Habitat Selection by Red Panda (Ailurus fulgens fulgens) in Gaoligongshan Nature Reserve, China
Habitat Selection by Red Panda (Ailurus fulgens fulgens) in Gaoligongshan Nature Reserve, China
Xu Liu1, 2, Liwei Teng2, Youzhong Ding3 and Zhensheng Liu2*
1Island Research Center, MNR, P.R.C, Fujian, China
2College of Wildlife and Protected Area,Northeast Forestry University, Harbin, Heilongjiang, China
3School of Life Sciences, East China Normal University, Shanghai, China
ABSTRACT
From August 2008 to January 2009 we studied habitat selection of red panda (Ailurus fulgens fulgens) in Gaoligongshan Nature Reserve using resource selection functions and resource selection index. Red panda preferred coniferous forest and broad-leaved coniferous forest on eastern and northern slopes located in the mid and upper parts of the hillside in the rainy season, containing larger diameter trees (>30 cm), a low tree density (<6/20 m2), high density bamboo (>70/m2 and 40~70/m2) and few stumps (<3/400 m2). In the dry season, red panda preferred coniferous forest and broad-leaved coniferous forest on eastern and southern slopes in mid and upper parts of the hillside, containing larger diameter trees (15~30 cm), good hiding conditions (visibility <10 m), a small number of stumps (<3/400 m2) and a high bamboo density (>70/m2 and 40~70/m2).
Article Information
Received 26 July 2019
Revised 11 January 2020
Accepted 20 February 2020
Available online 24 August 2021
(early access)
Published 22 April 2022
Authors’ Contribution
LT and ZL conceived and designed the research. YD revised the paper. XL conducted research and wrote the paper. ZL had primary responsibility for final contents.
Key words
Red panda, Habitat selection, Gaoligongshan, Resource selection functions, Resource selection index
DOI: https://dx.doi.org/10.17582/journal.pjz/20190726090725
* Corresponding author: [email protected]
0030-9923/2022/0004-1829 $ 9.00/0
Copyright 2022 by the authors. Licensee Zoological Society of Pakistan.
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
INTRODUCTION
Habitat protection is the key to protect wildlife. Habitat provides food, water and other resources necessary for shelter, reproduction and protection from predators (Yan et al., 1998; Ouyang et al., 2002; Wu et al., 2003; Liu et al., 2004). Patterns of habitat selection reveal habitat characteristics preferred by the species, habitat requirements, the complex relationship between species; and their environment provides a scientific basis for developing effective protection and management measures.
Red panda (Ailurus fulgens) are rare and specialized animals inhabiting the Himalayas in China, Nepal, India, Bhutan and Burma. China is critical to red panda and home to 6000‒7000 animals (Miles and John, 1984; Zhang et al., 2002; Han et al., 2004). Although red panda were once found in Sichuan, Yunnan, Tibet, Qinghai, Gansu, Guizhou and Shanxi (China), they are now confined to Sichuan, Yunnan and Tibet only. Red panda is listed as Category II species in Chinese Wild Animal Protection Law, as Endangered by the IUCN, and in CITES Appendix I (Wei et al., 1995; Yang et al., 2007). Red panda is threatened by deforestation, habitat loss, fragmentation, illegal trade and hunting, fishing and other external environmental pressures (Zhang, 2005; Liu et al., 2011).
Many studies have been conducted on habitat selection of red panda, but most focused on the subspecies mainly found in Sichuan (A. f. styani ), and conjunct habitat between red panda and giant panda (Ailuropoda melanoleuca) (Wang et al., 1998; Wei et al., 1999a; Wei et al., 2002; Zhang et al., 2004; Qi et al., 2009). Little is known regarding habitat selection by the nominate subspecies A. f. fulgens inhabiting Yunnan and surrounds (Hu, 1998; Zhang and Shi, 1999; Sangay et al., 2011; Saroj et al., 2012) or habitat differences between these two sub-species . Because of some shortcomings in design or methodology, some research results cannot fully reflect the micro-habitat selection of the nominate subspecies of red panda and fail to reveal the key factors affecting the micro-habitat selection of the nominate subspecies of red panda. Therefore, it is necessary to study the habitat selection of the nominate subspecies of the red panda. and Study the difference of habitat selection between the two subspecies is helpful for better protection and management of red panda. Resource selection functions can describe the habitat preferences of animals using the ratio of available resources to utilized resources (Wei et al., 1995; Yang et al., 2006). This method is crucial to understanding overall patterns of habitat selection and developing conservation and management strategies for threatened wildlife.
From August 2008 to January 2009, we established observation points throughout Gaoligongshan Nature Reserve in Yunnan to describe habitat selection patterns of red panda using resource selection functions and resource selection index. Because the climate difference between rainy season and dry season is obvious, the selection of habitat will change accordingly, hence we studied the selection of habitat of red panda both in rainy season and dry season. Our aim was to describe differences in habitat selection of nominate subspecies of red panda in rainy and dry seasons, and the habitat preferences of this subspecies in greater detail and compare the differences between A. f. styani and A. f. fulgens in habitat selection using published accounts of A. f. styani habitat selection and our data.
MATERIALS AND METHODS
Study area
Gaoligongshan Nature Reserve (24°56’~28°22’ N, 98°08’~98°50’ E) spans 400 km from north to south, has a total area of 4052 km2, and is the largest forest and wildlife nature reserve in Yunnan, China. The reserve has a higher altitude in the north and lower altitude in the south: the highest elevation is 5128 m above sea level, and the minimum altitude is 720 m. The dry season from November to April of the following year, is characterized by abundant sunshine and less precipitation. May-October is the wet season. Sunshine hours account for 40% of the whole year. Relative humidity is about 20% higher than that in dry season. The operational zone within the reserve covers 30 km2 and is concentrated 2800‒3400 m above sea level at Fengxue Yakou (Fig. 1); the terrain is steep and complex and the climate changes with altitude. The average temperature at Fengxue Yakou is 7oC, the highest is 12.5oC in August and the lowest is -0.5oC in January. The snow period is from December to March. The vegetation has been well-preserved and includes: (1) cool coniferous forest (elevation 2800~3400 m) dominated by scattered Yunnan hemlock (Tsuga dumisa) and huashan pine (Pinus armandii), understory shrubs include bamboo and azalea (Rhododendron protistum) and cover varies but is generally up to 70%; and (2) cold temperate shrub (altitude 3200~3400 m) mainly containing bamboo, Sorbus, rhododendrons, an upper story of fir (Abies delavayi) and lower story of herbaceous plants.
Field plots and data acquisition
Identifying traces of red panda
It is difficult to observe microhabitat selection by red panda directly in the field. Previous studies have indirectly measured red panda microhabitats using feces and evidence of feeding (Zhang, 2005). Here, Traces of eating are hard to judge, so here we did not use this as a basis for judgment. we used direct observation of red panda and feces as indicators of habitat use.
Microhabitat plots
We adopted the survey methods of Wei et al. (1995) used in Yele Nature Reserve. We crossed different vegetation types in the study area randomly, and established 12 transects, transects basically cover the research area. A site where a red panda or evidence of red panda habitat use was located formed the center and three separate plots were established: a 1 m × 1 m plot, a 20 m × 20 m plot and two 2 m × 10 m plots. We also set a 1 m × 1 m plot at the center of 1 / 4 plots of the 20 m × 20 m plot (i.e. 10 m × 10 m square plot). Within all plots we measured 18 variables, including i. Canopy density: canopy density of the 20 m × 20 m plots, divided into three categories of <50%, 50~75% and > 75%. ii. Slope: the slope of the 20 × 20 m plots as <40°, 40~60°, and >60°. iii. Aspect: the aspect of 20 m × 20 m plots as east (45~135°), south (135~225°), west (225~315°) or north (315~45°). iv. Slope position: the position of the entire 20 m × 20 m plot, divided into upper slope (slope of the hill or the top), middle slope (slope of the mountain or the middle) and lower slope (valley or slope bottom). v. Vegetation types: named by the appearance of dominant species, including conifer, coniferous forest, shrub grassland and bare land. vi. Bamboo density (plants / m2): the average bamboo in five 1 m × 1 m plots. vii. Bamboo height: the average height of bamboo in cm in five 1 m × 1 m plots (five bamboos were measured in each plot). viii. Tree density: the average number of trees in two 2 m × 10 m plots. ix. Tree DBH: the average diameter in cm at breast height of a tree closest to the center in each 10 m × 10 m plot. x. Tree distance (m): the average distance of a tree closest to the center in each 10 m × 10 m plot. xi. Fallen log density (plants): the average number of fallen trees in four 10 m × 10 m plots. xii. Fallen log size (cm): the average diameter of fallen trees closest to the center in each 10 m × 10 m plot. xiii. Fallen log distance (m): the average distance of a fallen log closest to the center in each 10 m × 10 m plot. xiv. Stump density (plant): the average number of tree stumps in four 10 m × 10 m plots. xv. Stump Size (cm): the average diameter of a tree stump closest to the center in each 10 m × 10 m plot. xvi. Stump distance (m): the average distance of a tree stump closest to the center in each 10 m × 10 m plot. xvii. Water distance (m): straight distance to the nearest water source in 20 m × 20 m plots classified as <500 m or > 500 m. xviii. Hiding conditions: the average maximum distance to a point 10 m high from each side in the 20 m × 20 m plots, classified as <10 m, 10~20 m or >20 m.
Contrast sample
To ensure the contrast sample adhered to the principles of randomness, we established the same number of contrast samples across the study area and measured the same habitat factors. In order to capture information about the impact of habitat selection by red panda, we used a Z-shaped transect line in the study area; the length of the line covered the study area. We set plots every 150 m along each line (with three independent plots) ensuring that the area of the contrast sample covered the entire study area (Zhang, 2005).
Data analysis
All statistical analyses were done in SPSS v17 (SPSS Inc., Chicago, USA). Statistical analyses included a single sample Kolmogorov-Smirnov test (for all data) to determine normality, independent-samples T test, Mann-Whitney u test, correlation analysis, a resource selection index and resource selection functions.
Meaning of resource selection functions (RSFs)
Resource selection function has obvious advantages compared to other methods of studying animal habitat preferences. It can better describe species’ preferences for using habitat resources and calculate the ratio of utilized resources to available resources (Zhang, 2005; Yang et al., 2007). The specific calculation method is as follows.
For a resource i in habitats, species have a selection rate of ωi =οi/πi, where οi is the proportion used in resource i, and πi= ai/a+, a + is all available resource units, and ai is the unit in which resource i can be used.
Because species’ habitat selection is often constrained by many factors, such as food, shelter and hydrothermal conditions, the resource selection function is generally expressed as a linear logarithmic model including several independent habitat variables: ω(x) = exp (β0+β1x1+β2x2+…+βkxk), where X represents different independent habitat variables and β represents selection coefficient. Then, the probability of species choosing habitats is: T(x) =exp(β0+β1x1+β2x2+…+βkxk)/[1+exp(β0+β1x1+β2x2+ …+βkxk)], When the value of T(x) is 1 or 0, that is to say, the selection coefficient β can be estimated by logistic regression coefficient (Wei et al.,1999; Zhang, 2005).
Logistic regression was first used in multivariate analysis in 1967. Now it is a standard statistical method to study the relationship between binary response variables (e.g. yes and no) or ordered response variables and a set of independent variables. At present, there are fixed modules in most statistical softwares (e.g. SPSS, SAS, etc.) (Hu and Du, 2002).
Method of calculating resource selection index
(1) Resource Selection Rate ωi
For resource i, species selection rate is: ωi=οi/πi, πi= ai/a+, where οi is the proportion used in resource i, a+ is all available resource units, and ai is the unit in which resource i can be used.
(2) Resource Selection Coefficient Wi and Resource Selection Index Ei
Wi=ωi /∑ωi ωi as resource selection rate
Ei= (Wi-1/n) / (Wi+1/n) n is the rank number of certain resources
Ei value is between - 1 and + 1,. If Ei > 0.1 means love, Ei = 1 means special love, Ei = 0 means random choice, Ei < 0.1 means almost random choice, Ei < - 0.1 means dislike, Ei = - 1 means no choice.
RESULTS
Habitat selection in the rainy season
Resource selection functions
Ensuring independence of variables in the resource selection function, we conducted correlation analysis between pairwise variable relationships. Two variables contain the same information if the correlation coefficient is greater than 0.5; when this occurred only one variable of greater biological significance was chosen for regression analysis. The correlation coefficient of the two sets of variables exceeded 0.5 (Table I).
Tree stump density, tree stump size and tree stump distance were measures of tree stump habitat use in this study. To take into account the importance and independence we tested the contribution of these three factors to habitat selection by red panda using principal component analysis. We believe that tree stump density and tree stump distance have greater biological significance hence these two factors were retained. Overall, we selected 17 environmental factors for the logistic regression: canopy density, slope, aspect, slope position, vegetation type, density of bamboo, bamboo height, tree density, tree DBH, tree distance, fallen log density, the size of fallen trees, fallen log distance, stump density, tree stump distance, distance to water source and hiding conditions.
Table I. Habitat variables with significant correlation coefficient between each other.
Habitat variables |
Correlation coefficient levels |
Significant |
Tree stump density and Tree stump size |
0.725 |
0.00 |
Tree stump size and Tree stump distance |
0.542 |
0.00 |
We normalized all parameters and did a logistic regression analysis using the forward / conditional method (based on assumptions for the probability of the likelihood ratio test and forward stepwise selection variables). The habitat model indicated that aspect, bamboo density, tree density, tree diameter at breast height and tree stump density explained red panda habitat selection (Table II). The red panda habitat resource selection function is logit (P) = -2.223-15.946 × tree diameter at breast height +6.828 × tree density -4.933 × bamboo density +4.615 × stump density +2.432 × slope. According to resource selection functions, red panda habitat selection probability is P = elogit (P) / (1 + elogit (P)). Correct model prediction was 95%.
Table II. The variables in the equation.
Variable and constant |
Selection coefficients β |
Standard error |
Wald Chi-square |
P |
|
Aspect |
2.432 |
1.650 |
2.173 |
0.140 |
|
Bamboo density |
-4.933 |
3.010 |
2.685 |
0.101 |
|
Tree density |
6.828 |
3.958 |
2.975 |
0.085 |
|
Tree size |
-15.946 |
9.596 |
2.762 |
0.097 |
|
Tree stump density |
4.615 |
2.999 |
2.367 |
0.124 |
|
Constant |
-2.223 |
1.801 |
1.524 |
0.217 |
Five factors play the most significant role in red panda habitat selection: aspect, bamboo density, tree density, tree size and tree stump density. According to the absolute number of the selection coefficient and the results of enter fitting, the five factors which significantly contribute to habitat selection can be ordered by their importance as tree size, tree density, bamboo density, stump density and aspect. The influence of tree size is the most important and key factor; tree density, bamboo density and stump density have greater impact and are second critical factor; the aspect is a secondary factor.
Habitat selection parameters
Habitat resource selectivity, the selection coefficient and selection index for red panda are shown in Table III. The results of the resource selection index show that red panda prefer a canopy density greater than 75%; slope of 40~60°; a western and northern aspect; slope position of 2800~3400 m; mixed coniferous and coniferous forest; a bamboo density greater than 70/m2 and 40~70 plants per square meter; bamboo height of less than 6 m; tree density of less than 6 plants / 20 m2; a tree DBH of more than 30 cm; tree distance of less than 1 m and 1~3 m, a fallen log density of less than five roots / 400 m2 and 5~10 roots / 400 m2; fallen trees size of 20~40 cm; distance to fallen tree of less than 2 m and 2~4 m; stump density of 3 / 400 m2; tree stump size of less than 30 cm; distance to stump of 3~5 m; and distance to water of less than 500 m. For hiding conditions, red panda prefer visibility less than 10 m.
In summary, the best habitat for red panda in the rainy season contains large diameter trees (>30 cm), a small tree density (<6 / 20 m2), large bamboo density (> 70 / m2 and 40~70 plants / m2), few stumps (<3 / 400 m2), an upper slope facing east or north and coniferous forests or mixed coniferous forest.
Habitat selection in the dry season
Resource selection functions
After correlation coefficient analysis (Table IV) we selected 13 environmental factors for the logistic regression: canopy density, slope, aspect, slope position, vegetation type, bamboo density, bamboo height, tree size, tree distance, fallen log size, stump density, water distance and hiding conditions.
Using identical methods as for our rainy season analysis we identified the following significant habitat variables: bamboo density, tree size, tree stump density and hiding conditions (Table V). The resource selection function for the dry season is logit (P) = -0.058-3.585 × tree size -2.088 × concealed conditions +1.569 × stump density -1.084 × bamboo density. According to the resource selection functions, the selection probability of red panda is P = elogit (P) / (1 + elogit (P)); the model correctly predicted 89.7%.
Table III. Habitat selection by the red panda in Gaoligongshan Nature Reserve
Habitat factors |
Category (i) |
Expected proportion used (πi) n=(30) |
Proportion used (oi) |
Resource selection rate (wi) |
Resource selection coefficient (Wi) |
Preference (Ei) |
Use |
<50 |
0.06667 |
0.03333 |
0.49993 |
0.20166 |
-0.24613 |
NP |
|
Canopy (%) |
50~75 |
0.40000 |
0.26667 |
0.66668 |
0.26892 |
-0.10696 |
NP |
>75 |
0.53333 |
0.70000 |
1.31251 |
0.52943 |
0.22729 |
P |
|
<40 |
0.23333 |
0.06667 |
0.28573 |
0.11321 |
-0.49293 |
NP |
|
Slope (°) |
40~60 |
0.70000 |
0.86666 |
1.23809 |
0.49056 |
0.19083 |
P |
>60 |
0.06667 |
0.06667 |
1.00000 |
0.39623 |
0.08621 |
AR |
|
45~135 |
0.53333 |
0.60000 |
1.12500 |
0.30474 |
0.09868 |
AR |
|
Aspect |
135~225 |
0.16667 |
0.06667 |
0.40000 |
0.10835 |
-0.39528 |
NP |
225~315 |
0.10000 |
0.10000 |
1.00000 |
0.27088 |
0.04009 |
AR |
|
315~45 |
0.20000 |
0.23333 |
1.16667 |
0.31603 |
0.11665 |
P |
|
Slope |
2800~3000 |
0.40000 |
0.43333 |
1.08333 |
0.50485 |
0.20463 |
P |
position |
3000~3400 |
0.53333 |
0.56667 |
1.06250 |
0.49515 |
0.19531 |
P |
>3400 |
0.06667 |
0.00000 |
0.00000 |
0.00000 |
-1.00000 |
NS |
|
Vegetation |
mixed broadleaf-conifer forest |
0.23333 |
0.23333 |
1.00000 |
0.46512 |
0.16505 |
P |
type |
coniferous forest |
0.66667 |
0.76667 |
1.15000 |
0.53488 |
0.23214 |
P |
Thicket |
0.10000 |
0.00000 |
0.00000 |
0.00000 |
-1.00000 |
NS |
|
Bamboo |
<40 |
0.16667 |
0.03333 |
0.20000 |
0.08397 |
-0.59756 |
NP |
density |
40~70 |
0.73333 |
0.86667 |
1.18182 |
0.49618 |
0.19632 |
P |
>70 |
0.10000 |
0.10000 |
1.00000 |
0.41985 |
0.11486 |
P |
|
Bamboo |
<4 |
0.13333 |
0.16667 |
1.25000 |
0.35140 |
0.02639 |
AR |
height |
4~6 |
0.30000 |
0.53333 |
1.77778 |
0.49977 |
0.19978 |
P |
>6 |
0.56667 |
0.30000 |
0.52941 |
0.14883 |
-0.38266 |
NP |
|
<6 |
0.03333 |
0.43333 |
13.0000 |
0.90179 |
0.46024 |
P |
|
Tree density |
6~10 |
0.33333 |
0.36667 |
1.10000 |
0.07631 |
-0.62745 |
NP |
>10 |
0.63333 |
0.20000 |
0.31579 |
0.02191 |
-0.87667 |
NP |
|
<15 |
0.66667 |
0.10000 |
0.15000 |
0.01345 |
-0.92241 |
NP |
|
Tree size |
15~30 |
0.30000 |
0.60000 |
2.00000 |
0.17937 |
-0.30029 |
NP |
>30 |
0.03333 |
0.30000 |
9.00000 |
0.80717 |
0.41547 |
P |
|
Tree |
<1 |
0.30000 |
0.33333 |
1.11111 |
0.42150 |
0.11680 |
P |
distance |
1~3 |
0.53333 |
0.60000 |
1.12500 |
0.42677 |
0.12292 |
P |
>3 |
0.16667 |
0.06667 |
0.40000 |
0.15174 |
-0.37437 |
NP |
|
Fallen log |
<5 |
0.53333 |
0.63333 |
1.18750 |
0.41007 |
0.10323 |
P |
density |
5~10 |
0.20000 |
0.26667 |
1.33333 |
0.46043 |
0.16012 |
P |
>10 |
0.26667 |
0.10000 |
0.37500 |
0.12950 |
-0.44041 |
NP |
|
Fallen log |
<20 |
0.46667 |
0.43333 |
0.92857 |
0.34491 |
0.01707 |
AR |
size |
20~40 |
0.36667 |
0.50000 |
1.36364 |
0.50651 |
0.20620 |
P |
>40 |
0.16667 |
0.06667 |
0.40000 |
0.14858 |
-0.38338 |
NP |
|
Fallen log |
<2 |
0.50000 |
0.56667 |
1.13333 |
0.42149 |
0.11679 |
P |
Continued on next page...... |
|||||||
Habitat factors |
Category (i) |
Expected proportion used (πi) n=(30) |
Proportion used (oi) |
Resource selection rate (wi) |
Resource selection coefficient (Wi) |
Preference (Ei) |
Use |
distance |
2~4 |
0.30000 |
0.36667 |
1.22222 |
0.45455 |
0.15385 |
P |
>4 |
0.20000 |
0.06667 |
0.33333 |
0.12397 |
-0.45783 |
NP |
|
Tree stump |
<3 |
0.70000 |
0.80000 |
1.14286 |
0.49485 |
0.19502 |
P |
density |
3~5 |
0.20000 |
0.16667 |
0.83333 |
0.36082 |
0.03960 |
AR |
>5 |
0.10000 |
0.03333 |
0.33333 |
0.14433 |
-0.39568 |
NP |
|
Tree stump |
<30 |
0.23333 |
0.50000 |
2.14286 |
0.60342 |
0.28832 |
P |
size |
30~50 |
0.50000 |
0.26667 |
0.53333 |
0.15018 |
-0.37878 |
NP |
>50 |
0.26667 |
0.23333 |
0.87500 |
0.24640 |
-0.14996 |
NP |
|
Tree stump |
<3 |
0.60000 |
0.70000 |
1.16667 |
0.40314 |
0.09479 |
AR |
distance |
3~5 |
0.36667 |
0.26667 |
0.72727 |
0.25131 |
-0.14030 |
NP |
>5 |
0.03333 |
0.03333 |
1.00000 |
0.34555 |
0.01799 |
AR |
|
Water |
<500 |
0.93333 |
0.96667 |
1.03571 |
0.67442 |
0.14851 |
P |
distance |
≥500 |
0.06667 |
0.03333 |
0.50000 |
0.32558 |
-0.21127 |
NP |
Hidden |
<10 |
0.53333 |
0.80000 |
1.50000 |
0.65563 |
0.13467 |
P |
conditions |
10~20 |
0.36667 |
0.16667 |
0.45455 |
0.19868 |
-0.43128 |
NP |
>20 |
0.10000 |
0.03333 |
0.33333 |
0.14570 |
-0.54872 |
NP |
Four factors play a significant role in habitat selection by red panda in the dry season: bamboo density, tree size, tree stump density and hiding conditions. According to the absolute number of the selection coefficient and the results of enter fitting, the four factors which significantly contribute to habitat selection can be ordered by their importance as tree size, hidden conditions, tree stump density and bamboo density. The influence of tree size is the most important key factor; hiding conditions has greater impact and is the second critical factor; and tree stump density and bamboo density are secondary factors.
Table IV. Habitat variables with significant correlation coefficient between each other.
Habitat variables |
Correlation coefficient levels |
Significant |
Tree density and Tree size |
-0.561 |
0.00 |
Fallen log size and Fallen log density |
0.602 |
0.00 |
Fallen log size and Fallen log distance |
0.563 |
0.00 |
Tree stump density and Tree stump size |
0.826 |
0.00 |
Tree stump density and Tree stump distance |
0.648 |
0.00 |
Habitat selection parameters
Habitat resources selectivity, the selection coefficient and selection index of red panda are provided in Table VI. The P indicates that red panda’s preference, NP indicates no preference and AP indicates random choice. In summary, the best habitat for red panda in the dry season contains larger diameter trees (15~30 cm), well concealed conditions (visibility <10 m), a small tree stump density (<3 / 400 m2), high bamboo density (> 70 / m2 and 40~70 plants / m2), upper slopes facing east or north with coniferous forests or mixed coniferous forests.
Table V. The variables in the equation.
Variable and constant |
Selection coefficients β |
Standard error |
Wald Chi-square |
P |
Bamboo density |
-1.084 |
0.371 |
8.511 |
0.004 |
Tree size |
-3.585 |
0.743 |
23.284 |
0.000 |
Tree stump density |
1.569 |
0.363 |
18.718 |
0.000 |
Hiding conditions |
-2.088 |
3580.674 |
0.000 |
1.000 |
Constant |
-0.588 |
318.992 |
0.000 |
0.999 |
DISCUSSION
Habitat selection by red panda (A. f. fulgens)
Wildlife will adopt different habitat selection strategies across different seasons because of seasonal changes in habitat, weather patterns, different physiological requirements and trade-offs between different habitat factors. Understanding seasonal changes in habitat selection is important for understanding seasonal variation in environmental factors and the scientific conservation and management of species (Zheng et al., 2006). In Gaoligongshan Nature Reserve, tree size, bamboo density and stump density have a major impact on red panda habitat selection both in the rainy and dry seasons. Red panda has the same requirements regarding the density of bamboo and tree stumps in the rainy season and dry season and these two factors are crucial to red panda because they determine its food supply and ability to reproduce.
Table VI. Habitat selection by the red panda in Gaoligongshan Nature Reserve.
Habitat factors |
Category (i) |
Expected proportion used (πi) n=(63) |
Proportion used (oi) |
Resource selection rate (wi) |
Resource selection coefficient (Wi) |
Preference (Ei) |
Use |
<50 |
0.14286 |
0.01587 |
0.11111 |
0.04652 |
-0.75505 |
NP |
|
Canopy (%) |
50~75 |
0.12698 |
0.14286 |
1.12500 |
0.47105 |
0.17121 |
P |
>75 |
0.73016 |
0.84127 |
1.15217 |
0.48243 |
0.18277 |
P |
|
<40 |
0.14286 |
0.04762 |
0.33333 |
0.13029 |
-0.43794 |
NP |
|
Slope |
40~60 |
0.63492 |
0.77778 |
1.22500 |
0.47883 |
0.17914 |
P |
>60 |
0.17460 |
0.17460 |
1.00000 |
0.39088 |
0.07946 |
AR |
|
45~135 |
0.71429 |
0.80952 |
1.13333 |
0.35897 |
0.17895 |
P |
|
Aspect (°) |
135~225 |
0.07937 |
0.07937 |
1.00000 |
0.31674 |
0.11776 |
P |
225~315 |
0.11111 |
0.09524 |
0.85714 |
0.27149 |
0.04121 |
AR |
|
315~45 |
0.09524 |
0.01587 |
0.16667 |
0.05279 |
-0.65131 |
NP |
|
2800~3000 |
0.38095 |
0.39683 |
1.04167 |
0.47496 |
0.17521 |
P |
|
Slope position |
3000~3400 |
0.52381 |
0.60317 |
1.15152 |
0.52504 |
0.22334 |
P |
>3400 |
0.09524 |
0.00000 |
0.00000 |
0.00000 |
-1.00000 |
NS |
|
Vegetation |
mixed broadleaf-conifer forest |
0.34921 |
0.38095 |
1.09091 |
0.49470 |
0.19488 |
P |
type |
coniferous forest |
0.55556 |
0.61905 |
1.11429 |
0.50530 |
0.20506 |
P |
Thicket |
0.09524 |
0.00000 |
0.00000 |
0.00000 |
-1.00000 |
NS |
|
<40 |
0.17460 |
0.04762 |
0.27273 |
0.11196 |
-0.49715 |
NP |
|
Bamboo |
40~70 |
0.77778 |
0.90476 |
1.16327 |
0.47753 |
0.17783 |
P |
density |
>70 |
0.04762 |
0.04762 |
1.00000 |
0.41051 |
0.10375 |
P |
<4 |
0.20635 |
0.14286 |
0.69231 |
0.24793 |
-0.14692 |
NP |
|
Bamboo |
4~6 |
0.47619 |
0.57143 |
1.20000 |
0.42975 |
0.12635 |
P |
height |
>6 |
0.31746 |
0.28571 |
0.90000 |
0.32231 |
-0.01681 |
AR |
<6 |
0.19048 |
0.58730 |
3.08333 |
0.77031 |
0.39594 |
P |
|
Tree |
6~10 |
0.50794 |
0.33333 |
0.65625 |
0.16395 |
-0.34062 |
NP |
density |
>10 |
0.30159 |
0.07937 |
0.26316 |
0.06574 |
-0.67052 |
NP |
<15 |
0.55556 |
0.11111 |
0.20000 |
0.04516 |
-0.76139 |
NP |
|
Tree size |
15~30 |
0.19048 |
0.55556 |
2.91667 |
0.65851 |
0.32785 |
P |
>30 |
0.25397 |
0.33333 |
1.31250 |
0.29633 |
-0.05876 |
AR |
|
<1 |
0.28571 |
0.30159 |
1.05556 |
0.39434 |
0.08384 |
AR |
|
Tree |
1~3 |
0.52381 |
0.58730 |
1.12121 |
0.41887 |
0.11371 |
P |
distance |
>3 |
0.19048 |
0.09524 |
0.50000 |
0.18679 |
-0.28174 |
NP |
<5 |
0.71429 |
0.79365 |
1.11111 |
0.48780 |
0.18812 |
P |
|
Fallen log |
5~10 |
0.19048 |
0.19048 |
1.00000 |
0.43902 |
0.13684 |
P |
density |
>10 |
0.09524 |
0.01587 |
0.16667 |
0.07317 |
-0.64000 |
NP |
Continued on next page...... |
|||||||
Habitat factors |
Category (i) |
Expected proportion used (πi) n=(63) |
Proportion used (oi) |
Resource selection rate (wi) |
Resource selection coefficient (Wi) |
Preference (Ei) |
Use |
<20 |
0.42857 |
0.33333 |
0.77778 |
0.25271 |
-0.13758 |
NP |
|
Fallen log |
20~40 |
0.31746 |
0.41270 |
1.30000 |
0.42238 |
0.11783 |
P |
size |
>40 |
0.25397 |
0.25397 |
1.00000 |
0.32491 |
-0.01280 |
AR |
<2 |
0.57143 |
0.58730 |
1.02778 |
0.36634 |
0.04717 |
AR |
|
Fallen log |
2~4 |
0.28571 |
0.31746 |
1.11111 |
0.39604 |
0.08597 |
AR |
distance |
>4 |
0.14286 |
0.09524 |
0.66667 |
0.23762 |
-0.16763 |
NP |
<3 |
0.39683 |
0.71429 |
1.80000 |
0.68354 |
0.34440 |
P |
|
Tree stump |
3~5 |
0.50794 |
0.25397 |
0.50000 |
0.18987 |
-0.27419 |
NP |
density |
>5 |
0.09524 |
0.03175 |
0.33333 |
0.12658 |
-0.44954 |
NP |
<30 |
0.26984 |
0.69841 |
2.58824 |
0.78216 |
0.40236 |
P |
|
Tree stump |
30~50 |
0.47619 |
0.25397 |
0.53333 |
0.16117 |
-0.34815 |
NP |
size |
>50 |
0.25397 |
0.04762 |
0.18750 |
0.05666 |
-0.70942 |
NP |
<3 |
0.79365 |
0.77778 |
0.98000 |
0.31562 |
-0.02730 |
AR |
|
Tree stump |
3~5 |
0.12698 |
0.14286 |
1.12500 |
0.36232 |
0.04167 |
AR |
distance |
>5 |
0.07937 |
0.07937 |
1.00000 |
0.32206 |
-0.01720 |
AR |
<500 |
0.73016 |
0.82540 |
1.13043 |
0.63597 |
0.11970 |
P |
|
Water distance |
≥500 |
0.26984 |
0.17460 |
0.64706 |
0.36403 |
-0.15737 |
NP |
<10 |
0.73016 |
0.85714 |
1.17391 |
0.56474 |
0.25767 |
P |
|
Hidden |
10~20 |
0.22222 |
0.12698 |
0.57143 |
0.27490 |
-0.09607 |
AR |
Conditions |
>20 |
0.04762 |
0.01587 |
0.33333 |
0.16036 |
-0.35037 |
NP |
In our study area, sheath bamboo and yunlong bamboo are the main feeding plants for red panda. The density of sheath bamboo is mostly greater than 40 plants / m2, while the density of yunlong bamboo is mostly less than 40 plants / m2, too low for red pandas to conceal themselves and avoid predators.
Stump density may be a habitat factor related to social and reproductive behavior. In the breeding season, red panda engage in marking behavior as a kind of olfactory communication of home range (Yang et al., 2006) and social class (Eason et al., 1999; Liu et al., 2004). In the estrus season, marking has other functions like gender identification, sexual selection and signaling information to conspecifics (Doty, 1986; Alock, 1989). The opposite sex is stimulated by sniffing these markings and they also induce synchronized estrus (Liu et al., 2004). Red panda mark using urine and information-secretion (Lan et al., 2011; Teng et al., 2013), and similar to the conclusions of Hu (1998). We believe that the density of stumps has important implications for the habitat choice of red panda. Red panda usually selects habitat with a stump density of three stumps / 400 m2; habitat with a stump density greater than 3 / 400 m2 is likely influenced by humans and red panda avoids these areas. Most of the time wildlife remains in concealed locations, and the ability to hide is particularly important to survival, especially for red panda. Bamboo is a food source of poor nutritional quality and therefore red panda must minimize energy expenditure (Wei et al., 1995) and spend a great deal of time resting. Tree branches and holes are primary resting places for red panda and large diameter trees having a strong bearing capacity are required. There is little difference in the choice of tree diameter in the rainy and dry seasons, and during both seasons red panda preferred a diameter greater than 15 cm.
Tree density is important to red panda in the rainy season. A large tree density is indicative of secondary forest where food resources are relatively scarce and the diameter at breast height is small. Red panda prefers habitat comprising a large tree density (representing primeval forest patches) with good hiding conditions and abundant food resources.
For the choice of slope direction, because of red panda preference for warmth, it will choose the sunny slope according to different seasons to ensure that its energy consumption is minimized. Red panda avoids too hot and too cold environments because of their small body size, and relatively low temperature and damp conditions of the study area means that red panda loses heat to the environment quickly. Retaining body heat is therefore very important for the red panda (Johnson et al., 1988).
Fallen trees were found to be important for red panda habitat selection. Fallen trees include partially collapsed logs between trees and fallen logs. These logs are extremely important for habitat selection by red panda, and the majority of red panda feces were in fact found around logs. For saving energy, red panda does not move too far away from its home range area, hence the place where feces were found is usually in the range of their activities, which is the preferred habitat also. Other habitat factors were found to play an important role in habitat selection in other red panda populations, such as water distance (Han et al., 2004) and human disturbance (Wang et al., 1998; Zhang et al., 1999) but were not important to the habitat preferences of red panda inhabiting Gaoligongshan. This is likely because this area contains abundant water resources all the year round and human interference in the nature reserve is minimal.
Comparison of habitat selection by A. f. fulgens and A. f. styani
The majority of studies into habitat selection by red panda have focused on A. f. styani. For example, red panda in the Xiangling Mountains prefers high density Bashania spanostachya (greater than 20 / m2), shorter and smaller bamboo (less than 260 cm; base diameter of less than 12 mm), and coniferous forest with a canopy density greater than 50% (Wei et al., 2002). In the Liangshan Mountains , vegetation type, water distance and human disturbance are the main ecological factors driving habitat selection by red panda; red panda prefers evergreen deciduous broad-leaved forest with a moderate density of Qiongzhuea macrophylla and moderate canopy density (Wei and Hu, 1992; Wei et al., 1995). In the Qionglai Mountains , water distance, bamboo base diameter and shrub density are key habitat selection factors for red panda, and slope, tree stump density and the density of fallen trees are second key factors (Zhang et al., 2002). Also, in these mountains, red panda prefers coniferous forests or mixed coniferous forest comprising a larger base diameter of cold bamboo (greater than 4 mm) and a canopy density greater than 80% (Yang et al., 2006; Zhang et al., 2009).
While there is variation amongst the habitat preferences of red panda inhabiting different mountain ranges, several similar habitat requirements are apparent. Red panda generally prefers habitat close to water with good bamboo growth on a southern slope . However, A. f. styani requires a high shrub density, large tree stumps and many fallen logs; whereas A. f. fulgens requires a certain tree diameter and a low density of tree stumps and fallen trees. A. f. styani is found at lower altitudes (1400‒3400 m) where there is a well-developed understory shrubbery, the large dense shrub provides a good shelter for red panda. A high number of tree stumps and fallen logs often results from human interference, thus red panda habitat selection avoids human interference. A. f. styani are also faced with interspecific competition from giant panda as these animals are sympatric in most areas and this competition may cause a narrowing of the red panda niche. A. f. fulgens inhabits higher altitudes (2000‒3600 m) where there is less understory hence red panda is mainly found in tree branches. Therefore, tree size and density become key habitat factors and selection for certain shrubbery characteristics is relaxed.
ACKNOWLEDGMENTS
We appreciate the help of all staff of Gaoligongshan Nature Reserve in field research, thank directions of my tutor, and really thank my family and ex-girlfriend (of Xu-Liu) for support.
Statement of conflicts of interest
The authors have declared no conflicts of interest.
REFERENCES
Alock, J., 1989. Animal behavior: An evolutionay approach (4rd edition) [M]. Sinauer Sunderlanda, Massachusetts, pp. 1-5961.
Doty, R. L., 1986. Odor guided behavior in mammals. Experientia, 42: 4-271. https://doi.org/10.1007/BF01942506
Qi, D.W., Hu, Y.B., Gu, X.D., Li, M. and Wei, F.W., 2009. Ecological niche modeling of the sympatric giant and red pandas on a mountain-range scale. Biodiv. Conserv., 18: 2127-2141. https://doi.org/10.1007/s10531-009-9577-7
Eason, P.K., Cobbs, G.A. and Trinca, K.G., 1999. The use of landmarks to define territorial boundaries. Anim. Behav., 58: 85-911. https://doi.org/10.1006/anbe.1999.1133
Han, Z.X., Wei, F.W., Zhang, Z.J., Li, M., Zhang B.W. and Hu J.C., 2004. Habitat selection by red pandas in Fengtongzhai Nature Reserve. Acta Theriol. Sin., 24: 185-192.
Hu, G., 1998. The preliminary study on the habitat selection of the red panda in Pianma of the Gaoligong Shan Mountains. J. Southw. Forest. Coll., 18: 184-188.
Hu, G. and Du, Y., 2002. The current distribution, population and conservation status of Ailurus fulgens in Yunnan. J. Northw. Forest. Univ., 17: 67-71.
Johnson, K.G., Schaller, G.B. and Hu, J., 1988. Comparative behavior of red and giant pandas in the Wolong Reserve, China. J. Mammal., 69: 552-564. https://doi.org/10.2307/1381347
Lan, C.Z., Liu, X., Diao, L.L., Liu, Z.S. and Zhang, M.M., 2011. Activity of captive red panda (Ailurus fulgens) during dry seasons. Chinese J. Wildl., 32: 191-193.
Liu, X., Zhang, M.H. and Liu, Z.S., 2011. Ecological research status of Ailurus fulgens, China. Chinese J. Wildl., 32: 38-40.
Liu, X.Q., Zhang, Z.J., Wei, F.W., Li, M., Li, C., Yang, Z. and Hu, J.C., 2004. Reproductive behavior variations and reproductive strategy in the captive red panda. Acta Theriol. Sin., 24: 173-176.
Liu, Z.S., Cao, L.R., Zhai, H., Hu, T.H. and Wang, X.M., 2004. Winter habitat selection by red deer (Cervus elaphus alxaicus) in Helan Mountain, China. Zool. Res., 25: 403-409.
Miles, S.R. and John, L.G. 1984. Ailurus fulgens, mammalian species. Am. Soc. Mammol., 222: 1-8. https://doi.org/10.2307/3503840
Ouyang, Z.Y., Li, Z.X., Liu, J.G., An, L., Zhang, H.M., Tan, Y.C. and Zhou, S.Q., 2002. The recovery processes of giant panda habitat in Wolong Nature Reserve, Sichuan China. Acta Ecol. Sin., 22: 1840-1849.
Sangay, D., Karl, V. and Rajanathan, R., 2011. Habitat correlates of the red panda in the temperate forests of Bhutan. PLoS ONE, 6: 1-11. https://doi.org/10.1371/journal.pone.0026483
Saroj, P., Achyut, A., David, R., Jennie, L. and Bikash, A., 2012. Summer diet and distribution of the red panda (Ailurus fulgens fulgens) in Dhorpatan Hunting Reserve, Nepal. Zool. Stud., 51: 701-709.
Teng, L.W., Liu, X. and Liu, Z.S., 2013. Activity rhythm of captive red panda (Ailurus fulgens) in Rainy seasons. J. econ. Anim., 17: 67-70.
Wang, W., Wei, F.W., Hu, J.C. and Yang, G., 1998. Habitat selection by red panda in Ma bian Dafengding reserve. Acta Theriol. Sin., 18: 15-20.
Wei, F.W. and Hu, J.C., 1992. Present Situation and protection of small pandas in Sichuan province. J. Sichuan Normal Univ. (Nat. Sci. Edt.), 03: 9-13.
Wei, F.W., Wang, W., Zhou, A., Hu, J.C. and Wei, Y., 1995. Preliminary study on food selection and feeding strategy of red pandas. Acta Theriol. Sin., 15: 259-266.
Wei, F.W., Feng, Z.J., Wang, Z., Zhou, A. and Hu, J., 1999a. Use of the nutrients in bamboo by the red panda (Ailurus fulgens). J. Zool., 248: 535-541. https://doi.org/10.1111/j.1469-7998.1999.tb01053.x
Wei, F.W., Rao, G., Li, M. and Feng, Z.J., 2002. Population genetic structure of red panda (Ailurus fulgens) in Qionglai and Xiangling mountains. Acta Theriol. Sin., 22(4):241-247.
Wu, Z.J. and Li, Y.M., 2003. Effects of habitat fragmentation on survival of animal populations. Acta Ecol. Sin., 23: 2424-2435.
Yan, Z.C. and Chen, Y.L., 1998. Habitat selection in animals. Chinese J. Ecol., 7: 3-49.
Yang, J.D., Zhang, Z.J., Li, M., Hu, J.C. and Wei, F.W., 2006. Home range of red pandas (Ailurus fulgens) in Fengtongzhai Nature Reserve, Si chuan, China. Acta Theriol. Sin., 26: 13-17.
Yang, J.D., Zhang, Z.J., Hu, J.C., Li, M. and Wei, F.W., 2007. Foraging characteristics and nutrition strategy of red pandas in Fengtongzhai Nature Reserve, Si chuan, China. Acta Theriol. Sin., 27: 249-256.
Zhang, J.S. and Shi, X.C., 1999. Habitat use of red pandas in Gaoligongshan, china. Chinese Wildl., 20: 34-35.
Zhang, Z.J., Hu, J.C. and Wu, H., 2002. Comparison of habitat selection of giant pandas and red pandas in the Qionglai Mountains. Acta Theriol. Sin., 22: 161-168.
Zhang, Z.J., Wei, F.W., Li, M., Zhang, B.W., Liu, X.H. and Hu, J.C., 2004. Microhabitat separation during winter among sympatric giant pandas, red pandas, and tufted deer: the effects of diet, body size, and energy metabolism. Can. J. Zool., 82: 1451-1458. https://doi.org/10.1139/z04-129
Zhang, Z.J., 2005. The habitat selection and activity rhythm of red panda (Ailurus julgens) in Fengtongzhai Nature Reserve. PhD thesis, Univ. Chinese Acad. Sci. Bei Jing, China.
Zhang, Z.J., Hu, J.C., Yang, J.D., Li, M. and Wei, F.W., 2009. Food habits and space-use of red pandas Ailurus fulgens in the Fengtongzhai Nature Reserve, China: food effects and behavioural responses. Acta Theriol., 54: 225-234. https://doi.org/10.4098/j.at.0001-7051.017.2008
Zheng, Y., Bao, Y.X., Ge, B.M. and Zheng, R.Q., 2006. Seasonal changes in habitat use by Black Muntjac (Muntiacus crinifrons). Acta Theriol. Sin., 26: 201-205.
To share on other social networks, click on any share button. What are these?