Related species
Distribution, abundance and ecology
Description & phenology
Uses and economic potential
Chemical-nutritive and industrial analysis
Historical production data
Yields and collection anal processing methods
Propagation and cultivation methods
Research contacts
Michael J. Balick
During the last decade there has been a great deal of study on the Oenocarpus-Jessenia palm complex. Widely used by people in: Lowland South America, it is the source of an important oil, beverage, and raw material for construction and handicrafts. Initial work on this palm was through collaborative activities between the Centro "Las Gaviotas" in Colombia, and the Botanical Museum of Harvard University in the US, commencing in 1975. Subsequently, numerous projects were begun at numerous sites in the Neotropics. This chapter focuses on Jessenia bataua subsp. bataua, the most widely used of the complex. Other species are also mentioned. The two major references on this group include a monograph (Balick 1986) and a domestication study (Balick 1988).
Family: Palmae
Species: Jessenia bataua (Martius) Burret
Synonyms: Oenocarpus bataua Martius, J. polycarpa Karsten, J. repanda Engel, J. oligocarpa Grisebach & Wendland e The three first synonyms are of J. bataua subsp. bataua, while the last is of J. bataua subsp. oligocarpa (Balick 1986).
Common names: patauá (Brazil, Suriname); milpesos, seje, palma de leche (Colombia); chapil (Ecuador); palma patavona (French Guiana); batawa (from the Carib, hence the specific name) (Guyana); ungurauy (Peru); jagua, yagua (Trinidad); seje, jagua (Venezuela) (Balick 1986).
Patauá's
importance to the people of northern South America is attested by
the number of common names attributed to it by the Amerindians,
and rural and urban populations in this region. Balick (1986)
lists 87 names, most from indigenous groups, and there are
probably many more.
Oenocarpus bacaba
Martius (bacaba: Brazil). Widely used in northern South America
as a source of vinho de bacaba, a thick, somewhat oily
juice prepared from the slurry of mesocarp and water. The bacaba
is a large, single-stemmed palm growing both in flooded and in
non-flooded areas in rainforest ecosystems. In the latter
ecosystem, bacaba may form high-density stands, called bacabais,
referred to as oligarchic stands (eg dominated by a few species)
by Peters et al. (1989). In fact, Oenocarpus bacaba,
O. distichus and J. bataua all
naturally form oligarchic forests, but their over harvest in the
past and in recent decades has led to the destruction or severe
reduction in stand density or the complete elimination of the
stands.
Oenocarpus balickii F. Kahn (sinamillo: Peru). This recently described species (Kahn 1990) is found in Amazonian Peru, Brazil, Colombia and perhaps elsewhere. It is distinguished from O. mapora by its solitary habit, greater number of pinnae and smaller fruit. It is common in well-drained sites in primary forest, where it can be found in great abundance. Its fruit is used to make a beverage, similar to that made from patauá.
Oenocarpus distichus Martius (bacaba-do-leque: Brazil). This species is the source of vinho de bacaba, a commonly consumed drink in southeastern Amazônia The bacaba-do-leque is distinguished from the bacaba by the striking profile formed by its opposite leaves; the latter species has a spiral leaf arrangement typical of most palms. This species is common on sandier, though humid soils in the seasonally dry forest areas of southeastern Amazônia
Oenocarpus makeru Bernal, Galeano & Henderson (makeru: Colombia). This species was recently described from the Caquetá River, Colombia (Bernal et al. 1991). It is especially interesting because it has some characteristics of Jessenia and this suggests that the generic concept of Martius (1823), lumping the two genera under Oenocarpus may be more appropriate. More complete collections are needed to confirm this, however. In the type locality ("Rio Caquetá, near the Chorro Córdoba, trail to the savanna") it is "abundant in the forest bordering an area of caatinga" (Bernal et al. 1991).
Oenocarpus mapora Karsten (bacabinha: Brazil). A common and widely used species in northwestern South America to southern Central America (to Costa Rica), this palm is a source of vinho de bacaba and palm hearts. This species is smaller and generally multistemmed. It is found as scattered individuals in upland or seasonally flooded sites The wood is used in house construction and for handicrafts.
Two
apparent hybrids exist in the wild, including O. bacaba
x J. bataua and O. bacaba x O.
minor. The presence of natural hybridization bodes well
for future breeding programs designed to improve yields,
tolerance to stress, reduced time to maturity, etc.
Patauá (Jessenia
bataua subspecies bataua) is found
throughout lowland northern South America, from Bolivia in the
south, to Panama in the north, and from Belém (Brazil) in the
east to the Chocó (Colombia) in the west.
Balick (1986, 1988) and Kahn (1988) report that patauá occurs both on well-drained upland soils (terra firma) and in seasonally or perennially flooded swamps (igapó and varzea). In the former ecosystem, patauá occurs as scattered individuals, frequently very numerous, although most of these are juvenile, acaulescent individuals (Kahn 1988). Mature palms may only occur at a rate of 1-2 individuals/ha. No botanical collections are reported above 950 m altitude (Balick 1986). In the latter ecosystem, patauá may be the dominant species over hundreds of hectares and forms the classic oligarchic forest described by Peters et al. (1989). Balick (1986, 1988) suggests that patauá, and palms in general, are more efficient at exploiting these high water stress ecosystems than are most dicots, due to their ability to adapt to such conditions. Peters et al. (1989) report as many as 100 mature and 900 immature palms/ha in some areas of Peru and Brazil, while Sirotti & Malagutti (1950) report up to 500 mature palms and an equal number of immature ones. Balick (1988), however, doubts that sejales of this density can produce fruit in quantities that would be comparable to yields derived from individual trees (see below).
While it
appears that patauá prefers the poorly drained, but more
nutrient-rich soils of the igapós and varzeas of
Amazônia, they probably are most abundant there because the
palms get substantial amounts of light and less competition from
surrounding vegetation. These soils are either very sandy, with
relatively high organic matter contents (igapó) or humic
gleys, with high silt, nutrients and organic matter (varzea).
On the terra firma they are frequently shaded
significantly, which probably explains the rarity of mature palms
in most areas. In fact, Kahn (1988) states that patauá requires
high light levels to fruit. Nonetheless, patauá does extremely
well on the terra firma if released from competition with the
surrounding vegetation. This is confirmed by observations of
high-density stands remaining in pastures in the Colombian Chocó
(Balick et al. 1988).
The patauá is a large
(15-25 m), single-stemmed palm, with a 15-25 cm stem diameter at
breast height. The 8-16 spirally arranged leaves are 3-10 m long,
of which the leaf sheath is 0.51.4 m, the petiole 0.2-1 m, the
rachis 3-8 m. The pinnae number 120-220 and are inserted at
regular intervals in a single plane along the rachis. The
inflorescence has a distinctive horsetail shape, called a
panicle, with 135-350 rachillae, each 70-120 cm long, and bears
from 500-4000 fruit, each weighing from 4-15 g, for a total
weight 2-32 kg/bunch. The small round to ovoid fruit have a dark
purple rind when ripe, containing a 1-3 mm thick, juicy/oily,
white or green or pink/purple mesocarp. The single seed contains
a ruminate endosperm (Balick 1986, 1988).
Leaves are
produced year round. A single inflorescence is produced in the
axil of each leaf (Balick 1986). Only 1-3 inflorescences reach
maturity during any one year, as developing inflorescences can
abort due to unfavorable nutrient status photoassimilate
reserves, or other physiological factors. This inflorescence
abortion often occurs during unfavorable periods for fruit set
and development. Collazos & Mejia (1988) found that patauá
flowers and fruits during periods of lower rainfall in western
Colombia and that the fruit take 10-14 months to ripen after
pollination.
Principal use: Mesocarp oil
Secondary uses: Food/beverage, medicinal, fiber
As with most palms, patauá
has multiple uses (Balick 1986, 1988). This discussion considers
its major potential - oil - its principal use. More complete
discussions can be found in the previously cited references.
Patauá's mesocarp oil is
almost identical to that of olive oil (Olea europaea)
in its physical appearance and fatty acid composition (Balick
1986, 1988) (see below, Table 2). The Amerindians have used the
patauá extensively since well before contact and consider it to
be the finest oil available from a forest plant. Since Latin
America produces very little olive oil and, in fact, this
production is decreasing, patauá has the potential to substitute
for Latin America's imports of this high-quality oil that is so
much in demand. FAO (1985) reports that Latin America produced
less than 1% of the world's olive oil in 1978, or about 13,000
MT. At least 40,000 MT were used in the region in 1974. This
disparity in production versus consumption of olive oil,
equivalent to about 27,000 MT, has probably expanded since those
data were collected, so the potential market may be much larger.
Since patauá oil is virtually identical to olive oil, it is likely that patauá oil could substitute for olive oil in most uses. There was a world shortage of olive oil during World War II and Brazil exported as much as 210 MT/year of patauá oil (Pereira Pinto 1951). Unfortunately, the harvesting of this oil resulted in the wholesale destruction of numerous massive oligarchic stands, which resulted in severe genetic and commercial erosion of patauá populations.
Unlike most
palm mesocarp oils, patauá oil is highly unsaturated, with
78±3% monounsaturated fatty acids and 3±1% polyunsaturated
fatty acids. This contrasts with olive oil's 77-80%
monounsaturated and 7-8% polyunsaturated fatty acids. With the
modern emphasis on unsaturated vegetable oils, patauá may even,
find a ready market in the developed countries.
Throughout Amazônia, and
northern South America, the Amerindians prepare patauá
"wine", actually a thick non-alcoholic juice with a
nutty flavor made from the fruit mesocarp crushed in water and
sieved, similar to vinho de bacaba. This is
a highly nutritious and energy-rich beverage. Balick (1988)
observed that the Amerindians put on weight and are healthier
during the patauá fruiting season than at other times of the
year and attributed this to consumption of the patauá drink. The
protein in this drink was shown to be of excellent quality (see
below, Table 3), which, combined with the oil and some minerals,
makes it an exceedingly nutritious, well-balanced beverage
(Balick & Gershoff 1981).
There are several Amerindian medicinal uses for the palm, some of which are worth further investigation. Alone or mixed with honey and lemon, patauá oil is considered a cure for minor bronchial and pulmonary infections. There was some work in Colombia that showed it's efficacy as a treatment for tuberculosis. The oil is also said to prevent hair loss, but this activity is unsubstantiated (Balick 1986).
The leaf
sheath and petiole have two types of fibers along their edge: a
strong stiff fiber used for blowgun darts and other hunting
equipment, and a soft, hair-like brown fiber that might be used
for rope. and weaving. These fibers could become an important
sub-product from patauá plantations or management areas (see
below).
An average patauá yields
two bunches, each weighing about 15 kg. Trees yielding up to 5
bunches have been observed in favorable agroecosystems (Balick
1988). Blaak (1988) points out that patauá has a
high-fruit/bunch ratio of 76-83% but a low oil/fruit ratio of
6.5-8% (Table 1). This gives an oil/bunch ratio of 5-6.5%.
Table 1. Patauá fresh fruit components (Blaak 1988)
Component |
mean±SD |
min. |
max. |
Fruit weight (g) |
8.0 ± 2.7 |
5.1 |
13.5 |
% pulp/fruit |
41.4 ± 3.2 |
35.6 |
44.7 |
% oil/fruit |
7.4 ± 0.7 |
6.6 |
8.1 |
Table 2 contrasts patauá oil with olive oil, which are both from the mesocarp. Note especially the high levels of unsaturated fatty acids. Note also the variation in fatty acid composition. Overall, these two oils show great chemical similarity.
Table 2. Fatty acid composition of patauá mesocarp oil and a comparison with olive oil (in % total oil).
#C |
Fatty acid |
patauá |
olive oil |
||
Jamieson (1943) |
Balick & Gershoff (1981)* |
Jamieson (1943) |
Balick & Gershoff (1981) |
||
C14: 0 |
- myristic |
- |
- |
1.0 |
- |
C16: 0 |
- palmitic |
8.8 |
13.2 ± 2.1 |
9.4 |
11.2 |
C16: 1 |
- palmitoleic |
- |
0.6 ± 0.2 |
- |
1.5 |
C18: 0 |
- stearic |
5.6 |
3.6 ± 1.1 |
1.4 |
2.0 |
C18: 1 |
- oleic |
76.5 |
77.7 ± 3.1 |
80.5 |
76.0 |
C18: 2 |
- linoleic |
3.4 |
2.7 ± 1.0 |
6.9 |
8.5 |
C18: 3 |
- linolenic |
- |
0.6 ± 0.4 |
- |
0.5 |
% unsaturated |
79.9 |
81.6 ± 4.7 |
87.4 |
86.5 |
|
* mean ± SD of 12 samples.
The dry patauá mesocarp contains about 7.4% protein, with an excellent balance of amino acids. Table 3 presents Balick & Gershoff's (1981) amino acid profile and a comparison of patauá with FAD/WHO's (1973) approximation of the essential amino acid profile of an ideal protein source. patauá is high for several essential Amino acids and only a little low for tryptophan and lysine. Patauá is, therefore, a protein with one of the highest biological values in the plant kingdom, and comparable to animal meat or human milk.
Table 3. Amino acid composition of patauá mesocarp protein* and a comparison with the FAO/WHO (1973) amino acid scoring pattern (Balick & Gershoff 1981).
Non-essential amino acids |
mg/g prot. |
Essential amino acids |
mg/g prot. |
FAO/WHO |
||
score |
% of score |
|||||
Aspartic acid |
122±8 |
Isoleucine |
47 ± 4 |
40 |
118 |
|
Serine |
54±3 |
Leucine |
78 ± 4 |
70 |
111 |
|
Glutamic acid |
96±5 |
Lysine |
53 ± 3 |
55 |
96 |
|
Pro Line |
75±8 |
Methionine |
18 ± 6 |
\ |
||
Glycine |
69±4 |
44 ± 9 |
35 |
126 |
||
Alanine |
58±4 |
Cystine |
26 ± 6 |
/ |
||
Histidine |
29±4 |
Phenylaline |
62 ± 3 |
\ |
||
Arginine |
56±2 |
105 ± 7 |
60 |
175 |
||
Tyrosine |
43 ± 5 |
/ |
||||
Threonine |
69 ± 6 |
40 |
173 |
|||
Valine |
68 ± 4 |
50 |
136 |
|||
Tryptophan |
9 ± 1 |
10 |
90 |
|||
* mean±SD from 7 samples, except Tryptophan from 3 samples.
Pereira Pinto (1951)
presents data on Brazilian exports of patauá oil immediately
before, during and after World War II. These are represented in
Figure 1. Patauá is not listed in the CACEX register of
Brazilian exports during the 1980's (CACEX 1981-88).
