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Article

Establishment and Expansion of Harmonia axyridis Pallas (Coleoptera: Coccinellidae) in Urban Green Areas in the Iberian Peninsula: From 2015 to 2021

by
Roberto Meseguer
1,
Belén Lumbierres
2 and
Xavier Pons
1,*
1
Department of Crop Protection and Forest Sciences, University of Lleida, 25198 Lleida, Spain
2
Laboratori d’Agricultura i Sanitat Vegetal de Catalunya, Departament d’Acció Climàtica, Alimentació i Agenda Rural, Generalitat de Catalunya, 25198 Lleida, Spain
*
Author to whom correspondence should be addressed.
Insects 2022, 13(8), 741; https://doi.org/10.3390/insects13080741
Submission received: 5 July 2022 / Revised: 13 August 2022 / Accepted: 15 August 2022 / Published: 17 August 2022
(This article belongs to the Special Issue Integrated Pest Management of Arthropods in Urban Green Spaces)
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Abstract

:

Simple Summary

Harmonia axyridis (Coleoptera: Coccinellidae) is a widespread invasive ladybird. In this study, we determine its occurrence and expansion in urban areas of the Iberian Peninsula after 2014. We also define the aphidophagous ladybird species complex in urban areas of the northeastern Iberian Peninsula and track any changes between 2015 and 2021. The expansion of the species mainly occurred in Catalonia (northeast Iberian Peninsula), where spring and summer populations on trees and shrubs and overwintering aggregations were recorded. The records of H. axyridis populations allow us to distinguish between two areas: one that has already been invaded and another that has not yet been invaded. The relative abundance of the ladybird species in each area is determined on a yearly basis. In the invaded area, H. axyridis became dominant two years after its detection, replacing Adalia bipunctata. This change in species prevalence is more pronounced in trees highly infested with aphids. In the not yet invaded area, changes in species dominance also occurred, and A. bipunctata replaced Oenopia conglobata from 2020 onwards. The yearly release of this ladybird in urban green areas for aphid control purposes could explain this shift. This study defines the current situation of H. axyridis in the Iberian Peninsula, and determines the main changes in ladybird species assemblages during the last few years.

Abstract

In the Western Palearctic region, Harmonia axyridis (Coleoptera: Coccinellidae) is mainly established in urban areas. In this study, we update its occurrence in urban areas of the Iberian Peninsula and determine its expansion after 2014. Changes in the ladybird species assemblage are also evaluated. We compile information about the records of H. axyridis in Spain from 2015 to 2021. In addition, we sample different locations to determine the relative abundances of the species composing the aphidophagous ladybird complex. The expansion of H. axyridis mainly occurred in Catalonia (Iberian Peninsula), where it is possible to identify two clear areas: one that has already been invaded and another that has not yet been invaded. Harmonia axyridis became the dominant species in the invaded area two years after it was first identified. This dominance is clearly shown on Liriodendron tulipifera and Tilia platyphyllos, where it accounted for more than 75% of the total collected individuals in the last year of the study. In the not-yet invaded area, Adalia bipunctata overcame Oenopia conglobata and became the prevalent species from 2020 onwards, likely due to its regular releases for aphid biocontrol. This study reveals that changes in ladybird species assemblages may not only be caused by invasive species, but also by biological control practices.

1. Introduction

Aphids (Homoptera: Aphididae) are widespread herbivores on plants of many ecosystems, including crops, forests, and urban vegetation [1]. They have the capacity to rapidly increase population size due to a high reproductive rate and short developmental time [2]. Fortunately, they have a large number of natural enemies that can stop or slow their population growth [3].
Ladybirds (Coleoptera: Coccinellidae) are among the most well-known aphid predators [3,4] and are considered to play a significant role as aphid control agents, especially in conservation strategies [5]. Each continent has a specific fauna of Coccinellidae [6], but the introduction of exotic species for aphid control may produce changes in this complex. In America, several aphidophagous species native to Europe (for example, Coccinella septempunctata L., Hippodamia variegata Goeze) were introduced for aphid control purposes, and their negative impacts have been well established [5,7,8]. In Europe, Hippodamia convergens Guérin-Meneville was introduced from North America, but there are no reports on its establishment [6,9]. The harlequin ladybird, Harmonia axyridis (Pallas), which is an East-Palearctic species native to Japan, China, Korea, Mongolia, and Siberia [10], was introduced to both North America and Europe. It has become established in many countries and has a well-documented impact on native ladybirds. Harmonia axyridis is able to prey on other ladybird species, avoid natural enemies, and better use food resources than the resident indigenous species; as a consequence, following their introduction, there was a change in the relative abundance of the ladybird complex [10,11,12,13,14,15,16,17].
In Spain, this coccinellid was introduced in Almería (southeastern Spain) for aphid control in 1995 [18]. Some adults were observed in the Canary Islands in 2003 and 2004 [19], and one single specimen was found in a public garden in Bilbao (northern Spain) in 2007 [20]. Despite this, no evidence of population establishment occurred [13,21] until Carbonell and Sesma [22] reported the occurrence of isolated individuals in several localities of Catalonia (northeastern Spain), and one overwintering aggregation quite close to the French border in 2013. Pons et al. [23] updated the status of this ladybeetle species in Spain and characterized an overwintering aggregation. Since then, some punctual new records of the occurrence of H. axyridis in the Iberian Peninsula have been made by citizen observers [24]. Nevertheless, no regular data on its expansion exists, and important changes may have occurred which could have led to a change in the relative abundance of the indigenous ladybird species.
The aims of the present study are as follows: (1) to update the occurrence of H. axyridis in the Iberian Peninsula and to determine its expansion after 2014; (2) to define the ladybird species composition in urban areas of the northeastern Iberian Peninsula; and (3) to track changes in the ladybird species assemblages throughout the study period.

2. Material and Methods

Firstly, we collected the available records from the literature on H. axyridis in Spain between 2015 and 2021, checking scientific databases (Web Science and Scopus), Spanish technical crop protection journals (Phytoma España, Vida Rural), technical reports from Spanish Agricultural services (Departament d’Acció Climàtica, Alimentació i Medi Rural, Generalitat de Catalunya; Ministerio de Agricultura, Pesca y Alimentación, Gobierno de España), Spanish entomological webpages and Google. The occurrence of winter aggregations after 2013–2014 was also recorded. Advisers and citizen observers informed us about their presence inside houses and buildings and, whenever possible, we visited them and recorded the number of individuals and color morphs in the aggregation.
We also prospected several locations in the northeastern Iberian Peninsula for the presence of ladybird aphidophagous species. Because H. axyridis spreads more rapidly into areas with a high proportion of urban land cover [11,25] and its preferential food tends to reach high densities in the vegetation of urban green areas [4], we monitored these types of habitats one or more times per season. In each of these locations, we selected trees and shrubs that we knew were likely to be infested by aphids at the sampling time. Each pair location/plant is referred to as a “site”. Vegetation in a site was inspected visually for 1 to 3 h (adding the sampling time of each observer), according to the number of plants to be inspected. The number of adults and larvae of each aphidophagous coccinellid species was determined, according to the recorder’s experience. When clusters of newly hatched larvae were found, they were brought to the laboratory and reared until we were able to determine the species. Because the number of samplings varied throughout a season and among sites, the total number of individuals observed of each species was standardized by dividing it by the number of samplings performed. The number of sites and the sampled plants are shown in Table S1.
With this information, a map with the expansion of H. axyridis in the northeastern Iberian Peninsula was drawn, showing the areas with and without the presence of this ladybird species. In order to determine changes in the ladybird species assemblages in these areas, we calculated the relative abundance of each ladybird species yearly from 2015 to 2021.
In one location, we regularly monitored two ornamental tree species between 2019 and 2021: tulip tree (Liriodendron tulipifera) and linden (Tilia platyphyllos), and we recorded the occurrence of aphidophagous ladybird species. These two plant species were selected because both usually support high densities of aphids (Illinoia liriodendri (Monell) on tulip tree, and Eucallipterus tiliae L. on linden). Samplings were performed every week or 15 days during the aphid infestation period (April–July). The sampling plan consisted of visual observation for 30 s of the tree canopy at two heights, at the low and the medium parts. The low canopy observation was made directly from the ground. For the upper canopy observation, a ladder was used, with the observer at 2.5 m above the ground level. The numbers of sampled trees were 50 and 30 tulip trees and linden, respectively, corresponding to 25% of the total number of planted trees in each sampling place. The number of adults and larvae of each aphidophagous coccinellid species was recorded. When clusters of newly hatched larvae were found, they were brought to the laboratory and reared until their identification at species level was possible. The relative abundance of each species each year was calculated.

Statistical Analysis

To compare differences between years in the relative proportions of the different coccinellid species, a chi-square test was carried out. Pairwise comparisons between years were then performed after applying the Bonferroni correction. When the number of individuals of one or several species was very low, they were grouped for analysis. All statistical analyses were performed using R version 4.0.3 (R Foundation for Statistical Computing, Vienna, Austria).

3. Results

The main species composing the aphidophagous ladybird complex in the urban green areas of the northeastern Iberian Peninsula were: Adalia bipunctata L., Adalia decempunctata L., Coccinella septempunctata L., H. axyridis, Hippodamia veriegata Goeze, Oenopia conglobata L., Propylea quatuordecimpunctata L., and Scymnus spp. The infrequent aphidophagous ladybirds recorded were: Myrhra octodecimguttata L., Harmonia quadripunctata (Pontoppidan), Chilocorus bipustulatus L., Oenopia lyncea Oliv., Tytthaspis sedecimpunctata L., Coccinula quatuordecimpustulata L., Calvia quatuordecimguttata L., Exochomus sp., Platynaspis sp., and Hyperaspis sp.

3.1. Occurrence of H. axyridis

By comparing the records reported before [23] and after 2014, this study revealed that H. axyridis has spread to more localities of the Iberian Peninsula (Figure 1a). However, most of these records correspond to isolated or small groups of adults that were photographed or observed by citizen scientists [24]. As far as we know, no records of winter aggregations have been reported in the Iberian Peninsula, except for those from Catalonia (Figure 1b).
The occurrence of H. axyridis in Catalonia is higher than in other parts of the Iberian Peninsula. Until now, spring and summer populations have been observed in more than 65 localities and 37 overwintering aggregations of between tens and hundreds of individuals have been reported in 5 different areas. The number of records after those reported in Pons et al. [23] has substantially increased (Figure 1b).
In Catalonia, the spread of H. axyridis has mainly occurred in the northern and eastern areas (Figure 1b). The isolated record in western Catalonia, belonging to the city of Lleida, corresponds to a solitary specimen that was found in 2014 inside a car coming from northeastern Catalonia. This individual was killed when detected [23]. No other specimens of H. axyridis have been found in the west, in a high number of urban areas (see Table 1a), on crops such as maize, alfalfa, cereals, orchards, etc., or in other habitats that are regularly sampled (authors unpublished). The records of the south of Catalonia come from localities of the Ebro delta area, where isolated individuals were photographed.
According to this information, we defined two areas in this region: one as the “invaded area” and the other as the “not yet invaded area” (Figure 1b).

3.2. Abundance of Ladybirds in the Not Yet Invaded and Invaded Areas

The not yet invaded area was dominated by O. conglobata until 2019, whereas A. bipunctata was the prevalent species in the last two years of the study (Table 1a). Adalia bipunctata was absent from this area until 2017, and its relative proportion increased over the years. The relative occurrence of H. variegata remained high every year and relatively stable. There were significant changes in the species occurrence over the study period (χ2 = 191.36; p < 0.0001; df: 36). Significant changes occurred in 2020 and 2021 (Table 1a and Table S2).
The invaded area was dominated by A. bipunctata until 2018. The appearance of H. axyridis was not recorded until 2017 and since this year there was a regular increase in its relative abundance in relation to the indigenous species (Table 1b). Significant changes in the relative abundance of ladybird species were also found over the study period in this area (χ2 = 771.15; p < 0.0001; df: 42). Yearly comparisons revealed that the H. axyridis arrival presupposed a significant shift in the coccinellid species complex composition in favor of the harlequin ladybird, with A. bipunctata being the most affected indigenous ladybird (Table 1a and Table S2).
Table
Table 1. Yearly relative (%) and absolute (in parentheses) abundances of the different ladybird species in (a) the not yet invaded and (b) invaded area (from 2015 to 2021). The ladybird species have been abbreviated as: Ha (H. axyridis), A2 (A. bipunctata), Oc (O. conglobata), A10 (A. decempunctata), C7 (C. septempunctata), Hvar (H. variegata), P14 (P. quatuordecimpunctata), and Scy (Scymnus spp.). Years with different letters in the right-hand column are significantly different at p < 0.05. * See discussion for the reason of the low recorded value.
Table 1. Yearly relative (%) and absolute (in parentheses) abundances of the different ladybird species in (a) the not yet invaded and (b) invaded area (from 2015 to 2021). The ladybird species have been abbreviated as: Ha (H. axyridis), A2 (A. bipunctata), Oc (O. conglobata), A10 (A. decempunctata), C7 (C. septempunctata), Hvar (H. variegata), P14 (P. quatuordecimpunctata), and Scy (Scymnus spp.). Years with different letters in the right-hand column are significantly different at p < 0.05. * See discussion for the reason of the low recorded value.
(a)
Ladybird Species
YearSample SitesA2OcA10C7HvarP14ScyDifferences between Years
201590 (0)48 (26)13 (7)4 (2)21 (11)4 (2)9 (5)bc
2016130 (0)48 (40)17 (14)3 (2)22 (18)1 (1)8 (7)c
2017164 (5)40 (48)12 (14)2 (3)28 (34)5 (6)9 (11)bc
20181611 (12)37 (41)12 (14)2 (2)27 (30)3 (4)6 (7)bc
20191315 (40)36 (97)8 (23)1 (2)34 (93)2 (7)4 (10)b
20201338 (117)30 (93)12 (36)<1 (1)14 (42)1 (4)5 (15)a
2021741 (33)18 (14)10 (8)4 (3)20 (16)4 (3)4 (3)a
(b)
Ladybird Species
YearSample SitesHaA2OcA10C7HvarP14ScyDifferences
between Years
2015130 (0)56 (178)8 (25)3 (10)3 (8)26 (84)2 (7)1 (4)f
201690 (0)53 (39)5 (4)9 (7)6 (5)29 (15)1 (1)3 (2)ef
2017106 (12)46 (98)8 (18)12 (26)5 (11)15 (31)4 (8)5 (10)de
20181617 (29)34 (57)12 (20)12 (20)4 (7)13 (23)4 (6)5 (9)d
20191952 (371)24 (172)6 (39)3 (22)2 (13)13 (95)<1 (1)<1 (2)c
20204243 (559)34 (442)7 (85)4 (56)1 (11)10 (128)<1 (4)1 (8)b
20211663 (279)25 (109)4 (17)3 (13)4 (18)<1 (2) *<1 (2)<1 (2)a

3.3. Changes in the Relative Abundance of the Aphidophagous Ladybird Species on L. tulipifera and T. platyphyllos

Harmonia axyridis was the dominant species during the three years of sampling on L. tulipifera, followed by A. bipunctata. The former’s relative yearly abundance increased significantly over the period of 2019–2021 (χ2 = 426.46; p < 0.0001; df: 12) (Figure 2, Table S3).
On T. platyphyllos, A. bipunctata was the prevalent species in 2019. However, a sharp increase in the abundance of H. axyridis relegated this species to second position from 2020. Changes in the species complex abundances were found over the study period (χ2 = 226.32; p < 0.0001; df: 10) (Figure 3). Yearly comparisons revealed significant differences between 2019 and 2020, but not between 2020 and 2021 (Table S3).

4. Discussion

The harlequin ladybird has an exceptional capacity to be successful in many new environments [26]. Its strong dispersal capacity makes this species capable of colonizing new areas with large enough aphid populations [10,27]. In the Western Palearctic region, H. axyridis is mainly established in urban areas [11,28,29], where aphid populations reach high densities on environmentally stressed plants (pollution, water, soil nutrient cycles) [25,30]. The focus on urban green spaces in our study allowed us to obtain the most informative data regarding the expansion of H. axyridis in the Iberian Peninsula since 2014, and the changes in the ladybird species assemblages after the establishment of this invasive species.
In the last two decades, much research has focused on the potential of the harlequin ladybird to invade new areas, the factors that may have led to such a successful expansion, and the consequences of this expansion. Some of these studies cast doubts on the invader’s ability to colonize Southern European regions, stressing that some biotic factors, such as the lower availability of food resources, may be playing a major role in preventing invasion by H. axyridis [31,32]. However, our study shows that the expansion of H. axyridis in the Iberian Peninsula [23] is in progress, especially in Catalonia (the northeast). Our findings regarding this expansion support predictions made by Poutsma et al. [33] and Amexia et al. [34] for the Mediterranean region and for the Iberian Peninsula, respectively. The expansion of H. axyridis in other southern European countries, like Bosnia-Herzegovina, Croatia, and Italy has been already reported [15,28,35,36].
Pons et al. [23] predicted a rapid spread of H. axyridis in crops due to the usual abundance of aphids during spring, as was reported by other European countries [37]. Amexia et al. [34] stated that the spread of H. axyridis in the northern Iberian Peninsula could be linked to vineyard areas, representing a risk for wine production as has already occurred in Canada [38], where damage to ripe bunches of grapes caused by this invasive ladybird species was reported during the harvest period. However, only a few adults of H. axyridis have been recorded in crop fields (authors unpublished), and surveys and interviews with vineyard farmers and wine producers in Catalonia have so far failed to detect the widespread presence of H. axyridis. Until now, its occurrence has mainly been restricted to urban areas. Harmonia axyridis prefers broadleaf arboreal host plants and concentrates in habitats with a high density of aphids [25]. The large aphid populations found on several trees in urban areas of Catalonia have likely facilitated the expansion of this invasive ladybird.
No regular reports of this species exist in southern areas of the Iberian Peninsula. The habitual high temperatures in these areas may be the key factor preventing its expansion. Recent studies have shown the detrimental effects of temperatures above 30 °C on the survival and fitness of this invasive species [39,40]. In addition, high temperatures can lead to a shortening of the period during which aphid populations are abundant enough to support the oviposition and development of coccinellids [32]. Nevertheless, new records from very hot climates [41] suggest that H. axyridis may be adaptable to extreme climates, so its potential spread to southern regions of the Iberian Peninsula should not be dismissed.
Pons et al. [23] stated that the impact of the establishment of the harlequin ladybird in the Iberian Peninsula would be similar to that already described in other European countries [42]. Some nuisance to humans in houses by overwintering aggregations have been reported in Spain, but no allergies or other skin reactions. Ecologically, the most concerning impact of the species’ expansion is the consequential changes in coccinellid assemblages [11,14,16,28,43,44,45,46,47].
Ladybirds are common aphid predators found in urban ecosystems [48,49]. Before the establishment of the harlequin ladybird, several aphidophagous species were prevalent in urban areas of Catalonia, including O. conglobata, A. bipunctata, H. variegata, A. decempunctata, and others [50,51]. This pattern is currently occurring in the not-yet invaded area, but it seems to have changed in the area where H. axyridis has spread and ladybird habitats overlap.
In the invaded area, H. axyridis has been established since 2017, and changes in the relative abundance of the species complex were recorded in 2019, 2020, and 2021. These changes were clearly observed on tulip trees and lindens. Kenis et al. [17] assessed the ecological risk posed by H. axyridis to 30 European native species and determined that A. bipunctata, A. decempunctata, and O. conglobata had the highest risk of displacement. Our results show that the most affected species may be A. bipunctata, because of the changes in population density observed on tulip trees and lindens. This is similar to the displacement of A. bipunctata already reported in other countries [17,30,47,52,53,54,55]. This can be explained due to the strong habitat overlap between H. axyridis and A. bipunctata [30], which may lead to strong competition between these two species. Harmonia axyridis is known to be the stronger competitor, due to its higher voracity, faster developmental time, and ability to gain more weight and to more quickly colonize resources [56,57]. Although several intraguild predation (IGP) studies have defined the two-spotted ladybird as the intraguild prey of H. axyridis [58,59], it seems that exploitative competition is the main cause of its decrease [47,60]. When H. axyridis reaches high numbers, A. bipunctata may be displaced to its ancestral habitats (i.e., natural or semi-natural habitats) [60]. The effect on the other species is not clear, and further studies are required to assess whether negative effects will arise from H. axyridis establishment. In the invaded area, the low relative abundance of H. variegata in 2021 was mainly due to the fact that its main host in urban areas, the oleander Nerium oleander, did not harbor large aphid populations, which may have caused the numbers recorded to be much lower than in previous years. An unexpected finding was the recording of a good number of C. septempunctata adults each year on tulip trees on just one of the summer sampling dates. The presence of only adults (no larvae were recorded at all) suggests that this ladybird uses tulip trees to obtain reserves before flying to other habitats or overwintering.
An interesting finding in the not-yet invaded area was the change in the most prevalent species. This was O. conglobata until 2019, but later A. bipunctata became the most abundant species. The reason for this shift is not clear. The advantages of one species may be due to its better performance in a concrete habitat, but no comparative studies between these two ladybirds have been done. However, some anthropogenic/human actions may enhance the success of one species. In many cities of the Iberian Peninsula, A. bipunctata has been widely released to control any aphid species (because it is the main aphidophagous ladybird that is commercially produced). We suggest that this could be the reason for the change in the relative abundance of the aphidophagous species in the not-yet invaded area. In areas where H. axyridis has already spread, releases of A. bipunctata are also undertaken annually. The results obtained in our study suggest that these regular releases have not had much of an effect on the dominance of H. axyridis.

5. Conclusions

The results of this study indicate the ongoing expansion of H. axyridis across the Iberian Peninsula. The expansion has thus far taken place mainly in Catalonia (northeast Iberian Peninsula), where two clear areas were defined: the invaded and the not yet invaded area. In the former, the presence of the exotic ladybird has been recorded since 2017, with it becoming the dominant species from 2019 onwards. The yearly increase of H. axyridis abundance was very clear on the ornamental trees L. tulipifera and T. platyphyllos, where it accounted for more than 75% of the total collected individuals in the last year of the study. In the not invaded area, O. conglobata was the prevalent species until 2020, when a sharp increase in the abundance of A. bipunctata relegated this species to second position. Such a shift could have had an anthropogenic origin, due to regular releases of A. bipunctata for aphid biocontrol. This study defines the current situation of H. axyridis in the Iberian Peninsula and points out that changes in the ladybird species assemblages may be caused not only by invasive species but also by biological control practices.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/insects13080741/s1, Table S1. Number of sampled urban areas and list of observed plants in both the not yet invaded and the invaded area. * Total number of sampled urban areas (not yet invaded area + invaded area); Table S2. Pairwise comparison between years to determine changes in the ladybird complex composition of the not yet invaded and the invaded area. Bold numbers indicate statistically significant differences; Table S3. Pairwise comparisons between years to determine changes in the ladybird complex composition of Liriodendron tulipifera and Tilia platyphyllos. Bold numbers indicate statistically significant differences.

Author Contributions

Conceptualization and methodology, R.M., B.L. and X.P.; validation, R.M. and X.P.; formal analysis, R.M. and X.P.; investigation, R.M., B.L. and X.P.; resources, X.P.; data curation, R.M. and X.P.; writing—original draft preparation, R.M. and X.P.; writing—review and editing, R.M., B.L. and X.P.; visualization, R.M. and X.P.; supervision, X.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

The authors would like to thank Sandra Las Heras, Jordi Senmartí, and Mònica Bedós for sharing information about the occurrence of H. axyridis. We also give thanks to TAC Osona and Vic, Manlleu, and Barcelona councils for allowing sampling in their urban green areas.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Blackman, R.L.; Eastop, V.F. Taxonomic issues. In Aphids as Crop Pest; van Emden, H.F., Harrington, R., Eds.; CAB International: Willingford, UK, 2007; pp. 1–29. [Google Scholar]
  2. Dixon, A.F.G. Parthenogenetic reproduction and the rate of increase in aphids. In Aphids, Their Biology, Natural Enemies and Control; Minks, A.K., Harrewijn, P., Eds.; Elsevier: Amsterdam, The Netherlands, 1987; Volume A, pp. 269–287. [Google Scholar]
  3. Völkl, W.; Mackauer, M.; Pell, J.K.; Brodeur, J. Predators, parasitoids and pathogens. In Aphids as Crop Pests; van Emden, H.F., Harrington, R., Eds.; CAB International: Willingford, UK, 2007; pp. 187–233. [Google Scholar]
  4. Majerus, M.E.N. Ladybirds (New Naturalist 81), 1st ed.; Harper-Collins: London, UK, 1994; p. 367. [Google Scholar]
  5. Michaud, J.P. Coccinellids in biological control. In Ecology and Behavior of the Ladybird Beetles (Coccinellidae); Hodek, I., Honek, A., van Emden, H.F., Eds.; Blackwell Publishing Ltd.: Chichester, UK, 2012; pp. 488–519. [Google Scholar]
  6. Roy, H.; Migeon, A. Ladybeetles (Coccinellidae). In BioRisk: Alien Terrestrial Arthropods in Europe; Chapter 8.4; Roques, A., Kenis, M., Lees, D., Lopez-Vaamonde, C., Rabitsch, W., Rasplus, J.Y., Roy, D.B., Eds.; Pensoft: Sofia, Bulgaria, 2010; pp. 293–313. [Google Scholar] [CrossRef]
  7. Evans, E.W.; Soares, A.O.; Yasuda, H. Invasions by ladybugs, ladybirds, and other predatory beetles. BioControl 2011, 56, 597–611. [Google Scholar] [CrossRef]
  8. Sloggett, J.J. Aphidophagous ladybirds (Coleoptera: Coccinellidae) and climate change: A review. Insect Conserv. Divers. 2021, 14, 709–722. [Google Scholar] [CrossRef]
  9. Soares, A.O.; Honek, A.; Martinkova, Z.; Brown, P.M.J.; Borges, I. Can native geographical range, dispersal ability and development rates predict the successful establishment of alien ladybird (Coleoptera: Coccinellidae) species in Europe? Front. Ecol. Evol. 2018, 6, 57. [Google Scholar] [CrossRef]
  10. Koch, R.L. The multicolored Asian lady beetle, Harmonia axyridis: A review of its biology, uses in biological control, and non-target impacts. J. Insect. Sci. 2003, 3, 32. [Google Scholar] [CrossRef] [PubMed]
  11. Adriaens, T.; San Martin y Gomez, G.; Maes, D. Invasion history, habitat preferences and phenology of the invasive ladybird Harmonia axyridis in Belgium. BioControl 2008, 53, 69–88. [Google Scholar] [CrossRef]
  12. Roy, H.; Wajnberg, E. From biological control to invasion: The ladybird Harmonia axyridis as a model species. BioControl 2008, 53, 1–4. [Google Scholar] [CrossRef]
  13. Brown, P.M.J.; Thomas, C.E.; Lombaert, E.; Jeffries, D.L.; Estoup, A.; Lawson Handley, L.J. The global spread of Harmonia axyridis (Coleoptera: Coccinellidae): Distribution, dispersal and routes of invasion. BioControl 2011, 56, 623–641. [Google Scholar] [CrossRef]
  14. Roy, H.E.; Adriaens, T.; Isaac, N.J.B.; Kenis, M.; Onkelinx, T.; San Martin, G.; Brown, P.M.J.; Hautier, L.; Poland, R.; Roy, D.B.; et al. Invasive alien predator causes rapid declines of native European ladybirds. Divers. Distrib. 2012, 18, 717–725. [Google Scholar] [CrossRef]
  15. Rondoni, G.; Athey, K.J.; Harwood, J.D.; Conti, E.; Ricci, C.; Obricky, J.J. Development and application of molecular gut-content analysis to detect aphid and coccinellids predation by Harmonia axyridis (Coleoptera: Coccinellidae) in Italy. Insect Sci. 2015, 22, 719–730. [Google Scholar] [CrossRef]
  16. Grez, A.A.; Zaviezo, T.; Roy, H.E.; Brown, P.M.J.; Bizama, G. Rapid spread of Harmonia axyridis in Chile and its effects on local coccinellids biodiversity. Divers. Distrib. 2016, 22, 982–994. [Google Scholar] [CrossRef]
  17. Kenis, M.; Adriaens, T.; Brown, P.M.J.; Katsanis, A.; San Martin, G.; Branquart, E.; Maes, D.; Eschen, R.; Zindel, R.; Van Vlaenderen, J.; et al. Assessing the ecological risk posed by recently establishes invasive alien predator: Harmonia axyridis as a case study. BioControl 2017, 62, 341–354. [Google Scholar] [CrossRef]
  18. Jacas, J.A.; Urbaneja, A.; Viñuela, E. History and future of introduction of exotic arthropod biological control agents in Spain: A dilemma? BioControl 2006, 51, 1–30. [Google Scholar] [CrossRef]
  19. Machado, A. El sarantontón asiático Harmonia axyridis (Pallas) presente en Canarias (Coleoptera: Coccinellidae). Vieraea 2006, 34, 71–72. [Google Scholar] [CrossRef]
  20. Goldazarena, A.; Calvo, D. First record of Harmonia axyridis (Coleoptera: Coccinellidae) from the Iberian Peninsula. Bol. Soc. Entomol Aragonesa 2007, 41, 437–439. [Google Scholar]
  21. Brown, P.M.J.; Adriaens, T.; Bathon, H.; Cuppen, J.; Goldazarena, A.; Hagg, T.; Kenis, M.; Klausnitzer, B.E.M.; Kovar, I.; Loomans, A.J.M.; et al. Harmonia axyridis in Europe: Spread and distribution of a non-native coccinellid. BioControl 2008, 53, 55–67. [Google Scholar] [CrossRef]
  22. Carbonell, R.; Sesma, J.M. Confirmada la presencia de Harmonia axyridis (Pallas, 1773) en la Península Ibérica. Primeras citas para Cataluña e Islas Baleares (Coleoptera: Coccinellidae). BV News 2013, 16, 12–17. [Google Scholar]
  23. Pons, X.; Roca, M.; Lumbierres, B.; Lucas, É. Characterization of a newly established aggregation of the invasive ladybeetle Harmonia axyridis and current status of the invader in Spain. Span. J. Agric. Res. 2015, 13, e1006. [Google Scholar] [CrossRef]
  24. Sesma, J.M.; Gil-Tapeado, D. La expansión de Harmonia axyridis (Pallas, 1973) en la Peninsula Ibérica (Coleoptera: Coccinellidae). BV News 2020, 9, 1–7. [Google Scholar]
  25. Purse, B.V.; Comont, R.; Butler, A.; Brown, P.M.J.; Kesel, C.; Roy, H.E. Landscape and climate determine patterns of spread for all colour morphs of the alien ladybird Harmonia axyridis. J. Biogeogr. 2015, 42, 575–588. [Google Scholar] [CrossRef]
  26. Soares, A.O.; Borges, I.; Borges, P.A.V.; Labrie, G.; Lucas, E. Harmonia axyridis: What will stop the invader? BioControl 2008, 53, 127–145. [Google Scholar] [CrossRef]
  27. Osawa, N. Population field studies on the aphidophagous ladybird beetle Harmonia axyridis (Coleoptera: Coccinellidae): Resource tracking and population characteristics. Popul. Ecol. 2000, 42, 115–127. [Google Scholar] [CrossRef]
  28. Roy, H.E.; Brown, P.M.J.; Adriaens, T.; Berkvens, N.; Borges, I.; Clusella-Trullas, S.; Comont, R.F.; De Clercq, P.; Eschen, R.; Estoup, A.; et al. The harlequin ladybird, Harmonia axyridis: Global perspectives on invasion history and ecology. Biol. Invasions 2016, 18, 997–1044. [Google Scholar] [CrossRef]
  29. Honek, A.; Martinkova, Z.; Strobach, J. Effect of aphid abundance and urbanization on the abundance of Harmonia axyridis (Coleoptera: Coccinellidae). Eur. J. Entomol. 2018, 115, 703–707. [Google Scholar] [CrossRef]
  30. Sloggett, J.J. Harmonia axyridis (Coleoptera: Coccinellidae): Smelling the rat in native ladybird declines. Eur. J. Entomol. 2017, 114, 455–461. [Google Scholar] [CrossRef]
  31. Soares, A.O.; Honek, A.; Martinkova, Z.; Skuhrovec, J.; Cardoso, P.; Borges, I. Harmonia axyridis failed to establish in the Azores: The role of species richness, intraguild interactions and resource availability. BioControl 2017, 62, 423–434. [Google Scholar] [CrossRef]
  32. Honek, A.; Dixon, A.F.G.; Soares, A.O.; Skuhrovec, J.; Martinkova, Z. Spatial and temporal changes in the abundance and compostion of ladybird (Coleoptera: Coccinellidae) communities. Insect Sci. 2017, 20, 61–67. [Google Scholar] [CrossRef]
  33. Poutsma, J.; Loomans, A.J.M.; Aukema, B.; Heijerman, T. Predicting the potential geographical distribution of the harlequin ladybird, Harmonia axyridis, using the CLIMEX model. BioControl 2008, 53, 103–125. [Google Scholar] [CrossRef]
  34. Amexia, O.M.C.C.; Sipos, J.; Burda, M.; Soares, A.M.V.M.; Soares, A.O. Factors influencing the introduction and spread of Harmonia axyridis in the Iberian Peninsula. Biol. Invasions 2019, 21, 323–331. [Google Scholar] [CrossRef]
  35. Kulijer, D. First record of invasive species Harmonia axyridis (Pallas, 1773) (Coleoptera: Coccinellidae) in Bosnia and Herzegovina. Acta Entomol. Serbica 2010, 15, 141–143. [Google Scholar]
  36. Stankovic, V.M.; Koren, T.; Stankovic, I. The harlequin ladybird continues to invade southeastern Europe. Biol. Invasions 2011, 13, 1711–1716. [Google Scholar] [CrossRef]
  37. Vandereycken, A.; Brostaux, Y.; Joie, E.; Haubruge, E.; Verheggen, F.J. Occurrence of Harmonia axyridis (Coleoptera: Coccinellidae) in field crops. Eur. J. Entomol. 2013, 110, 285–292. [Google Scholar] [CrossRef]
  38. Pickering, G.J.; Botezatu, A. A Review of Ladybug Taint in Wine: Origins, Prevention, and Remediation. Molecules 2021, 26, 4341. [Google Scholar] [CrossRef] [PubMed]
  39. Knapp, M.; Nedved, O. Gender and timing during ontogeny matter: Effects of a temporary high temperature on survival, body size and colouration in Harmonia axyridis. PLoS ONE 2013, 8, e74984. [Google Scholar] [CrossRef]
  40. Benelli, M.; Simon, R.; Francati, S.; Marchetti, E.; Dindo, M.L. Effect of two temperatures on biological traits and susceptibility to a pyrethroid insecticide in an exotic and native coccinellid species. Bull. Insectol. 2015, 68, 23–29. [Google Scholar]
  41. Biranvand, A.; Nedved, O.; Tomaszewska, W.; Al Ansi, A.N.; Fekrat, L.; Haghghadam, Z.M.; Khormizi, M.Z.; Noorinahad, S.; Senal, D.; Shakarami, J.; et al. The genus Harmonia (Coleoptera, Coccinellidae) in the Middle East region. Acta Entomol. Musei Natl. Pragae. 2019, 59, 163–170. [Google Scholar] [CrossRef]
  42. Majerus, M.; Strawson, V.; Roy, H. The potential impacts of the arrival of the harlequin ladybird, Harmonia axyridis Pallas (Coleoptera: Coccinellidae), in Britain. Ecol. Entomol. 2006, 31, 207–213. [Google Scholar] [CrossRef]
  43. Michaud, J.P. Invasion of the Florida citrus ecosystem by Harmonia axyridis (Coleoptera: Coccinellidae) and asymmetric competition with a native species. Cycloneda sanguinea. Environ. Entomol. 2002, 31, 827–835. [Google Scholar] [CrossRef]
  44. Lucas, E.; Labrie, G.; Vincent, C.; Kovach, J. The multicoloured Asian ladybeetle: Beneficial or nuisance organism? In Biological Control: A Global Perspective; Vincent, C., Goettel, M., Lazarovits, G., Eds.; CAB International: Willingford, UK, 2007; pp. 38–52. [Google Scholar] [CrossRef]
  45. Lucas, E.; Vincent, C.; Labrie, G.; Chouinard, G.; Fournier, F.; Pelletier, F.; Bostanian, N.; Coderre, D.; Mignault, M.P.; Lafontaine, P. The multicolored Asian ladybeetle Harmonia axyridis in Quebec agroecosystems ten years after its arrival. Euro. J. Entomol. 2007, 104, 737–743. [Google Scholar] [CrossRef]
  46. Bélanger, E.; Lucas, E. Dominance of the multi-coloured Asian lady beetle Harmonia axyridis in an undisturbed wild meadow ecosystem. Eur. J. Environ. Sci. 2011, 1, 7–14. [Google Scholar] [CrossRef]
  47. Bahlai, C.A.; Colunga-Garcia, M.; Gage, S.H.; Lamdis, D.A. The role of exotic ladybeetles in the decline of native ladybeetle populations: Evidence from long-term monitoring. Biol. Invasions 2015, 17, 1005–1024. [Google Scholar] [CrossRef]
  48. Gardiner, M.M.; Prajzner, S.P.; Burkman, C.E.; Alkbro, S.; Grewal, P.S. Vacant land conversion to community gardens: Influences on generalist arthropod predators and biocontrol services in urban greensapaces. Urban Ecosyst. 2014, 17, 101–122. [Google Scholar] [CrossRef]
  49. Grez, A.A.; Zaviezo, T.; Gardiner, M.M.; Alaniz, A.J. Urbanization filters coccinellids composition and functional trait distributions in greenspaces across greater Santiago, Chile. Urban For. Urban Green. 2019, 38, 337–345. [Google Scholar] [CrossRef]
  50. Lumbierres, B.; Pons, X.; Starý, P. Parasitoids and predators of aphids associated with public green areas of Lleida (NE Iberian Peninsula). Adv. Hortic. Sci. 2005, 19, 69–75. [Google Scholar]
  51. Pons, X.; Lumbierres, B. Control integrado de plagas en espacios verdes urbanos. In Hacia la Gestión Integrada de Plagas, Proceedings of the 12th Symposium Sanidad Vegetal, Sevilla, Spain, 23–25 January 2013; Consejería de Agricultura, Pesca y Medio Ambiente, Ed.; Servicio de Publicaciones y Divulgación—Consejería de Agricultura, Pesca y Medio Ambiente: Sevilla, Spain, 2013; pp. 145–184. [Google Scholar]
  52. Ottart, N. Impacts de la Coccinelle Invasive Harmonia axyridis sur les Populations de Coccinelles Indigenes a Bruxelles; TFE, Université Libre de Bruxelles, Ecole Interfacultaire de BioIngénieur: Brussels, Belgium, 2005. [Google Scholar]
  53. Durieux, D.; Fischer, C.; Brostaux, Y.; Sloggett, J.J.; Deneubourg, J.L.; Vandereycken, A.; Joie, E.; Wathelet, J.P.; Lognay, G.; Haubruge, E.; et al. Role of long-chain hydrocarbons in the aggregation behaviour of Harmonia axyridis (Pallas) (Coleoptera: Coccinellidae). J. Insect Physiol. 2012, 58, 801–807. [Google Scholar] [CrossRef] [PubMed]
  54. Brown, P.M.J.; Roy, H.E. Native ladybird decline caused by the invasive harlequin ladybird Harmonia axyridis: Evidence from a long-term field study. Insect Conserv. Divers. 2017, 11, 230–239. [Google Scholar] [CrossRef]
  55. Kenis, M.; Nacambo, S.; Van Vlaenderen, J.; Zindel, R.; Eschen, R. Long Term Monitoring in Switzerland Reveals That Adalia bipunctata Strongly Declines in Response to Harmonia axyridis Invasion. Insects 2020, 11, 883. [Google Scholar] [CrossRef]
  56. Labrie, G.; Lucas, E.; Coderre, D. Can developmental and behavioral characteristics of the multicolored Asian lady beetle Harmonia axyridis explain its invasive success? Biol. Invasions 2006, 8, 743–754. [Google Scholar] [CrossRef]
  57. Leppanen, C.; Alyokhin, A.; Gross, S. Competition for aphid prey between different lady beetle species in a laboratory arena. Psyche 2012, 2012, 890327. [Google Scholar] [CrossRef]
  58. Hautier, L.; Branquart, E.; Jansen, J.P.; Grégoire, J.C. Predation behaviour of Harmonia axyridis on Adalia bipunctata. IOBC/wprs Bulletin 2010, 58, 45–46. [Google Scholar]
  59. Katsanis, A.; Babendreier, D.; Nentwig, W.; Kenis, M. Intraguild predation between the invasive ladybird Harmonia axyridis and non-target European coccinellid species. BioControl 2012, 58, 73–83. [Google Scholar] [CrossRef]
  60. Zaviezo, T.; Soares, A.O.; Grez, A.A. Interspecific exploitative competition between Harmonia axyridis and other coccinellids is stronger than intraspecific competition. Biol. Control 2019, 131, 62–68. [Google Scholar] [CrossRef]
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Figure 1. Localities of (a) the Iberian Peninsula and Canary and Balearic islands (except Catalonia) and (b) Catalonia and Andorra (in purple) where H. axyridis was recorded in spring or summer. Black and red points correspond to records before and after 2015, respectively. Grey ovals indicate the areas were overwintering aggregations have been found. The straight black line separates the updated hypothetical invaded area from the not yet invaded area within Catalonia.
Figure 1. Localities of (a) the Iberian Peninsula and Canary and Balearic islands (except Catalonia) and (b) Catalonia and Andorra (in purple) where H. axyridis was recorded in spring or summer. Black and red points correspond to records before and after 2015, respectively. Grey ovals indicate the areas were overwintering aggregations have been found. The straight black line separates the updated hypothetical invaded area from the not yet invaded area within Catalonia.
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Figure 2. Relative abundance of the different ladybird species on L. tulipifera from 2019 to 2021.
Figure 2. Relative abundance of the different ladybird species on L. tulipifera from 2019 to 2021.
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Figure 3. Relative abundance of the different ladybird species on T. platyphyllos from 2019 to 2021.
Figure 3. Relative abundance of the different ladybird species on T. platyphyllos from 2019 to 2021.
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Meseguer, R.; Lumbierres, B.; Pons, X. Establishment and Expansion of Harmonia axyridis Pallas (Coleoptera: Coccinellidae) in Urban Green Areas in the Iberian Peninsula: From 2015 to 2021. Insects 2022, 13, 741. https://doi.org/10.3390/insects13080741

AMA Style

Meseguer R, Lumbierres B, Pons X. Establishment and Expansion of Harmonia axyridis Pallas (Coleoptera: Coccinellidae) in Urban Green Areas in the Iberian Peninsula: From 2015 to 2021. Insects. 2022; 13(8):741. https://doi.org/10.3390/insects13080741

Chicago/Turabian Style

Meseguer, Roberto, Belén Lumbierres, and Xavier Pons. 2022. "Establishment and Expansion of Harmonia axyridis Pallas (Coleoptera: Coccinellidae) in Urban Green Areas in the Iberian Peninsula: From 2015 to 2021" Insects 13, no. 8: 741. https://doi.org/10.3390/insects13080741

APA Style

Meseguer, R., Lumbierres, B., & Pons, X. (2022). Establishment and Expansion of Harmonia axyridis Pallas (Coleoptera: Coccinellidae) in Urban Green Areas in the Iberian Peninsula: From 2015 to 2021. Insects, 13(8), 741. https://doi.org/10.3390/insects13080741

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