Johnston's organ

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Illustration from the 1855 paper of Christopher Johnston Johnstons organ.jpg
Illustration from the 1855 paper of Christopher Johnston

Johnston's organ is a collection of sensory cells found in the pedicel (the second segment) of the antennae in the class Insecta. [2] Johnston's organ detects motion in the flagellum (third and typically final antennal segment). It consists of scolopidia arrayed in a bowl shape, each of which contains a mechanosensory chordotonal neuron. [3] [4] The number of scolopidia varies between species. In homopterans, the Johnston's organs contain 25 - 79 scolopidia. [5] The presence of Johnston's organ is a defining characteristic which separates the class Insecta from the other hexapods belonging to the group Entognatha. Johnston's organ was named after the physician Christopher Johnston (1822-1891) [6] father of the physician and Assyriologist Christopher Johnston.

Contents

Function

In fruit flies, midges and mosquitoes

In the fruit fly Drosophila melanogaster and Chironomus annularius , the Johnston's organ contains almost 480 sensory neurons. [7] In the mosquito, the Johnston's organ houses ~15 000 sensory cells in males, [8] comparable to that in the human cochlea, [9] and approximately half as many in females. [10] Distinct populations of neurons are activated differently by deflections of antennae caused by gravity or by vibrations caused by sound or air movement. [2] [11] This differential response allows the fly to distinguish between gravitational, mechanical, and acoustic stimuli. [2] [11]

The Johnston's organ of fruit flies, chironomids or mosquitoes can be used to detect air vibrations caused by the wingbeat frequency or courtship song of a mate. One function of the Johnston's organ is for detecting the wing beat frequency of a mate. [3] Production of sound in air results in two energy components: the pressure component, which is changes in air pressure; and the particle displacement component, which is the back and forth vibration of air particles oscillating in the direction of sound propagation. [12] Particle displacement has greater energy loss than the pressure component when getting further from the sound source, so for quiet sounds such as small flies, it is detectable only within a few wavelengths of the source. [12]

Another function of the Johnston's organ in fruit flies is to detect changes in the wing induced airflow during visually induced turns and control the magnitude of steering responses. [13] [14] During visually induced turns, antenna located opposite to the turn direction gets closer to the wing [13] . This increases the wing induced airflow and increases the activation of the neurons in the Johnston's organ. [13] [14] Increased activation of the Johnston's organ neurons works to reduce the wing stroke amplitude of the contralateral wing, providing a positive feedback loop to enhance the initial stages of the visually induced turns. [13] [14]

Insects, such as fruit flies and bees, detect sounds using loosely attached hairs or antennae which vibrate with air particle movement. [12] (Tympanal organs detect the pressure component of sound.) Near-field sound, because of the rapid dissipation of energy, is suitable only for very close communication. [12] Two examples of near-field sound communication are bee's waggle dance and Drosophila courtship songs. [12] In fruit flies, the arista of the antennae and the third segment act as the sound receiver. [12] Vibrations of the receiver cause rotation of the third segment, which channels sound input to the mechanoreceptors of the Johnston's organ. [12]

In hawk moths

The Johnston's organ plays a role in the control of flight stability in hawk moths. Kinematic data measured from hovering moths during steady flight indicate that the antennae vibrate with a frequency matching wingbeat (27 Hz). During complex flight, however, angular changes of the flying moth cause Coriolis forces, which are predicted to manifest as a vibration of the antenna of at about twice wingbeat frequency (~60 Hz). When antennae were manipulated to vibrate at a range of frequencies and the resulting signals from the neurons associated with the Johnston's organs were measured, the response of the scolopidia neurons to the frequency was tightly coupled in the range of 50–70 Hz, which is the predicted range of vibrations caused by Coriolis effects. Thus, the Johnston's organ is tuned to detect angular changes during maneuvering in complex flight. [15]

In honeybees

Dancing honeybees ( Apis mellifera ) describe the location of nearby food sources by emitted airborne sound signals. These signals consist of rhythmic high-velocity movement of air particles. These near-field sounds are received and interpreted using the Johnston's organ in the pedicel of the antennae. [16] Honeybees also perceive electric field changes via the Johnston's organs in their antennae and possibly other mechanoreceptors. Electric fields generated by movements of the wings cause displacements of the antennae based on Coulomb's law. Neurons of the Johnston's organ respond to movements within the range of displacements caused by electric fields. When the antennae were prevented from moving at the joints containing the Johnston's organ, bees no longer responded to biologically relevant electric fields. Honeybees respond differently to different temporal patterns. Honeybees appear to use the electric field emanating from the dancing bee for distance communication. [17] "Greggers_2018"Greggers U (12 September 2018). "ESF in bees". Freien Universität Berlin. Archived from the original on 2018-11-21. Retrieved 2013-06-11.</ref>

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<span class="mw-page-title-main">Halteres</span> Pair of small club-shaped insect organs

Halteres are a pair of small club-shaped organs on the body of two orders of flying insects that provide information about body rotations during flight. Insects of the large order Diptera (flies) have halteres which evolved from a pair of ancestral hindwings, while males of the much smaller order Strepsiptera (stylops) have halteres which evolved from a pair of ancestral forewings.

<span class="mw-page-title-main">Fly</span> Order of insects

Flies are insects of the order Diptera, the name being derived from the Greek δι- di- "two", and πτερόν pteron "wing". Insects of this order use only a single pair of wings to fly, the hindwings having evolved into advanced mechanosensory organs known as halteres, which act as high-speed sensors of rotational movement and allow dipterans to perform advanced aerobatics. Diptera is a large order containing an estimated 1,000,000 species including horse-flies, crane flies, hoverflies, mosquitoes and others, although only about 125,000 species have been described.

<span class="mw-page-title-main">Antenna (biology)</span> Paired appendages used for sensing in arthropods

Antennae, sometimes referred to as "feelers", are paired appendages used for sensing in arthropods.

<span class="mw-page-title-main">Mushroom bodies</span> Pair of structures in the brains of some arthropods and annelids

The mushroom bodies or corpora pedunculata are a pair of structures in the brain of arthropods, including insects and crustaceans, and some annelids. They are known to play a role in olfactory learning and memory. In most insects, the mushroom bodies and the lateral horn are the two higher brain regions that receive olfactory information from the antennal lobe via projection neurons. They were first identified and described by French biologist Félix Dujardin in 1850.

<span class="mw-page-title-main">Lateral line</span> Sensory system in fish

The lateral line, also called the lateral line organ (LLO), is a system of sensory organs found in fish, used to detect movement, vibration, and pressure gradients in the surrounding water. The sensory ability is achieved via modified epithelial cells, known as hair cells, which respond to displacement caused by motion and transduce these signals into electrical impulses via excitatory synapses. Lateral lines play an important role in schooling behavior, predation, and orientation.

Stimulus modality, also called sensory modality, is one aspect of a stimulus or what is perceived after a stimulus. For example, the temperature modality is registered after heat or cold stimulate a receptor. Some sensory modalities include: light, sound, temperature, taste, pressure, and smell. The type and location of the sensory receptor activated by the stimulus plays the primary role in coding the sensation. All sensory modalities work together to heighten stimuli sensation when necessary.

A mechanoreceptor, also called mechanoceptor, is a sensory receptor that responds to mechanical pressure or distortion. Mechanoreceptors are innervated by sensory neurons that convert mechanical pressure into electrical signals that, in animals, are sent to the central nervous system.

<span class="mw-page-title-main">Auditory system</span> Sensory system used for hearing

The auditory system is the sensory system for the sense of hearing. It includes both the sensory organs and the auditory parts of the sensory system.

The antennal lobe is the primary olfactory brain area in insects. The antennal lobe is a sphere-shaped deutocerebral neuropil in the brain that receives input from the olfactory sensory neurons in the antennae and mouthparts. Functionally, it shares some similarities with the olfactory bulb in vertebrates. The anatomy and physiology function of the insect brain can be studied by dissecting open the insect brain and imaging or carrying out in vivo electrophysiological recordings from it.

<span class="mw-page-title-main">Supraesophageal ganglion</span> Arthropod nervous system component

The supraesophageal ganglion is the first part of the arthropod, especially insect, central nervous system. It receives and processes information from the first, second, and third metameres. The supraesophageal ganglion lies dorsal to the esophagus and consists of three parts, each a pair of ganglia that may be more or less pronounced, reduced, or fused depending on the genus:

Chordotonal organs are stretch receptor organs found only in insects and crustaceans. They are located at most joints and are made up of clusters of scolopidia that either directly or indirectly connect two joints and sense their movements relative to one another. They can have both extero- and proprioceptive functions, for example sensing auditory stimuli or leg movement. The word was coined by Vitus Graber in 1882, though he interpreted them as being stretched between two points like a string, sensing vibrations through resonance.

<span class="mw-page-title-main">Tympanal organ</span> Hearing organ in insects

A tympanal organ is a hearing organ in insects, consisting of a membrane (tympanum) stretched across a frame backed by an air sac and associated sensory neurons. Sounds vibrate the membrane, and the vibrations are sensed by a chordotonal organ. Hymenoptera do not have a tympanal organ, but they do have a Johnston's organ.

<span class="mw-page-title-main">Arista (insect anatomy)</span> Bristle arising from the third antennal segment of an insect

In insect anatomy the arista is a simple or variously modified apical or subapical bristle, arising from the third antennal segment. It is the evolutionary remains of antennal segments, and may sometimes show signs of segmentation. These segments are called aristameres. The arista may be bare and thin, sometime appearing no more than a simple bristle; pubescent, covered in short hairs; or plumose, covered in long hairs.

A sense is a biological system used by an organism for sensation, the process of gathering information about the surroundings through the detection of stimuli. Although, in some cultures, five human senses were traditionally identified as such, many more are now recognized. Senses used by non-human organisms are even greater in variety and number. During sensation, sense organs collect various stimuli for transduction, meaning transformation into a form that can be understood by the brain. Sensation and perception are fundamental to nearly every aspect of an organism's cognition, behavior and thought.

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<span class="mw-page-title-main">Scolopidia</span>

A scolopidium is the fundamental unit of a mechanoreceptor organ in insects. It is a composition of three cells: a scolopale cap cell which caps the scolopale cell, and a bipolar sensory nerve cell.

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The lateral horn is one of the two areas of the insect brain where projection neurons of the antennal lobe send their axons. The other area is the mushroom body. Several morphological classes of neurons in the lateral horn receive olfactory information through the projection neurons.

<span class="mw-page-title-main">Subgenual organ</span>

The subgenual organ is an organ in insects that is involved in the perception of sound. The name refers to the location of the organ just below the knee in the tibia of all legs in most insects.

<span class="mw-page-title-main">Insect olfaction</span> Function of chemical receptors

Insect olfaction refers to the function of chemical receptors that enable insects to detect and identify volatile compounds for foraging, predator avoidance, finding mating partners and locating oviposition habitats. Thus, it is the most important sensation for insects. Most important insect behaviors must be timed perfectly which is dependent on what they smell and when they smell it. For example, olfaction is essential for locating host plants and hunting prey in many species of insects, such as the moth Deilephila elpenor and the wasp Polybia sericea, respectively.

References

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