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What Works in Conservation 2018

23 05 2018

Do you have a copy of this book? If not, why not?

This book is free to download. This book contains the evidence for the effectiveness of over 1200 things you might do for conservation. If you don’t have a copy, go and download yourself a free one here, right now, before you even finish reading this article. Seriously. Go. You’ll laugh, you’ll cry, it’ll change your life.

Why you’ll laugh

OK, I may have exaggerated the laughing part. ‘What Works in Conservation 2018’ is a serious and weighty tome, 660 pages of the evidence for 1277 conservation interventions (anything you might do to conserve a species or habitat), assessed by experts and graded into colour-coded categories of effectiveness. This is pretty nerdy stuff, and probably not something you’ll lay down with on the beach or dip into as you enjoy a large glass of scotch (although I don’t know your life, maybe it is).

But that’s not really what it’s meant for. This is intended as a reference book for conservation managers and policymakers, a way to scan through your possible solutions and get a feel for those that are most likely to be effective. Once you have a few ideas in mind, you can follow the links to see the full evidence base for each study at conservationevidence.com, where over 5000 studies have been summarised into digestible paragraphs.

The book takes the form of discrete chapters on taxa, habitats or topics (such as ‘control of freshwater invasives’). Each chapter is split into IUCN threat categories such as ‘Agriculture’ or ‘Energy production and mining’. For each threat there are a series of interventions that could be used to tackle it, and for each of these interventions the evidence has been collated. Experts have then graded the body of the evidence over three rounds of Delphi scoring, looking at the effectiveness, certainty in the evidence (i.e., the quality and quantity of evidence available), and any harms to the target taxa. These scores combine to place each intervention in a category from ‘Beneficial’ to ‘Likely to be ineffective or harmful’. Read the rest of this entry »

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Categories : amphibian, biodiversity, birds, captive breeding, climate change, conservation, conservation biology, conservation ecology, ecology, ecosystem, ecosystem function, ecosystem services, environmental policy, extinction, fish, fragmentation, function, governance, impact, invasive species, management, protected area, research, science, threatened species

Translocations: the genetic rescue paradox

14 01 2013

Harvesting and habitat alteration reduce many populations to just a few individuals, and then often extinction. A widely recommended conservation action is to supplement those populations with new individuals translocated from other regions. However, crossing local and foreign genes can worsen the prospects of recovery.

We are all hybrids or combinations of other people, experiences and things. Let’s think of teams (e.g., engineers, athletes, mushroom collectors). In team work, isolation from other team members might limit the appearance of innovative ideas, but the arrival of new (conflictive) individuals might in fact destroy group dynamics altogether. Chromosomes work much like this – too little or too much genetic variability among parents can break down the fitness of their descendants. These pernicious effects are known as ‘inbreeding depression‘ when they result from reproduction among related individuals, and ‘outbreeding depression‘ when parents are too genetically distant.

Location of the two USA sites providing spawners of largemouth bass for the experiments by Goldberg et al. (3): the Kaskaskia River (Mississipi Basin, Illinois) and the Big Cedar Lake (Great Lakes Basin, Wisconsin). Next to the map is shown an array of three of the 72-litre aquaria in an indoor environment under constant ambient temperature (25 ◦C), humidity (60%), and photoperiod (alternate 12 hours of light and darkness). Photo courtesy of T. Goldberg.

Recent studies have revised outbreeding depression in a variety of plants, invertebrates and vertebrates (1, 2). An example is Tony Goldberg’s experiments on largemouth bass (Micropterus salmoides), a freshwater fish native to North America. Since the 1990s, the USA populations have been hit by disease from a Ranavirus. Goldberg et al. (3) sampled healthy individuals from two freshwater bodies: the Mississipi River and the Great Lakes, and created two genetic lineages by having both populations isolated and reproducing in experimental ponds. Then, they inoculated the Ranavirus in a group of parents from each freshwater basin (generation P), and in the first (G1) and second (G2) generations of hybrids crossed from both basins. After 3 weeks in experimental aquaria, the proportion of survivors declined to nearly 30% in G2, and exceeded 80% in G1 and P. Clearly, crossing of different genetic lineages increased the susceptibility of this species to a pathogen, and the impact was most deleterious in G2. This investigation indicates that translocation of foreign individuals into a self-reproducing population can not only import diseases, but also weaken its descendants’ resistance to future epidemics.

A mechanism causing outbreeding depression occurs when hybridisation alters a gene that is only functional in combination with other genes. Immune systems are often regulated by these complexes of co-adapted genes (‘supergenes’) and their disruption is a potential candidate for the outbreeding depression reported by Goldberg et al. (3). Along with accentuating susceptibility to disease, outbreeding depression in animals and plants can cause a variety of deleterious effects such as dwarfism, low fertility, or shortened life span. Dick Frankham (one of our collaborators) has quantified that the probability of outbreeding depression increases when mixing takes place between (i) different species, (ii) conspecifics adapted to different habitats, (iii) conspecifics with fixed chromosomal differences, and (iv) populations free of genetic flow with other populations for more than 500 years (2).

A striking example supporting (some of) those criteria is the pink salmon (Oncorhynchus gorbuscha) from Auke Creek near Juneau (Alaska). The adults migrate from the Pacific to their native river where they spawn two years after birth, with the particularity that there are two strict broodlines that spawn in either even or odd year – that is, the same species in the same river, but with a lack of genetic flow between populations. In vitro mixture of the two broodlines and later release of hybrids in the wild have shown that the second generation of hybrids had nearly 50% higher mortality rates (i.e., failure to return to spawn following release) when born from crossings of parents from different broodlines than when broodlines were not mixed (4).

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