Matriphagy is the consumption of the mother by her offspring. [1] [2] The behavior generally takes place within the first few weeks of life and has been documented in some species of insects, nematode worms, pseudoscorpions, and other arachnids as well as in caecilian amphibians. [3] [4] [5]
The specifics of how matriphagy occurs varies among different species. However, the process is best-described in the Desert spider, Stegodyphus lineatus , where the mother harbors nutritional resources for her young through food consumption. The mother can regurgitate small portions of food for her growing offspring, but between 1–2 weeks after hatching the progeny capitalize on this food source by eating her alive. Typically, offspring only feed on their biological mother as opposed to other females in the population. In other arachnid species, matriphagy occurs after the ingestion of nutritional eggs known as trophic eggs (e.g. Black lace-weaver Amaurobius ferox , Crab spider Australomisidia ergandros). It involves different techniques for killing the mother, such as transfer of poison via biting and sucking to cause a quick death (e.g. Black lace-weaver) or continuous sucking of the hemolymph, resulting in a more gradual death (e.g. Crab spider). The behavior is less well described but follows a similar pattern in species such as the Hump earwig, pseudoscorpions, and caecilians.
Spiders that engage in matriphagy produce offspring with higher weights, shorter and earlier moulting time, larger body mass at dispersal, and higher survival rates than clutches deprived of matriphagy. In some species, matriphagous offspring were also more successful at capturing large prey items and had a higher survival rate at dispersal. These benefits to offspring outweigh the cost of survival to the mothers and help ensure that her genetic traits are passed to the next generation, thus perpetuating the behavior. [6] [7] [8] [9]
Overall, matriphagy is an extreme form of parental care but is highly related to extended care in the Funnel-web spider, parental investment in caecilians, and gerontophagy in social spiders. The uniqueness of this phenomenon has led to several expanded analogies in human culture and contributed to the pervasive fear of spiders throughout society. [10] [11]
Matriphagy can be broken down into two components:
Matriphagy generally consists of offspring consuming their mother; however, different species exhibit different variations of this behavior.
In many Black lace-weavers, Amaurobius ferox , offspring do not immediately consume their mother. A day after offspring emerge from their eggs, their mother lays a set of trophic eggs, which contain nutrition for the offspring to consume. [12] Matriphagy commences days later when the mother begins communicating with her offspring through web vibrations, drumming, and jumping. [12] [13] [7] Through these behaviors, offspring are able to detect when and where they can consume their mother. They migrate towards her and a couple of the spiderlings jump onto her back to consume her. [12] In response, the mother jumps and drums more frequently to keep her offspring off of her, however, they relentlessly continue attempting to get onto her back. [12] When the mother feels ready, she presses her body onto her offspring and allows them to consume her via sucking on her insides. [12] As they consume her, they also release poison into her body, causing a quick death. [12] The mother's body is kept for a few weeks as a nutritional reserve. [12]
Interestingly, matriphagy in this species is dependent on the developmental stage that the offspring are currently at. [12] If offspring, older than four days, are given to an unrelated mother, they refuse to consume her. [12] However, if younger offspring are given to an unrelated mother, they readily consume her. [12] Additionally, if a mother loses her offspring, she is able to produce another clutch of offspring. [12]
Mothers of one particular Australian species of the crab spider, Australomisidia ergandros (formerly in genus Diaea ), are only able to lay one clutch, unlike the Black lace-weaver. [9] They invest a significant amount of time and energy into storing nutrients and food into large oocytes, known as trophic eggs, similar to the Black lace-weaver. [9] However, these trophic eggs are too large to physically leave her body. [9] Some of the nutrients from the trophic eggs are liquefied into haemolymph, which can be consumed through the mother's leg joints by her offspring. [9] She gradually shrinks until she becomes immobile and dies. [9] [12]
In this species, it has been shown that this behavior may contribute to reducing cannibalism by siblings. [9]
Right after hatching, the hatchlings of the desert spider Stegodyphus lineatus rely solely upon their mother to provide them with food and nutrients. Their mother does this by regurgitating her bodily fluids, which contain a mixture of nutrients for them to feed on. [13] [7]
This behavior begins during mating. Mating causes an increase in the mother's production of digestive enzymes to better digest her prey. Consequently, she is able to retain more nutrients for her offspring to consume later. The mother's midgut tissues start to slowly degrade during the incubation period of her eggs. After her offspring hatch, she regurgitates food for them to feed on with the help of her already-liquefied midgut tissues. Meanwhile, her midgut tissues continue to degrade into a liquid state to maximize the amount of nutrients from the mother's body that her offspring will be able to obtain. As degradation continues, nutritional vacuoles form within her abdomen to amass all of the nutrients. Consumption begins when her offspring puncture her abdomen to suck up the nutritional vacuoles. After approximately 2–3 hours, the mother's bodily fluids are completely consumed, and only her exoskeleton remains. [13]
This species is only able to have one clutch, which might explain why so much time and energy is spent on taking care of offspring. Furthermore, matriphagy can also occur between offspring and mothers who have recently laid eggs that are not related. [13]
Anechura harmandi is the only species of Earwigs that has been currently documented to exhibit matriphagy. Mothers in this particular species of Earwigs have been found to reproduce during colder temperatures. [14] [15] This is mainly for the purpose of avoiding predation and maximizing their offspring's survival, since females are unable to produce a second clutch. [14] [15] Due to the cold temperature, there is a scarcity of available nutrients when the offspring hatch, which is why the offspring end up consuming their mother. [14] [15]
Matriphagy in this species of Pseudoscorpions is usually observed during times of food scarcity. [16] After their offspring hatch, mothers exit their nests and wait to be consumed. [16] Offspring follow their mothers out of the nest where they grab onto her legs and proceed to feed through her leg joints, similar to that of Australomisidia ergandros. [16]
Females of this species are able to produce more than one clutch of offspring if their first clutch was unsuccessful. [16]
Matriphagy in this species has been predicted to prevent cannibalism between siblings as well. [16]
The adaptive value of matriphagy is based on the benefits provided to the offspring and the costs borne by the mother. [2] Functionally analyzing matriphagy in this manner sheds light on why this unusual and extreme form of care has evolved and been selected for.
Unlike other milder forms of parental care, matriphagy necessarily costs the mother her life. Nevertheless, matriphagy may serve the mother's reproductive fitness, considering reproductive output, egg sac development, and number of young reared. The key question is whether the mother would produce more surviving offspring by evading matriphagy and reproducing again or by engaging in matriphagy and produces only one clutch.
In conclusion, offspring that engage in matriphagy benefit more than those that do not engage in this behavior. Furthermore, the progeny of females that escape matriphagy to lay a second brood are significantly less successful than those that ate their mother. Hence, enhanced fitness of the mother accounts for the evolution of this unusual and extreme form of parenting.
Matriphagy is one of the most extreme forms of parental care observed in the animal kingdom. However, in some species such as the Funnel-web spider Coelotes terrestris , matriphagy is only observed under certain conditions and extended maternal protection is the main method by which offspring receive care. In other organisms such as the African social velvet spider, Stegodyphus mimosarum and Caecilian amphibians, parental behavior closely related in form and function to matriphagy is used.
The ‘maternal social’ spider, Coelotes terrestris (Funnel-web spider) uses extended maternal care as a reproductive model for its offspring. Upon laying the egg sac, a C. terrestris mother stands guard and incubates the sac for 3 to 4 weeks. She stays with her young from the time of their emergence until dispersal approximately 5 to 6 weeks later. During the offsprings’ development, mothers will provide the spiderlings prey based on their levels of gregariousness. [17]
Protecting the egg sacs from predation and parasites yields a high benefit to cost ratio for the mothers. Fitness of the mother is highly correlated to offspring developmental state—a mother in better condition yields larger young that are better at surviving predation. The presence of the mother also protects the offspring against parasitism. In addition, the mother can keep feeding while guarding her progeny without any weight loss, allowing her to collect sufficient food for both herself and her offspring. [17]
Overall, costs of protecting the egg sac are low. Upon separation from egg sacs, 90% of females have the energy sustenance to lay new sacs, although it does induce a time loss of several weeks that could potentially affect reproductive success. [17]
In experimental conditions, costs arose if maternal care was not provided, with egg sacs drying out and developing molds, thus illustrating that maternal care is essential for survival. Experimental food-deprived broods reared by the mother induced matriphagy, where 77% of offspring consumed their mother upon birth. This suggests that matriphagy can exist under nutrient-limited conditions, but the costs generally outweigh the benefits when mothers have sufficient access to resources. [17]
Caecilian amphibians are worm-like in appearance, and mothers have thick epithelial skin layers. The skin on a caecilian mother is used for a form of parent-offspring nutrient transfer. In at least two species, Boulengerula taitana and Siphonops annulatus , the young feed on the mother's skin by tearing it off with their teeth. Because these two are not closely related, either this behaviour is more common than currently observed or it evolved independently. [18] The consumed skin then regenerates within a few days. [5]
The Taita African caecilian Boulengerula taitana is an oviparous (egg-laying) caecilian whose skin transforms in brooding females to supply nutrients to growing offspring. The offspring are born with specific dentition that they can use to peel and eat the outer epidermal layer of their mother's skin. Young move around their mother's bodies, using their lower jaws to lift and peel the mother's skin while vigorously pressing their heads against her abdomen. To account for this, the epidermis of brooding females can be up to twice the thickness of non-brooding females. [19]
Viviparous (developing in the mother) caecilians on the other hand, have specialized fetal dentition which can be used for scraping lipid-rich secretions and cellular materials from the maternal oviduct lining. The ringed caecilian Siphonops annulatus , an oviparous caecilian, exhibits characteristics similar to viviparous caecilians. Mothers have paler skin tones than non-attending females, suggesting that offspring feed on glandular secretions on the mother's skin—a process that resembles mammalian lactation. This scraping method is different from the peeling actions performed by oviparous caecilians. [19]
For both oviparous and viviparous caecilians, delayed investment is a common benefit. Providing nutrition through the skin allows for redirection of nutrients, yielding fewer and larger offspring than caecilians who only provide their offspring with yolk nutrients. [19] Rather than the mother sacrificing herself and solely being used for the offspring's nutrition, caecilian mothers supplement their offspring's growth; they provide enough nutrients for the offspring to survive, but not at the cost of their own life.
Stegodyphus mothers liquefy their inner organs and maternal tissue into food deposits. The African social velvet spider Stegodyphus mimosarum and the African social spider Stegodyphus dumicola are two social spider species that eat their mothers and other adult females, which is unique since social spiders do not tend to exhibit cannibalistic life history traits. In these specific spiders, deceased females are often found shriveled with shrunken abdomens. Offspring suck nutrients primarily from the dorsal part of the adult female's abdomen, and she may still be alive during this process. [20]
This behavior is not quite the same as matriphagy because Stegodyphus spiderlings are perfectly tolerant to other offspring, healthy conspecifics, and members of other species, suggesting that ordinary cannibalism is suppressed. Instead, the parental care exhibited is known as "gerontophagy", or the “consumption of old individuals” (geron = old person, phagy = to feed on). Gerontophagy is the final act of care for the offspring, and some offspring are found larger than others. This implies that some young spiders are already able to feed on prey by themselves and gerontophagy as a source of nutrition is supplemental rather than necessary. Thus, there exists the ‘cannibal's kin-dilemma’, which reveals a form of kin selection in social spiders. In this scenario, kin selection should counteract cannibalism of related individuals in social spiders, but any designated victim should prefer to be eaten by available close relatives. [20]
Those who have been exposed to matriphagy may be frightened by such a seemingly strange and bizarre natural behavior, especially since it is mainly observed in already feared organisms. Thus, matriphagy is often posed as perpetuation of a long held fear of arachnids in human society. [21]
In contrast, others may look to matriphagy as a leading example of purity, as it represents an instinctive form of altruism. Altruism in this case refers to an "intentional action ultimately for the welfare of others that entails at least the possibility of either no benefit or a loss to the actor," and is a highly popularized and desirable concept in many human cultures. [11] Matriphagy can be viewed as altruism, insofar as participating mothers "sacrifice" their survival for the welfare of their offspring. [11] Although participation in matriphagy is not truly an intentional action, mothers are nevertheless driven by natural selection pressures based on offspring fitness to engage in such behavior. [11] This in turn creates a cycle that perpetuates altruistic matriphagous behavior through generations. Such an example of altruism on a purely biological level differs severely from human standards of altruism, which are influenced by moral virtues such as rationality, trust, and reciprocity. [11]
Parent–offspring conflict (POC) is an expression coined in 1974 by Robert Trivers. It is used to describe the evolutionary conflict arising from differences in optimal parental investment (PI) in an offspring from the standpoint of the parent and the offspring. PI is any investment by the parent in an individual offspring that decreases the parent's ability to invest in other offspring, while the selected offspring's chance of surviving increases.
A trophic egg is an egg whose function is not reproduction but nutrition; in essence, the trophic egg serves as food for offspring hatched from viable eggs. In most species that produce them, a trophic egg is usually an unfertilised egg. The production of trophic eggs has been observed in a highly diverse range of species, including fish, amphibians, spiders and insects. The function is not limited to any particular level of parental care, but occurs in some sub-social species of insects, the spider A. ferox, and a few other species like the frogs Leptodactylus fallax and Oophaga, and the catfish Bagrus meridionalis.
Theridion grallator, also known as the Hawaiian happy-face spider, is a spider in the family Theridiidae that resides on the Hawaiian Islands. T. grallator gets its vernacular name of "Hawaiian happy-face spider" from the unique patterns superimposed on its abdomen, specifically those that resemble a smiley face. T. grallator is particularly notable because of its wide range of polymorphisms that may be studied to allow a better understanding of evolutionary mechanisms. In addition to the variety of color polymorphisms present, T. grallator demonstrates the interesting quality of diet-induced color change, in which its appearance temporarily changes as it metabolizes various food items.
Phryganoporus candidus, also known as the foliage web spider, is a small, subsocial jumping spider endemic to Australia. On average, they are 6–10 mm long and are a mottled brown colour, covered in silvery grey hair. They typically reside in arid and semi-arid locations, building their nests in various trees, bushes, and other plant-life. They have a mutualistic relationship with Acacia ligulata, and therefore prefer to build their nests in these trees.
Cannibalism is the act of consuming another individual of the same species as food. Cannibalism is a common ecological interaction in the animal kingdom and has been recorded in more than 1,500 species. Human cannibalism is also well documented, both in ancient and in recent times.
Spider cannibalism is the act of a spider consuming all or part of another individual of the same species as food. It is most commonly seen as an example of female sexual cannibalism where a female spider kills and eats a male before, during, or after copulation. Cases of non-sexual cannibalism or male cannibalism of females both occur but are notably rare.
Stegodyphus lineatus is the only European species of the spider genus Stegodyphus. Male S. lineatus can grow up to 12 mm long while females can grow up to 15 mm. The colour can range from whitish to almost black. In most individuals the opisthosoma is whitish with two broad black longitudinal stripes. Males and females look similar, but the male is generally richer in contrast and has a bulbous forehead. The species name refers to the black lines on the back of these spiders. S. lineatus is found in the southern Mediterranean region of Europe and as far east as Tajikistan.
Boulengerula taitana is a species of caecilian. It is endemic to the Taita Hills region of southeast Kenya. Boulengerula taitana are unique caecilians in appearance, fertilization type, and parental care. From their similar shape and presentation to worms, and their internalized fertilization, they set themselves apart from many other amphibians. D. taitana interactions between mothers and newly hatched young are unique in that the mother uses her own skin as a food resource for offspring. This species also has physiological adaptations in place to increase oxygen uptake and affinity to fit their underground lifestyle. The Boulengerula taitana differentiates itself from its close relatives in ways rarely documented and researched before.
The scissortail sergeant or striptailed damselfish is a large damselfish. It earns its name from the black-striped tail and sides, which are reminiscent of the insignia of a military Sergeant, being similar to those of the sergeant major damselfish. It grows to a length of about 16 centimetres (6.3 in).
Parental care is a behavioural and evolutionary strategy adopted by some animals, involving a parental investment being made to the evolutionary fitness of offspring. Patterns of parental care are widespread and highly diverse across the animal kingdom. There is great variation in different animal groups in terms of how parents care for offspring, and the amount of resources invested by parents. For example, there may be considerable variation in the amount of care invested by each sex, where females may invest more in some species, males invest more in others, or investment may be shared equally. Numerous hypotheses have been proposed to describe this variation and patterns in parental care that exist between the sexes, as well as among species.
Amaurobius ferox, sometimes known as the black lace-weaver, is a common nocturnal spider belonging to the family Amaurobiidae and genus Amaurobius. Its genus includes three subsocial species, A. fenestralis, A. similis and A. ferox, all three of which have highly developed subsocial organizations.
The six-spotted fishing spider is an arachnid from the nursery web spider family Pisauridae. This species is from the genus Dolomedes, or the fishing spiders. Found in wetland habitats throughout North America, these spiders are usually seen scampering along the surface of ponds and other bodies of water. They are also referred to as dock spiders because they can sometimes be witnessed quickly vanishing through the cracks of boat docks. D. triton gets its scientific name from the Greek mythological god Triton, who is the messenger of the big sea and the son of Poseidon.
Filial cannibalism occurs when an adult individual of a species consumes all or part of the young of its own species or immediate offspring. Filial cannibalism occurs in many species ranging from mammals to insects, and is especially prevalent in various types of fish species with males that engage in egg guardianship. The exact evolutionary purpose of the practice in those species is unclear and debated among zoologists, though there is consensus that it may have, or may have had at some point in species' evolutionary history, certain evolutionary and ecological implications.
Pisaurina mira, also known as the American nursery web spider, due to the web it raises young in, is a species of spider in the family Pisauridae. They are often mistaken for wolf spiders (Lycosidae) due to their physical resemblance. P. mira is distinguished by its unique eye arrangement of two rows.
Stegodyphus sarasinorum, also known as the Indian cooperative spider, is a species of velvet spider of the family Eresidae. It is native to India, Sri Lanka, Nepal, and Myanmar. This spider is a social spider that exhibits communal predation and feeding, where individuals live in large cooperatively built colonies with a nest or retreat constructed of silk woven using leaves, twigs, and food carcasses, and a sheet web for prey capture.
Vertebrate maternal behavior is a form of parental care that is specifically given to young animals by their mother in order to ensure the survival of the young. Parental care is a form of altruism, which means that the behaviors involved often require a sacrifice that could put their own survival at risk. This encompasses behaviors that aid in the evolutionary success of the offspring and parental investment, which is a measure of expenditure exerted by the parent in an attempt to provide evolutionary benefits to the offspring. Therefore, it is a measure of the benefits versus costs of engaging in the parental behaviors. Behaviors commonly exhibited by the maternal parent include feeding, either by lactating or gathering food, grooming young, and keeping the young warm. Another important aspect of parental care is whether the care is provided to the offspring by each parent in a relatively equal manner, or whether it is provided predominantly or entirely by one parent. There are several species that exhibit biparental care, where behaviors and/or investment in the offspring is divided equally amongst the parents. This parenting strategy is common in birds. However, even in species who exhibit biparental care, the maternal role is essential since the females are responsible for the incubation and/or delivery of the young.
Stegodyphus dumicola, commonly known as the African social spider, is a species of spider of the family Eresidae, or the velvet spider family. It is native to Central and southern Africa. This spider is one of three Stegodyphus spiders that lives a social lifestyle. This spider has been studied living in large natal colonies in large, unkempt webs. Each colony is composed mainly of females, where a minority act as reproducers, and a majority remain childless and take care of the young. Males live a shorter lifespan, during which they will largely remain in the natal nest. Females are known for extreme allomaternal care, since all females – even unmated virgin ones – will take care of the young until they are eventually consumed by the brood.
Vertical transmission of symbionts is the transfer of a microbial symbiont from the parent directly to the offspring. Many metazoan species carry symbiotic bacteria which play a mutualistic, commensal, or parasitic role. A symbiont is acquired by a host via horizontal, vertical, or mixed transmission.
Pardosa agrestis is a non-web-building spider in the family Lycosidae, commonly known as wolf spiders.
Pardosa pseudoannulata, a member of a group of species referred to as wolf-spiders, is a non-web-building spider belonging to the family Lycosidae. P. pseudoannulata are wandering spiders that track and ambush prey and display sexual cannibalism. They are commonly encountered in farmlands across China and other East Asian countries. Their venom has properties that helps it function as an effective insecticide, and it is, therefore, a crucial pesticide control agent.