The following pages link to Martin Tinker (Q138972):
Displayed 50 items.
- Comparative demography of sea otter populations (Q143649) (← links)
- Continuing sea otter population declines in the aleutian archipelago (Q144333) (← links)
- Stability and change in kelp forest habitats at San Nicolas Island (Q145193) (← links)
- Individual dietary specialization and dive behaviour in the California sea otter: Using archival time-depth data to detect alternative foraging strategies (Q146875) (← links)
- Ontogenetic and among-individual variation in foraging strategies of northeast Pacific white sharks based on stable isotope analysis (Q147506) (← links)
- The interaction of intraspecific competition and habitat on individual diet specialization: a near range-wide examination of sea otters (Q147916) (← links)
- Ecological drivers of variation in tool-use frequency across sea otter populations (Q148119) (← links)
- Complex trophic interactions in kelp forest ecosystems (Q148411) (← links)
- Concentration and retention of Toxoplasma gondii surrogates from seawater by red abalone (Haliotis rufescens) (Q151132) (← links)
- Characterizing species interactions to understand press perturbations: What is the community matrix? (Q151674) (← links)
- Trade-offs between energy maximization and parental care in a central place forager, the sea otter (Q151701) (← links)
- Foraging ecology (Q152264) (← links)
- Spatial and temporal variation in sea otter demography (Q152268) (← links)
- Individual variation in prey selection by sea otters: Patterns, causes and implications (Q154374) (← links)
- Lactation and resource limitation affect stress responses, thyroid hormones, immune function, and antioxidant capacity of sea otters (Enhydra lutris) (Q156604) (← links)
- Robust age estimation of southern sea otters from multiple morphometrics (Q156667) (← links)
- Sea otter population collapse in southwest Alaska: Assessing ecological covariates, consequences, and causal factors (Q156740) (← links)
- Predicting animal home-range structure and transitions using a multistate Ornstein-Uhlenbeck biased random walk (Q157320) (← links)
- Testing the nutritional-limitation, predator-avoidance, and storm-avoidance hypotheses for restricted sea otter habitat use in the Aleutian Islands, Alaska (Q233984) (← links)
- Timescales alter the inferred strength and temporal consistency of intraspecific diet specialization (Q234047) (← links)
- The cost of reproduction: differential resource specialization in female and male California sea otters (Q234124) (← links)
- Concentration and retention of Toxoplasma gondii oocysts by marine snails demonstrate a novel mechanism for transmission of terrestrial zoonotic pathogens in coastal ecosystems (Q234161) (← links)
- Evaluating potential conservation conflicts between two listed species: Sea otters and black abalone (Q234406) (← links)
- Effects of wildfire on sea otter (Enhydra lutris) gene transcript profiles (Q235083) (← links)
- Prey choice and habitat use drive sea otter pathogen exposure in a resource-limited coastal system (Q236797) (← links)
- Energetic demands of immature sea otters from birth to weaning: Implications for maternal costs, reproductive behavior and population-level trends (Q237029) (← links)
- An online database for informing ecological network models: http://kelpforest.ucsc.edu (Q237297) (← links)
- Dramatic increase in sea otter mortality from white sharks in California (Q237922) (← links)
- Permissible Home Range Estimation (PHRE) in restricted habitats: A new algorithm and an evaluation for sea otters (Q238212) (← links)
- The high cost of motherhood: End-lactation syndrome in southern sea otters (Enhydra lutris nereis) on the central California, USA, coast (Q238225) (← links)
- Rehabilitating sea otters: Feeling good versus being effective (Q238850) (← links)
- Asynchrony in craniomandibular development and growth in Enhydra lutris nereis (Carnivora: Mustelidae): Are southern sea otters born to bite? (Q239173) (← links)
- Mitogenomes and relatedness do not predict frequency of tool-use by sea otters (Q239343) (← links)
- Food abundance, prey morphology, and diet specialization influence individual sea otter tool use (Q239691) (← links)
- Ecosystem features determine seagrass community response to sea otter foraging (Q240064) (← links)
- Sea otters in a dirty ocean (Q242339) (← links)
- Recovery of a top predator mediates negative eutrophic effects on seagrass (Q244441) (← links)
- Gene transcription in sea otters (Enhydra lutris); development of a diagnostic tool for sea otter and ecosystem health (Q245229) (← links)
- Patterns of growth and body condition in sea otters from the Aleutian archipelago before and after the recent population decline (Q246366) (← links)
- Variation in δ13C and δ15N diet–vibrissae trophic discrimination factors in a wild population of California sea otters (Q247266) (← links)
- Persistent organic pollutants in the blood of free-ranging sea otters (Enhydra lutris ssp.) in Alaska and California (Q247280) (← links)
- Evidence for a novel marine harmful algal bloom: Cyanotoxin (Microcystin) transfer from land to sea otters (Q247522) (← links)
- Using ecological function to develop recovery criteria for depleted species: Sea otters and kelp forests in the Aleutian archipelago (Q247938) (← links)
- Population demographics, survival, and reporduction: Alaska sea otter research (Q249003) (← links)
- Studying sea otter foraging ecology: A review of some methodological approaches (Q249009) (← links)
- Mortality sensitivity in life-stage simulation analysis: A case study of southern sea otters (Q249106) (← links)
- Predicting community responses to perturbations in the face of imperfect knowledge and network complexity (Q250471) (← links)
- Food limitation leads to behavioral diversification and dietary specialization in sea otters (Q252419) (← links)
- Using demography and movement behavior to predict range expansion of the southern sea otter. (Q252577) (← links)
- Understanding and predicting ecological dynamics: Are major surprises inevitable (Q252993) (← links)