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Round and round they go and Galápagos giant tortoise

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The Galápagos tortoise or Galápagos giant tortoise (Chelonoidis nigra) is the largest living species of tortoise; this one is from the Island of Santa Cruz.

The Galápagos tortoise complex or Galápagos giant tortoise complex (Chelonoidis nigra) are the largest living species of tortoise. Modern Galápagos tortoises can weigh up to 417 kg (919 lb).[22] Today, giant tortoises exist only on two remote archipelagos: the Galápagos 1000 km due west of mainland Ecuador, and Aldabra in the Indian Ocean, 700 km east of Tanzania.

The Galápagos tortoises are native to seven of the Galápagos Islands, a volcanic archipelago about 1,000 km (620 mi) west of the Ecuadorian mainland. With lifespans in the wild of over 100 years, it is one of the longest-lived vertebrates. A captive individual lived at least 170 years. Spanish explorers, who discovered the islands in the 16th century, named them after the Spanish galápago, meaning "tortoise".[23]

Shell size and shape vary between populations. On islands with humid highlands, the tortoises are larger, with domed shells and short necks; on islands with dry lowlands, the tortoises are smaller, with "saddleback" shells and long necks. Charles Darwin's observations of these differences on the second voyage of the Beagle in 1835, contributed to the development of his theory of evolution.

Tortoise numbers declined from over 250,000 in the 16th century to a low of around 3,000 in the 1970s. This decline was caused by overexploitation of the species for meat and oil, habitat clearance for agriculture, and introduction of non-native animals to the islands, such as rats, goats, and pigs. The extinction of most giant tortoise lineages is thought to have also been caused by predation by humans or human ancestors, as the tortoises themselves have no natural predators. Tortoise populations on at least three islands have become extinct in historical time due to human activities. Specimens of these extinct taxa exist in several museums and also are being subjected to DNA analysis. Ten species of the original 15 survive in the wild; an 11th species (Chelonoidis abingdonii) had only a single known living individual, kept in captivity and nicknamed Lonesome George until his death in June 2012. Conservation efforts, beginning in the 20th century, have resulted in thousands of captive-bred juveniles being released onto their ancestral home islands, and the total number of the species is estimated to have exceeded 19,000 at the start of the 21st century. Despite this rebound, the species as a whole is classified as "vulnerable" by the International Union for Conservation of Nature.

Taxonomy
Early classification

The Galápagos Islands were discovered in 1535, but first appeared on the maps, of Gerardus Mercator and Abraham Ortelius, around 1570.[24] The islands were named "Insulae de los Galopegos" (Islands of the Tortoises) in reference to the giant tortoises found there.[25][26][nb 1]

Initially, the giant tortoises of the Indian Ocean and those from the Galápagos were considered to be the same species. Naturalists thought that sailors had transported the tortoises there.[27] In 1676, the pre-Linnaean authority Claude Perrault referred to both species as Tortue des Indes.[28] In 1783, Johann Gottlob Schneider classified all giant tortoises as Testudo indica ("Indian tortoise").[29] In 1812, August Friedrich Schweigger named them Testudo gigantea ("gigantic tortoise").[30] In 1834, André Marie Constant Duméril and Gabriel Bibron classified the Galápagos tortoises as a separate species, which they named Testudo nigrita ("black tortoise").[13]
Black and white photograph of Walter Rothschild straddling an adult Galápagos tortoise: Rothschild is a Victorian gentleman sporting a beard and top hat.
Walter Rothschild, cataloger of two Galápagos tortoise species
Recognition of subpopulations

The first systematic survey of giant tortoises was by Albert Günther of the British Museum, in 1875.[9] Günther identified at least five distinct populations from the Galápagos, and three from the Indian Ocean islands. He expanded the list in 1877 to six from the Galápagos, four from the Seychelles, and four from the Mascarenes. Günther hypothesized that all the giant tortoises descended from a single ancestral population which spread by sunken land bridges.[31] This hypothesis was later disproven by the understanding that the Galápagos, Seychelles, and Mascarene islands are all of recent volcanic origin and have never been linked to a continent by land bridges. Galápagos tortoises are now thought to have descended from a South American ancestor,[32] while the Indian Ocean tortoises derived from ancestral populations on Madagascar.[33][34]

At the end of the 19th century, Georg Baur[18] and Walter Rothschild[5][8][19] recognised five more populations of Galápagos tortoise. In 1905–06, an expedition by the California Academy of Sciences, with Joseph R. Slevin in charge of reptiles, collected specimens which were studied by Academy herpetologist John Van Denburgh. He identified four additional populations,[6] and proposed the existence of 15 species.[35] Van Denburgh's list still guides the taxonomy of the Galápagos tortoise, though now 10 populations are thought to have existed.[1]
Current species and genus names

The current specific designation of nigra ("black" – Quoy & Gaimard, 1824b[3]) was resurrected in 1984[36] after it was discovered to be the senior synonym (an older taxonomic synonym taking historical precedence) for the then commonly used species name of elephantopus ("elephant-footed" – Harlan, 1827[12]). Quoy and Gaimard's Latin description explains the use of nigra: "Testudo toto corpore nigro" means "tortoise with completely black body". Quoy and Gairmard described nigra from a living specimen, but no evidence indicates they knew of its accurate provenance within the Galápagos – the locality was in fact given as California. Garman proposed the linking of nigra with the extinct Floreana species.[7] Later, Pritchard deemed it convenient to accept this designation, despite its tenuousness, for minimal disruption to the already confused nomenclature of the species. The even more senior species synonym of californiana ("californian" – Quoy & Gaimard, 1824a[11]) is considered a nomen oblitum ("forgotten name").[37]

Previously, the Galápagos tortoise was considered to belong to the genus Geochelone, known as 'typical tortoises' or 'terrestrial turtles'. In the 1990s, subgenus Chelonoidis was elevated to generic status based on phylogenetic evidence which grouped the South American members of Geochelone into an independent clade (branch of the tree of life).[38] This nomenclature has been adopted by several authorities.[2][1][39][40]
Species
Main article: List of species of Galápagos tortoise
A map of the Galápagos with labels for names of the islands and their native species of tortoise
Galápagos archipelago annotated with ranges of currently recognised species of Galápagos tortoise, islands with surviving species are shaded.

Within the archipelago, up to 15 species of Galápagos tortoises have been identified, although only 11 survive to this day. Six are found on separate islands; five of them on the volcanoes of Isabela Island. Several of the surviving species are seriously endangered.[32] One of the species, C. abingdonii from Pinta Island, is considered extinct. The last known specimen, named Lonesome George, died in captivity on 24 June 2012; George had been mated with female tortoises of several other species, but none of the eggs from these pairings hatched. The species inhabiting Floreana Island (G. nigra)[41] is thought to have been hunted to extinction by 1850,[42][43] only 15 years after Charles Darwin's landmark visit of 1835, when he saw shells, but no live tortoises there.[44] The existence of the C. phantastica species of Fernandina Island is disputed, as it was described from a single specimen that may have been an artificial introduction to the island.[45][46][47] However, recent DNA testing shows that an intermixed, non-native population currently existing on the island of Isabela is of genetic resemblance to the species native to Floreana, suggesting that G. nigra has not gone entirely extinct.[41]

Prior to widespread knowledge of the differences between the populations (sometimes called races) from different islands and volcanoes, captive collections in zoos were indiscriminately mixed. Fertile offspring resulted from pairings of animals from different races. However, captive crosses between tortoises from different races have lower fertility and higher mortality than those between tortoises of the same race,[48][49] and captives in mixed herds normally direct courtship only toward members of the same race.[49]

The valid scientific names of each of the individual populations are not universally accepted,[10][46][50][51] and some researchers still consider each species to be a subspecies.[52][53] The taxonomic status of the various races is not fully resolved.[54]
Evolutionary history

All species of Galápagos tortoises evolved from common ancestors that arrived from mainland South America by overwater dispersal. Genetic studies have shown that the Chaco tortoise of Argentina and Paraguay is their closest living relative.[32] The minimal founding population was a pregnant female or a breeding pair.[32] Survival on the 1000-km oceanic journey is accounted for because the tortoises are buoyant, can breathe by extending their necks above the water, and are able to survive months without food or fresh water.[38] As they are poor swimmers, the journey was probably a passive one facilitated by the Humboldt Current, which diverts westwards towards the Galápagos Islands from the mainland.[55] The ancestors of the genus Chelonoidis are believed to have similarly dispersed from Africa to South America during the Oligocene.[38]

The closest living relative (though not a direct ancestor) of the Galápagos giant tortoise is the Chaco tortoise (Chelonoidis chilensis), a much smaller species from South America. The divergence between C. chilensis and C. nigra probably occurred 6–12 million years ago, an evolutionary event preceding the volcanic formation of the oldest modern Galápagos Islands 5 million years ago.[56] Mitochondrial DNA analysis indicates that the oldest existing islands (Española and San Cristóbal) were colonised first, and that these populations seeded the younger islands via dispersal in a "stepping stone" fashion via local currents.[57][58] Restricted gene flow between isolated islands then resulted in the independent evolution of the populations into the divergent forms observed in the modern species. The evolutionary relationships between the species thus echo the volcanic history of the islands.[32]
Species

Modern DNA methods have revealed new information on the relationships between the species:

Isabela Island

The five populations living on the largest island, Isabela, are the ones that are the subject of the most debate as to whether they are true species or just distinct populations or subspecies. It is widely accepted that the population living on the northernmost volcano, Volcan Wolf, is genetically independent from the four populations to the south and is therefore a separate species.[32] It is thought to be derived from a different colonization event than the others. A colonization from the island of Santiago apparently gave rise to the Volcan Wolf species (C. becki) while the four southern populations are believed to be descended from a second colonization from the more southerly island of Santa Cruz.[32] Tortoises from Santa Cruz are thought to have first colonized the Sierra Negra volcano, which was the first of the island's volcanoes to form. The tortoises then spread north to each newly created volcano, resulting in the populations living on Volcan Alcedo and then Volcan Darwin. Recent genetic evidence shows that these two populations are genetically distinct from each other and from the population living on Sierra Negra (C. guentheri) and therefore form the species C. vandenburghi (Alcedo) and C. microphyes (Darwin).[59] The fifth population living on the southernmost volcano (C. vicina) is thought to have split off from the Sierra Negra population more recently and is therefore not as genetically different as the other two.[59] Isabela is the most recently formed island tortoises inhabit, so its populations have had less time to evolve independently than populations on other islands, but according to some researchers, they are all genetically different and should each be considered as separate species.[59]

Floreana Island

Phylogenetic analysis may help to "resurrect" the extinct species of Floreana (C. nigra) – a species known only from subfossil remains.[43] Some tortoises from Isabela were found to be a partial match for the genetic profile of Floreana specimens from museum collections, possibly indicating the presence of hybrids from a population transported by humans from Floreana to Isabela,[53] resulting either from individuals deliberately transported between the islands,[60] or from individuals thrown overboard from ships to lighten the load.[18] Nine Floreana descendants have been identified in the captive population of the Fausto Llerena Breeding Center on Santa Cruz; the genetic footprint was identified in the genomes of hybrid offspring. This allows the possibility of re-establishing a reconstructed species from selective breeding of the hybrid animals.[61] Furthermore, individuals from the species possibly are still extant. Genetic analysis from a sample of tortoises from Volcan Wolf found 84 first-generation C. nigra hybrids, some less than 15 years old. The genetic diversity of these individuals is estimated to have required 38 C. nigra parents, many of which could still be alive on Isabela Island.[62]

Pinta Island

C. abingdonii Lonesome George at the Charles Darwin Research Station, in 2006

The Pinta Island species (C. abingdonii, now extinct) has been found to be most closely related to the species on the islands of San Cristóbal (C. chathamensis) and Española (C. hoodensis) which lie over 300 km (190 mi) away,[32] rather than that on the neighbouring island of Isabela as previously assumed. This relationship is attributable to dispersal by the strong local current from San Cristóbal towards Pinta.[63] This discovery informed further attempts to preserve the C. abingdonii lineage and the search for an appropriate mate for Lonesome George, which had been penned with females from Isabela.[64] Hope was bolstered by the discovery of a C. abingdonii hybrid male in the Volcán Wolf population on northern Isabela, raising the possibility that more undiscovered living Pinta descendants exist.[65]

Santa Cruz Island

Mitochondrial DNA studies of tortoises on Santa Cruz show up to three genetically distinct lineages found in nonoverlapping population distributions around the regions of Cerro Montura, Cerro Fatal, and La Caseta.[66] Although traditionally grouped into a single species (C. porteri), the lineages are all more closely related to tortoises on other islands than to each other:[67] Cerro Montura tortoises are most closely related to G. duncanensis from Pinzón,[55] Cerro Fatal to G. chathamensis from San Cristóbal,[55][68][69] and La Caseta to the four southern races of Isabela[55][69] as well as Floreana tortoises.[69]

In 2015, the Cerro Fatal tortoises were described as a distinct taxon, donfaustoi.[69][70] Prior to the identification of this species through genetic analysis, it was noted that there existed differences in shells between the Cerro Fatal tortoises and other tortoises on Santa Cruz.[71] By classifying the Cerro Fatal tortoises into a new taxon, greater attention can be paid to protecting its habitat, according to Adalgisa Caccone, who is a member of the team making this classification.[69][71]

Pinzón Island

When it was discovered that the central, small island of Pinzón had only 100–200 very old adults and no young tortoises had survived into adulthood for perhaps more than 70 years, the resident scientists initiated what would eventually become the Giant Tortoise Breeding and Rearing Program. Over the next 50 years, this program resulted in major successes in the recovery of giant tortoise populations throughout the archipelago.

In 1965, the first tortoise eggs collected from natural nests on Pinzón Island were brought to the Charles Darwin Research Station, where they would complete the period of incubation and then hatch, becoming the first young tortoises to be reared in captivity. The introduction of black rats onto Pinzón sometime in the latter half of the 19th century had resulted in the complete eradication of all young tortoises. Black rats had been eating both tortoise eggs and hatchlings, effectively destroying the future of the tortoise population. Only the longevity of giant tortoises allowed them to survive until conservation scientists and managers began to focus on Galapagos and the long path back to ecosystem restoration.[72]

Española

On the southern island of Española, only 14 adult tortoises were found, two males and 12 females. The tortoises apparently were not encountering one another, so no reproduction was occurring. Between 1963 and 1974, all 14 adult tortoises discovered on the island were brought to the tortoise center on Santa Cruz and a tortoise breeding program was initiated. In 1977, a third Española male tortoise was returned to Galapagos from the San Diego Zoo and joined the breeding group.[72] After 40 years' work reintroducing captive animals, a detailed study of the island's ecosystem has confirmed it has a stable, breeding population. Where once 15 were known, now more than 1,000 giant tortoises inhabit the island of Española. One research team has found that more than half the tortoises released since the first reintroductions are still alive, and they are breeding well enough for the population to progress onward, unaided.[73]

Species of doubtful existence

Species were described from three other islands, but their existence is based on scant evidence. The purported Rábida Island species (C. wallacei) was described from a single specimen collected by the California Academy of Sciences in December 1905,[35] which has since been lost. This individual was probably an artificial introduction from another island that was originally penned on Rábida next to a good anchorage, as no contemporary whaling or sealing logs mention removing tortoises from this island.[47] The C. phantastica species from Fernandina is known from a single specimen — an old male from the voyage of 1905–06.[35] No other tortoises or remains have been found on the island, suggesting the specimen was an artificial introduction from elsewhere.[46][47][60] Fernandina has neither human settlements nor feral mammals, so if this species ever did exist, its extinction must have been by natural means, such as volcanic activity.[46] The Santa Fe species has no binomial name, having been described from the limited evidence of bone fragments (but no shells, the most durable part) of 14 individuals, old eggs, and old dung found on the island in 1905–06.[35] The island has never been inhabited by man nor had any introduced predators.[60] The remains are considered artificial introductions,[46] possibly from camping at the good anchorage on the island.[60]
Description
File:Galapagos Riesenschildkröte Chelonoidis niger.ogvPlay media
Galápagos tortoise at the Rostock Zoo

The tortoises have a large bony shell of a dull brown or gray colour. The plates of the shell are fused with the ribs in a rigid protective structure that is integral to the skeleton. Lichens can grow on the shells of these slow-moving animals.[74] Tortoises keep a characteristic scute (shell segment) pattern on their shells throughout life, though the annual growth bands are not useful for determining age because the outer layers are worn off with time. A tortoise can withdraw its head, neck, and fore limbs into its shell for protection. The legs are large and stumpy, with dry, scaly skin and hard scales. The front legs have five claws, the back legs four.[35]
Gigantism

The discoverer of the Galápagos Islands, Fray Tomás de Berlanga, Bishop of Panama, wrote in 1535 of "such big tortoises that each could carry a man on top of himself."[75] Naturalist Charles Darwin remarked after his trip three centuries later in 1835, "These animals grow to an immense size ... several so large that it required six or eight men to lift them from the ground".[76] The largest recorded individuals have reached weights of over 400 kg (880 lb)[22][77] and lengths of 1.87 meters (6.1 ft).[3][78] Size overlap is extensive with the Aldabra giant tortoise, however taken as a species, the Galápagos tortoise seems to average slightly larger, with weights in excess of 185 kg (408 lb) being slightly more commonplace.[79] Weights in the larger bodied species range from 272 to 317 kg (600 to 699 lb) in mature males and from 136 to 181 kg (300 to 399 lb) in adult females.[35] However, the size is variable across the islands and species; those from Pinzón Island are relatively small with a maximum known weight of 76 kg (168 lb) and carapace length of approximately 61 cm (24 in) compared to 75 to 150 cm (30 to 59 in) range in tortoises from Santa Cruz Island.[80] The tortoises' gigantism was probably a trait useful on continents that was fortuitously helpful for successful colonisation of these remote oceanic islands rather than an example of evolved insular gigantism. Large tortoises would have a greater chance of surviving the journey over water from the mainland as they can hold their heads a greater height above the water level and have a smaller surface area/volume ratio, which reduces osmotic water loss. Their significant water and fat reserves would allow the tortoises to survive long ocean crossings without food or fresh water, and to endure the drought-prone climate of the islands. A larger size allowed them to better tolerate extremes of temperature due to gigantothermy.[81] Fossil giant tortoises from mainland South America have been described that support this hypothesis of gigantism that pre-existed the colonization of islands.[82]
Shell shape
Galápagos tortoise shell varieties
Tortoise of the C. abingdonii species has a distinctively saddle-shaped shell that flares above the neck and limbs.
Saddleback (C. abingdonii)
Tortoise of the chathamensis species has a slightly saddle-shaped shell.
Intermediate (C. chathamensis)
Tortoise of the C. porteri species has a rounded shell shaped like a dome.
Domed (C. porteri)

Galápagos tortoises possess two main shell forms that correlate with the biogeographic history of the species group. They exhibit a spectrum of carapace morphology ranging from "saddleback" (denoting upward arching of the front edge of the shell resembling a saddle) to "domed" (denoting a rounded convex surface resembling a dome). When a saddleback tortoise withdraws its head and forelimbs into its shell, a large unprotected gap remains over the neck, evidence of the lack of predation during the evolution of this structure. Larger islands with humid highlands over 800 m (2,600 ft) in elevation, such as Santa Cruz, have abundant vegetation near the ground.[51] Tortoises native to these environments tend to have domed shells and are larger, with shorter necks and limbs. Saddleback tortoises originate from small islands less than 500 m (1,600 ft) in elevation with dry habitats (e.g. Española and Pinzón) that are more limited in food and other resources.[55] Two lineages of Galápagos tortoises possess the Island of Santa Cruz and when observed it is concluded that despite the shared similarities of growth patterns and morphological changes observed during growth, the two lineages and two sexes can be distinguished on the basis of distinct carapace features. Lineages differ by the shape of the vertebral and pleural scutes. Females have a more elongated and wider carapace shape than males. Carapace shape changes with growth, with vertebral scutes becoming narrower and pleural scutes becoming larger during late ontogeny.

Evolutionary implications

In combination with proportionally longer necks and limbs,[35] the unusual saddleback carapace structure is thought to be an adaptation to increase vertical reach, which enables the tortoise to browse tall vegetation such as the Opuntia (prickly pear) cactus that grows in arid environments.[83] Saddlebacks are more territorial[78][84] and smaller than domed varieties, possibly adaptations to limited resources. Alternatively, larger tortoises may be better-suited to high elevations because they can resist the cooler temperatures that occur with cloud cover or fog.[50]

A competing hypothesis is that, rather than being principally a feeding adaptation, the distinctive saddle shape and longer extremities might have been a secondary sexual characteristic of saddleback males. Male competition over mates is settled by dominance displays on the basis of vertical neck height rather than body size[50] (see below). This correlates with the observation that saddleback males are more aggressive than domed males.[85] The shell distortion and elongation of the limbs and neck in saddlebacks is probably an evolutionary compromise between the need for a small body size in dry conditions and a high vertical reach for dominance displays.[50]

The saddleback carapace probably evolved independently several times in dry habitats,[78] since genetic similarity between populations does not correspond to carapace shape.[86] Saddleback tortoises are, therefore, not necessarily more closely related to each other than to their domed counterparts, as shape is not determined by a similar genetic background, but by a similar ecological one.[50]

Sexual dimorphism

Sexual dimorphism is most pronounced in saddleback populations in which males have more angled and higher front openings, giving a more extreme saddled appearance.[85] Males of all varieties generally have longer tails and shorter, concave plastrons with thickened knobs at the back edge to facilitate mating. Males are larger than females — adult males weigh around 272–317 kg (600–699 lb) while females are 136–181 kg (300–399 lb).[50]
Behavior
A tortoise somewhat submerged in a green outdoor pool full of algae
A tortoise bathing in a pool
Routine

The tortoises are ectothermic (cold-blooded), so bask for 1–2 hours after dawn to absorb the sun's heat through their dark shells before actively foraging for 8–9 hours a day.[46] They travel mostly in the early morning or late afternoon between resting and grazing areas. They have been observed to walk at a speed of 0.3 km/h (0.2 mph).[76]

On the larger and more humid islands, the tortoises seasonally migrate between low elevations, which become grassy plains in the wet season, and meadowed areas of higher elevation (up to 2,000 ft (610 m)[35]) in the dry season. The same routes have been used for many generations, creating well-defined paths through the undergrowth known as "tortoise highways".[51] On these wetter islands, the domed tortoises are gregarious and often found in large herds, in contrast to the more solitary and territorial disposition of the saddleback tortoises.

Tortoises sometimes rest in mud wallows or rain-formed pools, which may be both a thermoregulatory response during cool nights, and a protection from parasites such as mosquitoes and ticks.[51] Parasites are countered by taking dust baths in loose soil. Some tortoises have been noted to shelter at night under overhanging rocks.[87] - others have been observed sleeping in a snug depression in the earth or brush called a "pallet". Local tortoises using the same pallet sites, such as on Volcán Alcedo, results in the formation of small, sandy pits.[88]
Diet
An adult tortoise with a mouthful of green leaves.
A tortoise feeding

The tortoises are herbivores that consume a diet of cacti, grasses, leaves, lichens, berries, melons, oranges, and milkweed.[89] They have been documented feeding on Hippomane mancinella ('poison apple'), the endemic guava Psidium galapageium, the water fern Azolla microphylla, and the bromeliad Tillandsia insularis.[90] Juvenile tortoises eat an average of 16.7% of their own body weight in dry matter per day, with a digestive efficiency roughly equal to that of hindgut-fermenting herbivorous mammals such as horses and rhinos.[91]

Tortoises acquire most of their moisture from the dew and sap in vegetation (particularly the Opuntia cactus); therefore, they can survive longer than 6 months without water. They can endure up to a year when deprived of all food and water,[92] surviving by breaking down their body fat to produce water as a byproduct. Tortoises also have very slow metabolisms.[93] When thirsty, they may drink large quantities of water very quickly, storing it in their bladders and the "root of the neck" (the pericardium[46]), both of which served to make them useful water sources on ships.[92] On arid islands, tortoises lick morning dew from boulders, and the repeated action over many generations has formed half-sphere depressions in the rock.[46]
Senses

Regarding their senses, Charles Darwin observed, "The inhabitants believe that these animals are absolutely deaf; certainly they do not overhear a person walking near behind them. I was always amused, when overtaking one of these great monsters as it was quietly pacing along, to see how suddenly, the instant I passed, it would draw in its head and legs, and uttering a deep hiss fall to the ground with a heavy sound, as if struck dead."[76] Although they are not deaf,[35] tortoises depend far more on vision and smell as stimuli than hearing.[51]
Mutualism

Tortoises share a mutualistic relationship with some species of Galápagos finch and mockingbirds. Small groups of finches initiate the process by hopping on the ground in an exaggerated fashion facing the tortoise. The tortoise signals it is ready by rising up and extending its neck and legs, enabling the birds to reach otherwise inaccessible spots on the tortoise's body such as the neck, rear legs, cloacal opening, and skin between plastron and carapace. The birds benefit from the food source and the tortoises get rid of irritating ectoparasites.[94]

Some tortoises have been observed to insidiously exploit this mutualistic relationship. After rising and extending its limbs, the bird may go beneath the tortoise to investigate, whereupon suddenly the tortoise withdraws its limbs to drop flat and kill the bird. It then steps back to eat the bird, presumably to supplement its diet with protein.[95]
Two tortoises with their necks extended
A pair of tortoises engaging in a dominance display
Mating

Mating occurs at any time of the year, although it does have seasonal peaks between February and June in the humid uplands during the rainy season.[51] When mature males meet in the mating season, they face each other in a ritualised dominance display, rise up on their legs, and stretch up their necks with their mouths gaping open. Occasionally, head-biting occurs, but usually the shorter tortoise backs off, conceding mating rights to the victor. The behaviour is most pronounced in saddleback species, which are more aggressive and have longer necks.[85]

The prelude to mating can be very aggressive, as the male forcefully rams the female's shell with his own and nips her legs.[20] Mounting is an awkward process and the male must stretch and tense to maintain equilibrium in a slanting position. The concave underside of the male's shell helps him to balance when straddled over the female's shell, and brings his cloacal vent (which houses the penis) closer to the female's dilated cloaca. During mating, the male vocalises with hoarse bellows and grunts,[87] described as "rhythmic groans".[51] This is one of the few vocalisations the tortoise makes; other noises are made during aggressive encounters, when struggling to right themselves, and hissing as they withdraw into their shells due to the forceful expulsion of air.[96]
A tour guide holds up a tortoise egg and a small tortoise. The egg comfortably rests in the palm of a hand. It is spherical and the size of a billiard ball. It has a smooth, white surface with a light layer of soil on it. The tortoise is held by the other hand, above the egg. The width of the tortoise is only marginally wider than the egg.
A young tortoise and a tortoise egg
Egg-laying

Females journey up to several kilometres in July to November to reach nesting areas of dry, sandy coast. Nest digging is a tiring and elaborate task which may take the female several hours a day over many days to complete.[51] It is carried out blindly using only the hind legs to dig a 30 cm (12 in)-deep cylindrical hole, in which the tortoise then lays up to 16 spherical, hard-shelled eggs ranging from 82 to 157 grams (2.9 to 5.5 oz) in mass,[46] and the size of a billiard ball.[74] Some observations suggest that the average clutch size for domed populations (9.6 per clutch for C. porteri on Santa Cruz) is larger than that of saddlebacks (4.6 per clutch for C. duncanensis on Pinzón).[47] The female makes a muddy plug for the nest hole out of soil mixed with urine, seals the nest by pressing down firmly with her plastron, and leaves them to be incubated by the sun. Females may lay one to four clutches per season. Temperature plays a role in the sex of the hatchlings, with lower-temperature nests producing more males and higher-temperature nests producing more females. This is related closely to incubation time, since clutches laid early incubate during the cool season and have longer incubation periods (producing more males), while eggs laid later incubate for a shorter period in the hot season (producing more females).[97]
Early life and maturation

Young animals emerge from the nest after four to eight months and may weigh only 50 g (1.8 oz) and measure 6 cm (2.4 in).[51] When the young tortoises emerge from their shells, they must dig their way to the surface, which can take several weeks, though their yolk sac can sustain them up to seven months.[74] In particularly dry conditions, the hatchlings may die underground if they are encased by hardened soil, while flooding of the nest area can drown them. Species are initially indistinguishable as they all have domed carapaces. The young stay in warmer lowland areas for their first 10–15 years,[46] encountering hazards such as falling into cracks, being crushed by falling rocks, or excessive heat stress. The Galápagos hawk was formerly the sole native predator of the tortoise hatchlings; Darwin wrote: "The young tortoises, as soon as they are hatched, fall prey in great numbers to the buzzard".[76] The hawk is now much rarer, but introduced feral pigs, dogs, cats, and black rats have become predators of eggs and young tortoises.[98] The adult tortoises have no natural predators apart from humans; Darwin noted: "The old ones seem generally to die from accidents, as from falling down precipices. At least several of the inhabitants told me, they had never found one dead without some such apparent cause".[76]

Sexual maturity is reached at around 20–25 years in captivity, possibly 40 years in the wild.[99] Life expectancy in the wild is thought to be over 100 years,[100][101] making it one of the longest-lived species in the animal kingdom. Harriet, a specimen kept in Australia Zoo, was the oldest known Galápagos tortoise, having reached an estimated age of more than 170 years before her death in 2006.[102] Chambers notes that Harriet was probably 169 years old in 2004, although media outlets claimed the greater age of 175 at death based on a less reliable timeline.[103]

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Title Round and round they go
Released 10/10/2017 9:43 am
Copyright ESA/NASA
Description

Talk about an image making your head spin: ESA astronaut Paolo Nespoli took this stunning image of NASA astronauts Randy Bresnik and Mark Vande Hai during last week’s spacewalk.

During this excursion, the duo replaced part of the Station’s Canadarm2 robotic arm. The spacewalk took just under seven hours and saw the astronauts not only complete their main task but also accomplish some ‘get-ahead’ tasks.

Spacewalks are intensive for both crewmembers and ground support, so any opportunity to get ahead is welcomed.

This is the first of three spacewalks planned this month. Randy and Mark will venture out again on 10 October, followed by Randy and NASA astronaut Joe Acaba on 18 October.

The next spacewalks will again work on the robotic arm and replace some of the Station’s cameras.

Paolo will remain inside the Station and help the spacewalkers in and out of their suits. He will also be sure to take more stunning photographs.
Id 384993

http://www.esa.int/spaceinimages/Images/2017/10/Round_and_round_they_go

Darwin's development of theory of evolution
Three-quarter-length portrait of Charles Darwin aged about 30, with straight brown hair receding from his high forehead and long side-whiskers, smiling quietly, in wide lapelled jacket, waistcoat and high collar with cravat
Charles Darwin as a young man, probably subsequent to the Galápagos visit

Charles Darwin visited the Galápagos for five weeks on the second voyage of HMS Beagle in 1835 and saw Galápagos tortoises on San Cristobal (Chatham) and Santiago (James) Islands.[104] They appeared several times in his writings and journals, and played a role in the development of the theory of evolution.

Darwin wrote in his account of the voyage:

"I have not as yet noticed by far the most remarkable feature in the natural history of this archipelago; it is, that the different islands to a considerable extent are inhabited by a different set of beings. My attention was first called to this fact by the Vice-Governor, Mr. Lawson, declaring that the tortoises differed from the different islands, and that he could with certainty tell from which island any one was brought ... The inhabitants, as I have said, state that they can distinguish the tortoises from the different islands; and that they differ not only in size, but in other characters. Captain Porter has described* those from Charles and from the nearest island to it, namely, Hood Island, as having their shells in front thick and turned up like a Spanish saddle, while the tortoises from James Island are rounder, blacker, and have a better taste when cooked."[105]

The significance of the differences in tortoises between islands did not strike him as important until it was too late, as he continued,

"I did not for some time pay sufficient attention to this statement, and I had already partially mingled together the collections from two of the islands. I never dreamed that islands, about fifty or sixty miles apart, and most of them in sight of each other, formed of precisely the same rocks, placed under a quite similar climate, rising to a nearly equal height, would have been differently tenanted".[105]

Though the Beagle departed from the Galápagos with over 30 adult tortoises on deck, these were not for scientific study, but a source of fresh meat for the Pacific crossing. Their shells and bones were thrown overboard, leaving no remains with which to test any hypotheses.[106] It has been suggested[107] that this oversight was made because Darwin only reported seeing tortoises on San Cristóbal[108] (C. chathamensis) and Santiago[109] (C. darwini), both of which have an intermediate type of shell shape and are not particularly morphologically distinct from each other. Though he did visit Floreana, the C. nigra species found there was already nearly extinct and he was unlikely to have seen any mature animals.[44]
Line drawing of the HMS Beagle by F. G. King, a colleague of Darwin's: Galápagos tortoises were stacked in the lower hold.

However, Darwin did have four live juvenile specimens to compare from different islands. These were pet tortoises taken by himself (from San Salvador), his captain FitzRoy (two from Española) and his servant Syms Covington (from Floreana).[110] Unfortunately, they could not help to determine whether each island had its own variety because the specimens were not mature enough to exhibit morphological differences.[111] Although the British Museum had a few specimens, their provenance within the Galápagos was unknown.[112] However, conversations with the naturalist Gabriel Bibron, who had seen the mature tortoises of the Paris Natural History Museum confirmed to Darwin that distinct varieties occurred.[113]

Darwin later compared the different tortoise forms with those of mockingbirds, in the first[114] tentative statement linking his observations from the Galapagos with the possibility of species transmuting:

"When I recollect the fact that [from] the form of the body, shape of scales and general size, the Spaniards can at once pronounce from which island any tortoise may have been brought; when I see these islands in sight of each other and possessed of but a scanty stock of animals, tenanted by these birds, but slightly differing in structure and filling the same place in nature; I must suspect they are only varieties ... If there is the slightest foundation for these remarks, the zoology of archipelagos will be well worth examining; for such facts would undermine the stability of species."[115]

His views on the mutability of species were restated in his notebooks: "animals on separate islands ought to become different if kept long enough apart with slightly differing circumstances. – Now Galapagos Tortoises, Mocking birds, Falkland Fox, Chiloe fox, – Inglish and Irish Hare."[116] These observations served as counterexamples to the prevailing contemporary view that species were individually created.

Darwin also found these "antediluvian animals"[108] to be a source of diversion: "I frequently got on their backs, and then giving a few raps on the hinder part of their shells, they would rise up and walk away;—but I found it very difficult to keep my balance".[76]

5 October 2017

Dunes are prominent indicators of prevailing winds, as can be seen on this crater floor on Mars, imaged by ESA’s Mars Express on 16 May.
Dune field in a crater, plan view

Depressions such as impact craters can act as traps for sediments that have been blown in from elsewhere, accumulating in various patterns whipped up by strong winds.

The dune field in this unnamed 48 km-wide impact crater in the southern highlands of Mars includes sickle-shaped dunes known as barchans, and parallel ridges of dunes called transverse dunes.

A smoothly distributed sand sheet stretches between the dunes and the western wall of the crater.
Dune-filled crater in context

Barchans are the most common dune type found on Mars, and are also prevalent in Earth’s deserts. The shallower slope faces the wind, with the steeper, curved slope downwind, the ‘horns’ of the individual dunes pointing in the direction the wind is blowing. In this example, a southeasterly wind at the time of dune formation can be assumed.

Many nearby craters in this region also host dunes, and show a northwest shift of their dune fields relative to the crater centre, arguing for a uniform wind direction from the southeast.
Dune-filled crater topography

To the south of the dune field in the large crater, a single elongated transverse dune extends beyond the main field for several kilometres. Perhaps the underlying topography combined with near-surface winds caused the sediments to pile up here, or over time the smaller barchan dunes joined together.
Dune-filled crater in 3D

This scene is situated south of Tharsis, the largest volcanic province on Mars and home to Olympus Mons. Past volcanic activity in Tharsis produced vast amounts of basalt, fine pyroclastic deposits and ash, which were likely swept across the region to provide a source for the dark dune material observed in these craters today.

http://www.esa.int/Our_Activities/Space_Science/Mars_Express/Colourful_dunes_on_wind-swept_Mars

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Chelonoidis nigra[13] maoy kaliwatan sa bao nga gihulagway ni Jean René Constant Quoy ug Joseph Paul Gaimard ni adtong 1824. Ang Chelonoidis nigra kay sakop sa henero nga Chelonoidis, ug pamilya nga Testudinidae.[14][15] Giklaseklase sa IUCN ang kaliwatan sa madutlan.[1] Walay nalista nga matang nga sama niini.[14]


Ang mga gi basihan niini

Chelonoidis nigra. IUCN Red List of Threatened Species. Version 2012.2. International Union for Conservation of Nature (1996). Retrieved on 24/10/2012.
Valverde, J. (2004) Riesenschildkröten., Reptilia (Münster) 9 (6): 20-28
Ernst,C.H. and Barbour,R.W. (1989) Turtles of the World., Smithsonian Institution Press, Washington D.C. - London
Obst, F.J. (1985) Schmuckschildkroten: die Gattung Chrysemys, A. Ziemsen, Wittenberg Lutherstadt, Die Neue Brehm-Bucherei Heft 549 127 pp.
Pritchard, P.C.H. (1967) Scientific and common names of turtles of the world., Bulletin of the Ross Allen Reptile Institute 1967:1-10.
Garman, Samuel (1917) The Galapagos Tortoises, Memoirs of the Museum of Comparative Zoology 30 (4): 257-296 + 42 plates
Van Denburgh, John (1907) Expedition of the California Academy of Sciences to the Galapagos Islands, 1905-1906. I. Preliminary descriptions of four new races of Gigantic Land Tortoises from the Galapagos Islands, Proceedings of the California Academy of Sciences 1: 1-6
Rothschild, W. (1903) Note on Uroplates fimbriatus lichenius subspec. nov., Novitates Zoologicae, Zoological Museum, Tring, 10:490
Baur,G. (1889) On Meiolania and some points in the oseology of the Testudinata: a reply to Mr. G.A. Boulenger., Ann. Mag. nat. Hist. (6) 4: 37-46
Günther, A. (1874) Description of the living and extinct races of gigantic land-tortoises. Parts I. and II. introduction and the tortoises of the Galapagos islands., Ann. Mag. nat. Hist. (4) 14: 311-313
Duméril, A.M.C., and G. Bibron. (1835) Erpétologie Générale ou Histoire Naturelle Complète des Reptiles, Vol. 2., Librairie Encyclopédique de Roret, Paris, 680 p.
Harlan, R. (1827) Genera of North American Reptilia, and synopsis of the species., Journ. Acad. Nat. Sci. Philadelphia 5: 317-372
Quoy, J.R., and J.P. Gaimard. (1824) Zoologie. In: M.L. de Freycinet: Voyage Autour du Monde, Entrepris par le ministére et conformément aux instructions de s. exc. M. le Vicomte du Bouchage, Secrétaire d'etat au Department de la Marine, Exécuté sur les corvettes de S.M. l'Uranie et la Physi, Paris. iv + 712 pp.
Bisby F.A., Roskov Y.R., Orrell T.M., Nicolson D., Paglinawan L.E., Bailly N., Kirk P.M., Bourgoin T., Baillargeon G., Ouvrard D. (red.) (2011). Species 2000 & ITIS Catalogue of Life: 2011 Annual Checklist.. Species 2000: Reading, UK.. Retrieved on 24 september 2012.

TIGR Reptile Database . Uetz P. , 2007-10-02


Kahimtang na pagtipig

Madutlan (IUCN 3.1)[1]
Siyentipiko nga klasipikasyon
Ginharian: Animalia
Punoan: Chordata
Ilalum punoan: Vertebrata
Klase: Reptilia
Matang: Testudines
Pamilya: Testudinidae
Henero: Chelonoidis
Kaliwatan: Chelonoidis nigra
Siyentipikong ngalan
Chelonoidis nigra
Quoy & Gaimard 1824
Sinonimo

Geochelone nigrita CISNEROSHEREDIA 2006
Geochelone microphyes CISNEROSHEREDIA 2006
Geochelone hoodensis CISNEROSHEREDIA 2006
Geochelone guntheri CISNEROSHEREDIA 2006
Geochelone ephippium CISNEROSHEREDIA 2006
Geochelone darwini CISNEROSHEREDIA 2006
Geochelone chathamensis CISNEROSHEREDIA 2006
Geochelone becki CISNEROSHEREDIA 2006
Geochelone abingdonii CISNEROSHEREDIA 2006
Geochelone abingdoni VALVERDE 2004[2]
Geochelone nigra IVERSON 1992
Geochelone vicina ERNST 1989[3]
Geochelone vandenburghi ERNST 1989[3]
Geochelone porteri ERNST 1989[3]
Geochelone nigra KING 1989
Geochelone elephantopus ERNST 1989[3]
Chelonoidis elephantopus OBST 1985[4]
Chelonoidis elephantopus OBST 1985[4]
Chelonoidis elephantopus OBST 1985[4]
Geochelone elephantopus PRITCHARD 1967[5]
Geochelone elephantopus PRITCHARD 1967[5]
Geochelone elephantopus PRITCHARD 1967[5]
Geochelone elephantopus PRITCHARD 1967[5]
Geochelone elephantopus PRITCHARD 1967[5]
Geochelone elephantopus PRITCHARD 1967[5]
Geochelone elephantopus PRITCHARD 1967[5]
Geochelone elephantopus PRITCHARD 1967[5]
Geochelone elephantopus PRITCHARD 1967[5]
Geochelone elephantopus PRITCHARD 1967[5]
Geochelone elephantopus PRITCHARD 1967[5]
Testudo elephantopus MERTENS 1955
Testudo elephantopus MERTENS 1955
Testudo elephantopus MERTENS 1955
Testudo elephantopus MERTENS 1955
Testudo elephantopus MERTENS 1955
Testudo elephantopus MERTENS 1955
Testudo elephantopus MERTENS 1955
Testudo vandenburghi DE 1930
Testudo macrophyes GARMAN 1917[6]
Testudo typica GARMAN 1917[6]
Testudo clivosa GARMAN 1917[6]
Testudo hoodensis VAN 1907[7]
Testudo darwini VAN 1907[7]
Testudo chathamensis VAN 1907[7]
Testudo porteri Rothschild 1903[8]
Testudo becki Rothschild 1901
Testudo guntheri BAUR 1889[9]
Testudo abingdonii GÜNTHER 1877
Testudo vicina GÜNTHER 1874[10]
Testudo microphyes GÜNTHER 1874[10]
Testudo ephippium GÜNTHER 1874[10]
Testudo planiceps GRAY 1854
Testudo nigrita DUMÉRIL 1835[11]
Testudo schweiggeri DUMÉRIL 1835[11]
Testudo schweigeri Gray 1831
Testudo elephantopus HARLAN 1827[12]
Testudo nigra QUOY 1824[13]
Testudo californiana QUOY 1824[13]

Conservation

Several waves of human exploitation of the tortoises as a food source caused a decline in the total wild population from around 250,000[101] when first discovered in the 16th century to a low of 3,060 individuals in a 1974 census. Modern conservation efforts have subsequently brought tortoise numbers up to 19,317 (estimate for 1995–2009).[117]

The species C. nigra became extinct by human exploitation in the 19th century. Another species, C. abingdonii, became extinct on 24 June 2012 with the death in captivity of the last remaining specimen, a male named Lonesome George, the world's "rarest living creature".[118] All the other surviving species are listed by the IUCN as at least "Vulnerable" in conservation status, if not worse.
Chelonoidis porteri on Santa Cruz Island
Historical exploitation

An estimated 200,000 animals were taken before the 20th century.[46] The relatively immobile and defenceless tortoises were collected and stored live on board ships, where they could survive for at least a year without food or water (some anecdotal reports suggest individuals surviving two years[119]), providing valuable fresh meat, while their diluted urine and the water stored in their neck bags could be used as drinking water. The 17th-century British pirate, explorer, and naturalist William Dampier wrote, "They are so extraordinarily large and fat, and so sweet, that no pullet eats more pleasantly,"[120] while Captain James Colnett of the British Navy wrote of "the land tortoise which in whatever way it was dressed, was considered by all of us as the most delicious food we had ever tasted."[121] US Navy captain David Porter declared, "after once tasting the Galapagos tortoises, every other animal food fell off greatly in our estimation ... The meat of this animal is the easiest of digestion, and a quantity of it, exceeding that of any other food, can be eaten without experiencing the slightest of inconvenience."[92] Darwin was less enthusiastic about the meat, writing "the breast-plate roasted (as the Gauchos do "carne con cuero"), with the flesh on it, is very good; and the young tortoises make excellent soup; but otherwise the meat to my taste is indifferent."[122]

In the 17th century, pirates started to use the Galápagos Islands as a base for resupply, restocking on food and water, and repairing vessels before attacking Spanish colonies on the South American mainland. However, the Galápagos tortoises did not struggle for survival at this point because the islands were distant from busy shipping routes and harboured few valuable natural resources. As such, they remained unclaimed by any nation, uninhabited and uncharted. In comparison, the tortoises of the islands in the Indian Ocean were already facing extinction by the late 17th century.[123] Between the 1790s and the 1860s, whaling ships and fur sealers systematically collected tortoises in far greater numbers than the buccaneers preceding them.[124] Some were used for food and many more were killed for high-grade "turtle oil" from the late 19th century onward for lucrative sale to continental Ecuador.[125] A total of over 13,000 tortoises is recorded in the logs of whaling ships between 1831 and 1868, and an estimated 100,000 were taken before 1830.[119] Since it was easiest to collect tortoises around coastal zones, females were most vulnerable to depletion during the nesting season. The collection by whalers came to a halt eventually through a combination of the scarcity of tortoises that they had created and the competition from crude oil as a cheaper energy source.[126]

Galápagos tortoise exploitation dramatically increased with the onset of the California Gold Rush in 1849.[127] Tortoises and sea turtles were imported into San Francisco, Sacramento and various other Gold Rush towns throughout Alta California to feed the gold mining population. Galápagos tortoise and sea turtle bones were also recovered from the Gold Rush-era archaeological site, Thompson's Cove (CA-SFR-186H), in San Francisco, California.[128]

Population decline accelerated with the early settlement of the islands in the early 19th century, leading to unregulated hunting for meat, habitat clearance for agriculture, and the introduction of alien mammal species.[47] Feral pigs, dogs, cats, and black rats have become predators of eggs and young tortoises, whilst goats, donkeys, and cattle compete for grazing and trample nest sites. The extinction of the Floreana species in the mid-19th century has been attributed to the combined pressures of hunting for the penal colony on the relatively small island, the conversion of the grazing highlands into land for farming and fruit plantations, and the introduction of feral mammals.[129]

Scientific collection expeditions took 661 tortoises between 1888 and 1930, and more than 120 tortoises have been taken by poachers since 1990. Threats continue today with the rapid expansion of the tourist industry and increasing size of human settlements on the islands.[130] The tortoises are down from 15 different types of species when Darwin first arrived down to 11.[131]

Threats

Introduced mammals
Galapagos hawks prey on eggs and hatchlings
Poachers
Destruction of habitat
Characteristics that make tortoises vulnerable
Slow growth rate
Late sexual maturity
Can only be found on Galapagos Islands
Large size and slow moving[131]

Collection

The tortoises of the Galápagos’ island were not only hunted for the oil that they held for fuel but also once they were becoming more and more extinct people began to pay to have them in their collections, as well as being put into museums.[132]
Modern conservation
Galápagos tortoise on Santa Cruz Island (Galápagos)
Galápagos tortoise on Santa Cruz Island, Galápagos

The remaining species of tortoise range in IUCN classification from extinct in the wild to vulnerable. Slow growth rate, late sexual maturity, and island endemism make the tortoises particularly prone to extinction without help from conservationists.[67] The Galápagos giant tortoise has become a flagship species for conservation efforts throughout the Galápagos.
Two Galápagos tortoises occupy the foreground, apparently unconcerned by the presence of several tourists a few feet behind them. The tourists wear assorted sunglasses and sunhats, and most are taking pictures of the tortoises with their digital cameras.
Tourists see tortoises at the Charles Darwin Research Station

Legal protection

The Galápagos giant tortoise is now strictly protected and is listed on Appendix I of the Convention on International Trade in Endangered Species of Wild Fauna and Flora.[40] The listing requires that trade in the taxon and its products is subject to strict regulation by ratifying states, and international trade for primarily commercial purposes is prohibited. In 1936, the Ecuadorian government listed the giant tortoise as a protected species. In 1959, it declared all uninhabited areas in the Galápagos to be a national park[133] and established the Charles Darwin Foundation. In 1970, capturing or removing many species from the islands (including tortoises and their eggs) was banned.[134] To halt trade in the tortoises altogether, it became illegal to export the tortoises from Ecuador, captive or wild, continental, or insular in provenance. The banning of their exportation resulted in automatic prohibition of importation to the United States under Public Law 91-135 (1969).[135] A 1971 Ecuadorian decree made it illegal to damage, remove, alter, or disturb any organism, rock, or other natural object in the National Park.[136]

Captive breeding

With the establishment of the Galapagos National Park and the CDF in 1959, a review of the status of the tortoise populations began. Only 11 of the 14 original populations remained and most of these were endangered if not already on the brink of extinction. The breeding and rearing program for giant tortoises began in response to the condition of the population on Pinzón, where fewer than 200 old adults were found. All of the hatchlings had been killed by introduced black rats, for perhaps more than a century. Without help, this population would eventually disappear. The only thing preserving it was the longevity of the tortoise.[137] Its genetic resistance to the negative effects of inbreeding would be another.[132]

Breeding and release programs began in 1965 and have successfully brought seven of the eight endangered species up to less perilous population levels. Young tortoises are raised at several breeding centres across the islands to improve their survival during their vulnerable early development. Eggs are collected from threatened nesting sites, and the hatched young are given a head start by being kept in captivity for four to five years to reach a size with a much better chance of survival to adulthood, before release onto their native ranges.[98][117]

The most significant population recovery was that of the Española tortoise (C. hoodensis), which was saved from near-certain extinction. The population had been depleted to three males and 12 females that had been so widely dispersed that no mating in the wild had occurred.[138] Fruitless attempts to breed one of the tortoises, Lonesome George for example, is speculated to be attributed to a lack of postnatal cues,[139] and confusion over which would be the most appropriate genetic species would be the most appropriate to mate him with on the islands.[32] The 15 remaining tortoises were brought to the Charles Darwin Research Station in 1971 for a captive breeding program[140] and, in the following 33 years, they gave rise to over 1,200 progeny which were released onto their home island and have since begun to reproduce naturally.[141][142] One of the tortoises, Diego, is one of the main drivers of a remarkable recovery of the hoodensis species having fathered between 350 and 800 progeny.[143]

Island restoration

The Galápagos National Park Service systematically culls feral predators and competitors. Goat eradication on islands, including Pinta, was achieved by the technique of using "Judas" goats with radio location collars to find the herds. Marksmen then shot all the goats except the Judas, and then returned weeks later to find the "Judas" and shoot the herd to which it had relocated. Goats were removed from Pinta Island after a 30-year eradication campaign, the largest removal of an insular goat population using ground-based methods. Over 41,000 goats were removed during the initial hunting effort (1971–82).[144] This process was repeated until only the "Judas" goat remained, which was then killed.[145] Other measures have included dog eradication from San Cristóbal, and fencing off nests to protect them from feral pigs.[98]

Efforts are now underway to repopulate islands formerly inhabited by tortoises to restore their ecosystems (island restoration) to their condition before humans arrived. The tortoises are a keystone species, acting as ecosystem engineers[145] which help in plant seed dispersal and trampling down brush and thinning the understory of vegetation (allowing light to penetrate and germination to occur). Birds such as flycatchers perch on and fly around tortoises to hunt the insects they displace from the brush.[74] In May 2010, 39 sterilised tortoises of hybrid origin were introduced to Pinta Island, the first tortoises there since the evacuation of Lonesome George 38 years before.[146] Sterile tortoises were released so the problem of interbreeding between species would be avoided if any fertile tortoises were to be released in the future. It is hoped that with the recent identification of a hybrid C. abingdonii tortoise, the approximate genetic constitution of the original inhabitants of Pinta may eventually be restored with the identification and relocation of appropriate specimens to this island.[65] This approach may be used to "retortoise" Floreana in the future, since captive individuals have been found to be descended from the extinct original stock.[61]

Applied science

The Galapagos Tortoise Movement Ecology Programme is a collaborative project coordinated by Dr Stephen Blake of the Max Planck Institute for Ornithology. Its goal is to assist the Galapagos National Park to effectively conserve giant tortoises by conducting cutting-edge applied science, and developing an inspirational tortoise-based outreach and education programme. Since 2009, the project team have been analysing the movements of giant tortoises by tracking them via satellite tags. As of November 2014, the team have tagged 83 tortoises from four species on three islands. They have established that giant tortoises conduct migrations up and down volcanoes, primarily in response to seasonal changes in the availability and quality of vegetation.[147] In 2015 they will start to track the movements of hatchling and juvenile tortoises, supported by the UK's Galapagos Conservation Trust.[148]
See also

Amphibians and Reptiles portal iconTurtles portal

List of species of Galápagos tortoise
Galápagos wildlife

Notes

The first navigation chart showing the individual islands was drawn up by the pirate Ambrose Cowley in 1684. He named them after fellow pirates or English noblemen. More recently, the Ecuadorian government gave most of the islands Spanish names. While the Spanish names are official, many researchers continue to use the older English names, particularly as those were the names used when Darwin visited. This article uses the Spanish island names.

https://ceb.wikipedia.org/wiki/Chelonoidis_nigra
https://en.wikipedia.org/wiki/Gal%C3%A1pagos_tortoise

The Letters of an ‘Imbecile,’ the Sham, and Shame, of Eugenics

October 5, 2017

(Undark) – We now know that the Holmes opinion was both cruel and false — and is contradicted by a historic marker in Charlottesville, Virginia that has nothing to do with the Civil War, or the soldier-on-horseback monuments that have generated so much controversy recently. This much more obscure marker recalls Buck’s case and declares that she had no “hereditary defects.” Instead, she was the victim of a sham trial that began her trip to the Supreme Court, and provided justification for 60,000 poor or disabled people in 32 states who were sterilized under laws similar to Virginia’s Sterilization Act of 1924, which aimed to prevent people diagnosed with “insanity … idiocy, imbecility, feeble-mindedness or epilepsy” from reproducing.

Posted by Bioethics Pundit

Posted in Eugenics, General Bioethics, highlights, News, People, Reproductive Ethic

http://www.bioethics.com/archives/40302#.Wds4FJIIC84.facebook

Silicon Isn’t Just for Computers. It Can Make a Pretty Good Kidney, Too

October 6, 2017

(Wired) – Now, after more than 20 years of work, one team of doctors and researchers is close to offering patients an implantable artificial kidney, a bionic device that uses the same technology that makes the chips that power your laptop and smartphone. Stacks of carefully designed silicon nanopore filters combine with live kidney cells grown in a bioreactor. The bundle is enclosed in a body-friendly box and connected to a patient’s circulatory system and bladder—no external tubing required.

Posted by Bioethics Pundit

Posted in Clinical / Medical, Emerging Technologies, highlights, News, Organ Donation / Transplantation


Oct. 3, 2017
Metal with Memory: Shaping the Future of Aviation

While aeronautics researchers across the globe continue to develop technologies that will make air travel more efficient, more sustainable and safer, there is a group of NASA researchers who are altering the long-held view that wings have to stick straight out from an aircraft and stay that way.

Through NASA’s Convergent Aeronautics Solutions (CAS) Project, a team of engineers working within its Spanwise Adaptive Wing (SAW) project is investigating the feasibility of bending or shaping portions of an aircraft’s wings in-flight, potentially increasing performance and efficiency by reducing weight and drag.
Outer wing section of an F/A-18 research plane
The outer wing section of an F/A-18 research plane is disassembled at NASA’s Armstrong Flight Research Center in Edwards, California for delivery to NASA Glenn Research Center in Cleveland, Ohio.
Credits: NASA

The ability to fold wings isn’t new. Since the dawn of ship-based aviation, U.S. Navy aircraft have been required to fold their wings for space conservation. Currently, this type of wing folding, or actuation, happens only on deck and serves no aerodynamic purpose. Other aircraft, like the XB-70, have folded their wings in flight with success. However, these fold systems required bulky, multipart structures, including hydraulics, pneumatics and electric motors, which weigh hundreds of pounds and take up valuable space.

NASA’s engineers believe folding wings in-flight using advanced materials and technologies is a potential game-changer for future aircraft. The innovative actuation system that NASA and engineers from The Boeing Company are developing uses a revolutionary material that will accomplish this goal using less complex, lighter and more compact hardware than conventional systems.

That material is shape memory alloy (SMA), an engineered nickel-titanium alloy that can be trained to return to a desired shape after deformation by applying heat.

“By applying a temperature stimuli, you can trigger a physical change in the metal,” said Dr. Othmane Benafan, materials research engineer at NASA Glenn Research Center in Cleveland and the SAW project’s co-principle investigator. “It undergoes a reversible phase transformation much like ice melting and refreezing. The difference is it transitions from one solid state to another. The changes that happen at the atomic level are reversible, meaning the SMA is designed to bend and then return to its original shape once heat is applied.”

Much like folding a wing, SMA isn’t a new breakthrough. It is commercially available and its unique properties make it an attractive alternative to common actuators. However, current commercial SMAs have limited capabilities and can only be operated at or near room temperature.

The material NASA is developing is similar to these alloys, but with increased capabilities, higher operational loads, higher operating temperatures and energy density. The material has more predictable properties and can be accurately controlled, making it well-suited for aeronautics applications. It is also unique in regards to memory or “training,” because the rare microstructural features produce a better, more stable material.
Dr. Othmane Benafan
Dr. Othmane Benafan, co-principle investigator for the Spanwise Adaptive Wing Project, inspects a model of the shape memory alloy actuator and the outer wing section from an F/A-18 research plane.
Credits: NASA

For the SAW project, NASA is using SMA materials as torque-tube actuators. In this configuration, a single or group of trained SMA tubes are heated via internal heaters or external electrical coils, triggering them to twist and perform the desired actuation to drive a folding wing. Electrically-induced temperature change is only one possible stimuli. SMA can also be activated by using bleed air from the aircraft’s engines or simply through the ambient temperature changes experienced during flight. This compact, lightweight application, which is also extremely quiet, allows the entire actuator package to be attached at the wing hinge point. Conventional actuation approaches typically cannot fit in this area, leading to heavy and complex linkages or transmissions to drive a wing fold or similar aerodynamic surface.

But going from the test bench to replacing proven systems with SMA will require the development of a complete actuation and control system, and this is where Boeing’s expertise and previous experience comes in.

“We’ve done a lot of work with NASA to look at how we develop the material: how we melt it, how we forge it, how we turn it into a component, how we train it and how we integrate it into an aircraft,” said Jim Mabe, technical fellow at Boeing Research and Technology. “We’re not only developing the SMA technology, we’re developing everything around it to simplify integration. So, when requests do come in, we don’t have to do any of the science or research. We can quickly engineer an actuator according to application requirements. The way I look at it, putting SMA into an aircraft is becoming more of an engineering problem than a science problem because we’ve made huge strides maturing the science and processes.”

Being involved in NASA’s SAW project is just one of Boeing’s endeavors into wing shaping and SMA applications. Boeing previously used SMA as part of a flight test program in 2012, where it integrated a compact SMA torque tube actuator into a small trailing edge flap on a 737-800, one of Boeing’s ecoDemonstrator aircraft.

“We believe SMA could be something that will change the industry,” said Mabe. “This technology will eventually open the door to several different development approaches. And it’s not just limited to wings and flaps; there are other potential aircraft applications we can apply this material to as well.”

While NASA prepares to integrate SMA into SAW’s subscale flight-test of the Prototype-Technology Evaluation and Research Aircraft (PTERA) later this fall at NASA’s Armstrong Flight Research Center in Edwards, California, the team at NASA Glenn wants to get a head start on ground testing SMA actuators on a large-scale wing.

“This testing is critical as we want to move quickly from subscale into full-size demonstration in the coming years,” said Benafan. “It will allow us to better understand how SMA will work in a real wing at different loads and operating conditions.”

To do this, NASA Armstrong removed a wing section from one of its F/A-18 scientific research aircraft for testing at NASA Glenn. The F/A-18 was selected not only because of NASA’s access to the Boeing-built aircraft, but also for the wing-fold system required by the U.S. Navy.

The wing section, which was delivered to NASA Glenn in July, will have all of the factory fold mechanics removed, and it will be retrofitted with a 20,000-inch-pound SMA torque-tube actuator.

“We are using the F/A-18 wing as a test article to demonstrate the actuation concept at a much larger scale compared to what we have now, which is close to a few hundred inch-pounds” said Benafan. “We need to understand if scaling up is feasible from all aspects, including material performance, work densities and control of the actuators.”

When activated, the wing actuators will heat up and twist to move the 300-pound section over a 180-degree sweep. That can be 90 degrees from the flight-ready position to the vertical folded position, as well as moving 90 degrees down. More importantly, NASA wants to demonstrate actuation to any position desired within that 180-degree sweep.

Through the full-scale ground tests and the upcoming subscale flight test, the SAW project team is working to transform aircraft design through SMA-enhanced wing shaping. Ultimately, this shaping capability could increase aircraft performance during all phases of flight, including ground, subsonic and, possibly, supersonic.

SAW is a collaboration between NASA, The Boeing Company and Area-I, and it is part of NASA’s CAS project under the agency’s Transformative Aeronautics Concepts Program.

Jimi Russell
NASA Glenn Research Center
Last Updated: Oct. 3, 2017
Editor: Kelly Heidman

https://www.nasa.gov/feature/metal-with-memory-shaping-the-future-of-aviation

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