Biology:Rivacindela hudsoni
| Rivacindela hudsoni | |
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| R. hudsoni sighting in South Australia | |
Scientific classification 
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| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Arthropoda |
| Class: | Insecta |
| Order: | Coleoptera |
| Family: | Cicindelidae |
| Genus: | Rivacindela |
| Species: | R. hudsoni
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| Binomial name | |
| Rivacindela hudsoni (Sumlin, 1997)
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Rivacindela hudsoni is an Australian species of the family Cicindelinae or "tiger beetle" and is the fastest-running known insect.[1] The genus Rivacindela is contentiously treated as a subgenus of the broader Cicindela and are typically found in saline habitats such as dry salt lakes and salt streams and are flightless.[2] The species was discovered in South Australia and described in 1997, with an adult form of approximately 20–21mm in length and a running speed of 2.49m/s, or 120 body lengths per second.[3][2] The comprehensive phylogeny that defines the Rivacindela hudsoni is as follows: Animalia, Arthropoda, Insecta, Coleoptera, Carabidae, Cicindelinae, Rivacindela, Rivacindela hudsoni.[4]
Morphology
Egg
The first life stage of Rivacindela hudsoni is its egg form, inside of which the embryo develops.[5] Although a developmental period is not yet clearly described for this species due to its recent discovery, it can be inferred to be anywhere from 9 to 29 days when following the general trends of the family Cicindelinae.[5]
Larva
Once hatched, the organism is in its larval stage. Here, the Rivacindela hudsoni is white and grub-like with two tagmata (specialised body segments): the head and pronotum.[5] Both of these segments are highly chitinised, meaning there is a strong exoskeleton covering the larva which will be shed in order for the organism's metamorphosis and/or growth to occur.[6] On its lower back, the larva has a pair of large, forward facing hooks, used to anchor the organism to the substrate.[6] Further, it has mandibles for prey capture which originate below its eyes. [5] Not much is known of the pupal stage, as, in the same manner as all members of the Cicindelinae family, this stage of its life is completed entirely underground; it can take anywhere from three to 30 days to metamorphose.[7]
Adult
Like all insects, the Rivacindela hudsoni has three tagmata in its adult form.[3] These segments include the head, abdomen and a patterned thorax onto which six thin, uniramous appendages and two pairs of vestigial wings are attached.[7] The beetle's forewings are hardened to form a protective layer known as the elytra and are fused to the hindwings.[7] The species has two large eyes that together make the head wider than the thorax, underneath which a pair of filiform antennae are attached.[7] Surrounding the mouth is the labrum, onto which sharp projections and maxillae are attached next to a pair of sickle-like mandibles with both compound and simple teeth arranged along its length.[7] The average body length of R. hudsoni was recorded at 20.8mm.[2]
Physiology
Due to the R. hudsoni’s habitat being hot and dry, they rely on high resting metabolic rates to maintain optimal body temperatures at all times.[7] This is important as running speed is positively correlated with body temperature and therefore aids the beetles in prey capture.[7] This, combined with the length ratio of their femur and tibia, and the slender nature of the beetle’s legs is what allows them to run so quickly across substrates.[2]
Feeding
When eating, the R. hudsoni masticates food with their mandibles and pre-oral mill.[7] They utilise their mandibular glands in this process which secrete saliva across their teeth and mandibles.[8] Once the beetle’s meal passes this point, the food must travel through the three sections of the beetle’s digestive system. The first section is the foregut which is constituted by a crop, proventriculus and esophagus.[7] The beetle’s midgut is surrounded by ‘regenerative crypts’ of epithelial cells that are constantly replacing dead cells in this section of the gut. [9] The function of the midgut is to connect the foregut to the hindgut, which consists of the intestine and the rectum.[10]
R. hudsoni, like all tiger beetles, are fluid feeders.[4] This means they cannot consume and digest solids. To prevent this, the beetle’s hypopharyngeal membrane and epipharyngeal flap are covered by setae.[10] These hair-like structures point downwards and act as a filter to prevent any solid parts of the meal from entering the digestive tract.[10] Some studies have indicated that there is a possibility of extra-oral digestion in Cicindelinae, which would mean they regurgitate gut enzymes to break down food further in their mouths before it continues through to the foregut.[4] However, there is currently no complete evidence for this functionality.
Reproduction
The female R. hudsoni has gonads (or reproductive gland) that consist of two ovaries made of 8-30 tubes known as ovarioles.[4] These tubes converge to make two oviducts which in turn combine into a single oviduct.[4] Other parts of this system include the vagina and spermatheca where the sperm is stored within the female.[11] The eighth and ninth sections of a female’s abdomen are combined to form a telescopic ovipositor which she uses to deposit her eggs in a substrate once fertilised.[11]
The male R. hudsoni has both internal and external reproductive organs. The external organ is known as the aedeagus, which is the arthropod form of the penis.[4] On the inner wall of the aedeagus sits the endophallus and inside this is the male’s flagellum which is received by the female’s spermatheca during mating procedures.[11]
Behaviour
Larval hunting
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Once the larvae of the Rivacindela hudsoni hatch from the egg, they dig and reside in tunnels, anchoring themselves to the substrate via the pair of hooks on its back.[6] It is here that they move through their three larval developmental stages known as instars.[7] At the end of each instar, the organism moults its chitinized outer layer in order to grow.[7] These stages of growth are facilitated by the energy gained through the larvae's sedentary predatory behaviour.[7]
At this stage of its life, the Rivacindela hudsoni hunts using an ambush method of attack as it lies in wait for its arthropod prey to move in range of its mandibles.[6] Once the prey is in range, the larvae extends its body out of the burrow, grabs the organism with its mandibles and drags it back into the tunnel where it proceeds to kill and eat it.[7] At the end of the third instar, the larvae remain in a chamber situated in the depths of the burrow in which they pupate after blocking the tunnel's entrance.[5] Once the metamorphosis is complete, the adults dig out of the ground to begin the next stage of their lives.
Adult hunting
Adult Rivacindela hudsoni are diurnal, meaning they are active during the day with a period of rest and/or inactivity at night.[7] The hunting practises of these predatory flightless beetles are highly specialised due to the shift from bimodal locomotory status to a unimodal locomotory status, meaning the loss of flight and reduction to only running.[2] They have been observed to run in a zig-zag pattern which is closely followed by long, fast straight lines.[1] When running straight, the R. hudsoni were observed to run faster than any other recorded insect at 2.5m/s or 125 body lengths every second.[2] However, it has been observed that at high speeds, tiger beetles experience temporary blindness when chasing prey.[8] This is because the beetle cannot gather enough photons that reflect its prey to form an image of it, resulting in a stop-start mode of hunting made affordable by the its high speeds.[8] As a predator living in dry, saline environments, the R. hudsoni eats almost anything it can capture such as other beetles, caterpillars and ants while also taking advantage of other, larger meals as scavengers. Their feeding practises are not just to consume their prey whole. The beetles will slowly break down the prey’s cuticle to gain access to the soft, internal parts of its body.[10]
Thermoregulation
In the high temperatures of the Australian desert, the adult R. hudsoni spends up to 56% of its daily activity regulating its body temperature.[7] The time expended on this is determined by the number of available prey.[12] External tactics of thermoregulation observed include burrowing in cooler, wetter substrates, remaining still in shaded areas or shifting in and out of the shade throughout the day in an attempt to maintain an optimal body temperature of approximately 35°C.[12][6] Internally, the family Cicindelinae approach thermoregulation convectively as they "stilt" on their legs to optimise the positioning of their body above a higher heat boundary.[7] Concurrently, they orient their bodies in the direction of the sun to reduce the surface area of their body that is exposed to direct heat.[7]
Larvae use their burrow turrets as a thermoregulatory technique. Being only 2cm above the ground's surface to rise above the heat boundary in the same fashion as the adult's ‘stilt’ allows the larvae to be continuously active throughout the day.[7] In extreme cases such as high heat, the larvae will completely block their burrow and retreat to its depths.[7]
Reproduction
When a male R. hudsoni desires to mate, he will search for and chase a female displaying foraging behaviours such as intermittent sprints.[7] In the chase, males are often seen mounting both males and females of any species in an attempt to copulate.[7] Once he has sufficiently decreased the distance between himself and his target, he will leap onto the female's back, grabbing her thorax with his mandibles and her wings with his front two sets of legs.[13] This mating strategy is known as amplexus.[13] At this point, the female has the opportunity to exercise her choice over her mate as in most observed cases, the mounted female will attempt to remove the male by jumping, bucking and running around.[7] This behaviour is believed to be used for discerning the agility and strength of the male, allowing the female to mate with only those who rank high in those categories.[7]
After copulation, the male will maintain his mounted position for a longer than necessary length of time to deter or completely inhibit another male from mating with the same female.[13] It has been shown that for some species of Cicindelinae, actual copulation accounted for only 2.3% of the time spent in the amplexus.[7] This allows him to ensure his sperm will be the one to fertilise the female's egg. Studies have shown that the length of this amplexus is a determining factor of the distance between the mating site and oviposition.[13]
When the female is ready, she will lay her eggs individually in a carefully chosen substrate. The hairs on her thorax help her to determine the eligibility of the soil as a burrow for her eggs as they allow her to detect its composition and quality.[14] The female R. hudsoni's decision (as with all members of the Cicindelinae family) is dependent on a number of factors: soil temperature, soil type, salinity, moisture, and vegetation cover.[11][15] She expends the energy to do this as the burrow she lays her egg in will be used by the resultant larvae for all stages of its development, and thus her choice in oviposition will be a determining factor in the larvae's survival.[7] Once she has found a suitable spot, she uses her ovipositor which extends from her thorax to dig burrows in which she deposits an egg before refilling it with soil.[7]
Faunistics
Saline bodies of water are the most common habitat for Australian tiger beetles as they form a sort of haven for the insects which are surrounded by vast, arid deserts that cannot energetically support them.[1] Rivacindela as a genus is endemic to the Australian Eyrean region and its isolated evolution in this area gave the species its propensity for high speeds which have been shown to increase at higher surface temperatures.[16] The beetle was first recorded at 31°05'40.0"S 135°19'30.0"E by Sumlin in 1997.[3]
Sources
References
- ↑ 1.0 1.1 1.2 Sumlin, W. D. (1997). Studies on the Australian Cicindelidae XII: additions to Megacephala, Nickerlea and Cicindela with notes (Coleoptera). Bull. Worldwide Res, 4(4), 1–56
- ↑ 2.0 2.1 2.2 2.3 2.4 2.5 Kamoun, Sophien; Hogenhout, Saskia A. (1996). "Flightlessness and Rapid Terrestrial Locomotion in Tiger Beetles of the Cicindela L. Subgenus Rivacindela van Nidek from Saline Habitats of Australia (Coleoptera: Cicindelidae)". The Coleopterists Bulletin 50 (3): 221–230. ISSN 0010-065X. https://www.jstor.org/stable/4009161.
- ↑ 3.0 3.1 3.2 "Cicindela (Rivacindela) hudsoni Sumlin, 1997". https://bie.ala.org.au/species/urn:lsid:biodiversity.org.au:afd.taxon:4f6edc68-22c0-4d2a-a495-de92bcc60945. Retrieved 19 September 2020.
- ↑ 4.0 4.1 4.2 4.3 4.4 4.5 Gough, H. M., Duran, D. P., Kawahara, A. Y., & Toussaint, E. F. A. (2018). A comprehensive molecular phylogeny of tiger beetles (Coleoptera, Carabidae, Cicindelinae). Systematic Entomology, 44(2), 305–321
- ↑ 5.0 5.1 5.2 5.3 5.4 Brust, M. L., Hoback, W. W., & Knisley, C. B. (2005). Biology, Habitat Preference, and Larval Description of Cicindela cursitans Leconte (Coleoptera: Carabidae: Cicindelinae). The Coleopterists Bulletin, 59(3), 379–390
- ↑ 6.0 6.1 6.2 6.3 6.4 Pearson, D., & Volger, A. (2001). Tiger Beetles: The Evolution, Ecology, and Diversity of the Cicindelids. Cornell University Press, Ithaca
- ↑ 7.00 7.01 7.02 7.03 7.04 7.05 7.06 7.07 7.08 7.09 7.10 7.11 7.12 7.13 7.14 7.15 7.16 7.17 7.18 7.19 7.20 7.21 7.22 7.23 7.24 7.25 Pearson, D. L. (1988). Biology of Tiger Beetles. Annual Review of Entomology, 33(1), 123–147
- ↑ 8.0 8.1 8.2 Freidlander, B. (1998). When tiger beetles chase prey at high speeds they go blind temporarily, Cornell entomologists learn. Cornell Chronicle, Cornell University Press, Ithaca.
- ↑ Nardi, J. B., & Bee, C. M. (2012). Regenerative cells and the architecture of beetle midgut epithelia. Journal of Morphology, 273(9), 1010–1020
- ↑ 10.0 10.1 10.2 10.3 EVANS, M. E. G. (2009). The feeding method of Cicindela (Coleoptera: Cicindelidae). Proceedings of the Royal Entomological Society of London. Series A, General Entomology, 40(4-6), 61–66
- ↑ 11.0 11.1 11.2 11.3 Choudhuri, J. C. B. (1958). Experimental Studies on the Choice of Oviposition Sites by Two Species of Chorthippus (Orthoptera: Acrididae). The Journal of Animal Ecology, 27(2), 201
- ↑ 12.0 12.1 Dreisig, H. (1979). Daily activity, thermoregulation and water loss in the tiger beetle Cicindela hybrida. Oecologia, 44(3), 376–389
- ↑ 13.0 13.1 13.2 13.3 Shivashankar, T., & Pearson, D. L. (1994). A Comparison of Mate Guarding Among Five Syntopic Tiger Beetle Species from Peninsular India (Coleoptera: Cicindelidae). Biotropica, 26(4), 436
- ↑ Cornelisse, T. M., & Hafernik, J. E. (2009). Effects of soil characteristics and human disturbance on tiger beetle oviposition. Ecological Entomology, 34(4), 495–503
- ↑ Hoback, W. W., Golick, D. A., Svatos, T. M., Spomer, S. M., & Higley, L. G. (2000). Salinity and shade preferences result in ovipositional differences between sympatric tiger beetle species. Ecological Entomology, 25(2), 180–187
- ↑ Nachtigall, W. (1996). Locomotory Behaviour in a Population of the Tiger Beetle Species Cicindela hybrida on a Small, Hot, Sandy Area (Coleoptera: Cicindelidae). Entomologia Generalis, 20(4), 241–248
Wikidata ☰ Q14281564 entry
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