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Adult female zygiella x-notata
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Subphylum: Chelicerata
Class: Arachnida
Order: Araneae
Infraorder: Araneomorphae
Family: Araneidae
Genus: Zygiella
Species:
Z. x-notata
Binomial name
Zygiella x-notata
(Clerck, 1757)

Zygiella x-notata

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Zygiella x-notata, sometimes known as the missing sector orb weaver or the silver-sided sector spider,[1][2] is a spider species in the family Araneidae. They are solitary spiders, residing in daily-spun orb webs. Z. x-notata are a member of the genus Zygiella, the orb-weaving spiders. The adult female is easily recognized by the characteristic leaf-like mark on her posterior opisthosoma, caudal to the yellow-brown cephalothorax. 

The webs of Zygiella x-notata are known for their characteristic missing sector, lending to the common name of spider as the "missing sector orb weaver". This species is distributed widely around the world, primarily inhabiting areas of human occupancy in northern Europe.

Common prey include flying insects and other small insects. These get caught in the sticky spiral hub of the spider's orb web. Capture of prey occurs as the foreleg of Z. x-notata detects vibrations on the signal strand that connects the spider's retreat to the prey-capturing hub of the web. Webs are rebuilt daily by juvenile Zygiella x-notata and are renewed as needed by adult females. After sexual maturity, males discontinue web production in search of fecund females. After reproduction during the summer months, males die. Females produce an egg sac in late autumn and juveniles emerge in late spring. After several moults, juvenile females are ready to reproduce.

Description

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The adult female Zygiella x-notata have a body size of 5-11mm in length, while adult males have a body size up to 7mm.[3] In adult females, the carapace width is 1.5 mm. [4] The prosoma is yellow-brown, with a leaf-like mark on the opisthosoma. The abdomen has a silvery sheen due to guanine crystals below the skin.[2][3] Adult females are recognizable from their grey banded legs and pattern of dark grey waves on their dorsal side.[3] Adult males are smaller than adult females, and display a dark dorsal exterior with dark brown legs and cephalothorax. The male abdomen is smaller and less marked with a shiny cream color than the female abdomen.[5] In moderate climate, adults appear from July to October, sometimes even into December. In warmer regions, Z. x-notata are active all year.

The specific name x-notata is Latin for "x-shaped mark".[2]

Population Structure, Speciation, and Phylogeny

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Common names

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The common name missing sector orb weaver comes from the distinctive structure of Z. x-notata's web. Characteristically, this species is known to build a web with a missing sector containing solely a signal thread in the top half [6] The species has also been referred to commonly as the silver-sided sector spider.[3]

Subspecies and distribution

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  • Zygiella x-notata (Clerck, 1757) — Holarctic, Neotropical
  • Zygiella x-notata chelata (Franganillo, 1909) — Portugal
  • Zygiella x-notata percechelata (Franganillo, 1909) — Portugal

Habitat and Distribution

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Habitat

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Zygiella x-notata are common in areas inhabited by humans, including on boats and docks.[7][6] They are also found on urban vegetation like bushes, shrubs, and trees, as well as in more pristine environments.[7][8] Females construct an orb-web preferentially near human settlements, and this is where they live out their adult lives. [4] If their webs are disturbed, they retreat inside to stay safe from predators.[citation needed]

Distribution

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This species of orb-weaving spider inhabits areas of northern Europe and is invasive in some of the coastal areas of the Americas. They can also be found in some other locations around the world.[4] Zygiella x-notata is abundant in the west Palearctic region, and is also distributed across the Holarctic.[8][9]

Aggregations

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As urban colonizers, Zygiella x-notata often aggregate around human settlements. Ideal locations for web building include constructions such as walls, fences, and window frames, as these provide sufficient anchors for urban web development. Because these spaces are in high demand as optimal web building sites, they are often inhabited by multiple individual Zygiella x-notata spiders. Despite their characterization as solitary spiders, aggregations of up to 25 individual spiders per square meter have been observed on or near human constructions.[8]

Diet

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Juvenile feeding

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Juvenile zygiella x-notata characteristically build a new web each day until they read adulthood. [6]

Adult feeding

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Zygiella x-notata spin orb-webs which are used to capture and incapacitate prey. Rather than building a new web every day as juveniles do, adult female Z. x-notata build an initial web and renew it nearly every day as needed. [6] The female spider will sit in her retreat on the web, which is attached to a signal strand in the characteristic missing orb-web sector.[10][11] When prey are caught in the web, the female can thus detect its presence through vibrations in the signal strand. As these vibrations are detected, she climbs down the silken signal thread to the hub of the web where the prey has been trapped. [11] Prey type is dependent on the spider's native habitat and geographical location, but usually consists of flying prey such as Diptera.[4] Male Zygiella x-notata feed similarly to females as juveniles, but once they reach adulthood they no longer build webs in order to capture prey, rather focusing on successful reproduction. [12]

Predatory feeding behavior

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There are four stages of predatory behavior in Zygiella x-notata as described by Venner et al: first, the "waiting phase" occurs first, in which the spider is immobile in its retreat in the top corner of the web. A foreleg rests on the signal thread that spans from the spider's retreat to the hub of the web. Second is a "detection phase", where after prey has come into contact with the web, the spider moves toward it down the signal thread. Third is a "capture phase" in which the prey is incapacitated by the spider and subsequently moved back toward the retreat. Zygiella x-notata has been observed to bite and wrap its prey with silk during this phase as a means of incapacitation, prior to transportation to the retreat.[4] Finally, there is an "ingestion phase" where the spider eats the prey in its retreat and removes the prey's remains from the web. [10]

Vibratory signals in prey capture

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Zygiella x-notata spiders have the capacity to detect vibratory signals in both the air and via web vibrations. When building an orb-web to initiate the prey-capture behavior, female spiders can detect the presence of prey through air-borne vibrations. This stimulates web-spinning behaviors, even prior to prey capture.[13] Once vibratory signals are detected, Zygiella engages in several behavioral response patterns: 1) at least one leg is slightly moved; 2) the spider's front legs are repeatedly lifted off the signal thread; or 3) the spider walks out of its retreat and scurries down the signal thread to the hub of the web. In a characteristic and repeatable series of events, the spider exits the hub, rushing in the direction of the source of the initial vibratory signal. Once the spider has found the vibration's source, it touches the prey with its first pair of legs, grabs the prey using its first three pairs of legs, and bites it. Consequently, if no further vibrations (either threadborne or airborne) are detected once the spider has entered the hub of the web, Z. x-notata will actively vibrate the web to detect motionless dead prey or dirt particles hanging in the web. This "web-jerking" procedure, occurring through flexes in the spider's forelegs in contact with the web radii, is repeated until the spider finds a prey item in the web by following the anomalous vibration.[14]

Web

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Web type

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Zygiella x-notata spiders build an orb web in areas frequently occupied by humans. [10][6][7] The orb web has a spiral-like appearance with radii converging to a central hub. [10] During the early construction of the web, a nonsticky spiral is formed to later be replaced with a sticky spiral. Characteristic of the species, a "missing sector" is often present in the top half of the web that is crossed by a signal thread connecting the hub of the web to the spider's retreat. [6][10] The signal thread is variable in length, reaching anywhere from 4cm to 50cm long.[14]

Affects of prey on web-building

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The predatory feeding behavior of the missing sector orb weaver influences changes in web construction. Web building was found to be stimulated by the presence of prey, resulting in spiders in the presence of prey to spin their webs earlier than spiders in the absence of prey.[13] However, web building duration decreased in the presence of prey and thus web sizes were found to be smaller across the sample population. These characteristically smaller webs are spun with narrower web meshing, aiding in the quick capture of prey. Although these webs were smaller than webs built in the absence of prey, they provided a quick method to trap prey. This exemplifies Zygiella x-notata's capacity to sense changes in local prey availability.[13][15] A similar study conducted by Venner et al. found that this species of orb weaving spiders changes its web building behavior in response to new information detected during prey capture.[10] When the spiders experienced the act of capturing and consuming prey, they adapted their web construction and energy expenditure in anticipation of the next capture.

Construction

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Web construction occurs through an observable and repeatable process that becomes more organized with increasingly identical webs as the adult female spider ages. According to Anotaux et al. there are four steps to the process of web construction. First, the spider constructs an outer frame and radial threads. Second, she produces an auxiliary spiral. Third, she builds a sticky capture spiral meant to trap local prey. Finally, she remodels the center of the web - the hub - which connects to the signal thread as a prey detection device for the spider which lay in wait in her retreat.[6]

Longevity

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Juvenile Z. x-notata have been found to rebuild their webs daily in order to catch prey. [6] Web renewal typically occur at the end of the night for both juvenile and adult spiders. [10] Generally, the longevity of Zygiella x-notata webs is approximately one day.

Influence of ageing and experience on web construction

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Multiple studies have shown that the composition and construction frequency of Zygiella x-notata orb webs change with increasing age and experience in the resident female. [10][6][15][4] Anotaux et al. determined that older Z. x-notata invest less silk in the production of their webs as compared to younger spiders in both short- and long-lived varieties. Older adult female spiders were also found to have greater variation in their orb webs than younger adult females, reflecting a decline in locomotor functioning correlated with increased web irregularity in older age. [6] Venner et al. established a correlation between prey capture and ingestion, and web rebuilding practices among adult female Z. x-notata. Spiders who engaged in the four stages of predatory behavior and subsequently rebuilt their webs were found to invest less in the capture area of their newly built web. [10]

Web anomalies

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Spiders of the species Zygiella x-notata consider previous elements of web construction in the building of future webs. This is an imperfect process, susceptible to web building errors. Anomalies in web structure among this species have been found to result from positional modification of a spider on the radial strands of the web. When the spider's fourth leg is oriented peripherally to the web during web building, opposite the hub of the web, anomalies in web construction are common. In this position, the spider cannot detect the correct attachment position of the inner spiral to the next radial thread. Web anomalies are detrimental to spider success, as they can alter the performance of the web, including both prey capture ability and predation avoidance.[9]

Characteristic missing sector

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Zygiella x-notata is known for its flexibility in web building with the missed sector orb webs that are woven by this species. Even though the web construction behaviors are innate, there is a characteristic flexibility in these spiders when they alter their webs according to their advantage and safety. Based on its knowledge of its retreat, Zygiella species typically leave a missing sector especially when creating webs on a door or window frame. Sometimes after building the complete webs, spiders will go back through and fill in the missing sector or they will not fill in a certain sector as per circumstances. The process of creating the missing sector involves switching direction in that region during the spiral or biting through threads to remove spirals in that section after building the full web.[16]

Reproduction and Life Cycle

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Egg sacs

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Egg sacs are used in arachnid species to protect developing spiderlings against predators and parasites. The egg sac provides spiderlings with an adequate embryological microclimate suited to development. It also provides spiderlings with sufficient nutrients to survive through hatching.[17]

Zygiella x-notata is an iteroparous species, incurring multiple reproductive events throughout the course of an individual's lifetime. Females of the species Zygiella x-notata produce egg sacs in late autumn. Spiderlings emerge in mid-to-late spring of the following year.[17]

Structure
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The egg sacs of the species Zygiella x-notata are elliptical in structure. They range from a white to yellow-brown color. The eggs are protected by a series of complex airy structures consisting of sequential layers of silk. These layers of silk enclose and protect the eggs from predators, parasites, and the risks of premature hatching.[17]

The structural composition of Zygiella egg sacs is similar with that of most other spiders belonging to the same family, Araneidae. They are uniform in shape and structure, consisting of an inner basic layer, an intermediary double insulation layer, and an outer layer.[17] These layers are in place to provide the developing spiderlings with protection from harmful external ecosystems and predators.

Mating

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Male choosiness

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Adult male Zygiella x-notata have been found to be choosy for female mates in high competition environments. Bel-Venner et al. show that under conditions of weak intrasexual competition, males pair opportunistically with females, whereas in highly competitive environments, males selectively guard females according to their own competitive ability. [18] This demonstrated a particular size assortative mating behavior in the differential mating preferences of Z. x-notata males, where large males frequently chose to mate with larger, more fecund females, and smaller males chose to mate with smaller females. [18]

Mate guarding

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Premoult females are a vital resource in the reproductive success of male Zygiella x-notata. Prior to copulation, male spiders try to guard a female before her final moult, when she becomes sexually receptive. [12] By guarding the female, a male expects to be his guarded females first copulation after becoming sexually receptive. This provides a significant reproductive benefit to the male, as mate guarding tends to lead to reproductive success.

Bel-Venner & Venner studied the precopulatory mate guarding behavior of Zygiella x-notata. They found mate guarding to be a widespread phenomenon among their population of interest, and observed strong competition between males to guard females with the frequent action of male take-over. [12] As predicted by sexual selection theory, larger males were found to be more successful at guarding females and evicting smaller males from their guarding positions. [12] Although there is an energetic cost to mate-guarding, males who engage in this behavior incur differential reproductive success on the basis of increased body size and competitive ability.

Vibrational courtship

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The orb webs of female Zygiella x-notata spiders hang vertically under high tension conditions as two-dimensional sheets of silk. Male spiders of this species have been found to utilize the high tension of the web's silk threads to send vibrational courtship signals to the resident female.[11] A study conducted by Tarsitano & Kirchner analyzed the vibratory patterns associated with this courtship ritual. Male Z. x-notata were found to produce three types of vibrational courtship signals on the female's web. A periodic "pulling" signal, a "plucking" signal, and a "burping" signal were identified. The "pulling" and "plucking" signals are both performed by the male immediately prior to copulation as a means of arousing the resident female.[11] These signals involve the male using his forelegs to "pull" or "pluck" a segment of silk he previously threaded into the signal strand on the female's web. The third, "burping" signal is produced by the male as he approaches the female in her retreat, and is likely used to warn the female that he is a potential mate, and not prey. [11] This "burping" practice prevents the female from attacking the male as he begins engaging in the "pulling" and "plucking" pre-courtship signaling. The temporal patterning of these vibrational courtship signals enable the female to distinguish between a potential mate and potential prey items in her web.

Social Behavior

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Behavior in urbanized environments

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With a growing human population, many Zygiella x-notata have adapted to living on or near human constructions in urban, suburban, and rural areas. Urban environments provide orb web building spiders, such as Z. x-notata, with sufficient locations in which to build their webs. However, high quality web building sites are coveted by many individuals of both the Zygiella species and others. In urbanized environment, Zygiella x-notata exhibit high within-species aggression. This is in part due to the favorability of diverse, but stable, aggressiveness types in urban dwelling spiders. Aggressiveness may facilitate high density aggregations of spiders, observed to be up to 25 individuals per square meter. However, high aggression rates within a population could prove costly as a result of high incidences of injury and death due to inter-individual fighting. Consequently, this aggressive typology is constrained to urban dwelling Zygiella, indicating enhanced behavioral plasticity in the species.[8]

Predators

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Wasps

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Wasps are active predators of spiders, particularly engaging in predation behaviors during the spiders' reproductive period. Wasp attacks by the species Vespula germanica are common in Zygiella x-notata. Male spiders and smaller females are at greater risk of predation by wasps.[5]

Male preference

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Males are located for predation by wasps more frequently than females. There are multiple reasons why this occurs. First, adult male Zygiella x-notata do not produce orb webs and thus reside on window frames or other human structures. This leaves males at a disadvantage, as they can be more easily identified by wasps. Second, the dorsal side of the male, as well as the male's legs and cephalothorax, appear significantly darker than that of the female. When placed in contrast with their residence on human settlements, the dark color of the male is easily visible and thus preferentially located by wasps. Third, male spiders engage in mate guarding behaviors. While guarding their potential female mates, males are typically located on the female's web, outside of her retreat. Here, the male is vulnerable to predation due to his increased visibility.[5]

Predation avoidance

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Due to the significant threat of predation by wasps, Zygiella x-notata has developed defensive behaviors to avoid predation threats. One tactic used by Zygiella x-notata to escape predation by wasps is jumping from webs or off human constructions. In males particularly, this survival behavior consists of jumping down the frame of a window, where he can no longer be located by the wasp. In female spiders, predation avoidance involves a tactic known as "web cleaning". Females' web cleaning behavior involves throwing prey remains out of the web after eating. If either prey or an inanimate object remain stuck on the web, the females will remove the section of web containing the prey or object, and rebuild the section of web. This behavior decreases the predation risk to females by lowering the wasp's visibility threshold. Additionally, web cleaning behaviors often occur at night to reduce the risk of potential predation. During the day, the female remains in her retreat to reduce visibility to wasps, thereby reducing predation risk.[5]

Consequences of predation

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Consequences of predation by wasps include decreased reproductive success of an individual Zygiella x-notata as a result of capture by the wasp, displacement of the spider upon jumping from the web or other structures, and prey theft by the wasp. These all pose physiological and energetic costs to the spider, occasionally resulting in physical impairment or death.[5]

Physiology

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Leg anatomy

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The dorsal tibia of the walking legs and pedipalps contain a group of trichobothria. There is only one sensillum on the leg metatarsus.[14]

Invasive Species

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Zygiella x-notata is considered an invasive species in California, however they are not harmful to humans and they are not known to bite either. The only obstruction they seem to cause is disrupting garden work with their large webs.[19]

See also

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References

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  1. ^ "Spider News: Messy Webs and Tarantula Hearts | Science 2.0". www.science20.com. 27 August 2014. Retrieved 15 November 2020.
  2. ^ a b c Factsheet 6: Missing-sector Orbweaver (Zygiella x-notata), British Arachnological Society, 2016. Retrieved 27 November 2016
  3. ^ a b c d Smith, Taylor. "Discovering the daily activity pattern of Zygiella x-notata and its relationship to light" (PDF).{{cite web}}: CS1 maint: url-status (link)
  4. ^ a b c d e f Anotaux, Mylène; Toscani, Camille; Leborgne, Raymond; Châline, Nicolas; Pasquet, Alain (1 September 2014). "Aging and foraging efficiency in an orb-web spider". Journal of Ethology. 32 (3): 155–163. doi:10.1007/s10164-014-0404-6. ISSN 1439-5444.
  5. ^ a b c d e Pasquet, Alain; Cardot, Julien; Leborgne, Raymond (16 August 2007). "Wasp Attacks and Spider Defence in the Orb Weaving Species Zygiella x-notata". Journal of Insect Behavior. 20 (6): 553–564. doi:10.1007/s10905-007-9098-8. ISSN 0892-7553.
  6. ^ a b c d e f g h i j Anotaux, M.; Marchal, J.; Châline, N.; Desquilbet, L.; Leborgne, R.; Gilbert, C.; Pasquet, A. (1 November 2012). "Ageing alters spider orb-web construction". Animal Behaviour. 84 (5): 1113–1121. doi:10.1016/j.anbehav.2012.08.017. ISSN 0003-3472.
  7. ^ a b c Leborgne, Raymond; Pasquet, Alain (1 March 1987). "Influences of aggregative behaviour on space occupation in the spider Zygiella x-notata (Clerck)". Behavioral Ecology and Sociobiology. 20 (3): 203–208. doi:10.1007/BF00299734. ISSN 1432-0762.
  8. ^ a b c d Kralj-Fišer, Simona; Hebets, Eileen A.; Kuntner, Matjaž (25 July 2017). "Different patterns of behavioral variation across and within species of spiders with differing degrees of urbanization". Behavioral Ecology and Sociobiology. 71 (8). doi:10.1007/s00265-017-2353-x. ISSN 0340-5443.
  9. ^ a b Toscani, Camille; Leborgne, Raymond; Pasquet, Alain (31 July 2012). "Behavioural analysis of web building anomalies in the orb-weaving spiderZygiella x-notata(Araneae, Araneidae)". Arachnologische Mitteilungen. 43: 79–83. doi:10.5431/aramit4309. ISSN 1018-4171.
  10. ^ a b c d e f g h i Venner, Samuel; Pasquet, Alain; Leborgne, Raymond (1 March 2000). "Web-building behaviour in the orb-weaving spider Zygiella x-notata: influence of experience". Animal Behaviour. 59 (3): 603–611. doi:10.1006/anbe.1999.1327. ISSN 0003-3472.
  11. ^ a b c d e Tarsitano, Michael; Kirchner, Wolfgang (2001). "Vibrational courtship signals of Zygiella x-notata" (PDF). British Arachnological Society. 12: 26–32.
  12. ^ a b c d Bel-Venner, M. C.; Venner, S. (1 June 2006). "Mate-guarding strategies and male competitive ability in an orb-weaving spider: results from a field study". Animal Behaviour. 71 (6): 1315–1322. doi:10.1016/j.anbehav.2005.08.010. ISSN 0003-3472.
  13. ^ a b c Pasquet, Alain; Ridwan, Ahmad; Leborgne, Raymond. "Presence of potential prey affects web-building in an orb-weaving spider Zygiella x-notata". Animal Behaviour. 47: 477–480.
  14. ^ a b c Klärner, Diemut; Barth, Friedrich G. (1 December 1982). "Vibratory signals and prey capture in orb-weaving spiders (Zygiella x-notata, Nephila clavipes; Araneidae)". Journal of comparative physiology. 148 (4): 445–455. doi:10.1007/BF00619783. ISSN 1432-1351.
  15. ^ a b "Web-building management in an orb-weaving spider, Zygiella x-notata: influence of prey and conspecifics". Comptes Rendus Biologies. 327 (1): 84–92. 1 January 2004. doi:10.1016/j.crvi.2003.11.006. ISSN 1631-0691.
  16. ^ "Missing Sector Orb Spinner, Zygiella x-notata". britishspiders.org.uk. British Arachnological Society. Retrieved 5 November 2020.
  17. ^ a b c d Gheysens, T.; Beladjal, L.; Gellynck, K.; Nimmen, E. Van; Langenhove, L. Van; Mertens, J. (2005/08). "EGG SAC STRUCTURE OF ZYGIELLA X-NOTATA (ARACHNIDA, ARANEIDAE)". The Journal of Arachnology. 33 (2): 549–557. doi:10.1636/CS05-12.1. ISSN 0161-8202. {{cite journal}}: Check date values in: |date= (help)
  18. ^ a b Bel-Venner, M.c; Dray, S; Allainé, D; Menu, F; Venner, S (7 January 2008). "Unexpected male choosiness for mates in a spider". Proceedings of the Royal Society B: Biological Sciences. 275 (1630): 77–82. doi:10.1098/rspb.2007.1278. PMC 2562406. PMID 17956845.{{cite journal}}: CS1 maint: PMC format (link)
  19. ^ Skene, Jennifer (18 October 2010). "Spider Invaders". KQED. Retrieved 5 November 2020.
  • Le Guelte, Louis: Structure de la toile de Zygiella x-notata Cl. 1966.
  • Levi, Herbert Walter: "The orb-weaver genus Zygiella (Araneae, Araneidae)." in Bulletin of the Museum of Comparative Zoology, vol. 146, no. 5, Cambridge 1974. ISSN 0027-4100
  • Weissmann, Monika: Web-building and prey-capture in two orb-weavers. 1987.
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