Biology and Pre-Health
Biology Department
Figure 1. Possible niche relationships between two species.
A major goal in evolutionary biology is to understand how species differentiate and adapt to their distinct environments.
Ecological niche divergence is the process by which closely related species evolve different ecological roles by adapting to distinct resources or environmental conditions, often reducing competition.
Both biotic factors (e.g., diet and resource use) and abiotic factors (e.g., climate) are key drivers of this divergence.
Climate can influence species directly through physiological constraints and indirectly by shaping resource availability, while diet reflects how species utilize those resources.
Although both climate and diet contribute to niche divergence, the extent to which climatic differences drive dietary differences among closely related species remains unclear.
This study investigates the relationship between climate and diet in shaping niche divergence among sister species.
To do this, divergence was quantified along both climate (temperature and precipitation) and diet axes and compared across multiple mammalian families.
Sister species occupying similar climates will exhibit more similar diets, as climate acts as both a physiological constraint and a filter on resource availability.
Figure 2. Phylogeny of the order Carnivora. Families included in analyses are circled in red.
Species pairs were identified using published phylogenetic hypotheses within focal carnivore families.
Pairs were defined as terminal sister taxa, representing the two most closely related extant species sharing an immediate common ancestor exclusive of other taxa.
Phylogenetic relationships were cross-validated across multiple primary literature sources to ensure consistency of sister-pair assignments.
Divergence times (mya) for each species pair were obtained from TimeTree and cross-referenced with published molecular phylogenies when available.
When multiple estimates existed, consensus or most recent calibrated values were used to standardize comparisons across families.
Divergence time estimates were used to evaluate whether ecological niche divergence increased with evolutionary age.
→i, j: Species
→Cij: Shared Diet
→Si , Sj: Diet Proportions
Diet composition data was compiled from EltonTraits and supporting literature sources
Diet categories were standardized into broad resource groups (e.g. vertebrates, invertebrates, fruit)
Proportional diet data for each species were compared between sister species
Bray-Curtis dissimilarity was used to quantify dietary divergence, with values ranging from 0 (identical diets) to 1 (different diets)
→Pi, j: Frequency categories
→i, j: Species
→Di, j: Overlap
→S: # Climate space bins
Geographic occurrence records were compiled for each species and matched with WorldClim bioclimatic variables
Climatic niches were summarized using principle component analysis (PCA) to reduce multiple climate variables into major environmental gradients
Pairwise climatic divergence between sister species was quantified using Schoener’s D
Higher values indicated greater climatic differences
Dietary and climatic divergence metrics were compared across all species pairs
Pairwise values were evaluated across families to assess variation in niche divergence across taxonomic groups
Relationships between climate and diet were tested and compared with divergence time to determine whether environmental differences correspond with ecological differentiation
Figure 3. Diet divergence (Bray-Curtis dissimilarity) across species pairs grouped by family. Points represent individual species pairs; boxes show median and interquartile range.
Sister species exhibited a more consistent diet between one another in comparison to climate
Certain families (e.g. Mephitidae) had almost no variation in diet composition within sister species
Other families (e.g. Canidae) showed large variation between sister species
Climatic divergence varied across families, with most pairs showing moderate to high climatic differences
Several families exhibited broad variation, indicating that closely related species differ in climate niche overlap to varying degrees.
Some families showed consistently high climatic divergence, while others contained pairs occupying more similar climatic conditions
Figure 4. Climate divergence (Schoener’s D) across species pairs grouped by family. Points represent individual species pairs; boxes show median and interquartile range.
Figure 5. Relationship between climate and dietary niche divergence across mammalian sister-species pairs. Each point represents a single species pair, with climate divergence plotted on the x-axis and diet divergence on the y-axis. Point size corresponds to divergence time (millions of years), and color indicates taxonomic family.
Climate and diet divergence were weakly associated, indicating that climatic differentiation does not consistently correspond with trophic divergence across sister-species pairs.
Several species pairs exhibited high climate divergence but low diet divergence, suggesting conservation of feeding niches despite occupation of different environments.
In contrast, some pairs showed moderate to high diet divergence within similar climates, implying that resource partitioning can occur independently of broad-scale climate differences.
Figure 6. Relationship between climate divergence and log-transformed divergence time across mammalian sister-species pairs.
Climate divergence showed little relationship with divergence time, with both recent and older species pairs spanning similar levels of climatic differentiation.
Figure 7. Relationship between diet divergence and log-transformed divergence time across mammalian sister-species pairs.
Diet divergence also showed no strong temporal trend, indicating that trophic divergence may arise rapidly after speciation or remain conserved over long evolutionary timescales.
Log-transformed divergence time showed little relationship with climate divergence, with species pairs of varying ages exhibiting both low and high climatic differentiation (Figure 5).
The fitted trend for climate divergence was slightly positive but weak, suggesting that older sister-species pairs may accumulate modest climatic differences over time, though the overall effect was limited (Figure 6).
Diet divergence showed a weak negative relationship with log-transformed divergence time, indicating that older species pairs were not consistently more different in diet than recently diverged pairs (Figure 7).
Several recently diverged pairs already displayed moderate to high dietary divergence, suggesting that trophic niche shifts can occur early in the speciation process (Figure 3).
Conversely, some older species pairs retained low dietary divergence, consistent with long-term conservation of feeding ecology (Figure 3).
Wide scatter around both regression lines indicates that time since divergence alone is a poor predictor of niche differentiation in either climate or diet (Figure 6, 7).
These patterns suggest that ecological divergence may proceed episodically or under lineage-specific selective pressures, rather than increasing steadily with evolutionary age.
My hypothesis that sister species occupying similar climates will exhibit more similar diets was not supported, as the results suggest that multiple ecological pathways contribute to mammalian niche divergence, and that climate alone is not a strong predictor of dietary differentiation across sister species pairs.
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Critical Thinking: Analyzed and standardized variable ecological data (especially diet) to quantify divergence across species pairs.
Communication: Translated complex concepts like niche divergence and speciation into clear, organized visuals and explanations for diverse audiences.
Technology: Used R and ecological databases (e.g., EltonTraits, GloBI) to quantify and visualize niche divergence across species pairs.