring fitness was quantified as both survival until emergence and success as adults. There is evidence for a trade‐off between current and future reproduction, suggesting that the first assumption is met. In contradiction to the second assumption, one mortality factor, parasitism, increased proportionally with the number of bees in a brood cell. However, overall mortality until emergence significantly decreased with the number of bees in a brood cell as assumed by the theory. The determination of the optimum amount of investment per offspring is complicated because the sexes possibly differ in their relationship between amount of investment and fitness. Individual males received considerably fewer bees (2.2 ± 0.8) than females (3.8 ± 0.5). Two independent estimates of the investment specific survival suggested that sons with two bees had the highest fitness returns per single bee and, consistent with the prediction, most sons were provisioned with two bees. For daughters, four bees is probably the optimum amount and most daughters were provisioned with this number. In both sexes the variation of investment per offspring was less than expected by a Poisson distribution with the same mean. These findings support the view that parental investment is allocated in a way that optimizes the trade‐off between offspring number and investment per offspring. However, variation contradicting the hypothesis still occurred. This might be explained either by adaptive variation in the amount of investment per offspring, constraints in the adjustment of the optimum amount of investment, or problems in measuring parental investment.     

Points of view: Cannibalism and OSR -- a response to Kvarnemo

Reviews in Fish Biology and Fisheries -     

Influence of resource level on maternal investment in a leaf-cutter bee (Hymenoptera: Megachilidae)

Fisher's (1930) prediction of equal investment for each sexin a panmictic population is influenced by a number of ecologicalfactors, among which resource availability plays a major role,particularly when the population exists under changing resource availability.Rosenheim et al. proposed a multifaceted parental investment modelbased on the underlying assumption that individual females determine theirsex investment according to resource availability and oocyte availabilityto maximize reproductive success. The model predicts that greater availabilityof resources used for provisions will lead to (1) an increasein the proportion of females produced (when the female is thelarger sex) and (2) an increase in the amount of provisionsper offspring and thus an increase in offspring size. I testedthese predictions by a controlled experiment using a leaf-cutterbee, Megachile apicalis. I presented two levels of food resourcesto the nesting females, which were allowed to forage and nestin cages. The experimental results supported these parentalinvestment model's predictions.