Ankle Arthrodesis using Retrograde Nail in Case of Bosworth Fracture with Ankle Dislocation : A Rare Case Report.

Introduction: The Bosworth fracture is a distal fibula oblique fracture with proximal fibula posterior dislocation behind the posterior tibia tubercle. Extreme external rotation of the supinated foot causes it. These types of fractures and their treatment are infrequently described in the literatures. Case Report: A 72 -year-old female pillion rider on a two-wheeler had a Road traffic accident. The patient arrived at the emergency room with a Bosworth fracture along with an open ankle dislocation (Gustilo-Anderson Type 2B). She underwent a staged procedure in form of an external fixator and later on definitive fixation in the form of ankle fusion with retrograde nailing. Since there is very little information regarding treatment modality for an open Bosworth fracture with an ankle dislocation, this case report is very rare. Fracture united well within 8 weeks. Conclusion: These fractures in elderly patients with comorbidities if poorly managed can lead to severe consequences like an amputation. Awareness of these fractures patterns and their treatment can play a potential role in limb salvage.

Density-dependent growth and metamorphosis in the larval bronze frog Rana temporalis is influenced by genetic relatedness of the cohort.

Effects of density and kinship on growth and metamorphosis in tadpoles of Rana temporalis were studied in a 2 4 factorial experiment. Fifteen egg masses were collected from streams in the Western Ghat region of south India. The tadpoles were raised as siblings or in groups of non-siblings at increasing density levels, viz. 15, 30, 60 and 120/5 l water. With an increase in density level from 15 to 120 tadpoles/5 l water, duration of the larval stage increased and fewer individuals metamorphosed irrespective of whether they belonged to sibling or non-sibling groups by day 100 when the experiments were terminated. The size of individuals at metamorphosis declined significantly with increase in the density of rearing. However, at higher densities (60 and 120 tadpoles/5 l water) sibling group tadpoles performed better compared to mixed groups and took significantly less time to metamorphose. Also, more individuals of sibling groups metamorphosed compared to non-sibling groups at a given density. Mixed rearing retarded growth rates, prolonged larval duration resulting in a wider spectrum of size classes, and lowered the number of individuals recruited to terrestrial life. The study shows that interference competition occurred more strongly in cohorts of mixed relatedness than in sibling groups.

Members of opposite sex mutually regulate gonadal recrudescence in the lizard Calotes versicolor Agamidae).

Adult males and females of the seasonally breeding lizard Calotes versicolor were subjected to various social situations under semi-natural conditions to explain the role of socio-sexual factors in gonadal recrudescence. They were grouped as: (i) males and females, (ii) males and females separated by a wire mesh, (iii) same sex groups of males or females, (iv) castrated males with intact females and (v) ovariectomized (OvX) females with intact males from postbreeding to breeding phase. Specimens collected from the wild during breeding season served as the control group. Plasma sex steroid levels (testosterone in male and 17b-estradiol in female), spermatogenetic activity and vitellogenesis were the criteria to judge gonadal recrudescence. In intact males and females that were kept together, gonadal recrudescence and plasma sex steroids levels were comparable to those in wild-caught individuals. Gonadal recrudescence was at its least in all male and all female groups, and plasma sex steroids were at basal levels. Association with OvX females initiated testicular recrudescence but spermatogenetic activity progressed only up to the spermatid stage while males separated from females by wire mesh showed spermatogenetic activity for a shorter period. Females grouped with castrated males and those separated from males by wire mesh produced vitellogenic follicles. However, the total number and diameter of vitellogenic follicles, and plasma estradiol levels were lower than in the females grouped with intact males. The findings indicate that association with members of the opposite sex with progressively rising titers of sex steroids is crucial in both initiating and sustaining gonadal recrudescence in the lizard. Thus, members of the opposite sex mutually regulate gonadal recrudescence in the C. versicolor.

Pattern of plasma sex steroid hormone levels during reproductive cycles of male and female tropical lizard, Calotes versicolor.

Annual changes in gonadal activity and plasma sex steroid hormone levels in male and female Calotes versicolor [plasma testosterone (T) levels in males and 17 beta-estradiol (E(2)) and progesterone (P) levels in females] are described. In females both plasma E(2) (32.80 +/- 12.91 pg/ml) and P (1.72 +/- 0.79 ng/ml) levels are at their low levels during the postbreeding season when the gonads are regressed. With the onset of recruitment of vitellogenic follicles, E(2) levels begin to rise, reaching peak values (1306.00 +/- 407.01 pg/ml) when the follicles are preovulatory. During this time, plasma levels of P are low. Plasma E(2) levels decline (285.60 +/- 143.0 pg/ml) soon after ovulation, and circulating concentrations of P begin to rise, reaching peak value (19.24 +/- 10.03 ng/ml), during eggshell formation. In gravid females, at mid-gestation, the same pattern of E(2) secretion is found when a second set of follicles undergoes vitellogenesis. However, P levels remain low from mid-gestation (4.06 +/- 2.17 ng/ml) until oviposition. These findings suggest that high P levels are not needed for oviductal egg retention during late gestation and that low levels of P may facilitate growth of a new batch of vitellogenic follicles. In males, plasma levels of T are correlated with the spermatogenetic activity that accompanies breeding.

Effect of sex steroids on gonadal differentiation and sex reversal in the frog, Rana curtipes.

The bicolored frog, Rana curtipes, is endemic to Western Ghats of Southern India, having a prolonged larval life. In this species, gonadal differentiation is of the semidifferentiated type. The gonads initially differentiate into ovaries in all the individuals at Gosner stage 25. Later, in genetic males, the oocytes degenerate and testicular differentiation occurs at stages 30-31. Exposure of R. curtipes tadpoles to 50 microg/L of testosterone (T) or estradiol-17beta (E(2)) during stages 24-26 or 29-32 did not affect gonadal sex differentiation and proportion of males and females at metamorphosis. In all the groups, the sex ratio was almost 1:1 as in the controls. Likewise, exposure of tadpoles to low concentration of steroids (12.5 microg/L T or E(2)) throughout larval development was ineffective in altering the sex ratio or the gonadal sex differentiation. On the other hand, exposure to higher concentrations of steroids (25 and 50 microg/L) throughout the larval development (stages 25-45) significantly skewed the sex ratio toward the male or female direction, depending upon the sex steroid used. Thus, exposure to T or E(2) throughout the larval period could produce 93% males or 79% females, respectively, indicating the ability of these steroids to cause sex reversal. This study shows a possible absence of a "critical stage" that is sensitive to sex steroids for gonadal sex reversal in this frog.

Plasma progesterone levels and luteal activity during gestation and prolonged oviductal egg retention in a tropical lizard, Calotes versicolor.

Plasma progesterone (P) levels and luteal and adrenal activities were studied during normal gestation and unusual prolonged period of oviductal egg retention in a polyautochronic, multiclutched lizard, Calotes versicolor. The normal gestation period (approximately 15 days) was categorized into four stages: stage I--a few hours following ovulation, stage II--eggs with shell and embryo at primitive streak, stage III--embryonic stages 16-20, and stage IV--prior to ovipostion (stages 26-27). The gravid lizards maintained in captivity retained eggs in their oviducts for 45 days. Plasma P levels were low in stage I, increased significantly during stage II, declined in stage III, and reached their lowest in stage IV of gestation. 3Beta-hydroxysteroid dehydrogenase (3beta-HSDH) activity was greater in lutein cells at stage II and was present in traces in stage IV gestation. Interestingly, plasma P titers that were high in lizards with eggs retained longer though the corpora lutea (CL) showed a trace 3beta-HSDH activity. However, 3beta-HSDH activity was greater in the adrenocortical cells in these lizards than that in lizards during a normal gestation period. The present study on C. versicolor shows that the CL remains active and secretes P only during the early part of the gestation. The drop in P level during the later part of gestation might facilitate growth of a second set of vitellogenic follicles. During unfavorable conditions when the lizards are forced to retain eggs in the oviduct, the adrenal glands seem to secrete progesterone to help in egg retention and in inhibition of oviposition.

Pattern of gonadal sex differentiation, development, and onset of steroidogenesis in the frog, Rana curtipes.

Histomorphological changes and steroidogenic potential of the gonads during sexual differentiation and development were studied in Rana curtipes from tadpole stage 25 (Gosner) until maturity. In stage 25 tadpoles of smaller snout-vent length (SVL; 4-5 mm) the gonads were indifferent, containing a few somatic and germ cells, whereas in larger tadpoles (SVL > 7 mm) gonads were differentiated into ovaries with a central lumen. Onset of meiosis was seen in these ovaries. At stage 26, diplotene and first growth phase oocytes were found. With advancement in developmental stage and after metamorphosis the ovaries progressively enlarged due to increase in number and size of oocytes. Vitellogenesis began in the ovary of 4-month-old frogs. Females attained maturity 6 months after metamorphosis. The frogs showed amplexus and one frog spawned. Onset of testicular formation seen at stage 31 was associated with the degeneration of oocytes and infiltration of darkly stained somatic cells in the central region. By stage 35 all oocytes degenerated, leaving behind a large number of somatic and germ cells interspersed with each other. At stage 38, formation of seminiferous tubules enclosing spermatogonia and pre-Sertoli cells was seen. Initiation of meiosis was evident at metamorphic climax. Cysts of elongated spermatids associated with Sertoli cells were seen in 45-day-old frogs. Histochemically, delta(5)-3 beta-hydroxysteroid dehydrogenase activity was localized in the ooplasm, follicular cells, and interstitium of the ovary from stage 28 onward. The enzyme activity in the testis appeared in 45-day-old froglets. In R. curtipes gonadal differentiation is a semidifferentiated type since gonads initially differentiate into ovaries, and later, in the prospective males, the ovaries degenerate and transform into testes. The males attain maturity much earlier than the females. In R. curtipes gonadal sex differentiation precedes the onset of gonadal steroidogenesis.

The ontogeny of kin recognition in tadpoles of the toad Bufo melanostictus (Anura; bufonidae).

The ontogeny of kin recognition and influence of social environment on the development of kin recognition behaviour was experimentally investigated in tadpoles of Bufo melanostictus that lived in aggregations and showed low larval dispersion. Embryos and tadpoles of the toad were reared as (i) kin only, (ii) with kin and non-kin (separated by a mesh screen), and (iii) in isolation. They were tested for the ability to discriminate between (i) familiar siblings and unfamiliar non-siblings, (ii) familiar siblings and familiar non-siblings and, (iii) unfamiliar siblings and unfamiliar non-siblings. All tadpoles were fed on boiled spinach before conducting trials. Preference of test tadpoles to associate near the end compartments whether empty or containing members of specific stimulus groups was assessed using a rectangular choice tank. When tested in tanks with empty end compartments, the test tadpoles showed random distribution and thus no bias for the apparatus or the procedure. In the presence of kin/non-kin in the end compartments a significantly greater number of test tadpoles spent the majority of the time near familiar or unfamiliar kin rather than near familiar or unfamiliar non-kin. Kin discrimination ability persisted throughout larval development. Familiarity with siblings is not required for discriminating kin from non-kin, and kin discrimination ability is not modified following exposure to non-kin. Also, involvement of dietary cues is unlikely to be the prime mechanism of kin recognition in B. melanostictus unlike in some other anurans.

GnRH but not warm temperature induces recrudescence of quiescent testes in the tropical lizard Calotes versicolor (Daud.) during postbreeding phase.

The effects of temperature and various doses of GnRH on testicular recrudescence were studied in Calotes versicolor during the postbreeding (December-January) resting phase. Adult lizards (n = 51) were segregated into seven groups. Group I served as the initial control. Groups II, III, and IV were maintained at room temperature (23 +/- 1 degrees, range 17.5-25.5 degrees ) and natural photoperiod (12.25 h light:11.35 h dark). Groups V, VI, and VII were maintained at 30 +/- 1 degrees in an environmental chamber with 12 h light:12 h dark. Groups II and V received 0.2 ml saline, groups III and VI received 0.1 microgram GnRH/0.2 ml saline, and groups IV and VII received 0.5 microgram GnRH/0.2 ml saline on alternate days for 30 days. In the two groups that received 0.5 microgram GnRH, there was a significant increase in the diameter of the seminiferous tubules and Leydig cell nuclei, 3beta-HSDH activity in Leydig cells, and plasma testosterone level compared to those in other groups. There was no evidence of testicular recrudescence in lizards exposed to room/high temperatures treated with saline or 0.1 microgram GnRH. This study of C. versicolor shows that during the resting phase, high temperature per se does not stimulate testicular recrudescence, whereas 0.5 microgram GnRH does so. Also, the findings suggest that either higher brain centers regulating hypothalamus or hypothalamus itself become dormant, causing testicular inactivity (inactivation of hypophysial-testicular axis) during the postbreeding resting phase.

Interrelationship between food availability, fat body, and ovarian cycles in the frog, Rana tigrina, with a discussion on the role of fat body in anuran reproduction.

Long-term experiments were conducted to study the progression of vitellogenic cycles in Rana tigrina (an annual breeder) having different foraging backgrounds and held under conditions of weekly or daily food supply and in presence or absence of abdominal fat bodies. They were autopsied in June to assess fecundity. In nature an adult R. tigrina produces on an average 4,000 eggs/100 g body mass (b.m.) And spawns in June-July following monsoon rains. Weekly feeding from July to next breeding season, June resulted in a significant decrease in both fecundity (1700 eggs/100 g body b.m.) And mean size of eggs, compared to well-fed or wild-caught frogs. The abdominal fat bodies were barely seen in frogs fed weekly throughout, whereas in frogs fed weekly from July-December but daily from January onwards, the fat bodies became noticeable (1% of b.m.) And number and mean size of eggs increased significantly over those fed weekly throughout. Frogs captured in January possessed enlarged fat bodies (5% of b.m.), depicting a good foraging history. Maintenance of these frogs on a weekly feeding regimen led to an exhaustion of fat stores. They produced less number of eggs (2, 000/100 g b.m.) As compared to wild frogs but of normal size, whereas daily feeding slowed down a depletion of fat body mass and also significantly increased fecundity (3,000/100 g b.m.) Over the weekly fed individuals. Sham operation or fat body ablation in October or February had no significant effect on total fecundity per se (3,000-3,500 eggs/100 g b.m.) Compared to that of wild-caught frogs. However, eggs were significantly smaller due to fat body ablation despite daily feeding. The study shows that food abundance/fat bodies influence egg size and number in R. tigrina and that a direct or indirect functional relationship exists between fat body and ovarian cycles that are characteristically inverse to each other. J. Exp. Zool. 286:487-493, 2000.

Distribution of gonadotropin-releasing hormone immunoreactivity in the brain of Ichthyophis beddomei (Amphibia: Gymnophiona).

From a comparative viewpoint, we have investigated the presence and neuroanatomical distribution of gonadotropin-releasing hormone (GnRH)-immunoreactive material in the brain of a gymnophione amphibian, Ichthyophis beddomei. Immunocytochemical analysis of the adult brain and terminal nerves in both sexes shows the presence of neurons and fibers containing mammalian GnRH (mGnRH)- and chicken GnRH-II (cGnRH-II)-like peptides. With respect to GnRH-immunoreactive material, there are two distinct neuronal systems in the brain: one containing mGnRH, which is located in the forebrain and terminal nerve, and the other containing cGnRH-II, which is restricted to the midbrain tegmentum. Basically, this distribution pattern parallels that of many species of anurans and a urodele. Whereas the presence of cGnRH-II-immunoreactive fibers in the dorsal pallium of L. beddomei is a feature in common with a urodele amphibian, the total absence of cGnRH-II-like material in the median eminence is unique to this species. It is suggested here that the distribution profile of GnRH-like material within the brain and terminal nerve of I. beddomei represents a primitive pattern.

Kinetics of spermatogenesis in the Indian desert gerbil, Meriones hurrianae (Jerdon): seminiferous epithelial cycle, frequency of stages, spermatogonial renewal and germ cell degeneration.

The present study provides information on the germ cell associations, the pattern of spermatogonial cell renewal, percentage frequency distribution of different cellular associations and germ cell degeneration in the adult gerbil, M. hurrianae. Based on the formation of acrosomal system and the development of the spermatids as visualized with PAS-hematoxylin, 15 steps of spermiogenesis were identified. The first 12 steps were associated with 12 stages, and the other three steps were between the first 6 stages. The relative frequency was maximal for stage VII (14.24) and minimal for stage VIII (4.38), indicating stage VII to be of the longest and stage VIII of the shortest duration. On the basis of their shape, size and nuclear morphology, 6 types (A0, A1, A2, A3 In and B) of spermatogonia were identified in the gerbil. A-type spermatogonia are oval in shape. From A1 and A3 spermatogonia, progressive heterochromatinization was evident. The A3-spermatogonia divide to give rise to In spermatogonia which are smaller than A-type cells. The B-type spermatogonia are derived from In-type cells and are round in shape. These divide to give rise to first generation primary spermatocytes. Spermatogonia divide at fixed stages during the CSE, and they exhibit 5 peaks of mitosis. A-type spermatogonia divide during stages VI, IX, XII and I. In- and B-Types divide during stages II and V respectively. During stages XII and I, A3-type cells divide to give rise to In- as well as to A1-type cells, thus restoring the A-spermatogonial population. In this way A3-cells serve to renew the stem cells.(ABSTRACT TRUNCATED AT 250 WORDS)

Effect of synthetic nonapeptide (Thr-Cys-Ser-Val-Ser-Glu-Trp-Gly-Ile) on ovarian follicular development in the bull frog Rana tigrina (Daud).

Effect of synthetic nonapeptide (Thr-Cys-Ser-Val-Ser-Glu-Trp-Gly-Ile) representing the amino acid sequence 86-94 of human seminal plasma was studied on the ovarian follicular growth in the bullfrog R. tigrina during preparatory phase of reproductive cycle. Daily (except on Sundays) injections of 10 micrograms nonapeptide for one month caused a significant increase in ovarian weight and number of second growth phase (SGP) or vitellogenic oocytes. The results suggest that the nonapeptide is biologically active in amphibians also.

Effect of thyroxine, prolactin and adrenalin on the gravid ovaries of the frog Rana cyanophlyctis (Schn.).

The effects of thyroxine, prolactin and adrenalin on the gravid ovaries of R. cyanophlyctis were studied during late prebreeding period when vitellogenic growth of oocytes is complete or near completion. Specified doses of hormones were injected (ip) six days a week for one month. They were fed guppies ad libitum daily 6 days a week. Administration of 2 or 5 micrograms eltroxine (synthetic thyroxine) had no effect on ovaries or oviducts. Whereas, higher doses 8, 12 and 16 micrograms thyroxine caused significant (P < 0.05) decrease in the per cent weight of ovaries and oviducts. The mean diameter of the largest oocyte was also reduced significantly compared to the controls. There was an increase in the atresia of vitellogenic oocytes. Treatment with 100 micrograms prolactin also caused reduction in the per cent weight of ovaries and oviducts. However, mean diameter of the largest oocyte did not change significantly. Follicular atresia increased only moderately. Injection of 180 micrograms adrenalin bitartrate caused drastic decrease (P < 0.05) in the per cent weight of ovaries and oviducts and mean diameter of the largest oocyte. Many yolky follicles became atretic. The findings suggest that increase in the levels of thyroxine (beyond a certain limit), prolactin and adrenalin around the breeding period decrease the fecundity of the frog by inducing atresia of yolky oocytes. We conclude that the above hormones in excess quantities act as negative modifiers of ovarian activity in R. cyanophlyctis.

Effect of (d-Ala6) LHRH on hypophyseal gonadotrophs and ovary of adult frog, Rana tigrina (Daud.) during post-breeding regression phase.

Effects of synthetic luteinizing hormone-releasing hormone (LHRH, 1.5 micrograms) agonist on pituitary and ovary were studied in R. tigrina during November, the post-breeding regression phase. Injections (ip) were given 6 days a week for 30 days and frogs were sacrificed on day 31. Pituitary sections were stained with AB-PAS-OG. The staining intensity, cytoplasmic granulation and cell, nuclear and cytoplasmic areas of hypophyseal gonadotrophs (B2 cells) increased (P < 0.05) following LHRH administration. In controls, the B2 cells were small and faintly stained. LHRH treatment significantly increased ovarian weight over controls due to recruitment of medium sized second growth phase oocytes (MSGP) from the first growth phase (FGP) oocytes. Nearly 50% of oocytes from the FGP oocyte pool were recruited to SGP. Control frog ovaries lacked SGP oocytes. The results demonstrate that both ovary and pituitary of R. tigrina remain responsive to gonadotrophic and GnRH stimulation respectively during the post breeding regression phase.

Morphometric study of ovarian follicular growth during the estrous cycle of the laboratory-maintained Indian desert gerbil, Meriones hurrianae (Jerdon).

The pattern of changes in the population of healthy and regressing follicles in relation to the estrous cycle, was studied in the recently domesticated desert gerbil, Meriones hurrianae, which exhibits a longer cycle (proestrus: 1.5 days; estrus: 1 day; metestrus: 1.5 days; diestrus: 3 days). As the granulosa cell layers were not distinct, the follicles were classified on the basis of their morphology and size (group I: small preantral follicles; group II: large preantral follicles; group III: small antral follicles; group IV: medium-sized antral follicles; group V: large-sized follicles; group VI: Graafian follicles). Regressing follicles were classified likewise. Five animals were used for each stage of the cycle. One ovary from each gerbil was serially cut and stained with hematoxylin-eosin. Healthy and regressing follicles were found throughout the cycle. The follicular development occurred typically in a biphasic manner. In phase A, in which follicles reach the antral stage, the growth of oocytes and follicles is linearly correlated, whereas, in phase B, oocyte size remains stationary while follicle size increases due to accumulation of antral fluid. However, oocyte growth and nucleus growth are positively and linearly correlated (r = 0.74). The healthy follicles under 260 microns (groups I, II) do not fluctuate in the ovary of cyclic gerbils, whereas follicles in group III (261-350 microns) increase significantly (p < 0.05) at estrus and those of group IV in diestrus. Further, healthy group III follicles are reduced in diestrus while regressing follicles in group III increase. These findings thus suggest that the antral follicles are rescued from atresia at estrus.(ABSTRACT TRUNCATED AT 250 WORDS)

A study of ovarian follicular kinetics, oviduct, fat body, and liver mass cycles in laboratory-maintained Rana cyanophlyctis in comparison with wild-caught frogs.

Ovarian follicular dynamics and fluctuations in fat body, oviducal, and liver masses were studied in captive Rana cyanophlyctis in comparison with wild-caught frogs, sampled at monthly intervals over a period of 12 months. In both the captive and wild-caught frogs first growth phase (FGP) and second growth phase (SGP) or vitellogenic oocytes were produced throughout the period examined; however, changes in ovarian and oviducal weights were less marked in the former group. In the captive frogs SGP oocyte production was reduced by 50%, and, maximum ovarian weight and SGP oocyte number were attained 2-3 months earlier than in wild-caught controls. The FGP oocyte pool in laboratory-maintained frogs, however, was comparable with that of the corresponding wild-caught frogs. Captivity caused a threefold increase in atresia and reduced the number of oocytes reaching SGP. The depletion of fat stores in fat bodies during the later phases of captivity suggests that the deposition of lipids into oocytes (for SGP) was given priority over storage in the fat bodies. The low oviducal weights of captive frogs was correlated with a reduced number of SGP oocytes, which are the source of estrogen. On the other hand, liver weight remained high, indicating adequate hepatic vitellogenin synthesis. Possible reduction in its output was not detected, possibly due to the reduced number of follicles reaching SGP. The findings indicate that stress of captivity decreases gonadotrophins and estrogen levels. Oviducal growth is reduced in captive frogs.(ABSTRACT TRUNCATED AT 250 WORDS)

Kinetics of spermatogenesis in megachiropteran bat, Rousettus leschenaulti (Desmarset): seminiferous epithelial cycle, frequency of stages, spermatogonial renewal and germ cell degeneration.

The paper describes in detail the cytomorphology of different types of germ cells, the 10 typical cellular associations or stages of the cycle of seminiferous epithelium (CSE), frequency of appearance of these stages, pattern of spermatogonial stem cell renewal and per cent degeneration of various germ cells in R. leschenaulti. Of the 14 steps of spermiogenesis (stained with PAS-haematoxylin) the first 10 were associated with the stages I-X, whereas, the remaining were found in association with one of the first six stages. The frequency of appearance of the various stages ranged from 3.84% (stage V) to 19.84% (stage I). These observations indicate that stage V is of shortest duration and stage I is of the longest duration in the bat. Five types of spermatogonia (A1, A2, A3, In and B) were identified based on their shape, size and nuclear morphology. Type A spermatogonia are oval with a large nucleus containing 1 or 2 nucleoli. The chromatin showed progressive condensation from A1 to A3 so that the latter appeared darkest among all the A type spermatogonia. The In type derived from A3 are smaller but appear darker than A3 due to heterochromatin crusts along the inner border of the nucleus. The B type spermatogonia derived from In are round and possess single nucleolus. The B type spermatogonia divided mitotically before entering meiosis or the actual production of the primary spermatocytes. The various spermatogonia divided mitotically at fixed stages of the cycle giving rise to their next generations.(ABSTRACT TRUNCATED AT 250 WORDS)

No differences in pineal synaptic ribbon and spherule numbers in different stocks and strains of laboratory rats.

Previous studies have shown that the pineal glands of different stocks and strains of laboratory rats have different melatonin-forming capacities. In the present investigation a widely studied morphological parameter of the pineal, i.e. synaptic ribbon (SR) and synaptic spherule (SS) numbers, was explored in 6 different stocks and strains of laboratory rats, viz.:Han:WIST (albino), LEW/Han (albino), DA/Han (agouti), BN/Han (dark brown), LE/Han (black hooded) and (LEW x BN)/F1 (black with white belly). The rats were maintained under the usual laboratory conditions (lights on from 06.00-18.00 h) for 3 weeks and killed between 10.00-12.00 h, when they were 6 weeks old. The pineals were rapidly excised and processed for transmission electron microscopy. The morphology, distribution (in singles or groups, distant from, or near cell membrane etc.) and number of SR and SS per 20,000 microns2 area of pineal tissue were similar in all groups of rats studied. It is concluded that, in contrast to pineal gland size and melatonin synthesis, SR number is a fairly constant pineal parameter in different stocks and strains of laboratory rats and independent of pigmentation.

Kinetics of spermatogenesis in the wild squirrel Funambulus palmarum (Linnaeus).

The paper describes in detail the morphology and kinetics of germ cell associations, pattern of mitotic divisions, frequency distribution of different cellular associations (stages) and percent degeneration of various germ cells in the squirrel in which spermatogenesis in adults occurs all year round. Eighteen steps of spermiogenesis were identified based on the development of the acrosomal system using PAS-haematoxylin. These were appropriately divided into Golgi, acrosome, cap and maturation phases. Thirteen types of cellular associations or stages (I-XIII) were characterized along the length of the seminiferous tubule which repeated itself in space and time constituting the seminiferous epithelial cycle (CSE). Of the 18 steps of spermiogenesis, the first 13 were associated with stages I-XIII, respectively, and the rest with the first 9 stages. Spermiation occurred in stage IX. Seven types of spermatogonia [A0, A1, A2, A3, A4, intermediate (In) and B type] were identified based on their shape, size and nuclear morphology. A0 spermatogonia are pale in appearance with homogeneously distributed chromatin surrounded by a thin nuclear membrane. These are present in all stages. A1 are oval in shape and possess a thicker nuclear membrane. They are found in stages VI-X. The chromatin material undergoes progressive condensation from A1 to A4 making the last generation of spermatogonia appear darker. The In spermatogonia which are derived from A4 are morphologically similar to them but smaller in size. The B-type spermatogonia derived from the In types possess a typically round nucleus with uniformly condensed chromatin material underneath the nuclear membrane. The spermatogonia divide mitotically at fixed stages of the CSE giving rise to their next generations. Thus, A-type spermatogonia divide at stages X, XIII/I, IV and V, while In divide at stage VI. During each CSE of the squirrel, 5 peaks of mitosis occur. There is a single generation of B-type spermatogonia. These differentiate into primary spermatocytes and undergo meiosis or maturation divisions which enter to form spermatids. The A4 which divide differentially in stage VI give rise to In- and A1-type spermatogonia. Therefore, A4 spermatogonia form renewing stem cells. Based on the above pattern of spermatogonial mitosis a model for stem cell renewal in the squirrel is proposed. The percentage degeneration of germ cells varied with the cell type. During a single CSE of the squirrel, a total of 42.09% germ cells were found to degenerate. An attempt is made to compare and contrast the kinetics of spermatogenesis in the wild squirrel with that of the other rodents studied so far.