User:Yeapix/sandbox: Difference between revisions
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====Courtship==== |
====Courtship==== |
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[[File:The-Influence-of-Vibratory-Courtship-on-Female-Mating-Behaviour-in-Orb-Web-Spiders-(Argiope-pone.0053057.s003.ogv|thumb|The-Influence-of-Vibratory-Courtship-on-Female-Mating-Behaviour-in-Orb-Web-Spiders-(Argiope-pone.0053057.s003|A male ''Argiope keyserlingi'' engaging in vibratory courtship]] |
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Courtship in ''A. keyserlingi'' takes place on the female's web and mating takes place on a mating thread.<ref name="costsofcourtship">https://www.jstor.org/stable/4602073</ref> Male courtship behaviours are characterized by a series of vibratory signals from the male, including shudders, abdominal wags, and mating thread dances.<ref name="vibrcourtship"/> |
Courtship in ''A. keyserlingi'' takes place on the female's web and mating takes place on a mating thread.<ref name="costsofcourtship">https://www.jstor.org/stable/4602073</ref> Male courtship behaviours are characterized by a series of vibratory signals from the male, including shudders, abdominal wags, and mating thread dances.<ref name="vibrcourtship"/> |
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Below is a breakdown of the courtship process leading into [[Copulation (zoology)|copulation]]:<ref name="vibrcourtship"/> |
Below is a breakdown of the courtship process leading into [[Copulation (zoology)|copulation]]:<ref name="vibrcourtship"/> |
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Revision as of 09:20, 12 October 2024
Mating
Mate choice
In Argiope keyserlingi, mate choice dynamics differ between males and females, influenced by factors such as prior mating experiences and food availability. Virgin males tend to prefer virgin females,[1] while mated males display no discernible preference.[1] Female aggression towards courting males can vary based on the female's level of food satiation, with better-fed females showing more aggression.[1]
Sex pheromones
Female spiders embed contact pheromones into their web silk.[1] Males detect these pheromones through physical contact with the silk[1] to determine if the female has been mated already[1] and gain other information such as species identity and sexual receptivity[1][2]. A. keyserlingi is also known to use airborne pheromones, possibly to signal the female's location to males,[3] but the role of these in male mate choice is not known.[1]
Courtship
Courtship in A. keyserlingi takes place on the female's web and mating takes place on a mating thread.[4] Male courtship behaviours are characterized by a series of vibratory signals from the male, including shudders, abdominal wags, and mating thread dances.[5]
Below is a breakdown of the courtship process leading into copulation:[5]
- The male approaches the female by crawling along the outer threads surrounding the web.
- Once in the web, the male slowly makes his way to the the centre of the web (the hub), where the female is located.
- At the hub, the male ‘tastes’ the female by touching her legs and abdomen with his legs, then passing his legs through his mouth. This may last several minutes to over an hour, occurring in intervals with periods of rest.
- The male cuts a small section of the web above the female and constructs a mating thread, possibly reinforcing it with additional lines of silk.
- Hanging from the mating thread, the male produces vibrations by plucking and bouncing on the thread.
- The female moves onto the mating thread and exposes her genital opening (the epigyne).
- The male 'waggles' and begins copulation.
Shudders have been shown to have a strong influence on the female's time to enter a copulatory position.[5] Higher rates of shuddering correspond to greater female reluctance (higher delay),[5] as high shudder rates compromise the duration and quality of the shudder.[5] However, there is evidence that this reduces their risk of being cannibalised following copulation.[5]
Females may also display 'aggressive pumping' during courtship.[5] Males adjust their courtship behavior based on these signals, with higher rates of female pumping leading to higher delays in the male building the mating thread for copulation.[5]
Courtship behaviour is also affected by the age of both the male and female.[6] Males display longer shudders when courting older females[6] and older males take longer to approach females and perform more shudders.[6]
Sexual cannibalism
Argiope keyserlingi is a sexually cannibalistic species, with females potentially consuming the male after copulation. About 50% of males survive their first mating, but are always consumed following their second mating, resulting in a phenomenon where males never mate more than twice.[1][7] Research also indicates that each pedipalp cannot be used more than once,[7] suggesting males are also physiologically limited to two copulations. Levi suggests that the embolus, found on the pedipalp and involved in sperm transfer[8], may become damaged during copulation, preventing further mating[9].
Cannibalism in A. keyserlingi does not seem to be influenced by the female’s physical condition[10] or serve as a strategy to gain nutrients for egg production.[10][11]. It may function as a form of cryptic female choice,[10] allowing females to influence fertilization outcomes. Females can adjust the timing of cannibalism to limit the copulation duration,[10] and therefore amount of sperm transferred, favoring males with a smaller size.[10]
Despite no direct link to fecundity, females that consume the male will produce eggs with higher nutrient density.[11] Given the differences in nutrient composition between the spider and the egg and the species' sexual size dimorphism, post-copulatory feeding is not the source this energy[11] but instead, the energy is drawn from the female's somatic reserves.[11] Blamires suggests that protein uptake acts as a trigger to draw out the energy from these reserves.[11]
Distribution and habitat
The St Andrew's cross spider can be found mostly in rainforest margins, open forests, and heathlands of eastern Australia.[12] They can also be found in the northern segment of the Northern Territory, in the northern segment of Tasmania, in the western segment of Western Australia, near Tedi River of Papua New Guinea, in the Malakula island of Vanuatu, in all areas of Lord Howe Island.[citation needed] They construct medium-sized webs on low, shrubby vegetation.[12]
Individuals tend to prefer closed habitats, with preferences being determined by foliage density and predator density[13]. They avoid placing their webs within or between trees when there is bird presence[13]. Juveniles are exclusively found in closed habitats, likely to avoid insectivores like birds and lizards and to find more favourable vegetation for building webs.[13] A. keyserlingi may move into open habitats as subadults or adults, possibly due to requiring larger prey to sustain growth.[13]
Web
Web architecture
The web of the orb-weaving spider possesses meandering, bluish-white ribbons consisting of silk that can form either a full or partial cross through the center of the web. The purpose of the crucifix-like stabilimentum has long perplexed biologists, who first thought that the stabilimentum's purpose was to strengthen the web. Other ideas associate it with capturing prey or evading its predators.[12]
The architecture of the web is influenced by several factors, including the availability of space, air temperature, and prey abundance.[13] A. keyserlingi also adjusts the size and design of their webs depending on their feeding history. Food-deprived spiders invest more energy in web-building by producing more silk to increase their chances of catching prey. They tend to construct larger webs with a denser spiral arrangement,[14] presumably to increase the likelihood of prey capture.[15] In contrast, food-satiated spiders build smaller webs with larger mesh sizes,[14] which might help reduce exposure to predators[16] and conserve energy for reproduction.[17]
While the design of the stabilimentum is independent of the web's overall arrangement,[13] it is affected by factors such as prey populations,[13] light intensity, and temperature.[18][19] Spiders also modify their web decoration depending on food availability. Specifically, when food is more scarce, they reduce the number of silk bands (decorations) and when prey is plentiful, they increase the number of bands.[18]
Prey capture
The stabilimentum in the web of Argiope keyserlingi appears to function as a prey attractant.[20] One feature of the stabilimentum is that it effectively reflects ultraviolet light, making it attractive to flying insects. Research suggests that the stabilimentum uses UV light and/or blue light to exploit a visual bias in insects,[20][21] as most insect receptors are sensitive to both blue and UV light,[22] and many prey species of A. keyserlingi, including bees and flies, are attracted to UV light.[22]
However, the design of the stabilimentum also makes the web and the spider more visible to diurnal predators, such as birds and mantids.[13] The shape of the decoration can vary among a complete cross, a partial cross with one to three arms, or occasionally an absence of decoration. This variability can induce web-recognition problems for predators, potentially providing a form of camouflage or distraction.[12]
Once potential prey land on the web, the spider's attack strategy varies depending on the prey type. For example, A. keyserlingi wraps larger prey like bees and blowflies in silk before feeding, whereas it does not wrap smaller prey like Drosophila.[14]
Backup stuff
Old web section
The section with my stuff but not split into sections:
Its web possesses meandering, bluish-white ribbons consisting of silk that can form either a full or partial cross through the center of the web. The purpose of the crucifix-like stabilimentum has long perplexed biologists, who first thought that the stabilimentum's purpose is to strengthen the web. Other ideas associate it with capturing prey or evading its predators.[12] The web architecture is affected by availability of space, the air temperature and prey abundance.[13] The web decoration design is independent of the web's arrangement,[13] but is influenced by prey populations,[13] light intensity and temperature.[18][19] These decorations appear to function as a prey attractant.[20] One feature of the stabilimentum is that it effectively reflects ultraviolet light, making it attractive to flying insects. Research suggests that the stabilimentum uses UV light and/or blue light to exploit a visual bias in insects,[20][23] as most insect receptors are sensitive to both blue and UV light[22] and many A. keyserlingi prey species including bees and flies are attracted to UV light.[22] The design of the stabilimentum makes the web and the spider obvious to diurnal predators, especially birds and mantids. The shape of this decoration can vary from three shapes, a complete cross, a partial cross possessing one to three arms, or occasionally an absence of a decoration. This variability can induce web-recognition problems for predators. [12]
[1]
[10]
[5]
[7]
[11]
[2]
[13]
- ^ a b c d e f g h i j Gaskett, A., Herberstein, M., Downes, B., & Elgar, M. (2004). Changes in male mate choice in a sexually cannibalistic orb-web spider (Araneae: Araneidae). Behaviour, 141(10), 1197-1210. https://www.jstor.org/stable/4536195
- ^ a b Jason, Q. D., & Mark, A. (2017). Variation in the web-based chemical cues of Argiope keyserlingi. Journal of insect physiology. https://www.sciencedirect.com/science/article/pii/S0022191017300914
- ^ Krafft, B. (1982). The significance and complexity of communication in spiders. - In: Spider communication: Mechanisms and ecological significance (P.N. Witt & J.S
- ^ https://www.jstor.org/stable/4602073
- ^ a b c d e f g h i W ignall, A. E., & Herberstein, M. E. (1878). The influence of vibratory courtship on female mating behaviour in orb-web spiders. Argiope keyserlingi. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0053057 Cite error: The named reference "vibrcourtship" was defined multiple times with different content (see the help page).
- ^ a b c https://link.springer.com/article/10.1007/s00114-017-1527-8#Sec5
- ^ a b c Herberstein, M. E., Gaskett, A. C., Schneider, J. M., Vella, N. G. F., & Elgar, M. A. (2005). Limits to male copulation frequency: sexual cannibalism and sterility in St Andrew's Cross spiders (Araneae, Araneidae). Ethology, 111(11), 1050-1061. https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1439-0310.2005.01114.x
- ^ Foellmer, Matthias W. "Broken genitals function as mating plugs and affect sex ratios in the orb-web spider Argiope aurantia." (2008). https://www.researchgate.net/figure/A-Ventral-view-of-male-pedipalps-The-embolus-cap-of-the-male-s-left-palp-right-in_fig1_279901752
- ^ Levi, H. W. (1975). Mating behavior and presence of embolus cap in male Araneidae. In Proceedings of the 6th International Arachnological Congress (Vol. 1974, pp. 49-50). Amsterdam.
- ^ a b c d e f Elgar, M. A., Schneider, J. M., & Herberstein, M. E. (2000). Female control of paternity in the sexually cannibalistic spider Argiope keyserlingi. Proceedings of the Royal Society of London. Series B: Biological Sciences, 267(1460), 2439-2443. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1690835/
- ^ a b c d e f Blamires, Sean J. (June 2011). "Nutritional implications for sexual cannibalism in a sexually dimorphic orb web spider". Austral Ecology. 36 (4): 389–394. Bibcode:2011AusEc..36..389B. doi:10.1111/j.1442-9993.2010.02161.x. Cite error: The named reference "sexcan2nutr" was defined multiple times with different content (see the help page).
- ^ a b c d e f Cite error: The named reference
:0was invoked but never defined (see the help page). - ^ a b c d e f g h i j k l Blamires, S. J., Thompson, M. B., & Hochuli, D. F. (2007). Habitat selection and web plasticity by the orb spider Argiope keyserlingi (Argiopidae): do they compromise foraging success for predator avoidance?. Austral Ecology, 32(5), 551-563. https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1442-9993.2007.01727.x
- ^ a b c Herberstein, M. E., Abernethy, K. E., Backhouse, K., Bradford, H., De Crespigny, F. E., Luckock, P. R., & Elgar, M. A. (1998). The effect of feeding history on prey capture behaviour in the orbweb spider Argiope keyserlingi Karsch (Araneae: Araneidae). Ethology, 104(7), 565-571.
- ^ Chacon, P. & Eberhard, W. G . 1980: Factors affecting numbers and kinds of prey caught in artificial of Argiopr keyserlingi (Araneae: Araneidae). J. Arachnol. 21,91-106. spider webs, with considerations of how orb webs trap prey. Bull. Br. Arachnol. SOC.5,29-38.
- ^ Pasquet, A. 1984: Predatory-site selection and adaptation of the trap in four species of orb-weaving spiders. Biol. Behav. 9, 3-19
- ^ Sherman, P. 1994: The orb web: an energetic and behavioural estimator of a spider’s dynamic foraging and reproductive strategies. Anim. Behav. 48, 19-34.
- ^ a b c Herberstein, M. E., & Fleisch, A. F. (2003). Effect of abiotic factors on the foraging strategy of the orb‐web spider Argiope keyserlingi (Araneae: Araneidae). Austral Ecology, 28(6), 622-628. Cite error: The named reference "foragingstrat" was defined multiple times with different content (see the help page).
- ^ a b Bruce, M. J., Herberstein, M. E., & Elgar, M. A. (2001). Signalling conflict between prey and predator attraction. Journal of Evolutionary Biology, 14(5), 786-794.
- ^ a b c d Blamires, S. J., Hochuli, D. F., & Thompson, M. B. (2008). Why cross the web: decoration spectral properties and prey capture in an orb spider (Argiope keyserlingi) web. Biological Journal of the Linnean Society, 94(2), 221-229.
- ^ Li, D., Lim, M. L., Seah, W. K., & Tay, S. L. (2004). Prey attraction as a possible function of discoid stabilimenta of juvenile orb-spinning spiders. Animal Behaviour, 68(3), 629-635.
- ^ a b c d Briscoe, A. D., & Chittka, L. (2001). The evolution of color vision in insects. Annual Review of Entomology, 46(1), 471-510. 10.1146/annurev.ento.46.1.471 Cite error: The named reference "colorvision" was defined multiple times with different content (see the help page).
- ^ Li, D., Lim, M. L., Seah, W. K., & Tay, S. L. (2004). Prey attraction as a possible function of discoid stabilimenta of juvenile orb-spinning spiders. Animal Behaviour, 68(3), 629-635.