Applied Ecology and Forestry Science
ISSN (Print): ISSN Pending ISSN (Online): ISSN Pending Website: https://www.sciepub.com/journal/aefs Editor-in-chief: Romeo Ekoungoulou
Open Access
Journal Browser
Go
Applied Ecology and Forestry Science. 2024, 6(1), 1-9
DOI: 10.12691/aefs-6-1-1
Open AccessArticle

Invasive Acacia melanoxylon Impedes Growth of Commercial Tree Species in the Adjoining Forest Stands in Nabkoi and Timboroa Forest (Kenya)

Thomas Kiprotich Kiptoo1, 2, , James L. Kiyiapi1 and Francis K. Sang1

1Department of Forestry and Wood Science, School of Environmental Science and Natural Resource Management, University of Eldoret, P.O Box 1125-30100, Eldoret–Kenya

2Kenya Forest Service, P.O Box 30513-00100, Nairobi Kenya

Pub. Date: June 26, 2024

Cite this paper:
Thomas Kiprotich Kiptoo, James L. Kiyiapi and Francis K. Sang. Invasive Acacia melanoxylon Impedes Growth of Commercial Tree Species in the Adjoining Forest Stands in Nabkoi and Timboroa Forest (Kenya). Applied Ecology and Forestry Science. 2024; 6(1):1-9. doi: 10.12691/aefs-6-1-1

Abstract

Alien species invasion of the forest ecosystem may lead to structuring of the plant community structure. Invasive Acacia is one of the alien tree species in forests. The ecological relationship between Acacia melanoxylon invasion and forest ecology is not well understood in tropical humid forest ecosystems. Therefore, the main objective of this study was to determine the influence of A. melanoxylon on two commercial forest tree species (Cupressus lusitanica and Pinus patula) in a humid tropical forest (North Tinderet Forest, in Kenya). Transects measuring 500 m long were used for sampling the uninvaded and invaded sites. Along the transect, three 10 m × 10 m plots were systematically placed at 235 m intervals to enable counting and recording of trees (density), measuring diameter at breast height (DBH) > 1.3 m) as well as tree heights. The study established that the tree density, DBH and height of Pinus patula and Cupressus lusitanica, were significantly (P < 0.05) higher at the non-invaded sites compared to the invaded sites. These findings suggest that A. melanoxylon invasion reduced the growths and establishment of commercial tree species. It is thus recommended that future studies on ecological conditions for growth of A. melanoxylon should be conducted in controlled environment through growth response measurements which was not possible under the current study. Invasion by A. melanoxylon reduce the growth of commercial plantation tree species (Pinus patula and Cupressus lusitanica) therefore strategies for controlling growth of the A. melanoxylon should be done. Future studies should investigate how the nutrient uptake by the commercial plantation tree species is influenced by Acacia melanoxylon density.

Keywords:
ecological conditions acacia growth invasiveness tropical environment forest growth

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

References:

[1]  Montagnani, C., Gentili, R., Brundu, G., Caronni, S. and Citterio, S. (2022). Accidental Introduction and Spread of Top Invasive Alien Plants in the European Union through Human-Mediated Agricultural Pathways: What Should We Expect? Agronomy. 12: 423.
 
[2]  Fitzpatrick, B.M., McCartney-Melstad, E., Johnson, J. and Shaffer, H.B. (2024). New evidence contradicts the rapid spread of invasive genes into a threatened native species. Research Square.
 
[3]  Omondi, S.F., Githae, E.W. and Khasa, D.P. (2023). Long‐distance gene flow in Acacia senegal: Hope for disturbed and fragmented populations. Ecology and Evolution. 13: e10292.
 
[4]  Souza-Alonso, P., Rodríguez, J., González, L. and Lorenzo, P. (2017). Here to stay. Recent advances and perspectives about Acacia invasion in Mediterranean areas. Annals of Forest Science. 74: 1-20.
 
[5]  Vieites-Blanco, C. and González-Prieto, S.J. (2020). Invasiveness, ecological impacts and control of acacias in southwestern Europe–a review. Web Ecology. 20: 33-51.
 
[6]  Kim, E., Moon, J., Shim, J. and Hwang, E. (2024). Predicting invasive species distributions using incremental ensemble-based pseudo-labeling. Ecological Informatics. 79: 102407.
 
[7]  Alemayehu, B., Suarez-Minguez, J. and Rosette, J. (2024). Modeling the Spatial Distribution of Acacia decurrens Plantation Forests Using PlanetScope Images and Environmental Variables in the Northwestern Highlands of Ethiopia. Forests. 15: 277.
 
[8]  Zhang, R., Zeng, B., Chen, T. and Hu, B. (2024). Correction: Zhang et al. Genotype–Environment Interaction and Horizontal and Vertical Distributions of Heartwood for Acacia melanoxylon R. Br. Genes 2023, 14, 1299. Genes. 15: 221.
 
[9]  Kiptoo, T.K. and Kiyiapi, J.L.O. (2023). Impacts of Invasive Species on Commercial Forest Plantations in Africa-A Review. Journal of Aquatic Terrestrial Ecosystems. 1: 56-65.
 
[10]  Meira-Neto, J.A.A., Silva, N., Villa, P.M., da Silva, M.C.N.A., Tolentino, G.S., Buttschardt, T., Ulm, F. and Máguas, C. (2023). Metabolic groups of plants in neotropical hyperseasonal savannas threatened by Australian Acacia invasion. Wetlands Ecology and Management. 31: 401-417.
 
[11]  Anibaba, Q.A., Dyderski, M.K., Woźniak, G.B. and Jagodziński, A.M. (2023). Native plant community characteristics explain alien species success in post-industrial vegetation. NeoBiota. 85.
 
[12]  Khattak, W.A., Sun, J., Hameed, R., Zaman, F., Abbas, A., Khan, K.A., Elboughdiri, N., Akbar, R., He, F. and Ullah, M.W. (2024). Unveiling the resistance of native weed communities: insights for managing invasive weed species in disturbed environments. Biological Reviews.
 
[13]  Sitati, A., Nyaboke, L., Raburu, P. and Masese, F. (2021). Macroinvertebrate Structural Composition as Indicators of Water Quality in Headwater Streams. Africa Environmental Review Journal. 4: 110-122.
 
[14]  Liu, C., Groff, T., Anderson, E., Brown, C., Cahill Jr, J.F., Paulow, L. and Bennett, J.A. (2023). Effects of the invasive leafy spurge (Euphorbia esula L.) on plant community structure are altered by management history. NeoBiota. 81: 157-182.
 
[15]  Wu, X., Chong, P., Xu, E., Zhao, W., Jing, W., Jin, M., Zhao, J., Wang, S., Wang, R. and Ma, X. (2024). Relationships between Regeneration of Qinghai Spruce Seedlings and Soil Stoichiometry across Elevations in a Forest in North-Western China. Forests. 15: 267.
 
[16]  de los Ángeles García-Hernández, M. and López-Barrera, F. (2024). Direct seeding success of four threatened oak species in a peri-urban forest: effects of microhabitat and rodent exclusion. Forest Ecology and Management. 553: 121629.
 
[17]  Jennings, S., Wilkinson, G. and Unwin, G. (2003). Response of blackwood (Acacia melanoxylon) regeneration to silvicultural removal of competition in regrowth eucalypt forests of north-west Tasmania, Australia. Forest ecology and management. 177: 75-83.
 
[18]  Bai, X., Chen, Z., Chen, M., Zeng, B., Li, X., Tu, P. and Hu, B. (2024). Morphological, Anatomical, and Physiological Characteristics of Heteroblastic Acacia melanoxylon Grown under Weak Light. Plants. 13: 870.
 
[19]  Witt, A., Beale, T. and van Wilgen, B.W. (2018). An assessment of the distribution and potential ecological impacts of invasive alien plant species in eastern Africa. Transactions of the Royal Society of South Africa. 73: 217-236.
 
[20]  Schoeman, J., Allan, C. and Finlayson, C. (2019). Exploring the multiple meanings of adaptive management: A case study of the Lachlan Catchment in the Murray–Darling Basin. Environmental Management. 64: 470-482.
 
[21]  Kumar, A., Bhattacharya, T., Shaikh, W.A. and Biswas, J.K. (2024). Valorization of invasive plant and leaf litter wastes into biochar: Production, properties and potential for arsenic removal. Groundwater for Sustainable Development. 24: 101066.
 
[22]  Guareschi, S., Cancellario, T., Oficialdegui, F. and Clavero, M. (2024). Insights from the past: Invasion trajectory and niche trends of a global freshwater invader. Global Change Biology. 30: e17059.
 
[23]  Pathak, R., Negi, V.S., Rawal, R.S. and Bhatt, I.D. (2019). Alien plant invasion in the Indian Himalayan Region: state of knowledge and research priorities. Biodiversity and Conservation: 1-30.
 
[24]  Sarr, M.S., Seiler, J.R. and Sullivan, J. (2024). Effect of drought stress on the physiology and early growth of seven Senegalia (Acacia) Senegal (L.) Britton provenances. New Forests: 1-14.
 
[25]  Tomasetto, F., Duncan, R.P. and Hulme, P.E. (2019). Resolving the invasion paradox: pervasive scale and study dependence in the native‐alien species richness relationship. Ecology letters. 22: 1038-1046.
 
[26]  Vilizzi, L., Piria, M., Pietraszewski, D., Giannetto, D., Flory, S.L., Herczeg, G., Sermenli, H.B., Britvec, M., Jukoniene, I. and Petrulaitis, L. (2024). Development and application of a second-generation multilingual tool for invasion risk screening of non-native terrestrial plants. Science of The Total Environment: 170475.
 
[27]  Kusmana, C. and Suwandhi, I. (2019). Diversity of plant species and the presence of Invasive Alien Species (IAS) in the Sub-Montane Forest at Pakenjeng Region, Southern Part of Garut, West Java: IOP Conference Series: Earth and Environmental Science. IOP Publishing, pp. 012035.
 
[28]  Lowry, B.J., Lowry, J.H., Jarvis, K.J., Keppel, G., Thaman, R.R. and Boehmer, H.J. (2020). Spatial patterns of presence, abundance, and richness of invasive woody plants in relation to urbanization in a tropical island setting. Urban Forestry & Urban Greening. 48: 126516.
 
[29]  Campagnaro, T., Brundu, G. and Sitzia, T. (2018). Five major invasive alien tree species in European Union forest habitat types of the Alpine and Continental biogeographical regions. Journal for nature conservation. 43: 227-238.
 
[30]  Yadav, S.P.S., Mehata, D.K., Pokhrel, S., Ghimire, N.P., Gyawali, P., Katel, S. and Timsina, U. (2024). A comprehensive study of banmara (invasive alien plant species): Understanding the invasive potential and ecological consequences for biodiversity conservation, and management strategies. Journal of Agriculture and Food Research: 101031.
 
[31]  Chance, D.P., McCollum, J.R., Street, G.M., Strickland, B.K. and Lashley, M.A. (2019). Native Species Abundance Buffers Non-Native Plant Invasibility following Intermediate Forest Management Disturbances. Forest Science. 65: 336-343.
 
[32]  Erckie, L., Adedoja, O., Geerts, S., van Wyk, E. and Boatwright, J.S. (2022). Impacts of an invasive alien Proteaceae on native plant species richness and vegetation structure. South African Journal of Botany. 144: 332-338.
 
[33]  Jansen, C. and Kumschick, S. (2022). A global impact assessment of Acacia species introduced to South Africa. Biological Invasions. 24: 175-187.
 
[34]  Matos, F.A., Edwards, D.P., S. Magnago, L.F., Heringer, G., Viana Neri, A., Buttschardt, T., Dudeque Zenni, R., Tavares de Menezes, L.F., Zamborlini Saiter, F. and Reynaud Schaefer, C.E.G. (2023). Invasive alien acacias rapidly stock carbon, but threaten biodiversity recovery in young second-growth forests. Philosophical Transactions of the Royal Society B. 378: 20210072.
 
[35]  Impson, F., Hoffmann, J., Impson, O., Kleinjan, C. and Moran, V.C. (2024). Densities of a perennial invasive tree, Acacia cyclops, decline in the 20 years since inception of biological control with two seed-reducing agents, a flower-galling midge and a seed-feeding weevil. Biological Control: 105442.
 
[36]  Aweto, A.O. (2024). Is woody plant encroachment bad? Benefits of woody plant encroachment—A review. Landscape Ecology. 39: 1-12.
 
[37]  KNBS. (2019). The 2019 Kenya Population and Housing Census: Population by County and Sub-county. Kenya National Bureau of Statistics.
 
[38]  Weiß, C.H. (2007). Statsoft, inc., tulsa, ok: Statistica, version 8. Springer.
 
[39]  Kirkpatrick, L.A. (2015). A simple guide to IBM SPSS Statistics-Version 23.0. Cengage Learning.
 
[40]  Alkharpotly, A., Abd-Elkader, D.Y., Salem, M.Z. and Hassan, H.S. (2024). Growth, productivity and phytochemicals of Coriander in responses to foliar application of Acacia saligna fruit extract as a biostimulant under field conditions. Scientific Reports. 14: 2921.
 
[41]  Pometti, C.L., Bessega, C.F., Vilardi, J.C. and Saidman, B.O. (2012). Landscape genetic structure of natural populations of Acacia caven in Argentina. Tree genetics & genomes. 8: 911-924.
 
[42]  Huntley, B.J. (2023). The Arid Savanna Biome, Ecology of Angola: Terrestrial Biomes and Ecoregions. Springer. pp. 339-359.
 
[43]  Linders, T.E.W., Schaffner, U., Eschen, R., Abebe, A., Choge, S.K., Nigatu, L., Mbaabu, P.R., Shiferaw, H. and Allan, E. (2019). Direct and indirect effects of invasive species: Biodiversity loss is a major mechanism by which an invasive tree affects ecosystem functioning. Journal of Ecology. 107: 2660-2672.
 
[44]  Sikorska, D., Sikorski, P., Archiciński, P., Chormański, J. and Hopkins, R.J. (2019). You can’t see the woods for the trees: invasive Acer negundo L. in urban riparian forests harms biodiversity and limits recreation activity. Sustainability. 11: 5838.
 
[45]  Lorenzo, P., Rodríguez, J., González, L. and Rodríguez-Echeverría, S. (2017). Changes in microhabitat, but not allelopathy, affect plant establishment after Acacia dealbata invasion. Journal of Plant Ecology. 10: 610-617.
 
[46]  Chaves Lobón, N., González Félix, M. and Alías Gallego, J.C. (2023). Comparison of the Allelopathic Potential of Non-Native and Native Species of Mediterranean Ecosystems. Plants. 12: 972.
 
[47]  Abd El Gawad, A. and El-Amier, Y. (2015). Allelopathy and potential impact of invasive Acacia saligna (Labill.) wendl. on plant diversity in the Nile delta coast of Egypt. International Journal of Environmental Research. 9.
 
[48]  Ismail, N. and Metali, F. (2014). Allelopathic effects of invasive Acacia mangium on germination and growth of local paddy varieties. Journal of Agronomy. 13: 158-168.