Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1 -- 2786 2024-03-18 15:28:29 |
2 Reference format revised. Meta information modification 2786 2024-03-19 02:57:45 |

Video Upload Options

Do you have a full video?

Confirm

Are you sure to Delete?
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Potortì, A.G.; Messina, L.; Licata, P.; Gugliandolo, E.; Santini, A.; Di Bella, G. Snail Shell Waste in Food Industries. Encyclopedia. Available online: https://encyclopedia.pub/entry/56382 (accessed on 29 April 2024).
Potortì AG, Messina L, Licata P, Gugliandolo E, Santini A, Di Bella G. Snail Shell Waste in Food Industries. Encyclopedia. Available at: https://encyclopedia.pub/entry/56382. Accessed April 29, 2024.
Potortì, Angela Giorgia, Laura Messina, Patrizia Licata, Enrico Gugliandolo, Antonello Santini, Giuseppa Di Bella. "Snail Shell Waste in Food Industries" Encyclopedia, https://encyclopedia.pub/entry/56382 (accessed April 29, 2024).
Potortì, A.G., Messina, L., Licata, P., Gugliandolo, E., Santini, A., & Di Bella, G. (2024, March 18). Snail Shell Waste in Food Industries. In Encyclopedia. https://encyclopedia.pub/entry/56382
Potortì, Angela Giorgia, et al. "Snail Shell Waste in Food Industries." Encyclopedia. Web. 18 March, 2024.
Snail Shell Waste in Food Industries
Edit

Effective waste management has become an urgent societal challenge. Food waste is made up of items meant for human consumption that are lost, polluted, disposed of, or deteriorated; the reutilization of shells from mollusk waste is a severe problem in terms of environmental protection and the development of the circular economy. The properties of waste shells are presented and discussed, including their biological–natural origin and high calcium carbonate content. This could add social and innovation focus on shell waste management, getting a non-toxic, eco-sustainable, low-cost, biodegradable supplement to invest in. Furthermore, it has the potential to support the circular economy approach by creating a closed system that minimizes the use of natural resources and environmental contamination. 

shell waste food ecology circular economy waste valorization

1. Introduction

Effective waste management has emerged as a critical social issue, particularly with regard to waste reuse. Its utilization, especially in the case of biomass wastes [1] and challenging-to-handle waste, can advance cost-effectiveness and sustainability in the fields of food innovation and the green economy. More specifically, there is a need to research and develop agro-food waste treatment systems to minimize the impact on the environment [2]. One of the primary challenges is lowering the amount of waste produced by recycling and reusing it to create products with additional value to respect the circular economy and bioeconomy principles [3][4][5]. Using food waste as animal feed is a solution that addresses challenges related to food waste management and food safety but also reduces the need to develop conventional feeds, which is a resource and environmentally intensive effort [6]. Managing food waste is an achievable social, political, and environmental solution that promotes a circular economy. In the next years, there will be a significant rise in the need for food production due to the growing global population.
In these conditions, substantial amounts of food industry waste are gaining more and more attention from the scientific, political, and economical spheres. A third of the food produced for human use is lost or wasted worldwide, according to the Food and Agriculture Organization. Except for the retail and domestic phases of the global food supply chain, the FAO’s most current data from 2019 shows that 13.8% of food produced in 2016 was lost from farm to table, highlighting the need for improved waste management systems considering the depletion of natural resources. According to national and international regulatory frameworks, minimizing waste release and maximizing its value (while maintaining standards for food and feed safety and quality) are essential tactics for an efficient management system to generate a real food industry’s sustainability [7]. Reducing pollution and the quantity of scarce resources consumed are made possible by solid waste management, which also lowers costs and strengthens the green economy. Not only will the economy expand when this happens, but people will also live better, healthier lives.

2. Snail Shell Composition

In mollusks, shells are composed of more than 95% inorganic minerals such as phosphorus, manganese, iron, copper, zinc, sodium, potassium, and a tiny quantity of organic matrix [8][9]. In adults, calcium carbonate (CaCO3) is typically found as calcite and aragonite; in juvenile animals, it is frequently found as amorphous calcium carbonate (ACC) [10][11]. Unlike the restricted forms of inorganic substances, there is much diversity in the organic matrix, which includes proteins, lipids, and polysaccharides involved in regulating shell formation; the regulation of CaCO3 precipitation, encompassing nucleation, polymorph selection, and morphology modification via self-assembly and binding to the polysaccharide scaffold is largely dependent on shell proteins [8][12]. Active chemical substances found in snail shells include chitin (C8H13NO5)n, the primary organic material used to make chitosan. (C6H11NO4)n [13]. The membrane-shaped tissue of the mantle is divided into compartments by mineralizing cells that line its exterior and secrete both inorganic constituents and organic matrix. Therefore, the characterization of freshwater snail shell wastes is a prerequisite for promoting their diverse uses as biological materials. These substances have potential applications as biomaterials in the medical field. However, the habitat, environment, mineral content, and microorganisms of snails all have an impact on the bioactive component profile of their shells [14].

2.1. Proximate Composition of Snail Shell

Foods’ proximate composition is made up of their protein, carbohydrate, lipid, and moisture contents. The inclusion of these food components can be of great significance to the food industry, as they present an analytical opportunity for product development and quality control, allowing for improved product formulations and more rigorous quality assurance processes (QC) or regulatory reasons. The analysis of proximate composition conducted by Jatto et al. (2010) [15] showed a higher level of carbohydrate value, calculated as nitrogen free extract (NFE), as a soluble carbohydrate. In Achatina achatina species (African giant snail), it could lead to the use of these ingredients in the development of new ‘healthy’ products. The findings of a study carried out by Nkansah et al. (2021) [16] on three different snail species, such as Achatina marginata, Achatina fulica, and Achatina achatina, showed and confirmed that ash, which can range from 94.8% to 96.31%, is the primary component of the snail shell in Achatina marginata, indicating the quantity of carbon compounds and inorganic components.

2.2. Chitin and Chitosan

Natural aminopolysaccharides, chitin, and chitosan polymers have distinct structures, multifaceted characteristics, extremely complex functions, and a variety of uses in the biomedical and other industries [17][18][19], particularly in the health sector, are useful as antibacterial agents. It is now highly sought after as a novel functional biomaterial with enormous promise across a range of industries, in addition to being an underutilized resource [20][21]. When analyzing the content of chitin and chitosan compounds in different snail shell species of the class Gastropoda, such as Achatina achatina, Achatina fulica, and Archachatina marginata.
The results of the chitosan test obtained from these shell species against potentially dangerous bacterial strains showed that an inhibitory power of 34.33 mm against Staphylococcus aureus was observed at an optimal concentration of 500 ppm [22]. Additional test results demonstrating a sensitive response were obtained from patients with diabetic ulcers caused by the Staphylococcus aureus bacteria at concentrations between 300 and 700 ppm [23]. Achatina fulica species-derived snail shell chitosan was tested for its positive antibacterial activity on cotton fabric by observing how different soaking times affected Staphylococcus aureus growth activity. According to this study, the longer the cotton cloth is submerged in chitosan acetate (Achatina fulica), the more effective it is at inhibiting bacterial activity [24]. The potential of chitin and chitosan to mitigate the usage of synthetic food preservatives lies in their antibacterial and antifungal attributes. Additionally, N-carboxymethylated chitosan, a water-soluble derivative, exhibits antifungal properties. In comparison to synthetic wraps, chitosan-based films surpass in terms of decreased oxygen permeability and improved moisture transfer. 

2.3. Calcium Carbonate

As mentioned earlier, food waste is associated with nutrient losses. Chemical properties, together with the wide range of particle sizes, particle size distributions, and even different crystalline structures, make calcium carbonate an attractive starting material and the right carrier for various mixtures. Therefore, to increase the absorption of calcium from the diet, foods fortified with calcium are commercially available today [25]. Therefore, the calcium carbonate content of the snail shell needs to be extremely high in order for it to be considered a potential source for various industries, as Sundalian et al. (2022) have determined, finding that CaCO3 is the major component of the shells. In order to support the claim, Parveen et al. 2020 [26] attempted to clarify the physical and chemical characteristics of the shells of three Indian freshwater snails, namely, Bellamya bengalensis (Lamarck, 1882) (Gastropoda: Viviparidae), Pila globosa (Swainson, 1828) (Gastropoda: Ampullaridae), and Brotia costula (Rafinesque, 1833) (Gastropoda: Pachychalidae), for the assessment of the calcium carbonate content through field emission scanning electron microscopes (FE-SEM) and energy-dispersive spectroscopy (EDS) microstructure observation and characterization [27].
This increasing need to carry out the mineralogical properties characterisation analysis for snail shell powder in order to further elucidate its characteristic industry potentials also with energy dispersive X-ray (SEM/EDX), X-ray fluorescent (XRF) and the X-ray diffraction (XRD) analysis [28][29].
Images from scanning electron microscopy (SEM) and the corresponding energy dispersive X-ray spectroscopy (EDS) spectra of the shells confirm the high concentrations content (mean percentage of dry weight), supporting and somewhat validating the hypothesis that 95.0–99.9% of snail shells are made of calcium carbonate [30]. Strong calcium peaks, along with carbon and oxygen peaks and the incidence of magnesium and silicium peaks, are seen in the CaCO3 polymorphs.
These chemical properties, together with the wide range of particle sizes, particle size distributions, and even different crystalline structures, make calcium carbonate an attractive starting material and the right carrier for various mixtures. Therefore, commercially available foods fortified with calcium are available to increase the amount of calcium absorbed from the diet today [31]. Calcium supplementation is often used to prevent and treat osteoporosis. Several calcium salts and formulations are available on the market worldwide. Many calcium supplements contain additional ingredients such as vitamin K and magnesium. The most commonly available forms of calcium are calcium carbonate and calcium citrate.

2.4. Other Mineral Elements

Minerals serve a multitude of purposes, including forming the components of our bones, impacting the function of muscles and nerves, and controlling the body’s water balance [32]. Similar to vitamins and other vital nutrients found in food, different animal species have different mineral needs [33]. The two main categories of elements found in minerals are macro (major) and micro (trace). The ultra-trace elements fall into the third category. Calcium, phosphorus, sodium, and chloride are examples of macro minerals. Iron, copper, cobalt, potassium, magnesium, iodine, zinc, manganese, molybdenum, fluoride, chromium, selenium, and sulfur are examples of microelements [34]. The requirement for macrominerals is above 100 mg/dL, and the requirement for microminerals is below 100 mg/dL [35]. The ultra-trace elements, which have been identified in animals and are thought to be vital for these creatures, include boron, silicon, arsenic, and nickel. It is impossible to overstate the significance of mineral elements for plant, animal, and human nutrition.
As nutraceuticals, they have also acquired immense importance in recent animal science in that the nutritional and health-promoting effects of their constituents are considered to have beneficial pharmacological effects, contributing, for example, to the establishment of a normal physiological state of health, to the prevention of diseases and, consequently, to the improvement of production performance, and, as dietary supplements, they can reduce the use of antibiotics [36]
The chemical composition of giant African land snail shells, Archachatina marginata, collected from six southwestern States of Nigeria, was studied by Akinnusi et al. (2018) [37]. Eighteen locations throughout the states were used to gather snails, with three locations in each state. The concentrations of magnesium, calcium, iron, sodium, potassium, chloride, and phosphorus were measured in the shells, evidencing calcium as the most abundant mineral element (1618.89 mg/100 g) and chloride was the least abundant (6.37 mg/100 g). Shells from Lagos State had the lowest concentration (745.6 mg/100 g), while those from Ondo State had the highest total mineral concentration (780.0 mg/100 g), with no discernible difference between them and those from Ekiti State. The table displays the overall mean value of the chemical composition of the snail shells from the six southwestern States of Nigeria. All the mineral elements studied were found in the shells but in different concentrations. Calcium was the highest (260.75–279.68 mg/100 g). The phosphorus content in the shells varies between 196.27 mg/100 g and 206.08 mg/100 g. The shells analyzed collected from Ekiti State had the highest concentrations of Mg2+, Fe2+, and K+ (although not significantly different from those from Ondo State), while the highest Ca2+ levels were found in the shells from Ondo State. Those from Lagos State had the lowest concentrations of Mg2+, Fe2+, and K+

3. Food Industry Applications

Communities are trying to help solve the problem of sustainable use of existing shell waste, and many projects are being launched around the world to sensitize local people to its reuse as useful items. However, these practices are just a drop in the ocean until the valorization of shells and the development of new products become the main focus of the actual food industry [38]. The content of snail shells found in nature varies depending on the diet, including the influence of protein, microorganisms, and mineral content of the living environment, along with constant research about the active chemical compound content of several gastropod-class snail shells, which can be used as a reference basis for biomaterials, food industry preparations, animal feed, and pharmaceutical suppl

3.1. Functional By-Product Production

Traditional Chinese medicine (TCM) is an ancient and important ethnomedical document that still holds an important place in healthcare in China and is also embraced by the Chinese population worldwide [39]. Mollusks are an essential component of many TCM recipes that are used to treat various medical conditions, where shells are either consumed whole or ground into a powder or decocted (heated to extract essence). A number of conventional respiratory medications with Indian origins contain the ashes of burned mollusk shells or cuttlefish bones that have been processed into pills, pastes, and solutions [40]. Traditional Eastern Mediterranean healers used to treat skin conditions, rheumatism, and stomach ulcers by inhaling smoke from opercula from the Muricidae and Strombidae families [41][42]. A particular incentive for research into anti-inflammatory compounds stems from the fact that mollusks are used extensively in traditional medicine to treat symptoms of inflammation and that mollusks are the most important mollusk product used worldwide for the same purpose [42]. However, many European civilizations believed that burning opercula ash could heal split veins [43]. Shells from Monetaria moneta have been used in India to treat a variety of conditions, including asthma [44], and in Zimbabwe, snail shells have long been used as a treatment for topical abscesses [45]. Overall, TCM therapeutic formulations benefit from the contributions of four classes of mollusks: Poly-placophora, Cephalopoda, Bivalvia, and Gastropoda, which have 2, 3, 31, and 34 species, respectively [46].
A recent investigation by Chitprasert et al. (2023) [47] put an eye on the benefits of the use of CaCO3-like nanoparticles to encapsulate and promote the gastrointestinal digestion and bioactivity of vitexin in vitro to improve the bioaccessibility for functional food application. Calcium carbonate is the most common and cheapest form of calcium. For many patients, cost plays an important role. A study that evaluated the cost of calcium from foods and supplements found that calcium carbonate was the cheapest form of calcium, accounting for about a third of the cost of the cheapest food sources, such as frozen skim milk and calcium-fortified orange juice [48].
This investigation revealed that the bioaccessibility, in vitro, was significantly enhanced by this nanoencapsulation with CaCO3, guaranteeing higher antioxidant activity compared to the free vitexin. As a result, this study demonstrates that vaterite CaCO3 nanoparticles are intriguing delivery systems for vitexin meant for use in functional food applications. Furthermore, the CaCO3 nanoparticles are promising options for large-scale production and may raise the possibility of successful commercialization because of their established benefits and low cost [47].
Filter aids or clarifiers are currently used in industrial beer production to improve the quality and clarity of beer. These active ingredients help capture contaminants and/or suspended solids that form blockages or deposits [49]. Due to the high demand for these commercials, these raw materials are relatively expensive and not readily available; cost-effective and locally available alternative filter aids are needed. This can be achieved by finding alternatives to these commercial filter aids from some locally available sources, such as snail shell powder, which mainly consists of calcium compounds, specifically CaCO3, as opposed to diatomaceous earth, which mainly contains silica from the remains of diatoms. Therefore, the use of some of these locally available products as filter aids during brewing has the potential to yield products with desirable qualities comparable to those achieved using commercially available filter aids. This study demonstrated that snail shell powder showed a moderate clarifying effect during the beer-making process, even though the clarity of beer treated with eggshells and other filter aids was excellent [50]. Nevertheless, improving the production of snail shell powder by improving its methods and cost could enhance its use as a potential filter aid in beverage clarification, especially for the large quantities of single-use snail shell waste that are practically available.

3.2. Valorization in Livestock Feed Supplement

Crushed shells are an important calcium supplement (CaCO3) when included in livestock feed. Calcium supplementation is used to improve livestock health, especially bone health, as well as in laying hens as a supplement to improve eggshell quality and strength [51]. Replacing calcium in limestone with calcium in some marine shellfish increases bone development, egg production, and egg strength, weight, and thickness in chickens [52][53][54][55] and ducks [56]. It has been shown that, according to EU Regulation (EC) No. 1069/2009, shell waste can only be used as a feed additive if it does not contain meat in order to exempt it from classification as an animal by-product [57]. The allocation of standards is regulated by the respective authorities of each member state. Ultimately, the recovery of this species needs to consider the distance between shellfish production and farms, both from the perspective of environmental and economic sustainability [58].

References

  1. Yang, M.; Chen, L.; Wang, J.; Msigwa, G.; Osman, A.I.; Fawzy, S.; Rooney, D.W.; Yap, P.S. Circular economy strategies for combating climate change and other environmental issues. Environ. Chem. Lett. 2023, 21, 55–80.
  2. Chowdhary, P.; Gupta, A.; Gnansounou, E.; Pandey, A.; Chaturvedi, P. Current trends and possibilities for exploitation of Grape pomace as a potential source for value addition. Environ. Pollut. 2021, 278, 116796.
  3. Manca, M.L.; Casula, E.; Marongiu, F.; Bacchetta, G.; Sarais, G.; Zaru, M.; Escribano-Ferrer, E.; Peris, J.E.; Usach, I.; Fais, S.; et al. From waste to health: Sustainable exploitation of grape pomace seed extract to manufacture antioxidant, regenerative and prebiotic nanovesicles within circular economy. Sci. Rep. 2020, 10, 14184.
  4. Osorio, L.L.; Flórez-López, E.; Grande-Tovar, C.D. The Potential of Selected Agri-Food Loss and Waste to Contribute to a Circular Economy: Applications in the Food, Cosmetic and Pharmaceutical Industries. Molecules 2021, 26, 515.
  5. Kalli, E.; Lappa, I.; Bouchagier, P.; Tarantilis, P.A.; Skotti, E. Novel application and industrial exploitation of winery by-products. Bioresour. Bioprocess. 2018, 5, 46.
  6. Nath, P.C.; Ojha, A.; Debnath, S.; Sharma, M.; Nayak, P.K.; Sridhar, K.; Inbaraj, B.S. Valorization of Food Waste as Animal Feed: A Step towards Sustainable Food Waste Management and Circular Bioeconomy. Animals 2023, 13, 1366.
  7. FAO. The state of Food and Agriculture 2019. In Moving forward on Food Loss and Waste Reduction; FAO: Rome, Italy, 2019.
  8. Marin, F.; Luquet, G.; Marie, B.; Medakovic, D. Molluscan Shell Proteins: Primary Structure, Origin, and Evolution. Curr. Top. Dev. Biol. 2008, 80, 209–276.
  9. Checa, A.G. Physical and Biological Determinants of the Fabrication of Molluscan Shell Microstructures. Front. Mar. Sci. 2018, 5, 353.
  10. Weiss, I.M.; Tuross, N.; Addadi, L.; Weiner, S. Mollusc Larval Shell Formation: Amorphous Calcium Carbonate is a Precursor Phase for Aragonite. J. Exp. Zool. 2002, 293, 478–491.
  11. McDougall, C.; Degnan, B.M. The Evolution of Mollusc Shells. Wire. Dev. Biol. 2018, 7, e313.
  12. Marin, F.; Roy, N.L.; Marie, B. The Formation and Mineralization of Mollusk Shell. Front. Biosci. 2012, S4, 1099–1125.
  13. Pillai, C.K.S.; Paul, W.; Sharma, C.P. Chitin and Chitosan Polymers: Chemistry, Solubility and Fiber Information. Prog. Polym. Sci. 2009, 34, 641–678.
  14. Sundalian, M.; Husein, S.G.; Putri, N.K.D. Review: Analysis and benefit of shells content of freshwater and land snails from gastropods class. Biointerface Res. Appl. Chem. 2021, 12, 508–517.
  15. Jatto, E.O.; Asia, O.; Medjer, W.E. Proximate and Mineral Composition of Different Species of Snail Shell. Pac. J. Sci. Technol. 2010, 11, 416–419.
  16. Nkansah, M.A.; Agyei, E.A.; Opoku, F. Mineral and proximate composition of the meat and shell of three snail species. Heliyon 2021, 7, e08149.
  17. Chandy, T.; Sharma, C.P. Chitosan as a biomaterial. Biomater. Artif. Cells Artif. Organs 1990, 18, 1–24.
  18. Paul, W.; Sharma, C.P. Chitosan, a drug carrier for the 21st century: A review. STP Pharma Sci. 2000, 10, 5–22.
  19. Muzzarelli, R.A.A.; Guerrieri, M.; Goteri, G.; Muzzarelli, C.; Armeni, T.; Ghiselli, R.; Cornelissen, M. The biocompatibility of dibutyryl chitin in the context of wound dressings. Biomaterials 2005, 26, 5844–5854.
  20. Kumar, M.N.; Muzzarelli, R.A.; Muzzarelli, C.; Sashiwa, H.; Domb, A.J. Chitosan chemistry and pharmaceutical perspectives. Chem. Rev. 2004, 104, 6017–6084.
  21. Hirano, S. Chitin biotechnology applications. Biotechnol. Annu. Rev. 1996, 2, 237–258.
  22. Umarudin, U.; Surahmaida, S.; Alta, R.; Ningrum, R.S. Preparation, Characterization, and Antibacterial of Staphylococcus aureus Activity of Chitosan from Shell of Snail (Achatina fulica F.). BIOTA Biol. Dan Pendidik. Biol. 2019, 12, 22–31.
  23. Umarudin, U.; Surahmaida, S. Isolation, Identification, and Antibacterial Test of Gastropod Chitosan of Snail Shell (Achatina fulica) Against Staphylococcus aureus From Diabetic Ulcer. Simbiosa J. 2019, 8, 37–49.
  24. Rismawati, R.; Hasri, H.; Sudding, S. Kitosan Asetat Cangkang Bekicot (Achatina Fulica) Sebagai Antibakteri Pada Kain Katun. Jurnal Sainsmat Maret 2020, 9, 45–56.
  25. Agoha, E.E.C.; Mazi, E.A. Biopolymers from African Giant Snail Shells Waste: Isolation and Characterization. In World Congress on Medical Physics and Biomedical Engineering; IFMBE Proceedings; Abia State University Department of Food Science and Technology Umuahia, Nigeria, 7–12 September; Dössel, O., Schlegel, W.C., Eds.; Springer: Berlin/Heidelberg, Germany, 2009.
  26. Parveen, S.; Chakraborty, A.; Chanda, D.K.; Pramanik, S.; Barik, A.; Aditya, G. Microstructure Analysis and Chemical and Mechanical Characterization of the Shells of Three Freshwater Snails. ACS Omega 2020, 5, 25757–25771.
  27. Osseni, S.; Bonou, S.; Sagbo, E.; Ahouansou, R.; Agbahoungbata, M.; Neumeyer, D.; Verelst, M.; Mauricot, R. Synthesis of Calcium Phosphate Bioceramics Based on Snail Shells: Towards a Valorization of Snail Shells from Republic of Benin. Am. J. Chem. 2018, 8, 90–95.
  28. Ademolu, K.; Precious, O.; Ebenso, I.; Baratunde, I. Morphometrics and Mineral Composition of Shell Whorls in Three Species of Giant African Snails from Abeokuta, Nigeria. Folla Malacol. 2016, 24, 81–84.
  29. Kolawole, M.Y.; Aweda, J.O.; Abdulkareem, S. Archachatina marginata bio-shells as reinforcement material in metal matrix composites. Int. J. Automot. Mech. Eng. 2017, 4, 4068–4079.
  30. White, M.M.; Chejlava, M.; Fried, B.; Sherma, J. The concentration of calcium carbonate in shells of freshwater snails. Am. Malacol. Bull. 2007, 22, 139–142.
  31. Jia, H.X.; Han, J.H.; Li, H.Z.; Liang, D.; Deng, T.T.; Chang, S.Y. Mineral intake in urban pregnant women from base diet, fortified foods, and food supplements: Focus on calcium, iron and zinc. Biomed. Environ. Sci. 2016, 29, 898–901.
  32. Kim, M.H.; Choi, M.K. Seven dietary minerals (Ca, P, Mg, Fe, Zn, Cu, and Mn) and their relationship with blood pressure and blood lipids in healthy adults with self-selected diet. Biol. Trace Elem. Res. 2013, 153, 69–75.
  33. Soetan, K.O.; Olaiya, C.O.; Oyewole, O.E. The importance of mineral elements for humans, domestic animals and plants: A review. Afr. J. Food Sci. 2009, 4, 200–222.
  34. Eruvbetine, D.; Tajudeen, I.D.; Adeosun, A.T.; Olojede, A.A. Cassava (Manihot esculenta) leaf and tuber concentrate in diets for broiler chickens. Bioresour. Technol. 2003, 86, 277–281.
  35. Murray, R.K.; Granner, D.K.; Mayes, P.A.; Rodwell, V.W. Harper’s Biochemistry, 25th ed.; McGraw-Hill, Health Profession Division: New York, NY, USA, 2000; Volume 225.
  36. Alagawany, M.; Elnesr, S.S.; Farag, M.R.; Tiwari, R.; Yatoo, M.I.; Karthik, K.; Michalak, I.; Dhama, K. Nutritional significance of amino acids, vitamins and minerals as nutraceuticals in poultry production and health—A comprehensive review. Vet. Q. 2021, 41, 1–29.
  37. Akinnusi, F.A.O.; Oni, O.O.; Ademolu, K.O. Mineral composition of giant African land snail’s (archachatina marginata) shells from six south West States, Nigeria. Niger. J. Anim. Sci. 2018, 20, 485–489.
  38. Topić Popović, N.; Lorencin, V.; Strunjak-Perović, I.; Čož-Rakovac, R. Shell Waste Management and Utilization: Mitigating Organic Pollution and Enhancing Sustainability. Appl. Sci. 2023, 13, 623.
  39. Seong, N. Traditional Chinese medicine. In Singapore’s Health Care System: What 50 Years Have Achieved; Earn, C., Satku, K., Eds.; World Scientific Publishing: Singapore, 2015; p. 351.
  40. Gopal, R.; Vijayakumaran, M.; Venkatesan, R.; Kathiroli, S. Marine organisms in Indian medicine and their future prospects. Nat. Prod. Radian 2008, 7, 139–145.
  41. Benkendorff, K.; Rudd, D.; Nongmaithem, B.D.; Liu, L.; Young, F.; Edwards, V.; Avila, C.; Abbott, C.A. Are the Traditional Medical Uses of Muricidae Molluscs Substantiated by Their Pharmacological Properties and Bioactive Compounds? Mar. Drugs 2015, 18, 5237–5275.
  42. Lev, E. Practical Materia Medica of the Medieval Eastern Mediterranean According to the Cairo Genizah; Brill: Leiden, The Netherlands, 2007.
  43. Ratsch, C.; Müller-Ebeling, C. The Encyclopedia of Aphrodisiacs: Psychoactive Substances for Use in Sexual Practices; Park Street Press: South Paris, ME, USA, 2013.
  44. Krishna, K.M.; Singh, K.K. A critical review on Ayurvedic drug Kapardika (Cypraea Moneta Linn). Int. Res. J. Pharm. 2012, 3, 8–11.
  45. Gelfland, M.; Mavi, S.; Drummond, R.; Ndemera, B. The Traditional Medical Practitioner in Zimbabwe: His Principles of Practice and Pharmacopoeia; Mambo Press: Gweru, Zimbabwe, 1985.
  46. Ahmad, T.B.; Liu, L.; Kotiw, M.; Benkendorff, K. Review of anti-inflammatory, immune-modulatory and wound healing properties of molluscs. J. Ethnopharmacol. 2018, 210, 156–178.
  47. Chitprasert, P.; Dumrongchai TRodklongtan, A. Effect of in vitro dynamic gastrointestinal digestion on antioxidant activity and bioaccessibility of vitexin nanoencapsulated in vaterite calcium carbonate. LWT 2023, 173, 114366.
  48. Zalte, N. Calcium and Calcium salts. J. Assoc. Physicians India 2017, 65, 1–2.
  49. Wu, C. What Are Filter Aids? American Filtration and Separation Society (AFS): Nashville, TN, USA, 2018.
  50. Iwuouno, J. Potential of egg shell and snail shell powder in Sorghum Beer Clarification. Arch. Curr. Res. Int. 2019, 16, 1–10.
  51. Muir, F.V.; Harris, P.C.; Gerry, R.W. The Comparative Value of Five Calcium Sources for Laying Hens. Poult. Sci. 1976, 55, 1046–1051.
  52. Islam, M.A.; Nishibori, M. Use of extruded eggshell as a calcium source substituting limestone or oyster shell in the diet of laying hens. Vet. Med. Sci. 2021, 7, 1948–1958.
  53. Tahamtani, F.M.; Kittelsen, K.; Vasdal, G. Environmental enrichment in commercial flocks of aviary housed laying hens: Relationship with plumage condition and fearfulness. Poult. Sci. 2022, 101, 101754.
  54. Saki, A.; Rahmani, A.; Yousefi, A. Calcium particle size and feeding time influence egg shell quality in laying hens. Acta Sci. Anim. Sci. 2018, 41, 42926.
  55. Safaa, H.; Serrano, M.P.; Valencia, D.G.; Frikha, M.; Jiménez-Moreno, E.; Mateos, G.G. Productive Performance and Egg Quality of Brown Egg-Laying Hens in the Late Phase of Production as Influenced by Level and Source of Calcium in the Diet. Poult. Sci. 2008, 87, 2043–2051.
  56. Wang, S.; Chen, W.; Zhang, H.X.; Ruan, D.; Lin, Y.C. Influence of particle size and calcium source on production performance, egg quality, and bone parameters in laying ducks. Poult. Sci. 2014, 93, 2560–2566.
  57. Morris, J.P.; Backeljau, T.; Chapelle, G. Shells from Aquaculture: A Valuable Biomaterial, Not a Nuisance Waste Product. Rev. Aquac. 2019, 11, 42–57.
  58. de Alvarenga, R.A.F.; Galindro, B.M.; de Fátima Helpa, C.; Soares, S.R. The recycling of oyster shells: An environmental analysis using Life Cycle Assessment. J. Environ. Manag. 2012, 106, 102–109.
More
Information
Subjects: Others
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : , , , , ,
View Times: 79
Revisions: 2 times (View History)
Update Date: 19 Mar 2024
1000/1000