Abstract

BackgroundThe study of morphology is experiencing a renaissance due to rapid improvements in technologies for 3D visualization of complex internal and external structures. But 3D visualization of the internal structure of mesoscale objects — those in the 10–1000 μm range — remains problematic. They are too small for microCT, many lack suitable specific fluorescent markers for confocal microscopy, or they require labor-intensive stacking and smoothing of individual TEM images. Here we illustrate the first comprehensive morphological description of a complete mesoscale biological system at nanoscopic resolution using ultra-modern technology for 3D visualization — serial block-face scanning electron microscopy (SBF-SEM). The SBF-SEM machine combines an in-chamber ultramicrotome, which creates a serial array of exposed surfaces, with an SEM that images each surface as it is exposed. The serial images are then stacked automatically by 3D reconstruction software. We used SBF-SEM to study the spinneret (thread-producing) system of a small, tube-dwelling crustacean that weaves tubes of silk. Thread-producing ability is critical for the survival of many small-bodied animals but the basic morphology of these systems remains mysterious due to the limits of traditional microscopy.ResultsSBF-SEM allowed us to describe — in full 3D — well-resolved components (glands, ducts, pores, and associated nerves and muscles) of the spinneret system in the thoracic legs and body segments of Sinelobus sp. (Crustacea, Peracarida, Tanaidacea), a tube-building tanaid only 2 mm in body length. The 3D reconstruction by SBF-SEM revealed at nanoscale resolution a unique structure to the gland and duct systems: In each of three thread-producing thoracic segments, two separate ducts, derived from two separate glands located in the body, run through the entire leg and merge at the leg tip just before the spinneret pore opening. We also resolved nerves connecting to individual setae, spines and pores on the walking legs, and individual muscles within each leg segment.ConclusionsOur results significantly expand our understanding of the diversity of spinneret systems in the Crustacea by providing the first well-resolved view of spinneret components in the peracarid crustacean order, Tanaidacea. More significantly, our results reveal the great power of SBF-SEM technology for comprehensive studies of the morphology of microscopic animals.Electronic supplementary materialThe online version of this article (doi:10.1186/s12983-016-0146-0) contains supplementary material, which is available to authorized users.

Highlights

  • The study of morphology is experiencing a renaissance due to rapid improvements in technologies for 3D visualization of complex internal and external structures

  • Serial block-face scanning electron microscopy (SBF-SEM), the method used here, uses a robotic ultramicrotome-embedded within a scanning electronmicroscope

  • Critical information is lacking about the presence and ontogeny of spinneret systems in other tanaids, and in other crustacean groups, to conclude with confidence how often spinneret systems have evolved independently in the Crustacea. This first comprehensive description of the spinneret system in a tanaid provides new evidence for a distinctive morphology: two separate ducts, derived from two separated glands in each thread-spinning segment, that merge at the leg tip or the terminal spine before secretions are released

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Summary

Introduction

The study of morphology is experiencing a renaissance due to rapid improvements in technologies for 3D visualization of complex internal and external structures. Both confocal laser scanning microscopy (cLSM) and micro-computer tomography (micro-CT), have facilitated a “renaissance of morphology” [4, 5] as a crucial discipline in the biological sciences Even with these new technologies, three-dimensional data are still difficult to acquire for non-specific (unlabelled) meso-scale objects (roughly 10–1000 μm) in a sufficient resolution (see [6]), even though this size range is essential to understanding the diversity and evolution of many animal groups that include small-bodied members [7]. Serial block-face scanning electron microscopy (SBF-SEM), the method used here, uses a robotic ultramicrotome-embedded within a scanning electronmicroscope It offers a significant advance in fully automated three-dimensional reconstruction of meso-scale structures to be observed at nanometer resolution [8, 10]. Few biologists seem to realize that this technology offers great power for studying whole-body morphology of meso-scale organisms or objects [6, 12]

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