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Influence of the microhabitat on the trap construction of Myrmeleon brasiliensis (Neuroptera: Myrmeleontidae) larvae

Influência do microhabitat na construção de armadilhas de larvas de Myrmeleon brasiliensis (Neuroptera: Myrmeleontidae)

ABSTRACT

Antlion larvae of Myrmeleon brasiliensis (Návas, 1914) build their traps in a microenvironment with protection from the direct action of rain and other perturbations as well as microhabitats that are less protected from disturbances that can destroy the traps. Differences in microhabitats may affect the characteristics of the trap-building process due the high energy expenditure exerted in building and maintaining these traps, which led to the following question: Do antlion larvae of M. brasiliensis build larger traps in protected microhabitats? Considering the occurrence of M. brasiliensis larvae in two microhabitats and the measurements of the size of the larvae and their traps, the hypothesis was that larvae would occur in greater abundance and the trap size would be larger in more protected microhabitats. The results showed that antlions occurred in equal abundance in both microhabitats, but density was greater in the protected microhabitat. Even in months with more rainfall, M. brasiliensis larvae continued to forage throughout the year in the protected microhabitat and the investment in trap size was greater in this microhabitat. This suggests that the larvae of the protected microhabitat have an advantage, given that they have the possibility of foraging throughout the year.

KEYWORDS
Antlion; disturbance; foraging; traps

RESUMO

Larvas de formiga-leão Myrmeleon brasiliensis (Návas, 1914) constroem suas armadilhas em microhabitat com proteção da ação direta da chuva e outros intempéries e em microhabitats menos protegidos de perturbações que podem destruir suas armadilhas. Dado o alto gasto energético para a construção e manutenção das armadilhas das larvas de formiga-leão, diferenças entre microhabitats podem afetar características da construção da armadilha. O que levantou a questão: larvas em microhabitats mais protegidos investem mais no tamanho de suas armadilhas de captura de presas? Através de medidas da ocorrência de larvas nos dois microhabitats e através de medidas do tamanho da larva M. brasiliensis e de sua armadilha, foi previsto que as larvas ocorreriam em maior abundância em microhabitats protegidos e que o investimento no tamanho da armadilha seria maior em microhabitats com maior proteção. Os resultados deste trabalho mostraram que as larvas de formiga-leão ocorrem em igual abundância nos dois microhabitats e a que densidade é maior no microhabitat protegido. Os dados demonstram que as larvas M. brasiliensis permaneceram forrageando durante todo o ano no microhabitat protegido, mesmo em meses mais chuvosos, e o investimento em tamanho de armadilha foi maior nesse microhabitat. O que sugere, que as larvas do microhabitat protegido apresentam vantagem, dado de fato de terem a possibilidade de forragear durante todo o ano.

PALAVRAS-CHAVE
Formiga-leão; perturbação; forrageamento; armadilhas

Ecosystems vary in time and space, which affects the distribution of organisms (Wellnitz & Poff, 2001Wellnitz, T. & Poff, N. L. 2001. Functional redundancy in het-erogeneous environments: implications for conservation. Ecology Letters 4(3):177-179. https://doi.org/10.1046/j.1461-0248.2001.00221.x
https://doi.org/10.1046/j.1461-0248.2001...
; Brown, 2003Brown, B. L. 2003. Spatial heterogeneity reduces temporal variability in stream insect communities. Ecology letters 6(4):316-325. https://doi.org/10.1046/j.1461-0248.2003.00431.x
https://doi.org/10.1046/j.1461-0248.2003...
). Variations within a patch or microhabitat of an ecosystem (incidence of light, temperature, disturbances, and resource availability) can affect the individual behaviour of organisms (Lin & Shiraishi, 1992Lin, L. K. & Shiraishi, S. 1992. Home range and microhabitat utilization in the Formosan wood mouse, Apodemus semotus. Journal of the Faculty of Agriculture 37(1):13-27.). According to the theory of optimum foraging, such variations in each environment lead predators to select patches in which the energy return is greater (Charnov, 1976Charnov, E. L. 1976. Optimal foraging, the Marginal Value Theorem. Theoretical Population Biology 9(2):129-136. https://doi.org/10.1016/0040-5809(76)90040-X
https://doi.org/10.1016/0040-5809(76)900...
; Brown & Kotler, 2004Brown, J. S. & Kotler, B. P. 2004. Hazardous duty pay and the foraging cost of predation. Ecology Letters 7(10):999-1014. https://doi.org/10.1111/j.1461-0248.2004.00661.x
https://doi.org/10.1111/j.1461-0248.2004...
). The energy return of sit-and-wait trap-building predators must be calculated based on resource availability as well as the energy expended on the building and maintenance of the trap (Blackledge & Wenzel, 2001Blackledge, T. A. & Wenzel, J. W. 2001.State-determinate foraging decisions and web architecture in the spider Dictyna volucripes (Araneae Dictynidae). Ethology Ecology and Evolution 13(2):105-113. https://doi.org/10.1080/08927014.2001.9522778
https://doi.org/10.1080/08927014.2001.95...
; Scharf et al., 2009Scharf, I.; Golan, B. & Ovadia, O. 2009. The effect of sand depth, feeding regime, density, and body mass on the foraging behaviour of a pit-building antlion. Ecological Entomology 34(1):26-33. https://doi.org/10.1111/j.1365-2311.2008.01038.x
https://doi.org/10.1111/j.1365-2311.2008...
).

Larvae of some species of antlion (Neuroptera: Myrmeleontidae) build funnel-shaped traps in dry and sandy soil to capture their prey (Lucas & Stange,1981Lucas, J. R. & Stangem, L. A. 1981. Key and descriptions to the Myrmeleon larvae of Florida (Neuroptera: Myrmeleontidae). Florida Entomologist 64(2):207-216. https://10.2307/3494571
https://10.2307/3494571...
; New, 1991New, T. R. 1991. Neuroptera, p. 525-542. In: CSIRO ed. The Insects of Australia: a text book for students and research workers. Melbourne, Melbourne University Press. 1137p.). Trap size and successful capture of prey is proportional to the larvae size (Klokočovnik & Devetak, 2013Klokočovnik, V. & Devetak, D. 2013. Feeding rate affects pit size in pit-building antlion larvae Euroleon nostras (Neuroptera: Myrmeleontidae). Açoreana Suplemento 9:83-89.). Larvae of the antlion species Myrmeleon brasiliensis (Návas, 1914) were observed in Brazil in the state of Mato Grosso do Sul. Myrmeleon brasiliensis build traps ranging from 9.19 to 35.21 mm in diameter (Nonato & Lima, 2011Nonato, L. M. & Lima, T. N. 2011. El comportamiento de predación de los estadios larvales de Myrmeleon brasiliensis (Neuroptera, Myrmeleontidae). Revista Colombiana de Entomología 37:354-356.) and pass through three instars (each lasting an average of 26 days) prior to the formation of the pupae (Missirian et al., 2006Missirian, G. B.; Uchôa-Fernandes, M. A. &Fischer, E. A. 2006.Development of Myrmeleon brasiliensis (Navás) (Neuroptera, Myrmeleontidae), in laboratory, with different natural diets. Brazilian Journal Biology 23(4):1044-1050. http://dx.doi.org/10.1590/S0101-81752006000400009
http://dx.doi.org/10.1590/S0101-81752006...
).

In the natural environment, factors such as wind, falling vegetal matter, rainfall, and the transit of other animals can destroy the traps of antlion larvae (Gotelli, 1993Gotelli, N. 1993. Ant lion zones: causes of high-density predator aggregations. Ecology 74(1):226-237. https://doi.org/10.2307/1939517
https://doi.org/10.2307/1939517...
). The construction and maintenance of a trap requires the expenditure of energy (Burgess, 2009Burgess, M. G. 2009. Sub-optimal pit construction in predatory ant lion larvae (Myrmeleon sp.). Journal of Theoretical Biology 260(3):379-385. https://doi:10.1016/j.jtbi.2009.05.026
https://doi:10.1016/j.jtbi.2009.05.026...
; Lima & Silva, 2017Lima, T. N. & Silva, D. C. R. 2017. Effect of energetic cost to maintain the trap for Myrmeleon brasiliensis (Neuroptera, Myrmeleontidae) in its development and adult size. Brazilian Journal Biology 77(1):38-42. http://dx.doi.org/10.1590/1519-6984.08715
http://dx.doi.org/10.1590/1519-6984.0871...
) and larvae whose traps have been disturbed have a 50% lower growth rate compared to those whose traps have not been disturbed (Griffiths, 1980Griffiths, D. 1980. The feeding biology of ant-lion larvae: prey capture, handling and utilization. Journal of Animal Ecology 49(1):99-125. https://doi.org/10.2307/4279
https://doi.org/10.2307/4279...
).

Due to the influence of several factors at the trap construction of antlion larvae and the great abundance of M. brasiliensis in Mato Grosso do Sul State, the present study aiming to comprehend the influence of the microhabitat on the trap construction of M. brasiliensis larvae, as well as their density and abundance. For that were evaluated 1) the abundance of M. brasiliensis larvae, 2) the relation between larval abundance and rainfall, 3) the density of larvae, 4) the trap size build by larvae, and 5) the investment of the larvae in trap size in microhabitats with different degrees of disturbance, as well as their abundance.

MATERIALS AND METHODS

Observations were carried out in a forest reserve (800 ha) in the municipality of Aquidauana in the state of Mato Grosso do Sul, Brazil (20°26’25”S, 55°39’21”W). The reserve is situated in the Maracaju Hills, which extend in the north-south direction throughout nearly the entire state, with the southern limit near Aquidauana and the northern limit in the proximities of the municipality of Rondonópolis in the state of Mato Grosso (Boggianiet al., 1998Boggiani, P. C.; Coimbra, A. M.; Riccomini, C. & Gesicki, A. L. D. 1998. Recursos minerais não-metálicos do Estado de Mato Grosso do Sul, Brasil. Revista do Instituto de Geologia 19(1-2):31-41.). The Maracaju Hills are covered mainly by forested savanna, semi-deciduous seasonal forests, riparian vegetation, and plains (Damasceno et al., 2000Damasceno, J. D. A.; Nakajima, J. N. & Rezende, U. M. 2000. Levantamento florístico das cabeceiras dos rios Negro, Aquidauana, Taquari e Miranda no Pantanal, Mato Grosso do Sul, Brasil. In: Willink, P.W.; Chernoff, B.; Alonso, L.E.; Montambault, J.R. & Lourival, R. eds. Uma avaliação biológica dos ecossistemas aquáticos do Pantanal, Mato Grosso do Sul, Brasil. Washington, Conservation International, p. 152-162. (Boletim de Avaliação Biológica 18).). Altitude ranges from 240 to 700 m (ZEE-MS, 2008ZEE-MS. 2008. Zoneamento Ecológico Econômico. Mato Grosso do Sul, Governo do Estado de Mato Grosso do Sul. Available at <Available at https://www.semac.ms.gov.br/controle/ShowFile.php?id=18269 >. Accessed on 23 April 2018.
https://www.semac.ms.gov.br/controle/Sho...
).

Larvae of Myrmelon brasiliensis (Návas, 1914) are found in two microhabitats areas of the Maracaju Hills in the municipality of Aquidauana, Brazil; in which the observation occurred: 1) a trail that cuts through the reserve which is characterized as an exposed microhabitat, as the larvae have no protection from the direct action of the rain and where M. brasiliensis larvae are seen building their traps below plantlets and near tree trunks; and 2) on the slope of the rocky cliffs of the Maracaju Hills - reaching approximately 100 meters in height and are composed of sandstone of eolian sedimentation (BRASIL, 1982Brasil. 1982. Projeto RADAMBRASIL. Rio de Janeiro, Ministério das Minas e Energia. Secretaria - Geral. 416p. ; ZEE-MS, 2008ZEE-MS. 2008. Zoneamento Ecológico Econômico. Mato Grosso do Sul, Governo do Estado de Mato Grosso do Sul. Available at <Available at https://www.semac.ms.gov.br/controle/ShowFile.php?id=18269 >. Accessed on 23 April 2018.
https://www.semac.ms.gov.br/controle/Sho...
) -, which is characterized as a protected microhabitat where the action of the rain does not destroy the traps due to the slope of the cliff.

Monthly observations were carried out from August 2016 to July 2017. Antlion larvae of M. brasiliensis collected in the area were identified by the researcher Lionel Stange (University of Florida).

Four sampling points were established at both environment (trail and cliff). Each sampling point measured approximately 2 m² (four quadrants of 2 m²), in which the abundance of the larvae and trap diameters were determined. The abundance was calculated by counting all the traps within the each quadrant. Within each sampling point, quadrants measuring 0.25 m² were established for the estimation of larval density. The density was calculated by counting the number of larvae per 0.25 m². At the end of the monthly observations in each microhabitat, the diameter of the traps of 50 larvae was measured and the larvae were collected and taken to the Laboratório de Estudos da Biodiverside of the Universidade Federal de Mato Grosso do Sul for the measurement of body size (head-abdomen). All measurements were performed with the aid of digital calipers (precision: 0.01 mm). Rainfall data were obtained from a meteorological station situated in the study location belonging to the Universidade Estadual de Mato Grosso do Sul.

The t-test was used for the comparison of larval abundance; the Mann-Whitney test was used for the comparison of larval density as well as trap sizes in the two microhabitats. The correlation between abundance and rainfall in the two microhabitats was determined using Pearson’s correlation test. The association between larval size (head-abdomen) and trap size in the two microhabitats was determined using linear regression analysis. All analyses were performed using the MyStat free software (https://systatsoftware.com/downloads/download-mystat/).

RESULTS

Nine hundred eighty five Myrmelon brasiliensis larvae were counted building traps (500 in the protected microhabitat and 485 on the trail). No difference in abundance was found between the two microhabitats (t22 = 0.07; P = 0.47). Mean larval density was higher in the protected microhabitat (7.8 larvae/0.25 m) than the exposed microhabitat (3.8 larvae/0.25 m²) (t22 = -2.90; P = 0.01), with the highest density (12 larvae/0.25 cm²) occurring in the protected environment in June 2017. Larval density on the trail was zero in the period of March and April (no larvae counted) due to rainfall.

No significant correlation was found between the larval abundance and rainfall in the protected microhabitat (r = -0.4559; P = 0.13), while the larval abundance was negatively affected by rainfall on the trail (r = -0.5866; P = 0.04) (Fig. 1).

Fig. 1.
Abundance of Myrmelon brasiliensis (Návas, 1914) (Neuroptera: Myrmeleontidae) larvae and rainfall (mm) registered in the period from August 2016 to July 2017 in exposed and protected microhabitats, Aquidauana, MS, Brazil.

Mean trap size was significantly larger in the microhabitat protected by the rocky cliffs of the Maracaju Hills in comparison to that of the trail (U = 18.00; P = 0.02) (Fig. 2). The investment of the larvae in trap size was positively correlated with body size in both microhabitats (protected: r² = 0.35; P = 0.000; exposed: r² = 0.15; P = 0.01). However, the coefficient of variation (r²) was higher in the protected environment, demonstrating that trap size was better explained by the size of the larvae in this environment than those on the trail.

Fig. 2.
Average trap size (±SD) of Myrmelon brasiliensis (Návas, 1914) (Neuroptera: Myrmeleontidae) larvae registered in the period from Agust 2016 to July 2017 in exposed and protected microhabitats, Aquidauana, MS, Brazil.

DISCUSSION

The results demonstrated that Myrmelon brasiliensis larvae occur throughout the entire year, with no difference in their abundance between microhabitats with different degrees of disturbance. Nevertheless, larvae in protected environments invest more in the size of their traps. Traps build by larvae on the trail (exposed environment) were destroyed in rainy periods, impeding the larvae from foraging until the soil dried out again. In the area near the rocky cliff of the hill (protected environment), only larvae in the more peripheral portion of the area were affected by rainfall, whereas those closer to the sandstone cliff wall continued foraging throughout the year. Laboratory experiments have been demonstrated that M. brasiliensis larvae rebuild their smaller size traps after the rain, when the soil dries out again (within five days, on average) (Freire & Lima, 2019Freire, L. G. & Lima, T. N. 2019. Effect of rain on trap building by Myrmeleon brasiliensis in a riparian woodland from the Cerrado biome in Brazil. Entomologia Experimentalis et Applicata 167(6):1-5. https://doi.org/10.1111/eea.12788
https://doi.org/10.1111/eea.12788...
).

The disturbance caused by the rain increases the cost of trap maintenance. The foraging strategy adopted by some species of antlion larvae and other trap builders (e.g., spiders and worm lion larvae) reduces the energy expended on the search for and capture of prey, but not in the trap building itself (Blackledge & Wenzel, 2001Blackledge, T. A. & Wenzel, J. W. 2001.State-determinate foraging decisions and web architecture in the spider Dictyna volucripes (Araneae Dictynidae). Ethology Ecology and Evolution 13(2):105-113. https://doi.org/10.1080/08927014.2001.9522778
https://doi.org/10.1080/08927014.2001.95...
; Devetak & Arnett, 2015Devetak, D. & Arnett, A. E. 2015. Preference of antlion and wormlion larvae (Neuroptera: Myrmeleontidae; Diptera: Vermileonidae) for substrates according to substrate particle sizes. European Journal Entomology 112(3):500-509. https://doi.org/10.14411/eje.2015.052
https://doi.org/10.14411/eje.2015.052...
; Adar et al., 2016Adar, S.; Dor, R. & Scharf, I. 2016.Habitat choice and complex decision making in a trap-building predator. Behavior Ecology 27(5):1491-1498. https://doi.org/10.1093/beheco/arw071
https://doi.org/10.1093/beheco/arw071...
; Miler et al., 2018Miler, K.; Yahya, B. & Czarnoleski, M.2018. Different predation efficiencies of trap-building larvae of sympatric antlions and wormlions from the rainforest of Borneo. Ecological Entomology 43(2):255-262. https://doi.org/10.1111/een.12495
https://doi.org/10.1111/een.12495...
). Thus, being in an environment that causes less destruction to the traps can diminish energy expenditure. Moreover, development time is longer for larvae that do not forage (Lima & Silva, 2017Lima, T. N. & Silva, D. C. R. 2017. Effect of energetic cost to maintain the trap for Myrmeleon brasiliensis (Neuroptera, Myrmeleontidae) in its development and adult size. Brazilian Journal Biology 77(1):38-42. http://dx.doi.org/10.1590/1519-6984.08715
http://dx.doi.org/10.1590/1519-6984.0871...
).Therefore, the lifecycle of the larvae on the trail could be longer than that among the larvae on the slope of the cliff, which implies that larvae on the slope of the hill can become more abundant in the environment in a given moment due to natural selection. For example, in years with more rainfall, larvae in the protected microhabitat can maintain the emergence rate of adults and the laying of eggs, whereas those in the exposed environment may remain in the larval phase for a longer period of time, thereby contributing less to the population size in the area.

The density of the antlion larvae was greater in the protected microhabitat than on the trail. Studies have demonstrated that density affects the movements of larvae and the occurrence of cannibalism (Lima, 2016Lima, T. N. 2016. Cannibalism among Myrmeleon brasiliensis larvae (Návas, 1914) (Neuroptera, Myrmeleontidae). Acta Scientiarum, Biological Sciences 38(4):447-450. https://doi.org/10.4025/actascibiolsci.v38i4.32822
https://doi.org/10.4025/actascibiolsci.v...
; Lima & Lopes, 2016Lima, T. N. & Lopes, F. S. 2016. Efeito da densidade, perturbação e alimento no deslocamento de Myrmeleon brasiliensis (Navás 1914) (Neuroptera, Myrmeleontidae). Ecología Austral 26:166-170.). In the present study, despite the greater density in the protected microhabitat, mean trap size and the investment of the larvae in trap size were greater. Thus, the protection of the rain and other perturbations (e.g., wind and trampling of humans who use the trails) that the microhabitat offers enables a greater investment in trap size, which may result to greater success in the capture of prey (Nonato & Lima, 2011Nonato, L. M. & Lima, T. N. 2011. El comportamiento de predación de los estadios larvales de Myrmeleon brasiliensis (Neuroptera, Myrmeleontidae). Revista Colombiana de Entomología 37:354-356.).

The lifecycle of antlions ranges from six months to two years, depending on the availability of food resources (quantity and quality of prey items), photoperiod, temperature, and metabolic rate (Fisher 1989Fisher, M. 1989. Antlion life cycles in Nigeria. Journal of Tropical Ecology 5(2):247-250. https://www.jstor.org/stable/2559556
https://www.jstor.org/stable/2559556...
; Arnett & Gotelli, 1999Arnett, A. E. & Gotelli, N. J. 1999. Bergmann’s rule in the ant lion Myrmeleon immaculatus DeGeer (Neuroptera: Myrmeleontidae): geographic variation in body size and heterozygosity. Journal of Biogeography 26(2):275-283. https://doi.org/10.1046/j.1365-2699.1999.00271.x
https://doi.org/10.1046/j.1365-2699.1999...
, 2001Arnett, A. E. & Gotelli, N. J. 2001. Pit-building decisions of larval antlions: effects of larval age, temperature, food, and population source. Journal of Insect Behavior 14:89-97.https://doi.org/10.1023/A:1007853730317
https://doi.org/10.1023/A:1007853730317...
; Missiran et al., 2006Missirian, G. B.; Uchôa-Fernandes, M. A. &Fischer, E. A. 2006.Development of Myrmeleon brasiliensis (Navás) (Neuroptera, Myrmeleontidae), in laboratory, with different natural diets. Brazilian Journal Biology 23(4):1044-1050. http://dx.doi.org/10.1590/S0101-81752006000400009
http://dx.doi.org/10.1590/S0101-81752006...
). Moreover, environments will high disturbance levels can exert an influence on the characteristics of the emerging adults (body size and wingspan). As there is a positive correlation between body size and fecundity in insects (Honek, 1993Honek, A. 1993. Intraespecifc variation in body size and fecundity in insects: a general relationship. Oikos 66(3):483-492. https://doi.org/10.2307/3544943
https://doi.org/10.2307/3544943...
; Sokolovska et al., 2000Sokolovska, N.; Rowe, L. & Johansson, F. 2000. Fitness and body size in mature odonates. Ecological Entomology 25(2):239-248. https://doi.org/10.1046/j.1365-2311.2000.00251.x
https://doi.org/10.1046/j.1365-2311.2000...
), larvae who undergo situations of high energy expenditure due to the maintenance of their traps may become smaller and less fecund adults.

In general, predators select locations with a greater energy return during the search for prey (Charnov,1976Charnov, E. L. 1976. Optimal foraging, the Marginal Value Theorem. Theoretical Population Biology 9(2):129-136. https://doi.org/10.1016/0040-5809(76)90040-X
https://doi.org/10.1016/0040-5809(76)900...
; Pyke et al.,1977Pyke, G. H.; Pulliam, H. R. & Charnov, E. L. 1977. Optimal foraging: aselective review of theory and tests. Quarterly Review of Biology 52(2):137-154.). In the case of trap-building predators, however, the prey comes to them and greater energy is expended on the building and maintenance of traps rather than searching for prey (Beachly et al.,1995Beachly, W. M.; Stephens, D. W. & Toyer, K. B. 1995. On the economics of sit-andwait foraging: site selection and assessment. Behavior Ecology 6(3):258-268. https://doi.org/10.1093/beheco/6.3.258
https://doi.org/10.1093/beheco/6.3.258...
). The present findings demonstrate that the level of disturbance in microhabitats in which M. brasiliensis larvae build traps affects the foraging characteristics of these larvae, such as the investment in trap size for the capture of prey. Therefore, protected environments constitute an advantaged for pit-building antlion larvae, as the maintenance of foraging ensures the continual capture of prey and, consequently, a shorter lifecycle time and greater storage of energy for adult forms.

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    » https://doi.org/10.1023/A:1007853730317
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    » https://doi.org/10.1093/beheco/arw071
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    » https://doi.org/10.1093/beheco/6.3.258
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    » https://doi.org/10.1111/j.1461-0248.2004.00661.x
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    » https://doi:10.1016/j.jtbi.2009.05.026
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Publication Dates

  • Publication in this collection
    15 July 2020
  • Date of issue
    2020

History

  • Received
    06 Mar 2020
  • Accepted
    10 June 2020
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