Brachysternus prasinus

B. prasinus is often mistaken for the more well-known Hylamorpha elegans, also known as the San Juan beetle, which is another species native to the same habitat.^[3] It can be differentiated from other Brachysternus beetle species because they have a well-developed supraspiracular ridge on the abdomen of male B. prasinus as well as a deeply emarginate terminal sclerite which are on the legs of female B. prasinus. Additional identifiers that allow for the differentiation of B. prasinus among other related scarab beetle species include their clypeal apex (a part of the insect's head) that is weakly reflexed at its tip. Moreover B. prasinus have prothoracic legs. These prothoracic legs include femurs which are weakly rounded and dilated as well as tibia with weak pro tibial notches.

Male and female B. prasinus differ slightly in their body shape. Male B. prasinus have the apex of the terminal sternite quadrite (a part of an insect's thorax or abdomen) whereas females are categorized as having the apex of the terminal sternite moderately to deeply emarginate. In other words, the bottoms of female B. prasinus are slightly more rounded than those of their male counterparts.^[3]

There is a large amount of variation among Brachysternus and especially in B. prasinus. Due to this large amount of variation, there are several different morphotypes of B. prasinus. As a result, there have been many different proposed names for these varied morphotypes. One morphotype is endemic to the province of Maule which encompasses Carrizalillo and Constitución, as well as the region of Talca Alto de Vilches in central Chile. This morphotype is unique from other B. prasinus due to the fact that they have more dense setose dorsally on their upper body.^[3] While these setae on B. prasinus are typically orange in the central Chilean morphotype, the setose of B. prasinus are a darker metallic green color on the top of their body and a deeper chestnut color on the bottom part of their body. This difference is thought to be due to changes in genetics across different locations. However, it has been argued that many of these morphotypes do not differ significantly and therefore should not be categorized separately. Some argue that these differences in color and setae type are simply due to the fact that  B. prasinus have a vast range of normal phenotypes.^[3]

Brachysternus prasinus lives on the southwestern coast of South America in Chile as well as parts of Argentina. B. prasinus lives in the area spanning from the Valparaíso region to the Magallanes Province. B. prasinus is found in Argentina in the province of Neuquén and the Río Grande Department region which is a part of the Tierra del Fuego Province.^[3] B. prasinus are seen across a wide range of elevations. They are found anywhere from elevations at sea level to 2,000 meters high in Southwestern South America.^[3] Their geographic range is highly dependent on the availability and distribution of Nothofagus, the species which B. prasinus feeds on.^[3] These forests of Nothofagus are often called Valdivian rainforests. B. prasinus have been observed in the Nothofagus forests near the cities of Coquimbo and Llanquihue in Chile as well as the areas of Neuquén and Chubut in Western Argentina.^[3]

Brachysternus prasinus lives in Nothofagus forests. It is hypothesized that the larvae of B. prasinus feed on dead and decaying wood as well as other vegetation similar to other Ruteline larvae. Adult B. prasinus often fly at dusk to other nearby Nothofagus trees for sustenance.^[3] These Nothofagus forests consist mainly of the Nothofagus plant but also often include other plant species like: Araucaria (Araucariaceae), Saxegothaea (Pinaceae), Drimys (Winteraceae), and Chusquea (Poaceae). Most of these plant species are plentiful from the months of November to February. The Valdivian rainforest district has two types of Northofagus including the deciduous Nothofagus obliqua and Nothofagus alpina, which is also called N. nervosa.^[4]

There is not a significant amount of information currently known about the life cycle and stages of Brachysternus prasinus. However, B. prasinus life cycle includes the following stages: egg, pupa, larvae, and adult. The larvae of B. prasinus have been found alongside other Chilean beetle scarab species including the larvae of Hylamorpha elegans.^[5] The larvae have been known to feed on the roots of crops as well as rotting wood.^[3] The larvae appear white in color with a dark chestnut colored head. The abdomen area of the larvae is also slightly darker.^[6] There is not much known about the pupal stage of B. prasinus.^[5] These beetles have an annual life cycle like many other scarab beetles. They are thought to be in the larval stage from January to around the month of November. The pupal stage is thought to span sometime between September and November. Finally, the adult stage lasts from approximately the month of November to February.^[6]

Adult B. prasinus often fly at dusk to nearby Nothofagus trees for sustenance. It has been observed that the peak flight season for Brachysternus prasinus is at the end of December.^[7] Adult B. prasinus are attracted to lights at night and have been captured while flying by shining lights in the darkness.^[3]

The species is highly dependent on different olfactory cues in its environment. B. prasinus utilize chemoreception, which is the process which allows organisms to respond appropriately to environmental stimuli, especially through smells and tastes. This chemoreception is carried out by odorant receptors (ORs), ionotropic receptors (IRs), and gustatory receptors (GRs). These different receptors relate to key proteins in the chemical ecology of these insects and can provide information on the evolutionary processes of scarab beetle species like B. prasinus.^[7] Scientists have used relative levels of ORs, IRs, and GRs to analyze the relations of different Scarabaeidae including B. prasinus. Additionally, it has been found that there is a sizable sex-biased expression in different ORs in B. prasinus. In other words, male and female B. prasinus have differing levels of specific ORs which likely provides important information on the behavior and reproductive habits of the species; however, more data is needed on the subject. It has also been suggested that ORs play a role in detecting plant volatiles, a process that is crucial to the feeding habits of insects like B. prasinus.^[7]

Olfactory receptor neurons (ORNs) in scarab beetles like Brachysternus prasinus and Hylamorpha elegans are key to detection of different smells as well. ORNs are specifically tuned to recognize enantiomeric pheromones. Additionally, pheromone-degrading enzymes are present in the antenna of scarab beetles.^[8] These enzymes show high substrate specificity which is thought to allow these beetles to deactivate certain pheromones and odorants but not others. These pheromones and pheromone-degrading enzymes are key to the chemical communication of scarab beetles,^[8] about which not much is currently known.^[9]

Brachysternus prasinus are part of the family Scarabaeidae, which is a highly diverse family but many of these insects have become considered pests to farmers and scientists.^[10] B. prasinus are viewed as subterranean pests. These beetles can cause damage through their laval feeding habits on the roots of crops as well as adult feedings on the above ground portions of plants.^[10] As a result, B. prasinus are important in regard to South American agriculture as well as the Chilean economy.^[7] B. prasinus have been known to cause immense damage to crops of wheat, especially Triticum aestivum, as well as red clover (Trifolium pratense).^[9] These pests have been difficult for farmers and agriculturalists to control because it is hard to determine larval positions in the soil. Additionally, it is difficult to predict the activity of these beetles at night. Several different possible solutions have been proposed to diminish the effects of these beetle pests on crop outputs including chemical and biological controls. Chemical control entails using specific chemicals as pest repellent. Biological control entails the manipulation of different pathogens and sex pheromones of scarabs.^[10]