Chinese Journal of Applied Ecology ›› 2020, Vol. 31 ›› Issue (11): 3959-3968.doi: 10.13287/j.1001-9332.202011.037
• Reviews • Previous Articles Next Articles
ZOU Yao, HAN Chong-xuan*
Received:
2020-03-20
Accepted:
2020-08-19
Online:
2020-11-15
Published:
2021-06-10
Contact:
* E-mail: sendakingcat@nwsuaf.edu.cn
Supported by:
ZOU Yao, HAN Chong-xuan. Interaction between intestinal microorganisms and carbohydrates of mammals and its influence[J]. Chinese Journal of Applied Ecology, 2020, 31(11): 3959-3968.
Add to citation manager EndNote|Ris|BibTeX
URL: https://www.cjae.net/EN/10.13287/j.1001-9332.202011.037
[1] Valdes AM, Walter J, Segal E, et al. Role of the gut microbiota in nutrition and health. BMJ Clinical Research, 2018, 361: 17-22 [2] Maukonen J, Saarela M. Human gut microbiota: Does diet matter? Proceedings of the Nutrition Society, 2015, 74: 23-36 [3] 谭支良. 动物胃肠道微生态理论与实践. 应用生态学报, 2003, 14(1): 148-150 [Tan Z-L. Micro-ecology in animal stomach and digestive tracts-theory and practice. Chinese Journal of Applied Ecology, 2003, 14(1): 148-150] [4] 吴金凤, 熊金波, 王欣, 等. 肠道菌群对凡纳滨对虾健康的指示作用. 应用生态学报, 2016, 27(2): 611-621 [Wu J-F, Xiong J-B, Wang X, et al. Intestinal bacterial community is indicative for the healthy status of Litopenaeus vannamei. Chinese Journal of Applied Ecology, 2016, 27(2): 611-621] [5] Fndriks L. Roles of the gut in the metabolic syndrome: An overview. Journal of International Medicine, 2017, 281: 319-336 [6] Murugesan S, Nirmalkar K, Hoyo-Vadillo C, et al. Gut microbiome production of short-chain fatty acids and obesity in children. European Journal of Clinical Microbiology & Infectious Diseases, 2017, 37: 621-625 [7] Gill SR, Pop M, Deboy RT, et al. Metagenomic analysis of the human distal gut microbiome. Science, 2006, 312: 1355-1359 [8] Shortt C, Hasselwander O, Meynier A, et al. Systematic review of the effects of the intestinal microbiota on selected nutrients and non-nutrients. European Journal of Nutrition, 2017, 57: 25-49 [9] Sender R, Fuchs S, Milo R. Revised estimates for the number of human and bacteria cells in the body. PLoS Biology, 2016, 14(8): e1002533, doi: 10.1371/journal.pbio.1002533 [10] Nicholson JK, Holmes E, Kinross J, et al. Host-gut microbiota metabolic interactions. Science, 2012, 336: 1262-1267 [11] Augustin LS, Kendall CW, Jenkins DJ, et al. Glycemic index, glycemic load and glycemic response: An international scientific consensus summit from the International Carbohydrate Quality Consortium (ICQC). Nutrition Metabolism and Cardiovascular Disease, 2015, 25: 795-815 [12] Flint HJ, Scott KP, Duncan SH, et al. Microbial degradation of complex carbohydrates in the gut. Gut Microbes, 2012, 3: 289-306 [13] Meenu M, Xu B. A critical review on anti-diabetic and anti-obesity effects of dietary resistant starch. Critical Reviews in Food Science and Nutrition, 2018, 59: 3019-3031 [14] Wang Z, Wang L, Chen Z, et al. In vitro evaluation of swine-derived Lactobacillus reuteri: Probiotic properties and effects on intestinal porcine epithelial cells challenged with enterotoxigenic escherichia coli K88. Journal of Microbiology and Biotechnology, 2016, 26: 1018-1025 [15] Wang Q, Zheng Y, Zhuang W, et al. Genome-wide transcriptional changes in type 2 diabetic mice supplemented with lotus seed resistant starch. Food Chemistry, 2018, 264: 427-434 [16] Si X, Starappe P, Blanchard C, et al. Enhanced anti-obesity effects of complex of resistant starch and chitosan in high fat diet fed rats. Carbohydrate Polymers, 2017, 157: 834-841 [17] Ze X, Duncan SH, Louis P, et al. Ruminococcus bromii is a keystone species for the degradation of resistant starch in the human colon. Multidisciplinary Journal of Microbial Ecology, 2012, 6: 1535-1543 [18] Jiminez JA, Uwiera TC, Abbott DW, et al. Impacts of resistant starch and wheat bran consumption on enteric inflammation in relation to colonic bacterial community structures and short-chain fatty acid concentrations in mice. Gut Pathogens, 2016, 8: 1-20 [19] Abell GCJ, Cooke CM, Bennett CN, et al. Phylotypes related to Ruminococcus bromii are abundant in the large bowel of humans and increase in response to a diet high in resistant starch. FEMS Microbiology Ecology, 2008, 66: 505-515 [20] Connolly ML, Lovegrove JA, Tuohy KM. In vitro evalua-tion of the microbiota modulation abilities of different sized whole oat grain flakes. Anaerobe, 2010, 16: 483-488 [21] Leu L, Kevin R, Brown LI, et al. A symbiotic combination of resistant starch and bifidobacterium lactis facilitates apoptotic deletion of carcinogen-damaged cells in rat colon. Journal of Nutrition, 2005, 135: 996-1001 [22] Walker AW, Ince J, Duncan SH, et al. Dominant and diet-responsive groups of bacteria within the human colonic microbiota. ISME Journal, 2011, 5: 220-230 [23] Walker AW, Duncan SH, Harmsen HJM, et al. The species composition of the human intestinal microbiota differs between particle-associated and liquid phase communities. Environmental Microbiology, 2008, 10: 3275-3283 [24] Salyers AA, Vercellotti JR, West SE, et al. Fermentation of mucin and plant polysaccharides by strains of Bacteroides from the human colon. Applied and Environmental Microbiology, 1977, 33: 319-322 [25] Paturi G, Nyanhanda T, Butts CA, et al. Effects of potato fiber and potato- resistant starch on biomarkers of colonic health in rats fed diets containing red meat. Journal of Food Science, 2012, 77: 216-223 [26] Gareau MG, Sherman PM, Walker WA. Probiotics and the gut microbiota in intestinal health and disease. Nature Reviews Gastroenterology and Hepatology, 2010, 7: 503-514 [27] Zhang L, Li HT, Shen L, et al. Effect of dietary resis-tant starch on prevention and treatment of obesity-related diseases and its possible mechanisms. Biomedical and Environmental Sciences, 2015, 28: 291-297 [28] Martínez I, Kim J, Duffy PR, et al. Resistant starches types 2 and 4 have differential effects on the composition of the fecal microbiota in human subjects. PLoS One, 2010, 5(11): e15046, doi: 10.1371/journal.pone.0015046 [29] Metzler BU, Canibe N, Montagne L, et al. Resistant starch reduces large intestinal pH and promotes fecal lactobacilli and bifidobacteria in pigs. Animal, 2018, 13: 64-73 [30] Tian G, Wu X, Chen D, et al. Adaptation of gut microbiome to different dietary non-starch polysaccharide fractions in a porcine model. Molecular Nutrition & Food Research, 2017, 61: 1700012, doi:10.1002/mnfr.201700012 [31] Ramirez-Farias C, Slezak K, Fuller Z, et al. Effect of inulin on the human gut microbiota: Stimulation of Bifidobacterium adolescentis and Faecalibacteriumprausnitzii. British Journal of Nutrition, 2008, 101: 541-550 [32] Lattimer JM, Haub MD. Effects of dietary fiber and its components on metabolic health. Nutrients, 2010, 2: 1266-1289 [33] Leikin JB, Paloucek FP. Poisoning and Toxicology Handbook. 4th Ed. Hudson, OH, USA: Lexi-Comp Inc., 2008: 892-893 [34] Heinsbroek SEM, Williams DL, Welting O, et al. Orally delivered-glucans aggravate dextran sulfate sodium (DSS)-induced intestinal inflammation. Nutrition Research, 2015, 35: 1106-1112 [35] Ross AB, Pere-Trepat E, Montoliu I, et al. A whole-grain-rich diet reduces urinary excretion of markers of protein catabolism and gut microbiota metabolism in healthy men after one week. Journal of Nutrition, 2013, 143: 766-773 [36] Shabat SKB, Sasson G, Doron-Faigenboim A, et al. Specific microbiome-dependent mechanisms underlie the energy harvest efficiency of ruminants. The ISME Journal, 2016, 10: 2958-2972 [37] Arntzen M, Anikó V, Mackie RI, et al. Outer membrane vesicles from Fibrobacter succinogenes S85 contain an array of carbohydrate-active enzymes with versatile polysaccharide-degrading capacity. Environmental Microbiology, 2017, 19: 2701-2714 [38] Bensoussan L, Sarah M, Dassa B, et al. Broad phylogeny and functionality of cellulosomal components in the bovine rumen microbiome. Environmental Microbiology, 2016, 19: 185-197 [39] Israeli-Ruimy V, Bule P, Jindou S, et al. Complexity of the Ruminococcus flavefaciens FD-1 cellulosome reflects an expansion of family-related protein-protein interactions. Scientific Reports, 2017, 7: 42355, doi: 10.1038/srep42355. [40] Rubino F, Carberry C, Waters SM, et al. Divergent functional isoforms drive niche specialisation for nutrient acquisition and use in rumen microbiome. The ISME Journal, 2017, 11: 932-944 [41] Fernando SC, Purvis HT, Najar FZ, et al. Rumen microbial population dynamics during adaptation to a high-grain diet. Applied and Environmental Microbiology, 2010, 76: 7482-7490 [42] Mao SY, Huo WJ, Zhu WY. Microbiome metabolome analysis reveals unhealthy alterations in the composition and metabolism of ruminal microbiota with increasing dietary grain in a goat model. Environmental Microbiology, 2016, 18: 525-541 [43] Khafipour E, Plaizier JC, Aikman PC, et al. Population structure of rumen Escherichia coli associated with subacute ruminal acidosis (SARA) in dairycattle. Journal of Dairy Science, 2011, 94: 351-360 [44] Tian LM, Scholte J, Scheurink AJ, et al. Effect of oat and soybean rich in distinct non-starch polysaccharides on fermentation, appetite regulation and fat accumulation in rat. International Journal of Biological Macromo-lecules, 2019, 140: 515-521 [45] Nie Y, Lin QL, Luo FJ. Effects of non-starch polysaccharides on inflammatory bowel disease. International Journal of Molecular Sciences, 2017, 18: 1372-1397 [46] Carlotta DF, Duccio C, Monica DP, et al. Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa. Procee-dings of the National Academy of Sciences of the United States of America, 2010, 107: 14691-14696 [47] Burkitt DP. Epidemiology of large bowel disease: The role of fibre. Proceedings of the Nutrition Society, 1973, 32: 145-149 [48] Neyrinck AM, Possemiers S, Verstraete W, et al. Die-tary modulation of clostridial cluster XIVa gut bacteria (Roseburia spp.) by chitin-glucan fiber improves host metabolic alterations induced by high-fat diet in mice. Journal of Nutritional Biochemistry, 2012, 23: 51-59 [49] Cox LM, Cho I, Young SA, et al. The nonfermentable dietary fiber hydroxypropyl methylcellulose modulates intestinal microbiota. FASEB Journal, 2013, 27: 692-702 [50] Kaoutari AE, Armougom F, Gordon JI, et al. The abundance and variety of carbohydrate-active enzymes in the human gut microbiota. Nature Reviews Microbiology, 2013, 11: 497-504 [51] Xu XF, Xu PP, Ma CW, et al. Gut microbiota, host health, and polysaccharides. Biotechnology Advances, 2013, 31: 318-337 [52] McNeil NI. The contribution of the large intestine to energy supplies in man. American Journal of Clinical Nutrition, 1984, 39: 338-342 [53] Salyers AA, West SE, Vercellotti JR, et al. Fermentation of mucins and plant polysaccharides by anaerobic bacteria from the human colon. Applied and Environmental Microbiology, 1977, 34: 529-533 [54] Xu J. A genomic view of the human Bacteroides thetaiotaomicron symbiosis. Science, 2003, 299: 2074-2076 [55] Sonnenburg ED, Zheng H, Joglekar P, et al. Specificity of polysaccharide use in intestinal bacteroides species determines diet-induced microbiota alterations. Cell, 2010, 141: 1241-1252 [56] Doi RH, Kosugi A. Cellulosomes: Plant-cell-wall-degrading enzyme complexes. Nature Reviews Microbiology, 2004, 2: 541-551 [57] Gilad O, Jacobsen S, Stuer-Lauridsen B, et al. Combined transcriptome and proteome analysis of Bifidobacterium animalis subsp. lactis BB-12 grown on xylo-oligosaccharides and a model of their utilization. Applied and Environmental Microbiology, 2010, 76: 7285-7291 [58] Ley RE, Turnbaugh PJ, Klein S, et al. Human gut microbes associated with obesity. Nature, 2006, 444: 1022-1023 [59] Ley RE, Hamady M, Lozupone C, et al. Evolution of mammals and their gut microbes. Science, 2008, 320: 1647-1651 [60] Zhu L, Wu Q, Dai J, et al. Evidence of cellulose metabolism by the giant panda gut microbiome. Proceedings of the National Academy of Sciences of the United States of America, 2011, 108: 17714-17719 [61] Pope PB, Denman SE, Jones M, et al. Adaptation to herbivory by the Tammar wallaby includes bacterial and glycoside hydrolase profiles different from other herbivores. Proceedings of the National Academy of Sciences of the United States of America, 2010, 107: 14793-14798 [62] 任世恩, 南小宁, 许淼, 等. 野生和人工饲喂条件下甘肃鼢鼠肠道细菌多样性比较. 微生物学报, 2020, 60(4): 826-838 [Ren S-E, Nan X-N, Xu M, et al. Comparison of intestinal bacterial diversity of Gansu zokor under wild and artificial feeding conditions. Acta Microbiologica Sinica, 2020, 60(4): 826-838] [63] Li ST, Zhang C, Gu YY, et al. Lean rats gained more body weight than obese ones from a high-fibre diet. British Journal of Nutrition, 2015, 114: 1188-1194 [64] Maurice CF, Knowles SC, Ladau J, et al. Marked seasonal variation in the wild mouse gut microbiota. The ISME Journal, 2015, 9: 2423-2434 [65] Amato KR, Leigh SR, Kent A, et al. The gut microbiota appears to compensate for seasonal diet variation in the wild black howler monkey (Alouatta pigra). Microbial Ecology, 2015, 69: 434-443 [66] 杨静, 南小宁, 邹垚, 等. 不同因素对六盘山地区甘肃鼢鼠肠道细菌多样性的影响. 微生物学报, 2018, 58(8): 1382-1396 [Yang J, Nan X-N, Zou Y, et al. Effects of different factors on intestinal bacterial diversity of Eospalax cansus in the region of Liupan Mountains. Acta Microbiologica Sinica, 2018, 58(8): 1382-1396] [67] 刘占英. 绵羊瘤胃主要纤维降解细菌的分离鉴定及不同氮源对其纤维降解能力的影响. 博士论文. 呼和浩特: 内蒙古农业大学, 2008 [Liu Z-Y. Isolation and Identification of Major Cellulolytic Bacteria in Rumen of Sheep and Effects of Nitrogen Sources on Their Cellulolytic Activities. PhD Thesis. Hohhot: Inner Mongolia Agricultural University, 2008] [68] Sun BH, Wang X, Bernstein S, et al. Marked variation between winter and spring gut microbiota in free-ranging Tibetan,macaques (Macaca thibetana). Scientific Reports, 2016, 6: 26035, doi: 10.1038/srep26035 [69] Wong JMW, De SR, Kendall CWC, et al. Colonic health: Fermentation and short-chain fatty acids. Journal of Clinical Gastroenterology, 2006, 40: 235-243 [70] Koh A, De Vadder F, Kovatcheva-Datchary P, et al. From dietary fiber to host physiology: Short-chain fatty acids as key bacterial metabolites. Cell, 2016, 165: 1332-1345 [71] De VF, Kovatcheva-Datchary P, Goncalves D, et al. Microbiota-generated metabolites promote metabolic benefits via gut-brain neural circuits. Cell, 2014, 156: 84-96 [72] Hamer HM, Jonkers D, Venema K, et al. Review article: The role of butyrate on colonic function. Alimentary Pharmacology and Therapeutics, 2008, 27: 104-119 [73] Hamer HM, Jonkers D, Bast A, et al. Butyrate modulates oxidative stress in the colonic mucosa of healthy humans. Clinical Nutrition, 2009, 28: 88-93 [74] Dronamraju SS, Coxhead JM, Kelly SB, et al. Cell kinetics and gene expression changes in colorectal cancer patients given resistant starch: A randomised controlled trial. Gut, 2009, 58: 413-420 [75] Clarke JM, Topping DL, Bird AR, et al. Effects of high-amylose maize starch and butyrylated high-amylose maize starch on azoxymethane-induced intestinal cancer in rats. Carcinogenesis, 2008, 29: 2190-2194 [76] Rombeau JL, Kripke SA. Metabolic and intestinal effects of short-chain fatty acids. Journal of Parenteral and Enteral Nutrition, 1990, 14: 181S-185S [77] Psichas A, Sleeth ML, Murphy KG, et al. The short chain fatty acid propionate stimulates GLP-1 and PYY secretion via free fatty acid receptor 2 in rodents. International Journal of Obesity, 2015, 39: 424-429 [78] Chambers ES, Viardot A, Psichas A, et al. Effects of targeted delivery of propionate to the human colon on appetite regulation, body weight maintenance and adiposity in overweight adults. Gut, 2015, 64: 1744-1754 [79] Freeland KR, Wolever TMS. Acute effects of intravenous and rectal acetate on glucagon-like peptide-1, peptide YY, ghrelin, adiponectin and tumour necrosis factor-alpha. British Journal of Nutrition, 2010, 103: 460-466 [80] Frost G, Sleeth ML, Sahuri-Arisoylu M, et al. The short-chain fatty acid acetate reduces appetite via a central homeostatic mechanism. Nature Communications, 2014, 5: 3611, doi: 10.1038/ncomms4611 [81] Wajner M, Santos KD, Schlottfeldt JL, et al. Inhibition of mitogen-activated proliferation of human peripheral lymphocytes in vitro by propionic acid. Clinical Science, 1999, 96: 99-103 [82] Nilsson NE, Kotarsky K, Owman C, et al. Identification of a free fatty acid receptor, FFA2R, expressed on leukocytes and activated by short-chain fatty acids. Biochemical and Biophysical Research Communications, 2003, 303: 1047-1052 [83] Karaki S, Kuwahara A. Propionate-induced epithelial K+ and Cl-/HCO3- secretion and free fatty acid receptor 2 (FFA2 GPR43) expression in the guinea pig distal colon. European Journal of Physiology, 2011, 461: 141-152 [84] Kim MH, Kang SG, Park JH, et al. Short-chain fatty acids activate GPR41 and GPR43 on intestinal epithelial cells to promote inflammatory responses in mice. Gastroenterology, 2013, 145: 396-406 [85] Maslowski KM, Vieira AT, Ng A, et al. Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43. Nature, 2009, 461: 1282-1286 [86] Sina C, Gavrilova O, Forster M, et al. G-proteincoupled receptor 43 is essential for neutrophil recruitment during intestinal inflammation. Journal of Immunology, 2009, 183: 7514-7522 [87] Singh N, Gurav A, Sivaprakasam S, et al. Activation of Gpr109a, receptor for niacin and the commensal meta-bolite butyrate, suppresses colonic inflammation and carcinogenesis. Immunity, 2014, 40: 128-139 [88] Park J, Kim M, Kang SG, et al. Short-chain fatty acids induce both effector and regulatory T cells by suppression of histone deacetylases and regulation of the mTORS6K pathway. Mucosal Immunology, 2015, 8: 80-93 [89] Giannini G, Cabri W, Fattorusso C, et al. Histone deacetylase inhibitors in the treatment of cancer: Overview and perspectives. Future Medical Chemistry, 2012, 4: 1439-1460 [90] Gopal E, Miyauchi S, Martin PM, et al. Transport of nicotinate and structurally related compounds by human SMCT1 (SLC5A8) and its relevance to drug transport in the mammalian intestinal tract. Pharmaceutical Research, 2007, 24: 575-584 [91] Tong LC, Wang Y, Wang ZB, et al. Propionate ameliorates dextran sodium sulfate-induced colitis by improving intestinal barrier function and reducing inflammation and oxidative stress. Frontiers in Pharmacology, 2016, 7: doi: 10.3389/fphar.2016.00253 [92] Huang C, Song P, Fan P, et al. Dietary sodium butyrate decreases postweaning diarrhea by modulating intestinal permeability and changing the bacterial communities in weaned piglets. Journal of Nutrition, 2015, 145: 2774-2780 [93] Shen H, Lu Z, Xu Z, et al. Associations among dietary non-fiber carbohydrate, ruminal microbiota and epithe-lium g-protein-coupled receptor, and histone deacetylase regulations in goats. Microbiome, 2017, 5: 123, doi:10.1186/s40168-017-0341-z [94] Ma X, Fan PX, Li LS, et al. Butyrate promotes the recovering of intestinal wound healing through its positive effect on the tight junctions. Journal of Animal Science, 2013, 90: 266-268 [95] Kim M, Qie YQ, Park J, et al. Gut microbial metabolites fuel host antibody responses. Cell Host & Microbe, 2016, 20: 202-214 [96] Den BG, Bleeker A, Gerding A, et al. Short-chain fatty acids protect against high-fat diet-induced obesity via a PPARγ-dependent switch from lipogenesis to fat oxidation. Diabetes, 2015, 64: 2398-2408 [97] Zhang BB, Zhou G, Li C. AMPK: An emerging drug target for diabetes and the metabolic syndrome. Cell Metabolism, 2009, 9: 407-416 |
[1] | DIAO Hao-yu, WANG An-zhi, YUAN Feng-hui, GUAN De-xin, SUN Yu, WU Jia-bing. Applications of compound-specific isotope analysis in tree non-structural carbohydrates research: A review. [J]. Chinese Journal of Applied Ecology, 2020, 31(12): 4291-4300. |
[2] | WANG Xiao-yu, WANG Shou-le, TANG Yang, ZHOU Wang-ming, ZHOU Li, ZHONG Qing-lin, DAI Li-min, YU Da-pao. Characteristics of non-structural carbohydrate reserves of three dominant tree species in broadleaved Korean pine forest in Changbai Mountain, China. [J]. Chinese Journal of Applied Ecology, 2019, 30(5): 1608-1614. |
[3] | ZHANG Dou, JING Hang, WANG Guo-liang. Responses of non-structural carbohydrates content in leaves of different plant species in Pinus tabuliformis plantation to nitrogen addition. [J]. Chinese Journal of Applied Ecology, 2019, 30(2): 489-495. |
[4] | FENG Huan, MENG Pan-pan, DOU Qing, ZHANG Shou-xia, WANG Hai-hua, WANG Chun-yan. Advances in mechanisms of nutrient exchange between mycorrhizal fungi and host plants [J]. Chinese Journal of Applied Ecology, 2019, 30(10): 3596-3604. |
[5] | . Estimating nonstructural carbon content of tree crown considering its spatial variability: A case study on Juglans mandshurica and Ulmus japonica. [J]. Chinese Journal of Applied Ecology, 2015, 26(8): 2253-2264. |
[6] | SU Li-wei, LI Sheng, MA Shao-ying, WANG Ya-mei, CAO Bao-chen. Physiological response of the distribution of non-structural carbohydrates to water stress in wheat. [J]. Chinese Journal of Applied Ecology, 2015, 26(6): 1759-1764. |
[7] | GUO Zi-wu1, HU Jun-jing1,2, YANG Qing-ping1, LI Ying-chun1, CHEN Shuang-lin1, CHEN Wei-jun2. Influence of mulching management on the relationships between foliar non-structural carbohydrates and N, P concentrations in Phyllostachys violascens stand. [J]. Chinese Journal of Applied Ecology, 2015, 26(4): 1064-1070. |
[8] | DONG Yan-hong1, LIU Bin-bin2, ZHANG Xu1, LIU Xue-na1, AI Xi-zhen1,2, LI Qing-ming1,2,3. Responses of non=structural carbohydrate metabolism of cucumber seedlings to drought stress and doubled CO2 concentration. [J]. Chinese Journal of Applied Ecology, 2015, 26(1): 53-60. |
[9] | GONG Qing-tao1, LI Su-hong1,2, ZHANG Kun-peng1, WU Hai-bin1, LIU Wei1, ZHANG Xue-ping1, SUN Rui-hong1. Ovipositional preference of Grapholitha molesta. [J]. Chinese Journal of Applied Ecology, 2014, 25(9): 2665-2670. |
[10] | TIAN Mi1, CHEN Ying-long2, LI Min1, LIU Run-jin1. Structure and function of arbuscular mycorrhiza: A review. [J]. Chinese Journal of Applied Ecology, 2013, 24(8): 2369-2376. |
[11] | LI Yan-yan, ZHOU Xiao-rong, PANG Bao-ping, CHANG Jing. Effects of host plants on the life table parameters of experimental populations of Aphis gossypii. [J]. Chinese Journal of Applied Ecology, 2013, 24(5): 1435-1438. |
[12] | HE Zhang, LIU Ji-bing, CHEN Yong-ling, CHEN Zhong-zheng, DUAN Bi-sheng, HU Hao-yuan. Effects of different treatment methods of housefly pupae for the reproduction of Pachycrepoideus vindemmiae Rondani. [J]. Chinese Journal of Applied Ecology, 2013, 24(3): 795-800. |
[13] | XIE Hai-cui1, CAI Wan-zhi2, WANG Zhen-ying1, HE Kang-lai1. Effects of elevated atmospheric CO2 on plant, herbivorous insect, and its natural enemy: A review. [J]. Chinese Journal of Applied Ecology, 2013, 24(12): 3595-3602. |
[14] | WANG Ya-fei1,2, LI Hui1, LI Xiao-bin1,2. Isolation and characterization of petroleum catabolic broadhostrange plasmids from ShenFu wastewater irrigation zone. [J]. Chinese Journal of Applied Ecology, 2013, 24(11): 3289-3299. |
[15] | ZHANG Hai-yan, WANG Chuan-kuan, WANG Xing-chang, CHENG Fang-yan. Spatial variation of nonstructural carbohydrates in Betula platyphylla and Tilia amurensis stems. [J]. Chinese Journal of Applied Ecology, 2013, 24(11): 3050-3056. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||