Organisms at high altitude

Last updated
An Alpine chough in flight at 3,901 m (12,799 ft) Yellow-billed chough Pin Valley Spiti Himachal Jun18 D72 7201.jpg
An Alpine chough in flight at 3,901 m (12,799 ft)

Organisms can live at high altitude, either on land, in water, or while flying. Decreased oxygen availability and decreased temperature make life at such altitudes challenging, though many species have been successfully adapted via considerable physiological changes. As opposed to short-term acclimatisation (immediate physiological response to changing environment), high-altitude adaptation means irreversible, evolved physiological responses to high-altitude environments, associated with heritable behavioural and genetic changes. Among vertebrates, only few mammals (such as yaks, ibexes, Tibetan gazelles, vicunas, llamas, mountain goats, etc.) and certain birds are known to have completely adapted to high-altitude environments. [1]

Contents

Human populations such as some Tibetans, South Americans and Ethiopians live in the otherwise uninhabitable high mountains of the Himalayas, Andes and Ethiopian Highlands respectively. The adaptation of humans to high altitude is an example of natural selection in action. [2]

High-altitude adaptations provide examples of convergent evolution, with adaptations occurring simultaneously on three continents. Tibetan humans and Tibetan domestic dogs share a genetic mutation in EPAS1 , but it has not been seen in Andean humans. [3]

Invertebrates

Tardigrades live over the entire world, including the high Himalayas. [4] Tardigrades are also able to survive temperatures of close to absolute zero (−273 °C (−459 °F)), [5] temperatures as high as 151 °C (304 °F), radiation that would kill other animals, [6] and almost a decade without water. [7] Since 2007, tardigrades have also returned alive from studies in which they have been exposed to the vacuum of outer space in low Earth orbit. [8] [9]

Other invertebrates with high-altitude habitats are Euophrys omnisuperstes , a spider that lives in the Himalaya range at altitudes of up to 6,699 m (21,978 ft); [10] it feeds on stray insects that are blown up the mountain by the wind. [11] The springtail Hypogastrura nivicola (one of several insects called snow fleas) also lives in the Himalayas. It is active in the dead of winter, its blood containing a compound similar to antifreeze. Some allow themselves to become dehydrated instead, preventing the formation of ice crystals within their body. [12]

Insects can fly and kite at very high altitude. Flies are common in the Himalaya up to 6,300 m (20,700 ft). [13] Bumble bees were discovered on Mount Everest at more than 5,600 m (18,400 ft) above sea level. [14] In subsequent tests, bumblebees were still able to fly in a flight chamber which recreated the thinner air of 9,000 m (30,000 ft). [15]

Ballooning is a term used for the mechanical kiting [16] [17] that many spiders, especially small species such as Erigone atra , [18] as well as certain mites and some caterpillars use to disperse through the air. Some spiders have been detected in atmospheric data balloons collecting air samples at slightly less than 5 km (16000 ft) above sea level. [19] It is the most common way for spiders to pioneer isolated islands and mountaintops. [20] [21]

Fish

Naked carp in Lake Qinghai at 3,205 m (10,515 ft) Gymnocypris przewalskii 2013.JPG
Naked carp in Lake Qinghai at 3,205 m (10,515 ft)

Fish at high altitudes have a lower metabolic rate, as has been shown in highland westslope cutthroat trout when compared to introduced lowland rainbow trout in the Oldman River basin. [22] There is also a general trend of smaller body sizes and lower species richness at high altitudes observed in aquatic invertebrates, likely due to lower oxygen partial pressures. [23] [24] [25] These factors may decrease productivity in high altitude habitats, meaning there will be less energy available for consumption, growth, and activity, which provides an advantage to fish with lower metabolic demands. [22]

The naked carp from Lake Qinghai, like other members of the carp family, can use gill remodelling to increase oxygen uptake in hypoxic environments. [26] The response of naked carp to cold and low-oxygen conditions seem to be at least partly mediated by hypoxia-inducible factor 1 (HIF-1). [27] It is unclear whether this is a common characteristic in other high altitude dwelling fish or if gill remodelling and HIF-1 use for cold adaptation are limited to carp.

Mammals

The Himalayan pika lives at altitudes up to 4,200 m (13,800 ft) Himalayan Pika.JPG
The Himalayan pika lives at altitudes up to 4,200 m (13,800 ft)

Mammals are also known to reside at high altitude and exhibit a striking number of adaptations in terms of morphology, physiology and behaviour. The Tibetan Plateau has very few mammalian species, ranging from wolf, kiang (Tibetan wild ass), goas, chiru (Tibetan antelope), wild yak, snow leopard, Tibetan sand fox, ibex, gazelle, Himalayan brown bear and water buffalo. [29] [30] [31] These mammals can be broadly categorised based on their adaptability in high altitude into two broad groups, namely eurybarc and stenobarc. Those that can survive a wide range of high-altitude regions are eurybarc and include yak, ibex, Tibetan gazelle of the Himalayas and vicuñas llamas of the Andes. Stenobarc animals are those with lesser ability to endure a range of differences in altitude, such as rabbits, mountain goats, sheep, and cats. Among domesticated animals, yaks are perhaps the highest dwelling animals. The wild herbivores of the Himalayas such as the Himalayan tahr, markhor and chamois are of particular interest because of their ecological versatility and tolerance. [32]

Rodents

A number of rodents live at high altitude, including deer mice, guinea pigs, and rats. Several mechanisms help them survive these harsh conditions, including altered genetics of the hemoglobin gene in guinea pigs and deer mice. [33] [34] Deer mice use a high percentage of fats as metabolic fuel to retain carbohydrates for small bursts of energy. [35]

Other physiological changes that occur in rodents at high altitude include increased breathing rate [36] and altered morphology of the lungs and heart, allowing more efficient gas exchange and delivery. Lungs of high-altitude mice are larger, with more capillaries, [37] and their hearts have a heavier right ventricle (the latter applies to rats too), [38] [39] which pumps blood to the lungs.

At high altitudes, some rodents even shift their thermal neutral zone so they may maintain normal basal metabolic rate at colder temperatures. [40]

The deer mouse DiGangi-Deermouse.jpg
The deer mouse

The deer mouse ( Peromyscus maniculatus ) is the best studied species, other than humans, in terms of high-altitude adaptation. [1] The deer mice native to Andes highlands (up to 3,000 m (9,800 ft)) are found to have relatively low hemoglobin content. [41] Measurement of food intake, gut mass, and cardiopulmonary organ mass indicated proportional increases in mice living at high altitudes, which in turn show that life at high altitudes demands higher levels of energy. [42] Variations in the globin genes (α and β-globin) seem to be the basis for increased oxygen-affinity of the hemoglobin and faster transport of oxygen. [43] [44] Structural comparisons show that in contrast to normal hemoglobin, the deer mouse hemoglobin lacks the hydrogen bond between α1Trp14 in the A helix and α1Thr67 in the E helix owing to the Thr67Ala substitution, and there is a unique hydrogen bond at the α1β1 interface between residues α1Cys34 and β1Ser128. [45] The Peruvian native species of mice ( Phyllotis andium and Phyllotis xanthopygus ) have adapted to the high Andes by using proportionately more carbohydrates and have higher oxidative capacities of cardiac muscles compared to closely related native species residing at low-altitudes (100–300 m (330–980 ft)), ( Phyllotis amicus and Phyllotis limatus ). This shows that highland mice have evolved a metabolic process to economise oxygen usage for physical activities in the hypoxic conditions. [46]

Yaks

Domestic yak at Yamdrok Lake Bos grunniens at Yundrok Yumtso Lake.jpg
Domestic yak at Yamdrok Lake

Among domesticated animals, yaks ( Bos grunniens ) are the highest dwelling animals of the world, living at 3,000–5,000 m (9,800–16,400 ft). The yak is the most important domesticated animal for Tibet highlanders in Qinghai Province of China, as the primary source of milk, meat and fertilizer. Unlike other yak or cattle species, which suffer from hypoxia in the Tibetan Plateau, the Tibetan domestic yaks thrive only at high altitude, and not in lowlands. Their physiology is well-adapted to high altitudes, with proportionately larger lungs and heart than other cattle, as well as greater capacity for transporting oxygen through their blood. [47] In yaks, hypoxia-inducible factor 1 (HIF-1) has high expression in the brain, lung and kidney, showing that it plays an important role in the adaptation to low oxygen environment. [48] On 1 July 2012 the complete genomic sequence and analyses of a female domestic yak was announced, providing important insights into understanding mammalian divergence and adaptation at high altitude. Distinct gene expansions related to sensory perception and energy metabolism were identified. [49] In addition, researchers also found an enrichment of protein domains related to the extracellular environment and hypoxic stress that had undergone positive selection and rapid evolution. For example, they found three genes that may play important roles in regulating the bodyʼs response to hypoxia, and five genes that were related to the optimisation of the energy from the food scarcity in the extreme plateau. One gene known to be involved in regulating response to low oxygen levels, ADAM17, is also found in human Tibetan highlanders. [50] [51]

Humans

A Sherpa family Sherpa.jpg
A Sherpa family

Over 81 million people live permanently at high altitudes (>2,500 m (8,200 ft)) [52] in North, Central and South America, East Africa, and Asia, and have flourished for millennia in the exceptionally high mountains, without any apparent complications. [53] For average human populations, a brief stay at these places can risk mountain sickness. [54] For the native highlanders, there are no adverse effects to staying at high altitude.

The physiological and genetic adaptations in native highlanders involve modification in the oxygen transport system of the blood, especially molecular changes in the structure and functions of hemoglobin, a protein for carrying oxygen in the body. [53] [55] This is to compensate for the low oxygen environment. This adaptation is associated with developmental patterns such as high birth weight, increased lung volumes, increased breathing, and higher resting metabolism. [56] [57]

The genome of Tibetans provided the first clue to the molecular evolution of high-altitude adaptation in 2010. [58] Genes such as EPAS1 , PPARA and EGLN1 are found to have significant molecular changes among the Tibetans, and the genes are involved in hemoglobin production. [59] These genes function in concert with transcription factors, hypoxia inducible factors (HIF), which in turn are central mediators of red blood cell production in response to oxygen metabolism. [60] Further, the Tibetans are enriched for genes in the disease class of human reproduction (such as genes from the DAZ , BPY2 , CDY , and HLA-DQ and HLA-DR gene clusters) and biological process categories of response to DNA damage stimulus and DNA repair (such as RAD51 , RAD52 , and MRE11A ), which are related to the adaptive traits of high infant birth weight and darker skin tone and, are most likely due to recent local adaptation. [61]

Among the Andeans, there are no significant associations between EPAS1 or EGLN1 and hemoglobin concentration, indicating variation in the pattern of molecular adaptation. [62] However, EGLN1 appears to be the principal signature of evolution, as it shows evidence of positive selection in both Tibetans and Andeans. [63] The adaptive mechanism is different among the Ethiopian highlanders. Genomic analysis of two ethnic groups, Amhara and Oromo, revealed that gene variations associated with hemoglobin differences among Tibetans or other variants at the same gene location do not influence the adaptation in Ethiopians. [64] Instead, several other genes appear to be involved in Ethiopians, including CBARA1 , VAV3 , ARNT2 and THRB , which are known to play a role in HIF genetic functions. [65]

The EPAS1 mutation in the Tibetan population has been linked to Denisovan-related populations. [66] The Tibetan haplotype is more similar to the Denisovan haplotype than any modern human haplotype. This mutation is seen at a high frequency in the Tibetan population, a low frequency in the Han population and is otherwise only seen in a sequenced Denisovan individual. This mutation must have been present before the Han and Tibetan populations diverged 2750 years ago. [66]

Birds

Ruppell's vulture can fly up to 11.2 km (7.0 mi) above sea level Ruppelsvulture.jpg
Rüppell's vulture can fly up to 11.2 km (7.0 mi) above sea level

Birds have been especially successful at living at high altitudes. [67] In general, birds have physiological features that are advantageous for high-altitude flight. The respiratory system of birds moves oxygen across the pulmonary surface during both inhalation and exhalation, making it more efficient than that of mammals. [68] In addition, the air circulates in one direction through the parabronchioles in the lungs. Parabronchioles are oriented perpendicularly to the pulmonary arteries, forming a cross-current gas exchanger. This arrangement allows for more oxygen to be extracted compared to mammalian concurrent gas exchange; as oxygen diffuses down its concentration gradient and the air gradually becomes more deoxygenated, the pulmonary arteries are still able to extract oxygen. [69] [ page needed ] Birds also have a high capacity for oxygen delivery to the tissues because they have larger hearts and cardiac stroke volume compared to mammals of similar body size. [70] Additionally, they have increased vascularization in their flight muscle due to increased branching of the capillaries and small muscle fibres (which increases surface-area-to-volume ratio). [71] These two features facilitate oxygen diffusion from the blood to muscle, allowing flight to be sustained during environmental hypoxia. Birds' hearts and brains, which are very sensitive to arterial hypoxia, are more vascularized compared to those of mammals. [72] The bar-headed goose (Anser indicus) is an iconic high-flyer that surmounts the Himalayas during migration, [73] and serves as a model system for derived physiological adaptations for high-altitude flight. Rüppell's vultures, whooper swans, alpine chough, and common cranes all have flown more than 8 km (26,000 ft) above sea level.

Adaptation to high altitude has fascinated ornithologists for decades, but only a small proportion of high-altitude species have been studied. In Tibet, few birds are found (28 endemic species), including cranes, vultures, hawks, jays and geese. [29] [31] [74] The Andes is quite rich in bird diversity. The Andean condor, the largest bird of its kind in the Western Hemisphere, occurs throughout much of the Andes but generally in very low densities; species of tinamous (notably members of the genus Nothoprocta ), Andean goose, giant coot, Andean flicker, diademed sandpiper-plover, mountain parakeet, miners, sierra-finches and diuca-finches are also found in the highlands. [75] [76]

Cinnamon teal

Male cinnamon teal Sarcelle cannelle.jpg
Male cinnamon teal

Evidence for adaptation is best investigated among the Andean birds. The water fowls and cinnamon teal ( Anas cyanoptera ) are found to have undergone significant molecular modifications. It is now known that the α-hemoglobin subunit gene is highly structured between elevations among cinnamon teal populations, which involves almost entirely a single non-synonymous amino acid substitution at position 9 of the protein, with asparagine present almost exclusively within the low-elevation species, and serine in the high-elevation species. This implies important functional consequences for oxygen affinity. [77] In addition, there is strong divergence in body size in the Andes and adjacent lowlands. These changes have shaped distinct morphological and genetic divergence within South American cinnamon teal populations. [78]

Ground tits

In 2013, the molecular mechanism of high-altitude adaptation was elucidated in the Tibetan ground tit ( Pseudopodoces humilis ) using a draft genome sequence. Gene family expansion and positively selected gene analysis revealed genes that were related to cardiac function in the ground tit. Some of the genes identified to have positive selection include ADRBK1 and HSD17B7 , which are involved in the adrenaline response and steroid hormone biosynthesis. Thus, the strengthened hormonal system is an adaptation strategy of this bird. [79]

Other animals

Alpine Tibet hosts a limited diversity of animal species, among which snakes are common. There are only two endemic reptiles and ten endemic amphibians in the Tibetan highlands. [74] Gloydius himalayanus is perhaps the geographically highest living snake in the world, living at as high as 4,900 m (16,100 ft) in the Himalayas. [80] Another notable species is the Himalayan jumping spider, which can live at over 6,500 m (21,300 ft) of elevation. [29]

Plants

Cushion plant Donatia novae-zelandiae, Tasmania Cushion-plant-atop-Mount-Ossa.jpg
Cushion plant Donatia novae-zelandiae , Tasmania

Many different plant species live in the high-altitude environment. These include perennial grasses, sedges, forbs, cushion plants, mosses, and lichens. [81] High-altitude plants must adapt to the harsh conditions of their environment, which include low temperatures, dryness, ultraviolet radiation, and a short growing season. Trees cannot grow at high altitude, because of cold temperature or lack of available moisture. [82] :51 The lack of trees causes an ecotone, or boundary, that is obvious to observers. This boundary is known as the tree line.

The highest-altitude plant species is a moss that grows at 6,480 m (21,260 ft) on Mount Everest. [83] The sandwort Arenaria bryophylla is the highest flowering plant in the world, occurring as high as 6,180 m (20,280 ft). [84]

See also

Related Research Articles

<span class="mw-page-title-main">Hypoxia (medical)</span> Medical condition of lack of oxygen in the tissues

Hypoxia is a condition in which the body or a region of the body is deprived of adequate oxygen supply at the tissue level. Hypoxia may be classified as either generalized, affecting the whole body, or local, affecting a region of the body. Although hypoxia is often a pathological condition, variations in arterial oxygen concentrations can be part of the normal physiology, for example, during strenuous physical exercise.

<span class="mw-page-title-main">Hemoglobin</span> Oxygen-transport metalloprotein in red blood cells of most vertebrates

Hemoglobin, is the iron-containing oxygen-transport protein present in red blood cells (erythrocytes) of almost all vertebrates as well as the tissues of some invertebrate animals. Hemoglobin in blood carries oxygen from the respiratory organs to the other tissues of the body, where it releases the oxygen to enable aerobic respiration which powers the animal's metabolism. A healthy human has 12 to 20 grams of hemoglobin in every 100 mL of blood. Hemoglobin is a metalloprotein and chromoprotein.

<span class="mw-page-title-main">Globin</span> Superfamily of oxygen-transporting globular proteins

The globins are a superfamily of heme-containing globular proteins, involved in binding and/or transporting oxygen. These proteins all incorporate the globin fold, a series of eight alpha helical segments. Two prominent members include myoglobin and hemoglobin. Both of these proteins reversibly bind oxygen via a heme prosthetic group. They are widely distributed in many organisms.

<span class="mw-page-title-main">Bar-headed goose</span> Species of bird

The bar-headed goose is a goose that breeds in Central Asia in colonies of thousands near mountain lakes and winters in South Asia, as far south as peninsular India. It lays three to eight eggs at a time in a ground nest. It is known for the extreme altitudes it reaches when migrating across the Himalayas.

<span class="mw-page-title-main">Andean goose</span> Species of bird

The Andean goose is a species of waterfowl in tribe Tadornini of subfamily Anserinae. It is found in Argentina, Bolivia, Chile, and Peru.

<span class="mw-page-title-main">Polycythemia</span> Laboratory diagnosis of high hemoglobin content in blood

Polycythemia is a laboratory finding in which the hematocrit and/or hemoglobin concentration are increased in the blood. Polycythemia is sometimes called erythrocytosis, and there is significant overlap in the two findings, but the terms are not the same: polycythemia describes any increase in hematocrit and/or hemoglobin, while erythrocytosis describes an increase specifically in the number of red blood cells in the blood.

<span class="mw-page-title-main">Yellow-billed pintail</span> Species of bird

The yellow-billed pintail is a South American dabbling duck of the genus Anas with three described subspecies.

<span class="mw-page-title-main">Altitude training</span> Athletic training at high elevations

Altitude training is the practice by some endurance athletes of training for several weeks at high altitude, preferably over 2,400 metres (8,000 ft) above sea level, though more commonly at intermediate altitudes due to the shortage of suitable high-altitude locations. At intermediate altitudes, the air still contains approximately 20.9% oxygen, but the barometric pressure and thus the partial pressure of oxygen is reduced.

<span class="mw-page-title-main">Eastern deer mouse</span> Species of mammal

Peromyscus maniculatus is a rodent native to eastern North America. It is most commonly called the eastern deer mouse; when formerly grouped with the western deer mouse, it was referred to as the North American deermouse and is fairly widespread across most of North America east of the Mississippi River, with the major exception being the lowland southeastern United States.

Chronic mountain sickness (CMS) is a disease in which the proportion of blood volume that is occupied by red blood cells increases (polycythaemia) and there is an abnormally low level of oxygen in the blood (hypoxemia). CMS typically develops after extended time living at high altitude. It is most common amongst native populations of high altitude nations. The most frequent symptoms of CMS are headache, dizziness, tinnitus, breathlessness, palpitations, sleep disturbance, fatigue, loss of appetite, confusion, cyanosis, and dilation of veins.

<span class="mw-page-title-main">Effects of high altitude on humans</span> Environmental effects on physiology

The effects of high altitude on humans are mostly the consequences of reduced partial pressure of oxygen in the atmosphere. The oxygen saturation of hemoglobin determines the content of oxygen in blood. After the human body reaches around 2,100 metres (6,900 ft) above sea level, the saturation of oxyhemoglobin begins to decrease rapidly. However, the human body has both short-term and long-term adaptations to altitude that allow it to partially compensate for the lack of oxygen. There is a limit to the level of adaptation; mountaineers refer to the altitudes above 8,000 metres (26,000 ft) as the death zone, where it is generally believed that no human body can acclimatize. At extreme altitudes, the ambient pressure can drop below the vapor pressure of water at body temperature, but at such altitudes even pure oxygen at ambient pressure cannot support human life, and a pressure suit is necessary. A rapid depressurisation to the low pressures of high altitudes can trigger altitude decompression sickness.

<span class="mw-page-title-main">Himalayan wolf</span> Subspecies of mammal

The Himalayan wolf is a canine of debated taxonomy. It is distinguished by its genetic markers, with mitochondrial DNA indicating that it is genetically basal to the Holarctic grey wolf, genetically the same wolf as the Tibetan and Mongolian wolf, and has an association with the African wolf. No striking morphological differences are seen between the wolves from the Himalayas and those from Tibet. The Himalayan wolf lineage can be found living in Ladakh in the Himalayas, the Tibetan Plateau, and the mountains of Central Asia predominantly above 4,000 m (13,000 ft) in elevation because it has adapted to a low-oxygen environment, compared with other wolves that are found only at lower elevations.

Fabiola León-Velarde Servetto is a Peruvian physiologist who has devoted her research to the biology and physiology of high altitude adaptation. Born in Lima, Peru. She is the daughter of Carlos Leon-Velarde Gamarra and Juana Servetto Marti from Uruguay, and granddaughter of Angelica Gamarra. Under the mentorship of high altitude physiologist Carlos Monge Cassinelli, she obtained a BSc. in Biology (1979), an MSc (1981) and DSc (1986) in physiology at Cayetano Heredia University in Lima, Perú.

<span class="mw-page-title-main">EPAS1</span> Protein-coding gene in the species Homo sapiens

Endothelial PAS domain-containing protein 1 is a protein that is encoded by the EPAS1 gene in mammals. It is a type of hypoxia-inducible factor, a group of transcription factors involved in the physiological response to oxygen concentration. The gene is active under hypoxic conditions. It is also important in the development of the heart, and for maintaining the catecholamine balance required for protection of the heart. Mutation often leads to neuroendocrine tumors.

<span class="mw-page-title-main">EGLN1</span> Protein-coding gene in the species Homo sapiens

Hypoxia-inducible factor prolyl hydroxylase 2 (HIF-PH2), or prolyl hydroxylase domain-containing protein 2 (PHD2), is an enzyme encoded by the EGLN1 gene. It is also known as Egl nine homolog 1. PHD2 is a α-ketoglutarate/2-oxoglutarate-dependent hydroxylase, a superfamily non-haem iron-containing proteins. In humans, PHD2 is one of the three isoforms of hypoxia-inducible factor-proline dioxygenase, which is also known as HIF prolyl-hydroxylase.

Hypoxic ventilatory response (HVR) is the increase in ventilation induced by hypoxia that allows the body to take in and transport lower concentrations of oxygen at higher rates. It is initially elevated in lowlanders who travel to high altitude, but reduces significantly over time as people acclimatize. In biological anthropology, HVR also refers to human adaptation to environmental stresses resulting from high altitude.

Fish are exposed to large oxygen fluctuations in their aquatic environment since the inherent properties of water can result in marked spatial and temporal differences in the concentration of oxygen. Fish respond to hypoxia with varied behavioral, physiological, and cellular responses to maintain homeostasis and organism function in an oxygen-depleted environment. The biggest challenge fish face when exposed to low oxygen conditions is maintaining metabolic energy balance, as 95% of the oxygen consumed by fish is used for ATP production releasing the chemical energy of nutrients through the mitochondrial electron transport chain. Therefore, hypoxia survival requires a coordinated response to secure more oxygen from the depleted environment and counteract the metabolic consequences of decreased ATP production at the mitochondria.

High-altitude adaptation in humans is an instance of evolutionary modification in certain human populations, including those of Tibet in Asia, the Andes of the Americas, and Ethiopia in Africa, who have acquired the ability to survive at altitudes above 2,500 meters. This adaptation means irreversible, long-term physiological responses to high-altitude environments, associated with heritable behavioural and genetic changes. While the rest of the human population would suffer serious health consequences, the indigenous inhabitants of these regions thrive well in the highest parts of the world. These humans have undergone extensive physiological and genetic changes, particularly in the regulatory systems of oxygen respiration and blood circulation, when compared to the general lowland population.

Cynthia Beall is an American physical anthropologist at the Case Western Reserve University, Cleveland, Ohio. Four decades of her research on people living in extremely high mountains became the frontier in understanding human evolution and high-altitude adaptation. Her groundbreaking works among the Andean, Tibetan and East African highlanders are the basis of our knowledge on adaptation to hypoxic condition and how it influences the evolutionary selection in modern humans. She is currently the Distinguished University Professor, and member of the U.S. National Academy of Sciences and the American Philosophical Society.

Hypoxia inducible lipid droplet-associated is a protein that in humans is encoded by the HILPDA gene.

References

  1. 1 2 Storz JF, Scott GR, Cheviron ZA; Scott; Cheviron (2007). "Phenotypic plasticity and genetic adaptation to high-altitude hypoxia in vertebrates". J Exp Biol. 213 (pt 24): 4125–4136. doi:10.1242/jeb.048181. PMC   2992463 . PMID   21112992.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. Frisancho AR (1993). Human Adaptation and Accommodation. University of Michigan Press. pp. 175–301. ISBN   978-0472095117.
  3. Wang, G.D; Fan, R.X; Zhai, W; Liu, F; Wang, L; Zhong, L; Wu, H (2014). "Genetic convergence in the adaptation of dogs and humans to the high-altitude environment of the tibetan plateau". Genome Biology and Evolution. 6 (8): 206–212. doi:10.1093/gbe/evu162. PMC   4231634 . PMID   25091388.
  4. Hogan, C.Michael (2010). "Extremophile". In Monosson, E; Cleveland, C (eds.). Encyclopedia of Earth. Washington, D.C.: National Council for Science and the Environment. Archived from the original on 2011-05-11.
  5. Becquerel P. (1950). "La suspension de la vie au dessous de 1/20 K absolu par demagnetization adiabatique de l'alun de fer dans le vide les plus eléve". Comptes Rendus Hebdomadaires des Séances de l'Académie des Sciences (in French). 231: 261–263.
  6. Bakalar, Nicholas (26 September 2016). "Tardigrades Have the Right Stuff to Resist Radiation". The New York Times. ISSN   0362-4331.
  7. Crowe, John H.; Carpenter, John F.; Crowe, Lois M. (October 1998). "The role of vitrification in anhydrobiosis". Annual Review of Physiology . Vol. 60. pp. 73–103. doi:10.1146/annurev.physiol.60.1.73. PMID   9558455. Closed Access logo transparent.svg
  8. Space.com Staff (8 September 2008). "Creature Survives Naked in Space". Space.com . Retrieved 2011-12-22.
  9. Mustain, Andrea (22 December 2011). "Weird wildlife: The real land animals of Antarctica". NBC News . Retrieved 2011-12-22.
  10. Hingston, R.W.G. (1925). "Animal Life at High Altitudes". The Geographical Journal. 65 (2): 185–195. doi:10.2307/1782885. hdl: 2027/umn.319510004384116 . JSTOR   1782885.
  11. "Himalayan jumping spider". BBC Nature. Retrieved 2016-10-01.
  12. Pearson, Gwen (14 January 2014). "Snow Fleas". Wired.
  13. Mani, MS (1968). Ecology and Biogeography of High Altitude Insects. Springer. p. 118.
  14. Richards, OW (1930). "The humble–bees captured on the expeditions to Mt. Everest (Hymenoptera, Bombidae)". Annals and Magazine of Natural History. 10 (5): 633–658. doi:10.1080/00222933008673177.
  15. Dillon, M. E.; Dudley, R. (2014). "Surpassing Mt. Everest: extreme flight performance of alpine bumblebees". Biology Letters. 10 (2): 20130922. doi:10.1098/rsbl.2013.0922. PMC   3949368 . PMID   24501268.
  16. "Flying Spiders over Texas! Coast to Coast". Archived from the original on 2011-11-26.
  17. Maxim, Hiram Stevens (1908). "Flying Kites". Artificial and Natural Flight. p. 28.
  18. Valerio, C.E. (1977). "Population structure in the spider Achaearranea Tepidariorum (Aranae, Theridiidae)" (PDF). The Journal of Arachnology. 3: 185–190. Retrieved 2009-07-18.
  19. VanDyk, J.K. (2002–2009). "Entomology 201 - Introduction to insects". Department of Entomology, Iowa State University. Archived from the original on 8 June 2009. Retrieved 18 July 2009.
  20. Hormiga, G. (2002). "Orsonwells, a new genus of giant linyphild spiders (Araneae) from the Hawaiian Islands" (PDF). Invertebrate Systematics. 16 (3): 369–448. doi:10.1071/IT01026 . Retrieved 2009-07-18.
  21. Bilsing, S.W. (May 1920). "Quantitative studies in the food of spiders" (PDF). The Ohio Journal of Science. 20 (7): 215–260. Retrieved 2009-07-18.
  22. 1 2 Rasmussen, Joseph B.; Robinson, Michael D.; Hontela, Alice; Heath, Daniel D. (8 July 2011). "Metabolic traits of westslope cutthroat trout, introduced rainbow trout and their hybrids in an ecotonal hybrid zone along an elevation gradient" (PDF). Biological Journal of the Linnean Society. 105: 56–72. doi: 10.1111/j.1095-8312.2011.01768.x .
  23. Verberk, Wilco C.E.P.; Bilton, David T.; Calosi, Piero; Spicer, John I. (11 March 2011). "Oxygen supply in aquatic ectotherms: Partial pressure and solubility together explain biodiversity and size patterns". Ecology. 92 (8): 1565–1572. doi:10.1890/10-2369.1. hdl: 2066/111573 . PMID   21905423. S2CID   299377.
  24. Peck, L.S.; Chapelle, G. (2003). "Reduced oxygen at high altitude limits maximum size". Proceedings of the Royal Society of London. 270 (Suppl 2): 166–167. doi:10.1098/rsbl.2003.0054. PMC   1809933 . PMID   14667371.
  25. Jacobsen, Dean (24 September 2007). "Low oxygen pressure as a driving factor for the altitudinal decline in taxon richness of stream macroinvertebrates". Oecologia. 154 (4): 795–807. Bibcode:2008Oecol.154..795J. doi:10.1007/s00442-007-0877-x. PMID   17960424. S2CID   484645.
  26. Matey, Victoria; Richards, Jeffrey G.; Wang, Yuxiang; Wood, Chris M.; et al. (30 January 2008). "The effect of hypoxia on gill morphology and ionoregulatory status in the Lake Qinghai scaleless carp, Gymnocypris przewalskii". The Journal of Experimental Biology. 211 (Pt 7): 1063–1074. doi: 10.1242/jeb.010181 . PMID   18344480.
  27. Cao, Yi-Bin; Chen, Xue-Qun; Wang, Shen; Wang, Yu-Xiang; Du, Ji-Zeng (6 October 2008). "Evolution and regulation of the downstream gene of hypoxia-inducible factor-1a in naked carp (Gymnocypris przewalskii) from Lake Qinghai, China". Journal of Molecular Evolution. 67 (5): 570–580. Bibcode:2008JMolE..67..570C. doi:10.1007/s00239-008-9175-4. PMID   18941827. S2CID   7459192. Closed Access logo transparent.svg
  28. Smith, A.T.; Xie, Y.; Hoffmann, R.S.; Lunde, D.; MacKinnon, J.; Wilson, D.E.; Wozencraft, W.C.; Gemma, F. (2010). A Guide to the Mammals of China. Princeton University Press. p. 281. ISBN   978-1-4008-3411-2 . Retrieved 2020-09-21.
  29. 1 2 3 Canadian Broadcasting Company (CBC). "Wild China: The Tibetan Plateau". Archived from the original on November 13, 2012. Retrieved 2013-04-16.
  30. China.org.cn. "Unique Species of Wild Animals on Qinghai-Tibet Plateau" . Retrieved 2013-04-16.
  31. 1 2 WWF Global. "Tibetan Plateau Steppe". Archived from the original on 2013-06-15. Retrieved 2013-04-16.
  32. Joshi LR. "High Altitude Adaptations". Archived from the original on 2014-01-06. Retrieved 2013-04-15.
  33. Storz, J.F.; Runck, A. M.; Moriyama, H.; Weber, R. E.; Fago, A (1 August 2010). "Genetic differences in hemoglobin function between highland and lowland deer mice". The Journal of Experimental Biology. 213 (15): 2565–2574. doi:10.1242/jeb.042598. PMC   2905302 . PMID   20639417.
  34. Pariet, B.; Jaenicke, E. (24 August 2010). Zhang, Shuguang (ed.). "Structure of the altitude adapted hemoglobin of guinea pig in the R-state". PLOS ONE. 5 (8): e12389. Bibcode:2010PLoSO...512389P. doi: 10.1371/journal.pone.0012389 . PMC   2927554 . PMID   20811494.
  35. Cheviron, Z.A.; Bachman, G. C.; Connaty, A. D.; McClelland, G. B.; Storz, J. F (29 May 2010). "Regulatory changes contribute to the adaptive enhancement of thermogenic capacity in high-altitude deer mice". Proceedings of the National Academy of Sciences of the United States of America. 22. 109 (22): 8635–8640. Bibcode:2012PNAS..109.8635C. doi: 10.1073/pnas.1120523109 . PMC   3365185 . PMID   22586089.
  36. Yilmaz, C.; Hogg, D.; Ravikumar, P.; Hsia, C (15 February 2005). "Ventilatory acclimatization in awake guinea pigs raised at high altitude". Respiratory Physiology and Neurobiology. 145 (2–3): 235–243. doi:10.1016/j.resp.2004.07.011. PMID   15705538. S2CID   9592507. Closed Access logo transparent.svg
  37. Hsia, C.C.; Carbayo, J. J.; Yan, X.; Bellotto, D. J. (12 May 2005). "Enhanced alveolar growth and remodeling in guinea pigs raised at high altitude". Respiratory Physiology & Neurobiology. 147 (1): 105–115. doi:10.1016/j.resp.2005.02.001. PMID   15848128. S2CID   25131247. Closed Access logo transparent.svg
  38. Preston, K.; Preston, P.; McLoughlin, P. (15 February 2003). "Chronic hypoxia causes angiogenesis in addition to remodelling in the adult rat pulmonary circulation". The Journal of Physiology. 547 (Pt 1): 133–145. doi:10.1113/jphysiol.2002.030676. PMC   2342608 . PMID   12562951.
  39. Calmettes, G.; Deschodt-Arsac, V.; Gouspillou, G.; Miraux, S.; et al. (18 February 2010). Schwartz, Arnold (ed.). "Improved energy supply regulation in chronic hypoxic mouse counteracts hypoxia-induced altered cardiac energetics". PLOS ONE. 5 (2): e9306. Bibcode:2010PLoSO...5.9306C. doi: 10.1371/journal.pone.0009306 . PMC   2823784 . PMID   20174637.
  40. Broekman, M; Bennett, N.; Jackson, C.; Scantlebury, M. (30 December 2006). "Mole-rats from higher altitudes have greater thermoregulatory capabilities". Physiology and Behavior. 89 (5): 750–754. doi:10.1016/j.physbeh.2006.08.023. PMID   17020776. S2CID   35846450.
  41. Snyder LR (1985). "Low P50 in deer mice native to high altitude". J Appl Physiol. 58 (1): 193–199. doi:10.1152/jappl.1985.58.1.193. PMID   3917990.
  42. Hammond KA, Roth J, Janes DN, Dohm MR; Roth; Janes; Dohm (1999). "Morphological and physiological responses to altitude in deer mice Peromyscus maniculatus". Physiol Biochem Zool. 72 (5): 613–622. doi:10.1086/316697. PMID   10521329. S2CID   40735138.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  43. Storz JF, Runck AM, Sabatino SJ, Kelly JK, Ferrand N, Moriyama H, Weber RE, Fago A; Runck; Sabatino; Kelly; Ferrand; Moriyama; Weber; Fago (2009). "Evolutionary and functional insights into the mechanism underlying high-altitude adaptation of deer mouse hemoglobin". Proc Natl Acad Sci U S A. 106 (34): 14450–1445. Bibcode:2009PNAS..10614450S. doi: 10.1073/pnas.0905224106 . PMC   2732835 . PMID   19667207.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  44. Storz JF, Runck AM, Moriyama H, Weber RE, Fago A; Runck; Moriyama; Weber; Fago (2010). "Genetic differences in hemoglobin function between highland and lowland deer mice". J Exp Biol. 213 (Pt 15): 2565–2574. doi:10.1242/jeb.042598. PMC   2905302 . PMID   20639417.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  45. Inoguchi N, Oshlo JR, Natarajan C, Weber RE, Fago A, Storz JF, Moriyama H; Oshlo; Natarajan; Weber; Fago; Storz; Moriyama (2013). "Deer mouse hemoglobin exhibits a lowered oxygen affinity owing to mobility of the E helix". Acta Crystallogr F. 69 (Pt 4): 393–398. doi:10.1107/S1744309113005708. PMC   3614163 . PMID   23545644.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  46. Schippers MP, Ramirez O, Arana M, Pinedo-Bernal P, McClelland GB; Ramirez; Arana; Pinedo-Bernal; McClelland (2012). "Increase in carbohydrate utilization in high-altitude Andean mice". Curr Biol. 22 (24): 2350–2354. doi: 10.1016/j.cub.2012.10.043 . PMID   23219722.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  47. Wiener G, Jianlin H, Ruijun L (2003). The Yak (2 ed.). Regional Office for Asia and the Pacific Food and Agriculture Organization of the United Nations, Bangkok, Thailand. ISBN   978-9251049655.
  48. Wang, DP; Li, HG; Li, YJ; Guo, SC; et al. (2012). "Hypoxia-inducible factor 1alpha cDNA cloning and its mRNA and protein tissue specific expression in domestic yak (Bos grunniens) from Qinghai-Tibetan plateau". Biochem Biophys Res Commun. 348 (1): 310–319. doi:10.1016/j.bbrc.2006.07.064. PMID   16876112.
  49. Shenzhen, BGI (July 4, 2012). "Yak genome provides new insights into high altitude adaptation" . Retrieved 2013-04-16.
  50. Qiu, Q; Zhang, G; Ma, T; Qian, W; et al. (2012). "The yak genome and adaptation to life at high altitude". Nature Genetics. 44 (8): 946–949. doi: 10.1038/ng.2343 . PMID   22751099.
  51. Hu, Q; Ma, T; Wang, K; Xu, T; Liu, J; Qiu, Q (2012). "The Yak genome database: an integrative database for studying yak biology and high-altitude adaption". BMC Genetics. 13 (8): 600. doi:10.1186/1471-2164-13-600. PMC   3507758 . PMID   23134687.
  52. Tremblay, JC; Ainslie, PN (2021). "Global and country-level estimates of human population at high altitude". Proceedings of the National Academy of Sciences of the United States of America. 118 (18): e2102463118. Bibcode:2021PNAS..11802463T. doi: 10.1073/pnas.2102463118 . ISSN   0027-8424. PMC   8106311 . PMID   33903258.
  53. 1 2 Moore, Lorna G (2001). "Human genetic adaptation to high altitude". High Altitude Medicine & Biology. 2 (2): 257–279. doi:10.1089/152702901750265341. PMID   11443005.
  54. Penaloza, D; Arias-Stella, J (2007). "The heart and pulmonary circulation at high altitudes: healthy highlanders and chronic mountain sickness". Circulation. 115 (9): 1132–1146. doi: 10.1161/CIRCULATIONAHA.106.624544 . PMID   17339571.
  55. Frisancho AR (2013). "Developmental Functional Adaptation to High Altitude: Review". Am J Hum Biol. 25 (2): 151–168. doi:10.1002/ajhb.22367. hdl: 2027.42/96751 . PMID   24065360. S2CID   33055072.
  56. Beall CM (2006). "Andean, Tibetan, and Ethiopian patterns of adaptation to high-altitude hypoxia". Integr Comp Biol. 46 (1): 18–24. CiteSeerX   10.1.1.595.7464 . doi:10.1093/icb/icj004. PMID   21672719.
  57. Vitzthum, V. J. (2013). "Fifty fertile years: anthropologists' studies of reproduction in high altitude natives". Am J Hum Biol. 25 (2): 179–189. doi:10.1002/ajhb.22357. PMID   23382088. S2CID   41726341.
  58. Yi, X.; Liang, Y.; Huerta-Sanchez, E.; Jin, X.; et al. (2010-07-01). "Sequencing of 50 Human Exomes Reveals Adaptation to High Altitude". Science. American Association for the Advancement of Science (AAAS). 329 (5987): 75–78. Bibcode:2010Sci...329...75Y. doi:10.1126/science.1190371. ISSN   0036-8075. PMC   3711608 . PMID   20595611.
  59. Simonson, TS; Yang, Y; Huff, CD; Yun, H; et al. (2010). "Genetic evidence for high-altitude adaptation in Tibet". Science. 329 (5987): 72–75. Bibcode:2010Sci...329...72S. doi: 10.1126/science.1189406 . PMID   20466884. S2CID   45471238.
  60. MacInnis, MJ; Rupert, JL (2011). "'ome on the Range: altitude adaptation, positive selection, and Himalayan genomics". High Alt Med Biol. 12 (2): 133–139. doi:10.1089/ham.2010.1090. PMID   21718161.
  61. Zhang, YB; Li; Zhang; Wang; Yu (2012). "A preliminary study of copy number variation in Tibetans". PLOS ONE. 7 (7): e41768. Bibcode:2012PLoSO...741768Z. doi: 10.1371/journal.pone.0041768 . PMC   3402393 . PMID   22844521.
  62. Bigham, AW; Wilson, MJ; Julian, CG; Kiyamu, M; et al. (2013). "Andean and Tibetan patterns of adaptation to high altitude". Am J Hum Biol. 25 (2): 190–197. doi:10.1002/ajhb.22358. hdl: 2027.42/96682 . PMID   23348729. S2CID   1900321.
  63. Bigham, A; Bauchet, M; Pinto, D; Mao, X; et al. (2010). "Identifying signatures of natural selection in Tibetan and Andean populations using dense genome scan data". PLOS Genetics. 6 (9): e1001116. doi:10.1371/journal.pgen.1001116. PMC   2936536 . PMID   20838600.
  64. Alkorta-Aranburu, G; Beall; Witonsky; Gebremedhin; Pritchard; Di Rienzo (2012). "The genetic architecture of adaptations to high altitude in Ethiopia". PLOS Genetics. 8 (12): e1003110. arXiv: 1211.3053 . Bibcode:2012arXiv1211.3053A. doi:10.1371/journal.pgen.1003110. PMC   3516565 . PMID   23236293.
  65. Scheinfeldt, LB; Soi, S; Thompson, S; Ranciaro, A; et al. (2012). "Genetic adaptation to high altitude in the Ethiopian highlands". Genome Biol. 13 (1): R1. doi:10.1186/gb-2012-13-1-r1. PMC   3334582 . PMID   22264333.
  66. 1 2 Huerta-Sanchez, E; Jin, X; Asan; Bianba, Z; Peter, B.M; Vinckenbosch, N; Liang, Y (2014). "Altitude adaptation in Tibetans caused by introgression of denisovan-like DNA". Nature. 512 (7513): 194–197. Bibcode:2014Natur.512..194H. doi:10.1038/nature13408. PMC   4134395 . PMID   25043035.
  67. McCracken, K. G.; Barger, CP; Bulgarella, M; Johnson, KP; et al. (October 2009). "Parallel evolution in the major hemoglobin genes of eight species of Andean waterfowl". Molecular Evolution. 18 (19): 3992–4005. CiteSeerX   10.1.1.497.957 . doi:10.1111/j.1365-294X.2009.04352.x. PMID   19754505. S2CID   16820157.
  68. "How the Respiratory System of Birds Works". Foster and Smith. Retrieved 21 December 2012.
  69. Moyes, C.; Schulte, P. (2007). Principles of Animal Physiology (2nd ed.). Benjamin-Cummings Publishing Company. ISBN   978-0321501554.
  70. Grubb, B.R. (October 1983). "Allometric relations of cardiovascular function in birds". American Journal of Physiology. 245 (4): H567–72. doi:10.1152/ajpheart.1983.245.4.H567. PMID   6624925. Closed Access logo transparent.svg
  71. Mathieu-Costello, O. (1990). Histology of flight: tissue and muscle gas exchange. In Hypoxia: The Adaptations. Toronto: B.C. Decker. pp. 13–19.
  72. Faraci, F.M. (1991). "Adaptations to hypoxia in birds: how to fly high". Annual Review of Physiology. 53: 59–70. doi:10.1146/annurev.ph.53.030191.000423. PMID   2042973. Closed Access logo transparent.svg
  73. Swan, L.W. (1970). "Goose of the Himalayas". Journal of Natural History. 70: 68–75.
  74. 1 2 Tibet Environmental Watch (TEW). "Endemism on the Tibetan Plateau". Archived from the original on 2012-04-10. Retrieved 2013-04-16.
  75. Conservation International. "Tropical Andes: Unique Biodiversity". Archived from the original on 2013-04-23. Retrieved 2013-04-16.
  76. "How Do Birds Survive at High Altitudes?". The Wire. Retrieved 2021-01-27.
  77. McCracken, KG; Barger, CP; Bulgarella, M; Johnson, KP; et al. (2009). "Signatures of High‐Altitude Adaptation in the Major Hemoglobin of Five Species of Andean Dabbling Ducks". The American Naturalist. 174 (5): 610–650. doi:10.1086/606020. JSTOR   606020. PMID   19788356. S2CID   20755002.
  78. Wilson, RE; Peters, JL; McCracken, KG (2013). "Genetic and phenotypic divergence between low- and high-altitude populations of two recently diverged cinnamon teal subspecies". Evolution. 67 (1): 170–184. doi:10.1111/j.1558-5646.2012.01740.x. PMID   23289570. S2CID   8378355.
  79. Cai, Q; Qian, X; Lang, Y; Luo, Y; et al. (2013). "The genome sequence of the ground tit Pseudopodoces humilis provides insights into its adaptation to high altitude". Genome Biol. 14 (3): R29. doi:10.1186/gb-2013-14-3-r29. PMC   4053790 . PMID   23537097.
  80. Facts and Details (of China) (2012). "Tibetan Animals" . Retrieved 2013-04-16.
  81. Körner, Christian (2003). Alpine Plant Life: Functional Plant Ecology of High Mountain Ecosystems. Berlin: Springer. pp. 9–18. ISBN   978-3-540-00347-2.
  82. Elliott-Fisk, D.L. (2000). "The Taiga and Boreal Forest". In Barbour, M.G.; Billings, M.D. (eds.). North American Terrestrial Vegetation (2nd ed.). Cambridge University Press. ISBN   978-0-521-55986-7.
  83. "High Altitude Plants". Adventurers and Scientists for Conservation. Archived from the original on 2012-04-25. Retrieved 2017-01-07.
  84. Bezruchka, Stephen; Lyons, Alonzo (2011). Trekking Nepal: A Traveler's Guide. The Mountaineers Books. p. 275.