{"id":180624,"date":"2017-03-01T20:42:03","date_gmt":"2017-03-02T01:42:03","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/canidae-wikipedia\/"},"modified":"2017-03-01T20:42:03","modified_gmt":"2017-03-02T01:42:03","slug":"canidae-wikipedia","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/transhumanist\/canidae-wikipedia\/","title":{"rendered":"Canidae &#8211; Wikipedia"},"content":{"rendered":"<p><p>Canids[1]          Temporal range: 39.750Ma Late Eocene-Holocene                                                                            Major extant canid genera left-to-right, top-to-bottom:          Canis,          Cuon, Lycaon, Cerdocyon, Chrysocyon, Speothos,          Vulpes,          Nyctereutes, Otocyon and Urocyon                                      Scientific classification                                                Kingdom:                          Animalia                                      Phylum:                          Chordata                                      Class:                          Mammalia                                      Order:                          Carnivora                                      Suborder:                          Caniformia                                      Family:                          Canidae          G.          Fischer de Waldheim, 1817[2]                                      Genera and species                                      <\/p>\n<p>            See text          <\/p>\n<p>    The biological family Canidae    [3] is a lineage of carnivorans that    includes domestic dogs,    wolves,    foxes, jackals, dingoes, and many other    extant and extinct dog-like mammals. A member of this    family is called a canid (, ).[4]  <\/p>\n<p>    The cat-like feliforms and dog-like caniforms emerged    within the Carnivoramorpha 43 million years before    present.[5] The caniforms included the    fox-like Leptocyon genus whose various species    existed from 34 million years before present before branching    11.9 million YBP into Vulpini (foxes) and Canini (canines).[6]:1745  <\/p>\n<p>    Canids are found on all continents except Antarctica, having    arrived independently or accompanied human beings over extended    periods of time. Canids vary in size from the 2-m-long    (6ft 7 in) gray wolf to the 24-cm-long (9.4in)    fennec fox.    The body forms of canids are similar, typically having long    muzzles, upright ears, teeth adapted for cracking bones and    slicing flesh, long legs, and bushy tails. They are mostly    social animals, living together in family    units or small groups and behaving cooperatively. Typically,    only the dominant pair in a group breeds, and a litter of young    is reared annually in an underground den. Canids communicate by    scent signals and by vocalizations. They are very intelligent.    One canid, the domestic dog, long ago entered into a    partnership with humans and today remains one of the most    widely kept domestic animals.  <\/p>\n<p>    In the history of the carnivores, the family Canidae is    represented by the two extinct subfamilies designated as Hesperocyoninae and Borophaginae, and    the extant subfamily Caninae.[7]    This subfamily includes all living canids and their most recent    fossil relatives.[6]    All living canids as a group form a dental monophyletic relationship with the extinct    borophagines with both groups having a bicuspid (two points)    on the lower carnassial talonid, which gives this    tooth an additional ability in mastication. This together with the    development of a distinct entoconid    cusp and the broadening of the talonid of the first lower    molar,    and the corresponding enlargement of the talon of the upper    first molar and reduction of its parastyle    distinguish these late Cenozoic canids and are the essential    differences that identify their clade.[6]:p6  <\/p>\n<p>    Within the Canidae, the results of allozyme and chromosome analyses    have previously suggested several phylogenetic divisions:  <\/p>\n<p>    DNA analysis shows that the    first three form monophyletic clades. The wolf-like canids and the South    American canids together form the tribe Canini.[9] Molecular data imply a North    American origin of living Canidae some ten million years ago    and an African origin of wolf-like canines (Canis,    Cuon, and Lycaon), with the jackals being the    most basal of this group. The South    American clade is rooted by the maned wolf and bush dog, and    the fox-like canids by the fennec fox and Blanford's fox. The    grey fox and island fox are basal to the other clades, however    this topological difference is not strongly supported.[10]  <\/p>\n<p>    The cladogram below is based on the phylogeny of Lindblad-Toh    et al (2005),[10] modified to    incorporate recent findings on wolf-like Canis species    by Koepfli et al (2015).[11]  <\/p>\n<p>    The Canidae today includes a diverse group of some 34 species    ranging in size from the maned wolf with its long limbs to the    short-legged bush    dog. Modern canids inhabit forests, tundra, savannahs and    deserts throughout tropical and temperate parts of the world.    The evolutionary relationships between the species have been    studied in the past using morphological approaches but    more recently, molecular studies have enabled the investigation    of phylogenetic relationships. In some    species, genetic divergence has been suppressed    by the high level of gene flow between different populations and    where the species have hybridized, large hybrid zones    exist.[12]  <\/p>\n<p>    Carnivorans evolved from miacoids about 55 million years ago (Mya) during the late Paleocene.[13] Some five    million years later, the carnivorans split into two main    divisions: caniforms (dog-like) and feliforms (cat-like). By 40 Mya, the first    member of the dog family proper had arisen. Called Prohesperocyon wilsoni, its    fossilized remains have been found in what is now the    southwestern part of Texas. The chief features which identify    it as a canid include the loss of the upper third molar (part    of a trend toward a more shearing bite), and the structure of    the middle ear which has an enlarged bulla (the hollow bony structure    protecting the delicate parts of the ear).    Prohesperocyon probably had slightly longer limbs than    its predecessors, and also had parallel and closely touching    toes which differ markedly from the splayed arrangements of the    digits in bears.[14]  <\/p>\n<p>    The canid family soon subdivided into three subfamilies, each    of which diverged during the Eocene: Hesperocyoninae (about 39.74-15 Mya),    Borophaginae (about 34-2 Mya), and Caninae (about 34-0 Mya).    Caninae is the only surviving subfamily and all present-day    canids including wolves, foxes, coyotes, jackals, and domestic    dogs belong to it. Members of each subfamily showed an increase in body mass    with time, and some exhibited specialised hypercarnivorous diets that made them    prone to extinction.[15]:Fig. 1  <\/p>\n<p>      Evolution of the Canids    <\/p>\n<p>          -65        <\/p>\n<\/p>\n<p>          -60        <\/p>\n<\/p>\n<p>          -55        <\/p>\n<\/p>\n<p>          -50        <\/p>\n<\/p>\n<p>          -45        <\/p>\n<\/p>\n<p>          -40        <\/p>\n<\/p>\n<p>          -35        <\/p>\n<\/p>\n<p>          -30        <\/p>\n<\/p>\n<p>          -25        <\/p>\n<\/p>\n<p>          -20        <\/p>\n<\/p>\n<p>          -15        <\/p>\n<\/p>\n<p>          -10        <\/p>\n<\/p>\n<p>          -5        <\/p>\n<\/p>\n<p>          0        <\/p>\n<p>    By the Oligocene, all three subfamilies of canids    (Hesperocyoninae, Borophaginae, and Caninae) had appeared in    the fossil records of North America. The earliest and most    primitive branch of the Canidae was the Hesperocyoninae    lineage, which included the coyote-sized Mesocyon of the    Oligocene (38-24 Mya). These early canids probably evolved for    the fast pursuit of prey in a grassland habitat; they resembled    modern civets in    appearance. Hesperocyonines eventually became extinct in the    middle Miocene. One of the early members of the    Hesperocyonines, the genus Hesperocyon, gave rise to    Archaeocyon and Leptocyon. These    branches led to the borophagine and canine radiations.[16]  <\/p>\n<p>    Around 910 Mya during the Late Miocene, Canis, Urocyon, and Vulpes genera expanded from southwestern    North    America, where the canine radiation began. The success of    these canines was related to the development of lower carnassials that were    capable of both mastication and shearing.[16] Around 8 Mya, the    Beringian land    bridge allowed members of the genus Eucyon a means to enter Asia and they    continued on to colonise Europe.[17]  <\/p>\n<p>    During the Pliocene, around 45 Mya, Canis    lepophagus appeared in North America. This was small    and sometimes coyote-like. Others were wolf-like in    characteristics. Canis latrans (the coyote) is theorized    to have descended from Canis lepophagus.[18]  <\/p>\n<p>    The formation of the Isthmus of Panama, about 3 Mya, joined    South    America to North America, allowing canids to invade South America, where    they diversified. However the most recent common ancestor of    the South American canids lived in North America some 4 Mya and    the likelihood is that there were more than one incursion    across the new land bridge. One of the resulting lineages    consisted of the gray    fox (Urocyon cinereoargentus) and the now extinct    dire wolf    (Canis dirus). The other lineage consisted of the    so-called South American endemic species, the maned wolf    (Chrysocyon brachyurus), the short-eared dog    (Atelocynus microtis), the bush dog (Speothos    venaticus), the crab-eating fox (Cerdocyon thous)    and the South American foxes (Lycalopex    spp.). The monophyly of this group has been established by    molecular means.[17]  <\/p>\n<p>    During the Pleistocene, the North American wolf line    appeared, with Canis edwardii, clearly identifiable    as a wolf, and Canis rufus appeared,    possibly a direct descendent of Canis edwardii. Around    0.8 Mya, Canis ambrusteri    emerged in North America. A large wolf, it was found all over    North and Central America, and was eventually supplanted by its    descendant, the dire wolf, which then spread into South America    during the late Pleistocene.[19]  <\/p>\n<p>    By 0.3 Mya, a number of subspecies of the gray wolf (Canis    lupus) had developed and had spread throughout Europe and    northern Asia.[20] The gray wolf colonized North    America during the late Rancholabrean era across the Bering land    bridge, there being at least three separate invasions, with    each one consisting of one or more different Eurasian gray wolf    clades.[21] MtDNA studies have    shown that there are at least four extant C. lupus    lineages.[22] The    dire wolf shared its habitat with the gray wolf but became    extinct in a large-scale extinction event that occurred around    11,500 years ago. It may have been more of a scavenger than a    hunter; its molars appear to be adapted for crushing bones and    it may have died out as a result of the extinction of the large    herbivorous animals on whose carcases it relied.[19]  <\/p>\n<p>    In 2015, a study of mitochondrial genome sequences and whole    genome nuclear sequences of African and Eurasian canids    indicated that extant wolf-like canids have colonised Africa    from Eurasia at least 5 times throughout the Pliocene and    Pleistocene, which is consistent with fossil evidence    suggesting that much of African canid fauna diversity resulted    from the immigration of Eurasian ancestors, likely coincident    with Plio-Pleistocene climatic oscillations between arid and    humid conditions. When comparing the African and Eurasian    golden jackals, the study concluded that the African specimens    represented a distinct monophyletic lineage that should be    recognized as a separate species, Canis anthus (African golden wolf).    According to a phylogeny derived from nuclear sequences, the    Eurasian golden jackal (Canis aureus) diverged from the    wolf\/coyote lineage 1.9 million years ago but the African    golden wolf separated 1.3 million years ago. Mitochondrial    genome sequences indicated the Ethiopian wolf diverged from the    wolf\/coyote lineage slightly prior to that.[11]:S1  <\/p>\n<p>    Wild canids are found on every continent except Antarctica, and    inhabit a wide range of different habitats, including deserts, mountains, forests, and grasslands. They vary in size from the fennec    fox, which may be as little as 24cm (9.4in) in    length and weigh 0.6kg (1.3lb),[23] to the gray wolf, which may be up to 160cm    (5.2ft) long, and can weigh up to 79kg    (174lb).[24]    Only a few species are arboreal  the North American    gray fox, the closely related Channel Island fox,[25] and the raccoon dog habitually    climb trees.[26][27][28]  <\/p>\n<p>    All canids have a similar basic form, as exemplified by the    grey wolf, although the relative length of muzzle, limbs, ears    and tail vary considerably between species. With the exceptions    of the bush dog, raccoon dog, and some domestic breeds of Canis    lupus, canids have relatively long legs and lithe    bodies, adapted for chasing prey. The tails are bushy and the    length and quality of the pelage varies with the season. The    muzzle portion of the skull is much more elongated than that of    the cat family. The zygomatic arches are wide, there is a    transverse lambdoidal ridge at the rear of the    cranium and in some species, a sagittal    crest running from front to back. The bony orbits around    the eye never form a complete ring and the auditory bullae are    smooth and rounded.[29]  <\/p>\n<p>    All canids are digitigrade, meaning they walk on their toes.    The tip of the    nose is always naked, as are the cushioned pads on the    soles of the feet. These latter consist of a single pad behind    the tip of each toe and a more-or-less three-lobed central pad    under the roots of the digits. Hairs grow between the pads and    in the Arctic fox, the sole of the foot is densely covered with    hair at some times of year. With the exception of the four-toed    African hunting dog (Lycaon pictus),    there are five toes on the forefeet but the pollex (thumb) is    reduced and does not reach the ground. On the hind feet, there    are four toes, but in some domestic dogs, a fifth vestigial    toe, known as a dewclaw, is sometimes present but has no    anatomical connection to the rest of the foot. The slightly    curved nails are non-retractile and more or less blunt.[29]  <\/p>\n<p>    The penis in    male canids is supported by a bone called the baculum. It also contains a    structure at the base called the bulbus glandis which helps to create    a copulatory tie during mating, locking the    animals together for up to an hour.[30] Young canids are born    blind, with their eyes opening a few weeks after birth.[31] All living canids (Caninae) have    a ligament analogous to the nuchal ligament of ungulates used to maintain the posture of the    head and neck with little active muscle exertion; this ligament    allows them to conserve energy while running long distances    following scent trails with their nose to the ground.[32] However,    based on skeletal details of the neck, at least some    Borophaginae (such as Aelurodon) are believed to have lacked this    ligament.[32]  <\/p>\n<p>    Most canids have 42 teeth, with a dental formula of: 3.1.4.23.1.4.3.    The bush dog has only one upper molar with two below, the dhole    has two above and two below, and the bat-eared fox has three or    four upper molars and four lower ones.[29] The molar teeth are    strong in most species, allowing the animals to crack open bone    to reach the marrow. The deciduous, or baby teeth, formula    in canids is 3.1.33.1.3,    molars being completely absent.[29]  <\/p>\n<p>    Almost all canids are social animals and live together in    groups. In general, they are territorial or have a home range    and sleep in the open, using their dens only for breeding and    sometimes in bad weather.[33] In most    foxes, and in many of the true dogs, a male and female    pair work together to hunt and to raise their young. Gray    wolves and some of the other larger canids live in larger    groups called packs. African wild dogs have packs which    may consist of twenty to forty animals, and packs of fewer than    about seven individuals may be incapable of successful    reproduction.[34] Hunting in packs has the    advantage that larger prey items can be tackled. Some species    form packs or live in small family groups depending on the    circumstances, including the type of available food. In most    species, some individuals live on their own. Within a canid    pack, there is a system of dominance so that the strongest,    most experienced animals lead the pack. In most cases, the    dominant male and female are the only pack members to    breed.[35]  <\/p>\n<p>    Canids communicate with each other by scent signals, by visual clues and    gestures, and by vocalizations such as growls, barks, and    howls. In most cases, groups have a home territory from which    they drive out other conspecifics. The    territory is marked by leaving    urine scent marks, which warn trespassing    individuals.[36] Social behaviour is also    mediated by secretions from glands on the upper surface of the    tail near its root and from the anal glands.[35]  <\/p>\n<p>    Canids as a group exhibit several reproductive traits that are    uncommon among mammals as a whole. They are typically monogamous, provide    paternal care to their offspring, have reproductive cycles with    lengthy proestral and dioestral phases and have a copulatory tie    during mating. They also retain adult offspring in the social    group, suppressing the ability of these to breed while making    use of the alloparental care they can provide to help    raise the next generation of offspring.[37]  <\/p>\n<p>    During the proestral period, increased levels of oestradiol make the female attractive to the    male. There is a rise in progesterone during the oestral phase and    the female is now receptive. Following this, the level of    oestradiol fluctuates and there is a lengthy dioestrous phase    during which the female is pregnant. Pseudo-pregnancy    frequently occurs in canids that have ovulated but failed to    conceive. A period of anoestrus follows pregnancy or    pseudo-pregnancy, there being only one    oestral period during each breeding season. Small and    medium-sized canids mostly have a gestation period of fifty to sixty days    while larger species average sixty to sixty-five days. The time    of year in which the breeding season occurs is related to the    length of day, as has been demonstrated in the case of several    species that have been translocated across the equator to the    other hemisphere and experiences a six-month shift of phase.    Domestic dogs and certain small canids in captivity may come    into oestrus more frequently, perhaps because the photoperiod stimulus breaks down under    conditions of artificial lighting.[37]  <\/p>\n<p>    The size of a litter varies, with from one to sixteen or more    pups being born. The young are born small, blind and helpless    and require a long period of parental care. They are kept in a    den, most often dug into the ground, for warmth and    protection.[29] When    the young begin eating solid food, both parents, and often    other pack members, bring food back for them from the hunt.    This is most often vomited up from the adult's stomach. Where    such pack involvement in the feeding of the litter occurs, the    breeding success rate is higher than is the case where females    split from the group and rear their pups in isolation.[38] Young canids may take a year to    mature and learn the skills they need to survive.[39] In some species, such as the    African wild dog, male offspring usually remain in the natal    pack, while females disperse as a group, and join another small    group of the opposite sex to form a new pack.[40]  <\/p>\n<p>    Because the African wild dog (Lycaon pictus)    largely exists in fragmented small populations, its existence    is endangered. Inbreeding avoidance via mate    selection is characteristic of the species and has important    potential consequences for population persistence.[41] Inbreeding is rare within    natal packs. Computer-population simulations indicate that all    populations continuing to avoid incestuous mating will become    extinct within 100 years due to the unavailability of unrelated    mates.[41] Thus the impact of    reduced numbers of suitable unrelated mates will likely have a    severe demographic impact on the future viability of small wild    dog populations.  <\/p>\n<p>    Red wolves    primarily live in packs composed of a socially monogamous breeding pair    and offspring of different ages. Using long-term data on red    wolf individuals of known pedigree, it was found that    inbreeding among first-degree relatives was rare.[42] A likely mechanism for    avoidance of inbreeding is independent dispersal trajectories    from the natal pack. Many of the young wolves spend time alone    or in small non-breeding packs composed of unrelated    individuals. The union of two unrelated individuals in a new    home range is the predominant pattern of breeding pair    formation.[42]  <\/p>\n<p>    Among Ethiopian wolves, most females disperse    from their natal pack at about two years of age, and some    become \"floaters\" that may successfully immigrate into existing    packs. Breeding pairs are most often unrelated to each other,    suggesting that female-biased dispersal reduces    inbreeding.[43]  <\/p>\n<p>    Grey wolves and Arctic foxes also exhibit inbreeding avoidance.[44]  <\/p>\n<p>    Inbreeding is ordinarily avoided because it leads to a    reduction in progeny fitness (inbreeding depression) due largely    to the homozygous expression of deleterious recessive    alleles.[45]    Cross-fertilization between unrelated individuals ordinarily    leads to the masking of deleterious recessive alleles in    progeny.[46][47]  <\/p>\n<p>    On the basis of an analysis of data on 42,855 dachshund    litters, it was found that as the inbreeding coefficient    increased, litter size decreased and the percentage of    stillborn puppies increased, thus indicating inbreeding    depression.[48]  <\/p>\n<p>    One canid, the domestic dog, entered    into a partnership with humans a long time ago. This    partnership is documented as far back as 26,000 years ago, when    the footprints of a young boy aged about eight to ten were    found in Chauvet Cave in southern France, walking    alongside what was identified as a large dog or wolf.[49] The earliest recorded fossil of    a dog was found to be around 36,000 years ago in Goyet Cave in    Belgium.[50] Even earlier, wolves were found    fossilized in the same locations as humans at sites that date    back 300,000 years, showing how far back humans and wolves had    interactions with one another.[51] The fact that wolves    are pack animals with cooperative social structures may have    been the reason that the relationship developed. Humans    benefited from the canid's loyalty, cooperation, teamwork,    alertness and tracking abilities while the wolf may have    benefited from the use of weapons to tackle larger prey and the    sharing of food. Humans and dogs may have evolved    together.[52] The bond between humans and dogs    can be seen in the burial of dogs with their owners as early as    11,000 years ago in the Americas and 8,500 years ago in    Europe.[51]  <\/p>\n<p>    Among canids, only the gray wolf has widely been known to prey    on humans.[53] Nonetheless, at least two records have coyotes killing    humans,[54] and two have golden jackals    killing children.[55] Human    beings have trapped and hunted some canid species for their fur    and, especially the gray wolf, coyote and the red fox, for    sport.[56] Canids such as the dhole are now endangered in the wild because of    persecution, habitat loss, a depletion of ungulate prey species    and transmission of diseases from domestic dogs.[57]  <\/p>\n<p>    All extant species of family Canidae are in subfamily Caninae.  <\/p>\n<p>    Except where otherwise stated, the following classification is    based on a 1994 paper by Xiaoming Wang, curator of terrestrial    mammals at the Natural History    Museum of Los Angeles County on the systematics of the    subfamily Hesperocyoninae,[58] a 1999 paper by    Wang, together with the zoologists Richard H. Tedford and Beryl    E. Taylor on the subfamily Borophaginae,[59] and a 2009 paper by    Tedford, Wang and Taylor on the North American fossil    Caninae.[60]  <\/p>\n<p>     (Mya =    million years ago) (million years = in existence)  <\/p>\n<p>     (Mya =    million years ago)  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>View original post here:<br \/>\n<a target=\"_blank\" href=\"https:\/\/en.wikipedia.org\/wiki\/Canidae\" title=\"Canidae - Wikipedia\">Canidae - Wikipedia<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Canids[1] Temporal range: 39.750Ma Late Eocene-Holocene Major extant canid genera left-to-right, top-to-bottom: Canis, Cuon, Lycaon, Cerdocyon, Chrysocyon, Speothos, Vulpes, Nyctereutes, Otocyon and Urocyon Scientific classification Kingdom: Animalia Phylum: Chordata Class: Mammalia Order: Carnivora Suborder: Caniformia Family: Canidae G.  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/transhumanist\/canidae-wikipedia\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":5,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[15],"tags":[],"class_list":["post-180624","post","type-post","status-publish","format-standard","hentry","category-transhumanist"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/180624"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=180624"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/180624\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=180624"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=180624"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=180624"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}