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scientific name: Culex coronator (Dyar & Knab) (Insecta: Diptera: Culicidae)

Introduction - Distribution - Description - Life Cycle and Biology - Medical Importance - Surveillance - Selected References


Introduction (Back to Top)

Culex coronator (Figure 1) is a neotropical mosquito that was first described in Trinidad by Dyar and Knab in 1906 (Akaratovic and Kiser 2017, ITIS 2020). Coronator means ‘crown’ in Latin, which refers to the unique crown of spines found on the tip of the larval siphon of this mosquito species. Culex coronator is a common species collected throughout Mexico, Central America, and South America (Martinez-Palacios 1952, Carpenter and Lacasse 1955). Recently expanding its range northward into the continental United States, Culex coronator has also been documented sporadically in most southern states, with widespread distributions in eastern Texas, Florida, Georgia, and South Carolina. Culex coronator’s recent rapid range expansion throughout the southern United States may pose a public health risk since St. Louis Encephalitis virus (SLEV), West Nile (WNV), and Zika virus (ZIKV) have been isolated from wild Culex coronator mosquitoes (Aitken et al. 1964, Mackay et al. 2008, Unlu et al. 2010, Elizondo-Quironga et al. 2018). Additionally, the potential for Culex coronator to transmit SLEV and WNV has been shown (Hammon and Reeves 1943, Alto et al. 2014). However, Culex coronator’s role in their transmission cycles in nature is not clearly understood.


Figure 1. Lateral view of an adult female Culex coronator mosquito. Photograph by Nathan D. Burkett-Cadena, University of Florida.

Figure 1. Lateral view of an adult female Culex coronator mosquito. Photograph by Nathan D. Burkett-Cadena, University of Florida.


Culex coronator is one of five species in the Culex coronator complex of the subgenus Culex (Linnaeus) 1758. The other four species in this complex are Culex camposi (Dyar) 1925, Culex ousqua Dyar 1918, Culex usquatissmus Dyar 1922 and Culex usquatus Dyar 1918. This complex is well-distributed throughout Central and South America (Akaratovic and Kiser 2017).



Distribution (Back to Top)

Culex coronator is found throughout much of the southern United States and all countries from the US to Argentina (Martinez-Palacios 1952, Carpenter and Lacasse 1955, Rossi and Vezzani 2011, Sames et al. 2021; Figure 2). Culex coronator was first collected in the U.S. in 1920 in San Benito, Texas and is currently found in Alabama, Arizona, Arkansas, Florida, Georgia, Louisiana, Mississippi, New Mexico, North Carolina, Oklahoma, South Carolina, Tennessee, Texas, and Virginia (Dyar 1921, Darsie and Ward 2005, Smith et al. 2006, Akaratovic and Kiser 2017, Trimm et al. 2017, Sames et al. 2019, Wilke et al. 2020, Sames et al. 2021). Culex coronator was first reported in Florida in the western panhandle in 2005 and has since been documented in all 67 counties (Smith et al. 2006, Connelly et al. 2016, Sames et al. 2021, Boehmler et al. 2022).


Figure 2. Major global regions (shaded in red) where Culex coronator has been identified. Map created using mapchart.net by Sierra M. Schluep, University of Florida.

Figure 2. Major global regions (shaded in red) where Culex coronator has been identified. Map created using mapchart.net by Sierra M. Schluep, University of Florida.


Description (Back to Top)

Adults: Similar to other Culex mosquitoes, Culex coronator is brownish in color, has a blunt abdomen, and narrow wing scales. This species is a part of the Culex coronator complex, which shares morphological traits in most life stages. Molecular methods in conjunction with morphological taxonomy are typically needed to accurately identify specimens to species level. However, Laurito et al. (2018) provides a detailed assessment for distinguishing species in the complex using male genitalia. Prior studies have used the methods described in Laurito et al. (2018) to confirm that Culex coronator is the species that has expanded its distribution into the southern United States, suggesting other members of the complex have remained south of the border (Akaratovic and Kiser 2017).

Like other members of its subgenus, adult females of Culex coronator possess acrostichal setae (a row of setae arising from the central mid-line of the thorax; Figure 3), narrow, decumbent scales on their occiput (back of the head; Figure 3), and abdominal terga (the dorsal plates of each abdominal segment) with pale bands or patches along their basal boarders (Figures 3 and 4).


Figure 3. Dorsal view of an adult female Culex coronator showing acrostichal setae, the occiput with narrow, flat scales, and abdominal terga with basal pale bands. Illustrations by Nathan D. Burkett-Cadena, University of Florida.

Figure 3. Dorsal view of an adult female Culex coronator showing acrostichal setae, the occiput with narrow, flat scales, and abdominal terga with basal pale bands. Illustrations by Nathan D. Burkett-Cadena, University of Florida.


Figure 2. Guava root-knot nematode Meloidogyne enterolobii females are white and pear-shaped. Photograph by Will Rutter, USDA-ARS. Used by permission

Figure 4. Lateral view of an adult female Culex coronator. Photograph by Sierra M. Schluep, University of Florida.


Adult females of Culex coronator can be differentiated from almost all other members of the subgenus Culex in Florida by the presence of distinct basal and apical bands of pale scales on the tarsomeres of the hind legs (Figure 5). Additionally, the most apical hindleg tarsomere, hind tarsomere 5, has rings of pale scales both basally and apically with a band of dark scales in between (Figure 5). Culex coronator adults could be potentially confused with the adults of two other Culex species found in Florida that possess pale banding on the hind tarsi, Culex bahamensis Dyar and Knab and Culex tarsalis Coquillett. However, Culex coronator can be distinguished from Culex bahamensis and Culex tarsalis by the lack of a complete band of pale scales on the proboscis. Rather than a complete band, Culex coronator possesses a patch of pale scales on the underside of the proboscis (Figure 6). Also, the pleuron (lateral aspect of the thorax) of Culex coronator has alternating bands of dark and pale integument, giving the thorax a somewhat striped appearance (Figures 4 and 6).


Figure 3. Meloidogyne male at 400x magnification. Males are worm-shaped with rounded heads and tails. Photograph by Zane Grabau, University of Florida.

Figure 5. Adult female Culex coronator hindleg and close-up view of tarsomere 5 of the hind leg. Photograph by Nathan D. Burkett-Cadena, University of Florida.


Figure 6. Lateral view of an adult female Culex coronator, showing patch of pale scales on underside of proboscis (arrow). Photograph by Nathan D. Burkett-Cadena, University of Florida.

Figure 6. Lateral view of an adult female Culex coronator, showing patch of pale scales on underside of proboscis (arrow). Photograph by Nathan D. Burkett-Cadena, University of Florida.


Larvae: Culex coronator larvae have an elongate siphon (siphon index: 4.5-5.5) with an apical (at the tip) ring or crown of spines (Figure 7), a feature which differentiates the larvae of this mosquito from all other mosquitoes in Florida. On the head of Culex coronator larvae, seta 6-C (a hair-like structure located on the larval head) has 3 or more branches, like other members of the subgenus Culex. The pecten, a row of small spine-like structures on the siphon, are confined to the basal third of the siphon (Figure 7).


Figure 6. Lateral view of an adult female Culex coronator, showing patch of pale scales on underside of proboscis (arrow). Photograph by Nathan D. Burkett-Cadena, University of Florida.

Figure 7. Fourth instar larva of Culex coronator. A ring or crown of spines is visible near the terminal end of the siphon. Photograph by Nathan D. Burkett-Cadena, University of Florida.


Life Cycle and Biology (Back to Top)

Culex coronator mosquitoes possess a holometabolous (complete) life cycle containing four stages: eggs, larvae, pupae, and adults.

Eggs: An adult female Culex coronator lays eggs in a single clump, forming a floating egg raft with specialized structures that allow the eggs to remain vertically upright. Eggs in a raft typically hatch shortly after embryonic development is complete because they are generally not desiccation-resistant like some mosquito species in other genera, such as Aedes or Psorophora. The source of the blood meal may influence the number of eggs in a raft laid by Culex coronator, with avian blood meals producing a greater number of eggs than mammalian blood meals (Alto et al. 2014).

Larvae: Mosquito larvae pass through four instars (stages), growing in size during each instar. The list of potential Culex coronator larval habitat sites is diverse. Larvae may be found in stagnant or slow-moving ground pools and seeps, artificial containers, ditches, culverts, tire ruts, ground depressions, and even dredge sites (Dyar and Knab 1906, Pecor et al. 2002, Varnado et al. 2012, Alto et al. 2014, Yee and Skiff 2014, Sames et al. 2019). According to Connelly et al. (2016), Culex coronator larvae are found more commonly in open, sunlit aquatic habitats compared to those in shaded locations. Sames et al. (2019) found that in June to early September larvae favor partially shaded areas, while in late September to the end of the larval season, larvae can be found in larval habitats in full sun.

Because of its ability to occupy artificial containers in sunlit or partially shaded areas, Culex coronator has been documented co-occurring in larval habitats with medically significant mosquito species like Aedes albopictus, Culex nigripalpus, Culex quinquefasciatus, Culex restuans, and Culex salinarius (Moulis et al. 2008, Varnado et al. 2012, Yee et al. 2012, Alto et al. 2014). Yee and Skiff (2014) found that Culex coronator larvae have higher survivorship rates and faster developmental rates when supplied with a mixture of animal waste and leaf litter as opposed to leaf litter alone. Yee and Skiff (2014) also performed a competitive study between Culex coronator, Culex quinquefasciatus, and Aedes albopictus larvae and showed that Culex coronator developed and survived at similar rates as Culex quinquefasciatus. However, Culex coronator larval survivorship was reduced by 50% when reared with Aedes albopictus larvae. These results suggest that as larvae, Culex coronator may not be likely to outcompete Aedes albopictus but should not be negatively impacted by Culex quinquefasciatus (Yee and Skiff 2014).

Pupae: The mosquito pupa is a transitional stage between the larval stage and the adult stage. Pupae do not eat and generally reside at the surface of the water except when diving to avoid potential predators.

Adults: Adult Culex coronator mosquitoes are primarily active after dusk and are not typically known to enter houses (Moulis et al. 2008, Wilke et al. 2020). Adults are primarily mammalian blood feeders. Blood meals are frequently obtained from white-tailed deer, though other mammalian hosts like racoons, humans, horses, dogs, and cats have also been identified (Roberts and Hsi 1979, Brauch 2008, Mackay et al. 2010). In addition to taking blood meals from mammals, Culex coronator occasionally feeds on birds (Mackay et al. 2010). During times of drought when suitable oviposition (egg-laying) sites may be limited, gravid Culex coronator females can delay oviposition for several weeks, typically laying eggs following a rainfall event (Mackay et al. 2010). Culex coronator mosquitoes are known to overwinter as adults (Varnado et al. 2012).


Medical Importance (Back to Top)

Culex coronator mosquitoes have been collected from nature infected with SLEV, WNV, and ZIKV (Aitken et al. 1964, Mackay et al. 2008, Unlu et al. 2010, Elizondo-Quironga et al. 2018). Culex coronator has also been found to be a competent laboratory vector of SLEV and WNV (Hammon and Reeves 1943, Mackay et al. 2010, Alto et al. 2014). Though SLEV-, WNV-, and ZIKV-infected Culex coronator mosquitoes have been collected from the wild and their potential to transmit SLEV and WNV within the laboratory has been shown (Hammon and Reeves 1943, Aitken et al. 1964, Mackay et al. 2008, Unlu et al. 2010, Alto et al. 2014, Elizondo-Quironga et al. 2018), host feeding patterns determine the role of mosquitoes in a virus transmission cycle. So far Culex coronator has been found to predominantly take blood meals from white-tailed deer but is known to opportunistically take blood meals from both birds and humans (Roberts and Hsi 1979, Brauch 2008, Mackay et al. 2010). The opportunistic feeding on birds and humans could allow the transmission of SLEV and WNV from birds to humans and, in rare cases, of ZIKV from humans to humans. However, to better understand the role of Culex coronator in the transmission cycle of these viruses, more studies of its feeding behavior and infection prevalence in nature are needed.


Surveillance (Back to Top)

Culex coronator larvae have been successfully collected using cups, dippers, basters, and siphons from natural and artificial ground pool habitats like flooded depressions in fields, natural and concrete roadside ditches, culverts, and abandoned swimming pools as well as artificial container habitats like water troughs, tires, plastic tubs, and barrels (Connelly et al. 2016, Sames et al. 2019 and 2021). Commonly used methods to sample Culex coronator adults include the Centers for Disease Control and Prevention (CDC) miniature light trap baited with dry ice (Figure 8), the CDC gravid trap, and the BG-Sentinel trap (Debboun et al. 2005, Varnado et al. 2005, Goddard et al. 2006, Kelly et al. 2008, Moulis et al. 2008, Noden et al. 2015, Wilke et al. 2019, Wilke et al. 2021). Adults have been captured in many areas including near woodlands, swamps, pastures, neighborhoods, and recently in deforested and highly urbanized areas (Debboun et al. 2005, Varnado et al. 2005, Smith et al. 2006, Moulis et al. 2008, Wilke et al. 2021). In the U.S., Culex coronator can be collected year-round with peak abundance usually observed in the summer and fall months (Akaratovic and Kiser 2017, Wilke et al. 2019, Sames et al. 2021).


Figure 8. A CDC miniature light trap with a cooler containing dry ice hanging above it. Photograph by Eva A. Buckner, University of Florida.

Figure 8. A CDC miniature light trap with a cooler containing dry ice hanging above it. Photograph by Eva A. Buckner, University of Florida.


Selected References (Back to Top)

Authors: Sierra M. Schluep, sschluep@ufl.edu, Nathan D. Burkett-Cadena, nburkettcadena@ufl.edu, Derrick K. Mathias, d.mathias@ufl.edu, and Eva A. Buckner, eva.buckner@ufl.edu, University of Florida.
Photographs and maps: Eva A. Buckner, Nathan D. Burkett-Cadena, and Sierra M. Schluep, University of Florida.
Web Design: Kay Weigel
Publication Number: EENY-794
Publication Date: July 2022

Copyright University of Florida ~ An Equal Opportunity Institution
Featured Creatures Editor and Coordinator: Dr. Elena Rhodes, University of Florida