|Thermoregulation in animals|
|Ectotherm • Endotherm • Poikilotherm • Homeothermy • Heterothermy • Stenotherm • Eurytherm • Thermolabile • Thermostability • Gigantothermy • Kleptothermy • Bradymetabolism • Tachymetabolism • Thermogenesis|
An ectotherm, from the Greek εκτός (ektós) "outside" and θερμός (thermós) "hot", is an organism in which internal physiological sources of heat are of relatively small or quite negligible importance in controlling body temperature. Some refer to these organisms as "cold blooded". Such organisms (for example frogs) rely on environmental heat sources, which permits them to operate at very economical metabolic rates. Such animals live in environments in which temperatures are practically constant, as is typical of regions of the abyssal ocean. In contrast where temperature varies so widely as to limit the physiological activities of other kinds of ectotherms, many species habitually seek out external sources of heat or shelter from heat; for example, many reptiles regulate their body temperature by basking in the sun, or seeking shade when necessary in addition to a whole host of other behavioral thermoregulation mechanisms. In contrast to ectotherms, endotherms rely largely, even predominantly, on heat from internal metabolic processes.
In ectotherms, fluctuating ambient temperatures may affect the body temperature. Such variation in body temperature is called poikilothermy, though the concept is not widely satisfactory and the use of the term is declining. In small aquatic creatures such as Rotifera, the poikilothermy is practically absolute, but other creatures have wider physiological options at their disposal, and they can avoid ambient temperature changes, or moderate their effects.
Various patterns of behavior enable certain ectotherms to regulate body temperature to a useful extent. To warm up, reptiles and amnthoids find sunny places and adopt positions that maximise their exposure; at harmfully high temperatures they seek shade or cooler water. In cold weather, honey bees huddle together to retain heat. Butterflies and moths may orient their wings to maximize exposure to solar radiation in order to build up heat before take-off.  Gregarious caterpillars, such as the Forest Tent caterpillar, benefit from basking in large groups for thermoregulation.  Many flying insects, such as honey bees and bumble bees, also raise their internal temperatures endothermally prior to flight, by vibrating their flight muscles without violent movement of the wings (see insect thermoregulation). Such endothermal activity is an example of the difficulty of consistent application of terms such as poikilothermy and homiothermy.
In addition to behavioral adaptations, physiological adaptations help ectotherms regulate temperature. Diving reptiles conserve heat by heat exchange mechanisms, whereby cold blood from the skin picks up heat from blood moving outward from the body core, re-using and thereby conserving some of the heat that otherwise would have been wasted. The skin of bullfrogs secretes more mucus when it is hot, allowing more cooling by evaporation.
During periods of cold some ectotherms enter a state of torpor, in which their metabolism slows or, in some cases, such as the wood frog, effectively stops. The torpor might last overnight or last for a season, or even for years, depending on the species and circumstances.
Advantages and disadvantages
Ectotherms rely largely on external heat sources such as sunlight to achieve their optimal body temperature for various bodily activities. Accordingly they depend on ambient conditions to reach operational body temperatures. In contrast endothermic animals as a rule maintain nearly constant high operational body temperatures largely by reliance on internal heat produced by metabolically active organs (liver, kidney, heart, brain, muscle) or even by specialized heat producing organs like brown adipose tissue (BAT). Also as a rule, ectotherms have lower metabolic rates than endotherms at a given body mass. As a consequence, endotherms generally rely on higher food consumption, and commonly on food of higher energy content. Such requirements may limit the carrying capacity of a given environment for endotherms as compared to its carrying capacity for ectotherms.
Because ectotherms depend on environmental conditions for body temperature regulation, as a rule they are more sluggish at night and in early mornings. When they emerge from shelter, many diurnal ectotherms need to heat up in the early sunlight before they can begin their daily activities. In cool weather the foraging activity of such species is therefore restricted to the day time in most vertebrate ectotherms, and in cold climates most cannot survive at all. In lizards, for instance, most nocturnal species are geckos specialising in "sit and wait" foraging strategies. Such strategies do not require as much energy as active foraging, and do not as a rule require hunting activity of the same intensity. From another point of view, sit-and-wait predation may require very long periods of unproductive waiting. Endotherms cannot in general afford such long periods without food, but suitably adapted ectotherms can wait without expending much energy. Endothermic vertebrate species are therefore less dependent on the environmental conditions and have developed a higher variability (both within and between species) in their daily patterns of activity.
Contrast between thermodynamics and biological terminology
Note that because of historical accident, students encounter a source of possible confusion between the terminology of physics and biology. Whereas the thermodynamic terms "exothermic" and "endothermic" respectively refer to processes that give out heat energy and processes that absorb heat energy, in biology the sense is effectively inverted. The metabolic terms "ectotherm" and "endotherm" respectively refer to organisms that rely largely on external heat to achieve a full working temperature, and to organisms that produce heat from within as a major factor in controlling their bodily temperature.
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