Viral Diagnosis in Psittacine Birds: A Scientometric and Systematic Review of 47 Years.

The first reports of viruses in psittacine birds date back to the early 1970s. Here, we elucidate the differences among these previous studies and the advances achieved. The objective of this study was to carry out a comprehensive review using both scientometric and systematic methods to analyze the evolution of published studies on viruses in psittacine birds up to 2022. The search descriptors "virus", "diagnosis", and "Psittaciformes" were used to find the articles of interest for this study. A total of 118 articles were manually selected, and the scientometric data were organized using the software VOSviewer® version 1.6.18. The present review revealed that: (i) on average, 2.5 articles/year on the diagnosis of viral infection in psittacine birds were published since 1975; (ii) the most productive research groups are concentrated in three countries: Australia, the United States, and Germany; (iii) the most important virus in psittacine birds is the Circovirus, which causes psittacine beak and feather disease; (iv) the diagnostic method of choice is polymerase chain reaction (PCR); and (v) the most studied psittacine birds were those in the Psittacidae family that were kept in captivity.

First karyotype description of the species of Adenomera Steindachner, 1867 (Anura, Leptodactylidae) in the " thomei" clade.

The genus Adenomera Steindachner, 1867 currently comprises 29 nominal species, some of which are suggested to be cryptic species complexes. The present study was carried out with specimens of the "thomei" clade that encompasses three taxa distributed in the Atlantic Forest biome: Adenomerathomei Almeida et Angulo, 2006, Adenomera sp. L., and Adenomera sp. M. We used classical cytogenetics to describe the diploid number and karyomorphology of these three species collected in two different locations in the state of Bahia, Brazil. Our results revealed the diploid number 2n = 24 (FN = 34) with two pairs of metacentric chromosomes (pairs 1 and 5), three pairs of submetacentric chromosomes (pairs 2, 3, and 4), and seven pairs of telocentric chromosomes (pairs 6, 7, 8, 9, 10, 11, and 12). Further morphological, bioacoustic, and cytogenetic data (C-banding and AgNor) are needed to better delineate the lineages within the "thomei" clade.

Predicting the Invasion Risk by Anastrepha sororcula (Diptera: Tephritidae) in Distinct Geographic Regions.

The movement of endemic fruit flies to new habitats represents a major biological and economic threat. Anastrepha sororcula Zucchi, 1979 is widely distributed in Brazil and also in Colombia, Ecuador, and Paraguay. Here, we present the potential distribution of A. sororcula in endemic areas and project this model into other regions such as part of sub-Saharan Africa, Central America, and Asia to show areas around the world that this species can potentially establish. We combined geographic coordinates with climate data. The models were built using the maximum entropy (MaxEnt) algorithm. Many mango- and guava-producing countries exhibited climatic suitability for A. sororcula in the regions studied including the nine largest world producers: India, Brazil, Malawi, Kenya, Haiti, Cuba, Colombia, Madagascar, and the Democratic Republic of the Congo. Many of these countries showed ideal host plant availability and climatic conditions for the entry and establishment of A. sororcula. This study is a pioneer in the identification of representative areas in the world with climatic suitability for A. sororcula, which shows the importance of predicting areas at risk of invasion to monitor the movement and establishment of fruit fly species in new regions, which is fundamental to area-wide integrated pest management programs.

Fertility life table and biology of Tetrastichus giffardianus (Hymenoptera: Eulophidae) in the larvae of Ceratitis capitata (Diptera: Tephritidae).

Tetrastichus giffardianus is a gregarious koinobiont endoparasitoid of tephritids, including Ceratitis capitata, which is one of the most important fruit pests worldwide. The objective of this study was to evaluate the effect of constant temperatures on the biology and development of the egg-adult period of T. giffardianus in larvae/pupae of C. capitata to construct a fertility life table. The study was carried out in climatic chambers at constant temperatures of 15, 20, 25, 30, and 35 ± 1°C, 70 ± 10% relative humidity and a photophase of 12 h. Complete egg and larval development occurred only at temperatures of 20, 25, and 30°C. The mean longevity of males and females was inversely proportional to temperature. The time of development of the pre-imaginal period was influenced by temperature and ranged from 41 days at 20°C to 11 days at 25°C. The best T. giffardianus performance occurred at 25°C when the intrinsic rate of increase was 0.21, the mean generation time was 20.43 days, the time required to double the population was 3.33 days, and the finite rate of population increase (λ) was 1.23. The results of this study provided information for the establishment of mass rearing and an evaluation of the adaptability of T. giffardianus to different environments, which is necessary for the use of this parasitoid in the biological control of tephritid pests, particularly C. capitata.

Oil palm age and genotype interfere with defoliator lepidopteran infestation

The state of Pará has oil palm plantings of different ages and distinct genotypes. The understanding of which factors influence the occurrence and abundance of defoliating caterpillars in palm groves is paramount for control strategies based on integrated pest management (IPM). This study quantified the effect of oil palm age independently, and that of oil palm age and genotype, on the occurrence and abundance of defoliating caterpillars. Data were collected from 1994­2014 and consisted of counting the average number of caterpillars/leaf/parcel. For Opsiphanes invirae and Talima sp., leaf 17 was sampled; for Acharia spp., Euclea sp., Euprosterna elaeasa, Natada sp., and Automeris liberia, leaf 25 was sampled. For Oiketicus kirbyi, Antaeotricha sp., and Brassolis sophorae no specific leaf was considered. Palm trees were classified into three groups: young palm trees (0­8 years after planting), adult palm trees (9­19 years after planting), and old palm trees (over 20 years after planting). Talima sp. showed the highest population peak followed by O. invirae, Acharia spp., Elaeis elaeasa and Euclea sp. This study concludes that genotype has an impact on the infestation by defoliating caterpillars. Also, oil palms at reproductive age are more prone to higher infestation levels than young trees. While population levels of defoliating caterpillars are low in general, outbreaks are frequent. Importantly, intraspecific genotypes are more vulnerable than interspecific genotypes to infestations by defoliating caterpillars. This study contributes to the bioecological knowledge on defoliating caterpillars on oil palm and therefore provides important information to strengthen integrated pest management practices.

First record of Anastrepha bahiensis Lima (Diptera: Tephritidae) infesting fruits of Averrhoa carambola L. in the eastern Amazon, Brazil

ABSTRACT We report for the first time field infestation under natural conditions by Anastrepha bahiensis on star fruit (Averrhoa carambola L., Oxalidaceae) in the state of Pará, Eastern Amazon, Brazil. This report reinforces the importance of field infestation studies on fruit flies in the Brazilian Amazon.

Identifying Anastrepha (Diptera; Tephritidae) Species Using DNA Barcodes.

Molecular identification of fruit flies in the genus Anastrepha (Diptera; Tephritidae) is important to support plant pest exclusion, suppression, and outbreak eradication. Morphological methods of identification of this economically important genus are often not sufficient to identify species when detected as immature life stages. DNA barcoding a segment of the mitochondrial cytochrome oxidase I gene has been proposed as a method to identify pests in the genus. The identification process for these fruit flies, however, has not been explained in prior DNA barcode studies. DNA barcode methods assume that available DNA sequence records are biologically meaningful. These records, however, can be limited to the most common species or lack population-level measurements of diversity for pests. In such cases, the available data used as a reference are insufficient for completing an accurate identification. Using 539 DNA sequence records from 74 species of Anastrepha, we demonstrate that our barcoding data can distinguish four plant pests: Anastrepha grandis (Macquart) (Diptera; Tephritidae), Anastrepha ludens (Loew), Anastrepha serpentina (Wiedemann), and Anastrepha striata Schiner. This is based on genetic distances of barcode records for the pests and expert evaluation of species and population representation in the data set. DNA barcoding of the cytochrome oxidase I gene alone cannot reliably diagnose the pests Anastrepha fraterculus (Wiedemann), Anastrepha obliqua (Macquart), and Anastrepha suspensa (Loew).

Relevant genetic differentiation among Brazilian populations of Anastrepha fraterculus (Diptera, Tephritidae).

We used a population genetic approach to detect the presence of genetic diversity among six populations of Anastrepha fraterculus across Brazil. To this aim, we used Simple Sequence Repeat (SSR) markers, which may capture the presence of differentiative processes across the genome in distinct populations. Spatial analyses of molecular variance were used to identify groups of populations that are both genetically and geographically homogeneous while also being maximally differentiated from each other. The spatial analysis of genetic diversity indicates that the levels of diversity among the six populations vary significantly on an eco-geographical basis. Particularly, altitude seems to represent a differentiating adaptation, as the main genetic differentiation is detected between the two populations present at higher altitudes and the other four populations at sea level. The data, together with the outcomes from different cluster analyses, identify a genetic diversity pattern that overlaps with the distribution of the known morphotypes in the Brazilian area.

First description of the karyotype of a eucharitid wasp (Hymenoptera, Chalcidoidea, Eucharitidae).

The haploid karyotype of Kapala sp. (Eucharitidae), a parasite of the Neotropical ant Dinoponera lucida Emery, 1901 (Hymenoptera, Formicidae), is reported for the first time. It consists of four metacentric chromosomes. Chromosomes in the family Eucharitidae were unknown so far; therefore, our results confirm that multiple parallel chromosomal fusions have taken place in several lineages within the superfamily Chalcidoidea.

Numerical and structural chromosome variation in the swarm-founding wasp Metapolybia decorata Gribodo 1896 (Hymenoptera, Vespidae).

The Neotropical Polistinae wasps are diverse in taxonomy, social behavior, and nesting founding characteristics. Although some species in this group have been used as models for studies on wasp's biology, they are poorly known in terms of cytogenetics. Here we reported an intraspecific numerical-structural chromosome variation in the swarm-founding wasp Metapolybia decorata from the Brazilian Atlantic Rainforest using conventional and molecular cytogenetic techniques. The observed structural chromosome change involved a telomeric fusion that resulted in a chromosome number range of 2n = 34-36. The origin and geographic distribution of the variant chromosome forms as well as their frequency and maintenance in the studied populations are discussed. In addition, we reported a novel and geographically restricted deletion in the fused chromosomes indicating that the species is undergoing a continued process of karyotype evolution leading to fused chromosome stabilization by elimination of inactive centromeric sequences. Evidence of differences in the telomeric sequences of this wasp was also found by in situ hybridization using the motif (T2AG2)7 as probe.

Molecular characterization of constitutive heterochromatin in three species of Trypoxylon (Hymenoptera: Crabronidae: Trypoxylini) by CMA3/DAPI staining.

Previous cytogenetic analyses in Trypoxylon Latreille, 1796 have been basically restricted to C-banding. In the present study, base-specific CMA3 and DAPI fluorochrome staining were used to characterize the constitutive heterochromatin in three Trypoxylon species. The heterochromatin was GC-rich in all the species studied; however, in Trypoxylon nitidum F. Smith, 1856the molecular composition of the heterochromatinwasdifferent among chromosome pairs. Conversely, the euchromatin was AT-rich in the three species. These results suggest high conservatism in the euchromatic regions as opposed to the heterochromatic regions that have a high rate of changes. In this study, we report the karyotype of Trypoxylon rugifrons F. Smith, 1873which has the lowest chromosome number in the genus and other characteristics of the likely ancestral Trypoxylon karyotype.