Abstract
Fruiting in angiosperms is a complex process that is partially influenced by the external environment. In the case of invasive Alternanthera philoxeroides, introduction of this species to multiple global regions may have caused the failure of its sexual reproductive system due to genetic bottleneck and a propensity for clonal propagation. Alternanthera philoxeroides fruits rarely in its invaded ranges which raises questions regarding environmental stimuli that affect fruiting; we propose here that A. philoxeroides fruiting is partly caused by terrestrial conditions. Two instances of fruiting A. philoxeroides were observed in disparate locations in northern Mississippi, USA during 2022. Despite prolific fruiting in western Mississippi, no seeds germinated under any dormancy treatments at increasing durations. In both populations, fruiting was only observed in terrestrial forms of A. philoxeroides, even when nearby aquatic forms exhibited flowering but no fruiting. The exclusivity of fruiting to terrestrial A. philoxeroides seems to suggest drier conditions are an environmental trigger for A. philoxeroides fruiting. However, this process does not account for non-viability of seeds. Previous research suggests low genetic diversity can result in formation of nonviable seeds whether due to inbreeding depression or another unknown mechanism. We postulate that aquatic conditions present a barrier to A. philoxeroides fruiting and that if habitats transition from wet to dry, fruiting may be induced. However, environments are shifting and multiple A. philoxeroides haplotypes have been observed in the invaded range thus future work should assess the effects of terrestrial conditions on fruiting and seed viability in different A. philoxeroides haplotypes.
Data Availability
Data used in the preparation of this article will be made available by the corresponding author upon reasonable request.
References
Barrett SCH (2015) Influences of clonality on plant sexual reproduction. Proceedings of the National Academy of Sciences of the United States of America 112:8859–8866. https://doi.org/10.1073/pnas.1501712112
Barrett SCH, Colautti RI, Eckert CG (2008) Plant reproductive systems and evolution during biological invasion. Molecular Ecology 17:373–383. https://doi.org/10.1111/j.1365-294X.2007.03503.x
Cho L-H, Yoon J, An G (2017) The control of flowering time by environmental factors. The Plant Journal 90:708–719. https://doi.org/10.1111/tpj.13461
Clements D, Dugdale TM, Butler KL, Hunt TD (2014) Management of aquatic alligator weed (Alternanthera philoxeroides) in an early stage of invasion. Management of Biological Invasions 5:327–339
Comai L (2005) The advantages and disadvantages of being polyploid. Nature Reviews Genetics 6:836–846. https://doi.org/10.1038/nrg1711
Cortés-Flores J, Cornejo-Tenorio G, Urrea-Galeano LA et al (2019) Phylogeny, fruit traits, and ecological correlates of fruiting phenology in a Neotropical dry forest. Oecologia 189:159–169. https://doi.org/10.1007/s00442-018-4295-z
Du Y, Mao L, Queenborough SA et al (2020) Macro-scale variation and environmental predictors of flowering and fruiting phenology in the Chinese angiosperm flora. Journal of Biogeography 47:2303–2314. https://doi.org/10.1111/jbi.13938
Dugdale TM, Champion PD (2012) Control of alligator weed with herbicides: A review. Plant Protection Quarterly 27:70–82
European and Mediterranean Plant Protection Organization (2016) Alternanthera philoxeroides (Mart.) Griseb. EPPO Bulletin 46:8–13. https://doi.org/10.1111/epp.12275
Fredriksson GM, Wich SA, Trisno, (2006) Frugivory in sun bears (Helarctos malayanus) is linked to El Niño-related fluctuations in fruiting phenology, East Kalimantan, Indonesia. Biological Journal of the Linnean Society 89:489–508. https://doi.org/10.1111/j.1095-8312.2006.00688.x
Ghazoul J, Satake A (2009) Nonviable seed set enhances plant fitness: the sacrificial sibling hypothesis. Ecology 90:369–377. https://doi.org/10.1890/07-1436.1
Government of Canada CFIA (2014) Weed Seed - Sessile joyweed (Alternanthera sessilis). https://inspection.canada.ca/plant-health/seeds/seed-testing-and-grading/seeds-identification/alternanthera-sessilis/eng/1398289385833/1398289412685. Accessed 24 Sep 2022
Julien MH, Bourne AS, Low VHK (1992) Growth of the weed Alternanthera philoxeroides (Martius) Grisebach, (alligator weed) in aquatic and terrestrial habitats in Australia. Plant Protection Quarterly 7:102–108
Julien MH, Skarratt B, Maywald GF (1995) Potential Geographical Distribution of Alligator Weed and its Biological Control by Agasicles hygrophila. Journal of Aquatic Plant Management 33:55–60
Kapoor L, Simkin AJ, George Priya Doss C, Siva R (2022) Fruit ripening: dynamics and integrated analysis of carotenoids and anthocyanins. BMC Plant Biology 22:27. https://doi.org/10.1186/s12870-021-03411-w
Kita KK, de Souza MC (2003) Levantamento florístico e fitofisionomia da lagoa Figueira e seu entorno, planície alagável do alto rio Paraná, Porto Rico, Estado do Paraná Brasil. Acta Scientiarum Biological Sciences 25:145–155. https://doi.org/10.4025/actascibiolsci.v25i1.2091
Kittelson PM, Maron JL (2000) Outcrossing rate and inbreeding depression in the perennial yellow bush lupine, Lupinus arboreus (Fabaceae). American Journal of Botany 87:652–660. https://doi.org/10.2307/2656851
Lui-qing Y, Fuji Y, Yong-jun Z et al (2007) Response of Exotic Invasive Weed Alternanthera philoxeroides to Environmental Factors and Its Competition with Rice. Rice Science 14:49–55
Mendoza I, Peres CA, Morellato LPC (2017) Continental-scale patterns and climatic drivers of fruiting phenology: A quantitative Neotropical review. Global Planet Change 148:227–241. https://doi.org/10.1016/j.gloplacha.2016.12.001
Nathan R (2006) Long-Distance Dispersal of Plants. Science 313:786–788. https://doi.org/10.1126/science.1124975
Roberto MC, Santana NF, Thomaz SM (2009) Limnology in the Upper Paraná River floodplain: large-scale spatial and temporal patterns, and the influence of reservoirs. Brazilian Journal of Biology 69:717–725. https://doi.org/10.1590/S1519-69842009000300025
Roman J, Darling JA (2007) Paradox lost: genetic diversity and the success of aquatic invasions. Trends in Ecology & Evolution 22:454–464. https://doi.org/10.1016/j.tree.2007.07.002
Sosa AJ, Julien MH, Cordo HA (2003) New research on Alternanthera philoxeroides (alligator weed) in its South American native range. Proceedings of the XI International Symposium on Biological Control of Weeds. CISRO Entomology, Canberra, Austrailia, pp 180–185
Tanveer A, Ali HH, Manalil S et al (2018) Eco-Biology and Management of Alligator Weed [Alternanthera philoxeroides) (Mart.) Griseb.]: a Review. Wetlands 38:1067–1079. https://doi.org/10.1007/s13157-018-1062-1
Vogt GB, Qumbly, Jr. PC, Kay SH (1992) Effects of Weather on the Biological Control of Alligatorweed in the Lower Mississippi Valley Region, 1973–83. United States Department of Agriculture. Tech Bull 1766:1–143
Williams DA, Harms NE, Knight IA et al (2020) High genetic diversity in the clonal aquatic weed Alternanthera philoxeroides in the United States. Invasive Plant Science and Management 13:217–225. https://doi.org/10.1017/inp.2020.32
Williamson GB, Ickes K (2002) Mast fruiting and ENSO cycles – does the cue betray a cause? Oikos 97:459–461. https://doi.org/10.1034/j.1600-0706.2002.970317.x
Xu C-Y, Zhang W-J, Fu C-Z, Lu B-R (2003) Genetic diversity of alligator weed in China by RAPD analysis. Biodiversity Conservation 12:637–645. https://doi.org/10.1023/A:1022453129662
Acknowledgements
We thank the South Carolina Aquatic Plant Management Society and the MidSouth Aquatic Plant Management Society whose scholarships helped fund this and other important research on invasive Alternantera philoxeroides. We thank Weston Thompson and the rest of the Mississippi Department of Wildlife, Fisheries, and Parks for permitting the use of Muscadine Farms Wildlife Management Area. We thank Alejandro Sosa, PhD for providing insight into native A. philoxeroides reproduction in Argentina. We thank Ryan Folk, PhD, Nicholas Engle-Wrye, and the rest of the staff at the Mississippi State University herbarium (MISSA) for housing and digitizing A. philoxeroides vouchers used in the preparation of this article.
Funding
This research on invasive Alternantera philoxeroides was funded by the Gulf States Marine Fisheries Commission (grant # FWS-801–037-2021-MSU).
Author information
Authors and Affiliations
Contributions
Samuel A. Schmid, Gray Turnage, and Gary N. Ervin all contributed to the study conception and design. Material preparation, data collection and analysis were performed by Samuel A. Schmid. The manuscript was drafted by Samuel A. Schmid. Samuel A. Schmid, Gray Turnage, and Gary N. Ervin all critically revised subsequent versions of the manuscript. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Competing Interests
The authors declare no competing interests were operative in the preparation of this article.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
13157_2023_1662_MOESM1_ESM.docx
Supplementary file1 Text files of herbarium labels for voucher specimens Schmid 14 MISSA037070, Schmid 15 MISSA037071, Schmid 19 MISSA037072. (DOCX 13 KB)
Rights and permissions
About this article
Cite this article
Schmid, S.A., Turnage, G. & Ervin, G.N. Rare Production of Seeds by Invasive Alternanthera philoxeroides (Alligator Weed) in North America Observed in Terrestrial Populations. Wetlands 43, 12 (2023). https://doi.org/10.1007/s13157-023-01662-x
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s13157-023-01662-x