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Article

Size of Openings in Water-Holding Containers: Impact on Oviposition by Culex (Culex) Mosquitoes

Florida Medical Entomology Laboratory, Department of Entomology and Nematology, University of Florida-IFAS, 200 9th St. S.E., Vero Beach, FL 32962, USA
*
Author to whom correspondence should be addressed.
Insects 2019, 10(9), 257; https://doi.org/10.3390/insects10090257
Submission received: 30 July 2019 / Revised: 12 August 2019 / Accepted: 16 August 2019 / Published: 21 August 2019
(This article belongs to the Special Issue Vector Biology and Ecology)

Abstract

:
To assess how a grate covering a catch basin impacts oviposition by Culex mosquitoes, a field study was conducted in south Florida using containers with two types of covers, with openings of equal area, but different configurations. One opening mimicked a catch basin grate with 16 small openings, while the other cover had just one large opening. The number and presence of egg rafts in six of each container and cover combination was recorded over 18 nights at two field sites, consisting of a wastewater management facility area and residential subdivision. Three mosquito species, all belonging to the subgenus Culex accounted for more than 99% of total egg rafts collected: Culex nigripalpus (n = 1766), Culex quinquefasciatus (n = 754) and Culex coronator (n = 526). Approximately 90% of Cx. nigripalpus and Cx. coronator egg rafts were deposited in the containers with the large opening cover; whereas more Cx. quinquefasciatus egg rafts were laid in the containers with small opening covers than those of Culex nigripalpus and Culex coronator combined. Similar patterns of egg laying activity were noted at each sampling stations. These results suggest that for locating oviposition sites Culex quinquefasciatus may rely more on olfactory clues, while other Culex species depend more on visual clues.

1. Introduction

Culex nigripalpus Theobald and Culex quinquefasciatus Say are the most common Culex (Culex) mosquitoes in south Florida where they occur in a wide variety of aquatic habitats, such as, roadside swales, ponds, and numerous types of containers [1,2]. The females of both species will utilize highly nutrient-rich microhabitats as oviposition sites [3,4]. In small natural and man-made containers, for example cemetery vases and tank bromeliads, the immatures of Culex quinquefaciatus usually are much more abundant than those of Culex nigripalpus [5,6]. When two types of ovitraps were used to assess seasonal activity patterns of four species of Culex mosquitoes, Culex quinquefasciatus laid approximately equal numbers of egg rafts in both types of traps; whereas Culex nigripalpus deposited more than 90% of their egg rafts in the larger of two traps [7]. Identifying the specific factors responsible for trap selection by the two species is difficult because the traps varied not only in size, but also in shape and in the amount of nutrient rich water.
Containers baited with hay infusion or some other type of attractant are important components of gravid traps [8] and increasing both container and aperture size may result in improved capture rates for some species [9]. Distinguishing the impact of container size versus aperture size on mosquito collections can be problematic since larger containers often have larger apertures [10]. Storm water catch basins are an exception to this general pattern, because mosquitoes often must pass through the rather small openings for the size of each catch basin in the metal grates that cover catch basins. In south Florida, immatures of Culex quinquefaciatus are usually much more common than those of Culex nigripalpus in catch basins, even though these are relatively large containers [11].
The current study was designed to test the hypothesis that container aperture size influences Culex oviposition behavior in south Florida. A primary goal of this research was to acquire information that could be used to develop improved gravid traps, particularly for capturing Culex nigripalpus.

2. Materials and Methods

Experiments were conducted in Indian River County, FL at two field sites that were recommended by personnel from the Indian River Mosquito Control District. Culex (Culex) mosquitoes were abundant at both sites during the summer months (Figure 1). Site A was at the county’s west regional wastewater treatment facility wetlands (N 27.6170980, W 80.502280) where several ponds with various types of aquatic plants were being used to improve water quality conditions. Site B (N 27.5992620, W 80.4738990) was in subdivision with many undeveloped lots. Nearby was a citrus processing plant that used a spray field for the disposal of untreated wastewater.
For each site, an ovitrap was placed at six collecting stations that were separated by at least 30 meters. Most of the traps were located in safe, shaded areas to protect them from mowing machines and other types of disturbances. The ovitraps were black plastic vats (47cm L × 35 cm W × 13cm D) covered with a piece of black painted plywood (61 cm L × 48cm W × 1.2 cm D). One type of cover had just one large opening (ca. 600 cm2), while the other had 16 small openings (2.5cm L × 15.5cm W), a configuration mimicking what is typically found in grates covering stormwater catch basins (Figure 2). The total amount of opening space in two types of covers was equivalent (ca. 600 cm2). Covers were secured to the vats using strips of Velcro.
To attract gravid Culex mosquitoes, ovitraps were baited with 3.8 L of hay infusion, which was prepared with 5 g of hay and 130 mg liver powder/yeast mix (1:6) in 3.8 L of water and held for 3 days before being placed in an ovitrap. New hay infusion was added to the ovitraps just prior to each nightly sampling session. Sampling for egg rafts was conducted from July 15 to August 15, 2014, for total 18 days. For each station, half the ovitrap collections were taken using the cover with the large opening and half of the collections were taken using the cover with small openings. On any given collection date, three ovitraps at each site had a cover with a large opening and three ovitraps had a cover with small openings. Cover types were rotated so that on each successive collection date ovitraps had a different type of cover.
After each nightly collection, the deposited egg rafts in each vat were transferred individually in vials and stored in a bioclimatic chamber. Once the eggs hatched, the larvae were identified to species using local and regional guides [12,13].
The relationships inter-site variation and ovitrap cover types were analyzed by analysis of variance (ANOVA) to evaluate effects of each independent variable (vat opening types, sites, and time) on the number of egg rafts across three species.

3. Results

We obtained 3059 egg rafts throughout the study belonging to five species of Culex, subgenus Culex. The collected species were Culex nigripalpus, Culex quinquefasciatus, Culex coronator, Culex salinarius, and Culex interrogator. Most egg rafts were identified as Cx. nigripalpus (n = 1768, 57.8%), Cx. quinquefasciatus (n = 754, 24.6%), and Cx. coronator (n = 484, 16.4%). Among the egg rafts we collected, were two egg rafts of Cx. salinarius and three egg rafts of Cx. interrogator. In general, the number of egg rafts varied by opening type, site and date for the most common species (Table 1). Large numbers of egg rafts were collected on some occasions, with maximum numbers of egg rafts from any single container being 34, 164, and 32 for Cx. coronator, Cx. nigripalpus, and Cx. quinquefasciatus, respectively.
Among these Culex species, we found significantly more egg rafts in vats with the large opening (Table 1). The number of egg rafts of Cx. nigripalpus was a greater in vats with the single large opening (1614/1768) compared with other Culex species (Cx. quinquefasciatus: 477/754, Cx. coronator: 475/527). We found more egg rafts in vats with the large opening among these Culex species. However, the proportion of egg rafts of Cx. quinquefasciatus (477/754) in these vats was smaller than the other two Culex species (Cx. nigripalpus 1614/1768, Cx. coronator: 475/527) (Figure 3).
All the Culex species sampled during this study laid more egg rafts in the large opening vats (p < 0.0001). The oviposition behavior of Cx. nigripalpus was not affected by the sites or days, yet Cx. coronator was more abundant at site A than site B (p = 0.0031) but consistent during the experiment period. The total number of egg rafts at sites A and B was 195 and 289, respectively. Although Cx. quinquefasciatus was affected by all the tested factors, cover openings affected this species less than other factors (Table 1).

4. Discussion

Two of the five Culex species collected during this study are relatively new introductions to Florida. Cx. coronator was first detected in the northwest Florida in 2005 [14]. Within a few years it had spread throughout the state [15], occurring in aquatic habitats similar to those utilized by Cx. nigripalpus. In 2013, Cx. interrogator larvae were collected from a stormwater catch basin in Broward County. More recently, adults and immatures of this species have been collected in three additional counties in peninsular Florida [16]. Mosquito surveillance activities conducted by the Indian River Mosquito Control District during 2014 encountered relatively few Culex interrogator, especially when compared to collections of Cx. nigripalpus and Cx. coronator (Shroyer per. comm.). The scarcity of adult Cx. interrogator is the most likely reason why only few egg rafts of this species were collected. Cx. salinarius is a common mosquito in north Florida where it is most active during the spring; whereas in the southern part of the state this mosquito is less abundant and usually inactive during the summer months. These factors undoubtedly contributed to the paucity of Cx. salinarius egg rafts in our collections.
The land around our two study sites used to be dominated by citrus groves; however, many of them have been taken out of production. The abandoned citrus farms have been turned in pastures or cleared of trees for future residential developments (Figure 1). Due to a high-water table and poorly drained soils, most citrus trees in Indian River County are planted on raised beds usually two rows of trees with a drainage/irrigation ditch in between rows of citrus trees. These ditches often become a major source of mosquito production, particularly following major rainfall events or during an extended dry period when the ditches are flooded for irrigation [17]. Even when groves are abandoned, the ditches often persist, without proper maintenance, in pastures and in undeveloped tracts of land where they continue to provide aquatic habitats for Cx. nigripalpus, Cx. coronator and other mosquito species. Immatures of Cx. quinquefaciatus are not very common in these ditches, probably because the nutrient load in the water is usually not high enough to attract gravid females. Significantly more Cx. quinquefaciatius egg rafts were collected at Site B (subdivision: total 441 egg rafts) than at site A (wastewater wetlands: total 300 egg rafts). A spray field near site B was located around Citrus Packers (Figure 1) and receiving untreated wastewater from a citrus processing plant during the winter and spring just prior to the start of the current study (personal communication). This field and some nearby paddocks with small ponds, were likely the major production areas for the Cx. quinquefasciatus that deposited egg rafts in the ovitraps a Site B (Figure 1). By contrast, at Site A, the wastewater received a primary and a secondary treatment before being added to the constructed wetlands, hence this aquatic system was essentially unsuitable for Cx. quinquefasiatus.
Mosquitoes use both visual and olfactory cues to locate and select suitable oviposition sites [18,19,20,21]. Since all ovitraps contained the same amount of hay infusion and the same square centimeters opening to the outside, it seems reasonable to postulate that olfactory cues emanating from the two types traps were equivalent. Therefore, the preponderance of Cx. nigripalpus and Cx. coronator egg rafts in the traps with the one large opening relative to the traps with several small openings would seem to result from a visual response by these mosquitoes (Figure 3). Ovitraps with small openings may hinder the mosquito’s capacity to assess the water surface by acting like a blind. As Cx. quinquefasciatus prefers nutrient-rich aquatic habitats, it may place a greater reliance on olfactory cues than on visual cues when near a potential oviposition site. Metal grates covering stormwater catch basins probably affect these mosquitoes in a similar manner, because grate covers are unlikely to pose a barrier to Cx. quinquefasciatus oviposition.

5. Conclusions

In Florida, Cx. nigripalpus and Cx. quinquefasciatus are the primary vectors of West Nile and St. Louis encephalitis viruses [22,23,24,25]. The recent expansion of Cx. coronator populations throughout the state increases the potential for this mosquito to serve as a vector of West Nile virus [26]. Efforts to develop better gravid traps for mosquito and arbovirus surveillance have been focused mainly on various types of infusions and related attractant and the lesser extent other features of the traps [9,27,28,29,30,31]. Generally gravid traps capture far more Cx. quinquefasciatus females than Cx. nigripalpus females even during the summer months in areas where Cx. nigripalpus populations are more abundant than those of Cx. quinquefasciatus [29]. Commercially available gravid traps for Cx. mosquitoes have rather large collecting devises directly above the water-holding container. By either making these samplers smaller or by redeploying them to the side of the container may allow for enhanced collections of Cx. nigripalpus without adversely impacting collections of Cx. quinquefasciatus.

Author Contributions

G.F.O. and D.S. conceived and designed the experiments; G.F.O., D.S. and A.C. performed the experiments; G.F.O. and D.S. analyzed the data; G.F.O. and D.S. wrote the paper.

Funding

This study was supported by the Florida Department of Agriculture and Consumer Services (Project # 00117166: contract # 00080912), subcontract to D. Shin.

Acknowledgments

We thank D. Shroyer and B. Peery for advice on study sites. We also appreciate J. Day, C. Smartt, and N. Burkett-Cadena for commenting on the early version of this manuscript.

Conflicts of Interest

All authors declare no conflict of interest.

References

  1. Provost, M.W. The Natural History of Culex Nigripalpus. In St. Encephalitis in Florida; Florida State Board of Health Monograph Series: Jacksonville, FL, USA, 1969; Volume 12, pp. 46–62. [Google Scholar]
  2. Rey, J.R.; O’Meara, G.F.; O’Connell, S.M.; Cutwa-Francis, M.M. Mosquito production from four constructed treatment wetlands in peninsular Florida. J. Am. Mosq. Control Assoc. 2006, 22, 198–205. [Google Scholar] [CrossRef]
  3. O’Meara, G.F.; Evans, F.D.S. Seasonal Patterns of Abundance among three species of Culex mosquitoes in a south florida wastewater lagoon. Ann. Entomol. Soc. Am. 1983, 76, 130–133. [Google Scholar] [CrossRef]
  4. O’Meara, G.F.; Cutwa-Francis, M.; Rey, J.R. Seasonal variation in the abundance of Culex nigripalpus and Culex quinquefasciatus in wastewater ponds at two Florida dairies. J. Am. Mosq. Control Assoc. 2010, 26, 160–166. [Google Scholar] [CrossRef]
  5. O’Meara, G.F.; Cutwa, M.M.; Evans, L.F. Bromeliad-inhabiting mosquitoes in south Florida: Native and exotic plants differ in species composition. J. Vector Ecol. 2003, 28, 37–46. [Google Scholar]
  6. Leisnham, P.T.; LaDeau, S.L.; Juliano, S.A. Spatial and temporal habitat segregation of mosquitoes in urban Florida. PLoS ONE 2014, 9, e91655. [Google Scholar] [CrossRef] [PubMed]
  7. O’Meara, G.F.; Vose, F.E.; Carlson, D.B. Environmental factors influencing oviposition by Culex (Culex) (Diptera: Culicidae) in two types of traps. J. Med. Entomol. 1989, 26, 528–534. [Google Scholar] [CrossRef]
  8. Reiter, P. A portable battery-powered trap for collecting gravid Culex mosquitoes. Mosq. News 1983, 43, 496–498. [Google Scholar]
  9. Popko, D.A.; Walton, W.E. Large-volume gravid traps enhance collection of culex vectors. J. Am. Mosq. Control Assoc. 2016, 32, 91–102. [Google Scholar] [CrossRef]
  10. Derraik, J.G.; Slaney, D. Container aperture size and nutrient preferences of mosquitoes (Diptera: Culicidae) in the Auckland region, New Zealand. J. Vector Ecol. 2005, 30, 73–82. [Google Scholar]
  11. Rey, J.R.; O’Meara, G.F.; O’Connell, S.M.; Cutwa-Francis, M.M. Factors affecting mosquito production from stormwater drains and catch basins in two Florida cities. J. Vector Ecol. 2006, 31, 334–343. [Google Scholar] [CrossRef]
  12. Haeger, J.S.; O’Meara, G.F. Separation of 1st-instar larvae of 4 Florida Culex (Culex). Mosq. News 1983, 43, 76–77. [Google Scholar]
  13. Darsie, R.F.; Ward, R.A. Identification and Geographical Distribution of the Mosquitoes of North America, North of Mexico; University of Florida Press: Gainesville, FL, USA, 2005; p. 383. [Google Scholar]
  14. Smith, J.P.; Walsh, J.D.; Cope, E.H.; Tennant, R.A.; Kozak, J.A.; Darsie, R.F. Culex coronator dyar and knab: A new Florida species record. J. Am. Mosq. Control Assoc. 2006, 22, 330–332. [Google Scholar] [CrossRef]
  15. Connelly, C.R.; Alto, B.W.; O’Meara, G.F. The spread of Culex coronator (Diptera: Culicidae) throughout Florida. J. Vector Ecol. 2016, 41, 195–199. [Google Scholar] [CrossRef] [PubMed]
  16. Shin, D.; O’Meara, G.F.; Civana, A.; Shroyer, D.A.; Miqueli, E. Culex interrogator (Diptera: Culicidae), a mosquito species new to Florida. J. Vector Ecol. 2016, 41, 316–319. [Google Scholar] [CrossRef]
  17. Day, J.F.; Curtis, G.A. When It Rains, They Soar—and That Makes Culex Nigripalpus a Dangerous Mosquito. Am. Entomol. 1994, 40, 162–167. [Google Scholar] [CrossRef]
  18. Allan, S.A.; Day, J.F.; Edman, J.D. Visual ecology of biting flies. Annu. Rev. Entomol 1987, 32, 297–316. [Google Scholar] [CrossRef]
  19. Bentley, M.D.; Day, J.F. Chemical ecology and behavioral aspects of mosquito oviposition. Annu. Rev. Entomol. 1989, 34, 401–421. [Google Scholar] [CrossRef] [PubMed]
  20. Beehler, J.W.; Millar, J.G.; Mulla, M.S. Synergism between chemical attractants and visual cues influencing oviposition of the mosquito, Culex quinquefasciatus (Diptera: Culicidae). J. Chem. Ecol. 1993, 19, 635–644. [Google Scholar] [CrossRef] [PubMed]
  21. Day, J.F. Mosquito Oviposition Behavior and Vector Control. Insects 2016, 7, 65. [Google Scholar] [CrossRef]
  22. Day, J.F.; Curtis, G.A.; Edman, J.D. Rainfall-directed oviposition behavior of Culex nigripalpus (Diptera: Culicidae) and its influence on St. Louis encephalitis virus transmission in Indian River County, Florida. J. Med. Entomol. 1990, 27, 43–50. [Google Scholar] [CrossRef]
  23. Richards, S.L.; Mores, C.N.; Lord, C.C.; Tabachnick, W.J. Impact of extrinsic incubation temperature and virus exposure on vector competence of Culex pipiens quinquefasciatus Say (Diptera: Culicidae) for West Nile virus. Vector Borne Zoonotic Dis. 2007, 7, 629–636. [Google Scholar] [CrossRef]
  24. Richards, S.L.; Lord, C.C.; Pesko, K.; Tabachnick, W.J. Environmental and biological factors influencing Culex pipiens quinquefasciatus Say (Diptera: Culicidae) vector competence for Saint Louis encephalitis virus. Am. J. Trop Med. Hyg. 2009, 81, 264–272. [Google Scholar] [CrossRef]
  25. Day, J.F.; Tabachnick, W.J.; Smartt, C.T. Factors That Influence the Transmission of West Nile Virus in Florida. J. Med. Entomol. 2015, 52, 743–754. [Google Scholar] [CrossRef]
  26. Alto, B.W.; Connelly, C.R.; O’Meara, G.F.; Hickman, D.; Karr, N. Reproductive biology and susceptibility of Florida Culex coronator to infection with West Nile virus. Vector Borne Zoonotic Dis. 2014, 14, 606–614. [Google Scholar] [CrossRef]
  27. Reisen, W.K.; Meyer, R.P. Attractiveness of selected oviposition substrates for gravid Culex tarsalis and Culex quinquefasciatus in California. J. Am. Mosq. Control Assoc. 1990, 6, 244–250. [Google Scholar]
  28. Isoe, J.; Beehler, J.W.; Millar, J.G.; Mulla, M.S. Oviposition responses of Culex tarsalis and Culex quinquefasciatus to aged Bermuda grass infusions. J. Am. Mosq. Control Assoc. 1995, 11, 39–44. [Google Scholar]
  29. Allan, S.A.; Kline, D. Evaluation of various attributes of gravid female traps for collection of Culex in Florida. J. Vector Ecol. 2004, 29, 285–294. [Google Scholar]
  30. Burkett-Cadena, N.D.; Mullen, G.R. Field comparison of Bermuda-hay infusion to infusions of emergent aquatic vegetation for collecting female mosquitoes. J. Am. Mosq. Control Assoc. 2007, 23, 117–123. [Google Scholar] [CrossRef]
  31. Kesavaraju, B.; Kiyoguchi, D.; Dickson, S. Efficacy of gravid traps in trapping Culex pipiens. J. Am. Mosq. Control Assoc. 2011, 27, 320–322. [Google Scholar] [CrossRef]
Figure 1. Locations of the oviposition traps: (A) Wastewater management facility area; (B) Bella Terra: residential subdivision.
Figure 1. Locations of the oviposition traps: (A) Wastewater management facility area; (B) Bella Terra: residential subdivision.
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Figure 2. Vats with two different covers for characterizing Culex spp. oviposition behavior. (A) Hay infusion water in a vat.; (B) Ovitrap cover with storm drain type openings; (C) Ovitrap cover with a single large opening.
Figure 2. Vats with two different covers for characterizing Culex spp. oviposition behavior. (A) Hay infusion water in a vat.; (B) Ovitrap cover with storm drain type openings; (C) Ovitrap cover with a single large opening.
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Figure 3. Average number of egg rafts deposited by three Culex species in containers with two cover types, at sites A and B. Covers had 16 small openings or one large opening of equivalent total opening area. Bars represent standard error of the mean.
Figure 3. Average number of egg rafts deposited by three Culex species in containers with two cover types, at sites A and B. Covers had 16 small openings or one large opening of equivalent total opening area. Bars represent standard error of the mean.
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Table 1. Effect of cover opening configuration (top), site, and collection day (time) on oviposition in three Culex species using ANOVA.
Table 1. Effect of cover opening configuration (top), site, and collection day (time) on oviposition in three Culex species using ANOVA.
SourceSpeciesSum of SquaresTotal NumberProb > F
Opening TypeCx. nigripalpus9491.352928.3308<0.0001
Cx. coronator646.0412633.1189<0.0001
Cx. quinquefasciatus138.24096.96720.0089
SiteCx. nigripalpus7783.32182.11200.0209
Cx. coronator575.738902.68320.0031
Cx. quinquefasciatus1724.66557.9019<0.0001
TimeCx. nigripalpus713.75042.13050.1459
Cx. coronator10.858750.55670.4565
Cx. quinquefasciatus393.128119.8132<0.0001

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MDPI and ACS Style

Shin, D.; O’Meara, G.F.; Civana, A. Size of Openings in Water-Holding Containers: Impact on Oviposition by Culex (Culex) Mosquitoes. Insects 2019, 10, 257. https://doi.org/10.3390/insects10090257

AMA Style

Shin D, O’Meara GF, Civana A. Size of Openings in Water-Holding Containers: Impact on Oviposition by Culex (Culex) Mosquitoes. Insects. 2019; 10(9):257. https://doi.org/10.3390/insects10090257

Chicago/Turabian Style

Shin, Dongyoung, George F. O’Meara, and Ayse Civana. 2019. "Size of Openings in Water-Holding Containers: Impact on Oviposition by Culex (Culex) Mosquitoes" Insects 10, no. 9: 257. https://doi.org/10.3390/insects10090257

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