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Penguins Of Madagascar Sinhalal



The Penguins of Madagascar is an American computer-animated television series co-produced by DreamWorks Animation and Nickelodeon. It stars nine characters from DreamWorks' animated film Madagascar: the penguins Skipper, Rico, Kowalski, and Private; the lemurs King Julien, Maurice, and Mort; and Mason and Phil the chimpanzees. Characters new to the series include Marlene the otter and a zookeeper named Alice. It is the first Nicktoon co-produced with DreamWorks Animation. The series was executive-produced by Bob Schooley and Mark McCorkle, who were the creators of the animated series Buzz Lightyear of Star Command (a spin-off of Pixar's Toy Story franchise) and Disney Channel's Kim Possible.


Penguins (order Sphenisciformes /sfɪˈnɪsɪfɔːrmiːz/, family Spheniscidae /sfɪˈnɪsɪdiː/) are a group of aquatic flightless birds. They live almost exclusively in the Southern Hemisphere: only one species, the Galápagos penguin, is found north of the Equator. Highly adapted for life in the water, penguins have countershaded dark and white plumage and flippers for swimming. Most penguins feed on krill, fish, squid and other forms of sea life which they catch with their bills and swallow whole while swimming. A penguin has a spiny tongue and powerful jaws to grip slippery prey.[4]




Penguins Of Madagascar Sinhalal



The word penguin first appears in literature at the end of the 16th century.[8] When European explorers discovered what are today known as penguins in the Southern Hemisphere, they noticed their similar appearance to the great auk of the Northern Hemisphere, and named them after this bird, although they are not closely related.[9]


The birds currently known as penguins were discovered later and were so named by sailors because of their physical resemblance to the great auk. Despite this resemblance, however, they are not auks, and are not closely related to the great auk.[9][16] They do not belong in the genus Pinguinus, and are not classified in the same family and order as the great auk. They were classified in 1831 by Charles Bonaparte in several distinct genera within the family Spheniscidae and order Sphenisciformes.


The number of extinct penguin species is debated. Depending on which authority is followed, penguin biodiversity varies between 17 and 20 living species, all in the subfamily Spheniscinae. Some sources consider the white-flippered penguin a separate Eudyptula species, while others treat it as a subspecies of the little blue penguin;[19][20] the actual situation seems to be more complicated.[21] Similarly, it is still unclear whether the royal penguin is a separate species or merely a color morph of the macaroni penguin. The status of the rockhopper penguins is also unclear.


Some recent sources[3][28] apply the phylogenetic taxon Spheniscidae to what here is referred to as Spheniscinae. Furthermore, they restrict the phylogenetic taxon Sphenisciformes to flightless taxa, and establish the phylogenetic taxon Pansphenisciformes as equivalent to the Linnean taxon Sphenisciformes,[28] i.e., including any flying basal "proto-penguins" to be discovered eventually. Given that neither the relationships of the penguin subfamilies to each other nor the placement of the penguins in the avian phylogeny is presently resolved, this is confusing, so the established Linnean system is followed here.


The evolutionary history of penguins is well-researched and represents a showcase of evolutionary biogeography. Although penguin bones of any one species vary much in size and few good specimens are known, the alpha taxonomy of many prehistoric forms still leaves much to be desired. Some seminal articles about penguin prehistory have been published since 2005;[3][29][32][33] the evolution of the living genera can be considered resolved by now.


In any case, the gigantic penguins had disappeared by the end of the Paleogene, around 25 mya. Their decline and disappearance coincided with the spread of the Squalodontoidea and other primitive, fish-eating toothed whales, which certainly competed with them for food, and were ultimately more successful.[29] A new lineage, the Paraptenodytes, which includes smaller but decidedly stout-legged forms, had already arisen in southernmost South America by that time. The early Neogene saw the emergence of yet another morphotype in the same area, the similarly sized but more gracile Palaeospheniscinae, as well as the radiation that gave rise to the penguin biodiversity of our time.


Modern penguins constitute two undisputed clades and another two more basal genera with more ambiguous relationships.[32] To help resolve the evolution of this order, 19 high-coverage genomes that, together with two previously published genomes, encompass all extant penguin species have been sequenced.[38] The origin of the Spheniscinae lies probably in the latest Paleogene and, geographically, it must have been much the same as the general area in which the order evolved: the oceans between the Australia-New Zealand region and the Antarctic.[29] Presumably diverging from other penguins around 40 mya,[29] it seems that the Spheniscinae were for quite some time limited to their ancestral area, as the well-researched deposits of the Antarctic Peninsula and Patagonia have not yielded Paleogene fossils of the subfamily. Also, the earliest spheniscine lineages are those with the most southern distribution.


The genus Aptenodytes appears to be the basalmost divergence among living penguins.[3][39] They have bright yellow-orange neck, breast, and bill patches; incubate by placing their eggs on their feet, and when they hatch the chicks are almost naked. This genus has a distribution centred on the Antarctic coasts and barely extends to some Subantarctic islands today.


The geographical and temporal pattern of spheniscine evolution corresponds closely to two episodes of global cooling documented in the paleoclimatic record.[29] The emergence of the Subantarctic lineage at the end of the Bartonian corresponds with the onset of the slow period of cooling that eventually led to the ice ages some 35 million years later. With habitat on the Antarctic coasts declining, by the Priabonian more hospitable conditions for most penguins existed in the Subantarctic regions rather than in Antarctica itself.[41] Notably, the cold Antarctic Circumpolar Current also started as a continuous circumpolar flow only around 30 mya, on the one hand forcing the Antarctic cooling, and on the other facilitating the eastward expansion of Spheniscus to South America and eventually beyond.[29] Despite this, there is no fossil evidence to support the idea of crown radiation from the Antarctic continent in the Paleogene, although DNA study favors such a radiation.[41]


Penguin ancestry beyond Waimanu remains unknown and not well-resolved by molecular or morphological analyses. The latter tend to be confounded by the strong adaptive autapomorphies of the Sphenisciformes; a sometimes perceived fairly close relationship between penguins and grebes is almost certainly an error based on both groups' strong diving adaptations, which are homoplasies. On the other hand, different DNA sequence datasets do not agree in detail with each other either.


What seems clear is that penguins belong to a clade of Neoaves (living birds except for paleognaths and fowl) that comprises what is sometimes called "higher waterbirds" to distinguish them from the more ancient waterfowl. This group contains such birds as storks, rails, and the seabirds, with the possible exception of the Charadriiformes.[42]


Inside this group, penguin relationships are far less clear. Depending on the analysis and dataset, a close relationship to Ciconiiformes[33] or to Procellariiformes[29] has been suggested. Some think the penguin-like plotopterids (usually considered relatives of cormorants and anhingas) may actually be a sister group of the penguins and those penguins may have ultimately shared a common ancestor with the Pelecaniformes and consequently would have to be included in that order, or that the plotopterids were not as close to other pelecaniforms as generally assumed, which would necessitate splitting the traditional Pelecaniformes into three.[43]


A 2014 analysis of whole genomes of 48 representative bird species has concluded that penguins are the sister group of Procellariiformes,[44] from which they diverged about 60 million years ago (95% CI, 56.8-62.7).[45]


The distantly related puffins, which live in the North Pacific and North Atlantic, developed similar characteristics to survive in the Arctic and sub-Arctic environments. Like the penguins, puffins have a white chest, black back and short stubby wings providing excellent swimming ability in icy water. But, unlike penguins, puffins can fly, as flightless birds would not survive alongside land-based predators such as polar bears and foxes; there are no such predators in the Antarctic. Their similarities indicate that similar environments, although at great distances, can result in similar evolutionary developments, i.e. convergent evolution.[46]


Penguins are superbly adapted to aquatic life. Their wings have evolved to become flippers, useless for flight in the air. In the water, however, penguins are astonishingly agile. Penguins' swimming looks very similar to birds' flight in the air.[47] Within the smooth plumage a layer of air is preserved, ensuring buoyancy. The air layer also helps insulate the birds in cold waters. On land, penguins use their tails and wings to maintain balance for their upright stance.


The emperor penguin has the largest body mass of all penguins, which further reduces relative surface area and heat loss. They also are able to control blood flow to their extremities, reducing the amount of blood that gets cold, but still keeping the extremities from freezing. In the extreme cold of the Antarctic winter, the females are at sea fishing for food, leaving the males to brave the weather by themselves. They often huddle together to keep warm and rotate positions to make sure that each penguin gets a turn in the centre of the heat pack. 2ff7e9595c


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