The food-burying behavior has been reported in many mammals and birds, but was rarely observed in invertebrates. The red imported fire ants, Solenopsis invicta Buren, is an invasive pest in many areas of the world that usually performing food-burying during the foraging processes. However, the impacted factors and measureable patterns of this behavior is largely unknown. In the present study, food-burying vs food-transport behaviors of Solenopsis invicta were observed under laboratory and field conditions. When starved (no food was provided for 37 days) in the laboratory, food (sausage) was consumed by large numbers of ants, and few burying behaviors were observed. However, when food was provided until satiation of the colonies, food-transport was suppressed and significantly more soil particles were relocated on the food and graph paper square (where the food was placed) when compared with these colonies exposed to starved conditions. Videotapes showed that soil particles (1.47 ± 0.09 mm2) were preferentially placed adjacent to (in contact with) the food items at the beginning; and after the edges were covered, ants transported significantly smaller soil particles (1.13 ± 0.06 mm2) to cover the food. Meanwhile, larger particles (1.96 ± 0.08 mm2) were pulled/dragged around (but not in contact with) the food. Interestingly, only a small number of ants, mainly the small workers, were involved in food-burying, and the ants tended to repeatedly transport soil particles. A total of 12 patterns of particle transport were identified, and soil particles were most frequently picked from the foraging arena and subsequently placed adjacent to the food. In the field, almost all released food was actively transported by Solenopsis invicta workers, and no burying behavior was observed. Our results show that the food-burying behavior of Solenopsis invicta may be associated with the suppressed foraging activity, and the burying task may be carried out by certain groups of workers.

Aquilaria sinensis (Lour.) Gilg is an economically important tree species that produce the highly prized agarwood. In recent years, agarwood production has been seriously threatened by the outbreak of Heortia vitessoides Moore, a leaf-eating pest that shows gregariousness during the larval stage. However, little attention has been paid to the aggregation behavior of H. vitessoides larvae. In the present study, we collected 102 cohorts of H. vitessoides larvae (13,173 individuals in total) in the wild; 54 cohorts were comprised of the same-instar larvae, and 48 cohorts were comprised of larvae with different developmental stages (instars). In general, young larvae (<third instar) tended to form large aggregations, whereas older-instar larvae were either solitary or formed small aggregations. Laboratory studies showed a strong aggregation tendency in the newly hatched and second-instar larvae of H. vitessoides, whenever the individuals originated from the same or different sibling cohorts. In addition, all newly hatched larvae died within two days after they were isolated. When newly hatched larvae were initially assigned in 10-larvae cohorts (containing sibling individuals) or 20-larvae cohorts (either containing individuals originating from the same or different sibling cohorts), their larval survivorship, duration of larval stage, and adult emergence were not significantly different. Interestingly, combining avermectin-treated larvae (donors) with untreated ones (receptors) significantly decreased larval survivorship and adult emergence of receptors, indicating a horizontal transfer of avermectin among H. vitessoides larvae. This study enhances our understanding of the population ecology of H. vitessoides, and may bring novel insights into the management strategies against this pest.

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Eusocial insects have evolved diverse particle‐use behaviors. A previous study reported that red imported fire ants, Solenopsis invicta Buren, deposited soil particles on substances treated with essential balm, a fire ant repellent. We hypothesized that S. invicta modifies inaccessible surfaces by covering them with soil particles to facilitate food search and transportation. Here, laboratory experiments were conducted to study the particle‐covering behavior of S. invicta in response to viscose surfaces or surfaces treated with essential balm or liquid paraffin in the presence of real food (sausage) or non‐food objects (acrylic plates). S. invicta workers deposited significantly more soil particles on these three types of treated surfaces than on untreated surfaces. In addition, significantly more particles were relocated on viscose and paraffin‐smeared surfaces in the presence of food than in the presence of non‐food objects. The particle‐covering behavior on viscose surfaces was also observed in the field. Interestingly, when no soil particles were available, ants searched and transported food on viscose surfaces only if the surfaces were artificially covered with sufficient quantities of soil particles but could not do so on viscose surfaces without soil particles or with insufficient quantities of soil particles. In addition, ants actively relocated particles to cover viscose surfaces if the transportation distance was within 200 mm, whereas significantly fewer particles were relocated at longer transportation distances (400 mm). Our study provides a novel example of particle use by fire ants during foraging.

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