Species of arachnid
Top 3 Misumena vatia related articles
- 1 Taxonomy and phylogeny
- 2 Description
- 3 Habitat and distribution
- 4 Diet
- 5 Reproduction and life cycle
- 6 Mating
- 7 Parental care
- 8 Physiology
- 9 References
- 10 External links
|Female with prey silver-spotted skipper (Hesperia comma)|
|Male is much smaller than female|
Misumena vatia is a species of crab spider with a holarctic distribution. In North America, it is called the goldenrod crab spider or flower (crab) spider, as it is commonly found hunting in goldenrod sprays and milkweed plants. They are called crab spiders because of their unique ability to walk sideways as well as forwards and backwards. Both males and females of this species progress through several molts before reaching their adult sizes, though females must molt more to reach their larger size. Females can grow up to 10 mm (0.39 in) while males are quite small, reaching 5 mm (0.20 in) at most. Misumena vatia are yellow or white, and have the ability to change between these two colors based on their surroundings. They have a complex visual system, with eight eyes, that they rely on for prey capture and for their color-changing abilities. Sometimes, if Misumena vatia consume colored prey, the spider itself will take on that color.
Misumena vatia feed on common insects, often consuming prey much larger than themselves. They use venom to immobilize their prey, though they are harmless to humans. They face threats due to parasites and larger insects. For Misumena vatia, survival depends on the choice of hunting site. The spiders closely monitor multiple sites to see if others nearby are frequented by greater numbers of potential prey. The primary sex ratio is biased toward females. Females are stationary and choose a flower to settle on while males cover great distances searching for mates. Females do not emit pheromones, rather, they leave "draglines" of silk behind them as they move, which males follow. Females live longer than males, on average. After mating, females guard their nests until the young have hatched, after which they die.
Misumena vatia Intro articles: 3
Taxonomy and phylogeny
The species Misumena vatia was first described by Swedish archeologist and entomologist Carl Alexander Clerck in his book Aranei Svecici. Misumena vatia belongs to the family Thomisidae, or spiders known as crab spiders. The family includes more than 2000 species, which are found all over the world. The genus Misumena includes many other species which are found worldwide. Misumena vatia falls into the Thomisus clade. Other clades in the family Thomisidae include the Borboropactus clade, the Epidius clade, and the Stephanopis clade.
Close relatives include Mecaphesa asperata, which is also found in North America, as well as Central America and the Caribbean. It is similar in size and shape but is light-gray to brown with pink stripes on the abdomen and cephalothorax. It is also coated with hairs that are short and stiff.
Similar species of the Misumenoides and Misumenops genera tend to be found south of Misumena vatia’s home range, but some species, such as Misumenoides formosipes, are found in North America as well. Philodromidae is a closely related family of wandering spiders. These spiders differ from those in the family Thomisidae in that their front legs are of a similar length as their back legs. Thus, their hunting style is quite different.
Misumena vatia Taxonomy and phylogeny articles: 7
This species has a wide, flat body that is short and crab-like. It can walk sideways in addition to being able to move forward and backward. Of its eight legs, the first two pairs are the longest. These sets of legs are usually held open, as the spider uses them to capture its prey. Misumena vatia is harmless to humans, as its fangs are not powerful enough to penetrate human skin and its venom is too weak to harm larger animals.
These spiders may be yellow or white. This ultimately depends on the flower on which they are hunting (active camouflage). Younger females especially, which may hunt on a variety of flowers such as daisies and sunflowers, have a strong tendency to adapt to the color of the surrounding flower. However, the color-changing process is not instant and can require up to 25 days to complete. Older females need large amounts of relatively large prey to produce the best possible clutch of eggs. In North America, they are most commonly found in goldenrods, bright yellow flowers which attract large numbers of insects, particularly in autumn. It is often very hard even for a searching human to spot this spider on a yellow flower. These spiders are sometimes called 'banana spiders' because of their striking yellow color.
Females have light complexions, either white or yellow with darker sides. They may have some markings on the abdomen that can be brown or red. These markings are genetically determined and not affected by a background color change. Males are darker than females, with red or brown outer shells. They have a characteristic white spot in the middle that continues through the area around the eyes. Males specifically have two sets of red and white bands both dorsally and laterally. Similar species of the crab spiders appear in a variety of colors such as those of the genus Diaea, which can be lime green, or some species of Xysticus and Coriarchne which are brown.
These spiders change color based on visual cues. The color change is most obvious on females of this species. The ability of males and juveniles to change color has not been documented. Two other known spiders with this color change ability include Thomisus onustus and Thomisus spectabilis. Depending on the color of flower they see around them, they can secrete a liquid yellow pigment into the body's outer cell layer. The baseline color of the spider is white. In its white state, the yellow pigment is sequestered beneath the outer cell layer so that inner glands which are filled with white guanine are visible. They are able to match with greater accuracy to white flowers, such as Chaerophyllum temulum (the rough chervil) in particular, compared to yellow flowers based on the spectral reflectance functions. While the spider is residing on a white plant, it tends to excrete the yellow pigment instead of storing it in its glands. In order to change back to yellow, the spider must first produce enough of the yellow pigment. For this reason it takes these spiders much longer to turn from white to yellow than it does for them to go from yellow to white. The color change from white to yellow can take between 10 and 25 days while the opposite color change takes only about six days. The yellow pigments are kynurenine and 3-hydroxykynurenine. Color changes are induced by visual cues and spiders with impaired vision lose this ability.
Notably, spiders of this species sometimes choose to hunt on flowers that, to the human eye, they do not appear to match in color. For instance, they can be found hunting on the pink petals of the pasture rose (Rosa carolina). The spider appears white, or changes to white, causing it to stand out to human observers. Arthropods, on the other hand, serve as both predators and prey to Misumena vatia, and have photoreceptors that allow them to see ultraviolet, blue, and green light but oftentimes lack red receptors altogether. As a result, Misumena vatia is camouflaged, appearing dark on a dark background.
Misumena vatia is highly sexually dimorphic. Females are larger than males and tend to fall between 6–9 mm (0.24–0.35 in) in length. Males, on the other hand, are only 3–4 mm (0.12–0.16 in) long. The female's legs are white or yellow, while the male's first and second legs are brown or red and the third and fourth are yellow. Additionally, in concurrence with the male’s smaller size, the male Misumena vatia molts two fewer times than the female.
Other physical characteristics
Misumena vatia has two rows of eyes. Those in the anterior row are equally spaced and curved backward while those in the second row vary in appearance from animal to animal, and can be curved more or less than the first. The area around the eyes is narrower in the front than the back. The spider's hair is erect and can be either filiform or rod-shaped. The legs do not have spines, except under the tibia and metatarsal bones of the first two sets of legs. The appearance of the clypeus and the structure of the cephalothorax can be used to distinguish the genus Misumena within its subfamily.
Misumena vatia Description articles: 20
Habitat and distribution
Misumena vatia is found only in North America and Europe. Other species of crab spiders, however, can be found all over the world. The species prefers a temperate climate and generally inhabits forest biomes. Misumena vatia is terrestrial and can be found on several plants and flowers such as milkweed and goldenrod in North America, as well as trillium, white fleabane (Erigeron strigosus), ox-eye daisy (Chrysanthemum leucanthemum), red clover (Trifolium pratense) and buttercups (Ranunculus acris)."
Females of this species do not travel more than a few yards (meters) from their feeding location. They are attracted by the fragrance of flowers, though other visual and tactile clues also help them choose a territory. Their survival depends on their ability to choose a small area home to flowering plants which will attract prey. Males are highly motile and may disperse great distances as they search for mates. Additionally, spiderlings may travel great distances by ballooning, if they find the area around their nest to be lacking in resources. However, this is risky as there is no guarantee that the search for a new territory will be successful.
Misumena vatia hunts large prey with a low rate of success. Hunting success rate is highly dependent upon the spider's choice of hunting site. Before they lay their eggs, females are heavy and slow, which necessitates that they choose a hunting site on which to stay. When hunting on their preferred plant of milkweed, they monitor nearby umbels to see if another site would be more profitable. Over the course of a few hours, Misumena vatia may recognize and move to another nearby hunting site. Most often, they move to flowers that produce more nectar and attract more prey, however occasionally some intentionally and consistently pick less profitable sites to hunt on. Thus, the population is dimorphic in terms of patch choice behavior. The reason a minority might choose poorer hunting sites on purpose remains unknown.
Misumena vatia Habitat and distribution articles: 10
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Crab spiders are carnivorous, feeding on invertebrate insects such as flies, bees, butterflies, grasshoppers, dragonflies, and hoverflies. Bumblebees (Bombus appositus) provide the spider with the most biomass, but small syrphid flies (Toxomerus marginatus) are the prey captured most frequently. Other frequently captured prey include honeybees (Apis mellifera) and moths. Immature Misumena vatia commonly feed on smaller-sized prey such as thrips, aphids in the family Aphididae, and dance flies the in family Empididae. They may also use nectar and pollen as food sources when prey is scarce.
Misumena vatia is primarily dependent on its vision to hunt, so it typically finds and captures food during the day. Adult males search the upper stratum of field vegetation, where females are commonly found hunting, for potential mates. The spider can hunt bugs and insects larger than itself because it has the ability to use venom to immobilize its prey. Misumena vatia waits, camouflaging itself on a flowering plant or on the ground, for prey to pass by, and then grabs the prey with its forelegs. It immobilizes prey by injecting venom with its fangs. Unlike many spiders which wrap their prey in silk, Misumena vatia uses its fangs to suck the liquid out of prey until satiated. This is a form of external digestion, in which spiders inject digestive enzymes into prey. As a result, prey size is not a limiting factor for consumption.
Although Misumena vatia most often hunts during the daytime, there is evidence that it is sometimes driven to hunt at night due to an increase in nocturnal prey activity. This behavior occurs most commonly in response to increased night-time activity by moths in early September.
Misumena vatia has the ability to retain its excretions for at least 50 days and will not excrete when confined to small spaces or near its hunting sites. Excretion may alert predators to the spider's whereabouts.
Diet-induced color change
Misumena vatia can also change color as a result of prey consumption. Once consumed, colorful prey can show through the thin, transparent epidermis of the abdomen, affecting opisthosomal coloration. Ingestion of red-eyed fruit flies cause the abdomen to turn pink. Coloration changes caused by prey consumption revert to normal the normal white or yellow within 4–6 days after prey ingestion. Color change intensity is positively correlated with the amount of colorful prey consumed. Color change intensity also decreases with the spider's age. These spiders have been observed to have pink, orange, yellow, brown, green, or white opisthosomas depending on the prey consumed.
Misumena vatia Diet articles: 18
Reproduction and life cycle
Sex ratios among Misumena vatia vary from a ratio of 1.5 females per male at hatching to a ratio of 2.5–5.1 females per male by the time they reach adulthood. Since males must spend considerable time searching for females, they face danger from the environment, reducing their numbers. Males cannot mate multiple times in quick succession but require a two-day interval between matings. In nature, Misumena vatia produces a single brood. However, females are capable of producing another brood if artificially induced.
Female Misumena vatia prefer common milkweed (Asclepias syriaca) over spreading dogbane (Apocynum androsaemifolium), pasture rose (Rosa carolina), and chokecherry (Prunus virginiana) for nest construction. Females who lay eggs on milkweed have higher nesting success, which correlates with early survival of clutches. The nest appearance can vary widely, depending on the type of plant on which it is constructed. In the case of the pasture rose and the sensitive fern (Onoclea sinsibilis), nests consist of several small leaves bound together. These nests are more vulnerable to predators though, because they are not as tightly bound as those created on milkweed, and have a greater area that is covered only by silk.
A minority of males—only about ten percent—guard pre-reproductive females as they molt into their adult stage. Almost all males who guard such females mate with them after they have molted. The low level of mate guarding is related to the female-leaning sex ratio expressed by Misumena vatia. Males of this species tend to guard less frequently and exhibit less aggression than other closely related species, such as Misumenoides formosipes, which do not have a female-biased sex ratio.
In May and early June, males molt into adulthood, with the number of adult males peaking between June 5 to July 15. Females do not molt into adulthood until mid to late June, with numbers of adult females peaking around June 25. After males molt, their body mass does not increase, remaining at about 4 mg (0.00014 oz). Males, however, do undergo body changes as they enter the adult stage. Their front legs lengthen while the abdomen shrinks. Females live an average of two years and spend most of this time guarding their eggs sacs and the territory (flowers) on which they hunt. Males have shorter lifespans by about a month. Only near the end of the female's second year of life will she allow males onto her territory to mate. Females lay their eggs most commonly in the middle of the summer; these hatch after 3.5 weeks. Females usually die very soon after their eggs have hatched, during their second winter. Young undergo one molt within the egg sac, and emerge after hatching as second instars. They can sustain themselves for a few days with the nutrients from their yolk sacs.
Misumena vatia Reproduction and life cycle articles: 6
The much smaller males scamper from flower to flower in search of females and are often seen missing one or more of their legs. This may be due either to near misses by predators such as birds or to fighting with other males. Males exhibit a random pattern of searching for mates until they discover a female dragline. Females leave these draglines behind them as they search for prey. Males follow the draglines in search of potential mates. Unlike many spider species, the females do not deposit any pheromones on these lines. Males follow the lines mechanically rather than chemically. The tendency for a male to follow a line is highly influenced by its life stage and the stage of the female of interest. Adult males preferentially follow adult female and juvenile female draglines, while penultimate males do not display a specific preference. Male Misumena vatia are also more likely to follow lines laid by their own species than those of a related species.
Two males interested in the same female may compete, since encounters with females are relatively rare. This may include light touching, chasing, foreleg lashing, grappling, and biting between males. If the female is being guarded by an existing male, the guarding male may either fend off the challenger or be replaced. The male which finds the female of interest first has an advantage in any ensuing contest. In this species, unlike many other species of spider, older and younger males are generally the same size. While older males initiate contests more frequently than younger males, the nature of their attacks is less likely to include extensive bodily contact. Younger males win significantly more contests than older males. After a contest between males, the winner immediately mates with the female while the loser retreats.
When a male finds a female, he climbs over her head, over her opisthosoma and onto her underside, where he inserts his pedipalps to inseminate her. The male may wrap the female loosely with silk during copulation. Females have a pair of gonopores which the male pedipalp may enter for copulation. When the male inserts his pedipalp into the female's gonopore he will make rhythmic, vibratory movements that can last from 1–2 seconds. Gonopore contacts of less than 30 seconds will result in unfertilized eggs and a failed copulation. Matings last an average of four minutes.
Males can accurately identify the reproductive condition of potential mates. They prefer to mate with virgin females over those which have previously mated. Males mate for longer with virgin females and produce more pedipalp movements than during copulation with previously-mated females. Males are most likely to enter both gonopores of a virgin female, while they may only enter one gonopore of a previously-mated female. Females have a low probability of mating with a second male, but have a higher probability of mating with a second male than they do a third one.
The female then lays her eggs preferentially on plants from the Asclepias genus (milkweeds). When preparing to lay eggs, she first identifies a suitable location for her brood. She descends the plant stalk down to the leaf that she chooses and then rolls up the end of a leaf. She secures the leaf by spreading silk, creating a cocoon-like structure, and lays her eggs inside the nest she has created. She tends to lay her eggs at night. The young grow to be about 5 mm (0.20 in) by autumn and remain on the ground through winter. Their final molt, from penultimate instars to adults, occurs during May of the next year.
Because Misumena vatia employs camouflaging, it can focus more energy on growth and reproduction rather than on finding food and escaping from predators. As in many Thomisidae species, there is a positive correlation between female weight and egg clutch size, or fecundity. Selection for larger female body size thus increases reproductive success.
This species exhibits a high first-male sperm precedence, so providing a virgin female with a large sperm quantity is advantageous. Because there is a very limited number of virgin females available at any given time, there is strong selective pressure that favors males that provide large sperm quantities. The need to produce a large sperm quantity for each copulation prevents males from remating quickly. Additionally, females are likely to deny subsequent males after their first mating as further reproduction will interfere too strongly with the female's foraging success. More matings are also unfavorable because they can increase the risk of infection with sexually transmitted parasites or diseases.
In some cases, males can tell whether a female has mated previously from a distance. This may be due the female's heightened aggression that manifests after she has mated once. It is more common, however, that in order to assess the reproductive history of a given female, the male must first mount her, which is dangerous for the male as there is a chance the female may attack, capture, and kill him. Since females are difficult to locate and the cost of searching for them is so high, the risk is usually worthwhile to the male. In addition, since locating females is difficult, there is a low chance that another male has previously inseminated a given female, so it is therefore beneficial for males to provide large quantities of sperm. This adaptation is also beneficial in the case that a female loses her first brood. When a female has been inseminated with a large quantity of sperm, she may have enough to fertilize a second brood to replace the lost first brood.
Like many other arachnids and insects, Misumena vatia may express sexual cannibalism; however it is only considered moderately common. In cases of precopulatory sexual cannibalism, older males are more likely than younger males to be targets of attack, and are more likely to suffer death or injury as a result of such an attack, especially during the latter half of the mating season. This could be a result of a decreased ability among older males to evade attack from females. Older males do not tend to display riskier mating behavior than younger males. The size of the male does not influence its likelihood of being cannibalized during copulation. Females increase cannibalistic attacks as the mating season progresses. More males tend to be cannibalized after mid July, which could be a result of male aging but is more likely a result of increased female aggression during this time. Non-reproductive cannibalism is uncommon among Misumena vatia. However, it has been observed in individuals in roughly one percent of broods. In these broods, cannibalism tends to occur among spiderlings. Cannibalistic individuals can be up to three times larger than those who are non-cannibalistic.
Misumena vatia Mating articles: 11
Like many other species, Misumena vatia guards its nest to protect its vulnerable eggs from attack. Nest guarding increases the spider's overall reproductive success by protecting against predation from ichneumonid and dipteran egg predators. These spiders are usually observed guarding the nest by standing on its underside, the most vulnerable face of the nest. Most guarding spiders will remain by the nest until the young have begun to emerge from their eggs—about three weeks. A minority of spiders abandon their nests before spiderlings have hatched, while some may remain until all the young have hatched or longer. Most die within a few days of the hatching of their young.
Parasitization by the ichneumonid wasp, Trychosis cyperia, an egg predator, is common. The wasp deposits an egg in the nest and its larva feeds on the eggs. One attack can destroy the nest completely. Misumena vatia experience strong selection to minimize attack from wasps, which is why egg guarding by the female is important for reproductive success. Wasps tend to feed on small egg masses guarded by small spiders, as small spiders cannot defend their nests as effectively. Other known predators include ants, other spiders, birds, lizards, and shrews. When defending the nest from an approaching predator, females typically raise their front legs in a display otherwise observed when they are attacking prey.
Misumena vatia Parental care articles: 6
These spiders respond quickly to motion that is both within and outside of their visual range. To do so, they rely heavily on several types of mechanoreceptors. Tactile hairs sense touch, trichobothria sense air currents, and slit sensilla are sensitive to vibrations and mechanical stresses. While still important, vision plays a less important roll in prey detection. Remarkably, Misumena vatia fail to notice prey when it is stationary.
These spiders have two rows of four eyes each for a total of eight eyes. The antero-lateral (75 μm diameter) and postero-lateral (65 μm diameter) eyes are the larger in size of the four sets of eyes. The antero-median (59 μm diameter) are considered the principal eyes and along with the postero-median (55 μm diameter) constitute the smaller of the sets. All of the eyes other than the principal eyes are considered the secondary eyes. The antero-median eyes appear the clearest, while the other sets of eyes appear darker. The postero-median eyes look directly upward, and their field of view overlaps somewhat with that of the postero-lateral eyes. The antero-lateral and postero-lateral eyes also share a slight overlap in their visual fields. The antero-lateral eyes give these spiders a region of binocular vision. The organization of the antero-lateral, postero-median, and postero-lateral eyes allows these spiders to see nearly their entire upper visual environment.
The four pairs of eyes are similar in structure, all containing a retina, a dioptric apparatus, and a cellular vitreous body. The outermost layer of the eye is the lens. The columnar cells of the vitreous body stand between the lens and the retina, and their nuclei rest next to the retina. Three layers of pigment cells surround the vitreous body. The epidermis is the outer layer, and it contains electron-dense granules and electron-lucent inclusions of micro-crystals. The middle layer contains dark, pigment granules, and the innermost layer contains larger, dark, pigment granules inside glial cells. These layers prevent light that may enter through a nearby transparent cuticle from reaching the retina, keeping each eye isolated. The retina contains photoreceptor cells and other supporting cells.
The principle eyes have a complex and unique organization. They have three different photoreceptive segments. The periphery contains a half-circle of one type of rhabdomere, while the center is pigmented and contains two types of rhabdomeres. These spiders also have a "giant rhabdom" in the lowest layer of the center of the retina. Only the light entering along its optic axis stimulates this giant rhabdom, so the visual information comes in the shape of a dot. Misumena vatia can control the trajectory of the giant rhabdom by moving their eye muscles, which means these single points of visual information are integrated to generate the spider's visual field.
Vision plays an important role in the spider's substrate color matching. Misumena vatia have the necessary physiological machinery to see color, and are most sensitive to wavelengths of light between 340-520 nm. Misumena vatia's principle eyes have tiered retinas, with four layers containing different types of photoreceptors. These spiders have been proven to have green and UV photoreceptors, and likely have many other types which allow them to see a full range of colors. The secondary eyes are dichromal, meaning that they have two types of photoreceptors. Since Misumena vatia use their visual systems to inform color changes, they must be able to see color in their environment and on their own bodies. The visual field of the antero-lateral and antero-medial eyes allow the spider to see its legs, while the postero-lateral eyes see the opisthoma. Since the visual fields are so wide, these spiders see their own bodies and the color of their surroundings, which supports the idea that color matching is facilitated by the visual system.
Autotomy, the loss of one leg, can happen in a variety of critical situations, including fleeing from predators, fighting, and getting rid of parasites. The disadvantage is obvious, but most spiders can grow back lost limbs if the loss occurs during a juvenile stage and before the final molting.
The loss of an anterior leg is common among males. Over their lifetimes, approximately 30 percent of males will lose one of their anterior legs. One direct disadvantage of losing a leg is a decrease in mobility. Spiders with all eight legs have considerably higher body weights, showing that losing legs negatively impacts foraging and significantly decreases the speed with which they can move along lines. Since females are widely dispersed, the impairment of mobility adversely affects the male’s reproductive success.
Misumena vatia Physiology articles: 8
- Acorn, John and Sheldon, Ian. (2003). Bugs of Ontario Edmonton: Lone Pine Publishing
- Clerck, Carl; Bergquist, Carl; Borg, Eric; Gottman, Lorens; Salvius, Lars (1757). Svenska spindlar : uti sina hufvud-slägter indelte samt under några och sextio särskildte arter beskrefne : och med illuminerade figurer uplyste. Stockholmiae: Literis Laur. Salvii. doi:10.5962/bhl.title.119890.
- Morse, Douglass H. (2007). Predator Upon a Flower: Life History and Fitness in a Crab Spider. Cambridge, Massachusetts: Harvard University Press. ISBN 978-0-674-02480-9.
- Bern, Natural History Museum. "NMBE - World Spider Catalog". wsc.nmbe.ch. Retrieved 2021-03-22.
- Benjamin, Suresh P.; Dimitrov, Dimitar; Gillespie, Rosemary G.; Hormiga, Gustavo (2008). "Family ties: molecular phylogeny of crab spiders (Araneae: Thomisidae)". Cladistics. 24 (5): 708–722. doi:10.1111/j.1096-0031.2008.00202.x. S2CID 49532398.
- "Goldenrod crab spider - flower crab spider - Misumena vatia". Biodiversity of the Central Coast. Retrieved 2020-11-20.
- Haynes, Dean L. (31 May 2012). "Predatory Behavior of Philodromus rufus Walckenaer (Araneae: Thomisidae)". The Canadian Entomologist. 98 (2): 113–133. doi:10.4039/Ent98113-2 – via Cambridge University Press.
- Abraham, Barbara J. (1983). "Spatial and Temporal Patterns in a Sagebrush Steppe Spider Community (Arachnida, Araneae)". The Journal of Arachnology – via Biodiversity Heritage Library.
- "Misumena – Flower Crab Spider". usaspiders.com. Retrieved 12 May 2020.
- "Goldenrod Crab Spider". Prince William Conservation Alliance. Retrieved 25 October 2020.
- "Crab spider Misumena vatia". Spider and Harvestman Recording Scheme website. Retrieved 27 October 2020.
- Kaston, Elizabeth. How to Know the Spiders. McGraw-Hill Science/Engineering/Math.
- Comstock, John. The Spider Book. Forgotten Books.
- Insausti, Teresita C.; Casas, Jérôme (2008). "The functional morphology of color changing in a spider: development of ommochrome pigment granules". Journal of Experimental Biology. 211 (5): 780–789. doi:10.1242/jeb.014043. PMID 18281341.
- Chittka, Lars (2001). "Camouflage of Predatory Crab Spiders on Flowers and the Colour Perception of Bees (Aranida: Thomisidae / Hymenoptera: Apidae)". Entomologia Generalis. 25 (3): 181–187. doi:10.1127/entom.gen/25/2001/181.
- Oxford, G. S.; Gillespie, R. G. (1998). "Evolution and ecology of spider coloration". Annual Review of Entomology. 43 (1): 619–643. doi:10.1146/annurev.ento.43.1.619. PMID 15012400.
- Insausti, Teresita C.; Defrize, Jérémy; Lazzari, Claudio R.; Casas, Jérôme (2012). "Visual fields and eye morphology support color vision in a color-changing crab-spider". Arthropod Structure & Development. 41 (2): 155–163. doi:10.1016/j.asd.2011.11.003. PMID 22309704.
- "Misumena Vatia". Animal Diversity Web. Retrieved 17 October 2020.
- Anderson, Jill T.; Morse, Douglass H. (2001). "Pick-up lines: cues used by male crab spiders to find reproductive females". Behavioral Ecology. 12 (3): 360–366. doi:10.1093/beheco/12.3.360.
- "Crab Spider: Grasslands Predator Hiding in Plain Sight" (PDF). California Native Grasslands Association. Retrieved 2020-11-20.
- Morse, Douglass H. (1981). "Prey Capture by the Crab Spider Misumena vatia (Clerck) (Thomisidae) on Three Common Native Flowers". The American Midland Naturalist. 105 (2): 358–367. doi:10.2307/2424754. JSTOR 2424754.
- Vasconcellos-Neto, João; Messas, Yuri Fanchini; da Silva Souza, Hebert; Villanueva-Bonila, German Antonio; Romero, Gustavo Quevedo (2017). "Spider–Plant Interactions: An Ecological Approach". In Viera, Carmen; Gonzaga, Marcelo O. (eds.). Behaviour and Ecology of Spiders: Contributions from the Neotropical Region. Springer. pp. 165–214 . doi:10.1007/978-3-319-65717-2_7. ISBN 978-3-319-65717-2.
- Lockley, Timothy C.; Young, Orrey P.; Hayes, Jane Leslie (1989). "Nocturnal Predation by Misumena vatia (Araneae, Thomisidae)". Journal of Arachnology. 17 (2): 249–251. JSTOR 3705635.
- Morse, Douglass H. (2008). "Excretion behavior of adult female crab spiders Misumena vatia (Araneae, Thomisidae)". Journal of Arachnology. 36 (3): 612–614. doi:10.1636/ST07-96.1. JSTOR 25434338. S2CID 53062637.
- Schmalhofer, Victoria R. (2000). "Diet-Induced and Morphological Color Changes in Juvenile Crab Spiders (Araneae, Thomisidae)". Journal of Arachnology. 28 (1): 56–60. doi:10.1636/0161-8202(2000)028[0056:DIAMCC]2.0.CO;2. JSTOR 3706359.
- Morse, Douglass H. (2007). "Mating Frequencies of Male Crab Spiders, Misumena vatia (Araneae, Thomisidae)". Journal of Arachnology. 35 (1): 84–88. doi:10.1636/ST06-13.1. JSTOR 25067813. S2CID 86287483.
- Morse, Douglass H. (1994). "Numbers of Broods Produced by the Crab Spider Misumena vatia (Araneae, Thomisidae)". Journal of Arachnology. 22 (3): 195–199. JSTOR 3705422.
- Morse, Douglass H. (1990). "Leaf choices of nest-building crab spiders (Misumena vatia)". Behavioral Ecology and Sociobiology. 27 (4): 265–267. doi:10.1007/BF00164898. JSTOR 4600476. S2CID 20063676.
- Morse, Douglass H. (1989). "Nest Acceptance by the Crab Spider Misumena vatia (Araneae, Thomisidae)". The Journal of Arachnology. 17 (1): 49–57. JSTOR 3705404 – via JSTOR.
- Holdsworth, Andrew R.; Morse, Douglass H. (2000). "Mate Guarding and Aggression by the Crab Spider Misumena vatia in Relation to Female Reproductive Status and Sex Ratio". The American Midland Naturalist. 143 (1): 201–211. doi:10.1674/0003-0031(2000)143[0201:MGAABT]2.0.CO;2. JSTOR 3082995.
- Hu, Helen H.; Morse, Douglass H. (2004). "The effect of age on encounters between male crab spiders". Behavioral Ecology. 15 (5): 883–888. doi:10.1093/beheco/arh114.
- Morse, Douglass H. (2016). "Limb loss and limb regeneration of crab spiders Misumena vatia". Journal of Arachnology. 44 (2): 165–170. doi:10.1636/15-003. JSTOR 24892332. S2CID 89303822.
- Leonard, Anne S.; Morse, Douglass H. (2006). "Line-following preferences of male crab spiders, Misumena vatia". Animal Behaviour. 71 (3): 717–724. doi:10.1016/j.anbehav.2005.08.004. S2CID 53202836.
- Morse, Douglass H. (2010). "Male mate choice and female response in relation to mating status and time since mating". Behavioral Ecology. 21 (2): 250–256. doi:10.1093/beheco/arp183.
- Morse, Douglass H. (1987). "Attendance Patterns, Prey Capture, Changes in Mass, and Survival of Crab Spiders Misumena vatia (Araneae, Thomisidae) Guarding Their Nests". Journal of Arachnology. 15 (2): 193–204. JSTOR 3705729.
- "Misumena – Flower Crab Spider". usaspiders.com. Retrieved 12 May 2020.
- Fritz, Robert S.; Morse, Douglass H. (1985). "Reproductive success and foraging of the crab spider Misumena vatia". Oecologia. 65 (2): 194–200. Bibcode:1985Oecol..65..194F. doi:10.1007/BF00379217. JSTOR 4217515. PMID 28310665. S2CID 22817217.
- Head, Graham (1995). "Selection on Fecundity and Variation in the Degree of Sexual Size Dimorphism Among Spider Species (Class Araneae)". Evolution. 49 (4): 776–781. doi:10.1111/j.1558-5646.1995.tb02313.x. JSTOR 2410330. PMID 28565139.
- Morse, Douglass H.; Hu, Helen H. (2004). "Age Affects the Risk of Sexual Cannibalism in Male Crab Spiders (Misumena vatia)". The American Midland Naturalist. 151 (2): 318–325. doi:10.1674/0003-0031(2004)151[0318:AATROS]2.0.CO;2. JSTOR 3566748.
- Morse, Douglass H. (2011). "Cannibalism within nests of the crab spider Misumena vatia". Journal of Arachnology. 39 (1): 168–170. doi:10.1636/Hi10-32.1. JSTOR 23048796. S2CID 83891820.
- "Misumena vatia". BioKids. Retrieved 26 October 2020.
- Lutzy, Rebecca M.; Morse, Douglass H. (November 2008). "Effects of leg loss on male crab spiders Misumena vatia". Animal Behaviour. 76 (5): 1519–1527. doi:10.1016/j.anbehav.2008.04.025. ISSN 0003-3472. S2CID 53171226.
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