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Article

The Use of Artificial Neural Networks for Determining Values of Selected Strength Parameters of Miscanthus × Giganteus

by
Sławomir Francik
1,*,
Bogusława Łapczyńska-Kordon
1,
Norbert Pedryc
1,
Wojciech Szewczyk
2,
Renata Francik
3,4 and
Zbigniew Ślipek
1,5
1
Department of Mechanical Engineering and Agrophysics, Faculty of Production Engineering and Energetics, University of Agriculture in Krakow, Balicka 120, 30-149 Krakow, Poland
2
Department of Agroecology and Plant Production, University of Agriculture in Krakow, Al. Mickiewicza 21, 31-120 Krakow, Poland
3
Department of Bioorganic Chemistry, Chair of Organic Chemistry, Jagiellonian University Medical College, 30-688 Krakow, Poland
4
Institute of Health, State Higher Vocational School, Staszica 1, 33-300 Nowy Sącz, Poland
5
Technical Institute, State Higher Vocational School, Staszica 1, 33-300 Nowy Sącz, Poland
*
Author to whom correspondence should be addressed.
Sustainability 2022, 14(5), 3062; https://doi.org/10.3390/su14053062
Submission received: 31 December 2021 / Revised: 3 February 2022 / Accepted: 3 March 2022 / Published: 6 March 2022
(This article belongs to the Special Issue Computational Intelligence for Sustainable Development)

Abstract

:
The aim of this paper is to develop neural models enabling the determination of biomechanical parameters for giant miscanthus stems. The static three-point bending test is used to determine the bending strength parameters of the miscanthus stem. In this study, we assume the modulus of elasticity bending and maximum stress in bending as the dependent variables. As independent variables (inputs of the neural network) we assume water content, internode number, maximum bending force value and dimensions characterizing the cross-section of miscanthus stem: maximum and minimum stem diameter and stem wall thickness. The four developed neural models, enabling the determination of the value of the modulus of elasticity in bending and the maximum stress in bending, demonstrate sufficient and even very high accuracy. The neural networks have an average relative error of 2.18%, 2.21%, 3.24% and 0.18% for all data subsets, respectively. The results of the sensitivity analysis confirmed that all input variables are important for the accuracy of the developed neural models—correct semantic models.

1. Introduction

At the UN Sustainable Development Summit in 2015, the 2030 Agenda for Sustainable Development with the 17 Sustainable Development Goals was adopted. Goal number 7—“Clean and affordable energy” is related to activities for the development of sustainable and modern energy—renewable energy sources.
One of the very important applications of plant (lignocellulosic) biomass is its use as a renewable energy source. The percentage share of cellulose, hemicellulose and lignin in a given type of biomass may vary, which significantly affects its energy parameters and the possibility of using it for the production of biofuels [1]. Research is carried out on woody [2,3,4] and herbaceous biomass [5], but also pomaces, fruit stones, kernel shells and other residuals [6,7,8,9], and recently on so-called water biomass (algae) [10,11].
The giant miscanthus (miscanthus × giganteus) is one of the most productive plant species, which, thanks to the fast and abundant biomass production, can provide the required amounts of the raw material. It is characterized by a high biomass production potential, which means that it is used to establish industrial biomass plantations throughout Europe and the USA [12,13,14,15]. Giant miscanthus can be successfully used in the production of compact solid biofuels [16,17,18,19], biogas and bioethanol [20,21,22]. Miscanthus’ biomass is used in the production of technical papers, cardboard, packaging plywood or fibers for lining packaging. It can also be a substitute for plastics in the production of packaging [23]. Studies are carried out on miscanthus fibers to develop renewable construction materials—lightweight concrete [24].
The necessity to determine the mechanical properties of materials of plant origin is crucial in the process of designing specific machines for their processing, as well as in the selection of optimal conditions for their operation. It is difficult because the mechanical properties of these types of materials change depending on the environmental conditions (e.g., water content). The results of research on the biomechanical properties of industrial plant stems are used in designing better and more efficient biomass processing equipment (e.g., harvesting and grinding machines) [25,26,27,28,29,30,31,32]. Biomechanical properties can also be used as a selection criterion in a plant breeding program—assessing and adjusting stem mechanical traits may improve stem lodging resistance [33].
Typical laboratory tests aimed at determining the biomechanical properties of plant stems include: bending tests [27,28,29,33,34,35,36], compression tests along or across the stem [36,37], tensile tests [27,32,36], shearing tests [27,29,36] and cutting tests [26,27,28].
In the case of bending, the typical strength parameters determined in the studies of stems of various plants are the modulus of elasticity for bending [27,29,34,35,38] and maximum stress in bending [29,36,38], while the results of the studies conducted so far clearly confirm the influence of the water content and the internode on the values of these strength parameters [27,29,34,35].
Artificial neural network (ANN) is a robust data-modeling tool that is widely used in many applications, such as regression, classification and approximation-based learning processes. Implementation of artificial neural networks for different research proved to be very efficient and accurate. ANNs are characterized by very high accuracy in comparison with other models in certain applications [39,40,41,42,43,44,45].
ANNs are used in various scientific fields, including bioinformatics, biochemistry, medicine, meteorology, economic sciences, robotics, aquaculture, food security and climatology. An example of that is the use of ANNs to approximate the gas volumetric percentage in a gas-oil two phase flow [46]. Multilayer perceptron type ANNs have been used as well to enhance the spatial resolution in detector modules constituting the PET (positron emission tomography) scanner [47]. Artificial neural networks are also used in agriculture, agrophysics or agricultural engineering [16,40,41,43,44,45,48,49,50,51,52,53,54,55,56].
Many ANN applications are related to renewable energy sources (different uses of ANN models for better energy production predictions). Research addresses, for example, the use of ANNs to forecast solar radiation (the main problem for the best use of photovoltaic systems) and wind power forecasting [57,58,59,60,61].
In the field of engineering, ANN was used, among others, to detect accidental damage to the support bearings on the assembly conveyor [62] and to predict tool wear and surface roughness during turning [63]. Several papers have used ANNs to predict paper properties in order to achieve a high-performance process [64].
There are many uses of artificial neural networks in agriculture [49]. The multilayer perceptron neural network was developed to predict the normalized shear strength of organic soils without drainage [65]. ANNs are also employed to control and predict variables in agricultural drying processes, e.g., to identify the dynamics of said processes for tomato, tobacco and willow woodchips [45,66]. Feed-forward artificial neural networks were used to predict energy consumption in closed production plant systems [67]. One very important application area of artificial neural networks in agriculture is the modeling of the greenhouse environment (the greenhouse system is non-linear and variable with time) [68]. Many greenhouse environment predictive models [49,69,70,71,72,73], as well as greenhouse environment and greenhouse energy consumption control systems [74,75,76], have been developed.
The diversification of artificial neural networks applications is large, demonstrating the importance of this tool. They achieve high accuracy, are computationally efficient, and require no knowledge of the physical relationships between inputs and outputs [16,42,43,44,45,49,77,78,79,80,81].
The aim of the paper was to develop neural models enabling the determination of biomechanical parameters for giant miscanthus stems.
In the literature no information has been found on the creation of neural models for determining biomechanical parameters of plant stems, so our approach is innovative.

2. Materials and Methods

2.1. Gathering Experimental Data

The plant material used for the research (miscanthus stalks) was harvested in February and March. Samples were taken from individual internodes of miscanthus stalks (Figure 1a), then, the dimensions of the cross-section for each sample were determined (Figure 1b) and subjected to three-point bending strength tests (Figure 1c). Three-point bending tests were carried out in the laboratory of the Department of Mechanical Engineering and Agrophysics. The water content of miscanthus stalks was determined with the drying method, independently for each internode.
The static three-point bending test was used to determine the bending strength parameters of the miscanthus stem. The elliptical shape of the miscanthus stalk cross-section was adopted.
The modulus of elasticity for bending (MOEbend) and maximum stress in bending (σbend) for miscanthus stem was calculated from the equations:
MOE bend = Δ F bend · L 3 48 · I major · Δ f = ( F bend 2 F bend 1 ) · L 3 12 · π · ( f 2 f 1 ) · ( a 3 · b a 1 3 · b 1 )
σ bend   max = M bendmax · a I major = F bend · L · a π · ( a 3 · b a 1 3 · b 1 )
where:
  • MOEbend—modulus of elasticity bending (MPa),
  • ΔFbend—change in the value of the bending force in the range of the linear characteristic (N),
  • L—distance between supports (mm),
  • Imajor—moment of inertia around neutral axis (ellipse major axis) (mm4),
  • Δf—the deflection of the stem in the range of the linear characteristic (mm),
  • Fbend1—value of the initial bending force (N),
  • Fbend2—value of the main bending force (N),
  • f1—initial deflection of the stem (mm),
  • f2—stem deflection for Fbend2 (mm),
  • a—the length of the semi-minor axis of the ellipse (mm),
  • b—the length of the semi-major axis of the ellipse (mm),
  • a1—the semi-minor axis of the ellipse a minus the stalk wall thickness g (mm),
  • b1—the semi-major axis of the ellipse b minus the stalk wall thickness g (mm).
  • σbend max—maximum stress in bending (MPa),
  • Mbendmax—maximum bending moment about neutral axis (N·mm),
  • Imajor—moment of inertia around neutral axis (ellipse major axis), (mm4),
  • Fbend—maximum bending force value (N).
The static three-point bending tests of the stalks were performed in replicates of 15 for each of the five internodes and for each of the two humidities.

2.2. Semantic Models Formulation

The creation of an ANN model begins with adopting a semantic–conceptual model. Such a model should be logically resemble to the theory describing modeled phenomenon in the form of a system of objects and relations between them.
In the case of models using artificial neural networks, the development of a semantic model requires the selection of independent variables (network inputs) and dependent variable or variables (network outputs). If the goal is to determine the value of several dependent variables, better results are obtained by developing several neural models (one ANN for each variable) than one model with several outputs.
In this study, we assumed the modulus of elasticity bending and maximum stress in bending as the dependent variables (biomechanical parameters characterizing the strength of the miscanthus stem).
As independent variables (inputs of the neural network), we assumed water content Wcont, internode number NrNod, maximum bending force value Fbend and dimensions characterizing the cross-section of miscanthus stem: maximum stem diameter Dstem Max, minimum stem diameter Dstem min and stem wall thickness Thstem wall.
Four semantic models were formulated:
Model A: MOEbend = f (Wcont, NrNod, Dstem Max, Dstem min, Thstem wall),
Model B: σbend = f (Wcont, NrNod, Dstem Max, Dstem min, Thstem wall),
Model C: MOEbend = f (Wcont, NrNod, Dstem Max, Dstem min, Thstem wall, Fbend),
Model D: σbend = f (Wcont, NrNod, Dstem Max, Dstem min, Thstem wall, Fbend),
where:
  • MOEbend—modulus of elasticity bending (MPa),
  • σbend—maximum stress in bending (MPa),
  • Wcont—water content (kgwater·kgdry mass−1),
  • NrNod—internode number (-),
  • Dstem Max—maximum stem diameter (mm),
  • Dstem min—minimum stem diameter (mm),
  • Thstem wall—stem wall thickness (mm),
  • Fbend—maximum bending force value (N).
Semantic models A and B allow one to determine the values of the modulus of elasticity bending and maximum stress in bending without performing a three-point bending test. However, an additional variable introduced in models C and D (Fbend—maximum bending force value) requires an endurance test.

2.3. Selecting Neural Network’s Type and Carrying Out the Process of Learning

In preliminary studies, the accuracy of models using two different types of feed-forward ANNs—multilayer radial basis function networks and multilayer perceptron neural networks (MLP) networks were checked. As MLP networks demonstrated much greater accuracy in further research, only this type of network was used.
The number of neurons in the input and output layers is determined by the number of inputs and outputs from the neural network. In our research, the number of neurons in the input layer was 5 (for models A and B) and 6 (for models C and D), while there was 1 neuron in the output layer. The number of neurons in the hidden layer was changed from 3 to 11 in the course of a repeated process of network learning.
The development of neural models was performed using the specialized software Statistica Neural Networks (Dell Inc. (2016). Dell Statistica (data analysis software system), version 13, StatSoft, Inc., Tulsa, OK, USA). To obtain as accurate models as possible, we applied the procedure of multiple repeats using the function “Automatic Designer”. Such a procedure allows for obtaining accurate neural models, as the ANN learning process is stochastic.
For each of the four semantic models (Equations (3)–(6)), 100 ANNs with different architectures were developed, with the 10 most accurate networks for each of the four semantic models retained for further analysis.
The entire data set obtained from the measurements, consisting of 1050 patterns (7 water content, 10 internodes and 15 repetitions for each Wcont value and each internode) was randomly divided into learning, testing and validation subsets.
The learning subset is used to create neural models in the ANNs’ learning process. The other two subsets are not used in the learning process. The test subset is used to select the best ANNs, while the validation subset is used to assess the ability to generalize the acquired knowledge by the ANN—it allows one to assess the accuracy of the neural network for completely new data.
The division was carried out for groups of measurements—for the individual values of Wcont and NrNod (Figure 2), assuming that 70% are learning subset, 15% testing subset and 15% validation subset:
  • learning subset: Wcont = 0.219 (NrNod = 1, 2, 4, 7, 9); Wcont = 0.226 (NrNod = 1, 2, 4, 5, 6, 8, 9); Wcont= 0.298 (NrNod = 1, 4, 5, 6, 7, 8, 10); Wcont = 0.388 (NrNod = 1, 2, 3, 4, 5, 7, 8, 9, 10); Wcont = 0.412 (NrNod = 1, 2, 3, 6, 8, 9); Wcont = 0.470 (NrNod = 1, 2, 3, 5, 6, 8, 9, 10); Wcont = 0.481 (NrNod = 1, 2, 3, 5, 6, 8, 9, 10);
  • testing subset: Wcont = 0.219 (NrNod = 3, 6, 8); Wcont = 0.226 (NrNod = 3); Wcont = 0.388 (NrNod = 6); Wcont = 0.412 (NrNod = 4, 5, 7); Wcont = 0.470 (NrNod = 4, 7);
  • validation subset: Wcont = 0.219 (NrNod = 5); Wcont = 0.226 (NrNod = 7, 10); Wcont = 0.298 (NrNod = 2, 3, 9); Wcont = 0.412 (NrNod = 10); Wcont = 0.481 (NrNod = 4, 7).
In the learning process, four different activation functions were used: linear, logistic, hyperbolic tangent and exponential. The BFGS (Broyden-Fletcher-Goldfarb-Shanno) algorithm was used in the learning process. The BFGS algotithm is a quasi-Newton optimization method, which provides good convergence and is the most recommended technique for training neural networks [82,83,84].

2.4. Choosing and Assessing the Best Neural Models

As the criterion for selecting the best ANN, the value of root mean-square error (RMSE) was selected for testing the data subset, independently for the four adopted semantic models, calculated according to the formula:
RMSE = 1 n i = 1 n ( Y M E , i Y A N N , i ) 2
where:
  • RMSE—root mean-square error (MPa),
  • YME,i—measured value of output (MPa),
  • YANN,i—calculated by ANN value of output (MPa),
  • n—number of observations (-).
RSME is a commonly used statistical error to evaluate the model’s performance [54,73,75,85].
For the analysis of selected neural models, the mean absolute percentage error (MAPE) was used:
MAPE = 1 n i = 1 n | Y M E , i Y A N N , i Y M E , i | · 100 %
where:
  • MAPE—mean absolute percentage error (%),
  • |…|—absolute value (-).
  • YME,i—measured value of output (MPa),
  • YANN,i—calculated by ANN value of output (MPa),
  • n—number of observations (-).
In order to evaluate the assumed independent variables in the semantic models, a sensitivity analysis was performed for selected neural models. Sensitivity analysis, based on the value of the error quotient, allows one to determine which variables in the model are important for its accuracy. The greater the value of this quotient, the more important the input field is for the accuracy of the model.

3. Results

Figure 3, Figure 4, Figure 5 and Figure 6 summarize the RMSE values for all developed neural networks for the testing subsets. Based on these values, the best neural networks were selected. RMSE values for all subsets of data (learning, testing and validation) are provided in Appendix A (Figure A1, Figure A2, Figure A3 and Figure A4).
For the MOEbend variable, for the testing subset, the smallest RMSE error value = 78 MPa was calculated for the annA05 MLP 5-11-1 neural network (Figure 3). For σbend, the smallest error for the testing subset (RMSE = 3.9 MPa) was calculated for the annB01 MLP 5-11-1 network (Figure 4). For the neural networks developed in accordance with the C semantic model, the lowest RMSE value = 77 MPa for the testing subset was obtained for annC09 MLP 6-7-1 (Figure 5). The developed neural networks in accordance with the semantic model D, which allow for the determination of σbend, achieved very high accuracy. The minimum RMSE error value = 0.20 MPa (for the testing subset) had annD03 MLP 6-10-1 (Figure 6). The above neural networks were selected as the best and subjected to further analysis.
Figure 7 summarizes the MAPE error values for the selected four best neural models for the learning, testing and validation data subsets. MAPE values for all developed neural networks are included in Appendix B (Figure A5, Figure A6, Figure A7 and Figure A8).
The sensitivity analysis results for selected neural networks annA05, annB01, annC09 and annD03 are presented in Table 1 and Table 2 (for validation subset). Error ratio values (greater than 1) indicate that all adopted semantic models A, B, C and D are correct.
Table 3 lists the architecture, training algorithm and activation functions of the selected ANNs.
Figure 8 and Figure 9 show the MAPE error values for selected (best) models developed in accordance with the semantic models A, B, C and D (annA05, annC09, annB01 and annD03), for validation subsets. MAPE errors were calculated for individual measurement conditions—for the set levels of the independent variables Wcont and NrNod.
In Appendix C (Figure A9, Figure A10, Figure A11 and Figure A12), MAPE error values for all data subsets (learning, testing and validation) were compiled.

4. Discussion

Based on the conducted sensitivity analysis, it was demonstrated that four semantic models were correctly adopted—all input variables are important for the accuracy of selected neural models (annA05, annB01, annC09 and annD03).
For the annA05 network, which enables the determination of modulus of elasticity in bending (MOEbend) value, the values of the error quotient (Table 1) demonstrated that the most important inputs of the neural network are the minimum diameter of the stalk (Dstem min) and the thickness of the stalk wall (Thstem wall).
For the annC09 network (Table 2), the most important inputs of the neural network are the minimum diameter of the stalk (Dstem min). The internode number (NrNod) came second, and the maximum bending force (Fbend Max) came third as an additional network input compared to annA05.
A slightly different ranking of the neural network inputs occurred in the case of the annB01 model (Table 1), which made it possible to determine the maximum bending stress (σbend). The most important input (the highest value of the error quotient) is the stalk wall thickness (Thstem wall), followed by the minimum diameter of the stalk (Dstem min) and the water content (Wcont).
However, for the annD03 model, in which the maximum bending force was introduced as an additional network input, the ranking of the inputs is also different (Table 2). The first is Fbend Max, with 2.5 times the error quotient value compared to the second Dstem min, and about four times greater than the third Dstem Max. NrNod and Wcont, which are fifth and sixth in the ranking and have error quotient values several thousand times lower than Fbend Max.
Such order is understandable because the geometric dimensions of the cross-section of the stalk, which is a biocomposite pipe with an oval cross-section, determine the value of the moment of inertia that is used to calculate the modulus of elasticity and the maximum bending stress (σbend). The value of Fbend Max appears in the formula for calculating σbend. The significant influence of NrNod on the value of MOEbend may result from the fact that the internodes are formed by the miscanthus gradually, from the lowest to the highest. On the other hand, the influence of water content on biomechanical parameters of plants has been demonstrated in many studies.
Neural networks used to determine MOEbend, developed in accordance with the semantic models A and C, are characterized by similar accuracy. The MAPE error values are similar for the validation subset: 2.2–2.4% and 1.9–2.4% (Appendix B: Figure A5 and Figure A7). The MAPE values for the learning subset are at a similar level, and slightly higher for the testing subset (2.4–2.9%). The best ANNs selected (annA05 and annC09) have almost identical MAPE error values: 1.8% and 1.9% for the learning subset, 2.4% and 2.5% for the testing subset, and 2.3% and 2.2% for the validation subset (Figure 7).
Taking into account such small differences in errors between these ANNs and the fact that with the annC09 model it is necessary to carry out an endurance test in order to determine the Fbend Max value, the annA05 network is the more appropriate one. To determine the MOEbend value with similar accuracy, annA05 requires only knowledge of the dimensions of the stalk cross-sectional dimensions, internode number and water content.
In the case of neural models used to determine the σbend value (developed in accordance with the B and D semantic models), the differences in the MAPE error values are much greater.
For B-type neural networks, the MAPE error for the validation subset varies from 3.7% to 4.7% and for D models it is about 10 times smaller—from 0.20% to 0.44% (Appen-dix B: Figure A6 and Figure A8). The best-selected models (annB01 and annD03) have MAPE error values of 2.7% and 0.16% for the learning subset, 3.0% and 0.17% for the testing subset and 4.1% and 0.20% for the validation subset (Figure 7).
Such significant differences in the error values between the annB01 and annD03 networks mean that the annD03 network is the recommended model for determining the σbend value, despite the need to perform a bending test.
Figure 8 and Figure 9 enable detailed MAPE error analysis for selected models (annA05, annC09, annB01 and annD03), for validation data subset. The MAPE values calculated for individual Wcont and NrNod values (measurement conditions) were summarized—in groups of 15 repetitions. It can be determined for which water contents and internode numbers the ANNs are least accurate.
The MAPE errors for MOEbend-determining ANNs (Figure 8) are similar for both models (annA05 and annC09). In the case of the validation subset, these errors are smaller for high water contents (Wcont = 0.412 kgwater·kgdry mass−1 and 0.481 kgwater·kgdry mass−1). The maximum MAPE for annC09 (3.7%) is only slightly lower than that for annA05 (4.1%).
The highest value of MAPE for annA05 occurs for NrNod = 3 and Wcont = 0.412 kgwater·kgdry mass−1 (learning subset) and amounts to 6.4% (Appendix C, Figure A9). In addition, for annC09, the highest value of MAPE occurs for NrNod = 3 and Wcont = 0.412 kgwater·kgdry mass−1 and amounts to 6.7% (Appendix C, Figure A11). As there is the same “measuring point”, it can be concluded that the increase in error is the result of a particularly large data noise.
The most even distribution of MAPE values occurs for Wcont = 0.388 kgwater·kgdry mass−1, for annA05 from 0.7% to 2.6% (Appendix C, Figure A11) and for annC09 from 0.9% to 2.4% (Appendix C, Figure A11). On the other hand, the least uniform distribution of MAPE values was found for Wcont = 0.412 kgwater·kgdry mass−1, for both neural models. The spread of values is almost identical: for annA05 from 0.8% to 6.4%, and for annC09 from 0.7% to 6.7%.
The above analysis demonstrates that both developed neural models (annA05 and annC09) are similar in terms of error values for different Wcont and NrNod values. They are most accurate at Wcont = 0.388 kgwater·kgdry mass−1, for all internodes.
The MAPE errors for σbend-determining ANNs (Figure 9) are very different for both models (annB01 and annD03). In the case of the validation set, for annB01, these errors are smaller for high water contents (Wcont = 0.412 kgwater·kgdry mass−1 and 0.481 kgwater·kgdry mass−1). The maximum MAPE for annB01 is 9.2% and the lowest is 1.7% (Figure 9a). For annD03, the MAPE values are much smaller. For the validation set, the highest value is 0.31% and the lowest 0.13% (Figure 9b).
The highest MAPE value for annB01 occurs for NrNod = 5 and Wcont = 0.219 kgwater·kgdry mass−1 (validation subset) and amounts to 9.2% (Appendix C, Figure A10). On the other hand, for annD03, the highest MAPE value occurs for NrNod = 4 and Wcont = 0.470 kgwater·kgdry mass−1 (testing subset) and is 0.33% (Appendix C, Figure A12).
The most even distribution of MAPE values occurs for Wcont = 0.470 kgwater·kgdry mass−1, for annB01 from 2.2% to 3.7% (Appendix C, Figure A10), and for Wcont = 0.412 kgwater·kgdry mass−1, for annD03 from 0.12% to 0.20% (Appendix C, Figure A12). On the other hand, the least uniform distribution of MAPE values was found for Wcont = 0.219 kgwater·kgdry mass−1, for both neural models. The spread of values is: for annB01 from 2.1% to 9.2%, and for annD03 from 0.08% to 3.1%.

5. Conclusions

The four developed neural models, enabling the determination of the value of the modulus of elasticity in bending (annA05 and annC09) and the maximum stress in bending (annB01 and annD03), demonstrate sufficient and even very high accuracy. The neural networks, annA05, annC09 and annB01, respectively, have an average relative error of 2.18%, 2.21% and 3.24% for all data subsets. On the other hand, the average relative error for annD03 is an order of magnitude lower and amounts to 0.18%.
The results of the sensitivity analysis confirmed that all input variables are important for the accuracy of the developed neural models—correct semantic models.
To determine the MOEbend value, we propose the annA05 neural model, which requires only knowledge of the dimensions of the stalk cross-section, internode number and water content (the annC09 model is just as accurate but requires a three-point bending test). However, for the determination of the value of σbend, we propose the neural model annD03, which is about 18 times more accurate than annB01, although it has an additional input variable (Fbend obtained from the three-point bending test).
Our further research will be conducted towards increasing the operability of ANNs models used to determine the biomechanical parameters of miscanthus. We will try to develop a tool that will reduce the need to carry out labor-intensive strength tests when determining the MOEbend and σbend values for individual parts of the stem (individual internodes).

Author Contributions

Conceptualization, S.F. and Z.Ś.; methodology, S.F. and B.Ł.-K.; software, S.F. and N.P.; validation, S.F., W.S., R.F. and Z.Ś.; investigation, B.Ł.-K. and R.F.; data curation, S.F. and R.F.; writing—original draft preparation, S.F. and R.F.; writing—review and editing, S.F., B.Ł.-K., N.P., W.S. and Z.Ś.; visualization, N.P., W.S. and R.F.; supervision, S.F. and B.Ł.-K. All authors have read and agreed to the published version of the manuscript.

Funding

Article processing charges were financed from the subsidy of the Ministry of Education and Science for the Agricultural University of Hugo Kołłątaj in Krakow for the year 2022.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data is contained within the article.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A

Figure A1. RMSE error values for the MOEbend dependent variable, for the semantic model A (ANN with 5 inputs) for the learning, testing and validation data subsets.
Figure A1. RMSE error values for the MOEbend dependent variable, for the semantic model A (ANN with 5 inputs) for the learning, testing and validation data subsets.
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Figure A2. RMSE error values for the σbend dependent variable, for the semantic model B (ANN with 5 inputs) for learning, testing and validation data.
Figure A2. RMSE error values for the σbend dependent variable, for the semantic model B (ANN with 5 inputs) for learning, testing and validation data.
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Figure A3. RMSE error values for the MOEbend dependent variable, for the semantic model C (ANN with 6 inputs) for learning, testing and validation data.
Figure A3. RMSE error values for the MOEbend dependent variable, for the semantic model C (ANN with 6 inputs) for learning, testing and validation data.
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Figure A4. RMSE error values for the σbend dependent variable, for the semantic model D (ANN with 6 inputs) for learning, testing and validation data.
Figure A4. RMSE error values for the σbend dependent variable, for the semantic model D (ANN with 6 inputs) for learning, testing and validation data.
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Appendix B

Figure A5. MAPE error values for the MOEbend dependent variable, for the semantic model A (ANN with 5 inputs) for learning, testing and validation data.
Figure A5. MAPE error values for the MOEbend dependent variable, for the semantic model A (ANN with 5 inputs) for learning, testing and validation data.
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Figure A6. MAPE error values for the σbend dependent variable, for the semantic model B (ANN with 5 inputs) for learning, testing and validation data.
Figure A6. MAPE error values for the σbend dependent variable, for the semantic model B (ANN with 5 inputs) for learning, testing and validation data.
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Figure A7. MAPE error values for the MOEbend dependent variable, for the semantic model C (ANN with 6 inputs) for learning, testing and validation data.
Figure A7. MAPE error values for the MOEbend dependent variable, for the semantic model C (ANN with 6 inputs) for learning, testing and validation data.
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Figure A8. MAPE error values for the σbend dependent variable, for the semantic model D (ANN with 6 inputs) for learning, testing and validation data.
Figure A8. MAPE error values for the σbend dependent variable, for the semantic model D (ANN with 6 inputs) for learning, testing and validation data.
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Appendix C

Figure A9. MAPE error values for the MOEbend dependent variable for annA05 (MLP 5-11-1), depending on the internode number (NrNod) and water content (Wcont). Testing data: Wcont = 0.219 (NrNod = 3, 6, 8); Wcont = 0.226 (NrNod = 3); Wcont = 0.388 (NrNod = 6); Wcont = 0.412 (NrNod = 4, 5, 7); Wcont = 0.470 (NrNod = 4, 7). Validation data: Wcont = 0.219 (NrNod = 5); Wcont = 0.226 (NrNod = 7, 10); Wcont = 0.298 (NrNod = 2, 3, 9); Wcont = 0.412 (NrNod = 10); Wcont = 0.481 (NrNod = 4, 7). The remaining values not mentioned are the learning data subset.
Figure A9. MAPE error values for the MOEbend dependent variable for annA05 (MLP 5-11-1), depending on the internode number (NrNod) and water content (Wcont). Testing data: Wcont = 0.219 (NrNod = 3, 6, 8); Wcont = 0.226 (NrNod = 3); Wcont = 0.388 (NrNod = 6); Wcont = 0.412 (NrNod = 4, 5, 7); Wcont = 0.470 (NrNod = 4, 7). Validation data: Wcont = 0.219 (NrNod = 5); Wcont = 0.226 (NrNod = 7, 10); Wcont = 0.298 (NrNod = 2, 3, 9); Wcont = 0.412 (NrNod = 10); Wcont = 0.481 (NrNod = 4, 7). The remaining values not mentioned are the learning data subset.
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Figure A10. MAPE error values for the σbend dependent variable for annB01 (MLP 5-11-1), depending on the internode number (NrNod) and water content (Wcont). Testing data: Wcont = 0.219 (NrNod = 3, 6, 8); Wcont = 0.226 (NrNod = 3); Wcont = 0.388 (NrNod = 6); Wcont = 0.412 (NrNod = 4, 5, 7); Wcont = 0.470 (NrNod = 4, 7). Validation data: Wcont = 0.219 (NrNod = 5); Wcont = 0.226 (NrNod = 7, 10); Wcont = 0.298 (NrNod = 2, 3, 9); Wcont = 0.412 (NrNod = 10); Wcont = 0.481 (NrNod = 4, 7). The remaining values not mentioned are the learning data subset.
Figure A10. MAPE error values for the σbend dependent variable for annB01 (MLP 5-11-1), depending on the internode number (NrNod) and water content (Wcont). Testing data: Wcont = 0.219 (NrNod = 3, 6, 8); Wcont = 0.226 (NrNod = 3); Wcont = 0.388 (NrNod = 6); Wcont = 0.412 (NrNod = 4, 5, 7); Wcont = 0.470 (NrNod = 4, 7). Validation data: Wcont = 0.219 (NrNod = 5); Wcont = 0.226 (NrNod = 7, 10); Wcont = 0.298 (NrNod = 2, 3, 9); Wcont = 0.412 (NrNod = 10); Wcont = 0.481 (NrNod = 4, 7). The remaining values not mentioned are the learning data subset.
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Figure A11. MAPE error values for the MOEbend dependent variable for annC09 (MLP 6-7-1), depending on the internode number (NrNod) and water content (Wcont). Testing data: Wcont = 0.219 (NrNod = 3, 6, 8); Wcont = 0.226 (NrNod = 3); Wcont = 0.388 (NrNod = 6); Wcont = 0.412 (NrNod = 4, 5, 7); Wcont = 0.470 (NrNod = 4, 7). Validation data: Wcont = 0.219 (NrNod = 5); Wcont = 0.226 (NrNod = 7, 10); Wcont = 0.298 (NrNod = 2, 3, 9); Wcont = 0.412 (NrNod = 10); Wcont = 0.481 (NrNod = 4, 7). The remaining values not mentioned are the learning data subset.
Figure A11. MAPE error values for the MOEbend dependent variable for annC09 (MLP 6-7-1), depending on the internode number (NrNod) and water content (Wcont). Testing data: Wcont = 0.219 (NrNod = 3, 6, 8); Wcont = 0.226 (NrNod = 3); Wcont = 0.388 (NrNod = 6); Wcont = 0.412 (NrNod = 4, 5, 7); Wcont = 0.470 (NrNod = 4, 7). Validation data: Wcont = 0.219 (NrNod = 5); Wcont = 0.226 (NrNod = 7, 10); Wcont = 0.298 (NrNod = 2, 3, 9); Wcont = 0.412 (NrNod = 10); Wcont = 0.481 (NrNod = 4, 7). The remaining values not mentioned are the learning data subset.
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Figure A12. MAPE error values for the σbend dependent variable for annD03 (MLP 6-10-1), depending on the internode number (NrNod) and water content (Wcont). Testing data: Wcont = 0.219 (NrNod = 3, 6, 8); Wcont = 0.226 (NrNod = 3); Wcont = 0.388 (NrNod = 6); Wcont = 0.412 (NrNod = 4, 5, 7); Wcont = 0.470 (NrNod = 4, 7). Validation data: Wcont = 0.219 (NrNod = 5); Wcont = 0.226 (NrNod = 7, 10); Wcont = 0.298 (NrNod = 2, 3, 9); Wcont = 0.412 (NrNod = 10); Wcont = 0.481 (NrNod = 4, 7). The remaining values not mentioned are the learning data subset.
Figure A12. MAPE error values for the σbend dependent variable for annD03 (MLP 6-10-1), depending on the internode number (NrNod) and water content (Wcont). Testing data: Wcont = 0.219 (NrNod = 3, 6, 8); Wcont = 0.226 (NrNod = 3); Wcont = 0.388 (NrNod = 6); Wcont = 0.412 (NrNod = 4, 5, 7); Wcont = 0.470 (NrNod = 4, 7). Validation data: Wcont = 0.219 (NrNod = 5); Wcont = 0.226 (NrNod = 7, 10); Wcont = 0.298 (NrNod = 2, 3, 9); Wcont = 0.412 (NrNod = 10); Wcont = 0.481 (NrNod = 4, 7). The remaining values not mentioned are the learning data subset.
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Table A1. Weights and biases between the input layer and the hidden layer as well as those between the hidden layer and the output layer for the annA05 neural network.
Table A1. Weights and biases between the input layer and the hidden layer as well as those between the hidden layer and the output layer for the annA05 neural network.
Weights and Biases between
Input and Hidden Layers
Weights and Biases between
Hidden and Output Layers
Connections Connections
Input
Neuron
Hidden
Neuron
WeightsHidden
Neuron
Output
Neuron
Weights
Wcont1−1.90461MOEbend−2.0160
NrNod2.4885
Dsteam Max−2.7905
Dstem min3.1284
Thsteam3.6997
Bias−4.6094
Wcont21.77572MOEbend−0.3861
NrNod−10.4613
Dsteam Max3.1509
Dstem min2.6889
Thsteam6.5689
Bias3.5696
Wcont3−2.74733MOEbend−0.1412
NrNod−9.5350
Dsteam Max3.8914
Dstem min−1.6132
Thsteam9.4627
Bias2.6229
Wcont43.05434MOEbend−1.2546
NrNod−12.4148
Dsteam Max2.8839
Dstem min1.8528
Thsteam1.6986
Bias−3.9850
Wcont5−2.97335MOEbend9.3524
NrNod−12.8446
Dsteam Max−4.5719
Dstem min3.5891
Thsteam3.6138
Bias−5.1506
Wcont61.74906MOEbend0.3699
NrNod−4.3593
Dsteam Max2.5651
Dstem min3.7031
Thsteam4.6927
Bias−0.8075
Wcont7−2.83697MOEbend−2.1642
NrNod1.9192
Dsteam Max0.7166
Dstem min1.3162
Thsteam2.5379
Bias−5.0349
Wcont80.79758MOEbend−8.6974
NrNod−8.7901
Dsteam Max0.6474
Dstem min6.1603
Thsteam3.5364
Bias−11.3223
Wcont96.30979MOEbend−2.8854
NrNod−0.9085
Dsteam Max4.1519
Dstem min0.0516
Thsteam−4.4881
Bias3.2790
Wcont102.688110MOEbend2.3047
NrNod−8.4866
Dsteam Max1.7032
Dstem min0.7164
Thsteam−1.2511
Bias−2.2674
Wcont111.352711MOEbend−0.5312
NrNod0.3887
Dsteam Max5.3995
Dstem min0.9965
Thsteam−3.0340
Bias−2.9259
---BiasMOEbend2.9477
Table A2. Weights and biases between the input layer and the hidden layer as well as those between the hidden layer and the output layer for the annD03 neural network.
Table A2. Weights and biases between the input layer and the hidden layer as well as those between the hidden layer and the output layer for the annD03 neural network.
Weights and Biases between
Input and Hidden Layers
Weights and Biases between
Hidden and Output Layers
Connections Connections
Input
Neuron
Hidden
Neuron
WeightsHidden
Neuron
Output
Neuron
Weights
Wcont10.461611σbend1.52045
NrNod−0.03784
Dsteam Max−0.60342
Dstem min−2.48068
Thsteam−1.42360
Fbend Max1.11253
Bias−1.53380
Wcont20.900752σbend0.65696
NrNod−0.34368
Dsteam Max0.30125
Dstem min0.99976
Thsteam−0.25100
Fbend Max1.38583
Bias0.64301
Wcont30.116743σbend−2.56040
NrNod0.07561
Dsteam Max−0.10368
Dstem min−0.30686
Thsteam0.09658
Fbend Max−0.84279
Bias−0.83605
Wcont40.132374σbend−3.48714
NrNod−0.32838
Dsteam Max−0.52042
Dstem min−1.88645
Thsteam−1.19246
Fbend Max−3.61781
Bias−1.60437
Wcont50.077775σbend1.87011
NrNod0.21921
Dsteam Max−0.30698
Dstem min−0.54980
Thsteam0.01191
Fbend Max−0.10285
Bias0.50076
Wcont6−0.086136σbend−1.25730
NrNod0.30877
Dsteam Max0.06363
Dstem min0.35557
Thsteam−0.08044
Fbend Max−0.14423
Bias−0.38527
Wcont7−0.106447σbend4.13679
NrNod−0.10213
DsteamMax−1.39496
Dstemmin−1.47598
Thsteam−5.34947
Fbend Max3.03086
Bias−2.17910
Wcont8−0.674968σbend0.58499
NrNod0.36754
DsteamMax−0.50233
Dstemmin−0.30770
Thsteam−1.25587
Fbend Max−0.01521
Bias0.30264
Wcont9−0.314649σbend−0.64292
NrNod0.43811
DsteamMax−1.29949
Dstemmin−0.88291
Thsteam−1.54375
Fbend Max−2.38035
Bias−1.57620
Wcont100.3396610σbend−1.66961
NrNod−0.10133
DsteamMax1.85831
Dstemmin3.92750
Thsteam−0.52006
Fbend Max−1.86429
Bias1.13502
---Biasσbend1.16164

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Figure 1. Diagram of the performed research: (a) Scheme of miscanthus stem and internodes from which the samples were taken; (b) stand for determining the characteristic dimensions of samples: Dmin—minimum stalk diameter, Dmax—maximum stalk diameter and g—stalk wall thickness; (c) a scheme of a three-point bending test; (d) development of artificial neural networks.
Figure 1. Diagram of the performed research: (a) Scheme of miscanthus stem and internodes from which the samples were taken; (b) stand for determining the characteristic dimensions of samples: Dmin—minimum stalk diameter, Dmax—maximum stalk diameter and g—stalk wall thickness; (c) a scheme of a three-point bending test; (d) development of artificial neural networks.
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Figure 2. Division of data into individual subsets: L—learning subset; T—testing subset; V—validation subset.
Figure 2. Division of data into individual subsets: L—learning subset; T—testing subset; V—validation subset.
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Figure 3. RMSE error values for the MOEbend dependent variable, for the semantic model A (ANN with 5 inputs) for the testing data subset.
Figure 3. RMSE error values for the MOEbend dependent variable, for the semantic model A (ANN with 5 inputs) for the testing data subset.
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Figure 4. RMSE error values for the σbend dependent variable, for the semantic model B (ANN with 5 inputs) for the testing data subset.
Figure 4. RMSE error values for the σbend dependent variable, for the semantic model B (ANN with 5 inputs) for the testing data subset.
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Figure 5. RMSE error values for the MOEbend dependent variable, for the semantic model C (ANN with 6 inputs) for the testing data subset.
Figure 5. RMSE error values for the MOEbend dependent variable, for the semantic model C (ANN with 6 inputs) for the testing data subset.
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Figure 6. RMSE error values for the σbend dependent variable, for the semantic model B (ANN with 6 inputs) for the testing data subset.
Figure 6. RMSE error values for the σbend dependent variable, for the semantic model B (ANN with 6 inputs) for the testing data subset.
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Figure 7. MAPE error values for the best ANNs for the learning, testing and validation data subsets.
Figure 7. MAPE error values for the best ANNs for the learning, testing and validation data subsets.
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Figure 8. MAPE error values for the MOEbend dependent variable and for the validation data subset, depending on the internode number (NrNod) and water content (Wcont): (a) for annA05 (MLP 5-11-1); (b) for annC09 (MLP 6-7-1).
Figure 8. MAPE error values for the MOEbend dependent variable and for the validation data subset, depending on the internode number (NrNod) and water content (Wcont): (a) for annA05 (MLP 5-11-1); (b) for annC09 (MLP 6-7-1).
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Figure 9. MAPE error values for the σbend dependent variable and for the validation data subset, depending on the internode number (NrNod) and water content (Wcont): (a) for annB01 (MLP 5-11-1); (b) for annD03 (MLP 6-10-1).
Figure 9. MAPE error values for the σbend dependent variable and for the validation data subset, depending on the internode number (NrNod) and water content (Wcont): (a) for annB01 (MLP 5-11-1); (b) for annD03 (MLP 6-10-1).
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Table 1. Sensitivity analysis for selected neural models annA05 and annB051 for validation data subset.
Table 1. Sensitivity analysis for selected neural models annA05 and annB051 for validation data subset.
Dependent Variable
ANN Model
Independent Variables (ANN Inputs)
Wcont *NrNod *Dstem Max *Dstem min *Thstem wall *
MOEbend
annA05
(MLP 5-11-1)
Error quotient4.31.82.68.36.5
rank35412
σbend
annB01
(MLP 5-11-1)
Error quotient8.74.76.08.919.7
rank35421
* Wcont—water content (kgwater·kgdry mass−1), NrNod—internode numer (-), Dstem Max—maximum stem diameter (mm), Dstem min—minimum stem diameter (mm) and Thstem wall—stem wall thickness (mm).
Table 2. Sensitivity analysis for selected neural models, annC09 and annD03, for the validation data subset.
Table 2. Sensitivity analysis for selected neural models, annC09 and annD03, for the validation data subset.
Dependent Variable
ANN Model
Independent Variables (ANN Inputs)
Wcont *NrNod *Dstem Max *Dstem min *Thstem wall *Fbend Max *
MOEbend
annC09
(MLP 6-7-1)
Error quotient2.43.11.35.52.22.6
rank426153
σbend
annD03
(MLP 6-10-1)
Error quotient3.39.7482611,964702129,524
rank654231
* Wcont—water content (kgwater·kgdry mass−1), NrNod—internode numer (-), Dstem Max—maximum stem diameter (mm), Dstem min—minimum stem diameter (mm), Thstem wall—stem wall thickness (mm) and Fbend Max—maximum bending force value (N).
Table 3. Characteristic of selected neural models.
Table 3. Characteristic of selected neural models.
ANNType and Architecture of the Neural NetworkNeuron Number
in Input
Layer
Liczba
Neuronów in Hidden
Layer
Liczba
Neuronów in Ouput
Layer
Learning
Algorithm
Activation
Function
in Hidden
Layer
Activation
Function
in Ouput
Layer
annA05MLP 5-11-15111BFGS 170LogisticExponential
annB01MLP 5-11-15111BFGS 178LogisticExponential
annC09MLP 6-7-1671BFGS 82LogisticExponential
annD03MLP 6-10-16101BFGS 237LogisticLinear
BFGS—Broyden-Fletcher-Goldfarb-Shanno algorithm; MLP—multilayer perceptron.
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Francik, S.; Łapczyńska-Kordon, B.; Pedryc, N.; Szewczyk, W.; Francik, R.; Ślipek, Z. The Use of Artificial Neural Networks for Determining Values of Selected Strength Parameters of Miscanthus × Giganteus. Sustainability 2022, 14, 3062. https://doi.org/10.3390/su14053062

AMA Style

Francik S, Łapczyńska-Kordon B, Pedryc N, Szewczyk W, Francik R, Ślipek Z. The Use of Artificial Neural Networks for Determining Values of Selected Strength Parameters of Miscanthus × Giganteus. Sustainability. 2022; 14(5):3062. https://doi.org/10.3390/su14053062

Chicago/Turabian Style

Francik, Sławomir, Bogusława Łapczyńska-Kordon, Norbert Pedryc, Wojciech Szewczyk, Renata Francik, and Zbigniew Ślipek. 2022. "The Use of Artificial Neural Networks for Determining Values of Selected Strength Parameters of Miscanthus × Giganteus" Sustainability 14, no. 5: 3062. https://doi.org/10.3390/su14053062

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