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Soil Characterization - Science topic

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I need a work a guide to get a work that is done recently or dated back. Thank you.
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Dear Mukhtar,
According to what you have said regarding soil fertility, I did a search in Google scholar with keywords: soil fertility+Nigeria, and I found many interesting papers; some are linked below:
Soil fertility enrichment potential of Jatropha curcas for sustainable agricultural production: A case study of Birnin Kebbi, Nigeria:
Delineation of Soil Fertility Management Zones for Site-specific Nutrient Management in the Maize Belt Region of Nigeria:
Influence of compost supplemented with jatropha cake on soil fertility, growth, and yield of maize (zea mays L.) in a degraded soil of Ilorin, Nigeria:
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How can we diagnose the soil in the laboratory through its appearance that it is fertile or not fertile without conducting an analysis on it?
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You asked an interesting question on the relationship between soil physical appearance and soil fertility. Allow me to proceed as follows:
For a soil to be said to be fertile, it must have a sustainable supply of the right quality and quantities of soil ameliorates which translate to nutrients. There are a number of physical parameters that might indicate fertility status of a soil cohort. However, these factors are not a guarantee that the soil is fertile.
1.Soil Color
Generally, black -dark colored soils are a positive indicator of the soil fertility status of the soil. They are good absorbers of heat which activates microbial activity hence soil biomass recirculation. This is a common case in 2:1 and 2:2 clay minerals which are generally good nutrient suppliers.
On the other hand,light-bright colored soils such as 1:1 Montmorillonites are generally poor nutrient holders due to poor heat absorption capacity, greater reflection thus poor nutrient churning capacity.
2.Soil Texture/Structure
We shall all agree that this can be established by the naked eye.That,large grained soils are generally considered as poor nutrient suppliers as compared to middle grained soil such as Ferrasols,assuming all other factors remain constant. Average soil is directly proportional to water holding capacity, soil Rhizosphere aeration which in turn affects Biota Respiration.
Large grained soils such as sandy soils are loosely attached, prone to erosion. They are also poor water reservoirs due to increased percolation.
3.Vegetation Cover/Material
Related to point number 1 is vegetative cover. Material cover is directly proportional to soil nutrient fertility status. Such soils might have deeper top layer, zone A and B.A good covered soil shall harbor more soil microbes which accelerates decomposition.Humus,a product of decompostion,makes such soils appear much darker.
Conclusion
Whereas soil physical factors might an indicator of soil fertility status, farmers and researchers should be encouraged to do a completed soil laboratory tests. Some of the physical factors mentioned above could be as a results of other underlying causes such as parent material, soil pollution, environmental degradation etc. Instead of dealing with symptoms which might result to wrong diagnosis/prescription, I recommend soil laboratory analysis.
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we take samples from field that have sandy soil very lose soil and dry soil after measurement moisture content we find low bulk density around 0.8 g/cm3  , 1.3 g/cm3  and 1.7 g/cm3  
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As you know bulk density is mass of solid divided by total volume of soil. So in Sandy soil total volume is high as volume of solid + volume of pores are there. So as a result bulk density of sandy soils reduces.
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There are several method for determining organic matter in soil such as black and walkley and Tyurin method. Among them which on gives the most reliable results?
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we have worked on this point in the following manuscript:
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how we can find poisson's ratio using resonant coulmn (detail procedure )..??
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This is a good question.
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Our method consists of a potentiometric titration of a soil plus an electrolyte solution (0.01, 0.1 and 1.0 M KCl). Soil is stabilised during 1 hour and then HCl or NaOH is added in order to modify pH to 4.0 or 12.0 respectively. PZC should be found in the intersection of the three curves, but we are getting unexpected results. Could you recommend another method or a modification of the one I am performing. Thank you very much.
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Video link for determination of Point of zero charge (PZC)
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I will do mineralogical analysis and i have to separate different soil fractions. I will also use these fractions in further studies so i need enough amount of clay. What is the best method .
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You can separate silt from clay by centrifuge method after removing organic matter, calcium carbonate, and iron oxide, as described by Dekimpe 1976.
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Totally I have 7 boreholes for soil, each was dug to the depth of 60 cm (10 cm intervals). I've got to compare the differences in chemical parameters among each of the six layers. So, what statistical test are most suitable for this kind of data ? 
I consider using Dependent T-test for the data set. The reason is, for each depth (of all boreholes), soil data are completely independent. However, within a profile, soil sample of any specific depth is closely linked to its upper/lower samples. Is that appropriate ?   
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Dear Nguyen,
Among the variables analyzed, the compatibility with normal distribution of all variables analyzed can be evaluated using the Kolmogorov–Smirnov test.
Differences between groups can be established by Student’s t -test for normally distributed values and by Mann-Whitney U-test for nonparametric values.
Pearson's correlation coefficient can be searched to examine the relation between normally distributed variables.
Spearman’s correlation coefficient can be used for nonnormally distributed values. Statistical significance was defined as P <0.05 or <0.01 etc...
Best regards...
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Many researchers have given the values of OMC and MDD for bentonite based buffer materials corresponding to heavy compaction (higher compaction energy).
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In expansive soils, swelling increases with increasing dry density and decreasing moisture content. Therefore, standard compaction is better to be used for expansive soils to reduce swelling problem.
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As soil quality represent it's "fitness to use" or "capacity of soil to function to sustain productivity maintaining environmental quality and improved health".
What are the basic components which must be included while developing the soil quality index?
Minimum set of data required for SQI ?
Is it necessary to rotate all the components ?
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The components for soil quality index from the measured soil properties of the mineral soil cores, may include sample weight, bulk density, water content, coarse fragment content, water and salt pH, carbon (total, organic, and inorganic C), total nitrogen (N), 1 M NH4Cl exchangeable cations (sodium [Na], potassium [K], magnesium [Mg], calcium [Ca], aluminum [Al]), 1 M NH4Cl extractable trace elements (manganese [Mn], iron [Fe], nickel [Ni], copper [Cu], zinc [Zn], cadmium [Cd], lead [Pb]), 1 M NH4Cl extractable sulfur (S), and Bray 1 or Olsen extractable phosphorus (P). e SQI
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I would be interested to know how wildfire influence on soil environment in forests (cf. OM, TN, CEC, AP, Al, pH, K+,Na+,Ca+,Mg2+, Soil class), especially after surface fire.
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I think the suggested paper is interesting but it focuses on hydrology.
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I have a TGA analysis from a soil sample from room temp. to 600ºC.
I've noticed four different stages (slopes) in the mass loss curve. Those stages are expressed in the differential curve as well.
- Room temp. - 110ºC - Water (2% mass loss) - The soil have been previously dehydrated.
- from 170ºC to 300ºC - ? (0.83% mass loss)
- from 300ºC to 460ºC - ? (2.267% mass loss)
- form 460ºC to 560ºC - ? (2.18% mass loss)
I've read many articles but I am having some trouble adapting the case studies to my sample.
My sample is from an agricultural soil. I know that have an important clay proportion and some organic matter.
What does mean every slope (and mass loss associated) that I have in my sample?
Many thanks in advance for any kind of help!
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The diagram showed four characteristic regions:
The first region (< 100 ˚C) showed that mass loss which is mainly due to water volatilization.
The second region (170-300˚C), the mass loss is mainly due to decomposition of organic matter, mainly carboxylic and phenolic functional groups of the humic acids, fulvic acids and hydrocarbon compounds.
In the third region (360-460˚C) the mass loss could be due to carbon oxidation of the organic matter (RCH+O2 ® CO2 + H2O).
In the forth region (460-560˚C),the mass loss could be due to dehydroxilation of metallic hydroxides (M-OH ® MO + H2O, were M = Al, Fe, Mn and other metals).
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I have to isolate actinomycetes from soil, for which soil extract agar is required..It would helpful if a protocol is available to prepare soil extract. Not for soil extract agar
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I have attached some articles about preparing soil extract media.
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Expansive soil are highly problematic soil because of volume change behavior under its moisture conditions. There are different types of methods are available to stabilize the soil but its not better solution in many aspects for that, so i need what are the new cheap materials used to stabilize the expansive soil in effective manner.   
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Solid wastes are used as one of the stabilization methods (non-traditional methods) to improve the engineering characteristics of expansive soils and to make these soils suitable in construction. From the geotechnical engineering perspective, fly ash, quarry waste, silica fume, cement kiln dust, tire rubber, rice husk, etc. represent the waste materials having effectual features required by excellent soil admixtures. Different stabilization methods reviewed and discussed in the attached paper.
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I am building a database of fall-cone test penetration depth vs water content. The database has 120 soils approx. Looking for published and unpublished results to increase the number of entries.
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Dear Marcelo Llano
You can consider the data result shown in the following paper for Quaternary soils. The liquid limit for the soils has been determined using different methods including the fall-cone method.
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Hi -
Has anyone ever had the issue when they are doing Loss on ignition analysis in a muffler oven at 1000C? Previously I worked with a newer muffler oven and had no issues weighing and baking soils at 1000C. I recently started using an different muffler oven which is a little older, but is properly functioning. I baked my soils and crucibles at 550C and it was fine. I then turned it up to 1000C and baked it at 1000C for 6 hours and turned it down to 105C to take the crucibles out after cooling. However, after I took the crucibles out all of them seemed to be changing colors from neutral ceramic white to green from the bottom up. Also it looks like there are small crystals or precipitate forming on the crucibles, more densely from the bottom up. Attached are a couple of pictures. Does anyone have any experience with this or have any suggestions on how to get to the bottom of this or fix it?
Edit: I just want to note I tried to clean these crucibles with an HCl acid bath, and the greenness did not go away and the precipitate crystals seems to arise once it is fully dry again.
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I have also observed this. At elevated temperatures, some elements will dissolve into the solid solution of the crucible. Look into the ceramics literature on vitrification. I would not worry about the color change, nor would I be concerned about contamination unless you are ashing a sample for subsequent digestion and quantification of elements in the ash. If you're simply looking at soil carbon, the altered crucibles will continue to be fine. Disregard the etching and color change. Keep in mind though that some elements like potassium volatilize at high temperatures (> 500 C).
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Particle size distribution (PSD) aka soil texture is a major feature to understand soils.
Sand, silt and clay classes of mineral particles are so commonly used that they become part of the everyday landscape of agronomists, farmers and others.
However,
Why such size limits have been placed between these categories?
Is there a reason?
In addition, different countries may have different PSD classes (eg., 50 µm or 63 µm between silts and sands).
On which scientific basis has this been made?
To follow up on that,
Don't you think that a more modern approach to soil texture characterisation would be more helpful by measuring soil PSd on a continuous scale? rather than splitting between sand, silt and clays.
Indeed, two soil with the same PSD (lets say 30% sand, 30% silt and 40% clay) could be very different.
Within sands, particles could all be towards th coarse side, or conversely towards the fine side.
Same reasoning for the other classes.
Without solid reasons (physical perhaps?) to set the boundaries between sands, silts and clays, that system seems a bit arbitrary and old-fashioned, isn't it?
Shouldn't it be more useful to represent the frequency distribution of particles on a continuous scale to give a more precise picture of the actual texture of a soil.
New techniques such as laser diffraction seem to be useful to this end, and could give a more representative image of the distribution of the size of soil's mineral particles.
Futhermore, current method to determine soil PSD using sieving and sedimentation is extremely long and prone to errors in measurements.
Any thoughts on this?
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The % of sand, silt and clay in the soil established the nature or texture of soil. Hence, first we have to determine the % of these components of soil.
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I am analyzing soil samples from a volcanic area (relatively young), formed by Andosols (non-allophanic), I have run all the routine analyzes (oxalate, DCB, pyrophosphate extractions, CEC....) however I've realized that the Alo content is smaller than the Alp for some samples (all of them A horizons with high organic matter content while for the 'less' organic horizons the Alo is always higher than the Alp). As far as I understand the Alo content represents the organic-bounded + the amorphous Al content, while the Alp represents only the organically-bounded Al, hence the Alo content should be higher than the Alp. Is there any mechanism that could help me explaining this behavior?
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Dear Marlon
Andisol with a high content of humic compounds, the majority of the proportion of Al-amorphous will be complexed to Al-humic, so it makes sense that in Andisol with high organic content, Al-humic> Al-amorphous. Conversely, at andisol with low OM content, only a small portion of Al-amorphous complexed to Al-humic so that Alo> Alp content
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For a dynamic soil model with element type name "cinpe4", for boundary (on the left & right side and bottom), and " CPE4R " for body of soil model.
That is my basic model.
I want to use Abaqus to calculate the natural frequency of the model (modes f1 & f2).
How can I do it? Can I use "hinged or roller support" on boundary, or it is not necessary?
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can you send me you cae file?
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any methods to reduce NH4OAc background for IC analysis? or any alternate soil extraction procedures available for cation analysis with IC in order to determine CEC?
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Hi Nitish,
A soil sample is extracted with an excess of 1 M ammonium acetate solution. The amounts of exchangeable sodium, potassium, calcium and magnesium in the extract are determined by flame photometry (Na and k) and by atomic absorption spectrophometry (ca and Mg). lanthanum or strotium is added as a releasing agent to prevent formation of refractory compounds which may interfere with determinations (e.g. phosphate),
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The problem we face in gypsiferous soil is how to accurately estimate the texture when gypsum reaches more than 50% and often as much as 70% . I think when the ratio reaches this limit, the texture can not be properly estimated , If the gypsum is washed there will be a difference In the soil texture field and laboratory ... I hope to see your views and suggestions?
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I conducted CBR tests on unbounded aggregates. As you can see the CBR test results in the attachment, the curves concave up and there is a relatively enormous shift between two test results. Considering that two curves are parallel, it, somehow, can be concluded that two samples has comparable properties, but the presence of the shift make the interpretation of the results difficult.
Based on New Zealand and British standard these curves should not be corrected, however some references in the literature recommended correction of these type of curves (I attached the PDF file).
Question A- If I correct the curves (as explained in the PDF file) or shift the sample-2 the results for two replicated samples are comparable. Under this conditions, do I need to correct the CBR test results?
Question B- If I correct the curve and the resultant curve does not meet 2.5 mm penetration how can I interpret the CBR test results?
Question C- If I should not correct the curves what would be the CBR test results in my case?
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As per AASHTO T-193 if the curves start concave upwards they should be corrected by extending the linear portion of the curve until it intersects the x-axis (penetration) and use the intersection as the new origin of the axis.
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I mean after doing the compaction practice in various water contents and determining the dry density corresponding to each water content, what would be the equation of the resultant compaction curve? Assuming that there should be only one optimum water content, I think the quadratic curve can be the best option to fit the bell shaped results. However, I could not find anything in the literature (the compaction curve is drawn without presenting the equation or a line simply connected data).
I was wondering if you could introduce me any reference about this matter.
It is a matter of great importance to me to determine the optimum moisture content consistently for all of my materials.
I attached my data and the quadratic curve passing through them. could you please let me know what is the optimum moisture content in these compaction data series and what is the compaction curve for them?
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As we all know, soil have acid buffering capacity(ABC) and ABC is the decisive factor determining the rate of soil pH change, How do researchers reduce ABC in soil science research? Can ferrous ions have this function? How to reduce the role of ABC?
I look forward to and thank you for your help and answer.
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In order to understand how soil buffer capacity works, you need to learn about permanent charges (caused by soil minerals) and variable charges (caused by organic matter) and how the above charges respond to acidic (e.g. elemental-S, FeSO4) or alkaline (lime) soil conditioners. A typical laboratory work to assess soil buffer capacity could explain the above phenomenon ( ).
Organic matter does play a significant role in controlling buffer capacity of soils hence it is important to learn the basics of organic matter and soil pH (
I have worked on soil buffer capacity in the context of assessing the effect of urea hydrolysis in soil (which is a reverse process to adding FeSO4, since it causes soil pH to rise substantially), however, could not find any specific experimental work involving FeSO4 reaction with soil with wide ranging concentrations.
I am not sure within which context you are working on FeSO4. Are you assessing FeSO4 as a soil conditioner?
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These are the questions I faced in my literature review I could not find an answer for them. Just for the record, I am going to do the CBR test on laboratory compacted base materials in the pavement.
1- In which moisture content and dry density this test is accomplished (generally for the scientific purpose). I mean, CBR can be employed directly after the compaction or after soaking in water for four days. Should the CBR test be done with various moisture content? Should it be done in 95% of MDD (as the compaction in field is usually 95% of compaction in the lab)?
2- What is the number of layers in the compaction process (if the vibratory hammer is used for the compaction)? 2 or 3 layers?
3- What would be the weight of surcharges if the pavement design includes an asphalt layer of 10 cm and a basecourse of 30 cm and the materials are to be used in the base layer?
4- While soaking aggregates in water, what should be the elevation of water above the sample?
Kind regards,
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You can refer to AASHTO T 193.
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I have been searching for seafloor soil properties data-sets, but I cannot find any data. Is there anywhere you can refer me to?
Thanks in advance.
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The level of detail for a particular region will vary significantly and in all cases it is likely to be a lower level of detail than a site specific survey. I'm note sure from your question if you have a particular part of the world in mind. However, here is a link to data relevant to the UK continental shelf;
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I have to add water in one kilogram soil to make it about 80% field capacity level. What is the best way to measure the amount of water required to attain 80% field capacity in one kilogram soil?
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- Dry a quantity of soil in an oven at 60 ° C until a constant weight ;
- Weigh a quantity p1 (1 kg for example) of dry soil in a pot (the pot must be perforated below);
- Water the pot to saturation and place it in the dark to avoid evaporation;
- After 48 hours, weigh the pot again (p2);
FC = p2-p1
ex: if p2 = 1.2 kg ie FC = 200 g (100% FC)
you must add 200 g of water to your dry soil to have 100% FC and therefore 160 g to have the soil at 80% FC.
NB: Make at least 3 repetitions
If you do not want to dry all of your soil, once the FC determined. Calculate the amount of water present in your soil by making the difference between the weight of the soil and the weight of the dry soil. You will have the amount of water already present in your soil. Complete this quantity to achieve the desired FC.
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This is a rare opportunity to investigate the fire-invasion continuum by observing the conditions before, during and after fire. Likewise, these experiments may provide original data for other scientific domains. Much more information can be retrieved from these experimental burns, including for example: soil micro-fauna, soil biochemical characteristics, fungi etc. There is the possibility to relate these data not only with fire characteristics but also with the invaded-non-invaded status, by simply collecting samples in neighbour control plots. Therefore, we are willing for cooperation to retrieve more data from these experiments and we welcome the collaboration of researchers who may add valuable expertise to our team. You may take a look at the project description at https://www.researchgate.net/project/Aliens-Flames
Feel free to contact the PI using the e-mail jss@esac.pt.
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Dear Colleagues
Nowadays, risk of fire due to climate change and its consequences like drought is becoming and increasing problem in natural landscape etc.
Therefore, fire occur during summer occasionally for different reasons which affect the plantation etc.
I was wondering if the focus of your project is on special species or different species and aspects?
Kind Regards
Alireza
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I mean if I want to know the SOM weight percent, but I don't need to know what organic compounds the soil contains.
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This article can be useful:
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There are many microflora in soil such as bacteria, algae and fungi that affect soil properties
Are the bacteria present in the soil affecting soil erosion and physical and chemical properties such as pH, Ec, CEC, SAR, ESP, OM, TDS, SS, DR%, CaCo3, CaSo4, Fe, P, Cl, So4, K, N, Co3, Mg, Ca, Na, bulk density, Soil texture and heavy metal (Cu, Cd, Zn, pb)
IS there any link and articles and clues will be appreciated.
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OM is most important of all...
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Dear all,
I have collected soil samples up to a depth of 50m from surface during drilling. I need to interpret alternate cycles of dry and wet climate on the basis of soil types. What are the criteria to classify soils into Entisol, Vertisol, Alfisol, Oxisol etc. ? I would like to know the parameters like texture, color, amount of organic matter, presence of particular minerals, cation exchange capacity, and pH values to characterise the soil types. It would be really helpful if you kindly provide me the list or document where the parameters range are given to classify the soils.
Thanks & regards,
Ashok
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Please have a look at enclosed PDF..
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I want to know is there any suitable polymer stabilizer for weak (organic and clay)subgrade soils? precedencely organic soil.would you please guide me.
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 this article is good but  1: I cant download it and 2:it is for qatar sub grade soils that have more than 40% up 10mm grading but is helpfull and I asked from author p.df file.
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Although there are several correlations available in the literature to predict the properties and behavior of cohesive soils (clays/silts) by standard penetration test (SPT), however at the same time many textbooks mention that the use of SPT values for predicting properties of cohesive soils is not very reliable. What are the factors that influence the SPT values obtained in clays, and decrease their reliability to be used for the prediction of soil properties?
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I think the SPT N Values show wide variation in Clayey soils with a slight change in moisture content . We performed SPT Tests for a clay formation in dry season (June 2015) and got SPT N values in the range of 20-25
for the same site (formation ) the SPT N values were recorded in the Range of 02-05 only in December 2015 (It was after a rain spell)
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EC e is time consuming but yet its  the reference method when assessing the soil salinity of soil, i wonder if there any empirical equation linking the EC e , EC 1:5 and Soil texture?
thank you for your answers 
Kind regards 
Yacine Louadj
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The relation between ECe and EC 1:2.5 for South Gujarat coastal alluvial plain (Aquepts Ochrepts) is ECe = EC1:2.5 x 3.429+0..606. For getting this relationship we have analysed 500 soil samples 25 years back.
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Ca (gypsum) application reduces Na content in salt affected soil but due to poor drainage gypsum amendment might not be properly effective. Therefore, gypsum application with subsoil drainage might be the best option for reducing salt. So, I need to know which method is most suitable for subsoil drainage. 
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Please get the  0-100 cm weighted mean value of the saturated hydraulic conductivity data  of the soil profile first and get the same data after adding gypsum. The difference may suggest you which method to apply. Moreover  be sure about the presence of  soluble carbonate and bicarbonate salts  vis a vis  chloride and sulphate. In case  former two are more than the latter then surface application of gypsum will be appropriate  before transplanting rice crop. Please get some information on the similar lines from ICAR-CSSRI, Karnal, India website.
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I want to compare two soil maps with 6 soil classes.
Each class has an integer number from (1; 2;...;6).
My purpose of is to obtain:
i. General Kappa, Kappa location, Kappa histo, and
ii. Fuzzy Kappa
I have attempted Map Comparison Kit (MCK) available on http://mck.riks.nl/.
The problem is that when I import my files into the MKC, it displayed the
integer number as decimal MCK. e.g. 0.0 - 0.8; 0.8-1.7; 1.7-2.5; 2.5-3.3;
3.3-4.2; 4.2-5 instead of having the classes as 1;2;3;4;5;6. When I specify
“categorical” in the MCK legend editor it didn´t change the display to 1;2;3;4;5;6.
With the legend editor one could affect integer number to these class interval
( 1=0.0 - 0.8; 2=0.8-1.7; 3=1.7-2.5; 4=2.5-3.3; 5=3.3-4.2; 6=4.2-5) but it changes completely the spatial distribution of the soil classes as compared to the original map.
Does anyone has an idea how I can import my data in such a way to have it as integer number as in the original and not as decimal? or any other software which can help me achieve the
same purpose?
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Use Surfer GIS software. You can assign a numerical value for each soil class Eg 1, 2,3 .... and create conture map (Use soil class value as Z value. Of-course it is a kind of a iso height map too. It is vary easy. Be careful when editing the legends, as we use soil class numerical value for categorizing it. You can give a name at the legend editing. 
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I am developing a research strategy to ameliorate and utilize acid soils in tropical environment. I realized that liming is a widely used option for topsoil, I haven't come across options for subsoil acidity. 
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I endorse the comments from Dr Tapas, the best quality fruits like banana, citrus, mango, citrus ..all are produced despite subsoil acidity , which i emphasized in my  responses to almost similar question  flagged off by Dr Pal sir...stating that can we call acid soils chemically degraded..?
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I am using pvpp to absorb the humic acid of peat soil. i put it directly on eluted dna. Does anyone know how it affect the dna?
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I do not think so if you are trying to extract dna from a soil material.
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I would like to know what are the average estimates for ratios between readily available (let's say accessible by a single extraction with NH4Ac, or AgTU, or BaCl, or KCl...), and "fixed" poorly hydrated cations (as Cs+, K+, NH4+...) in soils. For example, Bolt et al (1963) found that 96% of K were readily available, while only 4% were "fixed" in an illitic soil.
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G. H. Bolt, M. E. Sumner and A. Kamphorst. A Study of the Equilibria Between Three Categories of Potassium in an Illitic Soil.
Soil Science Society of America (Proceedings / Soil Science Society of America), V 27 N 3, p. 294-299, May-Jun 1963 
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I would recommend:
De Vries, W. 1994; or Van Breemen, N. 1994 ... I did not read all of their research but I came a cross them often in this kind of studies.
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In most pedotransfer functions, field capacity and permanent welting point predicted using some easily measured data such as soil texture, bulk density and or organic matter percentage. None of the well known pedotransfer functions used the hygroscopic water as an input variable. Do you know any work used the soil hygroscopic water to predict field capacity and permanent welting point?
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Dear Younes- yes, such relation exits. Please find attached a relevant paper. With best wishes-
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I need to understand the point (2.) of the diagnostic criteria of lithological discontinuity of the WRB ?
point (2). a relative change of 20 percent or more in the ratios between coarse sand, medium sand, and fine sand.
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Dear Jerome,
Please note to the example on page 69 of World reference base
for soil resources 2014 (Update 2015).
The best,
ISA
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Soil organic matter (SOM) is renowned for being the best indicator of soil quality, due to its capacity of improving stability and sustainability of agricultural and forest systems, as well as the fact it is sensitive to changes caused by agricultural practices such as soil tillage, soil compaction, erosion, liming, within others. However, the simple measurement of the total SOM (Walkley-Black, Yeomans & Bremner, dry combustion method - CHNS/O Analyzer) has not been sensitive enough to detect small changes in the soil. Thus, many SOM fractionation techniques have been used for this soil quality diagnosis purpose, such as SOM light fraction, SOM heavy fraction, carbon of microbial biomass, etc. However, most of these methods are expensive and difficult to be performed in large-scale monitoring programs. So I wonder if you know among the SOM fractions, which one(s) are those with better correlation or sensitivity to soil disturbance due tillage or crop system? Which of the SOM attributes would you recommend to be monitored in the long term programs, considering the operational feasibility (field soil sampling and lab analysis) and low cost?
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Interesting discussion . Sensitivity of soil organic matter fraction is largely guided by ease of extraction , active fraction  ( For example humic acid , fulvic acid as part  POM of SOM ) is more labile in nature , and hence contributes towards soil structural stability . Any reduction /depletion in these fractions would indicate loss of soil stability or potential degradation..Loss of organic matter binding soil particles means  soil is fast approaching towards degradation
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How to make an assessment of the structural soil quality viable for farmers?
Evaluations are conducted through academic research. They are expensive and laborious and are restricted to academia and do not reach the farmers.
How to do viable analysis at the farmer level?
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There are a number of articles on this in the literature - several published over the years in Soil Use and Management. Links attached.
Regards
Andrew
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Even on drying in oven the structural water doesn't get removed. So what is the significance of this in soil mass and if it get removed what will be the consequences?
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Dear Dr. Kumar,
The oven drying of soil mass at 105 degree centrigrade temperature for 48 hour is often sufficient to remove water contained in micropores and also hygroscopic water retained by soil colloids. The removal of structural water which is a part of mineral structure is achieved at much higher temperature and it is recorded by Thermal Gravimetric Analysis (TGA) or also in Differential Thermal analysis (DTA). These techniques are used in identification and characterization of soil minerals in conjunction to x-ray diffraction.
I agree with the answer of Dr. Beauvais. The structural water imparts specific properties  to soil colloids. High temperature drying of clay minerals for example like that  of vermiculite will collapse the c-axis and reduce it to that of illite. Such drying will affect the entry of other molecules in the interlayer space of 2:1 type  clay minerals. This would also change the specific surface area of the mineral. Similar changes in the reactivity of  hydroxides and oxyhydroxides would occur.
Even in the case of soil organic matter oven drying even at much lower temperatures (around 100-105 centigrade) would induce the internal pairing of  proton donor and proton acceptor  groups making re-hydration of organic colloids difficult.
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I have found from few literature s that TGA/DSC is just a comparison to calculate the organic matter loss.
Thank you.
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Dear Hepsiba,
You do not need DSC for soil analysis. TGA alone is sufficient to measure the loss of organic materials although you will need a high temperature (approx 1000 oc) so you will need to use ceramic pans.
I also find it useful to perform PXRD before and after TGA analysis to show that I am not burning or changing any of the mineral content in the sample.
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Soil Characterization: That is to assess spatial properties of soil dividing the land into homogenous facets/units and ascertain the characteristics of each unit at least from the top 30 cm.
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In general 5-15 cm or sometimes 30 cm soil is considered as surface soil. After collection of soil samples from the entire area covering the fields in Zig-Zag way you have to mix the soil samples throughly removing debris and root materials to prepare for analysis in the laboratory. Then you can go for mechanical analysis either by Pipette method or Hydrometer method . After that to air dry samples you may analyse for Hydrogen ion concentration (pH)  by pH meter and Electrical conductivity using EC meter  to measure the water soluble salts. Then you go for measuring Water holding capacity, moisture equivalent, Field Capacity, Permanent Wilting Point, Sticky point etc. Beside this you must determine the soil color after using Munsell color disc or Cardboard Disc. Then you may go for the measuring the exchangeable iions i.e. C.E. C or A. E. C. After completing the physical analysis you may start for Chemical Analysis or Physico-Chemical Analysis like Organic Matter content,, N, P, K, Ca, Mg, S, B, Cu, Fe, Mn, Mo, Zn etc. You may also separate the Clay fraction may be by sodium chloride methods. If you want to do biological parameters then you have to do with the fresh soils and go for microbial count using dilution plate technique, microbial activity by FDA and dehydrogenase measurements, microbial biomass and different beneficial enzyme activities. Lot of Practical Analysis Book are available in the market. Most popular soil analysis books are: Methods of Soil Analysis written by M. L. Jackson and books written by C. A. Black. You may also consult other books like Soil and Plant Analysis written by C. S. Piper
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I got difficulty in getting a purified community DNA from soil due to high A260/280 value (>2.0). Can you suggest a modification on the protocol using the FastDNA Spin kit for soil? I have tried a lot of published modifications but still didn't work. I think my soil sample has very high amount of protein and humic acids. How can I get rid of these contaminants? By the way, my sample was taken from pot-grown cacao where the soil is naturally acidic and is treated with Biochar and Biofertilizer (Mykorich) for almost 7 months under nursery conditions. It's really difficult to extract a pure DNA. The DNA concentration I got is very little (more than 5.0 ng/ul but less than 15 ng/ul). Thanks for the help.
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You need to provide more information about your soil to help to determine what can go wrong in your extraction, as well as what improvement did you try:
- the actual pH value (until 5 it should not be a problem to extract DNA).
- soil type/soil texture
- size and type of beads used for bead beating
- bead beating time and speed
- type of improvement you tried
I think if you have difficulties to extract DNA it is because of the biochar which is a common problem. Have a look on the attached paper that test different protocols to extract DNA from biochar enriched soil, although they do not use the Fast DNA Spin kit. You might have to use a different kit, have you thought about it or you do not have the possibility?
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Can anyone suggest me a volume for practical soil physical properties and Geotechnical parameters ?
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Dear Mahmoud,
I recommend the following book for you:
Singh R.A. (1980) Soil physical analysis. New Delhi Kalyani Publishers, New Delhi, India. Accession No. 153484.
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I am working on a project which involves interacting with soil by some and i want to assess approximately its results, please give instructions in modules: property, step, interaction and mesh just to model that basically, i do not intend creating a very sophisticated analysis.
Thanks in advance
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Dear Parham,
Why not spend some time in the library there is a wealth of knowledge on soil mechanics and mechanical properties of soil.  The simplest for what you would require are the Attenberg limits and simple compaction models based around these and consolidation density.
You might even find it useful to read (Topp GC, Reynolds WD, Cook FJ, Kirby JM and Carter MR (1997). Chapter 2. Physical Attributes of Soil Quality.  In Soil Quality for Crop Production. (Eds E.G. Gregorich and M.R. Carter), Developments in Soil Science, 25 Elsevier, Amsterdam, 21-58.) which will get you started.
Regards,
Freeman Cook
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Your opinions please!
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More than over-use of fertilizers , i feel , the very basis of such over-use of fertilizers , why does it happen ..?. Is it the non-availability of soil test- based fertilizer recommendation , unable to interpret the situation in right perspective in the context of changing yield performance ..? 
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In tropical soil the ocurrence of plinthinte and laterites  os widespread.  But how long time it Takes? Isso there any article about that? How to predict the age?
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THanks a lot! 
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Does anyone know a way to convert the World Reference Base for Soil Resources classification to the hydrological soil group? In particular I would need a conversion table to SWAT soil classification
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The only way is to go trough the WRB soil classes and extract from the qualifier list the textural classe. Indeed in WRB, you will have the Reference Soil Group like Cambisol, Podzol. The latter are followed by qualifier expressing special features like the soil texture (clayic, siltic, arenic qualifiers).
Convert the limit textural class of your Hydrological Soil Group with the soil textural calculator (see attached)  and try to find those limits according to WRB qualifier to build a conversion table.
A rough conversion (I guess, to be verified  )will be :
Group A ->Arenic qualifier
Group B-> Loamic qualifier
Group C -> Siltic qualifer
Group D -> Clayic qualifier
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Salt affected soils globally cover over 800 million ha (8-10% of of world land area), with a significant proportion of cultivated land is  salt affected . Such soils are characterized by salinity and sodicity of various demensions , the origin of which can be traced either geogenic or lithogenic or even combination of both. It is uncommon sight  to see , a soil once reclaimed is put to use for better crop production and added to the  main stream of  cultivated soils , though  still called as reclaimed soils. In this background , i put up following questions to my learned colleagues to contribute handsomely and benefit all of us:
*Why dont we consider calcareous soils as a part of salt affected soils  ?
* Why salts do not accumulate in grains or edible parts of plants ?. What are the mechanistic insights for such physiological events? 
* Do we have sensors to  directly measure the salinity and sodicity in field? Or , alternatively , Is there any field diagnostic kit available for appraisal of salinity or sodicity right in the field?
*Which type of reclamation is more sustainable from environment point of view?
* How do you see the role(s) of salt tolerant microbes in reclamation and post-reclamation scenario of salt affected soils?  
* What is the best method of artificial recharge of ground water?
* What is the system of rice intensification , and what magnitude of success , it holds in salt affected soils?
* How do you see the success of bio-saline agriculture ? Is saline aquaponics  potentially promising ?
*How do you see the emerging issues on salinity and sodicity getting vitiated by consequences of climate change? How shall we reorient our objectives in this context?
Thanks and regards 
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Thank you Dr. Anoop Kumar,
You have raised questions which are highly relevant to present situation because significant area of the world, especially in arid and semi arid zones is going out of cultivation consistently. Thus, the limited resource of land is shrinking slowly and slowly while there is constant rise in the population with ever increasing demand for food, feed and shelter. This situation is expected to worsen with happening of climate change that will raise temperature and decrease water availability in areas already with short supplies. Both these factors of climate favor salination and sodication with the result of converting highly fertile lands into saline, sodic and saline sodic. Increased use of saline groundwater will aggravate the situation. Ultimately, world food security, already shaking, will be coming at stake. It was demand of the day that this situation should be discussed by scientists and researchers of the Researchgate and workable solutions be recommended. Your effort is highly appreciable to open this discussion.  I request to world scientists community to actively take part in this discussion.  
Now I answer sub-questions put forward by Dr. Kumar to keep discussion on the track.
*Why do not we consider calcareous soils as a part of salt affected soils  ?
-Because by definition (EC> 4 dS/m or SAR> 13 or both parameters more than this criteria)  these do not come under these soils. However, these are more prone to be converted into saline, sodic or saline sodeic soils under a little bit negligence of agronomic practices because factors favoring salination or sidication are already operative in these soils.
* Why salts do not accumulate in grains or edible parts of plants ?. What are the mechanistic insights for such physiological events? 
- Up to certain limits all plants and salt tolerant plants in particular, segregate salts into cell vacuoles or there is salt shredding mechanism developed in certain plants (Diplecna chloea, salt grass or Kallar grass). However, in acute cases or in certain plants (like sugarcane- you can taste salts in its juice) salts can accumulate in eating parts.  
* Do we have sensors to  directly measure the salinity and sodicity in field? Or , alternatively , Is there any field diagnostic kit available for appraisal of salinity or sodicity right in the field?
*Which type of reclamation is more sustainable from environment point of view?
-That type of reclamation which disturbs the ecosystem to the minimum extent. However, you have to get rid of accumulated salts at least once and definitely it will distrb the environment once. However, if the natural drainage of soils is good or you are using tile drainage, the salts will be taken away safely.
* How do you see the role(s) of salt tolerant microbes in reclamation and post-reclamation scenario of salt affected soils?  
-Like other favorable soil characters, microbial population is also affected badly due to salt accumulation. It may be finished totally in ultra salt affected soils. That is why, after completion of chemical, hydro-chemical and/or physical reclamation, inoculations are highly recommended. 
* What is the best method of artificial recharge of ground water?
- Keeping a balance between total rainfall of the year and pumping of water for irrigation and domestic purposes will not disturb the ecosystem but if you are disturbing it, the water table will go deep and deep. Artificial recharge dams are made in upstream and this water is allowed to move into affected areas which are to be recharged. However, these practices have not paid much practically and no area have gained its original water table despite all recharging efforts. Al-Batinah area of Sultanate of Oman can be quotes just as an example, though there are many in the world.  
* What is the system of rice intensification , and what magnitude of success, it holds in salt affected soils?
-Rice is included among the crops with highest delta of water. This may be bitter but its a hard fact that rice intensification is increasing salinity problem. Pumping of saline water to irrigate rice is bringing salts into soil surface and sub-surface, thus increasing total salt load into ecosystem. Even good quality river water when kept standing in rice fields concentrates due to evaporation and leave these salts in the sub-surface because the soil is already puddled to save irrigation water. too much can be said in this regard. But I will conclude with the words that salt balance studies must be undertaken to understand the facts.
* How do you see the success of bio-saline agriculture ? Is saline aquaponics  potentially promising ?
- Bio-Saline agriculture is a good practice but still did not contributed much that was required. You can grow salt tolerant plants. But our immediate need is food security in which contribution of this practice is not significant. Actually, it is secondary agriculture and useful to put salty lands to other uses and prevent further degradation. It must be adopted where appropriate but not replacement of reclamation where it is possible. 
*How do you see the emerging issues on salinity and sodicity getting vitiated by consequences of climate change? How shall we reorient our objectives in this context?
- We will be facing worst situation with regard to salinity in areas hit too much by climate change because the problem will highly increase there. We have to revisit of planning of agriculture in these areas, especially where there no supplies of canal/terrestrial water like Qatar. Green house/ aquaculture may be good selection for these areas 
Why do salt affected soils continue to pose potential threats to food security? - 
-As I explained earlier that land resource is shrinking due to salinity and other allied problems. Crop yields decrease significantly when grown in salt affected soils. This all contribute to threats to food security.
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My objective is to set the criteria of AEV, and screen some impossible results out of the data base.
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Typical region of air-entry value have been reported from 0.05 cm (0.005 bar) for coarse texture soils to 100 cm (0.1 bar) for fine-textured soils in different studies.
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I read the ASTM D 1883. In this Code only the duration of the soaking is proposed. There are other papers in which a controlled temperature for this test is introduced. Is there any idea regarding the temperature and chemical composition of the water. Is is a distilled water or tap water or anything else?
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Dear Ebrahim
The quality of water or in general the water type is not so important in CBR tests. However, it is the best practice to use river or well water located in the area of study.
All the best
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Ascribing doubting as respects making use of the CY Model in FLAC3D so as to mimic the behavior of clayey soil in the seismic analysis to being utilized the friction hardening in the aforesaid soil constitutive model based on the UBCSAND model subsequent to perusing the paper entitled “NON-ASSOCIATED PLASTICITY FOR SOILS, CONCRETE AND ROCK”. In short, are we allowed to exploit the friction hardening for clay? Additionally, is it rational to have the friction hardening and the cohesion hardening instantaneously?
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Dear Nesterina,
I am going to conduct the seismic analysis associated with saturated undrained cohesive soils. 
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I am looking for a reference or the raw data for any chemical characterization of Lufa Speyer soils (in particular Lufa 2.4) other than the particle size distribution provided by the supplier. I am looking for the elemental composition of the soils, trace metal distributions and description of any other parameters which might be useful in modeling the fate of contaminants in these soils. Many thanks
Rich
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Standard soils are used especially for permission studies according to GLP (Good Laboratory Practice) investigating leaching, degradation and metabolism, influence on soil microflora and fauna, adsorption/desorption characteristics of pesticides in soils as well as for pot experiments and other investigations in the laboratory and in the field. In guidelines of the German JKI (Julis-Kühn-Institut) and other relating guidelines (OECD) soils with certain characteristics are recommended. Standard soils are also used in very different experiments not concerning pesticides.
For these purposes LUFA Speyer offers Standard soil types differing especially in their organic matter content, particle size distribution and pH-value.
Analyses Data Sheet for Standard Soils according to GLP:http://www.lufa-speyer.de/images/stories/2016-STB-Bo-data_sheet.pdf
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examples of such efforts in India and elsewhere, costs and success achieved in such efforts and magnitude of such efforts.
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Micronized sulphur,S in water dispersible microgranular form,can be applied to crops in sulphur deficient soils in small application rates,may be 8-10 kg/ha.To my knowledge it it not intended for sodic soil reclamation as it is a costly material and can not be applied in tonnes as amendment.Can you give the cost of 50 or 100 kg  micronized S?
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I´m looking for information about the influence of  pH, Ca, P, Al and other soil characteristics in the uptake of fluoride by plants. Should I also consider the stomata absorption?
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discuss this with Matthew Taylor, he is an expert on Flouride
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Paddy responds to added zinc even at soil available zinc of 2 ppm. Any reasons for this?
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The key problem is that we cannot say with any certainty what value of, e.g. DTPA Zn, is critical without doing the experiment with the soil in question.  That is, it is a big leap of faith to regard a chemical extraction to be a measure of bioavailability.
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are any models available that could be used to determine contaminants dispersal from contaminated sites such as waste dumps ?
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contact Dr. Utermann at the German Environmental Agency : jens.utermann@uba.de!
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who can share soil phenolic measurement protocol
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see the attachment
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I need literature on this subject.
soil health and soil quality
Thank you
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Soil quality is how well soil does what we want it to do. More specifically, soil quality is the capacity of a specific kind of soil to function, within natural or managed ecosystem boundaries, to sustain plant and animal productivity, maintain or enhance water and air quality, and support human health and habitation. Soil Organic Matter and Soil Biology play a major role in soil Quality.
Soil health is a state of a soil meeting its range of ecosystem functions as appropriate to its environment. Soil Health Testing is an assessment of this status.
Actually these both terms are used interchangeably in literature. The new term referred above "Soil Security" may be accepted over time as well.
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We have collected a set of Soil volumetric water content data using Em50 data logger equipped with ECH2O 5TE sensors from five different soil layers. The soils are mostly saline sandy soil with the groundwater depth of 1 to 2.5 meters. We found some of the records for volumetric water content are up to 100 %, especially in the bottom layer, could it be possible? If yes, Could you please explain why?
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Dear Abdullah,
Perhaps the attached paper might help you figure this out. I also saw on the Decagon website that salinity can vary your readings by up to 10%, so that might be a contributing factor.
Regards,
Steve
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hi all,
I am writing stiffness matrix [D] for element stiffness between pile and swelling soil. because of complex behavior between pile and swelling soil, i choose anisotropic matrix.
How can i take account the water change in the stiffness [D] matrix or the volume change?
Please help
best regards,
abdo Ali
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thanks you so much, Ariadne Tsambani
...
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I looking for reference sheet of MAPEP MS 30.
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Hi.  Is this the handbook you need?
Also, in the www.id.energy.gov website, I have seen other links to MAPEP Series that might help you too. 
Cheers!
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Can agricultural practices change soil texture and/or soil structure? And...How can fertilization modified retention/release/transmission of water into soil, in particular infiltration rate? How is it possible? 
thank you!
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Agricultural practices interfere heavily in the quality of agro-ecosystems. The main changes in the structure and physical ground are through intensive mechanization, native vegetation removal, lack of conservation practices, while soil fertility is affected by the export of nutrients (through harvesting of crops), soil acidification, lixiação nutrients, pesticides (these interfere in the macro, meso, and micro fauna of soil that are responsible for global cycling of nutrients).
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As you know disturbed soil samples have different Time-Settlement curve because they don’t experience preconsolidation pressure.  I have some results from Oedometer test which are related to different mixture of Kaolin and Bentonite with water content equal to liquid limit. Time-Settlement curves for them don’t match with undisturbed soil samples and I can't use conventional methods like Casagrande or Taylor in order to obtain coefficient of consolidation.
Anyone can give me some suggestion?
Thanks in advance.
I attached one of my results.
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Dear Seyed,
you may found the following paper useful
A Method for Correcting Consolidation Parameters for Sample Disturbance Using Volumetric Strain.
Article · January 1996 with 4 Reads
DOI: 10.3208/sandf.36.3_123
you may request full-text from the author "Takaharu Shogaki" on research gate
best wishes
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I don't know of many farmers routinely employing a field-wide evaluation of soil compaction, but when I do it's always wtih a penetrometer. Some sample a few points and believe that behavior reflects the whole area (a true statistical inference error, in my opinion). Others take samples not paying attention to soil moisture. I don't know, isn't there a better option or instrument?
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Hallo Tiago,
According to your question I can give you the following reply: 
Suitable parameters to assess the soil compaction are i)  saturated water conductivity, ii) effective bulk density (= bulk density + (0.009 * clay content [%]  ) by pF 1.8 and 2.5, iii) the macroporosity by pF 1.8, iv) penetration resistance (dynamic - Panda sonde) by pF 2.2 - 2.7. The penetration resistance alone is not enough to assess quantitavely the degree of soil compaction.
Basically, the penetrometer is an excellent and an appropriate intrument to measure the hardness of the soil or wearing capacity of the soil (different from degree of soil compaction). Only with one parameter (penetration resistance) you take into consideration at the same time soil texture, soil sturcture, soil moisture,  ground cover, root density to evaluate the soil  trafficability.  We have observed that in special cases a wet soil (permanent meadow) can be harder than an arable dry soil...
Penetration resistance is an imortant parameter to describe stress propagation in the soil. Penetrometers are not predestinate to assess directly the degree of soil compaction.   
With my best regards,
Etienne
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What are the main properties of soils developing under lacustrine environments? The environment under which soil is deposited. 
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As Stuart Harris indicates, lacustrine sediments are very variable, although mostly fine grained.  Many lacustrine deposits are metres or dekametres deep ,and any tendency towards thixotropic 'quick clay' instability is particularly hazardous for structures that impose high loadings, e.g. high rise blocks in the Mexico City earthquake
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Is it possible to convert soil nutrient concentrations (i.e. TN, TC, etc.) represented as a percent to a mass/mass concentration (i.e. mg/kg)? If it helps bulk density and soil core depth is also provided. 
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Soil test reports generally express TN and TC as a percent (%) of dry mass.  As an example, if the report says soil contains 1.23% of TN, this means that there is 1.23 grams of TN in 100 grams of dry soil.
To convert TN or TC expressed in % to g/kg dry soil:
1.23% TN = (1.23/100) x 1000 = 12.3 g/kg dry soil
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Biochar is claimed to be useful in many respects in agriculture provided enough raw material is available for its preparation. Can we get some favourable role in salt stressed soil?
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 I am supplementing through one very good studies covering the subject , you have raised Dr Ghafoor. Remediating saline–sodic soils with organic amendments is increasingly seen as a cheaper and sustainable alternative to inorganic materials. The reclamation potential of biochar, biosolids and greenwaste composts applied to a saline–sodic soil was evaluated in a laboratory leaching experiment using moderate SAR reclaimed water. Treatments included biochar, biosolids co-compost, greenwaste compost (all applied at a 75 t ha−1 rate), gypsum (50% soil gypsum requirement), biochar + gypsum, biosolids + gypsum, greenwaste + gypsum and a non-amended control ( Chaganti et a. 2015, Agricultural Water Management  158: 255-265).l  All treatments were subjected to a one month incubation after which, soils were filled in columns and leached using reclaimed water until 7 PV of water had passed. Cumulative leachate losses of Na+, Ca2+, and Mg2+ were evaluated in addition to soil properties after leaching. Results show that leaching with moderate SAR water was effective in reducing the soil salinity and sodicity of all soils, irrespective of amendment application. However, incorporating biochar and composts significantly enhanced this effect. Salt leaching was higher in soils treated with organic amendments. Cumulative leachate losses of cations were significantly higher from biochar and compost treated soils compared to gypsum and unamended controls. 
Enclosed below two very interesting PDFs highlighting the role of biochars in remediation of sodic soils.
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What are the soil properties sensitive enough to differentiate soils of organic and conventional farms?
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one of the best indicators (at least under our clima conditions) is the number of earthworms per area unit.
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In extraction of soil moisture data from SMAP, is it necessary to have terrestrial measured soil moisture control data? If the answer is yes, how can I use some point SM data to control the coarse scale SMAP data?
In lack of the measured SM data, is it possible to use SMAP for extraction of SM data?
Many thanks!
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I think, you still need other source of SM to compare with your result. If you have point measurement of SM, you just get the SM of the corresponding pixel. Because the field measurement of SM might be more accurate, you could adjust the SMA SM to match well with the observed one.
Hope that it could help!
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Its generally seen that addition of biochar generally increases the pH of the acidic soil. So does it also increases the pH of the alkaline soil?
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