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Northeast and East Central AsiaNational Biodiversity
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| Funded by: United Nation Development Programme (UNDP) United Nation Environment Programme (UNEP) Global Environment Facility (GEF) |
Edited by: Bureau of Life Sciences and Biotechnology, Chinese Academy of Sciences (CAS) Institute of Zoology, Chinese Academy of Sciences (CAS) Biodiversity Working Group / China Council for International Cooperation on Environment and Development (BWG/CCICED) |
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¡ïLoss
of Water and Soil Became the Top Environmental Problem in China
¡ïThe
Environment Impact Assessment Law (Draft)
¡ïEndangered
Plants in the Three Gorges Area Cloned
¡ïSnow
Leopard Conservation in Kyrghyzstan
¡ïTurns
to Unregulated Markets for Wood
¡ïTo
be or not to be for Saker Falcon in Central Asian countries?
¡ïFeatures
of Invasive Species in China
¡ïPartial
List of Invasive Species in China
¡ï1591
Species of Wild Animals Recorded on Protection List
¡ïDegradation
in Protected Areas: The Case of Wolong Nature Reserve for Giant Pandas
¡ïChina
Commences to Establish State-level Ecological Function Reserves
¡ïCompilation
of China's Biodiversity Websites
ZHANG Jiyao, Deputy
Minister, Ministry of Water Conservancy, Indicated
Loss of Water and Soil Became the Top Environmental
Problem in China
In today¡¯s videophone meeting on
national protection of Mother River, Zhang Jiyao, the Deputy Minister of the
Ministry of Water Conservancy (MWC), indicated that: ¡°Loss of water and soil
has become the top environmental problem in China. There is no time to delay
to protect the Mother River.¡±
Results of the second remote sensing survey conducted by MWC recently showed
that after several years of comprehensive control, some successes have been
achieved. However, water and soil erosion through out of the country is still
very serious, and tendency of ecological deterioration had not yet effectively
halted, in particular, such situation in the West had no choice but to be harnessed
at once. Nowadays, the area of water and soil erosion is 3,670,000sq.km., among
which eroded by water is 1,790,000sq.km.. Water and soil erosion area in the
Middle Yellow River is 450,000 sq.km., and that in the Upper Yangtze River is
300,000 sq.km. The main impacts of water and soil erosion are desertification,
petrifaction, degradation of land and threatening survival of the local residents.
Moreover rivers and lakes are silted up, so as to promote the occurrence of
draught and flood.
It is reported that water and soil erosion, water shortage and water pollution
more and more frequently influence Chinese social economy and people¡¯s production
and living. In 2000, big and middle sized cities, such as Tianjin, Dalian, Yantai
and Weihai, etc., were in bad need of water. 70% reaches of Huai River, Tai
Lake and Yellow River suffered pollution in various degrees. 60% reaches of
Hai River and Songliao River, and even some water head were polluted.
WANG Haizhou, China Youth, 9/1/2001
Translated by WU Lihui
The Environment Impact Assessment Law (Draft)
Proposed to the 19th Standing Committee Meeting of the 9th Session of the National
People's Congress
To implement the sustainable development
strategy and prevent the side impacts on environment due to policies and programs,
exploitation and construction, the Environment and Resource Committee of the
National People¡¯s Congress Council drew up the Environment Impact Assessment
(EIA) Law (Draft) of People¡¯s Republic of China on the basis of comprehensive
survey, argumentation and suggestions from all sides. This draft was submitted
to the 19th Standing Committee Meeting of the 9th Session of the National People's
Congress held on Dec 22nd. LI Peng, Chairman of the Standing Committee, presided
over the meeting.
WANG Tao, Vice Director of the Environment and Resource Committee, gave the
explanation of this draft. He indicated that China is one of the developing
countries which firstly conduct the EIA system. In the Environmental Protection
Law of People¡¯s Republic of China (Try out) approved in 1979, this system was
set up as a rule of law for the first time. After the practice of more than
20 years, in the period of the 9th Five-year Plan the execution rate of this
system was up to 90%. The evaluation, examination and approval work is standardized
gradually, and the evaluation range also expands from infrastructure projects
to technical reformation projects and regional exploitation and construction
projects.
However,
along with the constant expanding of range and scale of economic activities,
harms to environment caused by regional exploitation, industrial development
and utilization of natural resource are increasingly distinct. Especially, those
environmental problems caused by relative policies and programs have already
become major threats to the sustainable development of China. WANG Tao said
that, ¡®China¡¯s economic development history of the recent several decades indicates
side impacts derived from some policies and programs developed by the government
and related departments, compared with that of the construction projects, are
heavier, last longer period and affect broader ranges¡¯.
WANG Tao indicated that China has conducted beneficial exploration and accumulated
some experiences in the development of EIA system. According to the experiences
and practices, this draft expands the range of EIA from single construction
projects to those policies and programs which are harmful to environment. The
achievement of this aim cannot only rely on amending existing laws, and the
constitution of a complete Environment Impact Assessment Law is indispensable.
DING Pin, China Environment News, 23/12/2000
Translated by QIN Hua, Picture by Emil Shukurov
Endangered Plants in the Three Gorges Area
Cloned
Recently, the Yichang Three-Gorge
Vivarium, Chinese Academy of Science starts to collect explants of endangered
dove tree (Davidia involucrata), Henry emmenopterys (Emmenopterys henri) and
Wilson buckeye (Aesculus wilsonii) for inoculation and culture, so as to conduct
fast asexual reproduction experiments on them in the plant clone laboratory.
Dove tree, Henry emmenopterys and Wilson buckeye are key protected plants of
China. The clone of these plants marks the formal beginning of rescue clone
experiments of the Yichang Three-Gorge Vivarium for threatened plants in the
Three Gorges Area. The first group of cloned seedlings of Three Gorges plants
may come into being in the culture bottles after one month, provided that experiments
go on wheels.
Beijing Evening Paper, 23/3/2001
Translated by QIN Hua
SNOW LEOPARD CONSERVATION IN KYRGHYZSTAN
was
held. On this conference specialists from 5 countries: Kazakhstan, Kyrghyzstan,
Uzbekistan, Russia and USA set main problems and key moments for leopard protection
through regional projects. An international community organization "Asia
- Irbis" was created, its main task is snow leopard protection on Central
Asian territory in former USSR borders. Sooner Tajikistan joined this organization.
Seminar's participants accepted an Appeal to the Governments of their countries
with a request to unite the efforts on leopard saving. In 2000 with SEN funds
3 short-term projects on work with the local people in Uzbekistan, Kazakhstan
and Kyrghyzstan were held. Future will show us how soon positive results will
appear. It is hard to believe that those measures are enough. It is important
to widen the field of those and new projects and programs in order to recruit
all local people to conservation of this unique and wonderful inhabitant of the
high mountains. Snow leopard should live in its native places!Dr. Valentina TOROPOVA
Ph.D. in biology sciences,
NGO ¡°Asia - Irbis¡±
Picture by Emil Shukurov
Turns to Unregulated Markets for Wood
PIANMA, China -- This Chinese town
hard on the border with Bur-ma smells of wood. Sawdust floats through the air
like pollen. Fires crackle in roadside restaurants. Pianma's tallest structure
is a mountain of logs more than 50 feet high. And trucks weighed down with timber
trundle through town daily.
Pianma, 1,500 miles southwest of Beijing on the far edge of Yunnan Province,
is one of China¡¯s gateways into the forests of northern Burma, where for the
last several years a massive, unregulated and largely unnoticed timber trade
has stripped bare hundreds of square miles of ancient tropical forests. As such,
Pianma is a vantage point to view the mounting appetite of the Chinese economic
giant that is emerging and spreading its reach to the rest of Asia and the world.
The economy -- at more than $4 trillion it is 22 times bigger than it was in
1978 -- has led the charge toward renewal of what many Chinese regard as their
rightful influence on the country¡¯s Asian neighbors. China is the biggest investor
in Mongolia, for instance, and buys more than half its cashmere. China has challenged
Russia for influence in several Central Asian countries, including Kazakhstan
and Kyrgyzstan, where Chinese investments vie with Moscow¡¯s and Chinese bicycles,
electronic goods and other gadgets are pushing Russia¡¯s out.
To the south, China has improved ties with Vietnam, and Chinese firms are some
of the most aggressive investors in that country. Chinese firms have also plowed
money into Nepal and Cambodia.
China¡¯s growing economic influence has sometimes aroused passions in the region.
Mongolia moved several years ago to ban Chinese firms from participating in
its privatization process. Government and cashmere industry officials routinely
blame China for the collapse of their textile industry. Local officials in Siberia
have spoken about their fears of a "Chinese invasion," although negotiations
are underway for Chinese crews to cut down trees in Russia.
Here in Pianma, where men saunter the streets with pistols and prostitutes gather
on street corners offering laborers a quick massage and more, people have been
trading lumber for years. But the boom, truckers and lumberjacks say, really
began in 1998. That was the year China issued a ban on logging to protect its
fast-disappearing forests and to halt massive soil erosion that contributed
to deadly floods.
"You have a situation where an environmentally beneficial policy in China
created incentives to destroy forests in other parts of the world," said
Jim Harkness, director of the China office of WWF, a conservation organization
formerly known as the World Wildlife Fund.
From 12 provinces in 1998, the logging
ban was extended to 18 in 2000. No logging is allowed in the upper reaches of
the Yangtze or Yellow rivers, Logging has been reduced in Northeastern, Inner
Mongolia, the northwestern Xinjiang territory and elsewhere. In all 740,000
wood workers have been laid off, according to research by WWF. China¡¯s timber
production plummeted 97 percent from 1997 to 2000, when only 1 million cubic
meters were produced.
Preparations for China¡¯s entry into the World Trade Organization have also sparked
an increase in timber imports. Tariffs on forestry products have fallen drastically
as China seeks to prepare for a more open trading system. In many places around
China¡¯s borders, no tariffs are charged for logs.
In that atmosphere, thousands of out-of-work laborers flooded this town and
regions all along the borders after 1998, looking for wood to feed an unquenchable
demand for chopsticks, furniture and paper. China¡¯s imports of logs skyrocketed
from less than 5 million cubic meters in 1998 to more than 10 million in 1999
and between 14 million and 15 million last year.
Steven Johnson, a statistician at the International Timber Trade Organization,
estimates that within a few years China will surpass the United States, Japan
and the European Union as the world¡¯s biggest importer of logs, although its
imports of all wood products are still a fraction of the world total.
"The logging ban played a role," a World Bank official said, "but
the trend was already there. As China gets richer, it¡¯s natural that it will
consume more wood."
On paper, Burma supplies less than 10 percent of the imports, or 740,000 cubic
meters, according to statistics collected by the timber trade group. But no
one in this swath of western Yunnan Province believes those numbers.
"I would say it's about twice that high," said Li Jiajing, a 44-year-old
driver, who said he moved 1,000 cubic meters last year of teak, Chinese hemlock,
walnut, dragon spruce and Chinese pine, One recent day, he was preparing an
18-cubic-meter truckload of three teak logs; the trunks were more than 10 feet
in diameter, hundreds of years old.
Timber company officials estimate
that more than 350,000 cubic meters move through Pianma alone each year.£ Large
amounts also come into China from Burma at towns farther south along the border£ºTengchong,
Yingjiang, Zhangfeng, Ruili and Wanding. And a Malaysian timber firm is building
a bridge across the Salween River, 60 miles north of Pianma near Fugong, to
bring in still more logs.
In 1998, there were only 13 small sawmills in Dehong prefecture, a center of
the new logging trade. Now there are more than 100. Another 100 have sprouted
up around Tengchong.
China's activities in the Burmese rain forests are mirrored on its northern
border. Imports of Russian logs have skyrocketed over the past two years and
outstrip the number from Burma. Russia now accounts for 42 percent of all blocks
that flow into China. But Russia¡¯s wood comes mostly from forests that specialize
in faster-growing softwood, while Burma's comes from tropical forests where
the trees are often hundreds of years old.
"It's an international tragedy because Burma possesses about half of mainland
Southeast Asia's forests," said Kirk Talbot, a Washington-based expert
on Southeast Asian forests. "The combination of a military-backed junta
[in Burma] and unquenchable appetites in China is creating a disaster."
In theory£¬the military-run Myanmar Timber Enterprise controls all Burma's lumber
exports. But the Chinese are not dealing with the government from Rangoon across
from Pianma, for Burma's political system has conspired to facilitate the denuding
of its forests.
In 1988, Burma's military-led government annulled the results of an election.
Concerned that thousands of dissidents who fled Rangoon would be armed by insurgents
who have operated for decades along Burma's northern border, Burma's genera..ls
cut a deal with the rebel forces: In exchange for permission to engage in business,
the insurgents promised not to arm the dissidents.
Logging concessions were a key sweetener. Burma's generals gave these local
leaders access to logging machinery and milling equipment. Chinese businesses
were soon operating in Burma, bringing in lumberjacks and truckers and cutting
down forests.
Burma and Yunnan, the neighboring Chinese province, are home to an abundance
plant and animal life, from a dizzying variety of rhododendron species to the
lesser panda. There are more than 12,000 recorded species of trees in the region,
one of the most biologically diverse in the world.
Deforestation has ravaged its forests, however. In 1949, the year of China's
Communist revolution, half of Yunnan province was forested, but today it is
less than10 percent. In Burma, forest cover has dropped from 21 percent in 1949
to less than 7 percent today.
Environmentalists in Yunnan say the damage to Burma's forests along the border
has been severe. In 1997, one Yunnan-based conservationist reported that Chinese
loggers had cleared 35 miles into Burma, This year logging has moved 60 miles
inside Burma, he said.
"Burma used to be covered in huge trees like our Gaoligong Shan area just
across our border," said the environmentalist, who recently journeyed to
the border region. "Now you can climb to the top of their mountains and
all you see are roads and logging trucks and barely any trees."
Most of China's deals are done with warlords in Burma's Kachin state, which
borders China.
"The warlords basically run one region and so they sell us all of their
mountains," said Wang Jian, a businessman based in Pianma. "We're
in a difficult position because they change warlords all the time. So our incentive
is, once we get the contract,£¬cut all the logs. So we clearcut. If we don¡¯t,
and they change the warlords we're going to have to pay him as well."
That has angered China¡¯s environmentalists, who note that while China bans the
logging of its own hardwood forests, its policies encourage lumberjacks and
smugglers to cut down rare trees and snare endangered animals in Burma and Laos.
But Kou Wenzhong, a senior official
in China's forestry department, said Chinese firms have a hard time making money
in the region despite the absence of regulation.
"We're trying to pay attention to Burma's environment as well," he
said in an interview in Beijing, "but when a warlord is changed over there,
they rip up the contract and things get very difficult. Lots of contracts have
been broken. There have been serious losses."
-- John Pomfret, Washington Post
Monday, March 26, 2001
To be or not to be for Saker Falcon in Central
Asian countries?
-- Realities and perspective of Saker
Falcon survival in Kazakhstan
Using big falcons in hunting for
birds - prey is a big part of cultural heritage of many nations that inhabit
huge Eurasian territories from Saudi Arabia in the West to Mongolia and China
in the East and from Russia in the North to Afghanistan, Pakistan and India
in the South. To the end of 20th
century traditional falcon hunting stayed mainly in countries of Close and Middle
East. Bird that is preferred by Arab hunters is Saker Falcon, because it is
used to living in the conditions of high temperature and dry air of arid zone
and also has excellent hunting characteristics.
As many other former Soviet Union republics, Kazakhstan was closed for foreigners
a long time and for international society is "terra incognita" in
some way. This, and also no demand for Saker falcon on the national market let
Saker falcon live freely until early 90s. This species was stable and its population
number counted by specialist was from 2 up to 5 thousands of pairs. When USSR
collapsed, new era of new independent countries' establishment began that also
opened a new page in the lives of flying, running and crawling inhabitants.
The most tragic is Saker Falcon destiny, that in several years from blooming
species went down to the species that are on the border of disappearing. Tragedy
sizes could be vividly illustrated by following fact: according to monitoring
results that was taken by Institute of Zoology specialists from 1985, to 2000
year in Kazakhstan from several thousands not more that 150-200 nesting pairs
remained. According to materials of international conference held in Mongolia
in July of 2000 that set a goal of discussing the problem falcon conservation
in Eurasia, it is not better in other republics of Central Asia. For example,
in Kyrghyzstan and Uzbekistan Saker falcon population number also decreased
down to critical point and is not more that 100 and 150 pairs accordingly.
So what has happened? Why on the border of millenniums, characterized by really
high level of science and technology developing, this ecological tragedy took
place, that put not only Saker falcon, but many other rare species of Central
Asia on the survival border? Who is guilty in what had happened? Is it possible
to change the situation, stop the hunting for this species and restore its normal
population number? It is necessary to give straight answers to those questions,
or else in the nearest future we will witness Saker falcons repeating Dinosaurs
destiny (knowing that we are guilty in it).
Saker falcon protection problem was pointed out in the first years of Kazakhstan
establishment. Mass hunting for big falcons of the republic began in 1992, when
the republic was crowded by a huge wave of hunters from many Arab East countries.
Their goal was easy - there was no strict nature-conserving laws, no problems
with customs, hard material circumstances of local people and totally corrupted
bureaucrats. According to experts' counts in the period from 1993 to 1995, yearly
up to a thousand birds were illegally taken out of the country! Because of understandable
reasons (international airport, good roads, and most importantly - high density
of Saker falcon nests) main target for falcon hunting was South-East of the
country, where, according to annual nesting territories monitoring results,
Saker falcon population from 1993 to 1998 reduced in 8-10 times. Many previously
densely inhabited by falcons mountain ridges nowadays are completely devastated.
At the same time with foreign citizens lots of Kazakhstan people took active
participation part in falcons hunting. Falcon rush was warmed up by many rumors
and reports on the radio and television about Saker falcons fabulously high
cost, that on the Saudi Arabia markets gets as high as 75 thousand dollars.
Hard material circumstances of country people, often pasturing cattle near nests
of birds-of-prey, and also many rural citizens that know about falcons existence
only from other people's conversations, stimulated people's desire to get "easy
money".
Beginning with 1993, the situation became worse every day, because pressing
on the species increased with lots of incoming groups and widening their "affairs"
geography. Non-professional local hunters were replaced by organized groups
that used government support. Hope for Saker falcon conservation became very
illusory, when this species became an instrument of national politics. Government
members, high-ranked workers of nature-conserving agencies, and in some cases
even representatives of science - all those people that wanted to correct their
material conditions provided an opportunity of illegal hunt and taking the birds
out of Kazakhstan.
Examples of right treat of Saker falcons are shown by Austria and Hungary that
are located on the West border of this species' area, and in the East a good
example of rational treat of national possession is Mongolia. Even with big
population numbers in the republic (about 3000 pairs) and not having it in the
national Red Data Book list, this country sells only several dozens of birds
a year, which doesn't harm the population. It is interesting that almost all
money got from this trade are put into ecological problems salvations.
Actions coordination of countries territory of which is inhabited by falcons
became possible thanks to big international scientific program, started by National
Ornithological Research Center (NARC, UAE) in 1989 that united international
society attempts, interested in conservations and rational use of species' resources.
Owing to this program annual monitoring of nesting territories of Saker falcon
was done in Kazakhstan and other republics of Central Asia, biology and seasonal
migrations were studied. Created in 1995 Middle-Eastern work group made recommendations
oriented on population numvers stabilization and its further increasing. Main
features of those recommendations is following:
1. transparency provided to all operations with falcons in Kazakhstan;
2. prohibition on taking adult birds out of the border of the country;
3. marking with microchips all falcons taken abroad for identification;
4. giving hunting permissions according to results of control of Kazakhstan
populations conditions;
5. developing of legal act that would control taking in, using and taking out
of the country falcons taking in donsiderations CITES requirements.
After the recommendations were given to the government "Temporary rules
on usage of Saker falcon and Houbara bustard on Kazakhstan territory" was
published. This legal act doesn't count most of the recommendations points and
leaves ways for illegal affairs. Even more strange is reaction of Ministry of
Ecology and Bioresources of information about species critical conditions in
the republic. Knowing that there is not more that 200 pairs, this Ministry in
the summer of 2000 demanded from Institute of Zoology sanction for catching
of 200 birds!
From the facts above it is clear that the destiny of Kazakhstan Saker falcon
is in the "right" hands. Last actions of Ministry of Ecology and Natural
resources of Republic of Kazakhstan give us reasons to think that bureaucrats
do everything to do till the end affair begun in the 1992 and use this species
resource completely. Only joining the Convention of International Trade by Endangered
Species (CITES) in 2000 leaves a hope that the government would be forced to
finally turn their face to the nature, to the law, and make everything needed
for conservation Saker falcon and all other endangered species that live on
the Kazakhstan territory.
A.S Levin, Member of Middle-Eastern work group on falcons
Features of Invasive Species in China
![]() |
| Removing Water hyacinth by hands in Dianchi, Yunnan. Picture by XIE Yan |
8. Intentional or unintentional introductions when restoring the natural vegetation.
![]() |
| Large scale planting of Eucalyptus in Return Farmland into Forest in Sichuan, Picture by XIE Yan |
For many years, government departments of agriculture, forestry, and
animal husbandry, as well as customs authorities in China, have paid great attention
to the potential harm of a small number of
alien species, leading to the quarantine of alien diseases and pests. However,
it was only a few years ago that the concept of invasive species was introduced
into China and the potential threats to China¡¯s natural heritage are not yet
widely recognized. Not enough attentions are paid to those have not caused severe
economic damage but are competing with and substituting for the endemic species
and changing the local ecosystems. Therefore, intentional or unintentional introductions
of alien species when restoring the natural vegetation on a large scale will
necessarily bring the great loss of Chinese abundant and endemic biodiversity
and beyond retrieval. At present, the introductions of alien species on a large
scale in China include:
Partial List of Invasive Species in China
Mammals£º
Nutria (Myocastor coypus)
Musk rat (Ondatra zibethicus)
Brown rat (Rattus norvegicus)
Birds£º 
Sulphur-crested cockatoo (Cacatua sulpurea)
Rainbow lorikeet (Trichoglossus haematotus)
Canada goose (Anser canadensis)
Reptiles:
(Trachemys scripta elegans)
Amphibians:
Bull frog (Rana catesbeiana)
Marine toad (Bufo marinus)
Fishes£º
Bighead (Aristichthys nobilis)
Gobies (Gobiidae)
Topmouth Gudgeon (Pseudorasbora parva)
Mosquito fish (Gambusia affinis)
Livebearers (Poeciliidae)
Perch (Perca fluviatilus)
Silver carp (Hypophthalmichthys molitrix)
Crustaceans£º
Crayfish (Procambius clarkii)
Mollusks£º
Amazonian snail (Ampullaria gigas)
Giant Africa snail (Achatina fulica)
Insects£º
(Termite)
Pine Scale (Hemiberlesia pitysophila)
American White Moth (Hyphantria cunea)
Banana moth (Opogona sacchari)
Loblolly pine mealybug (Oracella acuta)
Vegetable Leaf Miner (Liriomyza sativae)
American rice water weevil (Lissorhoptrus oryzophilus)
American Cockroach (Periplaneta americana)
German Cockroach (Blattella germanica)
Woolly Apple Aphid (Eriosoma lanigerum)
Grape Root Louse (Phylloxera vitifolii)
Nematode:
North American pinewood nematode (Bursaphelenchus xylophilus)
Fungi£º
Black Spot (Ceratocystis fimbriata)
Wildlife Diseases£º
Infectious Pancreatic Necrosis Virus in trout (IPNV)
Plants£º
Mexican Tea (Chenopodium ambrosioides)
Alligator weed (Alternanthera philoxeroides)
Spingflower Alternanthera (Alternanthera pungens)
Amaranth (Amaranthus)
Cacti (Cactaceae)
Golden Dewdrop (Duranta repens)
Love Apple (Solanum aculeatissimum)
Plantaiga (Plantaginaceae)
Venus' Looking-glass (Triodanis)
Tropic Ageratum (Ageratum conyzoides)
Ragweed (Ambrosia)
Fleabance (Conyza)
Daisy Fleabane (Erigeron annuus)
Crofton weed (Eupatorium adenophorum)
South American Climber (Mikania micrantha)
Tall goldenrod (Solidago altissma)
Common cordgrass (Spartina anglica)
Darnel ryegrass (Lolium temulentum)
Water hyacinth (Eichhornia crassipes)
Palmate-leaved Morning Glory (Ipomoea cairica)
Ivygourd (Coccinia cordifolia)
Common Lantana (Lantana camara)
Virginia Creeper (Parthenocissus quinquefolia)
Common Cat's Claw Vine (Macfadyena unguis-cati)
Trilobe Wedelia (Wedelia trilobata)
Castor-oil Plant (Ricinus communis)
Common Parthenium (Parthenium hysterophorus)
Madeira Vine (Anredera cordifolia)
Yellow Sweetclover (Melilotus officinalis)
White Sweetclover (Melilotus albus)
Tubeleaf Kalanchce (Kalanchoe tubifolia)
Weeping Lantana (Lantana montevidensis)
Oleanderleaf Nothoscordum (Nothoscordum gracile)
Tall Fescue (Festuca arundinacea)
Blue Trumpet Vine (Thunbergia graniflora)
Odor Eupatorium (Eupatorium odoratum)
Prickly Pear (Opuntia monacantha)
Coromandel Coast Falsemallow (Malvastrum coromandelianum)
Timothy (Phleum pratense)
Carpetgrass (Axonopus compressus)
Ramose Scouring Rush (Equisetum ramosissimum)
Caterpillar Grass (Paspalum dilatatum)
West African Pennisetum (Pennisetum clandestinum)
Knotroot Bristlegrass (Setaria geniculata)
Sudangrass (Sorghum sudanense)
Italian Ryegrass (Lolium multiflorum)
Bulbous Barley (Hordeum bulbosum)
Alfalfa (Medicago sativa)
Mexican Ageratum (Ageratum houstonianum)
Tinctorial Coreopsis (Coreopsis tinctoria)
Lance Coreopsis (Coreopsis lanceolata)
Corntfower (Centaurea cyanus)
Aztec Marigold (Tagetes erecta)
Whiteedge Morning Glory (Ipomoea nil)
Common Morning Glory (Ipomoea purpurea)
Four-o¡¯clock (Mirabilis jalapa)
Pink Woodsorrel (Mimosa pudica)
Corymb Wood Sorrel (Oxalis corymbosa)
Hemp (Cannabis indica)
Sensitiveplant-like Senna (Cassia mimosoides)
Sickle Senna (Cassia tora)
Panicled Fameflower (Talinum paniculatum)
Coffee Senna (Cassia occidentalis)
Common Pokeweed (Phytolacca americana)
Hawksbeard Velvetplant (Crassocephalum crepidioides)
Common Chicory (Cichorium intybus)
XIE Yan and LI Zhenyu
1591 Species of Wild Animals Recorded
on Protection List
On the List of National Protected
Terrestrial Animals Which Are Beneficial or of Important Economic and Scientific
Research Values (hereafter the ¡®List¡¯) recently issued by the State Forestry
Administration (SFA), 1591 species of wildlife are recognized as protected objects.
The List includes five classes: Mammalia, Aves, Amphibia, Reptilia and Insecta,
totaling 46 orders and 177 families. This group of protected terrestrial wildlife
does not include the 335 species on the List of State Key Protected Wildlife.
It is reported that China is very abundant in the wildlife resource, with 6266
species of vertebrate. In 1988, China constituted the State Wildlife Protection
Law, to which the List of Key Protected Wildlife is attached. All provinces,
autonomous regions and cities also accordingly drew up local list of protected
wildlife. However, the key protected wildlife by the state and local governments
only account for a small part of China¡¯s whole wildlife resource. Besides these,
there are still many wildlife species which have irreplaceable functions in
the maintenance of environment, and they are also important natural resource
for the sustainable development of national economy. According to the provision
of the State Wildlife Protection Law that ¡®The list of national protected terrestrial
wildlife which are beneficial or of important economic and scientific research
values and its amendment are established and publicized by the forestry administration
department of the State Council¡¯, the SFA prepared and issued the List.
The related principal of the SFA indicated that the issuance of the List further
pinpoints the range and responsibilities of the wildlife protection in China,
and establishes another statute base for the protection of wildlife. Implement
of this List will provide potential safeguard for the advance of balanced law
execution, macro control of gross resource wastage, and promotion of resource
increase and ecological equilibrium.
ZHAO Cheng, People¡¯s Daily, 31/8/2000
Translated by QIN Hua
Degradation in Protected Areas: The Case
of Wolong Nature Reserve for Giant Pandas
Jianguo Liu
,
* Marc Linderman
, Zhiyun Ouyang
, Li An
,
Jian Yang
, Hemin Zhang![]()
It is generally perceived that biodiversity is better protected from human activities after an area is designated as a protected area. However, we found that this common perception was not true in Wolong Nature Reserve (southwestern China), which was established in 1975 as a "flagship" protected area for the world-renowned endangered giant pandas. Analyses of remote sensing data from pre- and post-establishment periods indicate that the reserve has become more fragmented and less suitable for giant panda habitation. The rate of loss of high-quality habitat after the reserve's establishment was much higher than before the reserve was created, and the fragmentation of high-quality habitat became far more severe. After the creation of the reserve, rates of habitat loss and fragmentation inside the reserve unexpectedly increased to levels that were similar to or higher than those outside the reserve, in contrast to the situation before the reserve was created.
More than 12,700 protected areas have been established around the world, accounting
for 13.2 million km
(an
area greater than the United States or China), or 8.81% of Earth's land surface
(1). Although protected areas are generally believed to be the cornerstones
of biodiversity conservation (2-4) and the safest strongholds of wilderness
(2, 5, 6), human encroachments and threats are still very common in many protected
areas (7, 8). The problems of mismanagement and conservation politics have been
widely publicized (7, 9), but quantitative information about the deterioration
of protected areas is scant (10). It is not clear whether all protected areas
are effectively protected because there is little research comparing ecological
degradation before and after the protected areas were established.
Is the rate of ecological degradation lower after the establishment of a protected
area? To answer this question, we performed a case study of Wolong Nature Reserve,
Sichuan Province, southwestern China (102¡ã52' to 103¡ã24'E, 30¡ã45' to 31¡ã25'N).
We chose Wolong for three main reasons. First, it is the largest protected area
designated for conserving the endangered giant pandas [Ailuropoda melanoleuca
(11)] and contains approximately 10% of the wild panda population (12);
created in 1975, the reserve covers an area of approximately 200,000 ha (12).
Second, as in many other protected areas, there are local people residing in
Wolong. Third, Wolong is a "flagship" nature reserve and has received
exceptional financial and technical support from the Chinese government and
many international organizations, such as the World Wildlife Fund (WWF) (9).
To a large extent, Wolong's ecological fate represents the success or failure
of tremendous conservation efforts made by the Chinese government and many international
organizations (9).
We assessed the rates of change in forest cover and giant panda habitat before
and after Wolong was established as a nature reserve. Forest cover, slope, and
elevation are important factors affecting pandas (11, 12). We incorporated these
factors to estimate habitat suitability for pandas. In a process similar to
hurricane damage assessment examining pre- and post-hurricane conditions (13,
14), we quantified forest cover before and after the reserve's establishment,
using remotely sensed data obtained at three different time points (15). The
different sources of data used in our study are typical of many studies of land
use and land cover change (16-18), because it is unrealistic to obtain remote
sensing data on the same characteristics over a long period of time because
of changes in the sensors.
Neither aerial photography nor multi spectral data were available for the entire
time span of this study. Although cloud-free images with consistent phenology
were not available, leaf-off [Corona data and Landsat Multispectral Scanner
(MSS) data] versus leaf-on [Landsat Thematic Mapper (TM) data] conditions did
not contribute significantly to the forest and panda habitat analyses for two
reasons. First, our classifications were simple and consisted of only forest
and nonforest categories. Second, because the 1997 image was acquired during
leaf-on conditions, the analyses would give a more conservative estimate of
forest loss. The images taken at different times were classified by means of
photo interpretation, and the classifications were validated using several methods
to ensure high quality (19).
In the reserve, elevation ranges from 1200 to 6250 m above sea level. Pandas'
preferred areas are between 2250 and 2750 m above sea level (11, 12). [Because
of the limitations of abiotic factors such as elevation, even without human
impacts less than half of the reserve is suitable for the panda (12).] Data
on forest cover were obtained from the remote sensing analyses discussed above,
whereas the slope and elevation values for each pixel were calculated from a
digital elevation model that we developed using the topographic maps provided
by the reserve. Using previously established habitat analysis procedures (12)
and previous studies on pandas' biological requirements (11), panda habitat
suitability was defined and divided into four categories: highly suitable, suitable,
marginally suitable, and unsuitable (12). (Unsuitable habitat would be underestimated,
because information regarding several factors affecting panda habitat, such
as bamboo distribution, was not available for the entire reserve and was thus
not considered in this study.) We then calculated the numbers and sizes of habitat
patches as measures of the degree of habitat fragmentation (20) at each time
point, using the FRAGSTATS program (21).
The average rates of change per year (in the amount of panda habitat, the number
of habitat patches, and mean patch sizes) before and after the reserve's establishment
were calculated in order to make appropriate comparisons, because the lengths
of the pre-establishment period (1965-1974) and post-establishment period (1974-1997)
were different. [When calculating rates of changes during pre- and post-establishment
periods, we substituted the 1974 data for the data from 1975 (March), when the
reserve was officially established, because of a lack of cloud-free remote sensing
imagery from 1975. This data substitution should not generate a significant
bias, because according to our interviews with local residents and reserve managers,
human disturbance to the panda habitat in 1974 was not much greater than that
during the previous years.] We also compared rates of change in panda habitat
inside the reserve to those outside (where habitat is not protected), a method
similar to the methods of spatial comparisons used in past studies (4, 22, 23).
The "outside" was defined as a surrounding area (62,656 ha) within
3 km around the reserve boundary, because it shared similar biophysical characteristics
(such as elevation) with the reserve.
The quantity and quality of panda habitat inside the reserve continued to decrease
after the reserve was created (Fig. 1). More surprising, the rates of panda
habitat change demonstrated that high-quality habitats were more severely affected
after the reserve was established (Table 1). The rates of change (the loss of
the total habitat area, decrease in the number of habitat patches, and reduction
in the mean patch size) in highly suitable habitats were much higher after the
reserve was set up than before the reserve's establishment (Table 1). For suitable
habitats, the rate of loss of the total area after the reserve's establishment
was lower than that before the reserve was established, but the rate of reduction
in mean patch size was higher after the reserve was created. The number of habitat
patches actually increased after the reserve was established. For marginally
suitable habitats, the rates of loss and reduction in the number of patches
were lower after the reserve was established, whereas mean patch sizes increased
slightly. Rates of change (the increase in the total area, reduction in the
number of patches, and increase in mean patch sizes) in unsuitable habitats
were lower after the reserve was established. 
Fig. 1. Change in the amount
of panda habitat in Wolong Nature Reserve before and after the reserve was established
in March 1975. (A) Highly suitable habitat, (B) suitable habitat, (C) marginally
suitable habitat, and (D) unsuitable habitat.
Although the rates of habitat loss inside the reserve were lower than those
outside the reserve before the reserve was created, after the designation of
reserve status, the rates of habitat loss and fragmentation inside the reserve
unexpectedly and dramatically increased to levels that were similar to or higher
than those outside the reserve (Table 2). Furthermore, the differences in the
rates of loss and fragmentation between inside and outside the reserve were
particularly large for highly suitable habitats. For suitable abitats, the rate
of habitat loss inside the reserve reached the same level as that in the surrounding
area after the reserve was established. The rate of reduction in the mean patch
size inside the reserve became even higher than that outside the reserve after
the reserve's establishment. The amount of marginally suitable habitats increased
outside the reserve but decreased inside the reserve after the reserve was established.
The mean patch sizes of marginally suitable habitats continued to increase both
inside and outside the reserve after the reserve was created. Both the amounts
and mean patch sizes of unsuitable habitats inside and outside the reserve increased
over time. The gap between the rates of increase in the amount of unsuitable
habitats inside and outside the reserve has almost doubled since the reserve's
establishment. Although the ratios of rates of increase in the mean patch sizes
of unsuitable habitats inside the reserve to those outside the reserve slightly
decreased after the reserve was created, the rate of increase in the mean patch
sizes was still higher inside the reserve than outside.
Table 1. Ratios of mean annual rates of change (the amount of panda habitat, number of habitat patches, and mean patch size) after the reserve's establishment to those before the reserve was created. A ratio of >1 indicates that the absolute rate of change after the reserve's establishment was higher than that before the reserve was established. The signs within parentheses represent the directions of change ("+" indicates an increase and "-" indicates a decrease) before and after the reserve was established, respectively.
| Habitat type | Amount of habitat | Number of patches | Mean patch size |
| Highly suitable | 5.54 ( -, - ) | 1.85 ( -, - ) | 22.30 ( -, - ) |
| Suitable | 0.56 ( -, - ) | 0.78 ( -, +) | 1.11 ( -, - ) |
| Marginally suitable | 0.07 ( -, - ) | 0.25 ( -, - ) | 0.07 ( -, +) |
| Unsuitable | 0.46 (+, +) | 0.36 ( -, - ) | 0.52 (+, +) |
Table 2. Ratios of mean annual rates of change (the amount and mean patch size of panda habitats) inside the reserve to those outside the reserve, before and after the reserve was established. A ratio of <1 indicates that the absolute rate of change inside the reserve was lower than the rate outside the reserve; a ratio of >1 indicates that the absolute rate of change was higher. The signs within parentheses represent the directions of change ("+" indicates an increase and "-" indicates a decrease between two time points), inside and outside the reserve, respectively.
| Habitat type | Amount of habitat | Mean patch size | ||
| Before establishment | After establishment | Before establishment | After establishment | |
| Highly suitable | 0.29 ( -, - ) | 1.15 ( -, - ) | 0.05 ( -, - ) | 4.38 ( -, - ) |
| Suitable | 0.71 ( -, - ) | 0.98 ( -, - ) | 4.37 ( -, - ) | 4.79 ( -, - ) |
| Marginally suitable | 0.61 ( -, - ) | 0.96 ( -, + ) | 1.01 ( -, - ) | 0.88 ( +, +) |
| Unsuitable | 0.64 (+, +) | 1.17 (+, +) | 1.28 (+, +) | 1.16 (+, +) |
The loss and fragmentation of panda habitats in Wolong were directly due to forest loss and fragmentation, which took two major forms (Fig. 2). First, forest fragments next to non forest land continued to shrink and disappear. Second, large tracts of forest were divided into smaller tracts. The loss and fragmentation of the forest and of high-quality habitats were at least partially responsible for the dramatic decrease in the number of wild pandas in the reserve, from 145 in 1974 (11, 24) to 72 in 1986 (25). Based on wildlife-habitat relationships (26) and the decreasing frequency of finding pandas in the wild (as indicated by our personal observations and by interviews with reserve biologists and local residents), the current number of wild pandas in Wolong is likely to be even smaller.
Fig.
2. Forest distribution pattern across Wolong Nature Reserve in 1997 (left),
with illustration of loss and fragmentation of forest (center) and panda habitats
(right) within a representative area before and after the reserve was established.
Gray areas are forested; those shown in white are nonforested. Highly suitable,
suitable, marginally suitable, and unsuitable habitats are indicated in red,
yellow, green, and black, respectively.
By examining the human population
and activities in the reserve, it is not difficult to explain the much higher
rates of loss and fragmentation of high-quality panda habitat after Wolong was
designated as a protected area. There were 4260 local residents and 904 households
inside the reserve in 1995, whereas there were only 2560 people and 421 households
in 1975 when the reserve was established (12). This rapid increase in the local
population was mainly due to the high birth rate (about 2.5 children per woman
in 1997) in the reserve (12), because China's one-child policy does not apply
to the members of the minority ethnic groups who account for approximately 75%
of the local residents (27). The rate of increase in the number of households
was even higher than the rate of the population increase because more young
people established new households rather than staying with their parents and
grandparents to live a traditional life-style, in which several generations
live under one roof. In addition to the rapid increase in the population size
and the number of households, the population structure has experienced a dramatic
change (27). From 1982 to 1996, the labor force (people 20 to 59 years of age)
of local residents in the reserve jumped by 60% (27).
Local people in the reserve were the direct driving force behind the destruction
of the forest and of panda habitat (27). Most of the labor force are farmers,
and there are a variety of economic activities in the reserve, including agriculture,
fuel wood collection, timber harvesting, road construction and maintenance,
Chinese herbal medicine collection, and tourism. The reserve attracts thousands
of tourists each year, and the booming tourism has helped to transform the reserve
from a closed economy to an open economy. For example, the tourism has significantly
stimulated the extraction of natural resources such as fuel wood to produce
marketable goods. These human activities in the reserve have had very negative
impacts on the forest and on panda habitat (12). After the forests with easy
access or close proximity to people were exhausted, forests in more remote areas
at higher elevations (often high-quality panda habitat) became targets of destruction
through activities such as fuel wood collection. In comparison, households outside
the reserve have tighter restrictions on birth rate and have become less dependent
on fuel wood as they have switched to coal, electricity, and other types of
energy. These socioeconomic differences are among the causes of the discrepancy
between the rates of habitat loss and fragmentation inside and outside the reserve.
Biodiversity conservation is faced with a much greater challenge than previously
thought because even a flagship protected area such as Wolong was not better
protected after its establishment. Quantitative analyses of pre- and post-establishment
conditions inside and outside protected areas produce insightful results and
provide much-needed information to develop strategies for truly effective biodiversity
conservation. Because most of the world's protected areas have been established
since the early 1970s (1), satellite imagery has been obtained at periodic intervals
since 1972, and aerial photographs of many regions date back years or even decades
earlier (16), it is also feasible to assess the effectiveness of many protected
areas on the basis of their pre- and post-establishment conditions, using the
approach presented here. To better understand the effectiveness of protected
areas and develop more feasible policies, it is essential to integrate ecology
with human demography, human behavior, and socioeconomic (12, 28).
REFERENCES AND NOTES
1. International Union for Conservation of Nature and Natural Resources (IUCN),
United Nations List of Protected Areas (World Conservation Monitoring Centre
and IUCN Commission on National Parks and Protected Areas, IUCN, Gland, Switzerland,
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3. S. L. Pimm and J. H. Lawton, Science 279, 2068 (1998) [ISI]
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DC, 1996).
8. C. P. van Schaik, R. A. Kramer, in Last Stand: Protected Areas and The Defense
of Tropical Biodiversity, R. Kramer, C. van Schaik, J. Johnson, Eds. (Oxford
Univ. Press, New York, 1997), pp. 212-230.
9. G. B. Schaller, The Last Panda (Univ. of Chicago Press, Chicago, IL, 1994).
10. C. P. van Schaik, J. Terborgh, B. Dugelby, in Last Stand: Protected Areas
and The Defense of Tropical Biodiversity, R. Kramer, C. van Schaik, J. Johnson,
Eds. (Oxford Univ. Press, New York, 1997), pp. 64-89.
11. G. B. Schaller, J. Hu, W. Pan, J. Zhu, The Giant Pandas of Wolong (Univ.
of Chicago Press, Chicago, IL, 1985).
12. J. Liu, et al., Conserv. Biol. 13, 1360 (1999) [ISI].
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[ISI].
14. K. Basnet, G. E. Likens, F. N. Scatena, A. E. Lugo, J. Trop. Ecol. 8, 47
(1992) [ISI].
15. The remotely sensed data used were Corona photographs from 1965, Landsat
MSS data from 1974 (the year right before the reserve was established), and
Landsat TM data from 1997. The Corona data are stereo pair photographs acquired
20 January 1965 as part of the Corona photo reconnaissance satellite project
(U.S. Geological Survey Eros Data Center, Sioux Falls, SD). Both Landsat MSS
(3 January 1974) and Landsat TM data (27 September 1997) were obtained from
China's Satellite Ground Station (Beijing, China).
16. T. M. Lillesand, R. W. Kiefer, Remote Sensing and Image Interpretation (Wiley,
New York, ed,3,1994)
17. D. A. Stow, D. Collins, D. McKinsey, Geocarto International 3, 3 (1990)
.
18. J. R. Jensen, Introductory Digital Image Processing: A Remote Sensing Perspective
(Prentice Hall, Upper Saddle River, NJ, ed. 2, 1996).
19. All images were geo referenced to ground control points collected throughout
the reserve, using Global Positioning System (GPS) receivers (Pathfinder Pro
XRS) with sub meter accuracy. Because the Corona data are black-and-white photos,
we did a forest/non forest classification using photo interpretation (or visual
classification) to provide a consistent methodology for each of the three time
points (1965, 1974, and 1997). The area of interest within each Corona photo
was scanned into a digital image at 1200 dots per inch, giving a ground resolution
of approximately 10 m. The individual Corona images were then combined into
a single coverage and were classified on the basis of photo interpretation.
To enhance the classification accuracy, we used general vegetation delineations
on topographic maps, field observation information, interviews with local residents,
and observations of areas that were undisturbed over time. The Landsat MSS and
TM data were classified with the same procedure used for the Corona photos.
To provide consistency, the visual interpretations of the Landsat data were
done using false-color infrared images with similar band combinations (MSS bands
4, 5, and 6 and TM bands 2, 3, and 4), and the TM images (30 m by 30 m) were
degraded and resampled to a resolution of 80 m by 80 m. To validate the visual
interpretations, we surveyed 250 ground-truth plots (the size of each plot was
equal to 60 m by 60 m, or 2 ¡Á 2 TM image pixels) in the summers of 1998 and
1999 in the reserve, using GPS units (with 1- to 3-m accuracy after differential
corrections), and we used digital methods [supervised and unsupervised classifications
(16, 18)] based on all four MSS bands and on comparable TM bands to classify
the Landsat MSS and TM imagery¡£The overall correspondences between the digital
and visual classifications ranged from 82 to 87%. Based on standard accuracy
assessment methods (16), the accuracy for forest classifications of the 1997
TM data using visual and digital methods was between 80 and 88% when the results
were compared with the independent data from the ground-truth plots. The visual
and digital methods resulted in consistent total forest areas (the forest areas
resulting from the digital methods were only 0.61 to 5.76% different from those
resulting from the visual method). These testing results indicate that the visual
classifications in our study were of high quality and comparability
20. R. T. T. Forman, Land Mosaics: The Ecology of Landscapes and Regions (Cambridge
Univ. Press, Cambridge, 1995).
21. K. McGarigal, B. J. Marks, FRAGSTATS: Spatial Pattern Analysis Program for
Quantifying Landscape Structure (Version 2.0) (Oregon State Univ. , Corvallis,OR,
1994).
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K. S. Bawa, Conserv. Biol. 13, 407 (1999) [ISI].
23. T. M. Caro, et al., Afr. J. Ecol. 36, 303 (1998) [ISI].
24. Giant Panda Expedition, Acta Zool. Sin. 20, 162 (1974) (in Chinese)
25. China's Ministry of Forestry and WWF, Conservation and Management Plan for
Giant Pandas and Their Habitat (Beijing, China, 1989) (in Chinese).
26. M. L. Morrison, B. G. Marcot, R. W. Mannan, Wildlife-Habitat Relationships:
Concepts and Applications (Univ. of Wisconsin Press, Madison, WI, 1992).
27. J. Liu, Z. Ouyang, Y. Tan, J. Yang, H. Zhang, Popul. Environ. 21, 45 (1999)
[ISI].
28. J. Liu, Ed., Integration of Ecology with Human Demography, Behavior, and
Socioeconomics, Ecol. Model. (special issue), in press.
29. We thank S. Pimm, C. Lepczyk, J. Qi, and two anonymous reviewers for helpful
suggestions and comments on earlier drafts of this paper; D. Rutledge, A. Thomas,
and J. Xie for technical assistance; Q. Wang, S. Song, W. Taylor, and the Wolong
Nature Reserve for logistic support (especially the assistance of J. Huang,
Y. Tan, and S. Zhou); and NSF, NASA, NIH, the American Association for the Advancement
of Science/The John D. and Catherine T. MacArthur Foundation, Michigan State
University, the National Natural Science Foundation of China, the Ministry of
Science and Technology of China (grant number G2000046807), and China Bridges
International for financial support.
10.1126/Science.1058104
¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡
Department
of Fisheries and Wildlife, 13 Natural Resources Building, Michigan State University,
East Lansing, MI 48824, USA.
*To whom correspondence should be addressed. E-mail: jliu@panda.msu.edu
Department of Systems Ecology,
Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences,
Beijing, China.
China's Center for Giant Panda
Research and Conservation, Wolong Nature Reserve, Wenchuan County, Sichuan Province,
China.
China Commences to Establish State-level
Ecological Function Reserves
The State Environment
Protection Administration (SEPA) formally approved of setting up ten experimental
units of state-level ecological function reserves in nine provinces (or autonomous
regions) recently. According to the news promulgation meeting of SEPA held yesterday,
this is the first group of experimental units of state-level ecological function
reserves in China.
These nine provinces (or autonomous regions) are Inner Mongolia, Heilongjang,
Jiangxi, Hunan, Sichuan, Shaanxi, Gansu, Qinghai and Xinjiang. The ten experimental
units of state-level ecological function reserves include: Ke¡¯erqin Sandland
Reserve at the north foot of the Yinshan Mountain, Sanjiang (three-river) Plain
Reserve, Poyang Lake Reserve, Dongting Lake Reserve, Ruo¡¯ergai-Maqu Reserve,
Qinling Mountains Reserve, Heihe Watershed Reserve, Changjiang Headstream Reserve,
Huanghe Headstrem Reserve and Talimu River Reserve. The program drafts of Changjiang
Headstream, Huanghe Headstrem, Heihe Watershed and Ke¡¯erqin Sandland reserves
have already been finished in advance.
Beijing Evening Paper, 23/3/2001 Translated by QIN Hua
Compilation of China's Biodiversity
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Beijing Window of Popular Science¡Ãhttp://www.bjkp.gov.cn/kxbl/smqy/kp0824.htm
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Guilin Environmental Protection¡Ãhttp://www.gll-gx.org.cn/hb/zrsht.htm
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Stories of Xinjiang Wild Animals: http://public.xj.cninfo.net/huanbao/wild/
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China Environmental Protection International¡Ãhttp://www.65.com.cn/
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http://www1.im.ac.cn/typecc/index.html
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