Flexible ovipositor sheaths in parasitoid Hymenoptera (Insecta)

The structure of the ovipositor sheaths is examined in a number of parasitic wasps as well as a few non-parasitic taxa. Parasitic wasps in the families Aulacidae, Braconidae, Ichneumonidae, Megalyridae, and Stephanidae with a very elongate, external ovipositor have the lateral wall of the sheath finely transversely subdivided by narrow furrows. This makes the sheath highly flexible, allowing it to support the ovipositor proper during ovipositing. The taxa having such a flexible sheath all drill into wood to lay their eggs. Support at the tip of the ovipositor is crucial in the initial stages of oviposition. The flexible ovipositor sheath is possibly a very ancient trait, arising prior to the radiation of extant Apocrita. This is corroborated by their presence in fossil Hymenoptera from the Upper Jurassic. The occurrence of short and/or concealed ovipositors with rigid sheaths in many extant apocritan taxa must therefore be assumed to be the result of multiple reversals.     

Seasonal change in the spatial utilization of host mussels in relation to ovipositor length by female rosy bitterling Rhodeus ocellatus kurumeus

The seasonal changes in ovipositor length and utilization patterns of mussels for oviposition in the rosy bitterling Rhodeus ocellatus kurumeus (Cyprinidae) were investigated in a field experiment and field surveys during the breeding period (April to August). The mean length of ovipositors at oviposition was short at the start (early April) and end (July) of the breeding period. Females with long ovipositor at oviposition were collected between mid‐April and June. Mark‐and‐recapture data showed that ovipositor length at oviposition changed rhythmically throughout the breeding period, shortening and lengthening as the female entered the spawning and resting phase. The density of rosy bitterling embryos in mussels increased between April and June, peaking in May, but decreasing in July. The position of eggs on mussel gills varied from close to the exhalant siphon to deeper inside the gill during April, and periodically thereafter. There was a positive correlation between ovipositor length at oviposition and the distance from exhalant siphon of mussels to eggs deposited by females, suggesting that ovipositor length at oviposition determined the position of eggs deposited on a mussel gill. Because dissolved oxygen in mussel gills decreased with the density of bitterling embryos, suitable positions for embryo survival in gills changed with embryo density. By changing ovipositor length at oviposition, females might be able to spawn their eggs in a position that maximizes embryo survival. Thus, plasticity in ovipositor length at oviposition may play an important role as an adaptation of rosy bitterling in utilizing mussels when their quality as a spawning substratum fluctuates seasonally.     

Nature's Swiss Army knives: ovipositor structure mirrors ecology in a multitrophic fig wasp community

Background

Resource partitioning is facilitated by adaptations along niche dimensions that range from morphology to behaviour. The exploitation of hidden resources may require specially adapted morphological or sensory tools for resource location and utilisation. Differences in tool diversity and complexity can determine not only how many species can utilize these hidden resources but also how they do so.

Methodology and Principal Findings

The sclerotisation, gross morphology and ultrastructure of the ovipositors of a seven-member community of parasitic wasps comprising of gallers and parasitoids developing within the globular syconia (closed inflorescences) of Ficus racemosa (Moraceae) was investigated. These wasps also differ in their parasitism mode (external versus internal oviposition) and their timing of oviposition into the expanding syconium during its development. The number and diversity of sensilla, as well as ovipositor teeth, increased from internally ovipositing to externally ovipositing species and from gallers to parasitoids. The extent of sclerotisation of the ovipositor tip matched the force required to penetrate the syconium at the time of oviposition of each species. The internally ovipositing pollinator had only one type of sensillum and a single notch on the ovipositor tip. Externally ovipositing species had multiple sensilla types and teeth on their ovipositors. Chemosensilla were most concentrated at ovipositor tips while mechanoreceptors were more widely distributed, facilitating the precise location of hidden hosts in these wasps which lack larval host-seeking behaviour. Ovipositor traits of one parasitoid differed from those of its syntopic galler congeners and clustered with those of parasitoids within a different wasp subfamily. Thus ovipositor tools can show lability based on adaptive necessity, and are not constrained by phylogeny.

Conclusions/Significance

Ovipositor structure mirrored the increasingly complex trophic ecology and requirements for host accessibility in this parasite community. Ovipositor structure could be a useful surrogate for predicting the biology of parasites in other communities.     

寄生垂叶榕的两种非传粉榕小蜂的产卵行为

通过对两种果外产卵非传粉榕小蜂Philotrypesissp.和Sycoscaptersp.产卵行为的详细观察,发现两种小蜂产卵期都集中在榕果发育的间花期,并且只在进过传粉榕小蜂的榕果内产卵。这两种小蜂的产卵行为基本都可以分为寻找产卵位点、刺壁、产卵和回收产卵器等步骤。落在果面上的两种小蜂的繁殖雌蜂都通过触角敲击果面寻找产卵位点。产卵结束后,Philotrypesissp.大多数情况在原位收回产卵针,而Sycoscaptersp.必须向前爬行才能将产卵针从果内收回。为了争夺产卵位点,在同一榕果产卵的Philotrypesissp.繁殖雌蜂之间会进行打斗。而Sycoscaptersp.繁殖雌蜂之间未观察到打斗行为。两种小蜂产卵器长度虽显著长于各自产卵时榕果果壁厚度,但却显著短于其产卵时榕果果壁和子房层的总厚度,说明这两种小蜂采用产卵针直接刺穿小花子房的产卵模式。     

Divergence of ovipositor length and egg shape in a brood parasitic bitterling fish through the use of different mussel hosts

Bitterling fishes deposit their eggs on the gills of living mussels using a long ovipositor. We examined whether ovipositor length (OL) and egg shape correlated with differences in host mussel species in the family Unionidae among populations of the tabira bitterling (Acheilognathus tabira) in Japan. Bitterling populations that use mussels in the sub-family Anodontinae possessed longer ovipositors and more elongated eggs than those using mussels of Unioninae, as expected from the difference in host size between the sub-families (anodontine mussels are larger than unionine mussels). Based on a robust phylogeny of A. tabira populations, we demonstrated that the evolution of both OL and egg shape were correlated with host differences, but not with each other, suggesting that these traits have been selected for independently. Our study demonstrates how adaptive traits for brood parasitism may diverge with host shift due to different host availability and/or interspecific competition for hosts.     

Mechanical properties of the endophytic ovipositor in damselflies (Zygoptera, Odonata) and their oviposition substrates

Damselfly females use their ovipositor valves to saw aquatic plants in order to insert their eggs into the plant tissues. Stiffness of the plant substrata is therefore an important parameter for oviposition substrate choice by females. Using a force transducer combined with a motorised micromanipulator, the bending stiffness of the ovipositor at the axial compressional load was studied in seven European damselfly species and compared to the local stiffness of seven preferred plant substrates. The puncture force of tested plant samples ranged from 105 to 1500 mN, and their local stiffness ranged from 208 to 1776 N/m. The bending stiffness of the ovipositor was estimated as 173-409 N/m depending on the damselfly species. Using original and literature data, a significant positive correlation between mechanical properties of the ovipositor and preferred oviposition substrates was demonstrated. Possible behavioural adaptations to overcome high stiffness of plant tissues during oviposition are discussed.     

Deterred oviposition response of Monochamus alternatus (Coleoptera: Cerambycidae) to oviposition scars occupied by eggs

1 The oviposition behaviour and response of Monochamus alternatus females to oviposition scars were investigated in the laboratory. 2 Prior to oviposition, females gnawed at the bark surface of Pinus densiflora bolts to make a wound. Then females turned their bodies 180° to position their ovipositors over the wounds and inserted them under the bark through the wounds. After an oviposition, a jelly was deposited while the ovipositor was still inserted. The females then withdrew their ovipositors and rubbed the oviposition scars with the tips of their abdomens. 3 When searching females encountered oviposition scars, they stopped walking and drummed the surface and inside of the oviposition scars with their maxillary and labial palpi. 4 Eighty-six percent of females left oviposition scars containing single eggs after the palpation. By contrast, when females encountered oviposition scars containing no eggs, 76% of them began to gnaw at the scars and 64% deposited single eggs. The response to artificial oviposition scars was similar to that to vacant oviposition scars made by the females. 5 The results of various observations and experiments showed that the females could recognize oviposition scars and discriminate the scars occupied by single eggs from vacant ones, and suggested that the palpation of oviposition scars was the critical discrimination behaviour, indicating mediation by chemical cues.     

Manganese and zinc in the ovipositors and mandibles of hymenopterous insects

X-ray microanalysis of the ovipositor and mandibles of various hymenopterous insects has revealed the presence in many species of up to 10% wt/wt of either zinc or manganese in the cuticle. These metals appear to be involved in cuticular hardening, so helping to reduce abrasive wear. Zinc is found in the ovipositors of most Siricidae, Stephanoidea, and Chalcidoidea. In Ichneumonoidea and Cynipoidea, the metal involved is manganese. Megalyroidea are unique in the Hymenoptera in having both zinc and manganese in their ovipositors, though in different locations. Except for Bethylidae, no metals were detected in the ovipositors or stings of species that penetrate soft substrates or do not make holes at all. The cutting edge of the mandibles of many insects that chew their way through hard substrates during egress from their pupation sites almost invariably contain high concentrations of zinc, and this is present in many that lack metals in their ovipositor. The phylogenetic and ecological implications of metal occurrence are discussed.     

Oviposition Deterrence Is Likely an Effect,Not a Mechanism,in the Leaf Beetle <Emphasis Type="Italic">Chrysophtharta bimaculata</Emphasis> (Olivier) (Coleoptera: Chrysomelidae)

Oviposition deterrence is common in many insects as an evolutionary mechanism to reduce subsequent larval competition. We investigated a suspected case of oviposition deterrence by the paropsine chrysomelid, Chrysophtharta bimaculata. In paired choice tests, gravid females were found to prefer ovipositing on host leaves without conspecific eggs, confirming the presence of an apparent oviposition deterrence mechanism. Washing egg batches in water, hexane, or ethanol did not change this preference, suggesting that a soluble marking pheromone was not involved. Furthermore, it is unlikely that a plant-derived oviposition deterring substance is produced as beetles showed no significant oviposition preference between leaves which had been oviposited upon, but then had the eggs removed, and those that had never been oviposited upon. In trials using artificial leaves and mimic egg batches, “leaves” with “egg batches” placed near the tip of the leaf (the preferred site of oviposition in this species) were significantly less likely to be laid upon than artificial leaves where mimic eggs were placed away from the tip. In combination, the results strongly infer that oviposition deterrence in C. bimaculata is due to the mechanical blocking of the oviposition site by the first laid egg-batch, rather than a specific oviposition deterring cue. The apparent oviposition deterrence in this insect may well be an outcome or evolutionary effect of oviposition-site selection, rather than a clear adaptive mechanism to decrease larval competition.