Tunneling response of termites to a pre-formed tunnel

Subterranean termites move from place to place while foraging by tunneling through soil. During a period of foraging, they are likely to encounter a number of pre-formed tunnels created by, for example, tree roots or the breaking up of a zone of hard or compacted soil. We systematically observed the behavioral response of tunneling termites to such pre-formed, artificially constructed tunnels at widths, W, of 0.5, 1.0, 1.5, and 2.0mm, which mimicked pre-formed tunnels in the field. The two tunnels intersected at an angle, theta (=0 degrees , 10 degrees , 20 degrees , 30 degrees , 40 degrees , 50 degrees , and 60 degrees ) formed between the advance direction of a termite tunnel and the perpendicular direction of a pre-formed tunnel. For W=Wc (=0.5mm) and theta相似文献   

Tunnel formation by Reticulitermes flavipes and Coptotermes formosanus (Isoptera: Rhinotermitidae) in response to wood in sand.

The tunneling responses of two subterranean termite species, Coptotermes formosanus Shiraki and Reticulitermes flavipes (Kollar), to the presence of sound wood in laboratory arenas were studied. Branching pattern and the speed of tunnel construction between R. flavipes and C. formosanus also were compared. Patlak's residence index (rho) was generated using the length, width, speed of construction, and area of the primary tunnels built by termites. In the same allotted time, C. formosanus built wider and shorter primary tunnels, whereas R. flavipes built thinner and longer primary tunnels. The presence of wood did not affect termite tunnel formation. This lack of variation in tunnel formation parameters was evidenced by the inability of the termites to locate wood sources over distance, even as short as 2.5 mm, and by the similar tunneling behaviors in areas of the arena with or without wood. Patlak's model predicted the densities of tunnels with an error between 9 and 28%. in experiments with R. flavipes exposed to a range of 0-8,000 g of wood, and between 61 and 87% in experiments with C. formosanus. These results indicated that the residence index can provide a qualitative measure of the effect of habitat heterogeneity on the individual termite tunnels. The tunneling constructions strategy of these subterranean termites is discussed.     

Behavioral response of termites to tunnel surface irregularity

Subterranean termites construct underground tunnels, tens to hundreds of meters in length, in order to search for and transport resources. Diverse soil conditions surrounding the tunnels, such as soil pores and differing moisture concentrations, may cause different sized- and shaped-irregularities in the tunnels. To understand how individual termites respond to the irregularities, the present study monitored the movement of termites, Coptotermes formosanus Shiraki, in artificially excavated tunnels with rectangular irregularities of varying sizes in two-dimensional sand substrates. Termites tunneled at some of the irregularities and not at the others. The tunneling or non-tunneling behavior resulted from four different responses. The non-tunneling response may result from a behavioral adaptation that allows termites to avoid wasting energy that may be used in foraging.     

Minimizing moving distance in deposition behavior of the subterranean termite

Subterranean termite nests are located underground and termites forage out by constructing tunnels to reach food resources, and tunneling behavior is critical in order to maximize the foraging efficiency. Excavation, transportation, and deposition behavior are involved in the tunneling, and termites have to move back and forth to do this. Although there are three sequential behaviors, excavation has been the focus of most previous studies. In this study, we investigated the deposition behavior of the Formosan subterranean termite, Coptotermes formosanus Shiraki, in experimental arenas having different widths (2, 3, and 4 mm), and characterized the function of deposited particles. We also simulated moving distance of the termites in different functions. Our results showed that total amounts of deposited particles were significantly higher in broad (4 mm width) than narrow (2 mm) tunnels and most deposited particles were observed near the tip of the tunnel regardless of tunnel widths. In addition, we found that deposited particles followed a quadratic decrease function, and simulation results showed that moving distance of termites in this function was the shortest. The quadratic decrease function of deposited particles in both experiment and simulation suggested that short moving distance in the decrease quadratic function is a strategy to minimize moving distance during the deposition behavior.     

Effect of biotic and abiotic factors on the tunneling behavior of Coptotermes gestroi and Heterotermes tenuis (Isoptera: Rhinotermitidae)

Using bidimensional arenas, the construction and spatial dispersion of tunnels constructed by Coptotermes gestroi and Heterotermes tenuis (Rhinotermitidae) was determined under different laboratory conditions. Workers of both species showed an increase of the tunneled area with the rise in temperature. The activity of workers of C. gestroi also increased with the rise in soil moisture. Primary tunnels showed a high degree of dispersion in the arenas for all treatments. The presence of food did not influence the tunneling pattern of C. gestroi; but for H. tenuis there was a significant decrease in the number of tunnels. In addition, the type of substrate affected the tunneling pattern in both species. The understanding of food searching strategies of subterranean termites could contribute in the improvement of pest management programs based on the use of toxic baits.     

Influence of Guidelines and Passageways on Tunneling Behavior of Reticulitermes flavipes (Kollar) and R. virginicus (Banks) (Isoptera: Rhinotermitidae)

Tunneling behavior of laboratory-maintained cultures of Reticulitermes flavipes (Kollar) and R. virginicus (Banks) was examined to determine (1) if the termites build tunnels along preexisting wires or tunnels, and (2) whether tunnels are arranged to optimize search efficiency. Tunnel patterns were considered optimal if, for the number of tunnels present, the maximum area was explored. Termites entered either control arenas or arenas in which they encountered a wire or a pre-formed tunnel. Analyses revealed that R. flavipes and R. virginicus almost always follow pre-formed tunnels, but do not follow wires as readily. Within each species, the distributions of tunnels in treatment arenas were different from distributions in control arenas, most often when pre-formed tunnels were the treatment. Optimal tunnel arrangements in control arenas were found in 62% of R. flavipes patterns with 2 tunnels and in 43% of R. virginicus patterns with 2 tunnels. None of the 3-tunnel patterns from control arenas of R. flavipes and 29% of those of R. virginicus had optimal arrangements. Overall, the spatial arrangement of tunnels in control arenas was significantly different between R. flavipes and R. virginicus.     

Directional change in tunneling of subterranean termites (Isoptera: Rhinotermitidae) in response to decayed wood attractants

Wood discs decayed with brown rot fungi and polymer discs impregnated with acetone extract of decayed wood were embedded in sand of a two-dimensional foraging arena to evaluate their attractant potential in directing termite tunnels toward them. Termites were released near one arena corner and were guided to follow the physical guideline of the arena edges. In the absence of the attractants, termites generally formed a relatively linear tunnel along the edges. When decayed wood discs or treated polymer discs were placed in wet sand near one side of the arena, termite tunnels departed from the arena edges and were oriented toward them. The attraction distance ranged from 12 to 18 cm. The attractant properties were most likely water soluble and permeated through wet sand to cause termites to change their orientation. The results demonstrated that when such attractants are placed near a bait station in the field, they may be used to direct termite foraging toward the station.     

Tunnel geometry of the subterranean termite Reticulitermes grassei （Isoptera： Rhinotermitidae）in response to sand bulk density and the presence of food

The cryptic habits of subterranean termites restricts detailed analysis of their foraging patterns in situ, but the process is evidently dominated by tunnel constructions connecting the nest with woody resources discovered within the territory of each colony. In this study, tunnel formation and orientation were studied experimentally in the termite Reticulitermes grassei （Clement）, using 2-dimensional laboratory foraging arenas con- taining fine sand as the substratum. The building of exploratory tunnels over a 10-day period and the geometry of the resulting network are described. Fractal analysis showed that tunnel geometry had a fractal dimension, regardless of the total length tunnelled whether foragers encountered the food source or not. The bulk density of the sand in the arenas affected the distances tunnelled, with higher density reducing construction, but did not affect tunnel geometry. Tunnels were not discernibly orientated with respect to the positioning of the food source, even in a situation where termites had failed to find the food source at a distance of less than 50 mm, suggesting that volatiles from wood are not attractants.     

Simulation study to determine why only some termites are active during tunneling activity

It has been known that some termites are responsible for tunnel excavation for foraging, while others are not involved in the excavation. The biological reason for this is that the resting termites are a backup for the termites that have used up their energy in the tunneling activity. In this study, we build an agent‐based model (ABM) wherein agents (simulated termites) follow simple rules that govern their behavior. In this model, the agents are endowed with a directional vector that has been shown to exist in real termites, but they do not communicate through pheromonal or physical marking of excavation sites. They move toward the tunnel tips, tunnel when their progress in that direction is blocked, and transport the excavated soil. Using the model, we investigated the work efficiency of termites in constructing tunnels and transporting food; the efficiency was defined as the inverse value of tunnel connectivity plus tunnel expansion speed. Biologically, the connectivity is related to the energy to be used for termites to transport food through tunnels, and the tunnel expansion speed is related to the energy required for constructing tunnels. Simulation results showed that the efficiency was maximized at an intermediate number of termites. This means that termites were better to be inactive to maintain the high efficiency when too many workers are present in the colony. We briefly discuss the strength and weakness of the ABM and the values of this study in relation to termite foraging strategy.     

The influence of soil heterogeneity on exploratory tunnelling by the subterranean termite Coptotermes frenchi (Isoptera: Rhinotermitidae)

The exploration of sand-filled arenas by workers of an entire colony of the Australian, subterranean foraging, tree-nesting termite, Coptotermes frenchi Hill was investigated under laboratory conditions. The first experiment tested whether termite exploration of sand was influenced by the presence of gaps or objects in the sand. Gaps and objects were chosen to represent soil heterogeneity in the urban environment: gaps to represent tunnels dug by other animals, perspex strips to represent cables and pipes, and wood strips to represent roots. Termites always chose to explore gaps thoroughly before they began tunnelling in the sand. Significantly more and longer tunnels were excavated from the end of gaps at the far end of the arenas, and relatively little tunnelling occurred around and along objects. Termite density was significantly greater around and along wood compared with perspex blocks. The second experiment tested whether termite exploratory tunnelling was influenced by soil moisture. The termites tunnelled slowly in dry sand, but after discovering a patch of wet sand, increased tunnelling five-fold until it was completely explored, after which activity declined. Energy and water conservation may be behind these patterns of exploratory tunnelling as well as those seen in large field studies, but caution is urged when interpreting small scale laboratory experiments to explain large scale field data.     

Directional selection by the subterranean termite Coptotermes formosanus Shiraki (Isoptera: Rhinotermitidae) at tunnel intersections

Subterranean termites construct complicated tunnel networks for foraging below ground. Thus, they often encounter tunnel intersections during foraging activity. Directional selection by termites at intersections is likely to affect foraging efficiency because depending on their selection, the path length from food resources to the nest can vary significantly. In order to understand how termites are guided to choose the most economical path without the use of pheromones, we artificially excavated two tunnels of varying widths (W₁ and W₂; 2, 3, or 4 mm) that intersected at a 90° angle in each of nine soil‐filled arenas. We observed the directional selection of termites at intersections in arenas with combinations of W₁ (mm) and W₂ (mm) (W₁, W₂). For (W₁, W₂) = (2, 2) and (4, 4), termites statistically equally chose the three directions left, right, and straight, while for the (3, 3) arena combination, termites preferentially decided to go straight. On the other hand, for (W₁, W₂) = (2, 3) (2, 4), and (3, 4), termites advancing from narrower tunnels into intersections tended to turn right or left, while termites coming from the wider tunnel were more inclined to go straight. On the assumption that a wider tunnel is more frequently used by termites in the field, we can deduce that the wider tunnel may represent the most efficient/shortest path. Thus, this simple selection mechanism can prevent termites from deviating from the most economical path.     

Why is the number of primary tunnels of the formosan subterranean termite,Coptotermes formosanus Shiraki (Isoptera: Rhinotermidae), restricted during foraging?

Subterranean termites forage by digging a network of tunnels to come into contact with food sources. When 1000 termites (Coptotermes formosanus Shiraki) were placed in a laboratory arena, 6.7 primary tunnels were constructed. The aim of this study was to explain the empirical observation in which termites restrict the number of primary tunnels. To this end, we constructed a model to simulate termite tunnel patterns based on empirical data and to calculate food transportation efficiency, γ, for the tunnel patterns. The efficiency was defined as the ratio of the number of encountered food particles to the sum of the shortest length from the location of encountered food particles to the initial position of growth of the tunnel. The γ was maximized when the number of primary tunnels was 5 or 6, which was fairly consistent with the empirical number of primary tunnels. This result indicated that termites may restrict the number of their primary tunnels to improve the transportation efficiency, which is directly related to their survival.     

Effect of Average Worker Size on Tunneling Behavior of Formosan Subterranean Termite Colonies

The effect of a colony's average worker size on tunneling behavior of Coptotermes formosanus Shiraki (Isoptera: Rhinotermitidae) in laboratory foraging arenas was investigated. Large groups of foragers from four colonies were added to arenas and allowed to tunnel for a period of 22 days. Various aspects of the resulting tunnel galleries were analyzed using ANOVA and regression analysis. After the exclusion of one colony due to high mortality, the only parameters shown to differ significantly were tunnel width and tunnel segmentation. Larger workers tended to construct less segmented galleries with wider tunnels. Tunnel length was positively correlated to size on the first 2 days, but the relationship reversed by day 4. Tunneling on day 1 was positively correlated to the discovery of food items. Our results indicate that a foraging group's average worker size can affect tunnel pattern and that groups composed of larger workers are better tunnelers, but groups of smaller sized workers are able to make up the difference over time. Possible explanations for size-related variation in tunneling behavior are discussed.     

Measurement of the time required for termites to pass each other in tunnels of different curvatures

Subterranean termites construct complex tunnel networks for foraging. During travel in the tunnels, termites often encounter one another when passing in opposite directions. Such encounters are likely to affect the “movement efficiency,” which is the time required for a termite to travel a certain distance in a tunnel. In this study, we explored how individual–individual encounters affect movement efficiency in tunnels by measuring the time (τ) taken by two termites to pass one another in tunnels of different curvatures. Artificial tunnels of 5 cm in length and variable widths (W) of 2, 3, or 4 mm were made. Tunnel distance (D) was 2, 3, 4, or 5 cm. When D had a higher value, curvature was lower. When W = 2, τ was significantly shorter in the tunnel with D = 5 than in tunnels of D = 2, 3, or 4, whereas τ was statistically the same for D = 2, 3 and 4. When W = 3, τ was shorter in the tunnel with D = 5 than for D = 3 and 4, while τ was longer in the tunnel with D = 2 than for D = 3 and 4. When W = 4, τ was longer in the tunnels with D = 2 and 3 than for D = 4 and 5. Based on these observations, 3 types of termite behavior were identified: biased walking, backward walking, and zigzag walking. We considered these results in relation to foraging efficiency.     

Valuation of efficacy and nonrepellency of indoxacarb and fipronil-treated soil at various concentrations and thicknesses against two subterranean termites (Isoptera: Rhinotermitidae)

The efficacy and nonrepellency of indoxacarb (150 SC, 150 g [AI]/liter) and fipronil (Termidor SC, 9.1% [Al]) against field-collected eastern subterranean termite, Reticulitermes flavipes (Kollar), and the Formosan subterranean termite, Coptotermes formosanus Shiraki, were evaluated for mortality and penetration into treated soil in laboratory glass tube bioassays. Both insecticides were tested at five concentrations (0, 1, 10, 50, and 100 ppm) and two thicknesses (20 and 50 mm) of treated soil. Indoxacarb caused significantly greater mortality than controls at all treatment thicknesses of > or = 10 ppm, but not at 1 ppm. Concentration and treatment thickness of indoxacarb significantly affected termite mortality. Eastern subterranean termites were significantly more susceptible to indoxacarb than Formosan subterranean termites, but there were no intercolony differences in either species. Termites completely penetrated through all treatment thickness of indoxacarb-treated soil at all concentrations, except one of the six Formosan subterranean termite replicates of 50 mm at 50 ppm, when all termites were killed before tunneling through the treated soil. Fipronil resulted in significantly faster and greater termite mortality than indoxacarb at corresponding concentrations. Concentration and treatment thickness of fipronil also significantly affected termite mortality. There was no intercolony difference in susceptibility to either insecticide in either termite. Both termite species completely penetrated 20-mm treatments of all tested fipronil concentrations, as well as 50-mm soil treated with fipronil at < or = 10 ppm. At 50 and 100 ppm fipronil, termites tunneled only a mean of 87 +/- 0.21 and 47 +/- 0.18% deep into 50-mm treated soil, respectively, before death. Both insecticides demonstrated a delayed mode of activity and nonrepellency against the two termite species.     

Effects of concentration,distance, and application methods of Altriset (Chlorantraniliprole) on eastern subterranean termite (Isoptera: Rhinotermitidae)

The effects of various concentrations, distance, and application methods of Altriset (Chlorantraniliprole) were investigated against one of the most destructive termites, the eastern subterranean termite, Reticulitermes flavipes Kollar. Three laboratory experiments were conducted. First, we examined the concentration effect of treating the soil contiguously to established foraging tunnels at a fixed 1 m distance. The results demonstrated 100% termite control in 19 d posttreatment at 100 and 50 μg/g and 27% termite mortality at 25 μg/g. Second, we tested the distance effect of the soil treatment (2 and 4 m) on the efficacy of Altriset to the satellite termite populations at a fixed 50 μg/g concentration. This resulted in 100% termite control in 22 d posttreatment at both 2 and 4 m. Third, we examined the effect of differing application methods using 12.5 and 25 μg/g prior to the establishment of foraging tunnels at a fixed 1m distance. This illustrated 100% termite control in 9 d posttreatment at 25 μg/g and 12 d posttreatment at 12.5 μg/g. The third experiment demonstrated soil treatments that were applied prior to termite tunnel establishment had greater efficacy than applications made post tunnel construction. Our results provide a comprehensive understanding about the efficacy of Altriset treatments on eastern subterranean termites.     

Efficacy of vetiver oil and nootkatone as soil barriers against Formosan subterranean termite (Isoptera: Rhinotermitidae).

Vetiver oil and its components nootkatone and cedrene were assessed as sand treatments for their efficacy to disrupt food recruitment by Coptotermes formosanus Shiraki. Termites were required to tunnel through sand treated with vetiver oil, nootkatone, cedrene, or untreated sand to reach a food source. Results showed that sand treated with vetiver oil or nootkatone disrupted termite tunneling behavior. As a consequence, after 21 d, wood consumption and termite survival were significantly lower compared with cedrene-treated or untreated sand treatments. Sand treated with vetiver oil or nootkatone at 100 microg/g substrate were effective barriers to termites.     

The effect of soil compaction on growth and P uptake by Trifolium subterraneum: interactions with mycorrhizal colonisation

The effects of vesicular-arbuscular mycorrhizal (VAM) colonisation on phosphorus (P) uptake and growth of clover (Trifolium subterraneum L.) in response to soil compaction were studied in three pot experiments. P uptake and growth of the plants decreased as the bulk density of the soil increased from 1.0 to 1.6 Mg m^-3. The strongest effects of soil compaction on P uptake and plant growth were observed at the highest P application (60 mg kg^-1 soil). The main observation of this study was that at low P application (15 mg kg^-1 soil), P uptake and shoot dry weight of the plants colonised by Glomus intraradices were greater than those of non-mycorrhizal plants at similar levels of compaction of the soil. However, the mycorrhizal growth response decreased proportionately as soil compaction was increased. Decreased total P uptake and shoot dry weight of mycorrhizal clover in compacted soil were attributed to the reduction in the root length. Soil compaction had no significant effect on the percentage of root length colonised. However, total root length colonised was lower (6.6 m pot^-1) in highly compacted soil than in slightly compacted soil (27.8 m pot^-1). The oxygen content of the soil atmosphere measured shortly before the plants were harvested varied from 0.18 m³m^-3 in slightly compacted soil (1.0 Mg m^-3) to 0.10 m³m^-3 in highly compacted soil (1.6 Mg m^-3).     

Localized treatments using commercial dust and liquid formulations of fipronil against Coptotermes formosanus （Isoptera： Rhinotermitidae） in the laboratory

Use of proper application methods and formulations of termiticides are im- portant to reduce their negative impact to the environment. In this study, we conducted laboratory experiments to determine the effect of localized treatments with commercial dust and liquid formulations of fipronil against Formosan subterranean termites, Coptoter- mes formosanus Shiraki. The test arena consisted of a specially designed 16-chambered structure with a center chamber connected to 5 foraging chambers that themselves were connected to 10 additional foraging chambers. One peripheral chamber received a liquid or dust treatment and termites were released in the center chamber. Results showed that 〉 91% of the termites were dead within the 9-d test period despite the localized treatment of only 1 foraging chamber. Termites that were still alive after 9 d were transferred to an untreated dish and held for 10 more days. The majority of those termites were dead and the rest were moribund on day 19. Regardless of the specific dish treated, both formulations of fipronil were found to be highly efficacious. Termites did not exhibit repellency to either formulation. Our results suggest that localized （or spot） treatment with either commer- cially available dust or liquid formulations of fipronil can be a viable option for control of a termite infestation where complete soil drenching is not desirable.     

Rounding a corner of a bent termite tunnel and tunnel traffic efficiency

Subterranean termites construct underground tunnels, tens to hundreds of feet, to reach feeding sites and to transport food items to their nest. To ensure a high rate food return to the nest, an optimized tunnel should be constructed. We found that termites (Coptotermes formosanus Shiraki) fill the corner of a bent tunnel with soil particles excavated from tunnel tip where their digging behavior is activated. The corner-filling behavior, eventually, made a sharp corner smooth-rounded. In the present study, we showed that the corner-filling behavior could play an important role in improving the tunnel traffic efficiency. To do this, we compared the termites' time spent for passing corners between with a right-angled flat tip (RA-corner), corresponding to the sharp corner, and with a rounded tip (R-corner) corresponding to the smooth-rounded corner. As a result, the passing time in the R-corner was significantly shorter than in the RA-corner. In addition, tunnel width effect was discussed in terms of individual movement.