生物多样性 ›› 2024, Vol. 32 ›› Issue (12): 24239. DOI: 10.17520/biods.2024239 cstr: 32101.14.biods.2024239
吴芳芳, 刘娜, 何春梅, 原作强, 郝占庆, 尹秋龙*()
收稿日期:
2024-06-17
接受日期:
2024-10-13
出版日期:
2024-12-20
发布日期:
2024-12-28
通讯作者:
E-mail: 基金资助:
Fangfang Wu, Na Liu, Chunmei He, Zuoqiang Yuan, Zhanqing Hao, Qiulong Yin*()
Received:
2024-06-17
Accepted:
2024-10-13
Online:
2024-12-20
Published:
2024-12-28
Contact:
E-mail: Supported by:
摘要: 研究植物群落结构及多样性格局有利于揭示生物多样性维持机制。秦岭处于南北气候分界线和动植物区系的交汇过渡带, 区系成分丰富且起源古老, 植被类型多样, 群落结构复杂, 是研究过渡区植物群落结构及多样性分布格局的重要平台。参照美国史密森热带研究院热带森林研究中心的样地建设标准, 我们以秦岭皇冠25 ha大样地为核心, 在秦岭南坡中段海拔800-2,600 m地段设置10个1 ha (100 m × 100 m)的长期定位监测样地并进行群落调查, 对胸径(diameter at breast height, DBH) ≥ 1 cm的木本植物物种组成、区系特征、径级结构、优势种空间分布和物种多样性的海拔梯度格局进行初步研究。结果表明: (1)共调查到种子植物208种, 分属50科109属。温带区系成分的属占总属数的69.7%, 温带区系特征明显。随海拔上升, 植物群落稀有种、偶见种及科、属、种组成呈现先上升后下降的单峰格局。群落优势种沿海拔梯度具有明显的更替现象, 中海拔呈现阔叶栎林与针叶杉林过渡性质。(2)所有样地内木本植物径级分布总体呈倒“J”型。分海拔来看, 除了海拔1,600 m、2,000 m木本植物径级分布呈现双峰型, 其余海拔均呈现倒“J”型, 群落结构总体较为稳定。优势种在不同海拔空间点格局表现为1-10 m尺度内聚集分布, 随着尺度的增加, 逐渐转变为随机分布和均匀分布。随着海拔的升高, 去除生境异质性后, 聚集分布的尺度范围缩小, 随机分布的尺度范围增大。(3)随海拔上升, 物种丰富度呈显著的单峰分布格局, 峰值出现在海拔1,200-1,400 m之间。Shannon-Wiener多样性指数、Simpson优势度指数、Pielou均匀度指数沿海拔梯度的变化呈显著的双峰格局, 两个峰值均出现在海拔1,000-1,200 m和海拔2,000-2,200 m。β多样性(Bray-Curtis相异指数和Jaccard相异指数)随海拔的升高呈现单峰趋势。本文为亚热带-暖温带过渡区森林长期监测和基础数据库建设奠定了基础, 同时为该过渡区生物多样性保护和森林可持续经营提供了理论支持。
吴芳芳, 刘娜, 何春梅, 原作强, 郝占庆, 尹秋龙 (2024) 秦岭山地木本植物群落结构及多样性的海拔梯度格局. 生物多样性, 32, 24239. DOI: 10.17520/biods.2024239.
Fangfang Wu, Na Liu, Chunmei He, Zuoqiang Yuan, Zhanqing Hao, Qiulong Yin (2024) Elevational gradient pattern of woody plant community structure and diversity in the Qinling Mountains. Biodiversity Science, 32, 24239. DOI: 10.17520/biods.2024239.
样地编号 Plot no. | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
P1 | P2 | P3 | P4 | P5 | P6 | P7 | P8 | P9 | P10 | |
海拔 Elevation (m) | 800 | 1,000 | 1,200 | 1,400 | 1,600 | 1,800 | 2,000 | 2,200 | 2,400 | 2,600 |
坡度 Slope (°) | 32 | 23 | 32 | 29 | 26 | 24 | 13 | 24 | 25 | 16 |
坡向 Aspect (°) | 254 | 210 | 327 | 267 | 156 | 190 | 317 | 307 | 268 | 186 |
最大胸径 Maximun diameter at breast height (cm) | 56.0 | 57.5 | 78.0 | 71.8 | 66.7 | 55.0 | 62.1 | 58.2 | 53.9 | 58.5 |
平均胸径 Mean diameter at breast height (cm) | 8.13 | 8.07 | 7.11 | 5.76 | 14.25 | 11.35 | 13.90 | 5.99 | 6.72 | 22.49 |
胸高断面积之和 Sum of basal area (m2) | 30.28 | 53.54 | 33.37 | 39.61 | 48.83 | 57.95 | 28.74 | 28.83 | 12.75 | 23.48 |
立木密度 Stand density (ind./km2) | 3,562 | 3,869 | 3,488 | 5,033 | 1,981 | 3,078 | 1,193 | 3,878 | 1,708 | 503 |
种数 No. of species (S) | 39 | 53 | 80 | 79 | 57 | 60 | 46 | 49 | 39 | 18 |
属数 No. of genera | 33 | 46 | 54 | 59 | 43 | 41 | 31 | 30 | 26 | 13 |
科数 No. of families | 23 | 29 | 35 | 35 | 26 | 26 | 18 | 20 | 16 | 8 |
Shannon-Wiener多样性指数 Shannon-Wiener diversity index (H') | 1.83 | 3.00 | 3.09 | 3.01 | 2.92 | 3.26 | 3.03 | 2.86 | 2.33 | 1.52 |
Simpson优势度指数 Simpson dominance index (D) | 0.76 | 0.93 | 0.93 | 0.90 | 0.90 | 0.93 | 0.94 | 0.91 | 0.83 | 0.68 |
Pielou均匀度指数 Pielou evenness index (E) | 0.49 | 0.76 | 0.70 | 0.69 | 0.72 | 0.80 | 0.79 | 0.73 | 0.64 | 0.52 |
表1 海拔样地调查信息
Table 1 Information on elevation survey sample plots
样地编号 Plot no. | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
P1 | P2 | P3 | P4 | P5 | P6 | P7 | P8 | P9 | P10 | |
海拔 Elevation (m) | 800 | 1,000 | 1,200 | 1,400 | 1,600 | 1,800 | 2,000 | 2,200 | 2,400 | 2,600 |
坡度 Slope (°) | 32 | 23 | 32 | 29 | 26 | 24 | 13 | 24 | 25 | 16 |
坡向 Aspect (°) | 254 | 210 | 327 | 267 | 156 | 190 | 317 | 307 | 268 | 186 |
最大胸径 Maximun diameter at breast height (cm) | 56.0 | 57.5 | 78.0 | 71.8 | 66.7 | 55.0 | 62.1 | 58.2 | 53.9 | 58.5 |
平均胸径 Mean diameter at breast height (cm) | 8.13 | 8.07 | 7.11 | 5.76 | 14.25 | 11.35 | 13.90 | 5.99 | 6.72 | 22.49 |
胸高断面积之和 Sum of basal area (m2) | 30.28 | 53.54 | 33.37 | 39.61 | 48.83 | 57.95 | 28.74 | 28.83 | 12.75 | 23.48 |
立木密度 Stand density (ind./km2) | 3,562 | 3,869 | 3,488 | 5,033 | 1,981 | 3,078 | 1,193 | 3,878 | 1,708 | 503 |
种数 No. of species (S) | 39 | 53 | 80 | 79 | 57 | 60 | 46 | 49 | 39 | 18 |
属数 No. of genera | 33 | 46 | 54 | 59 | 43 | 41 | 31 | 30 | 26 | 13 |
科数 No. of families | 23 | 29 | 35 | 35 | 26 | 26 | 18 | 20 | 16 | 8 |
Shannon-Wiener多样性指数 Shannon-Wiener diversity index (H') | 1.83 | 3.00 | 3.09 | 3.01 | 2.92 | 3.26 | 3.03 | 2.86 | 2.33 | 1.52 |
Simpson优势度指数 Simpson dominance index (D) | 0.76 | 0.93 | 0.93 | 0.90 | 0.90 | 0.93 | 0.94 | 0.91 | 0.83 | 0.68 |
Pielou均匀度指数 Pielou evenness index (E) | 0.49 | 0.76 | 0.70 | 0.69 | 0.72 | 0.80 | 0.79 | 0.73 | 0.64 | 0.52 |
分布区类型 Distribution area types | 属数 No. of genera (%) |
---|---|
1. 世界分布 Cosmopolitan | 2 (1.8) |
2. 泛热带分布 Pantropic | 8 (7.3) |
3. 热带亚洲和热带美洲间断分布 Tropical Asia and Tropical American disjuncted | 5 (4.6) |
4. 旧世界热带分布 Old World Tropic | 2 (1.8) |
5. 热带亚洲至热带澳大利亚分布 Tropical Asia and Tropical Australia | 3 (2.8) |
6. 热带亚洲分布 Tropical Asia | 6 (5.5) |
热带小计 Tropical subtotal (2-6) | 24 (22.1) |
7. 北温带分布 North Temperate | 43 (39.4) |
8. 东亚和北美间断分布 East Asia and North America disjuncted | 13 (11.9) |
9. 旧世界温带分布 Old World Temperate | 3 (2.8) |
10. 温带亚洲分布 Temperate Asia | 1 (0.9) |
11. 地中海、西至中亚分布 Mediterranean, West Asia to Central Asia | 1 (0.9) |
12. 东亚分布 East Asia | 15 (13.8) |
温带小计 Temperate subtotal (7-12) | 76 (69.7) |
13. 特有分布 Endemic to China | 7 (6.4) |
合计 Total | 109 (100.0) |
表2 秦岭南坡中段海拔样地所有木本植物属的区系组成
Table 2 Floristic composition of all genera of woody plants in all elevation plots in the middle section of the southern slope of Qinling Mountains
分布区类型 Distribution area types | 属数 No. of genera (%) |
---|---|
1. 世界分布 Cosmopolitan | 2 (1.8) |
2. 泛热带分布 Pantropic | 8 (7.3) |
3. 热带亚洲和热带美洲间断分布 Tropical Asia and Tropical American disjuncted | 5 (4.6) |
4. 旧世界热带分布 Old World Tropic | 2 (1.8) |
5. 热带亚洲至热带澳大利亚分布 Tropical Asia and Tropical Australia | 3 (2.8) |
6. 热带亚洲分布 Tropical Asia | 6 (5.5) |
热带小计 Tropical subtotal (2-6) | 24 (22.1) |
7. 北温带分布 North Temperate | 43 (39.4) |
8. 东亚和北美间断分布 East Asia and North America disjuncted | 13 (11.9) |
9. 旧世界温带分布 Old World Temperate | 3 (2.8) |
10. 温带亚洲分布 Temperate Asia | 1 (0.9) |
11. 地中海、西至中亚分布 Mediterranean, West Asia to Central Asia | 1 (0.9) |
12. 东亚分布 East Asia | 15 (13.8) |
温带小计 Temperate subtotal (7-12) | 76 (69.7) |
13. 特有分布 Endemic to China | 7 (6.4) |
合计 Total | 109 (100.0) |
图2 秦岭南坡中段各海拔样地木本植物径级分布及总体径级分布
Fig. 2 Diameter class distribution of woody plants and the overall diameter class distribution along elevational gradients in the middle section of the southern slope of Qinling Mountains
图3 锐齿槲栎(a-f)和栓皮栎(g-l)沿海拔梯度在完全随机模型(CSR)和异质泊松模型(HP)的空间分布。g^obs (r): g(r)的观测值; g^theo (r): g(r)的理论值; 灰色部分为99%置信区间。
Fig. 3 Spatial distribution pattern of Quercus aliena var. acutiserrata (a-f) and Q. variabilis (g-l) under complete spatial randomness (CSR) model and heterogeneous Poisson (HP) model along elevational gradients. g^obs (r), Observed value of g(r); g^theo (r), Theoretical value of g(r); Gray part is the 99% confidence interval.
图4 华山松(a-f)和油松(g-n)沿海拔梯度在完全随机模型(CSR)和异质泊松模型(HP)的空间分布。g^obs (r): g(r)的观测值; g^theo (r): g(r)的理论值; 灰色部分为99%置信区间。
Fig. 4 Spatial distribution pattern of Pinus armandii (a-f) and P. tabuliformis (g-n) under complete spatial randomness (CSR) null model and heterogeneous Poisson (HP) null model along elevational gradients. g^obs (r), Observed value of g(r); g^theo (r), Theoretical value of g(r); Gray part is the 99% confidence interval.
图5 秦岭南坡中段沿海拔梯度群落丰富度指数(a)、Simpson优势度指数(b)、Shannon-Wiener多样性指数(c)、Pielou均匀度指数(d)的变化。R2表示模型拟合优度; P < 0.05表示结果具有统计显著性。
Fig. 5 Changes in species richness (a), Simpson dominance index (b), Shannon-Wiener diversity index (c) and Pielou evenness index (d) along an elevational gradient in the middle section of the southern slope of Qinling Mountains. R2 indicates the goodness of fit of the model and P < 0.05 indicates that the results are statistically significant.
图6 秦岭南坡中段沿海拔Bray-Curtis相异指数和Jaccard相异指数的变化趋势
Fig. 6 Changes in Bray-Curtis index and Jaccard index along an elevational gradient in the middle section of the southern slope of Qinling Mountains
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