Food quality influences ovarian development in Scyphophorus acupunctatus (Coleoptera: Dryophthoridae).
The agave weevil, Scyphophorus acupunctatus Gyllenhall (Coleoptera: Dryophthoridae), is considered a primary pest of agave (Agave spp.) (Asparagaceae) and tuberose (Polianthes tuberosa L.) (Asparagaceae) in Mexico (Solis-Aguilar et al. 2001; Camino et al. 2002; Figueroa-Castro et al. 2013). Currently, we maintain a colony of this weevil in order to develop and evaluate pest management methods for its control. Continuous mass rearing of this species under laboratory conditions is possible using an artificial meridic diet rather than rearing individuals on tuberose bulbs (Valdes-Estrada et al. 2012). However, it is unknown if ovarian development is affected by the artificial diet. Here we describe the sequence and stages of ovarian maturation in virgin S. acupunctatus weevils, as well as the influence that meridic and tuberose bulb diets may have on this developmental process.
Materials and Methods
Initially, S. acupunctatus larvae were obtained from tuberose crops in Mazatepec, (18.7334778[degrees]N, 99.3172222[degrees]W) and Yautepec (18.8289444[degrees]N, 99.09291667[degrees]W), Morelos, Mexico, from Dec 2015 to Dec 2016 and reared on tuberose bulbs in the laboratory. Upon emergence, adults were maintained in an environmental chamber at 25 [+ or -] 2 [degrees]C, 60% RH, 12:12 h (L:D) photoperiod. Individuals were separated by sex based on the criteria of Ramirez-Choza (1993) and females were kept individually in 30 mL plastic containers.
To determine the effect of diet on ovarian maturation, virgin S. acupunctatus were fed a meridic diet composed of agar, vitamins, sucrose, brewer's yeast, wheat bran, cholesterol, Wesson's salts, sorbic acid, ascorbic acid, methyl p-hydroxybenzoate, and distilled water (Valdes-Estrada et al. 2012). Another cohort was fed 5 mm wide tuberose bulb slices, previously hydrated in water for 20 min.
All females were dissected at 0, 5, 10, 15, 20, 30, 45, and 60 d of age (n = 12 for each age) under a stereoscopic microscope (Zeiss Discovery-V20, Thornwood, New York, USA). Ovaries were removed by pulling the ovipositor in a posterior direction until they were freed from the other tissues. Samples were stored at 4 [degrees]C in 5 mL Eppendorf tubes with water and thymol (May & Baker Ltd., Ongar, United Kingdom) solution of 0.5 mg per mL. Photomicrographs of dissected material were prepared using a Canon EOS 5D Mark II camera (Canon, Inc., Tokyo, Japan).
The proximal follicle area, length, and presence of mature follicles or relics were obtained from micrographs of dissected material. Only data from an ovariole of each weevil with the largest number of follicles were recorded. Length and area of the proximal follicle in each ovariole was measured using ImageJ software (National Institutes of Health, Bethesda, Maryland, USA). Follicle area was calculated using the formula of an ellipse (nab, where n = 3.1416, a = length/2, and b = width/2) (Perez-Mendoza et al 2004).
Ovarian development was classified based on the degree of follicular differentiation, maturity of the proximal follicle, and presence of follicular relics (or mature follicles) in the oviducts as reported by Grodowitz & Brewer (1987). Development was divided into 1 parous and 3 nulliparous stages. Nulliparous stages were classified as: nulliparous 1 (where the germarium and vitellarium are not differentiated and are without follicles); nulliparous 2 (well-defined ovarioles with multiple follicles, the proximal follicle transparent indicating that it had not completed maturation); and nulliparous 3 (proximal follicle more opaque [mature] and close to ovulation). In the parous stage the follicles pass through the lateral oviduct (ovulation) or have follicular relics at the base of the ovarioles.
The mean number of follicles, as affected by diet and age (as well as mean length and area of the proximal follicle in each ovariole), was subjected to a 2-way ANOVA and differences determined by Tukey's test (P < 0.05). Females (on d of emergence) did not contain follicles, so this age was not included in analysis. Therefore, only length and area of the proximal follicle of individuals [greater than or equal to] 10 d of age were included in the analysis (75% females possessed follicles). All analyses were performed using SigmaPlot 12.5 (Systat Software, Inc., San Jose, California, USA).
We found that the female reproductive system of virgin S. acupunctatus was composed of a pair of ovaries with 2 tubular ovarioles each (Fig. 1). Only 0.01% of the dissected females possessed an ovary with 3 ovarioles; when this occurred the ovary was not fully developed and possessed no mature follicles. Follicle oocytes were surrounded by a layer of follicular cells that constituted the follicular epithelium (Fig. 2A). Follicles were observed to develop gradually into the vitellarium, where the least mature follicles were located distally whereas the mature ones occurred proximally, close to the common oviduct (Fig. 2B). Mature follicles were filled with yolk that contained a germinal vesicle or defined nucleus (Fig. 2C).
Ovarian development of virgin S. acupunctatus consisted of 4 stages: 3 nulliparous (without ovulation) and 1 parous (with ovulation) (Fig. 3). Ovulation occurred when the mature oocyte passed through the lateral oviduct (Fig. 3 PA). Follicle reabsorption and ovulation can be estimated by the presence of follicular relics at the base of the ovariole (Fig. 3 PB). Follicular relics were primarily light yellow, spotted, or ring shaped whereas very few were dark brown.
Females fed the meridic diet experienced a delay in ovariole maturation compared with those fed on tuberose bulbs (Fig. 4). We noted that all females fed the meridic diet at 0 and 5 d of age possessed undifferentiated ovaries without follicles (nulliparous 1), whereas 17% of those that fed on tuberose bulbs at 5 d of age presented well-defined ovarioles with follicles (nulliparous 2). At 10 d, 75% of females fed the meridic diet were in stage nulliparous 2 as well as 83% of females fed on tuberose; however, the rest of the females (17%) had mature follicles close to ovulation (nulliparous 3). At 15 d, 92% of the females fed on tuberose had already ovulated or had follicular relics (parous), but only 17% of the females fed on a meridic diet reached that stage (Fig. 4). At 20 d of age, all females fed on tuberose reached the parous stage, whereas 17% of those fed the meridic diet were in nulliparous 3 stage then later reached the parous stage at 30 d.
We also found that the number of follicles found in ovaries depended on the type of diet (F = 31.22; df = 1, 154; P < 0.001), the age of the individual (F = 76.71; df = 6, 154; P < 0.01), and the interaction between these 2 variables (F = 2.42; df = 6, 154; P < 0.05). Females fed tuberose bulbs gradually increased their number of follicles up through 20 d of age followed by a decrease; individuals fed the meridic diet showed similar development but with a delay of 10 d (Fig. 5). The production of follicles in females fed on tuberose was significantly greater than that of females fed on a meridic diet at 10, 20, and 45 d of age.
Length of the proximal follicle of individual weevils containing the most mature oocyte (Fig. 6A) was not affected by diet (F = 2.73; df = 1, 129; P > 0.05), but was affected by age (F = 22.75; df = 5, 129; P < 0.001), as well as the interaction between these 2 factors (F = 3.16; df = 5, 129; P = 0.010). The length of the proximal follicle increased progressively with respect to age until 30 and 20 d of age in females fed the meridic diet and tuberose bulb, respectively. At 30 d of age, the proximal follicle length of females fed the meridic diet was significantly greater compared with individuals that fed on tuberose (Fig. 6A); however, at 45 d of age this relationship was reversed.
The proximal follicular area was not affected by diet (F = 0.05; df = 1, 119; P > 0.05) but was affected by age (F = 19.21; df = 5, 129; P < 0.001), and interaction of diet and age (F = 4.24; df = 5, 129; P < 0.001). The proximal follicle area increased gradually with time until 30 and 20 d of age in individuals fed on the meridic diet and tuberose bulbs, respectively (Fig. 6B). Maximum increase was observed at 30 and 60 d of age in females fed the meridic diet, whereas those fed on tuberose was 45 d. Moreover, females that fed on tuberose bulbs had a significantly smaller proximal follicle area than those fed the meridic diet at 30 d, reversing this relationship at 45 d of age.
We observed that the female reproductive system of virgin S. acupunctatus was formed by a pair of ovaries with 2 ovarioles. These characteristics were similar to that reported for other dryophthorids such as Cosmopolites sordidus Germar (Coleoptera: Dryophthoridae) (Gold et al. 2001; Uzakah 2017), Sitophilus oryzae L. (Coleoptera: Dryophthoridae) (Perez-Mendoza et al. 2004), Rhynchophorus ferrugineus Olivier (Coleoptera: Dryophthoridae) (Naggar et al. 2010), and the curculionids Anthonomus grandis Boheman (Coleoptera: Curculionidae) (Burke 1959; Grodowitz & Brewer 1987), Neochetina eichhorniae Warner (Coleoptera: Brachyceridae) (Grodowitz et al. 1997), Sitona cylindricollis FSrster (Coleoptera: Curculionidae) (Garthe 1970), and Sitophilus granarius L. (Coleoptera: Dryophthoridae) (Dinuta et al. 2009). Ovarioles of S. acupunctatus contained a bulky germarium and are probably of the meroistic, telotrophic type as reported in other weevils (Grodowitz et al. 1987, 1997; Naggar et al. 2010; Perez-Mendoza et al. 2004).
Ovaries of virgin S. acupunctatus females possessed follicles in different stages of maturation and appearance of relics. We noticed that there was no synchronization of proximal follicle maturation whereas the number of ovulations in each ovariole varied. These results are in agreement with that reported by Adams (2000), Perez-Mendoza et al. (2004), and Lenz et al. (2007) for other insect species. However, in our study it was not possible to determine if S. acupunctatus follicular relics were the result of reabsorption or ovulation as reported for N. eichhorniae and Prostephanus truncatus Horn (Coleoptera: Bostrichidae) (Grodowitz et al. 1997; Scholz et al. 1998).
We found that S. acupunctatus females fed on a tuberose or meridic diet contained close to mature follicles in ovarioles (Nulliparous 3) when 10 and 15 d old, respectively. These data are in agreement with Hernandez et al. (2012) where 14-d-old females were ready to mate. Our study also showed that females fed on tuberose bulbs were parous between 10 and 15 d old whereas those that fed on the meridic diet reached this stage between 15 and 20 d old. This developmental difference is consistent with that reported for other weevils, such as Ceutorhynchus assimilis Paykull (Coleoptera: Curculionidae), wherein females complete their ovarian development by feeding on their host plant, but not when they are fed a diet of water and sugar (Ni et al. 1990).
In summary, the ovarian classification described in this paper will help to assess sexual maturity and provide quantitative information about the physiological condition of field populations of S. acupunctatus females. This knowledge could provide valuable guidance in monitoring the effectiveness of pest management suppression programs for this weevil pest.
RAB, NRQ, MRM, and AJP are Comision de Operacion y Fomento de Actividades Academicas (COFAA) and Estimulos al Desempeno de los Investigadores (EDI) Fellows. M. Vega acknowledges funding from Consejo Nacional de Ciencia y Tecnologia (CONACyT) and Beca de Estimulo Institucional de Formacion de Investigadores (BEIFI), IPN. This research was funded by Secretaria de Investigacion y Posgrado (SIP) Grants 20141203 and 20150997 to RAB.
Adams TS. 2000. Effect of diet and mating status on ovarian development in a predaceous stink bug Perillus bioculatus (Hemiptera: Pentatomidae). Annals of the Entomological Society of America 93: 529-535.
Burke HR. 1959. Morphology of the reproductive systems of the cotton boll weevil (Coleoptera, Curculionidae). Annals of the Entomological Society of America 52: 287-294.
Camino LM, Castrejon GVR, Figueroa BR, Aldana LL, Valdes EME. 2002. Scyphophorus acupunctatus (Coleoptera: Curculionidae) attacking Polianthes tuberosa (Liliales: Agavaceae) in Morelos, Mexico. Florida Entomologist 85: 392-393.
Dinuta A, Bunescu H, Bodis I. 2009. Contributions to the knowledge of morphology of the granary weevil (Sitophilus granarius L.), major pest of the stored cereals. Bulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca. Agriculture 66: 9-66.
Figueroa-Castro P, Solis-Aguilar JF, Gonzalez-Hernandez H, Rubio-Cortes R, Herrera-Navarro EG, Castillo-Marquez LE, Rojas JC. 2013. Population dynamics of Scyphophorus acupunctatus (Coleoptera: Curculionidae) on blue agave. Florida Entomologist 96: 1454-1462.
Garthe WA. 1970. Development of the female reproductive system and effect of males on oocyte production in Sitona cylindricollis (Coleoptera: Curculionidae). Annals of the Entomological Society of America 63: 367-370.
Gold CS, Pena JE, Karamura EB. 2001. Biology and integrated pest management for the banana weevil Cosmopolites sordidus (Germar) (Coleoptera: Curculionidae). Integrated Pest Management Reviews 6: 79-155.
Grodowitz MJ, Brewer FD. 1987. Ovarian anatomy and physiological age-grading of the female boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae). Annals of the Entomological Society of America 80: 642-651.
Grodowitz MJ, Center TD, Freedman JE. 1997. A physiological age-grading system for Neochetina eichhorniae (Warner) (Coleoptera: Curculionidae), a biological control agent of water hyacinth, Eichhornia crassipes (Mart.) Solms. Biological Control 9: 89-105.
Hayes EJ, Wall R. 1999. Age-grading adult insects: a review of techniques. Physiological Entomology 24: 1-10.
Hernandez RMC, Valdes EME, Aldana LL, Gutierrez OM, Lopez-Martinez V. 2012. Comportamiento reproductivo de Scyphophorus acupunctatus Gyll. en laboratorio. Southwestern Entomologist 37: 243-246.
Klowden MJ. 2008. Physiological Systems in Insects, 2nd edition. Academic Press, Burlington, Massachusetts, USA.
Lenz JM, Grodowitz MJ, Kennedy JH. 2007. A physiological age-grading system for female Hydrellia pakistanae Deonier (Diptera: Ephydridae). Biological Control 42: 119-128.
Naggar SEME, Mohamed HF, Mahmoud EA. 2010. Studies on the morphology and histology of the ovary of red palm weevil female irradiated with gamma rays. Journal of Asia-Pacific Entomology 13: 9-16.
Ni X, McCaffrey JP, Stoltz RL, Harmon BL. 1990. Effects of postdiapause adult diet and temperature on oogenesis of the cabbage seedpod weevil (Coleoptera: Curculionidae). Journal of Economic Entomology 83: 2246-2251.
Perez-Mendoza J, Throne JE, Baker JE. 2004. Ovarian physiology and age-grading in the rice weevil, Sitophilus oryzae (Coleoptera: Curculionidae). Journal of Stored Products Research 40: 179-196.
Ramirez-Choza JL. 1993. Max del henequen Scyphophorus interstitialis Gylh. bioecologia y control. Serie: Libro Tecnico. Centro de Investigacion Regional del Sureste. Instituto de Investigaciones Forestales, Agricolas y Pecuarias. Secretaria de Agricultura, Ganaderia y Recursos Hidraulicos, Merida, Yucatan, Mexico.
Scholz D, Borgemeister C, Markham R, Poehling HM. 1998. Physiological age-grading and ovarian physiology of Prostephanus truncatus. Physiological Entomology 23: 81-90.
Solis-Aguilar JF, Gonzalez-Hernandez H, Leyva-Vazquez JL, Equihua-Martinez A, Flores-Mendoza FJ, Martinez-Garza A. 2001. Scyphophorus acupunctatus Gyllenhal, an agave tequilero pest in Jalisco, Mexico. Agrociencia 35: 663-670.
Tyndale-Biscoe M. 1984. Age-grading methods in adult insects: a review. Bulletin of Entomological Research 74: 341-377.
Uzakah RP. 2017. Age at sexual maturity of male and female banana weevils, Cosmopolites sordidus Germar (Coleoptera: Curculionidae). Acta Zoologica 1: 1-7.
Valdes-Estrada ME, Aldana-Llanos L, Jimenez-Perez A, Gutierrez-Ochoa M, Hernandez-Reyes MC. 2012. Diets for rearing Scyphophorus acupunctatus (Coleoptera: Curculionidae). Florida Entomologist 95: 497-500.
Maritza Vega-Petlacalco (1), Rene Arzuffi (1), Jorge Valdez (2), Mario Rodriguez-Monroy (1), Alfredo Jimenez-Perez (1), and Norma Robledo (1,*)
(1) Centro de Desarrollo de Productos Bioticos, Instituto Politecnico Nacional, Km. 6 Carretera Yautepec-Jojutla, Col. San Isidro.Yautepec, Morelos, C.P. 62731, Mexico; E-mails: email@example.com (M. V. P.); firstname.lastname@example.org (M. R. M.); email@example.com (A. J. P.); firstname.lastname@example.org (N. R.)
(2) Colegio de Postgraduados, Entomologia, Km 36.5 Carretera Mexico-Texcoco, Montecillo, Estado de Mexico, C.P. 56230, Mexico; E-mail: email@example.com (J. V.)
(*) Corresponding author; Email: firstname.lastname@example.org
Caption: Fig. 1. (A) Female reproductive system of Scyphophorus acupunctatus formed by 2 ovaries (ov), germarium (g), vitellarium (v), oocyte (o), lateral oviduct (lo), common oviduct (co), spermatheca (s), and genital chamber (gc); (B) Distal part of the germarium (g) with bulky appearance possibly with trophocytes, prefollicular cells, and oogonia, terminal filament (tf), trachea (tr), tracheoles (trl); and (C) Approach to the onset of vitellarium with oocytes in development, germinal vesicle (gv), interfollicular tissue (tif), trachea (tr), and tracheoles (trl).
Caption: Fig. 2. Follicles of Scyphophorus acupunctatus in different stages of development. (A) Oocyte (o) located in the distal part of the vitellarium, further developed oocyte surrounded by follicular epithelium (fe) showing germinal vesicle (gv), peritoneal sheath (sh), trachea (tr), tracheoles (trl); (B) Gradual maturation of follicles (fo) with yolk (yo) and germinal vesicle (gv); (C) Mature follicle located in the proximal part of the vitellarium with yolk (yo).
Caption: Fig. 3. Sequence of developmental stages of ovarian maturation of Scyphophorus acupunctatus females. N1: without follicles, no clear differentiation between germarium and vitellarium; N2: ovarioles begin to differentiate (germarium and vitellarium), follicles begin to form but not yet mature; N3: ovarioles completely differentiated, proximal follicle mature and ready to be ovulated, no follicular relics present; PA: follicles in oviducts; PB: presence of follicular relics. N = nulliparous.
Caption: Fig. 4. Ovarian maturation of Scyphophorus acupunctatus females (%) at different ages fed on meridic diet (left) and tuberose bulb (right), n = 12 of each age and type of diet.
#Caption: Fig. 5. Average number ([+ or -] SEM) of follicles per ovariole in Scyphophorus acupunctatus at 5, 10, 15, 20, 30, 45, and 60 d of age fed on meridic diet (solid bars) and tuberose bulbs (empty bars). Bars within the same age with different letters indicate significant differences (Tukey multiple comparison test, *P < 0.05).
Caption: Fig. 6. (A) Average length ([+ or -] SEM) and (B) area ([+ or -] SEM) of proximal follicles in female of Scyphophorus acupunctatus at 10, 15, 20, 30, 45, and 60 d of age fed on meridic diet (solid bars) and tuberose bulbs (empty bars). Bars within the same age with different letters indicate significant differences (Tukey multiple comparison test, *P < 0.05).
Please Note: Illustration(s) are not available due to copyright restrictions.
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|Author:||Vega-Petlacalco, Maritza; Arzuffi, Rene; Valdez, Jorge; Rodriguez-Monroy, Mario; Jimenez-Perez, Alfr|
|Date:||Sep 1, 2018|
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