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Dancing close together in the woods: mate-guarding behavior might explain sexual dimorphism in Chrysoprasis auriventris auriventris Redtenbacher, 1868 (Coleoptera: Cerambycinae)

ABSTRACT

A fortuitous observation of mate-guarding behavior of male Chrysoprasis a. auriventris is presented here. In our observation, a male hold onto the female's body using his forelegs and walks along with her while she lays the eggs into the trunk slits. While guarding the female, the male adopted aggressive postures and attacked rival males that approached her. We suggest that the mate-guarding behavior may explain the male's elongated mid and hindlegs in this species, under a functional perspective. Additionally, a new host plant association was recorded.

Keywords:
Functional morphology; Longhorn beetles; Mating; Post-copula behavior; Sexual selection

There is no question of the vast ignorance we have about biodiversity. The organization of such lack of knowledge as shortfalls (Brown and Lomolino, 1998Brown, J.H., Lomolino, M.V., 1998. Biogeography, 2nd ed. Sinauer, Sunderland.; Lomolino, 2004Lomolino, M.V., 2004. Conservation biogeography. In: Lomolino, M., Heaney, L. (Eds.), Frontiers of Biogeography: New Directions in the Geography of Nature. Sinauer Associates, Sunderland, pp. 293–296.; Cardoso et al., 2011Cardoso, P., Erwin, T.L., Borges, P.A.V., New, T.R., 2011. The seven impediments in invertebrate conservation and how to overcome them. Biol. Conserv. 144 (11), 2647-2655. http://doi.org/10.1016/j.biocon.2011.07.024.
http://doi.org/10.1016/j.biocon.2011.07....
; Diniz-Filho et al., 2013Diniz-Filho, J.A.F., Loyola, R.D., Raia, P., Mooers, A.O., Bini, L.M., 2013. Darwinian shortfalls in biodiversity conservation. Trends Ecol. Evol. 28 (12), 689-695. http://doi.org/10.1016/j.tree.2013.09.003.
http://doi.org/10.1016/j.tree.2013.09.00...
; Hortal et al., 2015Hortal, J., De Bello, F., Diniz-Filho, J.A.F., Lewinsohn, T.M., Lobo, J.M., Ladle, R.J., 2015. Seven Shortfalls that Beset Large-Scale Knowledge of Biodiversity. Annu. Rev. Ecol. Evol. Syst. 46 (1), 523-549. http://doi.org/10.1146/annurev-ecolsys-112414-054400.
http://doi.org/10.1146/annurev-ecolsys-1...
; Faria et al., 2021Faria, L.R.R., Pie, M.R., Salles, F.F., Soares, E.D.G., 2021. The Haeckelian shortfall or the tale of the missing semaphoronts. J. Zool. Syst. Evol. Res. 59 (2), 359-369. http://doi.org/10.1111/jzs.12435.
http://doi.org/10.1111/jzs.12435...
) was a very important advancement, both in terms of the systematization of the knowledge gaps, and also for enabling the emergence of more focused and well-constructed mitigation proposals (e.g., Assis, 2018Assis, L.C.S., 2018. Revisiting the Darwinian shortfall in biodiversity conservation. Biodivers. Conserv. 27 (11), 2859-2875. http://doi.org/10.1007/s10531-018-1573-3.
http://doi.org/10.1007/s10531-018-1573-3...
). When one assesses the very nature of these shortfalls, the importance of natural history becomes even greater (see e.g., Cotterill and Foissner, 2010Cotterill, F.P., Foissner, W., 2010. A pervasive denigration of natural history misconstrues how biodiversity inventories and taxonomy underpin scientific knowledge. Biodivers. Conserv. 19 (1), 291-303. http://doi.org/10.1007/s10531-009-9721-4.
http://doi.org/10.1007/s10531-009-9721-4...
). Hence, such advancements in our knowledge of natural history, mainly by a process of observation and interpretation (see Gilligan, 2009Gilligan, D., 2009. Natural history from the ground up: developing a college-level natural history program in the new millennium. J. Nat. Hist. 3, 24-29.), often rely on notable fortuitous observations and documentation (Burns and Low, 2022Burns, K.C., Low, J., 2022. The psychology of natural history. Trends Ecol. Evol. 37, 1029–1031. http://doi.org/10.1016/j.tree.2022.09.001.
http://doi.org/10.1016/j.tree.2022.09.00...
).

In this context, there is a strengthening of citizen science initiatives to address biodiversity (e.g., Lees and Martin, 2015Lees, A.C., Martin, R.W., 2015. Exposing hidden endemism in a Neotropical forest raptor using citizen science. Ibis 157 (1), 103-114. http://doi.org/10.1111/ibi.12207.
http://doi.org/10.1111/ibi.12207...
; Barahona-Segovia et al., 2017Barahona-Segovia, R.M., Castillo Tapia, R., Pañinao-Monsálvez, L., 2017. First record of Myopa metallica Camras, 1992 (Diptera: Conopidae: Myopinae) in Northern Chile after 46 years: a case study of the success of citizen science programs. J. Insect Biodivers. 5 (13), 1-8. http://doi.org/10.12976/jib/2017.5.13.
http://doi.org/10.12976/jib/2017.5.13...
; Di Cecco et al., 2021Di Cecco, G.J., Barve, V., Belitz, M.W., Stucky, B.J., Guralick, R.P., Hulbert, A.H., 2021. Observing the observers: how participants contribute data to iNaturalist and implications for biodiversity science. Bioscience 71 (11), 1179-1188. http://doi.org/10.1093/biosci/biab093.
http://doi.org/10.1093/biosci/biab093...
), which stimulates the participation of local communities in monitoring and reporting threats to biodiversity. There are many interesting reports where photographs taken in an unpretentious manner have led to important findings and the decrease of the Wallacean shortfall (e.g., Freitas et al., 2021Freitas, T.M.S., Stropp, J., Calegari, B.B., Calatayud, J., de Marco Junior, P., Montag, L.F.A., Hortal, J., 2021. Quantifying shortfalls in the knowledge on Neotropical Auchenipteridae fishes. Fish Fish. 22 (1), 87-104. http://doi.org/10.1111/faf.12507.
http://doi.org/10.1111/faf.12507...
).

Biodiversity shortfalls are also massive for Coleoptera, which is particularly true for long-horned beetles (Cerambycidae) (e.g., Hanks and Wang, 2017Hanks, L.M., Wang, Q., 2017. Reproductive Biology of Cerambycids. In: Wang, Q. (Ed.), Cerambycidae of the World: Biology and Pest Management. CRC Press, Boca Raton, pp. 133–159.). Cerambycidae (Coleoptera), encompassing about 35,000 described species, is one of families with the greatest number of species within the Phytophaga (Haddad et al., 2018Haddad, S., Shin, S., Lemmon, A. R., Lemmon, E. M., Švacha, P., Farrell, B., Ślipiński, A., Windsor, D., McKenna, D. D., 2018. Anchored hybrid enrichment provides new insights into the phylogeny and evolution of longhorned beetles (Cerambycidae). Syst. Entomol. 43 (1), 68-89. http://doi.org/10.1111/syen.12257.
http://doi.org/10.1111/syen.12257...
; Tavakilian and Chevillotte, 2022Tavakilian, G.L., Chevillotte, H., 2022. Titan: Base de Données Internationales sur les Cerambycidae ou Longicornes. Version 3.0. Available in: http://titan.gbif.fr/ (accessed 18 May 2023).
http://titan.gbif.fr/...
). Despite the vast taxonomic literature, very little is known about their behavior, as most observations refer to species of economic interest (Hanks and Wang, 2017Hanks, L.M., Wang, Q., 2017. Reproductive Biology of Cerambycids. In: Wang, Q. (Ed.), Cerambycidae of the World: Biology and Pest Management. CRC Press, Boca Raton, pp. 133–159.). Moreover, it is not surprising that a single and fortuitous observation could provide several pieces of information regarding the bionomics of a single species.

According to Napp and Martins (1997, 18p)Napp, D.S., Martins, U.R., 1997. Revisão do gênero Chrysoprasis A.-Serville, 1834 (Coleoptera, Cerambycidae, Cerambycinae, Heteropsini). III. Grupo chalybea. Rev. Bras. Entomol. 41, 17-41.Chrysoprasis a. auriventris may be identified by the following: "...metatibiae strongly flattened, middle and hind legs very elongated, metafemora subequal in length to elytra, surpassing the elytral apex by half of their length, prothorax elongated, subparallel-sided, antennae (male) surpass the elytral apex by V–VI antennomeres…” (freely translated). The elongated middle and hindlegs are usually found in males only, and the authors did not address the females or comment on the sexual dimorphism. It is noteworthy that differences in length of appendages, where males typically have longer mid- and hindlegs are common in Cerambycidae, especially in Lamiinae (see Nascimento and Santos-Silva, 2019Nascimento, F.E.L., Santos-Silva, A., 2019. The “Podus” complex: new species and notes on some Acanthocinini (Coleoptera, Cerambycidae, Lamiinae). Zootaxa 4629 (2), 195-210. http://doi.org/10.11646/zootaxa.4629.2.3.
http://doi.org/10.11646/zootaxa.4629.2.3...
). However, some functional context for traits as the sexually dimorphic elongation of appendages are yet to be explored.

In this contribution, we describe aspects of the mating behavior of Chrysoprasis a. auriventris and suggest the function of its elongated legs as a secondary sexual trait and provide morphological notes on females. Additionally, Parapiptadenia rigida (Benth.) Brenan (Fabaceae) is recorded as a host plant for the species.

The observation was carried out in the Iguaçu National Park (-25.6548° -54.4357°, 210 m a.s.l.), Foz do Iguaçu, Paraná, Brazil.

Behavioral observations were made using a DSLR camera (Nikon D7500) with a macro lens (Nikon Micro-Nikkor 55mm f/2.8) and a diffused flashlight, and videos were taken using a smartphone (LG G7 ThinQ). Specimens were not collected, so the subsequent identification relied on the recorded photographs and videos. The specimens were identified using the key proposed by Napp and Martins (1997)Napp, D.S., Martins, U.R., 1997. Revisão do gênero Chrysoprasis A.-Serville, 1834 (Coleoptera, Cerambycidae, Cerambycinae, Heteropsini). III. Grupo chalybea. Rev. Bras. Entomol. 41, 17-41., and by comparing them with type material photographs provided by Bezark (2023)Bezark, L.G., 2023. A Photographic Catalog of the Cerambycidae of the World. New World Cerambycidae catalog. Available in: http://bezbycids.com/byciddb/wdefault.asp?w=n/ (accessed 15 May 2023).
http://bezbycids.com/byciddb/wdefault.as...
. Additional material housed at the Danúncia Urban Entomological Collection (CEDU-UNILA) was also studied.

On October 27th, 2022, around noon, during a nature walk along the Bananeiras Trail (Iguaçu National Park) in an ecotourism activity, one of us (BMT) observed a small aggregation of longhorn beetles (C. a. auriventrisRedtenbacher, 1868Redtenbacher, L. 1868. Reise der österreichischen Fregatte Novara um die Erde in den Jahren 1857, 1858, 1859 unter den Befehlen des Commodore B. von Wüllerstorf-Urbair. Zoologischer Theil. Zweiter Band. I. Abtheilung. A. 1: Coleoptera. Karl Gerold’s Sohn, Wien, 249 pp.) on a fallen trunk of Parapiptadenia rigida (Benth.) Brenan. The beetles seemed to prefer the cross-sectional location of the wood, where the innermost wood parts were exposed. A female was observed probing the trunk with her exposed ovipositor, clearly looking for cracks in the wood where eggs could be laid. The male held onto the female's thorax with his forelegs, just behind the pronotum, and between first and second pair of legs, keeping himself on top parallelling the female’s body, and following her movements walking on his long mid- and hindlegs (Figure 1, Video 1).

Figure 1
A. and B. pair of Chrysoprasis auriventris auriventris Redtenbacher, 1868 engaged in the mateguarding behavior; C. female with the ovipositor inserted into a slit in the trunk; D. trunk of Parapiptadenia rigida (Benth.) Brenan. and the surroundings.

Meanwhile, some other single males were also observed trying to harass the ovipositing female. Hence, the guarding male turned his body perpendicular to the female and kicked the opponent away with his long middle and hind legs, without losing physical contact with the female (Video 2), and then quickly returned to the straddled position parallel to the female’s body.

In the original description by Redtenbacher (1868, 195p)Redtenbacher, L. 1868. Reise der österreichischen Fregatte Novara um die Erde in den Jahren 1857, 1858, 1859 unter den Befehlen des Commodore B. von Wüllerstorf-Urbair. Zoologischer Theil. Zweiter Band. I. Abtheilung. A. 1: Coleoptera. Karl Gerold’s Sohn, Wien, 249 pp., only antennal length was mentioned as dimorphic in this species: “The antennae are hairy on the underside, in males they are much longer than the body, in females only as long as this” (freely translated). Subsequent authors (i.e. Napp and Martins, 1997Napp, D.S., Martins, U.R., 1997. Revisão do gênero Chrysoprasis A.-Serville, 1834 (Coleoptera, Cerambycidae, Cerambycinae, Heteropsini). III. Grupo chalybea. Rev. Bras. Entomol. 41, 17-41.) also only emphasized the length of antennae and neglected the sexual dimorphism of mid- and hindlegs, much shorter in females. While in males the metafemora exceed the elytral apex by about half of their length, in females the metafemora exceed the elytral apex by about 1/10 (0.1) of their length.

The main goals of mating strategies utilized by male insects can be understood under two main contexts: (i) insemination of a larger number of females (partners of other rivals), or (ii) prevention of sexual partner from being inseminated by other males (Alcock, 1994Alcock, J., 1994. Post insemination associations between males and females in insects: the mate-guarding hypothesis. Annu. Rev. Entomol. 39 (1), 1-21. http://doi.org/10.1146/annurev.en.39.010194.000245.
http://doi.org/10.1146/annurev.en.39.010...
). This latter could rely on mate-guarding behaviors in which males prevent females from leaving their sites and/or that conspecific males approach their mates (see Parker, 1974Parker, G.A., 1974. Courtship persistence and female-guarding as male time investment strategies. Behaviour 48 (1-4), 157-184. http://doi.org/10.1163/156853974X00327.
http://doi.org/10.1163/156853974X00327...
; Alcock, 1994Alcock, J., 1994. Post insemination associations between males and females in insects: the mate-guarding hypothesis. Annu. Rev. Entomol. 39 (1), 1-21. http://doi.org/10.1146/annurev.en.39.010194.000245.
http://doi.org/10.1146/annurev.en.39.010...
; Simmons, 2001Simmons, L.W., 2001 Sperm Competition and its Evolutionary Consequences in the Insects. Princeton, Princeton University Press.).

Cerambycids basically adopt two mating strategies, the "resource defense polygyny", in which males are extremely territorial and defend the scarce resource (host plant), or the most common "female defense polygyny" strategy, in which females (not the host plants) are the limiting resource, and are thus guarded by the males preventing rival males from mating with guarded females (see Hanks and Wang, 2017Hanks, L.M., Wang, Q., 2017. Reproductive Biology of Cerambycids. In: Wang, Q. (Ed.), Cerambycidae of the World: Biology and Pest Management. CRC Press, Boca Raton, pp. 133–159.).

As mentioned, a main feature of the observed species is the length/ratio of the mid and hindlegs in relation to the body of males. Cerambycids typically exhibit sexually dimorphic traits such as antennal length, that is longer in males (Hanks et al., 1996aHanks, L.M., Millar, J.G., Paine, T.D., 1996a. Body size influences mating success of the Eucalyptus Longhorned Borer (Coleoptera: cerambycidae). J. Insect Behav. 9 (3), 369-382. http://doi.org/10.1007/BF02214016.
http://doi.org/10.1007/BF02214016...
, 1996bHanks, L.M., Millar, J.G., Paine, T.D., 1996b. Mating behavior of the Eucalyptus Longhorned Borer (Coleoptera: Cerambycidae) and the adaptive significance of long “horns”. J. Insect Behav. 9 (3), 383-393. http://doi.org/10.1007/BF02214017.
http://doi.org/10.1007/BF02214017...
). The functional context of some hyperallometric traits was observed, as the elongated forelegs of male harlequin beetle [Acrocinus longimanus (Linnaeus, 1758)], used as weapons against other males, and for guarding females and host plants (Zeh et al., 1992Zeh, D.W., Zeh, J.A., Tavakilian, G., 1992. Sexual selection and sexual dimorphism in the harlequin beetle Acrocinus longimanus. Biotropica 24 (1), 86-96. http://doi.org/10.2307/2388476.
http://doi.org/10.2307/2388476...
). Here we provide new data on the mating behavior and host plant of C. a. auriventris, a species of longhorn beetle with barely known natural history. We also present our interpretation of the elongated mid- and hindlegs of males under a functional context, as an evolutionary consequence of the mate-guarding behavior.

Finally, we emphasize the importance that a single – and at first unpretentious – natural history observation has in addressing biodiversity shortfalls. Based on this observation, this communication provides data that could be contextualized under at least four biodiversity shortfalls: (i) a species trait, the long legs, was treated under its ecological function (Raunkiaeran shortfall, Hortal et al., 2015Hortal, J., De Bello, F., Diniz-Filho, J.A.F., Lewinsohn, T.M., Lobo, J.M., Ladle, R.J., 2015. Seven Shortfalls that Beset Large-Scale Knowledge of Biodiversity. Annu. Rev. Ecol. Evol. Syst. 46 (1), 523-549. http://doi.org/10.1146/annurev-ecolsys-112414-054400.
http://doi.org/10.1146/annurev-ecolsys-1...
), (ii) information on its host plant was presented (Eltonian shortfall, Hortal et al., 2015Hortal, J., De Bello, F., Diniz-Filho, J.A.F., Lewinsohn, T.M., Lobo, J.M., Ladle, R.J., 2015. Seven Shortfalls that Beset Large-Scale Knowledge of Biodiversity. Annu. Rev. Ecol. Evol. Syst. 46 (1), 523-549. http://doi.org/10.1146/annurev-ecolsys-112414-054400.
http://doi.org/10.1146/annurev-ecolsys-1...
), (iii) the known distribution of the species was extended to western Paraná State (Wallacean shortfall, Lomolino, 2004Lomolino, M.V., 2004. Conservation biogeography. In: Lomolino, M., Heaney, L. (Eds.), Frontiers of Biogeography: New Directions in the Geography of Nature. Sinauer Associates, Sunderland, pp. 293–296.).

Acknowledgments

We express our sincere thanks to Antonio Santos-Silva (MZUSP) and Vanessa Moreira (UNILA) for provide helping with bibliography and José O. Silva Júnior (UFPR) for providing images of females of C. a. auriventris. We sincerely appreciate the critical review by the anonymous reviewers which helped us improving this short communication. FELN is grateful to the Programa de Pós-Graduação em Biodiversidade Neotropical (PPGBN-UNILA) and CAPES for postdoctoral fellowship (88887.809176/2023-00). LRRF is indebted to PRPPG-UNILA for financial support (PRPPG 137/2018, 80/2019 and 214/2021).

References

  • Alcock, J., 1994. Post insemination associations between males and females in insects: the mate-guarding hypothesis. Annu. Rev. Entomol. 39 (1), 1-21. http://doi.org/10.1146/annurev.en.39.010194.000245
    » http://doi.org/10.1146/annurev.en.39.010194.000245
  • Assis, L.C.S., 2018. Revisiting the Darwinian shortfall in biodiversity conservation. Biodivers. Conserv. 27 (11), 2859-2875. http://doi.org/10.1007/s10531-018-1573-3
    » http://doi.org/10.1007/s10531-018-1573-3
  • Barahona-Segovia, R.M., Castillo Tapia, R., Pañinao-Monsálvez, L., 2017. First record of Myopa metallica Camras, 1992 (Diptera: Conopidae: Myopinae) in Northern Chile after 46 years: a case study of the success of citizen science programs. J. Insect Biodivers. 5 (13), 1-8. http://doi.org/10.12976/jib/2017.5.13
    » http://doi.org/10.12976/jib/2017.5.13
  • Bezark, L.G., 2023. A Photographic Catalog of the Cerambycidae of the World. New World Cerambycidae catalog. Available in: http://bezbycids.com/byciddb/wdefault.asp?w=n/ (accessed 15 May 2023).
    » http://bezbycids.com/byciddb/wdefault.asp?w=n/
  • Brown, J.H., Lomolino, M.V., 1998. Biogeography, 2nd ed. Sinauer, Sunderland.
  • Burns, K.C., Low, J., 2022. The psychology of natural history. Trends Ecol. Evol. 37, 1029–1031. http://doi.org/10.1016/j.tree.2022.09.001
    » http://doi.org/10.1016/j.tree.2022.09.001
  • Cardoso, P., Erwin, T.L., Borges, P.A.V., New, T.R., 2011. The seven impediments in invertebrate conservation and how to overcome them. Biol. Conserv. 144 (11), 2647-2655. http://doi.org/10.1016/j.biocon.2011.07.024
    » http://doi.org/10.1016/j.biocon.2011.07.024
  • Cotterill, F.P., Foissner, W., 2010. A pervasive denigration of natural history misconstrues how biodiversity inventories and taxonomy underpin scientific knowledge. Biodivers. Conserv. 19 (1), 291-303. http://doi.org/10.1007/s10531-009-9721-4
    » http://doi.org/10.1007/s10531-009-9721-4
  • Di Cecco, G.J., Barve, V., Belitz, M.W., Stucky, B.J., Guralick, R.P., Hulbert, A.H., 2021. Observing the observers: how participants contribute data to iNaturalist and implications for biodiversity science. Bioscience 71 (11), 1179-1188. http://doi.org/10.1093/biosci/biab093
    » http://doi.org/10.1093/biosci/biab093
  • Diniz-Filho, J.A.F., Loyola, R.D., Raia, P., Mooers, A.O., Bini, L.M., 2013. Darwinian shortfalls in biodiversity conservation. Trends Ecol. Evol. 28 (12), 689-695. http://doi.org/10.1016/j.tree.2013.09.003
    » http://doi.org/10.1016/j.tree.2013.09.003
  • Faria, L.R.R., Pie, M.R., Salles, F.F., Soares, E.D.G., 2021. The Haeckelian shortfall or the tale of the missing semaphoronts. J. Zool. Syst. Evol. Res. 59 (2), 359-369. http://doi.org/10.1111/jzs.12435
    » http://doi.org/10.1111/jzs.12435
  • Freitas, T.M.S., Stropp, J., Calegari, B.B., Calatayud, J., de Marco Junior, P., Montag, L.F.A., Hortal, J., 2021. Quantifying shortfalls in the knowledge on Neotropical Auchenipteridae fishes. Fish Fish. 22 (1), 87-104. http://doi.org/10.1111/faf.12507
    » http://doi.org/10.1111/faf.12507
  • Gilligan, D., 2009. Natural history from the ground up: developing a college-level natural history program in the new millennium. J. Nat. Hist. 3, 24-29.
  • Haddad, S., Shin, S., Lemmon, A. R., Lemmon, E. M., Švacha, P., Farrell, B., Ślipiński, A., Windsor, D., McKenna, D. D., 2018. Anchored hybrid enrichment provides new insights into the phylogeny and evolution of longhorned beetles (Cerambycidae). Syst. Entomol. 43 (1), 68-89. http://doi.org/10.1111/syen.12257
    » http://doi.org/10.1111/syen.12257
  • Hanks, L.M., Millar, J.G., Paine, T.D., 1996a. Body size influences mating success of the Eucalyptus Longhorned Borer (Coleoptera: cerambycidae). J. Insect Behav. 9 (3), 369-382. http://doi.org/10.1007/BF02214016
    » http://doi.org/10.1007/BF02214016
  • Hanks, L.M., Millar, J.G., Paine, T.D., 1996b. Mating behavior of the Eucalyptus Longhorned Borer (Coleoptera: Cerambycidae) and the adaptive significance of long “horns”. J. Insect Behav. 9 (3), 383-393. http://doi.org/10.1007/BF02214017
    » http://doi.org/10.1007/BF02214017
  • Hanks, L.M., Wang, Q., 2017. Reproductive Biology of Cerambycids. In: Wang, Q. (Ed.), Cerambycidae of the World: Biology and Pest Management. CRC Press, Boca Raton, pp. 133–159.
  • Hortal, J., De Bello, F., Diniz-Filho, J.A.F., Lewinsohn, T.M., Lobo, J.M., Ladle, R.J., 2015. Seven Shortfalls that Beset Large-Scale Knowledge of Biodiversity. Annu. Rev. Ecol. Evol. Syst. 46 (1), 523-549. http://doi.org/10.1146/annurev-ecolsys-112414-054400
    » http://doi.org/10.1146/annurev-ecolsys-112414-054400
  • Lees, A.C., Martin, R.W., 2015. Exposing hidden endemism in a Neotropical forest raptor using citizen science. Ibis 157 (1), 103-114. http://doi.org/10.1111/ibi.12207
    » http://doi.org/10.1111/ibi.12207
  • Lomolino, M.V., 2004. Conservation biogeography. In: Lomolino, M., Heaney, L. (Eds.), Frontiers of Biogeography: New Directions in the Geography of Nature. Sinauer Associates, Sunderland, pp. 293–296.
  • Napp, D.S., Martins, U.R., 1997. Revisão do gênero Chrysoprasis A.-Serville, 1834 (Coleoptera, Cerambycidae, Cerambycinae, Heteropsini). III. Grupo chalybea. Rev. Bras. Entomol. 41, 17-41.
  • Nascimento, F.E.L., Santos-Silva, A., 2019. The “Podus” complex: new species and notes on some Acanthocinini (Coleoptera, Cerambycidae, Lamiinae). Zootaxa 4629 (2), 195-210. http://doi.org/10.11646/zootaxa.4629.2.3
    » http://doi.org/10.11646/zootaxa.4629.2.3
  • Parker, G.A., 1974. Courtship persistence and female-guarding as male time investment strategies. Behaviour 48 (1-4), 157-184. http://doi.org/10.1163/156853974X00327
    » http://doi.org/10.1163/156853974X00327
  • Redtenbacher, L. 1868. Reise der österreichischen Fregatte Novara um die Erde in den Jahren 1857, 1858, 1859 unter den Befehlen des Commodore B. von Wüllerstorf-Urbair. Zoologischer Theil. Zweiter Band. I. Abtheilung. A. 1: Coleoptera. Karl Gerold’s Sohn, Wien, 249 pp.
  • Simmons, L.W., 2001 Sperm Competition and its Evolutionary Consequences in the Insects. Princeton, Princeton University Press.
  • Tavakilian, G.L., Chevillotte, H., 2022. Titan: Base de Données Internationales sur les Cerambycidae ou Longicornes. Version 3.0. Available in: http://titan.gbif.fr/ (accessed 18 May 2023).
    » http://titan.gbif.fr/
  • Zeh, D.W., Zeh, J.A., Tavakilian, G., 1992. Sexual selection and sexual dimorphism in the harlequin beetle Acrocinus longimanus. Biotropica 24 (1), 86-96. http://doi.org/10.2307/2388476
    » http://doi.org/10.2307/2388476

Edited by

Associate Editor: Frederico Salles

Publication Dates

  • Publication in this collection
    30 Aug 2024
  • Date of issue
    2024

History

  • Received
    12 Mar 2024
  • Accepted
    12 July 2024
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