Ostrinia scapulalis explained

Ostrinia scapulalis, the adzuki bean borer or adzuki bean worm, is a species of moth in the family Crambidae. It was described by Francis Walker in 1859. It is one of 20 moths in the genus Ostrinia and is of Eurasian origin.[1] The larvae have a gray mid-dorsal line and can be light pink or beige. The adult adzuki bean borer has a yellowish-brown forewing with jagged lines and variable darker shading, with a wingspan that ranges from 20 to 32 mm. The moths of this species are nocturnal and tend to be attracted to light.[2]

The larvae mainly feed on Artemisia vulgaris, but may also feed on maize.[3] They are typically found in corn fields, gardens, and commercial crop plantations and they are usually active from April to October. They are primarily found in Japan, although they can be found in other regions of Asia and Europe as well.

Distribution

O. scapulalis is most commonly found in the western (from western Europe to Russia) and eastern (from eastern China to Japan) Palearctic regions. However, this species' distribution may be wider than that, and may even be continuous from Europe to Japan. Japan has a significantly large concentration of moths, and the bulk of studies performed there are conducted on the adzuki bean borer. The moth thrives in the habitats and the natural resources found in both the western and eastern Palearctic regions.[4]

Enemies

Diseases

Wolbachia bacteria is responsible for one of the most prevalent diseases for O. scapulalis. These bacteria are maternally transmitted and their presence can cause many reproductive abnormalities in arthropods such as the adzuki bean borer. Namely, the bacteria can convert genetic males into functional females in a process known as feminization. This can skew the sex ratio of a population, which may in turn lower reproductive rates.[5]

Predators

Predators of O. scapulalis include:

Parasites

The Ostrinia species are victim to many natural parasites:

While Lydella thompsoni and Pseudoperichaeta nigrolineata both are known to parasitize other hosts, Macrocentrus cingulum is primarily associated with Ostrinia. Certain parasites such as Trichogramma brassicae are also used for biological control.[7]

Defense mechanisms

The adzuki bean borer is able to emit ultrasonic pulses at 40 kHz. This can be used in the context of mating, but it can also be used to fend off predators that use ultrasound as a locating mechanism. The adzuki bean borer generates these pulses and flies erratically to confuse and escape predation, specifically from bats.

Parental care

Oviposition

The life cycle of O. scapulalis begins during oviposition. Oviposition behavior has been found to be influenced by oviposition-deterring pheromones (ODPs), also known as host-marking pheromones (MPs), that emanate from egg masses laid by other conspecific females. A female that is ready to oviposit tends to reject hosts that are marked with MPs to favor unmarked hosts.[8]

Life history

Sex ratio distorters

Multiple studies have shown that there is a significant amount of sex ratio distortion that occurs in O. scapulalis. There are predicted to be two mechanisms of sex ratio distortion in this moth. One involves the bacteria Wolbachia (SRw+ trait) and another does not (SRw– trait). These traits may have been inherited from a common ancestor between O. furnicalis and O. scapulalis. The physiological reason as to why these traits induce a female biased sex ratio is unknown. It is suggested that the trait appearance is due to feminization, male killing at the larval stage, or meiotic drive.[9]

Genetics

Subspecies

O. scapulalis is one of eight Ostrinia species that are found in Japan. There is an unusually low level of divergence between the adzuki bean borer and the other seven Ostrinia species. Specifically, O. orientalis and O. nubilalis have a low level of divergence from O. scapulalis. However, the adzuki bean borer is morphologically distinct from the other two. A recent study showed that there are major QTLs (quantitative trait loci) that are associated with the mating isolation between O. nubilalis and O. scapulalis. Specifically, the QTLs associated with pheromone characteristics were present on distinct linkage groups.[10] Additional studies are required to target other aspects of the moths' genetic architectures which may explain their reproductive isolation.

Other genetic differences may serve as the basis for other behavioral differences between the moths, such as the fact that O. scapulalis, a mugwort-race moth, emerges from the pupa 10 days earlier than maize-race moths.[11]

Mating

Mate searching behavior

In most species, females are viewed as the more choosy sex with regards to the attributes of a given male due to a larger investment in a single gamete (the ova) by the female. However, evidence shows that O. scapulalis demonstrates behavior that would indicate the opposite being true. Females may pursue males (using species-specific pheromones) and males vary their investment in females of varying quality due to a significant cost of copulation to the male. This cost includes activities such as the production of sperm, territorial guarding, and parental care. Males were found to invest less in females that were older, smaller, or water deprived, indicating that the adzuki bean borer does change its reproductive investment due to the quality of the mate.

This alteration in reproductive investment also changes with respect to the age of the males. More modulation occurs with older males, demonstrating that mate-searching behavior is influenced by female condition and male age.[12] While older males were found to have higher rates of mating success than younger males, this was merely found to be due to a higher frequency of courtship and not reflective of female preference.

Female/male interactions

Female pheremones

Recently, gas chromatography has been used in order to identify the female sex chromosomes of O. scapulalis. The pheromone cocktail has been identified as a combination of the following compounds: (Z)-11-tetradecenyl acetate (Z11–14:OAc) and (E)-11-tetradecenyl acetate (E11–14:OAc) in a ratio of 100:3. In any single sex pheromone gland of the female moth, there is approximately 6.6 ng of Z11–14: OAc and 2.4 ng of E11–14:OAc present on average though it varies significantly.[13] It has been shown that variations in the ratio of one chemical to the other is largely influenced by genetic factors. Wind tunnel bioassays have shown that the binary blend of the two pheromones impact male behavior in the same way that a virgin female does, thus linking male behavior to the pheromones released by virgin females.[14]

Male ultrasound courtship

The male adzuki bean borer is primarily known to produce ultrasounds during courtship. This helps with courtship since the ultrasound renders the female motionless making copulation easier. These emitted pulses continue for an extended period time at a frequency of 40 kHz. However, the amplitude of this modulation is significantly altered between different populations which has been especially correlated to the surrounding geography of the population.[15]

Other courtship behavior

Outside of using ultrasound, there are other courtship behaviors observed. The male adzuki bean borer generally approaches from the rear of the female. As it does so, he fans his wings to appear larger. The male then vibrates the raised wings and extends his genital claspers. His abdomen is also extended at the targeted female. If the display is successful, the female accepts the male. If the display is not successful, the female may walk or fly away.

Nuptial gifts

The male adzuki bean borer provides nuptial gifts to the female in the form of proteins, carbohydrates, minerals, and sugars that are included in the spermatophore. These nuptial gifts are known to significantly improve the female's reproductive output. For example, the protein is thought to help with egg production. The resources that are required of the male to do this generally are derived from larval sources. This proves to be at a substantial cost to the male. Since there is a trade off between investment in current reproduction and future reproduction, more investment in reproduction should be made towards the end of the moth's lifespan. As this idea predicts, older males were found to produce significantly larger spermatophores than younger males, thus indicating a greater reproductive effort.[16] In contrast, neither female fecundity nor longevity and longevity was affected by age.

Multiple mating

Polygyny is common in the adzuki bean borer. Males of the species mate multiply and are polygynous although the females of the species mate only once and are monandrous. Males follow the many traces of female pheromones and land close to females before performing a courtship ritual and mating (transferring spermatophores to the female). This results in the majority of parental care being provided by the female of the species since male desertion is common.

Physiology

Hearing

Sound generation

O. scapulalis is able to produce ultrasonic sounds. The moth does so by rubbing the rough scales of its wings against other rough scales that are found in the midsection of its thorax. This action is key to producing sounds at various frequencies depending on how fast or slow the moth takes this action. The average frequency of sound generated is 40 kHz.

Hearing organs

These moths have tympanal ears sensitive to ultrasound. Tympanal organs consist of a chordotonal organ wrapped in tracheal epithelial tissue. The tympanum is a thin piece of transparent tissue that vibrates in response to ultrasonic sound.[17] The tympanal organ is tuned to the sounds that bat calls make. Additionally, this kind of hearing is less prevalent in bat free areas. This suggests that the ears of these moths have evolved to fend off insectivores including bats that emit ultrasonic sounds.

Olfaction

Olfaction is primarily observed as a key factor in males. This is because males must be able to distinguish the female pheromones of its own species from those of other similar species. Male odorant receptors consist of olfactory sensilla.[18] These sensilla are small sensory organs that may protrude or lie under the cuticle of the moth. In the adzuki bean borer, they are specifically sensitive to pheromones.[19]

Diapause

Diapause is considered as a delay in animal development due to multiple environmental factors. O. scapulalis is known to partake in this behavior. The larvae of this species diapause throughout winter in the upper portion of the stem of their host plant. The moth's main host plant in which they diapause is the mugwort although they also are found in the maize and hop stems. The reason for the preference for the location of diapause is the identity of parasitoids found in both. Their prevalences differ between maize and mugwort resulting in differing benefits during diapause.[20]

Notes and References

  1. Book: Proceedings of the 10th International Symposium on Insect-Plant Relationships. Ishikawa. Yukio. Takanashi. Takuma. Kim. Choong-gon. Hoshizaki. Sugihiko. Tatsuki. Sadahiro. Huang. Yongping. 1999. Springer, Dordrecht. 9789048152476. Series Entomologica. 237–244 . 10.1007/978-94-017-1890-5_30.
  2. Web site: Genus Ostrinia . BugGuide.Net. 2017-10-24.
  3. http://rspb.royalsocietypublishing.org/content/277/1694/2703.full Divergence in behaviour between the European corn borer, Ostrinia nubilalis, and its sibling species Ostrinia scapulalis: adaptation to human harvesting?
  4. http://www.prodinra.inra.fr/prodinra/pinra/data/2008/05/PROD20081ae42803_20080523082002811.pdf Reconsidering the taxonomy of several Ostrinia species in the light of reproductive isolation: a tale for Ernst Mayr
  5. Fujii. Y.. Kageyama. D.. Hoshizaki. S.. Ishikawa. H. . Sasaki . T. . April 22, 2001 . Transfection of Wolbachia in Lepidoptera: The feminizer of the adzuki bean borer Ostrinia scapulalis causes male killing in the Mediterranean flour moth Ephestia kuehniella . Proceedings of the Royal Society of London B: Biological Sciences . 268. 1469. 855–859. 10.1098/rspb.2001.1593. 0962-8452. 11345332 . 1088680.
  6. August 22, 2000 . Moth hearing in response to bat echolocation calls manipulated independently in time and frequency. Proceedings of the Royal Society of London B: Biological Sciences . 267. 1453. 1627–1632. 10.1098/rspb.2000.1188. 0962-8452. 11467425. 1690724 . Jones . G . Waters . DA.
  7. Pélissié. B.. Ponsard. S.. Tokarev. Y. S.. Audiot. P.. Pélissier. C.. Sabatier. R.. Meusnier. S. . Chaufaux . J. . Delos. M.. February 1, 2010 . Did the introduction of maize into Europe provide enemy-free space to Ostrinia nubilalis? Parasitism differences between two sibling species of the genus Ostrinia . Journal of Evolutionary Biology . 23. 2. 350–361. 10.1111/j.1420-9101.2009.01903.x. 20002249. 163108. 1420-9101.
  8. Li. Guoqing. Ishikawa. Yukio. June 1, 2005 . Oviposition deterrents from the egg masses of the adzuki bean borer, Ostrinia scapulalis and Asian corn borer, O. furnacalis . Entomologia Experimentalis et Applicata . 115. 3. 401–407. 10.1111/j.1570-7458.2005.00282.x. 85326500. 1570-7458.
  9. Kageyama. Daisuke. Nishimura. Gen. Hoshizaki. Sugihiko. Ishikawa. Yukio. 2003-12-01. Two kinds of sex ratio distorters in a moth, Ostrinia scapulalis . Genome. 46. 6. 974–982. 10.1139/g03-083. 14663516. 0831-2796.
  10. Streiff. Réjane. Courtois. Brigitte. Meusnier. Serge. Bourguet. Denis . April 2014. Genetic mapping of two components of reproductive isolation between two sibling species of moths, Ostrinia nubilalis and O. scapulalis. Heredity . 112. 4. 370–381. 10.1038/hdy.2013.113. 24220089. 0018-067X. 3966120.
  11. Thomas. Yan. Bethenod. Marie-Thérèse. Pelozuelo. Laurent. Frérot. Brigitte. Bourguet. Denis. Pitnick . S.. February 1, 2003 . Genetic isolation between two sympatric host-plant races of the European corn borer, Ostrinia nubilalis Hübner. i. sex pheromone, moth emergence timing, and parasitism. Evolution. 57. 2. 261–273. 10.1554/0014-3820(2003)057[0261:GIBTSH]2.0.CO;2. 12683523. 33694680 . 0014-3820.
  12. Win. Aye T.. Kojima. Wataru. Ishikawa. Yukio. May 1, 2015 . Female Condition-dependent Allocation of Nuptial Gifts by Males in the Moth Ostrinia scapulalis (Lepidoptera: Crambidae). Annals of the Entomological Society of America. 108. 3. 229–234. 10.1093/aesa/sav010. 84156371. 0013-8746. free.
  13. Takanashi. Takuma. Huang. Yongping. Takahasi. K. Ryo. Hoshizaki. Sugihiko. Tatsuki. Sadahiro. Ishikawa. Yukio. January 1, 2005 . Genetic analysis and population survey of sex pheromone variation in the adzuki bean borer moth, Ostrinia scapulalis . Biological Journal of the Linnean Society . 84. 1. 143–160. 10.1111/j.1095-8312.2005.00421.x. 0024-4066. free.
  14. Huang. Yongping. Tatsuki. Sadahiro. Kim. Choong-Gon. Hoshizaki. Sugihiko. Yoshiyasu. Yutaka. Honda. Hiroshi. Ishikawa. Yukio. Identification of Sex Pheromone of Adzuki Bean Borer, Ostrinia scapulalis . Journal of Chemical Ecology . December 1997. 23. 12. 2791–2802. 10.1023/A:1022567111508. 40841708.
  15. Takanashi. Takuma. Nakano. Ryo. Surlykke. Annemarie. Tatsuta . Haruki. Tabata. Jun. Ishikawa. Yukio. Skals. Niels. October 4, 2010 . Variation in Courtship Ultrasounds of Three Ostrinia Moths with Different Sex Pheromones . PLOS ONE . 5. 10. e13144. 10.1371/journal.pone.0013144. 20957230. 1932-6203. 2949388. free.
  16. Thanda Win. Aye. Kojima. Wataru. Ishikawa. Yukio. April 1, 2013 . Age-Related Male Reproductive Investment in Courtship Display and Nuptial Gifts in a Moth, Ostrinia scapulalis . Ethology . 119 . 4 . 325–334. 10.1111/eth.12069. 1439-0310.
  17. Book: Lepidoptera, moths and butterflies. Volume 2, Morphology, physiology, and development . Kristensen, Niels P.. 978-3110162103. Berlin. 861527633.
  18. Miura. Nami. Nakagawa. Tatsuro. Tatsuki. Sadahiro. Touhara . Kazushige. Ishikawa. Yukio. April 29, 2009 . A male-specific odorant receptor conserved through the evolution of sex pheromones in Ostrinia moth species . International Journal of Biological Sciences . 5. 4. 319–330. 1449-2288. 2677733 . 19421342. 10.7150/ijbs.5.319.
  19. Book: Steinbrecht, Rudolf Alexander. 158–183. 10.1002/9780470514948.ch13. 8894297. Ciba Foundation Symposium 200 - Olfaction in Mosquito-Host Interactions. 200. Novartis Foundation Symposia. 2007. 9780470514948. Structure and Function of Insect Olfactory Sensilla.
  20. Calcagno. Vincent. Bonhomme. Vincent. Thomas. Yan. Singer . Michael C.. Bourguet. Denis. September 7, 2010 . Divergence in behaviour between the European corn borer, Ostrinia nubilalis, and its sibling species Ostrinia scapulalis: adaptation to human harvesting? . Proceedings of the Royal Society of London B: Biological Sciences . 277. 1694. 2703–2709. 10.1098/rspb.2010.0433. 0962-8452. 20410041 . 2982046.