Variation in age of primiparity in mountain goats estimated from horn growth increments

Variation in age of primiparity is important for population dynamics and wildlife management because it can affect population growth. Using a novel technique based on the trade-off between annual horn growth and reproduction, we estimated the age of primiparity for 2274 female mountain goats (Oreamnos americanus, de Blainville 1816) harvested across British Columbia, Canada, from 1976 to 2019. We then investigated spatio-temporal variation in the probability that harvested females were primiparous when aged three, four or five years and older using Bayesian ordinal regressions. We found that the probability of primiparity at three years decreased over time in nearly all mountain ranges. In the Coastal Mountain range, however, the probability of primiparity at age three significantly increased. These results suggest that the large coastal populations of mountain goats could be more resilient to harvest than other populations in British Columbia, which may be experiencing environmental effects promoting later primiparity. Models predicting age of primiparity from annual growth measures are a valuable tool for wildlife management and could help conservation of many species.

Reproductive effort affects subsequent horn growth in sexually dimorphic male ungulates

Trade-offs between reproductive effort and subsequent growth in males are not well explored, despite their relevance in questions of individual energy allocation. Regarding the growth of sexual secondary characters in polygynous breeding male mammals, indeed, no conclusive studies exist. We investigated in male Alpine ibex (Capra ibex) the relationship between their behavioral reproductive effort, current horn size, and subsequent horn growth. While controlling for age, no evidence was found for male behavioral reproductive effort during the rut being affected by their horn size. On the other hand, reproductive effort significantly decreased age-specific horn growth during the following summer. Our study provides evidence that growth of secondary sexual characters is traded against behavioral investments in reproduction in a male mammal. It bears important implications for the understanding of energy allocation between various life-history components and the evolutionary ecology of secondary sexual characters.

Horn growth patterns of Nubian ibex from the Sinai, Egypt

Documenting patterns of horn growth and horn-age relationships of Nubian ibex (Capra nubiana) can contribute to a more comprehensive understanding of their natural history, horn development in ibex in general, and future conservation of the species. Our specific objectives included (1) documenting age-horn growth patterns; (2) contrasting horn growth patterns of Nubian ibex with other ibex species; and (3) determining whether horn development accurately reflects age of Nubian ibex in Sinai, Egypt. As expected, all male and female horn measurements had significant relationships with age. Horn growth in males started plateauing at ca. age 7–8, whereas female horn growth started plateauing at ca. age 4–6. The extremely arid environment of Nubian ibex in the Sinai may account for the slowing of horn growth at a younger age than seen in populations of some other ibex species. We found a significant relationship between the number of horn ridges and age, indicating that counting horn ridges provides a viable method of aging males to within ±1 y. Thus counting horn ridges may be a useful and non-invasive method to determine age or age class, which can further our understanding of age structure, the natural history, and management of Nubian ibex populations.

Mechanical Nociceptive Threshold, Tissue Alterations and Horn Growth in Calves after Injection of Isoeugenol or Clove Oil under the Horn Bud

Disbudding of calves is a common, painful intervention. Due to cytotoxic and anesthetic properties, the injection of clove oil or its component isoeugenol may be less detrimental to animal welfare. We investigated mechanical nociceptive threshold (MNT), possible tissue alterations and horn growth for up to 12 weeks after injection of 1.5 mL clove oil (CLOV), isoeugenol (ISO) or saline (CON) or after hot-iron disbudding (BURN; with local anesthesia and sedation, n = 10/treatment). MNT was measured using von Frey filaments and a pressure algometer at four locations around the horn bud. There was a treatment*time point interaction (linear mixed model, p < 0.05). MNT decreased most strongly and for the longest time for BURN in most calves at least for 3 weeks. For ISO, the decrease was less distinct and most calves’ values returned to baseline after 1–2 weeks. MNT in CLOV was intermediate, with decreased values up to 3 weeks in some animals. 12 weeks after the treatment, horn growth was prevented in about 50% of the horns in CLOV and ISO. Tissue alterations such as swellings of the eyelids often occurred in CLOV, but less so in ISO. Our results suggest that injection of isoeugenol causes less pain and thus seems to be beneficial compared to hot-iron disbudding, while clove oil was not advantageous. Regarding the effectiveness of isoeugenol to prevent horn growth, more studies are needed.

Clove Oil Delays Rather Than Prevents Scur/Horn Growth in Dairy Cattle

The objective of this study was to evaluate if administration of clove oil prevents scur/horn growth in dairy cattle long term. At approximately 4 days of age, calves had one of four treatments assigned to each horn bud: (1) clove oil administered subcutaneously under the horn bud (CLOV, n = 132); (2) cautery disbudded and the horn bud removed (BUDOFF, n = 126); (3) cautery disbudded and the horn bud tissue left intact (BUDON, n = 129); (4) a liquid nitrogen filled probe applied to the horn bud area (CRYO, n = 131). At approximately 16 months of age, all cattle were checked for scur or horn development. A sub-set of scurs/horns from the CLOV cattle were removed to evaluate tissue and structural development. In total, 5% of CLOV buds developed into horns and 63% into scurs; 10% of the scurs looked like normally developed horns but they were not attached to the skull. Cautery disbudding prevented scur and horn development in cattle when the horn bud tissue was removed, but some scur growth was observed in the BUDON treatment. CRYO was 100% ineffective at preventing scur/horn growth. Injecting clove oil under the horn bud appeared to delay horn development, but not prevent it, when administered to 4 day old dairy calves.

The Insulin Signaling Substrate Chico and the Ecdysone Response Element Broad Both Regulate Growth of the Head Horns in the Asian Rhinoceros Beetle, Trypoxylus dichotomus

Males of the Asian rhinoceros beetle, Trypoxylus dichotomus, possess exaggerated head and thoracic horns that scale dramatically out of proportion to body size. While RNAi-mediated knockdowns of the insulin receptor suggest that the insulin signaling pathway regulates nutrition-dependent growth including exaggerated horns, the genes that regulate disproportionate growth have yet to be identified. We used RNAi-mediated knockdown of several genes to investigate their potential role in growth and scaling of the sexually dimorphic, exaggerated head horns of T. dichotomus. Knockdown of the insulin signaling substrate chico and the ecdysone response element broad caused significant decreases in head horn length, while having no or minimal effects on other structures such as elytra and tibiae. However, scaling of horns to body size was not affected by either knockdown. In addition, knockdown of phosphatase and tensin homolog, a negative regulator of the insulin signaling pathway, had no significant effects on any trait. Our results do not identify any candidate genes that may specifically mediate the allometric aspect of horn growth, but they do confirm the insulin signaling pathway as a mediator of conditional trait expression, and importantly implicate the ecdysone signaling pathway, possibly in conjunction with insulin signaling, as an additional mediator of horn growth.