Journal of Phytopathology and Pest Management 10(1): 37-48, 2023
pISSN: 2356-8577 eISSN: 2356-6507
Journal homepage: http://ppmj.net/
Corresponding author: Marotea Vitrac,
E-mail: maroteav@gmail.com
37
Copyright © 2023
Arthropod fauna and rats in organic sugarcane in Tahiti
Marotea Vitrac1*, Taivini Teai1, Ines Shili-Touzi2, François-Régis Goebel3
1Research Mixt Unity about Insular Ecosystems in Ocenia (UMR 241 EIO), University of French Polynesia, Punaauia, French Polynesia
2ADI-Suds, ISTOM Ecole supérieur d’Agrodéveloppement International, Angers, France
3Agroecology and Sustainable Intensification of Annual Crops Department, CIRAD, Agricultural Research for Development, Montpellier, France
Abstract
Keywords: Saccharum officinarum, noble canes, arthropods, rats, Tahiti, organic agriculture.
As organic sugarcane is promised to an important development in French Polynesia
thank to the high-quality rum produced in this part of the world, preliminary studies
on main biotic constraints were conducted on this crop between 2018 and 2021 to
better apprehend their control. Visual observations at regular intervals and captures
using different types of traps were carried out to collect and identify the arthropod
fauna in Tahiti Island. With no surprise, stemborer insects were the most important
pests of sugarcane in these different areas. We were also able to identify key
predators and parasitoids that are important to preserve for natural control of these
pests. Stem borers and rats are a big concern in most islands and like the other pests,
we make propositions here to implement some tactics of agroecological crop
protection.
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38
1. Introduction
No main agricultural crops (maize, soya,
wheat, beans) is cultivated in French Polynesia
due to the small size of the agricultural land
owned by farmers, generally between 0.5 to 10
ha. However, the sugarcane sector has strong
development potential in several islands of
French Polynesia and mainly in Tahiti as rum
sales from small specific productions are
increasing worldwide. Actually, the studies
conducted regarding arthropod fauna in the
islands of French Polynesia were mainly
related to vegetables and market gardening
which are the only cash crops since the end of
the twentieth century (Paulian, 1998). Despite
the isolation and geographical remoteness of
the islands of French Polynesia, an interesting
entomological richness in term of insect
species (harmful and useful) is observed and
most of the insects and mites were probably
introduced by humans through commercial
routes or by so-called passenger traffics
(Ryckewaert, 1984). In this context, the
sugarcane areas are still modest, around 50
hectares in total (whom 10 hectares under
organic certification standards) and this crop is
conducted according to organic farming
methods and produces an exceptional rum,
with an IGP (Protected Geographical
Indication) approach. In Polynesian farms,
Saccharum spp. modern canes are grown with
Saccharum officinarum noble canes (Vitrac et
al., 2018a). The presence of noble canes
guarantees a rum with a strong aromatic
character (non-published data). The use of this
type of canes, which are very sensitive to pests,
diseases and weeds (Vitrac et al., 2018b), is
unusual and it is mainly devoted to rum
industry. In such a context of strong
development of this crop in the near future, it is
necessary to carry out a preliminary inventory
of arthropod pests in order to prevent the crop
from heavy damage and yield loss, especially
regarding the high sensitivity of noble canes,
the development of diseases and the resulting
disturbance of the whole sector. This article
does not mention weeds, a topic that has
already been published (Vitrac et al., 2019a).
The focus of this study was put on arthropods
and rats, such as stem borers and their natural
enemies: predators and parasitoids according
to visual field inspections and the use of
different types of traps to investigate the
arthropod diversity. These studies, conducted
between 2018 and 2021 have made possible
their identification for the very first time in this
particular context of organic certified and
agroecological fields. As an example, it seems
that organic conversion had an effect on the
composition of saprophagous macrofauna
fields in Martinique island (Coulis, 2021)
where thousands of hectares of conventional
sugarcane were grown for more than 30 years.
Therefore, we wanted to know the type of
arthropod fauna living and developing in the
specific context of organic sugarcane. In the
manual of crop protection published in Tahiti
(Hammes et al., 1989; Hammes & Putoa,
1986), some insects such as Rhabdoscelus
obscurus Boisduval were already mentioned as
stem borer, but nothing regarding other borer
species such as Chilo saccariphagus or
Tetramoera schistaceana which causes
important damages and yield losses in China
(Pan et al., 2021). C. sacchariphagus and
Eldana saccharina are also mentioned as key
stem borers in Reunion Island (Goebel & Way,
2009) but these authors didn’t mention R.
obscurus. This situation is not unique and is
similar to what is observed in other countries
such as Australia and Fiji were no Lepidoptera
stem borers are found but R.obscurus is present
(Goebel & Salam, 2011). Moreover, the rats
are in the list of key pests of sugarcane in
Polynesia (Sechan, 1987; Hood et al., 1970). A
preliminary study has already been conducted
by Vitrac et al. (2018b), showing the high
sensitivity of S. officinarum noble canes). In
this study, preliminary results are presented
about the biodiversity of arthropods and rats in
sugar cane for the very first time and additional
information is given on the biology of pests
and their damage and explore possible avenues
for an agroecological management plan, such
as the push-pull technique, which use attractive
ER Yeşim, 2023
39
plants around or inside the sugarcane fields to
reduce pest populations by using selective
treatments only done inside these special areas
(Nibouche et al., 2019).
2. Materials and methods
2.1 Agricultural practices in organic sugarcane
production
All the fields studied were organic certified for
both European (UE) and Pacific rules
(NOAB). Vitrac et al. (2019a) defined the
following soil preparation and cultural
practices: before planting, the soil was worked
to a depth of 15 cm then furrowed in twin rows,
close together: 50 cm and distant from each
other of 1.60 m. This spacing of 1.60 m (inter
row) allows the passage of a small 4x4 tractor
of 16 Horsepower (HP) equipped with a rotary
cutter with blades allowing the mechanical
weeding over 1.1 m in width. The arrangement
in double rows makes it possible to densify the
planting, the double row having to end up
merging into a single and wide row. Due to the
scarcity of plant material from recent local
surveys, planting was carried out with 8-week-
old plants raised in the nursery from one-eye
cuttings (Poser et al., 2020). The seedlings
were manually transplanted into the furrows at
50 cm intervals and in staggered rows, their
survival rate was close to 100%. The weeding
on the row was carried out using a “serpette”,
the local name for a small manual hoe. Organic
compatible organo-mineral fertilization
consisted of three inputs of distillery vinasses
(20 t/ha, source of K), composted horse
manure (5 t/ha, source of NP) and crushed
dolomite (2 t/ha, source of CaMg), applied
directly, mainly in the rows at the foot of the
canes. These organic fertilizers were applied
for the first time after the first post-planting
weeding. Rainfall and temperatures were
recorded using an automatic gauge between
January 2018 and October 2020.
2.2 Experimental sites and observation plots
2.2.1 Afaahiti site
This site (17°45'15.8"S 149°15'24.1"W) was
free of any crop and is representative of natural
vegetation and biodiversity, allowing organic
certification. A plot of modern RRV sugarcane
variety (red color modern Saccharum spp.
variety found locally, non-published data) was
planted in April 2018 on 2 500 m2 with a light
slope of about 3%. Different trapping systems
(soil surface, aerial) were installed in May
2018 in an experimental design of 12 plots
(Figure 1) comprising a set of one pitfall trap
(white cylinder plastic container of 1 liter) and
one yellow sticky trap (50 × 30 cm fixed at 50
cm height) per plot. The pitfall traps were
buried in the soil, filled with a 100ml of
solution containing 10 g/l of saccharose and
were covered by yellowish roof to avoid water
from rainfall coming inside the trap. Yellow
color was chosen because of its attractiveness
regarding insects. The insects were captured,
identified and counted. Material was discarded
after counting and reinstalled at each period:
15/12/2018; 5/2/2019 only for pitfall traps and
25/3/2019; 15/5/2019; 15/7/2019 and 5/9/2019
for pitfall and sticky traps.
2.2.2 Toahotu site
This site (17°45'30.1"S 149°17'21.4"W) was
the first plantation of organic certified
sugarcane plants in 2013 on old pineapple
fields stopped in 2007. It was renewed and
grown with varieties of noble canes in 2016 on
3000 m2, a plot where most of the research
studies regarding noble varieties were usually
conducted from 2016 (Vitrac et al., 2018b). In
2019, 3rd ratoon was in process. No insect traps
(pitfall or sticky) were used on this site. Only
borers were monitored. No statistical analysis
ER Yeşim, 2023
40
was done regarding arthropods observations
and inventory because of the high variability
regarding the number of insects captured in our
traps (unnatural distribution of populations).
2.3 Observations of stem borers
In Afaahiti site, a sample of 6 stems for 12
plots (72 stems) were harvested at 3 periods of
time (15/5/2019; 15/7/2019 and 5/9/2019) and
were split open longitudinally to check the
presence or absence of stem borers (Figure 1).
Sampling in Toahotu site was conducted at the
same period: 15/5/2019; 15/7/2019 and
5/9/2019. Six stems were harvested at 10 m,
triplicates sampled on the same row, for the
same variety, in the middle row to avoid
border effects (18 canes per variety). Varieties
were the following: 2 nobles Saccharum
officinarum varieties found locally in 2014,
JRP (yellowish color cane, non-published
data) and RBV (light red purple striped color
cane, non-published data) and 2 modern ones,
RRV and B69566 (introduced from CIRAD
Visacane in 2016). In Toahotu site, samples
were also observed in September 2018. In this
case 3 bunches of 30 stalks were harvested on
10m. Triplicates were also sampled on the
same row, for the same variety, in the middle
row to avoid border effects.
Figure 1: Afaahiti experimental plot. Arthropods (aerial and soil fauna) and rats were
monitored during 10 months between December 2018 and September 2019 on this first
organic certified plantation of modern RRV sugarcane variety.
3% slope
S
rows of sugarcane
2m²N 6 5 4 3 2 1
S S S S
S S S S
S S S S
R R
1,2, [] 12: 12 plots S Sticky traps Pit fall traps
R : rat traps reproduced on each plots: sampled borer cane plants
10m R: counted stalks attacked by rtats on 10m
1
2
3
6
9
8
5
7
10m R
10m R
10m R
12
4
10
11
P
P
P
P
P
P
B
B
B
B
B
P
B
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41
2.4 Observations of rat populations
For both Afaahiti and Toahotu sites, two
mechanical traps for rat control were installed
in March 2019 on the 3rd ratoon of the variety
B69566 every time in border of plots, close to
the natural vegetation. These traps use a
chemical pheromone to attract them and a
mechanical killing system and allow us to
count killed rats (electronic counter). Control
and counting of killed rats were conducted
every 2 weeks between April and October
2019, and then these killed rats were removed
after each control. In addition, in July and
September 2019, the stalks attacked by rats
were counted on 3x10m inside the field on the
middle row of each plot for each site (Figure
1). A treatment with Brodifacoum (0.005%)
was applied in the first week of July 2019. The
same procedure was applied one year before,
in June and July 2018 in Toahotu site for four
varieties, modern ones as RRV and B69566
and also two noble canes as JRP and RBV.
2.5 Statistical analysis regarding stem borers
and rats
Data was analyzed using the statistical
software XLSTAT 19.4.45191. A population
probability law (normal distribution) and
descriptive statistical parameters such as mean
and standard deviations were processed.
Means comparison tests of Mann Whitney
(samples<30) were used to compare borers
populations between varieties sampled.
2.6 Sampling and identification of macrofauna
Rainfall and temperatures were recorded using
an automatic gauge between January 2018 and
October 2020 in Afaahiti site. In Figure (2),
the successive weeding operations since
planting are positioned in relation to the
harvests and the monthly rainfall. All
measurements were conducted on the row
located on the middle of each plot (grey
columns on Figure 1) to avoid border effects.
Figure 2: Pattern of rainfall and temperatures in Afaahiti site and successive operations since planting in April
2018 (black arrows show plantation and harvest in early October 2019). For all the macrofauna observations;
P: pitfall traps; S: sticky traps; B: borers. Discontinued black arrows (June and December 2018) shows
operations of maintenance (mechanical and manual weed removing).
ER Yeşim, 2023
42
All arthropods collected in the pitfall and
sticky traps for 10 months were photographed
at each period for each sample. For pitfall
traps, samples were kept in 90° alcohol
solution and identified by entomologists from
CIRAD, based in Montpellier, using the
database of images and morphological
characteristics observed under a
stereomicroscope. Regarding the borer
species, stalks were split opened to visualize
attacks and tunnels inside the internodes.
Damaged stalks were counted, and the insects
were collected and also kept in alcohol for
further identification.
3. Results and Discussion
3.1 Arthropods
The arthropods levels and diversity are
presented in Figure (3). In pitfall traps, 29
different arthropods were identified whom 15
of more than 1% represented 94.83% of the
global amount. The 5 most abundant species
represented 74.87% of the number of
arthropods captured; they were composed of
natural predators such as Chelisoches morio
(25.07%) and Coleoptera Coccinelidae
(22.79%) and also insect pests (Scolytidae,
8.63%). C. morio (Dermaptera, Forficulidae)
was the main species captured. This species is
an important natural predator of crop pests
(Zhong et al., 2016). Spiders as generalist
predators were also well represented in our
catches (3.51%). It was the most
representative group within the 10 species
found between 1 and 5%. It is also observed
the presence of the centipede Scolopendra sp.
(Myriapoda) (0.89%) which is a generalist
predator of many insect species. In the sticky
traps, we identified 25 different arthropods
whom 7 of more than 1% represented 88.15%
of the global amount. C. morio was also
captured (1.30%) in these traps where 87.47%
are flies. It was also noticed that the presence
of bees which are good pollinators is
interesting in organic sugarcane fields free of
pesticides.
Figure 3: Cumulative numbers of arthropods (abundance) from pitfall (left) and sticky
(right) traps with different levels from grey to black for each period of sampling.
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A global amount of 992 arthropods collected in
this context of organic agriculture during the
10 months of sampling and regarding the
observations, we found 14 orders and 33
families (Table 1). Atencio et al. (2019) also
found a great diversity in similar context of
agroecological sugarcane plantations with
4735 insects collected for 26 months.
Table 1: Identification of arthropods captured in our traps in Tahiti.
Order
Family
Genus
Species
Common name
Feeding
Role
Coleoptera
Curculionidae
Rhabdoscelus
obscurus
Cane weevil
Sugarcane
Pest
Coleoptera
Cetonidae
Protaecia
fusca
Mottled flower
Flowers, fruits
Pest
Coleoptera
Elateridae
Chalcolepidius
silbermanni
Click beetle
Roots
Pest
Coleoptera
Carabidae
Carabid beetle
Invertebrates
Predator
Coleoptera
Scolytidae
Xyloborus
perforans
Borer beetle
Wood
Pest
Coleoptera
Nitidulidae
Carpophilus
humeralis
Pineapple beetle
Pineapple, cane
Pest
Coleoptera
Staphylinidae
Small rove beetle
Invertebrates
Predator
Lepidoptera
Noctuidae
Spodoptera
mauritia
Armyworm
Leaves
Pest
Lepidoptera
Nymphalidae
Melanitis
leda solendra
Evening brown
Leaves
Pest
Lepidoptera
Crambidae
Marasmia
trapezalis
Leafeater moth
Leaves
Pest
Lepidoptera
Lycaenidae
Lampides
boeticus
Azuré porte-queue
Leaves
Pest
Hemiptera
Plataspidae
Brachyplatys
subaeneus
Black bean bug
Sap sucking
Pest
Dermaptera
Chelisochidae
Chelisoches
morio
Earwigs
Invertebrates
Predator
Neuroptera
Chrysopidae
Chrysoperla
congrua
Green lacewings
Invertebrates
Predator
Dyctioptera
Iridopterigydae
Tropidomantis
tenera
Preying mantis
Invertebrates
Predator
Orthoptera
Tettigoniidae
Conocephalus
longipennis
Meadow grasshopper
Invertebrates
Predator
Diptera
Tephritidae
Euaresta
bella
Fruit fly
flowers, fruits
Pest
Diptera
Syrphidae
Hover fly
Invertebrates
Predator
Diptera
Dolichopodidae
Green fly
Invertebrates
Predator
Hymenoptera
Vespidae
Polistes
olivaceus
Hornets
Invertebrates
Predator
Hymenoptera
Sphecidae
Pryonix
spp
Thread-waisted wasp
Invertebrates
Predator
Hymenoptera
Ichneumonidae
Ophion
spp
Parasitic wasp
Invertebrates
Predator
Hymenoptera
Formicidae
Solenopsis
geminata
Fire ant
Invertebrates
Predator
Blattodea
Blatellidae
Blatella
germanica
German cockroach
Invertebrates
Predator
Hemiptera
Lygaeidae
Nysius
spp
False chinch bug
Sap sucking
Pest
Hemiptera
Delphacidae
Peregrinus
maidis
Corn planthopper
Sap sucking
Pest
Hemiptera
Derbidae
Cedusa
spp
Blue panthopper
Sap sucking
Pest
Hemiptera
Pseudococcidae
Saccharicoccus
sachari
Pink mealybugs
Sap sucking
Pest
Hemiptera
Pseudococcidae
Antonina
graminis
Grey mealybugs
Sap sucking
Pest
Hemiptera
Aleyrodidae
Neomaskellia
bergii
Sugarcane whitefly
Sap sucking
Pest
Myriapoda
Scolopendridae
Scolopendra
Invertebrates
Predator
Myriapoda
Centipede
Invertebrates
Predator
Arachnida
Tetragnathidae
Spider
Invertebrates
Predator
Arachnida
Salticidae
Plexippus
paykulli
Spider
Invertebrates
predator
It is admitted that arthropods diversity and
abundance are low under conventional
sugarcane agriculture, but studies are scarce
and even mineral or organic fertilization does
have significant effects on diversity and
amounts on invertebrate populations (Chi et
al., 2020). Moreover Coulis (2021) found no
significant difference between organic (in
conversion) and conventional fields regarding
the diversity of soil macrofauna. However,
these studies were limited to the saprophagous
macrofauna and didn’t consider the arthropod
biodiversity of the aerial parts of sugarcane as
we did in this present study. In addition, the
impact of pesticides in the upper part of the
vegetation is generally higher as most of flying
predators and parasitoids live there and their
activity is obviously limited by the use of
chemical spraying (Snchez-Bayo, 2011).
Loranger et al. (1998) showed the influence of
pesticides under different agricultural systems
in a similar context in Martinique and their
clear impact on reducing arthropods’ presence
and activity. But as agriculture is still
underdeveloped in Tahiti, an interesting
richness in terms of insect species is generally
observed (Hammes et al., 1989; Ryckewaert,
1984) even if the use of pesticides can be very
ER Yeşim, 2023
44
high locally (Ryckewaert, 2004). It indicates to
us a good level of biodiversity in our organic
cultivated sugarcane fields.
3.2 Stem borers
The main species of stemborer found in
Tahitian sugarcane is Rhabdoscelus obscurus
Boisduval (Figure 4) already mentioned by
Hammes et al. (1989). No other borer species
were observed. The infestation levels are
indicated in Table (2). They are about 6,1% for
the lower average of 1,1 canes infested by 18
samples and 51.7% for the highest (RBV,
Toahotu, 2018). These percentages are
representative about what Goebel et al. (2005)
found in South Africa: between 7,3 and 26,1%
of infested canes. Considering all the results,
the noble variety RBV is the most infested,
followed by B69566 (unauthorized under IGP
approach in 2022). Damage levels by R.
obscurus increased from May to September
following the maturation of the canes. At this
stage, cane stems are ready to be harvested and
RBV variety could be used only to attract R.
obscurus without any other treatments. It is
similar to push-pull strategy used by Nibouche
et al. (2019) with Erianthus arundinaceus as a
trap crop for the sugarcane stem borer Chilo
sacchariphagus. The difference is that no
treatment is needed and RBV variety can be
used as a useful plant which could be
harvested at the same time as the rest of the
fields contrary to B69566 which is not
authorized under IGP approach in 2022. It is
possible to cultivate it because of its good
ratoon (Vitrac et al., 2019b) and we could
plant for example 1 to 10 rows of canes.
Another way of control, added to the use of
RBV variety, could be to find a specific
parasitoid like Pan et al. (2021) did, using
Trichogramma and sex pheromones for
trapping and control Chilo sacchariphagus
and Tetramoera schistaceana.
Figure 4: Rhabdoscelus obscurus (Coleoptera, Curculionidae) Boisduval: adults on
the left and larva on the right (black and white scale in mm) and inside an infested
cane. Comparison of damaged stalks with the presence of holes and healthy canes
(in middle). Photos of the author (2019).
In Table (2), we observed that no RRV canes
were infested by stem borers in Afaahiti in
2019 for the 72 canes sampled for the whole
period. This result is surprising because in
Toahotu site RRV variety was infested in 2018
and in 2019 (3rd ratoon). We can thus
hypothesize that some contexts (like Afaahiti
in 2019) are free of stemborers regarding the
first plantation. We can also note the low level
of infested JRP variety. This is the major
potential of S. officinarum noble cane variety
regarding the Polynesian rum industry (Vitrac
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45
et al., 2019b). Noble varieties produce less
sugar and less biomass than modern varieties
(Vitrac et al., 2019b), especially in the early
season of June and July. At this stage, B69566
and RRV modern varieties present a Brix of 1
degree more than noble RBV and JRP and
higher concentrations in sucrose make them
more attractive for pests including stem borers
in this case. With a push-pull approach, we
could implement an experiment comprising
several rows of B69566 (unauthorized under
IGP approach in 2022) outside the fields to be
harvested, to attract stem borers and detect
their presence by using mechanical +
pheromone trapping as an efficient warning
system.
Table 2: Number of canes infested by stem borers on experimental sites.
Site
15/05/2019
15/07/2019
05/09/2019
Average
Standard deviation
Average
Standard deviation
Average
Standard deviation
Afaahiti 2019
RRV
0
-
0
-
0
-
Toahotu 2019
RRV
0
- ns
2.1
0.52 *
3
0.55 **
B69566
2.3
0.52 **
4.3
0.52 **
1.1
0.41 *
JRP
0
- ns
1.2
0.41 *
1.1
0.41 *
RBV
3.3
0.55 **
1.1
0.41 *
3.2
0.55 **
Toahotu 2018
15/9/18
RRV
5.3
1.5 *
B69566
5.3
1.5 *
JRP
1.3
1.2 **
RBV
9.3
3.1 ***
3.3 Rats
As weeds are the main constraints during the
vegetation period of sugarcane (Vitrac et al.,
2019a), rats are the most damaging pests
during the maturation period particularly on
noble canes where rat damage can totally
destroy the cane stalks before harvest (Vitrac
et al., 2018b). The identified rat killed by traps
by morphological approach (Séchan, 1987)
was Rattus exulans. No Rattus Norvegicus,
Rattus rattus or mice were observed. In 1970,
Hood et al. have already shown the big impact
of rats (Ratttus exulans) on Hawaian Polynesian
plantations aged of 15 months, with 5% of
stalks attacked by month. This period can be
compared to our plantation in the period of
July. The Figure (5) shows the levels of trapped rats
which increased from April to July and then
decreased after the treatment in September. It
seems that the response to Brodifacoum
treatment was more effective in Toahotu site.
Newly strip damaged are still quite high in
September for both sites due to the increase of
rat populations from June where the sugar
maturation generally starts. Brodifacoum (and
other raticides) treatment is accepted under
organic certified following a specific protocol:
several plastic tubes containing the rat baits are
placed inside the fields, and two or three days
after bait consumption, these plastic tubes are
removed. As an alternative to these baits, a
local mixture can be done to produce natural
baits, using Glyricidia sepium which is present
in Tahiti and French Polynesia (Berkelaar,
2011). It has the same effect as chemical
products such as Brodifacoum stopping the
synthesis of K vitamin. We can see in Table
(3) the low level of attacked JRP variety as it
was observed for borers. Noble varieties produce
less sugar and less biomass than modern varieties
(Vitrac et al., 2019b) (even if such a difference
is not significant in our context), especially in
the early season of June and July.
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46
Figure 5: (Evolution of killed rats by mechanical trapping. The black arrow indicates a
treatment using Brodifacoum 0,05% in early July 2019 for both sites.
At this stage, B69566 and RRV modern
varieties present a Brix of 1 degree more than
noble RBV and JRP. With a push-pull approach, we
can implement an experiment comprising some
rows of B69566, which is significantly more
attacked than the other varieties (Table 3), outside
the fields (because unharvestable under IGP
approach in 2022), to attract rats and detect
their presence by using mechanical and pheromone
trapping as an efficient warning system.
Table 3: Rat damages in Toahotu site in 2018 and Brix degrees.
Toahotu
2018
June
July
Rat damages
Brix
Rat damages
Brix
Total
Average
Standard deviation
Average
Standard deviation
Total
Average
Standard deviation
Average
Standard deviation
RRV
31
10,33
3,06
13,70
2,14
23
7,67
3,21
16,32
0,32
B69566
36
12,00
8,72
14,92
1,92
52
17,33
4,62
15,01
1,80
JRP
0
-
-
15,55
1,05
0
-
-
14,50
1,14
RBV
0
-
-
12,24
1,07
0
-
-
15,20
0,09
4. Conclusion
In this study, we identified the main arthropods
problems in the context of organic sugarcane
in Tahiti. We also generated for the first time
in French Polynesia a preliminary list of
arthropods, comprising insect pests, natural
predators, and parasitoids in this agrosystem.
An interesting functional biodiversity is
present, and its richness is mainly due to the
organically certified fields cultivated by small
producers. At the moment, the whole area of
sugarcane in Tahiti and other islands of French
Polynesia is not strengthened by pests and
diseases. However, sugarcane areas will
probably grow rapidly, and it is of utmost
importance to encourage organic cultivation
that will be able to preserve biodiversity in a
sustainable way. A knowledge base system
associated with a decision support system for
pest management (Martin et al., 2020) should
be an integrated method to follow for the
sustainable production of noble canes. Having
considered this, it is not forgotten that these
old varieties were first abandoned because of
their susceptibility to diseases (Vitrac et al.,
2018a) and replaced by modern Saccharum
spp. varieties. A better knowledge of the
potential of these noble canes and their uses is
the first step to building a highly valuable
10
20
30
40
50
60
70
0
1
2
3
4
5
6
7
8
9
10
April May June July Aug. Sept.
Fresh stripe damaged
Killed rats
Afaahiti Toahotu
ER Yeşim, 2023
47
agroecological context to provide the best
sugarcanes to this rum industry. The push-pull
approach using different types of sugarcane
and also companion plants should be further
tested and proposed as an agroecological crop
protection strategy.
References
Abd Elhafiz A, Abd Elhafiz A, Gaur SS,
Hamdany N, Osman M, Lakshmi TVR,
2015. Chlorella vulgaris and Chlorella
pyrenoidosa live cells appear to be
promising sustainable biofertilizer to
grow rice, lettuce, cucumber and eggplant
in the UAE Soils. Recent Research in
Science and Technology 7: 1421.
Atencio VR, Goebel FR, Miranda RJ, 2019.
Entomofauna associated with sugarcane
in Panama. Sugar Tech 21(4): 605618.
Chi L, Huerta E, lvarez-Sols D, K-Quej V,
Mendoza-Vega J, 2020. Abundance and
diversity of soil macroinvertebrates in
sugarcane (Saccharum spp.) plantations
under organic and chemical fertilization
in Belize. Acta Zoolgica Mexicana
(nueva serie) 36: 119.
Coulis M, 2021. Abundance, biomass and
community composition of soil
saprophagous macrofauna in conventional
and organic sugarcane fields. Applied
Soil Ecology 164: 103923.
Hammes C, Putoa R, 1986. Catalogue des
insectes et acariens d’intért agricole en
Polynésie franaise. Centre ORSTOM de
Tahiti.
Hammes C, Chant H, Mu L, 1989. Manuel, de
défense des cultures en Polynésie française.
Office of Scientific and Technical
Research Overseas (ORSTOM), France.
Goebel R, Way MJ, Gossard C, 2005. The
status of Eldana saccharina
(Lepidoptera: Pyralidae) in the South
African sugar industry based on regular
survey data. In: Proceedings of the South
Africa Sugarcane Technologists
Association, pp. 337346.
Goebel FR, Way MJ, 2009. Crop losses due to
two sugarcane stem borers in Reunion
and South Africa. Sugar Cane
International 27(3): p. 107111.
Goebel FR, Sallam N, 2011. New pest threats
for sugarcane in the new bioeconomy and
how to manage them. Current Opinion in
Environmental Sustainability 3: 8189
Loranger G, Ponge JF, Blanchart E, Lavelle P,
1998. Influence of agricultural practices
on arthropod communities in a vertisol
(Martinique). European Journal of Soil
Biology 34(4): 157165.
Martin P, Silvie P, Marnotte P, Goebel FR,
2020. A decision support system for
determining sugarcane pest reservoir.
Sugar Tech 22: 655661.
Nibouche S, Tibere R, Costet L, 2019.
Erianthus arundinaceus as a trap crop for
the sugarcane stem borer Chilo
sacchariphagus: Field validation and
disease risk assessment. Crop Protection
124: 104877.
Pan X, Shang X, Wei J, Huang C, Nikpay A,
Goebel FR, 2021. Biological control of
sugarcane borers in the province of
Guangxi, China: the importance of
Trichogramma releases and sex
pheromones for field monitoring and
trapping. International Sugar Journal
123 : 190193.
Paulian R, 1998. Les insectes de Tahiti.
Editions Boube, Paris, France.
Poser C, Chabanne A, Martin J, Gueno JM,
Ribotte JC, Tumoine L, Le Bras J,
Christina M, Goebel FR, 2018. Farming
for the future: improving productivity
ER Yeşim, 2023
48
and ecological resilience in sugarcane
production systems, In: ISSCT
Agricultural Engineering, Agronomy and
Extension Workshop, Saint Gilles,
Réunion, France.
Ryckewaert P, 1984. Observations sur les
rhopalocres de Polynsie franaise.
Alexanor 14(4): 155159.
Ryckewaert P, 2004. Rapport de mission à
Tahiti du 22 mars au 2 avril 2004.
CIRAD-FLHOR, Montpellier, France, 16
p.
Snchez-Bayo F, 2011. Impacts of
Agricultural Pesticides on Terrestrial
Ecosystems. In: Ecological Impacts of
Toxic Chemicals. Centre for
Ecotoxicology, University of Technology
Sydney, Australia, pp. 6387.
Vitrac M, Martin J, Teai T, Shili-Touzi I,
Goebel FR, 2019a. Des cannes nobles
tahitiennes cultivées en bio anéanties par
le wedelia Sphagneticola trilobata : une
mésaventure à surmonter. In : 24e
Conférence du COLUMA : Journées
internationales sur la lutte contre les
mauvaises herbes. Végéphyl. Alfortville :
Végéphyl, 11 p. Conférence du
CCOLUMA : Journées internationales
sur la lutte contre les mauvaises herbes,
Orléans, France.
Vitrac M, Teai T, Goebel FR, Shili-Touzi I,
2019b. Noble sugarcanes and modern
cultivars in Tahiti relative to organic rum
production : description and key
characteristics. AGROFOR International
Journal 4(2): 2027.
Vitrac M., Teai, T., Goebel, F. R., 2018a.
Sugarcanes and the Saccharum genus in
French Polynesia: historical and future
potential uses. In: CIPAM 10: 10ème
Colloque International sur les Plantes
Aromatiques et Médicinales et
Cosmétopées, Punaauia, French
Polynesia.
Vitrac M, Teai T, Goebel FR, Shili-Touzi I,
2018b. Organic sugarcane cultivation in
Tahiti. AGROFOR International Journal
3(3): 3138.
Zhong B, Lv C, Qin W, 2016. Preliminary
study on biology and feeding capacity of
Chelisoches morio (Fabricius)
(Dermaptera:Chelisochidae) on
Tirathaba rufivena (Walker).
SpringerPlus 5: 1944.