Cerci (sg.: cercus) are paired appendages usually on the rear-most segments of many arthropods, including insects and symphylans. Many forms of cerci serve as sensory organs, but some serve as pinching weapons or as organs of copulation. [1] In many insects, they simply may be functionless vestigial structures.
In basal arthropods, such as silverfish, the cerci originate from the eleventh abdominal segment. As segment eleven is reduced or absent in the majority of arthropods, in such cases, the cerci emerge from the tenth abdominal segment. [2] It is not clear that other structures so named are homologous. In the Symphyla they are associated with spinnerets. [1]
Most cerci are segmented and jointed, or filiform (threadlike), but some take very different forms. Some Diplura, in particular Japyx species, have large, stout forcipate (pincer-like) cerci that they use in capturing their prey. [3]
The Dermaptera, or earwigs, are well known for the forcipate cerci that most of them bear, though species in the suborders Arixeniina and Hemimerina do not. It is not clear how many of the Dermaptera use their cerci for anything but defense, but some definitely feed on prey caught with the cerci, much as the Japygidae do. [3]
Crickets have particularly long cerci while other insects have cerci that are too small to be noticeable. However, it is not always obvious that small cerci are without function; they are rich in sensory cells and may be of importance in guiding copulation and oviposition.
In groups such as crickets and cockroaches, cerci play important sensory roles. They have been shown to be sensitive to puffs of air and low-frequency vibration, and thus trigger anti-predatory responses such as escape in response to certain predators. In field crickets, the range of frequency detection by the cerci spans from infrasonic sound to nearly 1 kHz. It is worth noting that in crickets, higher-frequency sound such as stridulation and ultrasonic bat calls are picked up by a separate tympanal organ, not the cerci. [4]
Some hexapods such as mayflies, silverfish and diplurans possess an accompanying third central tail filament which extends from the tip of the abdomen. This is referred to as the terminal filament and is not regarded as a cercus. [2]
Aphids have tube-like cornicles or siphunculi that are sometimes mistaken for cerci but are not morphologically related to cerci.
Like many insect body parts, including mandibles, antennae and stylets, cerci are thought to have evolved from what were legs on the primal insect form, [3] a creature that may have resembled a velvet worm, Symphylan or a centipede, worm-like with one pair of limbs for each segment behind the head or anterior tagma. [5]
The order Diplura is one of three orders of non-insect hexapods within the class Entognatha. The name "diplura", or "two tails", refers to the characteristic pair of caudal appendages or filaments at the terminal end of the body.
Antennae, sometimes referred to as "feelers", are paired appendages used for sensing in arthropods.
Earwigs make up the insect order Dermaptera. With about 2,000 species in 12 families, they are one of the smaller insect orders. Earwigs have characteristic cerci, a pair of forcep-like pincers on their abdomen, and membranous wings folded underneath short, rarely used forewings, hence the scientific order name, "skin wings". Some groups are tiny parasites on mammals and lack the typical pincers. Earwigs are found on all continents except Antarctica.
Symphylans, also known as garden centipedes or pseudocentipedes, are soil-dwelling arthropods of the class Symphyla in the subphylum Myriapoda. Symphylans resemble centipedes, but are very small, non-venomous, and only distantly related to both centipedes and millipedes. More than 200 species are known worldwide.
Forficula auricularia is a species complex comprising the common earwig. It is also known as the European earwig. It is an omnivorous insect belonging to the family Forficulidae. The name earwig comes from the appearance of the hindwings, which are unique in their resemblance to human ears when unfolded. The species name of the common earwig, auricularia, is a specific reference to this feature. The European earwig survives in a variety of environments. It is also a common household insect in North America. They are often considered a household pest because of their tendency to invade crevices in homes and consume pantry foods, though they may also act as beneficial species depending on the circumstances.
The name Apterygota is sometimes applied to a former subclass of small, agile insects, distinguished from other insects by their lack of wings in the present and in their evolutionary history; notable examples are the silverfish, the firebrat, and the jumping bristletails. Their first known occurrence in the fossil record is during the Devonian period, 417–354 million years ago. The group Apterygota is not a clade; it is paraphyletic, and not recognized in modern classification schemes. As defined, the group contains two separate clades of wingless insects: Archaeognatha comprises jumping bristletails, while Zygentoma comprises silverfish and firebrats. The Zygentoma are in the clade Dicondylia with winged insects, a clade that includes all other insects, while Archaeognatha is sister to this lineage.
The Archaeognatha are an order of apterygotes, known by various common names such as jumping bristletails. Among extant insect taxa they are some of the most evolutionarily primitive; they appeared in the Middle Devonian period at about the same time as the arachnids. Specimens that closely resemble extant species have been found as both body and trace fossils in strata from the remainder of the Paleozoic Era and more recent periods. For historical reasons an alternative name for the order is Microcoryphia.
In biology, a tagma is a specialized grouping of multiple segments or metameres into a coherently functional morphological unit. Familiar examples are the head, the thorax, and the abdomen of insects. The segments within a tagma may be either fused or so jointed as to be independently moveable.
The abdomen is the part of the body between the thorax (chest) and pelvis, in humans and in other vertebrates. The abdomen is the front part of the abdominal segment of the torso. The area occupied by the abdomen is called the abdominal cavity. In arthropods, it is the posterior tagma of the body; it follows the thorax or cephalothorax.
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.
The mesosoma is the middle part of the body, or tagma, of arthropods whose body is composed of three parts, the other two being the prosoma and the metasoma. It bears the legs, and, in the case of winged insects, the wings.
The Entognatha are a class of wingless and ametabolous arthropods, which, together with the insects, makes up the subphylum Hexapoda. Their mouthparts are entognathous, meaning that they are retracted within the head, unlike the insects. Entognatha are apterous, meaning that they lack wings. The class contains three orders: Collembola, Diplura and Protura. These three groups were historically united with the now-obsolete order Thysanura to form the class Apterygota, but it has since been recognized that the hexapodous condition of these animals has evolved independently from that of insects, and independently within each order. The orders might not be closely related, and Entognatha is now considered to be a paraphyletic group.
The metasoma is the posterior part of the body, or tagma, of arthropods whose body is composed of three parts, the other two being the prosoma and the mesosoma. In insects, it contains most of the digestive tract, respiratory system, and circulatory system, and the apical segments are typically modified to form genitalia. In a few of the most primitive insects, the metasomal segments bear small, articulated appendages called "styli", which are often considered to be vestigial. There are also pre-apical appendages in most insect orders, called cerci, which may be multi-segmented and almost resembling a posterior pair of antennae; these may be variously modified, or lost entirely. Otherwise, most adult insects lack appendages on the metasoma, though many larval insects have some form of appendages, such as prolegs or, in aquatic insects, gills.
Zygentoma are an order in the class Insecta, and consist of about 550 known species. The Zygentoma include the so-called silverfish or fishmoths, and the firebrats. A conspicuous feature of the order are the three long caudal filaments. The two lateral filaments are cerci, and the medial one is an epiproct or appendix dorsalis. In this they resemble the Archaeognatha, although the cerci of Zygentoma, unlike in the latter order, are nearly as long as the epiproct.
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.
The external morphology of Lepidoptera is the physiological structure of the bodies of insects belonging to the order Lepidoptera, also known as butterflies and moths. Lepidoptera are distinguished from other orders by the presence of scales on the external parts of the body and appendages, especially the wings. Butterflies and moths vary in size from microlepidoptera only a few millimetres long, to a wingspan of many inches such as the Atlas moth. Comprising over 160,000 described species, the Lepidoptera possess variations of the basic body structure which has evolved to gain advantages in adaptation and distribution.
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.
The subphylum Hexapoda or hexapods comprises the largest clade of arthropods and includes most of the extant arthropod species. It includes the crown group class Insecta, as well as the much smaller class Entognatha, which includes three orders of wingless arthropods that were once considered insects: Collembola (springtails), Protura (coneheads) and Diplura. The insects and springtails are very abundant and are some of the most important pollinators, basal consumers, scavengers/detritivores and micropredators in terrestrial environments.
Most insects reproduce oviparously, i.e. by laying eggs. The eggs are produced by the female in a pair of ovaries. Sperm, produced by the male in one testicle or more commonly two, is transmitted to the female during mating by means of external genitalia. The sperm is stored within the female in one or more spermathecae. At the time of fertilization, the eggs travel along oviducts to be fertilized by the sperm and are then expelled from the body ("laid"), in most cases via an ovipositor.
Grylloidea is the superfamily of insects, in the order Orthoptera, known as crickets. It includes the "true crickets", scaly crickets, wood crickets and other families, some only known from fossils.