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Article

Updating Ecological and Behavioral Aspects of the Sandfly Fauna in the Vale do Ribeira Region, São Paulo State, Brazil

by
Byara Freitas Guedes Oliveira
1,
Maria de Fátima Domingos
1,
Fredy Galvis Ovallos
2 and
Vera Lucia Fonseca de Camargo-Neves
3,*
1
Secretaria de Estado da Saúde de São Paulo, Superintendência de Controle de Endemias, Núcleo de Biologia e Comportamento de Vetores de São Vicente, São Vicente 11310-050, SP, Brazil
2
Faculdade de São Paulo—USP, Faculdade de Saúde Pública, Departamento de Epidemiologia, São Paulo 01246-904, SP, Brazil
3
Secretaria de Estado da Saúde de São Paulo, Superintendência de Controle de Endemias—Sucen, Departamento de Epidemiologia e Orientação Técnica, São Paulo 01027-000, SP, Brazil
*
Author to whom correspondence should be addressed.
Insects 2021, 12(11), 988; https://doi.org/10.3390/insects12110988
Submission received: 14 September 2021 / Revised: 25 October 2021 / Accepted: 30 October 2021 / Published: 2 November 2021
(This article belongs to the Special Issue Insect Vector-Focused Approaches for Disease Control)
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Abstract

:

Simple Summary

Analyzing the biological and ecological characteristics of arthropods constitutes the basis for the entomological surveillance of vector-borne diseases. This is accomplished in order to implement vector surveillance and control programs. Thus, with the objective to update the distribution of sandflies in the main transmission region of cutaneous leishmaniasis in the state of São Paulo, we carried out a study of fauna in a modified environment, considering its environmental characteristics and climatic variables. Ecological indices such as richness, abundance, diversity, and equitability of the sandfly fauna in the region are presented.

Abstract

Some ecological parameters and the distribution of vectors in the municipality of Eldorado, Vale do Ribeira Region, São Paulo, were studied. Entomological surveys were carried out from September 2019 to March 2021. It was observed that a few ecological parameters, including richness, abundance, diversity, and equitability, were typical of a modified environment, where artificial ecotopes maintain the presence of sandflies throughout the year. A total of 11,668 sandflies were captured. The presence of five taxa were observed in Eldorado, with low diversity and high dominance of Nyssomyia intermedia next to Ny. neivai, which are sympatric species. The results presented reinforce the importance of these species in anthropized areas in the transmission of cutaneous leishmaniasis (CL) agents and the need for entomological monitoring. Psathyromyia pascalei was encountered for the first time in the municipality, expanding the known area of distribution of this species in a modified environment.

1. Introduction

Cutaneous leishmaniasis (CL) is an infectious non-contagious chronic disease caused by several species of parasites in the genus Leishmania (Kinetoplastida, Trypanosomatidae). In Brazil, the most epidemiologically important species responsible for its dermotropic forms are Leishmania (Viannia) braziliensis (Vianna), Leishmania (Viannia) guyanensis (Floch), and Leishmania (Leishmania) amazonensis (Laison and Shaw). The clinical forms have different characteristics according to the infecting species, such as: cutaneous leishmaniasis (L. guyanensis), mucosal cutaneous leishmaniasis (L. braziliensis), diffuse cutaneous leishmaniasis (L. amazonensis), and disseminated leishmaniasis (L. braziliensis) [1]. The transmission of these parasites depends on the species of sandfly-vectors found in an area and distribution of the reservoir [1].
Sandflies are Diptera (Diptera, Psychodidae, Phlebotominae) whose females are hematophagous. Their average period of adulthood is 20 days, which is sufficient time for successful transmission of the protozoan. The species that have been identified as vectors of CL of the main etiological agent in the state of São Paulo (SSP), Leishmania braziliensis, are Nyssomyia intermedia (Lutz and Neiva), Nyssomyia whitmani (Antunes and Coutinho), Nyssomyia neivai (Pinto), Migonemyia migonei (França), Pintomyia pessoai (Coutinho and Barretto), and Pintomyia fischeri (Pinto) [2].
CL is widely distributed in the tropical and subtropical regions of the world, and Brazil has autochthonous cases in all Brazilian states. According to the Brazilian Ministry of Health (2020), in 2018, the national health notification system (Sinan) had 16,432 reported cases, with the mucosal form accounting for 5.6% of the cases, 6.7% in children under 10 years, with a detection rate of 7.8 cases per 100,000 inhabitants [3].
Between 2007 and 2019, the SSP contained 4577 registered autochthonous cases, with a detection coefficient of 1.0 case/100,000 inhabitants. The disease is a public health problem, given the high percentage of mucous forms that have been notified, which represent 21.4% of the total number of notified cases. The average for the period was 350 cases/year, of which 6.5% were recurring cases and 4.9% were cases in children under 10 years (SES-SP) (Source: SUCEN/CVE/CCD/SES-SP (2021)).
In the Vale do Ribeira, CL has been identified continuously since 1956 after the description of the first autochthonous cases by Forattini and Oliveira (1956) [4]. In the 1950s, after intense deforestation, CL almost disappeared in SSP, reappearing in the 1980s, with a significant increase in the disease [5]. The main vector of Le. braziliensis has been described as Ny. intermedia sensu lato, which has also been the most prevalent species in other regions of SSP [2,6,7,8]. The Vale do Ribeira region remains an important transmission area in the state, with the highest notification of CL cases in SSP (SES-SP). In the period from 1997 to 2019, 22.7% of the cases were reported with the place of infection in at least one of the 15 municipalities in the Vale do Ribeira region (SES-SP) (Camargo-Neves 2020, unpublished data). The municipality of Eldorado represented 15% of the reported cases in this region, thus highlighting its epidemiological importance (Camargo-Neves 2020, unpublished data) and no data reported of the sandfly fauna in this municipality. Whereas the sandfly fauna of the Vale do Ribeira was described as belonging to the Ny. intermedia complex, in this study we update the occurrence of sandfly species in an area of modified environment and ecological aspects of the fauna are analyzed.

2. Materials and Methods

Study area: Entomological surveys were carried out in the rural area of the municipality of Eldorado. This municipality is in the southern region of the ESP (−24.5020 S; −48.0849 W) in the Atlantic Forest biome, at an altitude of 64 m above sea level (Figure 1A). Average temperatures in recent years ranged from lows of 16.1 °C to highs of 25.2 °C (average annual variation of 7.4 °C). During this same period, the annual rainfall index was 1869 mm with a monthly average of 155 mm and annual relative humidity of 85% [9]. According to the last census carried out in 2010 [10], Eldorado has a population of 14,641 inhabitants, with 7205 inhabitants living in urban areas and 7436 (50.7%) in rural areas, indicating the population’s vulnerability considering they live in rural anthropized environments where the transmission cycle of CL occurs. With 1657 km2 and demographic density of 9.6 inhabitant per km2, the municipality is the fourth largest in territorial extension in the state of Sao Paulo. Economic activities include subsistence agriculture and livestock, in addition to plant extraction (banana culture) and tourism. Eldorado is one of the 29 municipalities in São Paulo considered a tourist resort [11,12].
The entomological captures were carried out in a residence located in a rural area called “pé do morro” (foothill), close to a forested area (Figure 1B). The peridomicile contained many domestic animals with the presence of dogs, chickens, and goats.
Entomological Collection: The entomological collections were conducted from September 2019 to March 2021 (except for the months of December/2019 and April/2020), for one night every fortnight. The collections were accomplished in a Shannon trap-type [13] (Figure 1C) tent operated by three catchers for an average period of three hours, starting 30 min after dusk.
The specimens were collected with the aid of a Castro’s aspirator or an electric aspirator (6V) and kept alive in entomological cages, where they were fed with a fructose or sucrose source, until their arrival at the Center for Biology and Behavior of Vectors in São Vicente, from the Endemic Control Superintendence, where they were killed, clarified, and identified according to Galati (2003) [14]. The initial and final temperature and humidity were recorded as well as the presence of animals during the capture period.
Data Analysis: Data were compiled in an Excel® spreadsheet. The variables collected were date, capture time; initial and final temperature and humidity; presence of animals; number of catchers, and the registration of species by sex.
To estimate density, hourly effort per month was calculated, considering the number of catchers, and nights of capture.
The species’ richness, species’ accumulation rate, and statistical abundance analysis were estimated using the EstimateS version 9 statistical package [15]. Richness (S) was calculated as the number of species collected per survey night; the accumulation curve was calculated using the Coleman rarefaction method. The estimate of the true number of species was given by the estimator CHAO 1 and 95% confidence interval. Shannon diversity index (H), Simpson dominance index (λ), and Gini–Simpson equity index (1 − λ) using the statistical package PAST version 4.05 [16] were calculated by the average total number of captured specimens/hour/month for each species for the period in question. The Shannon diversity index was also calculated for each entomological survey, and a species’ accumulation curve was plotted. Spearman’s non-parametric correlation test [17] was used to correlate temperature and humidity with species; scatter plots were plotted in Excel®.

3. Results

In the study period, 11,668 sandflies were captured, of which 6369 were males. The male:female ratio observed was 1:1.25.
The richness (S) was five taxa, with the resulting efficiency from the collection period equal to 100% (CHAO 1 = 5 [5.0 − 5.1]). Figure 2 charts the species accumulation curve considering all the captures conducted.
Of the specimens captured, 73.3% were identified as Ny. intermedia and 25.0% as Ny. neivai (Table 1). The following ecological indices were obtained: diversity H = 0.63; dominance λ = 0.60; and equity 1 − λ = 0.40.
Their seasonality was noted in a prominent peak in 2020, starting in spring and ending in summer, correlated with relative humidity (average of 81.1%) and temperatures around 22.4 °C (Table 2). Although no correlation was observed between the temperature (r = 0.09) and relative humidity (r = −0.34) (Figure 3), there was an increase in the sandflies’ density with higher temperatures and a decrease with the rise of the relative humidity of the air (Figure 3, Figure A1). The total hourly average number of sandflies for a month for Ny. intermedia was 42.6 and 15.0 for Ny. neivai, with the highest values being observed in the spring for both years (Table 2, Figure A1).

4. Discussion

Some ecological parameters and the distribution of vectors in the municipality of Eldorado, Vale do Ribeira Region, São Paulo, were studied. In the study area Ny. intermedia s.s. is the predominant species, which represented 73.3% of the total specimens captured. The high density of Ny. intermedia reinforces the importance of this sandfly species as transmission agent of CL in the area, which has been described by several studies since the mid-1950s [18].
In a modified environment, Ny. intermedia s.l. was appointed as the main vector of L. braziliensis [18,19], mainly due to its high density in anthropized environments. Similar observations were described by Gomes et al. (1980) [20] and by Gomes and Galati (1989) [21], in studies on the adaptive capacity of Ny. intermedia s.l. in artificial ecotopes within the Vale do Ribeira region. However, Marcondes (1996) [22], based on morphological characteristics, observed the existence of two species, Ny. intermedia s.s. and Ny. neivai, so far considered as the same species. Therefore, data presented in this study contributes to the updating of information on these species in CL transmission foci in the state of São Paulo.
In the studied area, the modified environment and the presence of artificial ecotopes dominated by Ny. intermedia s.s. and closely followed by Ny. neivai, which are sympatric species in the coastal region of São Paulo, suggest that the adaptation of these species to the anthropic environment is unchanged. This has been previously observed in other municipalities of the Vale do Ribeira [8,20,21,23,24] as well as in other endemic areas of Brazil [25,26,27,28,29].
According to Andrade-Filho et al. (2006) [30], both species present a remarkable intraspecific and intrapopulational variation gradient; are morphologically very close with similar behavioral aspects, and are collected both in forests and in modified environments. The epidemiological importance of these two species is due to their known anthropophilic characteristic and the natural infection found by several studies [18,31,32,33,34,35,36].
The anthropophilic characteristic can also be attributed to Ny. neivai, given that the collections were conducted using a Shannon trap with humans as bait. In addition, its importance as a vector has been recorded through natural infection by Leishmania (Viannia) sp or Leishmania braziliensis [37,38,39,40]. This taxon, as well as Ny. intermedia, is adapted to the modified environment and can bridge the gap between the natural environment and the altered environment. Casanova et al. (2005) [41], in a marking, capture, and recapture study, found that the largest recapture of Ny. neivai females using Shannon traps exposed in wild and forest edge environments, demonstrating the tendency of this species to remain at the forest’s edge. However, infection is likely to occur when dispersing to the forest environment, as Shannon traps located in peri-domestic habitat support the hypothesis that household transmission results from infected females in an enzootic cycle which probably remain close to the human population [42,43,44].
Two other species of major epidemiological importance were captured. The Migonemyia migonei and Pintomyia fischeri species are known to be present in a modified environment and anthropophilic, as previously described in this region of the Vale do Ribeira in foci of cutaneous leishmaniasis [2,8,21,44]. These species are involved in the transmission of L. braziliensis, and its infection with this parasite has been registered in several endemic regions of Brazil [36,45,46,47,48]. Furthermore, Mi. migonei next to Ny. intermedia and Pi. fischeri have endophilic behavior, and can be infected outside the home and transmit the parasite to humans at home, contributing to the continuing transmission as observed in the municipality of Eldorado.
The finding of Pi. fischeri, even in low abundance, as observed in the studied area, is relevant due to its strong relationship with human habitat—its high anthropophily—which leads to this species being identified as a secondary vector of cutaneous leishmaniasis. In Eldorado, the high density observed of the more prevalent species, such as Ny. intermedia and Ny neivai, may be more favorable to CL transmission, to the detriment of Pi. fischeri, a fact corroborated by Galati et al., (2009) [49]. Nevertheless, its role as a secondary vector cannot be ruled out, since this species was registered with infection of Leishmania (Vianna) flagellated forms in Rio Grande do Sul [50] and its experimental infection has been proven [51]. Among the epidemiologically important vector species of CL, Pi. fischeri was the only one that was not naturally infected in SSP [52] but has been frequently found in high abundance in other areas of CL transmission [2,53].
Furthermore, Mi. migonei is a putative vector of Leishmania infantum [54] along with Pi. fischeri, whose natural infection was recorded by Pita-Ferreira (2005) [36] and experimentally its vectorial capacity demonstrated [55]. In addition, its high anthropophily and their joint distribution with the human cases of visceral leishmaniasis [56] point to the role of these two species of sandflies in the transmission of L. (L). infantum in the absence of Lutzomyia longipalpis. Therefore, the risk of visceral leishmaniasis transmission in the studied area should not be ruled out because the main vector is absent. The introduction of the infection is mainly through domestic dog, which is the main reservoir in the domestic environment and because of the cinophilic characteristic of these species.
The detection for the first time of Psathyromyia pascalei (Coutinho and Barreto) in the municipality of Eldorado is noteworthy even though this species has been observed in other municipalities in the Vale do Ribeira region [57,58]. So far, there is no evidence of its vectorial capacity for the transmission of L. braziliensis [59]. This encounter may reflect the proximity of the forest to the collection site, but also evidence of the domiciliation of the species, which deserves attention. Entomological monitoring should continue to verify future variations in the abundance of this species.
For the ecological indices, the low species diversity (H = 0.63) could be related to the degree of anthropization, and the existence of food sources (domestic animals) enhances the development of species close to the household, as described in the literature [25,27]. Deforestation in the Atlantic Forest region may have favored the adaptation of Ny. intermedia, Ny neivai, Pi. fischeri, and Mi. migonei [42,43]. In this study, the first two species showed dominance, representing 98.8% of the taxa captured (λ = 0.60), corroborating the statement that Ny. intermedia s.l. thrives in a modified environment at the expense of other species. Still considering its role as the main vector of CL in the state of São Paulo, a correlation was observed between the presence of CL cases and the presence of Ny. intermedia s.l., in 88% in the investigated municipalities [2].
The male:female ratio observed was 1:1.25, which was also an expected result for the environment modified by the capture method employed. Gomes et al. (1982) [24] observed that this behavior would be an endogenous mechanism of the species in which males and females would occur in the same proportion, including being captured during copulation, in captures carried out on the ground with human bait. As this behavior has not been observed in another municipality in the region [6], it was perhaps influenced by the capture method used.
The great plasticity of the phlebotomine population was observed throughout the year. The two most abundant species showed greater preference for the periods of the year, with an average relative humidity of 81,1% and average temperatures of 22.4 °C (Table 2). This behavior was also observed by Salomón et al. (2002) [60], in which Ny. intermedia showed peaks of exceptional abundance after the rains, during the prior season. However, its occurrence throughout the year can be favored by the ecotopes present in the peridomicile of the area. The same author [60] highlighted that the behavior of the species can be influenced by microecological characteristics caused by human activity, such as the presence of chicken coops in the study area. As these habitats of sandflies are characterized by small variations in temperature and humidity, the two species could be present throughout the year, notably Ny. intermedia.
Climatic factors, such as temperature, rainfall, and relative humidity have been related with the occurrence of sandflies [24,44,60,61,62,63,64]. Barata et al. (2004) [65] observed the interference of climatic factors on the density population of sandfly in an urban area of the municipality of Porteirinha (Minas Gerais, Brazil), indicating a significant correlation between the number of sandflies captured and rainfall and humidity. However, temperature had no significant effect on the dynamics of these insects in the region, as was observed in Eldorado, SP. Rutledge and Ellenwood (1975) [66] suggest that the seasonality of sandflies is related to the patterns of rainfall distribution that act by modifying breeding conditions. The highest density peak was evidenced between spring and summer in the year 2020, and was also observed in the same period in the previous year but at lower density (Table 2, Figure A1). This was probably due to the high relative humidity, which negatively interfered with the density of Ny intermedia and Ny neivai. The sandflies are commonly found in high densities during the hot and humid months and sometime in drier months [60,63,64]. This behavior (in hot and humid months) is characteristic of Ny intermedia sl in the Vale do Ribeira region [24,44]. Moreover, the preference of Ny. neivai has been described in hot and humid periods in other regions of SSP [27].
Long periods of drought or the rainy season are enough to change the dynamics of sandfly populations, even in these micro-habitats. Although seasonality studies should be conducted for at least two consecutive years to produce reliable and consistent data, reducing the margin of error provided by atypical years, it was only possible to carry out 17 months of capture fortnightly; however, we verified a plateau by the curve of species accumulation after the 9th week of capture (Figure 2) and the expected richness (S = 5) given by the CHAO 1 estimate was the same obtained in the study period. Furthermore, our results are consistent with those of other authors who studied this aspect in other municipalities of the Vale do Ribeira [8,24,49].

5. Conclusions

Five taxa were collected in the studied area in the Vale do Ribeira, and Ny. intermedia and Ny. neivai were the predominant species. The results reinforce the importance of these species in anthropophilic areas in the transmission of CL agents and emphasize the need for entomological surveillance with a goal to detect natural infection of sandflies, especially for the early detection of Leishmania infantum. The encounter of Ps. pascalei stands out, as this was the first time that it was found in the municipality, expanding the distribution area of this species in a modified environment. Future studies could focus on evaluating the circulation of the Leishmania species in those sandflies and evaluating blood feeding patterns.

Author Contributions

Conceptualization, V.L.F.d.C.-N.; methodology, M.d.F.D., V.L.F.d.C.-N.; formal analysis V.L.F.d.C.-N.; investigation B.F.G.O.; resources, V.L.F.d.C.-N., M.d.F.D., B.F.G.O.; data curation B.F.G.O., V.L.F.d.C.-N.; writing—original draft preparation, V.L.F.d.C.-N., B.F.G.O.; writing—review and editing, V.L.F.d.C.-N., F.G.O.; field supervision, M.d.F.D.; project administration, V.L.F.d.C.-N.; funding acquisition, V.L.F.d.C.-N. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Fundação de Amparo à Pesquisa do Estado de São Paulo—Fapesp, grant number 2017/50345-5 and grant number 2018/23161-3 (scholarship B.F.G.O.), and the Superintendência de Controle de Endemias, Secretaria de Estado de Saúde de São Paulo.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We thank Nilton França Mathias and the team that carried out the entomological collections.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A

Insects 12 00988 g0a1 550
Figure A1. Monthly hourly average of sandflies captured and monthly average temperature and relative humidity. Eldorado, SP, September 2019 to March 2021. Note: In the months of December 2019 and April 2020 no surveys were carried out.
Figure A1. Monthly hourly average of sandflies captured and monthly average temperature and relative humidity. Eldorado, SP, September 2019 to March 2021. Note: In the months of December 2019 and April 2020 no surveys were carried out.
Insects 12 00988 g0a1

References

  1. Guimarães, L.H.; Machado, P.R.L.; Lessa, H.A.; Lessa, M.; D’Oliveira, A., Jr.; Carvalho, E.M. Aspectos Clínicos da Leishmaniose Tegumentar. Gaz. Médica Bahia 2005, 75, 66–74. [Google Scholar]
  2. Camargo-Neves, V.L.F.; Gomes, A.C.; Antunes, J.L.F. Correlação da presença de espécies de flebotomíneos (Diptera: Psychodidae) com registros de casos da leishmaniose tegumentar americana no Estado de São Paulo, Brasil. Rev. Soc. Bras. de Med. Trop. 2002, 35, 299–306. [Google Scholar] [CrossRef] [Green Version]
  3. BRASIL. Ministério da Saúde (MS). Casos de Leishmaniose Tegumentar. Brasil, Grandes Regiões e Unidades Federadas. 1990 a 2019. [Internet]. 2019. Available online: https://antigo.saude.gov.br/images/pdf/2020/August/25/LT-Casos.pdf (accessed on 1 March 2021).
  4. Forattini, O.P.; Oliveira, O. Um foco de leishmaniose tegumentar na zona sul do Estado de São Paulo, Brasil. Arq. Fac. Hig. Saúde Pública 1957, 11, 23–34. [Google Scholar] [CrossRef] [Green Version]
  5. Gomes, A.C.; Camargo-Neves, V.L.F. Estratégias e perspectivas de controle da leishmaniose tegumentar americana no Estado de São Paulo, Brasil. Rev. Soc. Bras. Med. Trop. 1998, 31, 553–558. [Google Scholar] [CrossRef] [PubMed]
  6. Da-Silva, L.M.R.; Cunha, P.R. A urbanização da leishmaniose tegumentar americana no município de Campinas—São Paulo (SP) e região: Magnitude do problema e desafios. An. Bras. Dermatol. 2007, 82, 515–519. [Google Scholar] [CrossRef] [Green Version]
  7. Condino, M.L.F.; Sampaio, S.M.P.; Henriques, L.F.; Galati, E.A.B.; Wanderley, D.M.V.; Corrêa, F.M.A. Leishmaniose tegumentar americana: Flebotomíneos de área de transmissão no município de Teodoro Sampaio, região sudoeste do estado de São Paulo, Brasil. Rev. Soc. Bras. Med. Trop. 1998, 31, 355–360. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Domingos, M.F.; Carreri-Bruno, G.C.; Ciaravolo, R.M.C.; Galati, E.A.B.; Wanderley, D.M.V.; Corrêa, F.M.A. Leishmaniose tegumentar americana: Flebotomíneos de área de transmissão, no município de Pedro de Toledo, região sul do Estado de São Paulo, Brasil. Rev. Soc. Bras. Med. Trop. 1998, 31, 425–432. [Google Scholar] [CrossRef] [Green Version]
  9. BRASIL. Climate-Data.org. Clima: Eldorado [Internet]. 2021. Available online: https://pt.climate-data.org/ (accessed on 1 March 2021).
  10. IBGE—Instituto Brasileiro de Geografia e Estatísticas. [Internet]. 2021. Available online: www.ibge.gov.br/cidadesat (accessed on 1 March 2021).
  11. Lepsch, I.F.; Saraiva, I.R.; Donzeli, P.L.; Marinho, M.A.; Sakai, E.; Guillaumon, J.R.; Pfeifer, R.M.; Mattos, I.F.A.; Andrade, W.J.; Silva, C.E.F. Macrozoneamento das Terras da Região do Rio Ribeira de Iguape, SP; Governo do Estado de São Paulo, Secretaria do Agricultura e Abastecimento, Coordenadoria da Pesquisa Agropecuária, Instituto Agronômico: São Paulo, Brasil, 1990; Volume 19, pp. 1–181. ISSN 0102-2032. [Google Scholar]
  12. Ferraz, M.V.; Barletta, G.A.; Tosetti, L.L.; Cofani-Nunes, J.V. Diagnóstico da arborizaçãourbana de Eldorado, São Paulo. Rev. Tree Dimens. ProFloresta 2017, 2, 22. [Google Scholar] [CrossRef]
  13. Shannon, R. Métodos para coleta e alimentação de mosquitos em estudos de febre amarela na selva. Am. J. Trop. Med. 1939, 19, 131–140. [Google Scholar] [CrossRef]
  14. Galati, E.A.B. Morfologia e taxonomia: Classificação de Phlebotominae. In Flebotomíneos do Brasil; Rangel, E.F., Lainson, R., Eds.; Editora Fiocruz: Rio de Janeiro, Brazil, 2003; pp. 23–51. [Google Scholar]
  15. Colwell, R.K. EstimateS: Statistical Estimation of Species Richness and Shared Species from Samples. Version 9. User’s Guide and Application. 2013. Available online: http://purl.oclc.org/estimates (accessed on 9 March 2021).
  16. Hammer, Ø.; Harper, D.A.T.; Ryan, P.D. Past: Paleontological Statistics Software Package for Education and Data Analysis. Palaeontol. Electron. 2001, 4, 9. Available online: https://palaeo-electronica.org/2001_1/past/past.pdf (accessed on 9 March 2021).
  17. Sokal, R.R.; Rohlf, F.J. Biometria, Principios y Métodos Estadísticos em la Investigación Biológica; H Blume: Madrid, Spain, 1979; Volume XII, 832p, ISBN 84-721466-7. [Google Scholar]
  18. Forattini, O.P.; Rabello, E.X.; Serra, O.P.; Galati, E.A.B.; Barata, J.M.S. Observações sobre a transmissão da leishmaniose tegumentar no Estado de São Paulo, Brasil. Rev. Saúde Pública 1976, 10, 31–43. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Forattini, O.P.; Santos, M.R. Nota sobre infecção natural de Phlebotomus intermedius Lutz & Neiva, 1912, por formas leptomonas, em um foco ativo de leishmaniose tegumentar americana. Arq. Hig. São Paulo 1952, 17, 171–174. [Google Scholar]
  20. Gomes, A.C.; Rabello, E.X.; Santos, J.L.F.; Galati, E.A.B. Aspectos ecológicos da leishmaniose tegumentar americana. 1- Estudo experimental da frequência de flebotomíneos em ecótopos artificiais com referência especial a Ps. intermedius. Rev. Saúde Pública 1980, 14, 540–546. [Google Scholar] [CrossRef]
  21. Gomes, A.C.; Galati, E.A.B. Aspectos ecológicos da leishmaniose tegumentar americana. 7. Capacidade vetorial flebotomínea em ambiente florestal primário do sistema da Serra do Mar, região do Vale do Ribeira, Estado de São Paulo, Brasil. Rev. Saúde Pública 1989, 23, 136–142. [Google Scholar] [CrossRef] [Green Version]
  22. Marcondes, C.B. A redescription of Lutzomyia (Nyssomyia) intermedia (Lutz & Neiva, 1912), and resurrection of L. neivai (Pinto, 1926) (Diptera, Psychodidae, Phlebotominae). Memórias Inst. Oswaldo Cruz 1996, 91, 457–462. [Google Scholar] [CrossRef] [Green Version]
  23. Gomes, A.C.; Santos, J.L.F.; Galati, E.A.B. Ecological aspects of American cutâneos leishmaniasis. 4. Observations on the endophilic behavior of the sandfly and vectorial role of Psychodopygus intermedius in the RibeiraValey region of the S. Paulo State, Brazil. Rev. Saúde Pública 1986, 20, 280–287. [Google Scholar] [CrossRef] [Green Version]
  24. Gomes, A.C.; Rabello, E.X.; Santos, J.L.F.; Galati, E.A.B. Aspectos ecológicos da leishmaniose tegumentar americana. 2. Ecótopo artificial como abrigo de Psychodopygus intermedius e observações sobre alimentação e reprodução sob influência de fatores físicos naturais. Rev. Saúde Pública 1982, 16, 149–159. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Silva, A.M.; Camargo, N.J.; Santos, S.R.; Massafera, R.; Ferreira, A.C.; Postai, C.; Cristovao, E.C.; Konolsaisen, J.F.; Bisetto, A., Jr.; Perinazo, R.; et al. Diversidade, distribuição e abundância de flebotomíneos (Diptera: Psychodidae) no Paraná. Neotrop. Entomol. 2008, 37, 209–225. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Dias, E.S.; França-Silva, J.C.; Silva, J.C.; Monteiro, E.M.; Paula, K.M.; Gonçalves, C.M.; Barata, R.A. Flebotomíneos (Diptera: Psychodidae) de um foco de leishmaniose tegumentar no Estado de Minas Gerais. Rev. Soc. Bras. Med. Trop. 2007, 40, 49–52. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Massafera, R.; Silva, A.L.; Carvalho, A.P.; Santos, D.R.; Galati, E.A.B.; Teodoro, U. Fauna de flebotomíneos do município de Bandeirantes, no Estado do Paraná. Rev. Saúde Pública 2005, 39, 571–577. [Google Scholar] [CrossRef] [Green Version]
  28. Lainson, R.; Rangel, E.F. Ecologia das leishmanioses: Transmissores de leishmaniose tegumentar americana. In Flebotomíneos do Brasil; Rangel, E.F., Lainson, R., Eds.; Fiocruz: Rio de Janeiro, Brazil, 2003; pp. 291–309. [Google Scholar]
  29. Teodoro, U.; La Salvia Filho, E.M.L.; Misuta, N.M.; Verginassi, T.G.; Ferreira, M.E.M.C. Leismaniose tegumentar americana: Flebotomíneos de área de transmissão no Norte do Paraná, Brasil. Rev. Saúde Pública 1991, 25, 129–133. [Google Scholar] [CrossRef] [Green Version]
  30. Andrade Filho, J.D.; Galati, E.A.B.; Falcão, A.L. Polymorphism, inter-population and inter-specific variation in Nyssomyia intermedia (Lutz & Neiva) and Nyssomyianeivai (Pinto) (Diptera, Psychodidae, Phlebotominae). Rev. Bras. Entomol. 2006, 50, 385–393. [Google Scholar] [CrossRef] [Green Version]
  31. Andrade-Filho, J.D.; Galati, E.A.B.; Falcão, A.L. Nyssomyia intermedia (Lutz & Neiva, 1912) and Nyssomyia neivai (Pinto, 1926) (Diptera: Psychodidae: Phlebotominae) geographical distribution and epidemiological importance. Memórias Inst. Oswaldo Cruz 2007, 102, 481–487. [Google Scholar] [CrossRef] [Green Version]
  32. Forattini, O.P.; Pattoli, D.B.G.; Rebello, E.X.; Ferreira, A.O. Infecção natural de flebotomíneos em foco enzoótico de leishmaniose no estado de São Paulo, Brasil. Rev. Saúde Públ. 1972, 6, 431–433. Available online: https://www.scielosp.org/article/rsp/1972.v6n4/431-433/ (accessed on 9 March 2021).
  33. Rangel, E.F.; Sousa, N.A.; Wermelinger, E.D.; Barbosa, A.F. Infecção natural de Lutzomyia intermedia Lutz & Neiva, 1912, em área endêmica de leishmaniose tegumentar no Rio de Janeiro. Mem. Inst. Oswaldo Cruz 1984, 79, 395–396. [Google Scholar] [CrossRef]
  34. Casanova, C.; Mayo, R.C.; Rangel, O.; Mascarini, L.M.; Pignatti, M.G.; Galati, E.A.B.; Gomes, A.C. Natural Lutzomyia intermedia (Lutz & Neiva) infection in the Valley of the Mogi Guaçú River, State of São Paulo, Brazil. Bol. Dir. Malariol. San. Amb. 1995, 35, 77–84. Available online: https://scholar.google.com/citations?user=nNEEE4QAAAAJ&hl=pt-PT (accessed on 9 March 2021).
  35. Silva, A.C.; Gomes, A.C. Estudo da Competência vetorial de Lutzomyia intermedia (Lutz & Neiva, 1912) para Leishmania (Viannia) braziliensis, Vianna, 1911. Rev. Soc. Bras. Med. Trop. 2001, 34, 187–191. [Google Scholar] [CrossRef] [PubMed]
  36. Pita-Pereira, D.; Alves, C.R.; Souza, M.B.; Brazil, R.P.; Bertho, A.L.; Barbosa, A.F.; Britto, C.C. Identifications of naturally infected Lutzomyia intermedia and Lutzomyia migonei with Leishmania (Viannia) braziliensis in Rio de Janeiro (Brazil) revealed by a PCR multiplex non-isotopic hybridization assay. Trans. R. Soc. Trop. Med. Hyg. 2005, 99, 905–913. [Google Scholar] [CrossRef]
  37. Silva, O.S.; Grunewald, J. Contribution to the sandfly fauna (Diptera: Phlebotominae) of Rio Grande do Sul, Brazil and Leishmania (Viannia) infections. Mem. Inst. Oswaldo Cruz 1999, 94, 579–582. [Google Scholar] [CrossRef] [Green Version]
  38. Cordoba-Lanus, E.; De Grosso, M.L.; Pinero, J.E.; Valladares, B.; Salomón, O.D. Natural infection of Lutzomyia neivai with Leishmania spp. in northwestwern Argentina. Acta Trop. 2006, 98, 1–5. [Google Scholar] [CrossRef]
  39. Oliveira, D.M.; Reinhold-Castro, K.R.; Bernal, M.V.Z.; Legriffon, C.M.O.; Lonardoni, M.V.C.; Teodoro, U.; Silveira, T.G.V. Natural infection of Nyssomyia neivai by Leishmania (Viannia) spp. in the State of Paraná, Southern Brazil, detected by multiplex polymerase chain reaction. Vector-Borne Zoonotic Dis. 2011, 11, 137–143. [Google Scholar] [CrossRef]
  40. Marcondes, C.B.; Bittencourt, I.A.; Stoco, P.H.; Eger, I.; Grisard, E.C.; Steindel, M. Natural infection of Nyssomyia neivai (Pinto, 1926) (Diptera: Psychodidae, Phlebotominae) by Leishmania (Viannia) spp. in Brazil. Trans. R. Soc. Trop. Med. Hyg. 2009, 103, 1093–1097. [Google Scholar] [CrossRef]
  41. Casanova, C.; Costa, A.I.P.; Natal, D. Dispersal pattern of the sandfly Lutzomyia neivai (Diptera: Psychodidae) in a cutaneous leishmaniasis endemic rural area in Southeastern Brazil. Mem. Inst. Oswaldo Cruz 2005, 100. [Google Scholar] [CrossRef] [Green Version]
  42. Gomes, A.C.; Barata, J.M.S.; Rocha e Silva, E.O.; Galati, E.A.B. Aspectos ecológicos da leishmaniose tegumentar americana. 6. Fauna flebotomínea antropofílica de matas residuais situadas na região centro-nordeste do estado de São Paulo. Rev. Inst. Med. Trop. São Paulo 1989, 31, 32–39. [Google Scholar] [CrossRef] [PubMed]
  43. Gomes, A.C.; Galati, E.A.B.; Casanova, C.; Domingos, M.F.; Marques, G.R.A.M.; Camargo-Neves, V.L.F. Analysis of the geographical distribution of leishmaniasis vectors in the state of São Paulo Brazil. Bol. Dir. Malariol. San. Amb. 1995, 35 (Suppl. 1), 143–146. Available online: https://scholar.google.com.br/scholar?hl=pt-BR&as_sdt=0,5&cluster=5861626702299990072 (accessed on 9 March 2021).
  44. Gomes, A.C.; Galati, E.A.B. Aspectos ecológicos da leishmaniose tegumentar americana. 5. Estratificação de atividade espacial e estacional de Phlebotominae (Diptera, Psychodidae) em áreas de cultura agrícola da região do Vale do Ribeira, Estado de São Paulo, Brasil. Mem. Inst. Oswaldo Cruz 1987, 82, 467–473. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Azevedo, A.C.R.; Rangel, E.F.; Queiroz, R.G. Lutzomyia migonei (França, 1920) naturalmente infectado por flagelados peripilares em Baturité, foco de leishmaniose tegumentar no Estado do Ceará, Brasil. Mem. Inst. Oswaldo Cruz 1990, 85, 479. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Queiroz, R.G.; Vasconcelos, I.A.B.; Vasconcelos, A.W.W.; Souza, R.N.; Fé Filho, N.M.; David, J.R. Infecções naturais em flebotomíneos de uma zona endêmica de leishmaniose tegumentar americana na serra de Baturité, Estado do Ceará, Nordeste do Brasil. Mem. Inst. Oswaldo Cruz 1991, 86, 256. [Google Scholar]
  47. Pessoa, S.B.; Coutinho, J.O. Infecção natural e experimental dos flebótomos pela Leishmania braziliensis, no Estado de São Paulo. O Hospital 1941, 20, 25–35. [Google Scholar]
  48. Young, D.G.; Arias, J.R. Flebotomíneos Vectores de Leishmaniasis en las Americas. OPAS Caderno Técnico 1992, 3, 28. [Google Scholar]
  49. Galati, E.A.B.; Fonseca, M.B.; Marassá, A.M.; Bueno, E.F.M. Dispersal and survival of Nyssomyia intermedia and Nyssomyia neivai (Diptera: Psychodidae, Phlebotominae) in a cutaneous leishmaniasis endemic area of the speleological province of Ribeira Valley, São Paulo State, Brasil. Mem. Inst. Oswaldo Cruz 2009, 104, 1148–1158. [Google Scholar] [CrossRef] [Green Version]
  50. Pita-Pereira, D.; Souza, G.D.; Pereira, T.A.; Zwetsch, A.; Brito, C.; Rangel, E.F. Lutzomyia (Pintomyia) fischeri (Diptera: Psychodidae: Phlebotominae), a probable vector of American Cutaneous Leishmaniasis: Detection of natural infection by Leishmania (Viannia) DNA in specimens from the municipality of Porto Alegre (RS), Brazil, using multiplex PCR assay. Acta Trop. 2011, 120, 273–275. [Google Scholar] [CrossRef]
  51. Diniz, M.M.C.D.S.L.; GalvisOvallos, F.; de Castro Gomes, C.M.; de Oliveira Lavitschka, C.; Galati, E.A.B. Host-biting rate and susceptibility of some suspected vectors to Leishmania braziliensis. Parasites Vectors 2014, 7, 139. [Google Scholar] [CrossRef] [Green Version]
  52. Leal MMCS. Estudo da Capacidade Vetorial de Pintomyua Fischeri (Pinto) (Diptera: Psychodidae) para Leishmania(Vianna) Braziliensis Viana. Brasil [Dissertação de Mestrado]; Faculdade de Saúde Pública Universidade de São Paulo: São Paulo, Brazil, 2013; Available online: https://teses.usp.br/teses/disponiveis/6/6132/tde-15082014-104825/pt-br.php (accessed on 9 March 2021).
  53. Moschin, J.C.; Ovallos, F.G.; Sei, I.A.; Galati, E.A.B. Ecological aspects of phlebotomine fauna (Diptera, Psychodidae) of Serra da Cantareira, Greater São Paulo Metropolitan region, state of São Paulo, Brazil. Rev. Bras. Epidemiol. 2013, 16, 190–201. [Google Scholar] [CrossRef] [PubMed]
  54. Guimarães, V.C.F.V.; Pruzinova, K.; Sadlova, J.; Volfova, V.; Myskova, J.; Brandão Filho, S.P.; Volf, P. Lutzomyia migonei is a permissive vector competent for Leishmania infantum. Parasites Vectors 2016, 9, 159. [Google Scholar] [CrossRef] [Green Version]
  55. Galvis-Ovallos, F.; Ueta, A.E.; Marques, G.O.; Sarmento, A.M.C.; Araujo, G.; Sandoval, C.; Tomokane, T.Y.; da Matta, V.L.R.; Laurenti, M.D.; Galati, E. Aparecida Bianchi Detection of Pintomyia fischeri (Diptera: Psychodidae) With Leishmania infantum (Trypanosomatida: Trypanosomatidae) Promastigotes in a Focus of Visceral Leishmaniasis in Brazil. J. Med. Entomol. 2021, 58, 830–836. [Google Scholar] [CrossRef]
  56. Galvis-Ovallos, F.; Silva, M.; Bispo, G.; Oliveira, A.; Gonçalves Neto, J.R.; Malafronte, R. “Canine visceral leishmaniasis in the metropolitan area of São Paulo: Pintomyia fischeri as potential vector of Leishmania infantum.” “Leishmaniose viscérale canine dans la région métropolitaine de São Paulo: Pintomyia fischeri comme vecteur potentiel de Leishmania infantum. Parasite 2017, 24, 2. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Shimabukuro, P.H.F.; Galati, E.A.B. Lista de espécies de Phlebotominae (Diptera, Psychodidae) do Estado de São Paulo, Brasil, com comentários sobre sua distribuição geográfica. Biota Neotro 2011, 11 (Suppl. 1), 685–704. [Google Scholar] [CrossRef] [Green Version]
  58. Camargo-Neves, V.L.F. Características da transmissão da Leishmaniose Tegumentar Americana no Estado de São Paulo, Brasil [Dissertação de Mestrado]; Faculdade de Saúde Pública Universidade de São Paulo: São Paulo, Brazil, 1999; Available online: https://scholar.google.com.br/citations?user=B4_Dz7cAAAAJ&hl=pt-BR (accessed on 9 March 2021).
  59. Eckert, J.; Souza, G.D. Flebotomíneos (Diptera: Psychodidae: Phlebotominae) no município de Estrela e primeiro registro de Lutzomyia pascalei (Coutinho & Barretto) no Rio Grande do Sul. Rev. Bras. Bioci. 2010, 8, 399–402. Available online: http://www.ufrgs.br/seerbio/ojs/index.php/rbb/article/view/1555 (accessed on 9 March 2021).
  60. Salomón, O.D.; Rossi, G.C.; Spinelli, G.R. Ecological aspects of phlebotomine ((Diptera, Psychodidae) in an endemic area of tegumentary leishmaniasis in the Northeastern Argentina, 1993–1998. Mem. Inst. Oswaldo Cruz 2002, 97, 163–168. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  61. Scorza, J.V.; Ortiz, I.; Gomez, I. Observaciones biologicas sobre algunos flebotomos de Rancho Grande (Venezuela). 6- Sobre los factores microclimáticos que determinan la endemicidad de la flebotomo fauna de “Rancho Grande”. Acta Biol. Venez. 1968, 6, 76–83. [Google Scholar]
  62. Miscevic, Z. Dependence of the flight of sandflies (Diptera, Phlebotomidae) in artificial light on the temperature and relative humidity. Acta Vet. 1981, 31, 32–39. [Google Scholar]
  63. Aguiar, A.M.; Soucasaux, T. Aspectos da ecologia dos flebótomos do Parque Nacional da Serra dos Órgãos, Rio de Janeiro: I- Frequência mensal em isca humana (Diptera, Psychodidae, Phlebotominae). Mem. Inst. Oswaldo Cruz 1984, 79, 179–209. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Zeledon, R.; Murrillo, J.; Gutierrez, H. Observaciones sobre la ecologia de Lutzomyia longipalpis (Lutz & Neiva, 1912) y posibilidades de existencia de leishmaniasis visceral en Costa Rica. Mem. Inst. Oswaldo Cruz 1984, 79, 455–459. [Google Scholar] [CrossRef] [Green Version]
  65. Barata, R.A.; França-Silva, J.C.; Fortes-Dias, C.L.; Costa, R.T.; Silva, J.C.; Vieira, E.P.; Prata, A.; Michalsky, E.M.; Dias, E.S. Phlebotomine sandflies in Porteirinha, an endemic area of American visceral leishmaniasis in the State of Minas Gerais, Brazil. Mem. Inst. Oswaldo Cruz 2004, 99, 481–487. Available online: https://www.scielo.br/j/mioc/a/ZWGRfh78ZM7N3CHj6Cr7Nzp/?lang=en&format=pdf (accessed on 9 March 2021).
  66. Rutledge, L.C.; Ellenwood, D.A. Production of phlebotomine sandflies on the open forest floor in Panama: The species complement. Environ. Entomol. 1975, 4, 71–77. [Google Scholar] [CrossRef]
Insects 12 00988 g001 550
Figure 1. (A) Study area located in the municipality of Bairro André Lopes, Eldorado-SP, Vale do Ribeira region, São Paulo, Brazil; (B) collection point, aspects of peridomicile and, (C) capture site with Shannon trap.
Figure 1. (A) Study area located in the municipality of Bairro André Lopes, Eldorado-SP, Vale do Ribeira region, São Paulo, Brazil; (B) collection point, aspects of peridomicile and, (C) capture site with Shannon trap.
Insects 12 00988 g001
Insects 12 00988 g002 550
Figure 2. Species accumulation curve by the mean (S means) of the observed richness (S) compared to the expected number (Coleman rarefaction) in each collection.
Figure 2. Species accumulation curve by the mean (S means) of the observed richness (S) compared to the expected number (Coleman rarefaction) in each collection.
Insects 12 00988 g002
Insects 12 00988 g003 550
Figure 3. Dispersion graphs of the monthly hourly average for the total number of sandflies captured, monthly average air temperature (A), and relative humidity (B).
Figure 3. Dispersion graphs of the monthly hourly average for the total number of sandflies captured, monthly average air temperature (A), and relative humidity (B).
Insects 12 00988 g003
Table
Table 1. Total sandflies captured and identified according to species and sex.
Table 1. Total sandflies captured and identified according to species and sex.
SPECIES♀♂∑%
Nyssomyia intermedia38514633848473.3
Nyssomyia neivai12801676295625.5
Mygonemyia migonei6127880.8
Pintomyia fischeri2313360.3
Psathyromyia pascalei140140.1
TOTAL5229634911578100.0
Shannon index (H)0.63
Simpson index (λ)0.60
Gini–Simpson index (1 − λ)0.40
Table
Table 2. Monthly hourly average of Nyssomyia intermedia, Nyssomyia neivai and the total number of sandflies captured, as well as, monthly average temperature and relative humidity.
Table 2. Monthly hourly average of Nyssomyia intermedia, Nyssomyia neivai and the total number of sandflies captured, as well as, monthly average temperature and relative humidity.
YearMonthMonthly Average
Temperature (°C)Humidity (%)Nyssomyia intermediaNyssomyia neivaiSandfly Total
2019SEP18.592.536.919.256.4
OCT23.583.04.63.48.3
NOV23.584.024.69.237.0
DEC-----
2020JAN24.190.52.90.25.3
FEB25.580.816.24.120.6
MAR25.078.00.40.00.4
APR-----
MAY19.574.33.40.43.8
JUN19.286.07.62.610.3
JUL18.078.351.76.659.4
AUG20.082.328.94.433.4
SEP20.685.344.417.362.1
OCT23.476.0160.362.3227.5
NOV24.368.8157.749.3208.5
DEC23.981.0178.972.2255.3
2021JAN25.485.32.42.14.4
FEB25.577.51.10.61.7
MAR22.875.53.01.23.0
Average total22.481.142.615.058.7
Minimum and Maximum values(18.0–25.5)(68.8–92.5)(0.4–178.9)(0.0–72.2)(0.4–255.3)
Note: For the months of December 2019 and April 2020 no surveys were carried out.
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Oliveira, B.F.G.; de Fátima Domingos, M.; Ovallos, F.G.; de Camargo-Neves, V.L.F. Updating Ecological and Behavioral Aspects of the Sandfly Fauna in the Vale do Ribeira Region, São Paulo State, Brazil. Insects 2021, 12, 988. https://doi.org/10.3390/insects12110988

AMA Style

Oliveira BFG, de Fátima Domingos M, Ovallos FG, de Camargo-Neves VLF. Updating Ecological and Behavioral Aspects of the Sandfly Fauna in the Vale do Ribeira Region, São Paulo State, Brazil. Insects. 2021; 12(11):988. https://doi.org/10.3390/insects12110988

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Oliveira, Byara Freitas Guedes, Maria de Fátima Domingos, Fredy Galvis Ovallos, and Vera Lucia Fonseca de Camargo-Neves. 2021. "Updating Ecological and Behavioral Aspects of the Sandfly Fauna in the Vale do Ribeira Region, São Paulo State, Brazil" Insects 12, no. 11: 988. https://doi.org/10.3390/insects12110988

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