Early ontogeny of tetra Markiana nigripinnis (Characiformes: Characidae)

The early development of Markiana nigripinnis is described by morphological characters, pigmentation, and morphometry. Larvae were obtained through semi-natural breeding, collected, fixed, and identified according to their development. Eighty individuals with standard lengths ranging from 3.1 to 24.3 mm were analyzed. Larvae are poorly developed at hatching, with a relatively large yolk sac and finfold. At the preflexion stage, the eyes are pigmented, the mouth and anus are functional, the yolk is completely absorbed, and the pectoral fin bud emerges. At flexion, the first rays of the caudal, anal, and dorsal fins become evident. The pelvic fin bud emerges only at the postflexion stage, in addition to the complete absorption of the finfold. Pigmentation is distributed throughout the body, with a greater concentration on the top of the head, around the mouth, and at the base of the caudal fin. The myomere total number ranged from 34 to 49 (16-23 preanal, and 18-27 postanal). Juveniles show morphological characteristics like adults. The fins ray number are pectoral: 11-13, pelvic: 5-7, dorsal: 8-11, caudal: 16-27, and anal 30-47. The morphometric relationships reveal variations in growth along the early ontogeny of the species.

O desenvolvimento inicial de Markiana nigripinnis foi descrito considerando os caracteres morfológicos, a pigmentação e a morfometria. Indivíduos foram obtidos por meio de reprodução seminatural, coletados, acondicionados, fixados e identificados conforme seu período e estágio de desenvolvimento. Foram analisados 80 indivíduos com comprimento padrão variando de 3,1 a 24,3 mm. As larvas são pouco desenvolvidas à eclosão, com saco vitelino relativamente grande e presença de membrana embrionária. Em pré-flexão, os olhos estão pigmentados, a boca e o ânus são funcionais, o vitelo é completamente absorvido e surge o botão da nadadeira peitoral. Em flexão, os primeiros raios das nadadeiras caudal, anal e dorsal tornam-se evidentes. O botão da nadadeira pélvica aparece somente em pós-flexão, além da completa absorção da nadadeira embrionária. A pigmentação se distribui pelo corpo todo, com maior concentração no topo da cabeça, ao redor da boca e na base da nadadeira caudal. O número total de miômeros variou de 34 a 49 (16-23 pré e 18-27 pós-anal). Os juvenis apresentaram características morfológicas semelhantes ao adulto. O número de raios das nadadeiras é peitoral: 11-13, pélvica: 5-7, dorsal: 8-11, caudal: 16-27 e anal 30-47. As relações morfométricas revelam variações no crescimento ao longo da ontogenia inicial da espécie.

Early life history of two Neotropical Triportheidae fish (Characiformes)

The early ontogeny of Triportheus albus and T. angulatus, two fish species of Triportheidae, is described using morphological, meristic, and morphometric characters. These species are exploited by subsistence fisheries and have potential as an alternative source of fish, given the decline in the natural stocks of other commercially important fish species in the Amazon. The specimens were collected in the open water limnetic zone, under of the macrophyte stands, and in subsurface areas near sandbars in the Amazon basin. Intra and interspecific morphometric analyzes were performed to evaluate growth models between species. The combination of color pattern, body morphology, morphometric proportions and myomeres number distinguishes the species from each other and from other congeners. Some morphometric relationships related to head as snout length and eye diameter as well as length from the snout to the origins of anal and length from the snout to the origins of pelvic, related with standard length were different between the two species of Triportheus, reflecting different growth models between them. An identification key for larvae and juveniles of some species of Triportheus from the Eastern Amazon is presented.(AU)

A ontogenia inicial de Triportheus albus e T. angulatus, duas espécies de peixes pertencentes a Triportheidae, é descrita usando caracteres morfológicos, merísticos e morfométricos. Essas espécies são exploradas pela pesca de subsistência e têm potencial como fonte alternativa de pescado, dado o declínio nos estoques naturais de outras espécies de peixes comercialmente importantes na Amazônia. Os espécimes foram coletados na zona limnética de águas abertas, sob bancos de macrófitas e em áreas subsuperficiais próximas a bancos de areia na bacia amazônica. Análises morfométricas, intra e interespecíficas, foram realizadas para avaliar modelos de crescimento entre as espécies. A combinação do padrão de coloração, morfologia corporal, proporções morfométricas e número de miômeros distingue as espécies entre si e de outras congêneres. Algumas relações morfométricas relacionadas à cabeça, como comprimento do focinho e diâmetro do olho, assim como o comprimento do focinho à origem da nadadeira anal e o comprimento do focinho à origem da nadadeira pélvica, relacionadas ao comprimento padrão foram diferentes entre as duas espécies de Triportheus, refletindo modelos distintos de crescimento entre elas. Uma chave de identificação para larvas e juvenis de algumas espécies de Triportheus da Amazônia Oriental é apresentada.(AU)

The correlation between body weight, body weight gain and blood parameters in pigs at birth and weaning / A correlação entre peso corporal, ganho de peso corporal e parâmetros sanguíneos em suínos ao nascimento e desmame

The aim of study was to determine the relationship between metabolic parameters, body weight and body growth of piglets at birth and weaning. The experiment included 80 piglets obtained from F1 generation sows. Body weight was measured at birth (BW0), 24h (BW1) after birth and on day 25 (at weaning, BW2). Blood sampling was performed at the beginning of life (3rd day after birth) and at weaning (21st day after birth). BW0 and BW1 positively correlated with cholesterol and negatively with urea values at the beginning of life and RBC values at weaning. BW2 positively correlates with albumin and cortisol values at the beginning of life, total proteins, and globulins at weaning, and negatively correlates with erythrocyte values at weaning. Piglet growth from birth to weaning (BWG2-0) correlates positively with total proteins, albumin, and cortisol at the beginning of life and total proteins at weaning. ROC analysis shows that MCHC, TPROT, GLOB, CHOL and AST at the beginning of life can distinguish fast-growing from slow-growing piglets from birth to weaning period. The use of blood parameters enables early recognition of growth rate in piglets, which can help to optimize all further steps to achieve the best possible growth.

O objetivo do estudo foi determinar a relação entre parâmetros metabólicos, peso corporal e crescimento corporal de leitões ao nascimento e desmame. A experiência incluiu 80 leitões obtidos de porcas da geração F1. O peso corporal foi medido ao nascimento (BW0), 24h (BW1) após o nascimento e no dia 25 (no desmame, BW2). A amostragem de sangue foi realizada no início da vida (3º dia após o nascimento) e no desmame (21º dia após o nascimento). BW0 e BW1 correlacionaram-se positivamente com o colesterol e negativamente com os valores de uréia no início da vida e com os valores de hemácias no desmame. BW2 correlaciona-se positivamente com os valores de albumina e cortisol no início da vida, proteínas totais e globulinas no desmame, e negativamente com os valores de eritrócitos no desmame. O crescimento do leitão desde o nascimento até o desmame (BWG2-0) se correlaciona positivamente com as proteínas totais, albumina e cortisol no início da vida e com as proteínas totais no desmame. A análise ROC mostra que MCHC, TPROT, GLOB, CHOL e AST no início da vida pode distinguir leitões de crescimento rápido de leitões de crescimento lento desde o nascimento até o desmame. O uso de parâmetros sanguíneos permite o reconhecimento precoce da taxa de crescimento em leitões, o que pode ajudar a otimizar todas as etapas posteriores para alcançar o melhor crescimento possível.

Thalassemia, a human blood disorder

Abstract A group of inherited blood defects is known as Thalassemia is among the worlds most prevalent hemoglobinopathies. Thalassemias are of two types such as Alpha and Beta Thalassemia. The cause of these defects is gene mutations leading to low levels and/or malfunctioning and globin proteins, respectively. In some cases, one of these proteins may be completely absent. and globin chains form a globin fold or pocket for heme (Fe++) attachment to carry oxygen. Genes for alpha and beta-globin proteins are present in the form of a cluster on chromosome 16 and 11, respectively. Different globin genes are used at different stages in the life course. During embryonic and fetal developmental stages, globin proteins partner with globin and are later replaced by globin protein. Globin chain imbalances result in hemolysis and impede erythropoiesis. Individuals showing mild symptoms include carriers of alpha thalassemia or the people bearing alpha or beta-thalassemia trait. Alpha thalassemia causes conditions like hemolytic anemia or fatal hydrops fetalis depending upon the severity of the disease. Beta thalassemia major results in hemolytic anemia, growth retardation, and skeletal aberrations in early childhood. Children affected by this disorder need regular blood transfusions throughout their lives. Patients that depend on blood transfusion usually develop iron overload that causes other complications in the body systems like renal or hepatic impairment therefore, thalassemias are now categorized as a syndrome. The only cure for Thalassemias would be a bone marrow transplant, or gene therapy with currently no significant success rate. A thorough understanding of the molecular basis of this syndrome may provide novel insights and ideas for its treatment, as scientists have still been unable to find a permanent cure for this deadly disease after more than 87 years since it is first described in 1925.

Resumo Um grupo de defeitos sanguíneos hereditários é conhecido como talassemia e está entre as hemoglobinopatias mais prevalentes do mundo. As talassemias são de dois tipos, como talassemia alfa e beta. As causas desses defeitos são as mutações genéticas que levam a níveis baixos e/ou proteínas de globina com mau funcionamento, respectivamente. Em alguns casos, uma dessas proteínas pode estar completamente ausente. As cadeias de globina e formam uma dobra ou bolsa de globina para a fixação de heme (Fe ++) para transportar oxigênio. Os genes das proteínas alfa e beta globina estão presentes na forma de um cluster nos cromossomos 16 e 11, respectivamente. Diferentes genes de globina são usados em diferentes estágios do curso de vida. Durante os estágios de desenvolvimento embrionário e fetal, as proteínas globina se associam à globina e, posteriormente, são substituídas pela proteína globina. Os desequilíbrios da cadeia de globina resultam em hemólise e impedem a eritropoiese. Indivíduos que apresentam sintomas leves incluem portadores de talassemia alfa ou as pessoas com traços de talassemia alfa ou beta. A talassemia alfa causa condições como anemia hemolítica ou hidropsia fetal fatal, dependendo da gravidade da doença. A beta talassemia principal resulta em anemia hemolítica, retardo de crescimento e aberrações esqueléticas na primeira infância. As crianças afetadas por esse distúrbio precisam de transfusões de sangue regulares ao longo da vida. Os pacientes que dependem de transfusão de sangue geralmente desenvolvem sobrecarga de ferro que causa outras complicações nos sistemas do corpo, como insuficiência renal ou hepática, portanto as talassemias agora são classificadas como uma síndrome. A única cura para as talassemias seria um transplante de medula óssea ou terapia genética sem atualmente uma taxa de sucesso significativa. Uma compreensão completa da base molecular dessa síndrome pode fornecer novos insights e ideias para seu tratamento, já que os cientistas ainda não conseguiram encontrar uma cura permanente para essa doença mortal depois de mais de 87 anos desde que foi descrita pela primeira vez em 1925.

Dry-eye syndrome in Shih Tzu dog: Ocular surface clinical and morphological aspects in the different stages of keratoconjunctivitis sicca / Síndrome do olho seco em Shih Tzu: aspectos clínicos e morfológicos da superfície ocular nas diferentes fases da ceratoconjuntivite seca

ABSTRACT: This study analyzed clinical and cyto-histomorphological parameters of the ocular surface of Shih Tzu dogs, non-carriers and carriers of quantitative keratoconjunctivitis sicca (KCS) at different stages. Thirty-five eyes from 23 male and female Shih Tzu dogs between two and eight years were evaluated in four groups: control group (CG - without KCS), mild KCS group (KCS1), moderate KCS group (KCS2), and severe KCS group (KCS3). Most clinical variables among KCS carrier groups worsened at the more advanced stages of the disease, with a negative correlation between the Schirmer tear test (STT-1) and tear film break-up time (TBUT). Squamous metaplasia, lymphoplasmacytic inflammatory infiltrate, and decrease in conjunctival goblet cells on histopathological examination comprised disease severity parameters. Quantitative KCS non-carried Shih Tzu dogs have qualitative and tear film distribution changes. The cytomorphological exam is limited to evaluating the inflammatory infiltrate and quantifying conjunctival goblet cells. However, intermediate epithelial cells were higher in healthy eyes compared to eyes with KCS in Shih Tzu dogs. Also, moderate and severe KCS carrier Shih Tzu dogs have qualitative dysfunction of the tear film. KCS in Shih Tzu dogs is common and chronic and may be responsible for the loss of vision of these animals. Early identification of the disease and routine evaluation can improve these dogs' quality of life and ocular health.

RESUMO: Este estudo analizou os parâmetros clinicos e cito-histomorfológicos da superfície ocular de cães da raça Shih Tzu, portadores e não portadores de ceratoconjuntivite seca quantitative (CCS) em diferentes estágios. Trinta e cinco olhos de 23 cães da raça Shih Tzu, machos e fêmeas, entre as idades de dois e oito anos foram avaliados em quatro grupos: grupo controle (GC - sem CCS), grupo CCS inicial (CCS1), grupo CCS moderada (CCS2) e grupo CCS severa (CCS3). A maioria das variáveis clínicas dentro os grupos portadores de CCS pioraram a medida que os estágios da doença avançam, com correlações negativas entre o teste lacrimal de Schirmer (TLS) e o tempo de ruptura do filme lacrimal (TRFL). Metaplasia escamosa, infiltrado inflamatório linfoplasmocítico e diminuição das células caliciformes no exame histopatológico compreenderam parâmetros de severidade da doença. Cães Shih Tzu não portadores de CCS quantitativa tem alterações qualitativas e na distribuição do filme lacrimal. O exame citomorfológico é limitado para a avaliação do infiltrado inflamatório e quantificação de células caliciformes. Entretanto, células inermediárias epiteliais são mais presents nos olhos saudáveis quando comparados aos olhos portadores de CCS em Shih Tzus. Também, Shih Tzus portadores de CCS nos estágios moderados e severos possuem disfunções qualitativas da lágrima. A CCS em Shih Tzu é comum, crônica e pode ser responsável pela perda de visão dos animais. A identificação precoce da doença e avaliações rotineiras podem aumentar a qualidade de vida e a saúde ocular nesses cães.

Antiparkinsoniano para tratamento de sequelas neurológicas causadas pela cinomose / Antiparkinsonian for treatment of neurological sequels caused by canine distemper

Background: Canine distemper (CD) is a highly contagious viral disease caused by the canine distemper virus (CDV). In dogs, CDV infection is characterized by the presentation of systemic and/or neurological signs with viral persistence in some organs, including the central nervous system (CNS). Neurological damages resulting from CD are a defiance for veterinarians, due to occasioned clinical sequels that influence the patient quality of life. The treatment of sequelae should seek to promote the resolution or decrease of the deleterious effects that impede the patient independence. Thus, the present report aims to describe the action of antiparkinsonian medication (levodopa associated with carbidopa) administered to 3 dogs who presented neurological sequels resulting from the canine distemper. Cases: Dog 1. A 9-month-old male mixed breed; Dog 2. A 6-month-old male Shih Tzu. Dog 3. A 8-years-old bitch mixed breed. All animals were referred for neurological care because presented neurological damages after distemper involvement. Only the Dog 2 was vaccinated to CD. Dog 1 (mixed male) had severe myoclonus, lack of proprioception, decreased of muscle tonus and paralysis in both pelvic limbs, associated with a marked thoracolumbar kyphosis. Dog 2 (a puppy Shih Tzu male) presented myoclonus in PL, proprioceptive loss in thoracic and pelvic limbs, absence of withdrawal reflex in thoracic and pelvic limbs, decrease in muscle tonus in pelvic limb and increase in thoracic limb. Dog 3 (adult unneutered bitch) presented intense myoclonus, absence of proprioception, decrease in muscle tonus and paresis of pelvic limb. All patients were treated with antiparkinsonian medication (levodopa 250 mg associated with carbidopa 25 mg) with following dosages: Dog 1 received a commercially available tablet, orally once a day for 30 days, while Dogs 2 and 3 had doses calculated by extrapolation allometric. For the Dog 2 it was prescribed 0.25 mg of levodopa and 0.025 mg of carbidopa daily for 30 days. Dog 3 was treated with 1 mg of levodopa and 0.1 mg of carbidopa patient day for the same period. Thirty days after starting the treatment, the 3 patients were evaluated again, and showed improvement of the motor signs, and the treatment was maintained. At the next return (30 days): Dog 1 showed significant improvement, however, Dog 2 started to present epileptic seizures and nystagmus that were treated with levetiracetam, while the Dog 3 not returned. As Dog 1 had a better prognosis, treatment was maintained for 1 year, with the frequency being changed from 24 h x 24 h to 48 h x 48 h after 30 days and 72x72 h after another 30 days. Unfortunately, Dog 2 had a worsening of epileptic condition and died, while Dog 3 died by road-kill. Discussion: The cases reported are uncommon, because not exist information about the use of antiparksonian to treatment of neurological damages occasioned by canine distemper. Although there are emerging therapies, such as the use of mesenchymal stem cells, that can reduce these sequels, the access is still restricted to a few professionals. Thus, the use of medications for demyelinating diseases, as antiparkinsonian, may be an alternative. In fact, the three reported patients showed recovery of the motor and sensorial damages observed, which corroborates with the possibility of a new treatment using antiparkinsonian or other drugs to demyelinating diseases.

Embryo biopsies for genomic selection in tropical dairy cattle

Genomic selection has transformed the livestock industry, enabling early-life selection of animals. Biopsy sampling of pre-implantation embryos has been described since 1968. However, it was only after 2010, with the advancement of molecular biology techniques such as whole genomic amplification and SNP Chips, that next-generation sequencing became commercially available for bovine embryos. It is now possible to make decisions about which embryos to transfer not only based on recipients' availability or embryo morphology but also on genomic estimates. This technology can be implemented for a wide spectrum of applications in livestock. In this review, we discuss the use of embryo biopsy for genomic selection and share our experience with Gir and Girolando Brazilian breeding programs, as well as future goals for implementing it in Brazilian bovine in vitro embryo production practices.(AU)

The impact of microplastics on female reproduction and early life

Plastic pollution in our environment is one of the most important global health concerns right now. Micro- and nanoplastics (MNPs) are taken up by both humans and animals, mainly via food and water, and can pass important epithelial barriers. Indications of plastics in the blood circulation have recently been shown in both humans and farm animals, but standardized methods to quantify the exact levels of MNPs to which we are exposed are currently lacking. Potential hazards of MNPs are being investigated very recently, including the impact that MNPs may have on reproduction. However, studies on mammalian reproduction are scarce, but a wealth of data from aquatic species indicates reproductive effects of MNPs. The first studies in rodent models demonstrate that MNPs reach the gonads after oral exposure and may impact offspring after maternal exposure during the gestational period. These effects may arise from the particles themselves or the presence of plastic contaminants that leach from plastics. Plastic contamination has been detected in human placentas, fetal fluid and the meconium of newborns, indicating the presence of plastics from the very first start of life. Currently there is a lack of studies that investigate the impact of MNP exposure during the periconception and embryonic period, whereas this is an extremely sensitive period that needs considerable attention with the growing amount of plastics in our environment.(AU)

Síndrome da feminização em cão com sertolioma / Feminization syndrome in a dog with Sertoli cell tumor

Background: The uncontrolled multiplication of Sertoli cells causes Sertoli cell tumor or Sertolioma. Because of this, the level of estrogen in the bloodstream increases rapidly and approximately 25% of dogs with this tumor develop feminization syndrome. Testicular neoplasms are more common in dogs than cats, and are often found in elderly patients. This work aims to describe the clinical signs of the feminization syndrome and the treatment instituted in a canine diagnosed with sertolioma. Case: A 18-year-old male canine, 19.5 kg of body mass, with an increase in testicular volume for about 2 years, was treated at the University Veterinary Hospital. On clinical examination, a matte and brittle coat, alopecia on the hind limbs and gynecomastia were observed. Also noted, non-harmonious aspect of the scrotum, pendular foreskin, atrophied right testicle and hyperplastic left, scrotal hyperthermia and absence of pain. In addition, as a result of the hyperestrogenism resulting from the neoplasm, the paraneoplastic syndrome of feminization, the patient also presented galactorrhea, pendular foreskin, atrophy of the penis and the contralateral testicle, dermatopathies, such as bilateral symmetrical alopecia of the flanks, easily removable hair and variable hyperpigmentation. Rectal body temperature of 38.6°C, clear lung auscultation and muffled cardiac auscultation. The results of laboratory tests showed changes such as thrombocytopenia, platelet counts below the reference levels, platelet count of 163,000/uL. There were no alterations that represented metastases in the imaging exams, such as in the chest X-ray in three incidences and in the abdominal ultrasonography. Then, we opted for the surgical procedure of orchiectomy, with the traditional technique of three clamps, associated with total ablation of the scrotum. Samples were sent to the histopathology laboratory and the diagnosis of sertolioma was confirmed. At 10, 30 and 90 days after the operation, the patient was reassessed for possible recurrences or alterations, but there were no complications or recurrence after the procedure. Discussion: Neoplasms of the male reproductive system are common in dogs. Sertolioma is considered one of the most frequent neoplasms in elderly dogs and that results in systemic clinical signs. This is in line with the 18-year-old dog described in the present report. In addition, it may result in clinical signs resulting from hyperestrogenism resulting from the neoplasm that is called paraneoplastic feminization syndrome. The characteristics of this syndrome are: gynecomastia, galactorrhea, pendular foreskin, atrophy of the penis and contralateral testicle, associated with dermatopathies, such as symmetrical bilateral alopecia. All these clinical signs were present. The diagnosis is made through complete anamnesis, complete clinical examination and complementary examination such as ultrasound help in the presumptive diagnosis, but only with histopathology can it be confirmed. In the clinical approach, histopathology was performed to close the diagnosis. Treatment is behind orchiectomy and total ablation of the scrotum, which was performed in the reported case. The treatment of choice was easy to apply, in addition to improving the patient's quality of life, promoting rapid post-surgical healing and an early return to normal life. However, for the effectiveness of the technique, the early diagnosis and collaboration of tutors is fundamental.

Nutritional secondary hyperparathyroidism in a puppy Leopardus geoffroyi (d'Orbigny and Gervais, 1844) / Hiperparatireoidismo secundário nutricional em filhote de Leopardus geoffroyi (d'Orbigny and Gervais, 1844)

Nutritional Secondary Hyperparathyroidism (NSH) is a metabolic disorder that mainly affects young animals. This disease causes imbalance between the levels of calcium and phosphorus, culminating in bone changes. Wild animals raised in captivity can develop the disease when they are given an inadequate diet. The aim of this study is to report the clinical findings, the complementary exams and the therapeutics utilized in a Leopardus geoffroyi (Geoffroy's cat) cub originated from captivity with NSH. The animal went through complementary imaging exams and biochemical evaluation that respectively revealed generalized osteopenia and pathological fracture of the right femur, reduction of serum calcium level and elevation of serum phosphorus level. The diagnosis of NSH was established by associating the history, clinical signs, and findings of ancillary exams. The treatment was based on diet correction, mineral and vitaminic supplementation and sun exposure. The NSH diagnosis was stablished by associating history, clinical signs, imaging exams findings and serum biochemicals. The early identification of this disease is of paramount importance, because in this way corrections can be made in food management, in order to provide successful clinical recovery and promote quality of life for wild captive animals.(AU)

O hiperparatireoidismo secundário nutricional (HSN) é uma desordem metabólica que acomete principalmente animais jovens. Essa doença cursa com desequilíbrio entre os níveis de cálcio e fósforo, culminando com alterações ósseas. Animais silvestres quando criados em cativeiro podem desenvolver a doença quando recebem uma dieta inadequada. O obje-tivo deste estudo é relatar os achados clínicos, os exames complementares e a terapêutica utilizada em um filhote de Leopardus geoffroyi (gato-do-mato-grande)proveniente de cativeiro com HSN. O animal passou por exames complementares de imagem e avaliação bioquímica que revelaram respectivamente osteopenia generalizada e fratura patológica de fêmur direito, redução dos níveis séricos de cálcio e elevação do fósforo. O diagnóstico de HSN foi estabelecido associando o histórico, sinais clínicos e achados dos exames complementares. O tratamento foi baseado na correção da dieta, suplementação mineral e vitamínica e exposição solar. A identificação precoce dessa doença é de suma importância, pois dessa forma podem ser feitas correções no manejo alimentar, afim de proporcionar a recuperação clínica com êxito e promover qualidade de vida para os animais selva-gens de cativeiro.(AU)

Carcinoma de células escamosas (cce) em cão na região prepucial: relato de caso / Squamous cell carcinoma (scc) in dog in the preputial region: case report / Carcinoma de células escamosas (cce) en perro de la región prepucial: reporte de un caso

A expectativa de vida dos animais de companhia vem aumentando devido as mudanças comportamentais e de cuidados dos tutores. Em analogia, com as idades cada vez mais avançadas, é comum o desenvolvimento de doenças associadas, sendo o tumor o mais comum entre elas. Todavia, as neoplasias mais comuns na clínica de pequenos animais estão associadas ao sistema tegumentar. O carcinoma de células escamosas (CCE), ou carcinoma espinocelular, é uma neoplasia de epitélio, maligno, de crescimento lento e de baixo potencial metastático. Sua etiologia ainda não é precisamente conhecida e a causa exógena mais comum e descrita pela literatura é a exposição à luz ultravioleta, gerando consequentes lesões nas estruturas genéticas e imunogênicas na pele. Além disso, essas lesões apresentam-se de forma mais comum em animais de pelagem clara, com grande exposição solar e em área anatômicas hipopigmentadas. O prognóstico varia de acordo com a localização e o estágio clínico, sendo favorável o diagnóstico realizado precocemente, e o tratamento consiste na avaliação clínica seguida do protocolo adequado O presente relato de caso tem como objetivo principal reunir e discutir informações associadas sobre o carcinoma de células escamosas em caninos e felinos, abordando aspectos clínicos e patológicos, a fim de facilitar o raciocínio sobre o CCE, desde sua abordagem inicial, até seu diagnóstico final e estadiamento.(AU)

The life expectancy of companion animals has been increasing due to behavioral and care changes of the guardians. In analogy, with the increasingly advanced ages, the development of associated diseases is common, the tumor being the most common among them. However, the most common neoplasms in the small animal clinic are associated with the integumentary system. Squamous cell carcinoma (SCC), or squamous cell carcinoma, is a malignant, slow-growing, low-potential metastatic epithelial neoplasm. Its etiology is not yet precisely known and the most common exogenous cause described by the literature is exposure to ultraviolet light, generating consequent lesions on the genetic and immunogenic structures in the skin. In addition, these lesions are more common in light-haired animals, with high exposure to the sun, and in hypopigmented anatomical areas. The prognosis varies according to the location and clinical stage, being favorable to the early diagnosis, and the treatment consists in the clinical evaluation followed by the appropriate protocol. The present case report has as its main objective to gather and discuss associated information about squamous cell carcinoma in canines and cats, addressing clinical and pathological aspects, in order to facilitate the reasoning about the CCE, from its initial approach, to its final diagnosis and staging.(AU)

La esperanza de vida de los animales de compañía ha ido en aumento debido a los cambios de comportamiento y cuidado de los guardianes. Por analogía, con las edades cada vez más avanzadas, el desarrollo de enfermedades asociadas es común, siendo el tumor el más común entre ellos. Sin embargo, las neoplasias más comunes en la clínica de animales pequeños se asocian con el sistema tegumentario. El carcinoma epidermoide (CCE), o carcinoma epidermoide, es una neoplasia epitelial metastásica maligna de crecimiento lento y bajo potencial. Su etiología aún no se conoce con precisión y la causa exógena más común descrita por la literatura es la exposición a la luz ultravioleta, generando lesiones consecuentes en las estructuras genéticas e inmunogénicas de la piel. Además, estas lesiones son más comunes en animales de pelo claro, con alta exposición al sol, y en áreas anatómicas hipopigmentadas. El pronóstico varía según la localización y el estadio clínico, siendo favorable al diagnóstico precoz, y el tratamiento consiste en la evaluación clínica seguida del protocolo adecuado. El presente reporte de caso tiene como objetivo principal reunir y discutir información asociada sobre el carcinoma epidermoide en caninos y gatos, abordando aspectos clínicos y patológicos, con el fin de facilitar el razonamiento sobre el CCE, desde su abordaje inicial, hasta su diagnóstico final y estadificación.(AU)

Thalassemia, a human blood disorder / Talassemia, uma doença do sangue humano

A group of inherited blood defects is known as Thalassemia is among the world's most prevalent hemoglobinopathies. Thalassemias are of two types such as Alpha and Beta Thalassemia. The cause of these defects is gene mutations leading to low levels and/or malfunctioning α and β globin proteins, respectively. In some cases, one of these proteins may be completely absent. α and β globin chains form a globin fold or pocket for heme (Fe++) attachment to carry oxygen. Genes for alpha and beta-globin proteins are present in the form of a cluster on chromosome 16 and 11, respectively. Different globin genes are used at different stages in the life course. During embryonic and fetal developmental stages, γ globin proteins partner with α globin and are later replaced by β globin protein. Globin chain imbalances result in hemolysis and impede erythropoiesis. Individuals showing mild symptoms include carriers of alpha thalassemia or the people bearing alpha or beta-thalassemia trait. Alpha thalassemia causes conditions like hemolytic anemia or fatal hydrops fetalis depending upon the severity of the disease. Beta thalassemia major results in hemolytic anemia, growth retardation, and skeletal aberrations in early childhood. Children affected by this disorder need regular blood transfusions throughout their lives. Patients that depend on blood transfusion usually develop iron overload that causes other complications in the body systems like renal or hepatic impairment therefore, thalassemias are now categorized as a syndrome. The only cure for Thalassemias would be a bone marrow transplant, or gene therapy with currently no significant success rate. A thorough understanding of the molecular basis of this syndrome may provide novel insights and ideas for its treatment, as scientists have still been unable to find a permanent cure for this deadly disease after more than 87 years since it is first described in 1925.

Um grupo de defeitos sanguíneos hereditários é conhecido como talassemia e está entre as hemoglobinopatias mais prevalentes do mundo. As talassemias são de dois tipos, como talassemia alfa e beta. As causas desses defeitos são as mutações genéticas que levam a níveis baixos e/ou proteínas de globina com mau funcionamento, respectivamente. Em alguns casos, uma dessas proteínas pode estar completamente ausente. As cadeias de globina α e β formam uma dobra ou bolsa de globina para a fixação de heme (Fe ++) para transportar oxigênio. Os genes das proteínas alfa e beta globina estão presentes na forma de um cluster nos cromossomos 16 e 11, respectivamente. Diferentes genes de globina são usados em diferentes estágios do curso de vida. Durante os estágios de desenvolvimento embrionário e fetal, as proteínas γ globina se associam à α globina e, posteriormente, são substituídas pela proteína β globina. Os desequilíbrios da cadeia de globina resultam em hemólise e impedem a eritropoiese. Indivíduos que apresentam sintomas leves incluem portadores de talassemia alfa ou as pessoas com traços de talassemia alfa ou beta. A talassemia alfa causa condições como anemia hemolítica ou hidropsia fetal fatal, dependendo da gravidade da doença. A beta talassemia principal resulta em anemia hemolítica, retardo de crescimento e aberrações esqueléticas na primeira infância. As crianças afetadas por esse distúrbio precisam de transfusões de sangue regulares ao longo da vida. Os pacientes que dependem de transfusão de sangue geralmente desenvolvem sobrecarga de ferro que causa outras complicações nos sistemas do corpo, como insuficiência renal ou hepática, portanto as talassemias agora são classificadas como uma síndrome. A única cura para as talassemias seria um transplante de medula óssea ou terapia genética sem atualmente uma taxa de sucesso significativa. Uma compreensão completa da base molecular dessa síndrome pode fornecer novos insights e ideias para seu tratamento, [...].

Thalassemia, a human blood disorder / Talassemia, uma doença do sangue humano

Abstract A group of inherited blood defects is known as Thalassemia is among the world's most prevalent hemoglobinopathies. Thalassemias are of two types such as Alpha and Beta Thalassemia. The cause of these defects is gene mutations leading to low levels and/or malfunctioning α and β globin proteins, respectively. In some cases, one of these proteins may be completely absent. α and β globin chains form a globin fold or pocket for heme (Fe++) attachment to carry oxygen. Genes for alpha and beta-globin proteins are present in the form of a cluster on chromosome 16 and 11, respectively. Different globin genes are used at different stages in the life course. During embryonic and fetal developmental stages, γ globin proteins partner with α globin and are later replaced by β globin protein. Globin chain imbalances result in hemolysis and impede erythropoiesis. Individuals showing mild symptoms include carriers of alpha thalassemia or the people bearing alpha or beta-thalassemia trait. Alpha thalassemia causes conditions like hemolytic anemia or fatal hydrops fetalis depending upon the severity of the disease. Beta thalassemia major results in hemolytic anemia, growth retardation, and skeletal aberrations in early childhood. Children affected by this disorder need regular blood transfusions throughout their lives. Patients that depend on blood transfusion usually develop iron overload that causes other complications in the body systems like renal or hepatic impairment therefore, thalassemias are now categorized as a syndrome. The only cure for Thalassemias would be a bone marrow transplant, or gene therapy with currently no significant success rate. A thorough understanding of the molecular basis of this syndrome may provide novel insights and ideas for its treatment, as scientists have still been unable to find a permanent cure for this deadly disease after more than 87 years since it is first described in 1925.

Resumo Um grupo de defeitos sanguíneos hereditários é conhecido como talassemia e está entre as hemoglobinopatias mais prevalentes do mundo. As talassemias são de dois tipos, como talassemia alfa e beta. As causas desses defeitos são as mutações genéticas que levam a níveis baixos e/ou proteínas de globina com mau funcionamento, respectivamente. Em alguns casos, uma dessas proteínas pode estar completamente ausente. As cadeias de globina α e β formam uma dobra ou bolsa de globina para a fixação de heme (Fe ++) para transportar oxigênio. Os genes das proteínas alfa e beta globina estão presentes na forma de um cluster nos cromossomos 16 e 11, respectivamente. Diferentes genes de globina são usados ​​em diferentes estágios do curso de vida. Durante os estágios de desenvolvimento embrionário e fetal, as proteínas γ globina se associam à α globina e, posteriormente, são substituídas pela proteína β globina. Os desequilíbrios da cadeia de globina resultam em hemólise e impedem a eritropoiese. Indivíduos que apresentam sintomas leves incluem portadores de talassemia alfa ou as pessoas com traços de talassemia alfa ou beta. A talassemia alfa causa condições como anemia hemolítica ou hidropsia fetal fatal, dependendo da gravidade da doença. A beta talassemia principal resulta em anemia hemolítica, retardo de crescimento e aberrações esqueléticas na primeira infância. As crianças afetadas por esse distúrbio precisam de transfusões de sangue regulares ao longo da vida. Os pacientes que dependem de transfusão de sangue geralmente desenvolvem sobrecarga de ferro que causa outras complicações nos sistemas do corpo, como insuficiência renal ou hepática, portanto as talassemias agora são classificadas como uma síndrome. A única cura para as talassemias seria um transplante de medula óssea ou terapia genética sem atualmente uma taxa de sucesso significativa. Uma compreensão completa da base molecular dessa síndrome pode fornecer novos insights e ideias para seu tratamento, já que os cientistas ainda não conseguiram encontrar uma cura permanente para essa doença mortal depois de mais de 87 anos desde que foi descrita pela primeira vez em 1925.

Pyometra in a tiger (Panthera tigris)

Background: Captive tigers can live a long life, around 26 years. Among the diseases described some of non-infectious origin are quite common, such as chronic kidney disease, spondylosis, and biliary cysts or tumors. On the other hand, pyometra has been frequently reported in lions, who have a higher risk of developing the disease than tigers and leopards. Pyometra is a disease with few descriptions in tigers and it may be related to the physiological features of the species. The animal is listed as Endangered on the International Union for the Conservation of Nature Red List of Threatened. The present report aims to describe the diagnosis and treatment of pyometra in a captive tigress. Case: A 7-year-old entire female tiger (Panthera tigris) weighing 140 kg was presented with a 3-day history of anorexia and prostration. For clinical examinations, collection of laboratory and imaging tests, the patient initially underwent dissociative anesthesia to allow catheterization of the cephalic vein and intravenous general anesthesia for orotracheal intubation followed by anesthetic maintenance in isoflurane. On general physical examination, the animal had normal colored mucosa, vital parameters within normal limits, and a body condition score of 6 on a scale of 9. There was no presence of vulvar secretion. The blood count and the biochemical exams showed values within the normal range for the species. The chest X-ray in the right and left views did not demonstrate pulmonary abnormalities. Ultrasonographic examination of the abdomen showed distension of the uterine body and horns, which have intraluminal hyperechoic fluid content without flocculation. Based on the imaging exam, the diagnosis was suggestive of pyometra. Exploratory celiotomy was performed via ventral midline, confirming the condition, which was treated by ovariohysterectomy. The surgical technique was performed as described for therapeutic ovariohysterectomy in dogs and cats. Culture of uterine content identified Escherichia coli. The histological analysis identified diffuse endometritis associated with follicular cysts. The tiger had complete recovery without any complications. The patient was releasing 13 days after the surgical procedure and in the last contact four months after the surgery, it was in perfect health conditions. Discussion: Pyometra in large exotic felids has been occasionally reported, mainly in animals more than 10 years of age. Although the tigress in the report is estimated to be seven years old. The patient in question started with anorexia and prostration and as there was already a history of cystic endometrial hyperplasia, a possible pyometra was suspected, despite being uncommon in the species. There was not vaginal discharge. The definitive diagnosis was by means of ultrasound examination and ovariohysterectomy was performed. Abdominal surgery for these large felids is complex, due to the intra-abdominal volume the flank approach or by laparoscopic is suggested, however in this case a ventral midline incision was performed without intercurrences and complications in the post-operative period. The surgical technique like that used in small animals was effective for the treatment of pyometra in the tigress with the use of ovariohysterectomy. Culture of uterine content identified Escherichia coli, which has been the most commonly isolated pathogen in pyometra of large felids. It was concluded that, as in bitches with pyometra, early diagnosis and surgical treatment is ideal for the patient's recovery.

Thalassemia, a human blood disorder / Talassemia, uma doença do sangue humano

A group of inherited blood defects is known as Thalassemia is among the world's most prevalent hemoglobinopathies. Thalassemias are of two types such as Alpha and Beta Thalassemia. The cause of these defects is gene mutations leading to low levels and/or malfunctioning α and β globin proteins, respectively. In some cases, one of these proteins may be completely absent. α and β globin chains form a globin fold or pocket for heme (Fe++) attachment to carry oxygen. Genes for alpha and beta-globin proteins are present in the form of a cluster on chromosome 16 and 11, respectively. Different globin genes are used at different stages in the life course. During embryonic and fetal developmental stages, γ globin proteins partner with α globin and are later replaced by β globin protein. Globin chain imbalances result in hemolysis and impede erythropoiesis. Individuals showing mild symptoms include carriers of alpha thalassemia or the people bearing alpha or beta-thalassemia trait. Alpha thalassemia causes conditions like hemolytic anemia or fatal hydrops fetalis depending upon the severity of the disease. Beta thalassemia major results in hemolytic anemia, growth retardation, and skeletal aberrations in early childhood. Children affected by this disorder need regular blood transfusions throughout their lives. Patients that depend on blood transfusion usually develop iron overload that causes other complications in the body systems like renal or hepatic impairment therefore, thalassemias are now categorized as a syndrome. The only cure for Thalassemias would be a bone marrow transplant, or gene therapy with currently no significant success rate. A thorough understanding of the molecular basis of this syndrome may provide novel insights and ideas for its treatment, as scientists have still been unable to find a permanent cure for this deadly disease after more than 87 years since it is first described in 1925.(AU)

Um grupo de defeitos sanguíneos hereditários é conhecido como talassemia e está entre as hemoglobinopatias mais prevalentes do mundo. As talassemias são de dois tipos, como talassemia alfa e beta. As causas desses defeitos são as mutações genéticas que levam a níveis baixos e/ou proteínas de globina com mau funcionamento, respectivamente. Em alguns casos, uma dessas proteínas pode estar completamente ausente. As cadeias de globina α e β formam uma dobra ou bolsa de globina para a fixação de heme (Fe ++) para transportar oxigênio. Os genes das proteínas alfa e beta globina estão presentes na forma de um cluster nos cromossomos 16 e 11, respectivamente. Diferentes genes de globina são usados em diferentes estágios do curso de vida. Durante os estágios de desenvolvimento embrionário e fetal, as proteínas γ globina se associam à α globina e, posteriormente, são substituídas pela proteína β globina. Os desequilíbrios da cadeia de globina resultam em hemólise e impedem a eritropoiese. Indivíduos que apresentam sintomas leves incluem portadores de talassemia alfa ou as pessoas com traços de talassemia alfa ou beta. A talassemia alfa causa condições como anemia hemolítica ou hidropsia fetal fatal, dependendo da gravidade da doença. A beta talassemia principal resulta em anemia hemolítica, retardo de crescimento e aberrações esqueléticas na primeira infância. As crianças afetadas por esse distúrbio precisam de transfusões de sangue regulares ao longo da vida. Os pacientes que dependem de transfusão de sangue geralmente desenvolvem sobrecarga de ferro que causa outras complicações nos sistemas do corpo, como insuficiência renal ou hepática, portanto as talassemias agora são classificadas como uma síndrome. A única cura para as talassemias seria um transplante de medula óssea ou terapia genética sem atualmente uma taxa de sucesso significativa. Uma compreensão completa da base molecular dessa síndrome pode fornecer novos insights e ideias para seu tratamento, [...].(AU)

Estudo anatômico das lesões de endocardiose em cães, prevalência e epidemiologia / Anatomical study of endocardiosis lesions in dogs, prevalence and epidemiology / Estudio anatómico de las lesiones de endocardiosis en el perro, prevalencia y epidemiología

O coração é composto por duas importantes valvas átrio-ventriculares, a tricúspide e a bicúspide ou mitral. As válvulas cardíacas asseguram o sentido do fluxo sanguíneo dos átrios para os ventrículos e destes para as artérias. A endocardiose é um processo degenerativo crônico progressivo das válvulas, que acomete especialmente os cães, denominada endocardiose ou "doença do cão velho". Embora qualquer das válvulas possa ser afetada, é a válvula mitral que é habitualmente envolvida, isoladamente ou em combinação com a válvula tricúspide. A sua prevalência tem sido associada a parâmetros como idade, sexo e raça, afetando especialmente animais adultos de raças de pequeno porte. A etiologia da endocardiose é desconhecida, mas parece haver uma base hereditária. As lesões macroscópicas iniciais consistem em pequenos nódulos nas margens livres da valva, ficando distorcidas e com suas dimensões reduzidas, mas significativamente espessas e de coloração opaca, branca ou reluzente. Microscopicamente, a endocardiose é vista como um processo degenerativo do tecido valvular com discreta infiltração de tecido conjuntivo fibroso. Em estágios iniciais a doença apresenta, à auscultação, murmúrios cardíacos de baixa intensidade, sem sinais de descompensação e é geralmente achado incidental durante a rotina de exame clínico. As cúspides fundem-se em sua inserção, mas separam-se em direção ao centro da abertura, ajustando-se estreitamente ao mesmo tempo quando a valva se fecha e suas bordas livres são espessas e irregulares, especialmente durante uma fase tardia da vida. Com isso, o objetivo do presente trabalho foi averiguar as principais lesões, a epidemiologia e o grau de prevalência da endocardiose em cães na região noroeste do estado do Rio Grande do Sul, o que se verificou que não há casos frequentes na rotina clínica de pequenos animais de endocardiose. Não sendo possível verificar se há um sexo mais predisposto a apresentar a endocardiose. As lesões observadas na macroscopia eram referentes a nódulos brilhantes, e na microscopia presença de colágeno causando o espessamento da cúspide, além de achados inflamatórios.(AU)

The heart is composed of two important atrio-ventricular valves, the tricuspid and the bicuspid or mitral valve. The heart valves ensure the direction of blood flow from the atria to the ventricles and from the ventricles to the arteries. Endocardiosis is a chronic progressive degenerative process of the valves that affects dogs in particular, called endocardiosis or "old dog's disease". Although any of the valves can be affected, it is the mitral valve that is usually involved, either alone or in combination with the tricuspid valve. Its prevalence has been associated with parameters such as age, sex, and breed, affecting especially adult animals of small breeds. The etiology of endocardiosis is unknown, but there appears to be a hereditary basis. The initial macroscopic lesions consist of small nodules on the free margins of the valve, becoming distorted and reduced in size, but significantly thickened and opaque, white or shiny in color. Microscopically, endocardiosis is seen as a degenerative process of the valvular tissue with a discrete infiltration of fibrous connective tissue. In early stages the disease presents, on auscultation, with low-intensity cardiac murmurs without signs of decompensation and is usually an incidental finding during routine clinical examination. The leaflets fuse at their insertion, but separate towards the center of the opening, fitting closely together when the valve closes, and their free edges are thick and irregular, especially during a late phase of life. Thus, the aim of this study was to investigate the main lesions, the epidemiology and the degree of prevalence of endocardiosis in dogs in the northwest region of the state of Rio Grande do Sul, which was found that there are no frequent cases in the clinical routine of small animals of endocardiosis. It was not possible to verify whether there is a sex more predisposed to present endocardiosis. The lesions observed at macroscopy were referring to bright nodules, and at microscopy the presence of collagen causing thickening of the leaflet, besides inflammatory findings.(AU)

El corazón está compuesto por dos importantes válvulas aurículo- ventriculares, la tricúspide y la bicúspide o válvula mitral. Las válvulas cardíacas aseguran la dirección del flujo sanguíneo de las aurículas a los ventrículos y de los ventrículos a las arterias. La endocardiosis es un proceso degenerativo crónico y progresivo de las válvulas que afecta sobre todo a los perros, denominado endocardiosis o "enfermedad del perro viejo". Aunque cualquiera de las válvulas puede verse afectada, es la válvula mitral la que suele estar implicada, ya sea sola o en combinación con la válvula tricúspide. Su prevalencia se ha asociado a parámetros como la edad, el sexo y la raza, afectando especialmente a animales adultos de razas pequeñas. La etiología de la endocardiosis es desconocida, pero parece tener una base hereditaria. Las lesiones macroscópicas iniciales consisten en pequeños nódulos en los márgenes libres de la válvula, que se distorsionan y reducen de tamaño, pero se engrosan significativamente y adquieren un color opaco, blanco o brillante. Microscópicamente, la endocardiosis se observa como un proceso degenerativo del tejido valvular con una discreta infiltración de tejido conectivo fibroso. En fases tempranas, la enfermedad se presenta, en la auscultación, con soplos cardíacos de baja intensidad sin signos de descompensación y suele ser un hallazgo incidental durante el examen clínico rutinario. Las valvas se fusionan en su inserción, pero se separan hacia el centro de la apertura, encajando estrechamente cuando la válvula se cierra, y sus bordes libres son gruesos e irregulares, especialmente durante una fase tardía de la vida. Por lo tanto, el objetivo de este estudio fue investigar las principales lesiones, la epidemiología y el grado de prevalencia de endocardiosis en perros de la región noroeste del estado de Rio Grande do Sul, que se encontró que no hay casos frecuentes en la rutina clínica de pequeños animales de endocardiosis. No fue posible verificar si existe un sexo más predispuesto a presentar endocardiosis. Las lesiones observadas en la macroscopia fueron referentes a nódulos brillantes, y en la microscopia la presencia de colágeno causando engrosamiento de la valva, además de hallazgos inflamatorios.(AU)

Early development of two commercially valuable fish from the lower Amazon River, Brazil (Characiformes: Serrasalmidae)

We described the early development of Myloplus asterias and M. lobatus, two fish species of the Serrasalmidae using morphological, meristic, and morphometric characteristics. These herbivores serrasalmids are heavily fished because of their commercial importance in the Amazon. The individuals were collected between 2016 and 2020 in the limnetic zone of open water and macrophyte stands in the Lower Amazon River floodplain. We tested different growth models to identify the development pattern of these species. During the initial ontogeny, these two species can be differentiated mainly by the myomeres total number, 37 to 39 in M. asterias vs. 40 to 41 in M. lobatus, the pigmentation pattern, and dorsal-fin ray numbers. These characteristics are effective in distinguishing these species from other serrasalmids. The morphometric relationships were also different between these two species, showing distinct patterns in growth between the analyzed features. An identification key for larvae of some sympatric Serrasalmidae species from the Amazon basin is presented. Our expectation is that this study will contribute to the knowledge of the initial ontogeny and the biology of fish species in the Neotropical region.(AU)

Descrevemos o desenvolvimento inicial de Myloplus asterias e M. lobatus, duas espécies de peixes da família Serrasalmidae usando características morfológicas, merísticas e morfométricas. Esses serrasalmídeos herbívoros são fortemente pescados devido à sua importância comercial na Amazônia. Os indivíduos foram coletados entre 2016 e 2020 na zona limnética de águas abertas e em bancos de macrófitas na planície de inundação do baixo rio Amazonas. Testamos diferentes modelos de crescimento para identificar o padrão de desenvolvimento dessas espécies. Durante a ontogenia inicial, essas duas espécies podem ser diferenciadas pelo número total de miômeros; 37 a 39 em M. asterias vs. 40 a 41 em M. lobatus; pelo padrão de pigmentação e número de raios da nadadeira dorsal. Essas características são eficazes para distinguir essas espécies de outros serrasalmídeos. As relações morfométricas também foram diferentes entre as duas espécies, com distintos padrões de crescimento entre as características analisadas. Uma chave de identificação para larvas de algumas espécies simpátricas de Serrasalmidae da bacia amazônica é apresentada. Nossa expectativa é que este estudo contribua para o conhecimento da ontogenia inicial e da biologia das espécies de peixes da região Neotropical.(AU)

Life history trait variations and population dynamics of Calophysus macropterus (Siluriformes: Pimelodidae) in two river systems of the Colombian and Peruvian Amazon

The catfish Calophysus macropterus is heavily exploited in the Amazon basin, yet its life history characteristics are poorly documented, hampering proper fisheries management. In order to fill this gap, monthly sampling in the upper Putumayo River and in the Amazonas, lower Marañón and Ucayali (AMU) rivers were carried out over several years (2013-2015 in the AMU, 2013-2017 in the Putumayo) to provide detailed information about its reproduction, growth and mortality patterns (using length frequency data). Reproduction, which occurs during the dry and early flooding season, was only observed in the upper Putumayo River and not in the sampled portion of the AMU system, suggesting that the species reproduces closer to the Andes than other pimelodid catfishes. Size at first sexual maturity did not differ significantly among sex or among river systems, ranging from 25-28 cm SL. In both river systems, females had a faster growth than males and both genders also tended to have a better growth in the AMU than in the upper Putumayo. Mortality and exploitation estimate all indicated overexploitation of the species in both river systems. The implications of these results for fisheries management and conservation are discussed.(AU)

El bagre Calophysus macropterus está fuertemente explotado en la cuenca Amazónica. Sin embargo, su ciclo de vida está poco documentado, lo que dificulta su gestión pesquera. Para llenar este vacío, se realizaron muestreos mensuales en el alto río Putumayo alrededor de Puerto Leguízamo y en el Amazonas y los ríos bajo Marañón y Ucayali (AMU) cerca de Iquitos durante varios años (2013-2015 en AMU, 2013-2017 en Putumayo) para generar información sobre su reproducción, crecimiento y mortalidad. La reproducción, que se produce durante la estación seca y el inicio de la inundación, sólo se observó en el curso superior del río Putumayo y no en la parte muestreada del sistema de la AMU, lo que sugiere que la especie se reproduce más cerca de los Andes que otros pimelodidos. El tamaño de primera madurez sexual no difirió entre sexos o entre sistemas fluviales, oscilando entre 25-28 cm. En ambos sistemas fluviales, las hembras tuvieron un crecimiento más rápido que los machos y ambos géneros también tendieron a tener un mejor crecimiento en el AMU que en el alto Putumayo. Estimaciones de mortalidad y explotación indicaron una sobreexplotación en ambos sistemas. Se discuten las implicaciones de estos resultados para la gestión y conservación de las pesquerías.(AU)

Notes on the biological development of the darkling beetle Blaps nefrauensis nefrauensis Seidlitz, 1893 (Coleoptera: Tenebrionidae)

Abstract Several endemic species of Blaps occur in Tunisia, and the species Blaps nefrauensis nefrauensis has been reported in Moulares (urban zone in west-central Tunisia), where it lives and reproduces in home gardens and old buildings. The aim of this work is to study the life cycle of the darkling beetle, considering both field and laboratory rearing conditions. As a result, the beetle species has different developmental stages (egg, larva, prepupa, pupa, and adult) that last about 15 months. Each year during the same period, adults emerge (early summer) and expire (late autumn), larvae hatch (late summer) and pupate (early summer). There is only one generation per year. Females began laying eggs in late July. The eggs were ovoid, white, and about 2.7 mm in length and 1.5 mm in width. Embryogenesis took an average of nine days. The first instar larvae were at initially only 4.5 mm long and ivory white in color. A brief description of the newly egg hatched larva was provided; thus, the nerve fibers innervating the apical setae in the antennae and ligula were detected. Further light microscopic examination of the embryo before hatching from the egg pointed out that the antennal sensilla are protected during the embryogenesis stage.

Resumo Várias espécies endêmicas de Blaps ocorrem na Tunísia, e a espécie Blaps nefrauensis nefrauensis foi relatada em Moulares (zona urbana no centro-oeste da Tunísia), onde vive e se reproduz em jardins domésticos e prédios antigos. O objetivo deste trabalho é estudar o ciclo de vida do besouro escuro, considerando as condições de criação em campo e em laboratório. Como resultado, a espécie de besouro tem diferentes estágios de desenvolvimento (ovo, larva, prepupa, pupa e adulto) que duram cerca de 15 meses. Todos os anos, durante o mesmo período, os adultos emergem (início do verão) e expiram (final do outono), as larvas eclodem (final do verão) e se tornam pupas (início do verão). Existe apenas uma geração por ano. As fêmeas começaram a botar ovos no final de julho. Os ovos eram ovóides, brancos, com cerca de 2,7 mm de comprimento e 1,5 mm de largura. A embriogênese demorou em média nove dias. As larvas de primeiro instar tinham inicialmente apenas 4,5 mm de comprimento e uma cor branca marfim. Foi fornecida uma breve descrição da larva recém-eclodida; assim, as fibras nervosas que inervam as cerdas apicais nas antenas e ligulas foram detectadas. Um exame microscópico de luz posterior do embrião antes da eclosão do ovo mostrou que as sensilas antenais são protegidas durante o estágio de embriogênese.

Environmental influences on the ichthyoplankton in hypersaline estuaries located in a Semiarid Northeastern Brazilian coast

Hypersaline estuaries are commonly found in the Semiarid Northeast Brazilian coast. However, the utilization of these estuaries by early life stages of fishes is less well documented. This study aimed to evaluate the effects of environmental factors on the ichthyoplankton, and to describe their spatial and temporal variation in two estuaries (Tubarão and Casqueira). The sampling were diurnally in four excursions carried out during two dry-season months (November and December 2017) and two rainy-season months (May and July 2018). A total of 423 larvae representing 30 species (14 families) and 2,762 eggs (five families) were collected. Although the community structures were similar in both estuaries, there was strong seasonal variation, with higher abundances observed during the dry season. Low rainfall was the primary environmental driver affecting ichthyoplankton in both estuaries. Other environmental factors, such as depth, water temperature, and channel width, were also predictor variables for the distribution of eggs and larvae. The ichthyoplankton was dominated by marine estuarine-dependent species in both estuaries, accounting for 76% of individuals. The presence of the early life stages of typically marine species suggests that hypersaline environments provide important nursery areas and play an essential role for some coastal fish species.(AU)

Os estuários hipersalinos são comumente encontrados na região semiárida da costa nordestina brasileira. No entanto, a utilização desses estuários pelos primeiros estágios de vida dos peixes é pouco documentada. O objetivo deste estudo foi avaliar os efeitos de fatores ambientais sobre o ictioplâncton e descrever sua variação espacial e temporal em dois estuários (Tubarão e Casqueira). As amostragens foram diurnas em quatro excursões realizadas em dois meses da estação seca (novembro e dezembro de 2017) e dois meses da estação chuvosa (maio e julho de 2018). Um total de 423 larvas representando 30 espécies (14 famílias) e 2.762 ovos (cinco famílias) foram coletadas. Embora as estruturas das comunidades fossem semelhantes em ambos os estuários, houve fortes diferenças de variação sazonal, com maiores abundâncias observadas durante a estação seca. A baixa precipitação foi o principal fator ambiental que afetou o ictioplâncton em ambos os estuários. Outros fatores, como profundidade, temperatura da água e largura do canal, também foram preditoras para a distribuição de ovos e larvas. O ictioplâncton foi dominado por espécies marinhas dependentes em ambos os estuários, representando 76% dos indivíduos. A presença de estágios iniciais de espécies tipicamente marinhas sugere que ambientes hipersalinos fornecem áreas de berçário importantes e desempenham um papel essencial para algumas espécies de peixes costeiros.(AU)