Abstract: Astrocaryum jauari Mart. (Arecaceae) is one of the commonest palm species occurring in nutritionally poor Amazonian black water floodplains. It is an emergent or subcanopy tree that grows on river banks and  slands, with a wide distribution along the entire flooding gradient, tolerating flood durations between 30 and 340 days. The species is important for fish nutrition in the floodplains, and is also used for hearts of palm. In the present study, the auto-ecology of A. jauari w,as analysed over a period of  two years in the Anavilhanas Archipelago, Rio Negro, Brazil, with a focus on phenology, fruit production, and seed dispersal. Fruit fall is annual and synchronized with high water levels, with a production of 1.6 ton of fruit ha^-1. The fruits are eaten by at least 16 species of fish which either gnaw the pulp, fragment the seed, or ingest the entire fruit, thus acting as dispersal agents. Besides ichthyocory, barochory (with subsequent vegetative propagation) is an important dispersal mode, enhancing the occurrence of large masses of individuals in the Anavilhanas islands and in the region of maximum palm heart extraction near Barcelos. Rev. Biol. Trop. 54 (4): 1171-1178. Epub 2006 Dec. 15.

Key words: Astrocaryum jauari, floodplains, Amazonia, Anavilhanas, Brazil, ichthyocory, barochory.

Floodplain forests of large rivers in the Amazon region are subjected to water level fluctuations of about 10 m every year, as the result of the sum of the precipitation in the  catchment area (Goulding 1983). The regular annual occurrence of an aquatic and a terrestrial phase is of high ecological importance (Junk et al. 1989) and led to the evolution of a specific vegetation (Kubitzki 1989, Prance 1979) highly adapted to survive partially or totally submerged periods of up to 210 days,  depending on the position of the individuals in the flooding gradient (Junk 1993).

According to the water properties of the related rivers and the flora, two major floodplain ecosystems can be distinguished, the nutritionally rich „várzea“ associated to white  water rivers like the Amazon, and the nutritionally poor „igapós“, associated to black water rivers like the Rio Negro (Sioli 1975, Prance 1980). Owing to the high acidity, mineral content and low light penetration in the igapós, aquatic herbaceous vegetation (Junk and Piedade 1997) and phytoplancton production  (Sioli 1976, Schmidt 1973) are very poor. Life in this ecosystem therefore strongly depends on the allochtone primary production of the riparian forests (Erwin and Adis 1982, Junk et al. 1989, Junk and Piedade 1997).

In flooded forests, several plants dispersed by animals developed hard pericarps to protect the seeds against the acids of their digestive apparatus (Cronquist 1974). In such environments, the sound of fruit falling into the water can attract dispersors like fish (van der Pijl 1969), particularly if the fruits are heavy like those of palm trees. One of these, Astrocaryum jauari Mart. (Fig. 1A, B), which is frequent in the black water floodplains of the Rio Negro and its affluents, produces fruits which are consumed by fish (Fig. 1C; Gottsberger 1978, Goulding 1980, 1983). The commercially important Characidae family, and especially two of the most important fish in terms of local consumption and exportation, Colossoma bidens (pirapitinga) and Colossoma macropomum (tambaquí), feed on A. jauari and disperse its seeds (Goulding 1980). However, the fish may act also as predators, since they posses strong mandibles able to triturate the hard seeds.

Also ]]> considerable. The traditional use by indigenous people has been documented: A. jauari provides fiber, food, and shelter (Gragson 1992). In Puerto Ayacucho in the State of Amazonas, venezuela, at least four indigenous groups (Piaroa, Curripaco, Guahibo and Baniva) from ten ]]> products in the economic support of their families (Narvaez and Stauffer 1999). Owing  to the high quality and tenderness of the hearts of palm, this species was exploited for more than 20 years, supplying all hearts of palm commercialized in Central Amazonia between 1978 and 1998 (Piedade 1985, Piedade et  ]]> al. 2003) before being replaced by Bactris gasipaes from plantations (Alírio Rocha, pers. comm. SHARP S/A).

Although the species is common and of ]]> high ecological importance, information about the vegetative and reproductive phenologies, and their timing with respect to the flood pulse, is completely missing. Dispersal mechanisms and their relationship with the local distribution and population structure as well as the contribution of fruits to the food chains are analyzed in the present study.

Material and methods

Study sites: Data on phenology and on fruit production were collected in the Anavilhanas Archipelago, Rio Negro, Central Amazon, at the Anavilhanas Ecological Floating  Station (AEFE) of the Brazilian Institute of Environment (Instituto Brasileiro de Meio Ambiente - IBAMA), about 100 km from the city of Manaus (between 2^o00’ ]]> o02’ S  of latitude and 60^o 27’ to 61^o07’ W of longitude). The main period of data collection was from August 1980 to November 1982. From this year to 1998 irregular field trips added occasional observations, and data about the commercial extraction of the palm tree were collected.
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Climate: The climate is hot and humid with mean minimum temperatures above 18 ºC (Ribeiro 1976). The most arid month (October) has a relative humidity above 60 %. Mean annual precipitation ranges between 1 000 and 2 500 mm (Fig. 2; ]]> river level fluctuations in the Anavilhanas Archipelago show a similar pattern and amplitudes like those measured at the harbour in Manaus, with an annual mean amplitude of 10 m (Fig. 2; Schmidt 1973).

Vegetation: In the study sites, the vegetation forms three strata and has low plant densities. The taller trees reach 15 to 20 m height, with some emergent individuals about 25 m high (Piedade 1985). During high water levels, the vegetation is partially or totally inundated. Medium height of mature A. jauari is 20 m, with dense tree crowns, which have 6 to 14 leaves (Boer 1965), each one with a mean length of 3 m. A. jauari may occur isolated but more frequently the species forms huge stands along the margins of rivers or lakes (Corrêa 1969, Goulding 1980). The species may form clones with 4 to 6 individuals differing in size but belonging to a single rhizome (Boer 1965).

Phenology and fruit production: Nine healthy, adult individuals of A. jauari were marked and the phenological status was recorded once a month. Presence or absence of flowers, young and mature fruits were recorded as well as fruit maturation time. In the period of fruit maturation, phenology was recorded at weekly intervals. Ten fruit bunches were collected from different individual trees, ]]> ascertain total number of produced fruits and fruit weight and size. Twenty fruits per bunch were weighed. Additionally, 250 seeds were collected from different bunches for chemical analyses which were performed in the INPA, Manaus. Water content (in percent, after oven drying at 80 °C to constant weight), and the contents ]]> calories and vitamin A were measured.

Dispersal: Dispersal syndromes were observed on the marked trees. To estimate predation, fruits were monitored for ten weeks as follows: 1 000 ]]> bunches (pre-dispersal predation), and 3 000 fruits were collected from the soil (post-dispersal predation). In order to establish the efficiency of water as a dispersal agent, 1 000 seeds were collected floating at the water surface and opened to analyse the embrional integrity. Systematical analyses of fish stomach ]]> were performed at the Ecological Station. To this information were added bibliographical data and interviews with local people.

Exploitation: Data on palm extractivism until 1998 were gained from the technicians of the Fábrica de Palmito Jauari, SHARP do Brasil S.A., Manaus/AM.

Results

Phenology and fruit production: The production of flowers and fruits of A. jauari occurs once every year. The great majority of the adult palms starts the production of flowers when the water of the rivers are sinking and precipitation is not very intense yet, especially in August and September (Fig. 2). The flowering period is short and is soon substituted by ]]> presence of small fruits which develop slowly. The fruits are mature when the river levels rise again, after about nine months, with abscission occurring mainly at high water levels in the months May to July (Fig. 2). No pre-dispersal predation was detected.

]]> Every individual of A. jauari produces four fruit bunchs every year, which are 90 cm long on average and have a mean fruit number of 106, with a mean weight per fruit of 17 g (Table 1).

The chemical analyses of fruits of A. jauari  (Table 2) show that the pulp and the seed consist mainly of water and carbohydrates, with a high percentage of fat (14.7 %) in the seed.

Dispersal: Since mean fruit weight is high ]]> Table 1), and morphological features enhancing flotation are completely lacking, the fruits sink to the bottom when they fall into water. If fruits were found floating, then the seeds were not viable and all deteriorated. As a consequence of topographical conditions, after abscission the fruits may fall and  be accumulated ]]> (barochoric dispersal, Fig. 3). under such conditions, some of the seeds may be predated by small coleoptera. They may also roll  away from the mother plant, in many cases aided by the action of water. The fruits found in these conditions are less in number, and  are located in ]]> Ichthyochoric dispersal plays a major role: a total of 16 fish species feed on the fruits of A. jauari (Table 3). These belong to five families, mainly to the Characidae. Ten of the 16 species were categorized as possible dispersers, although ]]> C. macropomum, C. bidens and Prachtocephalus hemiliopterus) may also act as predators since they do not only swallow the whole fruits, but  sometimes chew and destroy them with their  strong mandibles and teeth (Goulding 1980). This could not be measured and quantified in the present study. In the ]]> we did not observe any indications of other  vertebrates feeding on fruits of A. jauari.

Discussion

The distribution of A. jauari was quite variable among different islands, occurring on sites flooded for 270 to 340 days per year on ]]> they dominated in areas flooded for 30 to 200 days per year. This high amplitude of distribution was already pointed out by Huber (1906) for populations of A. jauari along the Rio Purus. It is possible because the palm is well-adapted anatomically and physiologically to hypoxic conditions (Schlüter et ]]> . 1993). Annual inundation for as long as 300 days, at water temperatures of 28 °C, produce neither leaf loss nor rotting of the roots. Well-developed aerenchyma permits gas transport from the branches to the roots. At a depth of 1.2 m beneath black waters, the leaves in the crowns of the plants show little decrease in the amount of ]]>

Phenological patterns between sites are quite similar. A. jauari synchronizes its flowering with the period in which precipitation is less intense. With the onset of high precipitations, the fruits are growing already -a process which may last nine months- and at highestwater levels the abscission of mature fruits is at its maximum. Perhaps this long period of maturation is necessary to reach the high energetic and vitaminic level of the fruits (Table 2), since the soils of the black water floodplains are extremely poor in nutrients (Sioli 1976). The long maturation phase is also ]]> for the synchronization of fruit production with high water levels and the related seed dispersal by fish. The high nutritional value of the fruits (Table 2) may be related to the ichthyochoric dispersal syndrome. The especially high content of vitamin A may be advantageous for fish to put up stock reserves in the form ]]> fat which are needed for gonads development in the low water period when food resources are scarce. Goulding (1980) found 52 entire fruits of A. jauari in only one individual of C. macropomum, and in one individual of C. bidens ]]> A. jauari fruits. The noise of fruits falling into the water attracts fish and thus contribuites to the success of the propagation mechanism.

All floating fruits were no longer viable, indicating that ]]> in A. jauari. Although Corner (1966) emphasizes that in the genus Astrocaryum dispersal by flotation is frequent and apparent, in the case of A. jauari the heavy fruits may eventually be transported submerged by currents, but definitely ]]>

The observed local increases of population density probably result from barochory, and from vegetative propagation which enhances the occurrence of large masses of individuals in the Anavilhanas islands, and of even higher densities in the region of maximum extractivism, near Barcelos.

Hydrochory is probably of neglectable importance, and ichthyochory is responsible for long distance dispersal helping to colonize new habitats. Van der Pijl (1969) states ]]> ichthyochory is a primitive dispersal mechanism which in floodplains of Amazonia and Borneo has been maintained in ancient plant groups. These primitive mechanisms of dispersal usually imply a huge production and loss of fruits, since these mechanisms are highly hazardous in terms of the possibility of finding an appropriate place ]]> they allow several opportunists to exploit the resource (Janzen 1970 1971, Fleming and Heithaus 1981).

Finally both, the intensive extraction of the palm, and the pressure over the populations of the most probable fish acting as ]]> lead to the impoverishment of food chains in black water Amazonian floodplains, and to the decline of densities of A. jauari and some of the economically important fish species.

Resumen

Astrocaryum jauari Mart. (Arecaceae) es una de las especies más comunes de palma en las llanuras de inundación por las llamadas “aguas negras”, aguas ricas en taninos que tienen pocos nutrientes para la fauna. Habita el subdosel que se desarrolla en riberas e islas, con una distribución amplia en toda la gradiente de inundación (resiste entre 30 y 340 días bajo el agua). La especie es importante para la nutrición de los peces y en la producción de palmito. La autoecología de A. jauari fue analizada por dos años en el Archipiélago Anavilhanas, río Negro, Brazil, con énfasis en fenología, producción de frutas, y dispersores de semillas. La caída de los frutos es anual y sincronizada con el aumento de los niveles de agua, con una producción de 1.6 ton de fruta ha^-1. Las frutas son comidas por al menos de 16 especies de peces que roen la pulpa o fragmentos de semilla, o ingieren la fruta entera y actúan como agentes dispersores. Además de la ictiocoria, la barocoria y la subsecuente progragación asexual son básicos para la alta densidad de la especie.

Palabras clave: Astrocaryum jauari, llanura de inundación, Amazonía, Anavilhanas, Brasil, ictiocoria, barocoria.

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