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Visits

1. New fossil endocarps of Sambucus (Adoxaceae) from the upper Plioce.. [1843]
2. Geometric morphometrics: A powerful tool for the study of shape ev.. [1496]
3. First discovery of Cucubalus (Caryophyllaceae) fossil, and its bio.. [1200]
4. A new Drynaria (Polypodiaceae) from the Upper Pliocene of Southwes.. [1017]
5. Integrating fossils in a molecular-based phylogeny and testing the.. [987]
6. Fossil fruits of Ailanthus confucii from the Upper Miocene of Wens.. [983]
7. Leaf physiognomy and climate: Are monsoon systems different? [967]
8. Using species distribution modeling to improve conservation and la.. [936]
9. Quantitative reconstruction of the Late Miocene monsoon climates o.. [930]
10. A new Quercus species from the upper Miocene of southwestern China.. [922]
11. Paleoclimatic estimation reveals a weak winter monsoon in southwes.. [920]
12. Nutlet micro-morphology of the genus Microula (Boraginaceae) from .. [889]
13. 海拔对高山栎光合气体交换和叶性状的影响 [856]
14. Late Miocene southwestern Chinese floristic diversity shaped by th.. [835]
15. Continuous existence of Zanthoxylum (Rutaceae) in Southwest China .. [805]
16. New Biogeographic insight into Bauhinia s.l. (Leguminosae): integr.. [750]
17. Evolution of stomatal and trichome density of the Quercus delavayi.. [712]
18. A Miocene leaf fossil record of Rosa (R. fortuita n. sp.) from its.. [691]
19. 若干重要地质事件对中国植物区系形成演变的影响 [639]
20. Rates of Water Loss and Uptake in Recalcitrant Fruits of Quercus S.. [616]
21. Phylogeographic analysis reveals significant spatial genetic struc.. [564]
22. 中国兰科毛兰属一新记录种——孟连毛兰 [561]
23. 青藏高原--现代生物多样性形成的演化枢纽 [560]
24. Warm-cold colonization: response of oaks to uplift of the Himalaya.. [558]
25. First occurrence of Cedrelospermum (Ulmaceae) in Asia and its biog.. [545]
26. Vegetation changes across the Eocene-Oligocene transition: Global .. [539]
27. Regional constraints on leaf physiognomy and precipitation regress.. [537]
28. 陆地生态系统与地球环境的协同演化 [528]
29. 槭属翅果种内形态变异性及对其化石鉴定的意义 [511]
30. Late Miocene vegetation dynamics under monsoonal climate in southw.. [501]
31. 新生代青藏高原生长对东亚水循环及生态系统的影响 [468]
32. The intensification of the East Asian winter monsoon contributed t.. [462]
33. Major declines of woody plant species ranges under climate change .. [452]
34. Himalaya to Hengduan: dynamics of alpine treelines under climate c.. [447]
35. The occurrence of Pinus massoniana Lambert (Pinaceae) from the upp.. [446]
36. 古近纪/新近纪之交青藏高原陆地生态系统的重大转折 [439]
37. New U-Pb dates show a Paleogene origin for the modern Asian biodiv.. [435]
38. Leaf form-climate relationships on the global stage: an ensemble o.. [431]
39. The oldest Mahonia (Berberidaceae) fossil from East Asia and its b.. [431]
40. Fossil seeds of Euryale (Nymphaeaceae) indicate a lake or swamp en.. [425]
41. A new positive relationship between pCO(2) and stomatal frequency .. [424]
42. Resilience of plant-insect interactions in an oak lineage through .. [423]
43. A global-scale test for monsoon indices used in palaeoclimatic rec.. [415]
44. An early Oligocene occurrence of the palaeoendemic genus Dipteroni.. [407]
45. Biotic interchange through lowlands of Tibetan Plateau suture zone.. [407]
46. Vegetation history of the central Tibetan region during the late O.. [402]
47. A tropical forest of the middle Miocene of Fujian (SE China) revea.. [398]
48. Large-scale dataset from China gives new insights into leaf margin.. [397]
49. The oldest fossil record of Bauhinia s.s. (Fabaceae) from the Tibe.. [397]
50. 西藏芒康似勾儿茶叶属(鼠李科)化石及其生物地理学意义 [387]
51. 中新世以来黄毛青冈复合群(Quercus delavayi complex)气孔及叶表皮毛密.. [385]
52. Fossil infructescence from southwestern China reveals Paleogene es.. [385]
53. 鹤庆栎(Quercus heqingensis n. sp.)的发现及其在古大气CO_2浓度重建中.. [383]
54. Occurrence of Christella (Thelypteridaceae) in Southwest China and.. [379]
55. Gradual expansion of moisture sensitive Abies spectabilis forest i.. [374]
56. The first fossil record of ring-cupped oak (Quercus L. subgenus Cy.. [372]
57. Organellomic data sets confirm a cryptic consensus on (unrooted) l.. [372]
58. Podocarpium (Fabaceae) from the late Eocene of central Tibetan Pla.. [370]
59. FIRST FOSSIL FRUITS AND LEAVES OF BURRETIODENDRON SL (MALVACEAE SL.. [369]
60. The first fossil Microsoroid fern (Palaeosorum ellipticum gen. et .. [368]
61. The first megafossil record of Goniophlebium (Polypodiaceae) from .. [365]
62. Tibetan Plateau: An evolutionary junction for the history of moder.. [362]
63. NEW MIDDLE MIOCENE FOSSIL WOOD OF WATARIA (MALVACEAE) FROM SOUTHWE.. [356]
64. Heterogeneous occurrence of evergreen broad-leaved forests in East.. [354]
65. East Asian origins of European holly oaks (Quercus section Ilex Lo.. [351]
66. 始新世-渐新世气候转折期的植被变化:全球信号与区域特征 [351]
67. Evolutionary History of Atmospheric CO2 during the Late Cenozoic f.. [350]
68. Artificial neural networks reveal a high-resolution climatic signa.. [349]
69. 中国兰科毛兰属一新记录种孟连毛兰 [342]
70. Miocene Ulmus fossil fruits from Southwest China and their evoluti.. [342]
71. Distribution of Cenozoic plant relicts in China explained by droug.. [341]
72. 日本中部地区上新世到更新世过渡时期的气候演变:来自水杉叶片化石稳定.. [341]
73. Late Pliocene temperatures and their spatial variation at the sout.. [339]
74. A new Tsuga species from the upper Miocene of Yunnan, southwestern.. [337]
75. A new Celastrus species from the middle Miocene of Yunnan, China a.. [336]
76. SEQUOIA MAGUANENSIS, A NEW MIOCENE RELATIVE OF THE COAST REDWOOD, .. [335]
77. Late Miocene Palaeocarya (Engelhardieae: Juglandaceae) from Southw.. [333]
78. A Miocene leaf fossil record of Rosa (R-fortuita n. sp.) from its .. [333]
79. The earliest fossil bamboos of China (middle Miocene, Yunnan) and .. [329]
80. Eocene Podocarpium (Leguminosae) from South China and its biogeogr.. [321]
81. 新生代特提斯海区域的气候演变及其驱动因素 [318]
82. 申请国家自然科学基金项目的一点体会 [316]
83. Climate evolution and its driving factors in the Tethys Sea region.. [315]
84. The effects of litter quantity and quality on soil nutrients and l.. [312]
85. Tree rings reveal recent intensified spring drought in the central.. [312]
86. Lake geochemistry reveals marked environmental change in Southwest.. [311]
87. Bauhinia (Leguminosae) Fossils from the Paleogene of Southwestern .. [310]
88. Wildfire associated with a deciduous broadleaved forest from the N.. [300]
89. Hemitrapa Miki (Lythraceae) from the earliest Oligocene of southea.. [298]
90. Variations in Leaf Morphological Traits of Quercus guyavifolia (Fa.. [295]
91. Fire dynamics under monsoonal climate in Yunnan, SW China: past, p.. [294]
92. Peaches Preceded Humans: Fossil Evidence from SW China [293]
93. A new fossil species of Cryptomeria (Cupressaceae) from the Rupeli.. [293]
94. A new fossil record of Palaeosinomenium (Menispermaceae) from the .. [293]
95. Oligocene Limnobiophyllum (Araceae) from the central Tibetan Plate.. [289]
96. 青藏高原是研究生物演化和环境演变的天然实验室 [286]
97. Habitat, climate and potential plant food resources for the late M.. [282]
98. 西藏始新世狭叶梅属(Palibinia)的发现及其地质学和生物学意义 [282]
99. The importance of tropical tree-ring chronologies for global chang.. [281]
100. Late Pliocene diversity and distribution of Drynaria (Polypodiacea.. [279]

Downloads

1. Vegetation changes across the Eocene-Oligocene transition: Global .. [477]
2. Integrating fossils in a molecular-based phylogeny and testing the.. [446]
3. Leaf physiognomy and climate: Are monsoon systems different? [418]
4. 青藏高原--现代生物多样性形成的演化枢纽 [408]
5. 陆地生态系统与地球环境的协同演化 [324]
6. Paleoclimatic estimation reveals a weak winter monsoon in southwes.. [318]
7. A Miocene leaf fossil record of Rosa (R. fortuita n. sp.) from its.. [318]
8. Continuous existence of Zanthoxylum (Rutaceae) in Southwest China .. [317]
9. The oldest fossil record of Bauhinia s.s. (Fabaceae) from the Tibe.. [314]
10. 古近纪/新近纪之交青藏高原陆地生态系统的重大转折 [304]
11. Geometric morphometrics: A powerful tool for the study of shape ev.. [303]
12. First occurrence of Cedrelospermum (Ulmaceae) in Asia and its biog.. [297]
13. Himalaya to Hengduan: dynamics of alpine treelines under climate c.. [296]
14. Late Miocene southwestern Chinese floristic diversity shaped by th.. [293]
15. 若干重要地质事件对中国植物区系形成演变的影响 [292]
16. Vegetation history of the central Tibetan region during the late O.. [291]
17. New fossil endocarps of Sambucus (Adoxaceae) from the upper Plioce.. [278]
18. Warm-cold colonization: response of oaks to uplift of the Himalaya.. [275]
19. Podocarpium (Fabaceae) from the late Eocene of central Tibetan Pla.. [270]
20. Biotic interchange through lowlands of Tibetan Plateau suture zone.. [261]
21. 西藏芒康似勾儿茶叶属(鼠李科)化石及其生物地理学意义 [259]
22. Fossil seeds of Euryale (Nymphaeaceae) indicate a lake or swamp en.. [257]
23. Wildfire associated with a deciduous broadleaved forest from the N.. [257]
24. Nutlet micro-morphology of the genus Microula (Boraginaceae) from .. [250]
25. Heterogeneous occurrence of evergreen broad-leaved forests in East.. [248]
26. 槭属翅果种内形态变异性及对其化石鉴定的意义 [239]
27. A new Drynaria (Polypodiaceae) from the Upper Pliocene of Southwes.. [238]
28. A new fossil record of Palaeosinomenium (Menispermaceae) from the .. [235]
29. 海拔对高山栎光合气体交换和叶性状的影响 [233]
30. The intensification of the East Asian winter monsoon contributed t.. [232]
31. Late Miocene vegetation dynamics under monsoonal climate in southw.. [223]
32. Leaf form-climate relationships on the global stage: an ensemble o.. [222]
33. Climate evolution and its driving factors in the Tethys Sea region.. [219]
34. 植物多样性对古新世-始新世极热事件全球增温的响应——来自化石和模型.. [216]
35. Organellomic data sets confirm a cryptic consensus on (unrooted) l.. [213]
36. The Paleogene to Neogene climate evolution and driving factors on .. [208]
37. 青藏高原是研究生物演化和环境演变的天然实验室 [206]
38. Evolution of East Asian subtropical evergreen broad-leaved forests.. [206]
39. Quantitative reconstruction of the Late Miocene monsoon climates o.. [204]
40. Rates of Water Loss and Uptake in Recalcitrant Fruits of Quercus S.. [199]
41. Tibetan Plateau: An evolutionary junction for the history of moder.. [197]
42. A new Quercus species from the upper Miocene of southwestern China.. [196]
43. New U-Pb dates show a Paleogene origin for the modern Asian biodiv.. [196]
44. First discovery of Cucubalus (Caryophyllaceae) fossil, and its bio.. [195]
45. Fossil infructescence from southwestern China reveals Paleogene es.. [194]
46. Evolution of stomatal and trichome density of the Quercus delavayi.. [190]
47. 申请国家自然科学基金项目的一点体会 [190]
48. Resilience of plant-insect interactions in an oak lineage through .. [184]
49. Using species distribution modeling to improve conservation and la.. [182]
50. Paleoclimate model-derived thermal lapse rates: Towards increasing.. [182]
51. Large-scale dataset from China gives new insights into leaf margin.. [181]
52. A tropical forest of the middle Miocene of Fujian (SE China) revea.. [180]
53. 鹤庆栎(Quercus heqingensis n. sp.)的发现及其在古大气CO_2浓度重建中.. [180]
54. An early Oligocene occurrence of the palaeoendemic genus Dipteroni.. [178]
55. NEW MIDDLE MIOCENE FOSSIL WOOD OF WATARIA (MALVACEAE) FROM SOUTHWE.. [174]
56. A Miocene leaf fossil record of Rosa (R-fortuita n. sp.) from its .. [172]
57. A global-scale test for monsoon indices used in palaeoclimatic rec.. [168]
58. Late Pliocene temperatures and their spatial variation at the sout.. [168]
59. The oldest Mahonia (Berberidaceae) fossil from East Asia and its b.. [167]
60. East Asian origins of European holly oaks (Quercus section Ilex Lo.. [162]
61. The early Oligocene establishment of modern topography and plant d.. [162]
62. A new positive relationship between pCO(2) and stomatal frequency .. [159]
63. The first fossil record of ring-cupped oak (Quercus L. subgenus Cy.. [158]
64. Gradual expansion of moisture sensitive Abies spectabilis forest i.. [155]
65. 始新世-渐新世气候转折期的植被变化:全球信号与区域特征 [153]
66. The effects of litter quantity and quality on soil nutrients and l.. [152]
67. Bauhinia (Leguminosae) Fossils from the Paleogene of Southwestern .. [151]
68. Miocene Dipteronia (Sapindaceae) samaras from South Korea and thei.. [151]
69. 日本中部地区上新世到更新世过渡时期的气候演变:来自水杉叶片化石稳定.. [150]
70. 我国西南植物区系的分异:椿榆属和臭椿属化石的启示 [150]
71. The importance of tropical tree-ring chronologies for global chang.. [150]
72. 中国兰科毛兰属一新记录种——孟连毛兰 [149]
73. Fossil involucres of Ostrya (Betulaceae) from the early Oligocene .. [149]
74. Phylogeographic analysis reveals significant spatial genetic struc.. [148]
75. The first megafossil record of Goniophlebium (Polypodiaceae) from .. [148]
76. Major turnover of biotas across the Oligocene/Miocene boundary on .. [148]
77. Late Miocene Palaeocarya (Engelhardieae: Juglandaceae) from Southw.. [146]
78. Miocene Ulmus fossil fruits from Southwest China and their evoluti.. [146]
79. A Middle Eocene lowland humid subtropical "Shangri-La" ecosystem i.. [145]
80. Regional constraints on leaf physiognomy and precipitation regress.. [144]
81. Pod fossils of Albizia (Fabaceae: Caesalpinioideae) from the late .. [143]
82. Leaf and infructescence fossils of Alnus (Betulaceae) from the lat.. [142]
83. Evolutionary History of Atmospheric CO2 during the Late Cenozoic f.. [140]
84. Oligocene Limnobiophyllum (Araceae) from the central Tibetan Plate.. [140]
85. Distribution of Cenozoic plant relicts in China explained by droug.. [138]
86. Occurrence of Christella (Thelypteridaceae) in Southwest China and.. [137]
87. 中新世以来黄毛青冈复合群(Quercus delavayi complex)气孔及叶表皮毛密.. [136]
88. The relationship between leaf physiognomy and climate based on a l.. [136]
89. Tsuga seed cones from the late Paleogene of southwestern China and.. [136]
90. Higher palaeoelevation in the Baoshan Basin: Implications for land.. [135]
91. Artificial neural networks reveal a high-resolution climatic signa.. [134]
92. Hemitrapa Miki (Lythraceae) from the earliest Oligocene of southea.. [130]
93. Biotic interchange through lowlands of Tibetan Plateau suture zone.. [127]
94. Understanding the evolution of biodiversity in Asia [123]
95. Early Oligocene vegetation and climate of southwestern China infer.. [122]
96. An updated chronostratigraphic framework for the Cenozoic sediment.. [121]
97. The occurrence of Pinus massoniana Lambert (Pinaceae) from the upp.. [119]
98. Effects of herbivores and litter on Lithocarpus hancei seed germin.. [117]
99. 西藏札达盆地上新世植物群及古环境 [115]
100. 西藏新生代植物近十年来的重要发现、认识及其意义 [113]