» Articles » PMID: 39583905

Spinneret Spinning Field Ontogeny and Life History Observations in the Spider (Araneae: Palpimanidae)

Overview
Journal J Arachnol
Date 2024 Nov 25
PMID 39583905
Authors
Affiliations
Soon will be listed here.
Abstract

As in other Palpimanidae, two pairs of posterior spinnerets present in typical Araneomorphae are vestigial in Kulczyński, 1909, with only the anterior lateral spinneret (ALS) pair prominent. Nevertheless, in late juvenile and adult females, spigots appear in the ancestral posterior spinneret region (PS). Consistent with these spigots serving cylindrical silk glands, females construct substantial egg sacs. While juveniles and adults exhibit a compressed PS, in postembryos it is fully extended. Piriform silk gland (PI) spigots form a linear array on ALSs from the 1 stadium, increasing in number during ontogeny by addition of PIs of the tartipore-accommodated (T-A) subtype (i.e., functional during proecdyses). The number of T-A PIs added from one stadium to the next and locations occupied by their spigots often exhibit a stereotypic pattern, especially consistent in early instars. The number of non-T-A PIs remains constant through ontogeny from the 1 stadium: one per ALS rather than the two per ALS inferred in a few araneoids. The secondary major ampullate silk gland (2° MaA) spigot, primitively uni-shafted among araneomorphs, has become modified into a multi-shafted spigot with extended base, the number of shafts increasing during ontogeny. However, the multiple ducts that connect to the shafts continue to be accommodated during proecdysis by a single enormous tartipore. Sexual dimorphism is present, with late stadium females having greater numbers of T-A PI spigots and 2° MaA spigot shafts. Observations are presented pertaining to feeding behavior, sexual cannibalism (absent), habitat, winter diapause, numbers of molts, and longevity.

References
1.
Wolff J, Michalik P, Ravelo A, Herberstein M, Ramirez M . Evolution of Silk Anchor Structure as the Joint Effect of Spinning Behavior and Spinneret Morphology. Integr Comp Biol. 2021; 61(4):1411-1431. DOI: 10.1093/icb/icab003. View

2.
Benavides L, Hormiga G . Taxonomic revision of the Neotropical pirate spiders of the genus Gelanor Thorell, 1869 (Araneae, Mimetidae) with the description of five new species. Zootaxa. 2016; 4064(1):1-72. DOI: 10.11646/zootaxa.4064.1.1. View

3.
Townley M, Horner N, Cherim N, Tugmon C, Tillinghast E . Selected aspects of spinning apparatus development in Araneus cavaticus (Araneae, Araneidae). J Morphol. 2018; 208(2):175-191. DOI: 10.1002/jmor.1052080204. View

4.
Coddington J, Chanzy H, Jackson C, Raty G, Gardner K . The unique ribbon morphology of the major ampullate silk of spiders from the genus Loxosceles (recluse spiders). Biomacromolecules. 2002; 3(1):5-8. DOI: 10.1021/bm010108m. View

5.
Pekar S, Liznarova E, Bocanek O, Zdrahal Z . Venom of prey-specialized spiders is more toxic to their preferred prey: A result of prey-specific toxins. J Anim Ecol. 2018; 87(6):1639-1652. DOI: 10.1111/1365-2656.12900. View