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The mouthparts of arthropods have evolved into a number of forms, each adapted to a different style or mode of feeding. Most mouthparts represent modified, paired appendages, which in ancestral forms would have appeared more like legs than mouthparts. In general, arthropods have mouthparts for cutting, chewing, piercing, sucking, shredding, siphoning, and filtering. This article outlines the basic elements of four arthropod groups: insects, myriapods, crustaceans and chelicerates. Insects are used as the model, with the novel mouthparts of the other groups introduced in turn. Insects are not, however, the ancestral form of the other arthropods discussed here.
Insect mouthparts exhibit a range of forms. The earliest insects had chewing mouthparts. Specialisation includes mouthparts modified for siphoning, piercing, sucking and sponging. These modifications have evolved a number of times. For example, mosquitoes and aphids both pierce and suck; however, female mosquitoes feed on animal blood whereas aphids feed on plant fluids. This section provides an overview of the individual mouthparts of chewing insects.
The labrum is a flat extension of the head (below the clypeus), covering the mandibles. Unlike other mouthparts, the labrum is a single, fused plate (though it originally was—and embryonically is—two structures). It is the upper-most of the mouthparts and located on the midline. It serves to hold food in place during chewing by the mandibles and thus can simply be described as an upper lip.
Chewing insects have two mandibles, one on each side of the head. They are typically the largest mouthpart of chewing insects, being used to masticate (cut, shred, tear, crush, chew) food items. They open outwards (to the sides of the head) and come together medially.
Paired maxillae cut food and manipulate it during mastication. Maxillae can have hairs and "teeth" along their inner margins. At the outer margin, the galea is a cupped or scoop-like structure, which sits over the outer edge of the labium. They also have palps, which are used to sense the characteristics of potential foods.
The labium is a single structure, although it is formed from two fused secondary maxillae. It can be described as the floor of the mouth and functioning in close the mouth of the insect. With the maxillae, it assists manipulation of food during mastication.
The hypopharynx is a somewhat globular structure, arising from the base of the labium. It assists swallowing. It performs the role of the tongue found in large vertebrates.
Myriapods comprise four classes of arthropod, each with a similar morphology: Class Chilopoda (centipedes); class Diplopoda (millipedes); class Pauropoda; and class Symphyla. Myriapod mouthparts are similar to those of chewing insects, although there is some variation between the myriapod classes. A labrum is present but sometimes is not obvious and forms an upper lip, often in association with an epistome. The labium is formed by first maxillae in diplopoda forming the gnathochilarium. The preoral cavity so-formed contains paired mandibles and any maxillae which are present.
Centipedes, in addition to their mouthparts, possess a pair of "poison claws", or forcipules. These, like the maxillipeds of crustaceans, are modified legs and not true mouthparts. [1] The forcipules arise from the first body segment, curving forward and to the midline. The tip is a pointed fang, which has an opening from a venom gland. The forcipules are used to capture and envenomate prey.
Crustaceans comprise a number of classes, with various feeding modes supported by a range of adaptations to the mouthparts. In general, however, crustaceans possess paired mandibles with opposing biting and grinding surfaces. The mandibles are followed by paired first and second maxillae. Both the mandibles and the maxillae have been variously modified in different crustacean groups for filter feeding with the use of setae.
Up to the first three pairs of legs are modified to maxillipeds, which assist manipulation of food items by passing food forward to the mandibles for chewing or to the maxillae for cutting into smaller pieces.
Filter feeding crustaceans have setae on modified appendages that act as filters. Filter feeding may have developed in association with swimming, with early morphological adaptations occurring on the appendages of the body trunk. Subsequent adaptations appear to have favored forward filtering appendages. Filtering appendages generate water currents that bring food items into reach for collection by setae. Other setae may be used to brush the filtering setae clean, and yet other setae may transport food items to the mouth.
Barnacles have thoracic appendages modified for feeding, the cirri, which filter suspended food particles from water currents and pass the food to the mouth.
Chelicerates comprise four classes of arthropod, with similar gross morphology but defining differences: Class Xiphosura (horseshoe crabs); class Eurypterida (the extinct eurypterids); class Arachnida (spiders, scorpions, ticks and mites); and class Pycnogonida (sea spiders). Chelicerates are in part defined by possessing chelicerate appendages, although crustaceans also possess chelate appendages. Chelicerates are more easily distinguished from other arthropods in lacking antennae and mandibles.
Chelicerae are chelate appendages that are used to grasp food. For example, in horseshoe crabs, they are like pincers, whereas in spiders, they are hollow and contain (or are connected to) venom glands and are used to inject venom to disable prey prior to feeding. In some spiders, the chelicerae have teeth, which are used to macerate prey items to assist digestion by secreted enzymes. Those spiders without toothed chelicerae inject digestive enzymes directly into their prey. Mites and ticks have a range of chelicerae. Carnivores have chelicerae that tear and crush prey, whereas herbivores can have chelicerae that are modified for piercing and sucking (as do parasitic species). In sea spiders, the chelicerae (also known as chelifores) are short and chelate and are positioned on either side of the base of the proboscis or sometimes vestigial or absent.
Sea spiders possess a tubular proboscis forward from the body trunk, at the end of which is the opening to the mouth. In those species that lack chelifores and palps, the proboscis is well developed and more mobile and flexible. In such cases, it can be equipped with sensory bristles and strong rasping ridges around the mouth.
The subphylum Chelicerata constitutes one of the major subdivisions of the phylum Arthropoda. Chelicerates include the sea spiders, horseshoe crabs, and arachnids, as well as a number of extinct lineages, such as the eurypterids and chasmataspidids.
Centipedes are predatory arthropods belonging to the class Chilopoda of the subphylum Myriapoda, an arthropod group which includes millipedes and other multi-legged animals. Centipedes are elongated segmented (metameric) creatures with one pair of legs per body segment. All centipedes are venomous and can inflict painful stings, injecting their venom through pincer-like appendages known as forcipules or toxicognaths, which are actually modified legs instead of fangs. Despite the name, no centipede has exactly 100 pairs of legs; number of legs ranges from 15 pairs to 191 pairs, always an odd number.
The jaw is any opposable articulated structure at the entrance of the mouth, typically used for grasping and manipulating food. The term jaws is also broadly applied to the whole of the structures constituting the vault of the mouth and serving to open and close it and is part of the body plan of humans and most animals.
Pedipalps are the secondary pair of forward appendages among chelicerates – a group of arthropods including spiders, scorpions, horseshoe crabs, and sea spiders. The pedipalps are lateral to the chelicerae ("jaws") and anterior to the first pair of walking legs.
The chelicerae are the mouthparts of the subphylum Chelicerata, an arthropod group that includes arachnids, horseshoe crabs, and sea spiders. Commonly referred to as "jaws", chelicerae may be shaped as either articulated fangs, or as a type of pincers. Some chelicerae, such as those found on nearly all spiders, are hollow and contain venom glands, and are used to inject venom into prey or a perceived threat. Both pseudoscorpions and harvestmen have structures on their chelicerae that are used for grooming.
An appendage is an external body part, or natural prolongation, that protrudes from an organism's body.
The decapod is made up of 20 body segments grouped into two main body parts: the cephalothorax and the pleon (abdomen). Each segment may possess one pair of appendages, although in various groups these may be reduced or missing. They are, from head to tail:
The arthropod leg is a form of jointed appendage of arthropods, usually used for walking. Many of the terms used for arthropod leg segments are of Latin origin, and may be confused with terms for bones: coxa, trochanter, femur, tibia, tarsus, ischium, metatarsus, carpus, dactylus, patella.
Insect mandibles are a pair of appendages near the insect's mouth, and the most anterior of the three pairs of oral appendages. Their function is typically to grasp, crush, or cut the insect's food, or to defend against predators or rivals. Insect mandibles, which appear to be evolutionarily derived from legs, move in the horizontal plane unlike those of vertebrates, which appear to be derived from gill arches and move vertically.
The anatomy of spiders includes many characteristics shared with other arachnids. These characteristics include bodies divided into two tagmata, eight jointed legs, no wings or antennae, the presence of chelicerae and pedipalps, simple eyes, and an exoskeleton, which is periodically shed.
The mouth is the body orifice through which many animals ingest food and vocalize. The body cavity immediately behind the mouth opening, known as the oral cavity, is also the first part of the alimentary canal which leads to the pharynx and the gullet. In tetrapod vertebrates, the mouth is bounded on the outside by the lips and cheeks — thus the oral cavity is also known as the buccal cavity — and contains the tongue on the inside. Except for some groups like birds and lissamphibians, vertebrates usually have teeth in their mouths, although some fish species have pharyngeal teeth instead of oral teeth.
The mandible of an arthropod is a pair of mouthparts used either for biting or cutting and holding food. Mandibles are often simply called jaws. Mandibles are present in the extant subphyla Myriapoda, Crustacea and Hexapoda. These groups make up the clade Mandibulata, which is currently believed to be the sister group to the rest of arthropods, the clade Arachnomorpha.
The (pan)arthropod head problem is a long-standing zoological dispute concerning the segmental composition of the heads of the various arthropod groups, and how they are evolutionarily related to each other. While the dispute has historically centered on the exact make-up of the insect head, it has been widened to include other living arthropods, such as chelicerates, myriapods, and crustaceans, as well as fossil forms, such as the many arthropods known from exceptionally preserved Cambrian faunas. While the topic has classically been based on insect embryology, in recent years a great deal of developmental molecular data has become available. Dozens of more or less distinct solutions to the problem, dating back to at least 1897, have been published, including several in the 2000s.
In arthropods, the maxillae are paired structures present on the head as mouthparts in members of the clade Mandibulata, used for tasting and manipulating food. Embryologically, the maxillae are derived from the 4th and 5th segment of the head and the maxillary palps; segmented appendages extending from the base of the maxilla represent the former leg of those respective segments. In most cases, two pairs of maxillae are present and in different arthropod groups the two pairs of maxillae have been variously modified. In crustaceans, the first pair are called maxillulae.
Insects have mouthparts that may vary greatly across insect species, as they are adapted to particular modes of feeding. The earliest insects had chewing mouthparts. Most specialisation of mouthparts are for piercing and sucking, and this mode of feeding has evolved a number of times independently. For example, mosquitoes and aphids both pierce and suck, though female mosquitoes feed on animal blood whereas aphids feed on plant fluids.
Arthropods are invertebrate animals in the phylum Arthropoda. They possess an exoskeleton with a cuticle made of chitin, often mineralised with calcium carbonate, a body with differentiated (metameric) segments, and paired jointed appendages. In order to keep growing, they must go through stages of moulting, a process by which they shed their exoskeleton to reveal a new one. They are an extremely diverse group, with up to 10 million species.
Insect morphology is the study and description of the physical form of insects. The terminology used to describe insects is similar to that used for other arthropods due to their shared evolutionary history. Three physical features separate insects from other arthropods: they have a body divided into three regions, three pairs of legs, and mouthparts located outside of the head capsule. This position of the mouthparts divides them from their closest relatives, the non-insect hexapods, which include Protura, Diplura, and Collembola.
Spiders are air-breathing arthropods that have eight legs, chelicerae with fangs generally able to inject venom, and spinnerets that extrude silk. They are the largest order of arachnids and rank seventh in total species diversity among all orders of organisms. Spiders are found worldwide on every continent except for Antarctica, and have become established in nearly every land habitat. As of August 2022, 50,356 spider species in 132 families have been recorded by taxonomists. However, there has been debate among scientists about how families should be classified, with over 20 different classifications proposed since 1900.
This glossary describes the terms used in formal descriptions of spiders; where applicable these terms are used in describing other arachnids.
Wingertshellicus is an extinct genus of arthropod that has been found in Hunsrück Slate, that is located in the Rhenish Massif in Germany, and lived about 405 million years ago, during the Lower Emsian.