|Thermoregulation in animals|
An ectotherm (from the Greek ἐκτός (ektós) "outside" and θερμός (thermós) "hot") is an organism in which internal physiological sources of heat are of relatively small or of quite negligible importance in controlling body temperature. Such organisms (for example frogs) rely on environmental heat sources, which permit them to operate at very economical metabolic rates.
Some of these animals live in environments where temperatures are practically constant, as is typical of regions of the abyssal ocean and hence can be regarded as homeothermic ectotherms. In contrast, in places 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. For home captivity of pet reptiles, owners can use a UVB/UVA light system to assist the animals' basking behaviour.
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 (like crabs) have wider physiological options at their disposal, and they can move to preferred temperatures, avoid ambient temperature changes, or moderate their effects. Ectotherms can also display the features of homeothermy, especially within aquatic organisms. Normally their range of ambient environmental temperatures is relatively constant, and there are few in number that attempt to maintain a higher internal temperature due to the high associated costs.
Various patterns of behavior enable certain ectotherms to regulate body temperature to a useful extent. To warm up, reptiles and many insects 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 and fall webworm, 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.
Pros and cons
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 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). Ectotherms typically 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 (see ambush predator). Such strategies do not require as much energy as active foraging and do not 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.
- Davenport, John. Animal Life at Low Temperature. Publisher: Springer 1991. ISBN 978-0412403507
- Jay M. Savage; with photographs by Michael Fogden and Patricia Fogden. (2002). The Amphibians and Reptiles of Costa Rica: a Herpetofauna Between Two Continents, Between Two Seas. Chicago, Ill.: University of Chicago Press. p. 409. ISBN 978-0-226-73538-2.CS1 maint: multiple names: authors list (link)
- Milton Hildebrand; G. E. Goslow, Jr. Principal ill. Viola Hildebrand. (2001). Analysis of vertebrate structure. New York: Wiley. p. 429. ISBN 978-0-471-29505-1.CS1 maint: multiple names: authors list (link)
- "Best Reptile UVA/UVB Light Bulbs (Reviewed + Best Deals From Amazon) – BuddyGenius". buddygenius.com. 4 January 2018. Archived from the original on 17 January 2018. Retrieved 6 May 2018.
- Lewis, L; Ayers, J (2014). "Temperature Preference and Acclimation in the Jonah Crab, Cancer borealis". Journal of Experimental Marine Biology and Ecology. 455: 7–13. doi:10.1016/j.jembe.2014.02.013.
- Willmer, Pat; Stone, Graham; Johnston, Ian. Environmental Physiology of Animals. Hoboken: Wiley, 2009. Ebook Library. Web. 01 Apr. 2016.
- McClure, Melanie; Cannel, Elizabeth; Despland, Emma (June 2011). "Thermal ecology and behaviour of the nomadic social forager Malacosoma disstria". Physiological Entomology. 36 (2): 120–127. doi:10.1111/j.1365-3032.2010.00770.x.
- Schowalter, T. D.; Ring, D. R. (2017-01-01). "Biology and Management of the Fall Webworm, Hyphantria cunea (Lepidoptera: Erebidae)". Journal of Integrated Pest Management. 8 (1). doi:10.1093/jipm/pmw019. Archived from the original on 2017-11-15.
- Rehnberg, Bradley (2002). "Heat Retention by webs of the fall webworm Hyphantria cunea (Lepidoptera: Arctiidae): infrared warming and forced convective cooling". Journal of Thermal Biology. 27 (6): 525–530. doi:10.1016/S0306-4565(02)00026-8.
- LOEWY, KATRINA. "LIFE HISTORY TRAITS AND REARING TECHNIQUES FOR FALL WEBWORMS (HYPHANTRIA CUNEA DRURY) IN COLORADO" (PDF). Journal of the Lepidopterists' Society. Archived from the original (PDF) on 2018-05-06. Retrieved 2017-11-15.
- Hunter, Alison F. (2000-11-01). "Gregariousness and repellent defences in the survival of phytophagous insects". Oikos. 91 (2): 213–224. doi:10.1034/j.1600-0706.2000.910202.x. ISSN 1600-0706.
- Hut RA, Kronfeld-Schor N, van der Vinne V, De la Iglesia H (2012). In search of a temporal niche: environmental factors. Progress in Brain Research. 199. pp. 281–304. doi:10.1016/B978-0-444-59427-3.00017-4. ISBN 9780444594273. PMID 22877672.