Ecosystems can undergo abrupt regime shifts as a result of many factors. Shifts between turbid and clearwater states are well understood for human‐impacted shallow lakes, but are not well understood in other types of lakes. Here we use long‐term data to describe abrupt shifts in water clarity in Trout Lake, an oligotrophic lake with a largely undeveloped watershed. For several decades mean summer water clarity averaged 4.5 m, but then around 2007 water clarity sharply increased and the “clear water regime” persisted for nearly a decade. Nutrient availability did not explain these changes, but rather they were explained by a classic top‐down trophic cascade. Around 2007, the population of the apex pelagic predator, Lake Trout, substantially increased. This was accompanied by a sharp decline in the lake's major pelagic prey fish, the zooplanktivorous Cisco. In turn, there was an increase in large‐bodied zooplankton taxa (calanoids, Daphnia), which reduced algal biomass. This clear water regime was then disrupted in 2014 by the invasion of a predatory zooplankton, Bythotrephes cederstroemi. This invasion corresponded to strong impacts on lower trophic levels (decrease in large‐bodied zooplankton and decreased water clarity), but more minor impacts on higher trophic levels (increased Cisco, decreased Lake Trout abundances)—in effect reversing the trophic cascade and shifting Trout Lake to a novel ecosystem state. Our study provides a long‐term, empirically based example of successive ecological regime shifts that occurred from the rise of an apex predator and a mid‐trophic level invasion in an undeveloped, oligotrophic lake.

Geometric morphology can be influenced by several biotic and abiotic factors, including predator–prey interactions and habitat structure. We measured the external morphology of Micropterus salmoides (largemouth bass, LMB) from two states in north-eastern United States, to assess the potential divergence of body shape. LMB varied in overall body shape (canonical variate analysis, P<0.001) between states, with Maine populations exhibiting shorter jaws (ANOVA, P<0.001) and thicker caudal peduncle depths (ANOVA, P<0.001) than the LMB in Pennsylvania. We propose that these observed differences in morphological traits suggest that jaw length may be influenced by prey availability and resource utilisation, whereas peduncle depth is better explained by surrounding habitat structure. These findings showed that body shape is variable and is influenced by a complex array of environmental factors, even over small latitudinal differences.

Objective: Here we determine how traditional morphometrics (TM) compares with geometric morphometrics (GM) in discriminating among morphologies of four forms of ciscoes of the Coregonus artedi complex collected from Lake Huron.Methods: One of the forms comprised two groups of the same deepwater cisco separated by capture depth, whereas the other three forms were shallow-water ciscoes.Result: Our three groups of shallow-water ciscoes were better separated (3% vs. 19% overlap) in principle component analysis (PCA) with TM data than with GM data incorporating semilandmarks (evenly spaced nonhomologous landmarks used to bridge between widely separated homologous landmarks). Our two deepwater cisco groups, comprising a putatively single form collected from different depths, separated more in PCAs with GM data (33% overlap) than in PCAs with TM data (66% overlap), an anomaly caused by greater decompression of the swim bladder and deformation of the body wall in the group captured at greater depths. Separation of the two deepwater cisco groups captured at different depths was not affected by the removal of semilandmarks. Assignment of forms using canonical variate analysis accurately assigned 86% of individuals using TM data, 98% of individuals using GM data incorporating semilandmarks, and 100% of individuals using GM data without semilandmarks. However, we considered assignments from the same form of deepwater cisco into separate groups as misassignments resulting from different capture depths, which reduced the accuracy of assignments with GM data incorporating semilandmarks to 66%. Conclusion:Our study implies that TM will continue to have an important role in morphological discrimination within Coregonus and other fishes similarly shaped.

The sexually dimorphic, enlarged major claw is a notorious trait among male fiddler crabs, but comes with potential locomotor costs. Possessing the ability to autotomize the enlarged claw is thus potentially advantageous to not only to escape a predator’s grip, but also to increase running performance. Previous studies concluded that autotomy either has no effect or even a negative effect on running performance. If the claw does not aid in locomotion, then shedding the enlarged claw that accounts for 40% of a fiddler crab’s mass should positively affect running performance. I therefore investigated autotomy and running performance in the Atlantic sand fiddler crab Leptuca pugilator (Bosc, 1801) with a focus on improving upon the methods of previous studies. Crabs were given substantial recovery time between collection, running trials, and autotomy induction. Maximum sprint speed was assessed by running crabs on a 1 m sand and mud track where individuals were significantly faster after autotomy of the enlarged claw (N = 64, t63=-7.25, P < 0.001). Intact running velocity was furthermore a significant predictor of autotomized running velocity (R2 = 0.194, P < 0.001). This study is the first to show a significant increase in fiddler crab sprint velocity after autotomy on a flat surface, and I propose where methodological pitfalls may have occurred in previous studies.

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