Next Article in Journal
Effects of the Changes of Particle Surface Electric Field and Interaction Force on the Reclaimed Soil Aggregate Structural Stability under the Application of Different Soil Conditioners
Previous Article in Journal
Genome-Wide Association Studies Revealed the Genetic Loci and Candidate Genes of Pod-Related Traits in Peanut (Arachis hypogaea L.)
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Effect of Environmental, Soil and Management Factors on Weed Flora of Field Pea in South-East Hungary

Department of Integrated Plant Protection, Plant Protection Institute, The Hungarian University of Agriculture and Life Sciences (MATE), 2100 Godollo, Hungary
*
Author to whom correspondence should be addressed.
Agronomy 2023, 13(7), 1864; https://doi.org/10.3390/agronomy13071864
Submission received: 31 May 2023 / Revised: 12 July 2023 / Accepted: 13 July 2023 / Published: 14 July 2023
(This article belongs to the Section Weed Science and Weed Management)

Abstract

:
Pea is a widely cultivated leguminous plant which also contributes to soil enrichment through nitrogen fixation and benefits crop rotations. However, large weed populations are a challenge for pea production, requiring effective management strategies. It is essential to highlight the influence of soil parameters, factors affecting the environment, and management practices on weed populations to develop effective weed control and maximize pea yield and ease of harvesting. In our study, a total of 31 pea fields were surveyed prior to harvest to determine the coverage of each weed species, with the aim of identifying the typical weeds in the study area. In addition, environmental, soil, and management factors were recorded for each field. Based on our hypotheses, these factors influence the weed composition, and these effects can be described by the dominance of weed species. In our study, summer annuals and geophytic perennials were common, with Echinochloa crus-galli and Convolvulus arvensis being most dominant. The analysis revealed that the year of data record, soil type, and farming system most significantly influenced weed composition. Weed species were observed to have varying responses to soil texture, salt concentration, and phosphorus content. The survey period, geographical factors, farming system, and tillage practices also played a role in determining weed flora. The findings suggest strong correlations between soil parameters and weed composition, highlighting the importance of soil management in weed control. The year of data collection had the greatest influence on weed infestation. Soil-related variables, such as soil type, also played a significant role. Farming systems had a smaller effect on weed composition. Comparing our results with previous country level weed surveys in Hungary, our results identified some unique characteristics in the weed flora of South-East Hungary.

1. Introduction

Peas, of the genus Pisum, are one of the most widely cultivated leguminous plants in Hungary; they are grown in more than 100 countries around the world for seed, feed and food [1]. In Hungary, the area of cultivation (approx. 12 thousand hectares dry peas and 17 thousand hectares green peas) has been declining in recent years [2,3].
The most important use of peas is in animal feed, as they have very favorable nutritional values. They have a protein content of 21–25% and have high amounts of carbohydrates and digestible nutrients (86–87%). They are rich in amino acids and have a high content of lysine and tryptophan, which are less abundant in cereal grains. This makes peas a key ingredient in animal feed mixtures. Peas are also a good source of human protein and are consumed worldwide [4]. The climatic conditions in Hungary are favorable for pea production [5].
Peas are also useful crops for crop rotation because they leave a very favorable soil condition: they do not deplete the soil water and nutrient supply; early harvesting of peas allows sufficient time for tillage before sowing the next crop; and due to Rhizobium bacteria, they enrich the upper soil layer with nitrogen [6]. Beyond use as a main crop, peas can also be used as a green manure, second crop, and can increase the yield of roadside crops [4].
Field pea is mostly an early spring-sown crop in Hungary, and at the beginning of the growing season this crop develops together with winter annual and early summer annual weed species. Thus, the pea crop is easily weeded in the early stages of development due to late canopy closure [4]. Peas do not have the same shading density as cereals in the later growing period either, so they may also have a serious weed problem at harvest [5,7,8].
The most important winter annual species damaging pea crops include Matricaria spp., Anthemis spp., Papaver rhoeas, and Galium aparine. Among the most important members of the early summer annuals, Sinapis arvensis, Raphanus raphanistrum and Avena fatua are of concern. At the end of the growing season, after the leaves of peas have dried, the summer annuals weeds, Chenopodium spp., Amaranthus spp., Echinochloa crus-galli, Solanum nigrum, and the sunflower (Helianthus annuus), become dominant, while the most common perennial weeds are Cirsium arvense, Convolvulus arversis, and Sorghum halepense. During harvesting, the poisonous berries of Solanum nigrum may fall among the peas, causing quality damage [9,10].
The structure and nutrient content of the soil greatly influence the appearance and location of weeds [11]. The different physical and chemical properties of soil all interact. For example, a slight change in soil chemistry has a strong influence on the emergence and growth of weeds, too. Plants do not generally prefer more acidic soils, but some weeds may have an advantage over the crop under these conditions. The competitiveness of the cultivated crop can be improved by adding lime [12] and by organic and mineral fertilization [13].
Fertilization, as a factor affecting soil properties in the long term, has a crucial role in the development of weed flora and weed population and competition [14]. According to Häkansson [15], one such example is Sinapis arvensis, an important weed but formerly a major problem in acidic soils, whereas nowadays its importance has declined partly due to liming and fertilizer use.
Salinization is one of the most critical soil factors for crop yields. Salinization affects 20% of arable farmland globally, including 33% of irrigated farmland. Agricultural crops show a variety of adverse responses to salt stress and salinity adversely affects several different soil properties [16]. Salinity also determines morphological, physiological, and biochemical processes, including seed germination, plant growth, and water and nutrient uptake [17,18]. Thus, salinity as an ecological indicator plays a crucial role in habitat preference [19] as well as in all aspects of plant development, from germination to growth and reproduction [20].
Climate change is of paramount importance in agriculture, as weather factors have a profound impact on the development of all crops, including not only main crops but also weeds [21]. Sudden changes in weather stress main crops, making them more susceptible and less competitive against weeds [22]. Temperature, precipitation, humidity, and CO2 concentration all play a crucial role in the geographic distribution of weeds, as they alter weed proliferation and competitive behavior in the crop [23,24]. Further northward expansion of several weeds such as Amaranthus retroflexus, Setaria spp., Digitaria sanguinalis, Sorghum halepense has been observed [25,26]. Milder and wetter winters tend to increase overwintering of annual weeds, but thermophilic annuals also grow with greater intensity and expand where summers are longer and warmer [27,28].
Precipitation patterns and the increasing droughts associated with climate change will alter the occurrence and spread of weeds, and thus their impact on crop production. Extreme weather conditions and drought-prone agricultural areas are expected to become more prevalent in the near future [29,30]. As a result, drought and flood seasons will become more frequent, which may also change the occurrence and further spread of weeds. Rainier years favor hydromorphic weed species, while in drier years C4 weeds are favored over C3 species [29].
Both crop rotation and soil tillage influence weed emergence. In general, reduced tillage systems, such as no-tillage, stratify the soil weed seed set closer to the soil surface, whereas intensive tillage provides a uniform distribution of weed seeds down to the tillage depth [31,32]. Weed species respond quite differently to different tillage regimes, with increasing cover of Mercurialis annua, Panicum miliaceum, or Datura stramonium and with decreasing cover of Avena fatua, Cirsium arvense, or Anthemis austriaca under reduced tillage [33].
Reducing the number of tillage operations and abandonment of soil rotation helps to reduce some weeds. The abundance of large seeded deep germinating weed species Abutilon theophrasti, Xanthium spp., Datura stramonium are declining. However, the incidence of small-seeded and broad-leaved weeds such as Chenopodium album, Amaranthus retroflexus, Ambrosia artemisiifolia, and annual grasses, e.g., Echinochloa crus-galli and Setaria species, has been observed [34]. In addition, it can promote the establishment and emergence of perennial weed species such as Epilobium ciliatum, Poa trivialis, Cirsium arvense, Taraxacum officinale, Equisetum arvense, and Elymus repens [35,36].
Weeds are the most damaging agricultural pest [37]. In recent years, the approvals of many pesticide active substances have been withdrawn or not renewed in the European Union. Herbicidal active substances and preparations are no exception [38]. The crop under study is a minor uses crop, which has not been previously managed by a wide range of herbicidal preparations. Due to the successive withdrawals of active substances, non-chemical weed control technologies and their effective application are becoming increasingly important. Furthermore, as these techniques are common practice in organic farming systems, the question of rethinking the management system may arise.
Field weed species show different adaptability to soil nutrients. They have fundamentally different nutrient requirements and are adapted to different nutrient supply levels [39]. Rumex acetosella, Spergula arvensis, and Scleranthus annuus tolerate Ca deficiency and are often referred to as acidophilic weeds, while Chenopodium album, Stellaria media, and Tripleurospermum inodorum prefer calcareous soils and are better able to use fertilizers than cultivated crops. The latter are also known as nitrophil weeds [40,41,42].
Weed infestations reduce yields by competing for moisture, nutrients, space, and light, and make harvesting peas more difficult. Weed control increases pea yield by an average of 63% [43,44], and pea yield loss ranges from 40–70% due to weed competition. In addition to herbicidal treatments, the weed suppressive ability of different cultivars plays a role in the above percentages [45]. Traits such as long stems, number of branches, leaf area, and rapid canopy development all influence the competitive effects of pea and weed interference. From the point of view of competitive ability, it is recommended to grow pea varieties with the largest, strongest growth habit and longer vines [46]. Timing is also an important factor. Early sown pea varieties are those that are less susceptible to weed infestation [47], but the extent of weed infestation can be reduced by higher seeding rates and the use of competitive varieties [48].
Since there are large differences in weed control between organic and conventional systems, conventional seeding rates are not appropriate for organic pea production. This is supported by results that show that increasing the seeding rate increases yield and plant competitiveness and reduces yield losses due to weeds. In organic farming systems, weed infestation can be effectively reduced by increasing the seeding rate [37,49]. The adjustment of the seeding rate to a higher seeding rate also plays a crucial role in the development of weed suppression. Several experiments involving pea stands confirm that weed suppression is improved in crops with higher stand density, resulting in lower weed infestation in plots with increased number of plants [50].
Based on the above, the hypotheses of our work were that soil, management, and environmental factors influence the weed composition of pea fields by affecting the ability of weed species to reproduce at different rates and that the influence of these factors can be described by the relative dominance of particular species, as indicators. Furthermore, the aims of the research included identifying the typical weeds in field pea in the study area and determining and comparing factors influencing the variation in weed flora.

2. Materials and Methods

2.1. Data Collection

The aim of our study was to examine the pre-harvest weed vegetation of pea fields. A total of 31 pea fields were examined between 2017 and 2020 in South-East Hungary (in the region of Gyomaendrőd and Szarvas cities; Figure A1) when weed vegetation was sampled between mid-June and late July depending on the pea maturity.
The study area is characterized by alluvial and meadow soils with poor water management and poor tillage resulting in high weed populations in general.
The surveyed fields were assessed in eight 1 × 1 m randomly placed quadrats. Each weed species was surveyed on the basis of coverage, i.e., the percentage of ground covered by aboveground plant parts [51]. The analyses were based on the field-level average for all species.
On all surveyed fields, soil and management variables and factors affecting the environment (named as ‘environmental variables’) were also recorded by soil analyses, other observations, or farmer interviews. Tillage was based on either ploughing to a depth of 30–34 cm or on loosening by shank ripper to a depth of 35–50 cm, depending on the field. Preceding crops within a three year period were classified into three groups, as winter crops (winter wheat, winter barley, spelt wheat, winter oil-seed rape), sprint row crops (maize, sunflower, oil-seed pumpkin) and spring dense crops (canary grass, spring pea), and the relative frequency (between 0 and 1) of these groups was calculated weighted by the years of production as 0.6 for previous crop #1, 0.3 for previous crop #2, and 0.1 for previous crop #3. Analysis included the relative frequency of these groups. (Table 1; Table A1) The cultivar, amount of seeds, and sowing date were also recorded but were excluded from the analyses as cultivar and amount of seeds was the same (Nanny and 150 kg ha−1) and sowing data varied little (all pea plants were sown on the first week of March) for the surveyed fields.

2.2. Statistical Analyses

In the first step in the analysis, cover values of each species were aggregated within the eight plots from each field to calculate the average weed composition of the individual fields. These field averages were examined via statistical analyses. To demonstrate the importance of each species generally, both the average cover value and frequency (on field level) were calculated across all examined fields. The intercorrelations were assessed by calculating generalized variance inflation factors (GVIF) prior to the analysis in case of all of soil, environmental, and management factors. During this process, ‘tillage depth’ (highly correlated with tillage method); ‘number of mechanical weed control applications’, ‘MCPB herbicides’, fertilizer rates (N, P2O5, and K2O) (all highly correlated with farming system where mechanical weed control and the abandonment of fertilizer use characterized organic fields, while fertilizer and herbicide [MCPB a.i.] use dominated in conventional fields.) and ‘spring dense preceding crops’ (highly correlated with other preceding crops) were removed from the analysis (Table 1). The rest of the variables showed only a limited collinearity, where the highest value of GVIF (adjusted by degree of freedom) was 4.11 [52].
The second step included the calculation of the Shannon diversity index [53] based on relative coverage of weed species of each field according to the following equation:
H = Ʃ i = 1 R p i ln p i
where R: number of species, pi: proportion of coverage of individuals belonging to ith species in the sample.
Calculated indexes were analyzed together with the soil, management and environmental variables not eliminated in the first step by analysis of covariance (ANCOVA) [54] and by Pearson correlation (numeric variables) [55] in case of significant (p < 0.05) variables of ANCOVA.
In the third step, aggregated cover values were subjected to Hellinger transformation [56] and were examined in a redundancy analysis (RDA) together with the soil, management and environmental data, with the aim of describing the effect of explanatory variables on weed composition. The number of explanatory variables was decreased by stepwise backward selection using a p < 0.05 threshold for type I error, which resulted a minimal adequate model which contained nine independent variables (Table 1). In the next step of the multivariate analysis, the gross and net effects of each explanatory variable of the reduced model were estimated, based on methods of Lososová et al. [57]. In the case of most partial RDAs there was only one constrained axis, except soil type and year (date of record), where three and four constrained axes had to be tested. Based on the results, a common rank of ‘importance’ was settled among all explanatory variables according to the R2 adj-values of the net effects of the partial RDA models. To show the connections between weed species and significant factors, for each pRDA model 10 species were identified that represented the highest explained variation in the constrained axis. The entire statistical analysis was conducted in the R Environment (R Development Core Team, version 4.1.3) using the Vegan add-on package (vegan 2.5-1).

3. Results

3.1. Weed Composition

According to Figure 1, more than half of the weed % cover was occupied by summer annuals (a total of 13.3%). Next to annuals, the % cover of geophyte perennials was next most important on the surveyed fields. The most abundant species with more than one percent coverage were Echinochloa crus-galli (summer annual; 6.0%), Convolvulus arvensis (geophyte; 4.5%), Cirsium arvense (geophyte; 1.7%), Xanthium italicum (summer annual; 1.6%), and Hibiscus trionum (summer annual, 1.4%). In addition to weed species, a range of crop volunteers also appeared, i.e., Triticum spelta, T. aestivum, and Brassica napus with coverage of 0.5%, 0.2%, and 0.1%.
As seen in the % cover values, the summer annuals and geophyte perennials were the most frequent weeds during surveys. Six of eight species with more than 50% frequency were annuals and two of them perennials with the highest frequency of Echinochloa crus-galli (74.2%), Convolvulus arvensis (67.7%), Cirsium arvense, Chenopodium album, Setaria viridis (all 64.5%). According to the analysis of % cover and frequency data together, it was apparent than some species (e.g., Xanthium italicum, Hibiscus trionum) had high % cover values but appeared only on a few fields, and conversely Chenopodium album was a general species on most fields with low % cover values (Figure 2).

3.2. Effect of Variables on Diversity

The analysis of covariance dedicated that diversity was affected only by a limited number of variables. However, a significant effect was detected for soil humus content (p = 0.035), soil K2O content (p = 0.042), and frequency of spring row preceding crops (p = 0.028); the Pearson correlation did not show a significant relationship with diversity for any of these variables.
The small effect on diversity prompted us to analyze the impact on individual weed species in more detail.

3.3. Effect of Variables on Weed Composition

According to the redundancy analysis (RDA), the weed composition was mainly affected by the year of data record (15.6%), soil type (10.0%), and farming system (5.8%) but a total of nine factors were significant in our model. The total explained variation in order of all included soil, environmental, and management factors was 21.3, 23.0 and 8.8%, respectively (Table 2).
The soil preference of surveyed weed species varied widely. Alluvial meadow soil was highly preferred by Xanthium italicum, Hibiscus trionum and Setaria viridis; clay soils by Tripleurospermum inodorum and Persicaria lapathifolia; and Convolvulus arvensis was the most abundant on fields with loamy-clay soil.
The weed composition was also well differentiated by soil texture. Fields with hard ground featured higher % cover values for summer annuals (Chenopodium spp., Echinochloa crus-galli, Tripleurospermum inodorum) but Xanthium italicum, wheat species, and Fallopia convolvulus exhibited higher % cover values in the case of loose soils. The % cover of Convolvulus arvensis and Hibiscus trionum was most influenced by high salt concentration, but other species (e.g., Fallopia convolvulus, Cirsium arvense) preferred low salt content soils. High phosphorus content most influenced the % cover of Hibiscus trionum and Amaranthus retroflexus, but Fallopia convolvulus and winter wheat volunteers grew poorly in those fields (Table 3).
The survey periods exhibited varying levels of weed species dominance year by year. The most important species were Stachys annua and Hibiscus trionum in 2017, Fallopia convolvulus and Chenopodium polyspermum in 2018, spelt wheat volunteers and Persicaria lapathifolia in 2019, and Echinochloa crus-galli and Datura stramonium in 2020.
The surveyed area was relatively flat (altitude 78–86 m above mean sea level) but this factor also resulted in differences in weed composition. Stachys annua and Triticum spelta were more important on upland fields but Cirsium arvense and Tripleurospermum inodorum were frequent on low-lying fields.
Approximately a 900 square kilometer large survey area (approx. 25 km by latitude and 36 km by longitude) was included in the data collection. In this landscape unit, the northern fields were more covered by Stachys annua and Ambrosia artemisiifolia but Hibiscus trionum and Cirsium arvense were more important in the south (Table 4).
Within the management variables, only farming system (with high collinearity to herbicide and fertilizer use and number of mechanical weed control applications) and tillage (collinearity to tillage depth) resulted in significant differences in weed flora.
Cirsium arvense, Hibiscus trionum, and Chenopodium spp. were the most problematic in organic fields, but conventional fields were infested mainly by Convolvulus arvensis and Stachys annua.
The abundance of Tripleurospermum inodorum, Ambrosia artemisiifolia, and Fallopia convolvulus was the highest in fields with the loosening type of tillage, whereas Hibiscus trionum and Persicaria lapathifolia appeared with higher frequency after ploughing (Table 5).
The ordination diagram of RDA of our experiment indicated a high correlation between soil texture, salt concentration, phosphorous content, and soil type; furthermore, latitude and altitude were also correlated with most soil parameters, but the effect of tillage seemed to have no correlation with these variables (Figure 3). The effects of farming systems and sampling year were less significant than the effect of soil parameters on weed composition.
Echinochloa crus-galli and Xanthium strumarium were frequently associated with high salt concentrations and organic farming but were less frequent in fields with higher phosphorous content and higher altitude. The effect of tillage was also indicated by the weed composition; Triticum aestivum and Chenopodium polyspermum were more abundant in ploughed fields, whereas Echinochloa crus-galli and Convolvulus arvensis preferred fields with the loosening type of tillage (Figure 3).

4. Discussion

The high total number of recorded weed species (38) illustrated the species richness of pea fields. The range of dominant weed species varied from field to field, but there were not clear relationships between the calculated diversity (Shannon) and the environmental, soil, and management variables.
The investigated areas were characterized by compacted soils with poor water management, unfavorable nutrient supply, and heavy weed infestations. In the studied production areas, it was particularly characteristic that unfavorable weather conditions during the sowing and emergence of peas might result in insufficient stocks, which was observed in both conventional and organic fields during the study period. These unfavorable growing conditions and improperly developing stands evidently provided space for emerging weeds in our current study.
In conventional farming, many herbicides can be used in pea culture, which can be effective against most weed species. On the other hand, in ecologically managed areas, post-emergence weed control is accomplished by possible weed harrowing and hoeing. In the course of the study, in some cases, % weed cover in organic areas was almost twice as much (18.1%) as in conventional areas (9.3%); these results were similar to those of Dorner [58] who demonstrated the weed cover of 9.8% on organic pea fields compared to 3.8% in conventional farming. This level of weed infestation seems high, but it may be tolerable in the case of a densely sown crop [59]. In addition to the weed cover, the weed flora also changed significantly by farming system (5.8% in RDA model), similar to previous works [60,61,62].
As the other significant management factor (3.0% in RDA model), the different tillage regimes (ploughing or loosening) also resulted in differences in weed composition. However, the loosening may result a near-surface layer with a high weed seedbank, where weed emergence is promoted regardless of the size of the weed seeds, and some of the seeds are ploughed into a deeper layer, so the germination of small seeded species is more restricted [31,63]. We found that the medium- (Hibiscus trionum [64], Persicaria lapathifolia [65], Chenopodium spp. [66]) and large-seeded (Xanthium spp. [67]) species were more reduced by ploughing in our study.
Examining the results further, it can be concluded that environmental factors had the greatest influence on weed infestation (23.1%). Of all the factors studied, the year of the survey (15.6%) had the greatest influence on weed infestation. In the case of survey periods, most of the difference can be explained by differences in rainfall [68]. In the survey area, the aggregated 20 year (2001–2020) average rainfall between January and June was 277 mm, compared to 184, 330, 328, and 293 mm between 2017 and 2020, respectively [69], and years with the most and least rainfall showed the largest differences. Similarly, Lososová et al. [57] found that increasing precipitation is one of the most determining factors in weed species composition associated with increasing altitude and decreasing temperature and soil condition. The effect of precipitation on weed vegetation has also been confirmed in a comparison of different European agroecological regions [70].
Soil-related variables were also prominent (21.3%), of which soil type (10.0%) had the greatest effect on weeds, similar to that described in [71]. However, the effect of soil type cannot be interpreted in isolation because it is related to other soil parameters [72]. High values of soil texture resulted in a high abundance of weed Chenopodium species; this effect was also detectable for Quinoa (Ch. quinoa) when clay-rich soil structure was combined with high nutrient (P, K) content [73]. The surveyed fields showed only a limited salinity, but weed composition was influenced by this factor, too, as assumed by Borhidi [19].
Field peas show higher weed infestation and weed biomass than other densely planted crops such as cereals [60,74]. Comparing our results with the results of the Sixth National Field Weed Survey on Hungary for winter wheat, for which the survey period was similar to our study, there were similarities between several species and cover values. For the top 20 weed species, six species were identical, including two weed species Chenopodium album and Fallopia convolvulus, which had cover values less than 0.2% different from each other. In addition, Ambrosia artemisiifolia, Tripleurospermum inodorum, Convolvulus arvensis, and Cirsium arvense were also found among the top 20 weed species in both studies [75]. On the other hand, the weed community of pea is more diverse and has higher evenness than cereals or pea-cereal intercropping [76].
There were also several differences between the results of our research and the Sixth National Field Weed Survey on Hungary for winter wheat. In our study, cereal (Triticum aestivum and T. spelta) and oilseed rape (Brassica napus) volunteers and several summer annuals, e.g., Echinochloa crus-galli, Xanthium italicum, Hibiscus trionum, Avena fatua, Setaria viridis, Datura stramonium, Chenopodium polyspermum, Persicaria lapathifolia, Stachys annua, Amaranthus retroflexus, and Anagallis arvensis were all prominent weeds. These results are in line with Dorner’s research [58], in which the summer annual Ambrosia artemisiifolia was the most dominant. In contrast, in the Sixth National Field Weed Survey [75], the most prominent weeds of winter wheat included mainly winter annuals, e.g., Stellaria media, Apera spica-venti, Veronica spp., Papaver rhoeas, Consolida spp., Galium aparine, Descurainia Sophia, Lamium spp., Capsella bursa-pastoris, and Anthemis arvensis, but sunflower (Helianthus annuus) and Lolium multiflorum were also dominant.
Patterns in weed frequency seen in our results differed from those in Northern Europe, where Viola arvensis, Chenopodium album, Stellaria media, Galeopsis spp., and Elymus repens were present in most fields (44, 43, 42, 39, and 34%, respectively) [62].

5. Conclusions

The unique nature of the weed flora of peas in comparison to the weed flora of cereals is not clear. However, both cereals and field pea are generally densely planted crops, and they have a similar growing season. The many identified differences may be based on less % cover of field pea than cereals prior to harvest.
Since several factors influence the weediness of agricultural land simultaneously, it is essential to monitor and analyze these variables at the same time because some variables may have confounding or opposing effects on each other.
Although weed control is the cornerstone of plant protection in organic farming, the management systems differed mainly in the amount of weeds, whereas the weed flora differed less, despite the absence of herbicide use and different nutrient management methods.
During the data preparation, several variables were eliminated because of collinearity. Tillage depth was correlated with the tillage method; the number of mechanical weed control applications, amount of MCPB herbicides and fertilizers (N, P2O5, and K2O) were highly correlated with the farming system; and spring dense preceding crops were highly correlated with other preceding crops. Additionally, several other factors did not have a significant effect on weed composition, such as soil chemistry, humus, CaCO3 and K2O content, longitude, and winter and spring row preceding crops. This elimination of various parameters in our analysis process suggests a need to survey these parameters on a longer gradient or limit the surveyed factors in further studies and have a greater focus on important key factors.
The year of the study and the soil parameters were found by the redundancy analysis to have the greatest effect on weed composition. The studied years differed most in terms of rainfall. However, variation in rainfall in the study years is consistent with variation in weed composition. The influence of this factor can only be demonstrated for the region under study or for a region like it. Likewise, the explanatory effect of soil variables can only be interpreted in areas characterized by similar soil parameters. The weed flora of different agroecological regions can vary considerably.
The effect of the extent of weed infestation and the weed flora on yield was not included in the research, although it is known that adequate management of weeds is largely responsible for the success of farming. In order to assess the usefulness of the soil, environmental, and management variables included in this research for farmer practice, further research should also examine the impact of these variables on yield.

Author Contributions

Conceptualization, E.B.K. and M.Z.; methodology, Z.D. and M.Z.; software, validation, formal analysis, M.Z.; investigation, E.B.K.; resources, E.B.K. and D.C.; data curation, E.B.K. and M.Z.; writing—original draft preparation, M.Z.; writing—review and editing, E.B.K., Z.D., D.C. and M.Z.; visualization, M.Z.; supervision, M.Z.; project administration, Z.D. and M.Z.; funding acquisition, E.B.K., Z.D. and M.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Plant Sciences PhD School of the Hungarian University of Agriculture and Life Sciences.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A

Table A1. Soil variables and measured values of sampling sites.
Table A1. Soil variables and measured values of sampling sites.
Nr of FieldSoil TypeSoil TextureSoil ReactionSoil Properties
SaltHumusCaCO3P2O5K2O
[Arany][pH KCl]m/m %mg · kg−1
1Loamy-clay soil457.080.033.112.91134356
2Alluvial meadow soil526.850.062.210.4257312
3Alluvial meadow soil536.730.062.050.5154309
4Alluvial meadow soil576.870.071.740.6346268
5Alluvial meadow soil606.180.071.960.1841253
6Alluvial meadow soil606.270.071.900.2545282
7Alluvial meadow soil636.170.072.080.3356273
8Alluvial meadow soil526.250.112.190.10132494
9Alluvial meadow soil546.700.111.820.24204385
10Loamy-clay soil466.530.032.550.08325309
11Loamy-clay soil486.960.033.251.30286383
12Clay soil525.630.063.750.08220501
13Loamy-clay soil496.570.053.320.08420455
14Alluvial meadow soil557.030.092.200.38136375
15Alluvial meadow soil566.100.081.990.2348278
16Alluvial meadow soil635.960.071.940.3541268
17Alluvial meadow soil636.250.081.970.2977266
18Clay soil525.730.073.380.08203481
19Clay soil535.830.063.660.10237541
20Loamy-clay soil496.570.063.370.11382480
21Loamy-clay soil496.530.043.260.08399437
22Loamy-clay soil496.820.053.680.42278546
23Loamy-clay soil496.570.053.320.08420455
24Alluvial meadow soil576.950.061.980.6568274
25Alluvial meadow soil596.240.051.850.2562281
26Alluvial meadow soil576.970.092.891.66338295
27Alluvial meadow soil546.940.092.721.58351425
28Loamy-clay soil506.900.043.730.38238523
29Loamy-clay soil476.810.053.570.43159465
30Loamy-clay soil506.860.063.480.51338515
31Loamy-clay soil496.770.063.660.44316538
Figure A1. Location of fields in the survey area.
Figure A1. Location of fields in the survey area.
Agronomy 13 01864 g0a1

References

  1. Lake, L.; Guilioni, L.; French, B.; Sadras, V.O. Field Pea. In Crop Physiology Case Histories for Major Crops; Sadras, V.O., Calderini, D.F., Eds.; Academic Press: Cambridge, MA, USA, 2021; pp. 320–341. [Google Scholar] [CrossRef]
  2. Hungarian Central Statistical Office. Available online: https://www.ksh.hu/stadat_files/mez/hu/mez0012.html (accessed on 30 May 2023).
  3. Hungarian Central Statistical Office. Available online: https://www.ksh.hu/stadat_files/mez/hu/mez0013.html (accessed on 30 May 2023).
  4. Endres, G.; Kandel, H. Field Pea Production; NDSU: Fargo, ND, USA, 2021; pp. 1–11. Available online: https://www.ndsu.edu/agriculture/sites/default/files/2021-12/a1166.pdf (accessed on 30 May 2023).
  5. Schüller, F. A borsó gazdasági jelentősége és felhasználása. In A borsó. Magyarország kultúrflórája; Mándy, G., Szabó, L., Ács, A., Eds.; Akadémiai kiadó: Budapest, Hungary, 1980; pp. 127–130. [Google Scholar]
  6. Nagy, J. Vetésforgó és vetésváltás. In Földműveléstan; Nyíri, L., Ed.; Mezőgazda kiadó: Budapest, Hungary, 1993; pp. 294–330. [Google Scholar]
  7. Ujvárosi, M. Gyomirtás; Mezőgazdasági kiadó: Budapest, Hungary, 1973; pp. 99–159. [Google Scholar]
  8. McKey, K.; Schatz, B.; Endres, G. Field Pea Production; NDSU: Fargo, ND, USA, 2003; pp. 1–8. Available online: https://agresearch.montana.edu/wtarc/producerinfo/agronomy-nutrient-management/Pulses/NDSUFactSheet.pdf (accessed on 30 May 2023).
  9. Reisinger, P. A borsó gyomnövényei. In Növényvédelem; Glits, M., Horváth, J., Kuroli, G., Petróczi, I., Eds.; Mezőgazda kiadó: Budapest, Hungary, 1997; pp. 305–307. [Google Scholar]
  10. Reisinger, P. Borsó. In Gyomnövények, Gyomirtás, Gyombiológia; Hunyadi, K., Béres, I., Kazinczy, G., Eds.; Mezőgazda kiadó: Budapest, Hungary, 2000; pp. 516–518. [Google Scholar]
  11. Nordmeyer, H.; Häusler, A. Einfluss von Bodeneigenschaften auf die Segetalflora von Ackerflächen (Impact of soil properties on weed distribution within agricultural fields). J. Plant Nutr. Soil Sci. 2004, 167, 328–336. [Google Scholar] [CrossRef]
  12. Hashem, A. Weedsmart: Does Soil pH Affect Weed Management? Available online: https://www.graincentral.com/cropping/weedsmart-does-soil-ph-affect-weed-management (accessed on 30 May 2023).
  13. Repsiene, R.; Ozeraitiene, D. Manuring effect on the soil properties and crop rotation yield. Agriculture 2006, 93, 199–209. [Google Scholar]
  14. Forcella, F. Real-time assessment of seed dormancy and seedling growth for weed management. Seed Sci. Res. 1998, 8, 201–210. [Google Scholar] [CrossRef]
  15. Hakansson, S. Weeds and Weed Management on Arable Land—An Ecological Approach; CABI: Cambridge, MA, USA, 2003; pp. 56–80. [Google Scholar]
  16. Hock, B.; Elstner, C.F. Limitation of salt stress to plant growth. In Plant Toxicology; Hock, B.; Elstner, C.F. Marcel Dekker Inc.: New York, NY, USA, 2002; pp. 91–224. [Google Scholar]
  17. Singh, R. Weed management in major kharif and rabi crops. In National Training on Advances in Weed Management; ICAR-DWR: Jabalpur, India, 2014; pp. 31–40. [Google Scholar]
  18. Akbarimoghaddam, H.; Galavi, L.; Ghanbari, A.; Panjehkeh, N. Salinity effects on seed germination and seedling growth of bread wheat cultivars. Trakia J. Sci. 2011, 9, 43–50. [Google Scholar]
  19. Borhidi, A. Social Behavior Types of the Hungarian Flora, Its Naturalness and Relative Ecological Indicator Values; Janus Pannonius University: Pécs, Hungary, 1993; p. 37. [Google Scholar]
  20. Bano, A.; Fatima, M. Salt tolerance in Zea mays (L.) following inoculation with Rhizobium and Pseudomonas. Biol. Fertil. Soils 2009, 45, 405–413. [Google Scholar] [CrossRef]
  21. Chauhan, B.S.; Kaur, P.; Mahajan, G.; Randhawa, R.K.; Singh, H.; Kang, M.S. Global Warming and its Possible Impact on Agriculture in India. Adv. Agron. 2014, 123, 65–121. [Google Scholar]
  22. Patterson, D.T. Weeds in a Changing Climate. Weed Sci. 1995, 43, 685–700. [Google Scholar] [CrossRef]
  23. Patterson, D.T.; Westbrook, J.K.; Joyce, R.J.V.; Lingren, P.D.; Rogasik, J. Weeds, insects, and diseases. Clim. Chang. 1999, 43, 711–727. [Google Scholar] [CrossRef]
  24. Tubiello, F.N.; Soussana, J.F.; Howden, S.M. Crop and pasture response to climate change. Proc. Natl. Acad. Sci. USA 2007, 104, 19686–19690. [Google Scholar] [CrossRef]
  25. Weber, E.; Gut, D. A survey of weeds that are increasingly spreading in Europe. Agron. Sustain. Dev. 2005, 25, 109–121. [Google Scholar] [CrossRef] [Green Version]
  26. Clements, D.R.; DiTommaso, A. Climate change and weed adaptation: Can evolution of invasive plants lead to greater range expansion than forecasted? Weed Res. 2011, 51, 227–240. [Google Scholar] [CrossRef]
  27. Walck, J.L.; Hidayati, S.N.; Dixon, K.W.; Thompson, K.; Poschlod, P. Climate change and plant regeneration from seed. Glob. Chang. Biol. 2011, 17, 2145–2161. [Google Scholar] [CrossRef]
  28. Hanzlik, K.; Gerowitt, B. Occurrence and distribution of important weed species in German winter oilseed rape fields. J. Plant Dis. Prot. 2012, 119, 107–120. [Google Scholar] [CrossRef]
  29. Ramesh, K.; Matloob, A.; Aslam, F.; Florentine, S.K.; Chauhan, B.S. Weeds in a Changing Climate: Vulnerabilities, Consequences, and Implications for Future Weed Management. Front. Plant Sci. 2017, 8, 95. [Google Scholar] [CrossRef] [Green Version]
  30. Giannini, A.; Biasutti, M.; Held, I.M.; Sobel, A.H. A global perspective on African climate. Clim. Chang. 2008, 90, 359–383. [Google Scholar] [CrossRef]
  31. Cardina, J.; Herms, C.P.; Doohan, G.J. Crop rotation and tillage system effects on weed seedbanks. Weed Sci. 2002, 50, 448–460. [Google Scholar] [CrossRef]
  32. Sosnoskie, L.M.; Herms, C.P.; Cardina, J. Weed seedbank community composition in a 35-yr-old tillage and rotation experiment. Weed Sci. 2006, 54, 263–273. [Google Scholar] [CrossRef]
  33. Pinke, G.; Giczi, Z.; Vona, V.; Dunai, É.; Vámos, O.; Kulmány, I.; Koltai, G.; Varga, Z.; Kalocsai, R.; Botta-Dukát, Z.; et al. Weed composition in Hungarian phacelia (Phacelia tanacetifolia Benth.) seed production: Could tine harrow take over chemical management? Agronomy 2022, 12, 891. [Google Scholar] [CrossRef]
  34. Búvár, G.; Hadászi, L.; Fodor, I. A forgatás nélküli talajművelés gyomszabályozási vonatkozásai. Gyak. Agrof. 2000, 11, 90–92. [Google Scholar]
  35. Rao, A.N.; Brainard, D.C.; Kumar, V.; Ladha, J.K.; Johnson, D.E. Preventive Weed Management in Direct-Seeded Rice: Targeting the Weed Seedbank. Adv. Agron. 2017, 144, 45–142. [Google Scholar] [CrossRef]
  36. Pekrun, C.; Claupein, W. The implication of stubble tillage for weed population dynamics in organic farming. Weed Res. 2006, 46, 414–423. [Google Scholar] [CrossRef]
  37. Mohler, C.L. Mechanical management of weeds. In Ecological Management of Agricultural Weeds; Liebman, M., Mohler, C.L., Staver, C.P., Eds.; Cambridge University Press: Cambridge, UK, 2001; pp. 139–209. [Google Scholar]
  38. Andersons Centre. Crop Production Technology. The Effect of the Loss of Plant Protection Products on UK Agriculture and Horticulture and the Wider Economy. Available online: https://theandersonscentre.co.uk/wp-content/uploads/2017/07/Andersons-Final-Report.pdf (accessed on 30 May 2023).
  39. Kismányoky, A. Effect of Agrotechnical Factors to Crop Plants and Weeds. Ph.D. Thesis, University of Pannonia, Keszthely, Hungary, 2010. Available online: http://konyvtar.uni-pannon.hu/doktori/2010/Kismanyoky_Andras_theses_en.pdf (accessed on 30 May 2023).
  40. Larcher, W. Physiological Plant Ecology, 4th ed.; Springer: Berlin/Heidelberg, Germany, 1955; pp. 28–40. [Google Scholar]
  41. Hanf, M. Ackerunkräuter Europas mit ihren Keimlingen und Samen, 4th ed.; Eugen Ulmer: Stuttgart, Germany, 1999; pp. 301–321. [Google Scholar]
  42. Zimdahl, R. Fundamentals of Weed Science, 5th ed.; Academic Press: Cambridge, MA, USA, 2007; pp. 260–281. [Google Scholar]
  43. Harker, K.N.; Blackshaw, R.E.; Clayton, G.W. Timing weed removal in field pea (Pisum sativum). Weed Technol. 2001, 15, 277–283. [Google Scholar] [CrossRef]
  44. Fernandez, A.L.; Sheaffer, C.C.; Wyse, D.L.; Michaels, T.E. Yield and weed abundance in early- and late-sown field pea and lentil. Agron. J. 2012, 104, 1056–1064. [Google Scholar] [CrossRef]
  45. Efthimiadou, A.; Karkanis, A.; Bilalis, D.; Efthimiadis, P. The phenomenon of crop-weed competition; a problem or a key for sustainable weed management? J. Food Agric. Environ. 2009, 7, 861–868. [Google Scholar]
  46. Spies, J.M.; Warkentin, T.D.; Shirtliffe, S.J. Variation in field pea (Pisum sativum) cultivars for basal branching and weed competition. Weed Sci. 2011, 59, 218–223. [Google Scholar] [CrossRef]
  47. Harker, K.N.; Clayton, G.W.; Blackshaw, R.E. Comparison of leafy and semileafless pea for integrated weed management. Weed Technol. 2008, 22, 124–131. [Google Scholar] [CrossRef]
  48. Lemerle, D.; Verbeek, B.; Diffey, S. Influences of field pea (Pisum sativum) density on grain yield and competitiveness with annual ryegrass (Lolium rigidum) in south-eastern Australia. Aust. J. Exp. Agric. 2006, 46, 1465–1472. [Google Scholar] [CrossRef]
  49. Wall, D.A.; Friesen, G.H.; Bhati, T.K. Wild mustard interference in traditional and semi-leafless field peas. Can. J. Plant Sci. 1991, 71, 473–480. [Google Scholar] [CrossRef] [Green Version]
  50. Marx, G.A.; Hagedorn, D.J. Plant population and weeds growth relation in canning peas. Weeds 1961, 9, 494–496. [Google Scholar] [CrossRef]
  51. Van Der Maarel, E.; Franklin, J. Vegetation ecology: Historical notes and outline. In Weed Ecology, 2nd ed.; Van Der Maarel, E., Franklin, J., Eds.; Wiley-Blackwell: Oxford, UK, 2013; pp. 1–27. [Google Scholar]
  52. Fox, J. Applied Regression Analysis and Generalized Linear Models, 2nd ed.; Sage Publications: Thousand Oaks, CA, USA, 2008. [Google Scholar]
  53. Shannon, C.E. A Mathematical Theory of Communication. Bell Syst. Tech. J. 1948, 27, 379–423. [Google Scholar] [CrossRef] [Green Version]
  54. Chambers, J.M.; Freeny, A.; Heiberger, R.M. Analysis of variance, designed experiments. In Statistical Models in S, 1st ed.; Chambers, J.M., Hastie, T.J., Eds.; Wadsworth & Brooks/Cole: Pacific Grove, CA, USA, 1992; pp. 145–194. [Google Scholar]
  55. Soper, H.E.; Young, A.W.; Cave, B.M.; Lee, A.; Pearson, K. On the distribution of the correlation coefficient in small samples. Appendix II to the papers of “Student” and R.A. Fisher. A co-operative study. Biometrika 1917, 11, 328–413. [Google Scholar] [CrossRef]
  56. Borcard, D.; Gillet, F.; Legendre, P. Numerical Ecology with R; Springer: New York, NY, USA, 2011; pp. 34–50. [Google Scholar]
  57. Lososová, Z.; Chytry, M.; Cimalová, S.; Kropác, Z.; Otypková, Z.; Pysek, P.; Tichy, L. Weed vegetation of arable land in Central Europe: Gradients of diversity and species composition. J. Veg. Sci. 2004, 15, 415–422. [Google Scholar] [CrossRef]
  58. Dorner, Z. Analysis of Weed Flora of Ecological Farming System at the Ecological Model Farm of Kishantos. Ph.D. Thesis, Szent István University, Gödöllő, Hungary, 2006. [Google Scholar]
  59. Menalled, U.D.; Adeux, G.; Cordeau, S.; Smith, R.G.; Mirsky, S.B.; Ryan, M.R. Cereal rye mulch biomass and crop density affect weed suppression and community assembly in no-till planted soybean. Ecosphere 2022, 13, e4147. [Google Scholar] [CrossRef]
  60. Lundkvist, A.; Salomonsson, L.; Karlsson, L.; Gustavsson, A.-M.D. Effects of organic farming on weed flora composition in a long term perspective. Eur. J. Agron. 2008, 28, 570–578. [Google Scholar] [CrossRef]
  61. Zalai, M.; Dorner, Z. Weed flora of cereals in different farming systems. Plant Breed. Seed Sci. 2010, 61, 15–23. [Google Scholar] [CrossRef]
  62. Salonen, J.; Hyvönen, T.; Jalli, H. Weed flora and weed management of field peas in Finland. Agric. Food Sci. 2005, 14, 189–201. [Google Scholar] [CrossRef]
  63. Feledyn-Szewczyk, B.; Smagacz, J.; Kwiatkowski, C.A.; Harasim, E.; Wozniak, A. Weed flora and soil seed bank composition as affected by tillage system in three-year crop rotation. Agriculture 2020, 10, 186. [Google Scholar] [CrossRef]
  64. CABI Digital Library. Available online: https://www.cabidigitallibrary.org/doi/10.1079/cabicompendium.27133 (accessed on 2 June 2023).
  65. CABI Digital Library. Available online: https://www.cabidigitallibrary.org/doi/10.1079/cabicompendium.42689 (accessed on 2 June 2023).
  66. CABI Digital Library. Available online: https://www.cabidigitallibrary.org/doi/10.1079/cabicompendium.12648 (accessed on 2 June 2023).
  67. CABI Digital Library. Available online: https://www.cabidigitallibrary.org/doi/10.1079/cabicompendium.56864 (accessed on 2 June 2023).
  68. Travlos, I.; Gazoulis, I.; Kanatas, P.; Tsekoura, A.; Zannopoulos, S.; Papastylianou, P. Key factors affecting weed seeds’ germination, weed emergence, and their possible role for the efficacy of false seedbed technique as weed management practice. Front. Agron. 2020, 2, 1. [Google Scholar] [CrossRef]
  69. Körös Valley District Environment and Water Directorate. Available online: http://www.kovizig.hu/04-vizrajz/04-hidrometeorologia/03-evi-csapadekadatok/evi-csapadekadatok.php (accessed on 2 June 2023).
  70. Glemnitz, M.; Radics, L.; Hoffmann, J.; Czimber, G. Weed species richness and species composition of different arable field types—A comparative analysis along a climate gradient from south to north Europe. J. Plant Dis. Prot. 2006, 20, 577–586. [Google Scholar]
  71. Pätzold, S.; Hbirkou, C.; Dicke, D.; Gerhards, R.; Welp, G. Linking weed patterns with soil properties: A long-term case study. Precis. Agric. 2020, 21, 569–588. [Google Scholar] [CrossRef] [Green Version]
  72. Li, X.; Guo, M.; Wang, H. Impact of soil texture and salt type on salt precipitation and evaporation under different hydraulic conditions. Hydrol. Process. 2022, 36, e14793. [Google Scholar] [CrossRef]
  73. Mobeena, S.; Thavaprakaash, N.; Vaiyapuri, K.; Djanaguiraman, M.; Geethanjali, S.; Geetha, P. Influence of different types of soils on the growth and yield of Quinoa (Chenopodium quinoa Wild.). J. Appl. Nat. Sci. 2023, 15, 365–370. [Google Scholar] [CrossRef]
  74. Mohler, C.L.; Liebmann, M. Weed Productivity and Composition in Sole Crops and Intercrops of Barley and Field Pea. J. Appl. Ecol. 1987, 24, 685–699. [Google Scholar] [CrossRef]
  75. Novák, R.; Magyar, M.; Simon, G.; Kadaravek, B.; Kadaravekné Guttyán, A.; Nagy, M.; Blazsek, K.; Erdélyi, K.; Farkas, G.; Gyulai, B.; et al. Change in the spread of common ragweed in Hungary in the light of the National Arable Weed Survey (1947–2019). In Proceedings of the International Ragweed Society Conference, Budapest, Hungary, 8–9 September 2022. [Google Scholar]
  76. Poggio, S.L. Structure of weed communities occurring in monoculture and intercropping of field pea and barley. Agric. Ecosyst. Environ. 2005, 109, 48–58. [Google Scholar] [CrossRef]
Figure 1. Mean % cover of most abundant weed species of surveyed pea fields.
Figure 1. Mean % cover of most abundant weed species of surveyed pea fields.
Agronomy 13 01864 g001
Figure 2. Most frequent weed species of surveyed fields.
Figure 2. Most frequent weed species of surveyed fields.
Agronomy 13 01864 g002
Figure 3. Ordination diagrams of the reduced redundancy analysis (RDA) model containing the significant explanatory variables for explanatory variables and species. (Arrow: numeric variable; triangle: factorial soil variable; square: factorial environmental variable; gray circle: factorial management variable; black circle: species).
Figure 3. Ordination diagrams of the reduced redundancy analysis (RDA) model containing the significant explanatory variables for explanatory variables and species. (Arrow: numeric variable; triangle: factorial soil variable; square: factorial environmental variable; gray circle: factorial management variable; black circle: species).
Agronomy 13 01864 g003
Table 1. Units and ranges of continuous variables and values of categorical variables.
Table 1. Units and ranges of continuous variables and values of categorical variables.
Variable (Unit)Range/Recorded or Calculated Values
Soil factors
    Soil type
    Soil texture (KArany)
    Soil pH (KCl) B
    Soil properties (m/m %)
        Salt
        Humus B
        CaCO3B
    Soil properties (mg kg–1)
        P2O5
        K2O B
Alluvial meadow soil, clay soil, loamy-clay soil
40–63
5.63–7.08

0.03–0.11
1.74–3.75
0.08–2.91

40.7–420
253–546
Environmental factors
    Altitude (m, AMSL)
    Latitude (°)
    Longitude (°) B
    Year
78–86
46.73990–46.97027
20.42458–20.90111
2017–2020
Management factors
    Tillage system
    Tillage depth (cm) A
    Farming
    Nr. of mechanical weed control applications A
    MCPB herbicide (g a.i. ha–1) A
    Preceding crops a
        Wintering crops B b
        Spring row crops B c
        Spring dense crops A d
    Amount of fertilizer (kg ha–1)
        N A
        P2O5 A
        K2O A
ploughing, loosening
30–50
conventional, organic
0–1
0–1200

0–1
0–0.7
0–0.7

0–63
0–22.5
0–22.5
A Variables not included into the analysis due to multicollinearity B Variables dropped during the backward selection process a Calculated by last three preceding crops: (precrop 1 × 0.6) + (precrop 2 × 0.3) + (precrop 3 × 0.1) b Winter wheat, spelt wheat, winter barley, winter oilseed rape c Maize, sunflower, oilseed pumpkin d Spring pea, canary grass.
Table 2. Effects of the explanatory variables on the weed composition.
Table 2. Effects of the explanatory variables on the weed composition.
FactorsdfGross EffectNet Effect
Explained
Variation (%)
R2adjExplained
Variation (%)
R2adjFp-Value
Soil type
Soil texture (Arany)
Soil salt content
Soil P2O5 content
Year
Altitude
Latitude
Farming
Tillage
2
1
1
1
3
1
1
1
1
23.2
20.0
14.4
12.9
29.4
13.6
14.9
23.5
12.1
0.18
0.17
0.11
0.10
0.22
0.11
0.12
0.21
0.09
10.0
2.9
4.9
3.5
15.6
3.5
3.9
5.8
3.0
0.12
0.03
0.06
0.04
0.18
0.04
0.05
0.08
0.04
5.56
3.20
5.52
3.91
5.82
3.92
4.38
6.44
3.31
0.001
0.002
0.001
0.002
0.001
0.001
0.002
0.001
0.009
Table 3. Names, score values, and fit of species giving the highest fit along the first constrained axis in the partial redundancy analysis (pRDA) models of soil variables in open-field pea experiment (Hungary, 2017–2020).
Table 3. Names, score values, and fit of species giving the highest fit along the first constrained axis in the partial redundancy analysis (pRDA) models of soil variables in open-field pea experiment (Hungary, 2017–2020).
SpeciesAx 1
Score
FitSpeciesAx 1
Score
Fit
Alluvial meadow soil (+ high; − low)Soil texture (Arany; + high; − low)
Xanthium italicum
Hibiscus trionum
Setaria viridis
Avena fatua
Triticum spelta
Anagallis arvensis
Chenopodium album
Triticum aestivum
Fallopia convolvulus
Convolvulus arvensis
0.41
0.28
0.13
0.11
0.11
−0.05
−0.13
−0.17
−0.33
−0.43
0.52
0.21
0.27
0.15
0.09
0.12
0.10
0.25
0.22
0.21
Chenopodium album
Echinochloa crus-galli
Chenopodium polyspermum
Tripleurospermum inodorum
Chenopodium hybridum
Triticum aestivum
Avena fatua
Fallopia convolvulus
Triticum spelta
Xanthium italicum
0.14
0.14
0.10
0.09
0.02
−0.06
−0.09
−0.11
−0.12
−0.12
0.11
0.03
0.11
0.05
0.05
0.03
0.10
0.02
0.10
0.05
Clay soil (+ high; − low)Salt content (+ high; − low)
Tripleurospermum inodorum
Persicaria lapathifolia
Chenopodium album
Triticum aestivum
Fallopia convolvulus
Setaria viridis
Avena fatua
Hibiscus trionum
Xanthium italicum
Convolvulus arvensis
0.23
0.22
0.16
0.14
0.13
−0.08
−0.10
−0.14
−0.15
−0.23
0.32
0.28
0.14
0.17
0.04
0.11
0.11
0.05
0.07
0.06
Convolvulus arvensis
Hibiscus trionum
Amaranthus retroflexus
Phragmites australis
Avena fatua
Anagallis arvensis
Chenopodium polyspermum
Tripleurospermum inodorum
Cirsium arvense
Fallopia convolvulus
0.25
0.20
0.08
0.06
0.05
−0.05
−0.09
−0.11
−0.13
−0.23
0.07
0.11
0.13
0.21
0.03
0.10
0.10
0.07
0.06
0.11
Loamy-clay soil (+ high; − low)Soil P2O5 content (+ high; − low)
Convolvulus arvensis
Fallopia convolvulus
Triticum aestivum
Anagallis arvensis
Setaria viridis
Triticum spelta
Persicaria lapathifolia
Cirsium arvense
Hibiscus trionum
Xanthium italicum
0.57
0.26
0.09
0.04
−0.08
−0.09
−0.17
−0.19
−0.20
−0.32
0.38
0.14
0.07
0.07
0.12
0.06
0.17
0.12
0.11
0.33
Hibiscus trionum
Amaranthus retroflexus
Avena fatua
Triticum spelta
Setaria viridis
Phragmites australis
Ambrosia artemisiifolia
Chenopodium polyspermum
Triticum aestivum
Fallopia convolvulus
0.16
0.08
0.08
0.06
0.05
0.05
0.05
0.04
−0.14
−0.19
0.07
0.13
0.07
0.03
0.05
0.14
0.04
0.02
0.16
0.08
Table 4. Names, score values and fit of species giving the highest fit along the first constrained axis in the partial redundancy analysis (pRDA) models of environmental variables in open-field pea experiment (Hungary, 2017–2020).
Table 4. Names, score values and fit of species giving the highest fit along the first constrained axis in the partial redundancy analysis (pRDA) models of environmental variables in open-field pea experiment (Hungary, 2017–2020).
SpeciesAx 1
Score
FitSpeciesAx 1
Score
Fit
2017 (+ high; − low)2018 (+ high; − low)
Stachys annua
Hibiscus trionum
Cirsium arvense
Chenopodium hybridum
Calystegia sepium
Sinapis arvensis
Persicaria amphibia
Trifolium repens
Chenopodium album
Echinochloa crus-galli
0.22
0.21
0.20
0.05
0.04
0.04
0.02
0.01
−0.20
−0.33
0.31
0.12
0.13
0.33
0.23
0.24
0.10
0.22
0.21
0.19
Fallopia convolvulus
Chenopodium polyspermum
Triticum aestivum
Anagallis arvensis
Amaranthus retroflexus
Phragmites australis
Lastuca serriola
Amaranthus albus
Avena fatua
Convolvulus arvensis
0.51
0.13
0.13
0.10
0.09
0.05
0.04
0.01
−0.12
−0.33
0.55
0.22
0.14
0.40
0.17
0.15
0.14
0.14
0.16
0.13
2019 (+ high; − low)2020 (+ high; − low)
Triticum spelta
Persicaria lapathifolia
Tripleurospermum inodorum
Brassica napus
Consolida regalis
Rubus caesius
Anagallis arvensis
Datura stramonium
Chenopodium polyspermum
Hibiscus trionum
0.17
0.17
0.16
0.06
0.04
0.03
−0.05
−0.09
−0.13
−0.20
0.21
0.16
0.15
0.14
0.14
0.13
0.10
0.14
0.22
0.11
Echinochloa crus-galli
Datura stramonium
Avena fatua
Ambrosia artemisiifolia
Bromus tectorum
Anagallis arvensis
Triticum aestivum
Persicaria lapathifolia
Tripleurospermum inodorum
Fallopia convolvulus
0.61
0.17
0.14
0.07
0.01
−0.04
−0.11
−0.13
−0.13
−0.14
0.64
0.53
0.22
0.06
0.10
0.07
0.11
0.09
0.11
0.04
Altitude (+ high; − low)Latitude (+ high; − low)
Stachys annua
Triticum spelta
Setaria viridis
Phragmites australis
Anagallis arvensis
Chenopodium album
Chenopodium polyspermum
Hibiscus trionum
Tripleurospermum inodorum
Cirsium arvense
0.18
0.12
0.08
0.05
0.03
−0.09
−0.11
−0.13
−0.14
−0.16
0.19
0.11
0.10
0.11
0.04
0.04
0.16
0.05
0.12
0.09
Stachys annua
Ambrosia artemisiifolia
Triticum spelta
Setaria viridis
Anagallis arvensis
Phragmites australis
Chenopodium album
Chenopodium polyspermum
Cirsium arvense
Hibiscus trionum
0.17
0.10
0.09
0.06
0.04
0.03
−0.11
−0.12
−0.15
−0.18
0.19
0.13
0.06
0.07
0.06
0.04
0.06
0.20
0.08
0.10
Table 5. Names, score values and fit of species with the highest fit along the first constrained axis in the partial redundancy analysis (pRDA) models of management variables in open-field pea experiment (Hungary, 2017–2020).
Table 5. Names, score values and fit of species with the highest fit along the first constrained axis in the partial redundancy analysis (pRDA) models of management variables in open-field pea experiment (Hungary, 2017–2020).
SpeciesAx 1
Score
FitSpeciesAx 1
Score
Fit
Farming (+ organic; − conventional)Tillage (+ loosening; − ploughing)
Cirsium arvense
Hibiscus trionum
Chenopodium polyspermum
Chenopodium album
Persicaria lapathifolia
Tripleurospermum inodorum
Chenopodium hybridum
Triticum spelta
Stachys annua
Convolvulus arvensis
0.22
0.21
0.15
0.11
0.10
0.10
0.02
−0.10
−0.14
−0.23
0.16
0.12
0.29
0.07
0.06
0.06
0.05
0.08
0.12
0.06
Tripleurospermum inodorum
Ambrosia artemisiifolia
Fallopia convolvulus
Anagallis arvensis
Amaranthus retroflexus
Chenopodium polyspermum
Chenopodium album
Xanthium italicum
Persicaria lapathifolia
Hibiscus trionum
0.15
0.14
0.12
0.03
−0.05
−0.05
−0.07
−0.08
−0.10
−0.15
0.13
0.29
0.03
0.04
0.04
0.03
0.02
0.02
0.06
0.07
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Kovács, E.B.; Dorner, Z.; Csík, D.; Zalai, M. Effect of Environmental, Soil and Management Factors on Weed Flora of Field Pea in South-East Hungary. Agronomy 2023, 13, 1864. https://doi.org/10.3390/agronomy13071864

AMA Style

Kovács EB, Dorner Z, Csík D, Zalai M. Effect of Environmental, Soil and Management Factors on Weed Flora of Field Pea in South-East Hungary. Agronomy. 2023; 13(7):1864. https://doi.org/10.3390/agronomy13071864

Chicago/Turabian Style

Kovács, Endre Béla, Zita Dorner, Dávid Csík, and Mihály Zalai. 2023. "Effect of Environmental, Soil and Management Factors on Weed Flora of Field Pea in South-East Hungary" Agronomy 13, no. 7: 1864. https://doi.org/10.3390/agronomy13071864

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop