1. Introduction
Curculio sayi (Gyllenhal) is truly the lesser of two weevils. Both C. sayi (the lesser chestnut weevil) and C. caryatrypes (Boheman) are principal pests of chestnut production in the United States. Females of these species lay eggs in developing nuts and the larvae that emerge from these eggs can cause massive losses in nut production. While the economic and ecological consquences of chestnut weevil infestation are serious, not much is known about these weevils due to the interesting history of chestnut trees and chestnut production in the United States.
American chestnut trees (
Castanea dentata) once dominated the forests of the Eastern United States. Up until the early 1900s, an estimated four billion trees, accounting for more than 50% of the total basal area in eastern forests, grew on 800,000 km
2 [
1]. A staple of early American life, chestnut trees provided tannin-rich, decay-resistant wood used in everything from furniture to housing to musical instruments [
2,
3]. The value of chestnut timber in Pennsylvania alone in 1912 was assessed at USD 55 million, equal to USD 1.4 billion today [
3]. The introduction of chestnut blight (
Cryphonectria parasitica) in the early 1900s devastated American chestnut forests [
1,
2,
4]. Few trees survived and stump sprouts became infected well before maturation, surviving only as small, multi-stemmed shrubs. Chestnuts, and their associated insect pests, disappeared from the national consciousness.
Because of this historical dynamic, very little is known about chestnut weevils in North America. Of what research is available, most of it was published well before the year 2000 and the increasing impact of anthropogenic climate and land-use changes of the 21st century. Early work [
5] recognized the prevalence and severity of these pests, documenting high levels of infestation reaching 100% in some cases, with large quantities being seized and destroyed due to ‘worms, worms excreta, worm-eaten chestnuts, and decayed chestnuts’ which ‘were therefore liable to seizure for confiscation’ [
6]. Early work also documented some aspects of the phenology and lifecycle of these weevils including how they are able to lay eggs inside developing chestnuts and details as to their development [
7].
While this work is historically important, it did not gain much attention until recent advances in chestnut breeding created a resurgence in the commercial chestnut industry. The recent development of high-yield chestnut varieties that are blight-resistant have increased the opportunities to expand production of this high-value specialty crop in the US [
8,
9,
10,
11,
12]. New varieties of trees can produce 1000 to 1500 lbs per acre annually with prices ranging between USD 2.50 and USD 10 per pound depending on the market. As growers recognize the potential of commercial chestnuts, acreage in the northeast and Great Lakes regions is increasing and nurseries are rushing to keep up with demand for new trees (Zarnowski and Zarnowski, personal communication, 2020). Accompanying this resurgence is a resurgence in another organism: the lesser chestnut weevil.
As more blight-resistant trees come into production, weevil populations are exploding. If left unchecked, weevil populations can develop rapidly, reaching high levels of infestation in as little as two years [
7,
13,
14]. Damage from this weevil is now recognized to be devastating in two forms. First, weevil larvae physically damage the nut and erode consumer confidence when emerging from purchased nuts. Second, larvae infestations are accompanied by fungal infections by
Aspergillus fungi [
15], which produce the diarrheagenic toxin emodin [
16].
Efforts to control this pest depend on understanding its phenology. Investigations into
C. sayi phenology recommenced in 2008 with work in Missouri that documented the emergence, adult activity, and lifecycle of the lesser chestnut weevil over three years [
13]. Interestingly, the greater chestnut weevil was not encountered [
13]. In 2019, chestnut growers in upstate New York began to have similar problems. Curiously, they commented, their phenologies did not match that reported in the literature from Missouri. In discussions with other colleagues and growers in the Northeast, two important anecdotal trends became readily apparent. First, the lesser chestnut weevils (not the greater) were rapidly emerging as a principal pest of chestnuts in the region, in some cases going from 0% to above 80% infestation in as little as two years. Second, literature and extension reports from southern states did not match experiences in the northeast. Growers would begin monitoring in early spring, not find any weevils, conclude there was no problem, and still find devastating infestation at the end of the season.
To begin to address these trends, we began working to better understand the phenology and monitoring of the lesser chestnut weevil as a first step to improving its management in the northeastern United States.
2. Materials and Methods
All
C. sayi weevils were collected from Rose Valley Farm (43°09′26.5″ N, 76°55′21.1″ W), an organic farm in upstate Rose, New York during the field seasons of 2019 and 2020. These weevils were collected from a mature (15+ years old) commercial chestnut stand containing a mix of American Chestnut Hybrids. Trees were approximately 7 m on center and formed a complete canopy after leafing out. Catkins (flowering) occurred in mid to late June and nut drop began in late September to early October. The soil type was Elnora Loamy Fine Sand [
17].
2.1. Phenology and Monitoring
To examine the phenology and evaluate the adult monitoring potentials of different trap types, three different traps were deployed to the mature chestnut stand at Rose Valley Farm at the beginning of the field season (May). Emergence traps were conical traps 1 m in diameter that were constructed similar to those described by (Keesey, 2008) from fine hardware cloth and placed directly over the soil under the mid-canopy of chestnut trees [
13]. Trunk traps (Circle Trunk Trap, Small GL-4000-06, Great Lakes IPM Vestaburg, MI) were affixed to tree trunks at breast height (1.35 m above the ground) and consisted of fine mesh screen wrapped such that it abutted the diameter of the tree and terminated in a clear plastic trap. Pyramid traps (Tedders Pyramid Trap, GL-5000-06, Great Lakes IPM, Vestaburg, MI, USA) were staked into the ground within 0.5 m of the tree trunk and consisted of black upright cardboard supports terminating in a clear plastic trap.
A total of 16 pyramid traps, 12 trunk traps, and 3 emergence traps were emplaced in the chestnut stand. Traps were monitored weekly following emplacement and all insects in the trap were collected for evaluation in the lab. Male and female
C. sayi totals for each trap were tallied on a biweekly basis in both 2019 and 2020. Specimens were examined for the presence of
C. caryatrypes using diagnostic characteristics described previously [
6,
7,
13,
18].
Degree days were also monitored for each season. Degree days were calculated with a base of 4 °C using the Baskerville–Emin method beginning April 1. Temperature data were collected by the Network for Environment and Weather Applications (NEWA) station at Butler (Tree Crisp), NY, less than 17 km from the chestnut stand.
2.2. Lifecycle
To evaluate the lifecycle of C. sayi, 25 late stage C. sayi larvae that had recently emerged (within 24 h) from fallen chestnuts were placed into each of 20 soil microcosms adjacent to the commercial chestnut stand described above. These microcosms were constructed using 5-gallon buckets (one 5-gallon bucket for each of the 20 microcosms) perforated with 15–20 large-diameter (~7 cm) holes screened with fine mesh and filled with soil from the chestnut stand. These buckets were then covered with the same fine mesh and buried such that the soil level of the microcosm was flush with that of the adjacent soil. This set up allowed the transit of soil microorganisms through the fine mesh but prevented both the escape of the C. sayi larvae through the soil and the escape of any emerged adults above the surface.
These microcosms were emplaced in November of 2020. The 25 larvae were placed at the surface of the soil and the screen covering affixed to prevent escape. Microcosms were left unperturbed and then removed for analysis in late April 2021. To examine these microcosms, the top screen was first removed and the surface examined for adult C. sayi. Following the surface examination, the surface height of the soil was marked on the side of the bucket and the soil of the microcosm finely and delicately excavated and passed through a mesh sieve to look for larvae, adults, pupae, and pupal cells.
2.3. Analysis
Data were collated in tabular form (comma-separated values) and then imported to R V4.2.0 using RStudio as an IDE. The weevil catch was modeled using generalized linear models based on Poisson distributions using the log link function. All possible models were considered (including all levels of interactions) and best fit models were selected based on examination of diagnostic residual plots, likelihood ratio tests, analysis of deviance, information criteria, and goodness of fit. Differences in grouping factors were evaluated using estimated marginal means and Tukey’s pairwise contrasts adjusted for the family-wise error rate. The Tidyverse package was used to facilitate analysis and plotting [
19]. The car, emmeans, and lmtest packages were use to assist in model development, analysis, and interpretation [
20,
21,
22].
4. Discussion
Observed
C. sayi population dynamics suggest that the upstate New York population is univoltine with a peak in mid to late October (
Figure 1A). This is in contrast to reports from Missouri that there are two distinctive waves of emergence [
13]. This difference could be attributed to differences in season dynamics;
C. sayi in Missouri begins emerging in late May [
13] when the weather is still rather cold (nighttime temperatures around 4 °C) in upstate New York. Trapped
C. sayi populations in upstate New York only began to rise when cumulative degree days began to exceed 2000 (
Figure 1B).
In upstate New York, the adult
C. sayi population dynamics were consistent across two field seasons with one large population spike towards the end of the season beginning in early September (
Figure 1A). These populations tended to peak in mid to late October; by early November, populations were in decline. In both seasons, male
C. sayi trap catch began to rise earlier than female
C. sayi trap catch.
A second point of comparison between monitoring reports outside of the northeast is trap efficacy. Work in Missouri demonstrated the efficacy of emergence traps for collecting adult weevils as they emerge from the soil. In fact, these ground-based emergence traps collected many more
C. sayi than and in advance of other trap types [
13]. In contrast, our emergence traps in upstate New York did not catch a single
C. sayi adult in either season. Much more effective were the trunk and pyramid traps. Pyramid traps caught more than three times more weevils than trunk traps and were the most effective means of monitoring adult
C. sayi populations (
Figure 2). These traps caught more than two times more male than female
C. sayi adults. Both the pyramid and trunk traps work by arresting adults as they emerge from the soil and climb to the canopy. While this may be true if
C. sayi adults emerge proximal to the host trees, this may not be the case at our field site. If adult weevils were emerging from the soil underneath the chestnut trees under observation, we would have expected to have collected at least a few given the trap placement. Additionally, the peak populations of adult weevils we collected came in mid to late October at a time when the nuts themselves were almost mature. It could be our
C. sayi were flying into the canopy of our commercial orchard from surrounding areas.
This could be supported by the flight ability of
C. sayi and the attractive nature of the chestnut canopy during flowering. While the average flight distances for male and female adult
C. sayi are 247.1 m and 226.6 m, respectively, the maximum observed flights are much longer, with a female 2 hr flight of more than 3 km and a male flight exceeding 2.5 km [
23]. If
C. sayi were flying into the chestnuts evaluated in this study, they were likely attracted to the flowering catkins. Chestnut catkins produce a number of key volatile organic compounds [
24] that are highly attractive to both male and female
C. sayi [
25].
The C. sayi lifecycle aligns closely with previous reports including the construction of a pupal chamber just below the soil surface. As in previous reports, no weevils or pupal chambers were found more than 10 cm below the soil surface. The mortality of our subterranean C. sayi was more than double that of previous reports which could be related to differences in soil types and the presence of other soil organisms in the microcosms. In line with previous reports, we recovered multiple life stages, including adults that had eclosed but not yet emerged.
These staggered life stages could point to a survival strategy that has been documented in the European cousin of
C. sayi: the chestnut weevil
Curculio elephas.
C. elephas uses a staggered strategy of emergence to distribute a single generation to emerge as adults over multiple years [
26,
27]. This plasticity enhances long-term chances of survival so that an entire generation does not emerge in one potentially bad year [
26,
27]. A similar strategy could be occurring in
C. sayi. Given the varied life stages we discovered after a single season and similar results from previous studies [
13], we suspect that a single generation of larvae may emerge as adults over multiple years.