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The hummingbird community and their floral resources in an urban forest remnant in Brazil

Comunidade de beija-flores e seus recursos florais em um fragmento florestal urbano no Brasil

Abstracts

The temporal and spatial resource use among hummingbirds was studied over 13 months in an urban forest remnant (Prosa State Park: PSP) in Campo Grande, Mato Grosso do Sul, Brazil. Hummingbird visitation was recorded at three ornithophilous and eleven non-ornithophilous species. Flower density was roughly constant during the study period, with the density of non-ornithophilous flowers being higher than that of ornithophilous ones. Mean values of nectar volume and concentration were similar between ornithophilous and non-ornithophilous species. Eight hummingbird species were observed at PSP: Amazilia fimbriata, Anthracothorax nigricollis, Chlorostilbon lucidus, Eupetomena macroura, Hylocharis chrysura, Florisuga fusca, Thalurania furcata and an unidentified species. Hummingbird visit frequencies to ornithophilous and non-ornithophilous flowers were similar. However, some non-ornithophilous species received a higher number of visits, which seems to be related to their large number of open flowers per plant per day. The number of feedings bouts of hummingbirds increased with the total number of flowers observed per focal plant. All recorded species of hummingbirds visited non-ornithophilous flowers, predominantly melittophilous and generalised entomophilous flowers. Hummingbird species recorded at PSP may be viewed as generalists, visiting a large number of non-ornithophilous species. Despite being an urban forest, PSP is relatively rich in hummingbird species, suggesting that it provides important shelter and foraging sites for hummingbirds in such an environment.

community; flowering phenology; forest fragment; hummingbirds; pollination


O uso temporal e espacial de recursos por beija-flores foi estudado ao longo de 13 meses em um remanescente florestal urbano (Parque Estadual do Prosa: PSP) em Campo Grande, Mato Grosso do Sul, Brasil. As visitas dos beija-flores foram registradas em três espécies ornitófilas e 11 não ornitófilas. A densidade de flores foi mais ou menos constante durante o período de estudo, com a densidade de flores não ornitófilas sendo maior que a de flores ornitófilas. Os valores médios de volume e concentração do néctar foram similares entre as espécies ornitófilas e não ornitófilas. Oito espécies de beija-flores foram observadas no PSP: Amazilia fimbriata, Anthracothorax nigricollis, Chlorostilbon lucidus, Eupetomena macroura, Hylocharis chrysura, Florisuga fusca, Thalurania furcata e uma espécie não identificada. A frequência de visitas dos beija-flores foi similar entre as espécies ornitófilas e não ornitófilas. Entretanto, algumas espécies não ornitófilas receberam um alto número de visitas, o que parece estar relacionado ao alto número de flores abertas por planta por dia. O número de turnos de visitas dos beija-flores aumentou com o número total de flores observadas por planta focal. Todas as espécies de beija-flores visitaram flores não ornitófilas, predominantemente flores de espécies melitófilas e entomófilas generalistas. Os beija-flores observados no PSP podem ser considerados generalistas, visitando um grande número de espécies não ornitófilas. Apesar de o PSP ser um fragmento florestal urbano, possui riqueza de espécies de beija-flores relativamente alta, sugerindo ser importante sítio de abrigo e forrageamento para os beija-flores neste ambiente.

comunidade; fenologia de floração; fragmento florestal; beija-flores; polinização


ECOLOGY

The hummingbird community and their floral resources in an urban forest remnant in Brazil

Comunidade de beija-flores e seus recursos florais em um fragmento florestal urbano no Brasil

Rodrigues, LC.I,* * e-mail: licleia@yahoo.com.br ; Araujo, AC.II

IPrograma de Pós-graduação em Ecologia e Conservação, Laborátorio de Ecologia, Universidade Federal de Mato Grosso do Sul – UFMS, CP 549, CEP 79070-900, Campo Grande, MS, Brazil

IIDepartamento de Biologia, Universidade Federal do Mato Grosso do Sul – UFMS, CP 549, CEP 79070-900, Campo Grande, MS, Brazil

ABSTRACT

The temporal and spatial resource use among hummingbirds was studied over 13 months in an urban forest remnant (Prosa State Park: PSP) in Campo Grande, Mato Grosso do Sul, Brazil. Hummingbird visitation was recorded at three ornithophilous and eleven non-ornithophilous species. Flower density was roughly constant during the study period, with the density of non-ornithophilous flowers being higher than that of ornithophilous ones. Mean values of nectar volume and concentration were similar between ornithophilous and non-ornithophilous species. Eight hummingbird species were observed at PSP: Amazilia fimbriata, Anthracothorax nigricollis, Chlorostilbon lucidus, Eupetomena macroura, Hylocharis chrysura, Florisuga fusca, Thalurania furcata and an unidentified species. Hummingbird visit frequencies to ornithophilous and non-ornithophilous flowers were similar. However, some non-ornithophilous species received a higher number of visits, which seems to be related to their large number of open flowers per plant per day. The number of feedings bouts of hummingbirds increased with the total number of flowers observed per focal plant. All recorded species of hummingbirds visited non-ornithophilous flowers, predominantly melittophilous and generalised entomophilous flowers. Hummingbird species recorded at PSP may be viewed as generalists, visiting a large number of non-ornithophilous species. Despite being an urban forest, PSP is relatively rich in hummingbird species, suggesting that it provides important shelter and foraging sites for hummingbirds in such an environment.

Keywords: community, flowering phenology, forest fragment, hummingbirds, pollination.

RESUMO

O uso temporal e espacial de recursos por beija-flores foi estudado ao longo de 13 meses em um remanescente florestal urbano (Parque Estadual do Prosa: PSP) em Campo Grande, Mato Grosso do Sul, Brasil. As visitas dos beija-flores foram registradas em três espécies ornitófilas e 11 não ornitófilas. A densidade de flores foi mais ou menos constante durante o período de estudo, com a densidade de flores não ornitófilas sendo maior que a de flores ornitófilas. Os valores médios de volume e concentração do néctar foram similares entre as espécies ornitófilas e não ornitófilas. Oito espécies de beija-flores foram observadas no PSP: Amazilia fimbriata, Anthracothorax nigricollis, Chlorostilbon lucidus, Eupetomena macroura, Hylocharis chrysura, Florisuga fusca, Thalurania furcata e uma espécie não identificada. A frequência de visitas dos beija-flores foi similar entre as espécies ornitófilas e não ornitófilas. Entretanto, algumas espécies não ornitófilas receberam um alto número de visitas, o que parece estar relacionado ao alto número de flores abertas por planta por dia. O número de turnos de visitas dos beija-flores aumentou com o número total de flores observadas por planta focal. Todas as espécies de beija-flores visitaram flores não ornitófilas, predominantemente flores de espécies melitófilas e entomófilas generalistas. Os beija-flores observados no PSP podem ser considerados generalistas, visitando um grande número de espécies não ornitófilas. Apesar de o PSP ser um fragmento florestal urbano, possui riqueza de espécies de beija-flores relativamente alta, sugerindo ser importante sítio de abrigo e forrageamento para os beija-flores neste ambiente.

Palavras-chave: comunidade, fenologia de floração, fragmento florestal, beija-flores, polinização.

1. Introduction

Hummingbirds depend on nectar to supply most of their energy requirements, and these birds are morphologically, physiologically and behaviourally adapted to visit flowers in search of this resource (Diamond et al., 1986). This dependence on nectar as a food makes hummingbirds the major group of vertebrate pollinators in the Neotropics (Bawa, 1990). Flowers adapted to hummingbird-pollination (ornithophilous) are an important component of neotropical plant communities, comprising 2-15% of angiosperm species in a given community (Feinsinger, 1983; Machado and Lopes, 2004; Ramírez, 2004).

Hummingbirds and hummingbird-visited flowers have been extensively studied in Central America and the Andes (Stiles, 1975; Wolf et al., 1976; Snow and Snow, 1980; Feinsinger et al., 1982; Kodric-Brown et al., 1984; Arizmendi and Ornelas, 1990; Cotton, 1998a), where many studies have taken a community approach (Snow and Snow, 1980; Feinsinger et al., 1982; Kodric-Brown et al., 1984; Arizmendi and Ornelas, 1990). In contrast, most studies in Brazil have focused on individual plant species (e.g. Araujo et al., 1994; Sluys and Stotz, 1995; reviewed in Mendonça and Dos Anjos, 2003, 2006a). Of the few previous community studies in Brazil, most have been based on observations of a few days or months (e.g. Snow and Snow, 1980; 1986; Snow and Teixeira, 1982). Studies carried out throughout the year are scarce and mainly concentrated in the Atlantic rainforest (e.g. Araujo, 1996; Sazima et al., 1996; Buzato et al., 2000; Araujo and Sazima, 2003). These Brazilian studies have shown some differences from those reported in Central America and the Andes (e.g. Feinsinger, 1976; Snow and Snow, 1980; Feinsinger et al., 1982), especially with regard to families of ornithophilous plants. In this sense, additional studies in Brazil might reveal different hummingbird-flower community structure (Fischer et al., 1996).

The importance of non-ornithophilous species as food for hummingbirds is not well documented. The few studies including ornithophilous and non-ornithophilous species as food resources have shown that hummingbirds can be broad generalists, with percentage of visits to non-ornithophilous species varying from 32 to 71% (Snow and Snow, 1986; Arizmendi and Ornelas, 1990; Araujo, 1996; Cotton, 1998b; Vasconcelos and Lombardi, 2001; Araujo and Sazima, 2003; Mendonça and Dos Anjos 2005). In Brazil, only two sites were studied regarding hummingbird-visited plant communities (including ornithophilous and non-ornithophilous species) throughout the year: one in the southeastern Atlantic rainforest (Araujo, 1996), and one in the southern Pantanal (Araujo and Sazima, 2003).

Most hummingbird species are habitat generalists (Feinsinger, 1976; Araujo and Sazima, 2003) frequently found in edges, secondary growth forests and open areas with a high abundance of flowers (Stiles, 1975; Cotton, 1998b; Borgella et al., 2001; Araujo and Sazima, 2003). Also, these birds are able to fly long distances, crossing open areas to use resources from different forest fragments (Stouffer and Bierregaard, 1995; Borgella et al., 2001). In human-altered landscapes, these fragments are important habitats for hummingbird populations that use these areas as breeding and/or foraging sites (Borgella et al., 2001). Despite the fact that there are some studies focused on hummingbird communities in forest fragments (Stouffer and Bierregaard, 1995; Borgella et al., 2001), studies reporting interactions of these birds with their floral resources in forest fragments are unknown.

Thus, the aims of our study are to investigate floral features and flowering phenology of ornithophilous and non-ornithophilous species visited by hummingbirds in a forest remnant in the Brazilian savanna (Cerrado). Additionally, it aims to record hummingbird species composition, seasonal occurrence of different hummingbird species and flower-visiting behaviour at the study site. Since the study area is a forest remnant, composed mainly of secondary plant species, we expect to record mainly medium-billed hummingbirds that are generalists in the use of floral resources (Feinsinger et al., 1982), including high proportions of non-ornithophilous species in their diet.

2. Material and Methods

This study was carried out at PSP, located in the urban perimeter of Campo Grande, Mato Grosso do Sul in central Brazil (20º 26' 34" S, 54º 38' 47" W). Prosa State Park is a forest fragment of about 140 ha that is isolated from other fragments and completely surrounded by urban areas. It is characterised by secondary vegetation, currently in late stage of regeneration, and includes distinct plant physiognomies such as riparian forest, savanna and cerradão, whose fauna and flora are poorly studied (Mato Grosso do Sul, 2000).

The hummingbird-visited plants at PSP were studied biweekly over 13 months (September 2002 – August 2003, October 2003). The flowering species were recorded in a preexisting trail measuring 6 m wide and 2100 m in length, of which 1100 m are located in riparian forest and 1000 m in cerradão, comprising a total sample area of 12600 m2. Mean flower density was calculated for each month using the number of flowers recorded per species per total sampling area (flowers/m2) (cf. Araujo, 1996). Growth form, number of open flowers as well as floral morphology (including corolla length) and colour were recorded. Voucher specimens of plant species were deposited at the Campo Grande Herbarium (CGMS/UFMS).

Pollination syndromes were determined using attributes of corolla morphology and predominat colours, presence of odour and period of anthesis. Typical ornithophilous species have odorless flowers with diurnal anthesis and tubular, red, pink, yellow or orange corollas (cf. Faegri and Pijl, 1980). The remaining species visited by hummingbirds were classified as non-ornithophilous. Non-ornithophilous species were divided into melittophilous (flowers adapted for bee pollination), chiropterophilous (flowers adapted for bat pollination) or sphingophilous (flowers adapted for sphingid pollination), according to floral characteristics described in Faegri and Pijl (1980). Additionally one species (Inga vera) was classified as generalist (species that could be pollinated by more than two pollinator groups, including vertebrate and invertebrate pollinators) and another species (Serjania glutinosa) as entomophilous (species that could be pollinated by species of more than two invertebrate groups).

Sugar concentration and volume of nectar were recorded between 06:30 AM – 08:00 AM (EST), from flowers bagged during the pre-anthesis period. Sugar concentration was measured with a pocket refractometer (cf. Araujo et al., 1994), and transformed in mg of sugar (cf. Galetto and Bernadello, 2005). Nectar volume was measured with graduated capillary tubes (cf. Galetto and Bernadello, 2005). These measures were made on one to nine flowers per flowering species. A t-test was used to compare the sugar concentration and nectar volume, as well as the total amount of sugar (mg of sugar) in nectar among flowers of ornithophilous and non-ornithophilous species.

The visits of hummingbirds were recorded by direct observation (focal observations) on 35 plant species, selected according to the following criteria: 1) ornithophilous species; 2) species reported as visited by hummingbirds in previous studies (e.g. Araujo, 2003) or with similar morphologies to these hummingbird-visited species; and 3) species with records of occasional visits by hummingbirds at the study site. Focal observations were made throughout the 12 months of study. Also, in October 2003, individuals of Inga vera, Jacaratia spinosa and Vitex cymosa were monitored to provide additional information about visitors. A Pearson correlation was used to verify if the hummingbird bill length and corolla length of legitimally visited species were related.

Hummingbird visits to flowers were recorded using 7 x 35 binoculars, mainly between 08:00 AM – 12:00 AM and 02:00 PM – 05:00 PM. Hummingbirds were identified during their visits to flowers (Ruschi, 1982; Grantsau, 1988) and males and females of species with evident sexual dimorphism were treated separately. Time and number of visits were recorded. Visits were classified as 1) legitimate when hummingbirds contacted anthers and/or stigmas in a way that could result in pollination, or 2) illegitimate when hummingbirds did not contact anthers and/or stigmas. Hummingbirds visiting behaviour, as well as the occurrence and outcome of agonistic interactions between them, were also recorded. Data on bill length of hummingbirds were based on Grantsau (1988), or on hummingbirds (Anthracothorax nigricollis and Thalurania furcata) captured in mist nets at the study site (M. Kinas, pers. comm.).

A Mann-Whitney U test was used to compare hummingbird visit frequencies (number of flowers visited per plant per minute divided by the number of observed flowers per plant) and density of flowers to ornithophilous and non-ornithophilous species. After data were transformed to log(n + 1), the analysis of covariance (ANCOVA) was done to determine whether the number of foraging bouts was affected by the number of flowers observed, and to determine if the number of agonistic interactions observed per plant per minute was affected by the total number of open flowers per plant, and by the category of plant species visited (ornithophilous or non-ornithophilous).

3. Results

3.1. Plants visited by hummingbirds

Hummingbirds visited 14 of the 35 plant species studied. Of the 14 visited plants, three were ornithophilous (Bromelia balansae, Heliconia sp. and Psiguria ternata), and 11 non-ornithophilous (Table 1). Hummingbirds were not recorded visiting flowers of the ornithophilous species Ruellia brevifolia, Palicourea marcgravii or Psychotria poeppigiana during focal observations (360, 280 and 240 minutes, respectively).

The dominant growth form of the ornithophilous species recorded at PSP was shrub (three species), followed by herbaceous (two species) and climber (one species). In contrast, most non-ornithophilous species were climbers (six species), four were trees, and one was a shrub (Table 1). In the ornithophilous group most species recorded had red or yellow tubular flowers, while in the non-ornithophilous group, recorded species presented cream, white or lilac bell flowers (Table 1). Mean corolla length of visited flowers ranged from 3.16 mm (Centrosema pubescens) to 41.1 mm (Arrabidaea triplinervea) among non-ornithophilous species, and from 14 mm (P. ternata) to 36.5 mm (Heliconia sp.) among ornithophilous species (Table 1). Mean nectar sugar concentration (t = –0.38, p = 0.72, N = 9) and mean nectar volume (t = 0.22, p = 0.83, N = 9), as well as the amount of sugar in nectar (t = –0.82, p = 0.43, N = 9) of ornithophilous species were similar to those of non-ornithophilous species (Table 1).

Flowering activity was highest in November, December and May (Table 2). Most (N = 9) of the non-ornithophilous species flowered in the dry season, and the ornithophilous species flowered mainly in the rainy season (Table 2). Pooling flowers by syndrome, density of non-ornithophilous flowers ranged up to 2.1 flowers/m2 compared to the much lower range of 0.001 flowers/m2 for ornithophilous flowers, these densities being statistically different (U-test, U = 64, p = 0.002, N = 33). Density of ornithophilous flowers did not vary throughout the year. In contrast, density of non-ornithophilous flowers had a peak in January and another in August (Figure 1). The mean number of open flowers per individual per day for the ornithophilous species was 3.11 ± 2.52 flowers/d (N = 106), ranging from 1.75 (P. poeppigiana) to 12 flowers/d (B. balansae). For the non-ornithophilous species this number was higher (t = 4.08, P = 0.002), 155.25 ± 252.90 (N = 314), ranging from 3.34 (B. rufa) to 1560 flowers/d (V. cymosa) (Table 1).


3.2. Hummingbird community

Eight species of hummingbirds, all in the Trochilinae subfamily, were recorded at PSP: Glittering-throated Emerald (Amazilia fimbriata fimbriata), Black-throated Mango (Anthracothorax nigricollis nigricollis), Glittering-bellied Emerald (Chlorostilbon lucidus lucidus), Swallow-tailed Hummingbird (Eupetomena macroura macroura), Gilded Hummingbird (Hylocharis chrysura chrysura), Black Jacobin (Florisuga fusca), Fork-tailed Woodnymph (Thalurania furcata furcata), and one unidentified species. In addition, Versicolored Emerald (Amazilia versicolor versicolor), Rufous-throated Sapphire (Hylocharis sapphirina sapphirina) and the Phaethornithinae Planalto Hermit (Phaethornis pretrei) were also recorded at PSP in 2002 and 2003 (M. Kinas, pers. comm.).

The largest number of hummingbird species (N = 8) was recorded visiting flowers in September 2002 and October 2003. In January and March, hummingbirds were not recorded visiting flowers of monitored plants (Table 2), although in January, H. chrysura was recorded catching insects in the studied transect. This species was recorded in most of the study months (eight months), followed by males of A. nigricollis (six months), E. macroura and C. lucidus (five months), males of T. furcata (four months), while other species were recorded in two or fewer months (Table 2).

Mean bill length of visiting hummingbirds ranged from 18.0 to 21.5 mm. The short-billed (<20 mm) and medium-billed (20 to 30 mm) hummingbirds, C. lucidus (19 mm), T. furcata (21.5 mm), A. fimbriata (18 mm) and F. fusca (21 mm), only visited flowers with short-tubed corollas (<30 mm). Hylocharis chrysura (19 mm), E. macroura (21 mm) and A. nigricollis (21 mm) visited both long (≥30 mm) and short-tubed flowers (<30 mm). Bill length of hummingbirds and corolla length of visited flowers were not correlated (r = 0.08, p = 0.7). The only plant species that received illegitimate hummingbird visits was C. pubescens whose flowers were visited by females of C. lucidus using holes probably made by insects in the base of the corolla. Hylocharis chrysura was the main visitor of the studied community, visiting 71.4% of plant species recorded as visited by hummingbirds (Table 3).

Frequency of hummingbird visits to flowers was similar for ornithophilous and non-ornithophilous species (U-test, U = 137, p = 0.25, N = 46). Among the ornithophilous species, P. ternata received the highest frequency of visits (0.024 ± 0.014 flowers visited.minute–1. number of observed flowers–1.plant–1, N = 5), while among non-ornithophilous species I. vera was the most visited one (0.032 ± 0.048 flowers visited.minute-1. number of observed flowers-1.plant-1, N = 8 (Table 1).

The number of feedings bouts of hummingbirds increased with the total number of flowers observed per focal plant (ANCOVA, F1,42 = 14.812, P = 0.0003) (Figure 2). However, ornithophilous versus non-ornithophilous (ANCOVA, F1,42 = 0.360, P = 0.551), as well as the interaction between syndrome and the number of flowers observed (ANCOVA, F1,42 = 1.123, P = 0.294) did not affect the number of feedings bouts.


Males of A. nigricollis visited flowers of A. triplinervea at intervals from 10 to 30 minutes, disappearing from the clumps of flowers after their visits. Similar behaviour was recorded for females of the hummingbird C. lucidus at flowers of C. pubescens and P. ternata. However, after visiting flowers of I. vera, J. spinosa and B. rufa, this hummingbird perched, and frequently chased away other hummingbirds which approached the clumps and tried to visit the flowers. Similar behaviour was recorded for H. chrysura (during visits to flowers of I. vera, J. spinosa and P. ternata), and for males of A. nigricollis, C. lucidus and T. furcata on flowers of I. vera and J. spinosa. Florisuga fusca exhibited variable intervals between visits to I. vera (5 to 50 minutes) as well as E. macroura in visits to flowers of P. ternata (5 to 15 minutes). Sometimes after their visits, these hummingbird species perched, but they were not observed chasing other individuals that approached the flowers. Other hummingbird species were occasional visitors and their behaviour patterns were not defined in this study.

Eighty-eight agonistic interactions were recorded between hummingbirds, a large number of them (N = 40) being recorded for one focal individual of J. spinosa. The largest number of agonistic interactions during flower visits were recorded between H. chrysura and females of C. lucidus (25 interactions), and for intraspecific interactions, among males of A. nigricollis (10 interactions). Eupetomena macroura was not displaced by any other hummingbird species, while H. chrysura and males of A. nigricollis were displaced by all hummingbird species, except males of C. lucidus (Table 4). The number of agonistic interactions observed per minute was not affected by the total number of open flowers per plant (ANCOVA, F1,42 = 1.084, p = 0.3), by syndrome (ANCOVA, F1,42 = 0.824, p = 0.36), or by interactions between the two factors (ANCOVA, F1,42 = 0.405, p = 0.52). During focal observations on I. vera and J. spinosa, sometimes two to four hummingbird individuals were recorded visiting the same plant at the same time. These individuals defended different clumps of flowers in the crown and agonistic interactions between them were frequent.

4. Discussion

4.1. Plants visited by hummingbirds

The number of hummingbird-visited species and of ornithophilous species at PSP is lower than those reported for Neotropical communities with less seasonal climates (e.g. Stiles, 1978; Feinsinger et al., 1982; Snow and Snow, 1986; Araujo, 1996; Sazima et al., 1996; Cotton, 1998b; Buzato et al., 2000; Dziedzioch, 2003). However, they are similar to those reported for capões in the southern Pantanal (Araujo and Sazima, 2003), a cerrado in São Paulo (Silberbauer-Gottsberger and Gottsberger, 1988), and a savanna in Venezuela (Ramírez, 2004), where climate is seasonal and plant physiognomy is similar to that of cerrado (Ramírez, 2004). The number of hummingbird-visited species at PSP is also similar to that reported for a tropical dry forest in Mexico (Arizmendi and Ornelas, 1990). The similarity between PSP and all these sites with regard to the number of plant species visited by hummingbirds and number of ornithophilous species may be related to their strong seasonality. Furthermore, in the Neotropics hummingbird pollination is more frequent in habitats with less seasonal climates where food availability for these birds is more constant throughout the year (Ramírez, 2004).

Despite the fact that six ornithophilous species were observed, hummingbirds visited only three of these plant species. The absence of visits to P. marcgravii, P. poeppigiana and R. brevifolia may be related to the small number of open flowers per plant per day, low number of individuals flowering each month (P. marcgravii, 4.42 ± 2.5 individuals/mo, N = 7; and P. poeppigiana, 1 ± 0 individuals/mo, N = 4), or the low nectar volume in P. marcgravii and R. brevifolia (Table 1). However, in other sites, hummingbird visits were reported for P. poeppigiana (Coelho and Barbosa, 2004). Also in a semideciduous forest in southeastern Brazil, R. brevifolia had a very low frequency of visits (Sigrist and Sazima, 2002). Additional efforts would probably result in records of visits of hummingbirds to flowers of these species.

Flowering peaks of species visited by hummingbirds occurred in the middle of the wet season (November-December) and the beginning of the dry season (May). In September-October more hummingbird species were recorded at PSP. This result may be related to the flowering of the non-ornithophilous species I. vera and J. spinosa, which have the highest number of open flowers per day during these months in the study site. In other studied communities, flowering peaks occur at the end of the dry season and/or throughout the wet season (Arizmendi and Ornelas, 1990; Sazima et al., 1996; Araujo and Sazima, 2003).

The high frequency of hummingbird visits to melittophilous and generalised entomophilous species at PSP may be explained by the high frequency of species exhibiting these pollination syndromes at the study site (91.6%), the large number of open flowers on these plants per day, their diurnal anthesis, and their nectar offerings, which were similar to those found in ornithophilous flowers (e.g. Arizmendi and Ornelas, 1990; Araujo and Sazima, 2003). Moreover, the flowering seasons of these species occur in the dry season, when there are few ornithophilous species flowering at the study site. These results indicate that the birds are not slaves to floral syndrome, a conclusion also reached for the capões in the southern Pantanal (Araujo and Sazima, 2003).

Furthermore, with the exception of C. pubescens which received illegitimate visits, hummingbirds were able to contact the reproductive parts of the flowers during their visits to most of the non-ornithophilous species, thus indicating that these plant species may be pollinated by hummingbirds. These observations agree with those of Waser et al. (1996), Arizmendi and Ornelas (1990), Araujo (1996) and Araujo and Sazima (2003). However, more detailed data on pollen transfer efficiency of hummingbirds foraging on non-ornithophilous species are necessary (Castellanos et al., 2003).

4.2. Comparison of seven Neotropical sites

The families with the largest number of species visited by hummingbirds at PSP were Bignoniaceae and Fabaceae, as reported for the Pantanal (Araujo and Sazima, 2003) and a tropical dry forest in Mexico (Arizmendi and Ornelas, 1990). In sites with less seasonal climates, Bromeliaceae was the family with more species visited by hummingbirds (Table 5). At PSP, as well as in the Pantanal (Araujo and Sazima, 2003), the most frequent growth form of the species visited by hummingbirds was climber, while in the Atlantic forest communities, epiphytic species were the most frequent (Snow and Snow, 1986; Araujo, 1996) (Table 5). The differences in family frequencies and growth forms between sites possibly reflect differences in floristic composition (Araujo and Sazima, 2003), which is related to historical and geological factors, as well as to climate differences between them.

Hummingbirds visited more non-ornithophilous species at PSP, (78.6%) than in other communities as, for example, in an Atlantic forest community (32%) (Snow and Snow, 1986), or in a tropical dry forest in Mexico (34.7%) (Arizmendi and Ornelas, 1990). However, some of these studies focused mainly on ornithophilous species (e.g. Snow and Snow, 1986; Arizmendi and Ornelas, 1990). Year-round studies that included non-ornithophilous species presented more similar proportions to that recorded at PSP, such as studies in the Pantanal (71%) (Araujo and Sazima, 2003), the Caribbean (57.1%) (Stiles, 1978), and in another Atlantic forest community (50%) (Araujo, 1996) (Table 5). The high frequency of non-ornithophilous species visited by hummingbirds at PSP may be related to the low frequency of ornithophilous species present at the site (4.8% of the total plant species, unpubl. data), in a similar way as suggested for the capões in the Pantanal (Araujo and Sazima, 2003).

4.3. Hummingbird community

The number of hummingbird species recorded at PSP is similar to those reported for Atlantic forest communities (e.g. Sazima et al., 1996; Buzato et al., 2000), a tropical dry forest in Mexico (Arizmendi and Ornelas, 1990), and forests fragments in the Amazon (Stouffer and Bierregaard, 1995), but greater than that reported for southern Pantanal (Araujo and Sazima, 2003). No long-billed hummingbirds were recorded during the study period, although the long-billed (32 mm) Phaethornis pretrei (Phaethornitinae) was recorded in the riparian forest at the study site in 2002 and 2003 (Kinas M., pers. comm.). Hummingbirds of this subfamily are more frequent in the understory of forested areas, such as riparian forests (Stiles, 1978, 1981; Cotton, 1998b), and they are often considered more specialised, visiting ornithophilous flowers with long and/or curved corollas with large amounts of nectar (Stiles, 1978; Sazima et al., 1996; Buzato et al., 2000; Fischer and Leal, 2006). The low frequency of flowers with these characteristics, as well as the small area of riparian forest at PSP may explain the low frequency of hummingbird species from the subfamily Phaethornithinae in the area.

Hylocharis chrysura was the only species considered resident at PSP. In other neotropical communities, the number of resident hummingbirds varies between one to four species (Feinsinger, 1976; Araujo, 1996; Sazima et al., 1996; Araujo and Sazima, 2003), depending upon the local richness of ornithophilous species.

In some hummingbird-plant communities, a strong relationship has been observed between bill length and corolla length of visited flowers (Snow and Snow, 1980; Kodric-Brown et al., 1984; Sazima et al., 1996). However, this relationship was not clear-cut at PSP. With the exception of a visit of H. chrysura to Cuspidaria cf. lateriflora, species with long corollas were visited only by medium-billed hummingbirds (A. nigricollis and E. macroura), which were the species with the longest bills recorded in this study. Although, those relationships are also mediated by other floral traits, such as corolla diameter and curvature (Temeles et al., 2002; 2009), that were not measured in this study.

According to the flower-visiting behaviour of hummingbirds at PSP, their community roles (cf. Feinsinger and Colwell, 1978) may be classified as follows: H. chrysura acted as territorialist in clumps of flowers of I. vera, J. spinosa and P. ternata. In other plant species, this hummingbird species acted as a generalist, making occasional visits. Females of C. lucidus acted as low-reward trapliners during visits to C. pubescens and as territorialists in clumps of flowers of I. vera, J. spinosa, and B. rufa. Males of A. nigricollis also modified their foraging strategy according to the visited plant species. They acted as low-reward trapliners during visits to A. triplinervea flowers and as territorialists during visits to clumps of flowers of I. vera and J. spinosa. Eupetomena macroura acted as a territory parasite of H. chrysura in visits to P. ternata and F. fusca, as a territory parasite of H. chrysura and females of C. lucidus in visits to I. vera. Males of T. furcata acted as territorialists during visits to I. vera and J. spinosa. The observed shift in foraging strategies of hummingbirds may occur in response to changes in the availability and spatial distribution of flowers, as well as in response to competition with other nectarivorous species (Feinsinger, 1976; Feinsinger and Colwell, 1978; Stiles, 1981; Mendonça and Dos Anjos, 2006b, Toledo and Moreira, 2008). When the number of flowers is low and dispersed in the habitat as, for example, flowers of C. pubescens and A. triplinervea, it is advantageous to act as a trapliner (Feinsinger and Chaplin, 1975). On the other hand, when flowers occur in clumps, as with flowers of I. vera and J. spinosa, hummingbirds often act as territorialists, defending these clumps of resources (Wolf et al., 1976; Snow and Snow, 1986; Arizmendi and Ornelas, 1990; Cotton, 1998b). The spatial distribution of hummingbird territories as recorded for I. vera and J. spinosa, is often observed in trees and shrubs with high densities of flowers (Stiles and Wolf, 1970; Feinsinger, 1976).

For the hummingbirds at PSP, size was related to dominance. Eupetomena macroura, the largest hummingbird species recorded at the study site, was not displaced by any other species. Males of A. nigricollis, the second largest species, displaced more (12 times) than was displaced (eight times). Moreover, about 45% of interactions of males of A. nigricollis were with other males of the same species. Smaller hummingbirds often interacted intraspecifically or interspecifically with hummingbirds of similar sizes. A similar pattern of dominance was reported for an Atlantic forest assemblage (Araujo, 1996) and agrees with the one proposed by Des Granges (1979).

In summary, despite the fact that PSP is an urban forest remnant, the hummingbird richness indicates that it may be a refuge and an important foraging site for hummingbirds. In periods of flower scarcity in this area, hummingbirds probably shift to other forest remnants or forage in urban areas near the study remnant, using PSP mostly as a refuge site. Also, data support our expectation of the predominance of generalist hummingbird species at PSP. Studies regarding hummingbird communities in fragmented areas (Stouffer and Bierregaard, 1995; Borgella et al., 2001) also have shown that short to medium-billed generalist hummingbirds are the most frequent ones. Furthermore, hummingbirds at the study site visited flowers of the non-ornithophilous species legitimally, thus indicating that these plant species may also be pollinated by hummingbirds, supporting the idea of Waser et al. (1996) of generalisation in some pollination systems. However, the role of hummingbirds as pollinators on non-ornithophilous species needs to be better evaluated through studies regarding pollen transfer efficiency by these birds.

Acknowledgements – We thank E. Fischer, C.G. Machado, J. Ragusa-Netto, M. Sazima, P. Wilson and G. Ritchison for critical comments; A. Pott, V. Pott and U. Rezende for plant identification; J. Raizer for help in statistical analysis. The Secretaria do Meio Ambiente de Mato Grosso do Sul provided permits for data collection at PSP. PROPP/UFMS provided funds for the English revision. Financial support was provided by CAPES. This manuscript is part of the Master's Degree thesis of L.C.R. in the Graduate Programme in Ecology and Conservation at the Universidade Federal de Mato Grosso do Sul, Brazil.

References

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ARAUJO, AC. and SAZIMA, M., 2003. The assemblage of flowers visited by hummingbirds in the capões of southern Pantanal, Mato Grosso do Sul, Brazil. Flora, vol. 198, p. 427-435.

ARAUJO, AC., FISCHER, EA. and SAZIMA, M., 1994. Floração seqüencial e polinização de três espécies de Vriesea (Bromeliaceae) na região de Juréia, sudeste do Brasil. Revista Brasileira de Botânica, vol. 17, p. 113-118.

ARIZMENDI, MC. and ORNELAS JF., 1990. Hummingbirds and their floral resources in a tropical dry forest in Mexico. Biotropica, vol. 22, p. 172-180. http://dx.doi.org/10.2307/2388410

BAWA, KS., 1990. Plant-pollinator interactions in tropical rain forests. Annual Review of Ecology and Systematics, vol. 21, p. 399- 422. http://dx.doi.org/10.1146/annurev.es.21.110190.002151

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DZIEDZIOCH, C., STEVENS, AD. and GOTTSBERGER, G., 2003. The hummingbird plant community of a tropical montane rain forest in southern Ecuador. Plant Biology, vol. 5, p. 331-3237. http://dx.doi.org/10.1055/s-2003-40802

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MENDONÇA, LB. and DOS ANJOS, L., 2003. Bird-flower interactions in Brazil: a review. Ararajuba, vol. 11, p. 195-205.

-, 2005. Beija-flores (Aves, Trochilidae) e seus recursos florais em uma área urbana do Sul do Brasil. Revista Brasileira de Zoologia, vol. 22, p 51-59.

-, 2006a. Flower morphology, nectar features, and hummingbirdvisitation to Palicourea crocea (Rubiaceae) in the Upper Paraná River floodplain, Brazil. Annals of the Brazilian Academy of Sciences, vol. 78, p 45-57.

-, 2006b. Feeding behavior of hummingbirds and perching birds on Erytrina speciosa Andrews (Fabaceae) flowers in an urban area, Londrina, Paraná, Brazil. Revista Brasileira de Zoologia, vol. 23, p 42-49.

RAMÍREZ, N., 2004. Ecology of pollination in a tropical Venezuelan savanna. Plant Ecolology, vol. 173, p. 171-189. http://dx.doi.org/10.1023/B:VEGE.0000029320.34895.7d

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SAZIMA, I., BUZATO S. and SAZIMA M., 1996. An assemblage of hummingbird-pollinated flowers in a montane forest in southeastern Brazil. Botânica Acta, vol. 109, p. 149-160.

SIGRIST, RM. and SAZIMA M., 2002. Ruellia brevifolia (Pohl) Ezcurra (Acanthaceae): fenologia de floração, biologia da polinização e reprodução. Revista Brasileira de Botânica, vol. 25, p. 35-42.

SILBERBAUER-GOTTSBERGER, I. and GOTTSBERG, G., 1988. A polinização de plantas do cerrado. Revista Brasileira de Biologia = Brazilian Journal of Biology, vol. 48, p. 651-663.

SLUYS, MV. and STOTZ, DF., 1995. Padrões de visitação a Vriesea neoglutinosa por beija-flores no Espírito Santo, sudeste do Brasil. Bromelia, vol. 2, p. 27-35.

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-, 1986. Feeding ecology of hummingbirds in the Serra do Mar, southeastern Brazil. El Honero, vol. 12, p. 286-296.

SNOW, DW. and TEIXEIRA, DI., 1982. Hummingbirds and their flowers in the coastal mountains of southeastern Brazil. Journal of Ornithology , vol. 123, p. 446-450. http://dx.doi.org/10.1007/ BF01643279

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-, 1978. Temporal organization of flowering among the hummingbird food plants of a tropical wet forest. Biotropica, vol. 10, p. 194- 210. http://dx.doi.org/10.2307/2387905

-, 1981. Geographical aspects of bird-flower coevolution, with particular reference to Central America. Annals of the Missouri Botanical Garden, vol. 68, p. 323-351. http://dx.doi.org/10.2307/2398801

STILES, FG. and WOLF, LL., 1970. Hummingbird territoriality at a tropical flowering tree. The Auk, vol. 87, p. 467-491.

STOUFFER, PC. and BIERREGAARD, ROJR., 1995. Effects of forest fragmentation on understory hummingbirds in Amazonian Brazil. Conservation Biology , vol. 9, p. 1085-1094. http://dx.doi.org/10.1046/j.1523-1739.1995.9051072.x-i1

TEMELES, EJ., LINHART, YB., MASONJONES, M. and MASONJONES HD., 2002. The role of flower width in hummingbird bill length-flower length relationships. Biotropica, vol. 34, p. 68-80.

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Received July 21, 2010

Accepted September 24, 2010

Distributed August 31, 2011

  • ARAUJO, AC. 1996. Beija-flores e seus recursos florais numa área de planície costeira do litoral norte de São Paulo. Campinas: Universidade Estadual de Campinas. Dissertação de Mestrado em Ciências Biológicas.
  • ARAUJO, AC. and SAZIMA, M., 2003. The assemblage of flowers visited by hummingbirds in the capões of southern Pantanal, Mato Grosso do Sul, Brazil. Flora, vol. 198, p. 427-435.
  • ARAUJO, AC., FISCHER, EA. and SAZIMA, M., 1994. Floração seqüencial e polinização de três espécies de Vriesea (Bromeliaceae) na região de Juréia, sudeste do Brasil. Revista Brasileira de Botânica, vol. 17, p. 113-118.
  • ARIZMENDI, MC. and ORNELAS JF., 1990. Hummingbirds and their floral resources in a tropical dry forest in Mexico. Biotropica, vol. 22, p. 172-180. http://dx.doi.org/10.2307/2388410
  • BAWA, KS., 1990. Plant-pollinator interactions in tropical rain forests. Annual Review of Ecology and Systematics, vol. 21, p. 399- 422. http://dx.doi.org/10.1146/annurev.es.21.110190.002151
  • BORGELLA, RJR., SNOW, AA. and GAVIN, TA., 2001. Species richness and pollen loads of hummingbirds using forest fragments in southern Costa Rica. Biotropica, vol. 33, p. 90-109.
  • BUZATO, S., SAZIMA, M. and SAZIMA, I., 2000. Hummingbird-pollinated floras at three Atlantic Forest sites. Biotropica, vol. 32, no. 4B, p. 824-841. http://dx.doi.org/10.1111/j.1744-7429.2000. tb00621.x
  • CASTELLANOS, MC, WILSON P. and THOMSON JD., 2003. Pollen transfer by hummingbirds and bumblebees, and the divergence of pollination modes in Penstemon. Evolution, vol. 57, p. 2742-2752. PMid:14761053
  • COELHO, CP. and BARBOSA, AAA., 2004. Biologia reprodutiva de Psychotria poeppigiana Mull. Arg. (Rubiaceae) em mata de galeria. Acta Botânica Brasílica, vol. 18, p. 481-489.
  • COTTON, PA., 1998a. Coevolution in Amazonian hummingbird-plant community. Ibis, vol. 140, p. 639-646.
  • -, 1998b. The hummingbird community of a lowland Amazonian rainforest. Ibis, vo. 140, p. 512-521.
  • DIAMOND, JM., KARASOV, WH., PHAN, D. and CARPENTER, FL., 1986. Digestive physiology is a determinant of foraging bout frequency in hummingbirds. Nature, vol. 320, p. 62-63.
  • Des GRANGES, JL., 1979. Organization of a tropical nectar feeding bird guild in a variable environment. Living Bird, vol. 17, p. 199-236.
  • DZIEDZIOCH, C., STEVENS, AD. and GOTTSBERGER, G., 2003. The hummingbird plant community of a tropical montane rain forest in southern Ecuador. Plant Biology, vol. 5, p. 331-3237. http://dx.doi.org/10.1055/s-2003-40802
  • FAEGRI, K. and VAN DER, PIJIL., 1980. The principles of pollination ecology Oxford: Pergamon Press.
  • FEINSINGER, P., 1976. Organization of a tropical guild of nectarivorous birds. Ecological Monographs, vol. 46, p. 257-291. http://dx.doi.org/10.2307/1942255
  • FEINSINGER, P., 1983. Coevolution and pollination In FUTUYMA, DJ. and SLATKIN, M. (Eds.). Coevolution. Sinauer Associates, Sunderland, Massachusetts. p. 282-310.
  • FEINSINGER, P. and CHAPLIN SB., 1975. On the relationship between wing disc loading and foraging strategy in hummingbirds. The American Naturalist, vol. 109, p. 217-24. http://dx.doi.org/10.1086/282988
  • FEINSINGER, P. and COLWELL RK., 1978. Community organization among neotropical nectar-feeding birds. American Zoologist, vo. 18, p. 779-795.
  • FEINSINGER, P., WOLFE JA. and SWARM LA., 1982. Island ecology: reduced hummingbird diversity and the pollination biology of plants, Trinidad and Tobago, West Indies. Ecology, vol. 63, p. 494-506.
  • FISCHER, E., BUZATO, S., ARAUJO, AC. and PIRATELLI, AJ., 1996. Polinização por beija-flores. In Anais V Congresso Brasileiro de Ornitologia, 1996. Campinas: UNICAMP.
  • FISCHER, E., and LEAL, IR., 2006. Success of Passiflora coccinea (Passifloraceae) in the Central Amazon. Brazilian Journal of Biology, vol. 66, p. 747-754. http://dx.doi.org/10.1590/S1519- 69842006000400019
  • GALETTO, L. and BERNARDELLO, G., 2005. Rewards in flowers: Nectar In DAFNI, A., KEVAN, PG. and HUSBAND, BC. (Eds.). Practical Pollination Biology Enviroquest Ltd.
  • GRANTSAU, R., 1988. Os beija-flores do Brasil Rio de Janeiro: Expressão e Cultura.
  • KODRIC-BROW, A., BROWN, JH., BYERS, GS. and GORI, DF., 1984. Organization of a tropical island community of hummingbirds and flowers. Ecology , vol. 65, p. 1358-1368. http:// dx.doi.org/10.2307/1939116
  • MACHADO, IC. and LOPES AV., 2004. Floral traits and pollination systems in the Caatinga, a Brazilian tropical dry forest. Annals of Botany, vol. 94, p 365-375.
  • Mato Grosso do Sul (Estado). Ministério Público, 2000. Plano de manejo do Parque Estadual do Prosa Campo Grande.
  • MENDONÇA, LB. and DOS ANJOS, L., 2003. Bird-flower interactions in Brazil: a review. Ararajuba, vol. 11, p. 195-205.
  • -, 2005. Beija-flores (Aves, Trochilidae) e seus recursos florais em uma área urbana do Sul do Brasil. Revista Brasileira de Zoologia, vol. 22, p 51-59.
  • -, 2006a. Flower morphology, nectar features, and hummingbirdvisitation to Palicourea crocea (Rubiaceae) in the Upper Paraná River floodplain, Brazil. Annals of the Brazilian Academy of Sciences, vol. 78, p 45-57.
  • -, 2006b. Feeding behavior of hummingbirds and perching birds on Erytrina speciosa Andrews (Fabaceae) flowers in an urban area, Londrina, Paraná, Brazil. Revista Brasileira de Zoologia, vol. 23, p 42-49.
  • RAMÍREZ, N., 2004. Ecology of pollination in a tropical Venezuelan savanna. Plant Ecolology, vol. 173, p. 171-189. http://dx.doi.org/10.1023/B:VEGE.0000029320.34895.7d
  • RUSCHI, A., 1982. Aves do Brasil: beija-flores. Rio de Janeiro: Expressão e Cultura. vol. 4/5.
  • SAZIMA, I., BUZATO S. and SAZIMA M., 1996. An assemblage of hummingbird-pollinated flowers in a montane forest in southeastern Brazil. Botânica Acta, vol. 109, p. 149-160.
  • SIGRIST, RM. and SAZIMA M., 2002. Ruellia brevifolia (Pohl) Ezcurra (Acanthaceae): fenologia de floração, biologia da polinização e reprodução. Revista Brasileira de Botânica, vol. 25, p. 35-42.
  • SILBERBAUER-GOTTSBERGER, I. and GOTTSBERG, G., 1988. A polinização de plantas do cerrado. Revista Brasileira de Biologia = Brazilian Journal of Biology, vol. 48, p. 651-663.
  • SLUYS, MV. and STOTZ, DF., 1995. Padrões de visitação a Vriesea neoglutinosa por beija-flores no Espírito Santo, sudeste do Brasil. Bromelia, vol. 2, p. 27-35.
  • SNOW, DW. and SNOW BK., 1980. Relationships between hummingbirds and flowers in the Andes of Colombia. Bulletin of the British Museum of Natural History (Zoology), vol. 38, p. 105-139.
  • -, 1986. Feeding ecology of hummingbirds in the Serra do Mar, southeastern Brazil. El Honero, vol. 12, p. 286-296.
  • SNOW, DW. and TEIXEIRA, DI., 1982. Hummingbirds and their flowers in the coastal mountains of southeastern Brazil. Journal of Ornithology , vol. 123, p. 446-450. http://dx.doi.org/10.1007/ BF01643279
  • STILES, FG., 1975. Ecology, flowering phenology, and hummingbird pollination of some Costa Rican Heliconia species. Ecology, vol. 56, p. 285-301. http://dx.doi.org/10.2307/1934961
  • -, 1978. Temporal organization of flowering among the hummingbird food plants of a tropical wet forest. Biotropica, vol. 10, p. 194- 210. http://dx.doi.org/10.2307/2387905
  • -, 1981. Geographical aspects of bird-flower coevolution, with particular reference to Central America. Annals of the Missouri Botanical Garden, vol. 68, p. 323-351. http://dx.doi.org/10.2307/2398801
  • STILES, FG. and WOLF, LL., 1970. Hummingbird territoriality at a tropical flowering tree. The Auk, vol. 87, p. 467-491.
  • STOUFFER, PC. and BIERREGAARD, ROJR., 1995. Effects of forest fragmentation on understory hummingbirds in Amazonian Brazil. Conservation Biology , vol. 9, p. 1085-1094. http://dx.doi.org/10.1046/j.1523-1739.1995.9051072.x-i1
  • TEMELES, EJ., LINHART, YB., MASONJONES, M. and MASONJONES HD., 2002. The role of flower width in hummingbird bill length-flower length relationships. Biotropica, vol. 34, p. 68-80.
  • TEMELES, EJ., KOULOURIS, CR., SANDER, SE. and KRESS, WJ., 2009. Effect of flower shape and size on foraging performance and trade-offs in a tropical hummingbird. Ecology, vol. 90, p. 1147- 1161. PMid:19537537. http://dx.doi.org/10.1890/08-0695.1
  • TOLEDO, MCB. and MOREIRA, DM., 2008. Analysis of the feeding habits of the swallow-tailed hummingbird, Eupetomena macroura (Gmelin, 1788), in an urban park in southeastern Brazil. Brazilian Journal of Biology, vol. 68, p. 419-426. PMid:18660974.
  • VASCONCELOS, MF. and LOMBARDI, JA., 2001. Hummingbirds and their flowers in the campos rupestres of southern Espinhaço Range, Brazil. Melopsittacus, vol. 4, p. 3-30.
  • WASER, NM., CHITTKA, L., PRICE, MV., WILLIAMS, NM. and. OLLERTON, J., 1996. Generalization in pollination systems, and why it matters. Ecology, vol. 77, p. 1043-1060.
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  • Publication Dates

    • Publication in this collection
      01 Sept 2011
    • Date of issue
      Aug 2011

    History

    • Received
      21 July 2010
    • Accepted
      24 Sept 2010
    Instituto Internacional de Ecologia R. Bento Carlos, 750, 13560-660 São Carlos SP - Brasil, Tel. e Fax: (55 16) 3362-5400 - São Carlos - SP - Brazil
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