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Phytoseiidae mites (Acari: Mesostigmata) in pastures from Goiás state, Brazil

Falchi, Vanessa L. 1 ; Ribeiro, Lana Letícia C. 2 ; Demite, Peterson R. 3 and Daud, Rodrigo D. 4

1Programa de Pós-Graduação em Biodiversidade Animal, Universidade Federal Goiás (UFG), 74690-900, Goiânia, Goiás, Brazil & TEIA - Laboratório de Taxonomia, Ecologia e Interações de Aracnídeos, Departamento de Ecologia, Instituto de Ciências Biológicas, Universidade Federal de Goiás, UFG, Campus II, 74690-900, Goiânia, Goiás, Brazil.
2Programa de Pós-Graduação em Biodiversidade Animal, Universidade Federal Goiás (UFG), 74690-900, Goiânia, Goiás, Brazil & TEIA - Laboratório de Taxonomia, Ecologia e Interações de Aracnídeos, Departamento de Ecologia, Instituto de Ciências Biológicas, Universidade Federal de Goiás, UFG, Campus II, 74690-900, Goiânia, Goiás, Brazil.
3Instituto Federal de Educação, Ciência e Tecnologia de Roraima, Campus Bonfim, Bonfim, Roraima, Brazil.
4Programa de Pós-Graduação em Biodiversidade Animal, Universidade Federal Goiás (UFG), 74690-900, Goiânia, Goiás, Brazil & TEIA - Laboratório de Taxonomia, Ecologia e Interações de Aracnídeos, Departamento de Ecologia, Instituto de Ciências Biológicas, Universidade Federal de Goiás, UFG, Campus II, 74690-900, Goiânia, Goiás, Brazil.

2025 - Volume: 65 Issue: 4 pages: 1158-1172

https://doi.org/10.24349/dxmj-hesj

Original research

Keywords

Brazilian savannah Cerrado livestock Poaceae Predatory mites

Abstract

Phytoseiidae mites are represented by more than 2,700 species commonly found in plants and soil with some species widely used in biological control programs worldwide. Knowledge of mite diversity in pastures and interactions between Phytoseiidae and grasses is essential for developing more efficient and sustainable management techniques for this crop. Here, we present a survey of Phytoseiidae species in pastures from Goiás State, Brazil, to contribute to the knowledge of the diversity and abundance of these predatory mites. We sampled 15 country properties in the Cerrado domain that had pasture crops used for cattle farming, for a total of 480 samples, from eight different Poaceae species. We recorded 21 species from 10 genera, including 11 new records for Goiás and two species collected for the first time since their original descriptions, namely Amblyseius atibaiensis Mineiro, Lofego and Sato and Proprioseiopsis biologicus Lofego, Demite and Moraes. Only Iphiseiodes zuluagai Denmark and Muma, Neoseiulus benjamini (Schicha), Proprioseiopsis mexicanus (Garman) and Proprioseiopsis biologicus Lofego, Demite and Moraes had previously been reported in Brazilian pastures, while the remaining species are new records in these ecosystems. Proprioseiopsis ovatus (Garman), N. benjamini and P. mexicanus were the most abundant species, whereas only a single individual was found for Amblyseius acalyphus Denmark and Muma, Amblyseius compositus Denmark and Muma, A. lofegoi, I. zuluagai, Neoseiulus gracilis (Muma), Metaseiulus (Metaseiulus) camelliae Chant and Yoshida-Shaul and Silvaseius barretoae Yoshida-Shaul and Chant. These results highlight pastures as reservoirs for predatory mites, with potential for biological control in agroecosystems. However, further studies are necessary to better understand this diversity.


Introduction

Phytoseiidae includes more than 2,700 valid species with 257 species recorded in Brazil (Demite et al. 2025). These mites occur primarily on plants (Schmidt 2013), but some species have also been found in soil samples (Moraes et al. 2024). Phytoseiids are natural predators of several phytophagous arthropod species and nematodes. Some species are also used in biological control programs to manage mite and insect pests on crops (McMurtry et al. 2013; Moraes et al. 2024). Because of these attributes, these mites are widely studied in several crops (Döker et al. 2023; Hyte et al. 2023; Möth et al. 2023).

Approximately 40.3% of the territory of the state of Goiás, Brazil, is represented by pastures used for livestock production (LAPIG 2023). Poaceae species are used for fodder and soil cover and are typically adopted by producers due to their high productivity (Shavanov 2021). Despite their ecological and agricultural relevance, studies on mites in Brazilian pastures remain scarce, particularly in the Cerrado biome (Flechtmann 2000, 2004; Flechtmann and Navia 2007; Lofego et al. 2009). Flechtmann (2000) described two new species, Aceria aristidae Flechtmann and Aceria zoostrix Flechtmann (Eriophyidae), on Aristida (Poaceae) in São Paulo. Flechtmann (2004) recorded 10 species of phytophagous mites occurring on Urochloa ruziziensis (R. Germ and C.M. Evrard) Crins (Poaceae) in the state of São Paulo, including description of two new species, namely Catarhinus brachiariae (Diptilomiopidae) Flechtmann and Eotetranychus herbicolus Flechtmann (Tetranychidae). Flechtmann and Navia (2007) reported the first occurrence of Tetranychus (Armenychus) graminae Flechtmann (Tetranychidae) in central Brazil, causing an elephant grass infestation. Furthermore, Lofego et al. (2009) recorded 21 phytoseiid mite species in Brazilian pastures, with the description of a new species, Proprioseiopsis biologicus Lofego, Demite and Moraes.

Understanding the biodiversity of agricultural systems is essential for elucidating the ecological interactions between mites and their host plants. Accordingly, our goal was to provide the first comprehensive survey of Phytoseiidae mites in cultivated pastures across Goiás State, documenting their diversity, abundance, and associations with their host grasses.

Material and methods

Study area

Phytoseiidae mites were sampled during the rainy season in pastures between November and December 2022 in 15 livestock farms from Brazabrantes, Caturaí, Inhumas, Itaberaí, Itauçu and Nova Veneza municipalities, Goiás State, Brazil. Between January and May of 2023, all the same farms were sampled once more, except for the Itauçu 1 (Figure 1, Table 1).

Figure 1. Sampling sites in pastures of livestock farms in the municipalities of Brazabrantes, Caturaí, Inhumas, Itaberaí, Itauçu e Nova Veneza, State of Goiás, Brazil.

All farms sampled were in the Cerrado domain and grew pastures of the species Cynodon nlemfuensis Vanderyst, Urochloa arrecta (Hack. Ex T. Durand and Schinz) Morrone and Zuloaga, Urochloa brizantha (Hochst. ex A.Rich.) R.D. Webster, Urochloa decumbes (Stapf) R.D.Webster, Urochloa humidicola (Rendle) Morrone and Zuloaga, Urochloa lorentziana (Mez) Morrone and Zuloaga, Urochloa plantaginea (Link) R.D. Webster, and Urochloa ruziziensis (R. Germ. and C.M. Evrard) Crins (Poaceae) for livestock production.

Table 1. Geographic coordinates of pastures for Phytoseiidae sampling in livestock farms from Brazabrantes, Caturaí, Inhumas, Itaberaí, Itauçu and Nova Veneza municipalities, Goiás State, Brazil.

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Locality Geographical coordinates
Nova Veneza 1 16°20’50.03”S, 49°20’43.87”W
Nova Veneza 2 16°19’59.92”S, 49°20’58.99”W
Nova Veneza 3 16°23’21.55”S, 49°16’13.98”W
Nova Veneza 4 16°20’7.40”S, 49°19’17.40”W
Itauçu 1 16°11’18.56”S, 49°38’16.62”W
Itauçu 2 16°7’12.72”S, 49°37’12.58”W
Caturaí 1 16°26’26.66”S, 49°29’40.34”W
Itaberaí 1 15°59’12.91”S, 49°43’50.48”W
Itaberaí 2 16°4’23.77”S, 49°57’33.50”W
Nova Veneza 5 16°23’15.44”S, 49°18’30.00”W
Brazabrantes 1 16°25’59.52”S, 49°20’4.78”W
Caturaí 2 16°26’2.36”S, 49°28’58.51”W
Inhumas 1 16°17’50.28”S, 49°35’13.20”W
Inhumas 2 16°20’44.16”S, 49°25’3.50”W
Brazabrantes 2 16°18’57.89”S, 49°21’4.07”W

Mites collection

We randomly established five sampling plots on each livestock farm, totalizing 480 samples. Each plot was represented by a 1-square-meter area in the pasture where we collected grasses. At each sampling plot, we collected 2 L of grasses in a recipient, including all plant extensions such as stalks, nodes, internodes and leaves, except for rhizomes. Then, the sampled grasses were kept in individual paper bags (one bag per sampling plot) in a Styrofoam box with ice for transport. In the laboratory, the grasses were immersed in a 5 L container of 30% alcohol, which was shaken vigorously to release the Phytoseiidae mites from the plants. After this procedure, the grasses were removed, and the solution was transferred to a 25 µm mesh sieve. The mites that were trapped in the mesh were transferred to a pot containing 70% alcohol.

The samples were observed under stereomicroscope and all mites found were mounted on microscope slides using Hoyer's medium (Moraes et al. 2024). Phytoseiidae mites were counted and identified to the species level under a phase-contrast optical microscope using specialized dichotomous keys for genera and subgenera (Chant and McMurtry 2007) and works on descriptions, redescriptions, and revisions of Phytoseiidae (e.g., Barbosa and Demite 2023; Ferragut and Navia 2024; Lofego et al. 2024).

The list of mites collected in pastures from the state of Goiás, Brazil, includes the following information about the examined material: collection locality, grass species, month of sampling in Roman numerals, year in Arabic numerals, and the number of individuals of each sex (indicated by symbols ♀ and ♂). Additionally, the list provides previous records and observations. We extracted the previous records of Phytoseiidae species from the Phytoseiidae Database (Demite et al. 2025), available at: http://www.lea.esalq.usp.br/phytoseiidae .

Results

We sampled 21 species from 10 genera of Phytoseiidae in pasture crops in Goiás State, Brazil. Among these, seven genera belonged to Amblyseiinae, and three to Typhlodrominae (Table 2).

Table 2. Composition and abundance of Phytoseiidae species sampled in pastures from 15 livestock farms in the state of Goiás, Brazil.

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Phytoseiidae species CNL* UAR UBR UDE UHU UPL URU
Amblyseiinae Muma
Amblyseius acalyphus Denmark and Muma 1
Amblyseius atibaiensis Mineiro, Lofego and Sato 27 4
Amblyseius compositus Denmark and Muma 1
Arrenoseius lofegoi Barbosa and Demite 1
Iphiseiodes zuluagai Denmark and Muma 1
Neoseiulus benjamini (Schicha) 1 57 1 2 1
Neoseiulus gracilis (Muma) 1
Neoseiulus paraibensis (Moraes and McMurtry) 1 5
Neoseiulus transversus Denmark and Muma 1 13 1 1 3 1
Proprioseiopsis biologicus Lofego, Demite ans Moraes 11
Proprioseiopsis mexicanus (Garman) 3 2 43 1 4 10
Proprioseiopsis neotropicus (Ehara) 2
Proprioseiopsis ovatus (Garman) 1 2 151 3 18
Proprioseiopsis pentagonalis (Moraes and Mesa) 8 3
Typhlodromalus aripo De Leon 2
Typhlodromalus clavicus Denmark and Muma 1
Typhlodromalus peregrinus Muma 2 1
Typhlodromips mangleae De Leon 5
Typhodrominae Wainstein
Metaseiulus (Metaseiulus) camelliae Chant and Yoshida-Shaul 1
Silvaseius barretoae Yoshida-Shaul and Chant 1
Typhlodromus (Anthoseius) transvaalensis (Nesbitt) 13 1

*Poaceae species codes: Cynodon nlemfuensis (CNL), Urochloa arrecta (UAR), Urochloa brizantha (UBR), Urochloa decumbes (UDE), Urochloa humidicola (UHU), Urochloa plantaginea (UPL) and Urochloa ruziziensis (URU).

Among the 21 species recorded, 11 are new records for Goiás State, and two were collected for the first time since their original descriptions, namely, Amblyseius atibaiensis and Proprioseiopsis biologicus.

In total, we collected 416 adult phytoseiid mites that were identified at the species level. The most abundant species was Proprioseiopsis ovatus, followed by Neoseiulus benjamini and Proprioseiopsis mexicanus. Only one individual was sampled for Amblyseius acalyphus, Amblyseius compositus, Arrenoseius lofegoi, Iphiseiodes zuluagai, Neoseiulus gracilis, Metaseiulus (Metaseiulus) camelliae and Silvaseius barretoae. Regarding host plants, U. brizantha hosted the highest richness and abundance of Phytoseiidae mites, followed by U. plantaginea and U. decumbens (Table 2). No phytoseiid mites were recorded on U. lorentziana. The following is a list of Phytoseiidae species sampled in pastures from livestock farms in Goiás State, Brazil.

Phytoseiidae Berlese

Amblyseiinae Muma

Amblyseius Berlese

Amblyseius acalyphus Denmark & Muma

Amblyseius acalyphus Denmark & Muma 1973: 242.

Amblyseius acalyphus — Moraes et al. 1986: 6, 2004: 12; Lofego et al. 2024: 9.

Amblyseius (Amblyseius) acalyphus — Denmark & Muma 1989: 75.

Specimens examined — Itaberaí 1: Urochloa brizantha, IV-2023 (1 ♀).

Previous records — Brazil - Goiás, Mato Grosso, Mato Grosso do Sul, Minas Gerais, Roraima, São Paulo; Guadeloupe.

Observation — this species was previously recorded in the state of Goiás on Bauhinia ungulata L. (Leguminosae), Psidium guajava L. (Myrtaceae), Schinus terebinthifolius Raddi (Anacardiaceae), Brosimum gaudichaudii Trécul (Moraceae) and Protium spruceanum (Bentham) Engler (Burseraceae) (Demite et al. 2017).

Amblyseius atibaiensis Mineiro, Lofego & Sato

Amblyseius atibaiensis Mineiro, Lofego & Sato 2012: 596.

Amblyseius atibaiensis — Lofego et al. 2024: 15.

Specimens examined — Brazabrantes 2: Urochloa brizantha, IV-2023 (6 ♀, 1 ♂). Caturaí 1: Urochloa brizantha, IV-2023 (2 ♀, 1 ♂), V-2023 (2 ♀). Inhumas 2: Urochloa plantaginea, IV-2023 (4 ♀). Itaberaí 1: Urochloa brizantha, IV-2023 (1 ♀, 1 ♂). Nova Veneza 3: Urochloa brizantha, III-2023 (1 ♂). Nova Veneza 4: Urochloa brizantha, III-2023 (2 ♀), IV-2023 (9 ♀), V-2023 (1 ♀).

Previous records — Brazil - São Paulo.

ObservationAmblyseius atibaiensis was first described based on individuals sampled from the soil and litter of coffee crops in São Paulo State, Brazil (Mineiro et al. 2012). Here, A. atibaiensis is recorded for the first time after its original taxonomy description.

Amblyseius compositus Denmark & Muma

Amblyseius compositus Denmark & Muma 1973: 240.

Amblyseius compositus — Moraes et al., 1986: 11, 2004: 21; Lofego et al. 2024: 23.

Amblyseius (Multiseius) compositus — Denmark & Muma 1989: 95.

Specimens examined — Nova Veneza 4: Urochloa brizantha, II-2023 (1 ♀).

Previous records — Brazil - Amazonas, Bahia, Espírito Santo, Goiás, Minas Gerais, Paraná, Pernambuco, Piauí, Rio Grande do Sul, Sergipe, São Paulo, Tocantins.

Observation — this species was previously recorded in Goiás State on P. guajava, S. terebinthifolius, Virola sebifera Fusée-Aublet (Myristicaceae), Cecropia pachystachya Trécul (Urticaceae), Inga edulis von Martius (Leguminosae), Protium spruceanum, Rhamnaceae sp., Rudgea viburnoides, Tocoyena formosa Schumann (Rubiaceae), Trichilia martiana De Candolle (Meliaceae) and an unidentified Myrtaceae species (Demite et al. 2017).

Arrenoseius Wainstein

Arrenoseius lofegoi Barbosa & Demite

Arrenoseius lofegoi Barbosa & Demite 2023: 50.

Arrenoseius lofegoi — Lofego et al. 2024: 87.

Specimens examined — Nova Veneza 3: Urochloa brizantha, IV-2023 (1 ♀).

Previous records — Brazil - Bahia.

ObservationArrenoseius lofegoi was found in sugarcane (Saccharum officinarum L., Poaceae) crops in the state of Bahia, Brazil (Barbosa and Demite 2023). Arrenoseius lofegoi was previously recorded in Goiás State by Rossetti et al. (2025)

Iphiseiodes De Leon

Iphiseiodes zuluagai Denmark & Muma

Iphiseiodes zuluagai Denmark & Muma 1972: 23.

Iphiseiodes zuluagai — Moraes et al. 1986: 61; 2004: 91; Lofego et al. 2024: 107.

Amblyseius zuluagai — Moraes & Mesa 1988: 79.

Specimens examined — Nova Veneza 4: Urochloa brizantha, II-2023 (1 ♀).

Previous records — Brazil - Acre, Alagoas, Amapá, Amazonas, Bahia, Ceará, Distrito Federal, Goiás, Maranhão, Mato Grosso, Mato Grosso do Sul, Minas Gerais, Pará, Paraná, Paraíba, Pernambuco, Rio de Janeiro, Rio Grande do Norte, Rio Grande do Sul, Rondônia, Roraima, Sergipe, São Paulo, Tocantins; Colombia; Cuba; Dominican Republic; Guadeloupe; Marie Galante; Martinique; Panama; Peru; Puerto Rico; Venezuela.

Observation — previous recorded in Goiás State on Campomanesia pubescens (von Martius ex De Candolle) O. Berg (Myrtaceae), Didymopanax vinosum (Cham and Schltdl) Marchal (Araliaceae), Harconia speciosa Gomes (Apocynaceae), Xylopia aromatica (Lamark) von Martius (Annonaceae), Byrsonima coccolobifolia Kunth (Malpighiaceae), Byrsonima intermedia de Jussieu (Malpighiaceae), Doliocarpus cf. dentatus (Fusée-Aublet) Standley (Dilleniaceae), Ouratea spectabilis von Martius Ex Engler (Ochnaceae), Annona crassiflora von Martius (Annonaceae), Kielmeyera cf. coriacea von Martius and Zucc (Calophyllaceae), Ouratea spectabilis (von Martius) Engler (Ochnaceae), Qualea grandiflora von Martius (Vochysiaceae), two unidentified species of the Myrtaceae (Rezende and Lofego 2011); Zeyheria montana von Martius (Bignoniaceae), Trichilia martiana De Candolle (Meliaceae), Roupala montana Fusée-Aublet (Proteaceae) (Demite et al. 2017), and Miconia albicans (Swartz) Steudel (Melastomataceae) (Moraes et al. 2022).

Neoseiulus Hughes

Neoseiulus benjamini (Schicha)

Amblyseius benjamini Schicha 1981: 203.

Amblyseius (Amblyseius) benjamini — Tseng 1983: 60.

Neoseiulus benjamini — Moraes et al. 1986: 72, 2004: 108; Lofego et al. 2024: 199.

Specimens examined — Brazabrantes 1: Urochloa brizantha, I-2023 (1 ♀); Cynodon nlemfuensis, IV-2023 (1 ♀). Brazabrantes 2: Urochloa brizantha, XI-2022 (1 ♂), I-2023 (1 ♂), III-2023 (1 ♀). Caturaí 1: Urochloa brizantha, XI-2022 (1 ♀), XII-2022 (1 ♂), II-2023 (1 ♀, 1 ♂). Caturaí 2: Urochloa brizantha, XI-2022 (1 ♀). Inhumas 1: Urochloa brizantha, XI-2022 (1 ♂), II-2023 (1 ♂), V-2023 (1 ♀). Inhumas 2: Urochloa plantaginea, III-2023 (1 ♀). Itauçu 2: Urochloa brizantha, XI-2022 (1 ♀). Nova Veneza 1: Urochloa brizantha, XI-2022 (3 ♀), I-2023 (1 ♀), III-2023 (1 ♀), IV-2023 (2 ♀, 1 ♂). Nova Veneza 2: Urochloa brizantha, XII-2022 (1 ♀, 1 ♂), I-2023 (1 ♀, 1 ♂). Nova Veneza 3: Urochloa brizantha, III-2023 (3 ♀), IV-2023 (3 ♀), V (1 ♀). Nova Veneza 4: Urochloa brizantha, XI-2022 (1 ♀), XII-2022 (3 ♀), III-2023 (6 ♀, 3 ♂), IV-2023 (4 ♀, 3 ♂), V-2023 (3 ♀). Nova Veneza 5: Urochloa brizantha, XII-2022 (1 ♀), V-2023 (1 ♀); Urochloa plantaginea, I-2023 (1 ♀). Itaberaí 1: Urochloa humidicola, XI (1 ♀); Urochloa ruziziensis, XI-2022 (1 ♀).

Previous records — Australia; Brazil - Bahia, Distrito Federal, Goiás, Mato Grosso do Sul, Minas Gerais, São Paulo, Tocantins; Chile; Martinique; South Africa.

Observation — previous recorded in Goiás on Trachypogon sp. (Poaceae) and Stryphnodendron adstringens (von Martius) Coville (Fabaceae) (Rezende and Lofego 2011).

Neoseiulus gracilis (Muma)

Cydnodromus gracilis Muma, 1962: 9.

Neoseiulus gracilis — Moraes et al. 1986: 81, 2004: 122; Lofego et al. 2024: 207.

Neoseiulus atrii (Karg) — (synonymy according to Moraes et al. 1997).

Specimens examined — Itauçu 2: Urochloa brizantha, XII-2022 (1 ♀).

Previous records — Brazil - Alagoas, Bahia, Paraíba, Pernambuco, Tocantins; Cuba; Saint Lucia, United States of America; Venezuela.

Observation — this is the first record of this species in Goiás State, Brazil.

Neoseiulus paraibensis (Moraes & McMurtry)

Amblyseius paraibensis Moraes & McMurtry 1983: 135.

Neoseiulus paraibensis — Moraes et al. 1986: 92, 2004: 137; Lofego et al. 2024: 217.

Specimens examined — Caturaí 2: Urochloa arrecta, XI-2022 (1 ♀); Nova Veneza 1: Urochloa brizantha, XI-2022 (1 ♀, 3 ♂). Nova Veneza 3: Urochloa brizantha, XI-2022 (1 ♂).

Previous records — Brazil - Paraná, Paraíba, Rio Grande do Sul, São Paulo; Colômbia; Costa Rica; Cuba; Martinique; Nicaragua; Panama; United States of America.

Observation — here, N. paraibensis is recorded for the first time in Goiás State, Brazil.

Neoseiulus transversus Denmark & Muma

Neoseiulus transversus Denmark & Muma 1973: 267.

Neoseiulus transversus — Moraes et al. 1986: 98, 2004: 148; Lofego et al. 2024: 221.

Specimens examined — Brazabrantes 1: Urochloa brizantha, XI-2022 (1 ♀, 1 ♂). Brazabrantes 2: Urochloa brizantha, XI-2022 (3 ♀), XII-2022 (1 ♂). Caturaí 1: Urochloa brizantha, I-2023 (1 ♀). Itaberaí 1: Urochloa ruziziensis, XII-2022 (1 ♀), Cynodon nlemfuensis, I-2023 (1 ♀). Itaberaí 2: Urochloa decumbens, XI-2022 (1 ♂); Urochloa humidicola, XI-2022 (1 ♀). Nova Veneza 3: Urochloa plantaginea, XI-2022 (1 ♂), I-2023 (1 ♀). Nova Veneza 4: Urochloa brizantha, XII-2022 (1 ♀), I-2023 (1 ♀). Nova Veneza 5: Urochloa brizantha, XI-2022 (1 ♀, 1 ♂), XII-2022 (1 ♀, 1 ♂).

Previous records — Argentina; Brazil - Bahia; Goiás; Maranhão; Minas Gerais; Paraíba; Pernambuco, Rio Grande do Sul, São Paulo.

ObservationNeoseiulus transversus has been previously recorded in Goiás State on soybean crops (Glycine max Merril, Fabaceae) (Cavalcante et al. 2017).

Proprioseiopsis Muma

Proprioseiopsis biologicus Lofego, Demite & Moraes

Proprioseiopsis biologicus Lofego, Demite & Moraes, in Lofego et al. (2009): 51.

Proprioseiopsis biologicus — Lofego et al. 2024: 113.

Specimens examined — Brazabrantes 2: Urochloa brizantha, V-2023 (9 ♀). Nova Veneza 1: Urochloa brizantha, XI-2022 (2 ♀).

Previous records — Brazil - São Paulo.

Observation — this species was formally described based on specimens collected from U. decumbens in São Paulo, Brazil (Lofego et al. 2009). This is the first report of P. biologicus since its original description.

Proprioseiopsis mexicanus (Garman)

Amblyseiopsis mexicanus Garman 1958: 75.

Typhlodromus (Amblyseius) mexicanus — Chant 1959: 92.

Amblyseiulus mexicanus — Muma 1961: 278.

Proprioseiopsis mexicanus — Moraes et al. 1986: 118, 2004: 181; Lofego et al. 2024: 117.

Typhlodromus mexicanus — Hirschmann 1962: 5.

Amblyseius mexicanus — Collyer 1964: 634.

Proprioseiopsis (Patinoseius) mexicanus — (synonymy according to Karg 1989).

Proprioseiopsis amotus (Zack) — (synonymy according to Denmark & Evans 2011).

Proprioseiopsis asetus (Chant) — (synonymy according to Denmark & Evans 2011).

Proprioseiopsis clausae (Muma) — (synonymy according to Denmark & Evans 2011).

Proprioseiopsis kogi (Chant and Hansell) — (synonymy according to Denmark & Evans 2011).

Proprioseiopsis putmani (Chant) — (synonymy according to Denmark & Evans 2011).

Proprioseiopsis temperellus (Denmark and Muma) — (synonymy according to Denmark & Evans 2011).

Proprioseiopsis tropicanus (Garman) — (synonymy according to Denmark & Evans 2011).

Proprioseiopsis tulearensis (Blommers) — (synonymy according to Denmark & Evans 2011).

Proprioseiopsis versutus (Zack) — (synonymy according to Denmark & Evans 2011).

Specimens examined — Brazabrantes 1: Urochloa brizantha, II-2023 (2 ♀); Cynodon nlemfuensis, XII-2022 (1 ♀), IV-2023 (1 ♀), V-2023 (1 ♀). Brazabrantes 2: Urochloa brizantha, XI-2022 (2 ♀). Caturaí 1: Urochloa arrecta, XII-2022 (1 ♀). Caturaí 2: Urochloa brizantha, III-2023 (2 ♀), IV-2023 (1 ♀), V-2023 (1 ♀); Urochloa arrecta, XI-2022 (1 ♀). Inhumas 1: Urochloa brizantha, XII-2022 (1 ♀), III-2023 (3 ♀). Inhumas 1: Urochloa brizantha, II-2023 (2 ♀), V-2023 (1 ♀). Inhumas 2: Urochloa brizantha, XII-2022 (3 ♀); Urochloa plantaginea, III-2023 (4 ♀), V-2023 (4 ♀). Itaberaí 1: Urochloa brizantha: II-2023 (1 ♀), V-2023 (4 ♀); Urochloa decumbens, I-2023 (1 ♀). Itaberaí 2: Urochloa humidicola, XII-2022 (1 ♀), I-2023 (1 ♀), III-2023 (1 ♀), IV-2023 (1 ♀). Itauçu 1: Urochloa brizantha, XII-2022 (1 ♀). Itauçu 2: Urochloa brizantha, XI-2022 (1 ♀). Nova Veneza 1: Urochloa brizantha, III-2023 (5 ♀). Nova Veneza 2: Urochloa brizantha, XII-2022 (1 ♀), III-2023 (2 ♀). Nova Veneza 3: Urochloa brizantha, IV-2023 (1 ♀), V-2023 (2 ♀). Nova Veneza 4: Urochloa brizantha, XII-2022 (1 ♀), IV-2023 (2 ♀), V-2023 (2 ♀). Nova Veneza 5: Urochloa brizantha, V-2023 (2 ♀); Urochloa plantaginea, III-2023 (1 ♀, 1 ♂).

Previous records — Australia; Benin; Brazil - Alagoas, Bahia, Distrito Federal, Maranhão, Mato Grosso do Sul, Paraná, Paraíba, Pernambuco, Piauí, Rondônia, São Paulo, Tocantins; Canada; China; Colombia; Costa Rica; Cuba; Galapagos; Ghana; Guadeloupe; Hawaii; Ivory Coast; Jamaica; Japan; Kenya; Madagascar; Martinique; Mexico; New Zealand; Nicaragua; Panama; Peru; Reunion Island; Rodrigues Island (Mauritius); Saudi Arabia; Taiwan; United Arab Emirates; United States of America.

Observation — this is the first record of this species in Goiás State, Brazil.

Proprioseiopsis neotropicus (Ehara)

Amblyseius neotropicus Ehara 1966: 133.

Proprioseiopsis neotropicus — Moraes et al. 1986: 119, 2004: 183; Lofego et al. 2024: 120.

Specimens examined — Nova Veneza 4: Urochloa brizantha, IV-2023 (1 ♀), V-2023 (1 ♀).

Previous records — Argentina; Brazil - Alagoas, Amazonas, Bahia, Mato Grosso, Mato Grosso do Sul, Minas Gerais, Pará, Paraná, Paraíba, Pernambuco, Rio Grande do Sul, Roraima, São Paulo; Colombia; Ecuador; French Guiana; Peru.

Observation — this is the first record of this species in Goiás State, Brazil.

Proprioseiopsis ovatus (Garman)

Amblyseiopsis ovatus Garman 1958: 78.

Typhlodromus (Amblyseius) ovatus — Chant 1959: 90.

Amblyseiulus ovatus — Muma 1961: 278.

Typhlodromus ovatus — Hirschmann 1962: 5.

Amblyseius ovatus — Schuster & Pritchard 1963: 246.

Amblyseius (Amblyseius) ovatus — Tseng 1983: 42.

Proprioseiopsis ovatus — Tuttle & Muma 1973: 11; Moraes et al. 1986: 121, 2004: 151; Lofego et al. 2024: 121.

Proprioseiopsis (Proprioseiopsis) ovatus — Karg 1989: 208.

Proprioseiopsis antonelli Congdon — (synonymy according to Denmark & Evans 2011).

Proprioseiopsis cannaensis (Muma) — (synonymy according to Denmark & Evans 2011).

Proprioseiopsis hundsonianus (Chant and Hansell) — (synonymy according to Denmark & Evans 2011).

Proprioseiopsis parapeltatus Wu and Chou — (synonymy according to Tseng 1983).

Proprioseiopsis peltatus (Van der Merwe) — (synonymy according to Tseng 1983).

Specimens examined — Brazabrantes 1: Urochloa brizantha, XI-2022 (1 ♀); Cynodon nlemfuensis, IV-2023 (1 ♀). Brazabrantes 2: Urochloa brizantha, II-2023 (1 ♀), III-2023 (3 ♀, 1 M), IV-2023 (3 ♀), V-2023 (4 ♀). Caturaí 1: Urochloa brizantha, XII-2022 (5 ♀), I-2023 (1 ♀), III-2023 (8 ♀, 2 ♂), IV-2023 (7 ♀, 1 ♂), V-2023 (7 ♀, 4 ♂). Caturaí 2: Urochloa arrecta, XI-2022 (1 ♀). Inhumas 1: Urochloa brizantha, XI-2022 (1 ♀), XII-2022 (1 ♀), IV-2023 (1 ♀), V-2023 (1 ♀). Inhumas 2: Urochloa plantaginea, III-2023 (4 ♀), V-2023 (7 ♀). Itaberaí 1: Urochloa brizantha, XII-2022 (2 ♀), IV-2023 (1 ♀), V-2023 (1 ♀). Itaberaí 2: Urochloa humidicola, I-2023 (1 ♀), IV-2023 (1 ♀), V-2023 (1 ♀). Itauçu 1: Urochloa brizantha, XII-2022 (1 ♀). Nova Veneza 1: Urochloa brizantha, XII-2022 (1 ♀), II-2023 (10 ♀), IV-2023 (2 ♀), V-2023 (1 ♀). Nova Veneza 2: Urochloa brizantha, XII-2022 (2 ♀), IV-2023 (19 ♀), V-2023 (18 ♀, 3 ♂). Nova Veneza 3: Urochloa brizantha, XI-2022 (1 ♀), III-2023 (2 ♀), IV-2023 (17 ♀). Nova Veneza 4: Urochloa brizantha, XI-2022 (1 ♀), III-2023 (12 ♀), IV-2023 (1 ♀, 1 ♂), V-2023 (2 ♀); Urochloa arrecta, XI-2022 (1 ♀). Nova Veneza 5: Urochloa plantaginea, I-2023 (1 ♀), III-2023 (1 ♀), IV-2023 (4 ♀), V-2023 (1 ♀).

Previous records — Argentina; Australia; Brazil - Alagoas, Bahia, Distrito Federal, Goiás, Mato Grosso, Mato Grosso do Sul, Minas Gerais, Pará, Paraná, Rio Grande do Sul, São Paulo; Canada; China; Colombia; Costa Rica; Cuba; DR Congo; Ecuador; Egypt; El Salvador; Fiji; French Guiana; Ghana; Grande Comore Island (Comoros); Guadeloupe; Guyana; Hawaii; Honduras; India; Ivory Coast; Japan; Lesotho; Madagascar; Malaysia; Malawi; Marie Galante; Martinique; Mayotte Island; Mozambique; New Caledonia; Papua New Guinea; Paraguay; Peru; Philippines; Puerto Rico; Reunion Island; Saudi Arabia; Sierra Leone; South Africa; Spain; Sri Lanka; Taiwan; Thailand; Turkey; United States of America; Venezuela; Zimbabwe.

ObservationProprioseiopsis ovatus has been previously recorded on Psidium guineense Swartz (Myrtaceae) and Guapira noxia (Netto) Lundell (Nyctaginaceae) in the state of Goiás (Demite et al. 2017).

Proprioseiopsis pentagonalis (Moraes & Mesa)

Amblyseius pentagonalis Moraes & Mesa, in Moraes et al. (1991): 127.

Proprioseiopsis pentagonalis — Moraes et al. 2004: 186; Lofego et al. 2024: 124.

Specimens examined — Inhumas 2: Urochloa brizantha, V-2023 (5 ♀); Urochloa plantaginea (Poaceae), V-2023 (3 ♀). Nova Veneza 3: Urochloa brizantha, IV-2023 (3 ♀).

Previous records — Brazil - Amazonas, Bahia, Maranhão, Piauí, São Paulo; Colombia; Guadeloupe.

Observation — this is the first record of this species in Goiás State, Brazil.

Typhlodromalus Muma

Typhlodromalus aripo De Leon

Amblyseius aripo De Leon 1967: 21.

Typhlodromalus aripo — Moraes & McMurtry 1983: 132; Moraes et al. 1986: 128, 2004: 195. Lofego et al. 2024: 169.

Specimens examined — Nova Veneza 1: Urochloa brizantha, II-2023 (1 ♀). Nova Veneza 4: Urochloa brizantha, II-2023 (1 ♂).

Previous records — Argentina; Benin; Brazil - Alagoas, Amazonas, Bahia, Ceará, Distrito Federal, Espírito Santo, Goiás, Maranhão, Mato Grosso, Mato Grosso do Sul, Minas Gerais, Pará, Paraná, Paraíba, Pernambuco, Piauí, Rio Grande do Norte, Rio Grande do Sul, Santa Catarina, Sergipe, São Paulo, Tocantins; Cameroon; Colombia; Congo; Costa Rica; El Salvador; Guadeloupe; Guyana; Jamaica; Kenya; Malawi; Mexico; Mozambique; Paraguay; Peru; Trinidad; Uganda.

ObservationTyphlodromalus aripo has previously been recorded in Goiás State on Virola sebifera Fusée-Aublet (Myristicaceae), Vernonanthura sp. (Compositae), Luehea divaricata von Martius (Malvaceae), Cecropia pachystachya Trécul (Urticaceae), Zeyheria montana von Martius (Bignoniaceae), Magonia pubescens de Saint-Hilaire (Sapindaceae), Schefflera macrocarpa (von Chamisso and von Schlechtendal) Frodin (Araliaceae), Tibouchina sp. (Melastomataceae) and unidentified species of Rubiaceae and Malpighiaceae (Demite et al. 2017).

Typhlodromalus clavicus Denmark & Muma

Typhlodromalus clavicus Denmark & Muma 1973: 257.

Typhlodromalus simus — Moraes et al. 1986: 134, 2004: 204; Lofego et al. 2024: 171.

Specimens examined — Brazabrantes 1: Cynodon nlemfuensis, V-2023 (1 ♀).

Previous records — Brazil - São Paulo, Tocantins; El Salvador; Honduras.

Observation — this is the first record of this species in Goiás State, Brazil.

Typhlodromalus peregrinus Muma

Typhlodromus peregrinusMum a 1955: 270.

Typhlodromalus peregrinus — Moraes et al. 1986: 132, 2004: 202; Lofego et al. 2024: 176.

Typhlodromus (Typhlodromopsis) peregrinus — De Leon 1959: 114.

Typhlodromus (Amblyseius) peregrinus — Chant 1959: 97.

Amblyseius (Typhlodromalus) peregrinus — Muma 1961: 288.

Amblyseius peregrinus — Muma and Denmark 1962: 60.

Amblyseius (Amblyseius) peregrinus — Van der Merwe 1968: 113.

Typhlodromalus evansi (Chant) — (synonymy according to Muma 1964).

Typhlodromalus primulae (Chant) — (synonymy according to Muma 1964).

Typhlodromalus robiniae (Chant) — (synonymy according to Muma 1964).

Typhlodromalus sextus (Garman, 1958) — (synonymy according to Denmark & Evans 2011).

Examined material — Nova Veneza 3: Urochloa plantaginea, XI-2022 (1 ♀). Nova Veneza 4: Urochloa brizantha, II-2023 (2 ♀);

Previous records — Argentina; Brazil - Acre, Alagoas, Amazonas, Bahia, Ceará, Goiás, Mato Grosso, Paraíba, Pernambuco, Rio de Janeiro, Rio Grande do Norte, Rio Grande do Sul, Sergipe, São Paulo, Tocantins; Colombia; Costa Rica; Cuba; Dominican Republic; Ecuador; Guadeloupe; Guatemala; Guyana; Hawaii; Honduras; Martinique; Mexico; Nicaragua; Peru; Puerto Rico; Suriname; United States of America; Venezuela.

ObservationTyphlodromalus peregrinus has previously been recorded on Protium spruceanum (Bentham) Engler (Burseraceae) in Goiás State (Demite et al. 2017).

Typhlodromips De Leon

Typhlodromips mangleae De Leon

Typhlodromips mangleae De Leon 1967: 28.

Typhlodromips mangleaem — Moraes et al., 1986: 143, 2004: 217; Lofego et al 2024: 251.

Amblyseius mangleae — Moraes & Mesa 1988: 75.

Specimens examined — Brazabrantes 1: Urochloa brizantha, (1 ♀). Nova Veneza 2: Urochloa brizantha, V-2023 (1 ♀). Nova Veneza 4: Urochloa brizantha, II-2023 (1 ♀), III-2023 (1 ♀), V-2023 (1 ♀).

Previous records — Brazil - Alagoas, Bahia, Ceará, Distrito Federal, Maranhão, Mato Grosso do Sul, Minas Gerais, Pará, Paraná, Pernambuco, Rio Grande do Sul, São Paulo, Tocantins; Colombia; Peru; Puerto Rico; Trindad.

Observation — this is the first record of this species in Goiás State, Brazil.

Typhlodrominae Wainstein

Metaseiulus Muma

Metaseiulus (Metaseiulus) camelliae (Chant & Yoshida-Shaul)

Typhlodromus camelliae Chant & Yoshida-Shaul 1983: 1053.

Typhlodromina camelliae — Moraes et al. 1986: 236.

Metaseiulus (Metaseiulus) camelliae — Moraes et al. 2004: 278.

Metaseiulus camelliae — Bellini et al. 2005 479.

Specimens examined — Itauçu 2: Urochloa brizantha, XII-2022 (1 ♀).

Previous records — Argentina; Brazil - Minas Gerais, Rio Grande do Sul, Santa Catarina, São Paulo; Chile; Uruguay.

Observation — this is the first record of M. (M.) camelliae in Goiás State.

Silvaseius Chant & McMurtry

Silvaseius barretoae Yoshida-Shaul & Chant

Cydnodromella barretoae Yoshida-Shaul & Chant 1991: 93.

Silvaseius barretoae — Chant & McMurtry 1994: 241; Moraes et al. 2004: 304.

Specimens examined — Itaberaí 1: Urochloa brizantha, IV-2023 (1 ♀).

Previous records — Argentina; Brazil - Mato Grosso, São Paulo; Costa Rica.

Observation — this is the first record of this species in Goiás State, Brazil.

Typhlodromus Scheuten

Typhlodromus (Anthoseius) transvaalensis (Nesbitt)

Kampimodromus transvaalensis Nesbitt 1951: 55.

Typhlodromus (Typhlodromus) transvaalensis — Chant 1959: 60.

Neoseiulus transvaalensis — Muma 1961: 295.

Typhlodromus (Neoseiulus) transvaalensis — Pritchard & Baker 1962: 222.

Mumaseius transvaalensis — Abbasova 1970: 1410.

Clavidromus transvaalensis — Muma & Denmark 1971: 238; Moraes et al. 1986: 182.

Anthoseius (Anthoseius) transvaalensis — Wainstein & Vartapetov 1973: 104.

Anthoseius transvaalensis — Beglyarov 1981: 21.

Typhlodromus (Anthoseius) transvaalensis — Chant & McMurtry 1994: 252; Moraes et al. 2004: 355.

Anthoseius (Clavidromus) transvaalensis — Kolodochka 2006: 145.

Typhlodromus (Anthoseius) jackmickleyi De Leon — (synonymy according to Muma & Denmark 1968).

Typhlodromus (Anthoseius) pectinatus Athias-Henriot — (synonymy according to Muma & Denmark 1968).

Specimens examined — Caturaí 1: Urochloa brizantha, XII-2022 (2 ♀). Inhumas: Urochloa brizantha, XII-2022 (1 ♀). Nova Veneza 1: Urochloa brizantha, III-2023 (1 ♀). Nova Veneza 2: Urochloa brizantha, I-2023 (1 ♀). Nova Veneza 3: Urochloa brizantha, XII-2022 (1 ♀), III-2023 (6 ♀). Itaberaí 1: Urochloa brizantha, IV (1 ♀). Itaberaí 2: Urochloa humidicola, XII-2022 (1 ♀).

Previous records — Algeria; Anjouan Island; Argentina; Australia; Queensland; Azerbaijan; Brazil - Amazonas, Bahia, Mato Grosso, Pará, Paraná, Pernambuco, Rio Grande do Sul, São Paulo, Tocantins; Cameroon; Cape Verde; China; Colombia; Costa Rica; Cuba; Egypt; Georgia; Guinea; Hawaii; India; Indonesia; Iran; Israel; Italy; Japan; Jordan; Kenya; Mexico; New Caledonia; Panama; Peru; Philippines; Reunion Island; Singapore; South Africa; Spain; Taiwan; United States of America.

ObservationTyphlodromus (Anthoseius) transvaalensis was previously recorded in Goiás State by Rossetti et al. (2025).

Discussion

The grass species used for pastures in Goiás State act as reservoirs for predatory mites. In the present study, 21 Phytoseiidae species were recorded in pastures used for livestock. These results were similar to the findings of Lofego et al. (2009), which in turn, reported 21 phytoseiid mites on grasses of the species U. decumbens, U. brizantha, U. ruziziensis, Melinis minutiflora, Urochloa lorentziana, and Pennisetum purpureum in São Paulo State. Previous studies on native plants in the Cerrado recorded 34 species of Phytoseiidae (Demite et al. 2017), while another survey reported 26 species of mites from the same family (Rezende and Lofego 2011). In the Pantanal biome, Mendonça et al. (2019) reported 35 Phytoseiidae species associated with native trees. Additionally, collections carried out in the Cerrado, Pantanal, and Amazon Forest recorded nine, 16, and 11 species, respectively (Conceição et al. 2021), while another sampling in the same biomes recorded five, five, and 17 phytoseiid species, respectively (Demite et al. 2021). Rossetti et al. (2025) recorded 19 phytoseiid species in remnants of Cerrado vegetation in the state of Goiás. Thus, pasture areas, although simplified ecosystems, can exhibit considerable diversity when compared to natural vegetation remnants.

Among Phytoseiidae species sampled, only I. zuluagai, N. benjamini, P. mexicanus and P. biologicus have been previously reported in Brazilian grasslands (Lofego et al. 2009). For the remaining species, this study provides the first record in Brazilian pasture crops. Proprioseiopsis ovata was the most abundant species in the evaluated pastures. Species from this genus are widely used in natural biological control. For example, P. mexicanus, the third most abundant phytoseiid species sampled here, is a generalist predator with the potential to control arthropod pests (Yuan et al., 2025). Proprioseiopsis mexicanus has also been recorded at high abundances during the wet season (Mailloux et al. 2010). Neoseiulus benjamini was the second most abundant species in pastures from livestock farms in Goiás State. This species was previously reported on monocotyledonous plants from the families Poaceae and Cyperaceae (Demite et al. 2017; Ferragut and Navia 2022).

Our results showed that Poaceae crops support a rich assemblage of Phytoseiidae species. Therefore, assessing the biodiversity in pastures is essential for crop management, as these grass species are widely used for soil cover in Brazilian agroecosystems (Flechtmann 2004; Aguilar-Fenollosa et al. 2011; Blanco-Pérez et al. 2020). These results highlights the importance of avoiding farm management practices that affect predator populations (Farfan et al. 2021). However, more studies are necessary to increase our knowledge of the biodiversity associated with pasture crops and the interactions between mites and grasses.

Acknowledgements

Financial support was provided by CAPES/FAPEG within the ''Apoio aos Programas de Pós-Graduação Emergentes e em Consolidação em Áreas Prioritárias nos Estados» Program [Proc. nº 202010267000426]. V.L. Falchi was supported by a scholarship from the ''Coordenação de Aperfeiçoamento de Pessoal de Nível Superior» (CAPES) and Fundação de Amparo à Pesquisa do Estado de Goiás (FAPEG). L.L.C. Ribeiro receives a scholarship from CAPES/FAPEG. To the researcher Antônio Carlos Lofego (Universidade Estadual Paulista – UNESP, São José do Rio Preto, São Paulo, Brazil) for providing the microscope used for the identification of Phytoseiidae. We also thank Maria Victória Cordeiro Gama (Universidade Federal de Goiás) for reviewing the manuscript.



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Date received:
2025-10-07
Date accepted:
2025-11-03
Date published:
2025-11-14

Edited by:
Kreiter, Serge

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2025 Falchi, Vanessa L.; Ribeiro, Lana Letícia C.; Demite, Peterson R. and Daud, Rodrigo D.
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