Temporal range: 40–0Ma
|Euperipatoides kanangrensis on a eucalyptus log, in which it normally resides.|
Sole class: Udeonychophora
|Global range of Onychophora: Peripatidae in green, Peripatopsidae in blue|
The velvet worms (Onychophora — literally "claw bearers") are a minor ecdysozoan phylum with ~180 species. These obscurely segmented organisms have tiny eyes, antennae, multiple pairs of legs and slime glands. They have variously been compared to worms with legs, caterpillars and slugs. Most common in tropical regions of the Southern Hemisphere, they prey on smaller animals such as insects, which they catch by squirting an adhesive mucus. In modern zoology, they are particularly renowned for their curious mating behaviour and for bearing live young.
The two extant families of velvet worms are Peripatidae and Peripatopsidae. They show a peculiar distribution, with the peripatids being predominantly equatorial and tropical, while the peripatopsids are all found in what used to be Gondwana.
Formerly considered part of Tracheata, velvet worms are now considered close relatives of the Arthropoda and Tardigrada, with which they form the taxon Panarthropoda. This makes them of palaeontological interest, as they can help reconstruct the ancestral arthropod.
- 1 Anatomy
- 2 Distribution and habitat
- 3 Slime
- 4 Behaviour
- 5 Ecology
- 6 Conservation status
- 7 Phylogeny
- 8 Evolutionary history
- 9 Taxonomy
- 10 Human uses
- 11 Classification
- 12 See also
- 13 Notes
- 14 References
- 15 External links
Velvet worms are segmented creatures with a flattened cylindrical body cross-section and rows of unstructured body appendages known as lobopods (informally: stub feet). The animals grow to between 0.5 and 20 cm (.2 to 8 in), with the average being about 5 cm (2 in), and have between 13 and 43 pairs of legs. Their skin consists of numerous, fine transverse rings and is often inconspicuously coloured orange, red or brown, but sometimes also bright green, blue, gold or white, and occasionally patterned with other colours.
Segmenting—outwardly inconspicuous and identifiable only in the regular spacing of the pairs of legs—is visible in the regular arrangement of skin pores, excretion organs and concentrations of nerve cells. The individual body sections are largely unspecialised; even the head develops only a little differently from the abdominal segments. Segmentation is apparently specified by the same gene as in other groups of animals and is activated in each case, during embryonic development, at the rear border of each segment and in the growth zone of the stub feet.
The stub feet that characterise the velvet worms are conical, baggy appendages of the body, which are internally hollow and have no joints. Although the number of feet can vary considerably between species, their structure is basically very similar. Rigidity is provided by the hydrostatic pressure of their fluid contents, and movement is usually obtained passively by stretching and contraction of the animal's entire body. However, each leg can also be shortened and bent by internal muscles. Due to the lack of joints, this bending can take place at any point along the sides of the leg.
In some species, two different organs are found within the feet:
- Crural glands are situated at the shoulder of the legs, extending into the body cavity. They open outwards at the crural papillae—small wart-like bumps on the belly side of the leg—and secrete chemical messenger materials called pheromones. Their name comes from the Latin cruralis meaning "of the legs".
- Coxal vesicles are pouches located on the belly side of the leg, which can be everted and probably serve in water absorption. They are only found within the family Peripatidae and are named from coxa, the Latin word for "hip".
On each foot is a pair of retractable, hardened (sclerotised) chitin claws, which give the taxon its scientific name: Onychophora is derived from the Greek onyches, "claws"; and pherein, "to carry". At the base of the claws are three to six spiny "cushions" on which the leg sits in its resting position and on which the animal walks over smooth substrates. The claws are used mainly to gain a firm foothold on uneven terrain.
Each claw is composed of three stacked elements, like Russian nesting dolls. The outermost is shed during ecdysis, which exposes the next element in — which is fully formed, so does not need time to harden before it is used. (This distinctive construction identifies many early Cambrian fossils as early offshoots of the onychophoran lineage.)
Apart from the pairs of legs, there are three further body appendages, which are at the head and comprise three segments:
- On the first head segment is a pair of slender antennae, which serve in sensory perception. They probably do not correspond directly to the antennae of the Arthropoda, but perhaps rather with their "lips" or labrum. At their base is found a pair of simple eyes, except in a few blind species. In front of these, in many Australian species, are various dimples, the function of which is not yet clear. It appears that in at least some species, these serve in the transfer of sperm-cell packages (spermatophores).
- On the belly side of the second head segment is the labrum, a mouth opening surrounded by sensitive "lips". In the velvet worms, this structure is a muscular outgrowth of the throat, so, despite its name, it is probably not homologous to the labrum of the Arthropoda and is used for feeding. Deep within the oral cavity lie the sharp, crescent-shaped "jaws", or mandibles, which are strongly hardened and resemble the claws of the feet, with which they are probably homologous;:146 early in development, the jaw appendages have a similar position and shape to the subsequent legs. The jaws are divided into internal and external mandibles and their concave surface bears fine denticles. They move backward and forward in a longitudinal direction, tearing apart the prey.
The surface of the mandibles is smooth, with no ornamentation. The cuticle in the mandibles (and claws) is distinct from the rest of the body. It has an inner and outer component; the outer component has just two layers (whereas body cuticle has four), and these outer layers (in particular the inner epicuticle) are dehydrated and strongly tanned, affording toughness.
- On the third head segment, to the left and right of the mouth, are two openings designated "oral papillae". Within these are a pair of large, heavily internally branched slime glands. These lie roughly in the centre of the body and secrete a sort of milky-white slime, which is used to ensnare prey and for defensive purposes. Sometimes the connecting "slime conductor" is broadened into a reservoir, which can buffer pre-produced slime. The slime glands themselves are probably modified crural glands.
All three structures correspond to an evolutionary origin in the leg pairs of the other segments.
Skin and musculature
Unlike the arthropods, velvet worms do not possess a rigid exoskeleton. Instead, their fluid-filled body cavity acts as a hydrostatic skeleton, similarly to many unrelated soft-bodied animals that are cylindrically shaped, for example sea anemones and various worms. Pressure of their incompressible internal bodily fluid on the body wall provides rigidity, and muscles are able to act against it.
The body wall consists of a non-cellular outer skin, the cuticula; a single layer of epidermis cells forming an internal skin; and beneath this, usually three layers of muscle, which are embedded in connective tissues.
The cuticula is about a micrometer thick and covered with fine villi. In composition and structure, it resembles the cuticula of the arthropods, consisting of α-chitin and various proteins, although not containing collagen. It can be divided into an external epicuticula and an internal procuticula, which themselves consist of exo- and endo-cuticula. This multi-level structure is responsible for the high flexibility of the outer skin, which enables the velvet worm to squeeze itself into the narrowest crevices. Although outwardly water-repellent, the cuticula is not able to prevent water loss by respiration, and, as a result, velvet worms can only live in microclimates with high humidity to avoid desiccation.
The surface of the cuticula is scattered with numerous fine papillae, the larger of which carry visible villi-like sensitive bristles. The papillae themselves are covered with tiny scales, lending the skin a velvety appearance (from which the common name is likely derived). It also feels like dry velvet to the touch, for which its water-repellent nature is responsible. Moulting of the skin (ecdysis) takes place regularly, around every 14 days, induced by the hormone ecdysone. The inner surface of the skin bears a hexagonal pattern.
At each moult, the shed skin is replaced by the epidermis, which lies immediately beneath it; unlike the cuticula, this consists of living cells. Beneath this lies a thick layer of connective tissue, which is composed primarily of collagen fibres aligned either parallel or perpendicular to the body's longitudinal axis. Within the connective tissue lie three continuous layers of unspecialised smooth muscular tissue. The relatively thick outer layer is composed of annular muscles, and the similarly voluminous inner layer of longitudinal muscles. Between them lie thin diagonal muscles that wind backward and forward along the body axis in a spiral. Between the annular and diagonal muscles exist fine blood vessels, which lie below the superficially recognisable transverse rings of the skin and are responsible for the pseudo-segmented markings.
Beneath the internal muscle layer lies the body cavity. In cross-section, this is divided into three regions by so-called dorso-ventral muscles, which run from the middle of the underbelly through to the edges of the upper side: a central midsection and on the left and right, two side regions that also include the legs.
The colouration of Onychophora is generated by a range of pigments.[clarification needed] The solubility of these pigments is a useful diagnostic character: in all arthropods and tardigrades, the body pigment is soluble in ethanol. This is also true for the Peripatidae, but in the case of the Peripatopsidae, the body pigment is insoluble in ethanol.
Haemocoel and circulation
The body cavity is known as a "pseudocoel", or haemocoel. Unlike a true coelom, a pseudocoel is not fully enclosed by a cell layer derived from the embryonic mesoderm. A coelom is, however, formed around the gonads and the waste-eliminating nephridia.
As the name haemocoel suggests, the body cavity is filled with a blood-like liquid in which all the organs are embedded; in this way, they can be easily supplied with nutrients circulating in the blood. This liquid is colourless as it does not contain pigments; for this reason, it only serves a limited role in oxygen transport. Two different types of blood cells (or haemocytes) circulate in the fluid: amoebocytes and nephrocytes. The amoebocytes probably function in protection from bacteria and other foreign bodies; in some species, they also play a role in reproduction. Nephrocytes absorb toxins or convert them into a form suitable for elimination by the nephridia.
The haemocoel is divided by a horizontal partition, the diaphragm, into two parts: the pericardial sinus along the back and the perivisceral sinus along the belly. The former encloses the tube-like heart, and the latter, the other organs. The diaphragm is perforated in many places, enabling the exchange of fluids between the two cavities.
The heart itself is a tube of annular muscles consisting of epithelial tissues, with two lateral openings (ostia) per segment. While it is not known whether the rear end is open or closed, from the front, it opens directly into the body cavity. Since there are no blood vessels, apart from the fine vessels running between the muscle layers of the body wall and a pair of arteries that supply the antennae, this is referred to as an open circulation.
The timing of the pumping procedure can be divided into two parts: diastole and systole. During diastole, blood flows through the ostia from the pericardial sinus (the cavity containing the heart) into the heart. When the systole begins, the ostia close and the heart muscles contract inwards, reducing the volume of the heart. This pumps the blood from the front end of the heart into the perivisceral sinus containing the organs. In this way, the various organs are supplied with nutrients before the blood finally returns to the pericardial sinus via the perforations in the diaphragm. In addition to the pumping action of the heart, body movements also have an influence on circulation.
Oxygen uptake occurs to an extent via simple diffusion through the entire body surface, with the coxal vesicles on the legs possibly being involved in some species. However, of most importance is gas exchange via fine unbranched tubes, the tracheae, which draw oxygen from the surface deep into the various organs, particularly the heart. The walls of these structures, which are less than three micrometers thick in their entirety, consist only of an extremely thin membrane through which oxygen can easily diffuse. The tracheae originate at tiny openings, the spiracles, which themselves are clustered together in dent-like recesses of the outer skin, the atria. The number of "tracheae bundles" thus formed is on average around 75 per body segment; they accumulate most densely on the back of the organism.
Unlike the arthropods, the velvet worms are unable to control the openings of their tracheae; the tracheae are always open, entailing considerable water loss in arid conditions. Water is lost twice as fast as in earthworms and forty times faster than in caterpillars. For this reason, velvet worms are dependent upon habitats with high air humidity.
The digestive tract begins slightly behind the head, the mouth lying on the underside a little way from the frontmost point of the body. Here, prey can be mechanically dismembered by the mandibles with their covering of fine toothlets. Two salivary glands discharge via a common conductor into the subsequent "throat", which makes up the first part of the front intestine. The saliva that they produce contains mucus and hydrolytic enzymes, which initiate in and outside the mouth digestion. Historically, the salivary glands probably evolved from the waste-elimination organs known as nephridia, which are found homologously in the other body segments.
The throat itself is very muscular, serving to absorb the partially liquified food and to pump it, via the oesophagus, which forms the rear part of the front intestine, into the central intestine. Unlike the front intestine, this is not lined with a cuticula but instead consists only of a single layer of epithelial tissue, which does not exhibit conspicuous indentation as is found in other animals. On entering the central intestine, food particles are coated with a mucus-based peritrophic membrane, which serves to protect the lining of the intestine from damage by sharp-edged particles. The intestinal epithelium secretes further digestive enzymes and absorbs the released nutrients, although the majority of digestion has already taken place externally or in the mouth. Indigestible remnants arrive in the rear intestine, or rectum, which is once again lined with a cuticula and which opens at the anus, located on the underside near to the rear end.
In almost every segment is a pair of excretory organs called nephridia, which are derived from coelom tissue. Each consists of a small pouch that is connected, via a flagellated conductor called a nephridioduct, to an opening at the base of the nearest leg known as a nephridiopore. The pouch is occupied by special cells called podocytes, which facilitate ultrafiltration of the blood through the partition between haemocoelom and nephridium. The composition of the urinary solution is modified in the nephridioduct by selective recovery of nutrients and water and by isolation of poison and waste materials, before it is excreted to the outside world via the nephridiopore. The most important nitrogenous excretion product is the water-insoluble uric acid; this can be excreted in solid state, with very little water. This so-called uricotelic excretory mode represents an adjustment to life on land and the associated necessity of dealing economically with water.
A pair of former nephridia in the head were converted secondarily into the salivary glands, while another pair in the final segment of male specimens now serve as glands that apparently play a role in reproduction.
The entire body—including the stub feet—is littered with numerous papillae: warty protrusions that carry a mechanoreceptive bristle (responsive to mechanical stimuli) at the tip, each of which is also connected to further sensory nerve cells lying beneath. The mouth papillae, the exits of the slime glands, probably also have a function in sensory perception. Sensory cells known as "sensills" on the "lips" or labrum respond to chemical stimuli and are known as chemoreceptors. These are also found on the two antennae, which can be regarded as the velvet worm's most important sensory organs. Except in a few (typically subterranean) species, one simply constructed eye (ocellus) lies laterally, just underneath the head, behind each antenna. This consists of a chitinous ball lens, a cornea and a retina and is connected to the centre of the brain via an optic nerve. The retina comprises numerous pigment cells and photoreceptors; the latter are easily modified flagellated cells, whose flagellum membranes carry a photosensitive pigment on their surface.
The rhabdomeric eyes of the Onychophora are thought to be homologous with the median ocelli of arthropods; this would imply that the last common ancestor of arthropods bore only median ocelli. However, the innervation shows that the homology is limited: the eyes of Onychophora form behind the antenna, whereas the opposite is true in arthropods.
Both sexes possess pairs of gonads, opening via a channel called a gonoduct into a common genital opening, the gonopore, which is located on the rear ventral side. Both the gonads and the gonoduct are derived from true coelom tissue.
In females, the two ovaries are joined in the middle and to the horizontal diaphragm. The gonoduct appears differently depending on whether the species is live-bearing or egg-laying. In the former, each exit channel divides into a slender oviduct and a roomy "womb", the uterus, in which the embryos develop. The single vagina, to which both uteri are connected, runs outward to the gonopore. In egg-laying species, whose gonoduct is uniformly constructed, the genital opening lies at the tip of a long egg-laying apparatus, the ovipositor. The females of many species also possess a sperm repository called the receptacle seminis, in which sperm cells from males can be stored temporarily or for longer periods.
Males possess two separate testes, along with the corresponding sperm vesicle (the vesicula seminalis) and exit channel (the vasa efferentia). The two vasa efferentia unite to a common sperm duct, the vas deferens, which in turn widens through the ejaculatory channel to open at the gonopore. Directly beside or behind this lie two pairs of special glands, which probably serve an auxiliary reproductive function; the rearmost glands are also known as anal glands.
A penis-like structure has so far only been found in males of the genus Paraperipatus but has not yet been observed in action. As previously mentioned, males of many Australian species exhibit special structures on the head, which apparently take over certain tasks in transferring sperm to the females. In the species Euperipatoides rowelli, sperm is collected by these structures, and, when a female is encountered, the worm inserts its head in the vagina.
Distribution and habitat
Velvet worms live in all tropical habitats and in the temperate zone of the Southern Hemisphere, showing a circumtropical and circumaustral distribution. Individual species are found in Central and South America; the Caribbean islands; equatorial West Africa and Southern Africa; northeastern India; Indonesia and parts of Malaysia; New Guinea; Australia; and New Zealand. Fossils have been found in Baltic amber, indicating that they were formerly more widespread in the Northern Hemisphere when conditions were more suitable.
All extant velvet worms are terrestrial (land-living) and prefer dark environments with high air humidity. They are found particularly in the rainforests of the tropics and temperate zones, where they live among moss cushions and leaf litter, under tree trunks and stones, in rotting wood or in termite tunnels. They also occur in unforested grassland, if there exist sufficient crevices in the soil into which they can withdraw during the day.
Two species live in caves, a habitat to which their ability to squeeze themselves into the smallest cracks makes them exceptionally well-adapted and in which constant living conditions are guaranteed. Since the essential requirements for cave life were probably already present prior to the settlement of these habitats, this may be described as exaptation. Agriculture has apparently made available new habitats for velvet worms; in any case, they are found in man-made cocoa and banana plantations in South America and the Caribbean.
Because the danger of desiccation is greatest during the day and in dry weather, it is not surprising that velvet worms are usually most active at night and during rainy weather. Under cold or dry conditions, they actively seek out crevices in which they shift their body into a resting state. Velvet worms are negatively phototactical: they are repelled by bright light sources.
The largest measured population density is very low, at approximately ten individuals per square meter; velvet worms are often difficult to find in their natural habitat.
The Onychophora forcefully squirt slime from their oral papillae; they do so either in defence against predators or to capture prey. The openings of the glands that produce the slime are in the papillae, a pair of highly modified limbs on the sides of the head below the antennae. The glands themselves are deep inside the body cavity, each at the end of a tube more than half the length of the body. The tube both conducts the fluid and stores it until it is required. The distance that the animal can propel the slime varies; usually it squirts it about a centimetre, but the maximal range has variously been reported to be ten centimetres, or even nearly a foot, although accuracy drops with range. It is not clear to what extent the range varies with the species and other factors. One squirt usually suffices to snare a prey item, although larger prey may be further immobilised by smaller squirts targeted at the limbs; additionally, the fangs of spiders are sometimes targeted.
The slime, which can account for up to 11% of the organism's dry weight, is 90% water; its dry residue consists mainly of proteins — primarily a collagen-type protein. 1.3% of the slime's dry weight consists of sugars, mainly glactosamine. The slime also contains lipids and the surfactant nonylphenol. Onychophora are the only organisms known to produce this latter substance. It tastes "slightly bitter and at the same time somewhat astringent".:760
The proteinaceous composition accounts for the slime's high tensile strength and stretchiness. Upon ejection, it forms a net of threads about 20 µm in diameter, with evenly spaced droplets of viscous adhesive fluid along their length. It subsequently dries, shrinking, losing its stickiness, and becoming brittle. Onychophora eat their dried slime when they can, which is appropriate, because it takes an onychophoran about 24 days to replenish an exhausted slime repository.
The lipid and nonylphenol constituents may serve one of two purposes. They may line the ejection channel, stopping the slime from sticking to the organism when it is secreted; or they may slow the drying process long enough for the slime to reach its target.
Velvet worms move in a slow and gradual motion that makes them difficult for prey to notice. Their trunk is raised relatively high above the ground, and they walk with non-overlapping steps.:21 To move from place to place, the velvet worm crawls forward using its legs; unlike in arthropods, both legs of a pair are moved simultaneously. The claws of the feet are only used on hard, rough terrain where a firm grip is needed; on soft substrates, such as moss, the velvet worm walks on the foot cushions at the base of the claws.
The actual locomotion is achieved less by the exertion of the leg muscles than by local changes of body length. This can be controlled using the annular and longitudinal muscles. If the annular muscles are contracted, the body cross-section is reduced, and the corresponding segment stretches, since its volume must remain constant due to the incompressible behaviour of the coelom's liquid contents; this is the usual mode of operation of the hydrostatic skeleton as also employed by other worms. Due to the stretching, the legs of the segment concerned are lifted and swung forward. Local contraction of the longitudinal muscles then shortens the appropriate segment, and the legs, which are now in contact with the ground, are moved to the rear. This part of the locomotive cycle is the actual leg stroke that is responsible for forward movement. The individual stretches and contractions of the segments are coordinated by the nervous system such that contraction waves run the length of the body, each pair of legs swinging forward and then down and rearward in succession. The organisms can reach speeds of up to four centimetres per second.
The brains of Onychophora, though small, are very complex; consequently, the organisms are capable of rather sophisticated social interactions. Behaviour may vary from genus to genus, so this article reflects the most studied genus, Euperipatoides.
They form social groups of up to fifteen individuals, usually closely related, which will typically live and hunt together. Groups usually live together; an example in drier regions would be in a region of the moist interior of a rotting log. Group members are extremely aggressive towards individuals from other logs. Dominance is achieved through aggression and maintained through submissive behaviour. After a kill, the dominant female always feeds first, followed in turn by the other females, then males, then the young. Social hierarchy is established by a number of interactions: higher-ranking individuals will chase, bite and crawl on top of their subordinates. Juveniles never engage in aggressive behaviour, but climb on top of adults, which tolerate their presence on their backs. When assessing other individuals, individuals often measure one another up by running their antennae down the length of the other individual. Once hierarchy has been established, paired individuals will often cluster together to form an aggregate; this is fastest in male-female pairings, followed by pairs of females, then pairs of males. Hierarchy is quickly established between individuals from a single group, but not between organisms from different groups; these are substantially more aggressive and very rarely climb one another or form aggregates.
Individuals within an individual log are usually closely related; especially so with males. This may be related to the intense aggression between unrelated females.
Velvet worms are ambush predators, hunting only by night, and are able to capture animals at least their own size, although it may take almost all of their slime-secreting capacity to capture a large prey item. They feed on almost any small invertebrates, including woodlice (Isopoda), termites (Isoptera), crickets (Gryllidae), book/bark lice (Psocoptera), cockroaches (Blattidae), millipedes and centipedes (Myriapoda), spiders (Araneae), various worms and even large snails (Gastropoda). Depending on their size, they eat on average every one to four weeks. They are considered to be ecologically equivalent to centipedes (Chilopoda).
Potential victims can be detected from up to four centimetres away and are investigated by the gentle application of the antennae. If they are judged to be a suitable size, slime is ejected to immobilise the prey item. The most energetically favourable prey are two-fifths the size of the hunting onychophoran. The onychophoran bites into the prey and injects saliva, which further reduces motion and may initiate digestion of the prey item's innards. Ninety percent of the time involved in eating a specimen is spent ingesting it; re-ingestion of the slime used to trap the insect is performed while the onychophoran locates a suitable place to puncture the prey, and this phase accounts for around 8% of the feeding time, with the remaining time evenly split between examining, squirting and injecting the prey.
Onychophora probably do not primarily use vision to detect their prey; although their tiny eyes do have a good image-forming capacity, their forward vision is obscured by their antennae; their nocturnal habit also limits the utility of eyesight. Air currents, formed by prey motion, are thought to be the primary mode of locating prey; the role of scent, if any, is unclear. The animals literally creep up on their prey, with their smooth, gradual and fluid movement escaping detection by predators. Once they reach their prey, they touch it very softly with their antennae to assess its size and nutritional value. After each poke, the antenna is hastily retracted to avoid detection by the prey individual. This investigation may last anywhere upwards of ten seconds, until the velvet worm makes a decision as to whether to attack it—or until it disturbs the prey and flees.[clarification needed] Hungry Onychophora spend less time investigating their prey and are quicker to apply their slime. Once slime has been squirted, Onychophora will stop at nothing to hound down and devour their prey, in order to recoup the energetic investment. They have been observed to spend up to ten minutes searching for removed prey, after which they return to their slime to eat it. In the case of smaller prey, they may opt not to slime it at all.
Subsequently, a soft part of the prey item (usually a joint membrane in arthropod prey) is identified, punctured with a bite from the jaws, and injected with saliva. This kills the prey very quickly and begins a slower process of digestion. While the onychophoran waits for the prey to digest, it salivates on its slime and begins to eat it (and anything attached to it). It subsequently tugs and slices at the earlier perforation to allow access to the now-liquefied innards of its prey.
In social groups, the dominant female is the first to feed, not permitting competitors access to the prey item for the first hour of feeding. Subsequently, subordinate individuals begin to feed. The number of males reaches a peak after females start to leave the prey item. After feeding, individuals clean their antennae and mouth parts before re-joining the rest of their group. Because it takes so long to ingest a prey item, hunting mainly happens around dusk; the onychophorans will abandon their prey at sunrise.
This predatory way of life is probably a consequence of the velvet worm's need to remain moist. Due to the continual risk of desiccation, often only a few hours per day are available for finding food. This leads to a strong selection for a low cost-benefit ratio, which can barely be achieved with a herbivorous diet.
Reproduction and life-cycle
All species are in principle sexually distinct and bear, in many cases, a marked sexual dimorphism: the females are usually larger than the males and have, in species where the number of legs is variable, more legs. The females of many species are fertilized only once during their lives, which leads to copulation sometimes taking place before the reproductive organ of the females are fully developed. In such cases, for example at the age of three months in Macroperipatus torquatus, the transferred sperm cells are kept in a special reservoir, where they can remain viable for longer periods.
Fertilization takes place internally, although the mode of sperm transmission varies widely. In most species, for example in the genus Peripatus, a package of sperm cells called the spermatophore is placed into the genital opening of the female. The detailed process by which this is achieved is in most cases still unknown, a true penis having only been observed in species of the genus Paraperipatus. In many Australian species, there exist dimples or special dagger- or axe-shaped structures on the head; the male of Florelliceps stutchburyae presses a long spine against the female's genital opening and probably positions its spermatophore there in this way. During the process, the female supports the male by keeping him clasped with the claws of her last pair of legs. The mating behavior of two species of the genus Peripatopsis is particularly curious. Here, the male places two-millimetre spermatophores on the back or sides of the female. Amoebocytes from the female's blood collect on the inside of the deposition site, and both the spermatophore's casing and the body wall on which it rests are decomposed via the secretion of enzymes. This releases the sperm cells, which then move freely through the haemocoel, penetrate the external wall of the ovaries and finally fertilize the ova. Why this self-inflicted skin injury does not lead to bacterial infections is not yet understood (though likely related to the enzymes used to deteriorate the skin or facilitate the transfer of viable genetic material from male to female).
- Ovipary occur solely in the Peripatopsidae, often in regions with erratic food supply or unsettled climate. In these cases, the yolk-rich eggs measure 1.3 to 2.0 mm and are coated in a protective chitinous shell. Maternal care is unknown.
- The majority of species are ovoviviparous: the medium-sized eggs, encased only by a double membrane, remain in the uterus. The embryos do not receive food directly from the mother, but are supplied instead by the moderate quantity of yolk contained in the eggs—they are therefore described as lecithotrophic. The young emerge from the eggs only a short time before birth. This probably represents the velvet worm's original mode of reproduction, i.e., both oviparous and viviparous species developed from ovoviviparous species.
- True live-bearing species are found in both families, particularly in tropical regions with a stable climate and regular food supply throughout the year. The embryos develop from eggs only micrometres in size and are nourished in the uterus by their mother, hence the description "matrotrophic". The supply of food takes place either via a secretion from the mother directly into the uterus or via a genuine tissue connection between the epithelium of the uterus and the developing embryo, known as a placenta. The former is found only outside the American continent, while the latter occurs primarily in America and the Caribbean and more rarely in the Old World. The gestation period can amount to up to 15 months, at the end of which the offspring emerge in an advanced stage of development. The embryos found in the uterus of a single female do not necessarily have to be of the same age; it is quite possible for there to be offspring at different stages of development and descended from different males. In some species, young tend to be released only at certain points in the year.
A female can have between 1 and 23 offspring per year; development from fertilized ovum to adult takes between 6 and 17 months and does not have a larval stage. This is probably also the original mode of development. Velvet worms have been known to live for up to six years.
Predators and parasites
The velvet worm's important predators are primarily various spiders and centipedes, along with rodents and birds, such as, in Central America, the Clay-coloured Thrush (Turdus grayi). Hemprichi's Coral Snake (Micrurus hemprichii) feeds almost exclusively on velvet worms. For defence, some species roll themselves reflexively into a spiral, while they can also fight off smaller opponents by ejecting slime.
The global conservation status of velvet worm species is difficult to estimate; many species are only known to exist at their type locality (the location at which they were first observed and described). The collection of reliable data is also hindered by low population densities, their typically nocturnal behaviour and possibly also as-yet undocumented seasonal influences and sexual dimorphism.
To date, only eleven species have been studied in sufficient detail to enable population estimates, of which three—Opistopatus roseus, Speleoperipatus spelaeus and Peripatopsis leonina—are considered critically endangered, the last being probably already extinct. Two species—Macroperipatus insularis and Tasmanipatus anophthalmus—are assessed by the IUCN as endangered, while four further species are listed as threatened.
The primary threat comes from destruction and fragmentation of velvet worm habitat due to industrialisation, draining of wetlands and "slash and burn" for agriculture. Many species also have naturally low population densities and closely restricted geographic ranges; as a result, relatively small localised disturbances of important ecosystems can lead to the extinction of entire populations or species. Collection of specimens for universities or research institutes also plays a role on a local scale.
There is a very pronounced difference in the protection afforded to velvet worms between regions: in some countries, such as South Africa, there are restrictions on both collecting and exporting, while in others, such as Australia, only export restrictions exist. Many countries offer no specific safeguards at all. Tasmania has a protection programme that is unique worldwide: one region of forest has its own velvet worm conservation plan, which is tailored to a particular velvet worm species.
In their present forms, the velvet worms are probably very closely related to the arthropods, a very extensive taxon that incorporates, for instance, the crustaceans, insects and arachnids. They share, among other things, an exoskeleton consisting of α-chitin and non-collagenous proteins; gonads and waste-elimination organs enclosed in true coelom tissue; an open blood system with a tubular heart situated at the rear; an abdominal cavity divided into pericardial and perivisceral cavities; respiration via tracheae; and similar embryonic development. Segmentation, with two body appendages per segment, is also shared. However, antennae, mandibles and oral papillae are probably not homologous to the corresponding features in arthropods, i.e., they probably developed independently.
Another closely related group are the comparatively obscure water bears (Tardigrada); however, due to their very small size, these lack some characteristics of the velvet worms and arthropods, such as blood circulation and separate respiratory structures. Together, the velvet worms, arthropods and water bears form a monophyletic taxon, the Panarthropoda, i.e., the three groups collectively cover all descendants of their last common ancestor.
Due to certain similarities of form, the velvet worms were usually grouped with the water bears to form the taxon Protoarthropoda. This designation would imply that both velvet worms and water bears are not yet as highly developed as the arthropods. Modern systematic theories reject such conceptions of "primitive" and "highly developed" organisms and instead consider exclusively the historical relationships among the taxa. These relationships are not as yet fully understood, but it is considered probable that the velvet worms' sister groups form a taxon designated Tactopoda, thus:
For a long time, velvet worms were also considered related to the annelids. They share, among other things, a worm-like body; a thin and flexible outer skin; a layered musculature; paired waste-elimination organs; as well as a simply constructed brain and simple eyes. Decisive, however, was the existence of segmentation in both groups, with the segments showing only minor specialisation. The parapodia appendages found in annelids therefore correspond to the stump feet of the velvet worms.
Within the Articulata concept developed by Georges Cuvier, the velvet worms therefore formed an evolutionary link between the annelids and the arthropods: worm-like precursors first developed parapodia, which then developed further into stub feet as an intermediate link in the ultimate development of the arthropods' appendages. Due to their structural conservatism, the velvet worms were thus considered "living fossils". This perspective was expressed paradigmatically in the statement by the French zoologist A. Vandel:
- Onychophorans can be considered highly evolved annelids, adapted to terrestrial life, which announced prophetically the Arthropoda. They are a lateral branch which has endured from ancient times until today, without important modifications.
Modern taxonomy does not study criteria such as "higher" and "lower" states of development or distinctions between "main" and "side" branches—only family relationships indicated by cladistic methods are considered relevant. From this point of view, several common characteristics still support the Articulata concept—segmented body; paired appendages on each segment; pairwise arrangement of waste-elimination organs in each segment; and above all, a rope-ladder-like nervous system based on a double nerve strand lying along the belly.
An alternative concept, most widely accepted today, is the so-called Ecdysozoa hypothesis. This places the annelids and Panarthropoda in two very different groups: the former in the Lophotrochozoa and the latter in the Ecdysozoa. Mitochondrial gene sequences also provide support for this hypothesis.
Proponents of this hypothesis assume that the aforementioned similarities between annelids and velvet worms either developed convergently or were primitive characteristics passed unchanged from a common ancestor to both the Lophotrochozoa and Ecdysozoa. For example, in the first case, the rope-ladder nervous system would have developed in the two groups independently, while in the second case, it is a very old characteristic, which does not imply a particularly close relationship between the annelids and Panarthropoda.
The Ecdysozoa concept divides the taxon into two, the Panarthropoda into which the velvet worms are placed, and the sister group Cycloneuralia, containing the threadworms (Nematoda), horsehair worms (Nematomorpha) and three rather obscure groups: the mud dragons (Kinorhyncha); penis worms (Priapulida); and brush-heads (Loricifera).
Particularly characteristic of the Cycloneuralia is a ring of "circumoral" nerves around the mouth opening, which the proponents of the Ecdysozoa hypothesis also recognise in modified form in the details of the nerve patterns of the Panarthropoda. Both groups also share a common skin-shedding mechanism (ecdysis) and molecular biological similarities. One problem of the Ecdysozoa hypothesis is the velvet worms' subterminal mouth position: unlike in the Cycloneuralia, the mouth is not at the front end of the body, but lies further back under the belly. However, investigations into their developmental biology, particularly regarding the development of the head nerves, suggest that this was not always the case and that the mouth was originally terminal (situated at the tip of the body). This is supported by the fossil record.
The "stem-group arthropod" hypothesis is very widely accepted, but some trees suggest that the onychophorans may occupy a different position; their brain anatomy is more closely related to that of the chelicerates than to any other arthropod.
Fossils from the early Cambrian bear a striking resemblance to the velvet worms. These fossils, known collectively as the lobopodians, were marine and may represent a stem group to the onychophorans or a grade from which arthropods and onychophora arose. They are found in the Cambrian, Ordovician (possibly), Silurian and Pennsylvanian[note 1] periods.
Historically, all fossil Onychophora and lobopods were lumped into the taxon Xenusia, further subdivided by some authors to the Paleozoic Udeonychophora and the Mesozoic/Tertiary Ontonychophora; living Onychophora were termed Euonychophora.
Importantly, none of the Cambrian fossils bear features that distinctively unite them with the Onychophora; none can be confidently assigned to the onychophoran crown or even stem group.
It is not clear when the transition to a terrestrial existence was made, but it is considered plausible that it took place between the Ordovician and late Silurian—approximately —via the intertidal zone.
The low preservation potential of the non-mineralised Onychophora means that they have a sparse fossil record. Stem-group members include Ilyodes (=Helenodora, Carboniferous), Tertiapatus dominicanus and Succinipatopsis balticus (Tertiary); crown group representatives are known only from amber—there is a single, partial specimen from the Cretaceous,[note 2] and a more comprehensive record in Eocene deposits from . But, in fact, some of these amber-borne specimens lack slime papillae and separate feet, thus may belong in the stem group.
The vagaries of the preservation process can make fossils difficult to interpret. Experiments on the decay and compaction of onychophora demonstrate difficulties in interpreting fossils; certain parts of living onychophora are only visible in certain conditions. The mouth may or may not be preserved; claws may be re-oriented or lost; leg width may increase or decrease; and mud may be mistaken for organs. More significantly, features seen in fossils may be artefacts of the preservation process: for instance, "shoulder pads" may simply be the second row of legs compressed coaxially onto the body; branching "antennae" may in fact be produced through decay.
The modern velvet worms form a monophyletic group, incorporating all the descendants of their common ancestor. Important common derivative characteristics (synapomorphies) include, for example, the mandibles of the second body segment and the oral papillae and associated slime glands of the third; nerve strands extending along the underside with numerous cross-linkages per segment; and the special form of the tracheae.
By 2011, some 180 modern species, comprising 49 genera, had been described; the actual number of species is probably about twice this. According to more recent study, 82 species of Peripatidae and 115 species of Peripatopsidae have been described thus far. However, among these 197 species, 20 are nomina dubia due to major taxonomic inconsistencies. The best-known is the type genus Peripatus, which was described as early as 1825 and which, in English-speaking countries, stands representative for all velvet worms.
All genera are assigned to one of two families, the distribution ranges of which do not overlap but are separated by arid areas or oceans:
- The Peripatopsidae exhibit relatively many characteristics that are perceived as original or "primitive". They have between 13 and 25 pairs of legs, behind or between the last of which is the genital opening (gonopore). Both oviparous and ovoviviparous, as well as genuinely viviparous, species exist, although the Peripatopsidae essentially lack a placenta. Their distribution is circumaustral, encompassing Australia, Tasmania, New Zealand, New Guinea, South Africa and Chile.
- The Peripatidae exhibit a range of derivative features. They are longer, on average, than the Peripatopsidae and also have more leg pairs, numbering between 22 and 43—the gonopore is always between the penultimate pair. There are no oviparous species—the overwhelming majority are viviparous. The females of many viviparous species develop a placenta with which to provide the growing embryo with nutrients. Distribution of the Peripatidae is restricted to the tropical and subtropical zones; in particular, they inhabit Central and northern South America, several Caribbean islands, West Africa, northern India, Malaysia and various Indonesian islands.
- Phylum Onychophora
- Class Onychophorida
- Order † Paronychophora (extinct)
- Order Euonychophora
- Family Peripatidae
- Family Peripatopsidae
- Genera: Acanthokara, Aethrikos, Akthinothele, Anoplokaros, Austroperipatus, Baeothele, Centrorumis, Cephalofovea, Critolaus, Dactylothele, Dystactotylos, Euperipatoides, Florelliceps, Hylonomoipos, Konothele, Lathropatus, Leuropezos, Mantonipatus, Metaperipatus, Minyplanetes, Nodocapitus, Occiperipatoides, Ooperipatellus, Ooperipatus, Opisthopatus, Paraperipatus, Paropisthopatus, Peripatoides, Peripatopsis, Phallocephale, Planipallipus, Regimitra, Ruhbergia, Sphenoparme, Symperipatus, Tasmania, Tasmanipatus, Tetrameraden, Vescerro, Wambalana
- Family † incertae sedis
- Genus † Helenodora
- Class Onychophorida
- Poinar, G. Jr. (2000). "Fossil Onychophorans from Dominican and Baltic Amber: Tertiapatus dominicanus n.g., n.sp. (Tertiapatidae n.fam.) and Succinipatopsis balticus n.g., n.sp. (Succinipatopsidae n.fam.) with a Proposed Classification of the Subphylum Onychophora". Invertebrate Biology 119 (1): 104–9. doi:10.1111/j.1744-7410.2000.tb00178.x.
- Holm, E.; Dippenaar-Schoeman, A. (2010). The Arthropods of Southern Africa. ISBN 978-0-7993-4689-3.
- Prothero, D. R.; Buell (llustrator), C. D. (2007). Evolution: What the Fossils Say and Why It Matters. New York: Columbia University Press. p. 193. ISBN 0-231-13962-4.
- Ruppert, E. E.; Fox, R. S.; Barnes, R. D. (2004). Invertebrate Zoology: A Functional Evolutionary Approach (7th ed.). Belmont, CA: Thomson-Brooks / Cole. ISBN 978-0-03-025982-1, p. 505
- Piper, R. (2007). Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals. Greenwood Press.
- Fishelson, L. (1978). Zoology 1 (3rd ed.). Israel: Hakibutz Hameuchad Publishing. p. 430.
- Smith, M. R.; Ortega Hernández, J. (2014). "Hallucigenia's onychophoran-like claws and the case for Tactopoda". Nature 514 (7522): 363–366. doi:10.1038/nature13576. PMID 25132546.
- Head patterning and Hox gene expression in an onychophoran and its implications for the arthropod head problem. Eriksson BJ, Tait NN, Budd GE, Janssen R, Akam M. Dev Genes Evol. 2010 Sep;220(3–4):117-22. doi: 10.1007/s00427-010-0329-1.
- Koenemann, Stefan; Jenner, Ronald (2005-04-27). Crustacea and Arthropod Relationships. ISBN 9781420037548.
- Eriksson, B. J.; Tait, N. N.; Budd, G. E. (2003). "Head development in the onychophoranEuperipatoides kanangrensis with particular reference to the central nervous system". Journal of Morphology 255 (1): 1–23. doi:10.1002/jmor.10034. PMID 12420318.
- Wright, J. C.; Luke, B. M. (1989). "Ultrastructural and histochemical investigations of peripatus integument". Tissue and Cell 21 (4): 605–625. doi:10.1016/0040-8166(89)90012-8. PMID 18620280.
- Campiglia, S; Lavallard, R (1990). Minelli, Alessandro, ed. Proceedings of the 7th International Congress of Myriapodology. p. 461. ISBN 9004089721.
- Maas, A.; Mayer, G.; Kristensen, R. M.; Waloszek, D. (2007). "A Cambrian micro-lobopodian and the evolution of arthropod locomotion and reproduction". Chinese Science Bulletin 52 (24): 3385. doi:10.1007/s11434-007-0515-3.
- Monge-Najera, J. (1995). "Phylogeny, Biogeography and Reproductive Trends in the Onychophora" (pdf). Zoological Journal of the Linnean Society 114 (1): 21–60. doi:10.1111/j.1096-3642.1995.tb00111.x.
- S. M. Manton (1937). "Studies on the Onychophora". J Exp Biol 14 (4): 470–472.
- Mayer, G. (2006). "Structure and development of onychophoran eyes: What is the ancestral visual organ in arthropods?". Arthropod Structure and Development 35 (4): 231–245. doi:10.1016/j.asd.2006.06.003. PMID 18089073.
- Eriksson, J. (2003). Evolution and Development of the Onychophoran Head and Nervous System. ISBN 91-554-5613-8.
- Kemp, S. (1913). "Preliminary note on a new genus of Onychophora from the N. E. Frontier of India". Records of the Indian Museum 9: 241–242.
- Kemp, S. (1914). "Onychophora. Zoological results of the Abor expedition, 1911–1912". Records of the Indian Museum 8: 471–492.
- Poinar, G. (1996). "Fossil Velvet Worms in Baltic and Dominican Amber: Onychophoran Evolution and Biogeography". Science 273 (5280): 1370–1371. Bibcode:1996Sci...273.1370P. doi:10.1126/science.273.5280.1370.
- Baer, A.; Mayer, G. (2012). "Comparative anatomy of slime glands in onychophora (velvet worms)". Journal of Morphology 273 (10): 1079–1088. doi:10.1002/jmor.20044. PMID 22707384.
- Benkendorff, K.; Beardmore, K.; Gooley, A. A.; Packer, N. H.; Tait, N. N. (1999). "Characterisation of the slime gland secretion from the peripatus, Euperipatoides kanangrensis (Onychophora: Peripatopsidae)". Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology 124 (4): 457–465. doi:10.1016/S0305-0491(99)00145-5.
- Holm, Erik, Dippenaar-Schoeman, Ansie; Goggo Guide; LAPA publishers (URL: WWW.LAPA.co.za) 2010
- Harmer, Sir Sidney Frederic; Shipley, Arthur Everett et alia: The Cambridge natural history Volume 5, Peripatus, Myriapods, Insects. Macmillan Company 1922
- Read, V. M. S. J.; Hughes, R. N. (1987). "Feeding Behaviour and Prey Choice in Macroperipatus torquatus (Onychophora)". Proceedings of the Royal Society B, Biological Sciences 230 (1261): 483. Bibcode:1987RSPSB.230..483R. doi:10.1098/rspb.1987.0030.
- Moseley, H. N. "On the Structure and Development of Peripatus capensis". doi:10.1098/rstl.1874.0022.
- Pfeiffer, F.; Zielińska, T. (2004). Walking: biological and technological aspects. CISM International Centre for Mechanical Sciences Courses and Lectures 467. Springer. ISBN 3-211-22134-4.
- Reinhard, J.; Rowell, D. M. (2005). "Social behaviour in an Australian velvet worm, Euperipatoides rowelli (Onychophora: Peripatopsidae)". Journal of Zoology 267: 1. doi:10.1017/S0952836905007090.
- Dias, S. C.; Lo-Man-Hung, N. F. (2009). "First record of an onychophoran (Onychophora, Peripatidae) feeding on a theraphosid spider (Araneae, Theraphosidae)". Journal of Arachnology 37: 116–117. doi:10.1636/ST08-20.1.
- Read, V. M. S. T. J. (1988). "The Onychophora of Trinidad, Tobago and the Lesser Antilles". Zoological Journal of the Linnean Society 93 (3): 225–257. doi:10.1111/j.1096-3642.1988.tb01362.x.
- Walker, M. H.; Tait, N. N. (2004). "Studies of embryonic development and the reproductive cycle in ovoviviparous Australian Onychophora (Peripatopsidae)". Journal of Zoology 264 (4): 333–354. doi:10.1017/S0952836904005837.
- 2007 IUCN Red List – Search
- Podsiadlowski, L.; Braband. A.; Mayer, G. (2008). "The Complete Mitochondrial Genome of the Onychophoran Epiperipatus biolleyi Reveals a Unique Transfer RNA Set and Provides Further Support for the Ecdysozoa Hypothesis". Molecular Biology and Evolution 25 (1): 42–51. doi:10.1093/molbev/msm223. PMID 17934206.
- Strausfeld, N. J.; Mok Strausfeld, C.; Loesel, R.; Rowell, D.; Stowe, S. (2006). "Arthropod phylogeny: onychophoran brain organization suggests an archaic relationship with a chelicerate stem lineage". Proceedings of the Royal Society B: Biological Sciences 273 (1596): 1857–1866. doi:10.1098/rspb.2006.3536. PMC 1634797. PMID 16822744.
- Grimaldi, D. A.; Engel, M. S.; Nascimbene, P. C. (2002). "Fossiliferous Cretaceous Amber from Myanmar (Burma): Its Rediscovery, Biotic Diversity, and Paleontological Significance". American Museum Novitates 3361: 1–71. doi:10.1206/0003-0082(2002)361<0001:FCAFMB>2.0.CO;2. ISSN 0003-0082. hdl:2246/2914.
- Budd, G. E. (2001). "Why are arthropods segmented?". Evolution and Development 3 (5): 332. doi:10.1046/j.1525-142X.2001.01041.x. PMID 11710765.
- Bergstrom, J.; Hou, X. (2001). "Cambrian Onychophora or Xenusians". Zoologischer Anzeiger - A Journal of Comparative Zoology 240 (3–4): 237–245. doi:10.1078/0044-5231-00031.
- Van Roy, P.; Orr, P. J.; Botting, J. P.; Muir, L. A.; Vinther, J.; Lefebvre, B.; Hariri, K. E.; Briggs, D. E. G. (2010). "Ordovician faunas of Burgess Shale type". Nature 465 (7295): 215. Bibcode:2010Natur.465..215V. doi:10.1038/nature09038. PMID 20463737.
- Von Bitter, P. H.; Purnell, M. A.; Tetreault, D. K.; Stott, C. A. (2007). "Eramosa Lagerstätte—Exceptionally preserved soft-bodied biotas with shallow-marine shelly and bioturbating organisms (Silurian, Ontario, Canada)". Geology 35 (10): 879. doi:10.1130/G23894A.1.
- Thompson, I.; Jones, D. S. (1980). "A Possible Onychophoran from the Middle Pennsylvanian Mazon Creek Beds of Northern Illinois". Journal of Paleontology 54 (3): 588–596. doi:10.2307/1304204 (inactive 2014-09-02). JSTOR 1304204.
- Budd, G. (2001). "Tardigrades as 'Stem-Group Arthropods': The Evidence from the Cambrian Fauna". Zoologischer Anzeiger - A Journal of Comparative Zoology 240 (3–4): 265–279. doi:10.1078/0044-5231-00034. ISSN 0044-5231.
- Poinar, G. (1996). "Fossil Velvet Worms in Baltic and Dominican Amber: Onychophoran Evolution and Biogeography". Science 273 (5280): 1370–1371. Bibcode:1996Sci...273.1370P. doi:10.1126/science.273.5280.1370.
- Monge-Nájera, J.; Xianguang, H. (2002). "Experimental taphonomy of velvet worms (Onychophora) and implications for the Cambrian 'explosion, disparity and decimation' model". Revista de Biología Tropical 50 (3–4): 1133–1138. ISSN 0034-7744.
- Zhang, Z.-Q. (2011). "Animal biodiversity: An introduction to higher-level classification and taxonomic richness". Zootaxa 3148: 7–12. ISBN 978-1-86977-849-1.
- Oliveira I. de S., Read V. M. St. J., Mayer G.; Read; Mayer (2012). "A world checklist of Onychophora (velvet worms), with notes on nomenclature and status of names". ZooKeys 211 (211): 1–70. doi:10.3897/zookeys.211.3463. ISSN 1313-2970. PMC 3426840. PMID 22930648.
- Turner, R. Lister (1924). "88. Malignant Witchcraft in Papua and the Use of Poisons Therein". Man 24: 117–119. JSTOR 2788723.
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