Nativa, Sinop, v. 9, n. 5, p. 567-572, 2021.
Pesquisas Agrárias e Ambientais
DOI: https://doi.org/10.31413/nativa.v9i5.12536 ISSN: 2318-7670
Tree species susceptibility to leaf-cutting ants attack in carbon
neutralization plantations
Vicente Toledo Machado de MORAIS JÚNIOR1, Laércio Antônio Gonçalves JACOVINE1,
Mateus Comine Frades da SILVA1, Bruno Leão Said SCHETTINI1*, Maria Paula Miranda Xavier RUFINO1,
Indira Bifano COMINI1, Paulo Henrique VILLANOVA1, Samuel José Silva Soares da ROCHA1
1Federal University of Viçosa, Viçosa, MG, Brazil.
*E-mail: blsschettini@gmail.com
(ORCID: 0000-0001-5227-1951; 0000-0001-5485-3090; 0000-0003-2717-0635; 0000-0001-6510-4511;
0000-0001-6594-2152; 0000-0003-1815-5783; 0000-0002-4187-2740; 0000-0001-6686-1936)
Recebido em 23/06/2021; Aceito em 16/12/2021; Publicado em 23/12/2021.
ABSTRACT: Greenhouse gas (GHG) emissions neutralize planting are one of the options for climate changes
mitigating. Leaf-cutter ants attack is a threat to the plantations proper development. Ants have selective
foraging, which makes it important to know this selectivity and, thus, choose more suitable species to
neutralization planting compose. Thus, the goal of the present study was to evaluate the tree species
susceptibility to be attacked by leaf-cutter ants in carbon neutralization plantations. The study was carried out
in mixed plantations in Viçosa-MG and a classification was created for the present species. The Damage Index
(DI) was created by multiplying the Mean of Severity (MS) and the Frequency of Attacks (FA). The species
were classified according to the indication for neutralization plantations (indicated, moderately indicated, and
not indicated) and potential species for the extraction of natural insecticides. From the 59 species evaluated, 22
were classified as suitable for neutralization plantations, 6 as moderately indicated, 24 as not indicated, and 7 as
potential species for extracting natural insecticides.
Keywords: forest carbon; pest control; carbon offset; mixed plantings.
Susceptibilidade de espécies arbóreas ao ataque de formigas cortadeiras
em plantações de neutralização de carbono
RESUMO: O plantio para neutralizar as emissões de gases de efeito estufa (GEE) é uma das opções para
mitigar as mudanças climáticas. O ataque de formigas cortadeiras é uma ameaça ao bom desenvolvimento
dessas plantações. As formigas possuem forrageamento seletivo, o que torna importante conhecer essa
seletividade e, assim, escolher espécies mais adequadas para compor o plantio de neutralização. Assim, o
objetivo do presente estudo foi avaliar a susceptibilidade de espécies arbóreas ao ataque de formigas cortadeiras
em plantios de neutralização de carbono. O estudo foi realizado em plantios mistos do programa Carbono Zero
em Viçosa-MG e, com base nessa avaliação, foi criada uma classificação para as espécies presentes. O Índice
de Danos (DI) foi criado pela multiplicação da Média de Severidade (MS) e da Frequência de Ataques (FA). As
espécies foram classificadas quanto à indicação para plantios de neutralização (indicada, moderadamente
indicada e não indicada) e espécies potenciais para extração de inseticidas naturais. Das 59 espécies avaliadas,
22 foram classificadas como aptas para plantios de neutralização, 6 como moderadamente indicadas, 24 como
não indicadas e 7 como espécies potenciais para extração de inseticidas naturais.
Palavras-chave: carbono florestal; controle de pragas; compensação de carbono; plantios mistos.
1. INTRODUCTION
The increase in greenhouse gas (GHG) emissions
resulting from the burning of fossil fuels (MAHBUB et al.,
2019), agricultural activities (TUBIELLO, 2019) and the
degradation of terrestrial environments, cause climate
changes on a global scale (ZHENG et al., 2019). The
intensification of the greenhouse effect is one of the causes
of the highest concentration of GHG in the atmosphere (LI
et al., 2019) and, in this context, the removal of CO2 in the
atmosphere and its fixation in the form of biomass by trees
is one of the viable options for mitigating GHG emissions
(DIMOBE et al., 2019). Plantations can neutralize activities
that generate quantifiable GHG emissions, based on some
strategies (MORAIS JUNIOR et al., 2019).
Among the many challenges to overcome in planting with
tree species for carbon neutralization, the control of leaf-
cutter ants stands out. Leaf-cutter ants are pests that cause a
significant negative impact (ZANETTI et al., 2014), as they
defoliate trees, cut off sprouting buds, cause leggy seedlings
and occur throughout the year. Leaf-cutter ants, in natural
environments, cause the removal of leaf area in plants
(ELIZALDE et al., 2019), which results in decreases in the
photosynthetic rate, influencing the shape of the bole, the
quantity and quality of the wood produced and even
influencing the survival of damaged trees. Ants of the genera
Atta fabricius and Acromyrmex mayr are the ones that cause the
Tree species susceptibility to leaf-cutting ants attack in carbon neutralization plantations
Nativa, Sinop, v. 9, n. 5, p. 567-572, 2021.
568
most damage and losses (RABELING et al., 2019; SEGRE;
TAYLOR, 2019).
The search for plants resistant to insect attack is a viable
alternative to contain pest populations, without causing
damage to the environment and without burden to producers
(SINGH; KAUR, 2018), which are not restricted only to
decreased production, but it also affects the resistance of
plants, leaving them more vulnerable to new attacks
(CABRAL, 2015).
Leaf-cutter ants have selectivity in choosing attacked
plants (ARENAS; ROCES, 2016). This selective capacity is
manifested during foraging, when choosing certain species,
and even, certain origins of the same forest species. Although
leaf-cutter ants are highly polyphagous insects, some
vegetables escape their attack almost completely because they
probably have chemical defenses against the ants themselves,
their fungus, or both. The selectivity of ants is related to the
physical properties of the leaves, such as: the presence and
density of trichomes, thickness and hardness, the latter two
being related to water content. Leaf-cutter ants also prefer
pioneer plant species, this is probably due to their low level
of chemical defenses and their high nutritional content
(COLEY et al., 1985).
The increase in the number of works in the control areas
is constant, especially related to the resistance of plants, in an
attempt to seek alternatives, or even to make possible an
association of different control strategies for leaf-cutter ants.
Thus, the objective was to evaluate the susceptibility of tree
species to the attack by leaf-cutter ants in carbon
neutralization plantations and to create a list that classifies the
resistance of tree species to the attack of these insects.
2. MATERIAL AND METHODS
The study was conducted at the GHG emissions
neutralization plantations of the Carbono Zero Program
belonging to the Federal University of Viçosa (UFV), at the
UFV Open Space of Events, in Viçosa-MG (20º45'35 “S and
42º52'29” O).
The climate in the region is the Cwa type, according to
the Köppen system, that is, mesothermal with hot and rainy
summers, and cold and dry winters. Red Latosol and Yellow
Alico soils predominate in the region on the tops of the hills
and Red-Yellow Podzolics on the terraces, the relief is
characterized by hills in the form of spikes, sectioned by the
natural drainage network and altitudes ranging from 650m to
800m.
The experiment was carried out in an area that has a
history of occurrence of leaf-cutter ants of the species Atta
sexdens (Hymenoptera: Formicidae) with impacts on tree
individuals (MORAIS JUNIOR et al., 2019). Whenever
necessary, the combat was carried out with the use of
sulfluramid-based insecticides. Evidence of high infestation
is the presence of regenerating forests of Mabea fistulifera
Mart., neighboring the planting areas, which have a symbiotic
relationship with leaf-cutter ants, close to the plantations
(PETERNELLI et al., 2004).
The plantations started in 2010, with one per year, with a
combination of forest species native to the region (Table 1),
spaced 2m x 2m. The neutralization plantations in the
evaluation period were 7, 6, 5, 4, 3 and 2 years old,
respectively. Most planting areas were covered by Urochola
decumbens (Stapf) R.D. Webster. The area was mowed to
reduce competition and 30 days before planting, the fight
against leaf-cutter ants was carried out using ant bait (0.3%
sulfluramid) and anticide was applied every 5 months (0.3%
sulfluramid) at the beginning and at the end of each planting
line. The monitoring of the area to control leaf-cutter ants,
crowning of the seedlings and controlling the scrubland were
performed periodically.
Biweekly assessments were carried out to evaluate the
incidence and severity of damage leaf-cutter ants attacks on
plants. Each plant was evaluated individually and always by
the same evaluator, with the same evaluation criteria.
The incidence and severity were evaluated in the
following plant compartments: leaves, barks, trunks,
branches, flowers, fruits, seeds, and exposed roots. The
herbivorism caused by leaf-cutter ants fits in the following
cases: partial leaf loss with semilunar shape on the leaf, leaves
cut between two consecutive evaluations and direct
observation of the action of leaf-cutter ants cutting or
transporting the leaves.
The degree of severity and the incidence of damage to
each tree were assessed according to the following scale of
scores: 0 - there was no injury/damage; 1 - there was at least
a little damage by leaf-cutter ants anywhere in the tree; 3 -
there was an intermediate situation of damage or a situation
of doubt between note 1 and note 5; 5 - there was an
exaggerated amount of damage caused by leaf-cutter ants
anywhere in the tree.
The analyses were performed excluding individuals who
died or suffered attacks by agents other than leaf-cutter ants.
The initial number of individuals of each species that were
assessed regarding the impacts of herbivorism by leaf-cutter
ants corresponded to the initial number of seedlings planted,
subtracting the excluded individuals (FERREIRA, 2015).
From the records of attacks by leaf-cutter ants, the mean of
severity (MS) and the frequency of attacks (FA) per individual
were calculated for each species, and a Damage Index (DI)
was created: DI = MS * FA. This index was used to classify
speciesThe classified species were divided into four groups
(Table 2).
Table 2. Classification of species according to their damage index.
Tabela 2. Classificação das espécies de acordo com seu índice de
dano.
Classification of species ID
Potential for extraction of natural insecticides < 0,04
Less susceptible to leaf-cutting ants 0,04 < 0,39
Moderately susceptible to leaf-cutter ants attack 0,40 < 0,60
Highly susceptible to leaf-cutter ants > 0,60
In the cases where the same species were analyzed in
more than one plantation, for classification purposes, the
highest score was considered.
3. RESULTS
In planting 1, Zeyheria tuberculosa was the species with the
highest DI. Dalbergia brasiliensis, Adenanthera pavonina and Inga
vera were species with considerable damage (Table 3). Psidium
cattleyanum, Schinus molle, Eremanthus erythropappus, Cedrela fissilis
and Syzygium cumini were not attacked. In plantation 2,
Citharexylum myrianthum was the species with the highest MS
followed by Pleroma granulosum and Genipa infundibuliformis.
Pseudopiptadenia contorta and Peltophorum dubium were the least
attacked species in this planting. The 3 years old planting
showed the highest damage index for the species evaluated.
Ceiba speciosa was the species that suffered the greatest attack.
Citharexylum myrianthum and Genipa infundibuliformis also stood
Schettini et al.
Nativa, Sinop, v. 9, n. 5, p. 567-572, 2021.
569
out as the most attacked. Peltophorum dubium and
Anadenanthera colubrina var. cebil were the species with the
lowest rates, repeating the low attack rates in relation to the
other species (Table 3).
Table 1. Number of individuals and species identified in each of the neutralization plantations evaluated.
Tabela 1. Número de indivíduos e espécies identificados em cada plantio de neutralização avaliado.
Species
Family
10
11
12
13
14
15
L.
Fabaceae
11
3
4
Albizia niopoides
(Spruce ex Benth.)
Burkart
Fabaceae
26
17
49
Albizia niopoides
(Spruce ex Benth.) Burkart
Fabaceae
12
15
Amburana cearenses
(Allemão) A.C. Sm.
Fabaceae
7
Anadenanthera colubrina
(Vell.) Brenan
Fabaceae
16
Anadenanthera colubrina
var.
cebil
(Griseb
.) Altschul
Fabaceae
27
29
52
15
16
6
Andira anthelmia
(Vell.) Benth
Fabaceae
10
7
16
Apuleia leiocarpa
(Vogel) J.F.Macbr.
Fabaceae
12
Pachira glabra
Pasq.
Malvaceae
4
14
16
15
Libidibia ferrea
var.
leiostachya
(Benth.)
L.P.Queiroz
Fabaceae
11
Cenostigma pluviosum
(DC.) E. Gagnon & G.P. Lewis
Fabaceae
1
5
Cariniana legalis
(Mart.) Kuntze
Lecythidaceae
2
Cassia grandis
L.f.
Fabaceae
13
11
8
Cedrela fissilis
Vell.
Meliaceae
3
7
5
Ceiba speciosa
(A. St.
-
Hil.) Ravenna
Malvaceae
6
12
20
Centrolobium tomentosum
Guillem. ex Benth.
Fabaceae
15
Clitoria fairchildiana
R.A. Howard
Fabaceae
8
Colubrina glandulosa
Perkins
Rhamnaceae
11
4
13
11
Copaifera
langsdorffii
Desf.
Fabaceae
Cybistax antisyphilitica
(Mart.) Mart.
Bignoniaceae
4
Citharexylum myrianthum
Cham.
Verbenaceae
4
4
11
7
10
8
Dalbergia brasiliensis
Vogel
Fabaceae
2
Dalbergia nigra
(Vell.)Allemão ex Benth.
Fabaceae
5
15
Enterolobium contortisiliquum
(Vell.) Morong
Fabaceae
2
16
9
Eremanthus erythropappus
(DC.) McLeish
Asteraceae
4
4
Eugenia uniflora
L.
Myrtaceae
12
Gallesia integrifolia
(Spreng.) Harms
Phytolaccaceae
8
Garcinia
gardneriana
(Planch. & Triana) Zappi
Clusiaceae
14
Genipa americana
L.
Rubiaceae
15
6
5
Handroanthus serratifolius
(Vahl) S. Grose.
Bignoniaceae
6
Handroanthus chrysotrichus
(Mart. ex DC.) Mattos
Bignoniaceae
5
18
15
Handroanthus impetiginosus
(Mart. ex DC.) Mattos
Bignoniaceae
4
Hymenaea courbaril
L.
Fabaceae
13
3
8
14
26
7
Ilex cerasifolia
Reissek
Aquifoliaceae
6
Inga vera
Willd
Fabaceae
28
18
28
Jacaranda mimosifolia
D. Don
Bignoniaceae
12
Joannesia princeps
Vell.
Euphorbiaceae
7
13
12
4
Lecythis pisonis
Cambess.
Lecythidaceae
6
11
3
15
4
Machaerium nyctitans
(Vell.) Benth.
Fabaceae
15
Metrodorea nigra
A.
St.
-
Hil.
Rutaceae
16
17
8
Astronium urundeuva
(M. Allemão) Engl.
Anacardiaceae
18
Paubrasilia echinata
(Lam.) Gagnon, H.C. Lima & G.P.
Lewis Fabaceae 12
Peltophorum dubium
(Spreng.) Taub.
Fabaceae
41
31
21
34
15
Piptadenia gonoacantha
(Mart.) J.F. Macbr.
Fabaceae
3
Chloroleucon tortum
(Mart.) Pittier
Fabaceae
Plathymenia reticulata
Benth.
Fabaceae
5
10
Pseudopiptadenia contorta
(DC.)
G.P. Lewis & M.P. Lima
Fabaceae
17
2
Psidium cattleyanum
Sabine
Myrtaceae
3
2
10
Psidium guajava
L.
Myrtaceae
3
13
Samanea inopinata
(Harms) Barneby & J.W. Grimes
Fabaceae
19
8
Sapindus saponaria
L.
Sapindaceae
6
4
14
17
Schinus molle
L.
Anacardiaceae
5
17
Schinus terebinthifolia
Raddi
Anacardiaceae
2
18
20
14
Schizolobium parahyba
(Vell.) Blake
Fabaceae
13
9
Senna macranthera
(DC. ex Collad.) H.S. Irwin &
Barneby Fabaceae 6 3 13 3
Sterculia striata
A. St.
-
Hil. & Naudin
Malvaceae
7
8
Syzygium cumini
(L.) Skeels
Myrtaceae
3
18
Tabebuia roseoalba
(Ridl.) Sandwith
Bignoniaceae
Pleroma granulosum
(Desr.) D. Don
Melastomataceae
5
5
Zeyheria tuberculosa
(Vell.) Bureau ex Verl
.
Bignoniaceae
14
6
6
9
Tree species susceptibility to leaf-cutting ants attack in carbon neutralization plantations
Nativa, Sinop, v. 9, n. 5, p. 567-572, 2021.
570
Leaf-cutter ants perform activities inside and outside the
colony (ELIZALDE; SUPERINA, 2019), in view of this,
physiological, behavioral and foraging aspects are relevant
points in their control, which is based on the use of
sulfluramid based compounds (FERRO et al., 2018). The
results obtained in this study are directly related to the daily
life of the implantation of carbon offset plantations in areas
with intense attacks by leaf-cutter ants. A possible strategy to
be adopted from these results to minimize the losses caused
by leaf-cutter ants is the use of species resistant to the attacks
(FOELKEL, 2009), which occur mostly in hot and rainy
periods (MACEDO; LANGENHEIM, 1989).
In the 4-year planting, Ceiba speciosa and Handroanthus
chrysotrichus were the species with the highest DI. Schinus
terebinthifolia and Cariniana legalis were the most resistant to the
attack of leaf-cutter ants. The 5-year planting, Ceiba speciosa
and Handroanthus serratifolius were the species with the highest
DI, and Schinus terebinthifolia and Dalbergia nigra were those
with the lowest DI (Table 4).
Table 3. Five species with the highest damage index in plantations 1, 2, 3, 4, 5 and 6.
Tabela 3. Cinco espécies com maior índice de dano nos plantios 1. 2, 3, 4, 5 e 6.
Planting 1 (2010) Planting 2 (2011)
Specie MS FA ID Specie MS FA ID
Z. tuberculosa 0,97 1,00 0,97
C. myrianthum 1,25 1,00 1,25
D. brasiliensis 0,92 1,00 0,92
P. granulosum 1,08 1,00 1,08
A. pavonina 0,85 0,82 0,70
G. infundibuliformis 1,03 1,00 1,03
I. vera 0,71 0,93 0,66
H. chrysotricha 1,00 1,00 1,00
S. saponaria 0,57 0,83 0,47
A. pavonina 1,22 0,67 0,82
Planting 3 (2012) Planting 4 (2013)
Specie MS FA ID
Specie MS FA ID
C. speciosa 2,85 1,00 2,85
C. speciosa 1,20 1,00 1,20
C. myrianthum 1,97 1,00 1,97
H. chrysotricha 0,76 1,00 0,76
G. infundibuliformis 1,40 1,00 1,40
B. glabra 0,70 1,00 0,70
S. inopinata 1,24 1,00 1,24
C. myrianthum 0,69 1,00 0,69
P. gonoacantha 1,08 1,00 1,08
C. glandulosa 0,62 0,92 0,57
Planting 5 (2014) Planting 6 (2015)
Specie MS FA ID
Specie MS FA ID
C. speciosa 1,63 1,00 1,63
G.integrifolia 1,25 1,00 1,25
H. serratifolius 0,78 0,78 0,61
L. pisonis 0,92 1,00 0,92
P. echinata 0,58 0,83 0,48
I. cerasifolia 0,89 1,00 0,89
C. tomentosum 0,60 0,67 0,40
C. antisyphilitica 0,88 1,00 0,88
B. glabra 0,52 0,75 0,39
B. glabra 0,65 0,87 0,57
Table 4. Five species with the lowest damage index in plantations 1, 2, 3, 4, 5 and 6
Tabela 4. Cinco espécies com maior índice de dano nos plantios 1. 2, 3, 4, 5 e 6.
Planting 1 (2010) Planting 2 (2011)
Specie MS FA ID Specie MS FA ID
P. cattleianum 0,00 0,00 0,00
A. macrocarpa 0,02 0,10 0,00
S. molle 0,00 0,00 0,00
M. nigra 0,03 0,06 0,00
E. erythropappus 0,00 0,00 0,00
A. hassleri 0,03 0,06 0,00
C. fissilis 0,00 0,00 0,00
P. dubium 0,03 0,01 0,00
S. jambolanum 0,00 0,00 0,00
P. contorta 0,00 0,00 0,00
Planting 3 (2012) Planting 4 (2013)
H.courbaril 0,14 0,88 0,12
S. macranthera 0,07 0,23 0,02
A. hassleri 0,17 0,67 0,11
C. grandis 0,05 0,15 0,01
A. macrocarpa 0,08 0,38 0,03
A. macrocarpa 0,01 0,07 0,00
P. dubium 0,07 0,24 0,02
S. tererebinthifolius 0,00 0,00 0,00
S. terebinthifolius 0,03 0,33 0,01
C. legalis 0,00 0,00 0,00
H.courbaril 0,14 0,88 0,12
S. macranthera 0,07 0,23 0,02
Planting 5 (2014) Planting 6 (2015)
Specie MS FA ID
Specie MS FA ID
A. macrocarpa 0,05 0,31 0,02
E. erythropappus 0,06 0,25 0,02
P. dubium 0,07 0,21 0,02
P. dubium 0,06 0,20 0,01
G. gardneriana 0,04 0,01 0,00
S. molle 0,01 0,12 0,00
S. terebinthifolius 0,03 0,14 0,00
M.urundeuva 0,01 0,06 0,00
D. nigra 0,02 0,20 0,00
D. nigra 0,00 0,00 0,00
Schettini et al.
Nativa, Sinop, v. 9, n. 5, p. 567-572, 2021.
571
4. DISCUSSION
The list can provide bases for indicating more resistant
species, which can decrease costs associated with replanting
and maintenance in carbon neutralization projects. In the
present study there is no pattern of attack according to the
level of ecological succession of the species, and it is not
possible to generalize based on this question. The mean of
severity varied between species, which indicates selective
foraging (COSTA et al., 2019; COSTA et al., 2017).
The number of species classified as indicated for GHG
neutralization plantations were 24, and 22 were classified as
not indicated. The group of species with DI between 0.04
and 0.39 can be seen as an indicator of the species that should
be used primarily in places where leaf-cutter ants are an
ecological filter to be overcome.
The behavior of ants is variable, which are classified as
generalists (BEGON; TOWNSEND, 2021), and as selectives
(WIRTH et al., 2007), according to the species preference. In
the current study, it was observed that leaf-cutter ants cut
leaves from most species, but the foraging was not the same
among them. These results show a behavior that is better
explained by the optimal foraging theory, where leaf-cutter
ants collect from all potential food sources so that the
colonies can have an idea of food distribution and, thus, they
become aware of the best cost-benefit choices, that is, many
plant species are visited by ants, but foraging is not
concentrated in all of them (BEGON; TOWNSEND, 2021).
Based on this behavior, the diet of leaf-cutter ants is
influenced by the richness of species in the plant community,
in other words, the more diverse the community is, more
species will be included in the foraging (DEL-CLARO;
TOREZAN-SILINGARDI, 2012). The differences in the
frequency and intensity of attacks between species are
probably related to evolutionary aspects in plant defense
(KOST et al., 2011).
Schinus molle, Schinus terebinthifolia, Pseudopiptadenia contorta,
Copaifera langsdorffii, Cariniana legalis, Platonia insignis and
Astronium urundeuva are species with DI less than 0.04 and that
are indicated for mixed plantations. They were also classified
in another group of species, because they may have potential
for studies to discover natural insecticides, taking into
account the natural rejection of ants by these species.
The species Adenanthera pavonina, Pachira glabra,
Citharexylum myrianthum, Ceiba speciosa, Cybistax antisyphilitica,
Dalbergia brasiliensis, Enterolobium contortisiliquum, Gallesia
integrifolia, Genipa americana, Handroanthus serratifolius,
Handroanthus chrysotrichus, Ilex cerasifolia, Inga vera, Joannesia
princeps, Lecythis pisonis, Metrodorea nigra, Piptadenia gonoacantha,
Samanea inopinata, Sapindus saponaria, Senna macranthera, Pleroma
granulosum, Zeyherya tuberculosa with DI greater than 0.60,
should be avoided. It is recommended to avoid these species
in plantations for carbon neutralization in areas with intense
attack of leaf-cutter ants.
The presence of specific toxic constituents such as
saponins or aluminum also influences the foraging of leaf-
cutter ants (FOLGARAIT et al., 1996). Less attacked species,
with DI below 0.04, such as anacardiaceae Schinus molle,
Schinus terenbinthifolia, Astronium urundeuva and the Copaifera
langsdorffii, Cariniana legalis and Garcinia gardneriana, may be an
indicative of species that contain those compounds, as they
are naturally avoided by leaf cutting ants.
Centrolobium tomentosum, Psidium cattleyanum, Paubrasilia
echinata, Sterculia striata, Andira anthelmia and Colubrina
glandulosa were classified in the group of those moderately
indicated with DI between 0.60 and 0.40. Plantations aiming
to neutralize GHG emissions from any activity are effective,
and the choice of species with greater resistance to ant attack
contributes to a greater success of these plantations. This fact
reinforces the need to conduct studies that relate the
susceptibility of forest species to the damage caused by leaf-
cutter ants.
5. CONCLUSIONS
Most species (98.3%) are attacked by leaf-cutter ants and
the mean of severity varied, indicating selective foraging. This
makes it possible to classify the species in: 29 in the group of
those not indicated, and within this group 7 of the species
have potential for the extraction of chemical compounds, 6
in the group of moderately indicated, 24 in the group of
indicated, which proves the selectivity of trees species by leaf-
cutter ants. The use of species resistant to the attack of leaf-
cutter ants should be prioritized to the carbon neutralization
project become more successful. On the contrary, those most
susceptible species should be avoided.
There are species very resistant or species that are not
attacked by leaf-cutter ants. Thus, these species can provide
efficient active ingredients in the fight against leaf-cutter ants,
so these species can be the target of biochemical and
physiological investigations in the search for new
formulations of insecticides on the market.
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