Temperature, urbanization and body color polymorphism in south Brazilian... 381 TEMPERATURE, URBANIZATION AND BODY COLOR POLYMORPHISM IN SOUTH BRAZILIAN POPULATIONS OF DROSOPHILA KIKKAWAI (DIPTERA, DROSOPHILIDAE)

Body color polymorphism of urban populations of cosmopolite fly Drosophila kikkawai Burla, 1954 was investigated in relation to its possible association with environmental temperature. Samples of D. kikkawai were collected in spring, summer, autumn and winter between 1987 to 1988, in zones with different levels of urbanization in the southern Brazilian city of Porto Alegre, Rio Grande do Sul. A clear association was observed between darker flies and both seasons with low temperatures and areas of low urbanization (where temperature is generally lower than in urbanized areas). Results of preliminary laboratory experiments involving six generations of flies grown in chambers at temperatures of 17o and 25oC confirmed this tendency to a relationship between body color and temperature, with allele frequency of the main gene involved in body pigmentation changing over time.


INTRODUCTION
Drosophila kikkawai Burla, 1954 is a cosmopolitan species of fruit fly (PINHEIRO & VALENTE, 1993).It belongs to the D. melanogaster species group and occurs both in domestic and disturbed non-domestic sites.TSACAS & DAVID (1978) suggested that the introduction of this species to South America and Africa occurred prior to, and independent of human activity, and ASHBURNER (1989) considered that this species had only recently spread from its origin in Southeast Asia to South America and Africa.This species is of interest to evolutionists because it presents discrete genetic polymorphisms, including various types of karyotypes (BAIMAI et al.,1986) and variable posterior abdominal segment pigmentation (FREIRE-MAIA, 1953).FREIRE-MAIA & FREIRE-MAIA (1964) observed higher frequencies of light-colored D. kikkawai females in populations collected in hot climates at different latitudes.It is also known that in some other Drosophila species, darker forms occur more commonly in samples collected in colder climates (HEED & BLAKE, 1963;LEE, 1963;GIBERT et al., 1996GIBERT et al., , 1998;;MACHADO et al., 2001).There are two different systems for explaining the abdominal color polymorphism in D. kikkawai, the earlier being that of FREIRE-MAIA et al. (1954) and FREIRE-MAIA (1964a), which states that geographical genetic differences in modifier genes affect this character and produce three phenotypes, dark/dark (CC genotype), dark/light (Cc genotype) and light/light (cc genotype).A more recent system is that of GIBERT et al. (1999), who worked with Indian populations of D. kikkawai and suggested co-dominance of the major gene involved in abdominal segment color and modifier gene effects to explain the dark/dark (DD), dark/ light (DL) and light/light (LL), phenotypes found in their studies.
In the southern Brazilian city of Porto Alegre, D. kikkawai is common in Drosophila assemblies where it is sympatric with some wild species that are in the process of colonizing the urban environment (VALENTE et al., 1989).Porto Alegre is located in the coldest area of Brazil, has four well-defined seasons and has a known urbanization pattern.The subject was an analysis of the variations of abdominal segment pigmentation and fluctuations of D. kikkawai populations in relation to environmental variables in Porto Alegre and attempts to detect some type of association between these variables as a function of time and the level of disturbance (urbanization) of the collection sites.

MATERIAL AND METHODS
Fruit fly populations were sampled by the authors in Porto Alegre city (30 o 02'S; 51 o 31'W; roughly 1,3 million inhabitants) between January 1987 and December 1988 by collecting pre-adults (eggs, larvae and pupae) from rotten fruits and trapping adult flies on closed banana baits (model of TIDON & SENE, 1988) placed in parks, squares and streets along transects correspondent to the main avenues of the city, in three different urbanization zones characterized by RUSZCZYK (1986RUSZCZYK ( /1987) ) in the 1980 decade: a highly urbanized zone mainly occupied by buildings where cover vegetation is less than 20% (high urbanization, HU); a zone of medium urbanization containing houses and some buildings and having 20 to 40% of cover vegetation (medium urbanization, MU); and a zone of low urbanization predominantly occupied by houses and having more than 40% cover vegetation (low urbanization, LU) (fig.1).Urbanization characteristics of the sampling site (percentage vegetation cover, distance from the center of the city, altitude) were recorded (tab.I).Climatic data (temperature, relative humidity and rainfall scores during the month of collection and the preceding month) for Porto Alegre were obtained from the 8 o Distrito de Meteorologia, Ministério da Agricultura do Brasil.
Drosophila kikkawai samples were sorted by sex and phenotypic color (dark, medium and light, fig.2-7), based on the color of their abdominal segments, according to the system of FREIRE-MAIA et al. (1954) andFREIRE-MAIA (1964a).Specimens testimony of these samples are deposited in the Drosophilid collection of the Departamento de Genética, Universidade Federal do Rio Grande do Sul (UFRGS).
Laboratory experiments were also performed to investigate the effect of temperature on abdominal color polymorphism in these populations.Seven virgin females of each phenotype were mated with seven males of the three different phenotypes to form three populations.This was done by mating CC, Cc and cc females with CC males (population 1, P1), Cc males (population 2, P2) and cc males (population 3, P3).Three replicates of all crosses and populations were maintained in chambers at constant temperatures of 25 o or 17 o C + 1 o C and 60% relative humidity, respectively, on standard culture medium (MARQUES et al., 1966).To obtain the next generations (G1-G6) the adult flies were transferred to new vials with fresh food, three times.The adult progeny was allowed to interbreed to produce the next generation and then their abdominal color polymorphism were analyzed.

RESULTS
Despite extensive sampling, involving more than 136 individual samplings and 33,650 flies, only about 613 (about 2%) D. kikkawai were captured in the two years of the study in Porto Alegre (tab.II).This species was present in each of the three urbanization zones of Porto Alegre, although it was most abundant in highly urbanized areas.Climatic conditions such as temperature, relative humidity and rainfall during the month of collection and the preceding month, as well as factors related to the urbanization of the sampling site such as percentage vegetation cover, distance from the center of the city and altitude were also considered for statistical purpose.
Multiple regression analysis was performed using the frequency of occurrence of D. kikkawai as the dependent variable versus all the other variables (urbanization and climatic data and collection date).No significant correlation results were obtained (F= 1.60658; p> 0.25< 0.10) for samples 45 to 79, in spite of the tendency observed for species distribution in the urbanized zones (figs.8-10).For these samples, however, only percentage of vegetation cover and the amount of built-up land used as co-variables were significant, suggesting a more specific role for these variables in the distribution of D. kikkawai.It seems that D. kikkawai was capable of exploiting several types of breeding sites, including native plants (Butia eriospatha (C.Mart.ex Drude) Becc., Table II.Characterization of Drosophila kikkawai samples in Porto Alegre city.Number and abdominal color phenotypes of flies emerged in the laboratory (P) and of the next generation (G1) (S, summer; A, autumn; W, winter; SP, spring; HU, high urbanization; MU, medium urbanization; LU, low urbanization; N, total flies; FCC, FCc and Fcc, absolute frequency of CC, Cc and cc females, respectively; % FCC, % FCc and % Fcc, relative frequency of CC, Cc and cc females, respectively; -no flies detected).Eugenia edulis Benth.& Hook.f. ex Griseb., Ficus organensis Miq., Psidium guajava L. and Syagrus romanzoffiana (Cham.)Glassman), exotic plants (Averrhoa carambola L., Citrus reticulata Blanco, Citrus sinensis (L.) Osbeck, Diospyros kaki L. f., Eriobotrya japonica (Thunb.)Lindl.and Prunus persica (L.) Batsch) and garbage, as well as the banana baits where the adult flies were captured.
The frequency distribution of the three phenotypic classes of first generation offspring of flies (and their respective inferred genotypes) collected during the study (tab.II, fig.9) showed that the effect of temperature on abdominal color polymorphism occurred in the wild D. kikkawai populations.Dark phenotypes were the most common during the coldest months (May to August) and the light phenotypes during hot months (December to March).This tendency was specially clear in samples of 1988.
When abdominal polymorphism was analyzed in relation to the urbanization levels of origin, a gradient was obtained (fig.10) showing that darker forms (CC and Cc) are associated with less urbanized areas.
For the laboratory experiments on the effects of temperature on body color, Table III.Phenotypic absolute number (both sexs) and gene frequency (%) of alelles C and c in relation to abdominal tergite pigmentation polymorphism of Drosophila kikkawai maintained in chambers at 25ºC and 17ºC, during 6 generations (G1-G6) (CC, dark; Cc, medium; cc, light; N, total flies analyzed per generation; P, parental generation).The tendencies observed in these experiments suggest some advantages for the C allele at lower temperatures.These findings are similar to those obtained for natural populations, where darker flies are more frequent in winter (fig.9) and in less urbanized zones (fig.10) where temperatures tend to be lower than in more urbanized zones.

DISCUSSION
In spite of the small number of Drosophila kikkawai specimens in the Porto Alegre samples, its presence was constant during the collection period, unlike other wild species such as Drosophila willistoni Sturtevant, 1916, Drosophila nebulosa Sturtevant, 1916, and Drosophila paulistorum Dobzhansky & Pavan, 1943 whose populations have shown clear peaks during several years of observation (VALENTE et al., 1989). of the C and c alleles in laboratory populations kept at 17° and 25°C.These finding suggests once again that the allele dark body color is favored at lower temperatures.
Color polymorphism in abdominal segments is not an uncommon phenomenon in Drosophila (review in PAYANT, 1986), and has been studied by DA CUNHA (1949), HEED & BLAKE (1963), NAPP MARTINEZ & CORDEIRO (1970) and MACHADO et al. (2001) in South American Drosophila polymorpha Dobzhansky & Pavan, 1943. DA CUNHA (1949) found that genes with a different mode of action are responsible for the control of the expression of abdominal pigmentation in populations of the northern part of South America compared with those from the rest of Brazil.These latitudinal differences may reflect, once again, a selective response to different temperatures.Perhaps such latitudinal differences can also explain the different pattern of phenotype variation found by GIBERT et al. (1999) in Indian populations of D. kikkawai compared with those found in Brazilian populations of this fly.
The physiological basis for the advantage of darker forms of D. kikkawai in winter months and in colder environments is still not completely clear.The association between darker bodies and lower temperatures (and vice-versa) can be explained by the thermal budget hypothesis, which states that dark bodies absorb solar radiation better than those of light ones.Consequently, darker forms are favored in their sexual performances, activities of locomotion and in flight when they are subject to low temperatures.
Fig. 8. Frequency of Drosophila kikkawai in the parental (P) generation for each urbanization level during the period from January 1987 to December 1988 (HU, high urbanization; MU, medium urbanization; LU, low urbanization).

Fig. 9 .
Fig. 9. Phenotype distribution (u medium; s light; n dark) of Drosophila kikkawai (G1 generation) according to seasons of collection during the years 1987 and 1988.Red dots represent the fluctuation of the average minimum temperatures (T) (S, summer; A, autumn; W, winter; SP, spring).
in the frequencies of the C (dark) and c (light) alleles in the three laboratory populations (P1, P2 and P3) after six generations in all the crosses maintained at the two different temperatures (tab.III).In population 1 at 25 o C, the frequency of the C allele tended to drop from 75 to 52% in the first generation (G1) and maintained values around 50% until the sixth generation (G6).The same population at 17 o C also presented a drop in the frequency of C, in the first generation (G1), although not so abrupt, with the C alelle varying around 55% until the sixth generation.Population 2 at 25 o C showed an abrupt fall in the frequency of the C allele from 50 to 22% between the parent (P) and the first generation, this frequency tending to be maintained at about 19% in subsequent generations.At 17 o C the fall was less abrupt, with stabilization occurring in the sixth generation at a C allele frequency of about 33%.With population 3, the C allele frequency at 25 o C decreased from 25 to 13% in the first generation and oscillated around 15 to 19% in the following generations, while at 17 o C the initial C allele frequency tended to increase until it attained 30% in the sixth generation.

Fig. 10 .
Fig. 10.Percent distribution (F %) of darker females (CC and Cc) in relation to all Drosophila kikkawai collected at each urbanization level in Porto Alegre city, in the parental (P) generation (HU, high urbanization; MU, medium urbanization; LU, low urbanization).

Table I .
Original data used to perform the multiple regression analysis of Drosophila kikkawai frequency and weather and urban action variables.Samples 1 to 44 were collected during 1982 to January 1987; samples 45 to 79 were collected during February 1987 to 1988 (S, sample; F, frequency (%) of flies; TEMP ANT MAX, TEMP ANT MIN, previous temperature of collection, maximum Iheringia, Sér.Zool., Porto Alegre, 93(4):381-393, 30 de dezembro de 2003