首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 31 毫秒
1.

Fertilization experiments in Norway spruce stands on nutrient-poor sites have been practised in Denmark since the eighteenth century. Until 1950, the main aim was to find a nitrogen (N) source that improved the survival of plants in the early growth phase. The N supply could be improved by intercropping with N 2 -fixing plants, and fertilization with phosphorus (P) and potassium (K) improved the growth of the N 2 fixers, thereby improving tree growth and survival. Positive responses of P and K in spruce cultures were seen in the 1960s, and in most cases the N response was dependent on the supply of P and K. Fertilization experiments in mature spruce stands began in the 1960s. Despite 20 yrs of experimentation, no trends can be deduced. The results discouraged fertilization aimed at increasing growth in mature stands, and fertilization stopped in 1989. After 1980, fertilizers were used in experiments aimed at clarifying the causes and effects of forest decline. Fertilization and liming counteracted soil acidification and increased needle nutrient concentrations when they were below deficiency levels. However, positive growth responses have only been recorded in some of the experiments where nutrient deficiencies were overcome. The experiments have not resulted in practical revitalization programmes. Future fertilization of Danish forests may be limited to systems where nutrient extraction is in excess of the carrying capacity of the ecosystem, and presumably where spruce plantations are converted to broadleaved forests. Finally, future events of deposition of acidifying compounds may necessitate counteractive measures.  相似文献   

2.
Several studies have shown the positive effect of nitrogen fertilization on conifer growth. In young Norway spruce (Picea abies) stands, an additional effect of including a mixture of other nutrients has often, but not always, been found. We studied effects of repeated fertilization in 28 stands with young Norway spruce in central Norway. The treatments consisted of plots without nutrient addition (Control), fertilization with 150?kg?N?ha?1 (150?N), and fertilization with 150?kg?N plus addition of P, K, Mg, B, Mn and Cu (150?N?+?mix), repeated three times with approximately eight years interval. There was a clear positive effect on volume increment of the 150?N and 150?N?+?mix treatments compared to Control, and the effect was significantly higher for 150?N?+?mix than for 150?N. Fertilization had a stronger effect in the first fertilization period than in the second, while the third period was intermediate. The effect of 150?N?+?mix was strongest at plots?>?300?m a.s.l. However, this correlation may be due to geological conditions rather than elevation. Further studies are needed to find out under which edaphic conditions a nutrient mixture will increase growth substantially in young spruce stands.  相似文献   

3.
A series of 15 field experiments was established to quantify the growth response of first‐thinning stands of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst) to whole‐tree harvesting and to estimate the need for nutrient compensation. The experiments were undertaken in Finland, Norway and Sweden and represent a wide range of site conditions. The site index (H 100) of Scots pine stands varied from 19 to 29 m, and that of Norway spruce stands from 28 to 36 m. Total amounts of biomass and nutrients removed were calculated based on data obtained from felled sample trees. During the first 5‐yr period the growth response to the removal of logging residues varied considerably in both pine and spruce stands. Regression analyses did not reveal any functions that explained the variation in results satisfactorily. In cases where whole‐tree harvesting influenced tree growth negatively, this effect was counteracted by compensatory fertilization. It was concluded that to determine the response of remaining trees to harvesting intensity reliably, the post‐harvest period analysed must be longer than 5 yrs.  相似文献   

4.
Early management of the regenerated seedlings shapes the future stand properties. To address these issues, pre-commercial thinning (PCT) and control treatments were applied to planted Norway spruce (Picea abies L. Karst) and naturally regenerated birch (Betula pendula Roth., Betula pubescens Ehrh.) stands in forest experiments in southern Sweden (lat. 56–57?N) containing 1.1–5.5?m tall saplings. The treatments were retention of 1000 or 2000?stems?ha?1 of Norway spruce, with no birch or birch at 1000?stems?ha?1. Treatments were replicated with and without annual removal of birch sprouts from stumps. The periodic annual increment (PAI) over five years was calculated for total stand volume and individual trees. The mean PAI of dominant trees was significantly higher both following all PCT treatments than controls, and following low rather than high-density PCT. Birch retention did not affect growth of the dominant trees but PAI was lower in plots with uncontrolled sprouting. The PAI of birch was significantly higher in low-density Norway spruce plots than in control plots and the high-density plots. The treatment response was significant even in stands with initial heights of only 1–2?m.  相似文献   

5.

Mean age, mean and top heights and yield were studied in 20 mixed stands of birch ( Betula pubescens Ehrh. and B. pendula Roth) and Picea abies (L.) Karst. and nine mixed stands of birch and Pinus sylvestris L. in south-eastern Norway. Each mixed stand and the adjacent pure coniferous stand (control) were growing under the same site conditions and had not been commercially thinned. There were no significant differences in mean age at breast height or in top heights between birch and conifers in the mixed stands, while mean height was significantly higher for birch than for spruce. A growth index was calculated based on total volume and age at breast height. For the spruce sites the growth in young mixed stands (birch < 17 m) was superior to that of pure spruce, while the difference was insignificant in older stands. The growth index correlated positively with the ratio between generatively and vegetatively regenerated birch trees, and negatively with the age of the oldest species in the mixture and with site quality. For the pine sites there was no significant difference in the growth index between mixed birch-pine and pure pine stands. A mixture effect of birch on the volume yield of spruce or pine could not be demonstrated.  相似文献   

6.
Since 1999–2002 the European Commission has funded and the European Forest Institute has coordinated the interdisciplinary RECOGNITION project aiming at elucidating the causes of the growth acceleration which has been observed in some forest tree species in several parts of Europe. Within this project, it was our task to identify and quantify long-term changes in the nutritional status of representative forest stands that potentially could explain this growth increase, using available long-term series of foliar analyses. An inquiry among 25 forest research institutions in Europe resulted in 28 Scots pine (Pinus sylvestris L.) and 21 Norway spruce (Picea abies [L.] Karst.) stands for this historical development investigation (HDI). The stands generally are control plots of fertilization experiments and are located mainly in Central Europe and in Scandinavia. The monitoring periods vary from 15–40 years. The foliar data were given to us by our partner organisations, subjected to rigorous tests for plausibility and comprehensively evaluated using mainly single linear regression approaches. Most Scots pine stands under study in Central Europe, which grow predominantly on naturally poor or devastated soils in regions with relatively high atmospheric N deposition, suffered from N deficiency at the start of the monitoring period, but exhibited a considerable improvement in N nutrition over the past decades. The increase in N levels was usually associated with an increase in the ratios of N and P, K, Ca, and Mg, although critical values of these ratios are far from being reached. For the majority of the investigated Scots pine stands in Central Europe, growth acceleration due to a better N supply is highly probable. In contrast, N seems to be far less important as a potential driving factor for long-term growth changes in Scots pine in Scandinavia. Norway spruce stands examined in Central Europe were, in general, initially well supplied with N and characterised by a decreasing trend in foliar N levels although they received considerable N deposition from the atmosphere. This decrease in concentrations of N and other macronutrients is believed to be mainly a dilution effect as indicated by a simultaneous increase in needle weights. Spruce in Finland also turned out to be adequately provided with N at most sample sites, and no general trend of improving N nutrition was detected.  相似文献   

7.

Stem form and taper changes after thinning and thinning combined with N fertilization were studied in 23 Norway spruce [Picea abies (L.) Karst.] and 46 Scots pine (Pinus sylvestris L.) stands in Sweden observed for 5-28 yrs. Average taper was calculated for the stem section 1.3-6.0 m above ground level and as the ratio between the diameter at breast height and total tree height for periods of 5-10 yrs. At the start of the experiment, before the first thinning, the dominant height was 12-15 m. Once 65% of the basal area had been removed in a single thinning from below, the remaining trees showed a strong increase in taper compared with trees in unthinned stands. Stems in stands treated with heavily recurrent thinnings from below also increased in taper, although the increases were not always statistically significant. Trees in thinned, N-fertilized Scots pine stands in middle and northern Sweden developed a more pronounced taper compared with stems in equally thinned, unfertilized stands.  相似文献   

8.
Abstract

The success of natural regeneration on patch clear-cuts in Norway spruce stands in Southern Finland was examined in terms of stocking and tree height. The experiment was established in mature spruce stands in the submesic Myrtillus (MT) site type. In each of the eight study sites, three plots were treated with clear-cutting and planting, clear-cutting with partial tree retention and planting, and patch clear-cutting without site preparation, respectively. In three of the study sites, one plot with patch clear-cutting and site preparation was established. Each plot was 1 ha, out of which three patches of 40×40 m were clear-cut in the patch treatments. 10–11 years after cutting, the patches had on average 1316 crop trees ha–1, of which 91% were spruces. Some 27% of the stands were up to the target stocking level (≥1600 ha?1), and 36% were at least satisfactory (≥1300 ha?1). Site preparation did not yield greater stocking levels on patches, but that result is ambiguous due to a difference in initial stocking. The average spruce tree height in the patches (0.76 m) was much smaller than in the case of clear-cutting and planting (2.42 m). In conclusion, the patches had been restocked tolerably well with spruce and birch for practical purposes during the 10- to 11-year period, but the regeneration process had been very slow compared to clear-cutting and planting.  相似文献   

9.
The aim of this study was to determine the effect of whole-tree harvesting (WTH) on the growth of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.) as compared to conventional stem harvesting (CH) over 10 and 20 years. Compensatory (WTH + CoF) and normal nitrogen-based (CH + F or WTH + F) fertilisation were also studied. A series of 22 field experiments were established during 1977-1987, representing a range of site types and climatic conditions in Finland, Norway and Sweden. The treatments were performed at the time of establishment and were repeated after 10-13 years at 11 experimental sites. Seven experiments were followed for 25 years.Volume increment was on average significantly lower after WTH than after CH in both 10-year periods in the spruce stands. In the pine stands thinned only once, the WTH induced growth reduction was significant during the second 10-year period, indicating a long-term response.Volume increment of pine stands was 4 and 8% and that of spruce stands 5 and 13% lower on the WTH plots than on CH during the first and the second 10-year period, respectively. For the second 10-year period the relative volume increment of the whole-tree harvested plots tended to be negatively correlated with the amount of logging residue. Accordingly, the relative volume increment decreased more, the more logging residue was harvested, stressing the importance of developing methods for leaving the nutrient-rich needles on site.If nutrient (N, P, K) losses with the removed logging residues were compensated with fertiliser (WTH + CoF), the volume increment was equal to that in the CH plots. Nitrogen (150-180 kg ha−1) or N + P fertilisation increased tree growth in all experiments except in one very productive spruce stand. Pine stands fertilised only once had a normal positive growth response during the first 10-year period, on average 13 m3 ha−1, followed by a negative response of 5 m3 ha−1 during the second 10-year period. The fertilisation effect of WTH + F and WTH + CoF on basal area increment was both smaller and shorter than with CH + F.  相似文献   

10.

This paper summarizes results from fertilization research carried out in Scots pine ( Pinus sylvestris L.) and Norway spruce [ Picea abies (L.) Karst.] stands growing on mineral soil in Finland. The use of needle and soil analyses to indicate nutrient status and the need for fertilization are discussed along with the possibilities of increasing tree growth in various site types and stages of stand development. Doses, types of fertilizer, application time, growth increase, wood quality and the profitability of fertilization are also discussed. The stand response in terms of soil acidity, biological activity, soil fauna and resistance of trees to nutrient addition are all reviewed. The effects of fertilization on understorey vegetation, mushrooms and berries, and leaching loss of nutrients are also included.  相似文献   

11.

Nitrogen (N) is the only nutrient that promotes forest growth when given individually. An extra stem growth of 15 m 3 ha -1 is obtained during a 10 yr period following an application of 150 kg N ha -1 . Larger growth increases have often been the result of more intensive N fertilization. Lime or wood ash give a minor growth stimulation on sites with a carbon (C) to N ratio below 30 in the humus layer, while the opposite effect prevails on N-poor sites. Nutrients given as soluble fertilizers are readily taken up by trees. Boron deficiency may be induced in northern Sweden after N fertilization or liming. The ground vegetation may be altered by single-shot N fertilization, but long-term effects occur only for intensive regimes. Lime or wood ash may modify the flora if soil pH is significantly altered: the change will be in response to N availability. Fruit-body production of mycorrhizal fungi is disfavoured by chronic N input, but also by lime or ash. However, the mycorrhizal structures on root tips are less affected. Faunistic studies are not common and those present are mostly devoted to soil fauna. A practical N dose of 150 kg N ha -1 has no clear effect, but higher doses may reduce the abundance in some groups. Hardened wood ash does not significantly affect the soil fauna. Lime favours snails and earthworms, while other groups are often disfavoured. The response of aquatic fauna to terrestrial treatments has hardly been studied. N fertilization generally results in insignificant effects on fish and benthic fauna. Lime and wood ash reduce the acidity of the topsoil, but practical doses (2-3 t ha -1 ) are too low to raise the alkalinity of runoff unless outflow areas are treated. N fertilizer use in forestry and N-free fertilizers lack effects on acidification. N fertilization may, however, be strongly acidifying if nitrification is induced and followed by nitrate leaching. N fertilization often results in increased long-term C retention in trees and soil, but does not promote significant N 2 O losses. N may temporarily reduce CH 4 oxidation in soil, but there are indications of a long-term opposite effect. Lime and poorly hardened wood ash may cause losses of C from N-rich soils. Only a few per cent of added N are leached to surface water following practical N fertilization, while N-free fertilizers do not induce N leaching. Soil incubations and soil-water studies suggest an increased risk for nitrate formation and leaching where lime or wood have been added to N-rich soils, but increased leaching to surface water has not been observed. Wood ash causes a temporal increase in bioavailability of cadmium (Cd). Other fertilizers may indirectly increase the availability of heavy metals. Wood ash may contain radioactive caesium 137Cs, but addition of such ash does not increase radioactivity in plants and soil.  相似文献   

12.
Temporal variation of leaf area index (LAI) in two young Norway spruce stands with different densities was monitored during eight consecutive growing seasons (1998–2005). We focused on: (1) LAI dynamics and above-ground mass production of both spruce stands and their comparison, (2) leaf area duration (LADU), crop production index (CPI) and leaf area efficiency (LAE) evaluation, and (3) thinning impact on the above-mentioned parameters. Also, we tried to deduce the most effective LAI value for the Norway spruce forest investigated. The LAI values of both spruce stands showed a typical seasonal course. To describe the LAI dynamics of the stand, we recommend taking LAI measurements within short time intervals at the time of budding and needle expansion growth (i.e., in early spring) and close to the LAI peak, when the twig growth has been completed. The reason was that after reaching the seasonal maximum, no significant differences between subsequently obtained values were found in the following 2 months. Therefore, we recommend this period for the estimation of seasonally representative LAI values, enabling the comparison of various spruce stands. The maximum hemi-surface LAI value reached 12.4. Based on our results, the most effective LAI values for maximum above-ground biomass production were within the range of 10–11. We found an LAI over these values to be less effective for additional production of above-ground biomass. In forest practice, thinning intensity is mostly described by percentage of stocking reduction. We want to show that not only thinning intensity, but also the type of thinning is important information. The type of thinning significantly affected the stand above-ground biomass increment, canopy openness, stand LAI and LAI efficiency. The stimulating effect of high-type thinning was observed; the LAE as well as the CPI increased. Low-type thinning had no such effects on LAE increments compared to the high-type thinning with similar intensity.
  相似文献   

13.
Incoming shortwave global radiation (Q g) and photosynthetically active radiation (PAR; Q pa as a fraction of full daylight, relative irradiance (%Q), were measured at the same time in young stands of Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.). Measurements were made on three levels above ground: 20 cm above ground and 50 and 15 % of stand height. Stands of three heights (75, 150 and 300 cm) were studied during two months. The stands were created by arranging young trees cut from natural stands, in nine quadratic spacings: 0.1, 0.2, 0.3, 0.4, 0.5, 0.7, 1.0, 1.4 and 2.0 m. The leaf area index (L) was estimated. Differences in %Q‐values for Q pa and Qg in the same species and at the same stand height and level of light measurements above ground were significant only in 150 and 300 cm stands. In 75 cm high stands of Scots pine, the %Q was <60% at spacings <0.2 m and in 75 cm high stands of Norway spruce, the %Q was <60% at spacings <0.3 m. Only at 0.1x0.1–0.3x0.3 m, %Q was <20% in Norway spruce stands. In 150 cm stands %Q<20% was measured at spacings <0.7 m in Norway spruce and <0.5 in Scots pine. In 300 cm stands of Norway spruce it was measured up to 1.2 and in Scots pine <1.1 m. Light extinction coefficients, K and Kg for spruce and pine stands were 0.17–0.40 and 0.16–0.31 respectively. Some practical implications of the study are presented. Lack of light (%Q<10%) as a single factor of seriously suppressed growth and development of broad‐leaved plants and suckers by competition in young stands of spruce and pine only occur in dense stands 0.3x0.3 m‐1.1xl.l m (8000–100000 stems/hectare). Competition by light on a regenerated area generally occurs in the level of 50% of tree height (150–300 cm) and higher due to the rapid growth of broad‐leaved trees (sprouts) compared with planted conifers but the light intensity at these levels %Q>10%.  相似文献   

14.
The individual tree growth in stands of mixed Norway spruce (Picea abies (L.) Karst.) and birch (Betula pendula Roth & Betula pubescens Ehrh.) is estimated using basal area and height growth functions for each species separately. The individual tree growth models are distant dependent and the number, size and proximity of neighbours are expressed as size‐ratio competition indices. The competition indices were calculated using a basal area factor gauge to define competitors. The tree growth functions are based on data from nine mixed stands of Norway spruce and birch. The recursive multivariate regression approach is used. The growth functions have standard deviation about the function/standard deviation about the mean (sf/sm) values between 31 and 61% and the evaluations made with root mean square error (rmse) give estimates which vary between 8 and 45 % of the observed mean value. These values are comparable with the precision reported in other studies. In the present investigation the distant dependent indices are important independent variables. It seems suitable to describe the change in growth conditions from retarded to released growth by means of size ratio competition indices. For birch, a positive effect on growth is obtained the more the total competition consists of Norway spruce. For Norway spruce a negative effect on growth is obtained the more the total competition consists of Norway spruce. The lower competitors have a positive effect on the growth of the spruce trees. The interpretation should be that it is better to have a small competitor than a larger one, not that small competitors as such have a positive effect on growth of Norway spruce.  相似文献   

15.
The nutrient status of Norway spruce in pure and in mixed-species stands   总被引:1,自引:0,他引:1  
Atmospheric deposition of N and S appears to have caused nutrient imbalance in Norway spruce stands in southern Sweden. This calls for a change of forest management to procedures that promote nutrient balance. Studies have shown lower soil acidity in Norway spruce/deciduous mixed stands than in spruce monocultures, but the tree nutrient status in such mixtures has not been much investigated so far.

The nutrient status of Norway spruce foliage and top mineral soil chemistry in monocultures and in stands mixed with beech, birch, or oak was investigated through paired comparisons on 30 sites in southern Sweden (27 sites) and eastern Denmark (three sites). In total, 45 mixed stands and 34 pure stands were included in the study.

Spruce needles from mixed stands had higher concentrations and ratios to N of K, P, and Zn than needles from pure spruce stands. Among the mixed stands, the K status appeared to be positively correlated with the percentage of deciduous tree basal area. Soil samples from mixed stands had a higher Mg concentration, base saturation, and BC/Al ratio than soil samples from pure stands. The spruce needle nutrient status was comparable in pure stands on fertile sites and in mixed stands on poor sites. We did not detect any differences in spruce tree growth between pure and mixed stands.

This paper discusses possible reasons for a positive effect on the tree nutrient status in mixed-species stands and the possibility of using mixed-species stands as a forest management procedure to avoid nutrient imbalance.  相似文献   


16.
A stand-based model for predicting basal-area mean diameter growth for Norway spruce (Picea abies (L.) Karst.) in young mixed stands of spruce and birch (Betula pendula Roth, B. pubescens Ehrh.) was developed and compared with two existing growth models developed for older stands. The main data were from experiments with four different pre-commercial thinning regimes. A multiplicative model with four independent variables was found suitable. The independent variables were total number of trees per hectare of all the species, site index, dominant height of spruce, and a measure of competition between birch and spruce, i.e. dominant height of spruce divided by the dominant height of birch multiplied by the proportion of spruce of total number of trees. The R2 value was 0.59 and the coefficient of variation was 12%. A test with an independent data set from the National Forest Inventory (NFI) indicated that the function developed in this study is suitable for young stands at medium to highly productive areas. Large deviations between observed and predicted growth for the two existing functions were revealed in highly productive stands. The tests based on data from the NFI also indicated that the existing function developed for spruce in older mixed stands is suitable for practical purposes for young stands.  相似文献   

17.

One-year-old seedlings of Norway spruce [Picea abies (L.) Karst.] from seed orchards and natural stands were compared with respect to growth cessation and autumn-frost hardiness. The correlation among traits related to growth, growth cessation and frost hardiness on the same plants in two sets of environmental conditions was assessed. Total height, the degrees of shoot lignification and frost hardiness, and the timing of height growth cessation and budset were recorded at two nurseries in central and northern Sweden. Nine seed-orchard seed-lots were compared with seed from 26 natural stands originating from 56° N to 66° N in Sweden. Latitude explained 55-87% of the statistical variation among stands in the analysed traits at the central nursery and 49-84% at the northern nursery. On average, the seed-orchard progeny performed similarly to progeny from natural stands located 1-2° south of the origin of the seed-orchard clones. Reference material representing a geographical gradient was found to be a valuable aid when interpreting the results of growth cessation and frost-hardiness evaluations.  相似文献   

18.
Many forest soils in Finland are poor in boron (B), especially otherwise fertile (nitrogen-rich) soils and peatlands. Boron deficiency causes growth disorders affecting young Norway spruce (Picea abies) stands. We studied the effects of B fertilization on the growth and morphology of Norway spruce seedlings. Boron was applied in a nursery and/or after planting in a nursery-field and on a reforestation site, both known to be low in B. The B applied in the nursery increased foliar B concentration in a linear relationship to the amount of B fertilizer but did not affect seedling growth and morphology. Even the highest foliar B concentration (approx. 400 mg kg?1) did not have harmful effects on the seedlings. Therefore, B fertilization in the nursery can be used for increasing B storage in needles. Boron fertilization at planting increased foliar B concentration in the first season. Afterward, the concentration decreased but remained above the deficiency limit for at least 4–5 years. In the B-poor nursery-field, nonfertilized seedlings began to produce multiple leaders in the second year. On the reforestation site, fewer multiple leaders were found. At the nursery-field site, height growth was stimulated by B fertilization at planting. In conclusion, 200–400 mg m?2 (2–4 kg ha?1) of B applied at planting has longer-lasting effects on seedling B status than does B fertilization applied in the nursery, and can improve seedling quality and growth in the first years after planting on B-poor sites.  相似文献   

19.
To avoid large clear‐cut areas in recreation areas, three experiments where group selection was used to transform even‐aged stands of Norway spruce (Picea abies (L.) Karst.) into uneven‐aged stands were started. Two of these group selection stands were compared with adjacent forests managed by the clear‐cut system on the basis of the opinion of seven voluntary groups. The respondents have given their judgement of the forest sites in a semantic differential test. All parties made assessments when visiting the forest sites. In addition, two of the groups made assessments of black and white photographs representing the forest sites. The methods used were found to be both reliable and valid. A very low correlation was obtained between the assessment of whole forest areas and the mean value of the assessments of the stands within the same area. According to this study, the group selection method is preferable to clear‐cutting in even‐aged stands of Norway spruce if the attitudes of the voluntary groups are to be met.  相似文献   

20.
Abstract

This study analysed the effects of young stand characteristics on optimal thinning regime and length of rotation periods for even-aged Norway spruce [Picea abies (L.) Karst.] stands. Stand development was based on a distance-independent, individual-tree growth model. The young stand data were collected from 12 well-stocked Norway spruce stands in southern Finland. Results showed that optimal thinning regimes and rotation period depend on site quality and initial stand characteristics. At the first thinning, optimal thinning type depended on initial density. Thinning from both ends of the diameter distribution turned out to be optimal for initially dense stands. At the second and subsequent thinnings, thinning from above was clearly superior. At a low interest rate, thinning from below was optimal for the first thinning regardless of stocking level. For the study data, optimal rotation periods varied from 61 to 92 years at 3% interest rate. The high variation in length of rotation period was due to the sensitivity of optimal length of rotation period to site qualities, initial stand structure and density.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号