Saturday, January 31, 2009
New Bird Species Discovered in Southern China
An international conservation group says the discovery of a new bird species in southern China suggests the region could be home to many other unknown birds.
Birdlife International Thursday announced the discovery of a new species of babbler in China's Nonggang region near its border with Vietnam.
Ornithologists Zhou Fang and Jiang Aiwu first spotted the fist-size dark brown bird with white specks on its chest in 2005.
They later determined it was an undescribed species and have since named it the Nonggang babbler, after the region where it was discovered.
The new species resembles a wren-babbler in that it prefers running to flying, and seems to spend most of its time on the ground foraging for insects.
Nigel Collar, an ornithologist at Birdlife International, says the discovery is "exciting evidence" that there could be many more unknown bird species in the region.
Ornithologist Zhou Fang warned the country's rapid development could threaten many biologically diverse areas in China before further discoveries are made.
About 100 of the babblers have been identified so far in the Nonggang Natural Reserve in southwestern China.
Friday, January 30, 2009
Carnivorous sea squirt amongst new species discovered off Tasmania
Scientific sub makes deep-sea discoveries
A four-week expedition to explore the deep ocean south-west of Tasmania has revealed new species of animals and more evidence of impacts of increasing carbon dioxide on deep-sea corals.
Dr Thresher, from CSIRO, said "We set out to search for life deeper than any previous voyage in Australian waters. We also gathered data to assess the threat posed by ocean acidification and climate change on Australia's unique deep-water coral reefs."
The survey through the Tasman Fracture Commonwealth Marine Reserve, south-west of Tasmania, explored the near vertical slice in the earth's crust, known as the Tasman Fracture Zone, which drops from approximately 2000 metres to over 4000 metres.
New species - Carnivorous sea-squirt
"Our sampling documented the deepest known Australian fauna, including a bizarre carnivorous sea squirt, sea spiders and giant sponges, and previously unknown marine communities dominated by gooseneck barnacles and millions of round, purple-spotted sea anemones."
All of these new species are located more than 2000 metres below the surface.
Deep water reefs dying
Modern-day deep-water coral reefs were found, however there is strong evidence that this reef system is dying, with most reef-forming coral deeper than 1300 metres newly dead.
"We need to closely analyse the samples and measurements we collected before we can determine what's caused this, as it could be the result of several factors, such as ocean warming, disease or increasing ocean acidity," Dr Thresher says.
"Mathematical models predict that we could be seeing impacts of ocean acidification in this region. If our analysis identifies this phenomenon as the cause of the reef system's demise, then the impact we are seeing now below 1300 metres might extend to the shallower portions of the deep-reefs over the next 50 years, threatening this entire community."
Fossilised coral reefs
Vast fields of fossil corals were discovered below 1400 metres, and dated to more than 10,000 years old. The samples collected will be used to determine the periods over the last millions of years when reefs have existed south of Tasmania. They will also provide ancient climate data that contribute to models of regional and global climate change, based on historical circulation patterns in the Southern Ocean.
The international research team aboard the research vessel RV Thomas G. Thompson deployed a deep diving, remotely operated submarine vehicle named Jason, belonging to the Woods Hole Oceanographic Institution. Jason, which is approximately the size of a small car, is capable of collecting samples and data, and photographing and filming areas as deep as 6000 metres. Jason made 14 dives lasting up to 48 hours each and reaching a maximum depth of 4010 metres.
The collaborative voyage of US and Australian researchers was led by chief scientists Dr Jess Adkins from the California Institute of Technology and Dr Ron Thresher from CSIRO's Climate Adaptation and Wealth from Oceans Flagships.
The $2m cost of bringing the RV Thompson and Jason to Australia was met by the US National Science Foundation (NSF). The research was also supported by: the Australian Department of Environment, Water, Heritage and Arts; CSIRO and the Commonwealth Environmental Research Facility (CERF) Marine Biodiversity Hub.
CSIRO initiated the National Research Flagships to provide science-based solutions in response to Australia's major research challenges and opportunities. The nine Flagships form multidisciplinary teams with industry and the research community to deliver impact and benefits for Australia.
Sunday, January 11, 2009
Endangered numbat population gets a boost in Western Australia
The future is looking up for Western Australia's native mammal emblem, the numbat, following the release of 13 numbats into a site near Ravensthorpe this month.
The Department of Environment and Conservation (DEC) translocated the numbats into Cocanarup Timber Reserve as part of the DEC wildlife recovery program Western Shield. DEC principal research scientist Tony Friend said six captive-bred numbats from Perth Zoo and seven wild numbats from Dryandra Woodland, near Narrogin, were released.
"In total two adult females, six subadult (born in January 2008) males and five subadult females were released into Cocanarup, as part of the third release of numbats at the reserve since 2006," Dr Friend said.
Cocanarup Timber Reserve
"Cocanarup Timber Reserve was chosen as a numbat translocation site as it is baited each month for fox control under the Western Shield baiting program, plus it is an area of eucalypt woodland with good densities of hollow logs and termites, both of which are required by numbats. All numbats are fitted with radio collars so they can be monitored throughout their lives, with the collars being changed every four months before the battery fails."
Breeding
Numbats mate mostly in early to mid January and the young only become independent in October, with translocations done in December while both adult females and their young can be moved and still be given time to settle in before the mating season.
The numbat is classified as ‘Vulnerable' on State and Federal lists but has recently been elevated to ‘Endangered' in the World Conservation Union (IUCN) Red List of Threatened Species.
Predation
"Numbats are constantly under threat from native predators, particularly birds of prey and carpet pythons, while additional predation by foxes and cats can determine whether a population survives or becomes extinct," Dr Friend said.
"Numbats eat only termites and the supply of termites is critical in areas with numbat populations. Several recent sightings of an uncollared numbat at Cocanarup, which is most likely the progeny of a translocated numbat, have caused great excitement and indicate that the translocation is working."
Funding for the translocation is provided by the Western Shield Translocation Plan and Federal Government Natural Heritage Trust funding through South Coast NRM.
Saturday, January 10, 2009
3. Endangered Animal of the Week: 5th-11th Jan 2009
Giant Panda (Ailuropoda Melanoleuca)
Status: Endangered
Population Trend: Decreasing
Found: China
Range: The giant panda is confined to south-central China. Currently, it occurs in portions of six isolated mountain ranges (Minshan, Qinling, Qionglai, Liangshan, Daxiangling, and Xiaoxiangling) in Gansu, Shaanxi and Sichuan Provinces (about 75% of the population inhabits Sichuan Province). The panda's total range encompasses approximately 30,000 sq km between 102–108.3° E longitude and 28.2–34.1° N latitude. This range highly overlaps that of the Asiatic black bear (Ursus thibetanus), although the ecological requirements of these species differ appreciably (Schaller et al. 1989).
Significant climatic changes combined with thousands of years of cultivation of lower and flatter habitats and hunting by humans caused the giant pandas’ range to shrink to a remnant at the rugged western fringe of a once more expansive area (Schaller et al. 1985). This species previously ranged throughout most of southern and eastern China, with fossils indicating presence as far south as northern Myanmar and northern Viet Nam and stretching north nearly to Beijing. Another related species, the pygmy giant panda (A. microta), now extinct, also once existed in this area. As recently as 1850, giant pandas existed in eastern Sichuan and Hubei and Hunan Provinces. By 1900, they occurred only in the Qinling Mountains and along the edge of the Tibetan plateau. Soon after 1900, the expansion of agriculture upstream along principal river valleys separated this distribution into separate regions in the six mountain ranges.
Population: Three range-wide surveys have been conducted, in the mid-1970s, mid-late1980s, and 2000–2002. All surveys were based on incidence of sign, but techniques varied, so results are not directly comparable. Present best estimates indicate a total wild population between 1,000–2,000. Greater protection of forests and from poaching in recent years suggest that panda populations should be increasing, but this has not been confirmed empirically.
Results from the most recent survey, coordinated by the State Forestry Administration (SFA) of China and World Wildlife Fund (WWF), indicated a total population of ~1600 individuals. This is over 40% higher than previous estimates. It is believed that the increase in the estimated number of pandas is due largely to differences in survey methodology and a larger search area, as well as possibly an actual increase in panda population size in some areas. Conversely, in other areas, habitat conditions were deemed to be worse and panda numbers lower in 2000–2002 than in the 1980s survey.
The most recent population estimate was based on differentiating individual pandas from measurements of bamboo fragments in scats. It is known that different age classes of pandas have different bite-sizes of bamboo (Schaller et al. 1985), but the validity of differentiating individuals of the same age class based on bite-sizes has not been well tested. Recent information on DNA-identified scats suggests that the bite-size method may underestimate population size in some cases (e.g., dense populations; Zhan et al. 2006).
Many surviving wild giant panda subpopulations have fewer than 50 individuals (Loucks et al. 2001). No major reductions in the genetic diversity of these populations is apparent, although they likely experienced modest genetic losses from a much larger ancestral population (Lü 2001). Some controversial research suggests that the Qinling (Shaanxi Province) population is a genetically isolated and distinct subspecies (Wan et al. 2005)
Habitat and Ecology: Giant pandas occupy temperate montane forests with dense stands of bamboo at altitudes of 1,200–4,100 m asl (more typically 1,500–3,000 m asl; Hu and Wei 2004). Habitat use depends both on the type and density of bamboo, the overstory (which influences the growth of bamboo), and the hillslope (Reid and Hu 1991). Giant pandas do not hibernate but they generally descend to lower elevations in the winter (Liu et al. 2002), and may take temporary shelter in hollow trees, rock crevices and caves.
Giant pandas spend about 55% of the day (both daytime and night-time) feeding, mainly on bamboo (Schaller et al. 1985, 1989). Bamboo comprises 99% of their diet. They utilize over 60 species of bamboo, but 35 species comprise their main food source (Hu and Wei 2004). They often use different species of bamboo in different elevational bands, varying use with the seasons (Pan et al. 2001, Loucks et al. 2003)
Pandas are often erroneously believed to be poor breeders, an impression rooted in the previous disappointing reproductive performance of captive animals (Lü et al. 2000). Studies of wild pandas, however, indicate that their reproductive rates are comparable to those of some other species of bears (Garshelis 2004, Harris 2004, Wang et al. 2004). Moreover, captive populations in China are now reproducing well.
Giant pandas are usually solitary, except during the mating season and while rearing a cub. During the March–May breeding season, females may breed with multiple males. Birthing, often in rock dens or hollow trees, occurs in August–September (Schaller et al. 1985, Zhu et al. 2001). One or two cubs are born, but the mother raises only one.
Threats: Restricted and degraded habitat is the greatest threat to giant pandas. Population fragmentation exists on two scales — six mountain ranges separated by agriculture, and within these, fragments of bamboo forest separated by patches of cleared lands and forest without a bamboo understory. The giant panda's range contracted as trees were removed in logging operations and land was cleared for farming. Populations of pandas thereby became small and isolated, and confined to high ridges, hemmed in by cultivation.
Chinese authorities have established a network of panda reserves, and linkages now exist among some of these, but small population size and small total range remains a threat to the viability of this species. Moreover, in some reserves, and especially in panda range outside reserves, habitat has become degraded by intensive human use (Liu et al. 2001).
A further threat to pandas relates to their reliance on bamboo for food. Bamboo is subject to periodic, synchronous (and hence large-scale) flowering and die-off (at intervals of 15–120 years). Before significant human encroachment of their habitat, pandas could move to areas with healthy bamboo when a die-off occurred. Studies following the latest major bamboo die-off in the early 1980s indicated that pandas were still able to survive by finding patches that had not flowered, and also by moving to alternate habitats and feeding on less-favoured species of bamboo (Johnson et al. 1988, Reid et al. 1989).
Poaching of pandas was a serious problem in the past, but it has greatly diminished, and is no longer considered a major threat. Markets for panda skins have virtually disappeared, and penalties for poaching pandas have become far more severe (including death sentences in some cases). Panda parts are not used in Traditional Chinese Medicine. However, giant pandas are still sometimes killed in snares set for musk deer and other species.
Conservation Actions: Giant pandas are considered a threatened and precious species in China. They are listed under Category 1 (maximum level of protection) of the Chinese Wildlife Conservation Law of 1988 and on Appendix I of CITES. In 1989 the Chinese Ministry of Forestry (now SFA) and WWF drafted a joint national conservation plan for the giant panda, which was eventually adopted by the Chinese government in 1992. This plan now guides conservation initiatives for this species.
Since poaching of pandas has been largely controlled, the major conservation issue is restoring their habitat (Reid and Gong 1999, Lü et al. 2000). Previous considerations to clone pandas have been largely abandoned. There are still plans to release captive animals (experimental tests of this are presently occurring), but this effort addresses mainly a problem of overcrowding in captivity (due to enormous success in captive breeding) rather than the wild situation. Reintroduction of captive animals may be limited by lack of suitable release sites with adequate habitat but few or no pandas, which are necessary conditions to avoid possible transmission of disease and social disruption of the wild population.
A concerted effort has been made to increase both the quantity and quality of panda habitat. Beginning in 1963, forest reserves were established specifically for the conservation of giant pandas. By 1990, 13 panda reserves had been established — presently there are nearly 60 (under either federal or provincial jurisdiction). Increasing linkages among these reserves is a conservation priority (Loucks et al. 2003).
In addition to creating new reserves, China has worked to increase and improve forested area outside reserves. Following extensive flooding in 1998, tied directly to deforestation, China implemented the Natural Forest Conservation Program to enhance forest cover throughout major river basins; this included a ban on logging in natural forests. Additionally, a “Grain-to-Green” policy has forced farmers to abandon agricultural fields on steep slopes and replant these areas with trees (for which they are given grain and cash subsidies). As a result of these policies, China has become first in the world in terms of forest area gained per year (FAO 2006). The suitability of many of these newly forested areas for pandas, though, is still questionable. Additionally, the rising pace of economic development, particularly in presently undeveloped areas, has created more road and hydro-power construction, causing more forest fragmentation.
Status: Endangered
Population Trend: Decreasing
Found: China
Range: The giant panda is confined to south-central China. Currently, it occurs in portions of six isolated mountain ranges (Minshan, Qinling, Qionglai, Liangshan, Daxiangling, and Xiaoxiangling) in Gansu, Shaanxi and Sichuan Provinces (about 75% of the population inhabits Sichuan Province). The panda's total range encompasses approximately 30,000 sq km between 102–108.3° E longitude and 28.2–34.1° N latitude. This range highly overlaps that of the Asiatic black bear (Ursus thibetanus), although the ecological requirements of these species differ appreciably (Schaller et al. 1989).
Significant climatic changes combined with thousands of years of cultivation of lower and flatter habitats and hunting by humans caused the giant pandas’ range to shrink to a remnant at the rugged western fringe of a once more expansive area (Schaller et al. 1985). This species previously ranged throughout most of southern and eastern China, with fossils indicating presence as far south as northern Myanmar and northern Viet Nam and stretching north nearly to Beijing. Another related species, the pygmy giant panda (A. microta), now extinct, also once existed in this area. As recently as 1850, giant pandas existed in eastern Sichuan and Hubei and Hunan Provinces. By 1900, they occurred only in the Qinling Mountains and along the edge of the Tibetan plateau. Soon after 1900, the expansion of agriculture upstream along principal river valleys separated this distribution into separate regions in the six mountain ranges.
Population: Three range-wide surveys have been conducted, in the mid-1970s, mid-late1980s, and 2000–2002. All surveys were based on incidence of sign, but techniques varied, so results are not directly comparable. Present best estimates indicate a total wild population between 1,000–2,000. Greater protection of forests and from poaching in recent years suggest that panda populations should be increasing, but this has not been confirmed empirically.
Results from the most recent survey, coordinated by the State Forestry Administration (SFA) of China and World Wildlife Fund (WWF), indicated a total population of ~1600 individuals. This is over 40% higher than previous estimates. It is believed that the increase in the estimated number of pandas is due largely to differences in survey methodology and a larger search area, as well as possibly an actual increase in panda population size in some areas. Conversely, in other areas, habitat conditions were deemed to be worse and panda numbers lower in 2000–2002 than in the 1980s survey.
The most recent population estimate was based on differentiating individual pandas from measurements of bamboo fragments in scats. It is known that different age classes of pandas have different bite-sizes of bamboo (Schaller et al. 1985), but the validity of differentiating individuals of the same age class based on bite-sizes has not been well tested. Recent information on DNA-identified scats suggests that the bite-size method may underestimate population size in some cases (e.g., dense populations; Zhan et al. 2006).
Many surviving wild giant panda subpopulations have fewer than 50 individuals (Loucks et al. 2001). No major reductions in the genetic diversity of these populations is apparent, although they likely experienced modest genetic losses from a much larger ancestral population (Lü 2001). Some controversial research suggests that the Qinling (Shaanxi Province) population is a genetically isolated and distinct subspecies (Wan et al. 2005)
Habitat and Ecology: Giant pandas occupy temperate montane forests with dense stands of bamboo at altitudes of 1,200–4,100 m asl (more typically 1,500–3,000 m asl; Hu and Wei 2004). Habitat use depends both on the type and density of bamboo, the overstory (which influences the growth of bamboo), and the hillslope (Reid and Hu 1991). Giant pandas do not hibernate but they generally descend to lower elevations in the winter (Liu et al. 2002), and may take temporary shelter in hollow trees, rock crevices and caves.
Giant pandas spend about 55% of the day (both daytime and night-time) feeding, mainly on bamboo (Schaller et al. 1985, 1989). Bamboo comprises 99% of their diet. They utilize over 60 species of bamboo, but 35 species comprise their main food source (Hu and Wei 2004). They often use different species of bamboo in different elevational bands, varying use with the seasons (Pan et al. 2001, Loucks et al. 2003)
Pandas are often erroneously believed to be poor breeders, an impression rooted in the previous disappointing reproductive performance of captive animals (Lü et al. 2000). Studies of wild pandas, however, indicate that their reproductive rates are comparable to those of some other species of bears (Garshelis 2004, Harris 2004, Wang et al. 2004). Moreover, captive populations in China are now reproducing well.
Giant pandas are usually solitary, except during the mating season and while rearing a cub. During the March–May breeding season, females may breed with multiple males. Birthing, often in rock dens or hollow trees, occurs in August–September (Schaller et al. 1985, Zhu et al. 2001). One or two cubs are born, but the mother raises only one.
Threats: Restricted and degraded habitat is the greatest threat to giant pandas. Population fragmentation exists on two scales — six mountain ranges separated by agriculture, and within these, fragments of bamboo forest separated by patches of cleared lands and forest without a bamboo understory. The giant panda's range contracted as trees were removed in logging operations and land was cleared for farming. Populations of pandas thereby became small and isolated, and confined to high ridges, hemmed in by cultivation.
Chinese authorities have established a network of panda reserves, and linkages now exist among some of these, but small population size and small total range remains a threat to the viability of this species. Moreover, in some reserves, and especially in panda range outside reserves, habitat has become degraded by intensive human use (Liu et al. 2001).
A further threat to pandas relates to their reliance on bamboo for food. Bamboo is subject to periodic, synchronous (and hence large-scale) flowering and die-off (at intervals of 15–120 years). Before significant human encroachment of their habitat, pandas could move to areas with healthy bamboo when a die-off occurred. Studies following the latest major bamboo die-off in the early 1980s indicated that pandas were still able to survive by finding patches that had not flowered, and also by moving to alternate habitats and feeding on less-favoured species of bamboo (Johnson et al. 1988, Reid et al. 1989).
Poaching of pandas was a serious problem in the past, but it has greatly diminished, and is no longer considered a major threat. Markets for panda skins have virtually disappeared, and penalties for poaching pandas have become far more severe (including death sentences in some cases). Panda parts are not used in Traditional Chinese Medicine. However, giant pandas are still sometimes killed in snares set for musk deer and other species.
Conservation Actions: Giant pandas are considered a threatened and precious species in China. They are listed under Category 1 (maximum level of protection) of the Chinese Wildlife Conservation Law of 1988 and on Appendix I of CITES. In 1989 the Chinese Ministry of Forestry (now SFA) and WWF drafted a joint national conservation plan for the giant panda, which was eventually adopted by the Chinese government in 1992. This plan now guides conservation initiatives for this species.
Since poaching of pandas has been largely controlled, the major conservation issue is restoring their habitat (Reid and Gong 1999, Lü et al. 2000). Previous considerations to clone pandas have been largely abandoned. There are still plans to release captive animals (experimental tests of this are presently occurring), but this effort addresses mainly a problem of overcrowding in captivity (due to enormous success in captive breeding) rather than the wild situation. Reintroduction of captive animals may be limited by lack of suitable release sites with adequate habitat but few or no pandas, which are necessary conditions to avoid possible transmission of disease and social disruption of the wild population.
A concerted effort has been made to increase both the quantity and quality of panda habitat. Beginning in 1963, forest reserves were established specifically for the conservation of giant pandas. By 1990, 13 panda reserves had been established — presently there are nearly 60 (under either federal or provincial jurisdiction). Increasing linkages among these reserves is a conservation priority (Loucks et al. 2003).
In addition to creating new reserves, China has worked to increase and improve forested area outside reserves. Following extensive flooding in 1998, tied directly to deforestation, China implemented the Natural Forest Conservation Program to enhance forest cover throughout major river basins; this included a ban on logging in natural forests. Additionally, a “Grain-to-Green” policy has forced farmers to abandon agricultural fields on steep slopes and replant these areas with trees (for which they are given grain and cash subsidies). As a result of these policies, China has become first in the world in terms of forest area gained per year (FAO 2006). The suitability of many of these newly forested areas for pandas, though, is still questionable. Additionally, the rising pace of economic development, particularly in presently undeveloped areas, has created more road and hydro-power construction, causing more forest fragmentation.
A new species of land iguana found in the Galapagos
A species of pink land iguana overlooked by Charles Darwin during his visits to the Galápagos Islands may provide evidence of the ancient animal's diversification in the archipelago.
Park rangers first noted the presence of a pink variety of iguana on the slopes of Volcano Wolf on the island of Isabela in 1986, but it was not until 2000 that scientists began to examine it.
On his visit to the Galápagos Islands in 1835, Darwin failed to explore the Volcan Wolf volcano on the island of Isabela, the only home of the "rosada" iguana, a newly identified species of the land iguana Conolophus.
Ancient divergence
Genetic analysis of the rosada and other species of land iguanas performed by Dr Gabriele Gentile of the University Tor Vergata in Rome show that the rosada iguana originated in the Galápagos more than five million years ago, and diverged from the island's other iguana populations when the archipelago was still forming.
The ancient divergence between the rosada and other land iguanas - prior to the formation of the Volcan Wolf volcano - provides evidence for one of the most ancient diversification events recorded in the Galápagos. It is thought that the Wolf volcano is just 350,000 years old so the iguanas were present long before the volcano was formed.
Critically Endangered
This newly recognized species of iguana is already endangered and probably in danger of extinction, Gentile warns. The pink iguanas are only found on the slope of the Wolf volcano, and Dr Gentile's team believes that fewer than 100 Rosadas still exist.
Dr Gentile said "Our studies would indicate that the population size is very small. We only collected 36 during the two years study; and last year a large research team hiked up Wolf Volcano and only found 10, and most of those were ones that we'd marked earlier."
These numbers are low enough to make rosada a Critically Endangered species.
Tanzania forests yield 17 new species of amphibians and reptiles
Despite the vicinity of a major road, the rainforests of the South Nguru Mountains in eastern Tanzania were virtually unexplored until 2004, particularly from a herpetological point of view.
Several surveys were conducted between 2004 and 2006 with the aim of providing a comprehensive list of the amphibian and reptile species of this overlooked hotspot of biological diversity. The surveys were carried out by Michele Menegon, a researcher from the Natural Science Museum of Trento, Italy, in collaboration with the Tanzanian NGO Tanzania Forest Conservation Group and the Frontier Tanzania Forest Research Program.
17 new species
The surveys have resulted in the discovery of 17 reptile and amphibian species new to science. These species are only known from the Nguru Mountains. Overall, the surveys recorded a total of 92 herpeto-faunal species of which 15 were species previously only known from other areas.
Conservation Urgently Needed
Pressure on the forests, particularly the lowland forests, remains high. A conservation planning process is now underway that is attempting to address the loss of these critically important forests. These results, documenting the high species richness and the outstanding number of endemics of the forests, strongly highlight the biological importance of the South Nguru Mountains and place them among the most important sites for the conservation of herpetofauna in Africa.
A paper summarizing the results of the surveys, is published in the current issue of the scientific journal Acta Herpetologica and can be downloaded here.
Other recent discoveries in Tanzania - New genus of monkey!
Despite being a relatively well known and studied country, there are still many surprises lurking in some of Tanzania's nooks and crannies. Recent discoveries include a New Species of Giant Elephant-Shrew and, amazingly, a new genus of monkey, the Kipunji which is critically endangered.
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