This study is aimed at evaluating the relationship between endogenous testosterone levels and antler development in male sambar deer (Rusa unicolor unicolor) inhabiting the Horton Plains National Park, Sri Lanka. Seven antler growth stages of sambar were documented based on phenotypic observations for the first time in Sri Lanka as (a) cast, (b) growing 1—single spike, (c) growing 2—antler fork into a Y as the second tine appears, (d) growing 3—velvet begins to harden as the third tine appears, (e) growth completed—velvet shedding begins, (f) hard antler, and (g) casting. Fecal samples were collected every month for a period of eighteen months from male sambar deer in different stages of the antler growth cycle, feeding in the wet patana grasslands of the park, and the fecal testosterone level was estimated by radioimmunoassay. Ten animals were randomly selected from each antler stage for the experiment. The results disclose that the highest concentrations of testosterone were recorded in the hard antler stage. Velvet shedding was preceded by an increase in the testosterone level, and it is the sudden drop in the testosterone concentration which triggers the antler casting. The casting stage corresponded with the lowest mean testosterone concentration. Although the study was able to conclude a clear relationship between the fecal testosterone levels of the male sambar deer in the Horton Plains National Park and their antler stages, there is no clear seasonality for the antler cycle.

Crop damage caused by fall armyworm (FAW), Spodoptera frugipera J.E. Smith (1797) (Lepidoptera: Noctuidae), has generated concern among agriculturists globally. In 2019, FAW was first reported in Sri Lanka, where it caused significant losses to corn crops. However, given that the two FAW biotypes – “rice strain” (R-FAW) and “corn strain” (C-FAW) – are morphologically identical, the biotype(s) present in Sri Lanka were unknown. The current study used the mitochondrial cytochrome c oxidase subunit I gene (mt-CO1) of FAW to biotype nine FAW samples collected in Sri Lanka. The resulting molecular phylogeny revealed that both R-FAW and C-FAW biotypes were present among the samples. In addition, we used the temperature-switch polymerase chain reaction (PCR) technique to develop a gel-based molecular marker. Two fragments were successfully amplified by the newly developed marker ABUOP0002, with fragment sizes of 341 bp from R-FAW and 204 bp from C-FAW. This demonstrates that ABUOP0002 can serve as a diagnostic gel-based molecular marker to identify the R-FAW and C-FAW biotypes from samples already identified to species level as S. frugiperda through taxonomical keys and provides a possible alternative to more expensive sequencing-based assays.

BackgroundAmong the diseases in rice (Oryza sativa L.), bacterial leaf blight (BLB) caused by Xanthomonas oryzae pv. oryzae results in devastating economic losses, both in terms of yield and quality. The Xa21 mapped to the rice chromosome 11, is known to convey resistance against BLB by its involvement in plant pathogen recognition and immunity responses. The closely-linked sequence-tagged site marker

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