Manuscript accepted on : 12 December 2020
Published online on: --
Plagiarism Check: Yes
Reviewed by: Dr. Ibrahim Hmmam
Second Review by: Dr. Evelyn Garwe
Final Approval by: Dr. Hifzur R. Siddique
Jitu Chutia, JyotishSonowal
, Bhaba Kumar Pegu
and Devid Kardong
Department of Life Sciences, Dibrugarh University, Dibrugarh, Assam. India. 786004. Corresponding Author Email: jituchutia.j.c@gmail.com
DOI : http://dx.doi.org/10.13005/bbra/2887
ABSTRACT: The present study focuses on proximate and mineral compositions on 12 freshwater edible macroinvertebrate species under phylum Arthropoda and Mollusca mostly preferred by the ethnic communities around the Poba reserve forest of Assam, India. The analysis revealed protein was the most abundant nutrient for all the species; followed by carbohydrates and fats. The highest protein content was in Lobothelphusafungosa, (50.50%), total carbohydrate in Bellamyabengalensis (22.54%) and fats in Sartorianaspinigera (16.32%). Ash, fibre and moisture were highest in Corbiculaassamensis (12.46%), Sartorianaspinigera (11.41%) and Pilaglobosa (63.72%) respectively. Among the minerals, Calcium, Copper, Iron, Manganese, and Zinc were recorded highest in Bellamyabengalensis (138.62 mg/100g) Macrobrachiumassamense (2.73 mg/100g), Sartorianaspinigera (35.02 mg/100g), Macrobrachiumassamense (11.42 mg/100g) and Lethocerusindicus (3.71 mg/100g) respectively. Heavy metals (Lead, Cadmium, Molybdenum and Mercury) were absent in all the species under study. The freshwater macroinvertebratesanalyzed could form a baseline for future non-conventional food resources of considerable nutritive value.
KEYWORDS: Entomophagy; Macroinvertebrate; Non-Conventional Food; Poba Reserve Forest
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Copy the following to cite this article: Chutia J, Sonowal J, Pegu B. K, Kardong D. Evaluation of Proximate and Heavy Metals in Twelve Edible Freshwater Macroinvertebrates of Poba Reserve Forest Assam, India. Biosci Biotech Res Asia 2020;17(4). |
Copy the following to cite this URL: Chutia J, Sonowal J, Pegu B. K, Kardong D. Evaluation of Proximate and Heavy Metals in Twelve Edible Freshwater Macroinvertebrates of Poba Reserve Forest Assam, India. Biosci Biotech Res Asia 2020;17(4). Available from: https://bit.ly/3ngz4vu |
Introduction
Aquatic macroinvertebrates refer to the small organisms that have no internal skeletal system and live part or all of their lives in water. They comprise a diverse group of organisms that includes insects, molluscs, annelids and crustaceans. They show their presence in aquatic bodies by swimming, clinging or burrowing in the bottom substrate. Many aquatic insects and molluscs species are consumed worldwide due to their taste and seasonal availability.
This practice of consumption was an old and well-established tradition in many parts of the world and recently has gained popularity and acceptance due to the promising source of nutrition challenges facing the world [1- 3].The trend has gradually been increasing from tropical countries to Western societies [4]. Generally, it is used as ingredient in many cooking recipes in countries like Africa, Asia, South America, and Australia [5]. It is reported that the majority of edible macroinvertebrates contains a rich nutrient concentration [6, 7]. As a part of their daily diet, it may be an important component in eliminating deficiency diseases related to malnutrition [8]. With the rapid increase in human population size, there would be tremendous pressure on animal source foods. It is projected that the world population would exceed 9 billion around 2050 and there will be a food crisis due to a reduction in food production [9]. To combat this crisis, one of the alternatives of a protein-rich source is edible insects [7]. It has been speculated that a 10% increase in the global animal protein supply through mass production of insects would largely eliminate the malnutrition problem and also decrease the pressure on other protein sources [9]. Therefore, insects and other forms of terrestrial and aquatic macroinvertebrates may offer an important resource for humans nutrition and are worthy of development in various bio-prospecting aspects [7]. Although there is a considerable amount of information on the entomophagy and nutrient contents of terrestrial insects,the information on aquatic macroinvertebrates is scanty. The proliferation rate of insects is very high and many of them are pest on crops causing economic damage to farmers. The consumption of such insects is part and partial of the traditional pest management practices. However many edible terrestrial andaquatic macroinvertebratesare disease vectors[10,11]. So understanding these issues and refinement of traditional food habits is a major concern of an entomophagous community.
![]() |
Figure 1: Map of study area (Poba reserve forest). |
Poba reserve forest (PRF) situated in the eastern part of Assam is a repository of a variety of aquatic fauna distributed heterogeneously in the aquatic bodies of the reserve forest. Many species of aquatic macroinvertebrates are used as non-conventional food by the ethnic communities inhabiting around the reserve forest.So far no detailed exploration on diversity and proximate nutrient analysis on aquatic macroinvertebrate fauna had been carried out. Realizing the paucity of information the present study was undertaken on 12 commonly preferred species by the consumers under phylum Arthropoda and Mollusca collected from different aquatic bodies of PRF. The inventorization of proximate nutrients composition may help the communities for the ideal quantity of intake of neutraceutically valuable invertebrate resources. Further, this information may encourage sustainable use of these alternative cheap sources of non-conventional food resources and for possible domestic and commercial uses.
Materials and Methods
Sample Collection
The samples were collected from different perennial and ephemeral water bodies of PRF (latitude 27˚50′11″N and Longitude 95˚17′45″E) of Assam, India covering an area of about 102.21 km2 of land. Some specimens were collected from local markets during the seasons of their availability. Collected specimens were brought to the laboratory, sorted and preserved in 80% ethanol for future uses. Identification of the recorded specimens was done following standard taxonomic keys [12-16] and available updated literature from IUCN along with the technical support of the Zoological Survey of India. Kolkata, India.
Proximate Analysis
Moisture, Ash, and fibre contents were carried out following standard methods [17]. Nitrogen was determined by the micro-Kjeldahlmethod [18]. Crude protein content was subsequently calculated by multiplying the nitrogen content by a factor of 6.25. Fat content was determined by using the Soxhlet extraction method [19]. Carbohydrate content was calculated by subtracting the sum of the weights of protein, fibre, ether extract and ash from the total dry matter and reported as nitrogen-free extractives [20].
Estimation of Minerals
Selected minerals were determined in an Inductively Coupled Plasma-Atomic Emission Spectrometry; (ARCOS, Simultaneous ICP Spectrometer, SPECTRO Analytical Instruments GmbH, Germany) after acid digestion of the tissue samples with nitric acid and perchloric acid (5:1v/v) respectively [21].
Statistical Analysis
Data of the analysis are presented as means ± standard error (SE). Mean differences in proximate and minerals concentrations among the twelve freshwater macroinvertebrates were determined with one-way ANOVA using LSD in SPSS (Version 21) Software. Significance was accepted at P ≤ 0.05 levels.
Results
The systematic position and taxonomic keys of the twelve recorded freshwater macroinvertebrates are listed in Table 1. Analysis of the proximate composition of the species depicts a fair amount of nutrients (Table 2). There were significant differences in the means of the proximate compositions among theanalyzedspecies (P< 0.05).The highest amount of moisture content was observed in Pilaglobosa(63.72%) and least in Sartorianaspinigera(45.72%).The ash content of the recorded species ranges from 3.29% to 12.46% highest in Corbiculaassamensis and least in Lamellidenscorrianus. The highest fibre content was recorded in Sartorianaspinigera(11.41%), Cybistertripunctatus(11.00%) andLethocerusindicus(11.31%) against the Lamellidenscorrianus(0.28%) having the least fibre content.For most of the species, crude protein was the most abundant substance ranged from 18.10%(Macrobrachiumassamense) to 50.50%(Lobothelphusafungosa). Lipid content was recorded highest in Sartorianaspinigera (16.32%) and least in Lamellidensmarginalis (2.05%). The mean value of carbohydrate content was 11.32 %, being highest in Bellamyabengalensis (22.54%), and lowest in Macrobrachiumassamense (5.25%).
Table 1: Systematic position and taxonomic keys of analysed freshwater Macroinvertebrates.
Class
|
Order
|
Family
|
Species | Taxonomic Keys |
Insecta
|
Coleoptera | Dytiscidae | Cybistertripunctatus(Olivier,1795)
|
Head transverse, slightly convex above, subrounded and slightly sloping in front, antennae filamentous, mandibles are heavily sclerotized, triangular and strongly toothed on the inner side lie closely above the lacinia and galea,the joint between the cardo and stipes is elbow-shaped, mesoscutellum composed of two lateral chitjnisedsclerites. |
Hemiptera | Belostomatidae
|
Lethocerusindicus(Lepeletier and servile,1825) | Body narrowly elliptical, Antennae small; hidden inside a groove ventrally, Rostrum sharp and stout, the interocular region is little wider than the eye width, Scutellum little broader than hemelytra, sharp claws, Mid and hind legs provided with thick sets of swimming hairs on the ventral side. | |
Malacostraca |
Decapoda |
Potamonidae | Lobothelphusafungosa(Alcock,1909) | The carapace is almost square, cervical groove is hard to make out, outer orbital angle and the lateral epibranchial tooth prominent, antero-lateral borders of the carapace are subcristiform. The epigastric crests are not so continuous with the postorbital crests, and the latter is sharper, especially in their outer half. |
Sartorianaspinigera
(Wood-Mason, 1871) |
Carapace wide, gently convex and smooth with a slightly concave free edge. The antero-lateral margin of carapace is sharp with an epibranchial spine, orbits without large spines, and a distinct H-shaped deep gastric groove. | |||
Paleomonidae | Macrobrachiumassamense(Tiwari,1958) | Body divided into head, thorax, and abdomen,head and thorax region joined to form cephalothorax which includes mandibles, flagella, rostrum and eye containing a stalk.The abdomen has six body segments with five pair of walking legs, last segments contain telson with two pairs of dorsal spines, Rostrum is slightly slender reaching to the distal end of scaphocerite, rostral tip slightly upturned; | ||
Gastropoda |
Architaenioglossa |
Viviparidae | Bellamyabengalensis(Lamarck,1822) | Shell thin, whorls gradually increasing, shallow sutures, rather straight sides. Spire and body whorl of almost equal height, less rounded, with straight sides, aperture sub-circular with narrow black margin. |
Ampullaridae | Pilaglobosa(Swainson, 1822) | Shell globose shaped, spacious, the upper surface of whorls obliquely flattened, suture not deep, spire depressed. | ||
Sorbeoconcha | Pachychilidae | Brotiacostula (Brandt, 1974) | Shell elongated, regularly increasing, prominent axial ribs with spires,sculpture with spiral ridges. | |
Bivalvia |
Unionoida |
Unionidae |
Parreysiacorrugata (Muller,1774) | Shell elliptical to oval, umbones prominent, ventral margin convex, cardinal teeth strong, not lamellar, greenish. |
Lamellidenscorrianus (Lea,1834) | Shell elongated and elliptical, periostracum smooth, dorsal margin straight with a dark brown and yellowish band. | |||
Lamellidensmarginalis (Lamarck, 1819) | Shell oblongated and ovoid-shaped, periostracum blackish-brown with a light brown border along the ventral margin, ventral margin slightly contracted in the middle | |||
Veneroida |
Cyrenidae |
Corbiculaassamensis (Prashad,1928) | Shell ovate, dorsal margin regularly arched convex, anterior side short and rounded, posterior broad and truncate, striae regular concentric, distinct, but not deep. |
Table 2: Percentage Proximate composition.(% per 100 g Dry tissue).
Freshwater
Macroinvertebrates |
Moisture | Ash | Fibre | Crude
Protein |
Total Carbohydrate | Crude
Lipid |
Sartorianaspinigera | 45.72a
±0.45 |
8.61a
±0.39 |
11.41a
±0.40 |
35.24a
± 1.38 |
9.05a
± 0.32 |
16.32a
± 0.39 |
Macrobrachiumassamense | 54.65b
± 0.58 |
11.00b
±0.26 |
6.04b
±0.31 |
18.10b
± 0.70 |
5.25b
± 0.11 |
9.11b
± 0.48 |
Parreysiacorrugata | 52.37c
±0.50 |
5.28c
±0.14 |
4.37c
±0.13 |
27.62c
± 1.02 |
7.56c
±0.26 |
11.22c
±0.19 |
Lamellidenscorrianus | 48.87d
±0.58 |
3.29d
±0.14 |
0.28d
±0.02 |
25.54c
±0.86 |
11.12d
±0.48 |
3.58de
±0.27 |
Lamellidensmarginalis | 58.62e
±0.46 |
8.55a
±0.20 |
1.90e
±0.25 |
38.35e
± 0.88 |
7.45c
±0.39 |
2.05e
±0.04 |
Corbiculaassamensis | 63.50f
±0.27 |
12.46b
±0.53 |
4.86c
±0.32 |
20.90f
± 0.46 |
7.89ca
±0.31 |
4.09de
±0.33 |
Pilaglobosa | 63.72f
±0.50 |
8.28a
±0.24 |
0.95de
±0.04 |
33.31a
± 1.01 |
12.11d
± 0.32 |
3.12de
± 0.29 |
Bellamyabengalensis | 56.80h
±0.27 |
10.52b
±0.32 |
6.47b
±0.15 |
35.67a
± 1.03 |
22.54g
± 0.60 |
2.53de
± 0.15 |
Cybistertripunctatus | 47.00a
±0.57 |
3.58d
±0.21 |
11.00a
±0.27 |
26.54c
± 0.99 |
19.54h
± 0.36 |
12.35c
± 0.50 |
Brotiacostula | 62.86i
±0.83 |
8.50a
±0.40 |
1.85e
±0.10 |
44.42h
± 0.96 |
21.89g
± 1.03 |
2.90de
± 0.27 |
Lethocerusindicus | 46.76a
±0.48 |
3.53d
±0.30 |
11.31a
±0.30 |
22.67cf
± 0.74 |
5.86b
± 0.29 |
13.21k
± 0.35 |
Lobothelphusafungosa | 53.03bc
±0.58 |
7.22a
±0.12 |
2.83e
±0.26 |
50.50j
± 1.30 |
5.59b
± 0.35 |
6.52g
± 0.37 |
Values with different alphabets in each column are significantly different at P ≤ 0.05 level.
The results of the analysis of selected minerals are given in Table 3. Calcium (Ca) content was highest in Bellamyabengalensis (138.62 mg/100g) and lowest in Parreysiacorrugata (5.44 mg/100g). The highest amount of Copper (Cu), Iron (Fe), Manganese (Mn) and Zinc (Zn) contents were observed in Macrobrachiumassamense(2.73 mg/100g), Sartorianaspinigera (35.02 mg/100g), Macrobrachiumassamense (11.42 mg/100g)andLethocerusindicus(3.71 mg/100g) and lowest in Cybistertripunctatus (0.08 mg/100g), Lobothelphusafungosa (0.76 mg/100g), Pilaglobosa (1.07 mg/100g) and Parreysiacorrugata (0.93 mg/100g) respectively. The presence of selected heavy metals Lead (Pb), Cadmium (Cd), Molybdenum (Mo), and Mercury (Hg) were not detected in any of the specimens.
Table 3: Mineral composition (mg/100g).
Freshwater
Macroinvertebrates |
Ca | Cd | Cu | Fe | Mn | Pb | Zn | Mo | Hg |
Sartorianaspinigera | 125.44a
±1.48 |
ND | 1.32a
±0.01 |
35.02a
±0.50 |
8.95a
±0.32 |
ND | 3.52a
±0.12 |
ND | ND |
Macrobrachiumassamense | 109.20b
±2.17 |
ND | 2.73b
±0.22 |
28.65b
±0.24 |
11.42b
±0.34 |
ND | 3.64a
±0.13 |
ND | ND |
Parreysiacorrugata | 5.44c
±0.45 |
ND | 0.13c
±0.01 |
6.85c
±0.26 |
7.35c
±0.09 |
ND | 0.93b
±0.02 |
ND | ND |
Lamellidenscorrianus | 113.25b
±0.08 |
ND | 0.56d
±0.01 |
8.64d
±0.23 |
2.86d
±0.14 |
ND | 1.52b
±0.08 |
ND | ND |
Lamellidensmarginalis | 98.43e
±0.84 |
ND | 1.32a
±0.09 |
4.24e
±0.10 |
7.95ac
±0.27 |
ND | 2.31d
±0.03 |
ND | ND |
Corbiculaassamensis | 114.62b
±1.19 |
ND | 0.87e
±0.04 |
8.52d
±0.15 |
2.38d
±0.10 |
ND | 2.13d
±0.04 |
ND | ND |
Pilaglobosa | 19.87g
±1.82 |
ND | 1.90f
±0.02 |
3.61e
±0.17 |
1.07f
±0.03 |
ND | 1.14b
±0.04 |
ND | ND |
Bellamyabengalensis | 138.62h
±1.03 |
ND | 0.38d
±0.32 |
5.91c
±0.24 |
1.24f
±0.05 |
ND | 3.61a
±0.19 |
ND | ND |
Cybistertripunctatus | 11.87i
±0.43 |
ND | 0.08c
±0.72 |
31.08f
±0.32 |
8.34ac
±0.20 |
ND | 1.68b
±0.15 |
ND | ND |
Brotiacostula | 19.87g
±0.95 |
ND | 1.94f
±0.83 |
3.61e
±0.17 |
1.09f
±0.08 |
ND | 1.14b
±0.01 |
ND | ND |
Lethocerusindicus | 125.21a
±1.30 |
ND | 0.59d
±0.02 |
26.05h
±0.04 |
10.21b
±0.10 |
ND | 3.71a
±0.20 |
ND | ND |
Lobothelphusafungosa | 129.62a
±0.85 |
ND | 0.41d
±0.64 |
0.76j
±0.08 |
6.37e
±0.09 |
ND | 2.06d
±0.03 |
ND | ND |
ND- Not detected
± Standard Error
Values with different alphabets in each column are significantly different at P ≤ 0.05 level.
Discussion
Studies on nutrient compositions of edible macroinvertebrates around the world show that most of them had a satisfactory amount of energy, protein, fats, fibres, minerals and vitamins [22-25].Although, some edible species such as Macrotermessubhyalinus is not rich in amino acids like tryptophan and lysine for compensating the nutritional gap [26].Reports on the nutritional aspects of some aquatic and terrestrial macroinvertebratesof the north-eastern region of India suggested the presence of many important nutrients [27-30].In the present study results of the analysis of proximate composition shows that there was a significant difference (P< 0.05) in the analyzed specimens (Table 2). The Variations in nutrient contents of edible macroinvertebrates aredue to the life stages, the prevalence of various biotic and abiotic factors in their habitats and diet [31-34].For example, the fatty acid composition of edible grasshopper Ruspoliadifferensis reported to be influenced by the plants on which they feed[35]. Methods of food processing also influence the nutrient content to a greater extend [31, 33].
![]() |
Figure 2: Photographs of some freshwater Macroinvertebrates from the study sites: A. Parreysiafavidens; B.Bellamyabengalensis; C. Barytelphusafungosa; D.Brotiacostula; E. Cybistertripunctatus;F. Lamellidenscorrianus; G. Lethocerousindicus; H. Macrobrachiumassamense; I. Pilaglobosa J.Parreysiacorrugata |
The present study revealed that the moisture content in Pilaglobosa was higher compared to other macroinvertebrate species under study. The high amount of moisture content in food materials makes them a risk of microbial deterioration and spoilage [36, 37]. The values (58.62%, 56.80%, 63.72%, 62.86%) obtained in this study were lower than the value (85.9%, 82.1%, 85.5%, and 83.2%) reported earlier [38] for Lamellidensmarginalis, Bellamyabengalensis, Pilaglobosa and Helix sp. respectively. Analysis of ash content of the studied specimens revealed 7.56% on average which corroborated with the ash content for Lethocerusindicus and Cybistertripunctatus[30] and higher than Lamellidensmarginalis, Bellamyabengalensis, Pilaglobosaand Helix sp. [38]. In general, the ash content of biological material is a reflection of the minerals contents in them and may be beneficial for the human body [39, 40].The present findings of mean protein content ranged from 18.10 to 50.50 % (Table 2). The protein content of Lamellidenscorrianus and Lamellidensmarginalis in the present study slightly varied with the findings of other reports [27, 38].The possible cause of variation in protein content may be associated with the reproductive stages of the specimens [41, 42].The carbohydrate content of the studied specimens ranges from 5.25 to 22.54 %which is higher than the report of Shantibala et al. (2014) [30].Carbohydrates serve as a source of energy for aquatic fauna and perform many major structural roles in cells [43]. Generally, the ratio for carbohydrate content is less compared to other nutrients in aquatic organisms and fluctuates widely in response to changes in its habitat conditions [44].The lipid content of the studied specimens ranges from 2.05 to 16.32 (Table 2) which is higher compared to the studies on mollusc and edible arthropods species [24, 27].Sartorianaspinigera(16.32%), Cybistertripunctatus(12.35%) and Lethocerusindicus (13.21%)had the highest crude lipid content species which could contribute a significant source of dietary lipids.The crude fiber contents of the macroinvertebrate species in this study were quite similar with the other insect species such as termites and Componotussp. [45, 46]. Crude fibre has a significant physiological role in the organism’s body in maintaining internal distension for proper peristaltic movement of the intestinal tract [47]. A diet with low fibre content is associated with constipation. Food materials with high fibre content have been used for weight control and fat reduction, as they give a sense of satiety even when a small amount of food is consumed [48].
Minerals are the most important factors for the human body in maintaining several physiological processes and are constituents of bones, teeth, tissue, blood, muscles and nerve cells. Many insect species contain a satisfactory amount of minerals such as iron which boast almost equal iron contents tobeef containing about 6 mg per 100 g of dry weight[33]. In the present study,the most abundant mineral was calcium ranged from 5.44 to 138.62 mg/100g (Table 3).The calcium content of Pilaglobosa (19.87 mg/100g), Bellamyabengalensis(138.62 mg/100g), Helixsp (19.87 mg/100g)andLamellidensmarginalis (98.43 mg/100g) was lower than the studies reported earlier[38].Calcium is an important nutrient that has a vital role in neuromuscular functioning, enzyme-mediated processes and blood clotting. Therefore a constant concentration of calcium in the body is necessary.The second most abundant mineral in the present study was iron which is a component of haemoglobin and myoglobin that acts as a carrier molecule and as a cofactor of various enzymes [49]. Most of the analyzed specimens have a considerable amount of iron (Table 3) compared to other terrestrial insects, such as Bombyxmori[50]. Minerals like Zinc and Copper are the sole components of many enzymes involved in many physiological activities [51]. Deficiency of zinc has become a major public health problem especially for developing children and maternal health. Deficiency of this mineral can cause retardation of growth, Delayed sexual maturation, skin lesions, increased susceptibility to infections[52].The present analyzedspecimens have zinc contents of 0.93 mg/100g(Parreysiacorrugata) to 3.71 mg/100g(Lethocerusindicus) which is lower than the amount for beef (12.5mg/100g) and palm weevil larvae (26.5mg/100g) [33].
Heavy metal contamination in the aquatic organism, generally in Mollusca is a serious concern as they occur at the very low trophic levels in the food chains. Snails can accumulate metals higher than any other group of invertebrates [53]. However, in the present study evaluation of minerals depicted devoid of heavy metal contents suggesting the studied species can be used for consumption. The absence of heavy metal alone can’t be considered for safe consumption. Some edible insects containnaturally content toxic substances such as cyanogenic glycosides[54]. Consumption of grasshopper and locust if consumed without removing their feet can cause intestinal blockage.Similarly,Chitin covering of the exoskeleton of many insects is generally indigestible and causes allergies [55].There is also a risk of microbial disease transmission as Intestinal microbiota of many terrestrial and aquatic insects could be a favourable growth medium for undesirable microorganisms[10, 11].
In different parts of the world Aquatic insects such as mayflies are well harvested and eaten in countries like China, Vietnam, Japan and New Guinea[56]. In Thailand, many aquatic species of Nepidae, Hydrophilidae, Dytiscidae, Nepidae, Notonectidae and Belostomatidaeare reported to be commonly used edible insects[57].In India, about 255 insect species are used as non-conventional food by different ethnic tribes during the seasons of their availability. Among these, the most preferred species belongs to the family of Coleoptera followed by Orthoptera, Hemiptera, Hymenoptera, Odonata, Lepidoptera and Isoptera[58, 59].
Many reports on entomophagy revealed that it is practiced in all seven states of the north-eastern region of India [60-62]. More recently the enormous diversity of insects and other macroinvertebrate fauna are speculated as one of the major sources of future therapeutic agents. Ironically the poor section of the society across various communities consumes a good number of insects and mollusc species available around their localities as traditional food habits to meet their therapeutic and nutritional requirements during the lean period.
However, detail scientific knowledge on this food practice is quite scanty among the user communities. Therefore the present study is a kind of scientific validation of these traditional food habits which may lead to the inventorization and utilization of bio-resources having nutritional and therapeutic potentials in a sustainable approach.
Conclusion
The result of the present work reflects that most of the analyzed freshwater macroinvertebrates have a fair amount of crude protein, carbohydrate, lipids and minerals.The studied macroinvertebrate species represented the most preferred and the cheapest source of protein among the ethnic communities of the study area. This practice of entomophagy should be encouraged as many people can’t afford protein-rich food such as fish or meat. At the same time more exploration and its identification, as well as proper scientific research on the nutritional and anti-nutritional composition, are needed to study the prevailing freshwater macroinvertebrate consumption in the study area which would prove beneficial as a local source of nutrients. Further, the information on nutritional aspects could be effectively used for better utilization of freshwater macroinvertebrates to combat malnutrition and undernourishment of the poor people of the society.
Acknowledgements
The authors are thankful to the Department of life sciences, Dibrugarh University, Assam and Z.S.I Kolkata for the technical support and facilities for carrying out this work.
Conflict of Interest
The authors have no conflict of interest.
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