Pacific Island Ecosystems at Risk (PIER)
RISK ASSESSMENT RESULTS: Low risk, score: 3 (low risk based on second screen)
|
Australian/New Zealand Weed Risk Assessment adapted for Hawai‘i. Research directed by C. Daehler (UH Botany) with funding from the Kaulunani Urban Forestry Program and US Forest Service Information on
Risk Assessments |
Enterolobium cyclocarpum (syn. Inga cyclocarpa (Jacq.) Willd. Mimosa cyclocarpa ); monkeysoap, ear tree |
Answer |
||
1.01 |
Is the species highly domesticated? |
y=-3, n=0 |
n |
1.02 |
Has the species become naturalized where grown? |
y=-1, n=-1 |
y |
1.03 |
Does the species have weedy races? |
y=-1, n=-1 |
n |
2.01 |
Species suited to tropical or subtropical climate(s) (0-low; 1-intermediate; 2-high) – If island is primarily wet habitat, then substitute “wet tropical” for “tropical or subtropical” |
See Append 2 |
2 |
2.02 |
Quality of climate match data (0-low; 1-intermediate; 2-high) see appendix 2 |
2 |
|
2.03 |
Broad climate suitability (environmental versatility) |
y=1, n=0 |
n |
2.04 |
Native or naturalized in regions with tropical or subtropical climates |
y=1, n=0 |
y |
2.05 |
Does the species have a history of repeated introductions outside its natural range? y=-2 |
?=-1, n=0 |
y |
3.01 |
Naturalized beyond native range y = 1*multiplier (see Append 2), n= question 2.05 |
y |
|
3.02 |
Garden/amenity/disturbance weed y = 1*multiplier (see Append 2) |
n=0 |
n |
3.03 |
Agricultural/forestry/horticultural weed y = 2*multiplier (see Append 2) |
n=0 |
n |
3.04 |
Environmental weed y = 2*multiplier (see Append 2) |
n=0 |
|
3.05 |
Congeneric weed y = 1*multiplier (see Append 2) |
n=0 |
n |
4.01 |
Produces spines, thorns or burrs |
y=1, n=0 |
n |
4.02 |
Allelopathic |
y=1, n=0 |
|
4.03 |
Parasitic |
y=1, n=0 |
n |
4.04 |
Unpalatable to grazing animals |
y=1, n=-1 |
n |
4.05 |
Toxic to animals |
y=1, n=0 |
y |
4.06 |
Host for recognized pests and pathogens |
y=1, n=0 |
n |
4.07 |
Causes allergies or is otherwise toxic to humans |
y=1, n=0 |
n |
4.08 |
Creates a fire hazard in natural ecosystems |
y=1, n=0 |
n |
4.09 |
Is a shade tolerant plant at some stage of its life cycle |
y=1, n=0 |
n |
4.1 |
Tolerates a wide range of soil conditions (or limestone conditions if not a volcanic island) |
y=1, n=0 |
y |
4.11 |
Climbing or smothering growth habit |
y=1, n=0 |
n |
4.12 |
Forms dense thickets |
y=1, n=0 |
n |
5.01 |
Aquatic |
y=5, n=0 |
n |
5.02 |
Grass |
y=1, n=0 |
n |
5.03 |
Nitrogen fixing woody plant |
y=1, n=0 |
y |
5.04 |
Geophyte (herbaceous with underground storage organs -- bulbs, corms, or tubers) |
y=1, n=0 |
n |
6.01 |
Evidence of substantial reproductive failure in native habitat |
y=1, n=0 |
n |
6.02 |
Produces viable seed. |
y=1, n=-1 |
y |
6.03 |
Hybridizes naturally |
y=1, n=-1 |
|
6.04 |
Self-compatible or apomictic |
y=1, n=-1 |
|
6.05 |
Requires specialist pollinators |
y=-1, n=0 |
n |
6.06 |
Reproduction by vegetative fragmentation |
y=1, n=-1 |
n |
6.07 |
Minimum generative time (years) 1 year = 1, 2 or 3 years = 0, 4+ years = -1 |
See left |
15 |
7.01 |
Propagules likely to be dispersed unintentionally (plants growing in heavily trafficked areas) |
y=1, n=-1 |
n |
7.02 |
Propagules dispersed intentionally by people |
y=1, n=-1 |
y |
7.03 |
Propagules likely to disperse as a produce contaminant |
y=1, n=-1 |
n |
7.04 |
Propagules adapted to wind dispersal |
y=1, n=-1 |
n |
7.05 |
Propagules water dispersed |
y=1, n=-1 |
y |
7.06 |
Propagules bird dispersed |
y=1, n=-1 |
n |
7.07 |
Propagules dispersed by other animals (externally) |
y=1, n=-1 |
n |
7.08 |
Propagules survive passage through the gut |
y=1, n=-1 |
y |
8.01 |
Prolific seed production (>1000/m2) |
y=1, n=-1 |
n |
8.02 |
Evidence that a persistent propagule bank is formed (>1 yr) |
y=1, n=-1 |
y |
8.03 |
Well controlled by herbicides |
y=-1, n=1 |
|
8.04 |
Tolerates, or benefits from, mutilation, cultivation, or fire |
y=1, n=-1 |
y |
8.05 |
Effective natural enemies present locally (e.g. introduced biocontrol agents) |
y=-1, n=1 |
|
Total score: |
3 |
Supporting data:
Source |
Notes |
|
1.01 |
no evidence |
|
1.02 |
USDA, ARS, National Genetic Resources Program. Germplasm Resources Information Network - (GRIN). [Online Database] National Germplasm Resources Laboratory, Beltsville, Maryland. Available: http://www.ars-grin.gov/cgi-bin/npgs/html/tax_search.pl?monkeysoap (22 October 2003) |
Distributional range: |
1.03 |
no evidence |
|
2.01 |
USDA, ARS, National Genetic Resources Program. Germplasm Resources Information Network - (GRIN). [Online Database] National Germplasm Resources Laboratory, Beltsville, Maryland. Available: http://www.ars-grin.gov/cgi-bin/npgs/html/tax_search.pl?monkeysoap (22 October 2003) |
Distributional range: |
2.02 |
||
2.03 |
(1)CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. (2)http://www.winrock.org/forestry/factpub/FACTSH/Enterolob.html |
(1) E. cyclocarpum is native to the seasonally dry, tropical
forest formation and becomes less frequent progressing from deciduous to
evergreen wet forest, where it occurs rarely and then only on disturbed
sites such as river banks (Janzen, 1983). Throughout most of the native
range, annual rainfall varies between 750 and 2500 mm with a 3- to 6-month
dry season (Francis, 1988; Stewart et al., 1992). It is a truly tropical
species and intolerant of frosts. Within the native range in Central
America, it is very abundant at low elevations on the Pacific coastal plains
but rarely found above 1000 m. |
2.04 |
USDA, ARS, National Genetic Resources Program. Germplasm Resources Information Network - (GRIN). [Online Database] National Germplasm Resources Laboratory, Beltsville, Maryland. Available: http://www.ars-grin.gov/cgi-bin/npgs/html/tax_search.pl?monkeysoap (22 October 2003) |
Distributional range: |
2.05 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
Location of introductions |
3.01 |
USDA, ARS, National Genetic Resources Program. Germplasm Resources Information Network - (GRIN). [Online Database] National Germplasm Resources Laboratory, Beltsville, Maryland. Available: http://www.ars-grin.gov/cgi-bin/npgs/html/tax_search.pl?monkeysoap (22 October 2003) |
naturalized in West Indies |
3.02 |
no evidence |
|
3.03 |
no evidence |
|
3.04 |
(1) http://www.co.collier.fl.us/natresources/exotics/other%20exotics.htm (2) http://www.hear.org/pier/prospective.htm |
(1) on a list of "Nusiance Plants" [NOT ON FLEPPC LIST] (2) on the list of "Prospective Invasive Species for Pacific Islands " (Have been found on some Pacific islands and appear to be exhibiting invasive characteristics in wildland ecosystems. Are known to be invasive in similar ecosystems elsewhere in the world and could potentially be a problem on Pacific islands. ) [NO CONCRETE EVIDENCE THAT THIS SPECIES IS A PROBLEM IN NATURAL AREAS ANYWHERE IN THE WORLD] |
3.05 |
no evidence |
|
4.01 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
no description of these traits |
4.02 |
(1) Chacko, K. C.; Pillai, P. K. C. (1997) Storage and
hot-water treatments enhance germination of guanacaste (Enterolobium
cyclocarpum ) seeds. International Tree Crops Journal, 1997, Vol.9, No.2,
pp.103-107, 7 ref. |
(1)AB: "When the solution (leachate) obtained after hot
water treatment was used for soaking paddy (Oryza sativa ) seeds,
germination was delayed, although the cumulative final germination was
unaffected. " |
4.03 |
no evidence |
|
4.04 |
(1) Carranza-Montaño, M. A.; Sánchez-Velásquez, L. R.;
Pineda-López, M. del R.; Cuevas-Guzmán, R. (2003) Forage quality and
potential of species from the Sierra de Manantlán (México) tropical dry
forest. Agrociencia (Montecillo), 2003, Vol.37, No.2, pp.203-210, 16 ref.
|
(1) AB: "We studied forage quality and potential production
for nineteen plant species (Chloris gayana, Andropogon gayanus, Panicum
maximum, Verbesina greenmanii, Viguiera dentata, Guazuma ulmifolia ,
Compositae sp., Brosimum alicastrum, Sideroxylon capiri, Prosopis laevigata,
Leucaena esculenta, Enterolobium cyclocarpum, Acacia macilenta, A.
farnesiana, Coursetia caribaea, A. riparia, A. cochliacantha, Albizia
tomentosa and Pithecellobium dulce ) in five tropical dry forest and three
grassland sites at ejido [common land] 'Zenzontla', Sierra de Manantlán
Biosphere Reserve (México). All sites are grazed by livestock of the ejido
peasants. The nineteen species (herbs, shrubs and trees) were identified as
being used as forage and were each evaluated for dry weight and chemical
composition. " |
4.05 |
(1) CAB International, (2000) Forestry Compendium Global
Module. Wallingford, UK: CAB International.Identification and typing of
potentially poisonous plants of the southern Pacific coast of Guatemala.
Toxicity of fruits of the tree |
(1) "a high-quality dry season fodder from the pods"; "The
dust from sawmilling E. cyclocarpum wood is a pungent irritant to mucous
membranes, can produce an allergic reaction in workers (Record and Hess,
1943; Echenique-Manrique and Plumptre, 1990), and can kill fish if dumped
into rivers (Little et al., 1974)." |
4.06 |
Suharti, M.; Irianto, R. S. B.; Santosa, S. (1994) Behaviour of the stem borer Xystrocera festiva Pascoe on Paraserianthes falcataria and integrated control. FT: Perilaku hama penggerek batang sengon Xystrocera festiva Pascoe dan teknik pengendalian secara terpadu. Buletin Penelitian Hutan, 1994, No.558, pp.39-53, 5 ref. |
AB: A study was made of the life cycle and behaviour of
Xystrocera festiva in plantations of Paraserianthes falcataria at 2
locations in South Sumatra, followed by laboratory investigations of its
rearing. The pest was shown to have various hosts (Acacia mangium, A.
auriculiformis, A. arabica [A. nilotica], Pithecellobium jiringa, P. dulce,
Samanea saman [Albizia saman] and Enterolobium cyclocalipum [E. cyclocarpum]
). The use of integrated control methods is suggested. |
4.07 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
"The dust from sawmilling E. cyclocarpum wood is a pungent irritant to mucous membranes, can produce an allergic reaction in workers (Record and Hess, 1943; Echenique-Manrique and Plumptre, 1990), and can kill fish if dumped into rivers (Little et al., 1974)." [SAW DUST IS NOT INHALED BY PUBLIC] |
4.08 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
E. cyclocarpum is native to the seasonally dry, tropical forest formation and becomes less frequent progressing from deciduous to evergreen wet forest, where it occurs rarely and then only on disturbed sites such as river banks [a single trunked, large tree - low fire risk] |
4.09 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
It is a strongly light demanding species and must receive adequate sunlight as a dominant or co-dominant from the sapling stage onwards |
4.1 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
Soil and physiography |
4.11 |
tree |
|
4.12 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
A giant, thornless, canopy tree to 30-40 m tall and 2-3 m stem diameter with a short, clear bole, often supported by small buttresses, heavy branching and a huge spreading rounded crown. |
5.01 |
terrestrial |
|
5.02 |
tree; Fabaceae (Mimosaceae) |
|
5.03 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
It is known to be nitrogen-fixing |
5.04 |
tree |
|
6.01 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
Genetic conservation |
6.02 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
Propagation is mainly by seed |
6.03 |
no evidence |
|
6.04 |
Rocha, O. J.; Lobo, J. A. (1997) Genetic diversity and outcrossing rates in the guanacaste tree (Enterolobium cyclocarpum Jacq.) in the dry forests of Costa Rica. ED: Bruns, S.; Mantell, S.; Trägardh, C.; Viana, A. M. Recent advances in biotechnology for tree conservation and management. Proceedings of an IFS Workshop, Florianópolis, Brazil, 15-19 September 1997., 1998, pp.65-81, 4 pp. of ref. |
AB: "E. cyclocarpum is a predominantly outcrossed species, as all estimates indicated that nearly 90% of the progeny produced from each tree resulted from cross fertilization. In addition, very low levels of biparental inbreeding (Tm-Ts was only about 5%) were found. Both spatial and temporal variation were found in the outcrossing rates; furthermore, significant variation was found among outcrossing rates estimated for individual trees. When the data were examined using the correlated mating model proposed by Ritland, significant variation in effective selfing rates among populations and among years was detectable. Also a positive correlation was found between effective selfing rate and correlation of selfing, indicating significant variation in selfing rates in space and time." [depends on genotype introduced] |
6.05 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
A large tree of E. cyclocarpum may bear several million flowers. Each flower lasts 24 hours, but pollination is thought to be mainly by night-flying insects such as moths and beetles (Janzen, 1982a). |
6.06 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
Although trees are known to resprout vigorously after cutting, pollarding or ring-barking, there are no reports of successful vegetative propagation by grafting or rooting cuttings, although stump planting is successful |
6.07 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
Seed production can start at 15-25 years of age |
7.01 |
no evidence |
|
7.02 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
E. cyclocarpum is generally considered to have been introduced throughout the tropics mainly as a roadside or garden tree |
7.03 |
no evidence |
|
7.04 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
Seed dispersal has been investigated in detail by Janzen (1981, 1982a, 1982b, 1982c) who suggested that the large indehiscent fruits were once eaten by large herbivores that are now extinct, and to a lesser extent by peccaries, tapirs and rodents, and that its seeds were dispersed by passing through them. This role has now been largely taken over, albeit imperfectly, by introduced horses and cattle. Seed dispersal by horses operates predominantly over distances of several 100 m to 1 km, i.e. similar to pollen flow distances, with more sporadic seed dispersal over much longer distances of 10-20 km (Janzen, 1981). |
7.05 |
Hunter, J. R. (1989) Seed dispersal and germination of Enterolobium cyclocarpum (Jacq.) Griseb. (Leguminosae: Mimosoideae): are megafauna necessary? Journal of Biogeography, 1989, Vol.16, No.4, pp.369-378, 49 ref. |
AB: Experiments with seeds of this tree from Central America show that scarification of the seed testa may be more beneficial than heat treatment in stimulating rapid germination, but that a humid environment and warm tropical temperatures are completely adequate for this process. The hypothesis that megafauna served and presently serve as principal agents of seed dispersal is questioned. Dissemination by water (hydrochory) is suggested as an alternative strategy. |
7.06 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
The full-sized green pods are heavily preyed on by Amazona parrots which remove the green seed contents (Janzen, 1983), and spiny pocket mice, Liomys salvini may consume up to 93% of dispersed seeds (Janzen, 1982d). [seed predators of UNRIPE pods] |
7.07 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
The pods are 3-4 cm wide, curved to form an almost complete circle 8-10 cm in diameter, and dark lustrous-brown. The seeds are extremely hard, dark brown, compressed ovoid-ellipsoid, 13-20 x 11 x 8 mm, with a pale pleurogram and are arranged in two rows with 10-15 and occasionally up to 22 seeds per pod. |
7.08 |
(1) Mora G., B.; Rojas A., D. (1988) Study of the viability
and percentage germination of seeds of Enterolobium cyclocarpum. [FT:
Estudio de la viabilidad y procentaje de germinación de la semilla de
Enterolobium cyclocarpum (Jacq.) Grisseb (Leguminosae). ]Tecnología en
Marcha, 1988, Vol.9, No.2, pp.39-41, 6 ref. |
(1) "2.77% of seeds subjected to animal digestion germinated
" |
8.01 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
An adult tree may produce 2000 pods, each with 10-16 seeds ;
A giant, thornless, canopy tree to 30-40 m tall and 2-3 m stem diameter with
a short, clear bole, often supported by small buttresses, heavy branching
and a huge spreading rounded crown. |
8.02 |
(1) Chacko, K. C.; Pillai, P. K. C. (1997) Storage and
hot-water treatments enhance germination of guanacaste (Enterolobium
cyclocarpum ) seeds. International Tree Crops Journal, 1997, Vol.9, No.2,
pp.103-107, 7 ref. |
(1) AB: " Seeds stored for two years recorded higher
germination (40-53%) than fresh seeds (13-31%) after hot and boiling water
pretreatments. Untreated and cold water treated seeds registered either nil
or negligible (3-9%) germination. " |
8.03 |
no evidence of being controlled |
|
8.04 |
CAB International, (2000) Forestry Compendium Global Module. Wallingford, UK: CAB International. |
resprout vigorously after cutting, coppicing or ring-barking |
8.05 |
no evidence |
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This page updated 30 September 2005