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Supresion de las moscas Drosophila ananassae debido a la competencia interespecifica con D. melanogaster bajo condiciones artificiales.

SUPPRESSION OF DROSOPHILA ANANASSAE FLIES OWING TO INTERSPECIFIC COMPETITION WITH D. MELANOGASTER UNDER ARTIFICIAL CONDITIONS

INTRODUCTION

Natural selection often operates through competition, allowing various forms to survive and establish under certain environmental conditions. It tends to eliminate, gradually or rapidly, forms exploiting identical niches. Charles Darwin (1859) in his book "Origin of species" stated that Intraspecific and interspecific competition among organisms are a part of natural selection. This competition can be the result of high reproductive potential of some species when compared to the environmental carrying capacity. The most severe form of interspecific competition exists when organisms of two species have the same requirements. On the basis of theoretical equations, Lotka (1925) and Volterra (1926) independently predicted that two species with identical needs and habits cannot survive in the same place if they compete for limited resources. If both types are found together in nature, they must differ in their ecology, or else there are fluctuations in the environment, favoring first one and then the other. Experiments on interspecific competition between similar species have also demonstrated the validity of this theory (Connell 1981; Crombie 1947; Denno et al. 1995; Gause 1934; Hochkirch & Groening 2012; Luan et al. 2012; Zhang et al. 2011; Zimmering 1948). Careful analysis of the instances in which both species survive has shown that they occupy slightly different niches (Gause 1934; Crombie 1947). According to Kohn and Orians (1962) competition between species reveals ecological differences permitting coexistence of stable populations of closely related species of various kinds of animals.

Drosophila turns out to be the apt model system for studying interspecific competition, because in the genus Drosophila one finds a large number of species, some showing high degrees of morphological and ecological similarities and also close genetical relationships (Tantawy 1964). No wonder, exhaustive studies have been done, especially involving sibling species of this genus to study interspecific competition (Nunney 1990). A practical way of studying interspecific competition in the laboratory is by co-culturing two species together in large population cages or in culture bottles. One may simply study the effect of co-culturing on the fecundity of the species involved or one can also check the effect of altering various ecological conditions such as larval density, temperature etc. on the fecundity of co-cultured populations of two species. Merrell (1951) cultured D. melanogaster and D. funebris together in food bottles and found that the proportion of D. funebris eggs reaching pupation decreased significantly in mixed larval populations. Interspecific competition between D. melanogaster and D. simulans, was studied in much detail by Barker & Podger (1970). They examined the effects of larval density and short-term adult starvation on fecundity, egg hatchability and adult viability. It was found that significant effect of larval density on fecundity was probably mediated through effects on adult body weight. D. melanogaster females raised in mixed species cultures were less fecund than those from pure cultures, while D. simulans showed the reverse effect. Increasing the larval density of the two species at 15[degrees]C and 25[degrees]C temperatures, causes a progressive reduction in per cent hatching (Tantawy & Soliman 1967; Miller 1964; Chiang & Hodson 1950; Birch 1955). Boggild & Keiding (1958) in their studies on house fly larvae found that harmful effects of crowding on adult emergence result from an increased incidence of collisions between larvae. This causes the metabolic rate to be increased and thus reduces the fraction of ingested food available for tissue formation. Tantawy & Soliman (1967) found that there was a gradual elimination of D. simulans by D. melanogaster in the two cages, irrespective of their initial percentage at 25[degrees]C. These results also supported the results of Moore (1952) and Barker (1963). The results from cages kept at 15[degrees]C indicate that the outcome of competition at 15[degrees]C is completely different from that at 25[degrees]C. At 15[degrees]C there is an increase in D. simulans at the expense of D. melanogaster. A similar experiment was done by Montchamp-Moreau (1983) involving the same species. The optimum temperature for D. simulans was found to be 20[degrees]C and for D. melanogaster it was 25[degrees]C as while at 25[degrees]C D. melanogaster eliminated D.simulans and at 20[degrees]C the reverse occurred in mix culture cage populations. D. pseudoobscura and D. subobscura, two species sympatric in the west coast of North America exhibited competition in the laboratory to such an extent that D. subobscura was completely eliminated in just a few generations of their being co-cultured. The outcome was no different when they were reared at different temperatures (Pascual et al. 1998).

In nature two competing species do not face a straight battle and there may be other species too which have their own impact on the competition. For example it was found that competition between two closely related species D. melanogaster and D. hydei was affected by a third distant species of an entirely different kingdom Aspergilus niger (Hodge et al. 1999). Not only other species but components of interspcific competition are also known to be affected under different environmental conditions, creating a geographic mosaic of outcomes (Joshi 2004; Joshi & Thompson 1995). Price et al. (2012) found that presence of mating rivals cause males of D. pseudoobscura to modulate sperm transfer through an increase in sperm transfer, alteration in ejaculate composition etc. In D. melanogaster Bretman et al. (2009) reported that males kept with rivals prior to mating, mated for a longer duration.

The present study aimed at comparing the viability of two species of Drosophila, i.e. D. ananassae Doleschall and D. melanogaster Meigen when they are cultured together in food bottles. Taxonomically both species belong to the melanogaster species group of the subgenus Sophophora. Drosophila ananassae falls in the ananassae subgroup and the ananassae complex and D. melanogaster belongs to the melanogaster subgroup (Bock & Wheeler 1972). Distribution wise both species are cosmopolitan. D. melanogaster being semi-domestic, occurring in orchards and gardens and D. ananassae, a domestic species is found at a closer proximity to human habitation, such as fruit markets, kitchens etc. It occupies a unique status among the Drosophila species because of certain unusual genetical features (Singh 2010). The morphological features of the two species enable easy distinction of the two species and their sexes as males of D. melanogaster possess black abdominal tip and a characteristic pattern of sex comb. The females of D. melanogaster are larger in size with more swollen abdomen and black thin stripes at abdominal segment junctions. Drosophila ananassae males do not possess black coloration at the abdominal tip and they have a number of thick hairs on the first and second tarsal segments forming a diffused sex comb pattern. The females of D. ananassae are light in color as they lack black abdominal stripes. Earlier experiments on interspecific competition involving D. melanogaster have been done with its sibling species. However, D. ananassae and D. melanogaster are quite distinct. Therefore, it would be interesting to see the degree of competition that exists between the two, and whether they are able to thrive in presence of each other. Experiments were conducted to determine at which stage(s) of the life cycle interspecific competition occurs between the two species.

MATERIAL AND METHODS

This study was done by taking two wild type species of Drosophila, D. ananassae and D. melanogaster. These two stocks have been reared in our laboratory for the last three years. D. ananassae was originally collected from Ranchi (Jharkhand state) and D. melanogaster was collected from Varanasi (Uttar Pradesh), as adult forms by net sweeping. The stocks of both species were maintained in the laboratory on simple yeast-agar culture medium at 24[degrees]C with a 12 hours cycle of light and darkness.

Virgin male and female flies from both species were collected and aged. Twenty pairs (ten pairs from each species) of seven day-old flies were then kept together in 250 ml cylindrical culture bottles (height 15 cm, base diameter 5 cm, mouth diameter 2.5 cm) containing 50 ml of food. After three days, all flies were discarded. Flies emerging from the bottles were separated according to species and sex and counted. Pure cultures were established to serve as controls. The number of progeny emerging from such control cultures were also counted. The experiment was repeated five times.

Mating behavior of D. ananassae and D. melanogaster flies was observed in the presence of each other. Ten pairs of seven day-old virgin male and female flies of both species were kept in an Elen-Wattiaux mating chamber and observed for one hour. When a pair commenced mating it was aspirated out. As a control, 10 pairs of D. ananassae and 10 pairs of D. melanogaster were observed separately in the mating chamber. The total number of matings (formed couples) and the time interval in minutes from release to pair formation was recorded. Six replicates of each mating combination were carried out. All mating experiments were done between 6:00 am to 11:00 am, as Drosophila exhibits peak mating activity during the morning hours. One way ANOVA was done to test whether there was any difference in the mean number of matings among the four groups, (D. ananassae alone, D. ananassae in presence of D. melanogaster, D. melanogaster alone and D. melanogaster in presence of D. ananassae). Bonferroni t- test were used for pair wise comparison between the groups.

Ten pairs of seven day-old virgin male and female flies of both the species were kept together in culture bottles (as described above). After three days males were discarded and females of each species were kept separately in fresh culture bottles, and allowed to lay eggs. They were not exposed to males of their own species so that the progeny produced was only the outcome of matings that occurred when both the species were housed together. Also the effect of initial exposure of the two species to each other, on their progeny recovery could be determined.

The two species were also co-cultured in the food bottles to study larval competition. Ten pairs of seven day-old virgin male and female flies of both species were kept in fresh food bottles for three days, after which the flies were discarded. Polytene chromosome preparations of the third instar larvae were made by lacto-aceto-orcein method, to identify whether the larvae were D. ananassae or D. melanogaster.

RESULTS

Drosophila ananassae flies were almost eliminated in number during the first generation itself, when reared in culture bottles along with D. melanogaster adults as very few D. ananassae, males could be recovered. The numbers of D. melanogaster (both males and females) counted in the bottles are given in Table 1. Also, the numbers of flies counted in the control sets are shown.

In the second set of experiments, where males and females of both the species were observed in Elen-Wattiaux mating chamber, it was found that males of both species largely courted females of their own species. However, occasionally, D. melanogaster males would unsuccessfully court a D. ananassae female. It was also observed that D. melanogaster males would interfere with the courtship rituals of D. ananassae males and chased away a courting D. ananassae male. The results of one way ANOVA (Table 2.) show that there is a significant difference between the mean number of matings in D. ananassae and D. melanogaster when they are confined alone in the mating chamber and when they are kept in presence of each other. Bonferonni t-tests (Table 3.) proved that there are significant reductions in the number of D. ananassae matings, when it is kept with D. melanogaster. Therefore the presence of D. melanogaster affects the mating propensity of D. ananassae. Figure 1 shows that as the number of D. melanogaster pairs decreases in the mating chamber after being aspirated out when a pair commenced mating, the number of matings of D. ananassae increases. The average data of the six sets of mating experiments with ten pairs of D. ananassae in the presence of 10 pairs of D. melanogaster was used. Figure 2 shows the effect of time on mating success in D. ananassae and D. melanogaster in different conditions. The graph was constructed with the pooled data of the six sets of mating experiments. It depicts that the number of matings in D. ananassae in first 10 minutes is very high, when they are alone in the mating chamber, compared to when they are confined with D. melanogaster. In the next 50 minutes, however, the number of matings remains almost the same under the two conditions. For D. melanogaster, the number of matings was found to be less when alone than when in the presence of D. ananassae.

Initial exposure of the two species to each other does not affect fecundity or larval development, as good D. ananassae and D. melanogaster cultures could be recovered from culturing females which had been exposed to males of the other species earlier.

From the mixed culture of the two species, larvae were also analyzed to identify which species they belonged to by observing their salivary gland chromosomes. Out of fifty four larvae examined only three were found to be D. ananassae and the remaining larvae were all identified as D. melanogaster. Thus, bulk mortality of D. ananassae occurs in or before the third instar larval stage, with only a handful remaining alive to reach the pupal stage and even less if any emerging as adults.

DISCUSSION

Our experiments demonstrate that D. ananassae flies cannot thrive when confined in the small space of a food bottle with D. melanogaster. A finding consistent with observation of their habits in their natural habitat (Bock & Wheeler 1972), where in the presence of one, the other prefers another niche. It has also been observed by the authors that in nature when there is abundance of D. melanogaster in a certain place, D. ananassae is found fewer in number.

To go deeper into understanding the nature of interspecific competition that exists between the two species, we planned different experiments and found that competition starts right at the level of courtship rituals and matings and lasts until the late larval stages and perhaps beyond until D. ananassae is eliminated completely or its development severely hindered. Though, it is not sure what the outcome would have been if the two species were co-cultured in larger enclosures, one thing is certain, if D. ananassae is almost eliminated in the first generation in food bottles, in larger enclosures too it would not take a number of generations for it to disappear.

Fitness of D. ananassae is reduced in presence of D. melanogaster as D. melanogaster males interfere with the courtship rituals of D. ananassae males and prevent fertilization. Therefore in the presence of D. melanogaster, D. ananassae mates more infrequently than normal.

D. ananassae females which have succeeded in mating, may face competition from D. melanogaster females for egg laying sites. Given that when they were exposed initially to D. melanogaster and separated from them latter, their egg laying was normal and resulted in good larval recovery. Therefore, fitness of D. ananassae is affected only as long as D. melanogaster is present.

It was not possible for us to utilize the first and second instar larval stages for species identification, as they are small, present deep inside the food and their polytene chromosome preparations are not very good. However, the fact that a few D. ananassae third instar larvae could be identified through polytene chromosomes, indicates that some D.ananassae larvae are able to fight and withhold the battle until the third larval stage, facing a tough competition from D. melanogaster.

We observed that out of few progeny of D. ananassae reaching the third instar larval stage owing to larval competition, fewer pupate and lesser hatch as flies. Similar result was found by Merrel (1951) on D. funebris and D. melanogaster. This may indicate that individuals surviving to stage display lower survival probabilities than those stemming from pure cultures.

A very interesting observation was that while in D. ananassae the number of mating is reduced in presence of D. melanogaster, with D. melanogaster just the opposite occurs, that is D. melanogaster mates more rapidly in the presence of D. ananassae than when held alone at similar densities.

Both these behaviors are the outcomes of competition, a proof that both the species compete with each other. In the face of competition while D. ananassae may be conserving the energy required in courtship and matings (an important cost of reproduction) and invest it in survival waiting for less restrictive conditions, D. melanogaster increases its mating rate, perhaps to serve the purpose of ousting the competitor with the weapon of numbers. Under our experimental conditions the strategy displayed by D. melanogaster is perhaps better, as clearly it wins the battle. Yet D. ananassae might be more successful under different environmental conditions.

Recibido: 18/09/2012; aceptado: 22/05/2013.

ACKNOWLEDGEMENT. We are highly grateful to Ms. Parul Banerjee for her help in the preparation of this manuscript. We are thankful to University Grants Commission, New Delhi for giving financial assistance to S K in the form of Project fellow. We thank anonymous reviewers for their very appropriate corrections and suggestions in the manuscript.

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ARVIND K. SINGH (1) & SANJAY KUMAR

(1) Genetics Laboratory, Department of Zoology, Banaras Hindu University, Varanasi-221005 INDIA. <aksbhu23@rediffmail.com>

Table 1. Number of adult progeny recovered from pure and
mixed adult cultures of D. ananassae and D. melanogaster in
bottles containing 50 ml of diet. (Rows represent different
replicates, N=5).

         Pure culture

D.                  D.
melanogaster        ananassae

[male]   [female]   [male]   [female]

84          28        65       112
72          80       150       105
114         90        40        34
188         85       260       167
314         85       473       339

         Mixed culture

D.                  D.
melanogaster        ananassae

[male]   [female]   [male]   [female]

 103        62        18        0
 125       136        0         0
  94        75        0         0
 250       203        0         0
 289       101        25        2

Table 2. Results of one-way ANOVA comparing the number of
matings among four mating combination groups of 7-day old
adult flies i. e. D. ananassae, D. melanogaster, D.
ananassae in presence of D. melanogaster and D. melanogaster
in presence of D. ananassae

Source of variation   df    SS      MS        F

Between groups        3    70.79   23.59   21.61 *
Within groups         20   21.83   1.09
Total                 23   92.62

* P < 0.001

Table 3. Pair wise comparison of the number of matings,
under different conditions in D. ananassae and D.
melanogaster Bonferroni t-test

Bonferroni t-test

ana(s) vs. ana(m) *   ana(s) vs. mel(s)     ana(s) vs. mel(m)
ana(m) vs. ana(s) *   ana(m) vs. mel(s) *   ana(m) vs. mel(m) *
mel(s) vs. ana(s)     mel(s) vs. ana(m) *   mel(s) vs. mel(m)
mel(m) vs. ana(s)     mel(m) vs. ana(m) *   mel(m) vs. mel(s)

* P < 0.05, ana(s) D. ananassae alone, ana(m) D. ananassae
in presence of D. melanogaster, mel(s) D. melanogaster alone,
mel(m) D.melanogaster in presence of D. ananassae.
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Author:K. Singh, Arvind; Kumar, Sanjay
Publication:Acta Zoologica Mexicana (nueva serie)
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