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Tecoma stans. (Drawn by W. Roux, first published in Henderson (1995), ARC-Plant Protection Research Institute, Pretoria.) 

Tecoma stans. (Drawn by W. Roux, first published in Henderson (1995), ARC-Plant Protection Research Institute, Pretoria.) 

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Tecoma stans (L.) Juss ex Kunth var. stans (Bignoniaceae), known as yellow bells, was introduced into South Africa as an ornamental plant and now invades roadsides, urban open spaces, watercourses and rocky sites in the subtropical and tropical areas of six South African provinces, and neighbouring countries. Although deemed to be an ‘emerging weed...

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... stans (L.) Juss ex Kunth var. stans (Bignoniaceae) (Fig. 1), commonly known as yellow bells, is an evergreen shrub or small tree that has a wide natural distribution in the tropical and subtropical parts of central Mexico and South Florida, spreading southwards through Central America, the Caribbean and South America as far as northern Argentina (Gentry 1992). In Mexico, T. stans flowers have ...
Context 2
... stans ( Fig. 1) is a morphologically variable, densely-leafed shrub to small tree that is approxi- mately 2-6 m tall, occasionally up to 10 m in height and up to 25 cm in stem-diameter (Gentry 1992). Descriptions of the plant are provided by Pelton (1964), Gentry (1992), andHenderson (2001). The leaves are 100-200 mm long with a bright green adaxial ...

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... Es cultivada como especie ornamental en los trópicos y subtrópicos, por la vistosidad de sus flores; de igual forma es utilizada como barrera rompe viento y como cobertura para evitar el crecimiento de malezas. Sus hojas poseen efectos antidiabéticos y sus flores pueden ser empleadas como forraje de bajos porcentajes de nutrientes (Hoyos 1990;Madire et al. 2011). ...
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... ex Kunth var. stans (Bignoniaceae), also known as yellow bells, is a fast-growing small tree or shrub that produces thousands of viable light-weight papery seeds (Madire et al., 2011). It is native to Mexico, the southern states of the USA and throughout Central America, including the Caribbean region (Madire, 2013;Pelton, 1964). ...
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... Tecoma stans (L.) Juss ex Kunth var. stans (Bignoniaceae), commonly known as yellow bells, is an invasive shrub or small tree in South Africa and neighbouring countries that grows aggressively and typically forms multi-stemmed shrubs after clearing (Madire et al., 2011). The plant has a wide natural distribution in tropical and subtropical parts of the Western Hemisphere (Pelton, 1964). ...
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... Mada polluta has since established and become abundant at a few sites in KwaZulu-Natal (KZN) and the Eastern Cape (EC) provinces, while very small populations of Pseudonapomyza sp. have been recorded in KZN, EC, Limpopo and Mpumalanga provinces. Due to the severity of T. stans invasions in South Africa, it has been argued that a suite of agents is required to attack various parts of the plant, including the root system and the reproductive organs (Madire et al. 2011a). The Mexican root-feeding flea beetle Heikertingerella sp. ...
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Despite potential negative interactions between biological control agents, the release of multiple agents against invasive alien weeds is often justified. The leaf-feeding beetle Mada polluta Mulsant (Coleoptera: Coccinellidae), released against Tecoma stans (L.) Juss ex Kunth var. stans in South Africa, has so far been unable to contain the weed. Consequently, the root-feeding flea beetle Heikertingerella sp. (Coleoptera: Galerucinae) was introduced to complement M. polluta. The effects of the interaction between the two beetles on their performance and on the target weed were studied on potted T. stans plants in a quarantine glasshouse to assess whether they were additive, synergistic or negative. There was no significant difference in the percentage survival of the P1 adults of either beetle when tested alone or in combination. Mada polluta produced significantly more F1 adult progeny than Heikertingerella sp. when tested alone, while both beetles produced significantly fewer offspring when tested in combination. Leaf damage by M. polluta alone was higher than that caused by Heikertingerella sp. alone, but in combination was not significantly higher than damage by M. polluta alone. Although both beetles on their own caused a significant reduction in leaf density relative to the control, leaf density was significantly lower when in combination. Despite significant reductions in plant height relative to the control, the differences between the three beetle treatments were not significant. Although competitive interactions caused a trade-off between agent proliferation and their impact on the growth of T. stans, these data need to be confirmed in the field.
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Forest fires are frequent disturbances in tropical dry forests that influence the ecological processes and ecosystem services they provide. These can alter the viability of the seeds present in the edaphic bank, reducing their germination potential and the subsequent emergence of seedlings, which are key processes for the regeneration of the natural forest. In this work, the effect of temperatures presented during forest fires in the seed bank on nine representative species of the tropical dry forest were evaluated. My main objective was to quantify the viability and germination potential of the seed bank so that the effectiveness of these species can be identified in programs of conservation and restoration of dry forests with recurrent fires. I observed that Caesalpinia pulcherrima, Cordia alba, Crescentia cujete, Enterolobium cyclocarpium, Hura crepitans, and Lonchocarpus cf. violaceus may tolerate the conditions of low intensity forest fires; however, only H. crepitans may resist higher temperatures which are typical of high- intensity fires. In contrast, the species Pithecellobium dulce, Tabebuia rosea and Tecoma stans turned out to be highly vulnerable to high temperatures related to the effect of fire, so their seed banks could disappear due to forest fires. In conclusion, the priority use of C. pulcherrima, E. cyclocarpium, C. alba, C. cujete, L. cf. violaceus and H. crepitans in programs of ecological restoration of dry forests with a high incidence of forest fires, due to these species might generate seed banks that guarantee the continuity of their populations.
... This species produces large quantities of seeds dispersed by the wind (Pelton, 1964), mainly in dry seasons (Rojas-Rodríguez & Torres-Córdoba, 2012). While the species is used to reforest degraded sites (Chízmar, De Gracia, & Hoyos, 2015;Otsamo, Adjers, Hadi, Kuusipalo, & Vuokko, 1997), it is considered highly invasive in many places where it has been introduced as an ornamental or medicinal plant (Da Silva, Reis, & Reis, 2008;Lorenzi, 2000;Madire, Wood, Williams, & Neser, 2011;Reis et al., 2014;Ziller, 2001). T. stans is typical of dry forests in a relatively early successional state or in places dominated by subxerophytic scrub vegetation and in welldrained and/or rocky soils, although it may also be found in areas of pre-mountain and mountain rainforest (Pelton, 1964). ...
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Seed germination and seed longevity under different environmental conditions are fundamental to understand the ecological dynamics of a species, since they are decisive for its success within the ecosystem. Taking this into account, seed germination and seed storage behavior of a pioneer species of tropical dry forest (Tecoma stans) were studied in the laboratory, to establish the effect of different environmental conditions on a local tree population. Two seed lots collected in July 2011, from Cali (Colombia), were evaluated under three alternating temperatures (20/30, 20/25, 25/30 ºC; 16/8 h) and four light qualities (12-hour white light photoperiod, darkness, and 15 minutes of red light -R and far red light -FR). Final germination was recorded for all treatments; for white light treatment the daily germination was recorded to calculate mean germination rate, mean germination time, and two synchronization indices. To assess the effect of light quality on physiological variables, a destructive germination test was carried out. For this test, another seed lot was evaluated under the same light conditions using an alternating temperature of 20/30 °C - 16/8 h, recording germination during six days for every treatment. In addition, seeds were stored at two different moisture contents (7.7, 4.1 %) and three storage temperatures (20, 5, -20 ºC), during two time periods (one and three months); a seed germination test was conducted for each treatment. Four replicates of 35 seeds per treatment were used for all experiments. Germination was high (GP > 90 %) with all alternating temperatures under white light, whereas under R, FR, and darkness germination was evenly successful at low temperatures, but at higher temperature, half of the seeds entered into secondary dormancy (GP= 45-65 %). However, mean germination rate and synchronization under R and FR decreased significantly in comparison to white light treatment and, consequently, mean germination time increased. Seed storage behavior of this species is orthodox due to the high germination (GP > 90 %) obtained under all treatments. In conclusion, T. stans seeds have a negative germination response at high incubation temperatures in the absence of white light, entering into a secondary dormancy. In contrast, an environment with a lower temperature and without white light delays the germination, but at the end seeds are able to reach the same germination values. This seed dependence on incident light in limiting conditions suggests a physiological mechanism on the seed tissues of this species, probably mediated by phytochromes. Finally, the orthodox seed storage behavior of T. stans is a reason to include this species in ex situ seed conservation programs for restoration and recovery of the tropical dry forest; however, long-term studies should be conducted in order to evaluate the maintenance of this characteristic throughout longer periods of time.