The findings reported below span three interrelated dimensions of Barind sheep performance under the smallholder conditions of the Barind tract: body weight trajectories from birth through 12 months of age, flock multiplication and foundation stock survival, and the cumulative burden of disease across the full monitored population. Each section presents quantitative findings followed by a contextual discussion that situates the results within the wider literature on indigenous sheep production in Bangladesh and comparable tropical environments.
3.1 Sex-Specific Growth Performance from Birth to 12 Months
Body weight data for the 90-lamb growth sub-cohort (46 males, 44 females) are presented in Table 1. At birth, mean day-old weight was 1.24 ± 0.12 kg for males and 1.20 ± 0.11 kg for females, giving a combined cohort mean of 1.22 ± 0.11 kg. These values sit comfortably within the range of 1.10–1.35 kg documented for indigenous Bangladeshi sheep breeds under semi-intensive management (Haque & Siddiqui, 2017; Pervage et al., 2009), and the narrow standard deviations at birth — smaller than those observed at any subsequent age point — are consistent with the homogenising effect of uterine environment on neonatal size in a population that has not been subjected to intensive selection for growth (Sarker & Alam, 2020).
Growth proceeded in a curvilinear trajectory, with the most rapid absolute weight gain occurring in the pre-weaning period (Table 1). By three months, males had reached 5.35 ± 0.99 kg and females 5.09 ± 0.75 kg — representing approximately four-fold increases over birth weight for both sexes. The between-sex difference widened marginally during the post-weaning phase, reaching a maximum divergence of 0.62 kg at six months (8.40 vs. 7.78 kg), before narrowing again at nine months (11.62 vs. 11.43 kg, a difference of only 0.19 kg) and settling at 0.53 kg at 12 months (15.84 vs. 15.31 kg). This non-monotonic pattern of sexual dimorphism — widening then contracting — is not unusual in indigenous breeds under variable resource environments; it likely reflects periods of feed scarcity during the dry season (November–March in the Barind tract) during which both sexes experience reduced nutritional planes, temporarily equalising their growth rates regardless of hormonal status (Musa et al., 2020).
The combined 12-month mean of 15.55 ± 3.44 kg represents an approximately 12.7-fold increase over birth weight — a figure consistent with expected allometric growth in this breed type and comparable to the 14.5–16.0 kg reported by Haque and Siddiqui (2017) for indigenous sheep in northern Bangladesh under similarly semi-intensive management. It exceeds the 13.2 kg documented for extensively managed sheep in the coastal zone of Bangladesh (Mia et al., 2015), suggesting that the combination of daily grazing and strategic concentrate supplementation during late pregnancy adopted in this study supported growth performance at the upper achievable range for the Barind ecosystem. The progressive widening of standard deviations with age — from approximately 0.11 kg at birth to 3.03–4.02 kg at 12 months (Table 1) — is, we think, one of the more practically important observations in this dataset. It reflects the cumulative divergence in growth outcomes attributable to variation in farmer management capacity, access to supplementary feed, and the timing and severity of disease events across the 40 participating households.
3.2 Statistical Comparison of Sex-Based Growth Differences
Independent-samples t-tests at each of the six age points consistently yielded non-significant results (all p > 0.05), with effect sizes (Cohen's d) ranging from negligible to small-to-medium (Table 2). The closest approach to statistical significance occurred at six months (t(88) = 1.99, p = 0.050, d = 0.43), which corresponds to the post-weaning period during which anabolic androgen levels in males begin to diverge from those of females and would be expected — in principle — to drive differential protein deposition rates. However, the current sample size (n = 90, split approximately equally between sexes) provided limited statistical power to detect an effect of this magnitude. A retrospective power analysis for the six-month comparison indicated that approximately 87 animals per sex group would be required to achieve 80% power at α = 0.05 for an effect size of d = 0.43 — roughly four times the number available at this age point. Future longitudinal studies with expanded cohorts should revisit this question, ideally with a pre-specified sample size calculation.
The non-significant sex effect through 12 months is broadly consistent with reported findings for other South Asian indigenous breeds under comparable production environments. Rahman et al. (2016) and Haque and Siddiqui (2017) both reported statistically equivalent pre-weaning growth rates in male and female indigenous sheep in Bangladesh, and Dar et al. (2013), working with exotic and crossbred sheep in Kashmir, found that significant sexual dimorphism in growth typically emerges only in breeds subjected to intensive selection for muscle growth — a selection pressure that indigenous Barind sheep have not experienced. The practical implication for smallholder farmers is perhaps more useful than the statistical result itself: resource-constrained households that preferentially feed male lambs in the expectation of faster growth are unlikely to see a meaningful return on that investment during the first 12 months of life under current management conditions.
3.3 Flock Multiplication and Foundation Stock Survival
The multiplication status of the 200 foundation animals across the 12-month monitoring period is summarized in Table 3. By study close, 228 lambs had been born to the 160 foundation ewes, representing a crude lambing rate of approximately 143% per ewe (228 ÷ 160), or 114% relative to the full foundation cohort of 200. This range is consistent with the 90–120% flock-level multiplication rates documented by Mowsume et al. (2023) for comparable smallholder systems in Bangladesh, and implies that the majority of foundation ewes produced at least one lamb during the 12-month period, with a proportion producing twins. The 1.43 lambs per ewe figure broadly aligns with the kidding rates reported by Pervage et al. (2009) for Barind sheep, though direct comparisons are complicated by variation in management conditions and the length of the observation window.
Of the 200 foundation animals, 62 died during the study period, yielding a foundation stock mortality rate of 31.0% (Table 3). This figure is considerably higher than the 14.5–18.7% mortality range documented in organized farm settings in South Asia (Dar et al., 2013; Musa et al., 2020), and — in our view — represents the most concerning finding of this study. It is worth noting that the 31.0% mortality reflects the denominator of 200 foundation stock animals specifically, and should not be conflated with the 14.49% cumulative disease incidence figure reported for the full 428-animal monitored population (which includes the 228 births). These are two distinct epidemiological measures, and the manuscript maintains this distinction throughout. The elevated foundation stock mortality likely reflects a combination of factors: the stress of procurement and translocation to diverse new household environments, varying levels of farmer management competence across the 40 participating households, and the absence, in the project's current health protocol, of pre-distribution quarantine or post-distribution intensive monitoring during the critical first 30–60 days. Kabir et al. (2019) documented similar mortality spikes in the initial post-distribution period in sheep development projects in Bangladesh, attributing them largely to translocation stress and concurrent infectious challenge.
The net flock expansion from 200 to 366 animals — an increase of 83% over 12 months — demonstrates that, despite the substantial foundation stock mortality, indigenous Barind sheep maintain a positive reproductive trajectory under smallholder conditions. Non-mortality attrition pathways — including sales, religious sacrifices (Kurbani/Akika), revolving fund transfers to new beneficiary farmers, and theft — are not disaggregated in Table 3 because the primary SPSS disposal codes (STATUS variable) recorded these under shared categories not uniformly applied across all farms. Disaggregating productive (sale, transfer) from non-productive (death, theft) exits from the flock in future project cycles would substantially improve the interpretability of flock performance data.
3.4 Cumulative Disease Incidence and Health Constraints
Across the full monitored population of 428 animals (200 foundation stock + 228 births), 62 disease events were recorded over 12 months, yielding a cumulative disease incidence of 14.49% (Table 4). It should be noted that this figure represents cumulative incidence — the proportion of the population experiencing at least one disease event during the observation period — rather than point prevalence in the strict epidemiological sense, and should be interpreted accordingly (Rothman et al., 2008). Animals experiencing more than one disease event were counted once per event category; the 62 recorded events represented 62 distinct clinical episodes across 58 individual animals (four animals experienced two disease events each).
Pneumonia emerged as the single most prevalent condition, accounting for 16 cases (3.74% of the total population; 25.8% of all disease events; Table 4). This finding is consistent with the well-established dominance of respiratory disease in sheep production systems across subtropical Bangladesh, and specifically with the role of Pasteurella multocida and Mannheimia haemolytica as leading causes of pneumonic pasteurellosis in sheep in Rajshahi District (Ahmed et al., 2016). The Barind tract's climatic transition from the warm, humid monsoon to the cool, dry winter — with minimum temperatures dropping below 10°C in December and January — creates conditions of heightened respiratory vulnerability in animals housed in poorly ventilated pens, and this seasonal pattern should inform the timing of preventive interventions in future cycles. Specifically, a booster Pasteurella vaccine administered in October, before the onset of the cool season, would be a low-cost, high-impact addition to the current health protocol.
Gastrointestinal parasitic infections ranked second (15 cases; 3.50% of population; 24.2% of events). The Barind tract's monsoon-flooded lowlands provide near-ideal habitat for Lymnaea snails — the intermediate host of Fasciola hepatica — and the warm, moist post-monsoon soil conditions sustain high burdens of free-living nematode larvae (Chowdhury et al., 2018). The bimonthly ivermectin-albendazole deworming protocol implemented in this study may have been insufficient to control Fasciola specifically, as albendazole in single-dose field use has limited efficacy against adult liver fluke; triclabendazole administered once annually after the monsoon recession (typically October–November) is the agent of choice for definitive fluke control in endemic zones (Ershaduzzaman et al., 2025). The SPSS dataset also coded anaemia separately (DISEASES = 3), and although insufficient cases were recorded for a separate reportable category, clinicians should be aware that anaemia in this population may represent an overlapping manifestation of hepatic fasciolosis rather than a distinct nutritional entity.
Malnutrition and starvation ranked third (12 cases; 2.80% of population), reflecting the predictable consequence of the Barind dry season, during which natural pasture desiccates, groundwater falls, and farmers with limited fodder storage capacity struggle to maintain adequate nutritional planes. Sarker and Alam (2020) have documented this feed gap in detail, noting that even brief periods of negative energy balance in late-pregnant ewes can substantially impair lamb birth weight and survival. The concentrate supplement provided during the final four weeks of pregnancy in this study partially addresses this window, but mid-lactation and post-weaning nutritional gaps for lambs remain inadequately covered. On-farm establishment of drought-tolerant fodder plots — Napier grass (Pennisetum purpureum) as a bulk roughage and Stylosanthes hamata as a protein-rich legume supplement — could substantially reduce malnutrition-related attrition during the lean season and is a feasible intervention within the resource constraints of Barind smallholders.
Accidents and predator attacks were the fourth-ranked category (10 cases; 2.34% of population; 16.1% of events), a figure that is particularly worth reflecting on because these are, in principle, entirely preventable losses — unlike infectious disease, which requires veterinary inputs and supply chains. Rahman et al. (2016) identified stray dog predation during daytime grazing as a major sheep loss pathway in the Barind area, and the present findings suggest this remains an unaddressed vulnerability even under the study's supervised management protocol. Simple, inexpensive interventions — securing perimeter fencing around grazing areas, training farmers on nighttime penning practices, and repairing gaps in existing sheep housing — could eliminate a meaningful fraction of the 31% foundation stock mortality.
Enteritis/diarrhoea (7 cases; 1.64%) and food poisoning (2 cases; 0.47%) were the least frequently recorded conditions. The relatively low diarrhoea prevalence may reflect the partial effectiveness of the colostrum management and pen hygiene protocols implemented in this study, though it could also reflect under-reporting of mild, self-limiting enteric disease — a limitation inherent in any farmer-reported surveillance system with fortnightly visit intervals. Food poisoning, though rare, resulted in two fatalities and highlights the need for farmer education on the identification and fencing-off of known toxic plant species in the Barind landscape.
3.5 Integrated Interpretation and Practical Implications
Taken together, the three datasets in this study present a coherent and — in some respects — sobering picture of the productive potential and health vulnerabilities of indigenous Barind sheep under smallholder farming conditions. The growth trajectory (1.22 kg at birth to 15.55 kg at 12 months, with non-significant sex differences throughout) confirms that the breed is capable of meaningful productive output under semi-intensive management, and that the management protocol implemented in this study — particularly the strategic concentrate supplementation and bimonthly deworming — supported growth performance at the upper range achievable in the Barind ecosystem. At prevailing live-weight market prices in the Rajshahi region (approximately BDT 400–450 per kilogram), a 12-month male animal weighing 15–16 kg represents roughly BDT 6,000–7,200 in market value, equivalent to several weeks of income for a marginal farming household.
However, the 31.0% foundation stock mortality — equivalent to losing roughly one in three distributed animals within 12 months — substantially erodes the economic viability of the model as currently implemented. Even allowing for the contribution of births (net flock expansion of 83%), a mortality rate of this magnitude represents an unacceptable economic risk for households that received the foundation animals as part of a poverty-reduction initiative. Three targeted interventions, if added to the existing protocol, would address the primary mortality drivers identified in this study. First, a 14-day post-distribution quarantine and observation period for all procured foundation animals, during which close health monitoring and a booster deworming and respiratory vaccination course could be administered, would reduce the high early mortality associated with procurement stress. Second, annual Pasteurella vaccination in October — before the cool season — would substantially reduce the leading infectious cause of death (pneumonia, 25.8% of events). Third, post-monsoon triclabendazole treatment (October–November) would address the fasciolicide gap in the current bimonthly deworming protocol. Collectively, these three additions represent a modest increase in per-animal health expenditure that is likely to be substantially outweighed by the reduction in preventable mortality.
This study has several limitations that should inform the interpretation of findings and the design of follow-up research. The growth cohort (n = 90) was adequate for the descriptive objectives of this baseline study but underpowered to detect small-to-medium sex effects, particularly at six months. The farm-level management heterogeneity across 40 households — which we believe is reflected in the widening variance of body weight with age — was not statistically controlled; a mixed-effects model accounting for farm as a random effect would provide more precise estimates of the true breed-level growth trajectory. Disease diagnosis relied on clinical assessment rather than laboratory confirmation for most categories, introducing the possibility of misclassification, particularly for conditions presenting with overlapping signs (e.g., parasitic anaemia vs. nutritional anaemia). Future studies should incorporate laboratory diagnostics — at minimum, faecal egg counts for helminths and nasal swabs for respiratory pathogens — to enable pathogen-specific incidence estimates and guide targeted treatment protocols.