Life cycle and feeding behaviour
Adult females preferentially oviposit on
Ricinus communis plants growing in calm, unpolluted environments, actively avoiding sites exposed to pollution. The eggs of
Ariadne merione are laid singly never in clusters on the underside of castor leaves, with each leaf typically bearing between one and five eggs. The eggs are white, opaque and covered with fine spikes. They are spherical in shape with a distinct central depression and have a mean diameter of 1.261±0.134 mm. The average incubation period from oviposition to larval emergence was 2.022±0.839 days. Prior to hatching, the eggs develop distinct black spots and after emergence, the empty eggshell becomes transparent
(Srivastava and Kumar, 2016) (Fig 3).
Larva
There were five larval instars in the development of
Ariadne merione butterfly. All instars were characterized by green colouration and feeds on the moulted skin.
First instar
The newly hatched first instar larvae of
Ariadne merione measured 2.618±0.286 mm in length and 0.613±0.092 mm in width. This stage lasted for an average of 2.422±0.499 days. First instar larvae exhibited relatively low feeding activity, restricting their damage to the scraping of the leaf epidermis, which resulted in fine, whitish feeding trails on the leaf surface. Upon emergence movement was limited and larvae typically remained close to the hatching site, feeding intermittently. With progressive growth, the larvae became markedly more active and mobile (Fig 4).
Second instar
The second instar larvae, measuring 4.554±0.660 mm in length and 1.311±0.228 mm in width, persisted for 2.156±0.475 days. At this stage, feeding activity increased and larvae began to consume softer parenchymatous tissues between veins, leaving behind fine veins intact. The body coloration and spination became more distinct, aiding in camouflage against the host foliage (Fig 5).
Third instar
The third instar larvae attained a length of 8.341±1.294 mm and a width of 2.736±0.402 mm, with the stage lasting 2.444±0.586 days. This instar marked the transition to voracious feeding behaviour. Larvae consumed large areas of the leaf lamina, creating irregular holes and in heavily infested plants, significant portions of the photosynthetic surface were lost. Feeding was both diurnal and nocturnal and larvae became more mobile, dispersing to adjacent leaves (Fig 6).
Fourth instar
The fourth instar stage lasted 2.622±0.650 days, with larvae measuring 11.751±3.125 mm in length and 3.621±0.922 mm in width. Feeding intensity further increased and larvae were capable of stripping entire leaf blades, leaving only the midribs and major veins intact. By this stage, the larval body appeared more robust and defensive behaviours, such as curling when disturbed, were more pronounced (Fig 7).
Fifth instar
The fifth instar was the longest larval stage, lasting 3.867±0.786 days. Larvae at this stage reached 19.322±3.290 mm in length and 5.201±0.789 mm in width. They were intensive feeders, capable of causing complete defoliation in localized infestations. Feeding damage was severe, with leaves either skeletonized or entirely consumed, drastically reducing the photosynthetic capacity of the host plant. The body coloration was darker and larvae displayed more active movement, often moving between plants in search of food (Fig 8).
Pupa
Upon completion of the larval period, pupation occurred. The pupae measured 18.208±1.095 mm in length and 6.347±0.320 mm in width and the pupal stage lasted 5.500±0.762 days. Pupae were typically attached to stems or the undersides of leaves using a silk girdle and cremaster. After the pupal duration, adults emerged and were subsequently released into their natural environment (Fig 9).
Following eclosion, the newly emerged adult butterfly remains stationary with its wings fully spread for several hours, allowing the wings to dry and harden before initiating flight. The dorsal (upper) surface of the wings displays a bright orange background intricately patterned with fine brown lines. The body is slender, with the head, thorax and abdomen exhibiting a matching orange coloration.
In contrast, the ventral (under) surface of the wings is predominantly brown, adorned with reddish-brown wavy transverse lines, providing camouflage when the butterfly rests with wings closed. Sexual dimorphism is evident: males can be distinguished from females by the presence of a distinct white brand on the hindwings. In lepidopteran terminology, a “brand” refers to a specialised patch of androconia scales a secondary sexual characteristic in male butterflies. These androconia scales function in pheromone dissemination, assisting in courtship communication. In
A.
merione, the brand is associated with minute pheromone-emitting organs on the hindwing, from which the scent is dispersed during mating interactions
(Darragh et al., 2017) (Fig 10).
The developmental duration and morphometric traits of egg and larval instars were presented in the Table 1, 2 and Fig 11, 12.
A pictorial key for the field identification of different developmental stages of
Ariadne merione (Common Castor Butterfly) was provided (Table 3).
According to
Crimmins et al., (2020), a comprehensive understanding of the developmental stages of an insect pest is fundamental to designing timely detection and control strategies. Such knowledge enables interventions to be applied at the most vulnerable points in the pest’s life cycle, thereby reducing crop losses and improving overall yield. Also, accurate identification of pest instars plays a pivotal role in enhancing integrated pest management (IPM) strategies, particularly through instar-specific biocontrol interventions. Morphometric benchmarks enable rapid field-level differentiation of larval stages, allowing pest managers to time biological control measures more effectively. Since early instars are generally more vulnerable to parasitoids and microbial agents, targeting these stages can improve control efficacy while minimizing insecticide use. Moreover, the observed morphological variation across instars supports selective monitoring and tailored interventions, reinforcing the practical utility of instar-wise susceptibility data in real-world IPM programs
(Wang et al., 2022).
In this context, the present study was undertaken to document the complete life cycle, growth patterns and behavioural traits of the common castor butterfly (
Ariadne merione), a significant defoliator of
Ricinus communis.
The findings reveal that larval feeding intensity increases substantially from the third instar onwards, when the caterpillars display pronounced voracity and cause visible foliar damage. Consequently, pest management actions should be initiated at or before this stage to prevent extensive defoliation and potential yield loss. Importantly, the present study provides precise data on the duration of each developmental stage of
A.
merione, which can be directly applied to the formulation of targeted control schedules. But there is a current lack of specific data on the economic threshold levels of Ariadne merione in castor crops, establishing precise threshold values remains an important area for future research to optimize integrated pest management strategies.
While the larval stage is destructive to castor crops, the adult butterfly performs beneficial ecological functions, particularly as a pollinator. This dual role highlights the need for a balanced pest management approach that mitigates agricultural damage without unnecessarily harming beneficial insect populations. One practical solution is the application of phytochemical-based biopesticides during the early larval instars. Such products, as noted by
Walia et al., (2017), exert considerably less impact on non-target organisms compared with conventional synthetic pesticides. In addition, the adoption of plant-derived biopesticides reduces reliance on chemical inputs in agriculture
(Jat et al., 2024; Pillai et al., 2020). In integrated pest management (IPM), semiochemicals offer a promising avenue for non-toxic control strategies by modulating pest insect behaviour. These compounds can serve as attractants in baited traps for effective population monitoring, or function as repellents and cues that lure natural enemies, thereby helping to suppress pest numbers below economically damaging thresholds
(Smart et al., 2014).
Preserving the adult butterfly population carries multiple ecological and socio-economic benefits. Beyond maintaining biodiversity, adult butterflies contribute to ecosystem stability, support food security through pollination services and hold cultural as well as aesthetic value
(Potts et al., 2016). By integrating early intervention with biological control measures, it is possible to limit pest damage while sustaining the positive ecological functions performed by the adult stage
(Ratto et al., 2022).
The implementation of such a strategy depends on rigorous field monitoring, accurate life stage identification and the timely execution of control measures. The present study’s life cycle and morphometric data provide a foundation for such decisions. Continued research should focus on refining these pest management tactics, with an emphasis on enhancing efficacy, minimizing non-target effects and ensuring long-term sustainability in castor agroecosystems.
Future research can also focus on the use of artificial intelligence in morphometric analysis, as illustrated by
Neupane et al., (2024). This marks a major leap forward in lepidopteran studies. By harnessing community-sourced photographs and applying deep learning techniques, their method enables automated identification and measurement of key morphological traits essential for determining the growth stages of monarch caterpillars. This AI-assisted approach not only accelerates the collection of extensive, high-resolution developmental data but also improves consistency and accuracy by reducing the subjective errors common in manual assessments. Moreover, integrating AI into this process expands public involvement in data gathering and opens new avenues for tracking population changes and developmental patterns in natural habitats-offering valuable contributions to ecological research and conservation efforts.