Andrew Adogwa’s research while affiliated with University of the West Indies, St. Augustine and other places

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Publications (55)


Figure 1. The MNTB of the Noctilio leporinus Bat. (A) A transverse section of the brainstem at the level of the motor nucleus of the trigeminal nerve of the N. leporinus bat. 1. Superior olivary nucleus 2. Superior paraolivary nucleus 3. Accessory superior olivary nucleus 4. Medial nucleus of the trapezoid body 5. Pyramid 6. Motor nucleus of the trigeminal nerve 7. Superior cerebellar peduncle; (B) Cells in the medial nucleus of the trapezoid body (MNTB) at the level of the motor nucleus of the trigeminal nerve of the N. leporinus bat. 1. Dense-staining, multipolar cells (12.5 to 25.0 µm diameter) 2. Light-staining, multipolar cells (12.5 to 25.0 µm in diameter) 3. Light-staining, round cells (5.0 µm in diameter); (C) Relatively more dark staining cells in the middle third of the MNTB at the level of the trigeminal nerve of the Noctilio leporinus bat. 1. Dense-staining, multipolar cells (12.5 to 25.0 µm diameter) 2. Light-staining, multipolar cells (12.5 to 25.0 µm in diameter) 3. Light-staining, round cells (5.0 µm in diameter); (D) Extensive fibres of the trapezoid body (TB) throughout the MNTB of the N. leporinus bat, at the level of the commissure of the inferior colliculus (IC). The large, light staining cells were seen predominantly (D-Dorsal, M-Medial, L-Lateral, V-Ventral).
Figure 2. The MNTB of Phyllostomus hastatus bat. (A) A transverse section of the brainstem at the level of the middle cerebellar peduncle of the P. hastatus bat. 1. Middle cerebellar peduncle 2. Superior paraolivary nucleus 3. Medial nucleus of the trapezoid body 4. Ventral nucleus of the trapezoid body 5. Fibres of the trapezoid body; (B) Medium-sized, dark-staining, round/ oval cells (12.5 to 17.5 μm diameter) in the caudal third of the MNTB of the P hastatus bat; (C) A transverse section at the rostral third of the MNTB of the P. hastatus bat. 1. Inferior colliculus 2. Medial nucleus of the trapezoid body 3. Fibres of the trapezoid body 4. Medial lemniscus 5. Fourth ventricle; (D) The fibres and cells of the rostral third of the MNTB of the P. hastatus bat (D-Dorsal, M-Medial, L-Lateral, V-Ventral).
Figure 3. The MNTB of Carollia perspicillata bat. (A) A transverse section of the brainstem at the level of the facial nucleus of the Carollia perspicillata bat. 1. Cerebellum 2. Facial nucleus 3. Pyramid 4. Medial nucleus of the trapezoid body 5. Superior olivary complex 6. Cochlear nucleus; (B) The predominant cells of the caudal third of the MNTB of the C. perspicillata bat. 1. Large, oval cells (12.5 to 25.0 µm in diameter) 2. Small round cells (5.0 µm diameter); (C) Three cell-types of the MNTB of the C. perspicillata bat. 1. Large, oval cells (12.5 to 25.0 µm in diameter) 2. Small round cells (5.0 µm in diameter) 3. Large multipolar cells (20.0 to 32.5 µm in diameter); (D) A transverse section of the brainstem at the level of the caudal inferior colliculus of the C. perspicillata bat. 1. Inferior colliculus 2. Cerebellum 3. Medial nucleus of the trapezoid body 4. Fibres of the trapezoid body.
Cytoarchitecture of the medial nucleus of trapezoid body of three neotropical species of bats (Noctilio leporinus, Phyllostomus hastatus, and Carollia perspicillata) with different foraging behavior
  • Article
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October 2020

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60 Reads

Brazilian Journal of Biology

I Gibbons

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A Adogwa

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The present study was taken to test the hypothesis that the medial nucleus of the trapezoid body (MNTB) of echolocating neotropical bats with different foraging behavior will exhibit morphological variations in relative size, degree of complexity and spatial distribution. The brains were collected from six male adult bats of each species: Noctilio leporinus (fish-eating), Phyllostomus hastatus (carnivorous/ omnivorous) and Carollia perspicillata (fruit-eating) and were double-embedded and transverse serial sections were cut and stained with cresyl fast violet. The results showed that the MNTB is well developed in all the bats in general and the mean length of the MNTB was 1160 ± 124 µm in N. leporinus, 400 ± 59 µm in P. hastatus and 320 ± 25µm in C. perspicillata. The body and brain weight do not reflect proportionately on the size of the MNTB in the present study. The hearing frequency spectrum did not covary with the size of the MNTB among the bats studied. The MNTB is clearly demarcated from the ventral nucleus of the trapezoid body (VNTB) only in P. hastatus. The MNTB comprised mainly three types of cells in all three bats: dense-staining multipolar cells (12.5 µm and 25.0 µm diameter); light-staining multipolar cells measuring (12.5 µm and 25.0 µm diameter) and light-staining round cells (5.0 µm diameter). The large sized MNTB was observed in N. leporinus, which suggests that it relies heavily on echolocation whereas P. hastatus and C. perspicillata use echolocation as well but also rely on hearing, smell and vision.

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Anatomical view of the (a) GI tract and (b) Stomach of Didelphis marsupialis insularis showing (O) Oesophagus; (S) Stomach; (L) Liver; (SI) Small Intestine; (LI) Large Intestine: Colon and Rectum; (Ca) Caecum; (Sp) Spleen; (D) Duodenum; (AV) Antrum Ventricularis; (IA) Incisura Angularis; (LC) Lesser Curvature; (GC) Greater Curvature; (P) Pyloric opening; (C) Cardiac opening
Comparative relative gut lengths in eight Didelphis marsupials as a percentage of total gastrointestinal tract length. (Information for seven marsupials obtained from (Cáceres, 2005)
Photomicrographs of Didelphis marsupialis insularis (a) Oesophagus (Caudal) (b) Stomach (Cardia) (c) Stomach (Fundus) (d) Stomach (Pylorus) (e) Oesophagus (Cranial) (f) Oesophagus (Caudal) showing (ST) Stratified Squamous epithelium; (MM) Muscularis mucosa; (SM) Submucosa; (OG) Oesophageal gland; (TM) Tunica muscularis; (SKM) Skeletal muscle; (CG) Cardiac glands; (FG) Fundic glands; (PG) Pyloric glands
Photomicrographs of Didelphis marsupialis insularis (a) Duodenum (b) Jejunum (c) Ileum (d) Caecum (e) Colon (f) Rectum showing (MM) Muscularis mucosa; (SM) Submucosa; (TM) Tunica muscularis; (M) Mucosa; (V) Villi; (PC) Plicae circulares
Anatomy and histology of the gastrointestinal tract of the neo‐tropical opossum (Didelphis marsupialis insularis, Allen 1902)

July 2019

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129 Reads

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11 Citations

The morphology of the gastrointestinal tract (GI) is a strong indicator of the dietary habits of a species. The goal of this study was to describe the gross and microanatomy of the digestive tract of the neo‐tropical opossum (Didelphis marsupialis insularis) and relate them to the animals’ food habits. GI tracts from 12 adult animals were used for this study. Results found the small intestine made up 65.9% of the GI tract, and the stomach was simple with a prominent caecum. Histologically, the oesophageal mucosa was non‐keratinized and glands were found throughout the oesophagus. The large intestine showed a great number of goblet cells, the jejunum possessed well‐developed villi, and Peyer's patches were absent in the ileum. The absence of keratinization of the epithelial lining of the oesophagus and stomach and a high lymphocytic infiltration throughout the small and large intestine reflected a more carnivorous diet, whereas the presence of a well‐developed caecum in the large intestine indicated the ability to digest plant matter. Overall, the morphology of GI tract of D. m. insularis displayed both carnivorous and herbivorous features, allowing us to conclude that it is an omnivorous animal.


Figure 1. Superior olivary complex of Noctilio leporinus bat. (A) transverse section of the brainstem at the level of the facial nucleus. 1. Cochlear nucleus, 2. Caudal cerebellar peduncle, 3. Superior olivary complex, 4. Cerebellum, 5. Fourth ventricle, 6. Facial nucleus; (B) the divisions of the caudal third of the superior olivary complex in the brainstem. 1. First division of the superior olivary complex (dashed left bracket indicates the folded region), 2. Second division of the superior olivary complex; (C). transverse section of the brainstem at the level of the motor nucleus of the trigeminal nerve. 1. Lateral superior olive, 2. Dorsal medial superior olive, 3. Ventral medial superior olive, 4. Nucleus of the trapezoid body, 5. Pyramids, 6. Motor nucleus of the trigeminal nucleus; (D) the divisions of the middle third of the superior olivary complex. LSO = Lateral superior olive, DMSO = Dorsal medial superior olive, VMSO = Ventral medial superior olive; (E) transverse section of the brainstem at the level of the inferior colliculus. 1. Lateral superior olive, 2. Dorsal medial superior olive, 3. Ventral medial superior olive, 4. Nucleus of the trapezoid body, 5. Middle cerebellar peduncle, 6. Lateral lemniscus, 7. Inferior colliculus; (F) the cell-types found in the superior olivary complex. 1. Dark-staining, elongated/multipolar cells, 2. Light-staining round cells measuring 7.5 µm.
Figure 2. Superior olivary complex of the Phyllostomus hastatus bat. (A) transverse section of the brainstem at the level of the facial nucleus. 1. Cochlear nucleus, 2. Caudal cerebellar peduncle, 3. Medial vestibular nucleus, 4. Fourth ventricle, 5. Facial nucleus, 6. Superior olivary complex; (B) the first (1) and second (2) divisions of the caudal third of the superior olivary complex; (C) transverse section of the brainstem at the level of the trigeminal nucleus. 1. Cochlear nucleus, 2. Trigeminal nucleus, 3. Fourth ventricle, 4. Superior olivary complex; (D) the three (3) divisions of the middle third of the superior olivary complex. 1. Lateral superior olive (LSO), 2. Dorsal medial superior olive (DMSO), 3. Ventral medial superior olive (VMSO); (E) transverse section of the brainstem at the level of the nucleus of the trapezoid body. 1. Fourth ventricle, 2. Dorsal medial superior olive (DMSO), 3. Nucleus of the trapezoid body; (F) the cells found in the superior olivary complex.
Figure 3. Superior olivary complex of the Carollia perspicillata bat (A) the brainstem at the level of the facial nucleus of the C. perspicillata bat. 1. Cerebellum, 2. Pyramids, 3. Nucleus of the trapezoid body, 4. Superior olivary complex, 5. Cochlear nucleus, 6. Facial nucleus; (B) the brainstem at the level of the middle cerebellar peduncle. 1. Cerebellum, 2. Nucleus of the trapezoid body, 3. Fibres of the trapezoid body, 4. Superior olivary complex, 5. Cochlear nucleus, 6. Middle cerebellar peduncle; (C) the brainstem at the level of the inferior colliculus. 1. Cerebellum, 2. Inferior colliculus, 3. Fibres of the trapezoid body, 4. Nucleus of the trapezoid body, 5. Superior olivary complex.
Cytoarchitecture of the superior olivary complex of three neotropical species of bats (Noctilio leporinus, Phyllostomus hastatus and Carollia perspicillata) with different foraging behavior

May 2019

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124 Reads

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5 Citations

Brazilian Journal of Biology

The understanding of the echolocation by studying different auditory nuclei of echolocating bats can be an important link in elucidating questions arising in relation to their foraging behavior. The superior olivary complex (SOC) is the primary center for processing the binaural cues used in sound localization since echo locating bats rely on acoustic cues to navigate and capture prey while in flight. The present study was taken to test the hypothesis that the SOC of echolocating neotropical bats with different foraging behavior will exhibit morphological variations in relative size, degree of complexity and spatial distribution. The brains were collected from six male adult bats of each species: Noctilio leporinus (fish eating), Phyllostomus hastatus (carnivorous/omnivorous) and Carollia perspicillata (fruit eating). They were double-embedded and transverse serial sections were cut and stained with cresyl fast violet. The SOC measured as 640 ± 70 µm in the N. leporinus bat, 480 ± 50 µm in the P. hastatus and 240 ± 30 µm in the C. perspicillata bat. The principal nuclei of the SOC of in all three bats were the LSO, MSO and MNTB. The MSO and LSO were very well developed in N. leporinus bats. The MSO of N. leporinus bat subdivided into DMSO and VMSO. The main cell type of cells present in MSO and LSO are dark staining multipolar cells in all the bats studied. The well-developed MSO and LSO of N. leporinus bats indicate that these bats are highly sensitive to low frequency sounds and interaural intensity differences, which help these bats to forage over water by using various types of echolocation signals. The average size of SOC in P. hastatus and C. perspicillata bats can be attributed to the fact that these bats use vision and smell along with echolocation to forage the food.


Anatomy and Histology of the Digestive Tract of the Cocrico (Oratalis ruficauda)

November 2018

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163 Reads

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Andrew Adogwa

Abstract: The Cocrico (Oratalis ruficauda), one of the national birds of Trinidad and Tobago has drastically reduced in number in the recent years due to illegal hunting in Tobago. The captive rearing and breeding of these birds was in serious consideration as a part of the conservation programme. The understanding of the normal biology of this bird is essential to make better captive breeding and rearing policies. But, there is a dearth of published data related to, or describing, the detailed anatomy and histology of this bird apart from relating to commercial poultry. Therefore, the present study aimed to study the anatomy and histology of the digestive tract of the species, which in turn helps in developing suggestions for improvements in rearing, and to get a better understanding of its growth and production. Five apparently healthy adult birds (2 males and 3 females) were euthanized with the permission of the Forestry Division, Tobago House of Assembly (THA). The gross anatomical observations were made by dissection and the specimens were collected and fixed in 10% buffered formalin and processed by routine histological methods and stained with H&E and histological observations were made. The esophagus extended from the pharynx to the proventriculus with an average length of 14.1 cm and dilated at the thoracic inlet to form a crop with average breadth of 2.92 cms. The mucosa lined by stratified squamous epithelium with non-keratinized type with series of tubular mucous glands. The tunica muscularis consisted of inner and outer layer of smooth muscles. The stomach made up of a proventriculus and gizzard with a narrow isthmus between them. The proventriculus was spindle-shaped and measured an average length of 2.63 cm whereas ventriculus was lens-shaped and measured an average of 3.10 cm. The mucosa of proventriculus was extensively folded with simple tubular glands whereas the gizzard presented low folds with branched glands. The intestines consisted small intestines (duodenum, jejunum and ileum), paired ceca and small colorectum, which contributed 70.7% of the digestive tract length. The villi were well developed in duodenum and decline in number in jejunum and ileum. The anatomy and histology of the digestive tract of the cocrico showed several similarities with chicken but notable differences like poorly developed crop, the absence of an esophageal tonsil, a relatively thin gizzard, under-developed caeca and the absence of caecal tonsils. Keywords: Process simulation, energy analysis, carbon dioxide removal, ammonia process


Didelphis species, Neo-tropical animals with the potential for intensive production: Part 2: Review of reproductive systems

July 2017

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108 Reads

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1 Citation

Tropical Agriculture

This review focuses on the information that is available on the reproductive biology of Didelphis. From the findings of over 60 scientific documents - beginning as early as 1704- it was found that opossums possess some very exclusive reproductive adaptations, including: short gestation period, paired spermatozoa and a temporary pseudo-vaginal canal. These findings, however, were based on investigation on one or two species of the genus only. An overall picture of the reproductive biology and any adaptations or differences between the six species in the genus was therefore not possible. In conclusion, many gaps remain and novel theories on the topic have yet to be proposed on tropical and neo-tropical opossum species. Therefore, further study into the reproductive biology of South American and Caribbean species is highly recommended. This will allow for a clearer understanding of the reproductive biology of this marsupial, which can be a guide in the development of an intensive animal production system in the tropics.


Fig. 2. Dorsal (A), Ventral (B) and Lateral(C) views of the pelvis of D.leporina 
Fig. 3. Cranial (A), Caudal (B), Medial (C) and Lateral (D) views, Proximal (E) and distal extremity (F) of the left femur and the lateral surface (G) of the patella of the D. leporina 
Fig. 4. Cranial (A), Caudal (B), Medial (C) and Lateral (D) views, Proximal extremity (E) and Distal distal extremity (G) of the left tibia and fibula of D. leporina 
Hind Limb Skeleton of the Orange Rumped Agouti (Dasyprocta leporina Linnaeus, 1758): Structural and Functional Perspective

March 2017

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2,308 Reads

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5 Citations

Annual Research & Review in Biology

The present study was aimed to document the anatomy of the hind limb skeleton from a structural and functional perspective for the better understanding of locomotor behavior of the orange rumped agouti (Dasyprocta leporina), a caviomorph rodent on the verge of domestication in Trinidad and Tobago. The study was carried out by collecting bones from 6 adult male and 6 adult female animals. The results showed that several features were indicative of emphasized parasagittal movements and stabilized joints. The well-developed ischial tuber, long and strongly built ilium with wide wing and close grouping of greater and lesser trochanter near the proximal tuberosity of the Original Research Article Venkatesan et al.; ARRB, 12(2): 1-12, 2017; Article no.ARRB.30949 2 femur imply that the animal possesses a well developed flexor-extensor muscle set adapted to quick movements (reaction). The rather elongated body of the calcaneus strengthened the good jumping ability of D. leporina. These features along with elongation of the shank and foot indicate that D. leporina exhibits a well-developed cursorial ability with high jumping potential.


Fig. 3. The cranial (A) and caudal (B) views of the radius and medial (C) and lateral (D) views of the ulna of the D. leporina. 1. Articular notch 2.Shaft 3, 4. Articular facet for the carpals 5. Styloid process of the radius 6. Olecranon process 7. Anconeus process 8. 9. Medial coronoid process 10. Lateral groove 11.Styloid process of the ulna 
Fig. 5. The dorsal (A) and palmar (B) views of the manus of the 2. Second metacarpal 3. Third metacarpal 4. Fourth metacarpal 5. Fifth metacarpal V 6. First phalanx 7. Second phalanx 8. 
Morphological Studies of the Forelimb Skeleton of the Orange Rumped Agouti (Dasyprocta leporina Linnaeus, 1758)

January 2015

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1,235 Reads

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8 Citations

Annual Research & Review in Biology

The aim of the study is to document the morphological details of the forelimb bones of the orange rumped agouti (Dasyprocta leporina). The bones were collected from 12 adult animals of both sexes. Each limb comprised of 47 bones (30 bones, 17 sesamoid bones). The clavicle was poorly developed while the metacromion process of the scapula was very well developed. The humerus was peculiar, displaying poorly developed deltoid tuberosity, teres tubercle and the crest of the humerus and complete absence of the musculospiral groove. The distal extremity of the humerus was wide and presented a well-developed lateral epicondyle. The radius and ulna were separated and the ulna was larger and longer. The radial tuberosity was absent and semilunar notch of the ulna was deeper. The proximal row of carpals comprised of only two bones viz., radio-intermediate and ulnar carpal along two sesamoid bones viz., radial and accessory sesamoid bones on the palmar face. The manus presented five long, relatively thin metacarpal bones and five digits. The first digit was shorter with two phalanges whereas the other digits presented three phalanges. In conclusion, the features in the forelimb bones of the D. leporina reflected a wide functional spectrum, which include fast running, digging and shoveling. However, predominant features of the forelimb typified the D. leporina as cursorial rodents. (


Table 1: Major morphological features of the female reproductive tract 
Figure 1: Ventral appearance of the Reproductive Tract of the female agouti in situ (A) and ex situ (B). The ovaries (O), uterine/fallopian tubes (UT), utero-tubal junction (UTJ), uterus (U), cervix (CX), vagina (V) and bladder (GB). Scale bar represents 20 cm.
Figure 3: Macroscopic examination of the Cervix and Uterus of the female agouti showing the Utero-tubal junction (UTJ), Uterus (U), Septum (S), Cervix at pelvic inlet (CX) and Fornix Vagina (FV). Scale bar represents 2 cm.  
Figure 5: Cross-section of the Cervix of a non-pregnant female agouti with thick walls (CXW), numerous folds (F) lined with simple columnar epithelium (CE). Scale bar represents 20 µm.  
Figure 2: Cross-section of the ovary of a nonpregnant female agouti with the Primary follicles in the cortex (PF) and the tunica albuginea (TA). Scale bar represents 25 µm  
Gross and microscopic anatomy of the reproductive tract of the female agouti (Dasyprocta leporina): A neotropical rodent with potential for food production

January 2014

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25,834 Reads

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20 Citations

Tropical Agriculture

This study investigated the gross and microscopic anatomy of the reproductive tract of five cage reared female agouti (Dasyprocta leporina). The ovaries were paired yellow ovoid bodies with a mean (± SD) length of 10 mm (± 2.1), held near the caudal pole of the kidneys. The ovarian cortex consisted of cellular connective tissue in which ovarian follicles were embedded. Highly vascularized tissue was noted in the ovarian medulla. The fallopian tubes increased in width caudally from the ovary to the uterus. Paired uterine horns converged to form the Y-shaped uterine body and the characteristic duplex uterus was separated by a septum. The cervix was found at the pelvic inlet and protruded into the proximal vaginal lumen as the fornix. The vagina had a mean (± SD) length of 7 cm (± 11.4), representing the longest portion of the reproductive tract. Differences in vaginal epithelium were evident, indicating that vaginal colpocytology may be used to evaluate the reproductive stage of the female agouti in captivity. The distance between the urethral aperture and the anus may be used to determine the sex of cage reared agouti, especially when the perineum seals the vaginal orifice. Keywords: Anatomy; Dasyprocta; Female Agouti; Histology; Reproduction


Figure 1: Ventral appearance of the Reproductive Tract of the female agouti in situ (A) and ex situ (B). The ovaries (O), uterine/fallopian tubes (UT), utero-tubal junction (UTJ), uterus (U), cervix (CX), vagina (V) and bladder (GB). Scale bar represents 20 cm.
Figure 2: Cross-section of the ovary of a nonpregnant female agouti with the Primary follicles in the cortex (PF) and the tunica albuginea (TA). Scale bar represents 25 µm
Figure 3: Macroscopic examination of the Cervix and Uterus of the female agouti showing the Utero-tubal junction (UTJ), Uterus (U), Septum (S), Cervix at pelvic inlet (CX) and Fornix Vagina (FV). Scale bar represents 2 cm.
Figure 5: Cross-section of the Cervix of a non-pregnant female agouti with thick walls (CXW), numerous folds (F) lined with simple columnar epithelium (CE). Scale bar represents 20 µm.
Major morphological features of the female reproductive tract
Gross and microscopic anatomy of the reproductive tract of the female agouti (Dasyprocta leporina): A neotropical rodent with potential for food production

January 2014

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270 Reads

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7 Citations

This study investigated the gross and microscopic anatomy of the reproductive tract of five cage reared female agouti (Dasyprocta leporina). The ovaries were paired yellow ovoid bodies with a mean (± SD) length of 10 mm (± 2.1), held near the caudal pole of the kidneys. The ovarian cortex consisted of cellular connective tissue in which ovarian follicles were embedded. Highly vascularized tissue was noted in the ovarian medulla. The fallopian tubes increased in width caudally from the ovary to the uterus. Paired uterine horns converged to form the Y-shaped uterine body and the characteristic duplex uterus was separated by a septum. The cervix was found at the pelvic inlet and protruded into the proximal vaginal lumen as the fornix. The vagina had a mean (± SD) length of 7 cm (± 11.4), representing the longest portion of the reproductive tract. Differences in vaginal epithelium were evident, indicating that vaginal colpocytology may be used to evaluate the reproductive stage of the female agouti in captivity. The distance between the urethral aperture and the anus may be used to determine the sex of cage reared agouti, especially when the perineum seals the vaginal orifice.


Fig. 1. Transverse section of the brainstem of N.leporinus showing (a) most caudal part (b) middle third and (c) rostral third of the MGB. (d) Dense staining multipolar cells (arrows) measuring 10 to 12 μm in diameter on the MGBm at the caudal MGB. (e) Light, round cells (arrows) measuring between 10 to 15 μm in diameter in the MGBv at the caudal MGB. (f) Spindle-like multipolar cells (arrows) measuring 25 μm in diameter in the MGBd of the caudal MGB. DS – Superficial part of the MGBd D- MGBd, DD – Deep part of the MGBd, V – MGBv, M – MGBm, HPC – Hippocampus, CC – Crus cerebri, SN – Substantia nigra, MZ – Marginal zone, DM – Medial portion of MGBd, VM – Medial portion of the MGBv, VL – Lateral portion of the MGBv. 
Fig. 3. Different types of cells in different regions of the MGB of the P. hastatus bat. (a) Large, light-staining round cells with a diameter of 15 μm (arrows) in the MGBd (b) Dark-staining elongated cells with a diameter of 13 μm (arrows) in MGBv (c) Dense, round light-staining cells with a diameter of 15 μm (arrows) in the MGBm. 
Cytoarchitecture of the Medial Geniculate Body of Three Species of Bats: Noctilio leporinus, Phyllostomus hastatus and Carollia perspicillata

October 2013

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142 Reads

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2 Citations

Annual Research & Review in Biology

The aim of the present study is to document cytoarchitectural details of Medial Geniculate Body (MGB) of the brain in three species of echolocating bats with different forage behavior. The brains were collected from six male adult bats of each species: Noctilio leporinus (fish-eating), Phyllostomus hastatus (carnivorous/ omnivorous) and Carollia perspicillata (fruit-eating) and were double-embedded and transverse serial sections were cut and stained with cresyl fast violet. The results showed that the mean length of the medial geniculate body was 1330 ± 115 µm in N. leporinus, 1210 ± 90 µm in P.hastatus and 790 ± 68 µm in C. perspicillata. The MGB of all three bats appeared to be divided into three divisions: dorsal (MGBd), ventral (MGBv) and medial (MGBm). These divisions were most distinct in the N. leporinus bat and least apparent in the C. perspicillata. In the N. leporinus, both dense-staining multipolar cells and light-staining round cells were located throughout the MGB. In the P. hastatus, the dense-staining multipolar cells were predominantly present in the ventral division of the middle third of the MGB, whereas light- staining round cells predominated at the rostral end of the MGB. Only light-staining round cells were seen throughout the MGB of the C. perspicillata. The large sized MGB and its clear subdivisions in N. leporinus suggests that it relies heavily on echolocation whereas P.hastatus and C. perspicillata use echolocation as well but also rely on hearing, smell and vision


Citations (34)


... Ovaries of the current guinea pigs were paired similar to other smallsized mammalian species such as female agouti (Dasyprocta leporina) which were related to guinea pigs (Singh et al., 2014). Differently, ovaries in the hamster found ovoid in shape and completely enclosed in a bursa (Chanut and Williams, 2016). ...

Reference:

Histomorphological and Histochemical Study of the Ovary and the Uterine Tubes of the Adult Guinea Pigs (Cavica porcellus)
Gross and microscopic anatomy of the reproductive tract of the female agouti (Dasyprocta leporina): A neotropical rodent with potential for food production

... In humans, horses, and rats, they are sac-shaped, while in pigs and bulls, they are compact and multilobulated (Badia and al., 2006). Some rodents exhibit a branched tubular structure (Mollineau and al., 2009). In Saharan gerbils, the seminal vesicles are paired and tortuous, as observed in all rodents. ...

The Gross and Micro Anatomy of the Accessory Sex Glands of the Male Agouti (Dasyprocta leporina)

... Measurements provided as a reference are based on individual reports and not as a relevant statistical mean of the species. References (Aparicio and Plana, 2021;Borges, 2004;Cury and Ambrósio, 2016;Leon-Alvarado and Ramírez-Chaves, 2017;Mollineau et al., 2006;Moreira et al., 2013;Rosenfield, 2020 Species that are rarely encountered in human-controlled environments are prone to retaining higher levels of inbreeding, resulting in increased rates of infertility and disease (Frankham, 2005). The initial step in advancing such biotechnologies is to gain an understanding of the basic anatomy and physiology of the reproductive tract (Comizzoli et al., 2000). ...

The Gross Anatomy of the Male Reproductive System of a Neotropical Rodent: the Agouti (Dasyprota leporina)

... These technologies, however, advocate the use of germplasm from animals that have died, while electroejaculation makes it possible to obtain semen samples from possible breeding animals kept in captivity [6], or even from animals captured in their natural habitats [7]. Despite this, the implementation of electroejaculation for D. leporina agoutis has been slow and is limited to studies that compared different devices associated with different electrical stimuli [8], using an anesthetic protocol based on the xylazine-ketamine combination previously stipulated for the species [9]. ...

IMPROVING THE EFFICIENCY OF THE PRELIMINARY ELECTROEJACULATION TECHNIQUE DEVELOPED FOR SEMEN COLLECTION FROM THE AGOUTI (DASYPROCTA LEPORINA)

... At each increase, the on and off sequence was repeated. At this point, the entire sequence was repeated until the animal ejaculated or 10 min had elapsed (Mollineau et al., 2008(Mollineau et al., , 2010. The various stages of erection were photographed with a Ni-kon D300s camera (Nikon Inc., Melville, NY, USA) with Micro Nikkor 105 mm lens. ...

A preliminary technique for electro-ejaculation of agouti (Dasyprocta leporina)

... This is the case of the common opossum, Didelphis marsupialis (Didelphidae), a neotropical marsupial of medium body size up to 3450 g of body weight and 109 cm of total body length ). This Opossum has an omnivorous diet, including small animals, fruits, insects, which may vary with the habitat and the season of the year (Tardieu et al. 2019;Cordero-Rodríguez 2000). ...

Anatomy and histology of the gastrointestinal tract of the neo‐tropical opossum (Didelphis marsupialis insularis, Allen 1902)

... These nuclei are surrounded by the medial nucleus of the trapezoid body (MNTB), and several periolivary cell groups (Heffner & Masterton, 1990;Moore & Moore, 1971;Schwartz, 1992;Stotler, 1953;Strominger & Hurwitz, 1976). LSO and MSO are present in most mammals, however they vary in morphology and most prominently in size, depending on the hearing ability of the species (Gibbons et al., 2019;Irving & Harrison, 1967;Schwartz, 1992). ...

Cytoarchitecture of the superior olivary complex of three neotropical species of bats (Noctilio leporinus, Phyllostomus hastatus and Carollia perspicillata) with different foraging behavior

Brazilian Journal of Biology

... The lappe was decribed as a frugivore, the manicou as an omnivore, the collared peccary as a pseudo-ruminant herbivore, and the red brocket deer was grouped with ruminants [12][13][14][15][16][17][18][19]. The manicou has a gestation period of three weeks [17,18]. ...

Didelphis species, Neo-tropical animals with the potential for intensive production: Part 2: Review of reproductive systems
  • Citing Article
  • July 2017

Tropical Agriculture

... Considering the greater anatomical diversity of the mammals and in particular the caviomorph rodents, it would be inappropriate to extrapolate the information from other caviomorph rodents to the D. leporina. The literature on the skeletal system of the D. leporina exists with the appendicular system (Sundaram et al., 2015(Sundaram et al., , 2017 but features of vertebrae, ribs and sternum remain unstudied. Since the axial musculoskeletal system represents the plesiomorphic propulsive engine of the vertebrate body and maintains a central role in locomotion in all craniates (Schilling, 2011), the study of the axial skeletal system is important to understand the locomotor behaviour of these fast runners. ...

Hind Limb Skeleton of the Orange Rumped Agouti (Dasyprocta leporina Linnaeus, 1758): Structural and Functional Perspective

Annual Research & Review in Biology

... Anatomical characterization of the capybara scapula demonstrates a spine that ends at the acromion and features a sizeable hamate process that projects caudodistally. This same anatomical structure has been described in rodents such as the mole rat (Spalax leucodon Nordmann) (Özkan 2004), the paca (Agouti paca) (Oliveira et al. 2018), the agouti (Dasyprocta azarae) (Sundaram et al. 2015), the African giant rat (Cricetomys gambianus waterhouse) (Olude et al. 2009) and the Gambian rat (C. gambianus) (Olawoye et al. 2011). ...

Morphological Studies of the Forelimb Skeleton of the Orange Rumped Agouti (Dasyprocta leporina Linnaeus, 1758)

Annual Research & Review in Biology