Tuesday, October 30, 2018

THE HIBERNATION

Hibernation is a state of inactivity and metabolic depression in endotherms. Hibernation refers to a season of heterothermy characterized by low body temperature, slow breathing and heart rate, and low metabolic rate. It is most commonly observed during the winter months. Although traditionally reserved for "deep" hibernators such as rodents, the term has been redefined to include animals such as bears and is now applied based on active metabolic suppression rather than any absolute decline in body temperature. Many experts believe that the processes of daily torpor and hibernation form a continuum and utilize similar mechanisms.[1][2] The equivalent during the summer months is aestivation.
Often associated with low temperatures, the function of hibernation is to conserve energy when sufficient food is unavailable. To achieve this energy saving, an endothermic animal decreases its metabolic rate and thereby its body temperature.[2] Hibernation may last days, weeks, or months depending on the species, ambient temperature, time of year, and the individual's body condition. Before entering hibernation, animals need to store enough energy to last through the duration of their dormant period, possibly as long as the entire winter. Larger species become hyperphagic, eating a large amount of food and storing the energy in fat deposits. In many small species, food caching replaces eating and becoming fat.[3]
Some species of mammals hibernate while gestating young, which are born either while the mother hibernates or shortly afterwards.[4] For example, female polar bears go into hibernation during the cold winter months in order to give birth to their offspring. The pregnant mothers significantly increase their body mass prior to hibernation, and this increase is further reflected in the weight of the offspring. The fat accumulation enables them to provide a sufficiently warm and nurturing environment for their newborns. During hibernation, they subsequently lose 15–27% of their pre-hibernation weight by using their stored fats for energy.[5]
True hibernation is restricted to endotherms; ectotherms by definition cannot hibernate because they cannot actively down-regulate their body temperature or their metabolic rate. Still, many ectothermic animals undergo periods of dormancy which are sometimes confused with hibernation. Some reptile species are said to brumate, but possible similarities between brumation and hibernation are not firmly established. Many insects, such as the wasp Polistes exclamans, exhibit periods of dormancy which have often been referred to as hibernation, despite their ectothermy.[6]

 
 Northern bat hibernating in Norway

Mammals




Bats hibernating in a silver mine



Obligate hibernation

Obligate hibernators are animals that spontaneously, and annually, enter hibernation regardless of ambient temperature and access to food. Obligate hibernators include many species of ground squirrels, other rodents, mouse lemurs, European hedgehogs and other insectivores, monotremes, marsupials, and even butterflies such as the small tortoiseshell.[7] These species undergo what has been traditionally called "hibernation": a physiological state wherein the body temperature drops to near ambient (environmental) temperature, and heart and respiration rates slow drastically.
The typical winter season for obligate hibernators is characterized by periods of torpor interrupted by periodic, euthermic arousals, during which body temperatures and heart rates are restored to more typical levels. The cause and purpose of these arousals is still not clear; the question of why hibernators may return periodically to normal body temperatures has plagued researchers for decades, and while there is still no clear-cut explanation, there are multiple hypotheses on the topic. One favored hypothesis is that hibernators build a "sleep debt" during hibernation, and so must occasionally warm up to sleep. This has been supported by evidence in the Arctic ground squirrel.[8] Other theories postulate that brief periods of high body temperature during hibernation allow the animal to restore its available energy sources[9] or to initiate an immune response.[10]
Hibernating Arctic ground squirrels may exhibit abdominal temperatures as low as −2.9 °C (26.8 °F), maintaining sub-zero abdominal temperatures for more than three weeks at a time, although the temperatures at the head and neck remain at 0 °C (32 °F) or above.[11]
Historically there was a question of whether or not bears truly hibernate since they experience only a modest decline in body temperature (3–5 °C) compared with the much larger decreases (often 32 °C or more) seen in other hibernators. Many researchers thought that their deep sleep was not comparable with true, deep hibernation, but recent research has refuted this theory in captive black bears.[12]
Black bear mother and cubs "denning"

Facultative hibernation

Unlike obligate hibernators, facultative hibernators only enter hibernation when either cold-stressed, food-deprived, or both. A good example of the differences between these two types of hibernation can be seen in prairie dogs: the white-tailed prairie dog is an obligate hibernator and the closely related black-tailed prairie dog is a facultative hibernator.[13]

Primates

While hibernation has long been studied in rodents, namely ground squirrels, no primate or tropical mammal was known to hibernate until the discovery of hibernation in the fat-tailed dwarf lemur of Madagascar, which hibernates in tree holes for seven months of the year.[14] Malagasy winter temperatures sometimes rise to over 30 °C (86 °F), so hibernation is not exclusively an adaptation to low ambient temperatures. The hibernation of this lemur is strongly dependent on the thermal behaviour of its tree hole: if the hole is poorly insulated, the lemur's body temperature fluctuates widely, passively following the ambient temperature; if well insulated, the body temperature stays fairly constant and the animal undergoes regular spells of arousal.[15] Dausmann found that hypometabolism in hibernating animals is not necessarily coupled with low body temperature.[16]

Bears

Hibernating bears are able to recycle their proteins and urine, allowing them both to stop urinating for months and to avoid muscle atrophy.[17][18][19][20]

Birds

Historically, Pliny the Elder believed swallows hibernated, and ornithologist Gilbert White documented anecdotal evidence in his 1789 book The Natural History of Selborne that indicated the belief was still current in his time. It is now understood that the vast majority of bird species typically do not hibernate, instead utilizing torpor. One known exception is the common poorwill (Phalaenoptilus nuttallii), for which hibernation was first documented by Edmund Jaeger.[21][22]

Dormancy in ectotherms

Because they cannot actively down-regulate their body temperature or metabolic rate, ectothermic animals (including fish, reptiles, and amphibians) cannot hibernate. However, they can experience decreased metabolic rates associated with colder environments and/or low oxygen availability (hypoxia) and exhibit dormancy. It was once thought that basking sharks settled to the floor of the North Sea and became dormant, but research by Dr. David Sims in 2003 dispelled this hypothesis,[23] showing that the sharks actively traveled huge distances throughout the seasons, tracking the areas with the highest quantity of plankton. Epaulette sharks have been documented to be able to survive for long periods of time without oxygen and at temperatures of up to 26 °C (79 °F)[24] as a means to survive in their shoreline habitat, where water and oxygen levels vary with the tide. Other animals able to survive long periods with no or very little oxygen include goldfish, red-eared sliders, wood frogs, and bar-headed geese.[25] However, the ability to survive hypoxic or anoxic conditions is not the same as, nor closely related, to endotherm hibernation.

Hibernation induction trigger

Hibernation induction trigger (HIT) is somewhat of a misnomer. Although research in the 1990s hinted at the ability to induce torpor in animals by injection of blood taken from a hibernating animal, further research has been unable to reproduce this phenomenon. Despite the inability to induce torpor, there are substances in the blood of hibernators that can lend protection to organs for possible transplant. Researchers were able to prolong the life of an isolated pig's heart with a HIT.[26] This may have potentially important implications for organ transplant, as it could allow organs to survive for up to 18 hours outside the human body. This would be a great improvement from the current 6 hours.
The supposed HIT is a mixture derived from blood serum, including at least one opioid-like substance. DADLE is an opioid that in some experiments has been shown to have similar functional properties.[27]

In humans

Researchers have studied how to induce hibernation in humans.[28][29] The ability to hibernate would be useful for a number of reasons, such as saving the lives of seriously ill or injured people by temporarily putting them in a state of hibernation until treatment can be given.
 

THE ANNA'S HUMMINGBIRD

Anna's hummingbird (Calypte anna), a medium-sized hummingbird native to the west coast of North America, was named after Anna Masséna, Duchess of Rivoli.[2] In the early 20th century, Anna's hummingbirds bred only in northern Baja California and southern California. The transplanting of exotic ornamental plants in residential areas throughout the Pacific coast and inland deserts provided expanded nectar and nesting sites, allowing the species to expand its breeding range.[2][3]
Anna's hummingbird.jpg
 
 Male flying in California, USA

Description

Female annas hummingbird hovering.jpg
 Female hovering

 Anna's hummingbird is 3.9 to 4.3 in (9.9 to 10.9 cm) long. It has an iridescent bronze-green back, a pale grey chest and belly, and green flanks. Its bill is long, straight, and slender. The adult male has an iridescent crimson-red derived from magenta to a reddish-pink crown and gorget, which can look dull brown or gray without direct sunlight and a dark, slightly forked tail. Females also have iridescent red gorgets, though they are usually smaller and less brilliant than the males'. Anna's is the only North American hummingbird species with a red crown.[3] Females and juvenile males have a dull green crown, a grey throat with or without some red iridescence, a grey chest and belly, and a dark, rounded tail with white tips on the outer feathers.
These birds feed on nectar from flowers using a long extendable tongue. They also consume small insects and other arthropods caught in flight or gleaned from vegetation. A PBS documentary shows how Anna's hummingbirds eat flying insects.[4] They aim for the flying insect, then open their beaks to capture the prey.
While collecting nectar, they also assist in plant pollination. This species sometimes consumes tree sap.[5] The male's call is scratchy and metallic, and it perches above head-level in trees and shrubs.[3] They are frequently seen in backyards and parks, and commonly found at feeders and flowering plants.
Anna's hummingbirds can shake their bodies 55 times per second to shed rain while in flight, or in dry weather, to remove pollen or dirt from feathers.[6] Each twist lasts four-hundredths of a second and applies 34 times the force of gravity on the bird's head.

Reproduction

A female incubates eggs in a camouflaged nest.
Two nestlings are fed by a female hummingbird.
Open-wooded or shrubby areas and mountain meadows along the Pacific coast from British Columbia to Arizona make up C. anna's breeding habitat. The female raises the young without the assistance of the male. The female bird builds a nest in a shrub or tree, in vines, or attached to wires or other artificial substrates. The round, 3.8-to-5.1-centimetre (1.5 to 2.0 in) diameter nest is constructed of plant fibers, downy feathers and animal hair; the exterior is camouflaged with chips of lichen, plant debris, and occasionally urban detritus such as paint chips and cigarette paper.[2] The nest materials are bound together with spider silk. They are known to nest as early as mid-December and as late as June, depending on geographic location and climatic conditions.[citation needed]
Unlike most northern temperate hummingbirds, the male Anna's hummingbird sings during courtship. The song is thin and squeaky, interspersed with buzzes and chirps, and is drawn to over 10 seconds in duration. During the breeding season, males can be observed performing an aerial display dive over their territories. The males also use the dive display to drive away rivals or intruders of other species. When a female flies onto a male's territory, he rises up about 130 ft (40 m) before diving over the recipient. As he approaches the bottom of the dive, the male reaches an average speed of 27 m/s (89 ft/s), which is 385 body lengths per second.[7] At the bottom of the dive, the male travels 23 m/s (51 mph), and produces a loud sound described by some as an "explosive squeak" with his outer tail-feathers.[8][9]
Anna's hummingbirds hybridize fairly frequently with other species, especially the congeneric Costa's hummingbird.[2] These natural hybrids have been mistaken for new species. A bird, allegedly collected in Bolaños, Mexico, was described and named Selasphorus floresii (Gould, 1861), or Floresi's hummingbird. Several more specimens were collected in California over a long period, and the species was considered extremely rare.[10] The specimens were the hybrid offspring of an Anna's hummingbird and an Allen's hummingbird. A single bird collected in Santa Barbara, California, was described and named Trochilus violajugulum (Jeffries, 1888), or violet-throated hummingbird.[11] It was later determined to be a hybrid between an Anna's hummingbird and a black-chinned hummingbird.[12][13]

Locomotion

During hovering flight, Anna's hummingbirds maintain high wingbeat frequencies accomplished by their large pectoral muscles via recruitment of motor units.[14] The pectoral muscles that power hummingbird flight are composed exclusively of fast glycolytic fibers that respond rapidly and are fatigue-resistant.[14]

Distribution

Anna's hummingbirds are found along the western coast of North America, from southern Canada to northern Baja California, and inland to southern and central Arizona, extreme southern Nevada and southeastern Utah, and western Texas.[2] They tend to be permanent residents within their range, and are very territorial. However, birds have been spotted far outside their range in such places as southern Alaska, Saskatchewan, New York, Florida, Louisiana, and Newfoundland.[15][16]
Anna's hummingbirds have the northernmost year-round range of any hummingbird. During cold temperatures, Anna's hummingbirds gradually gain weight during the day as they convert sugar to fat.[17][18] In addition, hummingbirds with inadequate stores of body fat or insufficient plumage are able to survive periods of subfreezing weather by lowering their metabolic rate and entering a state of torpor.[19]
The population of Anna's hummingbirds is an estimated 1.5 million, which appears to be stable, and they are not considered an endangered species.[1]

Gallery

THE CRAB- EATING FOXS

The crab-eating fox (Cerdocyon thous), also known as the forest fox, wood fox, or Maikong, is an extant species of medium-sized canid endemic to the central part of South America, and which appeared during the Pliocene epoch.[not in citation given][3] Like South American foxes, which are in the genus Lycalopex, it is not closely related to true foxes. Cerdocyon comes from the Greek words kerdo (meaning fox) and cyon (dog) referring to the dog-and fox-like characteristics of this animal.
 Crab-eating Fox.JPG

Origin

Cerdocyonina is a tribe which appeared around 6.0 million years ago (Mya) in North America as Cerdocyon avius becoming extinct by around 1.4–1.3 Mya. living about 4.7 million years. This genus has persisted in South America from an undetermined time, possibly around 3.1 Mya, and continues to the present in the same or a similar form to the crab-eating fox.[4]
As one of the species of the tribe Canini, it is related to the genus Canis. The crab-eating fox's nearest living relative, as theorized at present, is the short-eared dog. This relationship, however, has yet to be supported by mitochondrial investigations. Two subgenera (Atelocynus and Speothos) were long ago included in Cerdocyon.

Habitat

The crab-eating fox is a canid that ranges in savannas; woodlands; subtropical forests; prickly, shrubby thickets; and tropical savannas such as the caatinga, plains, and campo, from Colombia and southern Venezuela in the north to Paraguay, Uruguay and northern Argentina at the southernmost reaches of its range.[5] The crab-eating fox has also been sighted in Panama since the 1990s.[6]
Its habitat also includes wooded riverbanks such as riparian forest. In the rainy season, their range moves uphill, whilst in drier times they move to lower ground.[7] Their habitat covers all environments except rainforests, high mountains, and open grassy savannas. In some regions of their range, they are threatened with extirpation.

Taxonomy and evolution

Cerdocyon thous, C. avius and other species of the genus Cerdocyon underwent radiational evolution on the South American continent.[8] All close relatives of the crab-eating fox (Cerdocyon thous) are extinct. It is the only living representative at present of the genus Cerdocyon. Genetically, there are 74 diploid chromosomes (36 pairs).

Appearance

The crab-eating fox is predominantly greyish-brown, with areas of red on the face and legs, and black-tipped ears and tail. It has short, strong legs and its tail is long and bushy. It may reach an adult weight of 10 to 17 pounds (4.5 to 7.7 kg). The head and body length averages 64.3 centimetres (25.3 in), and the average tail length is 28.5 centimetres (11.2 in).[9] This fox weighs between 10 to 17 pounds (4.5 to 7.7 kg).[10][11] It is mainly nocturnal and also is active at dusk, spending its day in dens that were dug by other animals. It either hunts individually or lives in pairs; it eats crabs, lizards and different flying animals. It is easy to domesticate and farm, but its fur is not so highly valued as that of other species.
The coat is short and thick. Coloration varies from grey to brown, to yellowish, to pale, to dark grey. There is a black streak along the back legs, with a black stripe along the spine. On muzzle, ears and paws there is more-reddish fur. The tail, legs and ear tips are black. The ears are wide and round. The torso is somewhat narrow; legs are short but strong. The dense hairy tail stays upright when they are excited.

Life cycle and behaviour

The crab-eating fox creates monogamic teams for hunting; groups of several monogamic pairs may form during the reproductive season. The population distribution is as follows: some explorers show one individual distribution for 4 km2. One observation showed that one had changed from 0,6 to 0,9 km2 for one individual.[9] Territorialism was noticed during the dry season; during rainy seasons, when there is more food, they pay less attention to territory.[7] Hideouts and dens often are found in bushes and in thick grass, and there are typically multiple entrance holes per den. Despite being capable of tunnelling, they prefer to take over other animals' burrows. Hunting methods are adapted to type of prey. Several characteristic sounds are made by the crab-eating fox such as barking, whirring and howling, which occur often when pairs lose contact with one another.
Cerdocyon thous

Reproduction

The adult female gives birth to one or two litters per year, and the breeding pair is monogamous. The pair ranges the plains together. As a tropical animal, reproduction is not fixed to certain times of year, and takes place twice yearly. The reproductive period most often begins in November or December, and again in July. The birth of offspring follows after a 56-day gestation, typically in January, February or sometimes March[7], then again from September to October.

Diet

The crab-eating fox searches for crabs on muddy floodplains during the wet season, giving this animal its common name. It is an opportunist and an omnivore, preferring insects or meat from rodents and birds when available. Other foods readily consumed include turtle eggs, tortoises, fruit, eggs, crustaceans, insects, lizards and carrion. Their diet is varied and has been found to differ by different researchers, suggesting opportunistic feeding and geographical variation. During the wet season, the diet contains more crabs and other crustaceans, while during the dry season it contains more insects.[9] The crab-eating fox contributes to the control of rodents and harmful insects.

Threats

This fox is occasionally hunted, but the pelt is not valuable. They do not pose a danger to livestock. The crab-eating fox is not currently a species of concern for conservation; however, its habitat is slowly shrinking due to human activity such as agriculture, as well as feral dogs' encroachment on its territory, though the population is still stable. Despite the low value of their pelts, these canids are sometimes killed by locals, even though there has been no unambiguous proof that they attack farm animals. They are easy to domesticate, and often bred by local people. This does not, however, remove the threats to their population. The species is not protected at present.

Status of conservation

The Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) lists the fox as not threatened by extinction.[12] The IUCN lists the crab-eating fox as being of "Least Concern".[2]


 Cerdocyon thous
(Linnaeus, 1766)


 Crab-eating Fox area.png


 Crab-eating fox range
 

THE MANED WOLF

(Illiger, 1815)