1 Introduction

Yunnan in southwestern China has long been recognized as a hotspot for plant diversity(Wu, 1988; López-Pujol et al., 2006, 2011; Ruth et al., 2008; Turkington and Harrower, 2016). It is home to approximately 16, 000 higher plant species grouped into more than 2300 genera within 244 families, representing 6% of the world's total diversity of higher plant species(Wu, 1979), even though the region accounts for only 4% of the Chinese land surface. Nearly half of these plant species are endemic to Yunnan. In addition, almost all ecosystem types within China, including tropical seasonal rain forest, evergreen broad-leaved forest, sclerophyllous evergreen broad-leaved forest, deciduous broad-leaved forest, both warm and cold temperate coniferous forests, dry and warm valley scrubs as well as subalpine and alpine scrubs can be found in Yunnan(Writing Group of Yunnan Vegetation, 1987). This high diversity of plant taxa and vegetation types qualifies Yunnan as an outstanding place for botanical research. Yunnan also exhibited exceptional botanical richness in the geological past as revealed by the rich fossil record. To date, around 20 megafossil floras are known from the Cenozoic of Yunnan, and hundreds of fossil species, covering ferns, gymnosperms and angiosperms, have been documented. A summary of past plant diversity based on palaeobotanical data affords a better understanding of the modern botanical richness in this region.

In the present review, we compile palaeobotanical data from literature to document plant diversity in Yunnan throughout the Cenozoic. Only fossil taxa represented by megafossils are considered, i.e., leaves, wood, fruits, seeds and flowers. Pollen records are not considered, because they can be transported to Yunnan from elsewhere and cannot be identified to a fine enough taxonomic resolution. We first briefly introduce the research history of palaeobotany in Yunnan, then present known fossil families, genera and species to depict the diversity of Cenozoic plants and ecosystems, and analyze the inferred floristic characters and changes. We also summarize the Neogene climate evolution in Yunnan and related extinction events exemplified for selected plant taxa. The present review aims to facilitate access to the rich palaeobotanical record of Yunnan for both palaeobotanists and botanists.

2 Research history of palaeobotany in Yunnan

As a montane region, Yunnan has more than 150 Cenozoic sedimentary basins, many of which have yielded Cenozoic strata that bear plant fossils(Ge and Li, 1999). The region archives at least 20 megafossil floras, ranging from the early Oligocene to late Pliocene(Fig. 1). However, these fossil floras rarely attracted attention before the beginning of the last century. In 1920, Colani reported the first plant fossils recovered from Miocene sediments along the former railway connecting Kunming and Hanoi(Colani, 1920), but interest was transient as no more palaeobotanical studies followed for the next 57 years. In 1978, several Chinese paleobotanists, including Tao Jun-Rong, Guo Shuang-Xing and Li Hao-Ming, jointly published a monograph entitled “Cenozoic Plants of China”(Writing Group of the Cenozoic Plants of China, 1978). In that monograph, 301 plant fossil species, covering mosses, ferns, gymnosperms and angiosperms, were described systematically. Among them, 76 species came from five floras in Yunnan: the Oligocene Jinggu flora, the Miocene Duotan flora, the early Miocene Shuanghe flora, the late Miocene Xiaolongtan flora, and the late Pliocene Eryuan flora. In the 1980s, Tao and Chen(1983)described the late Miocene Bangmai flora, also known as the Lincang flora, from southwestern Yunnan which comprised 59 fossil species grouped into 48 genera within 28 families; Tao(1986)reported the late Pliocene Fudong flora from northwestern Yunnan which yielded 17 species grouped into four genera of three families. Unfortunately, published mostly in Chinese, these works have had limited international recognition.

During the last two decades, 10 Cenozoic megafossil floras from Yunnan have been studied as doctoral or master's research projects, e.g., the late Miocene Xianfeng flora, the late Pliocene Nanbanbang, Fudong, Longmen and Tuantian floras. A few are still being investigated for the subject of doctoral research, e.g., the middle Miocene Wenshan and Maguan floras(formerly dated as late Miocene, but recently moved to middle Miocene according to lake geochemical evidence; Lebreton-Anberrée et al., 2016). To the best of our knowledge, at least eight doctoral and two master's theses are freely accessible at universities or institutions in China, e.g., Lanzhou University, Kunming Institute of Botany, Chinese Academy of Sciences(Zhao, 2002; Xie, 2007; Wu, 2010; Su, 2010; Xing, 2010; Huang, 2012; Hu, 2013; Li, 2015; Wang, 2016; Zhu, 2016). Such theses usually present a full list of identified plant taxa that more or less reflects a given fossil flora(Wu, 2010; Huang, 2012; Zhu, 2016). Some of the authors have also interpreted the palaeovegetation or palaeoclimate accordingly(Wu, 2010; Su, 2010; Xing, 2010). Based on detailed palaeobotanical research, hundreds of fossil species have been published in a variety of international journals(e.g., Zhao et al., 2004; Xie et al., 2010; Xing et al., 2010, 2013; Su et al., 2011, 2013b; Huang et al., 2012, 2013; Wu et al., 2012; Hu et al., 2014; Jia et al., 2015; Li et al., 2015; Zhu et al., 2015, 2016; Huang et al., 2016a; Fig. 2). In addition to those targeted within doctoral or master's projects, research has begun on other fossil floras, such as the Oligocene Jinggu flora, the middle Miocene Sanzhangtian flora, and the late Miocene Shuitangba flora, and tens of fossil species have been described(e.g., Wen et al., 2013; Jacques et al., 2013; Wang et al., 2013; Meng et al., 2014, 2015; Xie et al., 2014; Zhang et al., 2015a, 2015b; Liang et al., 2016; Su et al., 2016; Fig. 2). It seems that the recent decades have witnessed an upward surge in palaeobotanical research in Yunnan.

3 Families, genera and species of fossil plants

Up to now, approximately 386 plant species(including morphospecies)belonging to 170 genera within 66 families have been documented from the Cenozoic of Yunnan and most of them are from the Neogene(see the Appendix). They include ferns, gymnosperms and angiosperms, of which ferns and gymnosperms are relatively few.

Fossil ferns from Yunnan comprise only nine species placed in five genera of four families: Davalliaceae, Equisetaceae, Osmundaceae and Polypodiaceae. The genus Drynaria in Polypodiaceae is the most diverse and has four different fossil species, which all came from the Neogene of western Yunnan(Su et al., 2011; Wu et al., 2012; Wen et al., 2013; Huang et al., 2016b). This may from a historical view explicate the establishment of the modern Drynaria diversity in the Hengduan Mountains, western Yunnan(Huang et al., 2016b). Fossil gymnosperms from Yunnan fall into 24 species grouped into 10 genera of two families, Pinaceae and Cupressaceae. The former has 15 fossil species belonging to four genera(Cedrus, Picea, Pinus and Tsuga), while the latter has nine fossil species belonging to six genera(Calocedrus, Cephalotaxus, Cupressus, Platycladus, Sequoia and Taiwania).

Similar to modern Yunnan, angiosperms were the most diverse plant group throughout the Cenozoic. A total of 353 fossil species of angiosperms grouped into 155 genera within 60 families are known from megafossil remains. At the family level, Fabaceae has 23 genera with fossil records and represents the most genus-rich family in the fossils, followed by Lauraceae which has 11 fossil genera(Table 1). Other angiosperm families having at least five genera of fossil plants are Rosaceae(8 genera), Fagaceae(7 genera), Juglandaceae(6 genera), Malvaceae(6 genera)and Rutaceae(5 genera). Angiosperm families having four genera of fossil plants include Anacardiaceae, Betulaceae, Hamamelidaceae, Poaceae and Rhamnaceae. Most families are represented by only one genus with fossil evidence, e.g., Buxaceae, Caryophyllaceae, Elaeagnaceae and Moraceae(Table 1). Further fossil finds will no doubt reveal more. For their diversity at the species level, Fagaceae having 79 fossil species is the most species-rich family, followed by Fabaceae and Lauraceae with 38 and 33 fossil species, respectively. There are seven other families having 10 or more fossil species, namely Juglandaceae(14 species), Ulmaceae(13 species), Sapindaceae(13 species), Salicaceae(12 species), Betulaceae(11 species), Anarcardiaceae(11 species)and Rosaceae(10 species). Most families, however, have only one or two fossil species, e.g., Euphorbiaceae, Oleaceae, Nymphaeaceae and Celastraceae(Table 1). Based on the above summary, Fabaceae, Fagaceae, Lauraceae, Juglandaceae and Rosaceae were among the most diversified families in the Cenozoic of Yunnan either at the generic level or at the species level. Today, Fagaceae and Lauraceae are two of the major families contributing to evergreen broad-leaved forests in Yunnan as well as in other parts of southern China(Writing Group of Yunnan Vegetation, 1987), and Fabaceae is among the most common families in tropical and subtropical forests in Yunnan. Rich fossil records of Fabaceae, Fagaceae and Lauraceae suggest that their dominance in the present evergreen broad-leaved forests of Yunnan seems to have been largely established at least by the Neogene. In addition, many other families that are widely seen in the modern broad-leaved forests were also found as fossils, e.g., Juglandaceae, Ulmaceae, Sapindaceae, Salicaceae, Betulaceae and Rosaceae. This suggests that themodern floristic composition at the family level in Yunnan was probably formed in the Neogene or before. Interestingly, some families such as Magnoliaceae and Theaceae that are important and frequent components today are not well represented in the fossil record(Table 1).

With respect to the species diversity of genera, six angiosperm genera have more than 10 fossil species, i.e., Quercus, Castanopsis, Lithocarpus, Acer, Cyclobalanopsis and Cinnamomum(Table 2; Fig. 3). Among them, Quercus is obviously the richest and has 36 fossil species; Castanopsis, Lithocarpus and Acer have 14, 13 and 11 fossil species, respectively; and Cyclobalanopsis and Cinnamomum each has 10 fossil species. It is worth explaining that different classifications of Quercus and Cyclobalanopsis exist. Some botanists consider Quercus and Cyclobalanopsis as two separate genera distinguished by the imbricate-scaled or lamellate structure of the e.g., Betula and Ficus both with four fossil species, Alnus and Carpinus with three, and Lindera and Mahonia with two(Table 2). Most of the genera have only one fossil species, e.g., Buxus, Citrus, Cornus and Sambucus. Notably, the genera that were species diverse in the Cenozoic mainly belong to Fagaceae(Querucs, Castanopsis, Lithocarpus and Cyclobalanopsis)and Lauraceae(Cinnamomum, Phoebe and Machilus), and as already mentioned, they are still diverse in modern forests of Yunnan. Other genera that have good fossil records are also important components of modern broad-leaved forests in Yunnan, e.g., Acer, Ulmus, Myrica, Rhus and Salix. This therefore suggests the idea that the composition of Neogene evergreen broad-leaved forests in this regionwas already similar to that today at the generic level.

4 Disappearance of some plant taxa

Molecular studies have been repeatedly interpreted as meaning that numerous plant groups in Yunnan experienced species diversification as a result of increasing environmental complexity(e.g., Wang et al., 2005; Yu et al., 2015). The other side of the historical emergence of new lineages, however, is species extinction. Although most families and genera recorded as fossils still exist, some genera disappeared from Yunnan after the Neogene. To date, there are seven genera with fossil evidence we do not encounter in the natural vegetation of the region. They are Cedrus, Sequoia, Berryophyllum, Cedrelospermum, Palaeocarya, Podocarpium and Wataria(Fig. 4).

Cedrus is a small genus of four extant species restricted to Mediterranean regions and the western Himalayas(Maheshwari and Biswas, 1970). In modern Yunnan, no Cedrus grows as a natural population. However, a recent fossil discovery of seeds and cone scales indicate that Cedrus occurred in northwestern Yunnan during the late Pliocene(Su et al., 2013b). The genus must have disappeared from this region soon after(Su et al., 2013b), as is also evidenced by the decline in its pollen occurrences(Tong et al., 1990; Wang and Shu, 2004; Xiao et al., 2010). Sequoia is a genus now endemic only to the western coast of North America(Waston and Eckenwalder, 1993). Like the situation with Cedrus, Sequoia also has a fossil representative in Yunnan. Fossils of cones and leafy shoots discovered from the middle Miocene Maguan flora in southeastern Yunnan closely resemble modern Sequoia, indicating its occurrence in the region at that time(Zhang et al., 2015a). The genus probably disappeared from Yunnan after the middle Miocene. This raises the question as to why Cedrus and Sequoia went extinct in Yunnan but survive in other regions. Investigations by Su et al.(2013b)and Zhang et al.(2015a)have demonstrated that the aridification of the dry season, associated with monsoon intensification, might have played a major role. Today, Yunnan has dry conditions from late autumn to early spring, whereas Mediterranean regions and the western coast of North America both have wet winters and springs. As seeds of Cedrus and Sequoia are recalcitrant, they germinate immediately upon their maturity in the autumn(Olson et al., 1990; Kumar et al., 2011). Unfortunately, dry conditions after autumn may prevent their seeds from germinating or their seedlings from developing new leaves. In contrast to modern climates, in the Neogene Yunnan had relatively humid conditions in the dry season(Xia et al., 2009; Sun et al., 2011; Xing et al., 2012; Su et al., 2013a; Huang et al., 2015a). Humid and suitable habitats might explain the historical existence of the two genera in this region. As precipitation in the dry season decreased, likely linked to the Asian monsoon intensification, as is elaborated below, the dry winter and spring ultimately led to the regional extinction of species that require a moister dry season(Su et al., 2013b; Zhang et al., 2015a).

Unlike Cedrus and Sequoia that have no living relatives in Yunnan but survive in other regions, the remaining five genera only have fossil representatives; in other words, they have gone extinct globally. Berryophyllum is an extinct genus morphologically similar to extant Lithocarpus, Canstanopsis and Cyclobalanopsis of Fagaceae(Zhou, 1996). The genus was widely distributed in Europe and North America from the Paleocene to Miocene(Jones and Dilcher, 1988; Zhou, 1996). In Yunnan, it has been described only from the Oligocene Jinggu flora in southern Yunnan. Cedrelospermum(Ulmaceae)is another extinct genus that was well represented in Europe(Hably and Thiébaut, 2002; and references therein)and North America(Manchester, 1987, 1989; Manchester and Tiffney, 2001). In Yunnan, one fossil species described as Cedrelospermum asiaticum has been reported from the middle Miocene Maguan flora in southeastern Yunnan(Jia et al., 2015). This species represents the first record of Cedrelospermum in Asia(Jia et al., 2015). Palaeocarya is morphologically similar to two modern genera, namely Engelhardia and Oreomunnea of Juglandaceae(Manchester, 1999). It has an excellent fossil record in the Northern Hemisphere, extending from the Pliocene deeply into the Eocene(Tanai and Uemura, 1983; Jähnichen et al., 1984; Manchester, 1987; Guo and Zhang, 2002; Jin, 2009; Meng et al., 2015). In Yunnan, Palaeocarya has been reported from the middle Miocene Wenshan flora in southeastern Yunnan(Meng et al., 2015)and the late Pliocene Tuantian flora in southwestern Yunnan(Xie et al., 2010). Podocarpium of Fabaceae is one of the most common legumes recorded from the Eocene to Pliocene(Xu et al., 2015). In Yunnan, the genus has one fossil species named P. poocarpum from the late Miocene Xiaolongtan flora in southern Yunnan(Guo and Zhou, 1992). The extinct genus Wataria, established by Terada and Suzuki(1998), is anatomically similar to Reeveia of Malvaceae. In Yunnan, Wateria yunnanica has been described from the middle Miocene Shengli flora in southern Yunnan on the basis of fossil wood(Li et al., 2015). This wood species represents the first fossil occurrence of the genus in China(Li et al., 2015).

5 Floristic characters and changes

Of the 20 megafossil floras from Yunnan considered here, those of late Miocene and late Pliocene age have been well studied and they are relatively abundant(Fig. 1). Hence these floras may readily reflect floristic characters of the two time slices in the region as well as their changes. Fossil floras of other stratigraphical phases are not considered in the present analyses, as they have been insufficiently studied from a formal systematic viewpoint.

There are four late Miocene floras known from Yunnan on the basis of which we look at the lateMiocene floristic characteristics: the Shuitangba, Xianfeng, Bangmai and Xiaolongtan floras. The late Miocene Shuitangba flora in northeastern Yunnan is dominated by subtropical representatives of Quercus as revealed by the pollen record(Chang et al., 2015), and Euryale in the aquatic ecosystem as reflected by recently recovered carpological remains(Huang et al., 2015b). The flora contains several temperate elements such as Corylus and Staphylea, and only a few pantropical ones such as Zanthoxylum. Thus the Shuitangba flora might represent a northern subtropical flora. The late Miocene Xianfeng and Xiaolongtan floras in eastern Yunnan are both dominated by the evergreen fagaceous elements such as Cyclobalanopsis, Lithocarpus and Quercus, as well as Lauraceae(Xia et al., 2009; Xing et al., 2012). In the Xiaolongtan flora, tropical and subtropical Fabaceae are relatively abundant(Guo and Zhou, 1992; Xia et al., 2009), but the percentage of tropical components(30-50%)is still belowthe minimumlevel(60%)that defines a tropical floristic region(Zhu, 2013). Therefore, the Xianfeng and Xiaolongtan floras represent two subtropical floras. By contrast, the late Miocene Bangmai flora in southwestern Yunnan contains more tropical genera, accounting for 60% of the fossil assemblage(Guo, 2011). Moreover, several genera are mainly or even merely distributed in tropical regions, such as Mucuna, Murraya, Neocinnamomum, Ormosia, Piper and Terminalia(Guo, 2011). According to the definition of a tropical floristic region by Zhu(2013), the late Miocene Bangmai flora would qualify as tropical. Thus we conclude that in the late Miocene three known floristic regions occurred in Yunnan: a northern subtropical floristic region in the northeast, a subtropical floristic region in the east, and a tropical floristic region in the southwest(Fig. 5A).

For the late Pliocene, seven fossil floras are known from Yunnan, i.e., the Nanbanbang, Fudong, Eryuan, Longmen, Tuantian, Yuanmou and Hunshuitang floras. The first four floras from the southern Hengduan Mountains in northwestern Yunnan are fairly distinguished by the dominance of mountain oaks, Quercus sect. Heterobalanus, suggesting sclerophyllous evergreen broad-leaved forests during the late Pliocene. This is well supported by the fact that seven out of the 20 fossil species from the Fudong flora belong to Quercus sect. Heterobalanus(Huang, 2012), and 1275 out of around 1500 fossil specimens from the Longmen flora belong to this section(Su, 2010). Today, sclerophyllous evergreen broad-leaved forests dominated by Quercus sect. Heterobalanus are widely distributed in northwestern Yunnan(Writing Group of Yunnan Vegetation, 1987). This pattern might have been largely established by the late Pliocene. Distinct from these four floras, the contemporary Tuantian flora in southwestern Yunnan was shown to contain many tropical to subtropical elements, accounting for about 53% of the recognized fossil taxa(Wu, 2010). They include Castanposis, Cyclobalanopsis and Quercus of Fagaceae, and Cinnamomum, Lindera and Machilus of Lauraceae(Wu, 2010), which collectively characterize a subtropical evergreen broad-leaved forest. The late Pliocene Hunshuitang flora in eastern central Yunnan is dominated by Cyclobalanopsis(Hu, 2013; Hu et al., 2014), also suggesting a subtropical evergreen broad-leaved forest. Hence in the late Pliocene of Yunnan, at least two kinds of floristic regions existed: sclerophyllous evergreen broad-leaved forests in the northwest that represented a subalpine floristic region, and subtropical evergreen broad-leaved forests in the southwest and eastern center that in each case represented a subtropical floristic region(Fig. 5B).

Based on the above discussions, Yunnan possibly witnessed different floristic features between the late Miocene and late Pliocene. This allows us to observe floristic changes from the late Miocene to late Pliocene through to today. In northern Yunnan, the proportion of temperate elements at the generic level has increased since the late Miocene(Jacques et al., 2014). This is best exemplified by the fact that sclerophyllous evergreen broad-leaved forests were apparently absent during the late Miocene, but were well established in the late Pliocene and are still seen today. In southern Yunnan, the percentage of tropical elements declined significantly, as was previously noticed by Jacques et al.(2014). Today, Yunnan is covered mainly by subtropical evergreen broad-leaved forests, with tropical forests being restricted to its southern most parts. Overall, it appears that thermophylic floras have moved southward since the late Miocene, purportedly in response to elevation changes(Jacques et al., 2014).

6 Areal type analyses of seed plants

Research into spatial distribution patterns of plants can help botanists to better understand the origin of a flora and its relationship with others. In China, this kind of study began in 1965(Wu, 1965). In 1991, Wu(1991)summarized the results of previous studies and proposed a term named “areal type” to reveal the distribution of a genus of seed plants. In that summary, 15 areal types of seed plants distributed in China were defined and described(Wu, 1991). They are 1. Cosmopolitan, 2. Pantropic, 3. Tropical Asia and Tropical America disjunct, 4. Old World Tropic, 5. Tropical Asia and Tropical Australasia, 6. Tropical Asia to Tropical Africa, 7. Tropical Asia(IndoeMalaysia), 8. North Temperate, 9. East Asia and North America disjunct, 10. Old World Temperate, 11. Temperate Asia, 12. Mediterranean, West Asia to Central Asia, 13. Central Asia, 14. East Asia, and 15. Endemic to China(Wu, 1991;Wu et al., 2003). In the present review, we apply the definitions by Wu(1991)to analyze the areal types of seed plant genera from the Cenozoic of Yunnan. To achieve the best spatial resolution, we focus only on the late Miocene and late Pliocene floras, because of their relative abundance in Yunnan(Tables 3 and 4).

The late Miocene Shuitangba flora is represented by seven areal types at the generic level, the Old World Temperate type of which being the most abundant, followed by the North Temperate type. The late Miocene Xianfeng flora is dominated by the North Temperate type followed by the Tropical Asia and Tropical America disjunct type and the East Asia and North America disjunct type(Fig. 6). The late Miocene Bangmai and Xiaolongtan floras comprise several areal types with each including various genera. The Pantropic type frequently occurred in both floras, with the number of genera being 16 and 9, respectively. Other important areal types are the East Asia and North America disjunct type, the Tropical Asia(IndoeMalaysia)type and the North Temperate type. It is interesting that the Pantropic type and Tropical Asia(IndoeMalaysia)type are best to well represented in the Bangmai and Xiaolongtan floras in southern Yunnan, whereas they are rare to absent in the Shuitangba and Xianfeng floras in northern Yunnan(Fig. 6). Because these two areal types of seed plants reflect a tropical floristic composition, the Bangmai and Xiaolongtan floras may have a higher percentage of tropical elements than the Shuitangba and Xianfeng floras. Moreover, it should be noted that the Bangmai and Xiaolongtan floras have similar compositions of areal types. This seems to disagree with the suggested subdivision of floristic regions, namely that the late Miocene Bangmai flora represented a tropical floristic region while the late Miocene Xiaolongtan flora represented a subtropical floristic region. However, the Pantropic type of the former is considerably richer than the latter, which apparently supports our floristic region division. Hence it can be concluded that in the late Miocene southern Yunnan had far more Pantropic type elements than northern Yunnan.

To reconstruct the situation in the late Pliocene, four fossil floras can be used: the Fudong, Eryuan, Longmen and Tuantian floras. As is shown, the first three floras from northwestern Yunnan have only a few areal types, meaning low diversity of areal types(Fig. 7). Interestingly, they are all dominated by the North Temperate type, suggesting temperate floristic features. This is in line with results of our floristic analyses that northwestern Yunnan represented a subalpine floristic region. Different from the Fudong, Eryuan and Longmen floras, the Tuantian flora in southwestern Yunnan is much more diverse with regards to areal types(Fig. 7). Although the North Temperate type is also dominant, the Tropical Asia(IndoeMalaysia)type and the East Asia and North America disjunct type are frequent. Other areal types include the Pantropic type, the Tropical Asia and Tropical America disjunct type, the Old World Tropic type, the Tropical Asia and Tropical Australasia type, and the Tropical Asia to Tropical Africa type, which are found mainly in tropical zones. Therefore, the Tuantian flora is closer to a tropical flora than the remaining three, as is also indicated by our floristic analyses. In short, late Pliocene plant assemblages in northwestern Yunnan were dominated exclusively by the North Temperate type, while in southwestern Yunnan the Tropical Asia(IndoeMalaysia)type and the East Asia and North America disjunct type also played important roles.

7 Palaeoclimates reflected by the fossil floras

Because plants only exist in a climate zone that they can tolerate, they reflect climate characteristics of their distributional ranges. Although a fossil flora can tell us the general climate situation(e.g., the late Miocene Bangmai flora dominated by tropical elements indicates a warm climate), quantitative climate results allow a better understanding of past climate. As methodologies develop, fossil floras become valuable proxies for quantitative reconstructions of palaeoclimates by using appropriate approaches. In Yunnan, 10 megafossil floras have been investigated quantitatively regarding their palaeoclimates. They are exclusively Neogene in age, i.e., the early Miocene Shuanghe flora(Sun et al., 2011), the early to middle Miocene Mangdan flora(Zhao et al., 2004), the middle Miocene Tuantian flora(Sun et al., 2011), the late Miocene Xianfeng, Xiaolongtan and Bangmai floras(Xia et al., 2009; Jacques et al., 2011; Xing et al., 2012), and the late Pliocene Fudong, Longmen, Eryuan and Tuantian floras(Sun et al., 2011; Xie et al., 2012; Su et al., 2013a; Huang et al., 2015a). The reconstructed palaeoclimate results provide insights into climate changes and monsoon development in Yunnan throughout the Neogene, and thus help us to better understand the environmental conditions under which plant diversity evolved.

In the Miocene, estimated temperatures indicate that northern Yunnan was much warmer than it is now, suggesting a significant cooling trend to the present(Sun et al., 2011; Xing et al., 2012). For example, the mean annual temperature(MAT)of the early Miocene Shuanghe flora was estimated to be 13.8e21.7 ℃ by Coexistence Approach(CA)and 18.2 ± 3.6 ℃ by Leaf Margin Analysis(LMA), compared to 12.3 ℃ today(Sun et al., 2011). By contrast, temperatures in southern Yunnan have changed only moderately since the Miocene(Zhao et al., 2004; Xia et al., 2009). For example, the MAT estimated from the early to middle Miocene Mangdan flora using the CA was 18.8e20.5 ℃, close to 19-21 ℃ at present(Zhao et al., 2004). The observed different patterns of temperature changes between northern and southern Yunnan might be attributed to the difference in latitude or altitude or both. Northern Yunnan clearly had higher latitude than southern Yunnan, which supports a previous interpretation that the late Cenozoic cooling of the Northern Hemispherewas more pronounced in higher latitudes than in lower ones(Uhl et al., 2007; Utescher et al., 2011). On the other hand, northern Yunnan underwent significant surface uplift during the Neogene due to the southeastern extrusion of the Tibetan Plateau(Zhang and Ding, 2003; Clark et al., 2005), whereas southern Yunnan remained almost at the same level(Jacques et al., 2014). The considerable altitude increase probably was the other factor leading to the observed surface temperature decline in northern Yunnan, while the relatively stable elevation in southern Yunnan may explain the almost unchanged temperature level. The relevant importance of latitude versus altitude in controlling temperature changes, however, is currently unanswerable.

Apart from this cooling trend, Yunnan has also been affected by an aridification since the Miocene. Palaeoclimate reconstructions indicate that environments were humid in Yunnan during the late Miocene, and thereafter a drying trend occurred(Xia et al., 2009; Jacques et al., 2011; Sun et al., 2011; Xing et al., 2012). For example, the late Miocene Xianfeng flora revealed a mean annual precipitation(MAP)of 1206e1613 mm, higher than the presentday value of 1011 mm(Xing et al., 2012). This post-Miocene aridification appears to be particularly pronounced in the dry season. Various palaeoclimate reconstructions indicate that Yunnan had higher precipitation in summer but less rainfall in winter during the late Miocene(Xia et al., 2009; Jacques et al., 2011; Xing et al., 2012)and late Pliocene(Xie et al., 2012; Su et al., 2013a; Huang et al., 2015a). For instance, during the late Miocene the mean monthly precipitation of the three wettest months was 150e250 mm, while that of the three driest months was less than 50 mm, suggesting a prominent precipitation seasonality. These palaeoclimate results also demonstrate that summer precipitation has increased while winter precipitation has decreased since the late Miocene(Jacques et al., 2011; Xing et al., 2012; Su et al., 2013a; Huang et al., 2015a), suggesting a strengthening of the precipitation seasonality in Yunnan.

8 Conclusion

Based on our integration of published palaeobotanical data from Yunnan, our summary reaches six key points as stated below.

(1) Yunnan has a rich Cenozoic plant fossil record which has been investigated extensively, particularly over the past two decades, with an increasing number of fossil taxa being reported. These fossil taxa are important for answering past plant diversity and floral evolution in this region.

(2) Plant species from the Cenozoic of Yunnan are diverse. To date, approximately 386 fossil species belonging to 170 genera of 66 families have been documented. They cover ferns, gymnosperms and angiosperms, of which angiosperms are by far the most diverse, including 353 species grouped into 155 genera of 60 families. In the fossil angiosperms, Fagaceae, Fabaceae, Juglandaceae, Lauraceae and Rosaceae are among the most diverse families; and Querucs, Castanopsis, Acer, Lithocarpus, Cyclobalanopsis and Cinnamomum are among the most species-rich genera.

(3) Most of the families and genera represented in the fossil record are still part of the modern natural vegetation in Yunnan, but some genera have disappeared, possibly as a result of an aridification and/or extension of the dry season. So far, seven genera are known to have become extinct in Yunnan, namely Berryophyllum, Cedrelospermum, Cedrus, Palaeocarya, Podocarpium, Sequoia and Wataria.

(4) In the late Miocene, Yunnan had three floristic regions: a northern subtropical zone in the northeast, a subtropical zone in the east, and a tropical zone in the southwest. In the late Pliocene, Yunnan had two kinds of floristic regions: a subalpine floristic region in the northwest, and two subtropical floristic regions separately in the southwest and in the eastern center. Floristic characters changed significantly from the late Miocene to late Pliocene through to today, presumably attributed to altitude changes.

(5) In the late Miocene, southern Yunnan had more elements of the Pantropic type than northern Yunnan, with the southwest being obviously the richest in the Pantropic type, in agreement with results from floristic analyses. Three areal types including the North Temperate type, the Tropical Asia and Tropical America disjunct type, and the East Asia and North America disjunct type, were common in most of Yunnan except for the northeast. In the Pliocene, vegetation of Yunnan was dominated by the North Temperate type, but southwestern Yunnan also had abundant genera of the Tropical Asia (Indo-Malaysia) type and the East Asia and North America disjunct type.

(6) In the Neogene, Yunnan was warmer and more humid than today. Since the late Miocene, temperature has declined significantly in northern Yunnan but has remained almost at the same level in southern Yunnan. Summer precipitation has increased while winter rainfall has decreased, suggesting an intensification of the precipitation seasonality to the present.

Appendix A. Supplementary data

Supplementary data related to this article can be found at http://dx.doi.org/10.1016/j.pld.2016.11.004.

Acknowledgements: This study was supported by the National Natural Science Foundation of China (No. U1502231), the Foundation of the State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences (No. 163108), and the foundation of the Yunnan Key Laboratory for Palaeobiology, Yunnan University (No. 2015DG007-KF01). We thank Dr. Shu-Feng Li (Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences) for help with this study; and professor Robert A. Spicer (The Open University) and the other anonymous reviewer for constructive comments in improving the manuscript. This work is a contribution to Neogene Climate Evolution in Eurasia (NECLIME).