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William Ortmans, Grégory Mahy & Arnaud Monty

Northern range edge equilibrium of Ambrosia artemisiifolia L. not achieved in Western Europe

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Notes de la rédaction

Received on June 16, 2016; accepted on February 21, 2017

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L’équilibre en bordure d’aire nord n’est pas atteint pour l’invasion d’Ambrosia artemisiifolia L. en Europe de l’Ouest

Description du sujet. La distribution géographique d’une espèce, indigène ou invasive, peut être limitée par l’environnement. Dans cette situation, le taux de croissance des populations au-delà de la bordure d’aire est inférieur au taux de remplacement, et un équilibre en bordure d’aire (Range edge equilibrium, REE) prend place. L’émergence d’un REE n’a jamais été spécifiquement testée chez une espèce invasive. En Europe de l’Ouest, l’espèce invasive Ambrosia artemisiifolia L. est très abondante dans les champs de tournesols du centre et du sud de la France, mais sa progression semble limitée vers le Nord. Actuellement, on ne sait pas si l’espèce a atteint un REE ou non. Des informations sur la réponse de l’espèce face à la compétition du tournesol sont également manquantes.

Objectifs. Ce travail adresse deux questions : En Europe de l’Ouest, A. artemisiifolia a-t-elle atteint un REE au nord de son aire d’invasion ? Comment la compétition du tournesol influence-t-elle l’espèce ?

Méthode. Des plantules d’A. artemisiifolia ont été plantées avec ou sans tournesols dans des quadrats installés dans un champ en Belgique, environ 250 km au nord du front d’invasion. L’année suivante, le taux de croissance des populations et la banque de graines ont été évalués.

Résultats. Le taux de croissance des populations et la banque de graines ont été relativement importants. La compétition du tournesol n’a pas eu d’impact significatif sur les performances des plants.

Conclusions. Les résultats réfutent l’hypothèse d’un équilibre au front d’invasion actuel et suggèrent un potentiel d’invasion significatif vers le Nord.

Mots-clés : Belgique, distribution géographique, espèce envahissante, facteur écologique, compétition interspécifique, expérimentation au champ, Helianthus annuus


Description of the subject. The geographic distributions of a species, be it native or alien, is expected to be limited at some point by environmental conditions. In this situation, a range edge equilibrium (REE) takes place, i.e., populations occurring beyond the edge have a growth rate reduced below replacement. The occurrence of REE has never been tested for an invasive species. In Western Europe, the invasive weed Ambrosia artemisiifolia L. has spread in most parts of southern and central France, where it can be found in very high densities in sunflower fields, but seems to be limited in its northwards expansion. It is currently unknown whether the range has reached a limit or not. Information about how the species responds to sunflower competition is also lacking.

Objectives. This work addressed two questions: Has the northern part of A. artemisiifolia invaded range in Western Europe reached REE? How is A. artemisiifolia performance influenced by sunflower competition?

Method. Plots were established in an agricultural field ca. 250 km north to the current invaded range, in Belgium. We planted A. artemisiifolia seedlings with or without sunflower competition. The following year, the population growth rates and the soil seed bank were assessed.

Results. The species established populations with relatively high growth rates and soil seed bank. Sunflower competition did not have a significant impact on plant performance.

Conclusions. The results invalidate the hypothesis of equilibrium at the current margin of A. artemisiifolia invaded range, and suggest a significant potential for invasion northwards.

Keywords : Belgium, invasive species, geographical distribution, Helianthus annuus, interspecific competition, field experimentation, ecological factors

1. Introduction

1Species distributions are essentially the expression of a species’ ecological niche in space (Sexton et al., 2009). At the range edge of a given species, further expansion of the range is limited by biotic or abiotic factors that impede new populations’ survival beyond the edge (Hutchinson, 1957). Despite some minor fluctuations due to temporal variability at the range edge (Sexton et al., 2009), the long-term distribution of most native species is stable, and the situation is described as being in a range edge equilibrium (REE) (Stanton-Geddes et al., 2012).

2Biological invasions consist of the spread of invasive alien species in a new range, where they historically have not been present (Mack, 1981). At first, this new range is expanding with the species colonizing new habitats (Monty & Mahy, 2009; Alexander & Edwards, 2010). But all species are limited at some point along environmental gradients in their introduced range, just as they are in their native range (Alexander & Edwards, 2010). Due to the damage that invasive species can cause, it is important to predict how far their range might expand. Species’ range limits are well-known for native species (Stanton-Geddes et al., 2012; Hargreaves et al., 2014), and there is increasing evidence of range limits for alien species (Sexton et al., 2009; Alexander & Edwards, 2010). However, as is best presently known, no studies have explicitly tested REE for invasive species. This test would allow determination of whether the invasion range may or may not expand further.

3The population growth rate is the rate at which the number of individuals in a population changes in a given time period. It informs on whether the number of individuals is increasing, stable or decreasing, and how fast it is changing. Conventionally, the factor by which population size increases per year is the finite growth rate, and is given the symbol λ. It is calculated as Nt+1/Nt (Sibly & Hone, 2002), where N is the number of individuals, and t and t+1 are two given consecutive years. The measurement of λ beyond the range edge can be used to test the hypothesis of a REE (Stanton-Geddes et al., 2012; Hargreaves et al., 2014). Finding that λ is reduced below replacement (λ < 1) beyond the edge would indicate that the species distribution is stable. Occurrences of a population beyond the edge do not automatically disprove REE. For example, casual populations may persist several years despite unsuitable environmental conditions that limit their reproduction. The occurrence of such populations can be attributable to repeated introductions by human activity (Richardson et al., 2000), or to the formation of a soil seed bank that recovers the population, e.g., after a disturbance event (Gioria et al., 2012).

4Ambrosia artemisiifolia L. (Common ragweed, Asteraceae) is an annual invasive weed that was introduced from North America to Europe more than a century ago (Heckel, 1906). The species is currently invading numerous European countries (Chauvel et al., 2006; Kazinczi et al., 2008; Smith et al., 2013), where it is causing a health crisis because of its allergenic pollen (Kazinczi et al., 2008; Smith et al., 2013). The invasion is mostly favored by human activity and mostly grows along roads, riverbanks, wastelands and cultivated fields (Bassett & Crompton, 1975). Because the sunflower and A. artemisiifolia are both from the Asteraceae family, chemical control of the species is often ineffective (Chollet et al., 1999). Despite the fact that some sunflower varieties (e.g. Clearfield, Express Sun) tolerate some herbicide application and therefore facilitate the chemical treatment of A. artemisiifolia, high densities of the plant can often be observed in sunflower fields (Genton et al., 2005; Fumanal et al., 2008a; Pinke et al., 2013).

5The species can show considerable phenotypic variation, both in terms of plant size (Leiblein-Wild & Tackenberg, 2014; Ortmans et al., 2016a) and seed traits (Fumanal et al., 2007a; Ortmans et al., 2016b). Plant height can vary from 0.1 to 2.5 m according to environmental conditions (Essl et al., 2015). A single plant can produce from 300 to 6,000 seeds on average, and this number can reach 14,000 when the conditions are favorable (Bassett & Crompton, 1975). In addition, the species lifecycle is characterized by a long-term persisting seedbank (Bassett & Crompton, 1975; Fumanal et al., 2008b) that appears to play a major role in the invasion process (Baskin & Baskin, 1980; Guillemin & Chauvel, 2011). This is especially problematic in cultivated fields, where the seeds are buried or recovered when the ground is plowed (Bassett & Crompton, 1975; Baskin & Baskin, 1980; Fumanal et al., 2008b; Guillemin & Chauvel, 2011; Gioria et al., 2012).

6In Europe, its invasive range is intensively studied (Chauvel et al., 2006; Kazinczi et al., 2008; Essl et al., 2009; Pinke et al., 2011; Skjøth et al., 2013; Smith et al., 2013; Essl et al., 2015; Ortmans et al., 2016). Currently, there are three main regions that are highly invaded in Europe (Skjøth et al., 2013; Smith et al., 2013; Essl et al., 2015): the southeast of France (the Rhône Valley; Chauvel et al., 2006), the north of Italy (the Po region) and a larger area including western Austria (Essl et al., 2009), southern Czech Republic, southern Poland, Slovakia, Hungary (Kazinczi et al., 2008; Pinke et al., 2011), Slovenia, Croatia, Bosnia and Herzegovina, Serbia, Ukraine, and Romania.

7North of these highly invaded areas, the species is also present in lower densities. The invasion has reached northern France, northeast Germany, northern Poland, the Belarus and Russia. For the moment, it is difficult to predict how far the invasion will extend. The distribution of A. artemisiifolia appears to be limited in Northern Europe by low autumnal temperature that kills the adult plants before seed production (Chapman et al., 2014; Skálová et al., 2015).

8In Western Europe, some populations have been recorded over the years in Belgium, The Netherlands and northern Germany. However, these populations do not appear to become invasive (Verloove, 2006; Brandes & Nitzsche, 2007; Martin & Lambinon, 2008). Based on the literature and pollen density maps (Skjøth et al., 2013; Smith et al., 2013) it is possible to approximately map the invaded range in Western Europe (Figure1). Furthermore, in Belgium, A. artemisiifolia is still considered a casual non-naturalized species, because the local climate is described as limiting the plant’s development (Lambinon et al., 2004; Verloove, 2006; Martin & Lambinon, 2008). In contrast, several authors have predicted that the species will probably increase its distribution northwards (Cunze et al., 2013; Chapman et al., 2014; Storkey et al., 2014; Leiblein-Wild et al., 2016). This situation leads to questions about whether the invasion will indeed stabilize. Given that A. artemisiifolia is highly detrimental to humans (Kazinczi et al., 2008; Smith et al., 2013), there is an urgent need to determine if the invaded range will expand or not.


9The species’ invasion appears to be linked to sunflower cultivation (Chollet et al., 1998; Genton et al., 2005; Fumanal et al., 2008a; Pinke et al., 2013; Ozaslan et al., 2016). Sunflower production could be one of the factors behind the success of the invasion, and studies aiming to understand how A. artemisiifolia thrives in agricultural habitats are therefore needed (Pinke et al., 2013; Ozaslan et al., 2016). In sunflower fields, the competition inflicted on weed species is not expected to be homogeneous all over the field. For example, in field margins, the sunflower densities could be reduced due to an edge effect (Sosnoskie et al., 2007). Furthermore, field margins are known to harbor more weeds and pest species than the rest of the field, and can serve as a stepping stone for the invasion of the center of the field or as a source population for the invasion of adjacent fields (Blumenthal & Jordan, 2001; Sosnoskie et al., 2007). In order to assess how sunflower competition can impact A. artemisiifolia, this factor was explicitly tested in our study.

10Specifically, the work presented here addressed the following questions:

11– Has the distribution of A. artemisiifolia in Western Europe reached a REE situation?

12– How is A. artemisiifolia performance influenced by sunflower competition?

13To answer these questions, a field experiment was established 250 km north of the current margin of the invaded range in Western Europe. There have been many occurrences of the species close to the study site (Bullock et al., 2012; Ortmans et al., 2016a), so this experiment does not risk introducing the species into a virgin territory. The experimental context was a sunflower field. Ambrosia artemisiifolia plants from eight different populations from France were left to grow and reproduce, with or without sunflower competition. To take into account the variation induced by the origin of the population, this factor was explicitly introduced into the analysis. After two growing seasons, and before the second seed rain, population finite growth rates were assessed, and the soil seed bank was quantified.

2. Materials and methods

2.1. Seed collection

14The seeds were collected in the nearest invaded area from Belgium, in France. The seed collection occurred in the autumn 2011 in eight populations (Figure 1). A population was defined as a set of individuals of the same species growing on a uniform landscape element, at a given moment. Populations’ habitat was either ruderal (riverbank, railroad, soil deposit) or agricultural (corn field, uncultivated field, and fallows). The seed collection was carried out on 20 to 40 plants by population, and the collected seeds were pooled by population. The seeds were stored in cold (5 °C) and dry conditions.

2.2. Experimental design

15Prior to the start of the experiment, circa 150 seeds per population were stratified for 6 weeks at 5 °C on wet paper filter. Then the seeds were sown in plastic trays containing a thin layer of moisturized soil from the study site. Trays were put in a greenhouse in order to induce germination, but without supplementary heating, ventilation or lightning. On the 1st of May 2013, we selected 48 seedlings at the same development stage (i.e., with only cotyledons) of each population to be transplanted into the field experiment.

16The field experiment was established approximatively 250 km north of the current invasion range, in Gembloux, Belgium (50.565°N latitude, 4.703°E longitude). The experiment was established in an open ground agricultural field that served as a fallow land for several years. The soil is mainly loamy, with a share of sand and a small part of clay, fairly rich and favorably drained. To mimic the agricultural conditions, a plowing followed by tillage was performed. We established 64 plots of 1.4 1.4 m (1.96 m2) following a grid, and we spaced each plot 30 cm away from one another. Each plot was randomly assigned to one of the eight populations (A to H), and six seedlings of that population were planted. We paid attention to plant each plant at least 35 cm from one another, and at least 40 cm away from a border, to avoid future seeds falling off the plot during the fruiting season.

17Four plots of each population (i.e., half the plots) were randomly selected to receive the sunflower competition. This competition was applied following the agricultural technical itinerary available on the website of the French Technical Institute for oilseeds, protein crops, and hemp and their chains (Cetiom, 2013). This itinerary informs about the density and spacing of sunflower rows used in French agriculture (i.e., a density of six sunflowers by square meter and a spacing of 50 cm between rows). Thus, on the 1st of May 2013, we sowed 12 sunflowers on three equidistant rows spaced by 50 cm in each plot, with the center row aligned to the middle of the plot. On the 1st of June 2013, we performed a second sowing to replace the dead sunflowers. Every two weeks, new weeds other than ragweed seedlings were pulled up by hand to imitate the low competition normally occurring in sunflower crops.

18On the first flower appearance, i.e., on the 31st of July 2013 a wood frame supporting a “pollen-proof” small mesh fabric (Plantex® Protectmax, Du Pont de Nemours, Puteaux, France) was installed above each plot. This fabric allowed water to flow but limited pollen dispersion. The aim of this installation was to reduce cross fertilization among populations, and the hazard that the pollen can cause to the nearby inhabitants. To avoid inducing too much changes in environmental conditions, e.g., a decrease in the light received by the plants, or an increase in temperature within the frame, the fabric was only fixed until the 31st of September 2013. To prevent this experiment from acting as a source population, or from being a new introduction focus, we took caution to limit seed dispersal. We installed a fence on the ground that delimitated each plot, consisting of a 2 mm mesh of 30 cm height, with the bottom 10 cm buried in the soil. This fence allowed the water to flow but prevented the released seeds from being carried away by runoff water.

19In the second growing year, on the 3rd of March 2014, we mimicked tillage by scratching the soil surface with a rake. On A. artemisiifolia seedlings’ first emergence, on the 27th of March 2014, we sowed once again sunflowers following the same protocol. The sowing occurred on the same plots as the previous year, to perpetuate the sunflower competition.

20Following the end of the experiment, all the remaining plants were hand pulled to avoid creating a new population at the experimental site. We did not plow the field, in order to avoid burying seeds that can therefore remain viable a long time (Baskin & Baskin, 1980). We then realized a stale seedbed to deplete the soil seedbank, and then we established a pasture that applies sufficient competition to limit the development of the plant. The pasture is monitored regularly and the new A. artemisiifolia plants are hand pulled.

2.3. Plant performance measurements

21In order to obtain a non-destructive measurement of the plant performance at the end of the first year, we measured the height and diameter of all the A. artemisiifolia plants on the 1st of October 2013. Then, we calculated a mean biovolume by plot as:


22where k is the number of plants within the plot, and D and H, respectively, the diameter and height. Biovolume is a non-destructive measurement that is highly correlated to the biomass (Sarmiento et al., 2012), and is therefore a useful measurement to take for the comparison of population growth performance.

23We let the plants produce and release seeds. Since the species has barochoric dispersal, we assumed that the large majority of the seeds fell within the plot.

24On the 14th of February 2014, the plants completely lost their seeds and leaves, and had the appearance of dead branches. At that moment, we cut the stems at the ground surface and removed them, in order to allow the monitoring of the plots, the mimicked tillage operation, the sunflower sowing, and the other weed species removal.

25The second year, on the 1st of August 2014, we counted the number of plants in each plot by a subsampling method. The subsamples consisted of three randomly placed frames of 290 cm² within the plot. The total number of offspring by plot was then assessed. We also calculated λ (i.e., the population finite growth rate of each plot) by dividing the assessed number of offspring in August 2014 by six (the number of transplanted parents in 2013).

26On the same date, the stems of all plants were cut at the ground surface and were paper bagged by plot. The paper bags were dried for four days at 80 °C then weighted to the nearest 1 g (Optiss BC5000V1, Tefal, Sarcelles, France) to determine the offspring biomass. The biomass of A. artemisiifolia is closely related to the quantity of pollen and seeds produced by the plant (Fumanal et al., 2007b), and is thus a proxy for the reproductive performance.

27Finally, to evaluate how a single seed rain can contribute to the population growth, we made an evaluation of the soil seed bank. Twenty carrots of 2 cm diameter and 10 cm depth were sampled randomly at the surface of each plot. The carrots were plastic bagged, moistened, and then stratified for 6 weeks at 5 °C. After the stratification, the soil in the bags was spread in a thin layer within 15.1 x 20.2 cm aluminum trays and the seeds were allowed to germinate in a heated greenhouse. The temperature was always above 15 °C, and we applied a photoperiod of 18 h per day/6 h per night. The trays were watered every 3 days to allow the germination. The germinations were recorded and snatched weekly during 16 weeks. The germination record stopped when no germination had occurred for 2 weeks. The dormant soil seed bank is thus assessed as the total number of germinations.

2.4. Climatic data

28In order to compare the weather that occurred during the two experimental years, the regional climate, annual mean temperature and precipitation data since 1998 were acquired on the website of the Royal Meteorological Institute of Belgium (2015). The weather station, which recorded the data, is located in Uccle, Belgium, and is representative of the regional climate occurring at the study site.

2.5. Statistical analysis

29The variations of the plant performance-related traits were analyzed with descriptive statistics (mean, standard error of the mean, minimum, and maximum). To explore the effect of the population and competition on plant performance, we used a mixed model analysis of variance (ANOVA). We included the competition as a fixed effect, and population as a random effect. The interaction between population and competition was included in the model. No variable transformation improved the homoscedasticity of the data. All statistical analyses were performed with Minitab® ver. 16.2.2 (Minitab Inc., State College, PA, USA).

3. Results

30The biovolume of the parent plants was very variable and ranged from 0.232 m³ to 2.630 m³. The offspring number was very superior to the number of parents, and varied from 431 to 4,789, depending on the plot. The λ by plot averaged 273. The offspring biomass by plot averaged 656 g. The dormant soil seed bank was lower than the number of offspring, but still averaged 306 seeds·m-2 by plots. The complete descriptive statistics are given in table 1.


31The results of the two-way ANOVAs showed that the competition exerted by sunflowers had a significant influence on the biovolume, but did not have a significant impact on the variables measured during the second growing year (i.e., offspring number, λ, offspring biomass, and dormant soil seed bank; Table 2). The populations only varied in terms of dormant soil seed bank (Table 2). The interaction between population and the competition was not significant for any response variable. The offspring biomass and the λ were not significantly influenced by the studied factors (Table 2). To represent the variation among the population of the measured trait for which a significant variation was found, bar graphs were drawn (Figure 2).



32The regional climatic data showed that the two considered years were different from the average temperature and precipitations that occurred over the last 15 years (Figure 3). The 2013 growing year was colder (10.1 °C) than the mean temperature between 1998 and 2012 (11.0 ± 0.121 °C). Conversely, 2014 was warmer (11.9 °C) than the average. Both years were drier (816 mm and 784 mm, respectively) than the average (882 ± 29.3 mm).


4. Discussion

33This experiment showed that A. artemisiifolia is able to develop populations with a λ significantly greater than 1 in agricultural conditions beyond its current invaded range. The hypothesis of equilibrium at the edge of the current invaded range is thus rejected.

34The processes that can limit the range expansion of an invasive species can be multiple (e.g., genetic constraints that impede local adaptation, too harsh environmental conditions that limit population growth, or dispersal limitations to suitable sites) (Monty & Mahy, 2009; Sexton et al., 2009; Alexander & Edwards, 2010; Monty et al., 2013; Hargreaves et al., 2014; Ortmans et al., 2016a). This study highlighted the possible presence of suitable habitats for A. artemisiifolia invasion north of the current invaded range, i.e. the agricultural fields. When introduced in one such habitat, we found that the species is able to grow and reproduce. Given this result, one can wonder why the species is not as present in Belgian agriculture as it is in French. Dispersal limitations could be one of the main explanations of a delay in the colonization north of the current invaded range. In France, sunflower production becomes scarce above the latitude of 48°N (Agreste, 2010). Agricultural machinery is known to spread A. artemisiifolia seeds (Bohren, 2006), and populations harbored in sunflower crops can act as a source for further invasion (Chollet et al., 1998). Despite the fact that the species can be dispersed by a lot of other human activities (reviewed in Essl et al., 2015), the lack of sunflower crops in the north could constitute a significant dispersal limitation. This situation may change in the future, because in France, the development of early flowering hybrids allows sunflower cultivation increasingly northwards (Jouffret et al., 2011; Cetiom, 2013). In addition, global warming might also allow sunflower cultivation further north in the future, which will probably have consequences on the invasion. An increase in the distribution of a weed species has already been reported as a result of the modification of agricultural practices. For example, the archeophyt weeds followed the culturing of cereals from the Middle East to Europe, thereby increasing greatly their invaded range (Fried et al., 2009).

35The sunflower competition impacted significantly the biovolume of the parent plant, but this factor did not have an impact the following year: the offspring biomass, the soil seed bank, and the lambda were left unaltered. This observation suggests that, despite a sensibility to interspecific competition (Leskovšek et al., 2012), the sunflower appears to be a poor competitor against A. artemisiifolia. The large spacing between the sunflower plants makes this kind of crop especially invasible by A. artemisiifolia. Since its development is relatively synchronized with the sunflower, the use of fertilizer or the suppression of the other weeds could also benefit A. artemisiifolia, and therefore increase the invasibility of this type of crop. Given the poor effect of the sunflower competition, the facilitation effect of field margin situations is probably of minor importance.

36We observed significant variation among populations for the dormant soil seed bank, and for the proportion of dormant seeds (Table 2; Figure 2). The population factor was almost significant for the offspring number (P = 0.052), and for the λ (= 0.052; Table 2). Variation among populations in the studied variables could emanate from genetic differentiation among populations, as already demonstrated in France (Genton et al., 2005; Leiblein-Wild et al., 2014). It can also be the result of a local adaptation to environmental conditions, even if this subject was assessed in another study on the same geographical scale and did not show any adaptation to local climatic data (Ortmans et al., 2016a). Phenotypic variation can also be attributable to variability in seed lots collected in the field (Ortmans et al., 2016b). Further research is needed to understand the drivers of population variation in the species (Chun et al., 2010).

37The seed bank size was variable across the plots, probably because of the spatial heterogeneity of the seed rain (Rabinowitz & Rapp, 1980). While created in a single seed rain, the seed bank was relatively important, with 306 (± 51) viable seeds·m-2 on average. In comparison, Fumanal et al. (2008b) showed that the soil seed bank of long-established and unmanaged populations in France can vary from 536 to 4,477 seeds·m-2 depending on populations. The seed bank created in our field was smaller, although in a comparable range. These observations reinforce the idea of an invasion potential to the north of France. In order to prevent the creation of an important seed bank and the population anchorage for years, the early detection of the newly established populations is of major importance, in order to make the eradication possible. To be complete, the eradication actions have to include the depletion of the soil seed bank. Several good practices can be applied to reach this objective. For example, interventions that stimulate weed germination during intercropping such as a stale seedbed or a stubble ploughing, will promote germinations and thus soil seed bank exhaustion (Infloweb, 2016). It is also advisable to avoid cultivating frequently and successively easy invasible crops (e.g. sunflowers or soya), to limit the production of new seeds. Plowing the plot should also be avoided because it buries the seeds that can therefore remain viable for a long time (Baskin & Baskin, 1980).

38To the best of our knowledge, there are no available data about finite growth rates of A. artemisiifolia invasive populations. It is therefore difficult to evaluate if the finite growth rate we measured in our field is uncommonly high, or not. The λ calculated in this study is related to recently introduced populations that are based on transplanted plants. The results should therefore be handled with caution. Nevertheless, the density of the offspring reached 1,020 ± 70 plants·m-2. This number is about ten times higher than the density of plants that Fumanal et al. (2008b) recorded in invasive populations occurring in agricultural habitats of France. Since this density was formed in a single year from a maximum of 6 plants by plot, the finite growth rate of our population thus appears quite important. If the populations were allowed to reproduce for another year, it is probable that the λ would have been closer to 1, given the already high density of plants observed the second year.

39The regional climatic data have shown that the considered years, although relatively similar, were slightly outside the range of temperatures and precipitations that the region normally undergoes. While regrettable from the perspective of having representative conditions of the local climate, this special year of 2013 highlights that even in drier and colder conditions, the species is still able to successfully establish populations north of its current range. This is very interesting because colder conditions are expected to limit the species distribution area (Allard, 1943; Chapman et al., 2014). In 2014, the warmer temperatures likely favored the offspring growth. Since growing conditions were different between 2013 and 2014 due to the larger number of growing plants, it is difficult to assess the gain from the warmer temperatures. Although not negligible, the 0.9 °C positive difference with the 15-year average is relatively low, especially in the context of global warming that is expected to lead to a larger temperature increase (Stocker et al., 2013).

5. Conclusions

40This work showed that when introduced into an agricultural habitat of Belgium, A. artemisiifolia was able to establish populations with an important finite growth rate. Despite the current rarity of the species in the agricultural fields of Belgium, the growth of the species does not appear to be limited in this habitat. Because of the links between the species’ invasion and the sunflower cultivation, great caution has to be exercised if this production extends northwards. North to the current invaded range, awareness actions in the agricultural sector should be raised to avoid the repeated occurrence of the species in the fields remaining unnoticed, and to allow control measures to be initiated in the early stage of the species’ establishment.


42The authors thank the Unité Mixte de Recherche (UMR) 1347 Agroécologie from the Institut National de Recherche Agronomique of France that collected the seeds. The authors are also grateful to the Fonds de la Recherche dans l’Industrie et dans l’Agriculture (FRIA) for funding this study.


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Pour citer cet article

William Ortmans, Grégory Mahy & Arnaud Monty, «Northern range edge equilibrium of Ambrosia artemisiifolia L. not achieved in Western Europe», BASE [En ligne], Volume 21 (2017), Numéro 1, 12-21 URL :

A propos de : William Ortmans

University of Liège - Gembloux Agro-Bio Tech. BIOSE department. Biodiversity and Landscape Unit. Passage des Déportés, 2. BE-5030 Gembloux (Belgium). E-mail:

A propos de : Grégory Mahy

University of Liège - Gembloux Agro-Bio Tech. BIOSE department. Biodiversity and Landscape Unit. Passage des Déportés, 2. BE-5030 Gembloux (Belgium).

A propos de : Arnaud Monty

University of Liège - Gembloux Agro-Bio Tech. BIOSE department. Biodiversity and Landscape Unit. Passage des Déportés, 2. BE-5030 Gembloux (Belgium).