Ultrasonography as a tool for monitoring in ovo chicken development. 1. Technique and morphological findings.

Preliminary studies were performed to develop a method for using real-time, B-mode ultrasonography (US) to directly image the internal morphology of the chicken egg and developing embryo. Different soft tissue interfaces will reflect US waves differentially. These reflected waves, or echoes are then converted into a two-dimensional image of internal morphology. A major limitation of diagnostic US is its inability to penetrate through gas or hard tissue (bone, shell) interfaces. Methodology development to overcome the acoustic obstacle presented by the eggshell and air cell constituted the initial part of the preliminary study. An acoustical window was achieved by creating a 2-cm fenestration through the large end of the eggshell, then filling the air cell with sterile saline. Morphological features of the yolk and embryo were recorded at 0, 2, 6, 9, 14, and 17 days of incubation. The second part of the preliminary study explores whether the acoustic window, once created, could then be closed, and if closed, whether egg viability could be maintained. A second concurrent trial was conducted with 32 eggs that were fenestrated, imaged, recorded, reclosed, and incubated. Two methods of closure were attempted: one using dialysis membrane and tape; the other using an eggshell allograft. Hatchability was partially retained with both window closure methods.

Ultrasonography as a tool for monitoring in ovo chicken development. 2. Effects of eggshell alteration and ultrasonography on embryonic and posthatch development.

The influence of creating and closing acoustic windows on embryonic and posthatch development for the purpose of chicken embryogenesis monitoring by real-time ultrasonography (US) was evaluated at 2, 6, 9, 14, and 17 days of incubation. Acoustic windows were closed using either a porous dialysis film and tape (FM) or an eggshell allograft attached with collodion (CP). Results from eggs closed in each manner with and without concurrent nonsterile US examination were compared with two control groups. Window creation reduced hatchability. The hatchability reduction was caused primarily by bacterial contamination. Contamination was more common in the FM eggs than in the CP eggs and was greater in eggs that also underwent US. Hatchability increased and contamination decreased when US was performed closer to hatch. Egg weight loss was increased after Day 6 of incubation in FM + US eggs treated on Day 2 and after Day 9 in all eggs with windows except CP eggs treated on Day 9 and CP + US eggs treated on Days 6 and 9. Hatch weight decreased in chicks from eggs that had windows, particularly in FM eggs.