Variation in ovariole number and egg size of species of Dacus (Diptera; Tephritidae) and their relation to host specialization

Abstract. 1. An analysis of the number of ovarioles/ovary is presented for fourteen species of Dacus ranging from broad generalists (D.tryoni (Frogg.)) to strict host specialists (D.aglaia Hardy). For eight species data on egg size and the incubation time of eggs is also presented. Interrelationships among these life history variables and their relationships to host specialization were examined. 2. There was a broad positive relationship between the breadth of the natural host range (i.e. excluding cultivated fruits) and ovariole number (and hence potential fecundity). Highly polyphagous species had thirty-five to forty ovarioles/ovary while the specialists ranged from eight to twenty. 3. D.musae (Tryon), a specialist on banana, was an exception having an ovariole number similar to that of the most polyphagous species. 4. There was no clear relationship between egg size and ovariole number across eight species, though monophages were not fully represented in this analysis. Among these eight species there was no significant relationship between wing length and egg length, nor was there any such relationship among individuals within species. 5. There was considerable variation among species in the incubation time (at 25°C) for eggs, ranging from 24 h for D.cucumis French to 53 h for D.cacuminatus (Hering). This variation was only weakly related to egg size, though D.cucumis produced the largest eggs of any species examined. 6. Possible explanations for a relationship between potential fecundity and host range are discussed in terms of the balance between the abundance of host resources for generalists and their predictability for specialists. However, the observed relationship between ovariole number and host range must remain tentative, given that only fourteen species from one genus have been examined. Considerably more data is required for other dacines, for species in other tephritid subfamilies, and for other phytophagous insect groups to determine whether the relationship is generally applicable.     

Ovary structure in a presocial insect,Elasmucha grisea (Heteroptera,Acanthosomatidae)

First generation egg clusters of Elasmucha grisea are more closely guarded than second generation clusters. The ovaries of this species are structured to enhance this behavior. The population of E. grisea from S-W Poland breeds in the spring (May–June) and late summer (July–August). The second generation clutches contain fewer eggs and are destroyed 3–4 days after oviposition by predators and parasitoids.The ovary structure in the studied species differs from that found in other Heteroptera. The average number of ovarioles per ovary is 24 while in the other investigated species the number of ovarioles per ovary is 6–7. Lateral oviducts are elongated and the ovarioles are arranged in a pennate pattern. Each ovariole contains only one growing ovarian follicle. Differentiation of the ovarioles and ovarian follicles is synchronised thus enabling simultaneous oviposition. A comparative analysis of the ovary structure during the life cycle, particularly the presence of atresive ovarian follicles in the ovarioles of egg- and nymph guarding females, as well as the shape and structure of the apical part of the tropharium all support the hypothesis of cooperation between females in E. grisea. A similar ovary structure has been observed in the Coccoidea (Hemiptera, Homoptera) which indicates presocial behavior.     

Habitat quality and reproductive investment in aphids

ABSTRACT.

• 1 Genetically identical vetch aphids, Megoura viciae (Buckton), showed a weak but significant positive relationship between reproductive investment (number of ovarioles) and weight, here used as an indicator of habitat quality.
• 2 Apterae reared on poor quality plants showed the same range in numbers (twelve to twenty-two) but on average fewer ovarioles than those reared on high quality plants.
• 3 The variability in ovariole number was determined prior to birth.
• 4 Under constant conditions the age of a mother does not affect the range of ovariole numbers or the proportion of her offspring in each ovariole class.
• 5 Apterae reared on poor quality host plants gave birth to proportionately fewer offspring with a high ovariole number than apterae reared on high quality plants.
• 6 Winged individuals gave birth to proportionately more offspring with a high number of ovarioles than apterae.
• 7 The control and ecological significance of the intramorph variation in reproductive tactics shown by many species of aphids is discussed in the light of these results.

     

Germ-cell cluster formation in the telotrophic meroistic ovary of <Emphasis Type="Italic">Tribolium castaneum</Emphasis> (Coleoptera,Polyphaga, Tenebrionidae) and its implication on insect phylogeny

Tribolium castaneum has telotrophic meroistic ovarioles of the Polyphaga type. During larval stages, germ cells multiply in a first mitotic cycle forming many small, irregularly branched germ-cell clusters which colonize between the anterior and posterior somatic tissues in each ovariole. Because germ-cell multiplication is accompanied by cluster splitting, we assume a very low number of germ cells per ovariole at the beginning of ovariole development. In the late larval and early pupal stages, we found programmed cell death of germ-cell clusters that are located in anterior and middle regions of the ovarioles. Only those clusters survive that rest on posterior somatic tissue. The germ cells that are in direct contact with posterior somatic cells transform into morphologically distinct pro-oocytes. Intercellular bridges interconnecting pro-oocytes are located posteriorly and are filled with fusomes that regularly fuse to form polyfusomes. Intercellular bridges connecting pro-oocytes to pro-nurse cells are always positioned anteriorly and contain small fusomal plugs. During pupal stages, a second wave of metasynchronous mitoses is initiated by the pro-oocytes, leading to linear subclusters with few bifurcations. We assume that the pro-oocytes together with posterior somatic cells build the center of determination and differentiation of germ cells throughout the larval, pupal, and adult stages. The early developmental pattern of germ-cell multiplication is highly similar to the events known from the telotrophic ovary of the Sialis type. We conclude that among the common ancestors of Neuropterida and Coleoptera, a telotrophic meroistic ovary of the Sialis type evolved, which still exists in Sialidae, Raphidioptera, and a myxophagan Coleoptera family, the Hydroscaphidae. Consequently, the telotrophic ovary of the Polyphaga type evolved from the Sialis type. Electronic supplementary material Supplementary material is available in the online version of this article at and is accessible for authorized users.     

Mayflies (ephemeroptera), the most “primitive” winged insects,have telotrophic meroistic ovaries

Germ line cell cluster formation in ovarioles of three different stages, each from a different mayfly species, was studied using ultra-thin serial sectioning. In the analysed ovariole of Cloeön sp., only one linear, zigzag germ line cell cluster was found, consisting of sibling cells connected by intercellular bridges which represent remnants of preceding synchronized mitotic cycles followed by incomplete cytokinesis. A polyfusome stretched through all sibling cells. At the tip of the ovariole, cytokinesis occurred without preceding division of nuclei; thus, intercellular bridges were lined up but the remaining cytoplasm between the bridges had no nuclei. The analysed Siphlonurus armatus vitellarium contained five oocytes at different stages of development. Each oocyte in the vitellarium was connected via a nutritive cord to the linear cluster of its sibling cells in the terminal trophic chamber. Each cluster had the same architecture as was found in Cloëon. The 3-dimensional arrangement and distribution of closed intercellular bridges strongly suggest that all five clusters are derived from a single primary clone. The position of oocytes within each cluster is random. However, each oocyte is embraced by follicular or prefollicular cells whilst all other sibling cells are enclosed by somatic inner sheath cells, clearly distinguishable from prefollicular cells. In the analysed ovariole of Ephemerella ignita, two small linear clusters were found in the tropharium beside two single cells, two isolated cytoplasmic bags with intercellular bridges but no nuclei, and some degenerating aggregates. One cluster was still connected to a growing oocyte via a nutritive cord. In all species the nurse cells remained small and no indications of polyploidization were found. We suggest that this ancient and previously unknown telotrophic meroistic ovary has evolved directly from panoistic ancestors.     

Ontogenesis of the ovary in a moth midge,Tinearia alternata Say (Diptera: Psychodidae)

In a psychodid, Tinearia alternata, the initial differentiation of the polytrophic ovary occurs during the early larval stages. Early in development, each ovary anlage is a solid organ subdivided into three distinct zones: the cortex houses germ cells and somatic interstitial tissue, while two other somatic regions will give rise to the oviduct calyx and anterior part of the lateral oviduct. Germ cell cluster formation precedes the development of ovarioles. Each ovariole houses only one functional egg chamber. All ovarioles within paired ovaries are developmentally synchronized. In the larval ovaries, the newly formed egg chambers and then the ovarioles are intermingeled with and surrounded by the somatic interstitial tissue of the ovary cortex. The interstitial cells give rise to all the somatic elements of the ovarioles. In the pupal ovaries, the remaining interstitial tissue degenerates; thus, the ovarioles protrude into the body cavity. The ovaries in psychodids develop relatively large and swollen oviduct calyxes that are equivalent to receptaculum seminis (spermatheca). The morphological differentiation of germ cells within the egg chambers starts during late larval/early pupal stages. Nurse cell nuclei contain prominent nucleoli and polytene chromosomes. Oocyte growth results from accumulation of yolk and then, in the final stages of oogenesis, from an inflow of cytoplasm from the nurse cells. J. Morphol. 236:167–177, 1998. © 1998 Wiley-Liss, Inc.     

Genetic Basis for Developmental Homeostasis of Germline Stem Cell Niche Number: A Network of Tramtrack-Group Nuclear BTB Factors

The potential to produce new cells during adult life depends on the number of stem cell niches and the capacity of stem cells to divide, and is therefore under the control of programs ensuring developmental homeostasis. However, it remains generally unknown how the number of stem cell niches is controlled. In the insect ovary, each germline stem cell (GSC) niche is embedded in a functional unit called an ovariole. The number of ovarioles, and thus the number of GSC niches, varies widely among species. In Drosophila, morphogenesis of ovarioles starts in larvae with the formation of terminal filaments (TFs), each made of 8–10 cells that pile up and sort in stacks. TFs constitute organizers of individual germline stem cell niches during larval and early pupal development. In the Drosophila melanogaster subgroup, the number of ovarioles varies interspecifically from 8 to 20. Here we show that pipsqueak, Trithorax-like, batman and the bric-à-brac (bab) locus, all encoding nuclear BTB/POZ factors of the Tramtrack Group, are involved in limiting the number of ovarioles in D. melanogaster. At least two different processes are differentially perturbed by reducing the function of these genes. We found that when the bab dose is reduced, sorting of TF cells into TFs was affected such that each TF contains fewer cells and more TFs are formed. In contrast, psq mutants exhibited a greater number of TF cells per ovary, with a normal number of cells per TF, thereby leading to formation of more TFs per ovary than in the wild type. Our results indicate that two parallel genetic pathways under the control of a network of nuclear BTB factors are combined in order to negatively control the number of germline stem cell niches.     

Differences in body sizes and physiological conditions among castes in the ponerine ant Cryptopone sauteri (Hymenoptera: Formicidae)

In several poneroid ant species, mated workers alone undertake reproduction. The reproductive systems of such species have been examined extensively. However, few studies have investigated species with alate queens, which reproduce after shedding their wings. We compared body sizes and the numbers of ovarioles between queens and workers in the ant Cryptopone sauteri with alate queens. We also compared ovariole development between the castes to evaluate their reproductive systems. Approximately 60% of the nests collected were queenless. We often detected unmated queens in the nests throughout the year, but did not obtain strong evidence for their reproduction. Although significant differences were observed in the number of ovarioles and body characteristics between the queens and workers, the differences were not as prominent as those observed in Formicinae and Myrmicinae. We propose two alternative hypotheses, failure of nuptial flight or postponement of reproduction, to explain the presence of unmated queens in the nests.     

SIMILARITIES AND DIFFERENCES IN ALTITUDINAL VERSUS LATITUDINAL VARIATION FOR MORPHOLOGICAL TRAITS IN DROSOPHILA MELANOGASTER

Understanding how natural environments shape phenotypic variation is a major aim in evolutionary biology. Here, we have examined clinal, likely genetically based variation in morphology among 19 populations of the fruit fly (Drosophila melanogaster) from Africa and Europe, spanning a range from sea level to 3000 m altitude and including locations approximating the southern and northern range limit. We were interested in testing whether latitude and altitude have similar phenotypic effects, as has often been postulated. Both latitude and altitude were positively correlated with wing area, ovariole number, and cell number. In contrast, latitude and altitude had opposite effects on the ratio between ovariole number and body size, which was negatively correlated with egg production rate per ovariole. We also used transgenic manipulation to examine how increased cell number affects morphology and found that larger transgenic flies, due to a higher number of cells, had more ovarioles, larger wings, and, unlike flies from natural populations, increased wing loading. Clinal patterns in morphology are thus not a simple function of changes in body size; instead, each trait might be subject to different selection pressures. Together, our results provide compelling evidence for profound similarities as well as differences between phenotypic effects of latitude and altitude.     

Germ cell cluster formation and cell death are alternatives in caste-specific differentiation of the larval honey bee ovary

Summary

Caste-specific differentiation of the female honey bee gonad takes place in the fifth larval instar. In queen larvae most ovarioles exhibit almost simultaneous formation of numerous germ cell clusters within the first 20 h after the last larval molt. Ultrastructurally distinctive fusomal cytoplasm connects these cystocytes. Germ cell differentiation is accompanied by morphological changes in somatic components of the ovarioles, the follicle and the terminal filament cells. Subsequently, queen ovarioles elongate and differentiate basal stalks that coalesce in a basal calyx. A second round of mitotic activity was found to occur in the late prepupal and early pupal queen ovary. This round may elevate germ cell numbers composing each cluster to levels observed in follicles of adult honey bee queens. In contrast, germ cell cluster formation does not occur in most of the 120–160 ovarioles of the larval worker ovary, but instead many cells in such ovarioles show signs of impending degeneration, such as large autophagic bodies. DNA extracted from worker ovaries did not reveal nucleosomal laddering, and ultrastructurally, chromatin in germ cell nuclei appeared intact. In the 4–7 surviving ovarioles of the small worker ovary, germ cell clusters were found with ultrastructural characteristics identical to those in queen ovarioles. The temporal window during which divergence in developmental pathways of the larval ovaries initiates shortly after the last larval molt coincides with caste-specific differences in juvenile hormone titer which have long been considered critical to caste-specific morphogenesis.     

QUANTITATIVE GENETICS OF OVARIOLE NUMBER IN DROSOPHILA MELANOGASTER. I. SEGREGATING VARIATION AND FITNESS

The number of ovarioles of the Drosophila melanogaster ovary is a trait thought to be associated with female fecundity, and therefore is expected to be under strong natural selection. This hypothesis may be tested by examining patterns of genetic and environmental variation for ovariole number in natural populations, and by determining the association between ovariole number and fitness in isogenic lines derived from a natural population. We measured ovariole number, and competitive fitness and its components, for 48 homozygous chromosome 3 substitution lines in a standard inbred background; and body size in a sample of 15 chromosome 3 substitution lines. We found significant segregating genetic variation for ovariole number, with a broad-sense heritability (H²) of 0.403 and correspondingly high coefficients of genetic variation (CV_C = 20.8) and residual variation (CV_R = 25.3). Estimates of quantitative genetic parameters for body size (H² = 0.191, CV_G = 2.15, and CV_R = 3.87) are similar to those previously reported for this trait. Although the isogenic chromosome 3 substitution lines varied significantly for components of fitness, there was no significant linear or quadratic association of ovariole number and body size with fitness. There was, however, highly significant sex × genotype interaction for fitness among these lines. This special case of genotype × environment interaction for fitness may contribute to the maintenance of genetic variation for fitness in natural populations.     

Seasonal cycle of colony structure in the Ponerine ant Pachycondyla chinensis in western Japan (Hymenoptera, Formicidae)

Investigation of reproductive strategies of ants in the subfamily Ponerinae is important for understanding of the evolution of social structure and of the significance of caste dimorphisms. The biology of species with mated and egg-laying workers (gamergates) has been studied for many species, however, little attention has been paid to species that reproduce via alate queens only. We investigated the seasonal cycle of changes in the colony structure of Pachycondyla chinensis reproduced by alate queens in western Japan, and found the following novel biological characteristics of this species. P. chinensis showed a remarkable caste dimorphism in ovariole numbers: workers had no ovaries while queens had 18 to 36 ovarioles in their ovaries. The nesting system seemed to be polydomous: 266 of 400 nests collected were queenless. The number of queenless nests increased during the reproductive season. Among the 134 queenright nests, 38 had several mated-queens without significant differences in ovary activation and the remaining 96 nests were monogynous. During winter to early spring, most nests were polygynous. After alate production, most of the old queens seemed to die or be expelled and replaced by new queens. Virgin dealated queens were often found and they seemed to have laid eggs. Received 3 August 2007; revised 19 December 2007; accepted 20 December 2007     

Ueber die imaginale Ovarvergrösserung im zusammenhang mit der Physogastrie beiOdontotermes badius Haviland (Insecta,Isoptera)

Zusammenfassung Das schlauchförmige Ovar vonOdontotermes badius wird in seiner ganzen Länge vom Ovidukt durchzogen, in den von allen Seiten annähernd 3 000 Ovariolen münden.Bei einem schwärmenden Weibchen sind nur die ersten 5–7 Ovariolen in ihrer Entwicklung soweit fortgeschritten, dass wenige Tage nach dem Schwärmen und Abwerfen der Flügel Eier abgelegt werden können. Die übrigen Ovariolen sind noch in einem frühen Stadium der Entwicklung. Es dauert mehrere Jahre bis alle Ovariolen das Stadium der vollen Reife erreicht haben.Zur imaginalen Entwicklung: Die Ovariolen nehmen an Länge zu. Die Zwischenräume zwischen ihnen werden grösser. Der Ovidukt wird länger und breiter. Die Längenzunahme der Ovariolen wird nicht beendet, sobald sie das Stadium der ersten Reife erreicht haben. Es besteht eine Beziehung zwischen dem Wachstum des Ovars und der weiteren Verlängerung der Ovariolen. Mit der Verlängerung der Ovariolen nehmen zu: Die Grösse des Germariums, die Zahl der Oocyten in der Wachstumsphase und die Zahl der zu gleicher Zeit Dotter-einbauenden Oocyten. Zu einer Neubildung von Ovariolen kommt es jedoch in der Imago nicht. Die Entwicklung setzt Ovarvorn ein. Die vorderen Ovariolen erreichen zuerst ihre maximale Länge. Die Ovariolen entwickeln sich jedoch nicht gleichmässig.Im Zusammenhang mit dem Wachstum des Ovars nehmen alle Organe des Abdomens an Grösse zu. Dabei kann es sich um Zellteilungen, Vergrösserung von Zellen und um Neubildung von Organen handeln.Im gleichaltrigen Männchen kommt es dagegen nur zu einer Hoden-Hypertrophie und zu einer Verlängerung des Mitteldarms.

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Summary On the growth of the imaginal ovary in connexion with the physogastric enlargement ofOdontotermes badius Haviland (Insecta, Isoptera).The tubelike ovary ofOdontotermes badius is penetrated at full length by the oviduct into which approximately 3,000 ovarioles are discharging from all sides.In the case of a swarming female only the anterior 5 to 7 ovarioles are sufficiently mature to ovulate a few days after dropping of the wings. The rest of the ovarioles are in very early stages of development and very short in length and it takes several years before all of the ovarioles become fully mature.The imaginal development of the ovary proceeds as follows: The ovarioles lengthen and the distances between them become larger while the oviduct becomes longer and wider. When an ovariole reaches the first stage of maturation and gives off mature oocytes the lengthening of the ovariole is incomplete. There is a correlation between the growth of the ovary and the further lengthening of an ovariole. Also the lengthening, of the ovarioles is correlated with an increase in number of germarium-cells, in the number of oocytes of the growing stage and in the number of occytes which deposit yolk simultaneously. But there is no new formation of ovarioles during the whole imaginal life.The development of the ovarioles is phased. Those at the anterior pole are starting first and consequently reaching the maximum length sooner than the ovarioles at the hind part of the ovary. All the ovarioles start to develop but some of them develop more slowly and reach the maximum length later.Growth of the ovaries is made possible by the enlargement of the abdomen. In connexion with this enlargement there is growth of all abdominal organs. We must distinguish between growth by cell division alone (e.g. epidermis, connectives, midgut, heart tube), by widening of the epithelium cells predominantly (e.g. spermatheca, accessory glands) and by formation of new tissue (e.g. malpighian tubules).

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Herrn ProfessorWeidner, Hamburg, danke ich für die Artbestimmung; HerrnJ. Stein für die Ausführung der Zeichnungen.     

Age‐related changes in the development of oocytes and testicular follicles after emergence in Stavsolus japonicus (Plecoptera)

Abstract Female stoneflies oviposit several times during the adult stage of their life cycle. The number of eggs within the deposited egg masses decreases at successive ovipositions. To clarify the reason for this decrease and to determine the conditions of testicular follicles, the patterns of development of oocytes and testicular follicles on different days after emergence are investigated in the systellognathan species Stavsolus japonicus (Okamoto) (Perlodidae). The size of the mature oocytes in the ovariole peaks a few weeks after emergence but decreases to the lowest level by 35 days after emergence. Several maturing oocytes can be observed in the ovarioles of individuals a few weeks after emergence but only one mature oocyte is observed at 35 days after emergence. The decreased number of eggs laid per mass by older individuals may therefore be due to the lower maturation of all the ovarioles.     

The roles of cell size and cell number in determining ovariole number in Drosophila

All insect ovaries are composed of functional units called ovarioles, which contain sequentially developing egg chambers. The number of ovarioles varies between and within species. Ovariole number is an important determinant of fecundity and thus affects individual fitness. Although Drosophila oogenesis has been intensively studied, the genetic and cellular basis for determination of ovariole number remains unknown. Ovariole formation begins during larval development with the morphogenesis of terminal filament cells (TFCs) into stacks called terminal filaments (TFs). We induced changes in ovariole number in Drosophila melanogaster by genetically altering cell size and cell number in the TFC population, and analyzed TF morphogenesis in these ovaries to understand the cellular basis for the changes in ovariole number. Increasing TFC size contributed to higher ovariole number by increasing TF number. Similarly, increasing total TFC number led to higher ovariole number via an increase in TF number. By analyzing ovarian morphogenesis in another Drosophila species we showed that TFC number regulation is a target of evolutionary change that affects ovariole number. In contrast, temperature-dependent plasticity in ovariole number was due to changes in cell-cell sorting during TF morphogenesis, rather than changes in cell size or cell number. We have thus identified two distinct developmental processes that regulate ovariole number: establishment of total TFC number, and TFC sorting during TF morphogenesis. Our data suggest that the genetic changes underlying species-specific ovariole number may alter the total number of TFCs available to contribute to TF formation. This work provides for the first time specific and quantitative developmental tools to investigate the evolution of a highly conserved reproductive structure.     

A test of three hypotheses for ovariole number determination in the grasshopper Romalea microptera

Ovariole number in insects determines potential fecundity and can be influenced by genes, environmental conditions during development and parental effects. In the present study, three hypotheses are tested for ovariole number determination in the grasshopper Romalea microptera (Beauvois), which exhibits both intra‐ and interpopulation variation in ovariole number. In hypothesis 1, variation in ovariole number is a result of genetic variation. In hypothesis 2, ovariole number is influenced by nutrition during development. In hypothesis 3, ovariole number is influenced by maternal nutritional status. Females from four treatments are compared: low‐food, high‐food, daughters of low‐food, and daughters of high‐food. There is a relationship between parent and offspring ovariole number despite different environments, supporting hypothesis 1. Also, ovariole numbers are slightly, but significantly lower in individuals fed a low‐food diet compared with a high‐food diet, supporting hypothesis 2. Hypothesis 3 is not supported: starved and well‐fed females produce eggs of similar mass, as well as offspring with similar numbers of ovarioles, suggesting that the nutritional status of mothers does not influence offspring mass or offspring ovariole number. The results imply that genetic variation and developmental conditions determine ovariole number in this species but maternal environment does not. These results conflict with previous studies of ovariole determination in grasshoppers and locusts.     

Morphology,ultrastructure, and germ cell cluster formation in ovarioles of aphids

The structure of aphid ovaries, including ovipare and virginopare morphs of five species, was investigated by light and electron microscopy. Aphids contain telotrophic meroistic ovarioles. The amount and distribution of cytoplasmic components of nurse cells, nutritive cords, and young oocytes are nearly identical to those known from scale insects and heteropterans. Each ovariole has a constant number of nurse cells and oocytes. In ovaries of ovipare morphs, the nurse cell nuclei enlarge by endomitosis (n = 2⁸n?2¹⁰n), whereas in virginopare morphs the nurse cell nuclei remain small (n = 2²n?2⁴n). Furthermore, in virginoparae the previtellogenic growth of oocytes is highly reduced, and vitellogenesis and chorionogenesis are blocked totally. Embryogenesis starts immediately after the shortened previtellogenic growth. In each ovariole, all germ cell descendants belong to one germ cell cluster that follows the 2ⁿ rule. The cluster normally contains 2⁵ = (32) cells, but other mostly smaller numbers also occur. In contrast to polytrophic meroistic ovarioles, more than one cell of each cluster will develop into an oocyte. In Drepanosiphum platanoides, 16 (2^n?1) nurse cells and 16 (2^n?1) oocytes exist in each cluster, whereas, in Metopolophium dirhodum, 8 (2^n?2) oocytes and 24 (2^n?1 + 2^n?2) nurse cells are normally found. In many ovarioles of Macrosiphum rosae, 21 nurse cells nourish 11 oocytes. Models of germ cell cluster formation in aphid ovaries are discussed.     

What determines the number of ovarioles in a fly ovary?

The relation between the size of a fly and the number of ovarioles in its ovary was investigated in Phormia regina and Sarcophaga bullata. Small flies of varying size were produced by taking larvae prematurely off the food. The smallest flies thus obtained were derived from larvae only $\text{1}\text{8}$ of the weight of a normal larva. The number of ovarioles in an ovary is directly proportional to the size of the fly and, in the extreme case, is about $\text{1}\text{5}$ the normal number in Sarcophaga and about $\text{1}\text{3}$ in Phormia. Larvae prematurely taken off the food, but fed again after starving for several days, grow to normal or almost normal size and develop ovaries with about the normal number of ovarioles. Small or re-fed Sarcophaga do not show any changes in the anatomy of individual ovarioles but in Phormia disorders in ovariole development and a consequent reduction of fertility are frequent. The number of ovarioles remains identical from the early pupal stage all through the development of the pharate fly and then through ovarian development in the adult fly: it is determined by the size of the larva when it was taken off the food. This shows that it is not lack of space in a small adult fly abdomen which determines the number nor the occurrence of degenerative processes during ovarian development.