New insights into the life history of Monochamus saltuarius(Cerambycidae: Coleoptera) can enhance surveillance strategies for pine wilt disease

Min Li · Yun Dai · Yang Wang · Lichao Wang ·Shouhui Sun · Fengmao Chen

Abstract Pine wilt disease was f irst discovered in Dongtang town, Liaoning Province, China, in 2017. Monochamus saltuarius Gebler is a new vector of pinewood nematode and the only known vector in Liaoning Province. The biology of this pest has not been reported thus far; therefore,it is necessary to study its life history. During 2018 and 2019, we collected 138 and 491 adult M. saltuarius beetles,respectively, to analyze their eclosion from larva to adult stage. In mid-March, overwintering larvae began to feed(on xylem) and seek nutrition in preparation for pupation and eclosion. The adults began to appear in mid-April, and the population reached its peak in late May. The life span of the adults was 28–76 days. After approximately 1 week of supplemental nutrition (feeding on twigs), adults began to mate and lay eggs. The egg stage of M. saltuarius lasted 4–8 days. The larvae in Dongtang town have 4 instars and overwinter in tunnels as 3rd–4th instars. The 1st-instar stage lasted 3–9 days, the 2nd-instar stage lasted 11–23 days, the 3rd-instar stage lasted 30–130 days, and the 4th-instar stage lasted 44–180 days. The pupal stage lasted 7–12 days, and the life span of the adults was 28–76 days. In this study we systematically monitored the life history of M. saltuarius for the f irst time. Our objective was to lay a foundation for improving control of this pinewood nematode vector.

Keywords Bursaphelenchus xylophilus · China · Pine sawyer · Life cycle · Vector

Introduction

Pine wilt disease is caused by pinewood nematode,Bursaphelenchus xylophilus(Steiner and Buhrer 1934), and represents one of the most serious global threats to conifer trees.The pinewood nematode, an invasive species native to North America, survives and successfully reproduces in East Asian conifer trees (Togashi and Jikumaru 2007). The pinewood nematode was accidentally introduced into Japan (Mamiya 1988) in the early twentieth century and subsequently introduced into China (Sun 1982), Korea (Han et al. 2008) and other countries (Rodrigues 2009), where it has caused massive local mortality of conifers (Foit et al. 2019). In 1982,pine wilt disease was f irst identif ied inPinus thunbergiiParl.in Nanjing city, Jiangsu Province where 256 dead trees were recorded within an area of 200 ha. Although this initial outbreak was fully controlled, the total loss of pine trees caused by pine wilt disease in China in recent decades has led to economic losses reaching hundreds of billions of Chinese yuan, and the disease is still expanding rapidly in China(Zhang 2010). In 2016 and 2017, pine wilt disease spread for the f irst time to Shahekou city, Dalian, and Fengcheng city, Dandong, Liaoning Province, both in northeast China,and caused pine tree deaths over large areas.

Similar to other disease-causing nematodes, the pinewood nematode requires an insect vector to be transported from one tree to another, and the vectors are cerambycid beetles in the genusMonochamus(Aikawa 2008). To date, 13 species ofMonochamusbeetles have been shown to transmit pinewood nematode. In North America,M. carolinensisOlivier(Linit 1990),M. scutellatusSay (Holdeman 1980),M. titillatorFabricius (Luzzi et al. 1984),M. obtususCasey (Akbulut and Stamps 2012),M. notatusDrury,M. marmoratorKirby andM. mutatorLeConte (Wingf ield and Blanchette 1983) are vectors ofB. xylophilus. In Asia,M. alternatusHope (Mamiya and Enda 1972), M. saltuarius(Sato et al.1987) andM. nitensBates (Harman 1985) can transportB.xylophilus.M. sutorLinnéand (Pajares et al. 2017) andM.urussoviFischer-Waldheim (Togashi et al. 2008) have been identified as vectors of pinewood nematode throughout Europe.Monochamus galloprovincialisOlivier (Akbulut et al. 2008; Pajares et al. 2010) was identif ied in Europe and North Africa and has been reported to be responsible for local pinewood nematode transmission.

BeforeM. saltuariuswas identif ied as a new pinewood nematode vector in China, it was known as a common pine forest pest in Liaoning, Jilin and Heilongjiang provinces that had not attracted much attention in these areas. In fact,M.saltuariushas long been recognized as one of the transmission vectors of the pinewood nematode in Japan (Jikumaru and Togashi 1995), South Korea (Kim et al. 2006) and other East Asian regions. In these regions, pinewood nematode has caused mass mortality of native pine species, considerable economic and environmental damage, and substantial annual losses of timber (Zhao et al. 2008). In Dandong, native conifer trees, such asPinus koraiensisSieb., Pinus armandiiFranch.,andLarix gmeliniiRupr.,have suf fered severe damage due to pine wilt disease carried byM. saltuariusinfected with the pinewood nematode. In other areas where pine wilt disease has not yet spread, the presence of vector insects must know for the risks of extension and possible damage to be properly assessed. Pest monitoring will identify where a pest is found and help to quantify its rate of movement into an area (Augustin et al. 2012 ). Every year, the General Station of Forest Pest Management surveys the national forest areas to conf irm current pinewood nematode epidemic areas in China, to address areas that have been classif ied as epidemic areas, and to strengthen the protection and monitoring of the areas around the epidemic areas (Li and Yao 2019).

The life cycle ofM. alternatushas been studied thoroughly worldwide. The behavior of adults, egg laying and larva development ofM. alternatuswere studied in detail using cages with twigs and pieces of logs (Zhou and Togashi 2006). However, little is known about its life cycle and biology in China. BecauseM. alternatusappeared only recently as a new vector of the Pinewood nematode in China, its biology and other characteristics are yet to be fully described.

Although pine wilt disease is currently present in only Liaoning Province among several provinces in northeast China, the consequences of beetles vectoring the pinewood nematode into other provinces are unknown. Monitoring the vectors of pinewood nematode has become a key strategy for the monitoring of pine wilt disease in China. Many trap designs have been developed to capture vectors of the pinewood nematode for population monitoring or for large-scale trapping ofMonochamusspp. (Xu et al. 2018).

Pine wilt disease might continue to spread to regions with a relatively cold climate and cause mortality in native pine species despite preventive ef forts by government agencies. Therefore, detailed understanding of the biology ofM. saltuariusis needed for the development of pest management strategies that can prevent the dissemination of the pinewood nematode and control pine wilt disease by ef ficiently controlling its vector. We studied the life history ofM. saltuariuswith the aim of providing a reliable reference for the prevention and control of pests and pinewood nematodes.

Materials and methods

Study area

Fig. 1 Locations of the test sites in Dongtang town. 1. Xiaolingziling(E118° 15′ 46″, N40° 26′ 58″), 2. Beishantou (E118° 16′ 58″, N40°26′ 30″), 3. Qiangwai (E118° 17′ 12″, N40° 26′ 26″), 4. Zhuangaizi(E118° 17′ 42″, N40° 25′ 17″), and 5. Tangling (E118° 17′ 43″, N40°24′ 14″)

Our study area was located in the pine wilt disease epidemic area of Dongtang town (Fig. 1). Five separate sites were selected for f ield trapping experiments. The f ive locations were Xiaolingziling (E118° 15′ 46″, N40° 26′ 58″), Beishantou (E118° 16′ 58″, N40° 26′ 30″), Qiangwai (E118° 17′ 12″,N40° 26′ 26″), Zhuangaizi (E118° 17′ 42″, N40° 25′ 17″)and Tangling (E118° 17′ 43″, N40° 24′ 14″); the minimum distance between sites was approximately 1200 m. Dongtang town has a mean annual temperature of 3.3 °C (data provided by the Dandong Meteorological Bureau), mean annual rainfall of 900–1000 mm, and mean relative humidity of 63%. The area is rich in soil and pine forest resources, and the predominant tree species areP. koraiensis,P. armandii,Pinus tabuliformisCarr. andL. gmelinii, all of which are reported to be susceptible to pine wilt disease (Han et al.2008; Nakamura et al. 2010; Shi et al. 2012; Yu et al. 2019).

Adult eclosion rules

We studied the acquisition of f light dynamics of adultM.saltuariusby capturing the beetles in Dongtang town over a two-year period from 2018 to 2019. Beetles were captured in improved commercial traps (F2 attractant traps supplied by Hangzhou Felomon Biotechnology Co., Ltd. China) (Zhang et al. 2018). The attractant core consisted of two components. The f irst component was a blend of alpha- and betapinene in a plastic bottle, and the second component was the aggregation pheromone 2-undecyloxy-1-ethanol dispensed as f lakes. Both components provided a release rate of 2.7 μg/day at 25 °C. The trap consisted of a top cover, a cross baf fle,a trap, a funnel and a collection bottle (Fig. 2 a). Twenty-f ive F2 attractant traps were hung approximately 3 m from the ground, with 30 m spacing between traps (Chen et al. 2014),and f ive traps were installed at each of the f ive sites in the pine wilt disease epidemic area of Dongtang town. The trees at each site were located in 50- to 60-year-old pure Korean pine forests.From the beginning of April to the beginning of September in 2018 and 2019, we checked traps and removed beetles for identif ication every 2 days in accordance with an established method for capturing adultMonochamusin pine forests (Pimentel et al. 2014). Traps were easy to deploy and monitor, making it feasible to sample geographically distant locations.

Adult mating and oviposition

Captured adult beetles were kept in covered f ield cages(2 m × 2.5 m × 2 m) with sidewalls made of 0.2-cm metal mesh. Newly cut wood was placed in the cages for the adults to lay eggs on, and the cut ends of the wood were sealed with paraf fin to prevent water loss. FreshP. koraiensistwigs were also placed in the cages for adult feeding. Every 7 days, the wood pieces supplied for oviposition were removed from the adult cages and placed in new cages to record the time to eclosion (Fig. 2 b).

Larval development

The f irst wood piece with eggs was placed in a cage on July 6, 2018. At the beginning of the experiment, it was necessary to observe egg hatching for several days, and 10 egg-laying slits were checked every day to inspect egg status. As the larvae developed, the observation schedule was modif ied to once every 15 days. The methods for observing insect stage and age were described by Wang (Wang 2002).Observations were performed in the egg-laying slits under the bark, in the phloem, and f inally in the sapwood until the larvae were located. The tunnel in the log caused by larval feeding was checked to determine the exact position of the larvae in the log. Larvae with a milky white body color and feces in the intestine were considered to be feeding, while those with empty intestines and of yellowish white to yellow color were considered to be in diapause. Monitoring was stopped in November (the larvae did not develop during the cold season) and started again in March of the following year until eclosion. The stage of each instar and the head width of the larvae were recorded from 2018 to 2019.

Fig. 2 Trap suspension apparatus and net f ield cages. Suspension mode of the F2 attractant trap ( a). Net cages containing logs for oviposition ( b)

Trap sample examination

Captured beetles were sent to Fengcheng Forestry Pest Control Laboratory for identif ication and classif ication. If an insect could not be sent to the laboratory immediately, it was placed in a freezer at 4 °C until the next sample delivery.Over two years of f ield trapping experiments, 1290 insects were collected (non-coleopteran insects were not counted in 2018), and among these insects, 16% could not be identif ied to species (mainly weevils and Scolytidae). CapturedM.saltuariuswere examined in detail and sexed.

Results

Dynamics of adult M. saltuarius occurrence

In 2018 and 2019, f ield trapping of adultM. saltuariusbegan on April 1 and ended on August 31. According to the results of two years of investigation, oneM. saltuariusgeneration was produced every year in Dongtang town (Figs. 3, 4).AdultM. saltuariusf lying dynamics peaked in late May.During this period, 39 adults eclosed in 2018, and 232 adults eclosed in 2019, accounting for 28% and 24% of the total adults in 2018 and 2019. Among these adults, the f lying dynamics peak in 2018 and 2019 occurred on May 27 and May 24, with 21 and 84 adult f lying events, respectively.Subsequently, the number of adult f lying events decreased signif icantly. Beginning on June 26, 2018, and July 5, 2019,M. saltuariusadult f lying decreased gradually. After July 21, 2018, essentially noM. saltuariuseclosed. In 2018 and 2019, the adult trapped ofM. saltuariuswere generally the same, as were the dates of peak occurrence.In 2018, 138 adults were trapped in the pine wilt disease epidemic area in Dongtang town, with a mean of 2.76 beetles per trap; the ratio of females to males was 2.14:1. The number of adults captured in 2019 was signif icantly higher than in 2018. A total of 491 adults were trapped in the epidemic area, with a mean of 9.82 beetles per trap; the ratio of females to males was 1.15:1 (Table 1).

Fig. 3 Adults of Monochamus saltuarius. Female adult ( a), male adult ( b). Bar = 5 mm

Fig. 4 Eclosion period of adult Monochamus saltuarius in Dongtang town

Mating and oviposition behaviors in M. saltuarius adults

Before mating, male and female adults required several to dozens of minutes for mutual adaptation. The mating times of each pair of adults dif fered after one mating. Some of the pairs separated immediately after mating, while others mated repeatedly. After one mating event, male and female adults could copulate with the same partner or copulate with a dif ferent partner. Thus, there was no individual specif icity between males and females. Mating occurred between one male and multiple females and also between one female and multiple males. Some male and female adults copulated atdif ferent times, and some copulated 4 times consecutively,usually for 1–2 min each time. Female adults copulated while feeding, and both males and females were provided supplemental nutrition after copulation. Before laying eggs,the females excavate slits into the tree trunk and then insert their ovipositor into the slit to lay eggs.

Table 1 Number of Monochamus saltuarius trapped in 2018 and 2019

M. saltuarius adult life span

New twigs were provided every 3 days to provide continuous supplemental nutrition for the adults in the cages. Daily observations revealed that the life spans of female and male adults were ranged from 28–76 to 37–69 days, respectively.Beetles lived only 5–16 days without feeding.

Larval development

In Dongtang town, two years are required forM. saltuariusto complete its life cycle (Table 2, Fig. 5). Old-instar larvae mainly survived through the winter in the xylem, and a few lived through the winter in the phloem. In the middle of March of the following year, the overwintering larvae began to move and continued to feed. In the f irst 10 days of April, the larvae began to eat, and pupation and adult eclosion began in mid-April. In the f irst 10 days of May,there were egg-laying slits (Fig. 5 a) in the wood. Females began to oviposit and larvae appeared in mid-May. July and August were the peak periods for egg hatching. The larvae successively overwintered starting in late October or early November. Due to dif ferences in climatic and forest conditions, the time of adult eclosion dif fered among the areas. The time of adults eclosion is very important for nematode spread because transmission occurs by the adult through feeding, swarming and breeding. The earliest eclosion of adults occurred within the f irst 10 days of April. Therefore, trap monitoring should start within the f irst 10 days of March.

Table 2 Life cycle of M.saltuarius in Dongtang town

Fig. 5 Monochamus saltuarius development process. Egg-laying slit ( a), egg under the egg-laying slit ( b), 1st-instar larva ( c), 2nd-instar larva( d), 3rd-instar larva ( e), 4th-instar larva ( f), pupa ( g), and entry and eclosion holes ( h). Bar = 2 mm

Eggs

The eggs (Fig. 5 a) ofM. saltuariuswere long and oval,approximately 0.43 cm in diameter, slightly concave in the middle, and uneven in size at the ends. The eggs were generally laid in the lowest part of the egg laying slit, with the small side facing down. When the bark was cut open, the outer layer of the egg cuticle was surrounded by turpentine.The egg casing had two layers: the outer layer was thick and light yellow and had a mesh-like structure that prevented the eggs from hatching due to soaking in turpentine. The inner layer was thin and had a white membrane with no such structure. The egg laying period occurred from the f irst 10 days of May to the last 10 days of August, and the peak egg laying period was from June to July. The duration of the egg stage typically ranged from 4 to 8 days, with the longest duration being 12 days.

Larvae

In Dongtang town, most larvae started to hatch in mid-May.June to July was the peak period for egg hatching. Of the 304 eggs observed by dissection, 23 were dry and black in appearance. These eggs might have been infected by fungi(Álvarez et al. 2015) or were unfertilized (Zhang and Linit 1998 ). No natural enemies, such as parasitoids, were found.The egg hatching rate reached 92%. When hatching, the larva used its upper jaw to bread the casing along the long axis of the egg and then exited the egg casing. After hatching, the larva did not eat the egg casing but, rather, fed on pine bark.

LarvalM. saltuariusdeveloped through 4 instars, with the larval stage lasting 245–332 days. Head width values for each age range are shown in Fig. 6 and Table 3.

The newly hatched larvae (Fig. 5 b) were white and approximately the same length as the egg casing. They f irst ate the phloem of the endodermis in pine trees. Brown matter could be seen in the digestive tract, and brown powdery excrement was found at the feeding mark of the endodermis.The 2nd-instar larvae (Fig. 5 c) gradually fed on the surface of the sapwood, forming a curved, shallow and irregular borehole. The borehole was f illed with brown powder, white borehole f ibers and frass. At this time, brown and white boreholes could be seen outside the bark; these marks were an early indicator of damage caused byM. saltuarius. The larvae grew for 15–30 days in the cortex and sapwood. The 3rd- (Fig. 5 d) and 4th-instar (Fig. 5 e) larvae began to bore into the xylem. Oblate and circular boreholes (Fig. 5 g) of 0.5–1.1 cm length and 0.2–0.5 cm diameter were observed in the xylem. When larvae passed through the phloem to the xylem, they generally approached from the sapwood to the center, and no vertical borehole was found. The larvae fed in an upward or downward direction after entering the section

Fig. 6 Frequency distribution of head capsule width for 320 larvae of Monochamus saltuarius from 2018 to 2019

horizontally. The length of the borehole was related to the size of the larva. The length of a large borehole containing a mature larva reached 10.3 cm, while short boreholes were 6.5 cm. The larva usually accumulated feces and bores under the bark, and the larvae present in the xylem expelled sawdust and feces outward. A large amount of sawdust accumulated under the bark near the mouth of the hole, forming a dense layer. After larval entry into the xylem, no sawdust or feces was seen outside the bark.

Beetles overwintered from October to March, during which time the larvae ceased their activity and almost completely stopped eating. Most of the 3rd–4th instar larvae overwintered in the bored tunnel, and a few of the 2nd–3rd instar larvae overwintered under the bark, mostly in the thick bark at the base of the trunk. The chambers of the mature larvae in the xylem were constructed before overwintering and were clean, without sawdust or feces.

After overwintering, the larvae continued to eat and then formed a pupal chamber, in which the mature larvae pupated. The length and diameter of the pupal chamber were both approximately 3.63 cm. The short diameter was 1.54 cm. Some larvae pupated under the bark. When the larvae pupated, they formed a circular tunnel that was deeper than the borehole. At f irst, the pupa (Fig. 5 f) was completely milky white. After 4–5 days, the pupa turned slightly yellow,and the compound eyes turned a light brown color. On the 6th day, the maxilla started to turn light reddish brown and f inally turned brown or blackish brown. Similar to the compound eyes, on the 7th day, the ends of the claws, appendages of the foot, and ends of the tibia and legs became light brown. On the 9th day, the elytra turned gray or grayish black, and on the 10th day, the legs and antennae, which were movable, began to unfold, but the wings were not hard.On the 11th–12th day, the elytra began to harden, and the beetles f inally completed their eclosion.

Table 3 Larval duration and head width of M. saltuarius in Dongtang town

Discussion

AlthoughM. saltuariusis found in many parts of the world,this species′ life history has not attracted much attention or research interest as a pest, probably becauseM. alternatusis present in the same areas.M. alternatus, by comparison,has caused environmental and economic losses and this insect is an ef ficient vector of pine wilt disease (Akbulut and Stamps 2012). In recent years, scholars have paid particular attention to the mating mode and other related aspects ofM. saltuarius(Kobayashi et al. 2003; Anbutsu and Togashi 2008).M. saltuariusis a new vector of the pinewood nematode in China. Based on the biological characteristics and life cycle ofM. saltuarius, it is necessary to formulate scientif ic control measures and determine appropriate control periods. At present, experiments are being carried out only in Dongtang town. The life cycle ofM. saltuariusin other areas of China needs to be further studied. The number of larval stages inM. saltuariushad not been conf irmation.Our results clearly show that there are four stages, and we determined their size characteristics. With regard to the age classes ofM. saltuarius, many scholars consider that beetles of the genusMonochamushave 5 age classes (Naves et al.2006; Liu et al. 2008), but Koutroumpa (Koutroumpa et al.2008) and Togashi (Togashi 1990) found thatM. galloprovincialisandM. alternatushave four larval instars. According to the age classif ication method recommended by these previous authors, only four age classes were observed inM.saltuarius. There are many reason for this dif ference; one possible reason is that summer in Dongtang town is short andM. saltuariusbegin to overwinter in October, at which point its development is suspended. In March, the weather gradually warms, and the insects start to move and eat. Due to the long dormancy period of beetles in this area, there is no signif icant dif ference between the 4th-instar larvae and 5th-instar larvae.

The number of beetles collected in the second year was approximately 3.5 times that collected in the f irst year. The ratio of males to females was 2.41:1 in 2018 but gradually returned to 1.15:1 in 2019. The increased proportion of female beetles in 2018 may be a response byM. saltuariusto excessive disruption of the local population by humans(Peer and Taborsky 2004). The entrapment records for 2019 show that the number actually increased greatly compared with that in the previous year. BecauseM. saltuarius, similar to other beetles, may adjust the sex ratio of its of fspring according to the environment and population, it is even more important to strengthen ef forts to protect pine trees from pine wilt disease.M. saltuariuslarvae conceal themselves by boring holes into and feeding on pine tree tissues, making control by chemical agents very dif ficult at this stage. The thorough cleaning of dead wood harboring a large number ofM. saltuariuslarvae before adult eclosion can signif icantly reduce the population density of this forest pest and is an ef fective measure for preventing and controlling this pest(Kwon et al. 2011). However, pine trees have a lag period between initial infestation and display of wilt symptoms;thus, visually healthy but infected trees could be a source of infection for a given period. At present, cleaning of dead wood generally occurs from December to January of the next year, but at that time, visually healthy but infected trees are likely to be ignored. Some of these trees can be distinguished by observing whether the trunk has the egg-laying slits or not, but the slit is too small to be found with high probability.

Monochamus saltuariusis exposed in only the adult stage, and this stage serves as a vector of the pinewood nematode. The pinewood nematode can be spread by the movement ofM. saltuarius. Reducing the density of adults in the forest in a timely manner is the key to controlling pine wilt disease. The duration before adult eclosion is long, and there are many rainy days during the peak active period in May, making it dif ficult to ef fectively use traditional chemical control methods. Due to the long-term use of chemical pesticides, some pests have developed strong pesticide resistance, and many natural enemies of pests have been killed in large quantities, leading to explosive population growth in some pests. Biological control can ef fectively overcome the above shortcomings and thus has broad application potential. The most environmentally friendly form of biological control of diseases and insect pests is the use of natural enemies or microorganisms,predatory birds or other measures. Through experiments,Cheng showed thatScleroderma guaniis a natural parasitic enemy of the larvae and pupae of Cerambycidae and can aid natural control of wood borers (Cheng et al.2003). Yan et al. ( 2014) found that the mortality rate ofMonochamusbeetles was as high as 64.6% in a control experiment withDastarcus helophoroides, and the ef fect was signif icant.

Before the occurrence of pine wilt disease in Liaoning Province, it was thought that the pinewood nematode could not survive in this area of China because of its annual mean temperature of 10 °C (Quan et al. 2005). However,some isolates of pinewood nematodes have evolved since they invaded Liaoning Province, becoming more virulent and better adapted to low temperatures than the pinewood nematode found in the warm areas of South China.M. saltuarius, which originated from high latitudes, has adapted to low temperatures. Therefore, it is very important to develop a deep understanding ofM. saltuariusecology in cold climates.

Conclusion

The larvae ofM. saltuariusin Dongtang town, Liaoning Province, developed through 4 instars and overwintered in the borehole with 3–4 instars. The egg stage was 4–8 days,the 1st-instar larval stage was 3–9 days, the 2nd-instar larval stage was 11–23 days, the 3rd-instar larval stage was 30–130 days, the 4th-instar larval stage was 44–180 days and the pupal stage was 7–12 days. Adults began to appear in the middle of April, and the population size peaked in late May. After approximately 1 week of supplementary nutrition, the adults began to mate and lay eggs. The life span of the adults was 28–76 days. The study of the pine sawyerM. saltuariusas a vector of the pine wilt nematode will provide fundamental data to establish ef fective prevention measures for addressing this devastating disease.

Authors’ contributionLM and CFM conceived and designed the research. LM conducted the experiments. SSH contributed new reagents. DY, WY and WLC analyzed the data. LM wrote the manuscript.All authors read and approved the manuscript.

Compliance with ethical standards

Conf lict of interestThe authors declare that they have no conf licts of interest. This article does not contain any experiments with human participants or animals performed by any of the authors.

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source,provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creat iveco mmons.org/licen ses/by/4.0/.