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The vast majority of embryological research on amphibians focuses on just a single genus of frogs, Xenopus. To attain a more comprehensive understanding of amphibian development, experimentation on non-model frogs will be essential. Here, we report on the early development, rearing, and embryological analysis of túngara frogs (genus Engystomops, also called Physaleamus). The frogs Engystomops pustulosus, Engystomops coloradorum and Engystomops randi construct floating foam-nests with small eggs. We define a table of 23 stages for the developmental period in the foam-nest. Embryos were immunostained against Lim1, neural, and somite-specific proteins and the expression pattern of RetinoBlastoma Binding Protein 6 (RBBP6) was analyzed by in situ hybridization. Due to their brief life-cycle, frogs belonging to the genus Engystomops are attractive for comparative and genetic studies of development.
Many frogs deposit their eggs in the water; other frogs, however, have evolved adaptations that diminish or eliminate the aquatic requirement for reproduction (Duellman and Trueb, 1986). A deviation of the aquatic reproductive mode occurs in the túngara frogs, genus Engystomops (= Physalaemus), Leiuperidae, and consists in the formation of foam-nests that float over temporary water. In Engystomops pustulosus, reproduction occurs during the rainy season; the male attracts the female with a characteristic call, and amplexus takes place. During amplexus, the male beats the egg-jelly with its legs and feet. This action produces a floating mass of white foam, in which numerous eggs are embedded (Davidson and Hough, 1969; Ryan and Rand, 2003). In this way, E. pustulosus eggs are placed over, and develop above water. Development in foam-nests that float over temporary water protects embryos from predators, including tadpoles of other frogs (Ryan, 1985). Moreover, the hardened surface of the nest may reflect solar radiation, decreasing heat absorption, and preventing internal desiccation. At hatching, the tadpoles fall into the water (Davidson and Hough, 1969; Ryan, 1985). Engystomops pustulosus is active at night and displays a complex reproductive behavior. The ecology, sexual selection and communication strategies of this frog have been extensively studied (reviewed in Ryan 1985; Ryan and Rand 2003; Ron et al., 2006).
Frogs of the genus Engystomops inhabit the forest floor in lowland regions from Central Mexico to the Amazon basin, and the lowlands of W Ecuador and NW Peru (reviewed by Ron et al., 2006). The widely studied, Engystomops pustulosus, occurs at the Smithsonian Tropical Research Institute in Panama, among other locations (Davidson and Hough, 1969; Ryan, 1985; Ron et al., 2006). Other congenerics that have been analyzed are Engystomops coloradorum, and E. randi, which inhabit the western lowlands of Ecuador (Ron et al., 2006). Mitochondrial DNA analysis of these three species revealed a close relationship. Accordingly, these frogs have been placed in the Engystomops pustulosus species group (Ron et al., 2006). In this study, we describe the early development of these Engystomops species, methods for the handling of eggs and embryos, and frog laboratory maintenance.
In a search for an anuran amphibian with synchronous oogenesis, Davidson and Hough (1969) determined that E. pustulosus was appropriate for developmental work. The environmental changes of wet and dry seasons were reproduced in the laboratory to analyze the modifications of oogenesis. Oogenesis changes from synchronous during the dry season to asynchronous in the wet season. During the dry season, many oocytes reach their full growth (stage 6) and remain in the ovary until reproduction is triggered by the first rains. Besides these large oocytes, only previtellogenic oocytes were detected in the ovary by the end of the dry season. In contrast, during the wet season, the full range of oocyte-sizes occurs in the ovary. After the first mating of the rainy season, ovarian oocytes grow, producing oocytes of all sizes. Thereafter, in preparation for the impending mating, the largest oocytes complete their growth. This adaptation facilitates repeated mating during the wet season. Maternal transcripts are retained in E. pustulosus embryos to the tadpole stage (Davidson and Hough, 1969; Hough et al., 1973).
Eggs of E. coloradorum and E. randi are small and white, and resemble Xenopus laevis albino embryos (del Pino et al., 2007). Furthermore, as in X. laevis, embryonic development occurs rapidly in comparison with the slow-developing embryos of the dendrobatid frog Colostethus (= Epipedobates) machalilla (Grant et al., 2006), and of the marsupial frog Gastrotheca riobambae (del Pino et al., 2007). Tail bud stage embryos of E. coloradorum and E. randi differ from X. laevis embryos in their general shape, in the mode of somitogenesis, and size of cranial neural crest cell streams (del Pino et al., 2007).
Analysis of Lim1 (Lhx1) gene expression at the protein level in gastrulae of E. coloradorum and E. randi allowed detection of the organizer, and of the dorsal mesoderm (del Pino et al., 2007; Venegas et al., 2009). In embryos of these frogs, elongation of the notochord overlaps with involution at the blastopore lip, as in X. laevis embryos (del Pino et al., 2007). In addition, in the mid gastrula, the prechordal plate and notochord were simultaneously recognized by the expression of the protein Lim1, a pattern equivalent with that of Xlim1 mRNA expression in X. laevis embryos (Taira et al., 1992; 1994a,b; Venegas et al., 2009). In contrast, in embryos of the dendrobatid frog C. machalilla, only the prechordal plate was recognized during gastrulation. Elongation of the notochord occurred after blastopore closure in this frog (Venegas et al., 2009). This uncoupling of developmental events associates with the modular nature of frog gastrulation (Ewald et al., 2004; Moya et al., 2007; del Pino et al., 2007; Venegas et al., 2009).
In this study, we immunostained Engystomops embryos with several antibodies, to detect the neural tube, cranial neural crest cells, somites, pronephros, and performed in situ hybridization to analyze the expression of the RetinoBlastoma Binding Protein 6 (RBBP6) during development. A particular advantage for developmental studies is the brief life-cycle of these frogs, which can be as short as 4 months in E. pustulosus (Davidson and Hough, 1969). Our aim is to provide a methodological base-line for further comparative studies of Engystomops development.
Development of E. pustulosus, E. coloradorum, and E. randi embryos in the foam-nest was divided into 23 stages (st). Development in the foam-nest lasted 3 days in all of these frogs. At hatching, the foam-nest became somewhat liquid and the tadpoles moved into the water. The criteria used to define the developmental stages are given in Table 1. Developmental stages from fertilization to the early neurula were defined according to the X. laevis table of development (st 1–14; Nieuwkoop and Faber, 1994). Thereafter, the generalized table of frog development (Gosner, 1960) was used to stage embryos, as the embryonic morphology of Engystomops deviated from that of X. laevis embryos (Table 1) The external views of embryos are provided to complement the description of developmental stages (Fig 1A–P, 2A–G). The free-living tadpoles were not studied.
The foam-nests of E. pustulosus, E. coloradorum, and E. randi measured about 5 cm in diameter and were 4–5 cm high. The white eggs and embryos of these frogs were effectively camouflaged in the white foam of the nest. Each nest contained 130 ± 60 eggs of 1.3 mm in diameter in E. coloradorum (21 foam-nests with a total of 2,072 eggs); and 110 ± 69 eggs of 1.1 mm in diameter in E. randi (17 foam-nests with a total of 1,952 eggs). The foam-nests of E. pustulosus contain an average of 238 ± 97 eggs, based on 68 foam-nests collected in the field at the Barro Colorado Island, Panama (Ryan, 1985). The means and standard deviations are given.
External views of cleavage stage embryos are shown in Fig. 1A–E, and of the blastula in Fig. 1F,G. In the three species analyzed, eggs had a uniform white appearance. Therefore, the animal hemisphere could not be detected at the one-cell stage (Fig. 1A). Similarly, a gray crescent could not be detected in these pale colored embryos. Cleavage was holoblastic and synchronous, and new cleavage furrows were detected every 20 minutes during the early cleavage cycles (Table 1). The first cleavage furrow divided the egg into two blastomeres (st. 2, not shown). At the next three cleavage cycles, new cleavage furrows developed, and divided the embryo into 4, 8, (st 3–4, Fig. 1B,C), 16, and 32 blastomeres (st 5–6; Fig. 1D,E). The planes of these cleavage furrows were equivalent with those of X. laevis embryos (Nieuwkoop and Faber, 1994). Animal blastomeres were smaller than the vegetal blastomeres, as shown for blastula stage embryos (st 7–9; Fig. 1F,G). Although the external appearance of these embryos is white, dark pigment was detected around nuclei of surface cells (Fig. 1F).
Development of the blastocoel is shown in Fig 3A–C. The blastocoel was detected as a small cavity in the animal region of 8-cell stage embryos (st 4, not shown). The blastocoel enlarged from cleavage to the onset of gastrulation (st 5–10.5; Fig. 3A–C,F). Dark pigment was detected around internal nuclei, as observed in the blastocoel roof (Fig. 3B), in the vegetal region (not shown), and in surface cells of the equatorial region (st 7; 1F). In spite of this light pigmentation, embryos had a white appearance. Transcripts of the gene RBBP6 were detected in animal cells of blastula stage embryos (Fig. 3D).
External views of the gastrula are given in Fig. 1H–L, ,3J.3J. The morphology of the gastrula, and the expression of the protein Lim1 is shown in Fig. 3E–G, J–N. A prominent dorsal blastopore lip developed in the subequatorial region at the onset of gastrulation (st 10.5; Fig. 1H, ,3E),3E), as in embryos of X. laevis. Time-lapse movies of gastrulation revealed that the blastopore closes asymmetrically, moving ventrally over the yolk plug as gastrulation proceeded (see supplementary material), as has been observed in X. laevis. The archenteron was small at 10.5 (Fig. 3F,G), and bottle cells were found at the anterior tip of the archenteron (Fig. 3G), as in X. laevis embryos. The thickness of the blastocoel roof decreased from 5–6 cell-layers in a large-cell blastula (st 7; Fig. 3B) to 3-layers in the mid gastrula (st 11; Fig. 3H), and finally to two cell layers in the late gastrula (st 12; Fig 3I). During gastrulation, the blastopore decreased in size until it was just a slit at st 13 (st 11–13; Fig. 1I–L). Some embryos of st 13, however, had a small yolk plug (Fig 1L, ,3L).3L). The dorsal blastopore lip of st 10.5 embryos of E. coloradorum gave a positive signal for the protein Lim1 (Fig. 3E), as previously detected in E. randi embryos (Venegas et al., 2009). In st 12 embryos (Fig. 3J), the archenteron elongated and became inflated (Fig. 3K), and the blastocoel was still large (Fig. 3K). In slightly more advanced embryos, the archenteron was fully elongated and inflated (st 13, Fig. 3L). Small remnants of the blastocoel were detected (Fig. 3L). Elongation of the notochord started in the mid gastrula, as detected by immunostaining against the protein Lim1 (not shown). The notochord of a st 12.5 embryo is shown in Fig. 3M. The notochord was covered by endoderm in the rostral region of st 13, and st 14 embryos (Fig. 3O). In the caudal region, however, the notochord was not covered by endoderm, and was exposed in the blastocoel roof plate (Fig. 3N). These findings are consistent with the previous observation that the mode of gastrulation in Engystomops resembles that in X. laevis (del Pino et al., 2007).
The morphology of the neurula, and the expression of neural and somite markers are shown in Fig. 4. External views of the neurula are given in Fig. 1M–P, ,4I.4I. The neural plate was detected in st 13–14 embryos (Fig. 3N, O). The open neural folds were detected in embryos of st 14 and were clearly visible in st 15 embryos (Fig. 1M–O). Neural folds were far more pronounced than those in X. laevis (Fig. 4G,H). Similarly, the gastrocoel roof plate was larger than in X. laevis (Fig. 3N, ,4H).4H). Transcripts of the gene RBBP6 were restricted to the presumptive eye region (st 14, Fig. 4A). Somites were detected in st 15 embryos (Fig. 4B,C). The neural folds were positive for antigen 2G9 in st 15 embryos (Fig. 4D). The protein Lim1 was used as marker of the notochord, specific cells of the cns, and pronephros (st 15; Fig. 4E,F). The notochord was covered by endoderm in the rostral region (Fig. 4G), and it was exposed in the caudal region of st 15 embryos (Fig. 4H), as detected previously in st 13–14 (Fig. 3N,O). The neural folds gradually closed in the midline during st 16 (Fig. 1P, ,4I).4I). The streams of cranial neural crest cells were detected by the expression of antigen 2G9 in st 16 embryos (Fig. 4J). Somites were detected by immunostaining against sarcomeric meromyosin in st 15 embryos (not shown) and became more clearly detectable in st 16 embryos (Fig. 4K). Somites contain numerous cells of round shape (Fig. 4L), a feature that greatly differs from the X. laevis mode of somitogenesis, which involves fewer cells and cell rotation (Radice et al., 1989).
External views of tail bud and more advanced embryos are given in Fig. 2A–G. Expression of neural and somite markers are shown in Fig. 5. Embryos were curved around a large yolky endoderm, and differed in shape from the elongated X. laevis tailbud (st 17–18; Fig. 2A–C, ,5A).5A). Prominent branchial arches were visible in living and fixed embryos (st 17; Fig. 2A–C). Transcripts of the gene RBBP6 were detected in the neural region (Fig. 5A). After immunostaining against antigen 2G9 rhombomeres and streams of cranial neural crest cells were visible (st. 17; Fig. 5B,C). Rhombomeres 3 and 5 were negative for antigen 2G9 (Fig. 5B,C). The branchial anterior stream was weakly stained in comparison with the mandibular, hyoid and branchial posterior streams of cranial neural crest cells (st 17; Fig. 5C). The expression pattern of antigen 2G9 in rhombomeres and streams of cranial neural crest cells is comparable with the previously detected expression in G. riobambae embryos (del Pino and Medina, 1998). The closed neural tube and optic vesicles were detected by immunostaining against NCAM (st 17; Fig. 5D). Embryos of st 17 had about 12 somites pairs, as detected by immunostaining against sarcomeric meromyosin (st 17; Fig. 5E). Pronephros, immunostained against Lim1, were larger than in st 15 embryos (Fig. 5F).
Embryos of st 18 were characterized by muscular activity (Table 1). Embryos of this stage acquired an elongated shape, somites were numerous, and the tail was longer (Fig. 5G).The heart was positive for sarcomeric meromyosin (Fig. 5G). Pronephros and pronephric ducts were fully developed in embryos of this stage, (Fig. 5H). Specific cns cells were Lim1-positive (not shown). Embryos developed the cement gland, which was clearly detectable at st 18 (not shown).
Buds of the external gills developed in st 19 embryos (not shown). Further development of the external gills occurred from st 20–23 (Fig. 2D–G). At hatching, external gills were small and contained 6 gill branches in the first pair and 5 branches in the second pair (St 23; Fig. 2G). The tail became gradually elongated from st 18–23, and embryos acquired the shape of a tadpole (Fig. 2C–D,F). The opercular fold was detected in st 22–23 embryos (not shown). A remarkable feature of Engystomops development is the almost complete absence of dark pigment during development in the foam nest. The body and the head developed some dark pigment in st 20–23 embryos (Fig. 2D–G). In spite of the limited pigmentation, hatching embryos had a white appearance (Fig. 2F). Embryos of the three species of Engystomops hatched at st 23 (Table 1).
Early development in E. pustulosus, E. coloradorum and E. randi greatly resembles X. laevis development. Eggs and early embryos are white, develop rapidly, and resemble X. laevis albino embryos in size and appearance. It should be noted, however, that blastomeres contain dark pigment in the Engystomops species analyzed. Pigment surrounds the nuclei, instead of being localized to the surface of animal blastomeres (Fig. 1F, ,3B).3B). The patterns of cleavage, blastula formation, and gastrulation resemble closely the developmental patterns observed in X. laevis embryos. Elongation of the notochord overlaps with other processes of gastrulation in these rapidly developing frogs, as in X. laevis. In contrast, in the slow developing embryos of the dendrobatid frogs, C. machalilla and G. riobambae, the process of notochord elongation occurs after blastopore closure (del Pino, 1996; Benítez and del Pino, 2002; Venegas et al., 2009). The limitations imposed by the aquatic reproductive mode of X. laevis and Engystomops may have favored the acceleration of early development and, consequently, the overlap of developmental process during gastrulation. Although early development of túngara frogs closely resembled the developmental pattern of X. laevis, more advanced embryos greatly differed from X. laevis. The external morphology of advanced embryos of Engystomops resembled the morphology of Rana embryos (Pollister and Moore, 1937), with a major difference in pigmentation, as foam-nest embryos of túngara frogs lack dark surface pigment.
Túngara frog embryos were staged according to the X. laevis table of stages only until st 14 (Nieuwkoop and Faber, 1994). Thereafter, the embryonic morphology differed from X. laevis. Differences detected included the general shape of tail bud embryos (st 17), pattern of somitogenesis, and size of the cranial neural crest cell-streams. Somitogenesis involves numerous small cells and cell intercalation in E. coloradorum and E. randi, whereas in X. laevis, each somite consists of cells, which are already elongated, and the mode of somitogenesis involves cell rotation (Radice et al., 1989; del Pino et al., 2007). Moreover, the neural plate and neural folds of túngara frog embryos are larger than in X. laevis. The cranial neural crest cell-streams of E. randi embryos are also more conspicuous than in X. laevis embryos and are comparable to the pattern observed in the marsupial frog G. riobambae (del Pino and Medina, 1998; del Pino et al., 2007). Therefore, although frogs of the genus Engystomops and X. laevis develop rapidly, and have a similar morphology of early development, there are important differences in their advanced morphogenetic patterns.
Methods used to study X. laevis development (Sive et al., 2000) were successfully adapted to analyze the embryogenesis of túngara frogs.
Ovulation in túngara frogs can be induced by adding water to terraria and by water spraying to simulate rain, as explained in the section on maintenance and reproduction. As in X. laevis, it is known that E. pustulosus responds with ovulation to the administration of human chorionic gonadotropin (hCG, Davidson and Hough, 1969). Additionally, phonotaxis is induced in adult E. pustulosus females with hCG, which will eventually cause the female to ovulate (Lynch et al., 2006). Ovulation was similarly triggered in three females of E. randi by the subcutaneal administration of three doses of 100, 200 and 300 IU of hCG, respectively. The hormone was administered at 3 days intervals.
We have found that embryos of E. pustulosus can be easily released from foam nests with an adaptation of the X. laevis de-jellying method (Sive et al., 2000). Foam nests were removed from terraria and placed onto the surface of de-jellying solution (3 % cysteine in 33 % MMR, pH7.2) in a wide beaker. The beaker was gently swirled for several minutes. At intervals, embryos dropped from the nest into the solution, and were immediately removed to a dish containing 33 % MMR (MMR solution was prepared according to Sive et al., 2000). In some cases, agitation of the foam with forceps hastened release of embryos. Embryos were then reared as per X. laevis.
In contrast, embryos of E. coloradorum and E. randi were maintained within the foam nest, and were gradually removed for analysis. The jelly layers were somewhat liquid and were successfully removed with forceps. In some instances, embryos were chemically dejellied according to the X. laevis method (Sive et al., 2000).
Embryos of the túngara frogs were handled according to X. laevis methods (Sive et al., 2000), including time-lapse recordings. To maintain embryos in the foam-nest we placed the foam-nests of E. coloradorum and E. randi in deep plastic dishes of about 15 cm in diameter that were half-filled with chlorine-free water. Dishes were covered with plastic film to prevent desiccation and were maintained at room temperature (18–22 °C). Some embryos were moved to a petri dish filled with 15 % Steinberg’s solution (Rugh, 1962) to study embryogenesis. Procedures for fixation, vibratome sectioning of embryos, and immunostaining were previously described (del Pino et al., 2004; Venegas et al., 2009).
Injections of mRNA into early cleavage stage embryos were straightforward using the same method employed for X. laevis (not shown). (Sive et al., 2000). We have also adapted the Xenopus in situ hybridization method. We cloned a partial cDNA for the RBBP6 gene out of E. pustulosus, and by in situ hybridization we found it to be expressed in the animal region of the blastula (Fig. 3D) and neural tissues, especially the presumptive eye (Fig 4A, ,5A).5A). We have also performed in situ hybridization to the Shroom2 gene (Lee et al., submitted manuscript).
Tadpoles, juveniles, and adults of E. pustulosus and E. randi were kept in terraria, with successful reproduction. Maintenance in captivity of E. pustulosus at the University of Texas, Austin, differed from the method employed with E. randi at the Pontificia Universidad Católica del Ecuador. Both methods are described.
The E. pustulosus rearing laboratory at The University of Texas, Austin is an adaptation of the enclosures used at the National Aquarium in Baltimore (Maryland, U.S.A.) and the San Antonio Zoo (Texas, U.S.A.). The laboratory has a daily light cycle of 12 hours and is maintained at 27–28°C with humidity at 30–50 % year round. Terraria are placed on wooden frames with a downward angle of 30° and include 5.5, 10 and 15 gallon glass aquaria that have a hole with a connector and plastic tubing to allow for drainage. A 2″ layer of autoclaved and rehydrated sphagnum moss covers the bottom of each terrarium. Moss is hydrated using room temperature chlorine-free water. Plastic huts made of plant pots and artificial plants are placed in terraria to act as refugia. Terrarium covers are made of plastic frames with mesh screens and lined with Velcro and weather-stripping to prevent escapes.
Reproduction is induced by adding a water pond (small container with rocks and chlorine-free water), increasing humidity, and sometimes simulating rainfall by spraying the terraria with chlorine-free water. Pairs produce a foam nest that is then transferred to a 5 gallon aquarium filled with chlorine-free water. Tadpoles hatch after two days.
Tadpoles are housed in aquaria filled with chlorine-free water and each day are fed JurassiDiet, a pellet food for aquatic reptiles. Within 6 weeks there are newly metamorphosed frogs. These frogs are fed wingless Drosophila only, while juvenile and adult frogs are fed a combination of Drosophila and 7-day hatched crickets three times per week.
Engystomops randi was maintained at the Herpetology Section of the Museum of Zoology of Pontificia Universidad Católica del Ecuador. Frogs were kept in terraria, which were stacked in shelves inside a room with controlled environmental conditions. The daily light-cycle was of 12-hours, and room-temperature fluctuated between 24–28 °C. Terraria measured 60 × 35 × 35 cm and were arranged as follows: Chlorine-free water filled the floor to a height of about 5 cm. The water was covered with a sheet of sturdy plastic mesh that was supported by legs. Small-sized gravel partially covered the plastic mesh. Terraria were slightly tilted, resulting in the formation of a shallow water pool of about 1 cm in depth in the gravel-free area. Water was changed every 2 months. Coconut shells and a plant, a Phylodendrum sp., provided hiding places. Each terrarium was covered with plastic mesh and two glass plates that were placed slightly apart from each other. This cover arrangement allowed aeration, prevented frogs from breaking away, and insured conditions of high humidity. Terraria with a lower water level did not contain water pools, and were used to keep young frogs. Foam-nests, embryos and tadpoles were maintained under equivalent conditions of light in 50 × 30 × 30 cm aquaria. The aquaria were half-filled with chlorine-free water, and the water temperature fluctuated between 24–26 °C. Pumps provided aeration. Water was changed at weekly intervals.
Tadpoles were fed with a mixture of dried and finely ground plant leaves and invertebrates, as follows: the water fern Azolla sp., Taraxacum, Spirulina, Cyclops, Daphnia, and Tubifex. Newly metamorphosed frogs were fed daily for about 10 days with collembola (Folsomia candida). Somewhat larger frogs received newly hatched crickets, Gryllus sp., as prey. Adults were fed every other day with 15-day-hatched crickets and Drosophila.
The presence of a water reservoir at the bottom of each terrarium was advantageous for the maintenance of substrate humidity. Additionally, when the water level of the reservoir was increased, a water pool was formed, and the frogs used it for reproduction. In contrast, reduction of the water level in the reservoir diminished or eliminated the water pool. Young adults of E. randi reproduced often, whereas one-year old and older frogs reproduced less frequently or not at all.
One terrarium contained 12 frogs (6 males and 6 females) collected from nature. In two additional terraria, we maintained 5 males and 5 female laboratory-raised frogs per terrarium. These frogs belonged to the first and second generations. We observed that reproduction occurred when the level of the water in the reservoir was increased until the pool was flooded. In contrast, reduction of the water level inhibited reproduction. Accordingly, we changed the water and flooded the terraria to induce reproduction.
The 32 E. randi adults produced a total of 80 foam-nests in two years (February 2006–March 2008). The monthly production ranged from 0–16, with an average of 3 ± 4 foam-nests per month (the mean and standard deviation are given). Foam-nests were removed and cultured in aquaria until metamorphosis. Development in the foam-nest took three days until hatching (observation of 9 foam-nests). Based on the analysis of 121 tadpoles (34 ± 6 days; mean and standard deviation are given), the aquatic tadpole stages lasted about one month until metamorphosis. A maximum of 20 juveniles were maintained per terrarium. Six months after metamorphosis, young frogs of the first and second generations produced foam-nests, an indication of sexual maturity (193 and 201 days, respectively).
Engystomops randi was successfully maintained in small terraria and reached adulthood in 7–8 months after fertilization. In contrast, Davidson and Hough (1969) maintained from 50 to 400 individuals of E. pustulosus in beds of sterilized earth placed in the floor of a room of 8 × 12 feet with controlled conditions of light, temperature, and humidity. Tadpoles of E. pustulosus required 3–4 weeks to reach metamorphosis, and young frogs reproduced 2–3 months after metamorphosis (Davidson and Hough, 1969).
Túngara frogs are attractive for developmental work due to the ease of their maintenance in captivity and rapid development. In addition, reproduction can be induced by increasing the environmental humidity and by flooding. The synchronous oogenesis, rapid development, and short life cycle of these frogs are attractive for studies that involve the induction of developmental mutations and genetic studies of development.
Embryos were immunostained in whole mount against Lim1, neural and somite-specific proteins. We used the monoclonal antibody MF-20 (Bader et al., 1982) against adult chicken pectoralis myosin to detect muscle development. The monoclonal antibody (4d) against NCAM from chick brain membranes (Watanabe et al., 1986) was used to detect the neural tube. These two antibodies were obtained from the Developmental Studies Hybridoma Bank (Iowa City, IA). The monoclonal antibody 2G9 against a neural antigen from X. laevis (Jones and Woodland, 1989) was used to detect the neural tube and the neural crest (del Pino and Medina, 1998). This antibody was donated by E. A. Jones (University of Warwick, Warwick, U.K.). Some embryos were immunostained with a polyclonal antibody against Lim1, donated by M. Taira (University of Tokyo, Japan). Secondary antibodies were sheep anti-rabbit IgG and sheep anti-mouse IgG. Both antibodies were conjugated to alkaline phosphatase (Roche Molecular Biochemicals, Mannheim, Germany). Immunostaining was done as previously described (del Pino et al., 2004; Venegas et al., 2009). Some sections were cleared, stained with Hoechst 33258 (Sigma-Aldrich, St. Louis, MO, USA), mounted in glycerol, and examined with fluorescent optics.
Engystomops pustulosus embryos fertilized naturally were de-jellied in 1/3 X modified Marc’s Ringer (MMR) with 3% (w/v) cysteine at pH 7.8. They were fixed at neurula stage and tailbud stage with 1X MEMFA and were dehydrated with 100% methanol (according to Sive et al., 2000).
To synthesize a probe for RBBP6 transcripts (RetinoBlastoma Binding Protein 6), partial RBBP6 cDNA was cloned into PCRII vector (Invitrogen) by using FirstChoice RLM-RACE Kit (Ambion) and the probe was synthesized with T7 polymerase (Promega). In situ hybridization for E. pustulosus was performed with X. laevis in situ hybridization protocol (Sive et al., 2000). RBBP6 expressing regions were colorized with alkaline phosphatase (AP) and BM purple AP substrate (Roche).
Foam nests of E. pustulosus were obtained from frogs maintained at The University of Texas at Austin. Engystomops pustulosus were collected at various times from the Panama Canal area in Panamá with permission of the Smithsonian Tropical Research Institute and with scientific collecting permits from Autoridad Nacional del Ambiente, Panama.
Six couples of E. randi were collected from 8 to 23 February, 2005 in Ecuador, Province of “El Oro”, road to the Puyango Forest. The altitude is of 288 meters above sea level. The geographic coordinates of this site are W 80.083319, S 3.88184. Three couples of E. coloradorum were collected on the 30 January 2005 from Ecuador, Province of Pichincha, secondary road near Tinalandia north bank of the Toachi river. The altitude of this site is of 938 meters above sea level, and the geographic coordinates are W 79.05028, S 0.29546. Frogs were collected by S. R. Ron, G. Romero, and E. Tapia. Authorization 016-IC-FAU-DNBAP-MA from the Ministry of the Environment allowed the collection of frogs from Ecuador.
Grant sponsors: EMP was supported by grants from Pontificia Universidad Católica del Ecuador: 2006, 2007, 2008, and The Academy for the Developing World (TWAS), Grant 07-017 LDC/BIO/LA-UNESCO FR 3240144821; JBW and CJL were supported by the NIH/NIGMS.
We thank L. A. Coloma, S. Ron, and other members of the Herpetology Section, Museum of Zoology of the Pontificia Universidad Católica del Ecuador for the donation of several E. coloradorum adults and for their help with the reproduction of E. randi (its reproduction received financial support from the research program “Balsa de los Sapos”). We thank E. A. Jones (University of Warwick, UK), and M. Taira (University of Tokyo, Japan) for the donation of antibodies. We acknowledge the help of O. D. Pérez, and P. Montenegro-Larrea with frog care and discussions, and the assistance of J. Davis and D. Davis with language revision of a previous version.
Supplementary material. Time-lapse movie of gastrulation in Engystomops pustulosus.