Abstract:The effect of temperature on the rate of spotted lanternfly, Lycorma delicatula (White) (Hemiptera: Fulgoridae), egg development was investigated for a population in Pennsylvania. Mean developmental duration (days ± SE) for egg hatch was evaluated at five constant temperatures of 19.9, 24.2, 25.1, 26.7, and 30°C using egg masses laid during the fall of 2018 and collected in 2019 from Berks Co., Pennsylvania. Base temperature thresholds for egg development were estimated using intercept and slope parameters by … Show more
“…Various biotic and/or abiotic factors seem to be involved in this relatively slow expansion of distribution in Hokuriku, Japan. The most likely factor is the influence of climate, as shown previously 22 , 30 , 31 . Hokuriku has a large amount of precipitation, including snowfall in winter.…”
Lycorma delicatula has expanded its distribution from China to Japan, Korea, and the USA, causing significant economic damage to vineyards in the latter two countries. However, in Japan, L. delicatula has long been limited to the Hokuriku region, central Japan, and no significant damage to crops has been reported since it was first reported there in 2009. Manipulation experiments and field observations in the Hokuriku region, where winter precipitation is extremely high, revealed that egg numbers and hatchability were significantly reduced in exposed places, especially when wax was excluded from the egg mass. Phylogenetic analysis showed that the population in Japan could be divided into at least two groups. Most L. delicatula samples from Hokuriku formed a clade with those from northwestern China. Samples from Okayama, where the distribution of L. delicatula was recently confirmed, had the same haplotype as those from central China, Korea, and the USA. These results suggest that environmental factors and genetic characteristics of L. delicatula are involved in the relatively slow expansion of its distribution in Hokuriku. Conversely, in Okayama, where precipitation is relatively low, the rapidly increasing haplotype in Korea and the USA was detected, leading to concerns that its distribution will expand further.
“…Various biotic and/or abiotic factors seem to be involved in this relatively slow expansion of distribution in Hokuriku, Japan. The most likely factor is the influence of climate, as shown previously 22 , 30 , 31 . Hokuriku has a large amount of precipitation, including snowfall in winter.…”
Lycorma delicatula has expanded its distribution from China to Japan, Korea, and the USA, causing significant economic damage to vineyards in the latter two countries. However, in Japan, L. delicatula has long been limited to the Hokuriku region, central Japan, and no significant damage to crops has been reported since it was first reported there in 2009. Manipulation experiments and field observations in the Hokuriku region, where winter precipitation is extremely high, revealed that egg numbers and hatchability were significantly reduced in exposed places, especially when wax was excluded from the egg mass. Phylogenetic analysis showed that the population in Japan could be divided into at least two groups. Most L. delicatula samples from Hokuriku formed a clade with those from northwestern China. Samples from Okayama, where the distribution of L. delicatula was recently confirmed, had the same haplotype as those from central China, Korea, and the USA. These results suggest that environmental factors and genetic characteristics of L. delicatula are involved in the relatively slow expansion of its distribution in Hokuriku. Conversely, in Okayama, where precipitation is relatively low, the rapidly increasing haplotype in Korea and the USA was detected, leading to concerns that its distribution will expand further.
“…(2.1), ν i (t) (units: day −1 ) denotes the rate of development for i ∈ I/{d}, and that of diapause advection for i = d. Due to insect poikilothermy, these advective rates depends on t through temperature, T (units: o C), so that ν i (t) = ν i (T (t)) ≥ 0. Development typically occurs when temperatures exceed some minimal threshold, T ν i ,1 , with development rates increasing with temperature until a plateau is reached at high tempertures [38]. We therefore restrict ourselves to nondecreasing, continuous functions ν i (T ) (i ∈ I/{d}) that satisfy: ν i (T ) = 0 for T < T ν i ,1 , and ν i (T ) → ν i,max > 0 as T → ∞.…”
Section: Mathematical Structurementioning
confidence: 99%
“…The relative developmental age variable, a, is defined for each of the four life stages with respect to the duration of each stage in typical developmental units. For all life stages of the system except diapausing eggs, the developmental unit is the spotted lanternfly degree day-a measure of heat accumulation, which, in turn, tracks development [38]. Developing individuals accumulate degree days throughout periods of exposure to sufficiently warm temperatures, and, once certain threshold degree day counts are reached, transition to the next life stage.…”
Section: Calibration Of the Model Parameters And Functionsmentioning
confidence: 99%
“…Development speeds in SLF are quantified by the degree day function, through which each temperature, T , is assigned a certain number of degree days by which an individual ages in one day of constant exposure to that temperature. The advection coefficients, ν i (T ), have the common piecewise-linear form of the degree day function [38] for i ∈ I/{d}:…”
Section: Calibration Of the Model Parameters And Functionsmentioning
Invasive pest establishment is a pervasive threat to global ecosystems, agriculture, and public health. The recent establishment of the invasive spotted lanternfly in the northeastern United States has proven devastating to farms and vineyards, necessitating urgent development of population dynamical models and effective control practices. In this paper, we propose a stage-and age-structured system of PDEs to model insect pest populations, in which underlying dynamics are dictated by ambient temperature through rates of development, fecundity, and mortality. The model incorporates diapause and non-diapause pathways, and is calibrated to experimental and field data on the spotted lanternfly. We develop a novel moving mesh method for capturing age-advection accurately, even for coarse discretization parameters. We define a oneyear reproductive number (R 0 ) from the spectrum of a one-year solution operator, and study its sensitivity to variations in the mean and amplitude of the annual temperature profile. We quantify assumptions sufficient to give rise to the low-rank structure of the solution operator characteristic of part of the parameter domain. We discuss establishment potential as it results from the pairing of a favorable R 0 value and transient population survival, and address implications for pest control strategies.
“…The invasion success of this pest may be partly due to its broad host range 2 , apparent capacity for dispersal 6 , 7 and its potential to occupy a wide range of climatic conditions and ecosystems, especially disturbed habitats where the preferred host Ailanthus altissima (Mill.) Swingle (Simaroubaceae) (tree-of-heaven) is abundant 3 , 8 , 9 .…”
Lycorma delicatula (spotted lanternfly) has a broad host range with a strong preference for the invasive host plant from its native range, tree of heaven (Ailanthus altissima); it had long been speculated that L. delicatula could not develop or reproduce without access to tree of heaven. In 2019, we found that this assumption was incorrect, but fitness was reduced in the absence of A. altissima in that the number of egg masses laid was dramatically fewer for insects reared on suitable non-A. altissima host plants that had recently been established. We hypothesized that longer established, larger trees (of the same species) would improve the fitness of L. delicatula in the absence of tree of heaven. In spring 2020, we examined insect performance with and without access to A. altissima by tracking development, survival, host tree association and oviposition in large enclosures with trees planted two years prior to the study. Each enclosure included one each of Juglans nigra, Salix babylonica and Acer saccharinum along with either one A. altissima or one Betula nigra; these trees had twice the diameter of the same trees the previous year. We reared nymphs with and without access to A. altissima, released them into the corresponding large enclosures as third instars, and monitored them from early July 2020 through November 2020. We also determined whether lack of access to A. altissima by parents of L. delicatula have any fitness effects on offspring performance. To ensure adequate adult populations for comparing fecundity between treatments, third instars were released into the multi-tree enclosures due to high mortality in earlier instars that occurred in a similar study in 2019. Insect survival was higher and development faster with access to A. altissima. Third and fourth instar nymphs were most frequently observed on A. altissima when it was present, while adults were equally associated with A. saccharinum and A. altissima. In the absence of A. altissima, nymphs were most frequently found on S. babylonica, while adults were most often on A. saccharinum. Females with access to A. altissima deposited nearly 7-fold more egg masses than those without access to A. altissima, which is consistent with the difference in egg mass numbers between the two treatments the previous year; thus, our hypothesis was rejected. The offspring of parents that had been reared without access to A. altissima showed similar survival and development time from egg to adult as offspring from parents that never had access to A. altissima. These findings suggest that managers need to be aware that even in the absence of A. altissima in the landscape, several hardwood host trees can be utilized by L. delicatula to develop and reproduce, but fitness without A. altissima is likely to still be reduced.
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