Resumo Apesar das dificuldades encontradas em se realizar análises cromossômicas em peixes de pequeno porte, os estudos citogenéticos em Lebiasinidae vêm crescendo nos últimos anos e demonstrando padrões diferenciados na evolução cromossômica entre os membros da família. Nesse contexto, o gênero Lebiasina tem mostrado preservar sua macroestrutura cariotípica, composta por 2n = 36 cromossomos, enquanto os demais gêneros geralmente apresentam 2n maiores. Este estudo tem como foco a citogenética comparativa de três espécies de Lebiasina, sendo uma delas analisada pela primeira vez aqui, através do emprego de técnicas convencionais e moleculares. Os resultados obtidos reforçam a trajetória evolutiva diferenciada do gênero Lebiasina, ao mesmo tempo em que evidenciam as particularidades genômicas que acompanham a evolução de cada uma das espécies. Neste contexto, os componentes repetitivos do genoma tiveram um papel importante na caracterização particular de cada uma das espécies. Também, é notável que L. minuta e L. melanoguttata, duas espécies que ocorrem exclusivamente no território brasileiro, apresentam maior proximidade citogenética entre elas do que com a espécie irmã transandina, L. bimaculata.

Abstract Despite several difficulties in chromosomal analyses of small-sized fishes, the cytogenetics of the Lebiasinidae was largely improved in the last years, showing differential patterns in the chromosomal evolution inside the family. In this context, it has been shown that genus Lebiasina preserves its karyotypic macrostructure, composed of 2n = 36 chromosomes, whereas the other genera generally present higher 2n. This study focused on the comparative cytogenetics of three Lebiasina species, one of them analyzed here for the first time, using conventional and molecular procedures. The results reinforced the differentiated evolutionary path of the genus Lebiasina while, at the same time, highlighted the genomic particularities that have accompanied the evolution of each species. In this sense, the repetitive components of the genome played a significant role in the differentiation of each species. It is also notable that L. minuta and L. melanoguttata, the two species that occur exclusively in the Brazilian territory, show greater chromosomal similarities to each other than to the trans-Andean sister species, L. bimaculata.

ABSTRACT The results of a cytogenetic study carried out in two female Miniature Pinscher who died after birth, one affected with meningoencephalocele (MEC) and the other apparently normal, are presented. The analysis of 156 metaphases (75 of the specimen with pathology and 81 without pathology) showed a typical unimodal female complement 2n = 78 (76, XX) in 95.06% of all metaphases in the normal puppy, while the puppy with ECM showed a multimodal karyotype with three chromosomally distinct cell lines: 2n = 78 (36%); 77 (28%); 76 (10.67%). The remaining 25.33% of cells corresponded to cells with less than 76 chromosomes. Statistical analysis of the medians of the chromosome counts using the Man-Whitney U test between the normal (median = 78; median range = 51.81) and affected (median = 77; median range = 26.69) puppies revealed highly significant differences (p=2.8192x10-13). It was not possible to establish a pattern that would allow to identify a specific aneuploidy but it was possible to verify that the numerical variation affected both the sex chromosomes and those of the first large acrocentric complement pair, as well as other remaining chromosomal elements, which suggests the occurrence of random non-disjunction processes in the cells of the MEC-affected puppy. This result constitutes the first evidence of association between a case of MEC and chromosomal mosaicism in dogs.

RESUMEN Se presentan los resultados de un estudio citogenético realizado en dos hembras caninas de raza Pinscher Miniatura que murieron después de nacer, una afectada con meningoencefalocele (MEC) y la otra aparentemente normal. El análisis de 156 metafases (75 del ejemplar con patología y 81 sin patología) mostró un complemento femenino unimodal típico 2n = 78 (76, XX) en el 95.06% de todas las metafases en el cachorro normal, mientras que el cachorro con MEC mostró un cariotipo multimodal con tres líneas celulares cromosómicamente distintas: 2n = 78 (36%); 77 (28%); 76 (10.67%). El 25.33% de células restantes correspondió a células con menos de 76 cromosomas. El análisis estadístico de las medianas de los recuentos de cromosomas mediante la prueba U de ManWhitney entre el cachorro normal (mediana = 78; rango medio = 51.81) y afectado (mediana = 77; rango medio = 26.69) reveló diferencias altamente significativas (p=2.8192x10-13). No fue posible establecer un patrón que permitiera identificar una aneuploidía específica, pero se pudo verificar que la variación numérica afectó tanto a los cromosomas sexuales y a los del primer par acrocéntrico grande del complemento, así como también otros elementos cromosómicos restantes, lo cual sugiere la ocurrencia de procesos de nodisyunción aleatoria en las células del cachorro afectado con MEC. Este resultado constituye la primera evidencia de asociación entre un caso de MEC y mosaicismo cromosómico en perros.

RESUMO Parodontidae é um grupo relativamente pequeno de peixes caraciformes neotropicais que consiste em três gêneros (Apareiodon, Parodon e Saccodon) com 32 espécies válidas. Uma vasta literatura citogenética está disponível sobre Apareiodon e Parodon, mas até o momento não há dados citogenéticos sobre Saccodon, um gênero que contém apenas três espécies com distribuição transandina. No presente estudo foi descrito o cariótipo de S. wagneri, baseado em métodos convencionais (coloração de Giemsa, Ag-NOR, bandas C) e moleculares (mapeamento de DNA repetitivo por hibridização fluorescente in situ). Um número cromossômico diplóide de 2n = 54 foi observado, e a presença de cromossomos sexuais heteromórficos do tipo ZZ/ZW foi revelada. O cromossomo W possui uma banda terminal heterocromática que ocupa aproximadamente metade do braço longo, sendo esta banda aproximadamente a metade do tamanho do cromossomo Z. O ensaio FISH mostrou uma sintenia dos genes 18S-rDNA e 5S-rDNA no par de cromossomos 14, e a ausência de sítios teloméricos intersticiais. Nossos dados reforçam a hipótese de uma estrutura cariotípica conservadora em Parodontidae e sugerem uma origem ancestral dos cromossomos sexuais nos peixes desta família.

ABSTRACT Parodontidae is a relatively small group of Neotropical characiform fishes consisting of three genera (Apareiodon, Parodon, and Saccodon) with 32 valid species. A vast cytogenetic literature is available on Apareiodon and Parodon, but to date, there is no cytogenetic data about Saccodon, a genus that contains only three species with a trans-Andean distribution. In the present study the karyotype of S. wagneri was described, based on both conventional (Giemsa staining, Ag-NOR, C-bands) and molecular (repetitive DNA mapping by fluorescent in situ hybridization) methods. A diploid chromosome number of 2n = 54 was observed in both sexes, and the presence of heteromorphic sex chromosomes of the ZZ/ZW type was detected. The W chromosome has a terminal heterochromatin band that occupies approximately half of the long arm, being this band approximately half the size of the Z chromosome. The FISH assay showed a synteny of the 18S-rDNA and 5S-rDNA genes in the chromosome pair 14, and the absence of interstitial telomeric sites. Our data reinforce the hypothesis of a conservative karyotype structure in Parodontidae and suggest an ancient origin of the sex chromosomes in the fishes of this family.

Tilapia is a freshwater fish native to Africa that has many characteristics that make it an excellent fish for aquaculture, but it is also considered one of the most dangerous invasive exotic species in the world due to its adaptability and reproductive potential. This essay analyzes the dilemma between the benefits of these fish as an alternative to contribute to agrifood security and the threat it poses to Ecuador's aquatic biodiversity. The absence of official information makes it necessary to investigate the effect of the invasions by tilapia in the rivers, lagoons and estuaries colonized by this species. The level of action to prevent, eradicate or control the tilapia in Ecuador has been very limited and therefore the need to establish strategies to prevent its spread to areas not yet invaded is imposed. Although the government of Ecuador has regulations that restrict the introduction of exotic species, the reality is that, in the case of the tilapia, far from establishing adequate controls, the culture of these fish is promoted without major objections. The possibility of adopting biocontrol strategies to eradicate and / or mitigate the consequences of the invasion by tilapia in the country and the need to promote educational campaigns to create a new environmental behavior, conscience and responsibility in society is discussed.

La tilapia es un pez dulceacuícola originario del África que posee muchas características que la convierten en un excelente pez para acuicultura, pero también es considerada como una de las especies exóticas invasoras más peligrosas del mundo debido a su adaptabilidad y potencial reproductivo. En este ensayo se analiza el dilema entre las bondades de estos peces como alternativa para contribuir con la seguridad agroalimentaria y la amenaza que representa para la biodiversidad acuática de Ecuador. La ausencia de información oficial hace necesario investigar el efecto de las invasiones por tilapia en los ríos, lagunas y esteros colonizados por esta especie. El nivel de acción para prevenir, erradicar o controlar la tilapia en Ecuador ha sido muy limitado y por lo tanto se impone la necesidad de establecer estrategias para evitar su propagación hacia áreas aún no invadidas. Aunque el gobierno de Ecuador posee regulaciones que restringen la introducción de especies exóticas, la realidad es que, en el caso de la tilapia, lejos de establecer controles adecuados, el cultivo de estos peces es impulsado sin mayores objeciones. Se discute la posibilidad de adoptar estrategias de control biológico para erradicar y/o mitigar las consecuencias de la invasión por tilapias en el país y la necesidad de fomentar campañas educativas para crear un nuevo comportamiento ambiental, conciencia y responsabilidad en la sociedad.

RESUMEN Comprender los efectos de los metales pesados en los ecosistemas acuáticos es de gran importancia debido a su potencial de bioacumulación en los diversos niveles tróficos y de inducir daños en el ADN. El mercurio, considerado uno de los metales pesados más peligrosos, causa fracturas cromosómicas (evento clastogénico) o disfunción del huso mitótico (evento aneugénico), y puede conducir a la formación de fragmentos de cromatina encapsulada en un núcleo separado más pequeño, generalmente denominado micronúcleo. En este trabajo se evalúa la sensibilidad del test de micronúcleos en el cíclido neotropical Andinoacara rivulatus (Günther 1860). Los peces fueron divididos en cuatro grupos de 16 individuos, y cada grupo se colocó en acuarios separados (140 L) provistos de agua filtrada y aireación constante. Los peces fueron expuestos al cloruro de mercurio (HgCl2) en dosis de 0.1, 0.25 y 0.50 mg/kg de peso corporal, administrada por inyección intraperitoneal (IP). Los peces del grupo control fueron inyectados con solución fisiológica. Se identificaron las siguientes anomalías en los eritrocitos: micronúcleos que varían en tamaño y posición en el citoplasma, núcleo con evaginaciones, células binucleadas núcleos con muesca (núcleos con una profunda invaginación hacia el centro). El examen de los frotis de sangre demostró un mayor nivel de eritrocitos micronucleados y con muesca en peces inyectados con HgCl2 que en los controles. Fueron detectadas diferencias significativas en la frecuencia de eritrocitos micronucleados y células con núcleos con muescas entre los grupos expuestos al mercurio. El análisis de regresión lineal reveló una relación positiva entre la frecuencia de eritrocitos micronucleados y con muescas (P< 0.0001), con un coeficiente de correlación moderadamente fuerte (R= 0.737). Se propone que, además de los dos mecanismos hasta ahora conocidos de formación de micronúcleos (daño del huso mitótico y rupturas cromosómicas), la fragmentación de la cromatina en núcleos con muesca probablemente a causa de la combinación de los efectos citotóxicos del mercurio y el estrés mecánico, podría ser un tercer mecanismo de génesis de micronúcleos.

Abstract Understanding the effects of heavy metals in aquatic ecosystems is of significant importance due to their potential to bioaccumulate at various trophic levels and induce damage in DNA. Mercury is considered one of the most dangerous heavy metals, causing chromosomal breakage (clastogenic event) or spindle dysfunction (aneugenic event), that can lead to the formation of encapsulated chromatin into a separate smaller nucleus, generally referred to as a micronucleus. We evaluated the sensitivity of the micronucleus test in the neotropical cichlid Andinoacara rivulatus (Günther 1860). The fish were divided into four groups of 16 individuals, and each group was placed in separate aquaria (140 L) provided with filtered water and constant aeration. Fish were exposed to mercury chloride (HgCl2) at doses 0.1, 0.25, and 0.50 mg/kg body weight, administered by intraperitoneal (IP) injection. Fish from the control group were injected with a physiologic solution. The following erythrocyte anomalies were identified: erythrocytes with micronuclei varying to some extent in size and position in the cytoplasm, blebbed nucleus, binucleated cell, nuclei showing a deep invagination toward the center (notched nuclei). Examination of blood smears demonstrated a higher level of micronucleus and notched erythrocytes in fish injected with HgCl2 than in the controls. There were significant differences in the frequency of micronucleated and notched erythrocytes among the groups exposed to mercury. Linear regression analysis revealed a positive relationship between the frequency of micronucleated and notched erythrocytes (P< 0.0001), with a moderately strong correlation coefficient (R= 0.737). We propose that, in addition to the two so far known mechanisms of micronucleus formation (spindle apparatus damage and chromosomal ruptures), chromatin fragmentation in notched nuclei resulting from a combination of the cytotoxic effects of mercury and mechanical stress, may be a third mechanism of micronuclei genesis.

Se presenta una descripción general de las técnicas básicas y moleculares más comúnmente empleadas para el estudio de los cromosomas en los peces, con ejemplos que demuestran la utilidad de la citogenética para resolver problemas de tipo taxonómico, particularmente cuando las características merísticas o morfométricas no permiten una clara diferenciación entre especies.

This document presents a general overview on the basic and molecular techniques more commonly employed for the study of chromosomes in fishes, with examples that demonstrate the usefulness of cytogenetics to resolve taxonomic problems, particularly when meristic or morphometric characteristic do not result in a clear differentiation between species.

We present a database containing cytogenetic data of Neotropical actinopterygian fishes from Venezuela obtained in a single laboratory for the first time. The results of this study include 103 species belonging to 74 genera assigned to 45 families and 17 out of the 40 teleost orders. In the group of marine fishes, the modal diploid number was 2n=48 represented in 60% of the studied species, while in the freshwater fish group the modal diploid complement was 2n=54, represented in 21.21 % of the studied species. The average number of chromosomes and the mean FN were statistically higher in freshwater fish than in marine fish. The degree of diversification and karyotype variation was also higher in freshwater fish in contrast to a more conserved cytogenetic pattern in marine fish. In contrast to the assumption according to which 48 acrocentric chromosomes was basal chromosome number in fish, data here presented show that there is an obvious trend towards the reduction of the diploid number of chromosomes from values near 2n=60 with high number of biarmed chromosomes in more basal species to 2n=48 acrocentric elements in more derived Actinopterygii.

Se presenta una base de datos que contiene los datos citogenéticos de peces Actinopterigios Neotropicales de Venezuela obtenidos por primera vez en un solo laboratorio. Los resultados de este estudio incluyen 103 especies pertenecientes a 74 géneros de 45 familias contenidas en 17 de los 40 órdenes de teleósteos. En el grupo de peces marinos, el número diploide modal fue 2n=48 representado en 60% de las especies estudiadas, mientras que en el grupo de peces de agua dulce el complemento diploide modal fue 2n=54, representado en el 21,21% de las especies estudiadas. El número de cromosomas y FN promedio fueron estadísticamente superiores en peces dulceacuícolas. El grado de diversificación y variación en el cariotipo también fue mayor en peces de agua dulce en contraste con un patrón citogenético más conservado en peces marinos. En contraposición a la suposición según la cual 48 cromosomas acrocentricos era el número cromosómico basal en los peces, los datos aquí presentados muestran que existe una evidente tendencia hacia la reducción del número de cromosomas desde valores cercanos a 2n=60 con alto número de cromosomas birrámeos en las especies más basales a 2n=48 elementos acrocéntricos en los actinopterigios más derivados.

El género Pterois contiene nueve especies válidas, nativas del Mar Rojo y el Océano Índico en el Pacífico occidental. P. volitans y P. miles son nativas del Indo-Pacífico, y fueron introducidas en las aguas de Florida como resultado de la liberación de peces confinados en acuario y han sido reconocidas recientemente como invasoras en el Atlántico Occidental y Mar Caribe (Costa Rica hasta Venezuela). Los estudios citogenéticos realizados hasta ahora en el género Pterois cubren solamente aspectos básicos de tres especies que incluyen a P. volitans del océano Indo-Pacífico. Debido a la ausencia de información detallada sobre las características cromosómicas de esta especie invasora, el objetivo del presente estudio fue investigar las características citogenéticas en ejemplares de Venezuela mediante técnicas convencionales y moleculares y comparar los resultados con los reportados para el área de distribución original. Para ello, se investigaron las características cariotípicas mediante tinción con Giemsa, bandeo-C, impregnación con Nitrato de Plata (Ag-NOR) e hibridación fluorescente in situ (FISH) dual para localizar los genes ribosomales 18S rDNA y 5S rDNA en cuatro ejemplares de pez león capturados en la Isla Margarita, Venezuela. La comparación de secuencias del gen 16S de los especímenes analizados con secuencias ya incluidas en el Genbank permitieron corroborar la identificación de P. volitans excluyendo así la posibilidad de una identificación errónea de P. miles. El número diploide fue 2n=48 (2m+10sm+36a) con un FN=60. Los cromosomas presentaron tamaños que disminuyen de manera uniforme dificultando la identificación de homólogos, excepto el único par metacéntrico y el par cromosómico número 2. El bandeo-C reveló tres pares de cromosomas bandas-C negativos, mientras que los restantes presentaron bloques bandas-C positivos en posición telomérica y, en algunos casos, intersticial. Sólo dos cromosomas mostraron bandas-C pericentroméricas. La tinción secuencial reveló las Ag-NOR localizadas en los extremos de los brazos cortos del par número dos y el ensayo FISH demostró que los genes 18S rDNA y 5S rDNA se localizan en ese mismo par. Se discute la co-localización de los genes 5S rDNA y 18S rDNA. La distribución de la heterocromatina constitutiva y localización de las NORs en los peces examinados difirió de la reportada para ejemplares de P. volitans del Océano Índico (Java), sugiriendo que durante la propagación de P. volitans han ocurrido reorganizaciones cromosómicas que involucran la heterocromatina.

The genus Pterois includes nine valid species, native to the Red Sea and Indian Ocean throughout the Western Pacific. P. volitans and P. miles are native to the Indo-Pacific, and were introduced into Florida waters as a result of aquarium releases, and have been recently recognized as invaders of the Western Atlantic and Caribbean Sea (Costa Rica to Venezuela). Thus far, cytogenetic studies of the genus Pterois only cover basic aspects of three species, including P. volitans from Indo-Pacific Ocean. Considering the lack of more detailed information about cytogenetic characteristics of this invasive species, the objective of the present study was to investigate the basic and molecular cytogenetic characteristics of P. volitans in Venezuela, and compare the results with those from the original distribution area. For this, the karyotypic characteristics of four lionfish caught in Margarita Island, Venezuela, were investigated by examining metaphase chromosomes by Giemsa staining, C-banding, Ag-NOR, and two-colour-Fluorescent in situ hybridization (FISH) for mapping of 18S and 5S ribosomal genes. Comparing the sequences of the 16S gene of the specimens analyzed, with sequences already included in the Genbank, we corroborated that our specimens identified as P. volitans are in fact this species, and hence exclude the possibility of a misidentification of P. miles. The diploid number was 2n=48 (2m+10sm+36a) with FN=60. Chromosomes uniformly decreased in size, making it difficult to clearly identify the homologues except for the only metacentric pair, and the pairs number two, the largest of the submetacentric series. C-banding revealed only three pairs of chromosomes negative for C-band, whereas all remaining chromosomes presented telomeric and some interstitial C-positive blocks. Only two chromosomes were C-banding positive at the pericentromeric regions. Sequential staining revealed Ag-NOR on the tips of the short arms of chromosome pair number two and the FISH assay revealed that 18S rDNA and 5S rDNA genes are co-located on this chromosome pair. The co-localization of 5S rDNA and 45S rDNA is discussed. Both constitutive heterochromatin and NOR location detected in samples examined in this study, differ from those reported for P. volitans in previous analysis of specimens collected in Indian Ocean (Java), suggesting the occurrence of chromosome microrearrangements involving heterochromatin during the spread of P. volitans.Rev. Biol. Trop. 62 (4): 1365-1373. Epub 2014 December 01.

La textura es la característica más valorada en los cefalópodos. Los factores que principalmente afectan la textura del pulpo son congelación, escaldado y cocción. El objetivo de esta investigación fue evaluar el efecto de la congelación, escaldado y diferentes tiempos de cocción sobre la textura y perfil electroforético de las proteínas de brazos de pulpo (Octopus vulgaris). Los ejemplares fueron capturados con nasa en las cercanías de la Isla de Margarita y transportados al laboratorio, donde fueron empacados y sometidos a: a) congelación a -27°C ó a -20 °C b) escaldado o no escaldado c) cocción por 25, 35 ó 45 min. Se determinó la fuerza de corte sobre tiras de brazo de pulpo mediante celda de Kramer. Extractos de proteínas fueron sometidos a electroforesis en gel de poliacrilamida-dodecil sulfato de sodio (SDS-PAGE) al 12 % según método Laemmli. Fue realizada evaluación sensorial de la preferencia de la textura empleando escala hedónica de 7 puntos y panel no entrenado. La textura del pulpo no resultó afectada ni por la temperatura de congelación ni el escaldado. El pulpo congelado, al cocerlo, fue más blando que el fresco. En la medida que aumentó el tiempo de cocción, el pulpo se ablandó más. La cocción no afectó significativamente la cadena pesada de miosina (MHC) (205 kD); sin embargo, causó aparición de agregados proteínicos más pesados, nuevas bandas y pérdida de definición de bandas. Las fracciones de miosina y de paramiosina resultaron más afectadas cuando el pulpo fue congelado previo a la cocción.

Texture is the most valuable feature in cephalopods. Factors that mainly affect the texture of octopus are: freezing, scalding and cooking. The aim of this study was to assess the effect of freezing, scalding and length of cooking time on the texture and electrophoretic pattern of proteins of octopus arms. Octopuses were trapped near Margarita Island and carried with ice to the laboratory where they were packed and subjected to: a) freezing at -27°C or at -20 °C b) scalding c) cooking for 25 min, 35 min or 45 min. Shear force was determined by Kramer cell on strips of octopus arms. SDS-PAGE was done according to the Laemmli method with 12% polyacrilamide gels. A sensory evaluation of the preference of texture was carried out using a hedonic scale of 7-points and a non-trained panel. Octopus texture was not affected by freezing temperature or scalding. Frozen octopus was softer after cooking than fresh. The longer the cooking time was, the softer the octopus was. Myosin heavy chain (MHC) was not significantly affected by scalding or cooking; however large aggregates heavier than MHC, new bands and loss of resolution of the bands appeared. Myosin and paramyosin bands were more affected by freezing prior to cooking.

This study reports the description of the karyotype of Mugil incilis from Venezuela. The chromosome complement is composed of 48 acrocentric chromosomes, which uniformly decrease in size. Therefore, the homologues can not be clearly identified, with the exception of one of the largest chromosome pairs, classified as number 1, whose homologues may show a subcentromeric secondary constriction, and of chromosome pair number 24, which is considerably smaller than the others. C-banding showed heterochromatic blocks at the centromeric/pericentromeric regions of all chromosomes, which were more conspicuous on chromosomes 1, given the C-positive signals include the secondary constrictions. AgNO3 and fluorescent in situ hybridization (FISH) with 45S rDNA demonstrated that the nucleolus organizer regions are indeed located on the secondary constrictions of chromosome pair number 1. FISH with 5S rDNA revealed that the minor ribosomal genes are located on this same chromosome pair, near the NORs, though signals are closer to the centromeres and of smaller size, compared to those of the major ribosomal gene clusters. This is the first description of co-localization of major and minor ribosomal genes in the family. Data are discussed from a cytotaxonomic and phylogenetic perspective.

Se presenta la primera descripción del cariotipo de Mugil incilis de Venezuela. El complemento cromosómico está compuesto por 48 cromosomas acrocéntricos uniformemente decrecientes en tamaño. Por lo tanto, los homólogos no pueden ser claramente identificados, con excepción de uno de los pares de mayor tamaño, clasificado como número 1, cuyos homólogos poseen una constricción secundaria subcentromérica, y el par de cromosomas número 24, considerablemente más pequeño que los otros. El bandeo-C reveló bloques heterocromáticos en las regiones centroméricas/pericentroméricas de todos los cromosomas, más conspicuas en el cromosoma 1 en el que las señales C-positivas se encuentra localizada precisamente en la constricción secundaria. La tinción con AgNO3 y la Hibridación Fluorescente in situ (FISH) con sonda 45S rDNA revelaron que las regiones organizadoras del nucléolo están ciertamente localizadas sobre la constricción secundaria del cromosoma número 1. FISH con 5S rDNA reveló que los genes ribosomales menores están ubicados en este mismo par cromosómico, en posición proximal a las NORs, aunque cercanas al centrómero y de menor tamaño en comparación con los clúster de genes ribosomales mayores. Ésta es la primera descripción de co-localización de genes ribosomales mayores y menores en la familia Mugilidae. Los datos se discuten bajo perspectivas citotaxonómicas y filogenéticas.

Despite their ecological and economical importance, fishes of the family Ariidae are still genetically and cytogenetically poorly studied. Among the 133 known species of ariids, only eight have been karyotyped. Cytogenetic analyses performed on Genidens barbus and Sciades herzbergii revealed that both species have 2n = 56 chromosomes and Cathorops aff. mapale has 2n = 52 chromosomes: Genidens barbus has 10 Metacentrics (M), 14 Submetacentrics (SM), 26 Subtelocentrics (ST), and 6 Acrocentrics (A), Sciades herzbergii has 14M, 20SM, 18ST and 4A, whereas Cathorops aff. mapale has 14M, 20SM, and 18ST. The nucleolus organizer regions (NORs) were found in a single chromosome pair on the short arm of a large-sized ST pair in Genidens barbus and on the short arm of a middle-size SM pair in Cathorops aff. mapale. Multiple NORs on the short arms of two large-sized ST pairs were found in Sciades herzbergii. The occurrence of diploid numbers ranging from 2n = 52 through 56 chromosomes and the presence of different karyotypic compositions, besides the number and position of NORs suggest that several numeric and structural chromosome rearrangements were fixed during the evolutionary history of this fish family.

Lutjanidae, comumente conhecidos como snappers, inclui 105 espécies, reunidas em quatro subfamílias. A despeito do grande número de espécies e de sua distribuição mundial, a família tem sido pouco estudada e as relações filogenéticas entre alguns de seus gêneros e espécies ainda é motivo de debates. Apenas um pequeno número de espécies foi citogeneticamente analisada. Esse estudo apresenta a primeira descrição do cariótipo de Rhomboplites aurorubens assim como dados relativos à distribuição de heterocromatina constitutiva e localização dos genes 18S rRNA e 5S rRNA. Espécimes de Ocyurus chrysurus da Venezuela foram também analisados quanto às mesmas características citogenéticas. Ambas as espécies têm cariótipos compostos de 48 cromossomos com um único braço, entretanto R. aurorubens tem um único par de cromossomos subtelocêntrico, o menor do complemento cromossômico, entre os outros cromossomos acrocêntricos. A heterocromatina C-positiva é limitada à região pericentromérica de todos os cromossomos. Ambas as species apresentam um único par com Regiões Organizadoras de Nucléolo, mas as RONs são localizadas em posições diferentes, em posição terminal no braço curto dos menores cromossomos de R. aurorubens e em posição paracentromérica no braço longo de um par de cromossomos grandes de O. chrysurus. Em O. chrysurus, os genes 5S rDNA estão localizados em um par de cromossomos de tamanho médio, enquanto em R. aurorubens eles são sintenicamente localizados com os genes 18S rDNA no par de cromossomos número 24. Os dados citogenéticos obtidos, junto com os dados morfológicos e moleculares disponíveis para a família reforçam a proposta de sinonimizar o gênero Ocyurus com Lutjanus. Uma revisão da citogenética dos Lutjanidae é também apresentada

Lutjanidae, commonly known as snappers, includes 105 species, grouped in four subfamilies. In spite of the high number of species and of its worldwide distribution, the family has been little investigated and the phylogenetic relationships among some of its genera and species are still cause for debate. Only a small number of the species has been cytogenetically analysed. This study reports the first description of the karyotype of Rhomboplites aurorubens as well as data concerning the distribution of the constitutive heterochromatin and the location of the 18S rRNA and the 5S rRNA genes. Specimens of Ocyurus chrysurus from Venezuela were also investigated for the same cytogenetic features. Both species have a 48 uniarmed karyotype, but R. aurorubens has a single subtelocentric chromosome pair, the smallest of the chromosome complement, among the other acrocentric chromosomes. The C-positive heterochromatin is limited to the pericentromeric regions of all chromosomes. Both species show a single chromosome pair bearing the Nucleolus Organizer Regions, but NORs are differently located, in a terminal position on the short arms of the smallest chromosomes in R. aurorubens and in a paracentromeric position in a chromosome pair of large size in O. chrysurus. In O. chrysurus, the 5S rDNA gene cluster is located on a medium-sized chromosome pair, whereas in R. aurorubens it is syntenic with the 18S rDNA gene cluster on chromosome pair number 24. The obtained cytogenetic data, along with previous cytogenetic, morphological and molecular data for the family, reinforce the proposal to synonymize genus Ocyurus with Lutjanus. A review of Lutjanidae cytogenetics is also included.

La introducción de organismos a un nuevo ambiente generalmente ocurre en escaso número de individuos, lo cual determina el llamado "cuello de botella", reduciendo la variación genética, mientras que la selección reduce aún más esta variación. Entonces, ¿Cómo estos exóticos son exitosos, expanden su rango de distribución bajo nuevas condiciones, evolucionan rápidamente y se convierten en invasores, si su variación genética es baja? En el presente trabajo, se consideran una serie de mecanismos que permitirían a las poblaciones introducidas adquirir nueva variación genética. Las adaptaciones epigenéticas, la hibridización, las mutaciones adaptativas, los transposones, la endosimbiosis, las mutaciones somáticas y recombinaciones mitóticas son postuladas como fuentes de nueva variación. Además se analiza el papel de la purificación y la regulación biótica en la invasión exitosa de algunas especies.

Given that the introduction of organisms into a new environment usually occurs in low numbers, reducing genetic diversity (the so-called bottleneck effect), and that selection further decreases diversity beyond that caused by the bottleneck, then how do some alien species, if their genetic variation is low under new conditions, succeed in evolving rapidly, becoming invasive and expanding their ranges? In this paper a series of mechanisms that allow the introduced population to acquire new genetic variations are considered. Various possible roles of epigenetic adaptation, hybridization, adaptive mutations, transposons, endosymbiosis, somatic mutations, and mitotic recombination are postulated as sources of new genetic variations. The roles of purging and biotic regulation in the successful invasions of some species is also analyzed.

A introdução de organismos a um novo ambiente geralmente ocorre em escasso número de indivíduos, o qual determina o chamado "efeito gargalo", reduzindo a variação genética, enquanto que a seleção reduz ainda mais esta variação. Como, então, podem estes exóticos ser bem sucedidos, expandir sua faixa de distribuição sob novas condições, evolucionar rapidamente e se converter em invasores, se sua variação genética é baixa? No presente trabalho, é considerada uma série de mecanismos que permitiriam às populações introduzidas adquirirem nova variação genética. As adaptações epigenéticas, a hibridização, as mutações adaptativas, os transposões, a endossimbiose, as mutações somáticas e recombinações mitóticas são postuladas como fontes de nova variação. Além disso, se analisa o papel da purificação e a regulação biótica na invasão bem sucedida de algumas espécies.

No presente estudo três espécies de Lutjaninae, Lutjanus analis, L. griseus e L. synagris foram analisadas através da coloração convencional com Giemsa, banda C e coloração com nitrato de prata para identificar as Regiões Organizadoras de Nucléolo (NORs) ativas. Hibridação fluorescente in situ (FISH) foi também aplicada para estabelecimento do número e localização dos agrupamentos de genes ribossômicos (18S e 5S rRNA). A contagem de células metafásicas revelou um número diplóide modal de 48 cromossomos acrocêntricos em L. analis e L. griseus. Dois citótipos foram observados em L. synagris: citótipo I com 2n=48 cromossomos acrocêntricos, encontrado em 19 espécimes, e citótipo II com 46 cromossomos acrocêntricos e um grande metacêntrico, encontrado em dois espécimes. O grande metacêntrico, que possivelmente se originou por um rearranjo Robertsoniano, não está relacionado com o sexo. Nas três espécies a heterocromatina constitutiva está localizada nas regiões centroméricas de todos os cromossomos. NORs foram detectadas no braço curto de um único par cromossômico, número 24 em L. analis e número 6 em ambos os citótipos de L. synagris. Em L. griseus, um polimorfismo de número de NORs foi observado, após coloração com prata e por FISH, as fêmeas apresentaram um máximo de três NORs e os machos um máximo de seis NORs. Em todas as espécies os genes ribossômicos 5S foram encontrados em um único par cromossômico. Os dados obtidos, somados aos demais previamente publicados para cinco outras espécies de Lutjanidae, mostram que na família há uma homogeneidade cromossômica, porém também são encontrados cariótipos derivados, originados por rearranjos Robertsonianos, assim como pela ocorrência de sítios múltiplos e variados de NORs.

In the present study, three species of Lutjaninae, Lutjanus analis, L. griseus and L. synagris, were analyzed by conventional Giemsa staining, C-banding and silver staining, to reveal active Nucleolus Organizer Regions (NORs). Fluorescent in situ hybridization (FISH) was also applied to establish the number and location of the ribosomal gene clusters (18S and 5S rRNA genes). Counts of diploid metaphasic cells revealed a diploid modal chromosome complement composed of 48 acrocentric chromosomes in both L. analis and L. griseus. Two cytotypes were observed in L. synagris: cytotype I, with 2n=48 acrocentric chromosomes, found in 19 specimens, and cytotype II, with 46 acrocentric chromosomes and one large metacentric, found in two specimens. The large metacentric, which possibly originated from a Robertsonian rearrangement, was not found to be sex-related. In the three species, constitutive heterochromatin is located in the centromeres of all chromosomes. NORs were detected on the short arms of a single chromosome pair, number 24 in L. analis and number 6 in both cytotypes of L. synagris. In L. griseus, a polymorphism of the NORs number was detected, by both Ag-staining and FISH, as females show a maximum of three NORs, and males a maximum of six NORs. In all species, minor ribosomal genes were found located on a single chromosome pair. The obtained data, along with those previously reported for other five Lutjanidae species, show that a general chromosome homogeneity occurs within the family, but that derived karyotypes based on Robertsonian rearrangements as well as multiple and variable NORs sites can also be found.

Cytogenetic analyses performed in Cephalosilurus apurensis, Microglanis aff. cottoides and Pseudopimelodus bufonius revealed that the three species have 2n = 54 chromosomes: C. apurensis presented six metacentric (M), 28 submetacentric (SM), 14 subtelolocentric (ST), and six acrocentric (A) chromosomes, while M. aff. cottoides showed 10M, 32SM, 10ST and 2A, and P. bufonius had 12M, 30SM and 12ST. The nucleolus organizer regions (NORs) were present on the short arm of a middle-sized ST pair, identified as pair 19, in C. apurensis NORs were found on the short arm of a middle-sized ST (pair 23) and on the long arm of a middle-sized ST (pair 22) in M. aff. cotttoides and on the short arm of three middle-sized ST pairs, identified as pairs 9, 10 and 11, in P. bufonius. C-banding revealed a very small amount of constitutive heterochromatin in the chromosomes of all species, including the NORs. The occurrence of 2n = 54 in all species of the family Pseudopimelodidae and its absence among species of the closely related Pimelodidae and Heptapteridae may be important in identifying Pseudopimelodidae species.