Telephone-pole beetle
The telephone-pole beetle is a beetle native to the eastern United States and the only known living representative of the otherwise extinct family Micromalthidae. Larvae of the beetle live in decaying wood and can be pests to wooden structures, lending them their common name, the 'telephone-pole beetle.'
The larvae of Micromalthus debilis start as tiny white creatures with well-developed legs, resembling carabid larvae. Larvae bore into moist, decaying chestnut and oak logs, creating galleries as they consume wood fibers. Adult beetles are dark brown to blackish with vestigial reproductive organs. Micromalthuss evolutionary history dates back millions of years, with fossil records found in various ambers. Their larvae infest timber, weakening structures and attracting fungi, as seen in South African gold mines in the 1930s.
The telephone-pole beetle used to have reproducing adults, but has evolved to become obligately paedogenetic, having asexually reproducing female larvae and sterlile adults that occasionally develop from the juveniles. The rare adult is sometimes referred to as a 'ghost adult' due to its vestigial existence. When a substantial number of adults are generated at once in laboratory experiments, they exhibit vestigial mating behavior, including sex-role reversal, with females exhibiting more aggression and competition for mates. Being one of few parthenogenetic haplodiploid species, the telephone-pole beetle is an interesting subject of coleopteran reproductive behavior and physiology.
Distribution
The species was historically endemic to eastern North America. Reports of the species are infrequent and it is unknown whether they are rare, or common and unrecognized. A recent survey found that the species had spread to every continent except Australia, with finds in South Africa, Hong Kong, Belize, Cuba, Brazil, Japan, Hawaii, Italy and Austria, the dispersal is likely connected to the timber trade.Taxonomy
Classification of M. debilis was historically controversial and unsettled. The species, first reported by John Lawrence LeConte in 1878, was long considered one of the Polyphaga, and placed in the Lymexylidae or Telegeusidae, or as a family within the Cantharoidea. However, characteristics of larvae, wings, and male genitalia show that it is in the suborder Archostemata, where it has been placed since 1999.Description
Larvae
Female-producing female larvaeThe thelytokous female larva resembles a carabid larva when first hatched. The first instar larva is the smallest in length, measuring about 1.26mm. The body is white, distinct lateral bulges are present, and the legs are well-developed. The second instar and subsequent instars have similar morphologies, with the head and body size and width increasing with each subsequent instar. The larvae measure between 2.7 and 3.3 millimeters in length. The head displays a light brown hue and notable sclerotization. In almost all segments, the cuticle covering the thorax and abdomen lacks pigmentation. The body is characterized by its slender, elongated form, maintaining parallel sides and cylindrical shape, featuring dorsal and ventral ampullae along with lateral bulges on numerous segments. The thorax is shorter than the combined length of abdominal segments I to III. In later instars, the body is slightly flatter, broader, and shorter. Legs are not present in second and older instars which is considered a trait unique to M. debilis.
Male-producing female larvae
The penultimate instar of the male-producing larva is vaguely described as having a dense white color due to much fat. The body is cylindrically shaped and marked by segmented constrictions.
Male larvae
Unlike female larvae, which resemble the carabid type when first hatched, male larvae resemble that of a weevil. The body is short and stubby with stump-like legs.
Adults
The adult beetle is elongated and a dark brown to blackish color, with brownish-yellow legs and antennae. The head is larger than the thorax, with large eyes protruding from either side. According to H.S. Barber, the adult female is responsible forFeeding
The larvae are wood-borers that feed on moist and decaying chestnut and oak logs. Telephone-pole beetle larvae infest timber by burrowing into the wood, where they feed and develop. They tunnel through the timber, creating galleries as they consume the wood fibers.Life cycle
The life cycle of M. debilis is one of the most complicated life cycles among beetles because it involves viviparity, hypermetamorphosis, parthenogenesis, and paedogenesis. The life cycle is also highly unusual because the larvae rarely mature into adults in both sexes. Haplodiploidy is another notable feature of this species, shared with only a few other species of Coleoptera; haploid males are hatched from eggs within the mother's body via haploid parthenogenesis, and diploid females are birthed live via diploid parthenogenesis.Females
Upon being birthed live, the larva emerges as a minute white creature with long, slender legs that resemble the carabid type. This stage is primarily focused on migration, with the young larvae crawling away from the location of their birth to find new areas within their habitat. During this phase, they may consume the remains of their mother before migration. After a period of wandering, the larvae begin to burrow into wood or other suitable substrates again. They feed minimally during this time and undergo their first molt, transforming into a legless form that resembles the larva of cerambycid beetles. This stage is characterized by the development of an inconspicuous anal armature. Additional molts occur in this form, likely to accommodate head growth and overall body development. The larvae continue to bore through wood, packing their galleries with dust as they progress. The color of their bodies may darken due to the accumulation of food in their alimentary tract. As the larvae near maturity, the eggs in the ovaries of what will become the paedogenetic form become visible. At this stage, the larvae reverse their position in the gallery, construct a cell, and enter an aestivation phase. During aestivation, their bodies gradually turn white as they consume all available food in their system.Depending on circumstances, the larvae may either pupate or undergo another molt, ultimately revealing the paedogenetic form, in which they can produce young. Paedogenesis is the process by which larvae reproduce by giving birth to more larvae without the production of adults and is a process exclusive to females. Once the paedogenetic form emerges, it typically takes around two weeks for the new generation to be born. The young larvae are born tail-first and begin the cycle anew, continuing the species' life cycle.
Males
Male larvae are hatched from a single, large egg that adheres to the male-producing larva's body for 8–10 days. The larvae feed on the mother's body and will grow rapidly. The male rarely pupates and transforms into the imago, and will often die as a larva. While male adults only develop from uni-oviparous paedogenetic females, adult females only develop from cerambycoid paedogenetic females.Larval sex ratio
In naturally occurring paedogenetic larvae, the sex ratio is strongly biased toward females. None of the three canonical explanations for biased sex ratios, local mate competition, local resource competition, and local resource enhancement, are likely explanations for the biased sex ratio in telephone-pole beetle larvae. Local mate competition selects for female-biased sex ratios when male siblings compete to fertilize their female siblings, but this is unlikely in this species which females tend to avoid mating with siblings. Local resource competition selects for biased sex ratios but typically involves competition between females for resources and thus selects for male-biased ratios. Lastly, local resource enhancement can select for biased sex ratios if the offspring of one sex increases the fitness of parents. However, because female offspring feed on the mother, there is more likely competition between female larvae, contradicting this explanation. As such, the cause of sex ratio deviation remains unclear.Adulthood
Adult telephone-pole beetles are unable to copulate, and adult females do not have the physiological mechanisms to reproduce because they are unable to lay eggs or produce live progeny, either sexually or by parthenogenesis. Limited observations and experiments on M. debilis have resulted in conflicting observational conclusions, particularly regarding the beetle's reproduction, in the existing literature. Pollock & Normack reported the existence of reproductive adult males, but this was based on the incorrect conclusions by Barber. However, all existing experimental literature states that adults are sterile.Since adults do not have a role in reproduction, they are not a physiological part of the life cycle. Thus, the rarity of adult development in the natural world may be an evolutionary response to the lack of their reproductive role. In laboratory settings, development into adults can be induced by high temperatures, but this also results in high mortality because only one out of hundreds of heat-treated larvae will survive and pupate into an adult.
The adult females live for about six days and males only live for around 12 hours, with a strongly biased sex ratio towards females. The adults of both sexes are sterile and are vestigial remnants of a time when the life cycle involved sexual reproduction. The loss of sexual reproduction is likely associated with its infection by Wolbachia bacteria.