Fireflies with or without prespermatophores: Evolutionary origins and life-history consequences

During mating, some male North American fireflies produce spermatophores from prespermatophores in their paired reproductive accessory glands. Other species of fireflies have neither prespermatophores nor spermatophores. To establish a pattern of spermatophore occurrence across firefly species, we examined the male internal reproductive system in 20 Japanese species belonging to 10 genera for the presence or absence of prespermatophores. Twelve species from seven genera produced prespermatophores, while eight species from three genera did not. Superimposed on a molecular phylogeny of Japanese fireflies based on mitochondrial 16S ribosomal DNA sequences, the basal group was prespermatophore producers. Prespermatophores appear to have been lost in two different lineages. Species without prespermatophores are characterized by degeneration of both the forewings and hindwings, and by body gigantism in females.     

Condition-dependent spermatophore size is correlated with male's age in a bushcricket (Orthoptera: Phaneropteridae)

During mating, male bushcrickets transfer a spermatophore that consists of a sperm-containing ampulla and a product of the accessory glands, the spermatophylax, which females directly ingest. In the present study, we demonstrate male spermatophore allocation in the bushcricket Poecilimon zimmeri . Males of this species show condition-dependent spermatophore investment. This investment depended upon the age at first mating of males, with older individuals transferring larger spermatophores than younger ones of the same body mass. Independently of age, heavier males transfer larger spermatophores, but the size of males (as measured by femur length) was not a good predictor. Heavier males allocate a lower proportion of their mass to spermatophores and reach their maximal investment point earlier than less heavy males. Spermatophylax production levelled off to a species specific maximum earlier than that of sperm investment (measured as ampulla mass), suggesting that males face high levels of sperm competition.  © 2009 The Linnean Society of London, Biological Journal of the Linnean Society , 2009, 96 , 354–360.     

Limits to Nuptial Gift Production by Male Fireflies, Photinus ignitus

Males of diverse insect species provide females with nuptial gifts, and limits on males' ability to produce these gifts may influence courtship behavior and mating systems. In the firefly Photinus ignitus, males transfer a complex spermatophore to females during mating. We provided firefly males unlimited access to responsive females to examine whether spermatophore production limits male mating success. Male spermatophore mass decreased significantly across sequential matings, and the percentage of successful matings declined during the second half of each male's life span. Male body mass explained a significant proportion of variation in size of the first spermatophore produced by P. ignitus males, but this relationship disappeared with second spermatophores. This study indicates that males' ability to produce spermatophores declines over their lifetime and that limits on nuptial giftproduction can constrain male mating success in Photinus fireflies.     

Fitness advantage from nuptial gifts in female fireflies

Abstract 1. In many insects, males provide nuptial gifts to females in the form of spermatophores, sperm-containing structures produced by male accessory glands.
2. The work reported here examined the influence of both spermatophore number and spermatophore size on female reproductive output in two related firefly beetles, Photinus ignitus and Ellychnia corrusca (Coleoptera: Lampyridae). Based on differences in adult diet, male spermatophores were predicted to increase female reproductive output to a greater extent in P. ignitus than in E. corrusca .
3. Female fecundity was significantly higher in triply mated females than in singly mated females in both species, with no difference between mating treatments in female lifespan or egg hatching success. No effects of second male spermatophore size on fecundity, lifespan, or egg hatching success were detected in either species.
4. These results suggest a direct fitness advantage from multiple mating for females in both species, although enhanced fecundity may be due either to allocation of spermatophore nutrients to eggs or to other substances transferred within the spermatophore acting as oviposition stimulants.     

Spermatophore formation in the pseudoscorpion Chthonius ischnocheles (Chthoniidae)

The reproduction of pseudoscorpions involves indirect sperm transfer by means of spermatophores. The spermatophores are the product of the male genital atrium. A functional interpretation of spermatophore formation in Chthonius ischnocheles is based on evidence from (a) a morphological study of the genital atrium, the associated accessory glands and the musculature (b) males sectioned during spermatophore production (c) histochemical tests on the glands and their secretions (d) biochemical analyses of one gland (posterior dorsal) and its secretion (e) the behaviour of males during this process and (f) the structure of the spermatophore.
The anterior region of the genital atrium is concerned with the production of the sperm packet. The encysted sperm and the seminal fluid from the prostatic reservoir are encapsulated in a sperm packet by a secretion from two pairs of anterior glands. The posterior region of the genital atrium is responsible for the formation of the spermatophore stalk and its distal elaboration, the two lateral collars. These parts of the spermatophore arise from the fibroin secretion of the posterior dorsal gland; the shape of the spermatophore collars is correlated with their mould, the medial diverticula. In addition the lateral glands secrete a light oil which accumulates on a thickening of the spermatophore stalk proximal to the collars. This suggested that this secretion acts as a pheromone to attract females to the spermatophore since in this species males produce their spermatophores in the absence of females.     

Nuptial gifts and sexual selection in photinus fireflies

The phenomenon of nuptial gift transfer during mating occursacross a remarkably wide range of taxa, and such male donationsare likely to influence both pre-copulatory and post-copulatorysexual selection. This paper reviews what is known about nuptialgifts in Photinus fireflies (Coleoptera: Lampyridae), and discussesthe adaptive significance of spermatophores in firefly matingsystems. During copulation Photinus males transfer a spiral,gelatinous spermatophore to the female: sperm are released intothe female's spermatheca for storage, while the remainder ofthe spermatophore disintegrates within a specialized gland.Radiolabelling studies indicate that male-derived protein isused to help provision the female's developing oocytes, andmultiply-mated females show increased fecundity. As most Photinusadults do not feed, these studies suggest that females shouldcontinue to forage for matings to supplement their diminishinglarval reserves, even after they have gained sufficient spermto fertilize their eggs. Male spermatophore mass declines acrosssequential matings, and smaller spermatophores are associatedwith lower paternity success in situations where males competefor fertilizations. Declining spermatophore size across sequentialmatings may thus lead to diminishing reproductive returns forfirefly males. Taken together, these results suggest that seasonalchanges in nuptial gift availability may contribute to reversalsof traditional courtship roles, with male choice and female-femalecompetition occurring as spermatophore availability declines.     

Correlated evolution of female neoteny and flightlessness with male spermatophore production in fireflies (Coleoptera: Lampyridae)

The beetle family Lampyridae (fireflies) encompasses ～100 genera worldwide with considerable diversity in life histories and signaling modes. Some lampyrid males use reproductive accessory glands to produce spermatophores, which have been shown to increase female lifetime fecundity. Sexual dimorphism in the form of neotenic and flightless females is also common in this family. A major goal of this study was to test a hypothesized link between female flight ability and male spermatophore production. We examined macroevolutionary patterns to test for correlated evolution among different levels of female neoteny (and associated loss of flight ability), male accessory gland number (and associated spermatophore production), and sexual signaling mode. Trait reconstruction on a molecular phylogeny indicated that flying females and spermatophores were ancestral traits and that female neoteny increased monotonically and led to flightlessness within multiple lineages. In addition, male spermatophore production was lost multiple times. Our evolutionary trait analysis revealed significant correlations between increased female neoteny and male accessory gland number, as well as between flightlessness and spermatophore loss. In addition, female flightlessness was positively correlated with the use of glows as female sexual signal. Transition probability analysis supported an evolutionary sequence of female flightlessness evolving first, followed by loss of male spermatophores. These results contribute to understanding how spermatophores have evolved and how this important class of seminal nuptial gifts is linked to other traits, providing new insights into sexual selection and life-history evolution.     

父方投资与性角色逆转现象: 螽斯类昆虫的婚礼食物及对性选择方向的影响

大多数动物在繁殖过程中,雌性在繁殖过程中要比雄性付出更大投资,如相对于精子较大的卵子细胞,较长的育幼时间等,因而在交配过程中,雌性具有选择权,而雄性之间相互竞争以取得与雌性的交配权。然而自然世界中并不总是竞争的雄性（competitive male）-选择的雌性（selective female）这种婚配形式。在螽斯类昆虫中,雄性同样具有较大的父方投资。在繁殖期间,雄性螽斯争相鸣叫,求偶,且在交配后要给予雌性特殊的营养物质-精包,供雌性取食。因此在特定情况下,雌性之间将进行竞争以获取雄性配偶,雄性变得更具有选择性。影响这种性角色逆转的主要因素是可获得资源的紧缺。父方投资理论和性选择理论预测雄性显著地对后代投资时,雌性将表现出典型的雄性特征,她们竞争追求性活跃的雄性,而雄性将表现出典型的雌性特征,对配偶具有选择性。螽斯类昆虫中这种特殊的性角色逆转现象符合性选择理论和父方投资理论的预测。     

Sexual transfer of prostaglandin precursor in the field cricket, Teleogryllus commodus

ABSTRACT. When injected into the haemolymph of newly emerged adult males of the field cricket, Teleogryllus commodus (Walker), [³H]arachidonic acid is incorporated into tissue phospholipids. Two reproductive tissues, testes and accessory glands, incorporate and preserve the labelled arachidonic acid for at least 49 days. With onset of circadian rhythm-controlled spermatophore production, radioactive arachidonic acid is incorporated into spermatophore phospholipids. After mating with untreated females, radioactivity was detected in spermathecae and in haemolymph from females. Some of the transferred radioactive arachidonic acid is subsequently converted into prostaglandins. Hence, males of T. commodus transfer prostaglandin synthetase activity and substrate by way of spermatophores during mating     

Pattern of sperm storage and migration in the reproductive tract of the swallowtail butterfly Papilio xuthus: cryptic female choice after second mating

Females of the swallowtail butterfly Papilio xuthus L. (Lepidoptera: Papilionidae) mate multiply during their life span and use the spermatophores transferred to increase their longevity as well as fecundity. Sperm from different males may be stored in the sperm storage organs (bursa copulatrix and spermatheca). To clarify the pattern of sperm storage and migration in the reproductive tract, mated females are dissected after various intervals subsequent to the first mating, and the type and activity of sperm in the spermatheca are observed. When virgin females are mated with virgin males, the females store sperm in the spermatheca for more than 10 days. Sperm displacement is found in females that are remated 7 days after the first mating. Immediately after remating, these females flush out the sperm of the first male from the spermatheca before sperm migration of the second male has started. However, females receiving a small spermatophore at the second mating show little sperm displacement, and the sperm derived from the small spermatophore might not be able to enter the spermatheca. Females appear to use spermatophore size to monitor male quality.     

Differential allocation of male-derived nutrients in two lampyrid beetles with contrasting life-history characteristics

Across diverse animal taxa, sperm is transferred from malesto females during mating within a spermatophore produced bymale accessory glands. In some insects, male spermatophoresprovide females with nutrients that may be used to increasereproductive output or for somatic maintenance, while in othersno such benefits have been detected. Boggs suggested that variationin the current function of spermatophores may be explained byconsidering ecological and life-history factors. This studyexamined spermatophore function in Ellychnia corrusca and Photinusignitus (Coleoptera: Lampyridae), two beetles that exhibit markeddifferences in adult diet, adult life span, and overwinteringstage. During mating, males of both species transfer to femalesa complex, proteinaceous spermatophore, which is subsequentlydigested in a specialized sac within the female reproductive tract.Males of each species were injected with ³H-radiolabeled aminoacid mixtures and mated with conspecific females. The fate of spermatophore-derivedproteins was determined by dissecting females at various timesafter mating with these radiolabeled males. Females of thesetwo species showed markedly different patterns of incorporationof spermatophorederived nutrients. P. ignitus females incorporatedthe majority (62%) of spermatophore-derived protein into maturingoocytes within 2 days after mating. In contrast, in E. corruscaa large percentage of radiolabel (46%) appeared in female fatbody at 6 days after mating, with a threefold lower allocationto maturing oocytes compared to P. ignitus. These findings supportthe prediction that short-lived, nonfeeding females are selectedto allocate a greater proportion of male-derived nutrients toreproduction, while longer-lived, feeding females are selectedto allocate a greater proportion to somatic reserves and maintenance.These results suggest that life-history characteristics maybe useful in explaining observed differences in spermatophorefunction across taxa.     

Male age, mating status and nuptial gift quality in a bushcricket

Female mate choice occurs in many animals, and in some species females prefer older males. Because older males have demonstrated their survival ability, they may be of higher genetic quality, providing genetic benefits to the offspring of their mates. However, in species where females receive direct benefits of matings, younger males may be more likely to provide more fertile or more nutritious ejaculates, so females may discriminate against older males. Males of the bushcricket Ephippiger ephippiger (Orthoptera: Tettigoniidae) produce large spermatophores at mating (>30% of body weight, circa 10% protein content). Female E. ephippiger discriminate against the song of older males. We examined the effects of male age and mating history on male reproductive investment (spermatophore size, sperm number, nitrogen content). Males produced spermatophores with significantly fewer sperm and of lower nitrogen content on their fourth mating, despite free access to food and a 1-week interval between matings, indicating that there is a cost of mating to males. There was no indication that older virgin males produced lower-quality spermatophores. Rather, older males produced bigger spermatophores of higher nutritional value and containing more sperm. Male age and mating history seem likely to be strongly correlated in the field. We conclude that female E. ephippiger probably prefer the songs of younger males, because in the field, this preference correlates with male mating history and therefore resources provided at mating. Thus, female preference for younger males could reflect discrimination against low-quality nuptial gifts.     

Cryptic female choice during spermatophore transfer in Tribolium castaneum (Coleoptera: Tenebrionidae)

Sexual selection in both males and females promotes traits and behaviors that allow control over paternity when female mates with multiple males. Nonetheless, mechanisms of cryptic female choice have been consistently overlooked, due to traditional focus on sperm competition as well as difficulty in distinguishing male vs. female influence over processes occurring during and after mating. The first part of this study describes morphology and transformation of Tribolium castaneum spermatophores inferred from dissecting females immediately after normal or interrupted copulations. T. castaneum males are found to transfer spermatophores as an invaginated tube that everts inside the female bursa and which is filled with sperm during copulation. This sequence of events makes it feasible for females to control the sperm quantity transferred in each spermatophore. Through manipulation of the male phenotypic quality (by starvation) and manipulation of female control over sperm transfer (by killing a subset of females), the second part of this study examines whether females use control over transferred sperm quantity as a cryptic choice mechanism. Fed males transferred significantly more sperm per spermatophore than starved males but only when mating with live females. These results suggest an active differentiation by live females against starved males and provide an evidence for the proposed cryptic female choice mechanism.     

Effects of male mating interval on spermatophore formation,transfer, and subsequent female receptivity and fecundity in the sorghum plant bug,Stenotus rubrovittatus

Males of the sorghum plant bug, Stenotus rubrovittatus (Matsumura) (Heteroptera: Miridae), transfer a spermatophore to females during copulation. After a 1‐day interval between the first and second copulation, males transferred both sperm and a spermatophore to females during the second copulation. However, when male mating interval was <1 h, they transferred sperm but no spermatophores to females during the second copulation. Therefore, the male mating interval probably produces two types of mated females, those with and those without a spermatophore. Mated females of S. rubrovittatus do not remate for at least 3 days after mating, even when courted, and lay more eggs than virgin females at the beginning of the oviposition period. The effects of spermatophores on female sexual receptivity and fecundity were examined using mated females with or without a spermatophore. Only one of the 40 (2.5%) mated females with a spermatophore remated, whereas 10 of the 26 (38.5%) without a spermatophore remated. Furthermore, mated females with a spermatophore laid more eggs than those without a spermatophore. These results suggest that spermatophores participate in reducing female sexual receptivity and enhancing female fecundity in S. rubrovittatus.     

When do the Costs of Spermatogenesis Constrain Sperm Expenditure? Remarks on the Pattern of the Spermatogenic Cycle

The costs of spermatogenesis constrain sperm expenditure when sperm production per day is limited. Thus, males are challenged to allocate available resources to sperm production and other life history functions. However, this prevailing assumption is not applicable to species in which spermatogenesis becomes quiescent during the breeding season. Males of these species prepare large quantities of sperm before the breeding season. Among these species, constraints on ejaculates have been intensively investigated in salamanders that deposit spermatophores. Although it is predicted that sperm expenditure should not be limited because of abundantly prepared sperm, spermatophore deposition is often limited during the breeding season when vas deferens are full of sperm. We tested a hypothesis regarding limited spermatophore deposition by measuring sperm quantity and volume of spermatophores sequentially deposited by male eastern newts Notophthalmus viridescens. A male newt rarely deposits more than three spermatophores per mating. If depletion of non‐sperm components of spermatophores limits spermatophore deposition, we predicted that spermatophore volume decreases while sperm quantity remains constant as a male deposits more spermatophores. Alternatively, some regulative mechanisms allow a limited portion of available sperm to be expended per mating, in which sperm quantity is predicted to decrease while the spermatophore volume remains constant. Finally, depletion of non‐sperm components may regulate sperm expenditure, which predicted that both spermatophore volume and sperm quantity decrease. We found that both sperm quantity and the spermatophore volume decreased as a male deposited more spermatophores during a single mating. Sperm expenditure was constrained without the costs involved in active spermatogenesis, and depletion of non‐sperm components likely regulate sperm quantity loaded in spermatophores. In dissociated spermatogenesis, constrained sperm expenditure do not mean that costly spermatogenesis is directly limiting male mating capacity but rather suggest that the evolution of physiological mechanisms regulating sperm expenditure per mating maximizes male reproductive success.     

Transfer and fate of male secretions deposited in the spermatophore of females of Acanthoscelides obtectus Say (Coleoptera Bruchidae)

During mating, males of Acanthoscelides obtectus deposit a spermatophore in the female genital tract. Spermatophore structure subsequently undergoes considerable modification, especially the central portion, which becomes vacuolated. Two methods were used to show that certain male secretions could thus pass into female haemolymph. When young males were injected with [¹⁴C]-arginine or [¹⁴C]-histidine, the accessory glands actively incorporated the isotope and the resulting spermatophores were radioactive. After mating, spermatophore radioactivity declined and then appeared in the haemolymph of females and in the oöcytes after a delay. Immunoelectrophoresis also showed that antigens appeared in the haemolymph of females after mating which reacted against male-gland antiserum. This technique, however, did not enable us to detect the presence of male antigens in the oöcytes formed after mating. The fate of some male secretions in the female and their physiological importance in the control of the female reproductive function were analysed in the present work.     

Spermatophore and Sperm Allocation in Males of the Monandrous Butterfly Pararge aegeria: the Female’s Perspective

In insects, spermatophore production represents a non‐trivial cost to a male. Non‐virgin males have been shown to produce small spermatophores at subsequent matings. Particularly in monandrous species, it may be an issue to receive a sufficiently large spermatophore at the first and typically only mating. Females of the monandrous Speckled wood butterfly Pararge aegeria (L.) produce fewer offspring after mating with a non‐virgin male. After mating, females spend all their active time selecting oviposition sites and typically ignore other males. Here, we show that females did not discriminate between a virgin male and a recently mated male in our laboratory experiments. We demonstrate that the number of eupyrene sperm bundles relative to spermatophore mass differed with subsequent male matings. Males transferred a significantly smaller spermatophore after the first copulation, but the spermatophore mass did not decrease further with subsequent matings. However, the number of eupyrene sperm bundles decreased linearly. Therefore, there was proportionally more eupyrene sperm in the male’s second spermatophore compared with the first and the later spermatophores. Such a pattern has been shown in polyandrous species. Hence, it suggests that differences in sperm allocation strategy between polyandrous and monandrous butterflies may be quantitative rather than qualitative. There was also a tendency for females that had mated with a recently mated male to have higher propensity to remate than did females that had mated with a virgin male. We discuss the results relative to the mating system in P. aegeria, including female remating opportunities in the field and male mate‐locating behaviour.     

Paternity Analysis in a Hexapod (Orchesella cincta; Collembola) with Indirect Sperm Transfer

In species where males and females interact during mating, the role of females in sexual selection cannot always be demonstrated unambiguously. Here we present a model system to study female choice for mates. Orchesella cinca is a soil-dwelling hexapod with indirect sperm transfer. Females and males do not interact physically for reproduction. We gave females the choice between spermatophores produced by two different males. Paternity analysis based on microsatellite variation revealed that offspring in one clutch were sired by one male only. Direct observations showed that after a female has taken up a spermatophore, the female's receptivity to further spermatophore uptake seem to end. Our results imply that the female is in full control of paternity.     

Postcopulatory female choice increases the fertilization success of novel males in the field cricket, Gryllus vocalis

Although recent studies have demonstrated that female crickets prefer novel males to previous mates, the relative contribution of pre- and postcopulatory behaviors to this advantage remain unknown, as do the reproductive consequences to males. I paired females either with previous or novel mates, and recorded the latency to mating and the time after mating at which the female removed the male's spermatophore, terminating sperm transfer. Females that mated with familiar males removed their spermatophores sooner than females that mated with novel males. Females paired with novel males also mated more quickly than females paired with familiar males, but this difference was not statistically significant. A molecular-based paternity analysis was used to determine whether the postcopulatory preference of females for novel males influences a male's fertilization success. Females were assigned to either mate three times with the same male and then once with a novel male, or four times with four different males. The paternity of the last male was higher when the female previously had mated repeatedly with the same male than when she had mated previously with different males. These results suggest that female spermatophore removal behavior influences male paternity such that novel males receive a fertility benefit.     

Determinants of paternity in a butterfly

Success in sperm competition is of fundamental importance to males, yet little is known about what factors determine paternity. Theory predicts that males producing high sperm numbers have an advantage in sperm competition. Large spermatophore size (the sperm containing package) also correlates with paternity in some species, but the relative importance of spermatophore size and sperm numbers has remained unexplored. Males of the small white butterfly, Pieris rapae (Lepidoptera: Pieridae), produce large nutritious spermatophores on their first mating. On their second mating, spermatophores are only about half the size of the first, but with almost twice the sperm number. We manipulated male mating history to examine the effect of spermatophore size and sperm numbers on male fertilization success. Overall, paternity shows either first male or, more frequently, second male sperm precedence. Previously mated males have significantly higher fertilization success in competition with males mating for the first time, strongly suggesting that high sperm number is advantageous in sperm competition. Male size also affects paternity with relatively larger males having higher fertilization success. This may indicate that spermatophore size influences paternity, because in virgin males spermatophore size correlates with male size. The paternity of an individual male is also inversely correlated with the mass of his spermatophore remains dissected out of the female. This suggests that females may influence paternity by affecting the rate of spermatophore drainage. Although the possibility of female postcopulatory choice remains to be explored, these results clearly show that males maximize their fertilization success by increasing the number of sperm in their second mating.