WILD EDIBLE PLANTS IN ENHANCING POST-DISASTER FOOD SECURITY, ORMOC CITY, PHILIPPINES
Article Highlights:
- Wild edible plants (WEPs) in Ormoc City, Philippines, serve as critical food sources during disasters, offering essential nutrients and aiding food security.
- Melastoma malabathricum is rich in calcium, magnesium, and manganese, while Diplazium esculentum provides high levels of iron, copper, and zinc.
- Wild fruits like Melastoma malabathricum, Annona montana, and Rubus fraxinifolius contribute significant Vitamin C to the local diet.
- These plants not only provide sustenance but also offer medicinal benefits, emphasizing the need for further research, conservation, and sustainable use.
ABSTRACT
Wild Edible Plants (WEPs) are a valuable resource for communities facing food insecurity, and their nutritional profiles can provide essential dietary needs, especially in disaster-prone regions like the Philippines. This paper explores the nutritional value of wild edible plants (WEPs) in Ormoc City, Leyte, Philippines, with a particular focus on their role in addressing food security issues during natural disasters. The research included surveying the WEPs used by the local community in Ormoc City and analyzing these plants' nutrient and mineral composition. The study's key findings included identifying 15 plant species from 13 families. Melastoma malabathricum showed the highest Ca, Mg and Mn content; while Diplazium esculentum leaves had the highest iron, copper and zinc content. Furthermore, relatively high vitamin C content was found in wild fruits M. malabathricum, Annona montana, and Rubus fraxinifolius. The plants analyzed were rich in essential nutrients, including minerals (Ca, Na, Mg, Mn, Fe, Cu and Zn), crude fiber and vitamin C. The different plants excelled in different nutritional aspects, suggesting a diverse dietary potential. These plants play a crucial role in the local community, providing not only sustenance but also medicinal applications. Further research and conservation efforts should be encouraged to harness the nutritional and economic potential of these plants while ensuring their sustainable utilization and preservation.
INTRODUCTION
Wild Edible Plants (WEPs) encompass non-cultivated plant species growing spontaneously in nature in their natural or semi-natural habitats, which are harvested from the wild and utilized as sources of sustenance (Demir et al., 2020); (Duguma, 2020); (Mahklouf, 2019). WEPs, which are a rich source of micronutrients (, 2023) play a vital role as alternative food resources for families facing food insecurity in many developing and underdeveloped nations grappling with issues, such as poverty, famine, and drought (Anbessa et al., 2024); (Mishra et al., 2021); (Guzo et al., 2023); (Ojelel et al., 2019). Many WEPs have nutritional profiles akin to those of cultivated crops like some of the common vegetables (, 2023); (Waheed et al., 2023), rendering them valuable in augmenting the essential dietary needs of rural communities ((Nyakoojo & Tugume, 2020); (Ojelel et al., 2019)).
The Philippines is a region frequently subjected to a range of natural disasters, and exposed to natural hazards (Asio, 2020); (Ipong et al., 2020); (Yoshioka et al., 2021); (Radtke et al., 2018). One example of this vulnerability occurred in 2013 when Typhoon Haiyan, one of the most powerful tropical cyclones ever recorded, severely impacted Ormoc City. Subsequently, in 2017, a 6.5-magnitude earthquake struck the city (Ipong et al., 2020). Following the disaster, affected communities relied heavily on external aid. However, due to the extensive damage, especially in remote areas, relief operations were delayed. As assessed by (Stumpf et al., 2014), food supply emerged as one of the critical challenges in the aftermath of Typhoon Haiyan. The nutritional evaluation of WEPs can establish options to achieve food and nutritional security (, 2023), in response to Sustainable Development goal of zero hunger.
In the Philippines, a number of studies documenting wild edible plants in the country, and knowledge regarding their nutritional value has been conducted ((Buenavista et al., 2022); (Cacatian & Tabian, 2023); (Tasani & Barcellano, 2024)). This study was premised on several assumptions: 1) less attention is given to WEPs as a potential alternative to enhance food security for the community; 2) WEPs contain essential nutrients and minerals that can address nutritional requirements of the community during a disaster, hence the need to analyze their nutritional content, and 3) there is a need to incorporate information about WEPs into policies enhancing food security of a community during a disaster.
Consequently, this study (a) surveyed the WEPs already utilized by the local community, (b) assessed the nutrient and mineral composition of WEPs found in Ormoc City to ascertain their contribution to food security, and (c) identified potential implications for the utilization of WEPs during times of disaster.
MATERIALS AND METHODS
Study Area
Ormoc City has a total land area of 46,430 ha and is subdivided into 110 barangays (the smallest administrative division in the Philippines). Half of the lands is in mountainous and hilly areas, with agriculture, comprising 26,298 ha (56.64%), being the main use. The city has 15,034 ha (32.38%) of forest lands and 2,672 ha (5.75%) of commercial areas (Dumalan, 2023). Ormoc City is located at 11°00'26.59" N, 124°36'28.46" E in an enclave fronting the Ormoc Bay. The ambient temperature of Ormoc City is 25.9 °C, relative humidity of 70.2%, wind speed 0.55 m/s at 104°, east (BP Integrated Technologies, Inc. 2019) and an average rainfall of 2,456 mm. Given its geographical location, Ormoc in general, is highly susceptible to natural hazards and extreme weather events.
Ormoc City’s land encompasses a wide variety of plants, including wild edible plants that can serve as alternative food sources in the event of a calamity. Wild edible plants were collected from Barangays Bagong, Cabintan, Gaas, and Lake Danao, in Ormoc City, Leyte, Philippines ( Figure 1) in March 2019.
Figure 1.Context map of the study sites in Ormoc City, Leyte
Data Collection
Permission to conduct the study was sought from the local government unit through the City Agriculture Office (CAO).
Qualitative Ethnobotanical Survey
A qualitative ethnobotanical survey was conducted in March 2019 through key informant (KI) interviews. The methods used in similar studies ((Cacatian & Tabian, 2023); (Rahim et al., 2019); (Nyakoojo & Tugume, 2020)) were employed. The barangays selected were based on anecdotal information (Nyakoojo & Tugume, 2020); (Nyakoojo & Tugume, 2020)provided by some of the personnel of the City Agriculture Office. The City Agriculture Office of Ormoc purposively provided one key informant each for Barangays Bagong, Cabintan, Gaas, and Lake Danao based on their wide knowledge of the plant diversity in the study areas, and they provided folk knowledge of plants. Guided field excursions and field works were used to collect plant samples (Cacatian & Tabian, 2023) as well as additional data on the identity of the plants. The research team was joined in the field by the key informants who also served as local guides and were asked to mention wild edible plants that came into their minds; information on the wild edible plants and their mode of collection and preparation prior to consumption were recorded. The recorded data included: 1) vernacular names of the plant; 2) habit; 3) edible parts; 4) mode of harvest/preparation/consumption; 5) availability of the plants; 6) conservation status; and 7) additional information about the plants.
Plant Collection and Identification
Approximately 600 g each of the plant samples were collected from the four study sites, i.e., Barangays Bagong, Cabintan, Gaas, and Lake Danao. Fresh fruit and leaf samples were carefully placed in plastic resealable bags and temporarily stored in styrofoam boxes with ice to prevent deterioration. Subsequently, the samples were transported to the University of the Philippines Cebu Biology laboratory for analysis. For plant identification purposes, fruit samples were preserved in 500 mL glass jars containing 95% ethanol. Leaves and stem samples were also collected to prepare plant vouchers. Initial plant identification was carried out using Co’s Digital Flora of the Philippines (Pelser et al., 2011). Digitized voucher specimens were then sent to the University of the Philippines Los Baños for verification.
Sample Preparation
Plant samples were meticulously collected, taking care to minimize external contamination. The collected samples (fruits, leaves, and tubers) were washed thoroughly with distilled water. Subsequently, the fruit samples were carefully sectioned by cutting them open or slicing them into thin, uniform pieces. A subset of the samples, earmarked for moisture content determination, underwent immediate processing (Islary et al., 2016).
The bulk of the samples were subjected to a thorough drying process, initially through air-drying for a duration of 24 hours under controlled laboratory conditions then dried in a hot air oven at 50 o C until their weight stabilized, indicating the complete removal of the moisture (Korish, 2016); (Nielsen, 2010). Upon achieving constant weight, all samples were pulverized to a fine, uniform consistency and placed in airtight plastic resealable bags (Islary et al., 2016); (Korish, 2016) to prevent moisture ingress. These bags were properly labelled then stored at room temperature.
Quantitative Proximate Analyses
The determination of the proximate composition of the WEPs was conducted in accordance with established protocols outlined by the Association of Official Analytical Chemists (A.O.A.C., 2000). These analyses were done in triplicate to ensure precision and reliability.
Determination of Moisture Content
Three grams of each fresh plant sample were carefully weighed and placed in a crucible that had been preheated to a constant weight in a hot air oven. The plant samples were subjected to controlled heating at a temperature of 105 °C to constant weight, which was confirmed when the difference in sample weights did not exceed 0.0005 g. Moisture content was calculated using Equation (1).
\documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \text{Moisture } (\%) = \frac{\text{Fresh weight} - \text{Dry weight}}{\text{Fresh weight}} \times 100 \end{document} …………… (1)
Determination of Crude Fiber Content
Two grams per pulverized sample was subjected to boiling in a 0.25 N sulfuric acid (H2 SO4 ) solution. Subsequently, the mixture was subjected to filtration using a muslin cloth, and the residue was washed three times with hot distilled water. The residue from the previous step was further processed with 100 mL 0.313 N sodium hydroxide (NaOH). The resultant mixture was again subjected to filtration, followed by washing with hot distilled water, 0.5 N H 2 SO 4 , and 50% ethanol. The final residue obtained was placed in a crucible and dried at 100 °C to constant weight. The dried sample was allowed to cool in a desiccator for several minutes and was then weighed, establishing the initial weight (C 1 ). Subsequently, the sample was incinerated in a muffle furnace at a maintained temperature of 550 °C for 5 hours and then cooled in a desiccator. After cooling, the sample was reweighed (final weight, C 2 ). The percentage of crude fiber was determined using Equation 2.
\documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \%\ Crude\ Fiber\ = \ \frac{{C_{1}}_{} - \ C_{2}}{\text{Weight\ of\ the\ original\ sample\ }}\ \times 100 \end{document} …………. (2)
Determination of Crude Fat Content (Soxhlet Method)
The quantification of crude fat content was conducted using the Soxhlet method with petroleum ether extraction. The Soxhlet extraction apparatus was prepared by heating the Soxhlet beakers to constant weight. The final weight of these beakers was recorded as a reference. Two grams of each of the pulverized plant samples were securely enclosed within improvised filter paper tea bags specially designed for this purpose; the sample-containing tea bags were then placed inside extraction thimbles which were positioned within the Soxhlet beakers. The apparatus was set up and run in a water bath to facilitate fat extraction. Subsequently, the Soxhlet beakers were subjected to drying to eliminate excess ether solution, with subsequent weighing performed until a constant weight was attained. The determination of crude fat content was computed using Equation (3).
\documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \text{Crude\ Fat\ }\left( \% \right) = \frac{\text{Weight\ of\ fat}}{\text{Weight\ of\ the\ sample}}\ \ X\ 100 \end{document} ………… (3)
Determination of Ash Content
Approximately 2 - 3 g of each of the samples were placed in a crucible preheated to a constant weight. The initial weight was recorded, along with the combined weight of the crucible and the sample. The sample in the crucible was subjected to high-temperature treatment in a muffle furnace at 550 °C for 6 hours. Following the ashing procedure, the crucible and its contents were allowed to cool in a desiccator to prevent moisture absorption. Subsequently, the ash weight was determined. The percentage of ash content was calculated using Equation (4).
\documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \text{Ash\ Content\ }\left( \% \right) = \frac{\text{Ash\ weight}}{\text{Weight\ of\ the\ plant\ sample}}\ \ X\ 100 \end{document} ……….. (4)
Determination of Total Solids
Total solids, representing the dry matter in the plant samples, was calculated by subtracting the moisture percentage from 100 (Equation 5).
Total solids = 100 − Moisture content ……… (5)
Determination of Oxalic Acid
Five grams each of the pulverized plant samples were mixed with 3 M sulfuric acid (H 2 SO 4 ) solution and stirred for 1 hour. The resulting mixture was filtered and then gently heated between 80 °C to 90 °C using a hot water bath. The solution was titrated against 0.05 M potassium permanganate (KMnO 4 ) solution, with the temperature of the mixture consistently maintained at 70 °C. The titration endpoint was identified by the persistence of a light pink color for 15 seconds. The oxalic acid content was determined by calculating the equivalent milligrams of oxalate in 1 mL of 0.05 M KMnO 4 solution.
Determination of Alkaloids Percentage
In a 250-mL beaker, 5 g each of the pulverized plant samples was added with 200 mL of 20% acetic acid solution (CH 3 COOH). The beaker containing the resulting solution was covered with a watch glass and allowed to stand for 4 hours. The mixture was then filtered and concentrated to 50 mL using a hot water bath; this was then added with concentrated ammonium hydroxide (NH 4 OH) until the precipitate was complete. The solution was allowed to settle for 3 hours and decanted. The supernatant was discarded and the resulting precipitate was washed with 20 mL of 0.1 M NH 4 OH. The solution was then filtered with a pre-weighed Whatman no. 1 filter paper; the filter paper containing the precipitate was air-dried before weighing. The total alkaloids percentage was determined using Equation (6).
\documentclass{article} \usepackage{amsmath} \begin{document} \displaystyle \text{Alkaloids\ }\left( \% \right) = \frac{\text{Weight\ of\ the\ residue}}{\text{Weight\ of\ the\ sample}}X100 \end{document} ……….. (6)
Determination of Vitamin C Content
The vitamin C content in the plant samples was determined following the methodology outlined by Rai and Panda (2014), with some modifications. Prior to the analysis, an extracting solvent was prepared by combining 0.75 g ethylenediaminetetraacetic acid (EDTA), 5.0 g oxalic acid (C 2 H 2 O 4 ), ammonium molybdate ((NH 4 ) 2 MoO 4 ), orthophosphoric acid (H 3 PO 4 ), 5% sulfuric acid (H 2 SO 4 ), and distilled water. From this solution, 11 mL was taken comprising 4 mL of EDTA, C 2 H 2 O 4 , 2 mL (NH 4 ) 2 MoO 4 , 1 mL 5% H 2 SO 4 , 1 mL H 3 PO 4 , and 3 mL distilled water. This solution was added to 2.0 g of finely pulverized plant sample and placed in a 15 mL test tube. The test tube was vigorously shaken and allowed to stand for approximately 15 minutes. Subsequently, the resulting mixture was filtered using Whatman no. 1 filter paper, with the residue being discarded, and the filtrate was measured for its absorbance at 520 nm. For standardization, a standard curve was constructed using various concentrations of vitamin C (100%, 75%, 50%, 25%, 10% and 5%). The same procedure was carried out with the standard solutions. The vitamin C content was calculated using the linear equation derived from the standard curve.
Mineral Analysis
One hundred grams of each of the ground samples were sent to Technolab Analytical Group in Mandaue City, Cebu, Philippines, for the determination of the mineral contents.
Data Analysis
All experiments were carried out in triplicates; for quantitative data, the values were expressed as mean ± standard deviation.
RESULTS AND DISCUSSION
Wild Edible Plants and Their Uses
A total of 15 plant species belonging to 15 genera and 13 families were documented (Table 1) during the Key Informant (KI) interview and during the field excursions, which was participated by 4 individuals recommended by the head of the City Agriculture Office. These individuals included farmers and forest rangers who had extensive knowledge of the local plant diversity. The family that was represented the most was Arecaceae, with 3 species, followed by the rest of the families, each having 1 taxon. The plant species mentioned frequently by the key informants was Rubus fraxinifolius, locally known as “binit” (Table 1). About 47% of the documented plants were trees, 33% were vines, 13% herbs, and 7% shrubs (Table 1). Out of the 15 plants mentioned, only 8 species were collected for nutrient analyses, as these were the only plants available for collection during the March 2019 sampling. Artocarpus blancoi, Dillenia philippinensis, Diplazium esculentum, Melothria pendula, and Passiflora edulis were also included by (Cacatian & Tabian, 2023) in the list of indigenous wild food resources in northwestern Cagayan, Philippines.
Of the 15 plant species identified, at least 3 species have already been commercialized, i.e., “kaong” (Arenga pinnata) (used as a food ingredient), “rattan” (Calamus sp.), and “mirinda” (Passion Fruit) (Passiflora edulis). Most of the mentioned plants, primarily fruits, can be consumed raw, but a few wild fruits can also be used as food additives or seasoning (katmon) (Dillenia philippinensis) and can be processed into wine (binit) (Rubus fraxinifolius). A number of edible plants serve other purposes, due to the medicinal value that they may possess (Ramnath & Razal, 2019). The fruits of “pipinong gubat” and “apitngaw” have been mentioned to have medicinal properties. “Pipinong gubat” (Melothria pendula) can be brewed into herbal tea, and “apitngaw” (Melastoma malabathricum) is believed to relieve toothache.
One notable wild edible plant in the study is the wild yam, locally known as “kut” (Dioscorea hispida). It is a thorny creeping plant that grows near rock boulders and alongside river streams. The plant contains dioscorine, a toxic compound characteristic of the family Dioscoreaceae. Due to this, the tuber must be thoroughly processed to remove the toxins before consumption. According to the KI, this process takes days or even weeks. “Kut” is a traditional food in Barangay Bagong and is usually harvested and consumed during the Catholic Holy Week celebration, where locals would make kakanin (local rice or root crop delicacies). The collection and consumption of this wild yam happens in adverse situations as the effort to include them more frequently in diets requires much processing (Ramnath & Razal, 2019).
Aside from wild edible fruits, some WEPs are cooked as vegetable dishes, such as “pugahan” (Caryota mitis) and “pako” (Diplazium esculentum) salad. The edible part of “pugahan”, aside from its fruits, is the ‘ubod’ or the heart of the palm. Locals cut open the base stem of the plant to reveal the ‘ubod,’ which, according to the KI, tastes like carabao meat when cooked. On the other hand, “pako” is an edible fern that can be consumed in salads or stir-fried with oyster meat or any other preferred ingredient. The plant can be harvested abundantly along the side of Lake Danao.
| Family | Scientific name | Common name | Local name | Habit | Edible parts | Method of preparation, consumption | Food category | Conservation status and availability |
|---|---|---|---|---|---|---|---|---|
| Annonaceae | Annona montana (Macfad) | Mountain soursop | Wild guyabano | Tree | Fruit | Consumed raw | Fruit | Not Threatened/ Available |
| Arecaceae | Arenga pinnata (Wurmb) Merr. | Sugar palm | Native kaong | Tree | Fruit | Processed | Fruit, Food Ingredient | Not Threatened/ Available |
| Arecaceae | Calamus sp. | Rattan Palm | Rattan | Vine | Ubod (heart of palm) | Cooked | Vegetable | Not Threatened/ Available |
| Arecaceae | Caryota mitis Lour. | Clustered Fishtail Palm | Pugahan | Tree | Ubod, Fruit | Cooked | Fruit, Vegetable | Not Threatened/ Available |
| Athyriaceae | Diplazium esculentum (Retz.) Sw. | Fiddlehead fern | Paku | Herb | Fronds (young shoots) | Cooked, salad | Vegetable | Not Threatened/ Available |
| Cucurbitaceae | Melothria pendula L. | Creeping cucumber | Pipinong gubat | Vine | Fruit | Consumed raw | Fruit, beverage | Not Threatened/ Available |
| Dilleniaceae | Dillenia philippinensis Rolfe | Philippines Simpoh | Katmon | Tree | Fruit | Cooked | Seasoning, Food Ingredient | Not Threatened/ Available |
| Dioscoreaceae | Dioscorea hispida Dennst. | Intoxicating yam | Kut, wild yam | Vine | Root, Tuber | Cooked | Staple | Not Threatened/ Available |
| Flacourtiaceae | Flacourtia jangomas (Lour.) Raeusch. | Indian Plum, Indian Cherry | Seriales | Tree | Fruit | Consumed raw | Fruit | Not Threatened/ Available |
| Melastomaceae | Melastoma malabathricum L. | Malabar gooseberry; Indian Rhododendron | Apitngaw | Shrub | Fruit, seeds | Consumed raw | Fruit | Not Threatened/ Available |
| Moraceae | Artocarpus blancoi (Elmer) Merr. | Antipolo (Tagalog) | Antipo | Tree | Fruit, seeds | Cooked, roasted seeds | Fruit, snack | Not Threatened/ Available |
| Myrtaceae | Decaspermum parviflorum (Lam.) A.J. Scott | Silky myrtle | Beri | Tree | Fruit | Consumed raw | Fruit | Not Threatened/ Available |
| Pasifloraceae | Passiflora edulis Sims | Passion fruit | Mirinda | Vine | Fruit | Consumed raw | Fruit | Not Threatened/ Available |
| Rosaceae | Rubus fraxinifolius (Poir) | Mountain raspberry | Binit | Vine | Fruit | Consumed raw, processed | Fruit | Not Threatened/ Available |
| Zingiberaceae | Alpinia elegans (C. Presl) K.Schum. | Tagbak (Tagalog) | Panaon | Herb | Fruit, Rhizome | Consumed raw | Fruit | Not Threatened/ Available |
Proximate Composition
The 8 species available for collection and analysis included Annona montana, Decaspermum parviflorum, Diplazium esculentum, Dillenia philippinensis, Dioscorea hispida, Flacourtia jangomas, Melastoma malabathricum, and Rubus fraxinifolius. The nutrient composition of these plants is summarized in Table 2. The parameters analyzed were moisture content, dry matter or total solids, ash content, crude fat, and crude fiber.
Moisture and Dry Matter
Measuring the amount of moisture in a plant is the first step in assessing the overall nutritional value of plants. A relatively high moisture content would reveal that the plant is more liable to microbial degradation (Datta et al., 2019). Low moisture content in plants indicates the presence of insoluble materials and entails longer shelf life with reduced susceptibility to microbial infection; this is determined by the amount of total solids in plants (the composition of plants excluding the water content).
As shown in Table 2 the wild edible fruits D. philippinensis (91.17 ± 0.40 g/100 g), M. malabathricum (78.10 ± 1.00 g/100 g), A. montana (78.51 ± 12.43 g/100 g), R. fraxinifolius (77.94 ± 1.20 g/100 g), and Decaspermum parviflorum (66.76 ± 0.64 g/100 g) had relatively higher moisture content. The edible fern, D. esculentum (89.21 ± 1.37 g/100 g) that grows in damp areas, and wild yam, D. hispida (63.46 ± 2.53 g/100 g), also exhibited high moisture content. The unripe fruits of Flacourtia jangomas had relatively low moisture content (27.90 ± 2.34 g/100g), which is typical of young, developing seed fruits.
Ash
Ash content, which represents the inorganic residue remaining after the complete oxidation of organic matter in food samples, indicates the availability of inorganic minerals in plants ((Datta et al., 2019); (Mundaragi et al., 2017); (, 2023); (Yiblet & Adamu, 2023)). As observed in Table 2, most of the wild plants collected had relatively high ash content exceeding up to 20% with D. parviflorum having the highest among the plants analyzed, followed by F. jangomas. The high ash content in these fruits, such as D. parviflorum and F. jangomas can be attributed to their unripe state and their large, multiple seeds. The relatively high ash content in other wild plants in the study indicated that these plants contained high amounts of minerals.
| Plant species | Plant part analyzed |
Moisture (g/100 g) |
Dry matter (g/100 g) |
Ash (g/100 g) |
Crude fat (g/100 g) |
Crude fiber (g/100 g) |
|---|---|---|---|---|---|---|
Annona montana |
Fruit (ripe) |
78.51 ± 12.43 | 21.49 ± 12.43 | 13.96 ± 1.06 | - | - |
Decaspermum parviflorum |
Fruit (unripe) |
66.76 ± 0.64 | 33.24 ± 0.53 | 20.80 ± 2.45 | 0.84 ± 0.58 | 5.72 ± 0.11 |
Diplazium esculentum |
Leaves |
89.21 ± 1.37 | 10.79 ± 1.37 | 9.74 ± 0.38 | 1.35 ± 0.81 | 13.52 ± 1.85 |
Dillenia philippinensis |
Fruit (ripe) |
91.17 ± 0.40 | 8.83 ± 0.40 | 7.00 ± 1.06 | 1.37 ± 0.06 | 7.15 ± 0.002 |
Dioscorea hispida |
Tuber |
63.46 ± 2.53 | 36.54 ± 2.53 | 9.96 ± 1.57 | 0.66 ± 0.499 | 3.88 ± 0.19 |
Flacourtia jangomas |
Fruit (unripe) |
27.90 ± 2.34 | 72.90 ± 2.34 | 12.42 ± 2.42 | 0.91 ± 1.10 | 14.63 ± 0.47 |
Melastoma malabathricum |
Fruit (ripe) |
78.10 ± 1.00 | 21.90 ± 1.00 | 6.72 ± 0.36 | - | - |
Rubus fraxinifolius |
Fruit (ripe) |
77.94 ± 1.20 | 22.06 ± 1.20 | 15.57 ± 0.08 | 6.97 ± 1.96 | 26.59 ± 1.17 |
Crude Fat and Crude Fiber
Crude fat, a term used to describe the amount of fats in feedstuffs, food, and plants, represents the combination of free lipids and other fat-soluble materials present in a sample that can be dissolved in the solvent being used for extraction (AAFCO Lab Methods and Services Committee 2014). The crude fat content among the analyzed plants ranged from 0.66 g/100 g to 6.97 g/100 g (Table 2), with R. fraxinifolius having the highest fat content and wild yam having the lowest among the samples.
Crude fiber is the most common measurement of fiber in plants. In this study, R. fraxinifolius had the highest crude fiber content at 26.59 g/100 g, followed by F. jangomas at 14.63 g/100 g and D. esculentum at 13.52 g/100 g. The rest have fairly moderate amounts of fiber content. The crude fiber contents of the fruits of R. fraxinifolius, F. jangomas and the leaves of D. esculentum are higher than the dietary fiber content of commonly consumed fruits and vegetables like apple, banana, asparagus, carrot, or broccoli (Vicente et al. 2014) . Although crude fiber does not represent the total dietary fiber and may underestimate the total amount of dietary fiber present in plants, the results may imply that these plants can be good alternative sources of fiber.
Mineral Content
Minerals are inorganic substances that comprise one of the four major classes of micronutrients, which are essential nutrients needed in small amounts in the body. Minerals can be classified into two classes: macroelements and microelements (trace elements) (Siddiqui et al., 2014). These minerals are found in plants, and the composition and quantity of these elements vary depending on factors such as the type of cultivar, growth conditions, type of substrate, fertilizers used, nutrients requirement of the plant, and growth stages of the plant at the time of harvest ((Jākobsone et al., 2015)).
The mineral composition of the wild edible plants in the study is presented in Table 3. The parameters analyzed include sodium (Na), potassium (K), calcium (Ca), magnesium (Mg), iron (Fe), copper (Cu), zinc (Zn), and manganese (Mn).
M. malabathricum had the highest sodium (74.9 mg/kg) and calcium (5,017 mg/kg) contents among all the plant samples, followed by R. fraxinifolius at 74.8 mg/kg for Na, and 1,476 mg/kg for Ca. The Na content of D. parviflorum was 67.2 mg/kg, while the Ca content of F. jangomas and A. montana was 1,675 mg/kg and 721 mg/kg, respectively. D. hispida had the least amount of calcium among the samples collected in Ormoc City. The calcium content of the plants tested was higher than in some cultivated vegetables like lettuce, cabbage, and spinach (Datta et al., 2019).
Results showed that the WEPs in this study are not good sources of potassium since the potassium levels in the samples were below the detection limit (< 0.01 mg/kg). The wild edible fruits from Ormoc City contained high amounts of magnesium ranging from 1,650 mg/kg to 20,802 mg/kg. M. malabathricum had the highest magnesium content (20,802 mg/kg) among all the plants analyzed, followed by R. fraxinifolius (19,116 mg/kg). Magnesium aids in preventing muscle degeneration, growth retardation, cardiomyopathy, immunologic dysfunction, and bleeding disorders, among others (Datta et al., 2019).
Among the plants analyzed, D. esculentum had the highest iron content (31.5 mg/kg), followed by D. philippinensis (30.6 mg/kg) and M. malabathricum (23.5 mg/kg). The remaining samples had iron levels below the detection limit. For copper, D. esculentum leaves had the highest copper content (38.5 mg/kg) among all the plants. Zinc concentration was high in D. esculentum (44.4 mg/kg), F. jangomas (34.1 mg/kg), and M. malabathricum, (28.9 mg/kg), while it was low in A. montana (0.39 mg/kg). Lastly, for manganese, M. malabathricum had the highest manganese content (298 mg/kg), while D. parviflorum had the lowest manganese concentration (3.2 mg/kg). Iron, zinc, copper, sulfur, manganese, and iodine, are consumed in smaller amounts (< 100 mg/dL) (Linkon et al., 2015). Although these microelements play essential roles in various metabolic processes in the body, they are needed only in small amounts, and their intake should be regulated.
The recommended dietary allowance (RDA) for calcium (1,000 mg/day), magnesium (400 mg/day), and iron (8 mg/day) (Datta et al., 2019)suggests that the plants can supplement the daily mineral requirement.
| Plant species | Plant part analyzed |
Fe (mg/kg) |
Cu (mg/kg) |
Zn (mg/kg) |
Mn (mg/kg) |
Na (mg/kg) |
K (mg/kg) |
Ca (mg/kg) |
Mg (mg/kg) |
|---|---|---|---|---|---|---|---|---|---|
| Annona montana | Fruit (ripe) | 6.34 | 9.91 | 0.39 | 7.12 | 15.3 | < 0.01* | 721 | 11,984 |
| Decaspermum parviflorum | Fruit (unripe) | 6.34 | 11.4 | < 0.01* | 3.2 | 67.2 | < 0.01* | 276 | 1,650 |
| Diplazium esculentum | Leaves | 31.3 | 38.5 | 44.4 | 19.4 | 51.9 | <0.01* | 355 | 13,294 |
| Dillenia philippinensis | Fruit (ripe) | 30.6 | 8.35 | < 0.01* | 13.9 | 69 | < 0.01* | 427 | 13,780 |
| Dioscorea hispida | Tuber | 7.01 | 11.7 | < 0.01* | 5.0 | 8.94 | < 0.01* | 7.31 | 2,744 |
| Flacourtia jangomas | Fruit (unripe) | < 0.01* | 13.2 | 34.1 | 82.5 | < 0.01* | < 0.01* | 1,675 | 4,129 |
| Melastoma malabathricum | Flower | 23.5 | 11.7 | 28.9 | 298 | 74.9 | < 0.01* | 5,017 | 20,802 |
| Rubus fraxinifolius | Fruit (ripe) | 12.4 | 10.1 | 15.1 | 31.5 | 74.8 | < 0.01* | 1,476 | 19,116 |
| Plant species | Plant part analyzed |
Vitamin C content (g/100 g) |
Alkaloids content (g/100 g) |
Oxalate content (g/100 g) |
|---|---|---|---|---|
| Annona montana | Fruit (ripe) | 72.47 ± 2.21 | - | 0.95 ± 0.01 |
| Decaspermum parviflorum | Fruit (unripe) | 16.15 ± 4.51 | 0.56 ± 0.001 | 0.0057 ± 0.002 |
| Diplazium esculentum | Leaves | 21.94 ± 6.55 | 0.68 ± 0.14 | 0.2 ± 0.02 |
| Dillenia philippinensis | Fruit (ripe) | 18.17 ± 3.90 | 0.72 ± 0.013 | 0.45 ± 0.01 |
| Dioscorea hispida | Tuber | 25.90 ± 2.93 | 0.50 ± 0.05 | 0.29 ± 0.01 |
| Flacourtia jangomas | Fruit (unripe) | 36.61 ± 2.90 | 0.98 ± 0.03 | 0.074 ± 0.007 |
| Melastoma malabathricum | Fruit (ripe) | 82.58 ± 14.27 | - | 0.30 ± 0.05 |
| Rubus fraxinifolius | Fruit (ripe) | 40.28 ± 8.03 | 1.36 ± 0.11 | 0.52 ± 0.03 |
Vitamin C
Vitamin C, chemically known as ascorbic acid, is an important factor in assessing the quality of fruits (Khilari & Sharma, 2016). In addition to the polyphenols present in plants, vitamin C also contributes to the antioxidative properties of plants. L-ascorbic acid cannot be synthesized in humans and must be, therefore, consumed from food sources. It is well known that plant-based foods, especially fruits, are generally high in vitamin C, making them good sources of ascorbic acid (Lykkesfeldt et al., 2014). Vitamin C plays a crucial role in various metabolic processes, such as the formation of bile salts, serotonin production, the reduction of allergic activity, and the scavenging of free radicals (Chambial et al., 2013).
As shown in Table 4, low vitamin C content was observed in D. philippinensis (katmon) fruits and unripe fruits of D. parviflorum and F. jangomas. Relatively high vitamin C content was found in M. malabathricum (82.58 ± 14.27 g/100 g), followed by A. montana (72.47±2.21 g/100 g), and R. fraxinifolius (40.28± 8.03 g/100 g). The edible fern D. esculentum (21.94 ± 6.55 g/100 g) and D. hispida (25.90 ± 2.93 g/100 g) had lower vitamin C content. Some of the fruits in this study could help supplement the recommended daily allowance of ascorbic acid for different life stages and groups aged 1- 70 years which is 15 to 120 mg per day (Ojelel et al., 2020).
Antinutrients (Alkaloids and Oxalate)
Compounds that have specific functions for plant growth or defense mechanism (H, 2014) but can be toxic and/or anti-nutritive in humans, are labeled as antinutrients; they result in health hazard affecting digestion and the absorption of essential nutrients ((Lo et al., 2018); (Popova & Mihaylova, 2019)). They bind to minerals and other nutrients and reduce their bioavailability and digestibility, excess consumption of these substances may have adverse effects and may lead to toxicity ( (Nath et al., 2022); (Lo et al., 2018); (Aina et al., 2012); (H, 2014)). Alkaloids are a group of naturally occurring nitrogen-containing compounds produced from secondary metabolic pathways in plants to protect plants from herbivory and pathogenic attacks ((Almeida AC et al., 2017)).
(Ifemeje et al., 2014)
The amounts of oxalate in the plants analyzed ranged from 0.95 g/100 g to 0.0057 g/100 g, with the highest observed in A. montana fruits and the lowest in D. parviflorum. Oxalates are substances that can bind with other minerals (e.g., calcium) and form insoluble salts (Petroski & Minich, 2020).
Summary of the Proximate Composition, Mineral Composition, Alkaloids and Oxalates
A total of 15 edible plant species, representing 13 families, were identified in the study. D. philippinensis had the highest moisture content, followed by M. malabathricum, A. montana, and R. fraxinifolius. Most of the wild plants collected had relatively high ash content exceeding up to 20% with D. parviflorum having the highest among the plants analyzed, followed by F. jangomas, indicating a rich mineral content. R. fraxinifolius had the highest crude fiber content, followed by F. jangomas and D. parviflorum. The rest had moderate amounts of fiber content.
The fruits of M. malabathricum exhibited the highest Ca, Na, Mg, and Mn content, as well as the highest vitamin C content. R. fraxinifolius had the second highest Na content, and F. jangomas had the second highest Ca content. D. esculentum leaves had the highest iron, copper and zinc content, and a relatively high magnesium content. D. philippinensis and M. malabathricum also had relatively high iron content. The remaining samples had iron levels below the detection limit.
The fruits of A. montana, R. fraxinifolius, and M. malabathricum showed a relatively high vitamin C content. R. fraxinifolius exhibited the highest alkaloids content and D. hispida the lowest, while oxalate content was highest in A. montana fruits and the lowest in D. parviflorum fruits.
WEPS Identified but not Collected and Analyzed
Although 7 out of the 15 plant species identified as edible were not collected and analyzed, studies indicate that they are also considered edible in other countries and regions.
The sap of Arenga pinnata may be converted to palm sugar, which has a low glycemic index, making it a healthier alternative to refined sugar, particularly for diabetics (Haagen & Lantican, 2014). In Bhutan, certain villages believe that soup made from the young shoot of Calamus sp., helps alleviate nausea (, 2006). Similarly, local communities in Central Kalimantan in Indonesia consider Calamus sp. a food source (Fambayun & Kalima, 2022). A study on consumption practices in Assam, India, revealed that Calamus sp. shoots are eaten in various forms, i.e., raw, boiled, fried, roasted, and often cooked with other ingredients, such as fish, meat, black gram pulses, etc. (Thakur & Sheth, 2015). Another study found that D. angustifolia, and D. fissa are the preferable rattan used for food by the community near peatland areas in Central Kalimantan, both for daily sustenance and cultural activities. (Fambayun & Kalima, 2022)
Although Caryota mitis and Alpinia elegans were identified by key informants in this study as edible, they are primarily valued for their medicinal properties ( (Dalisay et al., 2018); Naïve et al. 2019; (Shahria et al., 2017)). In Bangladesh the roots and fruits of Caryota mitis have been reported to be traditionally used by folk medicinal practioners of a number of villages for treatment of constipation and hemorrhoids (Shahria et al., 2017). Alpinia elegans, an endemic Philippine medicinal plant, is known for treating musculoskeletal diseases, hemoptysis, headache, migraine, stomachache, and as an anti-relapse for women. (Naïve et al. 2019; (Dalisay et al., 2018)).
Melothria pendula L., now naturalized in Peninsular Malaysia, mainland Sumatra, Borneo (Sabah), the Philippines, and Sulawesi, thrives in urban areas and grows spontaneously along roadsides, in gardens, open spaces, and ditches, burial grounds and abandoned land (Husaini et al., 2024). In parts of Mexico, it is used as food and in beverages (Guerrero-Torres et al., 2023), while in the Philippines, it is recognized as a common medicinal plant (Raju et al., 2021).
The fruit of Passiflora edulis is considered a rich source of vitamin A, thiamine, riboflavin, niacin, calcium, phosphorus, and vitamin C. In Colombia, its pulp is used to prepare juices and soft drinks (Jiménez et al., 2011). Among Brazilian passion fruit species, Passiflora edulis Sims is the most cultivated and valued for its flavor and aroma (T et al., 2021).
CONCLUSION
The plants analyzed in this study were rich in essential nutrients, including mineral (Ca, Na, Mg, Mn, Fe, Cu and Zn), crude fiber and vitamin C. The different plants excelled in different nutritional aspects, suggesting a diverse dietary potential. These plants play a crucial role in the local community, providing not only sustenance but also medicinal applications. Further research and conservation efforts should be encouraged to harness the nutritional and economic potential of these plants while ensuring their sustainable utilization and preservation. Additionally, incorporating information about WEPs into disaster preparedness and food security policies could help safeguard vulnerable communities in disaster-prone regions, like the Philippines.
References
- A.A.F.C.O.. Association of American Feed Control Officials. Internet. 2014. Publisher Full Text
- Aina V.O., Sambo B., Zakari A., Haruna M.S.H., Umar H., Akinboboye R.M., Mohammed A.. Determination of nutritional and anti-nutrient content of Vitis vinifera (Grapes) grown in Bomo (Area C) Zaria, Nigeria. Adv J Food Sci Tech. 2012; 4:445-48.
- Almeida AC Alves, FMRJ Dunder, LPB Manzo, ARM Souza-Brito, A Luiz-Ferreira. Recent trends in pharmacological activity of alkaloids in animal colitis: Potential use for inflammatory bowel disease. Evidence-Based Complementary and Alternative Medicine:1-24. 2017. DOI
- Anbessa B., Lulekal E., Getachew P., Hymete A.. Ethnobotanical study of wild edible plants in Dibatie District, Metekel zone, Benishangul Gumuz Regional State, Western Ethiopia. J Ethnobiol Ethnomed. 2024; 20(1)
- A.O.A.C.. Association of Official Analytical Chemists: Arlington (US; 2000.
- Asio J.M.. Disaster knowledge and household preparations of selected communities in Central Luzon, Philippines: Basis for enhanced community disaster education program. IJ-HuMaSS. 2020; 3(2):44-51.
- T Barbosa Santos, Araujo FPA Figueiredo Neto, Freitas STSouza Araújo JOliveira Vilar SBAJ Brito Araújo, MS Lima. Phytochemical compounds and antioxidant activity of the pulp of two Brazilian passion fruit species. Passiflora cincinnata Mast. and Passiflora edulis Sims. Int J Fruit Sci. 2021; 21(1):255-69.
- Technologies B.P.Integrated, Inc. Ormoc weather monitoring system display. 2019. Publisher Full Text
- Buenavista D.P., Mollee E.M., McDonald M.. Any alternatives to rice? Ethnobotanical insights into the dietary use of edible plants by the Higaonon tribe in Bukidnon Province, the Philippines. Regional Sustainability. 2022; 3(2):95-109.
- Cacatian S.B., Tabian J.L.T.. Floristic composition and diversity of indigenous wild food resources in northwestern Cagayan, Philippines. Biodiversitas. 2023; 24(4):2324-33. DOI
- Chambial S., Dwivedi S., Shukla K.K., John P.J., Sharma P.. Vitamin C in disease prevention and cure: An overview. Indian J Clin Biochem. 2013; 28:314-28. DOI
- Dalisay J.A.G.P., Bangcaya P.S., Naive M.A.K.. Taxonomic studies and ethnomedicinal uses of Zingiberaceae in the mountain ranges of northern Antique, Philippines. BFIJ (Biological Forum–An International Journal. 2018; 10(2):68-73.
- Datta S., Sinha B.K., Bhattacharjee S., Seal T.. Nutritional composition, mineral content, antioxidant activity and quantitative estimation of water soluble vitamins and phenolics by RP-HPLC in some lesser used wild edible plants. Heliyon. 2019; 5(3)DOI
- Demir E., Turfan N., Özer H., Üstün N.S., Pekşen A.. Nutrient and bioactive substance contents of edible plants grown naturally in Salıpazarı (Samsun. Acta Sci Pol-Hortoru. 2020; 19(1):151-60.
- Duguma H.T.. Wild edible plant nutritional contribution and consumer perception in Ethiopia. Int J Food Sci. 2020; 2020(1)
- Dumalan R.. State of the mangrove in Ormoc City. Conference Paper presented at the State of the Mangrove Summit: Central and Eastern Visayas Proceeding. 2023;34-44.
- Fambayun R.A., Kalima T.. Rattan: Its role for food-alternative of the community near the peatland areas in Central Kalimantan. IOP Conf Ser Earth Environ Sci. 2022; 959(1)
- H Fekadu Gemede. Antinutritional factors in plant foods: potential health benefits and adverse effects. Int J Food Sci Nutr. 2014; 3(4):284-89.
- Guerrero-Torres P., Hernández-Sandoval L., Casas A., L. Melothria, Mart. Crov Melothria. Springer International Publishing: Cham (CH; 2023.
- Guzo S., Lulekal E., Nemomissa S.. Ethnobotanical study of underutilized wild edible plants and threats to their long-term existence in Midakegn District. 2023.
- Ifemeje J.C., Egbuna C., Eziokwudiaso J.O., Ezebuo F.C.. Determination of the anti-nutrient composition of Ocimum gratissimum, Corchorus olitorius, Murraya koenigii Spreng and Cucurbita maxima. J Innov Sci Res. 2014; 3:127-33.
- Ipong L.G., Ongy E.E., Bales M.C.. Impact of magnitude 6.5 earthquake on the lives and livelihoods of affected communities: The case of barangay Lake Danao. 2020.
- Islary A., Sarmah J., Basumatary S.. Proximate composition, mineral content, phytochemical analysis and in vitro antioxidant activities of a wild edible fruit (Grewia sapida Roxb. Ex DC.) found in Assam of North-East India. J Investig Biochem. 2016; 5(1)DOI
- Haagen A., Lantican C.B.. Arenga pinnata (Wurmb) Merr.: Promising source of bioethanol and low glycemic index sugar. 2014.
- Husaini I.P.A., Widjaya A.H., Saripudin S., Yuliyanto P., Latifah D., Irsyam A.S.D., Rosleine D., Hariri M.R.. Melothria pendula L. (Cucurbitaceae): First report from Java and range extension in Sumatra, Indonesia. Check List. 2024; 20(2):553-58.
- Jākobsone I., Kantāne I., Zute S., Jansone I., Bartkevičs V.. Macro-elements and trace elements in cereal grains cultivated in Latvia. Proceedings of the Latvian Academy of Sciences, Section B, Natural Exact and Applied Sciences. 2015; 69(4):152-57.
- Jiménez A.M., Sierra C.A., Rodríguez-Pulido F.J., González-Miret M.L., Heredia F.J., Osorio C.. Physicochemical characterisation of gulupa (Passiflora edulis Sims. fo edulis) fruit from Colombia during the ripening. Food Res Int. 2011; 44(7):1912-18.
- Khilari V., Sharma P.. Studies on ascorbic acid content of some wild edible fruits from Ahmednagar District, Maharashtra (India. Int J Adv Res. 2016; 4:583-90.
- Korish M.. Nutritional evaluation of wild plant Cissus rotundifolia. Italian J Food Sci. 2016; 28(1):43-9.
- Linkon K.M.R., Satter M.A., Jabin S.A., Abedin N., Islam M.F., Lisa L.A., Paul D.K.. Mineral and heavy metal contents of some vegetables available in local market of Dhaka City in Bangladesh. J Environ Sci Toxicol Food Tech. 2015; 9:01-06.
- Lo D., Hsin-I W., Wan-Jen W., Ray-Yu Y.. Anti-nutrient components and their concentrations in edible parts in vegetable families. CABI Reviews. 2018; 2018(13):1-30. DOI
- Lykkesfeldt J., Michels A.J., Frei B.. Vitamin C. Adv Nutr. 2014; 5:16-8.
- Mahklouf M.. Ethnobotanical study of edible wild plants in Libya. European J Ecol. 2019; 5(2):30-40.
- Report of investigation for wild edible plants and their traditional knowledge in Bhutan. Journal of the Faculty of Agriculture, Shinshu University. 2006; 42(1/2):37-46.
- Mishra A., Swamy S.L., Thakur T.K., Bhat R., Bijalwan A., Kumar A.. Use of wild edible plants: Can they meet the dietary and nutritional needs of indigenous communities in Central India. Foods. 2021; 10(7)
- Mundaragi A., Devarajan T., Jeyabalan S., Bhat S., Hospet R.. Unexploited and underutilized wild edible fruits of Western Ghats in Southern India. Agronomy. 2017; 60:326-39.
- Naive M.A.K., Dalisay J.A.G.P., Maglangit E.P.T., Cafe G.C., Nuneza O.M.. Free radical scavenging effects of the Philippine endemic medicinal plant Alpinia elegans (Zingiberaceae. Gard Bull. 2019; 71(2):435-44.
- Nath H., Samtiyta M., Dhewa T.. Beneficial attributes and adverse effects of major plant-based foods and anti-nutrients on health: A review. Hum Nutr Metab. 2022; 28(3)DOI
- Nielsen S.S.. Springer: NewYork (US; 2010.
- Nyakoojo C., Tugume P.. Traditional use of wild edible plants in the communities adjacent Mabira Central Forest Reserve, Uganda. Ethnobot Res Appl. 2020; 20:1-14.
- Ojelel S., Mucunguzi P., Katuura E., Kakudidi E.K., Namaganda M., Kalema J.. Wild edible plants used by communities in and around selected forest reserves of Teso-Karamoja region, Uganda. Journal of Ethnobiol Ethnomed. 2019; 15(1)DOI
- Ojelel S., Mucunguzi P., Kalema J., Kakudidi E.K., Namaganda M., Katuura E.. Nutritional value of selected wild edible plants in Teso-Karamoja region, Uganda. Afr J Food Agric Nutr Dev. 2020; 20(4):16112-125.
- Pelser P., Barcelona J., Nickrent D.. Co’s Digital Flora of the Philippines. 2011. Publisher Full Text
- Petroski W., Minich D.M.. Is there such a thing as “anti-nutrients”? A narrative review of perceived problematic plant compounds. Nutrients. 2020; 12(10)
- Popova A., Mihaylova D.. Antinutrients in plant-based foods: A review. The Open Biotechnol J. 2019; 13:68-76.
- Radtke K., Mann H., Weller D., Kirch L., Prütz R.. Bündnis Entwicklung Hilft: Bochum (DE; 2018.
- Rahim B.Z., Qureshi R., Tareen R.B.. Nutritional and phytochemical screening of wild fruit of Berberis baluchistanica: An endemic species to Pakistan. Appl Ecol Environ Res. 2019; 17(6):12697-707. DOI
- Rai P.K., Panda L.L.S.. An Indo-Burma hotspot region. Air Qual Atmos Hlth 7:93-101. ; 2014.
- Raju R., Prakash T., Rahul R., Poonangadu S.S., Kumar S.S., Sonaimuthu P., Chua J.M.T., Capili J.T.. Phytochemical analysis of three common medicinal plants (Gliricidia sepium, Melothria pendula, and Pithecellobium dulce) in the Philippines. Sch Acad J Biosci. 2021; 3:84-8.
- Ramnath M., Razal R.A.. Wild Tastes in Asia: Coming Home to the Forest for Food. 2019.
- Shahria S.S., MSA Bhuiyan, M Rahmatullah. Caryota mitis Lour. (Arecaceae): A previously unreported plant for treatment of elevated blood glucose level in diabetic patients. Asian Journal of Pharmacognosy. 2017; 1(3):32-3.
- Siddiqui K., Bawazeer N., Scaria Joy S.. Variation in macro and trace elements in progression of type 2 diabetes. The Scientific World Journal. 2014; 2014:1-9.
- Stumpf J., Wee C., Liwag C.R.E.U.. Kuehne Foundation, NUS HumLog Centre Asia Pacific. ; 2014.
- Nutritional evaluation of some potential wild edible plants of North Eastern region of India. Front Nutr. 2023; 10(1052086)
- Tasani A., Barcellano E.. Diversity and utilization of wild plants and macrofungi: Its contribution to rural livelihood in Cabagan, Isabela, Philippines. The Journal of Emerging Research in Agriculture, Fisheries and Forestry (JERAFF. 2024; 4(1):72-81.
- Thakur P.K., Sheth M.. Traditional consumption and therapeutic beliefs of Calamus tenuis Roxb. edible shoots of forest village natives of Dibrugarh District of Assam, India. Int J Adv Res. 2015; 3(12):1530-38.
- Vincente A.R., Manganaris G.A., Ortiz C.M., Sozzi G.O., Crisosto C.H.. Academic Press: San Diego (US; 2014.
- Waheed M., Haq S.M., Arshad F., Bussmann R.W., Pieroni A., Mahmoud E.A., Casini R., Yessoufou K., Elansary H.O.. Traditional wild food plants gathered by ethnic groups living in semi-arid region of Punjab, Pakistan. Biology. 2023; 12(2)
- Yiblet Y., Adamu E.. Nutritional composition and phytochemical evaluation of some selected wild edible plants in Tach Gaint District, Northwestern Ethiopia. Sci World J. 2023; 2023(1)
- Yoshioka N., Era M., Sasaki D.. Towards integration of climate disaster risk and waste management: A case study of urban and rural coastal communities in the Philippines. Sustainability. 2021; 13(4)
Association of American Feed Control Officials (AAFCO) [Internet]. 2014. AAFCO Lab Methods and Services. Available from: https://www.aafco.org/Portals/0/SiteContent/Laboratory/Fat_Best_Practices_Working_Group/Crude_Fat_Methods_Considerations.pdf
Aina VO, Sambo B, Zakari A, Haruna MSH, Umar H, Akinboboye RM, Mohammed A. 2012. Determination of nutritional and anti-nutrient content of Vitis vinifera (Grapes) grown in Bomo (Area C) Zaria, Nigeria. Advance Journal of Food Science and Technology 4, 445–448.
Alves de Almeida AC, de-Faria FM, Dunder RJ, Manzo LPB, Souza-Brito ARM, Luiz-Ferreira A. 2017. Recent trends in pharmacological activity of alkaloids in animal colitis: potential use for inflammatory bowel disease. Evidence-Based Complementary and Alternative Medicine, 1–24. https://doi.org/10.1155/2017/8528210 DOI: https://doi.org/10.1155/2017/8528210
AOAC, 2000. Official methods of Analysis of Association of Official Analytical Chemists, Arlington, 17th edition.
Arquion RD, Galanida CC, Villamor B, Aguilar HT. 2015. Ethnobotanical study of indigenous plants used by local people of Agusan del Sur, Philippines. Asia Pacific Higher Education Research Journal 2, 11. DOI: https://doi.org/10.56278/apherj.v2i2.102
Ashagre M, Asfaw Z, Kelbessa E. 2016. Ethnobotanical study of wild edible plants in Burji District, Segan Area Zone of Southern Nations, Nationalities and Peoples Region (SNNPR), Ethiopia. Journal of Ethnobiology and Ethnomedicine 12. https://doi.org/10.1186/s13002-016-0103-1 DOI: https://doi.org/10.1186/s13002-016-0103-1
Bacchetta L, Visioli F, Cappelli G, Caruso E, Martin G, Nemeth E, Bacchetta G, Bedini G, Wezel A, van Asseldonk T, van Raamsdonk L, Mariani F, on behalf of the Eatwild Consortium, 2016. A manifesto for the valorization of wild edible plants. Journal of Ethnopharmacology 191, 180–187. https://doi.org/10.1016/j.jep.2016.05.061 DOI: https://doi.org/10.1016/j.jep.2016.05.061
Baldermann S, Blagojević L, Frede K, Klopsch R, Neugart S, Neumann A, Ngwene B, Norkeweit J, Schröter D, Schröter A, Schweigert FJ, Wiesner M, Schreiner M. 2016. Are neglected plants the food for the future? Critical Reviews in Plant Sciences 35, 106–119. https://doi.org/10.1080/07352689.2016.1201399 DOI: https://doi.org/10.1080/07352689.2016.1201399
Brahma J, Singh B, Rethy P, Gajurel P. 2014. Nutritional analysis of some selected wild edible species consumed by the Bodos tribes of Kokrajhar District, BTC, Assam. Asian Journal of Pharmaceutical and Clinical Research 7, 5.
Beyer J, Drummer OH, Maurer HH. 2009. Analysis of toxic alkaloids in body samples. Forensic Science International 185, 1–9. https://doi.org/10.1016/j.forsciint.2008.12.006 DOI: https://doi.org/10.1016/j.forsciint.2008.12.006
Chambial S, Dwivedi S, Shukla KK, John PJ, Sharma P. 2013. Vitamin C in disease prevention and cure: An overview. Indian Journal of Clinical Biochemistry 28, 314–328. https://doi.org/10.1007/s12291-013-0375-3) DOI: https://doi.org/10.1007/s12291-013-0375-3
Chua-Barcelo RT. 2014. Ethno–botanical survey of edible wild fruits in Benguet, Cordillera administrative region, the Philippines. Asian Pacific Journal of Tropical Biomedicine 4, S525–S538. https://doi.org/10.12980/APJTB.4.201414B36 DOI: https://doi.org/10.12980/APJTB.4.201414B36
FAO. 1999. Use and potential of wild plants in farm households [WWW Document]. Available from: http://www.fao.org/3/w8801e02.htm#P15_2035 (accessed 3.12.19).
Fekadu Gemede H. 2014. Antinutritional factors in plant foods: potential health benefits and adverse effects. International Journal of Nutrition and Food Sciences 3, 284-. https://doi.org/10.11648/j.ijnfs.20140304.18 DOI: https://doi.org/10.11648/j.ijnfs.20140304.18
Ghosh B. 2000. Polyamines and plant alkaloids. Indian Journal of Experimental Biology 38, 1087–1091.
Ifemeje JC, Egbuna C, Eziokwudiaso JO, Ezebuo FC. 2014. Determination of the anti-nutrient composition of Ocimum gratissimum, Corchorus olitorius, Murraya koenigii Spreng and Cucurbita maxima. Journal of Innovation and Scientific Research 3, 127–133.
Ismail, Hussin, Idri. 2007. Physical, chemical & mineralogical properties of fly ash. Journal of Nuclear and Related Technology Vol. 4, Special Edition 2007, 47-51.
Islary A, Sarmah J, Basumatary S. 2016. Proximate composition, mineral content, phytochemical analysis and in vitro antioxidant activities of a wild edible fruit (Grewia sapida Roxb. ex DC.) found in Assam of North-East India. J. Investig. Biochem. 5, 21. https://doi.org/10.5455/jib.20160422015354) DOI: https://doi.org/10.5455/jib.20160422015354
Israr B, Frazier RA, Gordon MH. 2013. Effects of phytate and minerals on the bioavailability of oxalate from food. Food Chem. 141, 1690–1693. https://doi.org/10.1016/j.foodchem.2013.04.130) DOI: https://doi.org/10.1016/j.foodchem.2013.04.130
Jākobsone I, Kantane I, Zute S, Bartkevics V. 2015. Macro-elements and trace elements in cereal grains cultivated in Latvia. Proceedings of the Latvian Academy of Sciences Section B Natural Exact and Applied Sciences 69. https://doi.org/10.1515/prolas-2015-0022 DOI: https://doi.org/10.1515/prolas-2015-0022
Ju Y, Zhuo J, Liu B, Long C. 2013. Eating from the wild: diversity of wild edible plants used by Tibetans in Shangri-la region, Yunnan, China. Journal of Ethnobiology and Ethnomedicine 9, 28. https://doi.org/10.1186/1746-4269-9-28 DOI: https://doi.org/10.1186/1746-4269-9-28
Khilari V, Sharma P. 2016. Studies on Ascorbic acid content of some wild edible fruits from Ahmednagar District, Maharashtra (India). International Journal of Advanced Research 4, 583–590. https://doi.org/10.21474/IJAR01/397 DOI: https://doi.org/10.21474/IJAR01/397
Linkon KMR, Satter MA, Jabin SA, Abedin N, Islam MF, Lisa LA, Paul DK. 2015. Mineral and heavy metal contents of some vegetables available In local market of Dhaka City in Bangladesh. Journal of Environmental Science, Toxicology, and Food Technology 9, 01–06.
Lykkesfeldt J, Michels AJ, Frei B. 2014. Vitamin C. Advances in Nutrition 5, 16–18. Available from: https://doi.org/10.3945/an.113.005157 DOI: https://doi.org/10.3945/an.113.005157
Marshall MR. 2010. Ash Analysis, in: Nielsen, S.S. (Ed.), Food Analysis. Springer DOI: https://doi.org/10.1007/978-1-4419-1478-1_7
Medak B, Singha LB. 2017. Nutritional contribution by wild plants as novel food to the ethnic tribes of Arunachal Himalaya, India. IOSR J. Pharm. Biol. Sci. 12, 73–79. Available from: https://doi.org/10.9790/3008-1203077379 DOI: https://doi.org/10.9790/3008-1203077379
Murray SS, Schoeninger MJ, Bunn HT, Pickering TR, Marlett JA. 2001. Nutritional composition of some wild plant foods and honey used by Hadza Foragers of Tanzania. J. Food Compos. Anal. 14, 3–13. Available from: https://doi.org/10.1006/jfca.2000.0960 DOI: https://doi.org/10.1006/jfca.2000.0960
Mundaragi A, Devarajan T, Jeyabalan S, Bhat S, Hospet R. 2017. Unexploited and underutilized wild edible fruits of Western Ghats in Southern India. Agronomy 60, 326–339.
Narzary H, Basumatary A. 2015. Proximate and vitamin C analysis of wild edible plants consumed by Bodos of Assam, India. J. Mol. Pathophysiol. 4, 128. Available from: https://doi.org/10.5455/jmp.20151111030040 DOI: https://doi.org/10.5455/jmp.20151111030040
Nath H, Samtiyta M, Dhewa T. 2022. Beneficial attributes and adverse effects of major plant-based foods and anti-nutrients on health: A review. Human Nutrition and Metabolism. Available from: https://doi.org/10.1016/j.hnm.2022.200147 DOI: https://doi.org/10.1016/j.hnm.2022.200147
Nielsen SS. 2010. Determination of moisture content, in: Nielsen, S.S. (Ed.), Food Analysis Laboratory Manual. Springer US, Boston, MA, pp. 17–27. Available from: https://doi.org/10.1007/978-1-4419-1463-7_3 DOI: https://doi.org/10.1007/978-1-4419-1463-7_3
Ojelel S, Mucunguzi P, Katuura E, Kakudidi EK, Namaganda M, Kalema J. 2019. Wild edible plants used by communities in and around selected forest reserves of Teso-Karamoja region, Uganda. Journal of Ethnobiology and Ethnomedicine 15. Available from: https://doi.org/10.1186/s13002-018-0278-8 DOI: https://doi.org/10.1186/s13002-018-0278-8
Ong H, Kim Y. 2017. The role of wild edible plants in household food security among transitioning hunter-gatherers: evidence from the Philippines. Food Security 9, 11–24. Available from: https://doi.org/10.1007/s12571-016-0630-6 DOI: https://doi.org/10.1007/s12571-016-0630-6
Pelser P, Barcelona J, Nickrent D. 2011. Co’s Digital Flora of the Philippines [WWW Document]. Cos Digit. Flora Philipp. Available from http://www.philippineplants.org/
Petroski, W. and Minich, D.M., 2020. Is there such a thing as “anti-nutrients”? A narrative review of perceived problematic plant compounds. Nutrients, 12(10), p.2929. DOI: https://doi.org/10.3390/nu12102929
Popova A, Mihaylova D. 2019. Antinutrients in Plant-based Foods: A Review. The Open Biotechnology Journal. 13, 68-76. Available from: http://dx.doi.org/10.2174/1874070701913010068 DOI: https://doi.org/10.2174/1874070701913010068
Radtke K, Mann H, Weller D, Kirch L, Prütz R. 2018. WorldRiskReport 2018 focus: Child protection and children’s rights. Bündnis Entwicklung Hilft
Rahim BZ, Qureshi R, Tareen RB. 2019. Nutritional and Phytochemical Screening of Wild Fruit of Berberis Baluchistanica --An Endemic Species to Pakistan. Applied Ecology & Environmental Research, 17(6). DOI: https://doi.org/10.15666/aeer/1706_1269712707
Rai PK, Panda LLS. 2014. Dust capturing potential and air pollution tolerance index (APTI) of some road side tree vegetation in Aizawl, Mizoram, India: an Indo-Burma hotspot region. Air Quality, Atmosphere & Health 7, 93–101. Available from: https://doi.org/10.1007/s11869-013-0217-8 DOI: https://doi.org/10.1007/s11869-013-0217-8
Seal T. 2012. Evaluation of Nutritional Potential of Wild Edible Plants, Traditionally Used by the Tribal People of Meghalaya State in India. Am. J. Plant Nutr. Fertil. Technol. Available from: https://doi.org/10.3923/ajpnft.2012.19.26 DOI: https://doi.org/10.3923/ajpnft.2012.19.26
Seal T, Chaudhuri K. 2016. Nutritional analysis of some selected wild edible plants consumed by the tribal people of Meghalaya state in India. Int. J. Food Sci. Nutr. 1, 39–43.
Seal T, Pillai B, Chaudhuri K. 2017a. Evaluation of nutritional potential of five unexplored wild edible plants consumed by the tribal people of Arunachal Pradesh State in India. J. Food Nutr. Res. 5, 1–5. https://doi.org/10.12691/jfnr-5-1-1
Seal, T, Pillai B, Chaudhuri K. 2017b. Nutritional potential of five unexplored wild edible plants consumed by the tribal people of Arunachal Pradesh state in India. Int. J. Food Sci. Nutr. 2, 101–105.
Siddiqui K, Bawazeer N, Scaria Joy S. 2014. Variation in macro and trace elements in progression of type 2 diabetes. The Scientific World Journal 2014, 1–9. Available from: https://doi.org/10.1155/2014/461591 DOI: https://doi.org/10.1155/2014/461591
Stumpf J, Wee C, Liwag C. 2014. Typhoon Yolanda Relief Response Report: A Supply Chain Perspective. Kuehne Foundation, NUS HumLog Centre Asia Pacific. Volume 14 – Mar.
Unuofin JO, Otunola GA, Afolayan AJ. 2017. Nutritional evaluation of Kedrostis africana (L.) Cogn: An edible wild plant of South Africa. Asian Pacific Journal of Tropical Biomedicine 7, 443–449. Available from: https://doi.org/10.1016/j.apjtb.2017.01.016 DOI: https://doi.org/10.1016/j.apjtb.2017.01.016
Copyright (c) 2025 Patricia Anne Nazareno, Prof/Dr., Prof/Dr., Ms.

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Authors who publish with this journal agree with the following terms:
- Authors retain copyright and grant the journal right of first publication, with the work 1 year after publication simultaneously licensed under a Creative Commons attribution-noncommerical-noderivates 4.0 International License that allows others to share, copy and redistribute the work in any medium or format, but only where the use is for non-commercial purposes and an acknowledgement of the work's authorship and initial publication in this journal is mentioned.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).




