Issue |
Cah. Agric.
Volume 33, 2024
Réduire l’utilisation des pesticides agricoles dans les pays du Sud : verrous et leviers socio-techniques / Reducing the use of agricultural pesticides in Southern countries: socio-technical barriers and levers. Coordonnateurs : Ludovic Temple, Nathalie Jas, Fabrice Le Bellec, Jean-Noël Aubertot, Olivier Dangles, Jean-Philippe Deguine, Catherine Abadie, Eveline Compaore Sawadogo, François-Xavier Cote
|
|
---|---|---|
Article Number | 26 | |
Number of page(s) | 9 | |
DOI | https://doi.org/10.1051/cagri/2024023 | |
Published online | 08 October 2024 |
Article de recherche / Research Article
Tithonia diversifolia: beneficial companion plant to control Yellow Aphids on sugarcane fields in Tanzania
1
CIRAD, UPR AIDA, F-34398, Montpellier, France
2
AIDA, Univ Montpellier, CIRAD, Montpellier, France
* Corresponding author : quentin.mace@cirad.fr
To find sustainable ways to protect its sugarcane areas from the key pest Sipha flava (Hemiptera: Aphididae) in north Tanzania, the local company TPC Limited funded a 6 months project in coordination with the French Agricultural Research Centre for International Development (CIRAD) to assess different agroecological practices, such as the use of companion plants around sugarcane fields. In this study, the influence of the flowering species Tithonia diversifolia located at the field edges as a potential banker plant for conservation biological control of the yellow sugarcane aphid was evaluated. Predatory species were identified by direct capture and/or regular observations and the intensity of aphid damage was evaluated through number of colonies. Twenty-four aphid predator species were identified being hosted by T. diversifolia, and the vicinity of this plant reduced by 86% the number of S. flava colonies in the sugarcane edges. These species belonged mostly to family Coccinellidae (ladybugs), Syrphidae (hoverflies), Chrysopidae (green lacewings), Dolichopodidae (long legged flies). This is the first paper evaluating T. diversifolia’s potential as a banker plant in sugarcane crops for pest control.
Résumé
Afin de trouver des moyens durables de protéger leurs parcelles de canne à sucre contre le ravageur Sipha flava (Hemiptera : Aphididae) dans le nord de la Tanzanie, la société locale TPC Limited a financé un projet de 6 mois en coordination avec le Centre de coopération internationale en recherche agronomique pour le développement (CIRAD) pour évaluer différentes pratiques agroécologiques, telles que l’utilisation de plantes compagnes autour des champs de canne à sucre. Dans cette étude, l’influence de l’espèce à fleurs Tithonia diversifolia, située en bordure de champ, en tant que potentielle plante de service pour la lutte biologique de conservation contre le puceron jaune de la canne à sucre, a été évaluée. Les espèces prédatrices ont été identifiées par capture directe et/ou observations régulières et l’intensité des dégâts causés par les pucerons a été évaluée par le nombre de colonies. Vingt-quatre espèces prédatrices de pucerons ont été identifiées comme étant hébergées par T. diversifolia, et la proximité de cette plante a réduit de 86% le nombre de colonies de S. flava dans les bordures de canne à sucre. Ces espèces appartenaient principalement à la famille des Coccinellidae (coccinelles), Syrphidae (syrphes), Chrysopidae (chrysopes vertes) et Dolichopodidae (mouches à longues pattes). Il s’agit du premier article évaluant le potentiel de T. diversifolia en tant que plante de service dans les cultures de canne à sucre pour la lutte contre les ravageurs.
Key words: Sugarcane / biological control / banker plant / Sipha flava / Tithonia diversifolia
Mots clés : Canne à sucre / lutte biologique / plante de service / Sipha flava / Tithonia diversifolia
© Q. Macé and F.-R. Goebel, Hosted by EDP Sciences 2024
This is an Open Access article distributed under the terms of the Creative Commons Attribution License CC-BY-NC (https://creativecommons.org/licenses/by-nc/4.0), which permits unrestricted use, distribution, and reproduction in any medium, except for commercial purposes, provided the original work is properly cited.
1 Introduction
The Yellow Sugarcane Aphid (YSA) Sipha flava (Hemiptera: Aphididae) is a pest insect originated from North America that arrived in Africa in 2006 (Abdelmajid, 2008) and reached the sugarcane plantations of Tanzania during the last decade, where it became a growing problem. The pest is currently managed using pesticides such as neonicotinoids, but the efficacity of this chemical control tends to decrease due to the development of resistance in the aphid population (Dedryver et al., 2010). To manage pests without affecting the environment ability to provide ecosystem services and to prevent inducing chemical resistance in pest population, alternative control ways have to be implemented (Tilman et al., 2002). Unlike chemical control, biological control is able to manage pest using beneficial arthropods that are already present in the field or by massively release them in the fields. This biological control can be increased by introducing new species, but this technique requires important knowledge of both the introduced species and the receiving environment in order to prevent attack on non-target species that can eventually end up on their decline (Louda et al., 2003). An effort-effective way to use biological control is to conserve the native species. Most beneficial arthropods regarding aphid management also feed on pollen, their population can be preserved and encouraged with the help of banker plants at the vicinity of the major crop. These companion plants provides food (nectar) and shelter for beneficial arthropods (Huang et al., 2011). Tithonia diversifolia (Fig. 1) is a flowering plant from the Asteraceae family native from Central America but widespread in the world as an invasive species. Yet, it is of no threat to the crops as the plant is rarely found within the plots in large number, and can be easily removed (Husson et al., 2010). Such invasiveness has not been observed at TPC in the estate over the last 25 yr. The ecology of T. diversifolia varies greatly depending on the climate, it can be annual or perennial and its flowering period remain inconstant yet its interest on biological control depends mostly to its capacity to provide pollen and nectar. In lower Kilimanjaro region, T. diversifolia can be found in scarce number along rivers, roads or planted in vicinity of small scale farmer crops. The role of semi-natural habitat in increasing species richness in the fields have been proven (Billeter et al., 2007) and suggests that landscape diversity increase the biological control (Gardiner et al., 2009). As well as being used as insecticidal plant when macerated (Dougoud et al., 2019), green manure (Jama et al., 2000), and being widely used for pasture in South America (Mauricio, 2017), T. diversifolia growing agronomic interest could be extended to pest management as a banker plant for agroecological diversification (Donatti-Ricalde et al., 2018). Studies on T. diversifolia as banker plant for conservation biocontrol is very scarce and the only referenced article found by the authors was produced by Calvert et al., 2019. In fact despite the interesting role of T. diversifolia in hosting anthocorid predators of thrips, this plant also attracted the thrips and made this plant species not applicable as a banker plant in greenhouse crops. Yet the need to introduce flowering plants in this Northern-Tanzanian sugarcane plantations to increase the biological control has been stressed several times (Jepson, 1956; Katundu, 1999 ; Goebel, 2021), so following their instructions T. diversifolia hedges have been implemented in the early 2000 at TPC sugarcane estate (Katundu, 1999). This study aims at evaluating the potential of T. diversifolia as a banker plant for the natural enemies of the Yellow Sugarcane Aphid S. flava and its edge effect in Tanzanian sugarcane fields.
Fig. 1 Tithonia diversifolia bordering a sugarcane field. Tithonia diversifolia en bordure d’un champ de canne à sucre. |
2 Material and methods
Surveys for insects and the Yellow Sugarcane Aphid (YSA) S. flava (Homoptera: Aphididae) were conducted in Moshi, Tanzania (3°31’59.2"S 37°19’37.5"E) monthly from May to August 2023 in the morning (8 am-11 am) after the long rainy season, with daily temperature ranging from 15 °C to 25 °C. During this period T. diversifolia remained systematically flowering. In the Northern part of Tanzania, the climate is semi-arid. The fields are located on a plateau at an average altitude of 800 m. Within the 15,000 ha of properties, 7,800 ha are cultivated with sugarcane monoculture. In between the sugarcane fields, the presence of flower is very scarce, represented by ornamental flowers around the water pump stations, flamboyant trees along the main road and few T. diversifolia hedges remaining in the Northern part of the property. The cultivated area is surrounded by TPC’s “Namalok” nature reserve on the South, the Pangani and Kikuletwa rivers on the West, and villages of small scale farmers on the East. The sugarcane complex is arbitrarily divided in 3 areas (East, North, South). For both East and North area, two fields with T. diversifolia hedges in their vicinity were selected. In East area (fields K3 & K5), both T. diversifolia hedges are oriented South-North, separated from the sugarcane fields by a 15 meters dirt pathway alternately occupied by grass or bare soil depending on herbicide applications. In North area, the T.diversifolia bordering the field N51 is oriented South-North while the one bordering the field N52 is oriented East-West. Both hedges are close (<5 meters) to the fields they are bordering. All the fields are comparable in size, from 30 ha to 44 ha and benefit from the same system of overhead sprinkler irrigation. For all rows of T. diversifolia along each field studied a transect of 100 meters was observed by spending 5 min every ten meters for a total duration of 50 min. Every insect in direct contact with T. diversifolia was recorded, whether it was on the leaves or flowers. For each new species encountered, the first individual was captured for further identification at the laboratory under a stereomicroscope based on the previous entomologist consultancy report (Conlong, 2019; Goebel, 2021). When necessary, additional captures were carried out to confirm species identification by consulting keys (Chen et al., 2013; Hounkpati, 2005; John et al., 2017; Jones et al., 2002; Siaumar et Kamal, 1977; Speight et Sarthou, 2012; Tomaszewska et Szawaryn, 2016) and contacting specialist entomologists, or the identification was limited to genus level, then were confirmed by FR Goebel, an entomologist from the French Agricultural Research Centre for International Development (CIRAD). The insects already identified were just counted and photographed. The same protocol of transect was applied for both the closest and farthest sugarcane field edges to the Tithonia rows, resulting in a triple transect per field studied (Fig. 2). Only the insects in direct contact with sugarcane were counted. Particular attention was paid to checking the underside of sugarcane blades, as this is where aphids are found. The aphids were counted by colonies; a colony is defined by the homogenous aggregation of at least 2 individuals. Based on laboratory rearing, all the black ladybug larvae were considered as belonging to the species Hippodamia variegata, and all hairy white larva as belonging to Scymnus suturalis. Only insect species were considered in this study even though numerous araneid species were also encountered. All the statistical analysis were realized on RStudio (version 2023.03.0+386). As no variable followed normal law (p<0.05 at Shapiro test), the equality of the medians were tested by Wilcoxon test. The species diversity were quantified using the Shannon diversity index H’ (Shannon et Weaver, 1948). The species evenness of the communities was quantified with the Pielou’s evenness index E (Pielou, 1966).
Fig. 2 Scheme of the monthly triple transect realized per field studied. Schéma du triple transect mensuel réalisé par champ étudié]. |
3 Results
Within the 16 triple transects observed on 4 different T. diversifolia rows, 64 insect species were identified. 24 of them were known as aphid predators (Tabs. 1–4): 13 Coccinellidae, 1 Chrysopidae, 1 Dolichopodidae, 1 Formicidae, 2 Mantidae, 1 Staphylinidae, 5 Syrphidae (Fig. 3). These predators represent 46.5% of the observed species on T. diversifolia. The species diversity greatly depends on the T. diversifolia location (Tab. 5). The major species observed is Epilachna varivestis (Coleoptera: Coccinellidae), a phytophagous ladybeetle that has never been observed in sugarcane fields and is therefore not a threat to this crop. The most observed aphid predator is Condylostylus sp. (Diptera: Dolichopodidae), a long-legged fly that represent 29.1% of the observed insects. The aphid predators from the Coccinellidae family represent 9.8% of the observed insects, with 44.2% of the observed Coccinellidae being Exochomus concavus. In the East area (K3 and K5), the species were more evenly distributed (E>0.80) than in the North area (E<0.60). In N51, E. varivestis, the pest of T. diversifolia, was the dominant species (46% of the observed species), whereas in N52 it was the aphid predator Condostylus sp. The T. diversifolia rows and their surrounding sugarcane fields shared a variable proportion from 3 to 7 shared aphids predator species (Tabs. 1 and 3). The only larvae identified in T. diversifolia is the pest E. varivestis. For each sugarcane field, the closest edges were less infested by S. flava than the farthest edges (reduction of 86.6%). Regarding the total study, the Yellow Sugarcane Aphid median from the sugarcane field edges bordering T. diversifolia (3.5 colonies) were significantly (p= 0.001) lower than the one from the farthest edges (64.5 colonies) (Fig. 4). Yet no significant difference in predator quantity was observed in between edges of sugarcane fields (p= 0.57). However, in total, the median YSA per predator ratio is significantly higher (p= 0.001) in the sugarcane edges at the opposite of T. diversifolia (10.87 YSA per predator) than in the adjacent edges (0.42 YSA per predator) (Fig. 5).
Aphid predators observed during the K3 transects.
Prédateurs de pucerons observés durant les transects K3.
Aphid predators observed during the K5 transects.
Prédateurs de pucerons observés durant les transects K5.
Aphid predators observed during the N51 transects.
Prédateurs de pucerons observés durant les transects N51.
Aphid predators observed during the N52 transects.
Prédateurs de pucerons observés durant les transects N52.
Fig. 3 Major aphid predators detected during T. diversifolia monitoring. Principaux prédateurs de pucerons détectés lors du suivi de T. diversifolia. |
Major insect species observed on Tithonia diversifolia per location.
Principales espèces d’insectes observées sur Tithonia diversifolia par site.]
Fig. 4 Average number of S. flava in sugarcane rows in the vicinity of T. diversifolia. Nombre moyen de S. flava dans les rangs de canne à sucre à proximité de T. diversifolia. |
Fig. 5 Average ratio of S. flava per aphid predator in the vicinity of T. diversifolia. Ratio moyen de S. flava par prédateur de pucerons à proximité de T. diversifolia. |
4 Discussion
The diversity of aphid predators hosted by T. diversifolia makes it an effective banker plant for beneficial arthropods protecting sugarcane fields. In addition, random observations on other T. diversifolia revealed the presence of other insects from the family of Coccinellidae (Chilocorus stigma, Cryptolaemus montrouzieri, Psyllobora vigintimaculata, Tenuisvalvae notata). The absence of any aphid predator larva in T. diversifolia suggests that aphid predators might lay their eggs in the sugarcane fields. And the development of these eggs is very important for consumption of aphid’s larvae. As the number of predators per YSA is significantly higher in the closest sugarcane field edges of T. diversifolia, and as the number of aphids is significantly higher in the closest sugarcane field edges of T. diversifolia, we can conclude that T. diversifolia is protecting the edges of sugarcane fields by hosting aphid predators that consume both the nectar from their flower and the aphids nearby, in addition to laying eggs in the sugarcane fields. The presence in between sugarcane plots could slow down the aphid spreading through the sugarcane fields.
Additionally to the aphid predators, some moth parasitoid species have been observed (Brachymeria kassalensis, Enicospilus purgatus), meaning that T. diversifolia could play a role in sugarcane protection from Lepidoptera moth borers and leaf feeders, such as Sesamia calamistis, Spodoptera sp., Eldana saccharina, even though those assertions remain speculative as no literature supports these host-prey possibility. Numerous species of parasitoid wasp (Fig. 6) from the scoliidae family, such as Campsomeriella caelebs, Campsomeriella madonensis, Campsomeris mansueta, Cathimeris sjostedti, Megameris pseudofasciatipennis, Megameris soleata, were already observed feeding on T. diversifolia (Katundu, 1999). This family of wasp are known to be good parasitoids of white grubs. Even though managing this plant in all infested sugarcane areas could enhance biological control, T. diversifolia is sometimes reported as an invasive species and should therefore not be introduced into new habitats until further research. However, concerning places where T. diversifolia has settled for decades and has never become an invasive weed in the fields even when it has been planted next to the crops, such as in TPC, promoting T. diversifolia semi-natural hedges could address a major factor restricting insect biological control in wide sugarcane monoculture area: the absence of flowers. Regarding the results of the experiments, planting T. diversifolia around sugarcane fields could act as semi-natural barrier slowing down the spread of YSA during their outbreak cycle in between rainy seasons. These hedges can be easily managed with the machinery used for sugarcane plantation and slashed when necessary. In the Eastern Africa context, the overgrowth of T. diversifolia could be manually reduced by cutting to feed the cattle of the herders, mainly Maasaï people, frequently met in TPC during their pastoralism activities. Because of its allelopathic properties inhibiting the germination and growth of other plant species (Kato-Noguchi, 2020), T. diversifolia could provide a natural weed control limiting the usage of herbicide. This study is the first to evaluate T. diversifolia in its capacity to increase biological control in sugarcane fields. Regarding its widespread habitat over the world, the applications could be important, particularly in African sugar estates. Therefore, additional investigations are needed to evaluate the potential of protection provided by T. diversifolia as a companion plant to sugarcane fields in an agroecological management plan.
Fig 6 Campsomeriella sp. observed on T. diversifolia. Campsomeriella sp. observé sur T. diversifolia.gr |
Acknowledgments
We thank Jean-Yves Rasplus (Inrae, France) and Pascal Rousse (ANSES, France) for their contribution to identification and/or confirmation of main predatory species. We also thank Jean-Baptiste Castagnet (France) for his identifications of scoliid wasps and our colleague from CIRAD José Martin for his advice on weed science. We are also very grateful to the TPC staff for technical assistance during this study, with particular regards to the Field Services Executive Officer of TPC Didier Bosquet for enabling this research to take place in the best possible conditions.
Conflicts of interest
No conflict of interest has been identified. This study has been made during an internship funded by the sugarcane company TPC Limited.
References
- Abdelmajid N. 2008. Première apparition de Sipha flava (Homoptera, Aphididae) sur la canne sucre au Maroc. EPPO Bulletin 38 (2): 220–222. https://doi.org/10.1111/j.1365-2338.2008.01207.x. [CrossRef] [Google Scholar]
- Billeter R, Liira J, Bailey D, Bugter R, Arens P, Augenstein I, et al. 2007. Indicators for biodiversity in agricultural landscapes: a pan-European study: Biodiversity in European Agro-ecosystems. Journal of Applied Ecology 45 (1): 141–150. https://doi.org/10.1111/j. 1365-2664. 2007.01393.x. [Google Scholar]
- Calvert F, Hollingsworth RG, Wall M, Follett PA. 2019. Survey of flowering plants in Hawaii as potential banker plants of anthocorid predators for thrips control. Journal of Asia-Pacific Entomology 22 (3): 638–644. DOI : https://doi.org/10.1016/j.aspen.2019.05.001. [Google Scholar]
- Chen XS, Wang XM, Ren SX. 2013. A review of the subgenus Scymnus of Scymnus from China (Coleoptera: Coccinellidae). Annales Zoologici 63 (3): 417–499. https://doi.org/10.3161/000345413 × 672483. [CrossRef] [Google Scholar]
- Conlong DE. 2019. Scoping visit to review the Yellow Sugarcane Aphid (Sipha Flava) at TPC sugarcane estate, Moshi, Tanzania. [Google Scholar]
- Dedryver CA, Le Ralec A, Fabre F. 2010. The conflicting relationships between aphids and men: A review of aphid damage and control strategies. Comptes Rendus Biologies 333 (6-7): 539–553. https://doi.org/10.1016/j.crvi.2010.03.009. [CrossRef] [PubMed] [Google Scholar]
- Donatti-Ricalde MG, de Sousa WB, Ricalde F MP, S Silva A de C, Abboud AC de S. 2018. Potential attraction of Tithonia diversifolia (Hemsl) A. Gray and Tithonia rotundifolia (Mill.) S. F. Blake (Asteraceae) for use in conservative biological control. Cadernos de Agroecologia 13 (1) https://doi.org/10.1038/s41598-022-20188-6. [Google Scholar]
- Dougoud J, Toepfer S, Bateman M, Jenner WH. 2019. Efficacy of homemade botanical insecticides based on traditional knowledge. A review. Agronomy for Sustainable Development 39 (4): 37. https://doi.org/10.1007/s13593-019- 0583-1. [CrossRef] [Google Scholar]
- Gardiner MM, Landis DA, Gratton C, DiFonzo CD, O’Neal M, Chacon JM et al. 2009. Landscape diversity enhances biological control of an introduced crop pest in the north-central USA. Ecological Applications 19 (1): 143–154. https://doi.org/10.1890/ 07-1265.1. [CrossRef] [PubMed] [Google Scholar]
- Goebel FR. 2021. Consultancy report on the Yellow Sugarcane Aphid (YSA), Sipha flava, a key pest at Tanzania Planting Company (TPC), Tanzania. Montpellier (France): Cirad, 31 p. [Google Scholar]
- Hounkpati K. 2005. Systematic studies of West African Lady Beetles (Coccinellidae: Coleoptera). Togo: Université de Lomé, 300 p. [Google Scholar]
- Huang N, Enkegaard A, Osborne LS, Ramakers PMJ, Messelink GJ, Pijnakker J, et al. 2011. The banker plant method in biological control. Critical Reviews in Plant Sciences 30 (3): 259–278. https://doi.org/10.1080/07352689.2011.572055. [CrossRef] [Google Scholar]
- Husson O, Charpentier H, Chabaud FX, Naudin K, Rakotondramanana, Seguy L. 2010. Flore des jachères et adventices des cultures. In : Manuel pratique du semis direct à Madagascar Antananarivo (Madagascar): GSDM, 64 p. [Google Scholar]
- Jama B, Palm CA, Buresh RJ, Niang A, Gachengo C, Nziguheba G, et al. 2000. Tithonia diversifolia as a green manure for soil fertility improvement in western Kenya: a review. Agroforestry Systems 49: 201–221. https://doi.org/10.1023/A:1006339025728. [CrossRef] [Google Scholar]
- Jepson WF. 1956. The biology and control of the sugar-cane chafer beetles in Tanganyika. Bulletin of Entomological Research 47 (2): 377–397. https://doi.org/10.1017/S0007485300046733. [CrossRef] [Google Scholar]
- John TS, Van Harten A, Ketelaar R. 2017. The hoverflies of the Arabian Peninsula. Arthropod fauna of the UAE 6: 572–612. [Google Scholar]
- Jones LA, Montgomery M, Yu G, Lu W. 2002. Recognition of imported lady beetles in the Tribe Scymnini released in Eastern North America. In Onken B, Reardon R, Lashomb J, eds. The hemlock woolly adelgid in the eastern United States symposium; 2002 February 5-7; East Brunswick, New Jersey: Agricultural Experiment Station and Rutgers University, pp. 335–343. [Google Scholar]
- Kato-Noguchi H. 2020. Involvement of Allelopathy in the invasive potential of Tithonia diversifolia. Plants 9 (6): 766. https://doi.org/10.3390/plants9060766. [CrossRef] [PubMed] [Google Scholar]
- Katundu JM. 1999. Biology and ecology of Cochliotis melolonthoides Gerst (Coleoptera: Scarabidae) on sugarcane in Tanzania. London (United-Kingdom): University of London. [Google Scholar]
- Louda SM, Pemberton RW, Johnson MT, Follett PA. 2003. Nontarget effects, the Achilles’s heel of biological control? Retrospective analyses to reduce risk associated with biocontrol introductions. Annual Review of Entomology 48 (1): 365–396. https://doi.org/10.1146/annurev.ento.48.060402.102800. [CrossRef] [PubMed] [Google Scholar]
- Mauricio RM. 2017. Feeding ruminants using Tithonia diversifolia as forage. Journal of Dairy, Veterinary & Animal Research 5 (4). https://doi.org/10.15406/jdvar.2017.05.00146. [CrossRef] [Google Scholar]
- Pielou EC. 1966. The measurement of diversity in different types of biological collections. Journal of Theoretical Biology 13: 131–144. https://doi.org/10.1016/0022-5193(66)90013-0. [CrossRef] [Google Scholar]
- Shannon C, Weaver W. 1948. The mathematical theory of communication. The Bell System Technical Journal 27 (379-423). https://doi.org/10.1002/j.1538-7305.1948.tb01338.x. [CrossRef] [Google Scholar]
- Siaumar N, Kamal S. 1977. Keys for identification of species of family syrphidae (diptera) in Egypt. Bulletin Mensuelle de La Société Linnéenne de Lyon 10 (8): 373. [Google Scholar]
- Speight M, Sarthou JP. 2012. StN keys for the identification of adult European syrphidae 2012, 134 p. [Google Scholar]
- Tilman D, Cassman KG, Matson PA, Naylor R, Polasky S. 2002. Agricultural sustainability and intensive production practices. Nature 418 (6898): 671–677. https://doi.org/10.1038/nature01014. [CrossRef] [PubMed] [Google Scholar]
- Tomaszewska W, Szawaryn K. 2016. Epilachnini (Coleoptera: Coccinellidae)—a revision of the world Genera. Journal of Insect Science 16 (1): 101. https://doi.org/10.1093/jisesa/iew082. [CrossRef] [Google Scholar]
Cite this article as: Macé Q, Goebel F-R. 2024. Tithonia diversifolia: beneficial companion plant to control Yellow Aphids on sugarcane fields in Tanzania Cah. Agric. 33: 26. https://doi.org/10.1051/cagri/2024023
All Tables
Aphid predators observed during the K3 transects.
Prédateurs de pucerons observés durant les transects K3.
Aphid predators observed during the K5 transects.
Prédateurs de pucerons observés durant les transects K5.
Aphid predators observed during the N51 transects.
Prédateurs de pucerons observés durant les transects N51.
Aphid predators observed during the N52 transects.
Prédateurs de pucerons observés durant les transects N52.
Major insect species observed on Tithonia diversifolia per location.
Principales espèces d’insectes observées sur Tithonia diversifolia par site.]
All Figures
Fig. 1 Tithonia diversifolia bordering a sugarcane field. Tithonia diversifolia en bordure d’un champ de canne à sucre. |
|
In the text |
Fig. 2 Scheme of the monthly triple transect realized per field studied. Schéma du triple transect mensuel réalisé par champ étudié]. |
|
In the text |
Fig. 3 Major aphid predators detected during T. diversifolia monitoring. Principaux prédateurs de pucerons détectés lors du suivi de T. diversifolia. |
|
In the text |
Fig. 4 Average number of S. flava in sugarcane rows in the vicinity of T. diversifolia. Nombre moyen de S. flava dans les rangs de canne à sucre à proximité de T. diversifolia. |
|
In the text |
Fig. 5 Average ratio of S. flava per aphid predator in the vicinity of T. diversifolia. Ratio moyen de S. flava par prédateur de pucerons à proximité de T. diversifolia. |
|
In the text |
Fig 6 Campsomeriella sp. observed on T. diversifolia. Campsomeriella sp. observé sur T. diversifolia.gr |
|
In the text |
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.