The complete larval development of the spider crab Maguimithrax spinosissimus (Lamarck, 1818) is re-described and illustrated in detail from laboratory-reared material. The development consisted of the typical pattern reported for the Majoidea, two zoeal stages and one megalopa. The complete larval development from hatching to first crab lasted 5–6 days at temperatures that ranged between 24–28 °C. Both zoeal stages of M. spinosissimus exhibited moderate reduction in the number of setae in the maxilla and maxillipeds, from the first to the second zoeal stage, when compared with other closely related species. Maguimithrax spinosissimus can be easily distinguished from other species belonging to the closely related genus Mithrax by the (i) setation of the endopod of the maxillule, maxilla and second maxilliped in both zoeal stages; (ii) setation of the scaphognathite of the maxilla in the first zoeal stage; (iii) setation of the basis of maxilliped I in the second zoeal stage and megalopa; (iv) morphology of the antennule and antenna in the second zoeal stage; and (v) setation of the antennule, coxal endite of maxilla, and exopod of second maxilliped in the megalopa. All these characters support the recent generic status of Maguimithrax within the Mithracidae. Additional morphological details, not available previously, are provided. This study will provide support for conservation strategies in this species.

The carapace and chelipeds ornamentation of the deep-water spider crab Rochinia umbonata (Stimpson, 1871), from the Western Atlantic undergo very dramatic ontogenetic changes. Since the also deep-water spider crab Rochinia confusa Tavares, 1991 is differentiated from R. umbonata mostly on the basis of these characters, R. confusa is regarded herein as an ontogenetic stage and, therefore, a junior subjective synonym of R. umbonata.

The porcellanid crab Porcellana sayana is, for the first time, reported to have a symbiotic association with the crab Stratiolibinia bellicosa. This is also the first record on the association between the porcelain crab P. sayana and a brachyuran crab on the Brazilian coastline. In addition, this is the second record of association of P. sayana with a Majoidea crab.

Morphometric and gonad maturity of Libinia spinosa on the coast of Mar del Plata, Argentina, were assessed. In both sexes various morphometric features were measured to determine the morphometric maturity, and through macroscopic inspection of gonads and analysis of its content, different stages of gonad maturity were described and the physiological maturity was estimated. In females, the carapace width ranged from 8 to 56.5 mm while in males from 4.6 to 81.97 mm. The size at which 50% of females were morphometrically mature was calculated at 40.6 mm. Based on the allometric growth of the abdomen, two morphometric groups of females were recognized as juvenile and adult phases. In males, results of principal component analysis showed that the most suitable variables that efficiently represent the size and sexual differentiation factor were the carapace width and cheliped length respectively. The size at which 50% of males were morphometrically mature was estimated at 58.9 mm. Based on the allometry of the cheliped growth, two morphometric groups were recognized as immature and mature phases. Males maintained under laboratory conditions moulted and growth was related to regular and terminal moults. Males reached their terminal moult at a wide size-range, from 48.5 mm to 61.4 mm of carapace width. This terminal moult coincided with the size of morphometric maturity. In both sexes four stages of gonad development were described, two corresponded to immature phases and two to mature phases. The size at which 50% of females and males reached gonad maturity was LC50 = 40.33 mm and LC50 = 33.6 mm, respectively. In females, both morphometric and gonad maturity occurred at a similar size. In males, gonad maturity is acquired prior to morphometric maturity, thus three different types of males were characterized: (1) those with small carapace width and cheliped, without spermatophores in their vas deferens; (2) those with large carapace width and small cheliped, bearing spermatophores in their vas deferens; and (3) those with large carapace width and cheliped, bearing spermatophores in their vas deferens.