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Yifan Zhao al. Int. Journal of Engineering Research and Application www.ijera.com
ISSN : 2248-9622, Vol. 6, Issue 11, ( Part -2) November 2016, pp.38-41
www.ijera.com 38 | P a g e
Biodiversity hotspots of magnolia species in China
Yifan Zhao, Xiang Xu, Yao Xu, Qingqing Sun, Huayong Zhang*
(North China Electric Power University, Research Center for Engineering Ecology and Nonlinear Science,
Beijing, 102206, China)
ABSTRACT
Magnolia is one of the most primitive angiosperm families. Here, we delineated the biodiversity hotspots of
magnolia species in China based on secondary published plant atlas. We found that magnolia species were
concentrated in southern China. Biodiversity hotspots identification algorithm revealed that roughly 1.6% of the
landmass in China supported 90% of magnolia species. Our results not only guide the biodiversity conservation
of magnolia species in China, but also improve the understanding of the hidden ecological processes. These will
be helpful for the further exploration of environmental determinants explaining the spatial pattern of magnolia
species richness.
Keywords-Biodiversity hotspots, Conservation, Ecological processes, Identification algorithm, Magnolia
species
I. INTRODUCTION
Magnoliaceae, the magnolia family, is one
of the most primitive extant lineages of angiosperms
(93.5-110 mya), and therefore has important
contributions towards our understanding of the
origin and diversification of flowering plants [1].
Conservation assessments published by the
International Union for the Conservation of Nature
(IUCN) show that at least 48% of magnolia species
are threatened with extinction in the wild, mainly as
a consequence of the extensive logging and habitat
loss due to agriculture and livestock farming [2].
Accordingly, there is an urgent need to identify the
biodiversity hotspots and thus to pinpoint the
conservation priority for this family [1, 2]. Magnolia
family comprises over 300 species which are mainly
distributed throughout southeastern Asia and tropical
America [2]. Asia is the home to approximately two-
thirds of the species and China is considered as the
country with the richest magnolia species all over
the world. Consequently, magnolia species in China
provides an excellent circumstance for
understanding the spatial structure in species
richness and exploring the underlying mechanisms.
In this paper, we aim to identify the biodiversity
hotspots of magnolia species in China. This work
may delineate the biodiversity distribution and
provide the management guidance for the
biodiversity conservation of magnolia species in
China.
II. MATERIALS AND METHODS
2.1. Species Richness Data
Based on the recently published book Atlas
of Woody Plants in China [5], we obtained
distribution maps for 111 magnolia species using
ArcGIS 10.3 [6].This book provides one of the most
comprehensive databases for species distribution in
China. It compiled the country level occurrence for
all 13,570 native woody species in China using
extensive literature (such as floras, references on
nature reserves, monographs of field investigations,
scientific articles and specimen records). 26 experts
on botany, ecology and taxonomy from different
regions of China have checked each species
distribution to improve the precision of this database
[5]. Magnolia species are mainly distributed in the
southern China: virtually all regions of Taiwan,
Hainan, Yunnan, Guangxi, Guangdong, Sichuan,
Guizhou, Chongqing, Hubei, Jiangxi, Fujian,
Zhejiang and Shanghai, part of Tibet, Gansu,
Shaanxi, Henan, Anhui and Jiangsu (Fig. 1). Only
one species Oyama sieboldii is distributed in the
northeastern China. Oyama sieboldii is widely
distributed both in the northeastern and southern
China. The 111 magnolia species comprise of 82
species characterized by the evergreen life-form, and
29 species with the deciduous life-form [5]. In order
to reduce the effect of area on species richness, we
divided the study area into equal-area quadrats of
100 km × 100 km with Albers cubic equal area
projection. We excluded the quadrats which cover
landmass < 50% of a full-sized quadrat to control
area effect, as done in previous studies [7]. 111
magnolia species distribution maps were overlaid
with the quadrats, and the number of species present
at each quadrat was counted as species richness.
RESEARCH ARTICLE OPEN ACCESS
Yifan Zhao al. Int. Journal of Engineering Research and Application www.ijera.com
ISSN : 2248-9622, Vol. 6, Issue 11, ( Part -2) November 2016, pp.38-41
www.ijera.com 39 | P a g e
Figure 1. Distribution of provinces in China.
2.2. Hotspots Identification
Biodiversity hotspots recognize the
significant clustering distribution of species, which
not only guide conservation efforts and ecological
management [3], but also somewhat indicate the
spatial pattern in species richness. We applied the
complementary algorithm [8], whose principle is
determining the smallest number of quadrats that
contain all the species, to identify biodiversity
hotspots for magnolia species in China. Initially, the
quadrat with the maximum number of species was
chosen. All species found in the first chosen quadrat
were then excluded from the further consideration.
Secondly, the quadrat with the maximum number of
species that were not already chosen was selected. If
two quadrats have the same species richness, we
selected the quadrat with higher weighted species
richness. Weighted species richness was calculated
by summing up weights of the species present within
this quadrat, and weight of each species was defined
as the number of all quadrats where each species
was found. This process was conducted iteratively
until all 111 species were contained in the chosen
quadrats. Quadrats consisting of 90% species were
identified as hotspots [9, 10].
III. RESULTS AND DISCUSSION
Three quadrats located in Guizhou and
Yunnan comprised more than 40 species. Species
richness was lowest in the northeast and central
regions of China, and Taiwan, where quadrats
harbored only one species. Typically, Jilin and
Liaoning contained only one species Oyama
sieboldii (small deciduous tree); Shandong merely
supported Liriodendron chinense (deciduous tree)
and Oyama sieboldii; Hebei simply harbored
Yulania liliiflora (deciduous shrub) and Oyama
sieboldii; Taiwan also merely consisted of two
species Michelia compressa (evergreen tree) and
Parakmeria kachirachirai (evergreen tree). The
complementary algorithm manifested that 26
quadrats, which covered 2.7% of China’s land,
included all magnolia species (111 species). 15
quadrats occupied 1.6% of the landmass in China
and included 90% of the magnolia species (100
species). Consequently, these 15 quadrats were
recognized as the biodiversity hotspots, which were
mostly situated in the southern Yunnan (Fig. 2).
Both morphological and molecular
evidences have revealed that Magnoliaceae can be
considered as one of the most primitive angiosperm
family [1]. Thus, magnolia species are exceptionally
important in researches on biogeography and plant
evolution [11]. Additionally, magnolia species are of
remarkable value owing to their timber, medicinal
and food products and ornamental values, which
make magnolia species act as the attractive flagship
for plant conservation [2]. Here, we delineated the
magnolia species distribution in China and
discovered that the highest species richness appeared
in the southern China and especially clustered in
Guizhou, Yunnan and Guangxi (Fig. 2). While, the
quadrats supporting the lowest species richness
occurred in the Tibetan Plateau, Sichuan, Gansu,
Shaanxi, Henan, Anhui, Shandong, Hebei, Liaoning,
Jilin and Taiwan.
Many magnolia species are assessed as
threatened with extinction, and therefore it is
urgently needed to recognize the biodiversity
hotspots for planning conservation actions [2]. To
achieve this goal, we employed the complementary
algorithm to select 15 quadrats (each quadrat
covered the area of 104 km2
) which encompassed
90% of 111 magnolia species in China as the
hotspots [8, 9, 10]. Most of the quadrats denoted as
hotspots were distributed in the high altitudes due to
the heterogeneous habitats for plant species in the
mountainous regions, which was consistent with
previous reports [4, 10, 12, 13]. Typically, the first-
order selected quadrat was located at the
southeastern Yunnan, which consisted of 44.
Yifan Zhao al. Int. Journal of Engineering Research and Application www.ijera.com
ISSN : 2248-9622, Vol. 6, Issue 11, ( Part -2) November 2016, pp.38-41
www.ijera.com 40 | P a g e
Figure 2. Biodiversity hotspots for magnolia species in China. (a) Geographical distribution of hotspots: the
value of each quadrat represented the selection order through the complementary algorithm; (b) Relationship
between the number of cumulative species and the number of cumulative area.
Magnolia species and thus covered many
endangered species (Fig. 2). For instance, the
critically endangered and narrowly distributed
species Michelia coriacea (evergreen tree) retains
high levels of genetic diversity, mostly at the within-
population level [11]. Consequently, conservation
measures should focus on the establishment of
numerous seedlings, both in and ex situ, to preserve
as much as possible of the existing genetic diversity
[11].
IV. CONCLUSION
In this study, we identified the biodiversity
hotspots of magnolia species (one of the most
primitive angiosperm families) in China by the
published plant species atlas and identification
algorithm. The results showed that southern China
supported the most magnolia species and 90% of
magnolia species were concentrated in roughly 1.6%
of the landmass of China. This identification of
magnolia biodiversity hotspots in China is helpful
for biodiversity conservation of magnolia species in
China. Further research on the hidden ecological
processes behind the biodiversity hotspots of
magnolia species in China are needed to conduct.
ACKNOWLEDGEMENTS
We acknowledge with great appreciation
the support provided by National Special Water
Programs (No. 2009ZX07210-009, No.
2015ZX07203-011, No. 2015ZX07204-007),
Department of Environmental Protection of
Shandong Province (SDHBPJ-ZB-08), the China
Scholarship Council (No. 201306730020), the
Chinese Natural Science Foundation (No.
39560023).
REFERENCES
[1] Z.L. Nie, J. Wen, H. Azuma, Y.L. Qiu, H.
Sun, Y. Meng, W.B. Sun, and E.A.
Zimmer, Phylogenetic and biogeographic
complexity of Magnoliaceae in the
Northern Hemisphere inferred from three
nuclear data sets, Mol. Phylogenet. Evol,
48, 2008, 1027-1040.
[2] M. Rivers, E. Beech, L. Murphy, and S.
Oldfield, The Red List of Magnoliaceae:
Revised and Extended, Botanic Gardens
Conservation International: Richmond,
UK, 2016.
[3] C. Marchese, Biodiversity hotspots: A
shortcut for a more complicated concept,
Global Ecology and Conservation, 3,
(2015), 297-309.
[4] N. Myers, R.A. Mittermeier, C.G.
Mittermeier, G.A.B. da Fonseca, and J.
Kent, Biodiversity hotspots for
conservation priorities, Nature, 403, 2000,
853-858.
[5] J.Y. Fang, Z.H. Wang, and Z.Y. Tang,
(Eds.), Atlas of Woody Plants in China:
Distribution and Climate (Springer and
Higher Education Press, 2011).
[6] Environmental Systems Resource Institute
(ESRI), ArcMap 10.3.1. (Redlands, CA:
ESRI, 2015).
[7] Z.H. Wang, J.H. Brown, Z.Y. Tang, and
J.Y. Fang, Temperature dependence, spatial
scale, and tree species diversity in eastern
Asia and North America, Proc. Natl. Acad.
Sci. U.S.A, 106, 2009, 13388-13392.
[8] A.P. Dobson, J.P. Rodriguez, W.M.
Roberts, and D.S. Wilcove, Geographic
distribution of endangered species in the
United States, Science, 275, 1997, 550-553.
[9] V. Kati, P. Devillers, M. Dufrêne, A.
Legakis, D. Vokou, and P. Lebrun,
Hotspots, complementarity or
representativeness? designing optimal
small-scale reserves for biodiversity
conservation, Biol. Conserv, 120, 2004,
471-480.
Yifan Zhao al. Int. Journal of Engineering Research and Application www.ijera.com
ISSN : 2248-9622, Vol. 6, Issue 11, ( Part -2) November 2016, pp.38-41
www.ijera.com 41 | P a g e
[10] Z.J. Zhang, Y.J. Yan, Y. Tian, J.S. Li, J.S.
He, and Z.Y. Tang, Distribution and
conservation of orchid species richness in
China, Biol. Conserv, 181, 2015, 64-72.
[11] X.F. Zhao, Y.P. Ma, W.B. Sun, X.Y. Wen,
and R. Milne, High genetic diversity and
low differentiation of Michelia coriacea
(Magnoliaceae), a critically endangered
endemic in southeast Yunnan, China,
ISPRS Int. J. Mol. Sci, 13, 2012, 4396-
4411.
[12] J. López-Pujol, F.M. Zhang, and S. Ge,
Plant biodiversity in China: richly varied,
endangered, and in need of conservation.
Biodivers, Conserv, 15, 2006, 3983-4026.
[13] Z.Y. Tang, Z.H. Wang, C.Y. Zheng, and
J.Y. Fang, Biodiversity in China’s
mountains, Front. Ecol. Environ, 4, 006,
347-352.

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Biodiversity hotspots of magnolia species in China

  • 1. Yifan Zhao al. Int. Journal of Engineering Research and Application www.ijera.com ISSN : 2248-9622, Vol. 6, Issue 11, ( Part -2) November 2016, pp.38-41 www.ijera.com 38 | P a g e Biodiversity hotspots of magnolia species in China Yifan Zhao, Xiang Xu, Yao Xu, Qingqing Sun, Huayong Zhang* (North China Electric Power University, Research Center for Engineering Ecology and Nonlinear Science, Beijing, 102206, China) ABSTRACT Magnolia is one of the most primitive angiosperm families. Here, we delineated the biodiversity hotspots of magnolia species in China based on secondary published plant atlas. We found that magnolia species were concentrated in southern China. Biodiversity hotspots identification algorithm revealed that roughly 1.6% of the landmass in China supported 90% of magnolia species. Our results not only guide the biodiversity conservation of magnolia species in China, but also improve the understanding of the hidden ecological processes. These will be helpful for the further exploration of environmental determinants explaining the spatial pattern of magnolia species richness. Keywords-Biodiversity hotspots, Conservation, Ecological processes, Identification algorithm, Magnolia species I. INTRODUCTION Magnoliaceae, the magnolia family, is one of the most primitive extant lineages of angiosperms (93.5-110 mya), and therefore has important contributions towards our understanding of the origin and diversification of flowering plants [1]. Conservation assessments published by the International Union for the Conservation of Nature (IUCN) show that at least 48% of magnolia species are threatened with extinction in the wild, mainly as a consequence of the extensive logging and habitat loss due to agriculture and livestock farming [2]. Accordingly, there is an urgent need to identify the biodiversity hotspots and thus to pinpoint the conservation priority for this family [1, 2]. Magnolia family comprises over 300 species which are mainly distributed throughout southeastern Asia and tropical America [2]. Asia is the home to approximately two- thirds of the species and China is considered as the country with the richest magnolia species all over the world. Consequently, magnolia species in China provides an excellent circumstance for understanding the spatial structure in species richness and exploring the underlying mechanisms. In this paper, we aim to identify the biodiversity hotspots of magnolia species in China. This work may delineate the biodiversity distribution and provide the management guidance for the biodiversity conservation of magnolia species in China. II. MATERIALS AND METHODS 2.1. Species Richness Data Based on the recently published book Atlas of Woody Plants in China [5], we obtained distribution maps for 111 magnolia species using ArcGIS 10.3 [6].This book provides one of the most comprehensive databases for species distribution in China. It compiled the country level occurrence for all 13,570 native woody species in China using extensive literature (such as floras, references on nature reserves, monographs of field investigations, scientific articles and specimen records). 26 experts on botany, ecology and taxonomy from different regions of China have checked each species distribution to improve the precision of this database [5]. Magnolia species are mainly distributed in the southern China: virtually all regions of Taiwan, Hainan, Yunnan, Guangxi, Guangdong, Sichuan, Guizhou, Chongqing, Hubei, Jiangxi, Fujian, Zhejiang and Shanghai, part of Tibet, Gansu, Shaanxi, Henan, Anhui and Jiangsu (Fig. 1). Only one species Oyama sieboldii is distributed in the northeastern China. Oyama sieboldii is widely distributed both in the northeastern and southern China. The 111 magnolia species comprise of 82 species characterized by the evergreen life-form, and 29 species with the deciduous life-form [5]. In order to reduce the effect of area on species richness, we divided the study area into equal-area quadrats of 100 km × 100 km with Albers cubic equal area projection. We excluded the quadrats which cover landmass < 50% of a full-sized quadrat to control area effect, as done in previous studies [7]. 111 magnolia species distribution maps were overlaid with the quadrats, and the number of species present at each quadrat was counted as species richness. RESEARCH ARTICLE OPEN ACCESS
  • 2. Yifan Zhao al. Int. Journal of Engineering Research and Application www.ijera.com ISSN : 2248-9622, Vol. 6, Issue 11, ( Part -2) November 2016, pp.38-41 www.ijera.com 39 | P a g e Figure 1. Distribution of provinces in China. 2.2. Hotspots Identification Biodiversity hotspots recognize the significant clustering distribution of species, which not only guide conservation efforts and ecological management [3], but also somewhat indicate the spatial pattern in species richness. We applied the complementary algorithm [8], whose principle is determining the smallest number of quadrats that contain all the species, to identify biodiversity hotspots for magnolia species in China. Initially, the quadrat with the maximum number of species was chosen. All species found in the first chosen quadrat were then excluded from the further consideration. Secondly, the quadrat with the maximum number of species that were not already chosen was selected. If two quadrats have the same species richness, we selected the quadrat with higher weighted species richness. Weighted species richness was calculated by summing up weights of the species present within this quadrat, and weight of each species was defined as the number of all quadrats where each species was found. This process was conducted iteratively until all 111 species were contained in the chosen quadrats. Quadrats consisting of 90% species were identified as hotspots [9, 10]. III. RESULTS AND DISCUSSION Three quadrats located in Guizhou and Yunnan comprised more than 40 species. Species richness was lowest in the northeast and central regions of China, and Taiwan, where quadrats harbored only one species. Typically, Jilin and Liaoning contained only one species Oyama sieboldii (small deciduous tree); Shandong merely supported Liriodendron chinense (deciduous tree) and Oyama sieboldii; Hebei simply harbored Yulania liliiflora (deciduous shrub) and Oyama sieboldii; Taiwan also merely consisted of two species Michelia compressa (evergreen tree) and Parakmeria kachirachirai (evergreen tree). The complementary algorithm manifested that 26 quadrats, which covered 2.7% of China’s land, included all magnolia species (111 species). 15 quadrats occupied 1.6% of the landmass in China and included 90% of the magnolia species (100 species). Consequently, these 15 quadrats were recognized as the biodiversity hotspots, which were mostly situated in the southern Yunnan (Fig. 2). Both morphological and molecular evidences have revealed that Magnoliaceae can be considered as one of the most primitive angiosperm family [1]. Thus, magnolia species are exceptionally important in researches on biogeography and plant evolution [11]. Additionally, magnolia species are of remarkable value owing to their timber, medicinal and food products and ornamental values, which make magnolia species act as the attractive flagship for plant conservation [2]. Here, we delineated the magnolia species distribution in China and discovered that the highest species richness appeared in the southern China and especially clustered in Guizhou, Yunnan and Guangxi (Fig. 2). While, the quadrats supporting the lowest species richness occurred in the Tibetan Plateau, Sichuan, Gansu, Shaanxi, Henan, Anhui, Shandong, Hebei, Liaoning, Jilin and Taiwan. Many magnolia species are assessed as threatened with extinction, and therefore it is urgently needed to recognize the biodiversity hotspots for planning conservation actions [2]. To achieve this goal, we employed the complementary algorithm to select 15 quadrats (each quadrat covered the area of 104 km2 ) which encompassed 90% of 111 magnolia species in China as the hotspots [8, 9, 10]. Most of the quadrats denoted as hotspots were distributed in the high altitudes due to the heterogeneous habitats for plant species in the mountainous regions, which was consistent with previous reports [4, 10, 12, 13]. Typically, the first- order selected quadrat was located at the southeastern Yunnan, which consisted of 44.
  • 3. Yifan Zhao al. Int. Journal of Engineering Research and Application www.ijera.com ISSN : 2248-9622, Vol. 6, Issue 11, ( Part -2) November 2016, pp.38-41 www.ijera.com 40 | P a g e Figure 2. Biodiversity hotspots for magnolia species in China. (a) Geographical distribution of hotspots: the value of each quadrat represented the selection order through the complementary algorithm; (b) Relationship between the number of cumulative species and the number of cumulative area. Magnolia species and thus covered many endangered species (Fig. 2). For instance, the critically endangered and narrowly distributed species Michelia coriacea (evergreen tree) retains high levels of genetic diversity, mostly at the within- population level [11]. Consequently, conservation measures should focus on the establishment of numerous seedlings, both in and ex situ, to preserve as much as possible of the existing genetic diversity [11]. IV. CONCLUSION In this study, we identified the biodiversity hotspots of magnolia species (one of the most primitive angiosperm families) in China by the published plant species atlas and identification algorithm. The results showed that southern China supported the most magnolia species and 90% of magnolia species were concentrated in roughly 1.6% of the landmass of China. This identification of magnolia biodiversity hotspots in China is helpful for biodiversity conservation of magnolia species in China. Further research on the hidden ecological processes behind the biodiversity hotspots of magnolia species in China are needed to conduct. ACKNOWLEDGEMENTS We acknowledge with great appreciation the support provided by National Special Water Programs (No. 2009ZX07210-009, No. 2015ZX07203-011, No. 2015ZX07204-007), Department of Environmental Protection of Shandong Province (SDHBPJ-ZB-08), the China Scholarship Council (No. 201306730020), the Chinese Natural Science Foundation (No. 39560023). REFERENCES [1] Z.L. Nie, J. Wen, H. Azuma, Y.L. Qiu, H. Sun, Y. Meng, W.B. Sun, and E.A. Zimmer, Phylogenetic and biogeographic complexity of Magnoliaceae in the Northern Hemisphere inferred from three nuclear data sets, Mol. Phylogenet. Evol, 48, 2008, 1027-1040. [2] M. Rivers, E. Beech, L. Murphy, and S. Oldfield, The Red List of Magnoliaceae: Revised and Extended, Botanic Gardens Conservation International: Richmond, UK, 2016. [3] C. Marchese, Biodiversity hotspots: A shortcut for a more complicated concept, Global Ecology and Conservation, 3, (2015), 297-309. [4] N. Myers, R.A. Mittermeier, C.G. Mittermeier, G.A.B. da Fonseca, and J. Kent, Biodiversity hotspots for conservation priorities, Nature, 403, 2000, 853-858. [5] J.Y. Fang, Z.H. Wang, and Z.Y. Tang, (Eds.), Atlas of Woody Plants in China: Distribution and Climate (Springer and Higher Education Press, 2011). [6] Environmental Systems Resource Institute (ESRI), ArcMap 10.3.1. (Redlands, CA: ESRI, 2015). [7] Z.H. Wang, J.H. Brown, Z.Y. Tang, and J.Y. Fang, Temperature dependence, spatial scale, and tree species diversity in eastern Asia and North America, Proc. Natl. Acad. Sci. U.S.A, 106, 2009, 13388-13392. [8] A.P. Dobson, J.P. Rodriguez, W.M. Roberts, and D.S. Wilcove, Geographic distribution of endangered species in the United States, Science, 275, 1997, 550-553. [9] V. Kati, P. Devillers, M. Dufrêne, A. Legakis, D. Vokou, and P. Lebrun, Hotspots, complementarity or representativeness? designing optimal small-scale reserves for biodiversity conservation, Biol. Conserv, 120, 2004, 471-480.
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