Abstract
Biological invasions and consequent mass development of aquatic macrophytes constitute a significant threat to aquatic environments. As a consequence, species invasiveness is becoming of great interest. Urochloa arrecta is a mass development invasive Poaceae that has caused many impacts in freshwaters in Brazil. Studies have described its remarkable tolerance to stressful conditions, but propagules resistance to desiccation while in dispersion is unknown. Here, we analyzed through a microcosm experiment U. arrecta’s small propagules regeneration after desiccation and without any sediment—thus simulating a transportation scenario. As expected, the longer the time of stress, the lower the propagule regeneration performance. Even so, the macrophyte propagules can survive up to six days off of water and any sediment. Even when the propagules seemed unviable, there was some degree of regeneration. As a consequence of the results, we state that removal and transportation of U. arrecta should be controlled considering the propagule viability.
References
Anderson LG, White PCL, Stebbing PD, Stentiford GD, Dunn AM (2014) Biosecurity and vector behaviour: evaluating the potential threat posed by anglers and canoeists as pathways for the spread of invasive non-native species and pathogens. PLoS ONE 9:e92788. https://doi.org/10.1371/journal.pone.0092788
Bando FM, Michelan TS, Thomaz SM (2016) Propagule success of an invasive Poaceae depends on size of parental plants. Acta Limnol Bras 28:e23
Barrat-Segretain MH, Bornette G (2000) Regeneration and colonization abilities of aquatic plant fragments: effect of disturbance seasonality. Hydrobiologia 421:31–39. https://doi.org/10.1023/A:1003980927853
Bora LS, Thomaz SM, Padial AA (2020) Evidence of rapid evolution of an invasive poaceae in response to salinity. Aquat Sci 82:76. https://doi.org/10.1007/s00027-020-00750-y
Carniatto N, Thomaz SM, Cunha ER, Fugi R, Ota RR (2013) Effects of an invasive alien Poaceae on aquatic macrophytes and fish communities in a neotropical reservoir. Biotropica 45:747–754. https://doi.org/10.1111/btp.12062
De Ventura L, Weissert N, Tobias R, Kopp K, Jokela J (2016) Overland transport of recreational boats as a spreading vector of zebra mussel Dreissena polymorpha. Biol Invasions 18:1451–1466
FARES, ALB, NONATO FA da S, MICHELAN, TS. (2020) New records of the invasive macrophyte, Urochloa arrecta extend its range to eastern Brazilian Amazon altered freshwater ecosystems. Acta Amazonica, 50(2), 133–137. https://doi.org/10.1590/1809-4392201903831
Ferreira FA, Pott A, Pott VJ, Latini RO, Resende DC (2016) Macrófitas aquáticas. In: Latini AO, Resende DC, Pombo VB, Coradin L (eds) Espécies exóticas invasoras de águas continentais no Brasil. Ministério do Meio Ambiente, Brasília, pp 657–726
Galvanese EF, Costa APL, Araújo ES et al (2022) Community stability and seasonal biotic homogenisation emphasize the effect of the invasive tropical tanner grass on macrophytes from a highly dynamic neotropical tidal river. Aquat Sci 84:30. https://doi.org/10.1007/s00027-022-00858-3
Hoffmann M, Reader U, Melezer A (2015) Influence of environmental conditions on the regenerative capacity and the survivability of Elodea nuttallii fragments. J Limnol 74:12–20
Hussner A, Heidbüchel P, Coetzee J et al (2021) From introduction to nuisance growth: a review of traits of alien aquatic plants which contribute to their invasiveness. Hydrobiologia 848:2119–2151. https://doi.org/10.1007/s10750-020-04463-z
Keane RM, Crawley MJ (2002) Exotic plant invasions and the enemy release hypothesis. Trends Ecol Evol 17:164–170
Kuntz K, Heidbüchel P, Hussner A (2014) Effects of water nutrients on regeneration capacity of submerged aquatic plant fragments. Ann Limnol 50:155–162
Li F, Zhu L, Xie Y, Jiang L, Chen X, Deng Z, Pan B (2015) Colonization by fragments of the submerged macrophyte Myriophyllum spicatum under different sediment type and density conditions. Sci Rep 5:11821
Li Y, Niu W, Cao X, Wang J, Zhang M, Duan X, Zhang Z (2019) Effect of soil aeration on root morphology and photosynthetic characteristics of potted tomato plants (Solanum lycopersicum) at different NaCl salinity levels. BMC Plant Biol 19:331
Lockwood JL, Cassey P, Blackburn T (2005) The role of propagule pressure in explaining species invasions. Trends Ecol Evol 20:223–228
Michelan T, Thomaz S, Carvalho P, Rodrigues R, Silveira M (2010) Regeneration and colonization of an invasive macrophyte grass in response to desiccation. Nat Conservação 8:133–139
Mitchell CE, Power AG (2003) Release of invasive plants from fungal and viral pathogens. Nature 421:625–627
R Core Team (2022) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. URL https://www.R-project.org/
Rejmánek M (2011) Invasiveness. In: Simberloff D, Rejmánek M (eds) Encyclopedia of biological invasions. University of California Press, Berkeley, pp 379–385
Ricciardi A, Cohen J (2007) The invasiveness of an introduced species does not predict its impact. Biol Invasions 9:309–315. https://doi.org/10.1007/s10530-006-9034-4
Santamaria L (2002) Why are most aquatic plants widely distributed? Dispersal, clonal growth and small-scale heterogeneity in a stressful environment. Acta Oecol 23:137–154
Sato RY, Costa APL, Padial AA (2021) The invasive tropical tanner grass decreases diversity of the native aquatic macrophyte community at two scales in a subtropical tidal river. Acta Bot Bras [online] 35:140–150. https://doi.org/10.1590/0102-33062020abb0360
Simberloff D, Martin J, Genovesi P, Maris V, Wardle DA, Aronson J, Courchamp F, Galil B, García-Berthou E, Pascal M (2013) Impacts of biological invasions: what’s what and the way forward. Trends Ecol Evol 28:58–66
Thiemer K, Schneider SC, Benoît OL, Demars BOL (2021) Mechanical removal of macrophytes in freshwater ecosystems: Implications for ecosystem structure and function. Sci Total Environ 782:146671
Torchin ME, Lafferty KD, Kuris AM (2002) Parasites and marine invasions. Parasitology 124:137–151
Torchin, M, Lafferty, K, Dobson A, McKenzie VJ, Kuris AM (2003) Introduced species and their missing parasites. Nature 421, 628–630. https://doi.org/10.1038/nature01346
Acknowledgements
A. A. Padial acknowledges the National scientific and technological development board (CNPQ) for continuous financial support (process number of current researcher scholarship: 308648/2021-8, see funding information for previous supports); L. S. Bora also acknowledges CAPES for student scholarship (financial code 001). This research had the support of Research Council of Norway (297202/E10), the German Federal Ministry of Education and Research (033WU005), the French Agence National de Recherche (No. ANR-18-IC4W-0004-06), the South African Water Research Commission (K5/2951), and the Araucária Foundation in Brazil (No. 186/2019) for funding of MadMacs (Mass development of aquatic macrophytes—causes and consequences of macrophyte removal for ecosystem structure, function, and services) in the frame of the collaborative international consortium of the 2017 call of the Water Challenges for a Changing World Joint Program Initiative (Water JPI).
Funding
This work was supported by the National Scientific and Technological Development Board (process numbers: 307984/2015-0, 402828/2016-0, 301867/2018-6, 308648/2021-8). Author Bora L.S has received research support from Personal Higher Education Improvement Coordination (CAPES, financial code 001) by student scholarship. This research had the support of Research Council of Norway (297202/E10), the German Federal Ministry of Education and Research (033WU005), the French Agence National de Recherche (No. ANR-18-IC4W-0004-06), the South African Water Research Commission (K5/2951), and the Fundação Araucária in Brazil (No. 186/2019) for funding of MadMacs (Mass development of aquatic macrophytes—causes and consequences of macrophyte removal for ecosystem structure, function, and services) in the frame of the collaborative international consortium of the 2017 call of the Water Challenges for a Changing World Joint Programme Initiative (Water JPI). This work has previously been published as a preprint on Research Square. https://doi.org/10.21203/rs.3.rs-2370056/v1.
Author information
Authors and Affiliations
Contributions
All authors contributed to the study’s conception and design. Material collection was made by both authors, and data collection and analysis were performed by LSB. All drafts of the manuscript were written by LSB and AAP. LSB and AAP read and approved the final manuscript.
Corresponding author
Ethics declarations
Conflict of interest
The authors have no relevant financial or non-financial interests to disclose.
Data availability
Complete data is available upon request to authors.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Bora, L.S., Padial, A.A. Propagule resistance of an invasive Poaceae as a trait of its invasiveness. Braz. J. Bot 46, 1089–1093 (2023). https://doi.org/10.1007/s40415-023-00952-2
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s40415-023-00952-2