Tierra de Oro Laboratory

Physiology and Ecology in the Pinyon-Juniper Savanna

Tag: eleodes

  • Bahia de los Angeles 2026

    It was a successful year for science and wildlife.

    Peninsular landscape on the trip down. 6/17/26

    Once again, I joined Dr. Drew Talley and Dra. Dr Natalia Rodriguez Revelo for a summer survey of the islands in Bahia de los Angeles, Baja California.

    Natalia and Drew on Jorobado. 6/19/26

    The work on the islands went well, and we got data regarding beetle populations from twelve islands. It is also a highlight of my year to spend the time with my best friend and our wonderful colleague.

    Although work on the islands can be challenging, we are usually done by late morning, and there is time for other activities. This year, I thought it would be interesting to test the thermal resilience of some of the beetle species. The specific idea is that beetles that produce defensive chemicals (like Eleodes does) would be more sensitive to extreme conditions such as high temperature when compared with undefended beetles (such as Philolithus in Santa Fe or Cryptoglossa in Bahia). This has been assumed to be the case, but has not been tested rigorously.

    My idea was simple: collect beetles from two species, one defended and one undefended, and test their survival at temperatures ranging from benign to lethal. My prediction would be that the undefended beetles would survive at higher temperatures than those that invest energy and water in defensive scent glands.

    We decided it was better to collect the experimental beetles on the mainland. The project was added to the permit application along with the other, ongoing projects. However, the permit only allowed us to survey the beetles on the mainland, not collect or test them. Nonetheless, sampling would allow us to determine where it would be best to find enough beetles for experiments in the future.

    Bahia de los Angeles dump. 6/18/26

    For our first sampling location, we set traps at the local dump. We reasoned that we could avoid protected areas and private property by sampling at the dump.

    We set nine pitfall traps, baited with oatmeal along an arroyo. After checking back every afternoon for three days, we had caught six Cryptoglossa muricata. It was good to find beetles that would be appropriate for experiments, but we needed at least two species, and about 40 of each. We thought it best to look elsewhere.

    One can see why beetles in the Cryptoglossini are called “death feigning beetles.” This C. muricata is quite alive, but waiting for me to go away. 6/20/26

    We thought that the Glendale Community College field station might be a better location, so we asked Jared Ocampo, an old friend and the station manager, for permission to set traps around the station. He agreed, and even helped us set the traps.

    Arroyo on the southern approach to the Glendale Station. 6/24/26

    We set a total of 24 traps in three sets of eight. One group was set in an arroyo to the south of the station, one set was placed in desert to the west, and the last was placed near the beach to the north. Rather than checking every day, we left the traps for two nights.

    The results were pleasing. We trapped more than sixty C. muricata, and ten Eleodes loretensis, along with a number of Stibia. This is an almost ideal result, in that E. loretensis is chemically defended, whereas C. muricata is not, and they are well-matched n terms of size and mass.

    The traps in the arroyo were the most productive, and those in the desert also caught a good number of beetles. Interestingly, those by the beach only trapped a few Cryptoglossa.

    Assuming that all goes equally well next year and we have the proper permit, we should be able to compare the temperature sensitivities of these two species that are highly similar except for the presence of chemical defense.

    As always, there is more to come.

  • One Project Becomes Two

    After working very hard this winter to submit a manuscript describing the most recent results of the project, I realized that it has really become two non-overlapping lines of inquiry.

    A few weeks ago, I submitted a manuscript titled “Batesian Mimicry and Thermal Resilience Among Tenebrionid Beetles from a New Mexican PiƱon-Juniper Savanna” to the Journal of Experimental Biology. The editor said some kind words about it, but ultimately rejected it because it did not fit comfortably into the aims of the journal. The main complaint was that a significant portion of the paper focused on the ecology of the beetles, rather than their physiology.

    It took a few days for me to realize that the paper had evolved into something different. Looking over the title, two things may stand out.

    Batesian Mimicry

    Thermal Resilience

    Those are really two separate concepts and analyzing either one can be performed relatively independently of the other. In other words, this was two incomplete papers rather than one solid story.

    Now begins the process of completing both of those stories.

    Mimicry

    Several lines of evidence address whether the Asidini Philolithus elatus and Stenomorpha rimata are Batesian mimics of the Amphidorine Eleodes obscura. For an organism to be a bona fide Batesian mimic it must

    • Resemble the model in the eyes (or ears or nose) of potential predators.
    • Be palatable
    • Be undefended (or at least to a potential predator)
    • Overlap the model in space and/or time so that predators can learn the association
    • Be relatively uncommon to prevent predators from discovering their mimicry

    The Asidini fulfill these criteria to varying degrees

    • The major argument for mimicry is that the Asidini look a lot like E. obscura, and are about the same size and mass.
    • A close relative of S. rimata, S. marginata, has been shown to be palatable to mice and skunks. Palatability of P. elatus is unknown.

    On the minus side:

    • P. elatus will regurgitate when handled, suggesting at least mild defense
    • Headstanding behavior, which contributes to the mimicry, is weak (P. elatus) or non-existent (S. rimata)
    • Both Asidini are at least as common as E. obscura during peak season, giving predators plenty of opportunity to learn that they are quite edible.
    • Stenomorpha rimata is present in late September and October, when Eleodes have disappeared from the surface, giving predators plenty of time to learn that they are tasty and undefended.

    I really need to know who the local predators are, so that I can make sense of all this. I hope to use the upcoming field season to find out who is eating beetles around here. Based on scats and scattered body parts, someone is eating them, but who?

    Thermal Resilience

    Maintenance of scent glands is costly, so E. obscura should either use more metabolic energy than the undefended P. elatus and S. rimata, or devote less energy to other aspects of fitness. Based on respirometry across a range of temperatures it would appear that all three species use the same amount of energy per unit time, but the Asidini have much higher survival at elevated temperatures.

    This is a nice partial story, but I need to know more about possible mechanisms. Two sets of experiments would be very helpful in completing this part of the story.

    • Testing survival across a full range of temperatures. I have only tested up to 40C, which is semi-lethal to Eleodes but does not strongly affect P. elatus or S. rimata. Although I am no fond of the idea, I need to test up to a temperature that is 100% lethal in order to have a complete picture of thermal resilience.
    • Because temperature induced lethality is associated with disrupted ionic regulation, it will be important to examine concentrations of ions in the hemolymph (blood) of E. obscura, P. elatus and S. rimata at high temperatures.

    If all goes well, I should have two papers ready by the end of the season. Wish me luck.