Contents & References of The effect of extracts of some medicinal plants from pastures of Ardabil province on rumen microbial population under laboratory conditions
List:
Chapter One: Introduction and review of past researches
1-1- Introduction. 2
1-2- Rumen contents and fermentation characteristics in ruminants. 3
1-2-1- Gases from fermentation 3
1-2-2- Volatile fatty acids 5
1-2-3- Ammonia nitrogen. 5
1-2-4- composition of microbial populations in different parts of the rumen. 6
1-3- rumen microorganisms. 6
1-3-1- Bacteria 7
1-3-2- Protozoa 8
1-3-3- Fungi 9
1-4- Importance of medicinal plants. 12
1-5- Effective factors in the production of herbal extracts. 13
1-5-1- specific organs that produce plant extracts. 13
1-5-2- secretory structure. 13
1-5-2-1- external secretory structure. 13
1-5-2-2- internal secretory structure. 13
1-5-3- Ecological factors. 14
1-5-4- Plant cultivation and processing 14
1-6- Botanical characteristics of the studied species. 14
1-6-1- Crambe orientalis plant 14
1-6-2- Heracleum persicum plant 18
1-6-3- Zosima absinthifolia plant. 21
1-6-4- Teucrium polium l. 23
1-6-5-Oregano plant (Oregano vulgare L.) 25
1-7- Gas test method 28
Chapter two: materials and methods
2-1- Study area and sampling method. 30
2-1-1- Sampling area. 30
2-1-2- Sampling time and transfer of samples to the laboratory 30
2-2- Gas test 31
2-2-1- Preparation of samples for gas test 31
2-2-2- Rumen liquid and buffer 31
2-2-3- Recording times of gas production 32
2-2-4- Advantages and disadvantages of gas test 32
2-2-5- Preparation of extracts for gas test 33
2-2-6- Preparation of feed sample and syringes 33
2-2-7- Preparation of rumen liquid. 34
2-2-8- Preparation of artificial saliva. 34
2-2-9- preparation of witness sample. 36
2-2-10- Injecting a mixture of artificial saliva and rumen fluid in syringes 36
2-2-11- Injecting extracts into syringes 37
2-2-12- Incubation and reading of produced gas. 38
2-2-13- Determining the volume of produced gas. 38
2-3- preparation of rumen liquid to prepare culture medium. 39
2-3-1-culture environment. 39
2-3-2- Preparation of 0.1% solution of the same. 41
2-3-3- Preparation of volatile fatty acid mixture 41
2-3-4- Preparation of mineral solution number I 41
2-3-5- Mineral solution number II 41
2-3-6- Preparation of culture medium. 42
2-3-7- distribution of cultivation medium. 42
2-3-8- Preparation of anaerobic dilution solution. 43
2-3-9- Preparation of fresh rumen fluid 44
2-3-10- Preparation of different dilutions of rumen fluid. 44
2-3-11- Inoculation and maintenance of the performed cultures 47
2-4- Estimation of the number of bacteria 48
2-5- Counting of protozoa 48
2-6- Counting of anaerobic fungi. 49
Chapter Three: Results
3-1- rumen parameters. 51
3-2- Comparison between different levels. 49
3-2-1- Comparison between the levels of Teucrium polium l (sage pea) extract 49
3-2-2- Comparison between the levels of Crambe orientale (Spideh) extract 50
3-2-3- Comparison between the levels of Heracleum persicum (Angelflower) extract 51
3-2-4- Comparison between the levels of Zosima absinthifolia (Zosima) extract 51
3-2-5- Comparison between the levels of Oregano vulgare L (Oregano) extract 51
3-2-6- Gas production of the rapidly decomposing part (a) 53
3-2-7- Gas production of the water-insoluble and slow-decomposing materials in the rumen (b) 53
3-2-8- Potential gas production (a+b) 54
3-2-9- Gas production rate constant (c) 55
3-3- Estimation of rumen microbial population. 56
3-3-1- Bacteria population estimation 56
3-3-1-1- Bacteria population estimation at zero hour 57
3-3-1-1-1- 100 mg/liter level 57
3-3-1-1-2- 200 mg/liter level 57
3-3-1-1-3- level 300 mg/liter 57
3-3-1-2- estimation of bacteria population at four hours after incubation. 57
3-3-1-2-1- level of 100 mg/liter 57
3-3-1-2-2- level of 200 mg/liter 58
3-3-1-2-3- level of 300 mg/liter 58
3-3-1-3- comparison of bacterial populations between the levels of each extract 58
3-3-1-3-1- Comparison of bacteria population between the levels of each57
3-3-1-2-1- level of 100 mg/liter 57
3-3-1-2-2- level of 200 mg/liter 58
3-3-1-2-3- level of 300 mg/liter 58
3-3-1-3- comparison of bacterial populations between the levels of each extract 58
3-3-1-3-1- Comparison of the bacterial population between the levels of each extract at zero hour 58
3-3-1-3-1-1- Comparison of the bacterial population between different levels of Crambe orientalis extract 58
3-3-1-3-1-2- Comparison of the bacterial population between different levels of Heracleum persicum extract. 58
3-3-1-3-1-3- comparison of bacterial populations between different levels of Zosima absinthi extract 59
3-3-1-3-1-4- comparison of bacterial populations between different levels of Teucrium polium extract. 59
3-3-1-3-1-5- Comparison of bacteria population between different levels of Oregano vulgare extract. 59
3-3-1-3-2- Comparison of the bacterial population between different levels of each extract at four hours 59
3-3-1-3-2-1- Comparison of the bacterial population between different levels of Crambe orientalis extract 59
3-3-1-3-2-2- Comparison of the bacterial population between different levels of Heracleum persicum extract. 59
3-3-1-3-2-3-Comparison of bacterial population between different levels of Zosima absinthi extract 60
3-3-1-3-2-4-Comparison of bacterial population between different levels of Teucrium polium extract. 60
3-3-1-3-2-5- comparison of bacteria population between different levels of Oregano vulgare extract. 60
3-3-2- Estimation of the number of protozoa and fungi 60
Chapter 4: Discussion
4-1- The effect of extracts on digestibility and gas production 48
4-2- How extracts work 51
4-3- Effect of extract on rumen pH. 52
4-4- The effect of the extract on rumen microbial population. 53
4-5- Chemical compounds of medicinal plant extracts. 57
4-6- General conclusion and suggestions 62
4-6-1- General conclusion. 62
4-6-2- Proposals 62
Resources. 63
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