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Article

Bioherbicidal Properties of Parthenium hysterophorus, Cleome rutidosperma and Borreria alata Extracts on Selected Crop and Weed Species

by
Mst. Motmainna
1,
Abdul Shukor Juraimi
1,*,
Md. Kamal Uddin
2,
Norhayu Binti Asib
3,
A. K. M. Mominul Islam
4 and
Mahmudul Hasan
1
1
Department of Crop Science, Faculty of Agriculture, Universiti Putra Malaysia, Serdang 43400, Selangor, Malaysia
2
Department of Land Management, Faculty of Agriculture, Universiti Putra Malaysia, Serdang 43400, Selangor, Malaysia
3
Department of Plant Protection, Faculty of Agriculture, Universiti Putra Malaysia, Serdang 43400, Selangor, Malaysia
4
Agro Innovation Laboratory, Department of Agronomy, Faculty of Agriculture, Bangladesh Agricultural University, Mymensingh 2202, Bangladesh
*
Author to whom correspondence should be addressed.
Agronomy 2021, 11(4), 643; https://doi.org/10.3390/agronomy11040643
Submission received: 1 February 2021 / Revised: 2 March 2021 / Accepted: 4 March 2021 / Published: 27 March 2021
(This article belongs to the Section Weed Science and Weed Management)

Abstract

:
Natural product-based herbicides could be the effective alternatives to synthetic chemical herbicides for eco-friendly weed management. This research, therefore, was conducted to identify the phytotoxic properties of Parthenium hysterophorus L., Cleome rutidosperma DC. and Borreria alata (Aubl.) DC. with a view to introducing them as a tool for natural herbicide development. The methanol extracts of these plants were examined on the germination and growth of Zea mays L., Oryza sativa L., Abelmoschus esculentus (L.) Moench and Amaranthus gangeticus L., Oryza sativa f. Spontanea Roshev. (Weedy rice), Echinochloa colona (L.) Link., Euphorbia hirta L., and Ageratum conyzoides L. under laboratory and glasshouse conditions. A complete randomized design (CRD) with five replications and randomized complete block design (RCBD) with four replications were laid out for laboratory and glasshouse experiments, respectively. In the laboratory experiment, three plant extracts of 0, 6.25, 12.5, 50, and 100 g L−1 were tested on survival rate, hypocotyl, and radicle length of eight test plant species. No seed germination of A. conzyoides, E. hirta, and A. gangeticus were recorded when P. hysterophorus extract was applied at 50 g L−1. C. rutidosperma had the same effect on those plants at 100 g L−1. In the glasshouse, similar extracts and concentrations used in the laboratory experiments were sprayed on at the 2–3 leaf stage for grasses and 4–6 for the broadleaf species. Tested plants were less sensitive to C. rutidosperma and B. alata compared to P. hysterophorus extract. Among the weeds and crops, A. conyzoides, E. hirta, A. esculentus and A. gangeticus were mostly inhibited by P. hysterophorus extract at 100 g L−1. Based on these results, P. hysterophorus was the most phytotoxic among the tested plant extracts and could be used for developing a new natural herbicide for green agriculture.

1. Introduction

Parthenium hysterophorus L., Cleome rutidosperma DC., and Borreria alata (Aubl.) DC. belong to the family Asteraceae, Cleomaceae, and Rubiaceae, respectively, and are invasive weeds in Malaysia. Their damage includes threats to biodiversity, exacerbation of allergies and dermatitis, mutagenesis in humans and livestock, and interference (competition and allelopathy) with field crops and rangelands [1,2,3]. Parthenium hysterophorus is native to Mexico and has been spreading like wildfire in different countries. At present, ten states of Malaysia are invaded by this weed, and the state Kedah is the worst infested area [4]. Yield losses between 21 to 50% have occurred due to P. hysterophorus in different crop fields [5]. The allelochemicals released from this plant may inhibit seedling growth and nutrient uptake by destroying the plants’ usable source of nutrients [6,7]. Cleome rutidosperma is native to tropical Africa and now naturalized in different regions of Asia, Australia, America, and the West Indies [2]. This weed is mainly found in sugarcane fields and causes more than 50% sugarcane yield reduction in the Philippines [2]. In Malaysia, C. rutidosperma is planted around the field edges by the farmers to divert the ovipositor of Plutella xylostella (diamondback moth) away from the crop field [2]. Moreover, the plant is considered as the alternate host of Meloidogyne javanica and Meloidogyne incognita [8]. Borreria alata is native to southern Mexico [9]. It is a common weed in sugarcane, rubber, oil palm, orchards, tea, chinchoa, cassava, and many annual upland crops such as maize, soybean, and rice. It has reduced the dry weight and height of young rubber by 12 and 17%, respectively [10].
While manual weed control is the best and most sustainable, herbicidal control is the more effective and rapid option for weed management. However, due to the migration of labor from agriculture to industry; and off-target toxicity including weed biotypes resistant to existing synthetic herbicides, researchers are motivated to think about alternatives [11]. In these circumstances, allelopathic plants or their isolated allelochemicals may play a key role. Allelopathic plants may exert either inhibitory or stimulatory effects on the germination and growth of other plants in their immediate vicinity. Recently, allelopathic plants or their allelochemicals are being utilized sporadically instead of synthetic herbicides to control weeds, and more attention has been paid by scientists to develop natural product-based herbicides from allelopathic plants [12,13,14,15,16]. Moreover, due to the presence of higher oxygen and nitrogen-rich molecules and having a relatively low halogen substitute, most of the allelochemicals are environment friendly [17]. Hence, the allelochemicals isolated from allelopathic plants can either be developed as a natural herbicide or used for templates to further develop novel synthetic herbicides with new modes of action [14,16].
In most of the allelopathic studies, laboratory bioassay has mainly been used by the researchers to identify allelopathic plants because of their rapid out return. Additionally, bioassay performance may help the researchers to predict the allelopathic potentials of a plant in glasshouse or field conditions [18]. However, a plant that showed strong allelopathic activity on target plants in s laboratory bioassay, might differ in glasshouse or field conditions due to the influence of several environmental determinants [19]. Plant crude extract with strong allelopathic potential has recently contributed greatly to weed management and controlling weeds [19,20,21,22]. Although the allelopathic properties of P. hysterophorus have been reported, the allelopathy of C. rutidosperma and B. alata are scant so far. In addition, most of the articles related to P. hysterophorus allelopathy were based on their laboratory bioassay results. Therefore, a detailed study of these plants under both laboratory and glasshouse conditions warrants due attention to evaluating their allelopathic potential. Hence, to explore the allelopathic properties of P. hysterophorus, C. rutidosperma, and B. alata on Zea mays L., Oryza sativa L., Abelmoschus esculentus (L.) Moench, Amaranthus gangeticus L., Oryza sativa f. spontanea Roshev (Weedy rice), Echinochloa colona (L.) Link., Euphorbia hirta L. and Ageratum conyzoides L., two experiments were conducted under laboratory and glasshouse conditions with a view to developing natural product-based bioherbicides.

2. Materials and Methods

2.1. Test Plants

Four cropspecies, e.g., Z. mays, O. sativa, A. esculentus, and A. gangeticus, and four weed species, e.g., Weedy rice, E. colona, E. hirta, and A. conzyoides were used in this research as test plants. The seeds of E. colona, Weedy rice, and O. sativa “MR 219” were collected from the rice fields of Sekinchan, Kuala Selangor, and Selangor, Malaysia, and other weed seeds (E. hirta and A. conzyoides) were collected from farm 15 at the Universiti Putra Malaysia. The seeds of Z. mays, A. esculentus, and A. gangeticus were purchased from Green World Genetics Sdn. Bhd., Kuala lumpur, Selangor, Malaysia.

2.2. Extraction Procedure

Whole plants of P. hysterophorus, C. rutidosperma, and B. alata at their maximum vegetative stage were collected from different locations of Universiti Putra Malaysia except P. hysterophorus which was collected from Ladang Infoternak, Sungai Siput, Perak, Malaysia. The collected weeds were washed carefully with running tap water for removing the dust particles, then air-dried in open trays under shaded conditions at room temperature for 3 weeks. Then, each species was chopped and crushed separately in a Willey mill. In a conical flask, 100 g powder of each species was soaked with 1000 mL methanol: distilled water (80:20, v/v), and paraffin was used for wrapping the flask. The flask was shaken using an Orbital shaker at 150 rpm agitation speed for 48 h at a room temperature (24–26 °C). The solution was filtered using four layers of cheesecloth then centrifuged for 1 h at 3000 rpm. Then a 0.2-μ, 15-mm syringe filter (Phenex, Non-sterile, Luer/Slip, LT Resources, Puchong, Selangor, Malaysia) was used to re-filter the solution. A rotary evaporator was used at 40 °C to evaporate the methanol from the extract. Sterile distilled water was used to obtain stock extract concentrations of 6.25, 12.5, 25, 50, and 100 g L−1 for bioassay. All extracts were refrigerated at 4 °C before they were used. The method described by Aslani et al. [23] was used in preparing methanol extracts for each species.

2.3. Laboratory Bioassay

2.3.1. Experimental Site

The experiment was conducted in a growth chamber at the Seed Technology Laboratory, Department of Crop Science, Faculty of Agriculture, Universiti Putra Malaysia (3°02′ N, 101°42′ E, 31 m elevation), Selangor, Malaysia from January to March 2019.

2.3.2. Experimental Treatments and Design

Healthy and uniform weed seeds were collected and then soaked for 24 h with 0.2% potassium nitrate (KNO3) and then rinsed with distilled water and incubated at room (24–26 °C) temperature until the radicle emerged about 1 mm. Twenty pre-germinated uniform seeds of each crop and weed species were placed in 9.0-cm-diameter plastic disposable Petri dishes, containing two sheets of Whatman No. 1 filter paper. Then the filter paper on the Petri dishes was moistened with 10 mL of P. hysterophorus, C. rutidosperma and B. alata methanol extract at six different concentrations: 0 (distilled water only), 6.25, 12.5, 25, 50, and 100 g L−1 separately. The Petri dishes were then moved to a growth chamber and incubated under fluorescent light (8500 lux) with a completely randomized design at the temperature of 30/20 °C (day/night), with a 12 h/12 h (day/night cycle). Relative humidity ranged from 30 to 50%. The lids of the Petri dishes were not sealed to allow gas exchange and to avoid an anaerobic condition.

2.3.3. Data Collection

After 7 days of germination, the survival rate, radicle and hypocotyl length of all seedlings were measured. The hypocotyl and radicle length was measured using Image J software [24] and the inhibitory effect was calculated by the equation stated below [23]
I = 100 (C − A)/C
where “I” is the inhibition amount (%), “C” is the mean length of the radicle and hypocotyl of the control, and “A” is the mean length of the radicle and hypocotyl of the methanol extracts.

2.4. Glasshouse Experiment

2.4.1. Experimental Site and Design

The glasshouse experiment was conducted from April to June 2020, at the faculty of Agriculture in Ladang 15, Universiti Putra Malaysia. Foliar application of P. hysterophorus, C. rutidosperma, and B. alata methanol extract was assessed for their suppressive effects on the growth and development of Weedy rice, E. colona, E. hirta, A. conyzoides, Z. mays, O. sativa, A. esculentus, and A. gangeticus. Pre-germinated seeds of test plants were sown in each pot (15 cm diameter × 12 cm height) and then covered with soil at a depth of 1 cm, and finally, the soil was moistened with tap water. After germination, only five equal-sized healthy seedlings of O. sativa, E. colona, E. hirta, A. conyzoides, and weedy rice, and one seedling (equal-sized healthy) of Z. mays, A. gangeticus, and A. tricolor were kept in each pot. The pots were arranged in a randomized complete block design with four replications. Methanol extracts of P. hysterophorus, C. rutidosperma, and B. alata were sprayed with 6.25, 12.5, 25, 50, and 100 g L−1 concentration at the 2–3 leaf stage (2 weeks old) for grasses and 4–6 leaf stage for broadleaf species (3 weeks old) with the help of a 1 L multipurpose sprayer (Deluxe pressure sprayer). Spray volume (100 mL m−2) was prepared using distilled water [25]. Plants in the control treatment were sprayed with 200 mL water without extract at two days intervals or when needed.

2.4.2. Data Collection

Three weeks after spray, the individual plant was separated into the root, shoot, and leaf fractions. Plant height (PH) and root length (RL) were measured using a 1 m ruler. The leaf area was determined using a leaf area meter (LI-3000, Li-COR, Lincoln, NE, USA) and expressed as cm2 plant−1. Fresh and dry weights were determined using a digital balance. Samples were dried in an oven at 60 °C for 72 h to take the dry weight of the samples. Total chlorophyll content indicated as SPAD value was measured by a chlorophyll meter, SPAD-502 (Menolta, Japan), as described by Mahdavikia et al. [26]

2.5. Statistical Analysis

A two-way analysis of variance (ANOVA) was performed to determine any significant differences between each treatment and the control for both experiments. The differences between the treatment’s means were pooled using the Tukey test with a 0.05 probability level. SAS (Statistical Analysis System) software, version 9.4 (Cary, NC, USA) was used to conduct the analysis. Probit analysis based on the percentage of inhibition of survival rate or radicle and hypocotyl length was used to measure ECs50, ECr50, and ECh50. ECs50, ECr50, and ECh50 were the effective doses capable of inhibiting 50% of survival rate, radicle, and hypocotyl length respectively. The most active extracts were determined as the index (Re) using the equation given below for each extract tested:
Rank (Re) = ECs50n (survival rate) + ECr50n (radicle) + ECh50n (hypocotyl)
where Re is the rank of the extract and ECs50n, ECr50n, and ECh50n are the concentrations of treatments that cause 50% inhibition on germination, root, and hypocotyl growth, respectively. The extract with the lowest Re values was considered as the most phytotoxic treatment and the least phytotoxic effect of the extract was observed for the highest Re value.

3. Results

3.1. Laboratory Experiment

3.1.1. Effect of Methanol Extracts on Survival Rate and Initial Growth of Weeds

The results showed that P. hysterophorus, C. rutidosperma, and B. alata extracts significantly influenced the survival rate as well as the hypocotyl and radicle length of the tested weed species (p < 0.05). The magnitude of inhibition increased with an increase in extract concentration (Table 1).
No survival rate was recorded in A. conyzoides and E. hirta when P. hysterophorus extract was applied at 50 g L−1. Meanwhile, no significant inhibition on the survival rate of all weed species was observed when C. rutidosperma and B. alata extracts were applied at a low concentration of 6.25 g L−1. However, C. rutidosperma and B. alata inhibited seed survival rate at the highest concentrations by 100% and 90%, respectively. The survival rate of A. conyzoides and E. hirta seeds was more sensitive to the extracts compared to Weedy rice and E. colona seeds.
The radicle length of the target weed was significantly reduced (p < 0.05) by P. hysterophorus extract at a concentration equal to or higher than 6.25 g L−1. The root growth of A. conyzoides, E. hirta, E. colona, and Weedy rice was reduced by 89.3%, 85.4%, 89.5%, and 88.7% when treated with C. rutidosperma extracts at the concentration of 50 g L−1. No radicle development of the test species was observed when P. hysterophorus extract was applied at the highest concentration, whereas up to 90% inhibition was observed by B. alata extract (Table 1). All extracts decreased the hypocotyl elongation of the target weeds. At the concentration of 50 g L−1, P. hysterophorus, C. rutidosperma, and B. alata extracts reduced the hypocotyl length of all tested weeds by 95–100%, 84–90%, and 76–81%, respectively. Therefore, the extent of inhibition of P. hysterophorus extract was higher compared to C. rutidosperma and B. alata extracts.

3.1.2. Effect of Methanol Extracts on the Survival Rate and Initial Growth of Crops

The survival rate, hypocotyl and radicle length of the tested crops were also significantly influenced by the methanol extract of P. hysterophorus, C. rutidosperma, and B. alata. The decrement of these parameters increased with the increase of the extract concentration when compared to the control (Table 2).
The survival rate of Z. mays, O. sativa, A. esculentus, and A. gangeticus were reduced by 46%, 100%, 85%, and 100%, respectively for P. hysterophorus extracts, 35%, 93%, 64%, and 100%, respectively for C. rutidosperma extract, and 21%, 85%, 46%, and 88%, respectively for B. alata extract at the highest concentration i.e., 100 g L−1 (Table 2). Parthenium hysterophorus showed the highest phytotoxic effect on A. gangeticus (100%) compared to the other crops at 50 g L−1.
The reduction in radicle length ranged from 93 to 100% for P. hysterophorus extract, 78 to 100% for C. rutidosperma extract, and 74 to 88% for B. alata extract at the highest concentration (100 g L−1). Extracts of P. hysterophorus, C. rutidosperma, and B. alata differed from each other in reducing the radicle length of tested crops compared to the control (Table 2). The P. hysterophorus extract exerted a higher effect in reducing the radicle length of the target crops. For instance, at 50 g L−1 of P. hysterophorus extract, the radicle growth of A. gangeticus was completely suppressed (100%) while in C. rutidosperma and B. alata extracts it was reduced by 89.2% and 77.4%, respectively.
Hypocotyl growth of all tested crops responded differently to P. hysterophorus, C. rutidosperma, and B. alata extracts. The highest concentration (100 g L−1) of P. hysterophorus extract resulted in a reduction of 80 to 100% in hypocotyl length of the tested species. On the other hand, 100 g L−1 of C. rutidosperma and B. alata extracts resulted in 67 to 100% and 65 to 82% hypocotyl length reduction, respectively. At the lowest concentration (6.25 g L−1), C. rutidosperma and B. alata did not show any significant effect on the hypocotyl growth of Z. mays. The hypocotyl length of test crops was reduced by arange of 10.8 to 100%, 1.4 to 100%, and 1.4 to 82.0% when treated with P. hysterophorus, C. rutidosperma and B. alata extracts, respectively.

3.1.3. Comparison of Methanol Extracts on Examined Initial Growth Parameters and Plants

The half inhibitory concentrations of each extract for all test species are shown in Table 3. The effectiveness of the P. hysterophorus extract was higher than the C. rutidosperma and B. alata extract, as the rank value of C. rutidosperma extract (598.3 g L−1) and B. alata extract (876.9 g L−1) were more than the P. hysterophorus (393.9 g L−1). The obtained EC50 showed differences among the response of test plants to the inhibitory effect of P. hysterophorus, C. rutidosperma, and B. alata (Table 3). The differences in the sensitivity of species to the extracts were also evident from the rank values of plants. Zea mays was the only species affected at higher concentrations i.e., 157.7, 206.3, and 329.3 g L−1 of P. hysterophorus, C. rutidosperma, and B. alata extracts, respectively. In other words, the Z. mays plant showed more tolerance, which indicates that only a high concentration of extracts could suppress this plant. The second less sensitive test plant (after Z. mays) was A. esculentus. The rank value of A. conyzoides, E. hirta, E. colona, Weedy rice, O. sativa, and A. gangeticus was 22.0, 22.6, 25.7, 26.6, 30.9, and 33.8 g L−1, respectively, when they were treated with P. hysterophorus extract. The rank values for these tested plant species were 39.9, 44.2, 39.9, 39.9, 54.3, and 50.9 g L−1, respectively for C. rutidosperma and 50.6, 51.6, 53.6, 55.0, 66.9, and 79.8 g L−1, respectively for B. alata extracts. Therefore, it was apparent that these tested plant species were most sensitive to P. hysterophorus extract.

3.2. Glasshouse Experiment

3.2.1. Effect of Methanol Extract on Plant Height, Root Length, Leaf Area, and Total Chlorophyll Content of Weeds

Data regarding the effect of the foliar spray of methanol extracts of P. hysterophorus, C. rutidosperma, and B. alata on control (%), plant height, and root length of tested weeds are presented in Table 4. Among all the tested weeds, only A. conyzoides was controlled by 80% and 100% when sprayed with P. hysterophorus at a concentration of 50 g L−1 and 100 g L−1, respectively. A similar trend was observed where an increase in the concentration of each treatment resulted in a remarkable reduction in plant height. Among the treatments, P. hysterophorus showed a more phytotoxic effect on the plant height of tested weeds compared to C. rutidosperma and B. alata at the highest concentration (100 g L−1). At the same concentration, P. hysterophorus extract caused 100%, 60.0%, 20.4%, and 19.2% reduction in plant height of A. conyzoides, E. hirta, Weedy rice, and E. colona, respectively. On the other hand, 8.1to 11.1% and 5.6 to 8.6% plant height reduction was achieved by C. rutidosperma and B. alata extracts, respectively for all tested weeds.
Among the tested weeds, the root length of A. conyzoides was inhibited completely (100%) when sprayed with 100 g L−1 P. hysterophorus extract. The inhibition of root length of all tested weeds ranged from 35.3 to 100%, 15.9 to 22.4%, and 14.6 to 16.5% at the same concentration (100 g L−1) of P. hysterophorus, C. rutidosperma, and B. alata, respectively.
Declined leaf area and total chlorophyll content of all tested weeds werealso observed with an increase in the foliar spray of methanol extracts of P. hysterophorus, C. rutidosperma, and B. alata. Similar to plant height and root length, the leaf area and total chlorophyll of A. conyzoides were most affected by the foliar spray of P. hysterophorus extract compared to the others (Table 5). Leaf area inhibition of A. conyzoides, E. hirta, Weedy rice, and E. colona ranged from 15 to 100%, 12 to 70%, 5.3 to 42.0%, and 5.6 to 35.3%, respectively when sprayed with an increased amount of P. hysterophorus extract. A similar trend was also observed for total chlorophyll. The inhibition percentage for leaf area and total chlorophyll of all tested weeds ranged from 15.3 to 19.4 and 12.0 to 18.90 when sprayed with the highest concentration of C. rutidosperma and B. alata extracts, respectively.

3.2.2. Effect of Methanol Extract on Total Fresh and Dry Weight of Weeds

Total fresh and dry weights of all tested weeds were significantly influenced by the foliar spray of P. hysterophorus extract in a concentration-dependent pattern compared to C. rutidosperma and B. alata extract (Table 5). The control obtained the highest fresh and dry weight. However, the reduction differed among the targeted species and the treatments. Parthenium hysterophorus extract reduced the fresh and dry weight of tested weeds from 35.3 to 100% and 43.0 to 100% at 100 g L−1 compared to the control, respectively. At 50 g L−1 concentration, the foliar spray of P. hysterophorus extract reduced 52.8% and 87.1% total fresh weight and 56.0% and 90% total dry weight of E. hirta and A. conyzoides, respectively. On the other hand, among the treatments, the highest fresh and dry weight was recorded when different concentrations of C. rutidosperma and B. alata extracts were applied on the tested weeds (Table 5).

3.2.3. Phytotoxic Effect of Methanol Extracts on Plant Height and Root Length of Crops

The effect of treatments on the development of tested crops at the maturity stage is shown in Table 6. The result indicated that the suppressive magnitude of applied extracts was species-dependent. Plant height of all tested crops except Z. mays was significantly influenced by the extract of P. hysterophorus compared to C. rutidosperma and B. alata extract. There was no significant difference between the activities of C. rutidosperma and B. alata at the lowest concentration. The highest plant height reduction (62.2%) occurred at 100 g L−1 concentration of P. hysterophorus for A. gangeticus, and only 20.4% plant height of O. sativa was reduced at the same concentration (Table 6).
Root lengths of all tested plants were significantly decreased by all the applied extracts. Among the species, root length was more reduced in A. gangeticus at 100 g L−1 concentration of P. hysterophorus with an inhibition index of 72.2% followed by 61.9%, 38.9%, and 38.6% in A. esculentus, Z. mays, and O. sativa, respectively. This indicates that the effects caused by the P. hysterophorus extract on the plant height and root length were more prominent at higher concentrations across the species. The C. rutidosperma and B. alata extracts were less phytotoxic on the plant height and root length of the tested crops compared to P. hysterophorus extract. The extract of C. rutidosperma inhibited the plant height and root length of the tested crops by 8.2 to 14.1% and 9.2 to 21.0%, respectively.

3.2.4. Phytotoxic Effect of Methanol Extracts on Leaf Area, Total Chlorophyll, Fresh and Dry Weight of Crops

Foliar spray of P. hysterophorus, C. rutidosperma,and B. alata extract had a significant effect on leaf area and chlorophyll content of the test species (Table 7). The effects of P. hysterophorus extracts showed a decline from 6.3 to 61.0% at the lowest (6.25 g L−1) to the highest (100 g L−1) concentrations on the leaf area of A. esculentus, while 3.88 to 37.97% was recorded in O. sativa. The chlorophyll content of all tested crops except O. sativa was significantly affected by the foliar spray of P. hysterophorus extract at the concentration of 6.25 g L−1. The test crop A. esculentus showed a 17.3% decrease in chlorophyll content compared to O. sativa when sprayed with P. hysterophorus extract at the highest concentration (100 g L−1). Leaf area and chlorophyll content of A. gangeticus was inhibited by 22.1% and 18.3% by C. rutidosperma extract and 16.9% and 19.0% by B. alata extract, respectively at 100 g L−1 concentration.
The foliar spray of P. hysterophorus, C. rutidosperma, and B. alata also had a significant effect on the total fresh and dry weight of all tested species and the effect was concentration-dependent (Table 7). Moreover, the effect of extracts on different tested species at the same concentration was varied. Total dry weight was decreased from 9.9 to 64.7% in A. esculentus followed by 13.3 to 58.1%, 8.1 to 39.4%, and 6.0 to 36.4% in A. gangeticus, O. sativa, and Z. mays, respectively with a foliar spray of P. hysterophorus extract at lowest (6.25 g L−1) to highest concentrations (100 g L−1). For A. gangeticus, 61.1% growth reduction was achieved by P. hysterophorus extract while 16.4% and 13.6% reduction were achieved by C. rutidosperma and B. alata extract, respectively. On the other hand, A. gangeticus obtained a relatively higher reduction (61.0%) of total fresh weight for P. hysterophorus extract compared to other tested species and applied extracts.

4. Discussion

The methanol extract of three Malaysian invasive weeds had the ability to affect survival rate (%) and seedling growth of four selected weed species (A. conyzoides, E. hirta, Weedy rice, and E. colona) and four crops (Z. mays, O. sativa, A. esculentus, and A. gangeticus), under laboratory conditions. All these extracts influenced the survival rate, hypocotyl and radicle growth of tested species in a dose-dependent manner. Extracts of P. hysterophorus and C. rutidosperma were the most promising because of their remarkable strength, potency, and regularity in inhibiting germination and seedling growth of all tested species. The inhibition of plant extracts on the germination process is thought to be associated with osmotic effects on the rate of imbibition, which ultimately inhibits the initiation of germination and, especially, cell elongation [25]. The P. hysterophorus extract at 50 g L−1 fully inhibited the seed germination and seedling growth of A. conyzoides, E. hirta, and A. gangeticus. The inhibitory effect of P. hysterophorus extract and residues on the growth and development of some field crops were also reported by Batish et al. [27], Singh et al. [28], Mersie and Singh [29].
Moreover, at 50 g L−1 concentration, C. rutidosperma also caused significant inhibition of all tested seeds. Ladhari et al. [30] reported the allelopathic properties of Cleome arabica L. and identified 11-α-acetylbrachy-carpone-22(23)-ene as the main allelopathic compound. Whereas, Ahmed et al. [31] stated that the asdamarane type triterpene, for instance, 11-α-acetylbrachy-carpone-22(23)-ene, 17-α-hydroxycabraleactone, and amblyone were responsible for the toxicity of Cleome amblyocarpa.
The inhibitory effect of the test extracts varied among the eight species examined, and A. conyzoides was more sensitive to tested extracts than the other tested plants. The present study is in agreement with Ishak and Sahid [32] who found that the extract of Leucaena leucocephala at 66.7 g L−1 reduced germination, hypocotyl, and radicle elongation of A. conyzoides by 48%, 47%, and 65%, respectively. Furthermore, the radicle length of the tested species was more sensitive to extracts compared to the germination percentage and the hypocotyl length. The greater sensitivity of radicle growth to the allelopathic plant extracts is because—radicles are the first organ that are exposed to the phytotoxic substances and a more highly permeable tissue than other organs [19,33,34], and/or a low mitotic division in the root apical meristem [35]. Moreover, the allelopathic substances can affect genes responsible for the cellular characterization of radicle tissues and endoderm, reducing its development [36].
The glasshouse experiment provided further evidence for the higher allelopathic potential of P. hysterophorus extract compared to C. rutidosperma and B. alata as observed in the laboratory. The results showed that P. hysterophorus extract at 50 g L−1 and 100 g L−1 significantly reduced the growth of 21-days-old A. conyzoides and E. hirta. The highest reduction of 100% was observed from the maximum concentration (100 g L−1) of P. hysterophorus extract at the mature stage of A. conyzoides. This type of dose-dependent inhibitory activity was reported by many researchers around the globe [19,34,37,38]. A greater decrease in plant height was recorded in A. conyzoides compared to other species. At 21 days after spray, only untreated A. conyzoides began flowering which indicates that the other treated plants might be suppressed by allelochemicals stress. Aslam et al. [39] reported the phytotoxic effect of Calatropis procera, Peganum harmala, and Tamarix aphylla on the shoot and root length of mustard and wheat, and wheat was sensitive to all three extracts at all the concentrations. Mulberry aqueous leaf extract suppressed shoot and root length, shoot and root dry matters of Bermuda grass by 90% and 80% at 100% concentrations, respectively [40]. Hassan et al. [41] also observed a decrease in shoot and root length of Zea mays and Vigna unguiculata treated with increased concentrations of Jatropha curcas extract.
Foliar spray of P. hysterophorus extract reduced dry weights and leaf area as the level of concentration increased across species although the species responded independently. The reduction in total dry weight was observed to be associated with a decrease in plant height and leaf area. Total dry weight and leaf area were mostly decreased in A. conyzoides and E. hirta, respectively. Leaf area reduction was higher in A. conyzoides and lower in Z. mays at 21 days after spraying with P. hysterophorus extract. This type of species-dependent inhibitory activity was also reported by several studies. For example, phytotoxins have an adverse impact on the growth of certain plants while having little or no inhibition in other plants at certain concentrations [42,43,44]. Several studies reveal a decline in leaf area of certain plant species using different extracts [45,46].
Chlorophyll is a determinant factor in photosynthesis and it was found to be lower in A. conyzoides among all tested species. The leaves of the tested plants appeared partially folded and this may lead to a decrease in photosynthetic activity [47]. Reduction of chlorophyll content in plants due to application of allelopathic plant extracts was also reported by Kamal [48], Siyar et al. [49], and Abdel-Farid [50].
It was also observed in the present study that the application of plant extracts in a foliar spray in laboratory conditions caused more inhibition compared to glasshouse conditions. Similar findings were also reported by Al-Humaid and El-Mergawi [21]. The inhibition by foliar spray may occur through various mechanisms such as suppressed hormone activity, a decreased rate of ion absorption, enzyme activity inhibition, reduce cell membrane permeability and also inhibit certain physiological processes such as photosynthesis, respiration, and protein formation. Thus, the seedling stage and the more mature stage of target plants vary in their sensitivities to plant extracts.

5. Conclusions

The study demonstrated that all the methanol extracts from three Malaysian invasive weeds (P. hysterophorus, C. rutidosperma, and B. alata) have allelopathic potential on the seed germination, growth, and development of tested plants. P. hysterophorus appeared as the most phytotoxic plant extract among the three. Moreover, the phytotoxic effect of the extracts was dependent on the target species, extract concentrations, and the extracted plant species. The growth and development of the tested plant species in the glasshouse were less affected compared to seed germination and growth under laboratory conditions. The only phytotoxic impact was provided by P. hysterophorus on the tested plant species in the glasshouse trial. Among the test species, A. conyzoides was more sensitive to P. hysterophorus extract. Taking into account the promising result of P. hysterophorus extract, this weed could be used for further study to develop a natural product-based herbicide for sustainable green agriculture. Identification and characterization of the most active phytotoxic compounds of the P. hysterophorus extract will be the first step of future studies.

Author Contributions

Conceptualization, A.S.J. and A.K.M.M.I.; methodology, A.K.M.M.I.; validation, A.S.J., M.K.U., N.B.A. and M.M.; formal analysis, M.M. and M.H.; investigation, M.M. and M.H.; resources, M.M. and A.S.J.; data curation, M.M.; writing—original draft preparation, M.M.; writing—review and editing, A.S.J. and A.K.M.M.I.; visualization, M.M. and M.H.; supervision, A.S.J. and N.B.A.; project administration, A.S.J. and M.M.; funding acquisition, A.S.J. All authors have read and agreed to the published version of the manuscript.

Funding

This research received funding from the Fundamental Research Grant Scheme (FRGS), Malaysia (FRGS/1/2017/WAB01/UPM/01/2) and Putra Grant UPM (GP-IPB/2017/9523400).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors are grateful to Fundamental Research Grant Scheme (FRGS), Malaysia (FRGS/1/2017/WAB01/UPM/01/2) and Putra Grant UPM (GP-IPB/2017/9523400) also sincerely acknowledges the University Putra Malaysia for providing facilities. We also express gratitude to Sabina Yeasmin, for editing the English of this manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Patel, S. Harmful and beneficial aspects of Parthenium hysterophorus: An update. 3 Biotech 2011, 1, 1–9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Ghosh, P.; Chatterjee, S.; Das, P.; Karmakar, S.; Mahapatra, S. Natural habitat, phytochemistry and pharmacological properties of a medicinal weed–Cleome rutidosperma DC. (Cleomaceae): A comprehensive review. Int. J. Pharm. Sci. Res. 2019, 10, 1605–1612. [Google Scholar] [CrossRef]
  3. Conserva, L.M.; Ferreira, J.C. Borreria and Spermacoce species (Rubiaceae): A review of their ethnomedicinal properties, chemical constituents, and biological activities. Pharmacogn. Rev. 2012, 6, 46–55. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Maszura, C.M.; Karim, S.M.R.; Norhafizah, M.Z.; Kayat, F.; Arifullah, M. Distribution, Density, and Abundance of Parthenium Weed (Parthenium hysterophorus L.) at Kuala Muda, Malaysia. Int. J. Agron. 2018, 2018, 1046214. [Google Scholar] [CrossRef]
  5. Safdar, M.E.; Tanveer, A.; Khaliq, A.; Riaz, M.A. Yield losses in maize (Zea mays) infested with parthenium weed (Parthenium hysterophorus L.). Crop Prot. 2015, 70, 77–82. [Google Scholar] [CrossRef]
  6. Hassan, G.; Khan, M.A.; Marwat, K.B.; Anwar, M.; Hashim, S. Efficacy of some forest species extracts on wheat and two major weeds of Arid Zone of NWFP. Jpn. J. Plant Sci. 2008, 2, 39–42. [Google Scholar]
  7. Safdar, M.; Tanveer, A.; Khaliq, A.; Naeem, M. Allelopathic action of parthenium and its rhizospheric soil on maize as influenced by growing conditions. Planta Daninha 2014, 32, 243–253. [Google Scholar] [CrossRef] [Green Version]
  8. Mamaril, E.C.; Alberto, R.T. Root-knot nematodes infecting some common weeds in vegetable growing areas of Sicsican. Int. Nematol. Netw. Newsl. 1989, 6, 37–39. [Google Scholar]
  9. Cherigo, L.; Lezcano, J.; Spadafora, C.; MartínezLuis, S. Evaluation of phytotoxic, cytotoxic and antiparasitic in vitro activities of Borreria verticillata, a weed of Panamanian coffee crops. Biosci. Res. 2012, 9, 82–86. [Google Scholar]
  10. Burgos, N.R.; Ortuoste, J.D. Weed Management in Natural Rubber. In Weed Control: Sustainability, Hazards, and Risks in Cropping Systems Worldwide; CRC Press: Cleveland, OH, USA, 2018; pp. 485–504. [Google Scholar] [CrossRef]
  11. Arafat, Y.; Shahida, K.; Lin, W.; Fang, C.; Sadia, S.; Ali, N.; Azeem, S. Allelopathic evaluation of selected plants extract against broad and narrow leaves weeds and their associated crops. Acad. J. Agric. Res. 2015, 3, 226–234. [Google Scholar]
  12. Cheng, F.; Cheng, Z. Research Progress on the use of plant allelopathy in agriculture and the physiological and ecological mechanisms of allelopathy. Front. Plant Sci. 2015, 6, 1020. [Google Scholar] [CrossRef]
  13. Cheema, Z.A.; Farooq, M.; Khaliq, A. Application of allelopathy in crop production: Success story from Pakistan (Chapter 6). In Allelopathy: Current Trends and Future Applications; Cheema, Z.A., Farooq, M., Wahid, A., Eds.; Springer: Berlin, Germany, 2013; pp. 113–144. [Google Scholar] [CrossRef]
  14. Islam, A.K.M.M.; Yeasmin, S.; Qasem, J.R.S.; Juraimi, A.S.; Anwar, P. Allelopathy of Medicinal Plants: Current Status and Future Prospects in Weed Management. Agric. Sci. 2018, 9, 1569–1588. [Google Scholar] [CrossRef] [Green Version]
  15. Islam, A.K.M.M.; Widhalm, J.R. Agricultural Uses of Juglone: Opportunities and Challenges. Agronomy 2020, 10, 1500. [Google Scholar] [CrossRef]
  16. Noguchi, H. Current research status of allelopathy of plants grown in Bangladesh. Fundam. Appl. Agric. 2019, 5, 1–9. [Google Scholar] [CrossRef]
  17. Soltys, D.; Krasuska, U.; Bogatek, R.; Gniazdowska, A. Allelochemicals as Bioherbicides—Present and perspectives. In Herbicides—Current Research and Case Studies in Use; Price, A.J., Kelton, J.A., Eds.; IntechOpen: London, UK, 2013. [Google Scholar] [CrossRef] [Green Version]
  18. Ozkan, T.G.I.; Urusak, E.A.; Appiah, K.S.; Fujii, Y.; Ozkan, I. First Broad Screening of Allelopathic Potential of Wild and Cultivated Plants in Turkey. Plants 2019, 8, 532. [Google Scholar] [CrossRef] [Green Version]
  19. Islam, A.K.M.M.; Hasan, M.M.; Yeasmin, S.; Abedin, M.A.; Kader, M.A.; Rashid, M.H.; Anwar, M.P. Bioassay screening of tropical tree sawdust for allelopathic properties and their field performance against paddy weeds. Fundam. Appl. Agric. 2019, 4, 906–915. [Google Scholar] [CrossRef]
  20. Rawat, L.S.; Maikhuri, Y.M.; Yateesh, N.K.; Jha, N.K.; Phondani, P.C. Sunflower allelopathy for weed control in agriculture systems. J. Crop Sci. Biotechnol. 2017, 20, 45–60. [Google Scholar] [CrossRef]
  21. Al-Humaid, A.; El-Mergawi, R.A. Herbicidal activities of seven native plants on the germination and growth of Phalaris minor, Echinochloa crusgalli, Portulaca oleracea and Lactuca sativa. J. Agric. Sci. Technol. 2014, 4, 843–852. [Google Scholar]
  22. Boari, A.; Vurro, M.; Calabrese, G.J.; Mahmoud, M.N.Z.; Cazzato, E.; Fracchiolla, M. Evaluation of Dittrichia viscosa (L.) Greuter Dried Biomass for Weed Management. Plants 2021, 10, 147. [Google Scholar] [CrossRef]
  23. Aslani, F.; Juraimi, A.S.; Ahmad-Hamdani, M.S.; Omar, D.; Alam, A.; Hashemi, F.S.G.; Hakim, A.; Uddin, K. Allelopathic effect of methanol extracts fromTinospora tuberculataon selected crops and rice weeds. Acta Agric. Scand. Sect. B Plant Soil Sci. 2014, 64, 165–177. [Google Scholar] [CrossRef]
  24. Mirmostafaee, S.; Azizi, M.; Fujii, Y. Study of Allelopathic Interaction of Essential Oils from Medicinal and Aromatic Plants on Seed Germination and Seedling Growth of Lettuce. Agronomy 2020, 10, 163. [Google Scholar] [CrossRef] [Green Version]
  25. El-Mergawi, R.A.; Al-Humaid, A.I. Searching for natural herbicides in methanol extracts of eight plant species. Bull. Natl. Res. Cent. 2019, 43, 22. [Google Scholar] [CrossRef]
  26. Mahdavikia, F.; Saharkhiz, M.J.; Karami, A. Defensive response of radish seedlings to the oxidative stress arising from phenolic compounds in the extract of peppermint (Mentha × piperita L.). Sci. Hortic. 2017, 214, 133–140. [Google Scholar] [CrossRef]
  27. Batish, D.R.; Singh, H.P.; Pandher, J.K.; Arora, V.; Kohli, R.K. Phytotoxic effect of Parthenium residues on the selected soil properties and growth of chickpea and radish. Weed Biol. Manag. 2002, 2, 73–78. [Google Scholar] [CrossRef]
  28. Singh, H.P.; Batish, D.R.; Pandher, J.K.; Kohli, R.K. Phytotoxic effects of Parthenium hysterophorus residues on three Brassica species. Weed Biol. Manag. 2005, 5, 105–109. [Google Scholar] [CrossRef]
  29. Mersie, W.; Singh, M. Allelopathic effect of parthenium (Parthenium hysterophorus L.) extract and residue on some agronomic crops and weeds. J. Chem. Ecol. 1987, 13, 1739–1747. [Google Scholar] [CrossRef] [PubMed]
  30. Ladhari, A.; Omezzine, F.; DellaGreca, M.; Zarrelli, A.; Zuppolini, S.; Haouala, R. Phytotoxic activity of Cleome arabica L. and its principal discovered active compounds. S. Afr. J. Bot. 2013, 88, 341–351. [Google Scholar] [CrossRef] [Green Version]
  31. Ahmed, A.A.; Mohamed, T.K.; Williams, H.J.; Scott, A.I.; Reibenspies, J.H. Structure Revision of Cleoamblynol A from Cleome amblyocarpa. Nat. Prod. Lett. 1997, 10, 239–244. [Google Scholar] [CrossRef]
  32. Ishak, M.S.; Sahid, I. Allelopathic effects of the aqueous extract of the leaf and seed of Leucaena leucocephala on three selected weed species. In AIP Conference Proceedings; American Institute of Physics: College Park, MD, USA, 2014; pp. 659–664. [Google Scholar] [CrossRef] [Green Version]
  33. Nishida, N.; Tamotsu, S.; Nagata, N.; Saito, C.; Sakai, A. Allelopathic Effects of Volatile Monoterpenoids Produced by Salvia leucophylla: Inhibition of Cell Proliferation and DNA Synthesis in the Root Apical Meristem of Brassica campestris Seedlings. J. Chem. Ecol. 2005, 31, 1187–1203. [Google Scholar] [CrossRef] [PubMed]
  34. Islam, A.M.; Hasan, M.; Musha, M.H.; Uddin, K.; Juraimi, A.S.; Anwar, P. Exploring 55 tropical medicinal plant species available in Bangladesh for their possible allelopathic potentiality. Ann. Agric. Sci. 2018, 63, 99–107. [Google Scholar] [CrossRef]
  35. Levizou, E.; Karageorgou, P.; Psaras, G.K.; Manetas, Y. Inhibitory effects of water soluble leaf leachates from Dittrichia viscosa on lettuce root growth, statocyte development and graviperception. Flora—Morphol. Distrib. Funct. Ecol. Plants 2002, 197, 152–157. [Google Scholar] [CrossRef] [Green Version]
  36. Franco, D.M.; Silva, E.M.; Saldanha, L.L.; Adachi, S.A.; Schley, T.R.; Rodrigues, T.M.; Dokkedal, A.L.; Nogueira, F.T.S.; De Almeida, L.F.R. Flavonoids modify root growth and modulate expression of SHORT-ROOT and HD-ZIP III. J. Plant Physiol. 2015, 188, 89–95. [Google Scholar] [CrossRef] [PubMed]
  37. Mousavi, S.S.; Karami, A.; Haghighi, T.M.; Alizadeh, S.; Maggi, F. Phytotoxic Potential and Phenolic Profile of Extracts from Scrophularia striata. Plants 2021, 10, 135. [Google Scholar] [CrossRef] [PubMed]
  38. Abd-Elgawad, A.M.; El Gendy, A.E.-N.G.; Assaeed, A.M.; Al-Rowaily, S.L.; Alharthi, A.S.; Mohamed, T.A.; Nassar, M.I.; Dewir, Y.H.; ElShamy, A.I. Phytotoxic Effects of Plant Essential Oils: A Systematic Review and Structure-Activity Relationship Based on Chemometric Analyses. Plants 2020, 10, 36. [Google Scholar] [CrossRef]
  39. Alam, A.; Juraimi, A.S.; Rafii, M.Y.; Hamid, A.A.; Aslani, F.; Hakim, M.A. Salinity-induced changes in the morphology and major mineral nutrient composition of purslane (Portulaca oleracea L.) accessions. Biol. Res. 2016, 49, 24. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Haq, R.A.; Hussain, M.; Cheema, Z.A.; Mushtaq, M.N.; Farooq, M. Mulberry leaf water extract inhibits bermudagrass and promotes wheat growth. Weed Biol. Manag. 2010, 10, 234–240. [Google Scholar] [CrossRef]
  41. Hassan, A.; Mukhtar, F.; Mohammed, I. Allelopathic effect of Jatropha curcas (Lin) leachate on germination and early seedling growth of five (5) agricultural crops in Kano, Nigeria. Bayero J. Pure Appl. Sci. 2014, 6, 53. [Google Scholar] [CrossRef] [Green Version]
  42. Ladhari, A.; Omezzine, F.; Rinez, A.; Haouala, R. Phytotoxicity of Daphne gnidium L. occurring in Tunisia. World Acad. Sci. Eng. Technol. 2011, 59, 1534–1537. [Google Scholar] [CrossRef]
  43. Schandry, N.; Becker, C. Allelopathic Plants: Models for Studying Plant–Interkingdom Interactions. Trends Plant Sci. 2020, 25, 176–185. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Imatomi, M.; Novaes, P.; Gualtieri, S.C.J. Interspecific variation in the allelopathic potential of the family Myrtaceae. Acta Bot. Bras. 2013, 27, 54–61. [Google Scholar] [CrossRef] [Green Version]
  45. Jabran, K.; Mahajan, G.; Sardana, V.; Chauhan, B.S. Allelopathy for weed control in agricultural systems. Crop Prot. 2015, 72, 57–65. [Google Scholar] [CrossRef]
  46. Algandaby, M.M.; El-Darier, S.M. Management of the noxious weed; Medicago polymorpha L. via allelopathy of some medicinal plants from Taif region, Saudi Arabia. Saudi J. Biol. Sci. 2018, 25, 1339–1347. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Amador-Vargas, S.; Dominguez, M.; León, G.; Maldonado, B.; Murillo, J.; Vides, G.L. Leaf folding response of a sensitive plant shows context-dependent behavioral plasticity. Plant Ecol. 2014, 215, 1445–1454. [Google Scholar] [CrossRef]
  48. Kamal, J. Impact of allelopathy of sunflower (Helianthus annuus L.) roots extract on physiology of wheat (Triticum aestivum L.). Afr. J. Biotechnol. 2011, 10, 14465–14477. [Google Scholar] [CrossRef] [Green Version]
  49. Siyar, S.; Majeed, A.; Muhammad, Z.; Ali, H.; Inayat, N. Allelopathic effect of aqueous extracts of three weed species on the growth and leaf chlorophyll content of bread wheat. Acta Ecol. Sin. 2019, 39, 63–68. [Google Scholar] [CrossRef]
  50. Abdel-Farid, I.B.; Massoud, M.S.; Al-Enazy, Y.; Latef, A.A.H.A.; Jahangir, M.; Gomaa, N.H. Allelopathic Potential of Haloxylonpersicum against Wheat and Black Mustard with Special Reference to Its Phytochemcial Composition and Antioxidant Activity. Agronomy 2021, 11, 244. [Google Scholar] [CrossRef]
Table 1. Effects of P. hysterophorus, C. rutidosperma, and B. alata methanol extracts on survival rate (%), hypocotyl, and radicle length (cm) of the tested weed species.
Table 1. Effects of P. hysterophorus, C. rutidosperma, and B. alata methanol extracts on survival rate (%), hypocotyl, and radicle length (cm) of the tested weed species.
Tested PlantsDose (g L−1)P. hysterophorusC. rutidospermaB. alata
Survival Rate (%)Hypocotyl Length (cm)Radicle Length (cm)Survival Rate (%)Hypocotyl Length (cm)Radicle Length (cm)Survival Rate (%)Hypocotyl Length (cm)Radicle Length (cm)
A. conyzoides0.00100.00 a ± 04.91 a ± 0.032.70 a ± 0.04100.00 a ± 04.94 a ± 0.022.72 a ± 0.04100.00 a ± 04.99 a ± 0.042.68 a ± 0.03
(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.2582.00 b ± 1.222.92 b ± 0.040.89 b ± 0.0299.00 a ± 13.56 b ± 0.071.30 b ± 0.0299.00 a ± 13.99 b ± 0.031.33 b ± 0.01
(18)(40.53)(67.04)(1)(27.93)(52.20)(1)(20.04)(50.37)
12.538.00 c ± 1.30.86 c ± 0.020.34 c ± 0.0172.00 b ± 22.23 c ± 0.020.86 c ± 0.0183.00 b ± 4.642.96 c ± 0.031.05 c ± 0.02
(62)(82.48)(87.40)(28)(54.86)(68.38)(17)(40.68)(60.82)
2513.00 d ± 1.280.41 d ± 0.010.17 d ± 0.0145.00 c ± 3.530.96 d ± 0.010.57 d ± 0.1242.00 c ± 2.551.88 d ± 0.050.82 d ± 0.01
(87)(91.65)(93.70)(55)(80.57)(79.04)(58)(62.32)(69.40)
500.00 e ± 00.00 e ± 00.00 e ± 018.00 d ± 1.220.62 e ± 0.020.29 e ± 0.0128.00 d ± 2.500.98 e ± 0.040.71 e ± 0.02
(100)(100)(100)(72)(87.44)(89.34)(72)(80.36)(73.51)
1000.00 e ± 00.00 e ± 00.00 e ± 00.00 e ± 00.00 f ± 00.00 f ± 05.00 e ±0.320.44 f ± 0.020.23 f ± 0.21
(100)(100)(100)(100)(100)(100)(95)(91.18)(91.42)
E. hirta0.00100.00 a ± 06.32 a ± 0.021.91 a ± 0.01100.00 a ± 06.26 a ± 0.021.98 a ± 0.03100.00 a ± 06.34 a ± 0.021.89 a ± 0.2
(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.2584.00 b ± 1.873.68 b ± 0.010.71 b ± 0.0396.00 a ± 1.874.29 b ± 0.011.32 b ± 0.0298.00 a ± 1.224.94 b ± 0.110.95 b ± 1.4
(16)(41.77)(62.83)(4)(31.47)(33.33)(2)(22.08)(49.74)
12.539.00 c ± 1.80.97 c ± 0.010.33 c ± 0.0278.00 b ± 23.16 c ± 0.20.71 c ± 0.0882.00 b ± 1.23.75 c ± 0.070.81 c ± 0.03
(61)(84.65)(82.72)(22)(49.52)(64.14)(18)(40.85)(57.14)
2512.00 d ± 1.220.52 d ± 0.10.16 d ± 0.0148.00 c ± 1.220.99 d ± 0.040.44 d ± 0.745.00 c ± 2.242.16 d ± 0.010.59 d ± 1.96
(88)(91.77)(91.62)(52)(84.19)(77.78)(55)(65.93)(68.78)
500.00 e ± 00.00 e ± 00.00 e ± 020.00 d ± 1.580.71 e ± 0.30.29 e ± 1.7729.00 d ± 1.871.20 e ± 0.040.45 e ± 0.02
(100)(100)(100)(80)(88.66)(85.35)(71)(81.07)(76.19)
1000.00 e ± 00.00 e ± 00.00 e ± 00.00 e ± 00.00 f ± 00.00 f ± 09.00 e ± 10.69 f ± 0.20.18 f ± 0.01
(100)(100)(100)(100)(100)(100)(91)(89.12)(90.48)
Weedy rice0.00100.00 a ± 04.89 a ± 0.12.13 a ± 0.08100.00 a ± 04.98 a ± 0.082.21 a ± 0.1100.00 a ± 04.91 a ± 0.142.02 a ± 0.02
(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.2587.00 b ± 2.553.23 b ± 0.060.80 b ± 0.0398.00 a ± 1.223.61 b ± 0.011.06 b ± 0.02 100.00 a ± 03.98 b ± 0.041.02 b ± 0.03
(13)(34.15)(62.44)(2)(27.51)(52.04)(0)(18.94)(49.50)
12.549.00 c ± 1.871.48 c ± 0.020.60 c ± 0.0274.00 b ± 1.872.33 c ± 0.020.72 c ± 0.0481.00 b ± 1.872.75 c ± 0.070.96 bc ± 0.02
(51)(69.92)(71.83)(26)(53.21)(67.42)(19)(44.38)(52.47)
2520.00 d ± 1.580.75 d ± 0.010.24 d ± 0.0144.00 c ± 10.99 d ± 0.030.45 d ± 0.0251.00 c ± 1.82.02 d ± 0.030.88 c ± 0.01
(80)(84.66)(88.73)(56)(80.12)(79.64)(49)(58.86)(56.43)
507.00 e ± 20.24 e ± 0.060.16 de ± 0.1315.00 d ± 3.530.77 e ± 0.010.25 d ± 0.0123.00 d ± 1.221.14 e ± 0.010.33 d ± 0.19
(93)(95.09)(92.49)(85)(84.54)(88.69)(77)(76.78)(83.66)
1000.00 e ± 00.00 e ± 00.00 e ± 00.00 e ± 00.00 e ± 00.00 e ± 07.00 e ± 1.270.46 f ± 0.020.11 e ± 0.9
(100)(100)(100)(100)(100)(100)(93)(90.63)(94.55)
E. colona0.00100.00 a ± 05.11 a ± 0.032.95 a ± 1.96100.00 a ± 05.00 a ± 0.042.94 a ± 0.04100.00 a ± 05.07 a ± 0.042.90 a ± 0.02
(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.2584.00 b ± 13.46 b ± 0.021.14 b ± 0.2498.00 a ± 1.223.62 b ± 0.021.25 b ± 0.02100.00 a ± 04.01 b ± 0.021.40 b ± 0.01
(16)(32.29)(61.35)(2)(27.6)(57.48)(0)(20.91)(51.72)
12.539.00 c ± 11.77 c ± 0.330.69 c ± 0.0174.00 b ± 1.872.01 c ± 0.340.91 c ± 0.0482.00 b ± 22.85 c ± 0.231.30 c ± 0.12
(61)(65.36)(76.61)(26)(59.8)(69.05)(18)(43.79)(55.17)
2517.00 d ± 2.550.88 d ± 0.560.36 d ± 0.0452.00 c ± 1.470.79 d ± 0.070.63 d ± 0.0255.00 c ± 1.582.03 d ± 0.711.09 d ± 0.01
(83)(82.78)(87.80)(48)(84.2)(78.57)(45)(59.96)(62.41)
504.00 e ± 10.19 e ± 0.490.12 e ± 0.0320.00 d ± 1.580.50 e ± 0.060.31 e ± 0.0125.00 d ± 2.741.08 e ± 0.580.41 e ± 0.57
(96)(96.28)(95.93)(80)(90)(89.46)(75)(78.70)(85.86)
1000.00 e ± 00.00 f ± 00.00 f ± 00.00 e ± 00.00 f ± 0.010.00 f ± 06.00 e ± 10.34 f ± 1.460.20 f ± 0.02
(100)(100)(100)(100)(100)(100)(94)(93.29)(93.10)
Data are expressed as mean ± standard error. Means with the same letters in the column for each extract are not significantly different at p > 0.05. Values inside the parenthesis are inhibition percentages relative to the control.
Table 2. Effects of P. hysterophorus, C. rutidosperma, and B. alata methanol extracts on survival rate (%), hypocotyl and radicle length (cm) of tested crops.
Table 2. Effects of P. hysterophorus, C. rutidosperma, and B. alata methanol extracts on survival rate (%), hypocotyl and radicle length (cm) of tested crops.
Tested PlantsDose (g L−1)P. hysterophorusC. rutidospermaB. alata
Survival Rate (%)Hypocotyl Length (cm)Radicle Length (cm)Survival Rate (%)Hypocotyl Length (cm)Radicle Length (cm)Survival Rate (%)Hypocotyl Length (cm)Radicle Length (cm)
O. sativa0.00100.00 a ± 03.16 a ± 0.026.17 a ± 0.16100.00 a ± 03.19 a ± 0.036.17 a ± 0.01100.00 a ± 03.18 a ± 0.036.19 a ± 0.24
(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.2591.00 b ± 2.912.06 b ± 0.282.88 b ± 0.03100.00 a ± 02.92 b ± 0.023.11 b ± 0.04100.00 a ± 03.01 b ± 0.753.34 b ± 0.1
(9)(34.81)(53.32)(0)(8.46)(49.59)(0)(5.35)(46.04)
12.558.00 c ± 31.03 c ± 0.222.00 c ± 0.0286.00 b ± 1.871.94 c ± 0.13.31 c ± 0.4288.00 b ± 1.222.14 c ± 0.162.41 c ± 0.03
(42)(67.40)(67.58)(14)(39.18)(62.56)(12)(32.70)(61.07)
2525.00 d ± 2.240.63 d ± 0.60.99 d ± 0.348.00 c ± 20.99 d ± 0.041.11 d ± 0.0360.00 c ± 1.581.13 d ± 0.121.95 d ± 0.02
(75)(80.06)(83.95)(52)(68.96)(82.01)(40)(64.46)(68.50)
5010.00 e ± 1.580.42 e ± 0.010.55 e ± 0.2622.00 d ± 1.220.70 e ± 0.130.87 e ± 0.0231.00 d ± 1.870.87 e ± 0.131.15 e ± 0.1
(90)(86.71)(91.08)(78)(78.06)(85.89)(69)(72.64)(81.42)
1000.00 f ± 00.00 f ± 00.00 f ± 07.00 e ± 1.240.44 f ± 0.190.24 f ± 0.0215.00 e ± 1.580.68 f ± 0.710.88 f ± 0.33
(100)(100)(100)(93)(86.21)(96.11)(85)(78.62)(85.78)
Z. mays0.00100.00 a ± 02.88 a ± 0.055.98 a ± 0.02100.00 a ± 02.79 a ± 0.35.90 a ± 0.23100.00 a ± 02.83 a ± 0.255.89 a ± 0.24
(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.25100.00 a ± 02.57 b ± 0.014.91 b ± 0.03100.00 a ± 02.75 a ± 0.145.10 b ± 0.02100.00 a ± 02.79 a ± 0.595.13 b ± 0.16
(0)(10.76)(17.89)(0)(1.43)(13.56)(0)(1.41)(12.90)
12.592.00 ab ± 22.14 c ± 0.023.28 c ± 0.25100.00 a ± 02.48 b ± 0.023.88 ± 0.22100.00 a ± 02.31 b ± 0.213.91 c ± 0.35
(8)(25.69)(45.15)(0)(11.11)(34.24)(0)(18.37)(33.62)
2585.00 b ± 2.241.15 c ± 0.21.98 d ± 0.3190.00 b ± 1.582.03 c ± 0.042.91 ± 0.3595.00 a ± 1.582.15 c ± 0.132.38 d ± 0.01
(15)(60.07)(66.89)(10)(27.24)(50.68)(5)(24.03)(59.59)
5075.00 c ± 3.530.91 e ± 0.351.02 e ± 0.0474.00 c ± 1.871.30 d ± 0.011.26 ± 0.0187.00 b ± 2.551.16 d ± 0.151.56 e ± 0.02
(25)(68.40)(82.94)(26)(53.41)(78.64)(13)(59.01)(73.51)
10054.00 d ± 1.870.56 f ± 0.310.39 f ± 0.4765.00 d ± 3.530.91 e ± 0.040.77 ± 0.0479.00 c ± 1.870.99 e ± 0.430.71 f ± 0.03
(46)(80.56)(93.48)(35)(67.38)(86.95)(21)(65.02)(87.95)
A. esculentus0.00100.00 a ± 08.71 a ± 0.045.00 a ± 0.03100.00 a ± 08.78 a ± 0.115.09 a ± 0.02100.00 a ± 08.62 a ± 0.15.02 a ± 0.33
(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.25100.00 a ± 06.52 b ± 0.033.23 b ± 0.15100.00 a ± 07.05 b ± 0.044.00 b ± 0.03100.00 a ± 07.67 b ± 0.034.28 b ± 0.15
(0)(25.14)(35.40)(0)(19.70)(21.41)(0)(11.02)(14.74)
12.591.00 b ± 1.874.44 c ± 0.012.64 c ± 0.35100.00 a ± 05.66 c ± 0.183.14 c ± 0.01100.00 a ± 06.77 c ± 0.023.98 c ± 0.03
(9)(49.02)(47.20)(0)(35.54)(38.31)(0)(21.46)(20.72)
2581.00 c ± 1.92.94 d ± 0.251.96 d ± 0.0190.00 a ± 3.163.91 d ± 0.292.35 d ± 0.1994.00 a ± 2.455.20 d ± 0.813.08 d ± 0.26
(19)(66.24)(60.80)(10)(55.47)(53.83)(6)(39.67)(38.64)
5050.00 d ± 1.581.85 e ± 0.031.05 e ± 0.170.00 b ± 5.472.84 e ± 0.021.98 e ± 0.2978.00 b ± 3.744.24 e ± 0.162.15 e ± 0.13
(50)(78.76)(79.00)(30)(67.65)(61.10)(22)(50.81)(57.17)
10015.00 e ± 1.51.09 f ± 0.120.29 f ± 0.0936.00 c ± 41.90 f ± 0.191.09 f ± 0.1254.00 c ± 2.453.00 f ± 0.041.29 f ± 0.06
(85)(87.48)(94.20)(64)(78.34)(78.58)(46)(65.20)(74.30)
A. gangeticus0.00100.00 a ± 03.10 a ± 0.162.02 a ± 0.02100.00 a ± 03.09 a ± 0.012.04 a ± 0.18100.00 a ± 03.06 a ± 0.032.08 a ± 0.25
(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.2586.00 b ± 1.872.33 b ± 0.231.20 b ± 0.21100.00 a ± 02.85 b ± 0.161.50 b ± 0.24100.00 a ± 03.02 a ± 0.281.86 b ± 0.18
(14)(24.84)(40.59)(0)(7.77)(26.47)(0)(4)(10.58)
12.570.00 c ± 3.531.15 c ± 0.390.44 c ± 0.0180.00 b ± 1.581.55 c ± 0.020.85 c ± 0.3388.00 b ± 2.552.28 b ± 0.160.96 c ± 0.2
(30)(62.90)(78.22)(20)(49.84)(58.33)(12)(25.49)(53.85)
2530.00 d ± 1.580.81 d ± 0.050.18 d ± 0.0944.00 c ± 2.451.05 d ± 0.210.51 d ± 0.2453.00 c ± 1.221.67 c ± 0.020.76 d ± 0.01
(70)(73.87)(91.09)(56)(66.02)(75.00)(47)(45.42)(63.46)
500.00 e ± 00.00 e ± 00.00 e ± 011.00 d ± 10.58 e ± 0.270.22 e ± 0.1123.00 d ± 1.241.02 d ± 0.170.47 e ± 0.06
(100)(100)(100)(89)(81.23)(89.21)(77)(66.67)(77.40)
1000.00 e ± 00.00 e ± 00.00 e ± 00.00 e ± 00.00 f ± 00.00 f ± 012.00 e ± 1.470.55 e ± 0.310.23 f ± 0.23
(100)(100)(100)(100)(100)(100)(88)(82.03)(88.94)
Data are expressed as mean ± standard error. Means with the same letters in the column for each extract are not significantly different at p > 0.05. Values inside the parenthesis are inhibition percentages relative to the control.
Table 3. EC50 and rank value (Re) of P. hysterophorus, C. rutidosperma, and B. alata methanol extract for the tested species.
Table 3. EC50 and rank value (Re) of P. hysterophorus, C. rutidosperma, and B. alata methanol extract for the tested species.
Target PlantsP. hysterophorusC. rutidospermaB. alata
ECs50ECh50ECr50Rank (Re)ECs50ECh50ECr50Rank (Re)ECs50ECh50ECr50Rank (Re)
g L−1
A. conyzoides10.937.153.9622.0422.3911.286.2739.9426.5917.266.7750.62
E. hirta11.146.914.5922.6423.4811.019.7344.2227.8116.447.3851.63
E. colona11.739.384.5425.6523.8410.595.4239.8528.6016.898.0853.57
Weedy rice13.478.724.4326.6221.8811.676.3839.9327.5517.909.5955.04
O. sativa15.719.016.1330.8527.8419.856.6354.3234.8324.737.3366.89
A. gangeticus15.6510.737.3833.7622.5916.8311.4650.8830.6431.7117.4779.82
A. esculentus46.7714.7213.2174.774.5623.4724.83122.86104.7047.3237.98190.00
Z. mays115.4626.2415.96157.66131.8652.0722.34206.27254.0750.4421.77329.28
Rank (Re)240.8692.8660.24393.92348.44156.7793.06598.27534.79222.69116.37876.85
ECs50, ECh50, and ECr50 are the concentration of extracts that inhibits 50% of germination, hypocotyl and radicle respectively and Rank is the sum of ECs50, ECh50, and ECr50.
Table 4. Effect of methanol extract of P. hysterophorus, C. rutidosperma, and B. alata on the control (%), plant height (cm) and root length (cm) of A. conyzoides, E. hirta, weedy rice, and E. colona.
Table 4. Effect of methanol extract of P. hysterophorus, C. rutidosperma, and B. alata on the control (%), plant height (cm) and root length (cm) of A. conyzoides, E. hirta, weedy rice, and E. colona.
Tested WeedsDose (g L−1)Control (%)Plant Height (cm)Root Length (cm)
PHCRBAPHCRBAPHCRBA
A. conyzoides00.00 a ± 00.00 a ± 00.00 a ± 056.79 a ± 0.8357.34 a ± 1.3357.57 a ± 0.6328.18 a ± 1.5327.59 a ± 2.1828.10 a ± 0.21
(0)(0)(0)(0)(0)(0)
6.250.00 a ± 00.00 a ± 00.00 a ± 051.98 b ± 0.5756.62 a ± 3.257.05 a ± 0.5623.92 c ± 1.1626.88 b ± 1.1727.78 a ± 0.76
(8.45)(1.27)(0.90)(15.09)(2.56)(1.12)
12.50.00 a ± 00.00 a ± 00.00 a ± 046.11 b ± 0.7956.40 a ± 3.457.02 a ± 2.3721.38 c ± 0.1926.77 b ± 2.2127.70 a ± 2.51
(18.75)(1.65)(0.94)(24.13)(2.97)(1.41)
2510.00 a ± 5.770.00 a ± 00.00 a ± 037.08 b ± 1.0055.87 a ± 4.656.34 a ± 4.7615.53 b ± 0.9926.23 a ± 1.7727.16 a ± 1.95
(34.72)(2.58)(2.13)(44.91)(4.92)(3.36)
5080.00 a ± 8.160.00 b ± 00.00 b ± 013.30 b ± 4.4654.03 a ± 0.4955.45 a ± 0.784.65 b ± 1.5725.10 a ± 0.8926.23 a ± 0.67
(76.69)(5.76)(3.70)(83.53)(9.00)(6.66)
100100.00 a ± 00.00 b ± 00.00 b ± 00.00 c ± 051.02 b ± 1.1153.75 a ± 0.490.00 c ± 021.41 b ± 0.2824.00 a ± 1.5
(100)(11.03)(6.63)(100)(22.40)(14.56)
E. hirta00.00 a ± 00.00 a ± 00.00 a ± 042.24 a ± 0.2242.51 a ± 0.4142.35 a ± 0.2129.87 a ± 0.2930.48 a ± 0.2030.24 a ± 0.3
(0)(0)(0)(0)(0)(0)
6.250.00 a ± 00.00 a ± 00.00 a ± 038.45 b ± 0.5941.65 a ± 0.3942.00 a ± 1.3726.23 b ± 0.929.94 a ± 0.3229.89 a ± 0.28
(8.98)(2.01)(0.82)(12.18)(1.77)(1.13)
12.50.00 a ± 00.00 a ± 00.00 a ± 035.93 b ± 3.4541.52 a ± 0.3841.74 a ± 0.7824.16 b ± 0.1129.37 a ± 1.3129.63 a ± 0.39
(14.93)(2.33)(1.43)(19.09)(3.64)(2.01)
250.00 a ± 00.00 a ± 00.00 a ± 031.01 b ± 4.6341.43 a ± 0.4541.39 a ± 1.2120.23 b ± 0.5828.76 a ± 0.2828.98 a ± 0.32
(26.59)(2.54)(2.24)(32.26)(5.62)(4.15)
5025.00 a ± 00.00 b ± 00.00 b ± 026.34 b ± 0.9840.25 a ± 0.3240.55 a ± 2.1314.46 b ± 2.527.81 a ± 0.3227.80 a ± 1.12
(37.64)(5.31)(4.23)(51.61)(8.76)(8.07)
10055.00 a ± 00.00 b ± 00.00 b ± 016.51 b ± 0.4838.34 a ± 0.2438.71 a ± 0.698.79 b ± 0.6524.50 a ± 0.8825.39 a ± 0.45
(60.91)(9.79)(8.59)(70.58)(19.62)(16.02)
Weedy rice00.00 a ± 00.00 a ± 00.00 a ± 079.64 a ± 2.5680.19 a ± 0.7280.04 a ± 2.1227.01 a ± 1.8826.79 a ± 0.6426.66 a ± 0.24
(0)(0)(0)(0)(0)(0)
6.250.00 a ± 00.00 a ± 00.00 a ± 077.86 b ± 1.9379.55 a ± 2.8979.92 a ± 0.5425.57 b ± 0.3726.25 a ± 0.8526.32 a ± 0.03
(2.24)(0.80)(0.16)(5.32)(2.01)(1.29)
12.50.00 a ± 00.00 a ± 00.00 a ± 077.51 c ± 1.3178.72 b ± 1.8379.48 a ± 1.4824.18 c ± 1.1225.77 b ± 0.1426.21 a ± 0.11
(2.67)(1.84)(0.70)(10.47)(3.80)(1.69)
250.00 a ± 00.00 a ± 00.00 a ± 073.61 c ± 0.6777.74 b ± 0.6578.65 a ± 1.0822.54 b ± 0.2325.32 a ± 1.225.44 a ± 1.2
(7.58)(3.06)(1.74)(16.55)(5.50)(4.58)
500.00 a ± 00.00 a ± 00.00 a ± 069.54 b ± 1.8176.29 a ± 2.6677.02 a ± 0.7520.09 b ± 0.4323.93 a ± 0.7724.61 a ± 0.25
(12.68)(4.87)(3.78)(25.60)(10.68)(7.69)
1000.00 a ± 00.00 a ± 00.00 a ± 063.38 c ± 1.3373.72 b ± 1.8775.55 a ± 0.9815.66 b ± 0.2621.96 a ± 0.4222.13 a ± 0.45
(20.41)(8.07)(5.61)(41.99)(18.03)(17.02)
E. colona00.00 a ± 00.00 a ± 00.00 a ± 081.77 a ± 0.2582.05 a ± 0.7282.47 a ± 1.2320.22 a ± 0.0320.11 a ± 0.1119.99 a ± 0.21
(0)(0)(0)(0)(0)(0)
6.250.00 a ± 00.00 a ± 00.00 a ± 080.61 b ± 1.0981.62 ab ± 0.2882.35 a ± 0.5419.08 b ± 0.0619.59 a ± 0.6219.65 a ± 0.28
(1.41)(0.53)(0.14)(5.61)(2.56)(1.68)
12.50.00 a ± 00.00 a ± 00.00 a ± 079.06 b ± 1.1381.12 a ± 1.8382.03 a ± 1.4718.20 b ± 0.2719.50 a ± 0.4119.57 a ± 0.03
(3.31)(1.14)(0.53)(9.78)(3.03)(2.09)
250.00 a ± 00.00 a ± 00.00 a ± 075.52 b ± 0.6280.12 a ± 0.5581.50 a ± 0.816.35 b ± 0.1318.93 a ± 0.6818.88 a ± 0.67
(7.64)(2.36)(1.17)(19.11)(5.86)(5.52)
500.00 a ± 00.00 a ± 00.00 a ± 071.52 b ± 2.1878.15 a ± 0.6579.64 a ± 0.3215.06 b ± 0.5618.16 a ± 0.2818.06 a ± 0.50
(12.53)(4.77)(3.43)(25.52)(9.69)(9.62)
1000.00 a ± 00.00 a ± 00.00 a ± 066.10 b ± 0.7975.38 a ± 0.8776.89 a ± 0.2113.07 b ± 0.2116.90 a ± 0.6317.07 a ± 0.76
(19.17)(8.13)(6.76)(35.32)(15.93)(14.62)
Data are expressed as mean. Means ± standard error with same letters in the row for each extract are not significantly different at p > 0.05. Values inside the parenthesis are inhibition percentages relative to the control. Note: PH = P. hysterophorus, CR = C. rutidosperma, BA = B. alata.
Table 5. Effect of methanol extract of P. hysterophorus, C. rutidosperma, and B. alata on leaf area (cm2), total chlorophyll (SPAD), total fresh weight (g pot−1), and total dry weight (g pot−1) of A. conyzoides, E. hirta, weedy rice, and E. colona.
Table 5. Effect of methanol extract of P. hysterophorus, C. rutidosperma, and B. alata on leaf area (cm2), total chlorophyll (SPAD), total fresh weight (g pot−1), and total dry weight (g pot−1) of A. conyzoides, E. hirta, weedy rice, and E. colona.
Tested WeedsDose (g L−1)Leaf Area (cm2) Total Chlorophyll (SPAD)Total Fresh Weight (g pot−1)Total Dry Weight (g pot−1)
PHCRBAPHCRBAPHCRBAPHCRBA
A. conyzoides0811.72 a ± 4.74816.68 a ± 2.53813.86 a ± 5.1233.61 a ± 0.1134.01 a ± 0.2833.45 a ± 0.0387.87 a ± 0.5789.01 a ± 0.4188.71 a ± 0.1512.06 a ± 0.2212.27 a ± 0.2112.10 a ± 0.19
(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.25682.81 b ± 1.85811.44 a ± 2.22813.04 a ± 5.1029.87 a ± 0.0233.14 a ± 0.0333.10 a ± 0.0276.18 b ± 0.4487.25 a ± 0.5687.69 a ± 0.3110.66 b ± 0.2311.94 a ± 0.2512.02 a ± 0.20
(15.87)(0.64)(0.10)(11.13)(2.56)(1.05)(13.30)(1.98)(1.15)(11.63)(2.69)(0.69)
12.5525.31 b ± 5.23806.17 a ± 2.39806.13 a ± 3.6726.74 b ± 0.2032.26 a ± 0.1732.69 a ± 0.0966.84 b ± 0.5786.84 a ± 0.4587.25 a ± 0.259.53 b ± 0.2011.65 a ± 0.2311.85 a ± 0.18
(35.28)(1.29)(0.95)(20.45)(5.16)(2.28)(23.92)(2.44)(1.65)(20.95)(5.07)(2.09)
25319.16 b ± 6.92785.42 a ± 3.01791.36 a ± 3.5824.43 c ± 0.0530.16 b ± 0.0131.44 a ± 0.1548.62 b ± 0.8084.03 a ± 0.4884.81 a ± 0.447.16 b ± 0.1811.23 a ± 0.1911.49 a ± 0.21
(60.69)(3.83)(2.76)(27.31)(11.32)(6.02)(44.69)(5.60)(4.40)(40.60)(8.50)(5.07)
50125.20 b ± 4.20750.16 a ± 3.60758.11 a ± 6.0515.09 b ± 1.1228.94 a ± 0.0229.33 a ± 0.0111.34 b ± 1.8180.83 a ± 0.5482.25 a ± 0.421.19 b ± 0.4310.71 a ± 0.2510.94 a ± 0.25
(84.54)(8.15)(6.85)(54.96)(14.91)(12.31)(87.05)(9.91)(7.28)(89.97)(12.70)(9.62)
1000.00 c ± 0675.67 b ± 3.06716.05 a ± 1.900.00 b ± 026.68 a ± 0.0326.65 a ± 0.020.00 b ± 074.08 a ± 0.2475.96 a ± 0.840.00 b ± 09.89 a ± 0.209.98 c ± 0.19
(100)(17.27)(12.01)(100)(21.55)(20.32)(100)(16.77)(14.38)(100)(19.42)(17.45)
E. hirta0116.96 a ± 0.27117.25 a ± 0.11117.02 a ± 0.6944.45 a ± 0.3045.07 a ± 0.2044.79 a ± 0.2423.37 a ± 0.1624.05 a ± 0.2523.76 a ± 0.227.70 a ± 0.067.88 a ± 0.087.69 a ± 0.43
(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.25100.24 b ± 0.40116.33 a ± 0.14116.82 a ± 0.1240.43 b ± 0.1644.33 a ± 0.0744.49 a ± 0.2320.80 b ± 0.1323.36 a ± 0.2723.35 a ± 0.476.73 b ± 0.047.50 a ± 0.057.51 a ± 0.45
(14.29)(0.78)(0.17)(9.03)(1.64)(0.66)(10.99)(2.87)(1.73)(12.63)(4.75)(2.40)
12.585.91 b ± 1.05115.54 a ± 0.26115.59 a ± 0.2637.60 b ± 0.1843.85 a ± 0.1143.75 a ± 0.2518.41 b ± 0.1123.14 a ± 0.2623.32 a ± 0.275.93 b ± 0.037.39 b ± 0.047.39 b ± 0.62
(26.54)(1.45)(1.22)(15.41)(2.71)(2.33)(21.21)(3.81)(1.86)(23.01)(6.15)(3.90)
2571.46 b ± 0.49112.79 a ± 0.63112.94 a ± 0.2335.30 b ± 0.0143.00 a ± 0.0442.52 a ± 0.2113.62 b ± 1.0822.52 a ± 0.2823.02 a ± 0.174.50 b ± 0.137.19 a ± 0.217.28 a ± 0.41
(38.90)(3.80)(3.49)(20.59)(4.59)(5.07)(41.68)(6.39)(3.13)(41.53)(8.72)(5.33)
5058.58 b ± 0.27108.54 a ± 0.86109.56 a ± 0.3830.30 c ± 0.0841.19 a ± 0.1740.37 b ± 0.2711.04 b ± 0.1021.99 a ± 0.2922.23 a ± 0.243.39 b ± 0.126.93 a ± 0.346.99 a ± 0.18
(49.91)(7.43)(6.37)(31.83)(8.61)(9.87)(52.75)(8.58)(6.43)(55.97)(12.08)(9.07)
10038.95 b ± 0.9699.28 a ± 0.72100.44 a ± 1.2921.88 b ± 0.5836.77 a ± 0.2137.37 a ± 0.247.04 b ± 0.1120.37 a ± 0.3020.41 a ± 0.191.92 b ± 0.066.43 a ± 0.646.41 a ± 0.49
(66.70)(15.32)(14.17)(50.75)(18.41)(16.57)(69.88)(15.31)(14.08)(75.13)(18.42)(16.64)
Weedy rice0227.23 a ± 0.19 226.87 a ± 0.13226.96 a ± 0.9733.65 a ± 0.1834.04 a ± 0.1833.74 a ± 0.2285.74 a ± 0.0885.56 a ± 0.1485.27 a ± 0.1420.03 a ± 0.1520.44 a ± 0.1220.28 a ± 0.03
(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.25220.65 b ± 0.30225.79 a ± 0.23225.81 a ± 0.2432.03 b ± 0.5433.41 a ± 0.1233.52 a ± 0.6479.14 b ± 0.1783.95 a ± 0.0784.17 b ± 0.1218.85 b ± 0.0819.98 a ± 0.0120.06 a ± 0.49
(2.89)(0.47)(0.51)(4.81)(1.87)(0.64)(7.69)(1.88)(1.28)(5.87)(2.26)(1.06)
12.5210.58 b ± 0.47222.16 a ± 0.27222.51 a ± 0.2528.81 c ± 0.2432.26 b ± 0.2233.01 b ± 0.3274.60 b ± 0.2281.86 a ± 0.1481.54 a ± 0.2217.54 b ± 0.1819.54 a ± 0.0319.67 a ± 0.07
(7.33)(2.08)(1.96)(14.40)(5.25)(2.16)(13.00)(4.32)(4.38)(12.41)(4.40)(3.01)
25182.94 b ± 3.12216.98 a ± 2.11215.72 a ± 0.9625.72 c ± 0.7631.61 b ± 0.0932.15 a ± 0.1368.56 b ± 0.5278.62 a ± 0.3779.56 a ± 0.1415.30 c ± 0.0518.62 b ± 0.0419.05 a ± 0.11
(19.50)(4.36)(4.95)(23.56)(7.14)(4.70)(20.03)(8.11)(6.69)(23.62)(8.89)(6.07)
50156.16 c ± 0.35204.41 b ± 1.99210.51 a ± 0.3124.34 c ± 0.3229.06 b ± 0.0729.88 a ± 0.1159.51 b ± 0.1274.00 a ± 0.2674.12 a ± 0.2313.62 b ± 0.0716.87 a ± 0.217.15 a ± 0.33
(31.28)(9.90)(7.25)(27.66)(14.62)(11.44)(30.59)(13.51)(13.07)(31.99)(17.47)(15.42)
100125.33 c ± 0.12182.76 b ± 0.48187.56 a ± 0.6022.12 c ± 0.4327.21 b ± 0.0828.32 a ± 0.6050.51 b ± 0.2367.88 a ± 0.4668.60 a ± 0.0911.61 c ± 0.0814.14 b ± 0.0614.71 a ± 0.55
(44.84)(19.44)(17.36)(34.26)(20.07)(16.06)(41.09)(20.66)(19.55)(42.02)(30.81)(27.47)
E. colona0337.61 a ± 0.29338.02 a ± 0.10337.05 a ± 0.4432.90 a ± 0.5532.81 a ± 0.5233.05 a ± 0.27167.46 a ± 0.26168.42 a ± 0.28168.36 a ± 0.2141.17 a ± 0.2941.77 a ± 0.2041.89 a ± 0.06
(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.25317.54 b ± 1.13329.60 a ± 0.73332.89 a ± 0.9631.32 a ± 0.4232.06 a ± 0.5032.71 a ± 0.28160.79 b ± 0.41167.00 a ± 0.24167.17 a ± 0.2638.13 b ± 0.1140.97 a ± 0.2141.41 a ± 0.05
(5.95)(2.49)(1.23)(4.79)(2.29)(1.04)(3.98)(0.84)(0.71)(7.38)(1.93)(1.13)
12.5304.54 b ± 2.27326.85 a ± 1.42324.64 a ± 0.9430.11 b ± 0.5031.28 ab ± 0.4332.20 a ± 0.22155.66 b ± 0.61164.69 a ± 0.28164.59 a ± 0.3535.83 b ± 0.1340.21 a ± 0.1940.74 a ± 0.08
(9.80)(3.30)(3.68)(8.49)(4.64)(2.58)(7.04)(2.21)(2.24)(12.95)(3.73)(2.75)
25273.88 b ± 1.43319.60 a ± 0.73317.62 a ± 1.3327.09 b ± 0.3930.09 a ± 0.4531.15 a ± 0.25144.59 b ± 0.93159.70 a ± 0.18161.44 a ± 0.2531.57 b ± 0.0639.39 a ± 0.2739.75 a ± 0.66
(18.88)(5.45)(5.77)(17.57)(8.16)(5.76)(13.65)(5.18)(4.11)(23.31)(5.71)(5.11)
50244.88 b ± 1.60302.10 a ± 1.35305.37 a ± 2.1225.57 b ± 0.0828.93 a ± 0.3828.96 a ± 0.42132.62 b ± 0.44152.36 a ± 0.58153.52 a ± 0.4128.04 b ± 0.3837.56 a ± 0.2237.98 a ± 0.19
(27.47)(3.63)(9.40)(22.21)(11.82)(12.40)(20.80)(9.53)(8.81)(31.88)(10.07)(9.33)
100194.72 b ± 0.52274.46 a ± 0.13273.37 a ± 2.1118.09 b ± 0.2825.53 a ± 0.0926.23 a ± 0.31108.79 b ± 1.17139.82 a ± 0.33141.25 a ± 0.5723.46 b ± 0.1833.64 a ± 0.3834.48 a ± 0.17
(42.32)(18.80)(18.90)(44.99)(22.11)(20.61)(35.03)(16.98)(16.10)(42.99)(19.46)(17.69)
Data are expressed as mean ± standard error. Means with the same letters in the row for each extract are not significantly different at p > 0.05. Values inside the parenthesis are inhibition percentages relative to the control. In the table, PH = P. hysterophorus, CR = C. rutidosperma, BA = B. alata.
Table 6. Effect of methanol extract of P. hysterophorus, C. rutidosperma, and B. alata on the control (%), plant height (cm), and root length (cm) of O. sativa, Z. mays, A. esculentus, and A. gangeticus.
Table 6. Effect of methanol extract of P. hysterophorus, C. rutidosperma, and B. alata on the control (%), plant height (cm), and root length (cm) of O. sativa, Z. mays, A. esculentus, and A. gangeticus.
Tested CropsDose (g L−1)Control (%)Plant Height (cm)Root Length (cm)
PHCRBAPHCRBAPH CRBA
O. sativa00.00 a ± 00.00 a ± 00.00 a ± 077.07 a ± 0.5676.99 a ± 0.6577.05 a ± 0.1727.38 a ± 0.1327.34 a ± 0.2227.72 a ± 0.45
(0)(0)(0)(0)(0)(0)
6.250.00 a ± 00.00 a ± 00.00 a ± 075.50 b ± 0.3276.50 a ± 1.1876.75 a ± 0.2226.05 b ± 0.7326.93 a ± 0.4227.3 a ± 1.22
(2.04)(0.64)(0.38)(4.84)(1.50)(1.52)
12.50.00 a ± 00.00 a ± 00.00 a ± 072.92 c ± 1.2775.91 b ± 2.1176.45 a ± 1.2124.96 b ± 0.1126.39 a ± 0.2027.01 a ± 0.32
(5.38)(1.41)(0.77)(8.85)(3.46)(2.56)
250.00 a ± 00.00 a ± 00.00 a ± 069.99 c ± 0.6474.92 b ± 0.7575.69 a ± 0.6323.10 b ± 0.0125.74 a ± 0.9826.41 a ± 0.53
(9.19)(2.69)(1.76)(15.64)(5.83)(4.73)
500.00 a ± 00.00 a ± 00.00 a ± 067.60 c ± 1.673.70 b ± 1.2274.50 a ± 1.8620.87 b ± 0.3224.48 a ± 1.2225.21 a ± 0.31
(12.21)(4.27)(3.31)(23.81)(10.45)(9.03)
1000.00 a ± 00.00 a ± 00.00 a ± 061.34 b ± 0.7070.66 a ± 0.9372.07 a ± 0.1316.81 c ± 0.1622.22 b ± 0.3023.28 a ± 0.82
(20.40)(8.22)(6.46)(38.61)(18.73)(16.00)
Z. mays00.00 a ± 00.00 a ± 00.00 a ± 0132.84 a ± 1.14131.73 a ± 0.40130.14 a ± 0.5138.29 b ± 0.7138.78 a ± 1.0738.64 a ± 0.21
(0)(0)(0)(0)(0)(0)
6.250.00 a ± 00.00 a ± 00.00 a ± 0129.45 a ± 0.26129.58 a ± 0.21129.73 a ± 2.4236.99 b ± 1.1738.17 a ± 0.8538.02 a ± 0.19
(2.53)(1.63)(0.32)(3.39)(1.57)(1.62)
12.50.00 a ± 00.00 a ± 00.00 a ± 0126.13 b ± 0.37129.30 a ± 1.23129.04 a ± 0.6835.79 b ± 0.2437.65 a ± 1.1837.64 a ± 2.60
(5.03)(1.85)(0.84)(6.52)(2.89)(2.60)
250.00 a ± 00.00 a ± 00.00 a ± 0121.02 c ± 1.16128.41 a ± 1.58127.56 b ± 0.2132.37 b ± 0.5436.99 a ± 0.5436.84 a ± 1.65
(8.87)(2.52)(1.98)(15.46)(4.59)(4.67)
500.00 a ± 00.00 a ± 00.00 a ± 0110.99 b ± 0.57125.03 a ± 0.98125.50 a ± 0.4130.00 b ± 0.7135.34 a ± 0.8735.52 a ± 0.84
(16.42)(5.08)(3.56)(21.66)(8.85)(8.09)
1000.00 a ± 00.00 a ± 00.00 a ± 097.39 b ± 0.49119.77 a ± 0.54120.71 a ± 0.3323.41 b ± 0.4532.41 a ± 0.1132.67 a ± 0.11
(26.67)(9.09)(7.25)(38.88)(16.41)(15.44)
A. esculentus00.00 a ± 00.00 a ± 00.00 a ± 030.13 a ± 1.2629.68 a ± 0.8029.46 a ± 0.9729.61 a ± 0.6429.91 a ± 0.8030.01 a ± 1.10
(0)(0)(0)(0)(0)(0)
6.250.00 a ± 00.00 a ± 00.00 a ± 027.27 b ± 1.1528.99 a ± 0.6829.22 ± 1.2826.13 b ± 1.1529.01 a ± 0.6829.12 a ± 0.28
(9.43)(2.32)(0.81)(11.74)(2.98)(2.96)
12.50.00 a ± 00.00 a ± 00.00 a ± 026.04 c ± 0.4928.60 b ± 1.1329.00 a ± 1.1022.74 c ± 0.4928.19 b ± 1.1329.00 a ± 0.32
(13.55)(3.63)(1.56)(23.21)(5.73)(3.35)
250.00 a ± 00.00 a ± 00.00 a ± 021.60 b ± 0.2828.14 a ± 0.5328.50 a ± 2.4418.29 c ± 0.5527.16 b ± 0.5327.92 a ± 0.44
(28.31)(5.17)(3.28)(38.24)(9.19)(6.95)
500.00 a ± 00.00 a ± 00.00 a ± 017.94 c ± 1.0327.07 b ± 0.9127.98 a ± 1.0516.29 b ± 1.0325.70 a ± 1.9126.12 a ± 0.48
(40.43)(8.78)(5.02)(45.00)(14.06)(12.96)
1000.00 a ± 00.00 a ± 00.00 a ± 015.09 b ± 0.4625.50 a ± 0.1726.39 a ± 0.4411.28 b ± 0.4623.62 a ± 0.0223.40 a ± 1.14
(49.91)(14.07)(10.44)(61.91)(21.00)(22.03)
A. gangeticus00.00 a ± 00.00 a ± 00.00 a ± 066.78 a ± 1.4067.02 a ± 1.1266.61 a ± 0.5829.57 a ± 1.4429.34 a ± 0.6429.19 a ± 0.69
(0)(0)(0)(0)(0)(0)
6.250.00 a ± 00.00 a ± 00.00 a ± 061.64 b ± 2.4165.83 a ± 0.6365.53 a ± 0.8725.04 b ± 0.7428.57 a ± 1.1628.63 a ± 0.81
(7.68)(1.78)(1.62)(15.32)(2.64)(1.92)
12.50.00 a ± 00.00 a ± 00.00 a ± 058.50 b ± 0.3165.26 a ± 0.1065.15 a ± 1.2921.18 c ± 1.0128.18 b ± 0.4328.53 a ± 0.61
(12.39)(2.63)(2.20)(28.37)(3.95)(2.26)
250.00 a ± 00.00 a ± 00.00 a ± 050.16 b ± 1.2764.24 a ± 0.2363.98 a ± 0.4118.24 c ± 0.6427.33 b ± 0.6127.88 a ± 1.84
(24.87)(4.15)(3.95)(38.33)(6.86)(4.50)
500.00 a ± 00.00 a ± 00.00 a ± 037.16 b ± 0.7662.71 a ± 1.1862.48 a ± 1.0413.91 b ± 0.9126.54 a ± 1.1126.18 a ± 0.18
(44.34)(6.43)(6.20)(52.96)(9.55)(10.33)
1000.00 a ± 00.00 a ± 00.00 a ± 025.22 b ± 0.6459.41 a ± 0.9259.21 a ± 0.918.23 b ± 1.2323.91 a ± 0.2424.54 a ± 0.33
(62.22)(11.36)(11.11)(72.15)(18.52)(15.94)
Data are expressed as mean ± standard error.Means with the same letters in the row for each extract are not significantly different at p > 0.05. Values inside the parenthesis are inhibition percentages relative to the control. Note: PH = P. hysterophorus, CR = C. rutidosperma, BA = B. alata.
Table 7. Effect of methanol extract of P. hysterophorus, C. rutidosperma,and B. alata on leaf area(cm2), total chlorophyll (SPAD), total fresh and dry weight (g pot−1) of O. sativa, Z. mays, A. esculentus, and A. gangeticus.
Table 7. Effect of methanol extract of P. hysterophorus, C. rutidosperma,and B. alata on leaf area(cm2), total chlorophyll (SPAD), total fresh and dry weight (g pot−1) of O. sativa, Z. mays, A. esculentus, and A. gangeticus.
Tested CropsDose (g L−1)Leaf Area (cm2)Total Chlorophyll (SPAD)Total Fresh Weight (g pot−1)Total Dry Weight (g pot−1)
PHCRBAPHCRBAPHCRBAPHCRBA
O. sativa0321.46 a ± 4.17324.19 a ± 2.80323.94 a ± 3.8036.93 a ± 0.2737.52 a ± 0.1737.13 a ± 0.0596.03 a ± 0.2595.54 a ± 0.2795.13 a ± 0.2417.17 a ± 0.1717.46 a ± 0.1317.09 a ± 0.07
(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.25309.02 a ± 5.01321.99 a ± 2.35323.29 a ± 3.8434.73 b ± 0.1536.74 a ± 0.2136.80 a ± 0.3789.67 b ± 0.1694.30 a ± 0.6494.34 a ± 0.2215.77 b ± 0.1516.88 a ± 0.116.66 a ± 0.06
(3.88)(0.67)(0.20)(5.95)(2.07)(0.89)(6.62)(1.29)(0.83)(8.11)(3.32)(2.50)
12.5297.94 b ± 4.60317.49 a ± 4.34319.23 a ± 3.6032.66 b ± 0.2035.79 a ± 0.2736.03 a ± 0.0784.23 b ± 0.6791.88 a ± 0.3192.67 a ± 0.2814.67 b ± 0.0516.10 a ± 0.0316.18 a ± 0.14
(7.32)(2.08)(1.45)(11.54)(4.59)(2.98)(12.28)(3.83)(2.58)(14.48)(7.76)(4.60)
25271.77 b ± 6.45312.09 a ± 2.70315.53 a ± 4.1929.13 b ± 0.2534.90 a ± 0.6835.17 a ± 0.0678.13 b ± 0.7488.69 a ± 0.5790.53 a ± 0.2513.15 b ± 0.0815.43 a ± 0.0515.59 a ± 0.31
(15.46)(3.73)(2.60)(21.12)(6.98)(5.28)(18.64)(7.16)(4.83)(23.35)(11.57)(8.77)
50239.77 b ± 4.37299.27 a ± 3.97299.84 a ± 4.3926.75 b ± 0.3632.37 a ± 0.6432.80 a ± 0.1870.44 c ± 0.3284.44 b ± 0.1885.82 a ± 0.3211.94 c ± 0.1314.18 b ± 0.4114.63 a ± 0.40
(25.42)(7.69)(7.45)(27.54)(13.70)(11.67)(26.64)(11.62)(9.78)(30.45)(18.76)(14.37)
100199.36 b ± 3.49273.47 a ± 2.62279.34 a ± 4.4224.25 b ± 0.3130.22 a ± 0.0930.55 a ± 0.1762.41 b ± 0.2576.52 a ± 0.7178.23 a ± 0.4710.39 b ± 0.2112.28 a ± 0.9112.74 a ± 0.09
(37.97)(15.63)(13.78)(34.33)(19.44)(17.72)(35.01)(19.90)(17.76)(39.44)(29.65)(25.45)
Z. mays02502.50 a ± 0.122503.48 a ± 0.682502.06 a ± 0.4039.43 a ± 0.2339.00 a ± 0.1738.84 a ± 0.08181.12 a ± 0.39181.53 a ± 0.30181.33 a ± 0.0922.11 a ± 0.1421.91 a ± 0.1522.00 a ± 0.20
(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.252401.58 b ± 0.502488.35 a ± 2.782485.81 a ± 2.8736.51 b ± 0.2038.06 a ± 0.7337.97 a ± 0.02169.67 b ± 0.51178.77 a ± 0.21179.02 a ± 0.4420.79 b ± 0.0321.5 a ± 0.1321.84 a ± 0.16
(4.03)(0.60)(0.65)(7.40)(2.41)(2.24)(6.32)(1.52)(1.28)(5.95)(1.88)(0.73)
12.52309.58 b ± 4.792464.60 a ± 2.532471.31 a ± 4.3734.39 b ± 0.0337.06 a ± 0.0736.92 a ± 0.23163.95 b ± 0.61176.02 a ± 0.39177.72 a ± 0.5219.44 c ± 0.0621.00 b ± 0.0721.30 a ± 0.03
(7.71)(1.55)(1.23)(12.78)(4.98)(4.92)(9.48)(3.03)(2.00)(12.06)(4.15)(3.19)
252083.63 b ± 0.202405.10 a ± 6.452408.29 a ± 4.3931.97 c ± 0.0435.83 a ± 0.0435.24 b ± 0.02152.29 c ± 0.14172.00 b ± 0.41173.67 a ± 0.4817.58 c ± 0.0120.53 b ± 0.0621.09 a ± 0.02
(16.74)(3.93)(3.75)(8.93)(8.13)(9.25)(15.92)(5.25)(4.23)(20.49)(6.27)(4.11)
501813.28 c ± 0.812291.75 b ± 0.152324.72 a ± 5.1428.31 c ± 0.6434.44 a ± 0.2532.38 b ± 0.03135.89 c ± 0.04161.34 b ± 0.29165.34 a ± 0.4215.46 c ± 0.0719.30 b ± 0.1120.a ± 0.07
(27.54)(8.46)(7.09)(28.11)(11.71)(16.62)(24.97)(11.12)(8.82)(30.08)(11.88)(6.76)
1001602.44 c ± 2.372108.13 b ± 0.662128.98 a ± 0.6424.69 c ± 0.2130.25 b ± 0.930.86 a ± 0.30123.37 b ± 0.19147.41 a ± 0.37149.17 a ± 0.7214.06 c ± 0.2017.50 b ± 0.1219.53 a ± 0.10
(35.97)(15.79)(14.91)(37.39)(22.43)(20.53)(31.88)(18.80)(17.74)(36.40)(20.13)(11.21)
A. esculentus01130.05 a ± 0.051129.76 a ± 0.281131.29 a ± 0.9352.97 a ± 0.2353.17 a ± 0.0653.45 a ± 0.24103.31 a ± 0.44103.68 a ± 0.03104.11 a ± 0.3413.46 a ± 0.2213.67 a ± 0.1913.38 a ± 0.04
(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.251059.36 b ± 0.291113.51 a ± 2.201117.54 b ± 2.7046.65 b ± 0.0252.45 a ± 0.1652.11 b ± 0.4395.53 b ± 0.61102.16 a ± 0.13102.85 a ± 0.1712.11 b ± 0.0313.22 a ± 0.0813.05 a ± 0.08
(6.26)(1.44)(1.22)(11.94)(1.35)(2.49)(7.53)(1.47)(1.21)(9.92)(3.26)(2.48)
12.5982.41 b ± 2.151103.51 a ± 2.541099.79 a ± 4.0944.12 b ± 0.0451.29 a ± 0.0450.80 a ± 0.2389.43 b ± 0.28101.51 a ± 0.19101.81 a ± 0.1510.82 b ± 0.3112.91 a ± 0.0912.55 a ± 0.39
(13.06)(2.32)(2.78)(16.71)(3.53)(4.95)(13.43)(2.10)(2.21)(19.53)(6.82)(6.22)
25878.41 c ± 0.011067.40 b ± 1.311077.30 a ± 0.1041.00 c ± 0.4347.65 b ± 0.1848.10 a ± 0.6476.26 b ± 0.4999.61 a ± 0.0699.17 a ± 0.228.87 c ± 0.0512.57 a ± 0.0512.30 b ± 0.03
(22.27)(5.52)(4.77)(22.60)(10.37)(10.00)(26.17)(3.93)(4.75)(34.04)(8.80)(8.11)
50611.10 c ± 0.131007.45 b ± 4.671044.80 a ± 4.8333.20 c ± 0.9144.89 b ± 0.4345.80 a ± 0.4564.18 b ± 0.3795.59 a ± 0.3196.60 a ± 0.416.84 b ± 0.0412.12 a ± 0.4612.13 a ± 0.10
(45.92)(10.83)(7.65)(37.32)(15.58)(14.31)(37.87)(7.81)(7.21)(49.16)(11.30)(9.36)
100441.26 c ± 0.23917.77 b ± 0.16956.01 a ± 0.3325.61 b ± 0.5642.97 a ± 0.8743.32 a ± 0.8543.04 b ± 0.3287.41 a ± 0.3088.33 a ± 0.704.74 b ± 0.4411.20 a ± 0.111.39 a ± 0.09
(60.95)(18.76)(15.49)(51.67)(19.18)(18.93)(58.33)(15.70)(15.15)(64.72)(17.99)(14.85)
A. gangeticus01354.77 a ± 0.471354.08 a ± 0.081353.84 a ± 0.2748.39 a ± 0.1047.94 a ± 0.2648.20 a ± 0.0198.90 a ± 0.3798.21 a ± 0.0698.22 a ± 0.2413.45 a ± 0.0513.04 b ± 0.0813.17 b ± 0.8
(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)(0)
6.251209.63 b ± 0.791333.94 a ± 4.351331.78 a ± 0.6441.86 b ± 0.0547.51 a ± 0.2447.24 a ± 0.1887.27 b ± 0.3296.30 a ± 0.1996.31 a ± 0.1211.67 b ± 0.0612.77 a ± 0.0712.75 a ± 0.05
(10.71)(1.49)(1.63)(13.48)(0.88)(1.99)(11.75)(1.94)(1.94)(13.25)(2.07)(3.18)
12.51111.88 c ± 2.141302.04 b ± 0.831313.19 a ± 4.1439.18 b ± 0.0446.76 a ± 0.1946.75 a ± 0.1475.47 b ± 0.0494.46 a ± 0.3695.08 a ± 0.5210.26 b ± 0.612.64 a ± 0.1812.61 a ± 0.22
(17.93)(3.84)(3.00)(19.02)(2.44)(3.00)(23.68)(3.82)(3.20)(23.70)(3.05)(4.22)
25958.32 c ± 0.111254.79 b ± 4.801292.78 a ± 3.8932.24 b ± 0.0245.51 a ± 0.2445.60 a ± 0.0364.29 b ± 0.3892.01 a ± 0.2492.89 a ± 0.288.45 b ± 0.1812.38 a ± 0.5412.47 a ± 0.14
(29.26)(7.33)(4.51)(33.37)(5.06)(5.38)(34.99)(6.32)(5.43)(37.19)(5.08)(5.25)
50807.70 c ± 3.201144.79 b ± 2.511242.28 a ± 4.0928.49 b ± 0.4943.01 a ± 0.4043.35 a ± 0.2550.19 c ± 0.0789.05 b ± 0.2690.32 a ± 0.446.94 b ± 0.112.08 a ± 0.1111.87 a ± 0.11
(40.38)(15.45)(8.24)(41.12)(10.28)(10.05)(49.25)(9.33)(8.04)(48.38)(7.30)(9.83)
100550.20 c ± 1.771054.91 b ± 1.651135.31 a ± 2.6524.93 b ± 0.2439.18 a ± 0.0339.04 a ± 0.0738.52 c ± 0.8282.07 b ± 0.2284.83 a ± 0.545.63 b ± 0.0711.26 a ± 0.1011.10 a ± 0.09
(59.39)(22.09)(16.14)(48.47)(18.26)(19.01)(61.04)(16.43)(13.64)(58.14)(13.67)(15.66)
Data are expressed as mean ± standard error. Means with the same letters in the row for each extract are not significantly different at p > 0.05. Values inside the parenthesis are inhibition percentages relative to the control. Note: PH = P. hysterophorus, CR = C. rutidosperma, BA = B. alata.
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Motmainna, M.; Juraimi, A.S.; Uddin, M.K.; Asib, N.B.; Islam, A.K.M.M.; Hasan, M. Bioherbicidal Properties of Parthenium hysterophorus, Cleome rutidosperma and Borreria alata Extracts on Selected Crop and Weed Species. Agronomy 2021, 11, 643. https://doi.org/10.3390/agronomy11040643

AMA Style

Motmainna M, Juraimi AS, Uddin MK, Asib NB, Islam AKMM, Hasan M. Bioherbicidal Properties of Parthenium hysterophorus, Cleome rutidosperma and Borreria alata Extracts on Selected Crop and Weed Species. Agronomy. 2021; 11(4):643. https://doi.org/10.3390/agronomy11040643

Chicago/Turabian Style

Motmainna, Mst., Abdul Shukor Juraimi, Md. Kamal Uddin, Norhayu Binti Asib, A. K. M. Mominul Islam, and Mahmudul Hasan. 2021. "Bioherbicidal Properties of Parthenium hysterophorus, Cleome rutidosperma and Borreria alata Extracts on Selected Crop and Weed Species" Agronomy 11, no. 4: 643. https://doi.org/10.3390/agronomy11040643

APA Style

Motmainna, M., Juraimi, A. S., Uddin, M. K., Asib, N. B., Islam, A. K. M. M., & Hasan, M. (2021). Bioherbicidal Properties of Parthenium hysterophorus, Cleome rutidosperma and Borreria alata Extracts on Selected Crop and Weed Species. Agronomy, 11(4), 643. https://doi.org/10.3390/agronomy11040643

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