Humans are rapidly transforming the structural configuration of the planet's ecosystems, but these changes and their ecological consequences remain poorly quantified in underwater habitats. Here, we show that the loss of forest-forming seaweeds and the rise of ground-covering 'turfs' across four continents consistently resulted in the miniaturization of underwater habitat structure, with seascapes converging towards flattened habitats with smaller habitable spaces. Globally, turf seascapes occupied a smaller architectural trait space and were structurally more similar across regions than marine forests, evidencing habitat homogenization. Surprisingly, such habitat convergence occurred despite turf seascapes consisting of vastly different species richness and with different taxa providing habitat architecture, as well as across disparate drivers of marine forest decline. Turf seascapes contained high sediment loads, with the miniaturization of habitat across 100s of km in mid-Western Australia resulting in reefs retaining an additional ~242 million tons of sediment (four orders of magnitude more than the sediments delivered fluvially annually). Together, this work demonstrates that the replacement of marine forests by turfs is a generalizable phenomenon that has profound consequences for the ecology of temperate reefs. | 5263 PESSARRODONA Et Al.

Temperate marine ecosystems globally are undergoing regime shifts from dominance by habitat-forming kelps to dominance by opportunistic algal turfs. While the environmental drivers of shifts to turf are generally well-documented, the feedback mechanisms that stabilize novel turf-dominated ecosystems remain poorly resolved. Here, we document a decline of kelp Saccharina latissima between 1980 and 2018 at sites at the southernmost extent of kelp forests in the Northwest Atlantic and their replacement by algal turf. We examined the drivers of a shift to turf and feedback mechanisms that stabilize turf reefs. Kelp replacement by turf was linked to a significant multi-decadal increase in sea temperature above an upper thermal threshold for kelp survival. In the turf-dominated ecosystem, 45% of S. latissima were attached to algal turf rather than rocky substrate due to preemption of space. Turf-attached kelp required significantly (2 to 4 times) less force to detach from the substrate, with an attendant pattern of lower survival following 2 major wave events as compared to rock-attached kelp. Turf-attached kelp allocated a significantly greater percentage of their biomass to the anchoring structure (holdfast), with a consequent energetic trade-off of slower growth. The results indicate a shift in community dominance from kelp to turf driven by thermal stress and stabilized by ecological feedbacks of lower survival and slower growth of kelp recruited to turf.

Individuals rarely have equal competitive abilities, with body size being one of the most important attributes affecting the mechanism (i.e. exploitative and interference) and consequences of competition. Competitive interactions within size-structured populations are complex and can have major implications for population dynamics, community structure and evolutionary processes. Destructive grazing of kelp beds by the green urchin Strongylocentrotus droebachiensis creates barrens where high-quality food is scarce and intraspecific competition may have an important role in structuring populations. In this study, we experimentally identified the mechanisms underlying size-asymmetric competition between small, medium, and large size classes of the green urchin. A field-based mesocosm experiment showed that small and medium sea urchins grew less and produced smaller gonads when competing for food with large conspecifics. Surprisingly, when food was provided ad libitum but large urchins were present, small individuals’ growth and foraging behavior were reduced, providing strong evidence for interference competition between small and large sea urchins. Interactions between medium and large sea urchins were, however, more influenced by exploitative competition, suggesting that sea urchins shift ontogenetically from a situation of intense interference competition to one dominated by exploitative competition. The size structure of the population can thus determine the relative importance of interference and exploitative competition. In turn, the importance of interference competition may influence size structure by inhibiting the growth of smaller urchins, a pattern consistent with the prediction of theoretical models. The consideration of size-asymmetric competitive interactions can lead to a better understanding of population size structure and dynamics.

Knowledge of urchin age structure is crucial for understanding their ecosystem impacts and improving their management. In sclerochronology, translucent and opaque growth bands (TGB, OGB) in urchin ossicles are used to estimate age. An essential premise for using this technique is that one TGB and one OGB are formed every year, independent of urchin size or ossicle type. TGB and OGB addition are associated with slow and fast growth, respectively, and assumed to be added seasonally due to changes in water temperature. However, these assumptions are not unanimously supported by experiments, and validation attempts have not generated consensus. We conducted an experiment on Strongylocentrotus droebachiensis to test the validity of these assumptions and reviewed the literature to assess the use and validation of sclerochronology in urchins. The experiment demonstrated that the addition of TGB and OGB was not strictly related to temperature and was not consistent across urchin size-classes or ossicle types. TGB were added in response to temporary stress, and no distinction on the basis of band width or pigmentation could be made between natural TGB and stress-induced TGB. Only 52% of articles that used sclerochronology for aging urchins attempted any validation, and when the methodology was put under scrutiny, it was usually found to be wanting. More detailed studies are needed to address variability in growth bands deposition and endogenous and exogenous factors affecting this process. Sclerochronology in urchins should not be used until standardized procedures are able to provide accurate and precise interpretation of growth band addition.

Regenerating structures critical for survival provide excellent model systems for the study of phenotypic plasticity. These body components must regenerate their morphology and functionality quickly while subjected to different environmental stressors. Sea urchins live in high energy environments where hydrodynamic conditions pose significant challenges. Adhesive tube feet provide secure attachment to the substratum but can be amputated by predation and hydrodynamic forces. Tube feet display functional and morphological plasticity in response to environmental conditions, but regeneration to their pre-amputation status has not been achieved under quiescent laboratory settings. In this study, we assessed the effect of turbulent water movement, periodic emersion, and quiescent conditions on the regeneration process of tube feet morphology (length, disc area) and functionality (maximum disc tenacity, stem breaking force). Disc area showed significant plasticity in response to the treatments; when exposed to emersion and turbulent water movement, disc area was larger than tube feet regenerated in quiescent conditions. However, no treatment stimulated regeneration to pre-amputation sizes. Tube feet length was unaffected by treatments and remained shorter than non-amputated tube feet. Stem breaking force for amputated and not amputated treatments increased in all cases when compared to pre-amputation values. Maximum tenacity (force per unit area) was similar among tube feet subjected to simulated field conditions and amputation treatments. Our results suggest the role of active plasticity of tube feet functional morphology in response to field-like conditions and demonstrate the plastic response of invertebrates to laboratory conditions.

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