Stable Isotopes for Measurement of Nutrient Dynamics during Pregnancy and Lactation

Author(s):  
David L. Hachey
2018 ◽  
Vol 26 (1) ◽  
pp. 69-81 ◽  
Author(s):  
Salvador Sánchez-Carrillo ◽  
Miguel Álvarez-Cobelas

The addition of stable isotopes (SI) of 13C and 15N has been used to study several aquatic processes, thus avoiding environmental disturbance by the observer. This approach, employed for the last three decades, has contributed to expanding our knowledge of food-web ecology and nutrient dynamics in aquatic systems. Currently, SI addition is considered a powerful complementary tool for studying several ecological and biogeochemical processes at the whole-aquatic-ecosystem scale, which could not be addressed otherwise. However, their contributions have not been considered jointly nor have they been evaluated with a view to assessing the reliability and scope of their results from an ecosystem perspective. We intend to bridge this gap by providing a comprehensive review (78 scientific publications reporting in situ 13C/15N additions at the whole-aquatic-ecosystem scale) addressing the main results arising from their use as tracers. Specifically, we focus on: (i) reasons for SI additions at the whole-ecosystem scale to study ecological processes, (ii) the paradigms resulting from its use and the insights achieved, (iii) uncertainties and drawbacks arising from these SI addition experiments, and (iv) the potential of this approach for tackling new paradigms. SI tracer addition at the ecosystem scale has provided new functional insights into numerous ecological processes in aquatic sciences (importance of subsidies in lakes; heterotrophy dominance in benthic food webs in lakes, wetlands and estuaries; the decrease in N removal efficiency in most aquatic ecosystems due to anthropogenic alteration; the recognition of hyporheic zones and floodplains as hot spots for stream denitrification; and high rates of internal N recycling in tidal freshwater marshes). However, certain constraints such as the high cost of isotopes, the maintenance of the new isotopic steady state, and avoidance of biomass changes in any compartment or pool during tracer addition bear witness to the difficulties of applying this approach to all fields of aquatic ecology and ecosystems. The future development of this approach, rather than expanding to larger and complex aquatic ecosystems, should include other stable isotopes such as phosphorus (P18O4).


2019 ◽  
Vol 214 ◽  
pp. 103662 ◽  
Author(s):  
Pierre Taillardat ◽  
Alan D. Ziegler ◽  
Daniel A. Friess ◽  
David Widory ◽  
Frank David ◽  
...  

2019 ◽  
Author(s):  
Marko J. Spasojevic ◽  
Sören Weber1

Stable carbon (C) and nitrogen (N) isotopes in plants are important indicators of plant water use efficiency and N acquisition strategies. While often regarded as being under environmental control, there is growing evidence that evolutionary history may also shape variation in stable isotope ratios (δ13C and δ15N) among plant species. Here we examined patterns of foliar δ13C and δ15N in alpine tundra for 59 species in 20 plant families. To assess the importance of environmental controls and evolutionary history, we examined if average δ13C and δ15N predictably differed among habitat types, if individual species exhibited intraspecific trait variation (ITV) in δ13C and δ15N, and if there were a significant phylogenetic signal in δ13C and δ15N. We found that variation among habitat types in both δ13C and δ15N mirrored well-known patterns of water and nitrogen limitation. Conversely, we also found that 40% of species exhibited no ITV in δ13C and 35% of species exhibited no ITV in δ15N, suggesting that some species are under stronger evolutionary control. However, we only found a modest signal of phylogenetic conservatism in δ13C and no phylogenetic signal in δ15N suggesting that shared ancestry is a weaker driver of tundra wide variation in stable isotopes. Together, our results suggest that both evolutionary history and local environmental conditions play a role in determining variation in δ13C and δ15N and that considering both factors can help with interpreting isotope patterns in nature and with predicting which species may be able to respond to rapidly changing environmental conditions.


Author(s):  
J. BERRY, ◽  
C. COOK, ◽  
T.F. DOMINGUES, ◽  
J. EHLERINGER, ◽  
L. FLANAGAN, ◽  
...  

2020 ◽  
Vol 637 ◽  
pp. 225-235 ◽  
Author(s):  
MA Ladds ◽  
MH Pinkerton ◽  
E Jones ◽  
LM Durante ◽  
MR Dunn

Marine food webs are structured, in part, by predator gape size. Species found in deep-sea environments may have evolved such that they can consume prey of a wide range of sizes, to maximise resource intake in a low-productivity ecosystem. Estimates of gape size are central to some types of ecosystem model that determine which prey are available to predators, but cannot always be measured directly. Deep-sea species are hypothesized to have larger gape sizes than shallower-water species relative to their body size and, because of pronounced adaptive foraging behaviour, show only a weak relationship between gape size and trophic level. Here we present new data describing selective morphological measurements and gape sizes of 134 osteichthyan and chondrichthyan species from the deep sea (200-1300 m) off New Zealand. We describe how gape size (height, width and area) varied with factors including fish size, taxonomy (class and order within a class) and trophic level estimated from stable isotopes. For deep-sea species, there was a strong relationship between gape size and fish size, better predicted by body mass than total length, which varied by taxonomic group. Results show that predictions of gape size can be made from commonly measured morphological variables. No relationship between gape size and trophic level was found, likely a reflection of using trophic level estimates from stable isotopes as opposed to the commonly used estimates from FishBase. These results support the hypothesis that deep-sea fish are generalists within their environment, including suspected scavenging, even at the highest trophic levels.


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