Structural diversity of forest communities on Baihuashan Mountain, Beijing

2008 ◽  
Vol 3 (2) ◽  
pp. 213-218
Author(s):  
Jingming Zheng ◽  
Xiuhai Zhao ◽  
Chunyu Zhang
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Gongqiao Zhang ◽  
Gangying Hui ◽  
Aiming Yang ◽  
Zhonghua Zhao

AbstractThis study brings insight into interpreting forest structural diversity and explore the classification of individuals according to the distribution of the neighbours in natural forests. Natural forest communities with different latitudes and distribution patterns in China were used. Each tree and its nearest neighbours form a structural unit. Random structural units (or random trees) in natural forests were divided into different sub-types based on the uniform angle index (W). The proportions of different random structural units were analysed. (1) There are only two types of random structural units: type R1 looks similar to a dumbbell, and type R2 looks similar to a torch. These two random structural units coexist in natural forests simultaneously. (2) The proportion of type R1 is far less than that of R2, is only approximately 1/3 of all random structural units or random trees; R2 accounts for approximately 2/3. Furthermore, the proportion of basal area presents the same trend for both random structural units and random trees. R2 has approximately twice the basal area of R1. Random trees (structural units) occupy the largest part of natural forest communities in terms of quantity and basal area. Meanwhile, type R2 is the largest part of random trees (structural units). This study finds that the spatial formation mechanism of natural forest communities which is of great significance to the cultivation of planted forests.


2014 ◽  
Vol 10 ◽  
pp. 113-121
Author(s):  
Mateusz Wilk ◽  
Julia Pawłowska ◽  
Marta Wrzosek ◽  
Michał Gorczak ◽  
Małgorzata Suska-Malawska

During a 35-month study on the decomposition of Sphagnum moss litter in poor fen and pine bog forest, an intensive colonization of litter-bags by mycorrhizal roots was observed during the decomposition process. Content of mycorrhizal roots in litter-bags, expressed as % mass of roots, was generally increasing during the decomposition in pine bog forest, and fluctuating during decomposition on poor fen, although in both cases the results were statistically insignificant. Two morphotypes of ericoid roots and two morphotypes of ectomycorrhizal roots were recorded from litter-bags on poor fen during the decomposition experiment, while in pine bog forest one morphotype of ericoid and nine morphotypes of ectomycorrhizal roots were recorded. Molecular identification of mycorrhizal roots succeeded only in the case of one ericoid and six putatively ectomycorrhizal morphotypes. Most morphotypes were recorded only once during the whole 35-month decomposition period, and only one ericoid and one ectomycorrhizal morphotypes were shared between the poor fen and pine bog forest communities.


2020 ◽  
Author(s):  
Dung Do

<p>Chiral molecules with their defined 3-D structures are of paramount importance for the study of chemical biology and drug discovery. Having rich structural diversity and unique stereoisomerism, chiral molecules offer a large chemical space that can be explored for the design of new therapeutic agents.<sup>1</sup> Practically, chiral architectures are usually prepared from organometallic and organocatalytic processes where a transition metal or an organocatalyst is tailor-made for desired reactions. As a result, developing a method that enables rapid assembly of chiral complex molecules under metal- and organocatalyst-free condition represents a daunting challenge. Here we developed a straightforward route to create a chiral 3-D structure from 2-D structures and an amino acid without any chiral catalyst. The center of this research is the design of a <a>special chiral spiroimidazolidinone cyclohexadienone intermediate</a>, a merger of a chiral reactive substrate with multiple nucleophillic/electrophillic sites and a transient organocatalyst. <a>This unique substrate-catalyst (“subcatalyst”) dual role of the intermediate enhances </a><a>the coordinational proximity of the chiral substrate and catalyst</a> in the key Aza-Michael/Michael cascade resulting in a substantial steric discrimination and an excellent overall diastereoselectivity. Whereas the “subcatalyst” (hidden catalyst) is not present in the reaction’s initial components, which renders a chiral catalyst-free process, it is strategically produced to promote sequential self-catalyzed reactions. The success of this methodology will pave the way for many efficient preparations of chiral complex molecules and aid for the quest to create next generation of therapeutic agents.</p>


2007 ◽  
pp. 13-22 ◽  
Author(s):  
T. K. Yurkovskaya

I have focused only on some features of structure in the taiga vegetation cover. In conclusion I would like to tell some words about the causes of complicated space structure of the taiga and tundra vegetation cover. The causes of latitudinal differentiation are climatic undoubtedly, but heterogeneity of vegetation cover within the limits of tundra and taiga subzones is accounted for different factors. In tundra abiogenic factors prevail, first of all the permafrost processes. That is the reason why tundra vegetation cover is so sensible to any disturbances and so hard regenerates after various transformations. In taiga the space structure is mostly the result of self-regulation and self- restoration of biota. The abiotic factors, certainly, play significant role, but they recede to the second plan. So we showed that in the north and middle taiga the structure of vegetation cover, during the Holocene up to present time, is determined in many respects by the increasing role of mires. Suffice it to look at the map of distribution of mires in order to estimate their role in vegetation cover of the easteuropean taiga (Yurkovskaya, 1980). So, the increase of mire area on the Russian Plain in m2/year per 1000 ha varies between 200 and 700, the average increas is ca 300—400 m2/year (Elina et all., 2000). The mires favour peniplenization and unite the separate areas of forest communities into the whole by means of forming the buffer paludificated territories (various hydrophilous variants of forest communities). But if mires, at all their stability, after destroying practically don't restore, the forests even after continuous cuttings restore their structure and composition through the series of successional stages unless an ecotope is damaged completely. Hence the space structure of taiga is the result, first of all, self development and self regulation of its vegetation cover. But, as it is known, at present time the process of destruction of natural biota has gone too far that the question arises not only about supporting its state and structure but also about the survival of the mankind itself. In this regard the vegetation map of Europe is the invaluable basis, which gives the starting point for all conservational, ecological and economical measures. But it is important to learn reading and using the map. And this is one of our actual goals.


2008 ◽  
Vol 159 (4) ◽  
pp. 80-90 ◽  
Author(s):  
Bogdan Brzeziecki ◽  
Feliks Eugeniusz Bernadzki

The results of a long-term study on the natural forest dynamics of two forest communities on one sample plot within the Białowieża National Park in Poland are presented. The two investigated forest communities consist of the Pino-Quercetum and the Tilio-Carpinetum type with the major tree species Pinus sylvestris, Picea abies, Betula sp., Quercus robur, Tilia cordata and Carpinus betulus. The results reveal strong temporal dynamics of both forest communities since 1936 in terms of tree species composition and of general stand structure. The four major tree species Scots pine, birch, English oak and Norway spruce, which were dominant until 1936, have gradually been replaced by lime and hornbeam. At the same time, the analysis of structural parameters indicates a strong trend towards a homogenization of the vertical stand structure. Possible causes for these dynamics may be changes in sylviculture, climate change and atmospheric deposition. Based on the altered tree species composition it can be concluded that a simple ≪copying≫ (mimicking) of the processes taking place in natural forests may not guarantee the conservation of the multifunctional character of the respective forests.


Sign in / Sign up

Export Citation Format

Share Document