• <tr id="yyy80"></tr>
  • <sup id="yyy80"></sup>
  • <tfoot id="yyy80"><noscript id="yyy80"></noscript></tfoot>
  • 99热精品在线国产_美女午夜性视频免费_国产精品国产高清国产av_av欧美777_自拍偷自拍亚洲精品老妇_亚洲熟女精品中文字幕_www日本黄色视频网_国产精品野战在线观看 ?

    東方百合明星無性快繁體系的建立

    2016-05-30 14:38:13???/span>楊美純王燕農(nóng)艷豐岑湘濤
    南方農(nóng)業(yè)學(xué)報 2016年9期

    ??? 楊美純 王燕 農(nóng)艷豐 岑湘濤

    Abstract:【Objective】Propagation system established with sterile leaves of Oriental lily Love Story as material to provide technical reference for industrialized production of its seed-bulbs. 【Method】Sterile scales and leaves from flower organs culture were used as material and MS was used as basic medium, adding different concentrations of 6-BA and 2,4-D to induce adventitious buds and bulb-lets; using different concentrations of sugar to induce bulb-lets expansion and rooting; perlite, peat and vermiculite were mixed as the transplanted matrix of bulb-lets. 【Result】MS+1.5 mg/L 6-BA was appropriate for inducing adventitious buds with sterile scales and induction rate was 75.0%; the suitable sterile leaves differentiation bulb-lets medium was MS+2.0 mg/L 2,4-D and induction rate was 91.7%; the MS medium added 70.0 g/L sugar was suitable to induce bulb-lets expansion and rooting; perlite∶peat∶vermiculite=1∶1∶1 was the best transplanted matrix of plant-lets with bulb-lets and roots, transplanting survival rate got 100.0% in this matrix.【Conclusion】Oriental lily Love Story could be established asexually rapid propagation system by sterile leaf.

    Key words: Oriental lily Love Story; tissue culture; bulblets; rapid propagation

    CLC number: S682.29 Document code: A Article:2095-1191(2016)09-1528-05

    摘要:【目的】以東方百合品種明星無菌葉為材料建立快繁體系,為其種球產(chǎn)業(yè)化生產(chǎn)提供技術(shù)支撐?!痉椒ā恳曰ㄆ鞴倥囵B(yǎng)獲得的無菌小鱗片及葉片為材料,以添加不同濃度6-BA、2,4-D的MS培養(yǎng)基誘導(dǎo)不定芽及小鱗莖產(chǎn)生;以不同濃度的蔗糖誘導(dǎo)小鱗莖的膨大及根的產(chǎn)生;以珍珠巖、草炭、蛭石的混合基質(zhì)作為小鱗莖移栽基質(zhì)?!窘Y(jié)果】用 6-BA誘導(dǎo)無菌小鱗片產(chǎn)生不定芽時以1.5 mg/L為宜,誘導(dǎo)率為75.0%;用2,4-D誘導(dǎo)無菌葉片產(chǎn)生小鱗莖時以2.0 mg/L為宜,誘導(dǎo)率為91.7%;添加70.0 g/L蔗糖的MS培養(yǎng)基適宜小鱗莖膨大及根的產(chǎn)生;帶小鱗莖及根的組培苗在珍珠巖∶草炭∶蛭石=1∶1∶1的基質(zhì)中移栽成活率最高,達(dá)100.0%?!窘Y(jié)論】東方百合品種明星可利用無菌葉片建立無性快繁體系。

    關(guān)鍵詞: 東方百合明星;無菌葉;小鱗莖;無性快繁

    0 Introduction

    【Research significance】Lily, a perennial herb bulbous plant, belongs to Lilium of Liliaceae. Oriental hybrids are one of the four cut-flower lily varieties being larger flower, rich color and fragrance, and have been preferred by majority of consumers. The bulbs of commercial Oriental lily have low reproductive rate, and are easily infected by virus and so on, so the qualities of their seed-bulbs and cut-flowers were declined gradually; while a large of fine quality bulbs could be produced through tissue culture technology in a short time to meet the demand of cut-flower market(Tang et al., 2003; Zhou et al., 2010; Liao et al., 2012). Therefore, to establish the asexual rapid propagation system of Oriental lily Love Story, could ensure its species cha-

    racteristics, and improve its propagation coefficient to shorten breeding period, which would provide technical references for industrial production of its seed-bulbs. 【Research progress】Currently, many studies on tissue culture of different lily varieties were carried out and reported. According to the source of explants, the used explants of lily can be divided into three categories viz., scale, leaf and floral organ. Scale is used as explants to induce adventitious buds. Fu et al.(2008) screened out fit concentration of NAA to differentiate adventitious buds derived from sterile scales of Oriental lily. Tiber by adopting orthogonal polynomial regression method and mathematical model. Wang et al.(2013) studied the effects of different types and concentrations of hormones on differentiation of adventitious buds derived from sterile scales of Tiber, Rodina and Constanta plantlets. The results showed that, 1.0 and 2.0 mg/L of 6-BA were suited for differentiation of adventitious buds from sterile scales of Tiber and Rodina, while KT and TDZ were not suited for them. For lily variety Constanta, 1.0 mg/L KT was more suitable for differentiation of adventitious buds. Leaf was also used as explants to induce adventitious buds, and 2,4-D in medium was found to be the important regulated factor on somatic embryogenesis of adventitious buds induction derived from scale leaves of Lilium brownie var. Viridulum(Liu et al.,1997). Zhao et al.(2005) compared the effects of NAA, 6-BA, TDZ, and 2,4-D on leaves to differentiate adventitious buds of five lily varieties, it found that different lily species presented different sensibility to exogenous hormones; TDZ used alone or combining with low concentration of 2,4-D were suited for Yellow Lilium regale and Polyana; 0.05 mg/L NAA was suited for Lilium var. Golden Sun lily and Red lily; 6-BA combing with low concentration of 2,4-D was more suited for Lilium var. Snow Queen lily. Floral organs were used as explants to induce adventitious buds. Liu et al.(2007) used floral organs of four lily varieties as explants for tissue culture, it found that different lily varieties showed different induction rates of adventitious buds from floral organ, and different floral organs of the same variety were also found to have significant differences in induction rate; the adventitious buds induced sequence from easy to hard in order was filament, receptacle, ovary, corolla, stylus and anther. By using floral organs of Lilium var. Manissa to induce adventitious buds, Nong et al.(2014) found that, 3.0 mg/L 6-BA had significant effect on differentiation of adventitious buds, its highest differentiation rate could be reached to 95.5%. 【Research breakthrough point】At present, the commercial seed-bulbs of Oriental lily are commonly cultured by using plantlets. So far, there are no relative researching reports on commercial seed-bulbs of Oriental lily Love Story in domestic, and its fewer clones derived from sterile leaves are reported. 【Solving problem】The present study aimed to establishing the asexually rapid propagation system of Oriental lily Love Story by sterile leaf, which would provide technical references for industrialized production of its seed-bulbs.

    1 Materials and methods

    1. 1 Experimental materials

    The sterile bulblets derived from flower organ culture of Oriental lily Love Story were used as materials.

    1. 2 Experimental methods

    1. 2. 1 Induction of adventitious buds The sterile scales were taken from the sterile bulblet with tweezers to cut out the top, the intermediate and bottom parts of leave were cut into 0.5 cm2 of pieces, followed by culturing in MS medium supplied with 0-2.0 mg/L 6-BA. The new growing adventitious buds were counted after culturing for 40 days.

    1. 2. 2 Bulblets induction of sterile leaves The sterile leaves derived from the above-mentioned induced adventitious buds were cut out the top, then the middle and lower parts were cut into about 1.0 cm to culture in MS medium supplied with 0-3.0 mg/L 2,4-D, the induced bulblets were counted after culturing for 50 days.

    1. 2. 3 Expansion culture and rooting induction of sterile bulblets The sterile above-mentioned bulblets induced by sterile leaves were inoculated on MS medium supplied with 30.0-90.0 g/L sugar for bulblets expansion and rooting induction. The multiple of enlargement, rooting rate and average roots per bulblet were counted after culturing for 90 days.

    1. 2. 4 Transplanting culture The 50% carbendazim was mixed with different transplanted matrix(perlite, peat, vermiculite, sawdust, garden soil) as the amount of 40 g/m3, followed by covering with plastic for 3 days. The rooting bulblets(>0.3 cm in diameter) were removed from the culture room to domesticate for 7 days in greenhouse. The roots of bulblets were washed out adhering media, the bulblets were divided into 2 groups according to its diameter(0.3-0.5 cm, >0.5 cm) and immersed in 0.1% carbendazim solution for 15 min, followed by transplanting into four different mixed matrixes with equal proportion of perlite, peat, vermiculite, sawdust, or garden soil. The survival rate and plant height of bulblets were counted after culturing for 30 days.

    The above-mentioned culture process conditions were as follows: 25-28 ℃ of the culture room temperature, 12-14 hours/day of lighting time companied with 1500-2000 lx of light intensity.

    2 Results and analysis

    2. 1 Effects of different concentrations of 6-BA on adventitious buds differentiated from sterile scales

    During the process of scale culture, the scales began to wrinkle on the surface after inoculating for 8 days, and the scale incision site of two ends appeared little beige bumps after 14 days, followed by greening and developed into adventitious buds after 25 days.

    From the results shown in Tab.1, it found that in the range of 0-2.0 mg/L 6-BA, the differentiation rate of adventitious buds showed change trends of increasing firstly and decreasing at latter with the increase of 6-BA dosage in MS medium. By adding with 1.5 mg/L 6-BA, the adventitious buds grew strong and differentiated well, and its differentiation rate reached the highest as 75.0%. The dense adventitious buds with a lot of callus found to be differentiated when added 2.0 mg/L 6-BA; because the induced adventitious buds were too dense and unhealthy, so it was not good for further multiplication. Therefore, MS+6-BA 1.5 mg/L was the suitable culture medium for differentiating adventitious buds of sterile scales.

    2. 2 Effect of 2,4-D on bulblets differentiated of sterile leaves

    During the culture process of leaf sections, it found that sterile leaves began to enlargement after inoculating for 7 days, subsequently, little yellowish protuberance was formed at the both ends of incision, and the bulblets were formed after 30 days of culture. The callus was not found during the whole culture process.

    From the results of Tab.2, it showed that in the range of 0.5-2.0 mg/L 2,4-D, the number and size of bulblets differentiated were increased gradually, while the leaf number presented decreasing trend. When MS medium added with 2.0 mg/L 2,4-D, the differentiation rate of bulblet reached the highest as 91.7%. With the increase of 2,4-D concentration(above 2.0 mg/L), the number of bulblet was decreased gradually, the diffe-

    rentiation rate decreased to 42.9% by supplying 3.0 mg/L 2,4-D in MS medium, and no leaf was found to grow on bulblet.

    2. 3 Effect of sugar on expansion and rooting of bulblet

    As shown in Tab.3, the results showed that the rooting rate of all bulblets could reach to 100.0% when MS added with 30.0-90.0 g/L sugar. The expansion times of bulblet gradually increased with the increase of sugar concentration, while the average roots of different treatments presented change trends of increasing firstly and decreasing at latter. By adding 90.0 g/L sugar in MS medium, the bulblet grew strong, and its expansion times reached the highest as 3.0, the average roots per bulblet reached 5.4. By supplying 70.0 g/L sugar in MS medium, although the expansion times of bulblet was 2.6, the average roots per bulblet reached the highest as 6.3. Taking into account both of expansion state and rooting effect, MS+70.0 g/L sugar was considered as the suitable culture medium for expansion and rooting of bulblet.

    2. 4 Effects of different transplanted matrices on transplanting survival rate

    After transplanting for 10 days, the rooting bulblets of different matrices treatments started to grow new leaves. From the results of Tab.4, it found that the survival rate of bulblets for the 1st matrix treatment(perlite, peat and vermiculite) reached to 100.0% when bulblet diameter were 0.3-0.5 and >0.5 cm in size, and their average height found to be the highest as 4.5 cm. Furthermore, the survival rates of bulblets with 0.3-0.5 cm in size were 12.5%-44.3% higher than those of bulblets with >0.5 cm in size for other 3 treatments. The survival rate and average height of bulblets for the 4th treatment(perlite, peat, vermiculite and sawdust) were found to be higher than the 3rd treatment(perlite, peat, vermiculite and garden soil), because that the ventilation ability and water permeability of added sawdust were better than that of garden soil. Being without supplement of vermiculite, the ventilation ability and water permeability of the 2nd treatment(perlite, sawdust and garden soil) were lower than the other three treatments added with ventilation, which resulted in the lowest survival rate. By comprehensive consideration, the matrix combination of perlite,peat and vermiculite(1∶1∶1) was more suitable for transplanting of Oriental lily love story.

    3 Discussion

    Lily traditional propagation modes include generative propagation and vegetative propagation. Generative propagation require long period and easily produce mutation, vegetative propagation was characterized by very low propagation coefficient for inducing adventitious buds by using scales investment method(Lan, 2011). Therefore, during propagation process of lily plantlets, the tissue culture and rapid propagation of lily bulb are of important significance to improve its propagation coefficient, get a lot of virus-free high-quality bulbs and keep its species characteristics.

    In recent years, there are many reports on the propagation system established of lily. By using the bulb scale and leaf of three oriental lily varieties as explants, Hu et al.(2007) studied the effects of 6-BA, KT, NAA and 2,4-D in MS medium on organogenesis of oriental lily. The results of adventitious buds and bulblets diffe-

    rentiated from scale indicated that, the small bulbs were wrapped tight when formed in culture medium added with 2,4-D, poorer quality bulblets with serious vitrification were found in medium with high concentration of 6-BA. It also found that 6-BA was very important to adventitious buds differentiation, while KT could obviously shorten differentiation time. The results of orthogonal test showed that, KT and 2,4-D had a little effects on the formation of adventitious buds; the result of adventitious buds differentiated leaves indicated that, the initiation culture time, differentiation efficient and types of leaves were found to be different being variety differences. In the present study, 6-BA was used to choose for adventitious buds differentiation of lily variety Love Story scales, it found that 1.5 mg/L 6-BA was suitable for differentiation of scales, adventitious buds and the differentiation rate reached to 75.0%, which was similar as the reported results of Liu and Lin(2002) and Wang et al.(2013).

    By comparing the effects of 2,4-D, IAA and NAA on callus formation of L. brownie var. Viridulum sterile leaves(Liu et al., 1997), it found that callus induction rate were higher than the other treatments whether 2,4-D used alone or combining with cytokinin. Cytological observations results showed that, during the process of somatic embryogenesis formation, somatic embryos could be obtained directly without callus inducing stage when supplied 2,4-D in culture medium. In the study of Oriental lily. Tiber leaves to induce callus by using 2,4-D in MS medium, Fu et al.(2008) found that after a period of culture, the surface of explants could induce small absinthe-green embossmen, which some of them could be formed into callus and others were directly formed into bulblets. This similar phenomenon was also observed in the present study by using 2,4-D to induce callus from leaves, and bulblets were found to directly form from small embossmen of explants surface without obvious callus.

    During the rooting process of lily plantlets, Wang and Lin(2005) indicated that both of 1/2MS and MS media were advantageous to plantlets rooting; Luo et al.(2000) found that MS medium without any hormones was the best medium for rooting induction of Longiflorum. During the culture process of bulblets expansion of Lilum davidi var. Unicolor(Hoog) Cotton , MS medium adding with 60.0-90.0 g/L sugar could significantly promote the bulblets formation, and the highest weight reached to 99.30 mg when added 90.0 g/L sugar in medium(Wei et al., 2014). As to the rooting culture of Manissa, the rooting rate found to be reached to 100.0% and the average roots was 6.9 when added 60.0 g/L sugar in MS medium. In this trial for inducing bulblets expansion and rooting of Oriental lily Love Story, the similar results were found by supplying 70.0 g/L sugar in MS medium, the expansion times of bulblet was 2.6 and the average roots per bulblet reached the highest as 6.3.

    The transplanting matrix is one of the important factors for plantlet survival of lily, different lily plantlets need different suitable transplanting matrices. Luo et al.(2000) tried to use river sand, peat and perlite alone or in combination(1∶1) to study the transplant survival rate of Longiflorum, the results indicated that the best matrix for transplant was river sand and peat with ratio of 1∶1; Li et al.(2014) adopted peat, vermiculite, humus soil and dry chicken manure as matrix with ratio of 1∶1∶1∶1 to transplant lily plantlets, and the survival rate of plantlets with >0.5 cm in diameter found to be 86.7%. The perlite and humous(3∶1) screened was the best mixed matrix for Acapulco, the survival rate found to be reached to 100.0% and the plantlet grew well(Zhao et al., 2003). In our experiment, the matrix combination of perlite, peat and vermiculite(1∶1∶1) was more suitable for transplanting of Oriental lily Love Story, the survival rate of bulblets in diameter of 0.3-0.5 and >0.5 cm could be achieved 100.0%.

    4 Conclusion

    The present results showed that, by using sterile scales of adventitious bud derived from flower organ culture as explants, the established rapid propagation system of Oriental lily Love Story could be used for its industrialized production of seed-bulbs.

    Reference:

    Fu W Q, Du S T, Chen J K, Yin H. 2008. Effects of NAA and 2,4-D on oriental lily scale and leaflet culture[J]. Journal of Northwest Forestry University, 23(2): 83-86.

    Hu F R, Xi M L, Liu G X, Shi J S. 2007. Study on organogenesis and somatic embryogenesis of oriental lily[J]. Journal of Nanjing Forestry University(Natural Sciences Edition),31(2):5-8.

    Lan Q. 2011. Rapid propagation in vitro and polyploid induction of Lilium[D]. Baoding: Agricultural University of Hebei.

    Li Y, Li S L, Li X, Meng C J, Li D L, Pan C F. 2014. Test-tube plantlet transplanting of Manissa[J]. Shaanxi Journal of Agricultural Sciences, 60(2): 30-32.

    Liao Q, Zhou B, Marbaha, Liu Q L, Sheng W. 2012. The inducing of OT oriental lily bulblet and establishing of regeneration system[J]. Xinjiang Agricultural Sciences, 23(5): 450-452.

    Liu L M, Lu S Q, Chen Y X, Yang M C. 2007. Tissue cultrue of lily floral organs. Guangxi Agricultural Sciences, 38(3):219-222.

    Liu M Z, Lin X Y. 2002. Effects of hormone on plant regeneration of lily(Lilium daviaii Duch)[J]. Guihaia, 22(2): 167-170.

    Liu X M, Zhou P H, Qu S C, Lu X Y, Luo Z M. 1997. In vitro induction of indefinite bubs and somatic embryoes from scale leaves of tetraploid ‘Longya Lily[J]. Acta Horticulturae Sinica, 24(4): 353-358.

    Luo F X, Xu G H, Jin L L, Sun X M, Zhu M. 2000. Studied on rapid propagation of Lilium × Longiflorum[J]. Journal of Shen-

    yang Agricultural University, 31(3):254-257.

    Nong Y F, Zhou S, Mou Y M, Cen X T, Su X H, Yang M C. 2014. Tissue culture and rapid propagation of OT hybrids lily Manissa floral organs[J]. Journal of Southern Agriculture, 45(5):715-719.

    Tang D Q, Huang D F, Tang K X, Qian H M, Fu J. 2003. Tissue culture of oriental lily from bulb scale[J]. Plant Physiology Communications, 23(5): 450-452.

    Wang F B, Wang F, Guan L L, Hu F R. 2013. Effect of plant hormone on differentiation of adventitious buds derived from sterile scales of oriental hybrids lily test-tube plantlets[J]. Jiangsu Agricultural Sciences, 41(6): 53 -55.

    Wang H F, Lin Y Y. 2005. Preliminary discussion of lily organization trains and striking root[J]. Journal of Qiongzhou University, 12(2):24-26.

    Wei L P,Wei S B, Bi Z Q, Han Y S, Zhang J Z. 2014. Regeneration propagation system establishment of bulb-let derived from scale of Lilium davidii var. Unicolor(Hoog) Cotton[J]. Journal of Southern Agriculture, 45(5): 742-784.

    Zhao Q F, Zeng X Y, Ding L, She L P, Zhang Y M. 2003. Study on tissue culture and clonal propagation of Acapulco[J]. Journal of Northwest Normal University(Natural Science), 39(1): 66-68.

    Zhao Y P, Zhang J D, Cheng J G. 2005. In vitro induction of adventitious buds from leaves and scale leaves of lily species[J]. Journal of Xian University of Arts & Science, 8(1): 21-23.

    Zhou H, Xie L, Guo H R, Zhang Z S. 2010. Research progress on tissue culture of Liliaceae plants[J]. Hubei Agricultural Sciences, 45(5): 742-784.

    (責(zé)任編輯 韋莉萍)

    自拍欧美九色日韩亚洲蝌蚪91| 成人亚洲精品一区在线观看| 制服人妻中文乱码| а√天堂www在线а√下载| 亚洲 欧美 日韩 在线 免费| 国产精品电影一区二区三区| e午夜精品久久久久久久| 大香蕉久久成人网| 天天添夜夜摸| 国产成年人精品一区二区| 国产又爽黄色视频| 精品电影一区二区在线| 国产伦一二天堂av在线观看| 国产99久久九九免费精品| 大码成人一级视频| 高清毛片免费观看视频网站| 亚洲黑人精品在线| 日韩三级视频一区二区三区| 国产又爽黄色视频| 少妇粗大呻吟视频| 亚洲人成网站在线播放欧美日韩| 中文字幕久久专区| 自拍欧美九色日韩亚洲蝌蚪91| 99香蕉大伊视频| 亚洲国产精品成人综合色| 精品国产乱码久久久久久男人| 19禁男女啪啪无遮挡网站| 男女下面进入的视频免费午夜 | 亚洲精品在线观看二区| 亚洲色图av天堂| 丝袜美足系列| 久久人妻av系列| 日韩欧美免费精品| 国产精品久久久人人做人人爽| 99久久久亚洲精品蜜臀av| 岛国在线观看网站| 怎么达到女性高潮| 老司机福利观看| 免费不卡黄色视频| 禁无遮挡网站| 欧美在线一区亚洲| 久久久精品欧美日韩精品| www.999成人在线观看| 精品一品国产午夜福利视频| 91字幕亚洲| 欧美日韩黄片免| 国产精品免费视频内射| 日日摸夜夜添夜夜添小说| 伦理电影免费视频| 亚洲av电影不卡..在线观看| 久久久久久亚洲精品国产蜜桃av| 在线观看日韩欧美| 欧美日韩亚洲综合一区二区三区_| 好男人电影高清在线观看| 亚洲精品一卡2卡三卡4卡5卡| 亚洲天堂国产精品一区在线| 熟女少妇亚洲综合色aaa.| 亚洲色图 男人天堂 中文字幕| 久久精品91无色码中文字幕| 99国产精品免费福利视频| 午夜a级毛片| 成人三级黄色视频| 亚洲国产欧美网| 怎么达到女性高潮| 精品国产乱子伦一区二区三区| 91麻豆av在线| 亚洲国产精品成人综合色| 欧美日韩亚洲综合一区二区三区_| 亚洲精品美女久久av网站| 久久人妻av系列| 日本在线视频免费播放| 无人区码免费观看不卡| 麻豆av在线久日| 亚洲第一av免费看| 亚洲人成网站在线播放欧美日韩| 亚洲午夜理论影院| 亚洲第一电影网av| 91在线观看av| 久久久久久久精品吃奶| 国产xxxxx性猛交| 国产三级在线视频| 动漫黄色视频在线观看| 777久久人妻少妇嫩草av网站| 日日夜夜操网爽| 一级a爱视频在线免费观看| 又大又爽又粗| av在线天堂中文字幕| 亚洲精品一区av在线观看| 亚洲成人久久性| 妹子高潮喷水视频| 村上凉子中文字幕在线| 老汉色av国产亚洲站长工具| 男女下面插进去视频免费观看| 久久久久九九精品影院| a在线观看视频网站| 国产三级黄色录像| 搡老妇女老女人老熟妇| 很黄的视频免费| 国产aⅴ精品一区二区三区波| 91九色精品人成在线观看| 精品卡一卡二卡四卡免费| 亚洲三区欧美一区| 在线天堂中文资源库| 国产极品粉嫩免费观看在线| 国产亚洲精品一区二区www| 麻豆久久精品国产亚洲av| 一a级毛片在线观看| 美女高潮到喷水免费观看| 日韩大码丰满熟妇| 成人三级做爰电影| 男男h啪啪无遮挡| 国产精品国产高清国产av| 日韩欧美国产一区二区入口| 岛国视频午夜一区免费看| 久久人妻熟女aⅴ| 男人操女人黄网站| svipshipincom国产片| 国产精品秋霞免费鲁丝片| 午夜久久久在线观看| 丝袜美足系列| 夜夜看夜夜爽夜夜摸| 91成人精品电影| 黄色女人牲交| 国产成年人精品一区二区| 亚洲黑人精品在线| 91麻豆av在线| 午夜两性在线视频| 欧美激情极品国产一区二区三区| 亚洲人成电影免费在线| 日本在线视频免费播放| 法律面前人人平等表现在哪些方面| 亚洲欧美一区二区三区黑人| 精品免费久久久久久久清纯| 国产麻豆成人av免费视频| 日本在线视频免费播放| 色尼玛亚洲综合影院| 亚洲第一电影网av| 久久国产精品影院| 久久婷婷人人爽人人干人人爱 | 久久久国产成人精品二区| 人妻久久中文字幕网| 正在播放国产对白刺激| 50天的宝宝边吃奶边哭怎么回事| 啦啦啦韩国在线观看视频| 中文字幕精品免费在线观看视频| 亚洲中文日韩欧美视频| 亚洲专区字幕在线| 欧美性长视频在线观看| 欧美不卡视频在线免费观看 | 长腿黑丝高跟| 人人妻人人爽人人添夜夜欢视频| 久热这里只有精品99| 美女高潮喷水抽搐中文字幕| 久久国产乱子伦精品免费另类| 99久久久亚洲精品蜜臀av| 夜夜看夜夜爽夜夜摸| 国产亚洲精品综合一区在线观看 | 9热在线视频观看99| 后天国语完整版免费观看| 亚洲男人天堂网一区| 波多野结衣av一区二区av| 国产熟女午夜一区二区三区| 一级a爱片免费观看的视频| 亚洲欧美激情在线| 久久精品亚洲熟妇少妇任你| 欧美一级毛片孕妇| 久久精品91无色码中文字幕| www.www免费av| 在线观看免费日韩欧美大片| av福利片在线| 91麻豆av在线| 日本在线视频免费播放| 亚洲情色 制服丝袜| 亚洲精品av麻豆狂野| 久久青草综合色| 婷婷六月久久综合丁香| 久久狼人影院| 久久久久精品国产欧美久久久| 国产蜜桃级精品一区二区三区| 亚洲中文字幕日韩| 成人欧美大片| 十分钟在线观看高清视频www| 老司机午夜十八禁免费视频| 欧美另类亚洲清纯唯美| netflix在线观看网站| 国产一区二区三区视频了| 巨乳人妻的诱惑在线观看| 亚洲av日韩精品久久久久久密| 亚洲人成电影观看| 久久久久久久久免费视频了| 国产精品国产高清国产av| av天堂在线播放| 国产三级黄色录像| 精品国产一区二区久久| 热re99久久国产66热| 999精品在线视频| 女人高潮潮喷娇喘18禁视频| 日本欧美视频一区| 国产亚洲精品久久久久5区| 一进一出抽搐动态| 成熟少妇高潮喷水视频| 午夜激情av网站| 久久国产乱子伦精品免费另类| 久久狼人影院| 1024视频免费在线观看| 日韩欧美在线二视频| 日韩国内少妇激情av| 村上凉子中文字幕在线| 久久人妻熟女aⅴ| av片东京热男人的天堂| 一区二区三区国产精品乱码| 成人国产一区最新在线观看| 亚洲精品国产精品久久久不卡| 欧美色视频一区免费| 亚洲精品国产色婷婷电影| 精品福利观看| 欧美黄色淫秽网站| x7x7x7水蜜桃| 色尼玛亚洲综合影院| 久久国产亚洲av麻豆专区| 精品国产超薄肉色丝袜足j| 亚洲,欧美精品.| 欧美成人一区二区免费高清观看 | 欧美国产精品va在线观看不卡| 韩国精品一区二区三区| 男女午夜视频在线观看| 久久中文字幕一级| 一级毛片女人18水好多| 精品人妻在线不人妻| 在线观看日韩欧美| 亚洲精品一卡2卡三卡4卡5卡| 亚洲久久久国产精品| 后天国语完整版免费观看| 50天的宝宝边吃奶边哭怎么回事| 一区二区三区高清视频在线| 欧美日本中文国产一区发布| 美女 人体艺术 gogo| 精品国产国语对白av| 国产精品1区2区在线观看.| 国产真人三级小视频在线观看| 久久久久久久精品吃奶| 高清在线国产一区| 久久精品91蜜桃| 人人妻人人爽人人添夜夜欢视频| tocl精华| 国产精品野战在线观看| 黑人巨大精品欧美一区二区蜜桃| 久久久久久大精品| 如日韩欧美国产精品一区二区三区| 操出白浆在线播放| 婷婷六月久久综合丁香| 国产成人精品久久二区二区免费| 亚洲情色 制服丝袜| 黑人操中国人逼视频| 免费在线观看视频国产中文字幕亚洲| 麻豆一二三区av精品| 日本三级黄在线观看| 熟女少妇亚洲综合色aaa.| 国产精品野战在线观看| 欧美激情久久久久久爽电影 | www.自偷自拍.com| 精品一品国产午夜福利视频| 91老司机精品| 欧美日韩瑟瑟在线播放| 国产极品粉嫩免费观看在线| 九色国产91popny在线| 国产99白浆流出| 国产一区二区在线av高清观看| 日韩欧美在线二视频| 亚洲人成77777在线视频| 大型av网站在线播放| 国产区一区二久久| 亚洲国产日韩欧美精品在线观看 | 日日爽夜夜爽网站| 国产私拍福利视频在线观看| 人妻久久中文字幕网| 此物有八面人人有两片| 后天国语完整版免费观看| 免费无遮挡裸体视频| 91成年电影在线观看| 日韩欧美国产在线观看| 日韩 欧美 亚洲 中文字幕| 非洲黑人性xxxx精品又粗又长| 少妇 在线观看| 精品国产乱码久久久久久男人| 国产99久久九九免费精品| 久久婷婷人人爽人人干人人爱 | 久久精品国产清高在天天线| 午夜福利成人在线免费观看| 国产av在哪里看| 99在线视频只有这里精品首页| 亚洲精品一卡2卡三卡4卡5卡| 国内毛片毛片毛片毛片毛片| 丁香六月欧美| 亚洲久久久国产精品| 色尼玛亚洲综合影院| 国产在线观看jvid| 成人国语在线视频| 国产亚洲精品第一综合不卡| 久99久视频精品免费| 久久香蕉精品热| 亚洲精品中文字幕一二三四区| 午夜日韩欧美国产| 欧美激情极品国产一区二区三区| 人人澡人人妻人| 亚洲片人在线观看| 91麻豆av在线| 日本欧美视频一区| 精品欧美一区二区三区在线| 国产av在哪里看| 欧美日韩一级在线毛片| 在线观看免费视频日本深夜| 一级片免费观看大全| av电影中文网址| 黄色视频不卡| 中文字幕久久专区| 国产欧美日韩精品亚洲av| 国产精品 欧美亚洲| 精品久久久久久,| 很黄的视频免费| 午夜视频精品福利| 后天国语完整版免费观看| 黑人巨大精品欧美一区二区mp4| 免费女性裸体啪啪无遮挡网站| 国产成人免费无遮挡视频| 人人妻人人爽人人添夜夜欢视频| av天堂久久9| 日韩 欧美 亚洲 中文字幕| 国产97色在线日韩免费| 国产精品影院久久| 热99re8久久精品国产| 99久久久亚洲精品蜜臀av| 大香蕉久久成人网| 妹子高潮喷水视频| 午夜精品在线福利| 激情视频va一区二区三区| av超薄肉色丝袜交足视频| 亚洲国产日韩欧美精品在线观看 | 久久中文字幕人妻熟女| 91精品国产国语对白视频| АⅤ资源中文在线天堂| 国产高清videossex| 国产真人三级小视频在线观看| 十分钟在线观看高清视频www| 久久久久亚洲av毛片大全| 久久香蕉激情| 午夜视频精品福利| 欧美日韩福利视频一区二区| 久久婷婷成人综合色麻豆| 国产精品久久视频播放| 欧美成人午夜精品| 国产精品 国内视频| 少妇熟女aⅴ在线视频| 午夜福利免费观看在线| 久久精品国产综合久久久| 美女高潮到喷水免费观看| 成人欧美大片| 久久久久久大精品| 色播在线永久视频| 成在线人永久免费视频| 搞女人的毛片| 日韩av在线大香蕉| 久久国产精品影院| 久久性视频一级片| 亚洲精品国产区一区二| 欧美色视频一区免费| 国产一级毛片七仙女欲春2 | 看免费av毛片| 久久久国产欧美日韩av| 中文字幕另类日韩欧美亚洲嫩草| 久久中文看片网| 国产av精品麻豆| 1024视频免费在线观看| 丰满人妻熟妇乱又伦精品不卡| 黄网站色视频无遮挡免费观看| 欧美黄色片欧美黄色片| 国产成人一区二区三区免费视频网站| 女性被躁到高潮视频| 美女午夜性视频免费| 久久中文字幕一级| 黄色丝袜av网址大全| 97碰自拍视频| 少妇裸体淫交视频免费看高清 | 日韩欧美国产在线观看| 精品一区二区三区视频在线观看免费| 女性生殖器流出的白浆| 国产精品一区二区在线不卡| 亚洲国产精品sss在线观看| 给我免费播放毛片高清在线观看| 黑人操中国人逼视频| 国产私拍福利视频在线观看| 夜夜夜夜夜久久久久| 一二三四在线观看免费中文在| 啪啪无遮挡十八禁网站| 亚洲专区国产一区二区| 黄片大片在线免费观看| 女人被躁到高潮嗷嗷叫费观| 日本一区二区免费在线视频| 亚洲av成人不卡在线观看播放网| 老司机午夜十八禁免费视频| 丁香欧美五月| 色综合欧美亚洲国产小说| 久久久久亚洲av毛片大全| 两人在一起打扑克的视频| 女人高潮潮喷娇喘18禁视频| 99久久综合精品五月天人人| 啦啦啦免费观看视频1| 欧美一级毛片孕妇| 在线永久观看黄色视频| 两个人看的免费小视频| 美女高潮到喷水免费观看| 久久久久久久久中文| 99国产综合亚洲精品| 国产伦一二天堂av在线观看| 精品国产乱码久久久久久男人| 女人爽到高潮嗷嗷叫在线视频| 国产精品av久久久久免费| 99国产精品一区二区三区| 亚洲国产精品成人综合色| 少妇 在线观看| 桃红色精品国产亚洲av| 亚洲国产欧美日韩在线播放| 国产成人一区二区三区免费视频网站| 国产成人系列免费观看| www.熟女人妻精品国产| 国产蜜桃级精品一区二区三区| 久久人妻av系列| АⅤ资源中文在线天堂| 91九色精品人成在线观看| 69精品国产乱码久久久| 精品一品国产午夜福利视频| 叶爱在线成人免费视频播放| 黑人欧美特级aaaaaa片| 亚洲精品在线美女| 女生性感内裤真人,穿戴方法视频| 精品久久久久久成人av| 韩国精品一区二区三区| a在线观看视频网站| 岛国在线观看网站| 久久天堂一区二区三区四区| 免费观看精品视频网站| 国产精品精品国产色婷婷| 国产成+人综合+亚洲专区| 成人亚洲精品一区在线观看| 欧美性长视频在线观看| 日韩大码丰满熟妇| 午夜精品国产一区二区电影| 久久久久国产精品人妻aⅴ院| 老汉色av国产亚洲站长工具| 欧美日本视频| 亚洲av第一区精品v没综合| 国产精品99久久99久久久不卡| 男人的好看免费观看在线视频 | 免费在线观看亚洲国产| 亚洲第一av免费看| 最新美女视频免费是黄的| 日本精品一区二区三区蜜桃| 波多野结衣巨乳人妻| 制服丝袜大香蕉在线| 国产乱人伦免费视频| 日韩大码丰满熟妇| 亚洲 国产 在线| 国产亚洲欧美98| 国产真人三级小视频在线观看| 亚洲精品国产一区二区精华液| 亚洲第一青青草原| 久久 成人 亚洲| 叶爱在线成人免费视频播放| 老熟妇乱子伦视频在线观看| tocl精华| 涩涩av久久男人的天堂| 国产成人啪精品午夜网站| 亚洲,欧美精品.| 久久国产亚洲av麻豆专区| 午夜亚洲福利在线播放| 侵犯人妻中文字幕一二三四区| 麻豆国产av国片精品| 最好的美女福利视频网| 国产亚洲欧美精品永久| 免费在线观看完整版高清| 丁香六月欧美| 国产伦人伦偷精品视频| 少妇 在线观看| 欧美日韩一级在线毛片| 日韩成人在线观看一区二区三区| 国产精品一区二区在线不卡| 午夜福利免费观看在线| 日韩精品中文字幕看吧| 国产av又大| 久久人人精品亚洲av| 99久久综合精品五月天人人| 99精品欧美一区二区三区四区| 精品久久久久久久人妻蜜臀av | 国产精品电影一区二区三区| 亚洲九九香蕉| 久久久久国产精品人妻aⅴ院| 国产亚洲av嫩草精品影院| 久久久久亚洲av毛片大全| 人妻久久中文字幕网| 男女床上黄色一级片免费看| 亚洲国产日韩欧美精品在线观看 | 色综合欧美亚洲国产小说| 欧美午夜高清在线| 亚洲 欧美一区二区三区| 亚洲狠狠婷婷综合久久图片| 欧美日韩精品网址| 如日韩欧美国产精品一区二区三区| 人人妻人人澡欧美一区二区 | 亚洲av成人av| 好看av亚洲va欧美ⅴa在| 亚洲精华国产精华精| 精品国产超薄肉色丝袜足j| x7x7x7水蜜桃| 两个人免费观看高清视频| 可以在线观看毛片的网站| 少妇裸体淫交视频免费看高清 | 很黄的视频免费| 日韩精品免费视频一区二区三区| 欧美久久黑人一区二区| 90打野战视频偷拍视频| 午夜激情av网站| 久99久视频精品免费| 国产又色又爽无遮挡免费看| 国产在线精品亚洲第一网站| 久久久久久大精品| 亚洲va日本ⅴa欧美va伊人久久| 久久精品91无色码中文字幕| 午夜精品国产一区二区电影| 美女扒开内裤让男人捅视频| 国产成年人精品一区二区| 午夜福利影视在线免费观看| 国产高清有码在线观看视频 | 久久人妻av系列| 精品久久久久久久毛片微露脸| 国产精品免费视频内射| 操出白浆在线播放| 婷婷六月久久综合丁香| 看片在线看免费视频| 国产成人精品无人区| 一区二区三区激情视频| 首页视频小说图片口味搜索| 中文字幕人妻丝袜一区二区| 国产亚洲精品av在线| 十八禁人妻一区二区| 乱人伦中国视频| 丰满人妻熟妇乱又伦精品不卡| av有码第一页| 激情在线观看视频在线高清| 国产国语露脸激情在线看| 久久狼人影院| 成人欧美大片| 欧美在线一区亚洲| 老汉色∧v一级毛片| 色综合欧美亚洲国产小说| 亚洲熟妇熟女久久| 岛国在线观看网站| 日本一区二区免费在线视频| 国产av一区二区精品久久| 丰满人妻熟妇乱又伦精品不卡| 黄色女人牲交| 91麻豆av在线| 国内久久婷婷六月综合欲色啪| 成人三级黄色视频| 欧美成人免费av一区二区三区| 久久人人97超碰香蕉20202| bbb黄色大片| 亚洲全国av大片| 日本vs欧美在线观看视频| 国产高清视频在线播放一区| bbb黄色大片| 精品一区二区三区视频在线观看免费| 欧美人与性动交α欧美精品济南到| 妹子高潮喷水视频| 久久香蕉激情| 国产av在哪里看| 国产成人一区二区三区免费视频网站| 夜夜看夜夜爽夜夜摸| 51午夜福利影视在线观看| 成年版毛片免费区| 高清毛片免费观看视频网站| 国产高清视频在线播放一区| 很黄的视频免费| 国产精品香港三级国产av潘金莲| √禁漫天堂资源中文www| 88av欧美| 真人做人爱边吃奶动态| 国产精品自产拍在线观看55亚洲| 欧美乱色亚洲激情| 亚洲aⅴ乱码一区二区在线播放 | 97超级碰碰碰精品色视频在线观看| 国产一卡二卡三卡精品| 精品久久久久久久久久免费视频| 成人亚洲精品一区在线观看| 亚洲国产日韩欧美精品在线观看 | 久久久国产成人精品二区| 宅男免费午夜| 亚洲国产精品合色在线| 日韩有码中文字幕| 美女大奶头视频| 精品国内亚洲2022精品成人| 1024视频免费在线观看| 午夜影院日韩av| 窝窝影院91人妻| a在线观看视频网站| 欧美在线黄色| 国产1区2区3区精品| 桃红色精品国产亚洲av| 色av中文字幕| 99国产精品一区二区三区| АⅤ资源中文在线天堂| 欧美乱色亚洲激情| 美女高潮到喷水免费观看| 搞女人的毛片| 国产成人精品无人区| 不卡一级毛片|