CN111781163A - A method for eliminating the influence of soil particle size on the detection of soil parameters in discrete near-infrared bands - Google Patents
A method for eliminating the influence of soil particle size on the detection of soil parameters in discrete near-infrared bands Download PDFInfo
- Publication number
- CN111781163A CN111781163A CN202010712428.4A CN202010712428A CN111781163A CN 111781163 A CN111781163 A CN 111781163A CN 202010712428 A CN202010712428 A CN 202010712428A CN 111781163 A CN111781163 A CN 111781163A
- Authority
- CN
- China
- Prior art keywords
- soil
- absorbance
- particle size
- detected
- granularity
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002689 soil Substances 0.000 title claims abstract description 459
- 238000001514 detection method Methods 0.000 title claims abstract description 70
- 238000000034 method Methods 0.000 title claims abstract description 42
- 239000002245 particle Substances 0.000 title claims description 162
- 238000002835 absorbance Methods 0.000 claims abstract description 173
- 238000012937 correction Methods 0.000 claims abstract description 61
- 238000002329 infrared spectrum Methods 0.000 claims abstract description 23
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 98
- 229910052757 nitrogen Inorganic materials 0.000 claims description 49
- 238000013145 classification model Methods 0.000 claims description 11
- 238000004590 computer program Methods 0.000 claims description 10
- 230000000694 effects Effects 0.000 claims description 3
- 235000019580 granularity Nutrition 0.000 claims 22
- 238000012512 characterization method Methods 0.000 claims 1
- 230000003595 spectral effect Effects 0.000 description 23
- 238000010586 diagram Methods 0.000 description 16
- 238000004891 communication Methods 0.000 description 6
- 238000012706 support-vector machine Methods 0.000 description 5
- 238000004497 NIR spectroscopy Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 238000013528 artificial neural network Methods 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 238000007619 statistical method Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000004720 fertilization Effects 0.000 description 1
- 239000003041 laboratory chemical Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000003333 near-infrared imaging Methods 0.000 description 1
- 238000009659 non-destructive testing Methods 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/35—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light
- G01N21/359—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light using near infrared light
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/35—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light
- G01N21/3563—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light for analysing solids; Preparation of samples therefor
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N2021/3129—Determining multicomponents by multiwavelength light
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
Abstract
Description
技术领域technical field
本发明涉及光谱检测技术领域,具体涉及一种土壤粒度对离散近红外波段检测土壤参数影响的消除方法。The invention relates to the technical field of spectral detection, in particular to a method for eliminating the influence of soil particle size on soil parameters detected in discrete near-infrared bands.
背景技术Background technique
基于离散近红外波段对土壤参数进行检测,不仅可以有效降低检测成本,而且所建立的土壤参数预测模型也都取得了较好的预测结果。然而,基于离散近红外波段进行土壤参数检测面临着土壤粒度造成的严重干扰。The detection of soil parameters based on discrete near-infrared bands can not only effectively reduce the detection cost, but also the established soil parameter prediction models have achieved good prediction results. However, soil parameter detection based on discrete near-infrared bands faces serious interference caused by soil particle size.
现有技术中,通常采用将土壤研磨后过筛处理来消除土壤粒度干扰,但该方法费时费力,不能够应用于运用离散近红外波段进行在线土壤检测时的土壤粒度干扰消除。此外,针对连续近红外光谱常用的微分方法等也不适用于离散近红外波段。In the prior art, the soil particle size interference is usually eliminated by sieving the soil after grinding, but this method is time-consuming and labor-intensive, and cannot be applied to the soil particle size interference elimination when using discrete near-infrared wavebands for online soil detection. In addition, the differential methods commonly used for continuous near-infrared spectroscopy are not suitable for discrete near-infrared bands.
发明内容SUMMARY OF THE INVENTION
本发明实施例提供一种土壤粒度对离散近红外波段检测土壤参数影响的消除方法,用以解决现有技术中基于离散近红外波段进行土壤参数检测时面临土壤粒度造成的严重干扰,土壤参数检测精度差的问题。The embodiment of the present invention provides a method for eliminating the influence of soil particle size on soil parameters detected by discrete near-infrared bands, so as to solve the serious interference caused by soil particle size when soil parameters are detected based on discrete near-infrared bands in the prior art. problem of poor accuracy.
第一方面,本发明实施例提供一种土壤粒度对离散近红外波段检测土壤参数影响的消除方法,包括:In a first aspect, an embodiment of the present invention provides a method for eliminating the influence of soil particle size on soil parameters detected in discrete near-infrared bands, including:
确定待检测土壤在近红外光谱扫描下的多个检测波段的原始吸光度;Determine the original absorbance of multiple detection bands of the soil to be detected under near-infrared spectral scanning;
基于所述待检测土壤在特征波段的原始吸光度,确定所述待检测土壤的粒度修正系数;所述特征波段是基于多个土壤粒度下的土壤样本在近红外光谱扫描下的多个预设波段的样本原始吸光度确定的;Determine the particle size correction coefficient of the soil to be detected based on the original absorbance of the soil to be detected in the characteristic waveband; the characteristic waveband is a plurality of preset wavebands based on the near-infrared spectrum scanning of soil samples with multiple soil particle sizes The original absorbance of the sample is determined;
基于所述待检测土壤的粒度修正系数,对所述待检测土壤的每一检测波段的原始吸光度进行修正,并基于修正结果确定所述待检测土壤的土壤参数。Based on the particle size correction coefficient of the soil to be detected, the original absorbance of each detection band of the soil to be detected is corrected, and the soil parameters of the soil to be detected are determined based on the correction result.
可选地,所述基于所述待检测土壤在特征波段的原始吸光度,确定所述待检测土壤的粒度修正系数,包括:Optionally, determining the particle size correction coefficient of the soil to be detected based on the original absorbance of the soil to be detected in the characteristic waveband, including:
基于所述待检测土壤在特征波段的原始吸光度,确定用于表征所述待检测土壤的土壤粒度的吸光度比值;Based on the original absorbance of the soil to be detected in the characteristic waveband, determine an absorbance ratio used to characterize the soil particle size of the soil to be detected;
基于所述待检测土壤的吸光度比值,以及基准土壤粒度的吸光度比值,确定所述待检测土壤的粒度修正系数。Based on the absorbance ratio of the soil to be detected and the absorbance ratio of the reference soil particle size, the particle size correction coefficient of the soil to be detected is determined.
可选地,所述基准土壤粒度的吸光度比值是基于所述基准土壤粒度下的土壤样本在近红外光谱扫描下的特征波段的样本原始吸光度确定的。Optionally, the absorbance ratio of the reference soil particle size is determined based on the original sample absorbance of the soil sample under the near-infrared spectrum scanning of the soil sample under the reference soil particle size.
可选地,所述特征波段是基于如下方法得到的:Optionally, the characteristic band is obtained based on the following method:
对所述多个土壤粒度下的土壤样本进行近红外光谱扫描,确定所述土壤样本的多个预设波段的样本原始吸光度;performing near-infrared spectrum scanning on the soil samples under the plurality of soil particle sizes, and determining the original sample absorbance of the soil samples in a plurality of preset wavelength bands;
基于每一土壤样本的多个预设波段的样本原始吸光度,确定所述土壤样本在每一土壤粒度下的标准偏差值,以及综合标准偏差值;Determine the standard deviation value of the soil sample under each soil particle size, and the comprehensive standard deviation value based on the original absorbance of the sample in multiple preset bands of each soil sample;
基于所述土壤样本在每一土壤粒度下的标准偏差值,以及综合标准偏差值,确定所述特征波段。The characteristic band is determined based on the standard deviation value of the soil sample at each soil particle size, and the integrated standard deviation value.
可选地,所述基于所述土壤样本在每一土壤粒度下的标准偏差值,以及综合标准偏差值,确定所述特征波段,之后还包括:Optionally, the characteristic band is determined based on the standard deviation value of the soil sample under each soil particle size and the comprehensive standard deviation value, and further includes:
基于所述土壤样本的特征波段的样本原始吸光度,确定所述土壤样本的样本吸光度比值;Determine the sample absorbance ratio of the soil sample based on the original sample absorbance of the characteristic waveband of the soil sample;
基于所述土壤样本的样本吸光度比值和土壤粒度,建立土壤粒度分类模型,以验证所述样本吸光度比值对土壤粒度的表征能力。Based on the sample absorbance ratio and soil particle size of the soil sample, a soil particle size classification model is established to verify the ability of the sample absorbance ratio to characterize soil particle size.
可选地,所述特征波段为1361nm和1870nm。Optionally, the characteristic wavelength bands are 1361 nm and 1870 nm.
可选地,所述土壤样本包括4个粒度等级和6个全氮浓度梯度,4个粒度等级为0.2mm、0.45mm、0.9mm和2.0mm,6个全氮浓度等级为0g/kg、0.04g/kg、0.08g/kg、0.12g/kg、0.16g/kg和0.2g/kg。Optionally, the soil sample includes 4 particle size grades and 6 total nitrogen concentration gradients, the 4 particle size grades are 0.2 mm, 0.45 mm, 0.9 mm and 2.0 mm, and the 6 total nitrogen concentration grades are 0 g/kg, 0.04 g/kg, 0.08 g/kg, 0.12 g/kg, 0.16 g/kg and 0.2 g/kg.
第二方面,本发明实施例提供一种土壤粒度对离散近红外波段检测土壤参数影响的消除装置,包括:In a second aspect, an embodiment of the present invention provides a device for eliminating the influence of soil particle size on soil parameters detected in discrete near-infrared bands, including:
吸光度确定单元,用于确定待检测土壤在近红外光谱扫描下的多个检测波段的原始吸光度;The absorbance determination unit is used to determine the original absorbance of the soil to be detected in multiple detection bands under near-infrared spectral scanning;
系数确定单元,用于基于所述待检测土壤在特征波段的原始吸光度,确定所述待检测土壤的粒度修正系数;所述特征波段是基于多个土壤粒度下的土壤样本在近红外光谱扫描下的多个预设波段的样本原始吸光度确定的;A coefficient determination unit, configured to determine the particle size correction coefficient of the soil to be detected based on the original absorbance of the soil to be detected in the characteristic waveband; the characteristic waveband is based on the near-infrared spectrum scanning of soil samples with multiple soil particle sizes The original absorbance of the samples of multiple preset bands is determined;
修正检测单元,用于基于所述待检测土壤的粒度修正系数,对所述待检测土壤的每一检测波段的原始吸光度进行修正,并基于修正结果确定所述待检测土壤的土壤参数。The correction detection unit is configured to correct the original absorbance of each detection band of the soil to be detected based on the particle size correction coefficient of the soil to be detected, and determine soil parameters of the soil to be detected based on the correction result.
第三方面,本发明实施例提供一种电子设备,包括存储器、处理器及存储在存储器上并可在处理器上运行的计算机程序,所述处理器执行所述计算机程序时实现如第一方面所述的土壤粒度对离散近红外波段检测土壤参数影响的消除方法的步骤。In a third aspect, an embodiment of the present invention provides an electronic device, including a memory, a processor, and a computer program stored in the memory and executable on the processor, and the processor implements the first aspect when the processor executes the computer program The steps of the method for eliminating the influence of soil particle size on detection of soil parameters in discrete near-infrared bands.
第四方面,本发明实施例提供一种非暂态计算机可读存储介质,其上存储有计算机程序,所述计算机程序被处理器执行时实现如第一方面所述的土壤粒度对离散近红外波段检测土壤参数影响的消除方法的步骤。In a fourth aspect, an embodiment of the present invention provides a non-transitory computer-readable storage medium on which a computer program is stored, and when the computer program is executed by a processor, implements the soil particle size versus discrete near-infrared method described in the first aspect. Steps in the elimination method of band detection soil parameter effects.
本发明实施例提供的土壤粒度对离散近红外波段检测土壤参数影响的消除方法,根据待检测土壤在近红外光谱扫描下的特征波段的原始吸光度,确定待检测土壤的粒度修正系数,对多个检测波段的原始吸光度进行修正,基于修正结果确定待检测土壤的土壤参数,减小了土壤粒度对离散近红外波段的干扰,提高了土壤参数检测精度。In the method for eliminating the influence of soil particle size on soil parameters detected in discrete near-infrared wavelength bands provided by the embodiment of the present invention, the particle size correction coefficient of the soil to be detected is determined according to the original absorbance of the soil to be detected in the characteristic band under near-infrared spectral scanning. The original absorbance of the detection band is corrected, and the soil parameters of the soil to be detected are determined based on the correction results, which reduces the interference of soil particle size on the discrete near-infrared band and improves the detection accuracy of soil parameters.
附图说明Description of drawings
为了更清楚地说明本发明实施例或现有技术中的技术方案,下面将对实施例或现有技术描述中所需要使用的附图作一简单地介绍,显而易见地,下面描述中的附图是本发明的一些实施例,对于本领域普通技术人员来讲,在不付出创造性劳动的前提下,还可以根据这些附图获得其他的附图。In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the following briefly introduces the accompanying drawings that need to be used in the description of the embodiments or the prior art. Obviously, the accompanying drawings in the following description These are some embodiments of the present invention. For those of ordinary skill in the art, other drawings can also be obtained according to these drawings without creative efforts.
图1为本发明实施例提供的土壤粒度对离散近红外波段检测土壤参数影响的消除方法的流程示意图;1 is a schematic flowchart of a method for eliminating the influence of soil particle size on discrete near-infrared band detection soil parameters provided by an embodiment of the present invention;
图2为本发明实施例提供的土壤全氮浓度检测方法的流程示意图;2 is a schematic flowchart of a method for detecting soil total nitrogen concentration provided in an embodiment of the present invention;
图3为本发明实施例提供的标准偏差值与预设波段的关系曲线图;3 is a graph showing the relationship between a standard deviation value and a preset band provided by an embodiment of the present invention;
图4为本发明实施例提供的土壤粒度分类模型分类结果示意图;4 is a schematic diagram of a classification result of a soil particle size classification model provided by an embodiment of the present invention;
图5为本发明实施例提供的土壤全氮浓度检测样本原始吸光度示意图;5 is a schematic diagram of the original absorbance of a soil total nitrogen concentration detection sample provided by an embodiment of the present invention;
图6为本发明实施例提供的土壤全氮浓度检测样本修正吸光度示意图;6 is a schematic diagram of the corrected absorbance of a soil total nitrogen concentration detection sample provided in an embodiment of the present invention;
图7为本发明实施例提供的基于原始吸光度的土壤全氮浓度预测结果示意图;7 is a schematic diagram of a prediction result of soil total nitrogen concentration based on original absorbance provided by an embodiment of the present invention;
图8为本发明实施例提供的基于修正吸光度的土壤全氮浓度预测结果示意图;8 is a schematic diagram of a prediction result of soil total nitrogen concentration based on corrected absorbance provided by an embodiment of the present invention;
图9为本发明实施例提供的基于参照吸光度的土壤全氮浓度预测结果示意图;9 is a schematic diagram of a prediction result of soil total nitrogen concentration based on reference absorbance provided by an embodiment of the present invention;
图10为本发明实施例提供的土壤粒度对离散近红外波段检测土壤参数影响的消除装置的结构示意图;10 is a schematic structural diagram of a device for eliminating the influence of soil particle size on soil parameters detected in discrete near-infrared bands according to an embodiment of the present invention;
图11为本发明实施例提供的电子设备的结构示意图。FIG. 11 is a schematic structural diagram of an electronic device provided by an embodiment of the present invention.
具体实施方式Detailed ways
为使本发明实施例的目的、技术方案和优点更加清楚,下面将结合本发明实施例中的附图,对本发明实施例中的技术方案进行清楚、完整地描述,显然,所描述的实施例是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有作出创造性劳动前提下所获得的所有其他实施例,都属于本发明保护的范围。In order to make the purposes, technical solutions and advantages of the embodiments of the present invention clearer, the technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments These are some embodiments of the present invention, but not all embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those of ordinary skill in the art without creative efforts shall fall within the protection scope of the present invention.
近年来,随着变量施肥作业、智慧农田管理及农业可持续发展的需求,实时准确地提供农田土壤参数检测值变得越发紧迫。传统的实验室化学方法对土壤参数进行检测不仅费时、成本高而且污染环境。采用光谱技术对土壤参数进行快速无损的检测是一种性价比更好的选择,然而实验室使用的光谱仪及早期开发的基于光谱技术的土壤参数检测仪大多采用分光仪作为元件进行土壤参数检测,分光仪不仅价格昂贵而且很不适应农田的恶劣环境。基于离散近红外波段开发的土壤参数检测仪对土壤参数进行检测成为当前的研究热点,然而,该方法面临土壤粒度造成的严重干扰。In recent years, with the needs of variable fertilization operations, smart farmland management and sustainable agricultural development, it has become more and more urgent to provide real-time and accurate detection of farmland soil parameters. The detection of soil parameters by traditional laboratory chemical methods is not only time-consuming, costly, but also polluting the environment. It is a more cost-effective choice to use spectroscopic technology for rapid and non-destructive testing of soil parameters. However, most of the spectrometers used in laboratories and soil parameter detectors based on spectroscopic technology mostly use spectrometers as components to detect soil parameters. The instrument is not only expensive but also not suitable for the harsh environment of farmland. The detection of soil parameters by a soil parameter detector based on discrete near-infrared bands has become a current research hotspot. However, this method faces serious interference caused by soil particle size.
针对现有技术的不足,图1为本发明实施例提供的土壤粒度对离散近红外波段检测土壤参数影响的消除方法的流程示意图,如图1所示,该方法包括:In view of the deficiencies of the prior art, FIG. 1 is a schematic flowchart of a method for eliminating the influence of soil particle size on soil parameters detected in discrete near-infrared bands according to an embodiment of the present invention. As shown in FIG. 1 , the method includes:
步骤110,确定待检测土壤在近红外光谱扫描下的多个检测波段的原始吸光度;
具体地,对影响农田土壤环境质量的因素进行检测,可以确定农田环境质量及其变化趋势。土壤检测参数可以包括全氮、全磷、有机质、有效硼等。本发明实施例对土壤检测参数不作具体限定,后文内容以土壤全氮浓度检测为例来进行说明。Specifically, by detecting the factors affecting the environmental quality of farmland soil, the environmental quality of farmland and its change trend can be determined. Soil testing parameters can include total nitrogen, total phosphorus, organic matter, available boron, etc. The embodiments of the present invention do not specifically limit the soil detection parameters, and the following content will be described by taking the detection of soil total nitrogen concentration as an example.
对待检测土壤扫描时,可以选用基于离散近红外波段的车载式土壤全氮检测仪。运用多个检测波段的近红外光谱对待检测土壤进行扫描,得到待检测土壤在每一检测波段的近红外光谱扫描下的原始吸光度。When scanning the soil to be detected, a vehicle-mounted soil total nitrogen detector based on discrete near-infrared bands can be selected. Using the near-infrared spectrum of multiple detection bands to scan the soil to be detected, the original absorbance of the soil to be detected under the scan of the near-infrared spectrum of each detection band is obtained.
近红外光谱扫描的多个检测波段可以根据实际测量需求进行选择。Multiple detection bands of near-infrared spectral scanning can be selected according to actual measurement requirements.
例如,对待检测土壤进行全氮浓度检测,近红外光谱的检测波段可以选择1070nm、1130nm、1245nm、1375nm、1550nm、和1680nm。For example, to detect the total nitrogen concentration of the soil to be detected, the detection bands of the near-infrared spectrum can be selected from 1070 nm, 1130 nm, 1245 nm, 1375 nm, 1550 nm, and 1680 nm.
步骤120,基于待检测土壤在特征波段的原始吸光度,确定待检测土壤的粒度修正系数;特征波段是基于多个土壤粒度下的土壤样本在近红外光谱扫描下的多个预设波段的样本原始吸光度确定的;Step 120: Determine the particle size correction coefficient of the soil to be detected based on the original absorbance of the soil to be detected in the characteristic waveband; the characteristic waveband is the original sample of the soil sample in multiple preset wavebands under the near-infrared spectral scanning based on multiple soil particle sizes. Absorbance is determined;
具体地,采用近红外光谱对待检测土壤进行扫描时,土壤粒度会对扫描得到的原始吸光度产生一定程度的干扰。粒度修正系数,是为了尽可能消除因土壤粒度干扰造成的测量偏差,而对近红外光谱扫描得到的原始吸光度进行修正处理的系数。Specifically, when the soil to be detected is scanned by near-infrared spectroscopy, the soil particle size will interfere with the original absorbance obtained by scanning to a certain extent. The particle size correction coefficient is a coefficient for correcting the original absorbance obtained by near-infrared spectroscopy in order to eliminate the measurement deviation caused by the interference of soil particle size as much as possible.
特征波段是多个波段中能够通过对应的原始吸光度反映土壤粒度的波段。特征波段是基于多个土壤粒度下的土壤样本在近红外光谱扫描下的多个预设波段的样本原始吸光度确定的,特征波段的样本原始吸光度即通过近红外光谱对多个土壤粒度下的土壤样本进行扫描时所得的原始吸光度。本发明实施例对于特征波段的数量不作具体限定,优选地,特征波段的数量可以选择两个。The characteristic band is the band that can reflect the soil particle size through the corresponding raw absorbance. The characteristic band is determined based on the original absorbance of the soil samples in multiple preset bands under the near-infrared spectral scanning of the soil samples under multiple soil particle sizes. The raw absorbance obtained when the sample was scanned. The embodiment of the present invention does not specifically limit the number of characteristic bands, and preferably, two can be selected for the number of characteristic bands.
根据特征波段的原始吸光度,确定待检测土壤的粒度修正系数,例如,可以根据特征波段1361nm和1870nm的原始吸光度的平均值确定待检测土壤的粒度修正系数,也可以根据特征波段1361nm和1870nm的原始吸光度与其他波段的原始吸光度的差值确定待检测土壤的粒度修正系数。Determine the particle size correction coefficient of the soil to be tested according to the original absorbance of the characteristic wavelength bands. For example, the particle size correction coefficient of the soil to be tested can be determined according to the average value of the original absorbance of the characteristic wavelength bands of 1361 nm and 1870 nm, or the original absorbance of the characteristic wavelength bands of 1361 nm and 1870 nm. The difference between the absorbance and the original absorbance of other wavelength bands determines the particle size correction coefficient of the soil to be tested.
步骤130,基于待检测土壤的粒度修正系数,对待检测土壤的每一检测波段的原始吸光度进行修正,并基于修正结果确定待检测土壤的土壤参数。Step 130: Correct the original absorbance of each detection band of the soil to be detected based on the particle size correction coefficient of the soil to be detected, and determine soil parameters of the soil to be detected based on the correction result.
具体地,根据待检测土壤的粒度修正系数,对待检测土壤的每一检测波段的原始吸光度进行修正,得到修正结果,即待检测土壤的每一检测波段的修正吸光度,基于修正结果确定待检测土壤的土壤参数。Specifically, according to the particle size correction coefficient of the soil to be detected, the original absorbance of each detection band of the soil to be detected is corrected to obtain a correction result, that is, the corrected absorbance of each detection band of the soil to be detected, and the soil to be detected is determined based on the correction result. soil parameters.
例如,根据特征波段1361nm和1870nm的原始吸光度确定了待检测土壤的粒度修正系数P,使用粒度修正系数P对波段1070nm、1130nm、1245nm、1375nm、1550nm和1680nm的原始吸光度分别进行修正,得到每一检测波段的修正吸光度,利用BP神经网络建立土壤全氮预测模型,将每一检测波段的修正吸光度作为参数输入预测模型进行土壤全氮浓度预测。For example, the particle size correction coefficient P of the soil to be tested is determined according to the original absorbance of the characteristic bands of 1361 nm and 1870 nm, and the particle size correction coefficient P is used to correct the original absorbance of the bands of 1070 nm, 1130 nm, 1245 nm, 1375 nm, 1550 nm and 1680 nm respectively. The modified absorbance of the detection band was used to establish a soil total nitrogen prediction model using BP neural network, and the corrected absorbance of each detection band was used as a parameter to input the prediction model to predict the soil total nitrogen concentration.
本发明实施例提供的土壤粒度对离散近红外波段检测土壤参数影响的消除方法,根据待检测土壤在近红外光谱扫描下的特征波段的原始吸光度,确定待检测土壤的粒度修正系数,对多个检测波段的原始吸光度进行修正,基于修正结果确定待检测土壤的土壤参数,减小了土壤粒度对离散近红外波段的干扰,提高了土壤参数检测精度。In the method for eliminating the influence of soil particle size on soil parameters detected in discrete near-infrared wavelength bands provided by the embodiment of the present invention, the particle size correction coefficient of the soil to be detected is determined according to the original absorbance of the soil to be detected in the characteristic band under near-infrared spectral scanning. The original absorbance of the detection band is corrected, and the soil parameters of the soil to be detected are determined based on the correction results, which reduces the interference of soil particle size on the discrete near-infrared band and improves the detection accuracy of soil parameters.
基于上述实施例,步骤120,包括:Based on the above embodiment,
基于待检测土壤在特征波段的原始吸光度,确定用于表征待检测土壤的土壤粒度的吸光度比值;Based on the original absorbance of the soil to be tested in the characteristic wavelength band, determine the absorbance ratio used to characterize the soil particle size of the soil to be tested;
基于待检测土壤的吸光度比值,以及基准土壤粒度的吸光度比值,确定待检测土壤的粒度修正系数。Based on the absorbance ratio of the soil to be tested and the absorbance ratio of the reference soil particle size, the particle size correction coefficient of the soil to be tested is determined.
具体地,特征波段1361nm和1870nm的原始吸光度分别为A1361和A1870,确定表征待检测土壤的土壤粒度的吸光度比值R,用公式表示为:Specifically, the original absorbances of the characteristic wavelength bands 1361 nm and 1870 nm are A 1361 and A 1870 respectively, and the absorbance ratio R representing the soil particle size of the soil to be tested is determined, which is expressed by the formula as:
基准土壤粒度的吸光度比值为则可以确定待检测土壤的粒度修正系数P,用公式表示为:The absorbance ratio of the reference soil particle size is Then the particle size correction coefficient P of the soil to be tested can be determined, which is expressed as:
基于上述任一实施例,基准土壤粒度的吸光度比值是基于基准土壤粒度下的土壤样本在近红外光谱扫描下的特征波段的样本原始吸光度确定的。Based on any of the above embodiments, the absorbance ratio of the reference soil particle size is determined based on the original absorbance of the soil sample under the near-infrared spectral scanning of the characteristic wavelength band of the soil sample under the reference soil particle size.
具体地,可以选择土壤粒度为0.2mm的土壤作为基准土壤。使用土壤粒度为0.2mm的多个土壤样本,对于每一土壤样本,在特征波段的近红外光谱扫描下得到样本原始吸光度,进一步得到该土壤样本的吸光度比值。将多个土壤样本的吸光度比值的平均值作为基准土壤粒度的吸光度比值。Specifically, soil with a soil particle size of 0.2 mm can be selected as the reference soil. Using multiple soil samples with a soil particle size of 0.2 mm, for each soil sample, the original absorbance of the sample was obtained under the near-infrared spectrum scanning of the characteristic band, and the absorbance ratio of the soil sample was further obtained. The average value of the absorbance ratios of multiple soil samples was taken as the absorbance ratio of the reference soil particle size.
基于上述任一实施例,特征波段是基于如下方法得到的:Based on any of the above embodiments, the characteristic band is obtained based on the following method:
对多个土壤粒度下的土壤样本进行近红外光谱扫描,确定土壤样本的多个预设波段的样本原始吸光度;Perform near-infrared spectral scanning on soil samples under multiple soil particle sizes to determine the original absorbance of the soil samples in multiple preset bands;
基于每一土壤样本的多个预设波段的样本原始吸光度,确定土壤样本在每一土壤粒度下的标准偏差值,以及综合标准偏差值;Determine the standard deviation value of the soil sample under each soil particle size and the comprehensive standard deviation value based on the original absorbance of the sample in multiple preset bands of each soil sample;
基于土壤样本在每一土壤粒度下的标准偏差值,以及综合标准偏差值,确定特征波段。Based on the standard deviation value of the soil sample at each soil particle size, and the integrated standard deviation value, the characteristic band is determined.
具体地,对多个土壤粒度下的土壤样本进行近红外光谱扫描,确定土壤样本的多个预设波段的样本原始吸光度。根据美国材料检测协会(ASTM)对近红外光谱区的定义,近红外光谱为780nm-2526nm的区域。本发明实施例中,预设波段为近红外光谱850nm-2500nm内的波段。各个预设波段均为等间隔的波段,且各波段起点和终点依次相接,实现对近红外光谱范围的最大覆盖。Specifically, near-infrared spectrum scanning is performed on soil samples under multiple soil particle sizes to determine the original absorbance of the soil samples in multiple preset wavelength bands. According to the definition of the near-infrared spectral region by the American Society for Testing and Materials (ASTM), the near-infrared spectrum is the region of 780nm-2526nm. In the embodiment of the present invention, the preset wavelength band is a wavelength band within 850 nm-2500 nm of the near-infrared spectrum. Each preset waveband is an equally spaced waveband, and the start and end points of each waveband are connected in sequence to achieve maximum coverage of the near-infrared spectral range.
根据土壤样本的多个预设波段的样本原始吸光度,确定土壤样本在每一土壤粒度下的标准偏差值,以及综合标准偏差值。综合标准偏差值为土壤样本整体的标准偏差值。According to the original absorbance of the sample in multiple preset bands of the soil sample, the standard deviation value of the soil sample under each soil particle size and the comprehensive standard deviation value are determined. The comprehensive standard deviation value is the standard deviation value of the soil sample as a whole.
此处,土壤样本在任一土壤粒度j下的标准偏差值可以通过如下公式得到:Here, the standard deviation value of the soil sample at any soil particle size j It can be obtained by the following formula:
式中,i为预设波段的序号,j为土壤粒度等级序号,N为任一土壤粒度下土壤样本数量,W为任一土壤粒度下土壤样本的序号,W==1,2,3…N,为土壤粒度等级为j的土壤样本在预设波段为i的近红外光谱扫描下的样本原始吸光度,为土壤粒度等级为j的N个土壤样本在预设波段为i的近红外光谱扫描下的样本原始吸光度的平均值。In the formula, i is the serial number of the preset band, j is the soil particle size grade serial number, N is the number of soil samples under any soil particle size, W is the serial number of soil samples under any soil particle size, W==1,2,3… N, is the original absorbance of the soil sample with the soil particle size class j under the near-infrared spectral scan of the preset band i, is the average value of the original absorbance of the samples under the near-infrared spectral scanning of the preset band i of N soil samples with soil particle size grade j.
根据土壤样本在每一土壤粒度下的标准偏差值,以及综合标准偏差值,确定特征波段。例如,可以绘制土壤样本在每一土壤粒度下的标准偏差值与预设波段的关系曲线,以及综合标准偏差值与预设波段的关系曲线,确定特征波段。According to the standard deviation value of the soil sample under each soil particle size and the comprehensive standard deviation value, the characteristic band is determined. For example, the relationship curve between the standard deviation value of the soil sample under each soil particle size and the preset band, and the relationship curve between the integrated standard deviation value and the preset band can be drawn to determine the characteristic band.
基于上述任一实施例,基于土壤样本在每一土壤粒度下的标准偏差值,以及综合标准偏差值,确定特征波段,之后还包括:Based on any of the above embodiments, based on the standard deviation value of the soil sample under each soil particle size and the comprehensive standard deviation value, the characteristic band is determined, and the following further includes:
基于土壤样本的特征波段的样本原始吸光度,确定土壤样本的样本吸光度比值;Determine the sample absorbance ratio of the soil sample based on the sample original absorbance of the characteristic band of the soil sample;
基于土壤样本的样本吸光度比值和土壤粒度,建立土壤粒度分类模型,以验证样本吸光度比值对土壤粒度的表征能力。Based on the sample absorbance ratio and soil particle size of soil samples, a soil particle size classification model was established to verify the ability of the sample absorbance ratio to characterize soil particle size.
具体地,根据土壤样本的特征波段的样本原始吸光度,确定土壤样本的样本吸光度比值。Specifically, the sample absorbance ratio of the soil sample is determined according to the original sample absorbance of the characteristic waveband of the soil sample.
为验证样本吸光度比值对土壤粒度的表征能力,建立土壤粒度分类模型,将土壤样本的样本吸光度比值作为输入变量,得到土壤粒度分类结果,与土壤样本的土壤粒度进行对比。土壤粒度分类模型可以基于SVM(Support Vector Machine,支持向量机)模型建立,本发明实施例对于土壤粒度分类模型的选取不作具体限定。In order to verify the ability of the sample absorbance ratio to characterize soil particle size, a soil particle size classification model was established, and the sample absorbance ratio of the soil sample was used as an input variable to obtain the soil particle size classification result, which was compared with the soil particle size of the soil sample. The soil particle size classification model may be established based on an SVM (Support Vector Machine, support vector machine) model, and the embodiment of the present invention does not specifically limit the selection of the soil particle size classification model.
基于上述任一实施例,特征波段为1361nm和1870nm。Based on any of the above embodiments, the characteristic wavelength bands are 1361 nm and 1870 nm.
具体地,通过使用850nm-2500nm范围内的近红外光谱对不同土壤粒度的土壤样本进行扫描后,运用上述实施例中的方法分析得到特征波段为1361nm和1870nm。Specifically, after using the near-infrared spectrum in the range of 850nm-2500nm to scan soil samples with different soil particle sizes, the characteristic wavelength bands are 1361nm and 1870nm after analysis using the method in the above embodiment.
基于上述任一实施例,土壤样本包括4个粒度等级和6个全氮浓度梯度,4个粒度等级为0.2mm、0.45mm、0.9mm和2.0mm,6个全氮浓度等级为0g/kg、0.04g/kg、0.08g/kg、0.12g/kg、0.16g/kg和0.2g/kg。Based on any of the above embodiments, the soil sample includes 4 particle size grades and 6 total nitrogen concentration gradients, 4 particle size grades are 0.2mm, 0.45mm, 0.9mm and 2.0mm, 6 total nitrogen concentration grades are 0g/kg, 0.04g/kg, 0.08g/kg, 0.12g/kg, 0.16g/kg and 0.2g/kg.
下面通过一个土壤全氮浓度检测的实施例对上述方法进行说明。图2为本发明实施例提供的土壤全氮浓度检测方法的流程示意图,如图2所示,土壤全氮浓度检测过程的详细执行步骤如下:The above method will be described below through an example of soil total nitrogen concentration detection. 2 is a schematic flowchart of a method for detecting soil total nitrogen concentration provided by an embodiment of the present invention. As shown in FIG. 2 , the detailed execution steps of the soil total nitrogen concentration detection process are as follows:
第一步,将采样得到的标准土壤(全氮浓度为0g/kg)进行烘干处理,烘干温度为85℃,烘干时间为24h。烘干后的土壤样本分为6组,每组4个。使用尿素制成的氨素溶液对土壤样本进行配置,氨素溶液浓度分为1至6个等级。等级1氨素含量为0g/kg,等级2氮素含量为0.04g/kg,等级3氮素含量为0.08g/kg,等级4氮素含量为0.12g/kg,等级5氮素含量为0.16g/kg,等级6氮素含量为0.2g/kg。In the first step, the sampled standard soil (with a total nitrogen concentration of 0 g/kg) was dried at a drying temperature of 85°C and a drying time of 24 hours. The dried soil samples were divided into 6 groups of 4 each. Soil samples were prepared using ammonia solutions made from urea, with concentrations ranging from 1 to 6. The ammonia content of grade 1 is 0g/kg, the nitrogen content of grade 2 is 0.04g/kg, the nitrogen content of grade 3 is 0.08g/kg, the nitrogen content of
在土壤样本配置时,还可以模拟实际农田耕作层夏季平均土壤含水率(7%),对土壤样本进行配置。When configuring the soil samples, the soil samples can also be configured by simulating the average soil moisture content (7%) of the actual farmland plough layer in summer.
土壤配置完成后,进行烘干处理,对所有土壤样本进行过筛,分别为10目筛(2.0mm)、20目筛(0.9mm)、40目筛(0.45mm)和80目筛(0.2mm)。最终得到4组不同粒径的土壤样本,每组包含6个全氮浓度等级,每个全氮浓度等级包含4个土壤样本。总计获得96个不同粒径和全氮浓度下的土壤样本。表1为对土壤样本进行统计分析后得到的数据。After the soil configuration is completed, drying treatment is performed, and all soil samples are sieved into 10-mesh sieve (2.0mm), 20-mesh sieve (0.9mm), 40-mesh sieve (0.45mm) and 80-mesh sieve (0.2mm) ). Finally, 4 groups of soil samples with different particle sizes were obtained, each group contained 6 levels of total nitrogen concentration, and each level of total nitrogen concentration contained 4 soil samples. A total of 96 soil samples with different particle sizes and total nitrogen concentrations were obtained. Table 1 shows the data obtained after statistical analysis of soil samples.
表1土壤样本统计分析Table 1 Statistical analysis of soil samples
第二步,对4个土壤粒度梯度和6个全氮浓度等级的96个土壤样本进行近红外光谱扫描,获得850nm-2500nm波段范围内的样本原始吸光度值其中,i为预设波段序号,波段间隔为3nm,则i=850,853,856…,2500。m为土壤样本序号,m=1,2,3…,96。In the second step, 96 soil samples with 4 soil particle size gradients and 6 total nitrogen concentration levels were scanned by near-infrared spectroscopy to obtain the original absorbance values of the samples in the range of 850nm-2500nm. Wherein, i is the preset band sequence number, and the band interval is 3nm, then i=850, 853, 856..., 2500. m is the soil sample serial number, m=1,2,3...,96.
第三步,对4个土壤粒度下的土壤样本单独计算标准偏差值并计算所有96个土壤样本的综合标准偏差值j是土壤粒度等级序号,j=1为0.2mm下全部24个土壤样本,j=2为0.45mm下全部24个土壤样本,j=3为0.9mm下全部24个土壤样本,j=4为2.0mm下全部24个土壤样本。The third step is to calculate the standard deviation value separately for the soil samples under 4 soil particle sizes and calculate the combined standard deviation value for all 96 soil samples j is the soil particle size grade number, j=1 is all 24 soil samples under 0.2mm, j=2 is all 24 soil samples under 0.45mm, j=3 is all 24 soil samples under 0.9mm, j=4 is All 24 soil samples under 2.0mm.
图3为本发明实施例提供的标准偏差值与预设波段的关系曲线图,如图3所示,共5条曲线,分别为土壤样本在4个土壤粒度(Soil particle size)下的标准偏差值与预设波段的关系曲线,以及综合标准偏差值与预设波段的关系曲线,可以得到土壤粒度的特征波段为1361nm和1870nm。FIG. 3 is a graph showing the relationship between the standard deviation value and the preset band provided by the embodiment of the present invention. As shown in FIG. 3 , there are 5 curves in total, which are the standard deviations of soil samples under 4 soil particle sizes respectively. The relationship curve between the value and the preset band, as well as the relationship curve between the comprehensive standard deviation value and the preset band, the characteristic bands of soil particle size can be obtained as 1361nm and 1870nm.
第四步,根据土壤样本在特征波段1361nm和1870nm的样本原始吸光度,确定土壤样本的样本吸光度比值Rm,用公式表示为:The fourth step is to determine the sample absorbance ratio R m of the soil sample according to the original absorbance of the soil sample in the characteristic wavelength bands of 1361 nm and 1870 nm, which is expressed as:
式中,m为土壤样本序号,为土壤样本在特征波段1870nm的样本原始吸光度,为土壤样本在特征波段1361nm的样本原始吸光度。where m is the soil sample serial number, is the original absorbance of the soil sample in the characteristic wavelength band 1870nm, It is the original absorbance of the soil sample at the characteristic wavelength band 1361nm.
第五步,基于SVM(Support Vector Machine,支持向量机)建立土壤粒度分类模型,将样本吸光度比值Rm作为单一输入变量,验证比值Rm对土壤粒度分类的准确性。The fifth step is to establish a soil particle size classification model based on SVM (Support Vector Machine), and use the sample absorbance ratio R m as a single input variable to verify the accuracy of the ratio R m for soil particle size classification.
图4为本发明实施例提供的土壤粒度分类模型分类结果示意图,如图4所示,将土壤粒度分类模型得到的预测土壤粒度(Predicted soil particle size)与实际土壤粒度(Measured soil particle size)相对比,样本吸光度比值Rm能够很好地表征对土壤粒度的分类。对土壤粒度分类准确率进行统计,如表2所示:FIG. 4 is a schematic diagram of a classification result of a soil particle size classification model provided by an embodiment of the present invention. As shown in FIG. 4 , the predicted soil particle size (Predicted soil particle size) obtained by the soil particle size classification model is relative to the actual soil particle size (Measured soil particle size). The sample absorbance ratio Rm can well characterize the classification of soil particle size. Statistics on the accuracy of soil particle size classification are shown in Table 2:
表2土壤粒度分类准确率统计Table 2 Accuracy statistics of soil particle size classification
由此可知,根据土壤样本在特征波段1361nm和1870nm的样本原始吸光度确定的样本吸光度比值Rm对土壤粒度分类的准确性为93.8%,满足实际应用需求。It can be seen that the accuracy of the sample absorbance ratio Rm determined according to the original absorbance of the soil samples in the characteristic wavelength bands of 1361nm and 1870nm for soil particle size classification is 93.8%, which meets the needs of practical applications.
第六步,基于特征波段的原始吸光度,确定土壤样本的粒度修正系数Pm,用公式可以表示为:The sixth step, based on the original absorbance of the characteristic band, determine the particle size correction coefficient P m of the soil sample, which can be expressed as:
式中,m为土壤样本序号,为土壤样本在特征波段1870nm的样本原始吸光度,为土壤样本在特征波段1361nm的样本原始吸光度,为以0.2mm为基准土壤粒度下土壤样本在1870nm和1361nm处的吸光度比值平均值。where m is the soil sample serial number, is the original absorbance of the soil sample in the characteristic wavelength band 1870nm, is the original absorbance of the soil sample in the characteristic wavelength band 1361nm, is the average value of the absorbance ratio of soil samples at 1870nm and 1361nm with 0.2mm as the benchmark soil particle size.
第七步,利用粒度修正系数Pm,对土壤样本的原始吸光度值进行修正,获得修正后的土壤吸光度值用公式可以表示为:The seventh step is to use the particle size correction coefficient P m to obtain the original absorbance value of the soil sample Make corrections to obtain the corrected soil absorbance value The formula can be expressed as:
式中,i为预设波段序号,m为土壤样本序号。In the formula, i is the preset band serial number, m is the soil sample serial number.
图5为本发明实施例提供的土壤全氮浓度检测样本原始吸光度示意图,如图5所示,土壤全氮浓度为0.068g/kg时的单一土壤样本在6个离散近红外波段(1070nm、1130nm、1245nm、1375nm、1550nm和1680nm)处的五条曲线,分别为原始土壤样本的吸光度值(Original spectrum),土壤粒度(Soil particle size)分别为2.0mm,0.9mm,0.45mm和0.2mm时的土壤样本的原始吸光度值。Figure 5 is a schematic diagram of the original absorbance of the soil total nitrogen concentration detection sample provided by the embodiment of the present invention. As shown in Figure 5, when the soil total nitrogen concentration is 0.068g/kg, a single soil sample has six discrete near-infrared bands (1070nm, 1130nm , 1245nm, 1375nm, 1550nm and 1680nm), the absorbance values of the original soil samples (Original spectrum), the soil particle size (Soil particle size) were 2.0mm, 0.9mm, 0.45mm and 0.2mm. The raw absorbance value of the sample.
图6为本发明实施例提供的土壤全氮浓度检测样本修正吸光度示意图,如图6所示,土壤全氮浓度为0.068g/kg时的单一土壤样本在6个离散近红外波段(1070nm、1130nm、1245nm、1375nm、1550nm和1680nm)处的五条曲线,分别为原始土壤样本的吸光度值(Original spectrum),土壤粒度(Soil particle size)分别为2.0mm,0.9mm,0.45mm和0.2mm时的土壤样本的样本修正吸光度值。Figure 6 is a schematic diagram of the corrected absorbance of the soil total nitrogen concentration detection sample provided by the embodiment of the present invention. As shown in Figure 6, when the soil total nitrogen concentration is 0.068g/kg, a single soil sample has six discrete near-infrared bands (1070nm, 1130nm) , 1245nm, 1375nm, 1550nm and 1680nm), the absorbance values of the original soil samples (Original spectrum), the soil particle size (Soil particle size) were 2.0mm, 0.9mm, 0.45mm and 0.2mm. The sample corrected absorbance value of the sample.
第八步,使用基于离散近红外波段的车载式土壤全氮检测仪,选择波段为1070nm、1130nm、1245nm、1375nm、1550nm和1680nm的近红外光谱对待检测土壤进行扫描,得到待检测土壤的原始吸光度。The eighth step, use the vehicle-mounted soil total nitrogen detector based on discrete near-infrared bands, select the near-infrared spectrum of 1070nm, 1130nm, 1245nm, 1375nm, 1550nm and 1680nm to scan the soil to be tested to obtain the original absorbance of the soil to be tested. .
根据第一步至第七步中的方法,利用特征波段1361nm和1870nm的原始吸光度,确定待检测土壤的粒度修正系数,对待检测土壤的原始吸光度进行修正,得到待检测土壤的修正吸光度。According to the methods in the first to seventh steps, the original absorbance of the characteristic wavebands 1361nm and 1870nm is used to determine the particle size correction coefficient of the soil to be tested, and the original absorbance of the soil to be tested is corrected to obtain the corrected absorbance of the soil to be tested.
此外,作为对比,将待检测土壤在土壤粒度为0.2mm下的吸光度作为参照吸光度。In addition, as a comparison, the absorbance of the soil to be tested at a soil particle size of 0.2 mm was used as the reference absorbance.
利用BP神经网络建立土壤全氮浓度预测模型,分别将待检测土壤的原始吸光度、修正吸光度和参照吸光度输入至土壤全氮浓度预测模型,得到各自的全氮浓度预测结果,如表3所示:The BP neural network is used to establish the prediction model of soil total nitrogen concentration, and the original absorbance, corrected absorbance and reference absorbance of the soil to be tested are respectively input into the prediction model of soil total nitrogen concentration, and the respective prediction results of total nitrogen concentration are obtained, as shown in Table 3:
表3基于不同土壤吸光度的模型准确度统计Table 3 Model accuracy statistics based on different soil absorbances
图7为本发明实施例提供的基于原始吸光度的土壤全氮浓度预测结果示意图,图8为本发明实施例提供的基于修正吸光度的土壤全氮浓度预测结果示意图,图9为本发明实施例提供的基于参照吸光度的土壤全氮浓度预测结果示意图,如图7、图8和图9所示,与基于参照吸光度的土壤全氮浓度预测结果(图9)相比,基于原始吸光度的土壤全氮浓度预测结果(图7)误差较大,基于修正吸光度的土壤全氮浓度预测结果(图8)更接近于实际情况,减小了土壤粒度对离散近红外波段的干扰,提高了土壤参数检测精度。Fig. 7 is a schematic diagram of a prediction result of soil total nitrogen concentration based on original absorbance provided by an embodiment of the present invention, Fig. 8 is a schematic diagram of a predicted result of soil total nitrogen concentration based on corrected absorbance provided by an embodiment of the present invention, and Fig. 9 is provided by an embodiment of the present invention The schematic diagram of the prediction results of soil total nitrogen concentration based on reference absorbance, as shown in Figure 7, Figure 8 and Figure 9, compared with the prediction results of soil total nitrogen concentration based on reference absorbance (Figure 9), the original absorbance-based soil total nitrogen concentration The concentration prediction result (Fig. 7) has a large error, and the soil total nitrogen concentration prediction result (Fig. 8) based on the corrected absorbance is closer to the actual situation, which reduces the interference of soil particle size on discrete near-infrared bands and improves the detection accuracy of soil parameters. .
其中,图7、图8和图9中土壤全氮实测值是通过使用凯氏定氮仪对待检测土壤进行测量得到的。Among them, the measured values of soil total nitrogen in Figure 7, Figure 8 and Figure 9 are obtained by using a Kjeldahl nitrogen analyzer to measure the soil to be tested.
基于上述任一实施例,图10为本发明实施例提供的土壤粒度对离散近红外波段检测土壤参数影响的消除装置的结构示意图,如图10所示,该装置包括:Based on any of the above embodiments, FIG. 10 is a schematic structural diagram of a device for eliminating the influence of soil particle size on soil parameters detected in discrete near-infrared bands according to an embodiment of the present invention. As shown in FIG. 10 , the device includes:
吸光度确定单元1010,用于确定待检测土壤在近红外光谱扫描下的多个检测波段的原始吸光度;an
系数确定单元1020,用于基于待检测土壤在特征波段的原始吸光度,确定待检测土壤的粒度修正系数;特征波段是基于多个土壤粒度下的土壤样本在近红外光谱扫描下的多个预设波段的样本原始吸光度确定的;The
修正检测单元1030,用于基于待检测土壤的粒度修正系数,对待检测土壤的每一检测波段的原始吸光度进行修正,并基于修正结果确定待检测土壤的土壤参数。The
具体地,吸光度确定单元1010用于确定待检测土壤在近红外光谱扫描下的多个检测波段的原始吸光度。系数确定单元1020,用于基于待检测土壤在特征波段的原始吸光度,确定待检测土壤的粒度修正系数。修正检测单元1030,用于基于待检测土壤的粒度修正系数,对待检测土壤的每一检测波段的原始吸光度进行修正,并基于修正结果确定待检测土壤的土壤参数。Specifically, the
本发明实施例提供的土壤粒度对离散近红外波段检测土壤参数影响的消除装置,根据待检测土壤在近红外光谱扫描下的特征波段的原始吸光度,确定待检测土壤的粒度修正系数,对多个检测波段的原始吸光度进行修正,基于修正结果确定待检测土壤的土壤参数,减小了土壤粒度对离散近红外波段的干扰,提高了土壤参数检测精度。The device for eliminating the influence of soil particle size on soil parameters detected in discrete near-infrared wavelength bands provided by the embodiment of the present invention determines the particle size correction coefficient of the soil to be detected according to the original absorbance of the characteristic band of the soil to be detected under near-infrared spectral scanning, and determines the particle size correction coefficient of the soil to be detected. The original absorbance of the detection band is corrected, and the soil parameters of the soil to be detected are determined based on the correction results, which reduces the interference of soil particle size on the discrete near-infrared band and improves the detection accuracy of soil parameters.
基于上述任一实施例,系数确定单元1020包括:Based on any of the above embodiments, the
比值确定子单元,用于基于待检测土壤在特征波段的原始吸光度,确定用于表征待检测土壤的土壤粒度的吸光度比值;The ratio determination subunit is used to determine the absorbance ratio used to characterize the soil particle size of the soil to be detected based on the original absorbance of the soil to be detected in the characteristic wavelength band;
系数确定子单元,用于基于待检测土壤的吸光度比值,以及基准土壤粒度的吸光度比值,确定待检测土壤的粒度修正系数。The coefficient determination subunit is used for determining the particle size correction coefficient of the soil to be tested based on the absorbance ratio of the soil to be tested and the absorbance ratio of the reference soil particle size.
基于上述任一实施例,基准土壤粒度的吸光度比值是基于基准土壤粒度下的土壤样本在近红外光谱扫描下的特征波段的样本原始吸光度确定的。Based on any of the above embodiments, the absorbance ratio of the reference soil particle size is determined based on the original absorbance of the soil sample under the near-infrared spectral scanning of the characteristic wavelength band of the soil sample under the reference soil particle size.
基于上述任一实施例,特征波段是基于如下方法得到的:Based on any of the above embodiments, the characteristic band is obtained based on the following method:
对多个土壤粒度下的土壤样本进行近红外光谱扫描,确定土壤样本的多个预设波段的样本原始吸光度;Perform near-infrared spectral scanning on soil samples under multiple soil particle sizes to determine the original absorbance of the soil samples in multiple preset bands;
基于每一土壤样本的多个预设波段的样本原始吸光度,确定土壤样本在每一土壤粒度下的标准偏差值,以及综合标准偏差值;Determine the standard deviation value of the soil sample under each soil particle size and the comprehensive standard deviation value based on the original absorbance of the sample in multiple preset bands of each soil sample;
基于土壤样本在每一土壤粒度下的标准偏差值,以及综合标准偏差值,确定特征波段。Based on the standard deviation value of the soil sample at each soil particle size, and the integrated standard deviation value, the characteristic band is determined.
基于上述任一实施例,基于土壤样本在每一土壤粒度下的标准偏差值,以及综合标准偏差值,确定特征波段,之后还包括:Based on any of the above embodiments, based on the standard deviation value of the soil sample under each soil particle size and the comprehensive standard deviation value, the characteristic band is determined, and the following further includes:
基于土壤样本的特征波段的样本原始吸光度,确定土壤样本的样本吸光度比值;Determine the sample absorbance ratio of the soil sample based on the original sample absorbance of the characteristic band of the soil sample;
基于土壤样本的样本吸光度比值和土壤粒度,建立土壤粒度分类模型,以验证样本吸光度比值对土壤粒度的表征能力。Based on the sample absorbance ratio and soil particle size of soil samples, a soil particle size classification model was established to verify the ability of the sample absorbance ratio to characterize soil particle size.
基于上述任一实施例,特征波段为1361nm和1870nm。Based on any of the above embodiments, the characteristic wavelength bands are 1361 nm and 1870 nm.
基于上述任一实施例,土壤样本包括4个粒度等级和6个全氮浓度梯度,4个粒度等级为0.2mm、0.45mm、0.9mm和2.0mm,6个全氮浓度等级为0g/kg、0.04g/kg、0.08g/kg、0.12g/kg、0.16g/kg和0.2g/kg。Based on any of the above embodiments, the soil sample includes 4 particle size grades and 6 total nitrogen concentration gradients, 4 particle size grades are 0.2mm, 0.45mm, 0.9mm and 2.0mm, 6 total nitrogen concentration grades are 0g/kg, 0.04g/kg, 0.08g/kg, 0.12g/kg, 0.16g/kg and 0.2g/kg.
图11为本发明实施例提供的电子设备的结构示意图,如图11所示,该电子设备可以包括:处理器(Processor)1110、通信接口(Communications Interface)1120、存储器(Memory)1130和通信总线(Communications Bus)1140。其中,处理器1110、通信接口1120和存储器1130通过通信总线1140完成相互间的通信。处理器1110可以调用存储器1130中的逻辑命令,以执行如下方法:FIG. 11 is a schematic structural diagram of an electronic device provided by an embodiment of the present invention. As shown in FIG. 11 , the electronic device may include: a processor (Processor) 1110, a communication interface (Communications Interface) 1120, a memory (Memory) 1130, and a communication bus (Communications Bus) 1140. The
确定待检测土壤在近红外光谱扫描下的多个检测波段的原始吸光度;基于待检测土壤在特征波段的原始吸光度,确定待检测土壤的粒度修正系数;特征波段是基于多个土壤粒度下的土壤样本在近红外光谱扫描下的多个预设波段的样本原始吸光度确定的;基于待检测土壤的粒度修正系数,对待检测土壤的每一检测波段的原始吸光度进行修正,并基于修正结果确定待检测土壤的土壤参数。Determine the original absorbance of the soil to be detected in multiple detection bands under near-infrared spectral scanning; determine the particle size correction coefficient of the soil to be detected based on the original absorbance of the soil to be detected in the characteristic band; the characteristic band is based on the soil under multiple soil particle sizes. The original absorbance of the sample in multiple preset bands under near-infrared spectral scanning is determined; based on the particle size correction coefficient of the soil to be detected, the original absorbance of each detection band of the soil to be detected is corrected, and based on the correction results, the to-be-detected is determined. Soil parameters of the soil.
此外,上述的存储器1130中的逻辑命令可以通过软件功能单元的形式实现并作为独立的产品销售或使用时,可以存储在一个计算机可读取存储介质中。基于这样的理解,本发明的技术方案本质上或者说对现有技术做出贡献的部分或者该技术方案的部分可以以软件产品的形式体现出来,该计算机软件产品存储在一个存储介质中,包括若干命令用以使得一台计算机设备(可以是个人计算机,服务器,或者网络设备等)执行本发明各个实施例所述方法的全部或部分步骤。而前述的存储介质包括:U盘、移动硬盘、只读存储器(ROM,Read-Only Memory)、随机存取存储器(RAM,Random Access Memory)、磁碟或者光盘等各种可以存储程序代码的介质。In addition, the above-mentioned logic commands in the
本发明实施例还提供一种非暂态计算机可读存储介质,其上存储有计算机程序,该计算机程序被处理器执行时实现以执行上述各实施例提供的方法,例如包括:Embodiments of the present invention further provide a non-transitory computer-readable storage medium on which a computer program is stored, and when the computer program is executed by a processor, it is implemented to perform the methods provided by the foregoing embodiments, for example, including:
确定待检测土壤在近红外光谱扫描下的多个检测波段的原始吸光度;基于待检测土壤在特征波段的原始吸光度,确定待检测土壤的粒度修正系数;特征波段是基于多个土壤粒度下的土壤样本在近红外光谱扫描下的多个预设波段的样本原始吸光度确定的;基于待检测土壤的粒度修正系数,对待检测土壤的每一检测波段的原始吸光度进行修正,并基于修正结果确定待检测土壤的土壤参数。Determine the original absorbance of the soil to be detected in multiple detection bands under near-infrared spectral scanning; determine the particle size correction coefficient of the soil to be detected based on the original absorbance of the soil to be detected in the characteristic band; the characteristic band is based on the soil under multiple soil particle sizes. The original absorbance of the sample in multiple preset bands under near-infrared spectral scanning is determined; based on the particle size correction coefficient of the soil to be detected, the original absorbance of each detection band of the soil to be detected is corrected, and based on the correction results, the to-be-detected is determined. Soil parameters of the soil.
以上所描述的装置实施例仅仅是示意性的,其中所述作为分离部件说明的单元可以是或者也可以不是物理上分开的,作为单元显示的部件可以是或者也可以不是物理单元,即可以位于一个地方,或者也可以分布到多个网络单元上。可以根据实际的需要选择其中的部分或者全部模块来实现本实施例方案的目的。本领域普通技术人员在不付出创造性的劳动的情况下,即可以理解并实施。The device embodiments described above are only illustrative, wherein the units described as separate components may or may not be physically separated, and the components shown as units may or may not be physical units, that is, they may be located in One place, or it can be distributed over multiple network elements. Some or all of the modules may be selected according to actual needs to achieve the purpose of the solution in this embodiment. Those of ordinary skill in the art can understand and implement it without creative effort.
通过以上的实施方式的描述,本领域的技术人员可以清楚地了解到各实施方式可借助软件加必需的通用硬件平台的方式来实现,当然也可以通过硬件。基于这样的理解,上述技术方案本质上或者说对现有技术做出贡献的部分可以以软件产品的形式体现出来,该计算机软件产品可以存储在计算机可读存储介质中,如ROM/RAM、磁碟、光盘等,包括若干命令用以使得一台计算机设备(可以是个人计算机,服务器,或者网络设备等)执行各个实施例或者实施例的某些部分所述的方法。From the description of the above embodiments, those skilled in the art can clearly understand that each embodiment can be implemented by means of software plus a necessary general hardware platform, and certainly can also be implemented by hardware. Based on this understanding, the above-mentioned technical solutions can be embodied in the form of software products in essence or the parts that make contributions to the prior art, and the computer software products can be stored in computer-readable storage media, such as ROM/RAM, magnetic A disc, an optical disc, etc., includes several commands to cause a computer device (which may be a personal computer, a server, or a network device, etc.) to perform the methods described in various embodiments or some parts of the embodiments.
最后应说明的是:以上实施例仅用以说明本发明的技术方案,而非对其限制;尽管参照前述实施例对本发明进行了详细的说明,本领域的普通技术人员应当理解:其依然可以对前述各实施例所记载的技术方案进行修改,或者对其中部分技术特征进行等同替换;而这些修改或者替换,并不使相应技术方案的本质脱离本发明各实施例技术方案的精神和范围。Finally, it should be noted that: the above embodiments are only used to illustrate the technical solutions of the present invention, but not to limit them; although the present invention has been described in detail with reference to the foregoing embodiments, those of ordinary skill in the art should understand: it can still be Modifications are made to the technical solutions described in the foregoing embodiments, or some technical features thereof are equivalently replaced; and these modifications or replacements do not make the essence of the corresponding technical solutions depart from the spirit and scope of the technical solutions of the embodiments of the present invention.
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010712428.4A CN111781163B (en) | 2020-07-22 | 2020-07-22 | A method for eliminating the influence of soil particle size on the detection of soil parameters in discrete near-infrared bands |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010712428.4A CN111781163B (en) | 2020-07-22 | 2020-07-22 | A method for eliminating the influence of soil particle size on the detection of soil parameters in discrete near-infrared bands |
Publications (2)
Publication Number | Publication Date |
---|---|
CN111781163A true CN111781163A (en) | 2020-10-16 |
CN111781163B CN111781163B (en) | 2021-05-14 |
Family
ID=72763877
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202010712428.4A Active CN111781163B (en) | 2020-07-22 | 2020-07-22 | A method for eliminating the influence of soil particle size on the detection of soil parameters in discrete near-infrared bands |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN111781163B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113791041A (en) * | 2021-08-05 | 2021-12-14 | 北京农业信息技术研究中心 | Adaptive correction method and detection equipment for soil heavy metal detection equipment |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010129874A1 (en) * | 2009-05-07 | 2010-11-11 | Solum, Inc. | Measurement of nitrate-nitrogen concentration in soil based on absorption spectroscopy |
CN103134770A (en) * | 2013-02-01 | 2013-06-05 | 中国农业大学 | Method for eliminating influence on infrared spectrum detection of soil total nitrogen content from moisture |
CN105486663A (en) * | 2016-02-29 | 2016-04-13 | 上海交通大学 | Method for detecting stable carbon isotopic ratio of soil through near infrared spectrum |
CN107421911A (en) * | 2017-05-10 | 2017-12-01 | 浙江大学 | A kind of preprocess method of the soil nitrogen detection based on portable near infrared spectrometer |
WO2017223435A1 (en) * | 2016-06-23 | 2017-12-28 | The Taxas A&M University System | Vis-nir equipped soil penetrometer |
CN107607486A (en) * | 2017-09-25 | 2018-01-19 | 中国农业大学 | A kind of total soil nitrogen detection method and device |
CN108828016A (en) * | 2018-05-23 | 2018-11-16 | 北京农业智能装备技术研究中心 | A kind of self-operated measuring unit and method of the soil organism |
CN110793898A (en) * | 2019-10-22 | 2020-02-14 | 浙江大学 | Method for quantitatively analyzing spatial distribution of 3D pores with different sizes in soil column |
CN111153750A (en) * | 2020-01-03 | 2020-05-15 | 青岛农业大学 | A kind of fertilizer and detection method for promoting Suaeda salsa to repair coastal severe saline-alkali land |
-
2020
- 2020-07-22 CN CN202010712428.4A patent/CN111781163B/en active Active
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010129874A1 (en) * | 2009-05-07 | 2010-11-11 | Solum, Inc. | Measurement of nitrate-nitrogen concentration in soil based on absorption spectroscopy |
US20120147368A1 (en) * | 2009-05-07 | 2012-06-14 | Solum, Inc. | Automated Soil Measurement Device |
CN103134770A (en) * | 2013-02-01 | 2013-06-05 | 中国农业大学 | Method for eliminating influence on infrared spectrum detection of soil total nitrogen content from moisture |
CN105486663A (en) * | 2016-02-29 | 2016-04-13 | 上海交通大学 | Method for detecting stable carbon isotopic ratio of soil through near infrared spectrum |
WO2017223435A1 (en) * | 2016-06-23 | 2017-12-28 | The Taxas A&M University System | Vis-nir equipped soil penetrometer |
CN107421911A (en) * | 2017-05-10 | 2017-12-01 | 浙江大学 | A kind of preprocess method of the soil nitrogen detection based on portable near infrared spectrometer |
CN107607486A (en) * | 2017-09-25 | 2018-01-19 | 中国农业大学 | A kind of total soil nitrogen detection method and device |
CN108828016A (en) * | 2018-05-23 | 2018-11-16 | 北京农业智能装备技术研究中心 | A kind of self-operated measuring unit and method of the soil organism |
CN110793898A (en) * | 2019-10-22 | 2020-02-14 | 浙江大学 | Method for quantitatively analyzing spatial distribution of 3D pores with different sizes in soil column |
CN111153750A (en) * | 2020-01-03 | 2020-05-15 | 青岛农业大学 | A kind of fertilizer and detection method for promoting Suaeda salsa to repair coastal severe saline-alkali land |
Non-Patent Citations (6)
Title |
---|
乔星星 等: ""粒径对土壤光谱特性的影响"", 《山西农业科学》 * |
兰红 等: ""基于ArcGIS Engine的土壤氮肥空间分布成图系统"", 《农业机械学报》 * |
周鹏 等: ""基于Windows 平台的车载式土壤全氮快速检测系统软件"", 《农业机械学报》 * |
朱琦 等: ""土壤粒径对近红外光谱检测土壤养分建模的影响"", 《工业控制计算机》 * |
李民赞 等: ""基于卤钨灯光源和多路光纤的土壤全氮含量检测仪研究"", 《农业机械学报》 * |
苏芮: ""土壤粒径对麦田土壤全氮高光谱监测的影响"", 《中国优秀硕士学位论文全文数据库(电子期刊)》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113791041A (en) * | 2021-08-05 | 2021-12-14 | 北京农业信息技术研究中心 | Adaptive correction method and detection equipment for soil heavy metal detection equipment |
CN113791041B (en) * | 2021-08-05 | 2024-05-10 | 北京农业信息技术研究中心 | Self-adaptive correction method of soil heavy metal detection equipment and detection equipment |
Also Published As
Publication number | Publication date |
---|---|
CN111781163B (en) | 2021-05-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106918567B (en) | A kind of method and apparatus measuring trace metal ion concentration | |
CN108680515B (en) | Single-grain rice amylose quantitative analysis model construction and detection method thereof | |
CN110672546A (en) | A modeling method of distiller's grains model based on portable near-infrared spectrometer | |
CN105891147A (en) | Near infrared spectrum information extraction method based on canonical correlation coefficients | |
CN104062257A (en) | Method for determining total flavone content of solution based on near infrared spectroscopy | |
CN108169165B (en) | Maltose mixture quantitative analysis method based on terahertz spectrum and image information fusion | |
CN107247033B (en) | The method of identifying the maturity of Huanghua pear based on the fast decay elimination algorithm and PLSDA | |
CN110455726B (en) | Method for predicting soil moisture and total nitrogen content in real time | |
CN109540837B (en) | A method for rapid detection of lignocellulose content in ramie leaves by near infrared | |
CN111398213A (en) | A method for judging the eligibility of fermented grains model | |
CN110887800B (en) | A Data Calibration Method for Spectroscopic Water Quality Online Monitoring System | |
CN117312968A (en) | Method for predicting organic matter content of saline-alkali farmland soil | |
CN110609011A (en) | Near-infrared hyperspectral detection method and system for starch content of single-kernel corn seeds | |
CN114002162A (en) | Soil organic carbon content estimation methods, equipment, storage media and program products | |
CN110231306A (en) | A kind of method of lossless, the quick odd sub- seed protein content of measurement | |
CN116337783A (en) | Multi-point calibration method and system for gas analyzer | |
CN101769867A (en) | Nondestructive testing method for quality of compost products | |
CN119534381B (en) | Quick detection method and system for evaluating quality of sesame oil | |
CN111781163A (en) | A method for eliminating the influence of soil particle size on the detection of soil parameters in discrete near-infrared bands | |
WO2020248961A1 (en) | Method for selecting spectral wavenumber without reference value | |
CN109324018B (en) | A method for improving the accuracy of basic data for protein content modeling by near-infrared spectroscopy | |
CN111579526A (en) | A method for characterizing near-infrared instrument variance and correction | |
CN113984708B (en) | Maintenance method and device for chemical index detection model | |
CN113740293B (en) | Urea detection and analysis method and device based on near-infrared modeling | |
CN110646371A (en) | A kind of determination method of water content of tobacco flavor and fragrance |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |