Transcription factor Tox2 is required for metabolic adaptation and tissue residency of ILC3 in the gut.

Group 3 innate lymphoid cells (ILC3) are the major subset of gut-resident ILC with essential roles in infections and tissue repair, but how they adapt to the gut environment to maintain tissue residency is unclear. We report that Tox2 is critical for gut ILC3 maintenance and function. Gut ILC3 highly expressed Tox2, and depletion of Tox2 markedly decreased ILC3 in gut but not at central sites, resulting in defective control of Citrobacter rodentium infection. Single-cell transcriptional profiling revealed decreased expression of Hexokinase-2 in Tox2-deficient gut ILC3. Consistent with the requirement for hexokinases in glycolysis, Tox2-/- ILC3 displayed decreased ability to utilize glycolysis for protein translation. Ectopic expression of Hexokinase-2 rescued Tox2-/- gut ILC3 defects. Hypoxia and interleukin (IL)-17A each induced Tox2 expression in ILC3, suggesting a mechanism by which ILC3 adjusts to fluctuating environments by programming glycolytic metabolism. Our results reveal the requirement for Tox2 to support the metabolic adaptation of ILC3 within the gastrointestinal tract.

Transcriptional and epigenetic regulation in thymic epithelial cells.

The thymus is required for the development of both adaptive and innate-like T cell subsets. There is keen interest in manipulating thymic function for therapeutic purposes in circumstances of autoimmunity, immunodeficiency, and for purposes of immunotherapy. Within the thymus, thymic epithelial cells play essential roles in directing T cell development. Several transcription factors are known to be essential for thymic epithelial cell development and function, and a few transcription factors have been studied in considerable detail. However, the role of many other transcription factors is less well understood. Further, it is likely that roles exist for other transcription factors not yet known to be important in thymic epithelial cells. Recent progress in understanding of thymic epithelial cell heterogeneity has provided some new insight into transcriptional requirements in subtypes of thymic epithelial cells. However, it is unknown whether progenitors of thymic epithelial cells exist in the adult thymus, and consequently, developmental relationships linking putative precursors with differentiated cell types are poorly understood. While we do not presently possess a clear understanding of stage-specific requirements for transcription factors in thymic epithelial cells, new single-cell transcriptomic and epigenomic technologies should enable rapid progress in this field. Here, we review our current knowledge of transcription factors involved in the development, maintenance, and function of thymic epithelial cells, and the mechanisms by which they act.

Transcriptional Regulation of Yin-Yang 1 Expression through the Hypoxia Inducible Factor-1 in Pediatric Acute Lymphoblastic Leukemia.

Yin-Yang transcription factor 1 (YY1) is involved in tumor progression, metastasis and has been shown to be elevated in different cancers, including leukemia. The regulatory mechanism underlying YY1 expression in leukemia is still not understood. Bioinformatics analysis reveal three Hypoxia-inducible factor 1-alpha (HIF-1α) putative binding sites in the YY1 promoter region. The regulation of YY1 by HIF-1α in leukemia was analyzed. Mutation of the putative YY1 binding sites in a reporter system containing the HIF-1α promoter region and CHIP analysis confirmed that these sites are important for YY1 regulation. Leukemia cell lines showed that both proteins HIF-1α and YY1 are co-expressed under hypoxia. In addition, the expression of mRNA of YY1 was increased after 3 h of hypoxia conditions and affect several target genes expression. In contrast, chemical inhibition of HIF-1α induces downregulation of YY1 and sensitizes cells to chemotherapeutic drugs. The clinical implications of HIF-1α in the regulation of YY1 were investigated by evaluation of expression of HIF-1α and YY1 in 108 peripheral blood samples and by RT-PCR in 46 bone marrow samples of patients with pediatric acute lymphoblastic leukemia (ALL). We found that the expression of HIF-1α positively correlates with YY1 expression in those patients. This is consistent with bioinformatic analyses of several databases. Our findings demonstrate for the first time that YY1 can be transcriptionally regulated by HIF-1α, and a correlation between HIF-1α expression and YY1 was found in ALL clinical samples. Hence, HIF-1α and YY1 may be possible therapeutic target and/or biomarkers of ALL.

Automatic discovery of 100-miRNA signature for cancer classification using ensemble feature selection.

BACKGROUND: MicroRNAs (miRNAs) are noncoding RNA molecules heavily involved in human tumors, in which few of them circulating the human body. Finding a tumor-associated signature of miRNA, that is, the minimum miRNA entities to be measured for discriminating both different types of cancer and normal tissues, is of utmost importance. Feature selection techniques applied in machine learning can help however they often provide naive or biased results. RESULTS: An ensemble feature selection strategy for miRNA signatures is proposed. miRNAs are chosen based on consensus on feature relevance from high-accuracy classifiers of different typologies. This methodology aims to identify signatures that are considerably more robust and reliable when used in clinically relevant prediction tasks. Using the proposed method, a 100-miRNA signature is identified in a dataset of 8023 samples, extracted from TCGA. When running eight-state-of-the-art classifiers along with the 100-miRNA signature against the original 1046 features, it could be detected that global accuracy differs only by 1.4%. Importantly, this 100-miRNA signature is sufficient to distinguish between tumor and normal tissues. The approach is then compared against other feature selection methods, such as UFS, RFE, EN, LASSO, Genetic Algorithms, and EFS-CLA. The proposed approach provides better accuracy when tested on a 10-fold cross-validation with different classifiers and it is applied to several GEO datasets across different platforms with some classifiers showing more than 90% classification accuracy, which proves its cross-platform applicability. CONCLUSIONS: The 100-miRNA signature is sufficiently stable to provide almost the same classification accuracy as the complete TCGA dataset, and it is further validated on several GEO datasets, across different types of cancer and platforms. Furthermore, a bibliographic analysis confirms that 77 out of the 100 miRNAs in the signature appear in lists of circulating miRNAs used in cancer studies, in stem-loop or mature-sequence form. The remaining 23 miRNAs offer potentially promising avenues for future research.

Rapid and extensive karyotype diversification in haploid clinical Candida auris isolates.

Candida auris is a newly emerged pathogenic microbe, having been identified as a medically relevant fungus as recently as 2009. It is one of the most drug-resistant yeast species known to date and its emergence and population structure are unusual. Because of its recent emergence, we are largely ignorant about fundamental aspects of its general biology, life cycle, and population dynamics. Here, we report the karyotype variability of 26 C. auris strains representing the four main clades. We demonstrate that all strains are haploid and have a highly plastic karyotype containing five to seven chromosomes, which can undergo marked alterations within a short time frame when the fungus is put under genotoxic, heat, or osmotic stress. No simple correlation was found between karyotype pattern, drug resistance, and clade affiliation indicating that karyotype heterogeneity is rapidly evolving. As with other Candida species, these marked karyotype differences between isolates are likely to have an important impact on pathogenic traits of C. auris.

Nitrate assimilation pathway (NAP): role of structural (nit) and transporter (ntr1) genes in Fusarium oxysporum f.sp. lycopersici growth and pathogenicity.

The tomato pathogen Fusarium oxysporum f.sp. lycopersici possesses the capability to use nitrate as the only nitrogen source under aerobic and anaerobic conditions and to activate virulence-related functions when cultivated in the presence of nitrate, but not in ammonium. The genome of F. oxysporum f.sp. lycopersici encodes three paralogs nitrate reductase (NR) genes (nit1, nit2 and nit3) and one predicted ortholog of the Aspergillus nidulans high-affinity nitrate/nitrite transporters NtrA and NtrB, named ntr1. We set out to clarify the role of nit1, nit2, nit3 and ntr1 genes in nitrate assimilation and in the virulence of F. oxysporum f.sp. lycopersici. Quantitative RT-PCR analysis revealed that only nit1, nit2 and ntr1 are expressed at significant levels during growth in nitrate as the only nitrogen source. Targeted deletion of nit1 and ntr1, but not of nit2 or nit3, severely impaired growth of F. oxysporum on nitrate as nitrogen source, indicating that Nit1 and Ntr1 proteins are involved in nitrate assimilation by the fungus; biochemical analysis of nit mutants indicated that Nit1 and Nit2 enzymes contribute to about 50 and 30% of the total NR activity, respectively. In addition, a spontaneous chlorate-resistant mutant derived from F. oxysporum 4287, denoted NitFG, was characterized, showing inability to grow in nitrate under aerobic and anaerobic conditions and low levels of NR activity, in spite of its increased transcription levels of nit1 and nit2 genes. Tomato plant infection assays showed that NitFG and ∆ntr1 mutants induced an earlier death in tomato plants, whereas the single mutants ∆nit1, ∆nit2 and ∆nit1∆nit2 double mutant showed a mortality rate similar to the wild-type strain. Taken together, these results indicate that the Nit1 and Ntr1 proteins are important for nitrate assimilation of F. oxysporum f.sp. lycopersici incubated under aerobic and anaerobic conditions and that this metabolic process is not essential for the virulence of the fungus. These observations open new questions about the role of Nit1, Nit2, and Nit3 proteins in other routes of nitrate metabolism in this pathogenic fungus and in the possible regulatory role that can be exerted by the AreA protein in these routes.

DNA Oxidation Photoinduced by Norharmane Rhenium(I) Polypyridyl Complexes: Effect of the Bidentate N,N'-Ligands on the Damage Profile.

ReI -polypyridyl complexes have interesting and distinctive photochemical and photosensitizing properties. This work describes the capability to induce (or photoinduce) DNA damage of three ReI -complexes with a naturally occurring alkaloid called norharmane (nHo) as ligand: [Re(CO)3 (nHo)(L)]CF3 SO3 where L=2,2'-bipyridine (ReBpy), phenanthroline (RePhen) or dipyrido[3,2-a:2',3'-c]phenazine (ReDppz). The interaction of the complexes with DNA was investigated by steady-state and time-resolved spectroscopy. Data show that the mode and strength of interaction depend on the chemical structure of the bidentate ligand. The complexes show a major static contribution to the overall interaction, giving rise to the formation of noncovalent adducts with DNA, and the particular trend observed was RePhen>ReDppz>ReBpy. Photo-oxidation at the purine bases represents the major DNA damaging mechanism. RePhen also induces single-strand breaks in a yield similar to that of base damage, suggesting an additional photosensitizing pathway. We also performed the Ames test to evaluate the cytotoxic and mutagenic properties of both non-irradiated and photoexcited complexes. RePhen, but not the other complexes, turned out to be both toxic and phototoxic for the bacteria.

Association studies to transporting proteins of fac-ReI(CO)3(pterin)(H2O) complex.

A new synthetic route to acquire the water soluble complex fac-ReI(CO)3(pterin)(H2O) was carried out in aqueous solution. The complex has been obtained with success via the fac-[ReI(CO)3(H2O)3]Cl precursor complex. ReI(CO)3(pterin)(H2O) has been found to bind strongly with bovine and human serum albumins (BSA and HSA) with intrinsic-binding constants, Kb, of 6.5 × 105 M-1 and 5.6 × 105 M-1 at 310 K, respectively. The interactions of serum albumins with ReI(CO)3(pterin)(H2O) were evaluated employing UV-vis fluorescence and absorption spectroscopy and circular dichroism. The results suggest that the serum albumins-ReI(CO)3(pterin)(H2O) interactions occurred in the domain IIA-binding pocket without loss of helical stability of the proteins. The comparison of the fluorescence quenching of BSA and HSA due to the binding to the Re(I) complex suggested that local interaction around the Trp 214 residue had taken place. The analysis of the thermodynamic parameters ΔG0, ΔH0, and ΔS0 indicated that the hydrophobic interactions played a major role in both HSA-Re(I) and BSA-Re(I) association processes. All these experimental results suggest that these proteins can be considered as good carriers for transportation of ReI(CO)3(pterin)(H2O) complex. This is of significant importance in relation to the use of this Re(I) complex in several biomedical fields, such as photodynamic therapy and radiopharmacy.

The Inhibitory Activity of Plants from Central Argentina on p-Hydroxyphenylpyruvate Dioxygenase. Isolation and Mechanism of Inhibition of a Flavanone from Flourensia oolepis.

The enzyme 4-hydroxyphenylpyruvate dioxygenase catalyzes the second step in the tyrosine degradation pathway. In mammals, this enzyme is the molecular target of drugs used for the treatment of metabolic disorders associated with defects in the tyrosine catabolism, mainly the fatal hereditary disease tyrosinemia type 1. This study evaluated the inhibitory effect of 91 extracts on 4-hydroxyphenylpyruvate dioxygenase from mostly native plants from central Argentina. Flourensia oolepis ethanol extract showed itself to be the most effective, and bioguided fractionation yielded pinocembrin (1) as its active principle. This flavanone, with an IC50 value of 73.1 µM and a KI of 13.7 µM, behaved as a reversible inhibitor of the enzyme and as a noncompetitive inhibitor. Molecular modeling studies confirmed the inhibitory potency of 1 and explained its activity by means of in silico determination of its binding mode in comparison to inhibitors of known activity, cocrystallized with 4-hydroxyphenylpyruvate dioxygenase. The main structural determinants that confer its potency are discussed. Analysis of the binding mode of the flavanone 1 with 4-hydroxyphenylpyruvate dioxygenase revealed the basis of the noncompetitive reversible mechanism of inhibition at the molecular level, which seems to be a common feature in this ubiquitous family of natural compounds. The resulting information may establish the basis for obtaining novel 4-hydroxyphenylpyruvate dioxygenase inhibitors for the treatment of tyrosinemia type 1 and other disorders associated with tyrosinase catabolism.

Solvent dependent switching of 3MLLCT and 1IL luminescent states in [ClRe(CO)3(bathocuproinedisulfonate)]2-: spectroscopic and computational study.

Steady state and time-resolved luminescence experiments and calorimetric studies, as well as time-dependent density functional theory calculations performed on [ClRe(CO)(3)(Bathocuproinedisulfonate)](2-), show that the photophysical properties of the Re(I) anionic complex are determined by the balance between intraligand ((1)IL) and metal-ligand-to-ligand charge transfer ((3)MLLCT) excited states. In organic solvents, (3)MLLCT states prevail and the usual expected behavior is observed: bathochromic shift of the emission maximum, a reduced luminescence quantum yield and the shortening of the excited-state lifetime upon increasing the polarity of the solvent. In addition, singlet oxygen ((1)O2) is generated with high quantum yields (Φ(Δ) ≈ 0.5 in CH(3)CN) due to the quenching of the (3)MLLCT luminescence by (3)O2. The total quenching rate constant of triplet state by oxygen, k(q), reach values between 2.2 and 2.4 × 10(9) M(-1) s(-1) for the organic solvents studied. In CH(3)CN, the fraction of triplet states quenched by O2 which yield (1)O2, f(O2)T, is nearly unity. In aqueous solution, where no singlet oxygen is generated, the luminescence of the Re(I) complex is of (1)IL character with a emission quantum yield (Φ(em)) strongly pH dependent: Φ(em,(pH=2))/Φ(em,(pH=10)) ≈ 5.6. The variation of the pH of the solution tunes the photophysical properties of the Re(I) complex by changing the relative amount of the different species existing in aqueous solutions: [ClRe(CO)3(BCS)](2-), [(OH)Re(CO)3(BCS)](2-) and [(H2O)Re(CO)3(BCS)](−). TD-DFT calculations show that the percentage of charge transfer character of the electronic transitions is substantially higher in the organic solvents than in aqueous solutions, in agreement with the increase of (1)IL character of HOMO in [(H2O)Re(CO)3(BCS)](−) relative to [ClRe(CO)3(BCS)](2-).

Revision of the acutidens group of Mago (Araneae: Salticidae: Amycinae).

Of all the amycines, the acutidens group of species of Mago is one of the most commonly collected groups throughout the Amazon. Redescriptions of M. acutidens Simon and M. longidens Simon by Galiano initially helped separating the two species, but then it became clear that we were dealing with a group of several similar species demanding revision. In order to make identification possible, we present here a revision of this newly proposed group of species, providing illustrations of the male palp and epigyne for all the recognized species. The female of M. longidens Simon is described for the first time. Besides the new records for both M. acutidens and M. longidens, we present M. jurutiensis sp. nov. and M. similis sp. nov. from Juruti, Pará, Brazil, M. delicatus sp. nov. from several localities in the Brazilian states of Amazonas and Pará, and M. balbina sp. nov. from Presidente Figueiredo, Amazonas. Maps with collecting records for all species of the group are presented.

On the boundary of the jumping spider genus Rhyphelia Simon, 1902 (Araneae: Salticidae: Euophryini), with description of ten new species.

In this paper we synonymize Soesilarishius Makhan, 2007 with Rhyphelia Simon, 1902. We give new illustrations of the male holotype of the type species Rhyphelia variegata Simon, 1902 for comparisons, and describe the closely related Rhyphelia brevistylus sp. nov. () from the state of Bahia, Brazil. Additionally, we describe nine other new species from different Brazilian regions: Rhyphelia barbado sp. nov. () from Bahia, Rhyphelia bilineata sp. nov. () from Minas Gerais, Rhyphelia cotriguacuensis sp. nov. () from Mato Grosso, Rhyphelia gallina sp. nov. () from Acre, Rhyphelia novalima sp. nov. () and Rhyphelia okay sp. nov. () from Minas Gerais, Rhyphelia otti sp. nov. () from Rio Grande do Sul, Rhyphelia planaria sp. nov. () from So Paulo, and Rhyphelia tocantinensis sp. nov. () from Tocantins.

Snowflake: visualizing microbiome abundance tables as multivariate bipartite graphs.

Current visualizations in microbiome research rely on aggregations in taxonomic classifications or do not show less abundant taxa. We introduce Snowflake: a new visualization method that creates a clear overview of the microbiome composition in collected samples without losing any information due to classification or neglecting less abundant reads. Snowflake displays every observed OTU/ASV in the microbiome abundance table and provides a solution to include the data's hierarchical structure and additional information obtained from downstream analysis (e.g., alpha- and beta-diversity) and metadata. Based on the value-driven ICE-T evaluation methodology, Snowflake was positively received. Experts in microbiome research found the visualizations to be user-friendly and detailed and liked the possibility of including and relating additional information to the microbiome's composition. Exploring the topological structure of the microbiome abundance table allows them to quickly identify which taxa are unique to specific samples and which are shared among multiple samples (i.e., separating sample-specific taxa from the core microbiome), and see the compositional differences between samples. An R package for constructing and visualizing Snowflake microbiome composition graphs is available at https://gitlab.com/vda-lab/snowflake.

Lipolytic system of the tomato pathogen Fusarium oxysporum f. sp. lycopersici.

The lipolytic profile of Fusarium oxysporum f. sp lycopersici was studied by in silico search and biochemical enzyme activity analyses. Twenty-five structural secreted lipases were predicted based on the conserved pentapeptide Gly-X-Ser-X-Gly-, characteristic of fungal lipases, and secretion signal sequences. Moreover, a predicted lipase regulatory gene was identified in addition to the previously characterized ctf1. The transcription profile of thirteen lipase genes during tomato plant colonization revealed that lip1, lip3, and lip22 were highly induced between 21 and 96 h after inoculation. Deletion mutants in five lipase genes (lip1, lip2, lip3, lip5, and lip22) and in the regulatory genes ctf1 and ctf2 as well as a Δctf1Δctf2 double mutant were generated. Quantitative reverse transcription-polymerase chain reaction expression analyses of structural lipase genes in the Δctf1, Δctf2, and Δctf1Δctf2 mutants indicated the existence of a complex lipase regulation network in F. oxysporum. The reduction of total lipase activity, as well as the severely reduced virulence of the Δctf1, Δctf2, and Δctf1Δctf2 mutants, provides evidence for an important role of the lipolytic system of this fungus in pathogenicity.

Photosensitized generation of singlet oxygen from Re(I) complexes: a photophysical study using LIOAS and luminescence techniques.

Quantum yields and efficiencies of (1)O2 ((1)Δg) production along with photophysical properties for a number of Re(I) complexes in acetonitrile solutions are reported. Two different classes of Re(I) complexes, L(S)-CO2-Re(CO)3(bpy) (L(S) = 2-pyrazine, 2-naphthalene, 9-anthracene, 1-pyrene, 2-anthraquinone) and XRe(CO)3L (X = CF3SO3, py; L = bpy, phen), were probed as photosensitizers for (1)O2 ((1)Δg) production in air-saturated acetonitrile solutions. Depending on the nature of the Re(I) complex, the excited state responsible for the generation of (1)O2 ((1)Δg) is either a metal-to-ligand charge transfer ((3)MLCT) or a ligand centered ((3)LC) state. With L(S)-CO2-Re(CO)3(bpy) complexes, (1)O2 ((1)Δg) is produced by oxygen quenching of (3)LC states of anthracene and pyrene with high quantum yields (ΦΔ between 0.8 and 1.0), while the complexes bearing the ligands L(S) = 2-anthraquinone, 2-pyrazine, and 2-naphthalene did not yield (1)O2. XRe(CO)3L complexes generate (1)O2 ((1)Δg) mainly by oxygen quenching of their (3)MLCT luminescence with an efficiency of (1)O2 ((1)Δg) formation close to unity. Bimolecular rate constants for the quenching of the XRe(CO)3L complexes' emission by molecular oxygen range between 1 × 10(9) and 2 × 10(9) M(-1) s(-1), and they are all ≤ (1/9)kd, in good agreement with the predominance of the singlet channel in the mechanism of (1)O2 ((1)Δg) generation using these Re(I) complexes as photosensitizers. All the experimental singlet oxygen efficiencies are consistent with calorimetric and luminescence data for the studied complexes. With L(S)-CO2-Re(CO)3(bpy) complexes, calorimetric experiments were utilized in the calculation of the quantum yields of triplet formation; namely φT = 0.76 and 0.83 for the triplet states of anthracene and pyrene, respectively.

Nine new species of Soesilarishius from Brazil (Araneae: Salticidae: Euophryinae).

Nine new species of Soesilarishius Makhan, 2007 are described from Brazil, raising the genus member list up to 20 species. Soesilarishius chaplini sp. nov., S. paxiuba sp. nov. and S. muiratinga sp. nov. are described from the state of Pará. Soesilarishius bicrescens sp. nov., S. excentricus sp. nov. and S. flagellator sp. nov. are described from the state of Piauí. Soesilarishius inacrochelis sp. nov. and S. cearensis sp. nov. are described from the state of Ceará. Soesilarishius tabernarius sp. nov. is described from the state of Bahia. Both sexes are described for the new species, except for S. inuiratinga, S. bicrescens, S. excentricus and S. tabernarius, whose females remain unknown.

Revision of Breda and proposal of a new genus (Araneae: Salticidae).

The genus Breda Peckham & Peckham, 1894 is revised and nine valid species are redescribed and illustrated. The monotypic Paradescanso Vellard, 1924 is established as a new junior synonym of the genus. Breda modesta (Taczanowski, 1878) comb. nov. is transferred from Balmaceda Peckham & Peckham. The following synonymies are also established: Paradescansofallax Vellard, 1924 = Breda apicalis Simon, 1901 syn. nov.; B. quinquedentata Badcock, 1932 = B. apicalis Simon, 1901 syn. nov.; B. leucoprocta Mello-Leitão, 1940 = B. modesta (Taczanowski, 1878) syn. nov.; B. spinimanu (Mello-Leitão, 1941) = B. modesta (Taczanowski, 1878) syn. nov. The females of B. bicruciata (Mello-Leitão, 1943) and B. bistriata (C.L. Koch, 1846) are described and illustrated for the first time, as well as the male of B. lubomirskii (Taczanowski, 1878). Both sexes of Breda akypueruna sp. nov. and males of B. nanica sp. nov. and B. paraensis sp. nov., all three from the Amazon, are described and illustrated, increasing the present member list up to 13 species. Druzia gen. nov. is proposed to include B.flavostriata Simon, 1901. The Australian "Breda" jovialis (L. Koch, 1879) is tentatively transferred to Ocrisiona Simon.

First description of the male genitalia in a short-tailed whipscorpion (Arachnida: Schizomida), description of the female, and comments on pygidial glands and cuticular ultrastructure of Surazomus algodoal Ruiz & Valente, 2017.

The male genitalia of Surazomus algodoal Ruiz & Valente, 2017 are described. Since this is the first attempt to describe male genitalia in the schizomids, we propose new terminology to describe the sclerites of the male genital chamber in the order. We believe that the male genitalia may provide a large set of characters for taxonomic research in schizomids, as the female genitalia have proven to do. The setae and other cuticular structures were investigated using light and scanning electron microscopy (SEM). The female of S. algodoal is described for the first time, including the genitalia, and we highlight the sexual dimorphism present in the species. We also present descriptions of: 1) microtrichia, with respect to their presence/length/distribution, 2) cuticular sensilla, glandular openings and other cuticular structures, proposing new terminology, 3) setae of the pedipalpal trochanter and tarsus. Some changes on the terminology of setae of pedipalpal tibia are also given. These advances may be useful for description in other schizomids. The pygidial glands, mostly ignored in modern papers, were assessed and commented upon.

On the taxonomy of the jumping spider genus Matinta Ruiz & Maddison, 2019, with a taxonomic revision of the vicana species-group (Araneae: Salticidae: Amycini).

The male of Matinta opiparis (Simon, 1900) is redescribed based on fresh material, and the female is described for the first time. Matinta tatianae sp. nov. (male) is described from Acre and Par, Brazil. The vicana species-group of Matinta is revised, as follows: the males of M. silvae (Crane, 1943), M. fonsecai (Soares & Camargo, 1948), and M. vicana (Simon, 1900), and the female of M. silvae are redescribed based on fresh material. Three new species of the group are described: Matinta maddisoni sp. nov. from Morona Santiago, Ecuador (); Matinta pereirae sp. nov. from Amazonas, Brazil (); and Matinta aragog sp. nov. from French Guiana (). Detailed description of cheliceral dentition is given and commented. We conclude that the complex dentition within Amycini should be revised and more carefully studied.

Boosting precision crop protection towards agriculture 5.0 via machine learning and emerging technologies: A contextual review.

Crop protection is a key activity for the sustainability and feasibility of agriculture in a current context of climate change, which is causing the destabilization of agricultural practices and an increase in the incidence of current or invasive pests, and a growing world population that requires guaranteeing the food supply chain and ensuring food security. In view of these events, this article provides a contextual review in six sections on the role of artificial intelligence (AI), machine learning (ML) and other emerging technologies to solve current and future challenges of crop protection. Over time, crop protection has progressed from a primitive agriculture 1.0 (Ag1.0) through various technological developments to reach a level of maturity closelyin line with Ag5.0 (section 1), which is characterized by successfully leveraging ML capacity and modern agricultural devices and machines that perceive, analyze and actuate following the main stages of precision crop protection (section 2). Section 3 presents a taxonomy of ML algorithms that support the development and implementation of precision crop protection, while section 4 analyses the scientific impact of ML on the basis of an extensive bibliometric study of >120 algorithms, outlining the most widely used ML and deep learning (DL) techniques currently applied in relevant case studies on the detection and control of crop diseases, weeds and plagues. Section 5 describes 39 emerging technologies in the fields of smart sensors and other advanced hardware devices, telecommunications, proximal and remote sensing, and AI-based robotics that will foreseeably lead the next generation of perception-based, decision-making and actuation systems for digitized, smart and real-time crop protection in a realistic Ag5.0. Finally, section 6 highlights the main conclusions and final remarks.