Corm damage caused by banana weevils Cosmopolites sordidus (Germar) collected from different banana growing regions in Uganda

Abstract

Background

In this study, both healthy tissue culture plantlets and maiden suckers of the Nakitembe cultivar were used to assess the damage level variation caused by banana weevils collected from different banana growing regions. Seventy-nine (79) tissue culture plantlets and fifty (50) suckers were established in buckets in a randomized complete block design for 5 months. Ten adult weevils (5 females and 5 males) were introduced at the base of each plant, and the buckets were covered with a weevil proof mesh. Weevil damage was estimated as a percentage at 60 days after the weevil introduction by estimating the peripheral damage (PD), total cross section corm damage (XT) and above the collar damage (ACD).

Results

The results showed high differences in the PD, XI, XO and XT caused by weevils from the different zones. PD and XT ranged from 4.8–50.4 to 4.2–43.8%, respectively, caused by weevils collected from Kabale and Rakai, Kabale and Wakiso, respectively, while XI and XO varied from 0.0–42.9 to 8.3–40.4%, respectively, caused by banana weevils collected from Kabale and Rakai, Kabale and Rakai, respectively. Banana weevils from Rakai caused the highest ACD of 40.4% and no such damage was caused by banana weevils collected from western Uganda. Average ACD in suckers was 19.6% and significantly higher than that in tissue culture plants (8.5%).

Conclusions and recommendations

Corm damage assessment suggests the existence of banana weevil biotypes but it is recommended that follow-up studies be carried out to confirm this phenomenon.

* Research

* Open Access

Corm damage caused by banana weevils Cosmopolites sordidus (Germar) collected from different banana growing regions in Uganda

* Charles K. Twesigye1Email author,

* Kenneth Ssekatawa1,

* Andrew Kiggundu2,

* Wilberforce Tushemereirwe2,

* Enock Matovu3 and

* Eldad Karamura4

Agriculture & Food Security2018 7:73

https://doi.org/10.1186/s40066-018-0224-y

© The Author(s) 2018

* Received: 11 October 2017

* Accepted: 5 October 2018

* Published: 19 October 2018

Abstract

Background

In this study, both healthy tissue culture plantlets and maiden suckers of the Nakitembe cultivar were used to assess the damage level variation caused by banana weevils collected from different banana growing regions. Seventy-nine (79) tissue culture plantlets and fifty (50) suckers were established in buckets in a randomized complete block design for 5 months. Ten adult weevils (5 females and 5 males) were introduced at the base of each plant, and the buckets were covered with a weevil proof mesh. Weevil damage was estimated as a percentage at 60 days after the weevil introduction by estimating the peripheral damage (PD), total cross section corm damage (XT) and above the collar damage (ACD).

Results

The results showed high differences in the PD, XI, XO and XT caused by weevils from the different zones. PD and XT ranged from 4.8–50.4 to 4.2–43.8%, respectively, caused by weevils collected from Kabale and Rakai, Kabale and Wakiso, respectively, while XI and XO varied from 0.0–42.9 to 8.3–40.4%, respectively, caused by banana weevils collected from Kabale and Rakai, Kabale and Rakai, respectively. Banana weevils from Rakai caused the highest ACD of 40.4% and no such damage was caused by banana weevils collected from western Uganda. Average ACD in suckers was 19.6% and significantly higher than that in tissue culture plants (8.5%).

Conclusions and recommendations

Corm damage assessment suggests the existence of banana weevil biotypes but it is recommended that follow-up studies be carried out to confirm this phenomenon.

Keywords

* Variation

* Banana weevil

* Corm damage

Background

The banana weevil Cosmopolites sordidus (Germar) is the most challenging insect pest of Musa spp globally. In most regions of East Africa, the East African highland banana (EAHB) (Musa sp. AAA) is the staple food crop mainly produced by subsistence farming, while plantain (Musa spp. AAB) is a significant staple in much of West and Central Africa [1, 2]. Uganda produces approximately 9.2 million metric tons annually hence making it the second leading banana producer in the world with the highest per capita consumption that is estimated at 450 kg/person/year [3, 4]. The EAHB is used to make a dish branded matooke in Uganda and is mainly grown for consumption and as a source of rural income which offers the best profits to family labor [5, 6]. Both EAHB and Musa spp. AAB banana cultivars are highly susceptible to the banana weevil [1, 2].

Highland cooking (Musa AAA-EA) and beer bananas (Musa AAA-EA, ABB and AB) comply the most important staple food crop for the East African Great Lakes region. The fruit is consumed on farm, sold in local markets or transported by traders to urban centers. An extended harvest period ensures food and income sources throughout the year. Highland bananas reduce soil erosion on steep slopes and are principal sources of mulch for maintaining and improving soil fertility. East Africa represents a secondary center of crop diversity, while highland cooking cultivars are unique to the region (Stover and Simmonds, [7].

Uganda is Africa’s leading producer and consumer of bananas. In recent years, drastic yield declines in traditional banana growing areas such as Mpigi, Luwero, Mukono and Iganga districts have led to the replacement of cooking bananas with beer types and/or annual crops (e.g., cassava and sweet potatoes) (Karamura et al. [8]. Planting of annual crops necessitates frequent opening of the land, thereby accelerating soil erosion. In Uganda, as elsewhere in the region, banana production constraints include a pest complex (weevils, nematodes and diseases) which causes serious yield losses and shortened plantation life [9]). However, pest infestation levels are unknown and yield losses have been neither quantified nor partitioned among constraints. Farmers have identified weevils and deteriorating soil fertility as their most important problems but causal factors were frequently confused and damage by nematodes, and pathogens were often attributed to other factors (Gold et al. [9]).

However, each of the banana groups suffers from its own pest and disease constraints. For example, banana weevils and nematodes are highly damaging to highland cooking banana and plantain production, while Fusarium wilt is the key constraint to dessert bananas and ABB and AAB brewing bananas (Sengooba [10]; Sebasigari and Stover [11]. Soil degradation, due to increasing pressure on the land, associated with socioeconomic factors, also reduces production. A combination of these factors has been blamed for the “banana decline”; mean production in this region has dropped steadily, from 10 (1970) to 4.5 t/ha on subsistence farms (Gold et al. [12], Karamura et al. [13], Okech et al. [14] Tinzaara et al. [15]). This has had a negative effect on both food and household income security for local populations. Yet, research results in the region indicate that 30–40 t/ha can be obtained.

The decline in production and total destruction of highland banana in central Uganda and western Tanzania was attributed to banana weevils and consequently included the banana weevil among the principal limiting factors of banana production in East Africa [16, 17]. Eggs are laid by the female into the corm and pseudostem base of the banana plant and the resultant larvae tunnel through the corm hence damaging it. This hampers water and nutrient uptake as well as weakening the plant anchorage into the soil. Therefore, banana weevil attack can interfere with crop establishment, reduce bunch size, result in toppling plants, lead to mat dying-out and shortened plantation life [2, 16, 18].

Presently, there is no single control strategy that offers absolute control for banana weevils. Therefore, integrated pest management (IMP) strategy combining an array of methods such as habitat management (cultural control), biological control, host plant resistance, botanicals, and in some cases application of pesticides was deemed effective in the control of banana weevils [19]. Pesticides have been widely used by farmers but they are not highly recommended because of their broad spectrum, high cost and possibility of banana weevils developing resistance as a result of overuse [16, 17]. Therefore, the most promising control strategy in integrated pest management is host plant resistance to banana weevils which offers the potential to provide long term and sustainable crop protection to subsistence farmers at little cost [20]. Unfortunately, development of resistant cultivars through conventional breeding has resulted into hybrids with undesirable cooking traits since the majority of resistant cultivars are non cooking types presenting a problem to breeders, as cooking types are staple because of consumer preference [21]. Therefore, host plant resistance without altering the cooking traits of the staple cooking bananas can be achieved by breeding genetically modified plants which are resistant to banana weevils.

However [22], using Random Amplified Polymorphic DNA (RAPD), reported existence of banana weevil biotypes in Uganda. This is supported by different yield losses caused by banana weevils in different banana growing regions. Total destruction of banana plantation in central Uganda and negligible losses in Western Uganda was documented [23, 24].

The main objectives of this study were to: (1) establish the variation in corm damage caused by banana weevils collected from different banana growing regions in potted experiments under the same environmental conditions and (2) provide an insight into the existence of banana weevil biotypes that are essential in screening banana plants resistant to weevils.

Methods

Site description and source of materials

This study was carried out at National Agricultural Research Laboratories, Kawanda, situated at 0°25′N, 32°32′E, 1190 M above sea level, 13 km north of Kampala. Nakitembe suckers used in this study were collected from the National Banana Research Program, Uganda, banana plantations, whereas Nakitembe tissue culture plantlets were obtained from the Tissue Culture Laboratory at the National Agricultural Research Laboratories, Kawanda. Nakitembe was the cultivar of choice in this study, because Nakitembe tissue culture plantlets were available at an advanced stage in the Tissue Culture Laboratory. Before being used in potted experiments, sucker corms were pared and the entire pared corm was immersed in boiling water for 1 min to ensure that they were completely free from the weevils [25].

Sources of banana weevil

Weevils were captured from farmers’ banana plantations in the districts of Kabale, Ntungamo, Mbale/Sironko, Wakiso, Rakai, Bushenyi/Mbarara, Masaka, Kabarole (Fortportal) and Mukono using pseudostem traps on the basis of a grid map produced for diagnostic surveys of banana-based cropping systems [26].

Maintenance of weevils

Banana weevils were reared in an entomology laboratory in perforated plastic containers at room temperature. They were maintained on fresh Mbwazirime cultivar corm pieces that were changed regularly to avoid building up of rotting corm materials. All the test weevils were kept in these containers for at least 1 month before use in the experiments for acclimatization, and they were sexed using methods described by [27] whereby weevils were observed using a hand lens and males were differentiated from females on the basis of punctuations on their rostrums spreading beyond the point of antennae insertion.

Corm damage assessment experimental design

Seventy-nine (79) Nakitembe tissue culture plantlets and fifty (50) Nakitembe corms were planted in twenty liter perforated buckets with sterile soil mixed with farm yard manure and left to establish in a randomized complete block design with adequate watering for 5 months. The number of tissue culture plantlets and corms used was different due to their availability. Furthermore, the number of banana plants challenged with weevils was determined by the availability of weevils collected from each district as shown in Table 2. After 5 months, five adult female and five adult male weevils which were previously reared in an entomology laboratory were put in each of the ninety-six (96) buckets after which they were enclosed by a weevil proof net to prevent escape or entry of foreign weevils. The remaining thirty-three (33) plants were not challenged with weevils and therefore used as control. The plants were uprooted 2 months after introduction of the weevils. Roots were peeled off the corm, and peripheral damage (PD) was determined by estimating the percentage corm surface damage (Fig. 1).

Fig. 1 Fig. 1

Fig. 1

Potted banana plants wrapped in buckets after introducing adult weevils

A cross section of the corm was made 1 cm below the collar to determine the upper inner cross section damage, UXI (upper inner cylinder damage) and upper outer cross section damage UXO (upper cortex damage) by estimating the percentage damage of the upper inner cylinder region and upper cortex region, respectively (Fig. 2). A second cross section was made 3–5 cm depending on the size of the corm below the first cross section to determine the lower inner cross section damage, LXI (lower inner cylinder damage), and lower outer cross section damage, LXO (lower cortex damage), by estimating the percentage damage of the lower inner cylinder region and lower cortex region, respectively. Percentage corm damage was estimated by dividing the corm exposed cross section surface into four equal quarters. Area covered by galleries in each quarter was approximated out of 25%. Percentage cross section damage per corm circumference was computed by summing the percentage damage in all the four quarters.

Fig. 2 Fig. 2

Fig. 2

Diagrams illustrating estimation of percentage cross section circumference corm damage

The upper outer cross section damage UXO was added to the lower outer cross section damage LXO, and the mean was calculated to get the percentage total outer cross section damage XO. The average percentage of the upper inner cross section damage (UXI) and the lower inner cross damage (LXI) was calculated to acquire the percentage total inner cross section damage XI. The average of total inner cross section damage XI and total outer cross section damage XO was established to attain the percentage total cross section damage XT. A cross section.0.1 cm above the collar region was made to determine the above collar damage, ACD, by estimating the percentage damage on the cut section.

This experiment was repeated once to compare the results, and collected data were transformed using Arcsine transformation method to reduce the non-normality and heterogeneity of variance before the means were separated. The transformed data were subjected to analysis of variance (ANOVA) using the general linear model (GLM) on a Statistical Analysis Software (SAS) (v.9.2; SAS Institute [28], and the means for corm damage generated were separated using Student–Newman–Keuls test at 5% level of significance.

Results

Evaluation of corm damage caused to banana plants established from tissue banana plantlets and suckers

Mean percentages of PD, ACD, XI, XO and XT (± SE) for both tissue culture plants and suckers were compared, and the results showed no significant difference (p ≤ 0.05) in PD, XI, XO and XT levels caused both to tissue culture plant and suckers but ACD level caused was significantly different (p ≤ 0.05) between tissue culture plants and suckers as displayed in Table 1. However, in general, all the different damage types were higher in suckers than in tissue culture plants.

Table 1

Mean percentage peripheral damage, PD, percentage above the collar damage, ACD, percentage inner cross section damage, XI, percentage outer cross section damage, XO and percentage total cross section damage, XT, based on plant type

Plant type

No. of banana plants

PD (%)

ACD (%)

XI (%)

XO (%)

XT (%)

Tissue culture

79

23.0 ± 3.6A

8.5 ± 1.5B

18.3 ± 3.1A

19.9 ± 2.6A

19.1 ± 2.7A

Sucker

50

24.2 ± 4.7A

19.6 ± 4.6A

27.7 ± 5.6A

21.9 ± 4.7A

24.8 ± 5.0A

Mean values in each column accompanied by the same letter are not significantly different (p < 0.05) (Student–Newman–Keuls test rankings) and values accompanied by letter (s) which are not similar are significantly different (p > 0.05)

Comparison of corm damage caused by banana weevils collected from the different banana growing regions

Mean percentage peripheral damage (PD) (± SE) ranged from 4.8 to 50.4% and 0.0 for control. PD caused by weevils from Rakai and Fortportal was higher than PD caused by weevils from Masaka, Wakiso, Mukono, Sironko, Mbarara, Ntungamo, Mbale and Kabale. Student–Newman–Keuls test rankings indicate insignificant difference (p < 0.05) in PD caused by weevils from different sources as displayed in Table 2.

Table 2

Mean percentage peripheral damage, PD, percentage above the collar damage, ACD, percentage inner cross section damage, XI, percentage outer cross section damage, XO and percentage total cross section damage, XT, caused by banana weevils from different regions

Weevil source

No. of banana plants

PD (%)

ACD (%)

XI (%)

XO (%)

XT (%)

Rakai

16

50.4 ± 0 9.0A

40.4 ± 6.9A

42.9 ± 9.7BA

40.4 ± 7.6A

41.7 ± 8.4BA

Kyenjojo

05

50.0 ± 12.2A

0.0 ± 0.0C

23.5 ± 7.9BA

36.2 ± 11.1BA

29.9 ± 9.0BAC

Masaka

15

39.0 ± 08.7AB

10.4 ± 5.1BC

34.0 ± 9.5BA

31.4 ± 7.6BA

32.7 ± 8.0BAC

Wakiso

12

38.4 ± 10.3AB

31.9 ± 7.2AB

51.2 ± 11.6A

36.4 ± 9.5BA

43.8 ± 10.1A

Mukono

07

30.7 ± 06.1AB

9.3 ± 4.9BC

37.0 ± 8.4BA

37.2 ± 8.3BA

37.7 ± 8.3BAC

Sironko

12

27.6 ± 10.0AB

11.3 ± 6.4BC

11.8 ± 4.8BA

12.6 ± 3.2BA

12.2 ± 3.7BAC

Mbarara

06

23.3 ± 12.8AB

0.0 ± 0.0C

18.7 ± 9.8BA

23.2 ± 8.2BA

20.9 ± 8.5BAC

Ntungamo

07

20.7 ± 10.3AB

0.0 ± 0.0C

19.0 ± 9.4BA

18.6 ± 7.8BA

18.8 ± 8.3BAC

Mbale

10

13.1 ± 07.5AB

21.1 ± 9.0ABC

10.8 ± 10.0BA

8.8 ± 6.9BA

9.8 ± 8.4BAC

Kabale

06

4.8 ± 03.8AB

0.0 ± 0.0C

0.0 ± 0.0B

8.3 ± 0.8BA

4.2 ± 3.4BC

Control

33

0.0 ± 0.0B

0.0 ± 0.0C

0.0 ± 0.0B

0.0 ± 0.0B

0.0 ± 0.0C

Mean values in each column accompanied by the same letter are not significantly different (p < 0.05). (Student–Newman–Keuls test rankings) and values accompanied by letter (s) which are not similar are significantly different (p > 0.05)

For mean percentage above collar damage (ACD) (± SE), Student–Newman–Keuls test rankings indicate significant difference (p > 0.05) between ACD caused by weevils from Rakai, Wakiso, Mbale, Sironko, Masaka, Mukono and Kabale, Ntungamo, Fortportal, Mbarara and control as shown in Table 2. In general, there was no ACD caused by weevils collected from western Uganda.

There is no significant difference in cross section damage (mean percentage inner cross section damage (XI), outer cross section damage (XO) and total cross XT) caused by weevils collected from different banana growing regions as indicated by the Student–Newman–Keuls test rankings in Table 2. However, the results showed high damage levels caused by weevils from central and southern Uganda and low damage levels caused by weevils collected from eastern and Southwest and Mid-west Uganda (Figs. 3, 4).

Fig. 3 Fig. 3

Fig. 3

Cross section of corms showing percentage weevil damage ranging from 0 to 100% 2 months after introduction of adult weevils

Fig. 4 Fig. 4

Fig. 4

Representative banana pseudostems showing above the collar damage caused by banana weevil collected from different sites

Discussion

Corm damage variation

The results of the study revealed that the damage types caused by banana weevils collected from different regions had slight differences. This study revealed that there is a significant difference in above the collar damage (ACD) caused by weevils collected from different banana growing regions. ACD is where banana weevil larvae and adults bore in a region immediately above the corm, and it is a rare case which has not yet been studied. It is interesting to note that ACD clusters the weevils into two main populations; the western (Mid-west and Southwest regions) Uganda population (Kabale, Ntungamo, Mbarara/Bushenyi and Kyenjojo) and central, south and eastern Uganda population (Masaka, Rakai, Wakiso, Mukono, Mbale and Sironko).

The results showed that there are low peripheral damage (PD), low total cross section damage (XT) and no ACD caused by weevils from western Uganda and this explains why the yield loss caused by banana weevils in western (Mid-west and Southwest regions) Uganda is negligible. The report [20] is in agreement with these findings. Western region had the highest yield of banana in Uganda at 6.0 metric tons/hectare, whereas banana weevils collected from central (Wakiso and Mukono) and southern Uganda (Masaka and Rakai) caused significantly very high ACD as compared to the weevils from western Uganda (Mid-west and Southwest regions).

Since XT measures the extent to which the larvae could penetrate deep into the corm, internal corm damage directly affects the yield and survival of the banana plant [12], therefore, high ACD and XT caused by banana weevils collected from central and southern (Central and South regions) Uganda in pot experiments provide an insight into why banana weevils caused a yield loss of 20–60% in the central and up to 100% in southern Uganda as reported by [15, 30]. This is supported by the report [29] which showed that central Uganda had the lowest yield in metric tons/hectare (3.3 M t/Ha).

Weevils collected from eastern Uganda caused high ACD second to that of central and southern Uganda but not significantly different while significantly different from that caused by weevils from western (Mid-west and Southwest regions) Uganda. Follow-up field visits in a natural setting showed high level of ACD in Rakai district.

Relatively high ACD but the lowest inner cross section damage (XI), outer cross section damage (XO) and XT support the fact that no much yield loss due to banana weevils has been reported in the districts of Mbale, Sironko and Kapchorwa. This is evidenced by the eastern region ranking the second producers of banana in Uganda in metric tons/hectare at 5.6 M t/Ha [29].

The variation in the corm damage levels caused by banana weevils collected from different banana growing regions in potted experiments supports the existence of banana weevil biotypes. However, earlier studies associate dissimilarities in corm damage levels to difference in environmental conditions. [17, 22, 23] observed that the mean fraction weevil damage was greater in Masaka than in Bushenyi. They attributed this difference to variation in temperature as a result of altitude.

This indicates that banana growing regions on higher altitudes (Eastern, Western, Mid-west) are less affected by banana weevils compared to those found on lower altitudes (central and southwestern) because areas on higher altitude experience low environmental temperature which does not support high rate banana weevil growth [30]. The results showed no significant difference (p ≤ 0.05) in PD, XI, XO and XT levels caused both to tissue culture plant and suckers but ACD level caused was significantly higher in suckers than in tissue culture plantlets.

All the different damage types were higher in suckers than in tissue culture plants because tissue culture corms are too small to support many banana weevil larvae. The larvae exhibit cannibalism [31] and when they happen to meet they feed on each other hence reducing on the larvae load in tissue culture plantlet corms and therefore lower percentage damage than the larger corms. Suckers possess very big corms supporting a large number of banana weevil larvae. The chances of these larvae meeting are minimal. Large number of larvae in a corm results in higher percentage damage in suckers.

Conclusions

Corm damage assessment revealed that banana weevils from eastern, central and southern Uganda cause more damage than those from Southwestern and Mid-west Uganda in potted experiments. Therefore, corm damage assessment study has provided methodologies for further studies like evaluating the resistance of genetically modified banana plants to banana weevils. Other physiological and behavioral studies should be carried out such as response to sex hormones (pheromones), pesticide resistance and life cycle tables to support the molecular work already done.

Declarations

Authors’ contributions

KS, AK, EK and CT designed the study, KS conducted the experiments, KS, AK and CT analyzed the data, KS and CT wrote the manuscript. All authors read and approved the final manuscript.

Acknowledgements

The authors would like to thank Bioversity International for funding the research and National Agricultural Laboratories Kawanda for providing laboratory facilities and office space to KS.

Competing interests

All authors declared that they have no competing interests.

Availability of data and materials

All data generated or analyzed during this study are included in this published article (and its additional files).

Consent for publication

Not applicable.

Ethics approval and consent to participate

Not applicable.

Funding

This project was funded by Bioversity International through the National Banana Research Programme.

Publisher’s Note

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Authors’ Affiliations

(1)

Department of Biological Sciences, Faculty of Science, Kyambogo University, P.O. Box 1, Kyambogo, Kampala, Uganda

(2)

Uganda National Banana Research Programme, National Agricultural Research Laboratories, Kawanda, P.O. Box 7065, Kampala, Uganda

(3)

College of Veterinary Medicine Animal Resources and Biosecurity, CoVAB, Makerere University, P.O. Box 7062, Kampala, Uganda

(4)

Coordinator Bioversity International East and South Africa, P.O. Box 24384, Plot 106, Katalima Road, Naguru, Kampala, Uganda

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