Resumo A análise da capacidade de combinação fornece informações úteis para a seleção dos pais, também informações sobre a natureza e a magnitude das ações dos genes envolvidos. A melhoria das safras envolve estratégias para aumentar a potencialidade da produção e os componentes de qualidade. Visando ao aprimoramento dos respectivos caracteres em cabaça-amarga, capacidade de combinação e parâmetros genéticos para 19 caracteres, foram estimados a partir de uma técnica de análise dialélica completa 6 × 6. Os resultados revelaram que as variâncias, devido à capacidade geral de combinação (GCA) e capacidade específica de combinação (SCA), foram altamente significativas para a maioria dos caracteres importantes. Indicou a importância das ações gênicas aditivas e não aditivas. As variâncias GCA foram maiores em magnitude do que as variâncias SCA para todos os caracteres estudados, indicando a predominância dos efeitos do gene aditivo em sua herança. O pai P2 (BG 009) apareceu como o melhor combinador geral para o início; P1 (BG 006) para número de frutos, peso médio de um único fruto e produção de frutos; P4 (BG 027) para número de nó da primeira flor fêmea e dias para a maturidade do fruto da semente; P3 (BG 011) para comprimento do fruto e espessura da polpa do fruto; P5 (BG 033) para peso de 100 sementes; e P6 para o número de nós por videira principal. O efeito SCA, bem como o efeito recíproco, também foi significativo para a maioria dos personagens importantes em cruzamentos diferentes.

Abstract Combining ability analysis provides useful information for the selection of parents, also information regarding the nature and magnitude of involved gene actions. Crops improvement involves strategies for enhancing yield potentiality and quality components. Targeting the improvement of respective characters in bitter gourd, combining ability and genetic parameters for 19 characters were estimated from a 6×6 full diallel analysis technique. The results revealed that the variances due to general combining ability (GCA) and specific combining ability (SCA) were highly significant for most of the important characters. It indicated the importance of both additive and non-additive gene actions. GCA variances were higher in magnitude than SCA variances for all the characters studied indicating the predominance of the additive gene effects in their inheritance. The parent P2 (BG 009) appeared as the best general combiner for earliness; P1 (BG 006) for number of fruits, average single fruit weight and fruit yield; P4 (BG 027) for node number of first female flower and days to seed fruit maturity; P3 (BG 011) for fruit length and thickness of the fruit flesh; P5 (BG 033) for 100-seed weight; and P6 for number of nodes per main vine. The SCA effect as well as reciprocal effect was also significant for most of the important characters in different crosses.

Bones of forelimb were studied from a prepared skeleton of an adult female Asian elephant (Elephas maximus) in Anatomy Museum of Chittagong Veterinary and Animal Sciences University to understand the morphological form and structure of Asian elephant forelimb. The angle was approximately 123 between caudal border of scapula and caudal border of humerus. The scapula, humerus and bones of the antebrachium (particularly the ulna) were massive bones. The bones of manus were the short and relatively small. The dorsal border of scapula extended from the level of proximal extremity of first rib to the middle of the 6th rib. Ventral angle of scapula articulated with humerus by elongated shaped glenoid cavity (cavitas glenoidalis) of scapula and head of humerus (caput humeri). The major tubercle (tuberculum majus) of humerus was situated laterally to the head, which had smaller cranial part with large caudal part and extended cranially to the head. The crest of minor tubercle (tuberculum minus) was present as the rough line on the mediocaudal surface of humerus that ends in a slight depressed or elevated area, known as teres major tuberosity (tuberositas teres major). The lateral supracondyler crest (crista supra condylaris lateralis) at the caudal surface of the shaft limit the musculo-spiral groove in body of humerus. The radius and ulna are twin bones of forearm and the attachment between ulna and radius occurs in such a way, the radius articulates craniomedially with the ulna in the proximal part. But the shaft spirals laterally over the cranial surface of the ulna to articulate distally with the medial aspect of the ulna. There were 8 carpal bones, 5 metacarpal bones and 5 digits. The comparative size of the proximal and distal raw of carpal bones were ulnar carpal > radial > intermediate > accessory carpal and IV > III > II > I respectively. The gradual lengths of the metacarpal bones were III > IV > II > V > I. Digits I and V were vertical and digit II, III and IV were horizontal.

En el Museo de Anatomía de la Universidad de Veterinaria y Ciencias de Animales de Chittagong fueron estudiados los huesos del miembro torácico de un esqueleto preparado de un elefante asiático (Elephas maximus), hembra adulta, para analizar su morfología y estructura. El ángulo entre el margen caudal de la escápula y el margen caudal del húmero era de aproximadamente 123°. La escápula, húmero y los huesos del antebrazo (en particular la ulna) eran huesos macizos. Los huesos de las manos eran cortos y relativamente pequeños. El margen dorsal de la escápula se extendía desde el nivel de la porción proximal de la primera costilla para la parte media de la sexta costilla. El ángulo ventral de la escápula está articulado con el húmero por la cavidad glenoidea (cavitas glenoidalis), de forma alargada, de la escápula y la cabeza del húmero (caput humeri). El principal tubérculo (tuberculum majus) del húmero estaba situado lateralmente a la cabeza, que tenía una parte craneal pequeña y una mayor parte caudal, extendiéndose cranealmente en la cabeza. La cresta del tubérculo menor (tuberculum minus) estaba presente como la línea áspera sobre la superficie mediocaudal del húmero que termina en una pequeña zona deprimida o elevada, conocida como tuberosidad redonda mayor (tuberositas teres major). La cresta supracondilar lateral (crista supra condylaris lateralis) en la superficie caudal del eje limita la ranura músculo-espiral en el húmero. El radio y la ulna son huesos gemelos del antebrazo y la unión entre la ulna y el radio se produce de tal manera, que el radio articula, craneal y medialmente, con la ulna en la porción proximal. Pero el eje en espiral está ubicado lateralmente sobre la superficie craneal de la ulna para articular distalmente con la cara medial de la ulna. Se identificaron 8 huesos del carpo, 5 metacarpianos y 5 dígitos. El tamaño comparativo de las porciones proximal y distal de los huesos del carpo fue ulna > radial > Intermedio> carpiano accesorio y IV > III > II > I, respectivamente. Las longitudes graduales de los huesos metacarpianos eran III > IV > II > V > I. Dígitos I y V eran verticales y dígitos II, III y IV fueron horizontales.

Recent excavated skeleton of an adult female Asian Elephant (Elephas maximus), died in dystokia in Bangladesh was used for macro anatomical study. Some unique morphological features of bones of hind limb were observed. Pelvic canal was more oval and the wings of ilium were wider. Rump slope was about 36°. Angle between femur and tibia was close to 180°. In Femur, the major trochanter was located at the lower level of head. Minor trochanter, fovea capitis and trochanteric ridge were absent. Supracondyloid fossa was shallow but the intercondyloid fossa was deep. Posterior surface of patella possessed a blunt vertical ridge. The articular surfaces of both tibial condyles were clearly concave. The tibia and the fibula were articulated proximally and distally with keeping a wide interosseous space. Instead of tibial tuberosity, there was an elongated triangular depression in proximal part. There were six tarsal bones arranged in three rows. The comparative size of the distal tarsal bones were III+IV > I > II. The comparative lengths of the metatarsal bones were III > II > IV > V> I. Digits I and V were the most vertical and digit III was the most horizontal. The proximal phalanx was the biggest of all.

Fue utilizado para su estudio anatómico macrocroscópico, el esqueleto de un elefante asiático (Elephas maximus) hembra adulta, excavado recientemente y con muerte por distocia en Bangladesh. Se observaron algunas características morfológicas únicas de los huesos de los miembros posteriores. El canal pélvico era más ovalado y las alas del ilion eran más amplias. La pendiente de la rabadilla era de unos 36° aproximadamente; el ángulo entre el fémur y la tibia era próximo a los 180°. En el fémur, el trocánter mayor se encontraba en el nivel inferior de la cabeza. El trocánter menor, la fovea capitis y cresta del trocánter estuvieron ausentes. La fosa supracondílea era superficial, mientras que la fosa intercondílea era profunda. La superficie posterior de la patela poseía una cresta vertical sobresaliente. Las superficies articulares de ambos cóndilos tibiales eran claramente cóncavas. La tibia y la fíbula se articulan proximal y distalmente, manteniendo un amplio espacio interóseo. En lugar de la tuberosidad tibial, había una depresión triangular alargada en parte proximal. Se observaron seis huesos del tarso dispuestos en tres filas. El tamaño relativo de los huesos del tarso distal eran III + IV > I > II. Las longitudes comparativas de los huesos metatarsianos fueron III > II > IV > V > I. Los dígitos I y V fueron los más verticales y el dígito III fue el más horizontal. La falange proximal fue la de mayor tamaño.