Trevyn A. Toone (He/they) 1,2,3 , Sam J. Ahler (They/he) 4,5 , Julie E. Larson (She/her) 4,5,6 , Justin C. Luong (He/him) 7,8 , Francisco Martínez-Baena 9,10 , Carlos A. Ord oñez-Parra (He/him) 11 , Mateus C. Silva (He/him) 12 , Isabelle B. C. van der Ouderaa (She/her) 13 Scientists who identify as lesbian, gay, bisexual, transgender, queer, or members of other marginalized sexual orientations and gender identities (LGBTQ+) face serious disparities compared to their non-LGBTQ+ peers. Restoration science presents additional risks for LGBTQ+ researchers, including extensive time in the field-sometimes in locations that are hostile to LGBTQ+ people or create discomfort around gender expression and sexual orientation. At the same time, restoration science is uniquely positioned to create change: the same principles that shape ecosystem restoration also provide a blueprint for cultivating inclusion in science. We present 10 recommendations for LGBTQ+ inclusion based on four guiding restoration principles: (1) Context is key; (2) Healthy environments require support; (3) Success needs to be defined; and (4) A diverse future is worth striving for. We provide concrete actions that individuals and institutions can take and emphasize the positive outcomes that LGBTQ+ inclusion can generate for a healthier restoration community.
BackgroundThe trade in manta ray gill plates has considerably increased over the last two decades. The resulting increases in ray mortality, in addition to mortality caused by by-catch, has caused many ray populations to decrease in size. The aim of this study was to ascertain how yearling and juvenile growth and survival, and adult survival and reproduction affect reef manta ray (Manta alfredi) population change, to increase our understanding of manta ray demography and thereby improve conservation research and measures for these fish.MethodsWe developed a population projection model for reef manta rays, and used published life history data on yearling and juvenile growth and adult reproduction to parameterise the model. Because little is known about reef manta ray yearling and juvenile survival, we conducted our analyses using a range of plausible survival rate values for yearlings, juveniles and adults.ResultsThe model accurately captured observed variation in population growth rate, lifetime reproductive success and cohort generation time in different reef manta ray populations. Our demographic analyses revealed a range of population consequences in response to variation in demographic rates. For example, an increase in yearling or adult survival rates always elicited greater responses in population growth rate, lifetime reproductive success and cohort generation time than the same increase in juvenile survival rate. The population growth rate increased linearly, but lifetime reproductive success and cohort generation time increased at an accelerating rate with increasing yearling or adult survival rates. Hence, even a small increase in survival rate could increase lifetime reproductive success by one pup, and cohort generation time by several years. Elasticity analyses revealed that, depending on survival rate values of all life stages, the population growth rate is either most sensitive to changes in the rate with which juveniles survive but stay juveniles (i.e., do not mature into adults) or to changes in adult survival rate. However, when assessing these results against estimates on population growth and adult survival rates for populations off the coasts of Mozambique and Japan, we found that the population growth rate is predicted to be always most sensitive to changes in the adult survival rate.DiscussionIt is important to gain an in-depth understanding of reef manta ray life histories, particularly of yearling and adult survival rates, as these can influence reef manta ray population dynamics in a variety of ways. For declining populations in particular, it is crucial to know which life stage should be targeted for their conservation. For one such declining population off the coast of Mozambique, adult annual survival rate has the greatest effect on population growth, and by increasing adult survival by protecting adult aggregation sites, this population’s decline could be halted or even reversed.
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