SHORT NOTE

EGG LAYING AND ALBUMEN GLAND COMPOSITION OF MARGINATA DURING GROWTH PHASES

PUESTA DE HUEVOS Y COMPOSICIÓN DE LA GLÁNDULA DEL ALBUMEN DE ARCHACHATINA MARGINATA DURANTE LAS FASES DE CRECIMIENTO

Ademolu, K.O.1*; Taiwo, B.E.1; Jayeola, O.A.1 and Ajayi, O.1

1Biological Sciences Department. University of Agriculture. Abeokuta. Nigeria. *[email protected]

ADDITIONAL KEYWORDS PALABRAS CLAVE ADICIONALES Snail.Reproductive capability. Caracol. Capacidad reproductiva.

SUMMARY The egg laying pattern and albumen gland amilasa y cellulasa, seguidas en orden decrecien- composition in three growth phases of Archacha- te por juveniles y crías. En la fase juvenil hay mayor tina marginata: snailet, juvenile and adult were concentración de proteína, glucosa y lípidos en la investigated in this study. The juvenile stage laid glándula del albumen. Se registraron fuertes rela- the highest number of snails (9.3) followed by the ciones positivas entre número de huevos, y glu- adult stage (4.7), while no egg was laid by the cosa, proteína y lípidos de la glándula del albumen. snailet phase. However, the eggs laid by the adult Puede inferirse que en la etapa juvenil de A. phase were significantly (p<0.05) heavier than marginata, son mayores el potencial y la capaci- those laid by the juvenile stage. The adult stage dad reproductiva. had the biggest albumen gland (7.30±0.1cm) and the highest lipase, proteinase, α-glucosidase, INTRODUCTION amylase and cellulase activities followed by the juvenile stage, while the snailet had the least The search for cheap protein by values. However, results of organic composition citizens of developing countries like Nigeria of the albumen gland show that juvenile phase has is enormous because of the fluctuating a statistically higher protein, glucose and lipid economy. In recent time, attention has been composition than the other two growth phases. shifted to a new branch of study, that is, Correlation analysis showed a strong positive micro livestock- the rearing of invertebrate relationship between egg number and albumen gland glucose, protein and lipid composition It can and lower like grasscutters, rabbits thus be inferred that juvenile stage of A. marginata and snails. Snails are unique because of has the best reproductive capability and potential. their simple nature and ability to feed on wide varieties of feeds including household RESUMEN wastes. Generally, snails pass through three Se analizó el modelo de puesta y la composi- growth stages namely: Infantile (snailet), ción de las glándulas del albumen de Archachatina juvenile and mature (adult) phase (South, marginata en tres fases de crecimiento: cría, 1992). Ademolu et al. (2009) had earlier juvenil y adulto. La puesta fue mayor en la etapa A. juvenil (9,3) seguida de la adulta (4,7), no hubo observed that the juvenile phase of puesta de huevos en las crías. Los huevos de la marginata recorded a significantly higher etapa adulta fueron más pesados (p<0,05) que los concentration of glucose and lipids in their de la juvenil. Los adultos tuvieron las glándulas de haemolymph than other growth phases. albumen más grandes (7,30 cm) y las mayores Studies by different scientists have actividades lipasa, proteinasa, α−glucosidasa, shown that size and total number of eggs

Recibido: 26-4-12. Aceptado: 20-12-12. Arch. Zootec. 62 (240): 603-606. 2013. ADEMOLU, TAIWO, JAYEOLA AND AJAYI laid by snails differ from one to by sensitive weighing balance (PM-Mettler another and various reasons have been -K) and tape rule respectively. adduced for this observation, namely: tract Nine (9) snails from each group were size (Idokogi and Osinowo, 1998), genetic used for the chemical analysis of the albu- make-up and haemolymph characteristics men gland. The activities of amylase, α- (Ademolu et al., 2009). Nevertheless, the glucosidase, cellulase, lipase and proteinase knowledge of the properties of the albumen were determined following the method of gland - site of egg coating and fertilization AOAC (1990). Similarly, the organic contents can provide an insight into this age variation of the albumen gland were determined as in egg laying pattern and ultimately assist in follows - protein was analysed by Biuret better production of A. marginata in method (Henry et al., 1977), while glucose captivity. The thrust of this work is to exa- was determined colorimetrically (Baumni- mine the egg laying pattern and albumen ger, 1974). Lipid content was assayed by gland composition of A. marginata during method of Grant (1987). three growth phases. All data collected from this study were subjected to one-way analysis of variance MATERIALS AND METHODS (ANOVA) and wherever there were signi- ficant values, means separation was done The study was carried out in the Animal by SNK-test. Correlation analysis was also House of the Department of Biological done to determine the relationship between Sciences, Federal University of Agriculture, the egg number and the organic content of Abeokuta, Nigeria (7010'N and 302'E). Nine the albumen gland. plastic cages (30 x 40 x 24 cm) were filled with top loamy soil up to 5cm before introducing RESULTS the snails. A total of forty-five (45) Giant African The juvenile stage laid the highest land snails - A. marginata were purchased number of eggs followed by the adult stage, from the snail pen of the Department of while the snailet phase did not lay egg at all. Forestry and Wildlife Management. The However, the adult snails laid significantly snails were in three growth phases namely: bigger eggs (table I). Also, the adult stage snailet (±100.5 g), juvenile (±133.2 g) and had the heaviest and biggest albumen gland adult (±211.7 g) as earlier described by followed by the juvenile stage the smallest Idokogi and Osinowo (1998). The cages was observed in the snailet (table I). The housing the snails were cleaned every day color of the albumen gland of the experimen- before feeding and the top loamy soil tal snails varies from cream color in snailet replaced every 2 weeks. The snails were fed phase to golden yellow in the adult phase ad libitum for 12 week with fresh pawpaw (table I). The shape and texture of the gland leaves and water. The eggs laid during the are bean-like and soft respectively for the 3 experiment were recorded and incubated in phases of life. cans containing loamy soil. The albumen gland of adult A. marginata Snails were dissected following the recorded higher enzymatic activities for all method of Segun (1975). The albumen gland the enzymes than the other two phases of was carefully removed from the herma- development (table II). Statistical analysis phroditic duct with a pair of sterile scissor showed that the albumen gland of the into a clean petri dish. The colour and texture juvenile stage had a significantly (p<0.05) of the gland was observed by feeling with higher concentrations of lipid and glucose the fingers. The weight and width of albu- than both adult and snailet phases. Addi- men gland from the three groups were taken tional analysis (r2) of the number of eggs

Archivos de zootecnia vol. 62, núm. 240, p. 604. EGG LAYING AND ALBUMEN GLAND COMPOSITION OF ARCHACHATINA MARGINATA

DISCUSSION Table I. Egg laying pattern and albumen gland in A.marginata. (Producción de huevos y The egg laying pattern of different glándula del albumen en A. marginata). phases of development of A. marginata reveals that the juvenile stage laid the Snailet Juvenile Adult highest number of eggs followed by the adult stage. However, the smaller number of Egg laying eggs laid at the adult stage might possibly eggs laid 0.00 9.3±0.02a 4.7±0.01b be due to degenerating of some reproductive egg weight, g 0.00 1.93±0.1b 3.70±0.03a organs due to age. The juvenile stage is a Albumen gland growing and active phase of snails and thus Weight, g 1.0c±0.01 3.4b±0.3 11.0a±0.1 has the ability to produce higher number of Length, cm 2.5c±0.1 4.6b±0.2 7.3a±0.1 eggs. Idokogi and Osinowo (1998) reported Width, cm 0.7±0.03 1.0±0.02 1.6±0.4 that snailets have rudimentary reproductive Colour Cream Cream Golden yellow structures, suggesting that they were not Texture Soft Soft Soft sexually matured and this might explain their Shape Bean Bean Bean inability to lay any egg. The higher enzy- abcMean values on the same row having the same matic activities of the adult phase albumen superscript are not significantly different (p>0.05). gland suggests the ability of the gland cells to digest the substrates of those enzymes better and this might likely explains the laid and the organic concentration of the bigger sizes of the eggs laid by them as there albumen gland revealed a strong positive are more nutrients available for the growth relationship between them. The r2 values for of the eggs cells. In a related study, Maha glucose, protein and lipid were 0.99, 0.61 et al. (2009) reported that steroid hormones and 0.90 respectively. were abundantly present in the tissues of Biomphalaria alexandrina snails while low levels were recorded in juvenile snails. The Table II. Enzymatic activities and compo- low level in juvenile stage probably indi- sition of the albumen gland of A. marginata. cates the commencement of reproductive (Actividad enzimática y composición de la glándu- activities unlike the adult stage where the la del albumen de A. marginata). process is well established. The coloration of the albumen gland Snailet Juvenile Adult becomes intense as the snail ages su- ggesting level of growth. The color of tissues Enzymes (nmol) like muscles suggests their age and growth Cellulase 3.3±0.2 5.4±2.1 6.2±1.1 level (Odiete, 1999). Juvenile stage had a Amylase 5.1±0.1 6.5±0.4 7.5±0.1 significantly higher concentration of glucose α-glucosidase 7.1±0.1b 8.5±0.3ab 9.8±0.1a and lipid in its albumen gland relative to other Lipase 2.1±0.3b 4.3±0.1ab 5.9±0.2a stages of development. Similarly, a signi- Proteinase 9.3±0.1 10.9±0.7 11.6±0.5 ficantly higher concentration of glucose and Composition lipids was reported in the haemolymph of Protein, g/L 30.0±0.3b 58.6±1.3a 42.4±0.4ab juvenile A. marginata (Ademolu et al., 2009). Glucose, mg/dL 6.0±0.1b 16.10±1.1a 4.10±3.1b Lipids and glucose are rich energy metabo- Lipids, mg/dL 54.4±0.2b 89.30±0.6a 62.1±0.2b lites that supply the cells with much needed abMean values on the same row having the same energy at this phase of development. The superscript are not significantly different (p>0.05). higher number of eggs laid during this phase might not have been unconnected to the

Archivos de zootecnia vol. 62, núm. 240, p. 605. ADEMOLU, TAIWO, JAYEOLA AND AJAYI high concentration of these metabolites. a particular snail, as there existed a strong The albumen gland organic composition positive relationship between albumen might suggests the number of eggs laid by gland composition and number of eggs laid.

REFERENCES

Ademolu, K.O.; Idowu, A.B. and Jayeola, O.A. snail. Archachatina marginata. Proceeding on 2009. Changes in Haemolymph Biochemical Silver Anniversary of Nigerian Society for Ani- values during different growth phases in African mal Production (NSAP). Abeokuta, 21-25 March. giant , Archachatina marginata pp. 415-416. (Swainson). Nig J Anim Prod, 36: 161-166. Maha, R.; Abdul-Hamid, A.Z.; Mamlouk, E.T. and AOAC. 1990. Association of official Analytical Said, N. 2009. Assessment of steroids during Chemsit. Ed. W. Horwitz. 13th adition. Washing- maturation and infection of Biomphalaria ton, D.C. 1141 pp. alexandrina snails, an intermediate host of Baumniger, R.N. 1974. Analytical Chemistry. Schistosoma mansoni. Biohealth Sc Bulletin, Cambridge Press. London. pp. 83-85. 1: 7-12. Grant, G.H. 1987. Amino acids and Protein: Odiete, W.O. 1999. Basic Animal Physiology. Fundamentals of clinical chemistry. WB Sander Diversified Resources Ltd. Lagos. Company. Philadelphia. USA. pp. 326-329. Segun, O.A. 1975. The Giant Land Snail Henry, R.J.; Canon, D.C. and Winkalman, J.W. Archachatina (Calachatina) marginata (Swam- 1977. Clinical Chemistry: Principle and Technique son). Dissection guide of common tropical ani- 2nd ed. Harper and Row Publishers. New York. mal. Ethiope publishing house. Benin City. Nigeria. pp. 54-56. pp. 13-16. Idokogi, E.A. and Osinowo, O.A. 1998. Investigation South, A. 1992. Terrestrial Slugs: Biology, ecology on the reproductive system of the African land and control. Chapman and Hall. USA. pp. 9-19.

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